Saturday, September 12, 2015

COSMETICS AND BATHROOM PRODUCTS:EYE SHADOW

EYE SHADOW

Ancient Egyptian women developed the art of decorating the eyes by applying dark green color to the lower lid and blackening the upper lid with kohl, a preparation composed of antimony and soot. Egyptians also used powdered charcoal, powdered galena, or soot alone to achieve the same eyelid-darkening effect. Semiprecious stones such as lapis lazuli and malachite were also ground and used as eye shadows. In addition, the Romans adopted the technique of using kohl to darken the eyelids. In the Middle Ages, the Crusaders found eyelid-coloring cosmetics widely used in the Middle East, and it was they who spread the use of these types of cosmetics throughout Europe. Elizabethan women used an iri- descent eye shadow made of ground mother of pearl. By the nineteenth century, research in France led to the development of more and better eye cosmetics at decreased cost.

Eye shadow is a cosmetic product applied to the eyelids for coloring. Modern eye shadow is mostly composed of a petroleum jelly base with fats (e.g., mineral oil or jojoba oil) and waxes (e.g., beeswax, lanolin, or ozokerite). It is colored with dyes that include ultramarine colors (organic polymers containing aluminum, oxygen, silicon, sodium, and sulfur) such as blue, pink, or violet, iron oxides of various shades, carbon black (a form of carbon resembling charcoal), carmine, bismuth oxychloride, manganese violet, chromium hydroxide greens, bronze powder, alumi- num powder, ferric ferrocyanide, ferric ammonium ferrocyanide, zinc oxide (ZnO), or titanium dioxide (TiO2). As titanium dioxide is a white opaque powder, it may serve as a base, allowing other included colored dyes to be viewed by muting the natural color of the skin. Eye shadow may also contain additional chemicals to enable a longer shelf-life and manufacturing consistency for the product, including talc, aloe, binders (e.g., octyl palmitate), and preservatives (e.g., parabens, imidazolidinyl urea, or BHA). A typical composition may be approximately 60 percent petroleum jelly, 10 percent fats and waxes, 6 percent lanolin (grease in sheep’s wool), and the remainder dyes, pigments, and preservatives. Un- fortunately, the addition of synthetic chemical preservatives is often the source of consumer allergic reactions, including contact dermatitis.

COMMON MATERIALS AND OF fiCE SUPPLY PRODUCTS:TI NTED WINDOWS.

TI NTED WINDOWS

As energy consumption continues to grow in the United States, companies are looking to make homes more energy efficient. It is estimated that 2 percent of all energy consumed can be attributed to the inefficiency of household windows. Improving window technology could save billions of dollars spent on heating, lighting, and cooling costs for consumers nationwide. The concept of adjustable darkness windows in households began with the development of photochromic materials. Photochromic materials darken upon exposure to light and block ultraviolet radiation from the sun, reducing the strain on your air conditioner in the summer. These materials have been used for some time in consumer eyewear but have not made the transition to window coatings. The main reason is that such windows respond to light only and are not manually controlled. During the winter, photochromic windows would also exclude desirable warming ultraviolet radiation. An adjustable window film that could be darkened or lightened depending on conditions would be ideal to reduce energy consumption regardless of the season. Liquid crystalline displays (LCDs), which are found in watches, computers, and a variety of other electronic devices, work by aligning their crystals to allow light to pass through. In the absence of an electrical current, the liquid crystals are randomly aligned and appear as dark spots that form the numbers and letters that we see on an LCD display. LCD-based windows are already found in homes and offices around the world. With a flick of the switch, they turn from transparent to dark. These materials are used primarily in user-controllable privacy windows. The drawback to LCD-based devices is the lack of control over the darkness of the window. This problem is addressed in a new technology called a suspended particle device, which allows a window to change from dark to clear by applying an external electrical current. These devices are a sandwich of two glass panes coated with conductive material that hold a liquid suspension of particles. The particles align themselves when an external current is applied to the conductive glass coating, allowing light to pass through the glass. When the current is removed, the suspended particles move back to a random orientation to block light and darken the glass. Varying the applied voltage produces different shades of darkness for the glass.

COMMON MATERIALS AND OF fiCE SUPPLY PRODUCTS:RUBBER CEMENT AND SPRAY PAINT.

RUBBER CEMENT

Rubber cement is commonly used as an adhesive that serves to bond two objects together with a degree of flexibility. In the early 1800s, a viscous mixture of natural rubber dispersed in benzene or gasoline was used to cement seams of garments to ensure that they would be watertight. This mixture was later used to completely waterproof wool and cotton garments. The ability of rubber cement to form a durable and flexible bond is the main reason it is chosen as an office adhesive product. Little has changed in the formulation of rubber cement from the 1800s. Because of the flammability and toxicity of benzene and gasoline, these solvents are no longer found in modern rubber cement formulations. Today, rubber cement is a mixture of natural or synthetic rubber dispersed in isopropyl alcohol and heptane. These solvents, although safer, should not be considered innocuous. Isopropanol may cause reproductive disorders, and heptane is extremely flammable. For these reasons, rubber cement should be used in a ventilated area and away from open flames. Inhalation may cause irritation to the nose, throat, and lungs. Ingestion is equally hazardous, causing burns to the esophagus and gastrointestinal tract.

SPRAY PAINT

The idea of delivering a controlled spray of liquid was developed in the early 1930s by Eric Rotheim. This delivery system is used for a number of applications in industry and in homes. The design of the spray can is very simple. The metal can contains a propellant, paint, and a nozzle for delivering the spray. You may have noticed that the bottom of a spray can has a concave shape. This is done to strengthen the can and allow pressure within the can to be distributed to the walls of the can. The propellant is a fluid or gas stored under pressure and expels the paint out of the can. The propellant is generally a substance that is a gas at room temper- ature and pressure. Under pressure, the propellant is liquefied and will remain liquid even though it is well above its boiling point. The other liquid, in this case liquid paint, is also stored in the sealed metal can. In the metal can container, a long plastic tube runs from the valve at the top of the can all the way to the bottom of the can. The curved shape of the bottom of the can ensures that no paint is wasted in the bottom of the can. The nozzle has a very fine opening that serves to break the liquid paint into small droplets, ensuring controlled coverage of the paint. When the valve on the nozzle is opened, the pressure within the can is reduced, allowing the liquefied propellant to form a gaseous layer at the top of the can. The pressure exerted by this gas layer forces the paint at the bottom of the can to travel up the plastic tube connected to the nozzle, where it is released as a fine spray. You may have noticed that spray cans instruct you to shake the can for several minutes before painting. A small plastic or metal ball inside the can mixes up the propellant and paint to ensure a uniform consistency of paint as it is expelled from the nozzle. Until the 1980s, most manufacturers used chlorofluorocarbons (CFCs) as propellants in spray cans. It has been concluded that the use of CFCs is harmful to the ozone layer, and CFC-based propellants were phased out. Today, the most popular alternative propellant is liquefied petroleum gas, which does not harm the ozone layer but must be used with care because of its extreme flammability.

COMMON MATERIALS AND OF fiCE SUPPLY PRODUCTS:RECYCLED PAPER AND RECYCLED PLASTIC.

RECYCLED PAPER

Recycled paper is paper that contains fiber from waste paper. The United States has more than 500 paper mills that currently use at least some recycled materials in production. Recycled paper is made by collecting large amounts of used paper and washing the paper to remove any ink that may be present. The paper is then literally beaten to a pulp by machines and bleached, most commonly with chlorine bleaches, to make the paper white. Once a uniform white pulp is obtained, the paper goes to a forming section, followed by a series of presses that remove the water from the pulp. The wet paper moves on to a drying stage, where the moisture content is reduced and the thickness is reduced by rolling through a number of steel rollers. It is estimated that for one ton of paper the recycling process saves over 7,000 gallons of water, 500 gallons of oil, and 600 pounds of air pollution! The practice of collecting paper for recycling is common today. The majority of recovered paper comes from businesses and industry, where the recovery rate approaches nearly 70 percent. Paper seems to be one of the most benign items with regard to human health. In the earlier years of paper recycling, a bleaching by-product called dioxin was found throughout the pulp and paper manufacturing process. Dioxin is one of the most toxic human-made chemicals known. Pulp and paper mills using chlorine-based methods of whitening create dioxin when the chlorine reacts with chemicals present in the wood and other fibers. It is interesting that chlorinated toilet paper contains the highest amounts of these harmful chemicals.

RECYCLED PLASTIC

Plastics are well known for their desirable properties of being lightweight, strong, and formed into a variety of shapes. In fact, modern plastics might just be too durable. Millions of tons of plastics are buried in land- fills and will never be broken down by nature. To address the environ- mental impact of this problem, a vigorous recycling program has been enacted to reuse plastics and minimize their effect on the environment. Plastics recycling has been a great success for polyethylene terephthalate, which is used in soda bottles, and high-density polyethylene, which is used in numerous applications from plumbing to computers. One of the biggest problems of plastics recycling is the great diversity of plastics that are collected. Certain polymers do not mix, bond, or adhere well to one another. A recycled product derived from mixed plastics can have inferior strength and durability. In cases in which plastics cannot be separated into recyclable material, they may be used as fuels in incinerators because of their large heat value. To ensure success in the recycling processes, the source materials must be relatively clean, homogeneous, and free of con- tamination. In the recycling process, homologous plastics are reduced in size to very small pieces that are heated, cleansed of impurities, and formed into small pellets. These small pellets are sold to manufacturers and can be reincorporated into a variety of products. Polystyrene coffee cups are recycled and commonly used as inexpensive stuffing for toys or beanbag chairs. Polyethylene soda bottle material may be used to make trash cans, flower pots, traffic cones, and plastic lumber. Mixed plastics that are not incinerated are used to produce extruded plastic lumber, shipping pallets, fencing, and park benches.

COMMON MATERIALS AND OF fiCE SUPPLY PRODUCTS:POLARIZED SUNGLASSES AND RECHAR GEABLE BA TTERIES.

POLARIZED SUNGLASSES

How light waves interact with matter has been studied at great length throughout centuries. Sunlight and other light sources transmit light as waves at perpendicular angles to the direction of travel. In 1669, a Danish mathematician, Erasmus Bartholinus, performed the first comprehensive experiments concerning the interaction of light with transparent calcite crystals, which is considered the first account of polarized light waves. In 1932, Edwin Land developed a synthetic film of quinine sul- fate and iodine embedded in nitrocellulose and trademarked the name Polaroid. This material had a very interesting property. It allowed only light waves that were cohesive, or traveling in the same direction, to pass through the lens. In practice, this reduced the ambient light reaching the eye by more than 50 percent, making the material ideal for sunglasses. It also significantly reduced sun glare from objects by allowing only a frac- tion of the glaring light to pass through the lenses. Today, polarized sun- glasses are made by stretching an amorphous polymer of polyvinyl alcohol that aligns the molecules and sandwiching this layer between sheets of transparent material such as glass. These sunglasses are used in a variety of activities, such as driving, skiing, boating, and playing sports. Polarized sunglasses help reduce glare and filter out a significant amount of light without distorting images.

RECHAR GEABLE BA TTERIES

Many consumers are familiar with rechargeable batteries that are common in many everyday devices, such as cellular phones, laptop computers, and digital cameras. These batteries are constructed very much like a normal dry cell or alkaline battery. Typically, they contain nickel, cobalt, zinc, or cadmium and an electrolyte of potassium, sodium, or lithium hydroxide. The most common rechargeable batteries are based on a nickel/cadmium design with a cadmium anode and a nickel oxide cath- ode. These batteries operate very much like other batteries with one major difference. When the chemical reaction has been completed and no electron gradient exists between the anode and the cathode, these batteries can be recharged by an external current that reverses the flow of electrons from the cathode to the anode. This reestablishes the electron gradient between the two ends of the battery and allows the battery to be reused after charging is complete. This process can be repeated as many as 1,000 times before the batteries lose their ability to be recharged. Rechargeable batteries are not as new as you might think. The most common rechargeable battery is the lead-acid battery, which has been found in automobiles for the better part of a century. Rechargeable bat- teries undergo a reversible reaction, providing electrons to power devices and being recharged by reversing the chemical reaction to pump electrons back into the battery. Rechargeable batteries may leak when recharged, and the contents are harmful if swallowed and cause burns from the caustic electrolyte materials. As such, it is important to be sure that bat- teries are never connected improperly, short circuited, or exposed to high temperatures.

COMMON MATERIALS AND OF fiCE SUPPLY PRODUCTS:PENCILS AND PENS

PENCILS

The origins of the modern pencil date back to the mid 1500s, when graphite was discovered in the Seathwaite Valley in England. Soon there- after, graphite was used as a writing instrument. The real breakthrough came when French chemist Nicholas Conte discovered a process of firing a mixture of clay and graphite in varying proportions to create writing instruments of different hardnesses. These kiln-fired mixtures were encased in wood, and the pencil was born. In the United States, William Monroe manufactured wooden pencils in the early 1800s. Mass production of pencils in the United States began during the Civil War, when machinery for the production of pencils began to make handmade pencils obsolete. The mass production of pencils led to other related advances, such as the rubber eraser, first patented by Hyman Lipman in Philadelphia, and the mechanical pencil sharpener. Pencils do not contain lead, as is commonly thought. Instead, graphite, a form of carbon, is used along with various binders to modify the hardness of the pencil.

PENS

The history of the ink pen dates back many centuries, to the days of writing with a quill and ink with a charcoal base. Modern pens are much different than the reed, quill, or fountain pen of centuries ago. These older designs had several significant drawbacks, such as the uneven flow of ink, the slow drying of the ink documents, and the laborious cleanup associated with keeping the pens in good writing condition. The first improvement was the switch to faster-drying ink. Quick-drying ink was already used to print newspapers, but it was not until a Hungarian journalist, Laszlo Biro, developed a pen that used fast-drying ink that pens became practical for consumers. Biro developed a pen that used a tiny metal ball rotating inside a metal tube to keep the ink in the pen from drying out and let the ink flow out at a controlled rate. These “ballpoint pens” were patented by Biro in 1943, with the patent eventually being acquired by the British government so that the pens could be used by Royal Air Force crews. Milton Reynolds produced the first commercial ballpoint pen in the United States in 1945, selling thousands of pens until the more inexpensive BIC ballpoint pens were introduced on the American market in the mid 1950s. The development of new inks for use in these pens was a laborious trial-and-error process. Inks using linseed, rosin, or wood oil are darkened with dyes to produce different colors. Carbon gives plant oil ink a black appearance, chromium produces green and orange colors, cadmium colors the ink red, and iron in the form of ferrous sulfate gives the widely used blue ink color.

COMMON MATERIALS AND OFfiCE SUPPLY PRODUCTS:ALKALINE BA TTERIES AND CORR ECTIONFLUID.

ALKALINE BA TTERIES

Alkaline batteries are common in electronic devices used in everyday life; however, the way in which they produce electricity is little understood. They are typically constructed with a high-surface-area zinc anode (the positive end) and a manganese dioxide cathode (the negative end). Inside the battery case is a potassium hydroxide electrolyte that is gelled with a cellulose derivative. This electrolyte allows electrons to flow from the anode to the cathode. When the circuit is completed, this flow of electrons powers the electronic device. Although there are many different types of batteries, the construction is typically the same. What varies from battery to battery is the composition of the anode, cathode, and electrolyte. Alkaline batteries were derived from the older “dry cell”-type batteries and were put into commercial production in the early 1950s. A battery is nothing more than a contained chemical reaction that creates an electron potential gradient. The zinc anode is oxidized to form zinc hydroxide-releasing electrons. The manganese dioxide at the cathode is reduced by electrons from the zinc, which are carried to the cathode through the electrolyte solution. Although this is the most common type of alkaline battery in use, some alkaline batteries use mercury and silver in their construction. These metals, especially mercury, can be highly toxic and can be problematic to dispose of properly. Batteries may rupture when exposed to excess heat that accelerates the chemical reaction. This may release harmful flammable or corrosive materials that can result in serious chemical burns and skin irritation.

CORR ECTIONFLUID

The invention of White Out and other correction fluids was spawned by the need of Edwin Johanknecht for a correction fluid that worked on photostatic paper. In 1971, Johanknecht and his partners incorporated their new business, White-Out Products, Inc., providing correction fluid to users all over the world. Correction fluids usually contain a proprietary mixture of solvents and whiteners that act much like a thin fast- drying paint. Typically, methyl chloroform (1,1,1-trichloroethane) is used as a fast-drying solvent in which pigments such as titanium dioxide and other colorants are suspended. Correction fluid is brushed across the paper to cover mistakes and once dry can be written or typed over. Although the product is marketed for consumer use, there are a number of hazards associated with it. Inhalation of large amounts of solvent vapor may cause unconsciousness and may irritate the mucus membranes of susceptible individuals. It can also have a long-term effect on the central nervous system and cause abnormal heartbeats in humans. The dried correction fluid can be especially hazardous if burned, releasing small amounts of phosgene, hydrogen chloride, and chlorine. The formula will react with strong bases and oxidizing agents as well as reactive metals. For these reasons, it is important that correction fluid be used according to the manufacturer’s instructions.

AUTOMOTIVE AND GENERAL REPAIR PRODUCTS:WINDSHIELD WIPER FLUID AND WOOD GLUE

WINDSHIELD WIPER FLUID

Windshield wiper fluid is composed of methanol, water, and a detergent to help remove dirt accumulated on automotive windshields. Methanol was first produced from the destructive distillation of wood—hence the common name “wood alcohol.” Industrially, it is produced from natural gas (methane) but can also be produced from almost all organic materials, such as coal, wood, agricultural wastes, and garbage. High-temperature decomposition of these materials results in carbon dioxide, carbon monoxide, and hydrogen gases. These gases are catalytically converted to methanol, which is an important starting material for a number of industrial chemicals, such as formaldehyde plastics (Bakelite), antifreeze, rocket fuel, and polyester plastics.

The freezing point of methanol is –97.8 degrees centigrade; therefore, it remains liquid even at frigid winter temperatures. Mixing methanol with ice has the effect of depressing the freezing point of water; a mix- ture of water and methanol has a freezing point less than that of pure water alone. Thus, it helps to remove accumulated snow and ice on the windshield and prevents the windshield from becoming covered with ice. Methanol is highly toxic. Inhalation of methanol can lead to abdominal cramps, weakness, dizziness, and confusion. Ingestion of even small amounts of methanol can lead to blindness and death. Because of the inherent toxicity of methanol, several alternatives have been used for keeping windshields clear of ice and dirt. Ethanol-based washer fluids have been used successfully without the toxicity problems associated with methanol- based products.

WOOD GLUE

Wood glue, or polyvinyl acetate (PVA) glues, are the most common adhesives on the market. Glues come in a variety of formulas, all only slightly different, and specific to what they are designed to glue. In general, PVA glues are designed to work on porous materials and clean up easily because they are water based. They need pressure and air circulation to adhere to surfaces and maintain the strength of the bond. These glues are relatively safe consumer products because they do not emit any harmful fumes and are not hazardous to touch. PVA glues are only toxic if ingested.

AUTOMOTIVE AND GENERAL REPAIR PRODUCTS:SYNTHETIC MOTOROIL AND WD-40

SYNTHETIC MOTOROIL

Synthetic motor oils are made of a synthesized hydrocarbon base oil of hydrogenated polydecene, decanoic acid esters, zinc alkyl dithiophos- phate, and synthetic poly alpha olefins. Most synthetic oils also contain additives, detergents, and corrosion inhibitors as well as viscosity modifiers. It is believed that the first synthesized polymeric hydrocarbons were synthesized in 1877, yet it was not until 1929 that the commercial development of synthetic lubricants was undertaken. Because of the availability of commercial petroleum-based lubricants, these synthetic lubricants were ultimately unsuccessful. The advent of commercial jet travel spurred the development of the first commercially successful synthetic lubricant, Mobil 1, in 1975. This lubricant had superior resistance to thermal breakdown and lower friction properties than petroleum-based products.

Synthetic oils are used in engines to lubricate moving parts and protect them from wear and high temperatures. Detergents are added to synthetic formulations to reduce the deposits of contaminants on vital engine components, and corrosion inhibitors are added to reduce the effect of rust from the water produced in the combustion process.

Synthetic oils are somewhat safer than petroleum-based lubricants and do not cause any significant effects to the eyes, skin, or respiratory tract. Continuous exposure has been shown to cause cancer in laboratory animals. Brief or intermittent contact is not expected to pose any significant health problems in humans. Synthetic oils are related to petroleum-based lubricants with one significant difference. Whereas petroleum lubricants contain a variety of carbon chain lengths, synthetic lubricants contain specific compounds and polymers that help them adhere to the moving metal parts to combat friction. Other synthetic oils are used as hydraulic fluids, brake fluids, and antifreeze in automobiles.

WD-40

WD-40 is a proprietary formula composed of aliphatic petroleum distillates, petroleum base oil, carbon dioxide, and other nonhazardous ingredients. In 1953, the Rocket Chemical Company set out to create a line of rust prevention solvents and degreasers for use in the aerospace industry. On the fortieth attempt, they succeeded in formulating an effective water-displacing/lubricating formula, which they called WD-40. This product worked so well that it was used to protect the outer skin of the Atlas Missile from oxidation. It worked so well that employees of Rocket Chemical would sneak out cans of the formula for use in their own homes. The company produced a consumer version of the product in 1958, and since then people have used WD-40 on virtually everything.

WD-40 works by displacing moisture and forms a thin protective film on metal surfaces that protects the surface from oxidation and corrosion. It contains 60 to 70 percent aliphatic petroleum distillates, 15 to 25 per- cent petroleum base oil, and 2 to 3 percent carbon dioxide as a propellant. The volatile aliphatic hydrocarbons contained in the formula give WD-40 its characteristic odor and allow the formula to penetrate through rusted metal pieces. WD-40 has a much lower viscosity than standard light machine oils and is thought to contain tertiary alkyl amines, which have remarkably low surface tensions, providing low-temperature lubrication. Also important is the interfacial tension between WD-40 and water, because this is a measure of how fast the product will displace water out of the nooks and crannies of a rusty screw thread. This displacement is achieved with surfactants. Long-chain alcohols or quaternary ammonium salts may be some of the secret ingredients that help displace water and provide a temporary protective film to prevent corrosion.

WD-40 may cause headache or dizziness if inhaled and may cause dry- ing or irritation of the skin upon contact. Eye contact and ingestion are especially dangerous and may lead to vomiting, severe irritation, and chemical pneumonitis if entering the lungs. As such, this product should only be used in well-ventilated areas with proper protective equipment such as gloves and eye protection. The petroleum base of WD-40 is essentially a narrow-boiling kerosene fraction and has a flash point of less than fifty degrees centigrade. It should never be used in the vicinity of open flames and should be considered extremely flammable.

AUTOMOTIVE AND GENERAL REPAIR PRODUCTS:RADIA TORFLUID AND SUPER GLUE

RADIA TORFLUID

The active ingredient in radiator fluid is ethylene glycol, a two-carbon diol, which is used because of its low freezing point and high boiling point. A fluorescein dye is often added to readily identify antifreeze and make it less palatable to animals. Radiators are used with internal combustion engines to cool the engine block and pistons and maintain their specified operating temperatures. An engine’s water pump circulates the coolant through the engine block and back to the radiator, where the heat is dissipated by passage through air-cooled coils. Initially, water was circulated to cool automobile engines. In areas with cold winters, the water would freeze and destroy the delicate thin-walled coils in the radi- ator, causing leaks that lead to overheating. Ethylene glycol has a freez- ing point lower than the frigid temperatures that caused water-cooled engine problems. Ethylene glycol has the added advantage that the boil- ing point is higher than that of water, allowing the fluid to operate over a wider range of temperatures than alternative substances. The tempera- ture of the engine is controlled by the radiator fluid removing heat from the engine through the radiator, and the maximum coolant temperature is controlled with a high-temperature thermostat to control the flow rate of the liquid cooling the engine.

Ethylene glycol has a characteristically sweet smell that makes it irre- sistible to animals. The bright green or red fluorescein dye is added to warn humans and animals of the inherent danger associated with the in- gestion of antifreeze. If antifreeze is swallowed, it causes central nervous system depression followed by respiratory and cardiac distress. If untreated, ingestion leads to cardiac failure, renal failure, and brain damage.

SUPER GLUE

Superglue is ethyl-2-cyanoacrylate, which when applied to surfaces bonds and polymerizes, forming a strong bond between materials. It was discovered accidentally by an employee of Kodak Research Labs who was trying to develop an optically clear plastic for gun sights during World War II. He found that everything that the acrylate monomers touched would stick together so well that it was difficult to get the pieces apart once the acrylate cured.

Superglue is an acrylic resin that bonds to most materials instantly, and the polymerization is triggered by the hydroxide ions in water. It undergoes a process called anionic polymerization, in which the cyanoacry- late monomers link together when they come into contact with water. The chains form a durable plastic mesh that continues to cross-link until the polymer strands can no longer move. These polymers bind the surfaces being glued together by millions of polymeric strands, giving the bond exceptional strength. It is primarily used in repair work on consumer items but has recently been used successfully by forensic examiners to develop latent fingerprints and to close surgical wounds without stitches.

The polymerization process of cyanoacrylates is so fast that it can react with the water present on skin, causing it to bond skin instantly. As such, it should be handled with extreme care, because a small amount rubbed in the eye can instantly bond eyelids shut. It causes irritation of the nose, throat, and lungs from the noxious vapors of the acrylate monomer. There are different commercially available chemical variants that have slightly different setting properties and viscosities depending upon the application.

AUTOMOTIVE AND GENERAL REPAIR PRODUCTS:MOTOR OIL

MOTOR OIL

The distillation of crude oil or coal tar produces high-boiling components that are commonly used as lubricants such as motor oil. Solvent extraction and hydrogen refining are used to remove unwanted components and to increase the percentage of saturated hydrocarbons present. Modern lubricants must have good viscosity and temperature characteristics to meet the requirements of modern internal combustion engines. Corrosion and oxidation inhibitors are also added to increase the service life of the engines.

The discovery of petroleum oil’s lubricant properties dates back to the 1850s, when it was discovered that oil was able to withstand high and low temperatures without losing its lubricant properties. In the late 1860s, a method of steam heat distillation of crude oil was used to obtain high-viscosity petroleum oil that was capable of withstanding the high heats associated with maintaining the lubrication of combustion engines of the era. Vacuum Oils Co., the forerunner of Mobile Corp., successfully marketed these petroleum lubricants to machinery owners to reduce wear and repair costs on expensive machinery used in millwork. These oils had extraordinary performance characteristics, such as the ability to reduce friction and wear, the ability to function dependably at temperature extremes, and the ability to withstand rigorous and lengthy engine operation without chemical breakdown. These properties would be invaluable in the new internal combustion engines of the time.

A machine’s sliding or rolling surfaces must be separated to avoid friction and severe wear. This was accomplished by using lubricants with viscosities. Lubrication exists as long as a continuous thick film of oil separates the solid surfaces at all the points of wear, cooling and preserving metal parts from oxidation. In the internal combustion engine, oil must reliably lubricate bearings within the crankcase, pistons, and piston rings at temperatures at which fuel is being burned within the cylinder. Since oils change viscosity with respect to temperature, the ideal oil will protect moving parts equally at all temperatures. The principle of hydrodynamic lubrication, or coating the metal surfaces with a film of oil that will ad- here to the surface, is essential to avoid piston wear in the engine. This thin coat of oil reduces friction and as a consequence the operating temperature of the engine, preserving the moving metal components in the engine.

Motor oils are hazardous to the environment and to humans having direct contact with them. Although motor oils can withstand greater temperatures than other petroleum products, such as gasoline, they are still highly flammable. Like most other petroleum distillates, motor oil is carcinogenic, mutagenic, and has adverse effects on the human reproductive system. Because of its higher boiling point, it is not a significant

inhalation hazard and tends not to be absorbed through the skin readily. Prolonged exposure can lead to contact dermatitis. Motor oil that has been used should be discarded with care to avoid environmental contamination. Motor oils are less dense than water and are immiscible with water. Environmental contamination from oil is problematic in that there is no natural mechanism to break down the oil, so it accumulates in sedimentary deposits and eventually finds its way into the food chain, causing toxic effects. A typical barrel of crude oil ends up as gasoline for cars, kerosene for aircraft, diesel fuel for heavy vehicles, and lubricant oil for engines. A myriad of everyday products use products or by-products of the refining process.

AUTOMOTIVE AND GENERAL REPAIR PRODUCTS:GASOLINE.

GASOLINE

Gasoline is a mixture of petroleum hydrocarbons (organic molecules com- posed of carbon and hydrogen) that in general contain chains of four to twelve carbons. It is primarily used as a motor vehicle fuel, although it is also used as a solvent in industry. The first cars were fueled by kerosene, but they knocked and were notoriously unreliable and needed constant repair. Scientists realized that the premature ignition or knocking was attributable to vapors present in the hot engine. Gasoline from the distillation of coal tar eventually replaced kerosene as an automotive fuel, and when combined with antiknock agents such as tetraethyllead became a standard fuel for the automotive industry in the late 1930s. Concerns about environmental pollution from automobiles burning leaded gasoline paved the way for the unleaded gasoline formulations of the 1970s, and lead was completely removed from gasoline in the early 1990s with the advent of the Clean Air Act.

When gasoline is burned in an internal combustion engine, carbon di- oxide, water, and heat are produced. A gallon of gasoline contains approximately 13 million kilojoules of energy and is primarily made up of hydrocarbons with seven to eleven carbons. The gasoline vapor is ignited by the spark plug of the engine to drive the pistons, which transfer the energy to drive the automobile. Pollutants such as unburned gasoline hy- drocarbons as well as nitrogen-containing compounds are removed in the catalytic converter. The familiar octane number that consumers see at the gasoline pump refers to gasoline’s tendency to produce knocking in the engine. Isooctane is arbitrarily given a rating of 100 and n-heptane is given a rating of 0. When different hydrocarbons are blended or mixed with gasoline, the combustion in the cylinders of the engine is measured and compared with the octane scale. The higher the rating, the more efficient the combustion in the engine. Higher-octane gasolines are blended to produce very efficient combustion, which is why consumers pay more at the pump for high-octane gasoline.

Gasoline is extremely flammable in the liquid and vapor phases. It can accumulate a static charge through flow or agitation, potentially causing an explosion if the static is not dissipated. In addition to the physical hazards, gasoline is a carcinogen and causes central nervous system depression. The vapors are harmful if inhaled into the lungs. Coal tar also produces other fractions that include kerosene, diesel fuel, home heating oil, Vase- line, paraffin wax, and tar. These compounds all differ in the average length of their carbon chains, and their production depends on the frac- tional distillation of coal tar or crude oil.

AUTOMOTIVE AND GENERAL REPAIR PRODUCTS:AIR BAGS AND FUEL ADDITIVES

AIR BAGS

Air bags have been mandatory in automobiles since 1998 and have decreased the risk of dying in an accident by nearly 30 percent. The tech- nology behind air bags was first proposed during World War II to pre- vent injuries during a crash landing in an aircraft. Typically, air bags are located on the steering wheel or on the dashboard. They are intended to slow a passenger’s speed to zero with little or no damage to the person. The air bag is made up of three major components. The bag is made of a thin nylon or equivalent fabric, which is folded compactly behind the dashboard or inside a small space in the center of the steering wheel. It typically contains a small amount of cornstarch or talcum powder to keep the nylon pliable during storage. The inflation system consists of a reac- tion between sodium azide and potassium nitrate to produce a large vol- ume of nitrogen gas to inflate the bag. The sensor, which indicates the collision, is located in the bumpers of the automobile. The sensor is a switch that closes an electrical circuit when a collision above ten to fifteen miles per hour is detected. The electrical circuit triggers the chemical reaction in the inflation system and the air bag inflates in under one- twenty-fifth of a second. The reaction of the inflation system is so fast that the air bag is inflating at over 200 miles per hour! For this reason, it is important that passengers be seated at an appropriate distance from the air bag to avoid potential injuries from the air bag itself. Air bags can seriously harm children from the rapid inflation, and it is recommended that children under the age of one year not ride in the front seat of a vehicle equipped with air bags.

FUEL ADDITIVES

Since the mid 1920s, gasoline for consumer engines has contained the additive tetraethyllead, which improves fuel performance by preventing “knocking” in the cylinders of the engine. This knocking or preignition reduces engine efficiency, damages pistons, and reduces the power out- put of the internal combustion engine. Tetraethyllead, the most com- mon fuel additive of the past century, is a toxic liquid that killed more than fifty chemical workers during its early development and manufac- turing. Nevertheless, motor companies, oil companies, and the govern- ment authorized the manufacture and used of tetraethyllead in gasoline throughout the world.

In the late 1960s, new antipollution initiatives were enacted to reduce nitrogen oxides, carbon monoxide, and lead pollutants from automotive exhaust. Nitrogen oxides were responsible for the brown haze that hung over cities that can still be seen today. The advent of the catalytic con- verter, a small canister that contained heavy metal catalysts embedded on a ceramic support, helped oxidize carbon monoxide and reverse the reac- tion that produced nitrogen oxides. However, lead in the exhaust stream deactivated the catalysts in the catalytic converter. The only solution was to remove tetraethyllead from the gasoline.

Since the 1970s, tetraethyllead has not been added to gasoline, and oil refiners were pressed to increase the octane value of gasoline. One op- tion involved externally oxygenating fuels by adding alcohols such as methanol, ethanol, and tertiary butyl alcohol as well as ether combina- tions such as methyl tertiary butyl ether (MTBE). The petroleum indus- try preferred MTBE to alcohol blends because it was somewhat easier to handle. Ethanol was seen as a viable solution but has long been resisted by the petroleum industry. Along with boosting octane, oxygenated fuels have lower hydrocarbon and carbon monoxide emissions and have been used to fight city smog since the late 1980s. The reformulated gasolines (RFGs) proposed by the petroleum industry reduce pollutants such as hydrocarbons, toxic aromatic compounds, and nitrogen oxides from the combustion of gasoline. RFGs reduced hydrocarbon emissions by at least 15 percent in major cities and reduced the cancer risk associated with gasolines with high benzene content.

Reformulated gasoline blends have several advantages over gasohol (gasoline-alcohol mixtures) and MTBE blends. RFG blends evaporate less readily because they have a lower vapor pressure, and they have lower benzene and sulfur contents. Gasoline blends, as well as other petroleum distillates, are an inhalation hazard to humans. Hydrocarbon distillates have been shown to cause cancer in laboratory animals. The products from the combustion of gasoline, specifically carbon monoxide and nitrogen oxides, have been linked to the dissipation of the protective ozone layer

surrounding the earth and are responsible for a significant number of health problems in cities plagued with smog.

COMMON HOUSEHOLD AND LAWN PRODUCTS:FIREEXTINGUISHER

FIREEXTINGUISHER

Fire is a chemical reaction between the oxygen in the atmosphere and a fuel source. Fuels do not catch fire simply because they are surrounded by oxygen; the fuel must be heated for the combustion to take place. When a fuel is heated to its ignition temperature, the heat starts to decompose the fuel and release volatile gases. These gases formed from the decomposition of complex molecules react with oxygen to form water, carbon dioxide, and other products. The gases rise up through the air and make up the flame that emits heat and light. The heat produced by combustion keeps the fuel at the ignition temperature, so the fire continues to burn as long as fuel and oxygen are still present. The three essential elements to the fire are heat, oxygen, and fuel. Fire extinguishers are designed to remove one or more of these essential elements so the fire will cease this self-sustaining combustion. One of the best ways to remove heat is by dumping large amounts of water onto the fire. This cools the fuel below the ignition temperature as the water is converted to steam, interrupting the combustion cycle. It is also possible to remove the oxy- gen surrounding the fire by covering the fuel with a nonflammable mate- rial such as baking soda. This smothering effect separates the fuel from the atmospheric oxygen, again interrupting the combustion process.

Modern fire extinguishers operate on these two principles: removing heat or oxygen from the fire. A fire extinguisher is a metal cylinder that is filled with water or a smothering material with a mechanism to deliver the material from a safe distance. The extinguisher usually expels the water or smothering agent by pressure. A siphon tube leads from the bottom of the metal cylinder to the top of the extinguisher. The area above the active agent is pressurized with carbon dioxide. When the handle of the extinguisher is depressed, the carbon dioxide pressure forces the active agent through the siphon tube and out the nozzle of the extinguisher. If the extinguisher is aimed toward the fire, the water or smothering agent is delivered to cool or smother the fire.

Water is by far the most commonly used fire suppression material and one of the most effective. However, it is important that water not be used on fires involving electricity or flammable liquids. Most flammable liquids are less dense than water and will continue to burn while floating on top of the water. In these situations, the water serves only to spread the fire and will never effectively remove the heat as intended. Since water will also conduct electricity, there is the potential of electrocution should a water extinguisher be used on an electrical fire. Water extinguishers are intended to extinguish fires in which wood, plastic, or paper are the pri- mary fuels and should not be used on electrical or flammable liquid fires.

Another popular extinguishing material is ordinary compressed carbon dioxide. Because carbon dioxide is heavier than air, it displaces the oxy- gen surrounding the fire, halting the combustion of the fuel. However, carbon dioxide extinguishers do little to cool the temperature of the fuel, and the carbon dioxide quickly dissipates. This can result in the fire reig- niting. Ordinary baking soda (sodium bicarbonate), potassium bicarbon- ate, and ammonium phosphate are common smothering agents used in “dry chemical” fire extinguishers. These bicarbonates decompose and re- lease carbon dioxide that displaces oxygen. Combined with the insula- tion from the dry material, it works by smothering the fire.

Most fire extinguishers contain small amounts of fire suppressant ma- terial and should only be used on relatively small fires. Some of these agents work by displacing oxygen from the atmosphere surrounding the fire. This can be hazardous to persons in the area, who may become as- phyxiated because of the lack of breathable oxygen. The active agents in dry chemical extinguishers can be extremely hazardous if inhaled.

COMMON HOUSEHOLD AND LAWN PRODUCTS:INSECTICIDES AND WATER SOFTENERS

INSECTICIDES

Insecticides are used by farmers and homeowners to reduce the effect of various insects on crops, flowers, lawns, and ornamental plants. There are virtually hundreds of insecticides, many of which were developed as a consequence of early research on nerve gas weapons and which work to eliminate insects in a variety of ways. The way in which a particular pesti- cide kills an insect is called the mode of action and is a convenient way to classify the numerous available pesticides. Most traditional insecticides work on the nervous system. These chemicals are typically absorbed through the insect’s skin and affect the nerve impulses of the insect, causing paralysis and brain death. Some pesticides act to slow the pro- duction of energy needed for the insect to survive and are typically used in fumigation; the insects die after a period of lethargy. Insects have an external skeleton called an exoskeleton, of which the protein chitin is a major component. Chemicals that inhibit the synthesis of this protein kill pests because they cannot shed their exoskeleton and grow a new one. These are very specific for certain pests and have been used with great success against fleas and termites. Unfortunately, pesticides affect humans just as much as the insects they are intended to kill. The body weight of humans is much higher than that of insects, so a much smaller dose is required to kill an insect than to kill a human. However, pesticides and chronic exposure can lead to very severe health problems. Many of these chemicals can be absorbed through the skin and are acutely toxic if inhaled. As such, appropriate precautions should be taken when using insecticides, such as wearing protective garments and always following the manufacturer’s instructions.

WA TER SOFTENERS

Most people are familiar with discoloration or stains that are a result of problem water in the home. Red and brown stains caused by iron, blue and green stains caused by copper, and white scales caused by magne- sium and calcium are found in most homes with problem water. The process of softening water removes the minerals calcium and magnesium that are typically found in potable water. The removal of these elements is essential not only to make the water taste better but to prevent prob- lems associated with the deposits of these minerals in the water pipes. If these minerals are allowed to build up in pipes, they reduce water flow and pipes can eventually become completely clogged. One solution is to distill the water or to use water filters to remove the minerals. This approach is impractical because of the high cost associated with filtering or distill- ing all of the water used in the household. A more cost-effective approach, water softening, removes magnesium and calcium by a replacement pro- cess. A water softener contains a bed of small plastic beads or a zeolite matrix, which is saturated with sodium chloride. As water flows through the softener, the calcium and magnesium are replaced by sodium ions. This process is called ion filtration. The undesirable calcium and magne- sium remain in the softener and sodium ions are introduced to the water supply. Sodium does not cause precipitation problems, and the effects of hard water are eliminated.

COMMON HOUSEHOLD AND LAWN PRODUCTS:FERTILIZER.

FERTILIZER

Plants require a number of different chemical elements to grow. The elements carbon, hydrogen, and oxygen are readily available from water and air and are required for plants to thrive. Other essential elements required by the plant are called macronutrients and include nitrogen, phosphorus, and potassium. These elements are basic building blocks for the amino acids that make up proteins and ultimately plant cells. These elements are the key to healthy plants. Molecules that make up the membranes of cells all contain phosphorus (phospholipids), nitrogen is important for the synthesis of amino acids, which all contain nitrogen, and potassium is essential to the metabolism of plant cells. If these macronutrients are absent, it severely limits the growth rate of the plant. The decay of dead plants in the soil is a source of these essential elements. Nature recycles the elements from dead plants to produce healthy growing plants. The purpose of fertilizers is to provide the elements that the plant needs to grow in easily available forms. Many fertilizers supply nitrogen, phosphorus, and potassium. The availability of these macronutrients seems to be the major limiting factor in plant growth. Carefully reading a bag of fertilizer, one will notice a series of three numbers on the bag. These numbers tell you the available percentage of nitrogen, phosphorus, and potassium found in the fertilizer. Although fertilizers mainly provide these macro- nutrients, a number of other elements, called micronutrients, are required in much lesser amounts to help plants grow. When looking at the periodic table, it is interesting to observe that only twenty-five of these elements are considered to be essential for plants and animals. Trace elements required for normal plant growth include boron, copper, iron, manganese, zinc, and molybdenum. Copper is important in the reproductive stage of the plants. Deficiencies in copper limit the yield and quality of the fruits and seeds, the products of reproduction humans typically con- sume. Manganese and molybdenum are essential for nitrogen metabo- lism and fixation. Iron is critical for photosynthesis and respiration. Zinc is essential for sugar regulation and enzymes that control plant growth. One danger of fertilizers is inherent to the available nitrogen source. Nitrogen in the form ammonium nitrate is the most widely used and can make up 10 to 40 percent by weight of a bag of fertilizer. Unfortunately, ammonium nitrate is a powerful explosive, and fertilizers can be misused with disastrous results, as in the Oklahoma City bombing.

COMMON HOUSEHOLD AND LAWN PRODUCTS:ALUMINUM CANS AND FOIL.

ALUMINUM CANS AND FOIL

In the 1800s, aluminum was believed to be so rare that it was considered more valuable than gold or silver and used only for jewelry. This is surprising, since aluminum is the third most abundant element found on earth. In the early 1900s, extraction procedures had improved greatly, making aluminum widely available at reasonable cost. Ideas for using aluminum in food storage began to evolve because of the favorable prop- erties of this metal. Aluminum is lightweight, nontoxic, and easy to shape, it does not rust, and it can be easily recycled. These properties made aluminum an ideal material for packaging. In the 1950s, Coors Brewery partnered with a company called Aluminum International to develop an aluminum can for beer. This product was first marketed in 1958 and is the first commercial use of an aluminum beverage can. By 1964, a competing company, Reynolds Metals Co., became the first commercial sup- plier of twelve-ounce aluminum beverage cans that are still considered the standard today. Another development based upon the desirable properties of aluminum was thin foil. This aluminum foil was superior to papers and plastic because it protected contents from moisture and oxygen. Today, aluminum cans and foils are found with coatings of plastic to further protect the integrity of the stored product.

LIGHTING:NEON LIGHTS

NEON LIGHTS

The technology behind how a neon light works is very different from that of normal incandescent lights. Electroluminescence, or the conversion of electricity directly into light, is the operating principle of neon lights. Neon lights are used in advertising signs and are made of long narrow glass tubes that are often bent in different shapes. These tubes can emit light in a variety of colors. The construction of a neon light is much like that of a fluorescent light tube. The glass tube is filled with a gas such as neon, argon, or krypton at low pressure. At both ends of the tube are metal electrodes. When a high voltage is applied to the electrodes, the gas ionizes, causing electrons to flow through the gas. These electrons excite the gas atoms and cause them to emit photons that we can see in the form of visible light. Neon gives off a characteristic red light, and other gases emit other colors of light. The main difference between a neon light and a fluorescent light is the lack of a phosphor coating. In a neon light, the visible light is produced directly from the excited gas and is visible to the human eye. Another example of electroluminescence is seen in Indiglo watches and alarm clocks. These oper- ate in a very similar manner to neon lights. A high voltage is applied to a thin panel that is coated with a layer of a conductor and a layer of phos- phor. When the voltage is applied, the phosphor emits visible light with- out emitting heat.

LIGHTING:LIGHT-EMITTING DIODES.

LIGHT-EMITTING DIODES

Light-emitting diodes, commonly called LEDs, function like tiny light bulbs and are found virtually everywhere. A diode is a simple semiconductor device that has a varying ability to conduct electrical current. In a LED, the conductor material is typically aluminum-gallium-arsenide (AlGaAs). In pure AlGaAs, all of the atoms bond perfectly, leaving no mobile electrons that could potentially conduct electricity. A “doped” semiconductor has additional atoms that either add mobile electrons or create holes where electrons can go. This doping process increases the conductivity of the material. Semiconductors doped with extra electrons are know as N-type materials, since they have extra negatively charged particles that tend to migrate toward positively charged areas. Semiconductors with holes are known as P-type materials, since they effectively have extra positively charged particles. Electrons jump from hole to hole, moving from a negatively charged area to a positively charged area. A diode is simply a section of N-type semiconductor bonded to a section of P-type material with electrodes on each end. When no voltage is present, the N-type material fills the holes from the P-type material at the junction between the two layers. In this arrangement, all of the holes are filled and the material behaves as an insulator. To get electrons moving, the N-type section is attached to the negative end of a circuit and the P- type section to the positive end of the circuit. The free electrons in the N-type section are repelled by the negative electrode and attracted to the positive electrode. The holes in the P-type material move in the opposite direction, migrating toward the negative end of the circuit. As such, this arrangement only conducts electricity in one direction. The interaction between electrons and holes has an interesting effect in that it produces light. As the electrons move across a diode, they can fall into empty holes in the P-type layer. As these electrons drop from their mobile state to a lower orbital, the electrons release energy in the form of photons. For example, the atoms in a standard silicon diode are arranged so that the electrons release a relatively small amount of energy, producing infrared light. These diodes are ideal for use in remote controls, among other products. The gap between the conduction band and the lower orbitals determines the frequency of the photons emitted; in other words, it con- trols the color of light produced. By adjusting the properties of the materials used for the P-type and N-type semiconductors, virtually any color of light can be produced from LEDs. The main advantage of LEDs is their efficiency compared with normal incandescent lights. These devices are tailored to produce a specific wavelength of visible light. As such, they produce very little heat because they do not produce infrared light unless they are intended to do so.

LIGHTING:INCANDESCENT LIGHTS

INCANDESCENT LIGHTS

Light is a form of energy that can be released by an atom. Photons, the most basic unit of light, are made up of many small particle-like packets that have energy but no mass. Atoms release these photons when excited electrons revert back to their ground state energy. The excitement of these electrons, specifically how much energy is released, determines the wavelength of the emitted light and hence the color of the light. Incan- descent light bulbs are very simple in construction and theory of operation. At the base of the light bulb, there are two metal contacts that connect to the ends of an electrical circuit. The metal contacts are attached to a thin metal filament, usually made of tungsten, and the globe of the bulb is filled with an inert gas to prevent the metal from burning in the presence of oxygen. When the bulb is connected to a power supply, an electric current flows from one contact to the other through the filament. As the electrons move through the filament, they continually bump into the atoms that make up the filament. This constant impact vibrates the atoms and heats the filament atoms to the point at which electrons may temporarily be boosted to a higher energy level. As these electrons return to their ground state, they release energy in the form of photons or light. The metal filament is heated to over 2,200 degrees centigrade, at which point the photons released are at a wave- length that humans can see, otherwise known as visible light. A great deal of energy is given off by incandescent lights that cannot be seen by humans. These wavelengths of infrared light are responsible for the heat that a light bulb emits. Approximately 10 percent of the light an incandescent bulb emits is visible; hence, incandescent bulbs are inefficient, wasting a majority of energy generating heat instead of light.

LIGHTING:HALOGEN LIGHTS.

HALOGEN LIGHTS

A halogen light is very similar in construction and operation to an incandescent light bulb. However, improvements in the design increase the amount of visible light produced and reduce the amount of infrared (nonvisible) light emitted. A halogen lamp uses a tungsten filament just like an incandescent bulb, but it is encased in a much smaller quartz envelope. This small envelope is so close to the filament that ordinary glass would melt. Inside this envelope, a gas from the halogen group, a group of reactive gases found in group 7 on the periodic table, is used to react with the heated tungsten metal. These gases, because of their high reactivity, combine with the tungsten metal vapor and redeposit them on the filament. This process of recycling the filament metal helps the filament last much longer than that in an ordinary incandescent light bulb. It is also possible to get the filament much hotter, producing more light. The proximity of the quartz envelope to the filament is why halogen lights become extremely hot compared with ordinary light bulbs.

LIGHTING:GLOW STICKS

GLOW STICKS

Light is a form of energy that can be emitted through a variety of processes. All of these processes rely on the same basic principle: energy excites an atom’s electrons, and when these electrons return to their ground state they emit particles of light called photons. A light stick uses a chemical reaction instead of electricity to excite the atoms in a material. The chemical reaction typically involves several different steps. A typical commercial light stick holds a solution of hydrogen peroxide, phenyl oxylate ester, and a fluorescent dye. To produce light, the hydrogen per- oxide oxidizes the phenyl oxylate ester to produce phenol and an unstable peroxyacid ester. This unstable ester decomposes, resulting in an additional phenol molecule and a cyclic peroxy compound. The peroxy compound then decomposes to form carbon dioxide. As a result of these decompositions, energy is released to the dye, where the electrons jump to a higher energy level. As they return to their ground state energy, they release energy in the form of photons that we see as visible light. The light stick is simply a housing for the two solutions involved in the reaction and prevents the chemical reaction from happening until the two solutions are allowed to mix with each other. The hydrogen peroxide is kept in a small glass vial inside the solution of dye and phenyl oxylate ester. When you bend the plastic stick, the glass vial is broken and the two solutions begin to react with each other. Many factors determine how long the reaction will last. As a result, light sticks may produce light from several minutes to as long as several hours.

LIGHTING:FLUOR ESCENT LIGHTS.

FLUOR ESCENT LIGHTS

To understand how fluorescent lights work, it is helpful to remember that light results from the energy emitted when excited electrons return to their ground state. A fluorescent light contains a central element in a long sealed glass tube. This tube is typically filled with an inert gas, such as argon, and a small bit of mercury vapor. In addition, a phosphor powder is coated along the inside of the glass tube. When current is applied to the ends of the tube, electrons migrate through the gas from one end of the tube to the other. As the electrons move through the tube, some of them collide with gaseous mercury atoms. This collision promotes electrons in the mercury atom to a higher energy level. As these elec- trons revert back to their original energy level, they emit energy in the form of photons. The wavelength of the light emitted is a function of the energy difference between the ground state and the excited state. In a fluorescent tube, the mercury atoms release photons in the ultraviolet wavelength of the spectrum. This ultraviolet light is converted to visible light by the phosphors that coat the interior surface of the tube. When the photons emitted from the mercury collide with the phosphor coating, they transfer their energy, bumping the electrons of the phosphor to a higher energy level. The phosphor then releases photons as emitted light in the visible wavelengths. The phosphor is responsible for giving off the characteristic white light that we are familiar with. Varying com- positions of phosphors can give different color fluorescent lights. As dis- cussed later, incandescent bulbs waste a great deal of energy producing infrared light that is not seen by the human eye. Since fluorescent lamps yield a greater amount of visible light under the same circumstances, they are typically about five times more efficient than incandescent light bulbs. In contrast to traditional light sources, such as incandescent and halogen bulbs, fluorescent lights require a much higher voltage to operate. This is because of the greater resistance the electrons encounter moving through a gas instead of through a filament. It takes some time to heat the electrons in the tube to a temperature at which they will start to emit radiation in the form of photons. This is why fluorescent tubes sometimes take a second to light up when the current is applied. Trans- formers, which convert normal voltage to a much higher voltage, are used to apply higher-energy electrons to the light tube and ensure that the atoms emit photons of the proper wavelength. Fluorescent light tubes do contain a small amount of mercury vapor that can be toxic to humans. Therefore, great care should be exercised when cleaning up broken fluorescent light tubes.

LIGHTING:CANDLES

CANDLES

Candles are an operationally simple device for providing heat and light by means of a controlled flame. A candle is made up of two parts, the fuel made of wax, and the wick made from absorbent string. The wax fuel source is typically paraffin wax that is a heavy hydrocarbon that comes from the refinement of crude oil. Paraffin wax is very flammable and, much like other oils from petroleum refinement, it must be very hot for burning to take place. Once the combustion of the wax has started, it can be very difficult to put out. A candle controls the burning process by allowing only a small amount of the wax to burn. The wick of the candle is made of an absorbent material that absorbs liquid wax and carries it to the end of the wick by capillary action. When a candle is lit, the heat of the flame melts the wax on and near the wick. The wick absorbs the liquid wax, and the heat of the flame vaporizes the wax. It is actually the vaporized paraffin wax being emitted from the wick that produces the flame observed. You may have noticed that you can relight a candle by touching a flame to the smoke leaving a candle just after it has been extinguished. This smoke is actually paraffin vapor that is still hot enough to exist in the gaseous form. Touching a lit match to this stream of vapor allows the flame to run down the vapor trail and relight the wick of the candle. It is also interesting to observe that the wick does not burn significantly. This is because the heat required to vaporize the wax actually cools the wick and protects it from burning. Paraffin wax consists of hydro- carbons with typically between eighteen and thirty-six carbons in their chain. This mixture of chain lengths is actually essential for the success of wax as a candle fuel. Shorter-chained hydrocarbons tend to have lower melting points and boiling points. The shorter-chain hydrocarbons tend to vaporize first and provide the heat necessary to vaporize the longer hydrocarbon chains. In this way, the mixture of chain lengths ensures an easy-lighting candle that burns for a long period of time.

CLEANING PRODUCTS:TOILET BOWL CLEANERS.

TOILET BOWL CLEANERS

Toilet bowl cleaners are formulated to prevent or remove stains caused by hard water minerals (e.g., calcium [Ca], magnesium [Mg], etc.) and rust deposits resulting from iron (Fe) oxidation. These products allow for and contribute to the maintenance of a toilet bowl with pleasant odors, and some products contain active ingredients that disinfect. Most toilet bowls are manufactured from ceramic material with an applied tight glaze covering to prevent the soaking of water into the porous china-like materials. This glaze coating is relatively resistant to the decay- ing effects of acidic chemicals, so many toilet cleaning products contain a fair amount of acidic active ingredients. The buildup that forms within toilet bowls is mainly derived from calcium carbonate deposited from hard water minerals, along with discoloration attributable to iron com- pounds and the growth of fungal organisms. Acids readily dissolve cal- cium carbonate. The classic active ingredient for solid crystalline toilet bowl cleansing products is anhydrous granular sodium bisulfate (NaHSO4). This chemical is mainly sulfuric acid for which one of the hydrogen ions has been neutralized by sodium hydroxide. The addition of sodium bisulfate to water within the bowl will yield a highly acidic pH of approximately 1, which provides an environment for the cleaning away of most hard water deposits, iron stains, and residual bowl-adhering fecal matter.

Many common liquid toilet bowl cleansers now contain 7 percent to 9 percent hydrochloric acid (HCl), citric acid (2-hydroxy-1,2,3-propanetricarboxylic acid; C6H8O7), or some other acidic material. Hydrochloric acid is an especially good product for removing calcium carbonate-based hard water deposits and iron deposits (Fe2O3) because of the very high solubility of the chloride salts of calcium and iron in solution.

CLEANING PRODUCTS:SCOURING POWDERS.

SCOURING POWDERS

Scouring, or abrasive, cleansers are formulated to remove dense accumulations of soils commonly located in small household hard surface areas.

Most scouring powdered cleansers mainly consist of an insoluble abrasive powder (approximately 80 percent concentration), such as screened silica (SiO2), feldspar, calcite, or limestone, with the size of the abrasive particles approximately 44 micrometers or smaller. The remainder of the product formulation often consists of calcium carbonate (CaCO3) or similar alkaline salts (e.g., sodium carbonate), with an additional 2 per- cent grease-dissolving surfactants (e.g., anionic surfactants) and, in some cases, fragrance/perfume, color/dye and approximately 1 percent anhydrous chlorine bleach (e.g., sodium dichloro-S-triazinetrione dihydrate), which also acts as a disinfectant. Scrubbing with a small amount of water causes the abrasive ingredients to physically remove stains and deposits from hard surfaces such as porcelain tubs, sinks, cookware (e.g., pots and pans), bathroom fixtures, ceramic tiles, and outdoor grills. Organic- based stain material is then absorbed into the porous powder and rinsed away with the wash water.

Baking soda (sodium bicarbonate; NaHCO3) is also a mild abrasive cleanser. This chemical absorbs food odors readily, making it appropriate for cleaning areas constantly in contact with foods, including certain types of countertops and the inside of the refrigerator.

CLEANING PRODUCTS:OVEN CLEANERS.

OVEN CLEANERS

Oven cleaners are formulated to remove burned-on and baked-on greasy soils and other food-based soils from the walls of ovens used for food preparation. Usually dispensed in aerosol form with thickeners and propellants, the primary active ingredient of oven cleaners is sodium hydroxide. These cleaners are formulated into a thick consistency to ensure that the product will cling to vertical surfaces within an oven. A strong alkali will react with fat (e.g., triglycerides) to produce soap plus glycerine. After oven cleaner application, the greasy deposits on the oven walls are converted to soaps upon reaction with sodium hydroxide. Thus, the sodium hydroxide also reacts with some of the fatty grease, converting it to soap (i.e., saponification), which then is available to assist in cleaning and emulsifying the remainder of the grease within the oven via a detergent action. The resulting mixture can be removed with a dampened sponge or cloth. The extremely high-temperature oven-cleaning cycle settings of many modern household ovens ensures the ease of greasy dirt removal once the saponification process is completed. However, it is recommended that the consumer wear protective rubber gloves while wiping off the mixture, as the highly alkaline sodium hydroxide is extremely caustic and potentially very damaging to fingernails and skin tissues.

CLEANING PRODUCTS:METAL/J EWELRY CLEANERS.

METAL/J EWELRY CLEANERS

Metal cleaners are formulated to remove various types of soils from metal- ware and leave behind a polished finish. Brass and copper (Cu) objects react slowly with environmental air to form compounds that result in a blackened and tarnished finish, which obscures the beauty of the metals. Tarnish, the end result of the oxidation of metal, is the principal type of soil found on most metalware. Metals primarily used for decorative jewelry (e.g., rings, bracelets, necklaces, etc.), including gold (Au), platinum (Pt), and silver (Ag), are also subject to chemicals (e.g., skin acids, sulfur- containing compounds) that create an oxidizing environment and subsequent tarnishing effect. In fact, most gold and silver jewelry items are almost always a mixture of metals. For example, most gold jewelry is alloyed with copper, zinc, nickel (Ni), or silver, and silver is frequently mixed with some copper and zinc, to strengthen the metals to withstand the wear and tear of usage. Platinum usually shows the least effects of oxidation, due to the purity and composition of this metal. Brass is simply a metal alloy composed mostly of copper, with a small inclusive fraction of zinc. As such, metal objects, which nearly all contain some amount of copper, may react with oxygen and sulfur compounds (e.g., hydrogen sulfide) to form CuO and CuS, respectively.

Although there are many techniques used to clean such objects, commercial products are often simple solutions of ammonia within a hydro- gen-based solvent, with the additional inclusion of a very fine and mild abrasive called diatomaceous earth (DE). DE is nearly pure silica, in the form of SiO2, with a very porous characteristic. DE consists of the skeletons of small aquatic unicellular algal organisms called diatoms, which have survived evolutionary processes for approximately 100 million years. Placed in the taxonomic family Bacillariophyceae, the cell walls of these creatures are made of silica. Because silica is more dense than seawater or freshwater, the presence of silica tends to cause diatoms to sink into the water depths. As such, DE is collected from the bottom of ancient lake beds and is currently mined and used for many commercial and industrial purposes. Thus, within metal cleaners, DE acts as an abrasive, and the alkaline ammonia dissolves any greasy residue on the metalware. In addition, the ammonia reacts with the CuO or CuS to form the soluble ammonia complex of copper, which is Cu(NH3)42+. The greasy tarnish residue can then be washed away with clean water and a damp cloth.

CLEANING PRODUCTS:GLASS CLEANERS

GLASS CLEANERS

Glass cleaners are primarily liquids formulated to clean smooth glass-based areas such as windowpanes and mirrors. They loosen and dissolve oily soils located on glass, provide a shiny surface, and usually evaporate and dry quickly without leaving a streaking residue. One of the more common glass cleaner formulations contains isopropyl alcohol (CH3CH2CH2OH or CH3CHOHCH3) diluted with water. In some cases, ammonia (NH3) or vinegar (acetic acid; CH3COOH) is added for increased cleaning effi- ciency. Both ammonia and vinegar cut through greasy films, but alkaline ammonia vapors are highly irritating to the throat and entire respiratory system; thus, ammonia-based products should never be used for cleaning in a closed space. Ammonia-based glass cleaners do not leave a streaking residue, as both the ammonia and the water evaporate soon after application.

CLEANING PRODUCTS:DRAIN CLEANERS.

DRAIN CLEANERS

Drain cleaners/openers are formulated to unclog kitchen sink and bathroom/lavatory drain traps. Most sinks are synthesized of steel coated with enamel, and the drain trap beneath is usually made of brass or polyvinyl chloride. Brass is an alloy consisting mostly of copper (Cu), with a key additional incorporation of zinc (Zn). Although copper is relatively unreactive toward both bases and acids, zinc reacts easily with acids and slowly with bases. When such drains become clogged, it is usually because of the accumulation of greasy/fatty soap scum, hair, and related unwanted products. Thus, the classic key active ingredient in drain cleaners is the caustic alkaline chemical sodium hydroxide (NaOH), also referred to as “lye,” either in solid form with small chips of aluminum or as a concentrated liquid. When added to the product, the aluminum metal reacts with the sodium hydroxide solution to form hydrogen gas (H2), which initiates a bubbling effect within the clog, thereby creating a stirring and agitation action.

Liquid and gel-based drain cleaners marketed for consumer household use can contain a combination of sodium hydroxide, sodium hypochlorite (NaOCl; bleach), sodium silicate (abrasive), and various detergents (surfactant cleaning action). In general, the sodium hydroxide reacts with the water in the pipe to generate a significant amount of heat, which melts away most of the greasy clog. The melted substances are thus bro- ken down into simpler substances that can be rinsed away. A strong alkali will react with fat (e.g., triglycerides) to produce soap plus glycerine. Thus, the sodium hydroxide also reacts with some of the fatty grease, converting it to soap (i.e., saponification), which then is available to assist in cleaning and emulsifying the remainder of the grease within the pipe by a detergent action. If hair is the primary drain-clogging culprit (e.g., in shower drains), the bleaching agent included in the drain cleaner will degrade the keratin protein-based hair strands via oxidation, helping to unclog the drain.

Drains that simply possess slow water drainage, which are not truly blocked/plugged, can often be cleaned with slow-acting drain cleaners formulated with enzymes designed to degrade large insoluble organic (carbon-based) molecules into many smaller, water-soluble molecules. Examples of such enzymes include amylase (which breaks complex starches into glucose monosaccharide units), lipase (which breaks fats into glycerol and fatty acid units), protease (which breaks proteins into amino acid units), and cellulase (which breaks cellulose into glucose monosaccharide units).

CLEANING PRODUCTS:AMMONIA-BASED ALL-PURPOSE CLEANERS.

AMMONIA-BASED ALL-PURPOSE CLEANERS

Historically, ammonia (NH3) was first synthesized from coal tar. How- ever, these solutions were quite murky in appearance. In the early 1900s, before the onset of World War I, two German scientists, F. Haber and K. Bosch, developed the Haber-Bosch process, which involved the synthetic process of reacting nitrogen (N2) gas and hydrogen (H2) gas to form high quantities of pure ammonia gas. Natural gas (methane, CH4) is first reacted with steam to produce carbon dioxide (CO2) and hydrogen gas in a two-step process. Hydrogen gas and nitrogen gas are then reacted via the 1919 Nobel Prize-winning Haber-Bosch process to produce ammonia. These two scientists determined the conditions (extremely high temperatures and high pressures [steam]) and the catalysts (e.g., iron oxides and oxides of other common elements) necessary to produce ammonia gas. This colorless clear gas with a pungent odor is then easily liquefied for many uses. In fact, soap is often added to pure clear ammonia solutions to enhance consumer comfort compared with that of the originally marketed murky product.

Fresh household aqueous ammonia solutions range in concentrations of up to 10 percent actual ammonia. Such solutions are appropriate for use in loosening baked-on greasy soil or burned-on food particles. Diluted with water, ammonia solutions remove grease-based soils from glass surfaces, including mirrors and windows. Mixed with a detergent/surfactant, ammonia readily removes waxes from vinyl floor coverings (e.g., linoleum floors). This cleaner is not recommended for use on aluminum, asphalt tile, or woodwork, as it may lead to pitting, staining, and/or erosion of these materials. Ammonia-based solutions are excellent cleaners because they dissolve tough greasy stains without leaving a filmy residue. Both the ammonia and water evaporate after cleaning use. However, ammonia vapor is highly alkaline and caustic; therefore, it is potentially very irritating to the human respiratory system. In addition, it is extremely hazardous to mix ammonia with bleach. Potential noxious gases released from this reaction combination include chloramines (NH2Cl, NHCl2), hydrazine (NH2NH2), nitrogen trichloride (NCl3), and hydrochloric acid (HCl), all of which are toxic.

BABY PRODUCTS:DIAPER RASH TREATMENTS.

DIAPER RASH TREATMENTS

Many factors contribute to the initiation of diaper rash, including excess moisture, rubbing and friction, skin contact with urine and feces, and/or allergic reaction to the diaper material or to creams, powder, or wipes. While true diaper rash (irritant diaper dermatitis) is most common in babies between the ages of four and fifteen months, incontinent adults risk developing this preventable skin problem as well, as the chronic use of diapers is the common factor in both population groups. In general, infant skin is much less of an effective barrier than that of children (over the age of three) and adults. Because of the thin, soft, and water-containing nature of baby skin, substances are more easily permeable. Areas subject to a high concentration of moisture and soil provide a favorable environment for bacterial growth. Thus, if these types of irritants remain in contact with infant skin over an extended period of time, a rash may develop. The occlusive nature of a diaper tends to inhibit the evaporation of moisture from the skin surface, eventually leading to skin decomposition and an increase in bacterial colonization. Some bacteria produce ammonia through the degradation of urinary urea, and ammonia can then be used as a nutritional substrate, resulting in the growth of even more bacteria. The added presence of feces may contribute urease, which also degrades urinary urea to ammonia. Ammonia will raise the pH of the skin, and this increase in alkalinity facilitates further bacterial growth. In addition, urine may enhance the irritant activity of chemicals by increasing the permeability of the skin and directly acting as an irritant. Diaper rash, characterized by reddened and warm skin, typically occurs in all areas in close contact with the diaper, including the buttocks, upper thighs, lower abdomen, and genitalia.

While prevention of diaper rash may be achieved by keeping the skin dry, preventing urine and feces from mixing together, and retaining an acidic pH on the skin, most cases of diaper rash are treated with products sold in toothpaste-like tubes or plastic jars obtained without prescription. Nearly all brands are formulated with skin protectants such as zinc oxide (ZnO; used in skin healing; antiseptic properties), petrolatum (a semi- solid mixture of hydrocarbons derived from petroleum), and/or dimethicone (silicone emollient). Other products added to diaper rash creams and ointments might include solvents (e.g., benzyl alcohol), opacifying agents (e.g., glyceryl oleate), lubricants (e.g., mineral oil, cod liver oil), emulsifiers (e.g., ozokerite, propylene glycol), humectants (e.g., sorbitol), preservatives (e.g., benzoic acid, borax, BHA, or methylparaben), fragrances, and additional skin protectants and/or wound-healing products, including allantoin, beeswax, silicone, calamine, kaolin, lanolin, and ceresin (earth wax). Specialty brands may also have added products such as vitamins (e.g., cholecalciferol [vitamin D], vitamins A and D [in cod liver oil], and vitamin E), talc (mineral; provides softness), topical starch (cornstarch), extracts of aloe vera (skin wound healing), Peruvian balsam (skin-healing stimulant; antiseptic), and/or bismuth subnitrate (forms a protective coating over inflamed skin areas). However, some of the above secondary ingredients have been known to elicit allergic reactions in some infants.

Baby Products:BABY WIPES.

BABY WIPES

Because of the very thin, soft, and hydrated nature of baby skin, most types of chemical substances are easily permeable. In general, areas subject to a high concentration of moisture and soiling agents may provide a favorable environment for bacterial colonization. Areas of baby skin such as the buttocks, upper thighs, lower abdomen, pubic area, and groin that are subject to repetitive exposure to soiling agents, including urine and feces, require constant cleansing to avoid skin ailments (e.g., dermatitis).

Commercially available over-the-counter baby wet wipe products are manufactured to be minimally disruptive to the epidermal barrier and thus suitable for use on intact or compromised, irritated skin. While pre- moistened wipes generally differ in cleansing lotion formulation (emollients, preservative, pH, etc.) and fibrous composition, the wipes should be suitable for daily cleansing of the diapered area, even for infants with sensitive skin. Wipes should also be chemically formulated to avoid causing significant changes in the natural pH of pubic and buttock skin, as skin pH changes may exacerbate bacterial growth. In general, commercial baby wipes usually contain active cleansing ingredients such as purified water, potassium laureth phosphate, or chlorine dioxide. In addition, emollients and skin moisturizers such as propylene glycol, aloe barbaden- sis or aloe vera gel, polysorbate 20, cocamphodiacetate, sodium coco PG dimonium chloride phosphate, or glycerin may be added, along with emul- sifiers such as cetyl hydroxyethylcellulose or PEG-75 lanolin. Vitamins (e.g., tocopheryl acetate [vitamin E acetate]), pH-buffering agents (e.g., tetra- sodium EDTA, malic acid, citric acid), fragrance, and preservatives (e.g., sodium hydroxymethylglycinate, iodopropynyl butylcarbamate, DMDM hydantoin, methylparaben, propylparaben, 2-bromo-2-nitropropane-1,3- diol [alcohol], methylchlorisothiazolinone, methylisothiazolinone, quater- nium 15, and potassium sorbate) may also be added. Some consumers have found the extensive use of alcohols, fragrances, and preservatives in commercial wipes to be drying and irritating to the delicate tissues of their children and choose to use homemade wiping cloths with a simple cleansing solution such as purified water, mild soap, and skin-lubricating mineral or natural herbal oil.

Cellulose fibers and an adhesive binder characterize the fibrous compo- sition of most wipes. Often, special applications involve the depositing of cellulose fibers with the assistance of an electrostatic field to promote the properties of moisture absorbency and bulkiness with high absorption capacity. High-quality premoistened wipes are usually marketed in converted quarter-folded or flat-pack forms within a resealable plastic container.

Baby Products:BABY OIL

BABY OIL

Common baby oil is mineral oil derived from petroleum mixed with a small amount of fragrance. Baby oil has a number of uses, including prevention of scars, treatment for diaper and heat rash, sunburn relief, and treatment of canker sores. The purpose of using baby oil is to lock moisture into the skin. Typically, a small amount of baby oil is used after a bath or shower and increases the shine of the skin, making it appear healthier. Additionally, there are hundreds of formulations derived from plants, animals, and petroleum that are generically called “baby oil.” Some animal oils, such as emu oil, has been used as baby oil. This natural formulation contains a large number of very diverse chemical com- pounds that have potentially useful properties. Emu oil is said to have antibacterial, anti-inflammatory, moisturizing, and skin-penetrating properties. Baby oil is a chemical substance that is so common it is often thought to be innocuous. Unfortunately, the hydrocarbons present in mineral oil can be very hazardous to a baby. If a child aspirates baby oil, the lungs become coated with the oil. This blocks oxygen from reaching the bloodstream by inhibiting proper respiration. The inhalation of baby oil can lead to serious cases of chemical pneumonia.

HEALTH AND MEDICAL PRODUCTS:WART REMOVERS.

WART REMOVERS

Common cutaneous warts are hyperkeratotic papulonodules that most often appear on the hands, arms, and legs of an individual. The Latin word for wart is verruca, meaning “little hill” or “eminence.” Of all the diseases that plague humankind, warts are thought by many to possess the highest number of folk remedy treatments. Throughout history, treatments for warts included application of plant extracts (e.g., willow bark), paring with a sharp penknife, burning with the ash of wine lees, use of corrosives (e.g., brimstone), and rubbing with pork fat, potatoes, green walnuts, broom straws, or intestines of black chickens. Ointments were often rubbed on warts and consisted of a variety of substances, such as dandelion juice, castor oil, and onion juice. Other types of treatments included rubbing warts with the blood of frogs or pigs, or with new pennies, or tying slugs to the wart. Most cures for warts, however, were based on the theory of transferring the warts to another person, animal, or object. While early eighteenth-century thought suggested that warts might be “congealed nutritious juices” that had seeped from damaged underlying nerve filaments up through the skin, it was not until the end of the nineteenth century that the infectious nature of warts was recognized. Soon afterward, in the early twentieth century, it was suggested that warts were caused by a virus, and by the 1950s, confirmation of this theory was possible with the visualization of virus particles using the electron microscope.

Warts are common, contagious, and usually benign proliferations of skin and mucosa caused by human papillomaviruses (HPV), which are double-stranded DNA viruses. The word papilloma is derived from pa- pilla, meaning pustule or pimple, and the suffix oma, meaning tumor. HPV is widespread in human populations, and currently more than 150 types of HPV have been identified. Thus, infection of epidermal cells with HPV can manifest in benign cutaneous tumors as warts. Warts are filled with overgrown skin cells containing live HPV virus particles. Cutaneous (nongenital) warts are generally classified by their clinical features and morphology (e.g., common, flat, filiform) or location (e.g., plantar [undersurface of the foot]). Warts are usually spread by direct skin-to-skin inoculation of the virus from one person to another. Self- inoculation may also occur, especially with direct cutting of the wart, as any trauma that introduces breaks in the stratum corneum facilitates epi- dermal infection. Interestingly, the virus can resist desiccation, freezing, and prolonged storage outside of host cells. Thus, HPV may remain on and contaminate various surfaces (e.g., clothing, towels, floors, instruments) and subsequently infect scratched or broken skin via direct con- tact. While the incubation period for HPV ranges from one to six months, the latency period is suspected to last three or more years.

Because papillomaviruses are specialized for replication in external epithelia, infection is usually confined to the epithelium exposed to the external environment and does not result in systemic dissemination of the virus. While viral replication occurs in differentiated epithelial cells in the upper epidermal layer, viral particles are also often located in the deep epidermal basal layer. The epidermis becomes thickened and hyperkeratotic, and keratinocytes (keratin-containing cells) in the epidermal granular layer become vacuolated as a result of viral infection. The mechanisms by which virions penetrate the stratum corneum and infect viable keratinocytes is poorly understood, as there is a lack of practical in vitro culture systems available for these viruses to serve as study aids.

While the natural history of cutaneous HPV infections is for spontaneous regression within a few months or years, treatments (via medical personnel or the consumer) are frequently used to avoid potential viral spreading, wart enlargement, and individual social discomfort. Home remedies include the use of a pumice stone to remove the callus and/or warm water soaks (forty-five degrees centigrade) for thirty minutes daily for approximately six weeks. Most over-the-counter wart treatments func- tion by chemically destroying the epidermis in which the virus is present and are recommended for the removal of only cutaneous common warts (with typical raised, rough “cauliflower-like” appearance) and plantar warts. These treatments include topical once- or twice-daily application of solutions or pastes containing keratolytic agents such as salicylic acid [2-hydroxybenzoic acid; C6H4(OH)CO2H] and/or lactic acid as an active ingredient. By dissolving the intercellular cement substance, salicylic acid desquamates the horny virus-infected layer of the skin without affecting the structure of the viable epidermis. Treatment duration with this caustic agent depends on the size of the wart and the degree of skin discomfort tolerable to the consumer but generally requires up to twelve weeks. A flexible collodion (a liquid that dries to a long-acting film) or pad/disc-type product containing 15 to 40 percent salicylic acid is often applied directly to the wart lesion to lengthen chemical action time and allow enhanced chemical penetration into the skin epidermis. Such products can contain additional inactive ingredients such as solvents (e.g., acetone, alcohol, ether), fragrances (e.g., from camphor, menthol), emollients (e.g., polysorbate 80, propylene or polyethylene glycol), preservatives (e.g., quaternium-15, denatonium benzoate), thickeners (e.g., karaya gum base, ethylcellulose), and natural products historically thought to in- crease wart healing (e.g., castor oil, plant extracts derived from willow bark naturally containing salicylic acid). Therapeutic effects are usually enhanced by frequently removing dead surface keratin manually.