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Thursday, March 27, 2014

AUTOMOBILE POLLUTION


INTRODUCTION
Motor vehicle emissions are composed of the by-products that come out of the exhaust systems or other emissions such as gasoline evaporation. These emissions contribute to air pollution and are a major ingredient in the creation of smog in some large cities. A 2013 study by MIT indicates that 53,000 early deaths per year occur because of vehicle emissions.
The three main types of automotive vehicles used in our country are: (a) passenger cars powered by four stroke gasoline engines, (b) scooters and auto rickshaws powered by small two stroke gasoline engines, and (c) large buses and trucks powered mostly by four stroke diesel engines. Emissions from gasoline powered engines are generally classified as:
1.   (a)   Exhaust emissions (b) Crank-case emissions and (c) Evaporative emissions
Of the hydrocarbons emitted by a car with no controls, the exhaust emission gases account for roughly 65%, evaporation from the fuel tank and carburettor for roughly 15% and blowby or crank-case emission about 20%. CO, nitrogen oxides and lead compounds are emitted almost exclusively in exhaust gases. Diesel powered vehicles create relatively less pollution problems than gasoline engines. It exhausts only about one tenth of CO released by gasoline engine. Blowby is negligible in diesel engine since cylinder contains only air in compression stroke. Evaporative emissions are also low because the diesel engine uses closed injection fuel system and because the fuel is less volatile than gasoline. The major problem of diesel engine is smoke and odour.

EXHAUST EMISSION
The important exhaust emissions from gasoline engine are carbon monoxide, unburnt hydrocarbons, nitrogen oxides and particulates containing lead compounds. The emissions vary with air fuel ratio, spark timings and the engine operating conditions. To meet the exhaust emission standards for carbon monoxide and hydrocarbons, automobile manufacturers have used two basic methods.
1.      Inject air into the exhaust manifold near the exhaust valves, where exhaust gas temperature is highest, thus inducing further oxidation of unoxidised or partially oxidised substances.
2.      Design cylinders and adjust air-fuel ratio, spark timing and other variables to reduce the amount of hydrocarbons and carbon monoxide in the exhaust to the point where air injection is not required.
Device used to control hydrocarbon emissions falls in three classes
1.      Devices that modify engine operating conditions such as intake manifold, vaccum breakers, carburation mixture improvers, throttle retarders etc
2.      Devices that treat exhaust gases such as after burners, catalytic converters, absorbers and adsorbers and filters
3.      Use of modified or alternate fuels

CRANK-CASE EMISSIONS           
Crank-case emissions consist of engine blowby which leaks past the piston mainly during the compression stroke and of oil vapours generated into the crank-case. Worn out piston rings and cylinder liner may greatly increase the blowby. These gases mainly contain hydrocarbons and account nearly for 25% of total hydrocarbon emission from a passenger car. It can be reduced by eliminating the positive crank-case ventilation (PCV) system. These systems recycle crank-case ventilation air and blowby gases to the engine intake instead of venting them to the atmosphere.

EVAPORATIVE EMISSIONS
An average Indian passenger car would emit about 20 kg of hydrocarbon through evaporation annually. For controlling the evaporation of fuel from the carburettor and fuel system, systems are being developed that store vapours in the crank-case or in a charcoal canister that absorbs hydrocarbons for recycling to the engine. Mechanical methods are used to control evaporative emissions.
The exhaust gas pollutants comprise of HCs, carbon monoxide, nitrogen oxides and lead compounds. It essentially constitutes the fuel evaporation from the fuel tank and carburettor and consists of HCs alone.

PHOTOCHEMICAL SMOG
The deleterious effects of automobile pollutants include toxic effects of CO and lead compounds and the formation of photochemical smog. The chief culprits in the smog are the volumetrically lower concentrations of unburnt or partially burnt HCs and nitrogen oxides. The relative concentration of either pollutant varies with the engine operation.
The necessary conditions for smog formation are:
1.      Sufficient quantities and concentration of unburnt HCs and nitrogen oxides in the atmosphere.
2.      Stagnant atmospheric conditions produced by meteorological thermal inversions
3.      Strong sunlight

  Hydrocarbons + Nitric oxide + Sunlight                photochemical smog

AIR- FUEL RATIO
The decrease in air-fuel ratio increases the HC content (expressed as wt % of supplied fuel) in the exhausts of passenger cars at idle, but does not have any effect at part throttle. On the basis of experiments conducted on single cylinder engine operating at full throttle on propane, Daniel reported that ‘relative HC concentration’ measured with a dispersive infra-red analyser decreased with an increasing AF ratio and reached a minimum at an AF ratio leaner than stoichiometric. Methane and acetylene are two HCs most greatly affected by AF ratio.

Spark timing
The HC emission generally decreases as the spark is retarded at constant power. A 100 retard from the optimum economy value causes 7-18% reduction as measured by a flame-ionisation analyser.

Combined effect of AF ratio and Spark Timing
The reductions in HC emission due to leaner AF ratios and due to retarded spark timing are additive, but while the former improves fuel economy, the latter impairs it. However, these fuel economy effects tend to balance each other when both methods are employed.
  
This chart shows the resultant gases from burning petrol at different AFRs. Rich mixtures are cooler but you can see the increased Hydrocarbon emissions as the excess fuel is unused. Nitrogen oxides are low from the cooler temps, but Carbon Monoxide is far higher with the lack of free oxygen to convert the CO to CO2. Lean mixtures around 16:1 AFR produce the best economy, but the extra heat oxidises the Nitrogen in the air increasing air pollution, but with low CO levels.
  
CONTROL OF EXHAUST EMISSIONS

Two main approaches to minimize exhaust emissions are:
1.      Modification in the engine design and operating variables
2.      Treatment of exhaust gases after emission from the engine

Modification in the engine design and operating variables
1.      Use of leaner idle mixtures
2.      Use of leanest possible mixture and maximum spark retard compatible with good power output and drivability
3.      Use of minimum valve-over-lap necessary
4.      Pre-treatment of mixture to improve vaporisation and mixing of fuel with air

Exhaust treatment devices
The basic technique is to provide oxidation of HC and CO emission from the engine. Exhaust oxidation devices fall into two categories:
1.      Promotion of after burning  of pollutants by exhaust heat conservation, introduction of additional air and by providing sufficient volume to ensure adequate reaction time,
2.      Use of catalytic converters
Catalytic converters depend on the action of a catalyst containing certain exotic chemicals to convert HC and CO emissions to their oxidised products. Extra air is introduced by an engine driver blower. Vanadium pentoxide (V2O5) is one of the successful catalysts used so far.

CONTROL OF EVAPORATIVE EMISSIONS
There are two main sources of evaporative emissions: fuel tank and carburettor.
Principal factors governing fuel tank emissions are fuel volatility and ambient temperature. Insulation of the fuel tank to reduce temperature, sealed and pressurised fuel systems, and vapour collection systems have all been explored to reduce tank emissions.
Carburettor emissions may be divided into two categories, running losses occurring during engine operation and hot soak losses occurring when the vehicle is parked. On account of internal venting of carburettor the running losses are insignificant. Carburettor losses are substantial only during hot soak following a period of vehicle operation. The fuel voltality and carburettor design also greatly affect the carburettor emissions.

CONTROL OF CRANK-CASE EMISSIONS
These consists of engine blowby gases, ventilation air and crank-case lubricant fumes. New engines equipped with Positive Crank-case Ventilation System (PVC) return crank-case vapours through a vaccum valve, back to downstream side of the carburettor. Recycling burns hydrocarbons in the cylinders, dropping overall population by 25%.

ALTERNATIVES
1.      Electric cars
Even though the electric car promises a great future of pollution-free cars, its wide use for vehicular application may accentuate and aggravate the problem. Power generating steps have to be stepped up which is difficult. Furthermore more fuel has to be burnt at power plant on an equivalent basis to supply power to these cars.
2.      Natural gas
Compressed natural gas can essentially eliminate the pollutants but supply and proved reserves are limited.
3.      Wankel engine
This engine being compact has more space available for emission-control-equipment, can operate on fuel of low octane rating and what is more important, NOx emissions are 30% of those of piston engines. However hydrocarbon emissions are decidedly higher and CO emissions equal.
4.      Gas turbine
A properly designed automative gas turbine offers significant potential for alleviating air pollution caused by conventional otto-cycle engines. Because of high air-fuel ratios associated with gas turbines, CO and HCx emissions are usually negligible. NOx concentration is 100ppm with 200% excess air in a gas turbine as compared to 1200 ppm in as SI engine. However NOx emissions are comparable in magnitude. \
5.      Ammonia-fuelled SI engine
The use of ammonia will reduce two main pollutants: CO and HCx. The emission of NH3 in engine exhaust is to be avoided because of its irritating odour and toxic effect. This can be minimized by adding hydrogen in small quantities (2%) which will act as a combustion promoter in accelerating the burning of ammonia.
6.      Unleaded-gasoline powered SI engine

Lead compounds are toxic and conductive to more exhaust HC emissions. The most immediate benefit accruing from the removal of lead from gasoline is a 20ppm reduction in HC emissions in new cars. This reduction is effected by the process of natural oxidation of the hydrocarbons in the exhaust gas which is apparently inhibited by the presence of lead. The lead deposit is also responsible for spark plug fouling which increases HC emissions.

Monday, March 17, 2014

METALS AS DISINFECTANTS

1.     INTRODUCTION
Pathogen-free drinking water is a priority for the safety of human health concerned with waterborne infectious diseases. Increasing urbanization has aggravated the problem of microbial contamination in most of drinking water sources resulting into outbreaks and sporadic incidences of water transmitted diseases mainly gastroenteritis, cholera, dysentery, typhoid, poliomyelitis and hepatitis. Although there are a number of popular methods such as filtration, ozonisation, reverse osmosis and UV radiation, chlorination is the most popular globally used method for drinking water disinfection, particularly in piped supplies at community level. Recent analytical studies have revealed that chlorination of water produces numerous disinfection by-products (DBPs) after the reaction of residual chlorine with natural organic compounds such as humic and fulvic acids in water. Many of such DBPs have been reported to be mutagenic/ carcinogenic. To overcome this problem, there is a pressing need to replace chlorination with a safer and appropriate alternative process.
Certain metals like mercury, silver and copper with an oligodynamic property have been found to be biocidal with the capability to disinfect the water. Among these, silver is more appropriate as it is non-toxic and an efficient water disinfectant. Silver has been known as an effective biocide against viruses, bacteria, protozoa, algae, yeasts and moulds. Silver has strength, malleability, ductility, high reflectance of light, temperature resistance and electrical as well as thermal conductivity. Silver is used for electroplating, currency, ornaments, utensils, mirror plating, sweet coating, photography, electrical/electronic instrumentation, solar energy, medical (dental) applications and scientific research. The use of pots and pitchers made up of silver for storage of drinking water is an age-old tradition which indicates that its bactericidal property was well known to our ancestors.
2.     SILVER AS DISINFECTANT
The antimicrobial effects of silver (Ag) have been recognized for thousands of years. In ancient times, it was used in water containers and to prevent putrefaction of liquids and foods. In ancient times in Mexico, water and milk were kept in silver containers. Silver was also mentioned in the Roman pharmacopoeia of 69 B.C.
In 1884, silver nitrate drops were introduced as a prophylactic treatment for the eyes of new-borns, and this became a common practice in many countries throughout the world to prevent infections caused by Neisseria gonorrhoeae transmitted from infected mothers during childbirth. In 1928, the “Katadyn Process” based on the use of silver in water at low concentrations, was introduced.
Silver ions have the highest level of antimicrobial activity of all the heavy metals. Gram-negative bacteria appear to be more sensitive than gram-positive species. Kawahara et al. posited that some silver binds to the negatively charged peptidoglycan of the bacterial cell wall. Because gram-positive species have a thicker peptidoglycan layer than do gram-positive species, perhaps more of the silver is prevented from entering the cell.
Generally speaking, the observed bactericidal efficacy of silver and its associated ions is through the strong binding with disulphide (S–S) and sulfhydryl (–SH) groups found in the proteins of microbial cell walls. Through this binding event, normal metabolic processes are disrupted, leading to cell death. The antimicrobial metals silver (Ag), copper (Cu), and zinc (Zn) have thus found their way into a number of applications.
2.1.  Applications And Uses
a)      Drinking Water
Chlorine has been used as the principal disinfectant for drinking water since the early 1900s. In the 1970s, it was discovered that chlorination caused the formation of numerous chlorinated compounds in water, including trihalo-methanes and other disinfection by-products (DPB), that are known to be hazardous to human health. There is therefore a need to assess alternative disinfectants.
Silver electrochemistry experiments suggest that silver may have potential as a chlorine alternative in drinking water disinfection in applications in which chlorine may be considered too hazardous. Silver has been used as an effective water disinfectant for many decades, primarily in Europe. It has also been used to treat recycled water aboard the MIR space station and aboard NASA space shuttles.
Both the Environmental Protection Agency (EPA) and the World Health Organization (WHO) regard silver as safe for human consumption. Only argyria (irreversible skin discoloration) occurs with the ingestion of gram quantities of silver over several years or by the administration of high concentrations to ill individuals. There have been no reports of argyria or other toxic effects caused by silver in healthy persons (World Health Organization 1996). Based on epidemiological and pharmacokinetic data, a lifetime limit of 10 grams of silver can be considered a No Observable Adverse Effect Level (NOAEL) for humans (World Health Organization 1996). In the United States, no primary standards exist for silver as a component in drinking water. The EPA recommends a secondary non-enforceable standard of 0.1 mg/L (100 ppb) (Environmental Protection Agency 2002). The World Health Organization (1996) has stated this amount of silver in water disinfection could easily be tolerated because the total absorbed dose would only be half of the NOAEL after 70 years. Silver has been used as an integral part of EPA- and National Sanitation Foundation (NSF)-approved point-of-use (POU) water filters to prevent bacterial growth. Home water purification units (e.g., faucet-mounted devices and water pitchers) in the United States contain silverized activated carbon filters along with ion-exchange resins (Gupta et al. 1998). Today, some 50 million consumers obtain drinking water from POU devices that utilize silver (Water Quality Association 2001). These products leach silver at low levels (1–50 ppb) with no known observable adverse health effects. Such filters have been shown to prevent the growth of Pseudomonas flu-rescens and Pseudomonas aeruginosa in water; however, several studies have raised questions about their efficacy. Reasoner et al. (1987) established that bacterial colonization of such devices occurs within a matter of days and may result in a large number of bacteria in the product water.
b)     Cooling Towers/Large Building Water Distribution Systems
Cooling towers provide cooling water for air compressors and industrial processes that generate heat. They provide an ideal environment and a suitable balance of nutrients for microbial multiplication. Chlorine is a popular method for controlling such bacterial growth, but there are difficulties in maintaining disinfection efficacy, particularly at a high temperature or pH. Chlorination can also cause corrosion of cooling tower facilities.
Ag/Cu ionization has been used in cooling towers to control bacterial growth. In a study by Martinez et al. (2004), an appreciably reduced chlorine concentration of 0.3 parts per million (ppm or mg/L) was combined with 200 ppb Ag and 1.2 ppm Cu. This method had an appreciable impact on levels of coliform bacteria, iron-related bacteria, sulphate-reducing bacteria and slime-forming bacteria in a cooling tower.
Large hot water distribution systems in hospitals and hotels have also often been attributed as a source of contaminating bacteria.  Contaminated systems are usually treated by either superheating the water with flushing of the distal sites (heat-flush), by hyper chlorination, or by installing Ag/Cu ionization units. Greater bacterial reductions have been observed with Ag/Cu ionization than with the heat-flush method. Ag/Cu ionization is known to provide long-term control and may be used in older buildings in which the pipes could be damaged by hyper chlorination. Such systems are easy to install and maintain, are relatively inexpensive, and do not produce toxic by-products.
One microorganism that has been commonly isolated from cooling towers is Legionella pneumophila, the causative agent of Legionnaires’ disease. Many outbreaks have been linked to cooling towers and evaporative condensers. L. pneumophila is also commonly isolated from the periphery of hot water systems in large buildings such as hospitals, hotels, and apartment buildings where temperatures tend to be lower. Ag/Cu systems have been in common use in hospitals to control Legionella for more than a decade. Mietzner et al. reported that one such ionization system maintained effective control of L. pneu-mophila for at least 22 mon. Legionella may develop a tolerance to silver after a period of years, requiring higher concentrations to achieve the same effect.
c)  Recreational Waters
Bacteria, protozoa, and viruses may occur naturally in recreational waters or be introduced into swimming pools by bathers or through faulty connections between the filtration and sewer systems. Species carried by bathers include the intestinal Streptococcus faecalis and Escherichia coli, as well as skin, ear, nose, and throat organisms such as Staphylococcus aureus, Staphylococcus epidermidis, Streptococcus salivarius, Pseudomonas aeruginosa, and Mycobacterium marinum (Singer 1990). Mild to serious illnesses caused by ingestion of or contact with contaminated water can be the result of improperly maintained pools, spas, and hot tubs.
In recent years, there has been a rapid increase in the number of public, semipublic, and private pools built in Europe and America. Adequate disinfection of such waters is becoming an increasingly important health issue. Traditionally, chlorine-based products are used for disinfection of swimming pools. Chlorine produces harmful DBPs caused by the halogenation of organic compounds (urine, mucus, skin particles, hair, etc.) released into the water by swimmers. Thus, there is also a need for alternative disinfectants for recreational waters.
Silver (Ag2SO4) at a low concentration (10 ppb) has been shown to kill more than 99.9% of heterotrophic bacteria in swimming pools within 30 min. Silver has been used commercially in pools, but it is too slow to be used as a primary disinfectant. Regulatory agencies in some countries have recommended its use only in combination with another disinfectant. Electrolytic generation of Ag and Cu ions allows ppb concentrations to be maintained in a convenient and reproducible manner.
d) Food and Dietary Supplements
Silver has been used to treat vinegar, fruit juices, and effervescent drinks and wine. It is also available in Mexico as col-loidal silver in gelatin (‘Microdyn’) for use as a consumer fruit and vegetable wash and in the U.S. as an alternative health supplement or in silver citrate complexes as food additives.
e) Medical Applications
Silver has been used in numerous medical applications. In dentistry, silver nitrate is effective against a number of oral bacteria including gram-negative periodontal pathogens and gram-positive streptococci that cause. Dental amalgams contain approximately 35% Ag(0) and 50% Hg(0). It is unclear whether sufficient Ag(0) is released and oxidized to Ag(I) to produce an antimicrobial effect; however, the release of Hg(II) selects for metal-resistant bacteria. New amalgams have therefore been introduced that contain silver alone.
Silver salts have traditionally been administered to the eyes of new born infants to prevent neonatal eye. Silver ions are the most commonly used topical antimicrobial agents used in burn wound care in the Western world. Both silver nitrate and silver sulphadiazine have also been used as topical antiseptics for cutaneous wounds. A topical cream containing 1.0% silver sulphadiazine and 0.2% chlorhexidine digluconate has been marketed as Silvazine in the U.S.
Silver sulphadiazine has recently been incorporated directly into bandages used on burns and large open wounds. Unlike silver nitrate, silver sulphadiazine does not react with sulfhydryl groups or proteins. Thus, its action is not diminished in the wound. Nevertheless, the silver is still the antimicrobial portion of the molecule. Two commercial silver-coated dressings (Acticoat and Silverdin) prevented muscular invasion by P. aeru-ginosa in experimental burns in rats. P. aeruginosa and S. aureus populations were similarly affected by Silverlon, an FDA-approved wound dressing.
Silver has also been used to coat vascular, urinary, and peritoneal catheters, prosthetic heart valve sewing rings, vascular grafts, sutures, and fracture fixation devices. Plastic indwelling catheters coated with silver compounds retard the formation of microbial biofilms. Manal et al. (1996) determined that the adherence of four strains of E. coli was decreased by 50%–99% in comparison to silicone and latex catheters. In two separate clinical studies, 10%–12% of patients with silver-treated catheters developed bacteriuria (>100 microorganisms/mL) versus 34%–37% of patients with standard Foley catheters after 3 d. The onset of bacteria was thus delayed in comparison to latex catheters. Gentry and Cope (2005) also found a 33.5% reduction in catheter-associated urinary tract infections following the introduction of silver-coated catheters.
The complex of silver with antibiotics on the surfaces of polytetrafluoro ethylene vascular grafts has been examined in a number of studies. Silver increased the elution and prolonged the duration of ciprofloxacin release in one such study.
f) Antimicrobial Surfaces/Materials
Silver may be added to polymers to confer antimicrobial activity. The result is consumer products such as washing machines, refrigerators, and ice machines that have incorporated silver. Silver has been added to plastics to produce items such as public telephones and public toilets (in Japan), toys, and infant pacifiers.  Johnson Matthey Chemicals (UK) utilizes an inorganic composite with immobilized slow-release silver as a preservative in their cosmetics. Synthetic fabrics with silver are popular in items such as sportswear, sleeping bags, bed sheets, and dishcloths. These fabrics are believed to reduce the level of bacterial contamination and thus odours.
Silver may also be added to inorganic ceramics (e.g., zirconium phosphate, zeolite) that are able to trap metal ions and may then be added to other materials (e.g., paints, plastics, waxes, polyesters) to confer antimicrobial properties. Zeolite ceramic (Sodium aluminosilicate) has a porous three-dimensional crystalline structure in which ions can reside; it has a strong affinity for silver ions and can electrostatically bind up to 40% silver (wt/wt). Zeolites act as ion exchangers, releasing silver into the environment in exchange for other. The amount of silver released is dependent upon the concentration of cations in the environment (Kawahara et al. 2000). The bactericidal activity of Ag-zeolite appears to result from both the effect of silver ions (Matsumura et al. 2003) and the generation of reactive oxygen species, under aerated conditions, such as superoxide anions, hydroxyl radicals, hydrogen peroxide, and singlet oxygen.
Studies on stainless steel surfaces coated with zeolites containing 2.5%Ag and 14% Zn ions demonstrated significant reductions in L. pneumophila (Rusin et al. 2003), S. aureus (Bright et al. 2002), Campylobacter jejuniSalmonella  typhimurium,  Listeria monocytogenes,  and  Escherichia  coli O157:H7 (Bright KR, Gerba CP, unpublished data). Vegetative cells of Bacillus subtilis, B. anthracis, and B. cereus were also inactivated by at least three orders of magnitude within 24 hr by a Ag/Zn-zeolite whereas Bacillus spores were completely resistant under the same conditions.
2.2.  Antimicrobial Efficacy
The antimicrobial effect of silver has been demonstrated in numerous and varied applications against many different types of microorganisms including bacteria, viruses, and protozoa.

3.      COPPER AS DISINFECTANT
In the last few decades, work has been done on the antimicrobial properties of copper and its alloys against a range of micro-organisms threatening public health in food processing and healthcare applications. The use of copper and copper alloys for frequently touched surfaces such as door and furniture hardware, bed rails, light switches and food preparation surfaces can help limit microbial infections in hospitals and food dispensing organizations. Michels, et al. show that increasing the copper content of alloys increases antimicrobial effectiveness. The contact killing is so rapid that the production of protective biofilms is not possible. The specific mechanism by which copper affects cellular structures is not yet proven, but the active agent of cell destruction is generally considered to be the copper ion. Recent studies showed that large amounts of copper ions were taken up by E. coli over 90 min, when cells were applied to copper coupons via an aqueous suspension (a standing drop). When cells were plated on copper using minimum liquid and a drying time of 5 seconds, the accumulation of copper ions by cells was even more dramatic, reaching a high concentration in a fraction of the time.
The copper ion level of cells remained high throughout the killing phase, suggesting that cells become overwhelmed by their intracellular copper. The grain structure of the copper material affects ion diffusion and hence affects bacterial destruction by copper ions. The US Environmental Protection Agency (EPA) registers five copper alloys with public health claims. All of the alloys have minimum nominal copper concentrations of 60%. Registration of copper and certain copper alloys such as brass and bronze means that the EPA recognizes these solid materials’ antimicrobial properties. Products made from any of the registered alloys are legally permitted to make public health claims relating to the control of organisms that pose a threat to human health. Laboratory studies conducted under EPA-approved protocols have proven copper’s ability to kill, within 2 hours of contact time, more than 99.9% of the following disease-causing bacteria: Staphylococcus aureus, Enterobacter aerogenes, Escherichia coli O157:H7, Pseudomonas aeruginosa, Vancomycin-resistant Enterococcus faecalis (VRE) and MRSA.

3.1.  Copper surface generation
In order to make use of the antimicrobial ability of copper, surfaces that contact skin and foods should be composed of copper or copper alloy. This can be accomplished with solid copper equipment or by means of copper surface coating. In general, cost considerations favour copper coatings over solid structural copper. Various metal spray techniques are available for the purpose of depositing a copper surface onto implements that can transmit microorganisms, and it is desired to identify an optimal deposition method. Accordingly, three metal spray techniques are evaluated with respect to the anti-microbial activity of the copper surfaces produced by each.

3.2.  Plasma spray
The plasma spray process shown in Figure 1 uses a DC electric arc to generate a stream of high temperature ionized plasma gas, which acts as the spraying heat source. The coating material, in powder form and carried by an inert gas, is injected into the plasma jet where it is melted and propelled towards the substrate.
The plasma spray gun includes a copper anode and tungsten cathode, which are both water cooled. Plasma gas (argon, nitrogen, hydrogen, helium) flows around the cathode and through the anode, which is shaped as a constricting nozzle. The plasma, containing suspended metal droplets, exits in the anode nozzle and is directed toward a surface, where the particles deposit.
1
Figure 1 Plasma spray

3.3.  Arc spray
The arc spray process shown in Figure 2 creates an arc between two metallic wires acting as consumable electrodes. A DC voltage is applied between the wires, and an arc discharge is created at the contact of the wires. The wire electrodes are melted by the electric arc and a compressed air jet disperses the molten droplets and propels them onto a surface.
2
Figure 2 Arc spray

3.4.  Cold spray
The cold spray process shown in Figure 3 imparts super-sonic velocities to metal particles by placing them in a heated nitrogen or helium gas stream that is expanded through a converging–diverging nozzle. The powder feed is inserted at high pressure at the nozzle entrance. The particles, entrained within the gas, are directed towards a surface, where they are embedded on impact, forming a strong bond with the surface. The term “cold spray” has been used to describe this process due to the relatively low temperatures (100-500°C) of the expanded gas stream that exits the nozzle. Subsequent spray passes increase the structure thickness. The adhesion of the metal powder to the substrate, as well as the cohesion of the deposited material, is accomplished in the solid state.
The relatively low porosity of the cold spray coating results from particle packing caused by high velocity impact. Another characteristic of high velocity impacts is the creation of grain dislocations and work hardening. The low oxide content of cold sprayed deposits occurs because the particle temperature remains low and thus inhibits oxidation.
The spray techniques described each produce impacting metal particles in distinct temperature and velocity ranges. These temperatures and velocities create metal coatings with different characteristics with respect to the presence of oxides, porosity, grain dislocations, and hardness.
Because of these metallurgic differences, it is reason-able to assume that the coatings will exhibit differences in antimicrobial efficiency. Table 1 gives the particle temperatures and impact velocities, as well as the porosity and oxide ranges of the resulting deposits.

3
Figure 3 Cold spray
                                                                         
4.      CONCLUSION
Both the EPA and the WHO regard silver as safe for human consumption. It does not pose a risk to human health (World Health Organization 1996) and, in contrast to numerous other commonly utilized disinfectants, is not considered a hazardous substance. Silver inactivates a wide variety of micro-organisms such as bacteria, viruses, and protozoa, alone or in combination with other disinfectants, although this effect is not instantaneous.
The significant anti-microbiologic differences between coatings produced by different spray techniques demonstrate the importance of the copper application technique and of the resulting deposition structure. The cold spray technique showed superior anti-microbial effectiveness caused by the high impact velocity imparted to the sprayed particles which results in high dislocation density and high ionic copper diffusivity. The cold spray process is a mature technology which is currently in use for a variety of applications requiring various metal coatings. The cold spray process can readily apply copper coatings onto touch surfaces.

REFERENCES
  1. Nadia Silvestry-Rodriguez, Enue E. Sicairos-Ruelas,Charles P. Gerba, and Kelly R. Bright; “Silver as a Disinfectant” Rev Environ Contam Toxicol 191:23–45
  2. Champagne and Helfritch; “A demonstration of the antimicrobial effectiveness of various copper surfaces” Champagne and Helfritch Journal of Biological Engineering 2013, 7:8
  3. Satya P. Pathak,  K. Gopal; “Evaluation of bactericidal efficacy of silver ions on Escherichia coli for drinking water disinfection” Environ Sci Pollut Res (2012) 19:2285–2290

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