Activated carbon






Activated carbon


Activated carbon, also called activated charcoal, is a form of carbon processed to have small, low-volume pores that increase the surface area[1][2] available for adsorption or chemical reactions.[3]Activated is sometimes substituted with active.


Due to its high degree of microporosity, one gram of activated carbon has a surface area in excess of 3,000 m2 (32,000 sq ft)[1][2][4] as determined by gas adsorption.[1][2][5] An activation level sufficient for useful application may be obtained solely from high surface area. Further chemical treatment often enhances adsorption properties.


Activated carbon is usually derived from charcoal and is sometimes used as biochar. When derived from coal or corn[2][1] it is referred to as activated coal. Activated coke is derived from coke.




Contents






  • 1 Uses


    • 1.1 Industrial application


    • 1.2 Medical uses


    • 1.3 Analytical chemistry applications


    • 1.4 Environmental applications


    • 1.5 Agriculture uses


    • 1.6 Distilled alcoholic beverage purification


    • 1.7 Fuel storage


    • 1.8 Gas purification


    • 1.9 Chemical purification


    • 1.10 Mercury scrubbing




  • 2 Production


  • 3 Classification


    • 3.1 Powdered activated carbon


    • 3.2 Granular activated carbon


    • 3.3 Extruded activated carbon


    • 3.4 Bead activated carbon (BAC)


    • 3.5 Impregnated carbon


    • 3.6 Polymer coated carbon


    • 3.7 Woven carbon




  • 4 Properties


    • 4.1 Iodine number


    • 4.2 Molasses


    • 4.3 Tannin


    • 4.4 Methylene blue


    • 4.5 Dechlorination


    • 4.6 Apparent density


    • 4.7 Hardness/abrasion number


    • 4.8 Ash content


    • 4.9 Carbon tetrachloride activity


    • 4.10 Particle size distribution




  • 5 Modification of properties and reactivity


  • 6 Examples of adsorption


    • 6.1 Heterogeneous catalysis




  • 7 Reactivation and regeneration


    • 7.1 Thermal reactivation


    • 7.2 Other regeneration techniques




  • 8 See also


  • 9 References


  • 10 External links





Uses


Activated carbon is used in methane and hydrogen storage,[1][2]air purification, decaffeination, gold purification, metal extraction, water purification, medicine, sewage treatment, air filters in gas masks and respirators, filters in compressed air, teeth whitening, and many other applications.



Industrial application


One major industrial application involves use of activated carbon in metal finishing for purification of electroplating solutions. For example, it is a main purification technique for removing organic impurities from bright nickel plating solutions. A variety of organic chemicals are added to plating solutions for improving their deposit qualities and for enhancing properties like brightness, smoothness, ductility, etc. Due to passage of direct current and electrolytic reactions of anodic oxidation and cathodic reduction, organic additives generate unwanted breakdown products in solution. Their excessive build up can adversely affect plating quality and physical properties of deposited metal. Activated carbon treatment removes such impurities and restores plating performance to the desired level.



Medical uses


Main article: Activated charcoal (medication)



Activated charcoal for medical use


Activated carbon is used to treat poisonings and overdoses following oral ingestion. Tablets or capsules of activated carbon are used in many countries as an over-the-counter drug to treat diarrhea, indigestion, and flatulence.


However, it is ineffective for a number of poisonings including strong acids or alkali, cyanide, iron, lithium, arsenic, methanol, ethanol or ethylene glycol.[6]


Incorrect application (e.g. into the lungs) results in pulmonary aspiration, which can sometimes be fatal if immediate medical treatment is not initiated.[7]



Analytical chemistry applications


Activated carbon, in 50% w/w combination with celite, is used as stationary phase in low-pressure chromatographic separation of carbohydrates (mono-, di-trisaccharides) using ethanol solutions (5–50%) as mobile phase in analytical or preparative protocols.



Environmental applications




Activated carbon is usually used in water filtration systems. In this illustration, the activated carbon is in the fourth level (counted from bottom).


Carbon adsorption has numerous applications in removing pollutants from air or water streams both in the field and in industrial processes such as:



  • Spill cleanup


  • Groundwater remediation


  • Drinking water filtration

  • Air purification


  • Volatile organic compounds capture from painting, dry cleaning, gasoline dispensing operations, and other processes.


During early implementation of the 1974 Safe Drinking Water Act in the US, EPA officials developed a rule that proposed requiring drinking water treatment systems to use granular activated carbon. Because of its high cost, the so-called GAC rule encountered strong opposition across the country from the water supply industry, including the largest water utilities in California. Hence, the agency set aside the rule.[8] Activated carbon filtration is an effective water treatment method due to its multi-functional nature. There are specific types of activated carbon filtration methods and equipment that are indicated – depending upon the contaminants involved.[9]


Activated carbon is also used for the measurement of radon concentration in air.



Agriculture uses


Activated carbon (charcoal) is an allowed substance used by organic farmers in both livestock production and wine making. In livestock production it is used as a pesticide, animal feed additive, processing aid, nonagricultural ingredient and disinfectant.[10] In organic winemaking, activated carbon is allowed for use as a processing agent to adsorb brown color pigments from white grape concentrates.[11]



Distilled alcoholic beverage purification


See also: Lincoln County Process

Activated carbon filters (AC filters) can be used to filter vodka and whiskey of organic impurities which can affect color, taste, and odor. Passing an organically impure vodka through an activated carbon filter at the proper flow rate will result in vodka with an identical alcohol content and significantly increased organic purity, as judged by odor and taste.[citation needed]



Fuel storage


Research is being done testing various activated carbons' ability to store natural gas[2][1] and hydrogen gas.[1][2] The porous material acts like a sponge for different types of gases. The gas is attracted to the carbon material via Van der Waals forces. Some carbons have been able to achieve bonding energies of 5–10 kJ per mol. The gas may then be desorbed when subjected to higher temperatures and either combusted to do work or in the case of hydrogen gas extracted for use in a hydrogen fuel cell. Gas storage in activated carbons is an appealing gas storage method because the gas can be stored in a low pressure, low mass, low volume environment that would be much more feasible than bulky on-board pressure tanks in vehicles. The United States Department of Energy has specified certain goals to be achieved in the area of research and development of nano-porous carbon materials. All of the goals are yet to be satisfied but numerous institutions, including the ALL-CRAFT program,[1][2][12] are continuing to conduct work in this promising field.



Gas purification


Filters with activated carbon are usually used in compressed air and gas purification to remove oil vapors, odor, and other hydrocarbons from the air. The most common designs use a 1-stage or 2 stage filtration principle in which activated carbon is embedded inside the filter media.


Activated carbon filters are used to retain radioactive gases within the air vacuumed from a nuclear boiling water reactor turbine condenser. The large charcoal beds adsorb these gases and retain them while they rapidly decay to non-radioactive solid species. The solids are trapped in the charcoal particles, while the filtered air passes through.



Chemical purification


Activated carbon is commonly used on the laboratory scale to purify solutions of organic molecules containing unwanted colored organic impurities.


Filtration over activated carbon is used in large scale fine chemical and pharmaceutical processes for the same purpose. The carbon is either mixed with the solution then filtered off or immobilized in a filter.



Mercury scrubbing


Activated carbon, often infused with sulfur[13] or iodine, is widely used to trap mercury emissions from coal-fired power stations, medical incinerators, and from natural gas at the wellhead. This carbon is a special product costing more than US$4.00 per kg.[citation needed]


Since it is often not recycled, the mercury-laden activated carbon presents a disposal dilemma.[14] If the activated carbon contains less than 260 ppm mercury, United States federal regulations allow it to be stabilized (for example, trapped in concrete) for landfilling.[citation needed] However, waste containing greater than 260 ppm is considered to be in the high-mercury subcategory and is banned from landfilling (Land-Ban Rule).[citation needed] This material is now accumulating in warehouses and in deep abandoned mines at an estimated rate of 100 tons per year.[citation needed]


The problem of disposal of mercury-laden activated carbon is not unique to the United States. In the Netherlands, this mercury is largely recovered[citation needed] and the activated carbon is disposed of by complete burning.



Production


Activated carbon is carbon produced from carbonaceous source materials such as bamboo, coconut husk, willow peat, wood, coir, lignite, coal, and petroleum pitch. It can be produced by one of the following processes:




  1. Physical activation: The source material is developed into activated carbons using hot gases. Air is then introduced to burn out the gasses, creating a graded, screened and de-dusted form of activated carbon. This is generally done by using one or a combination of the following processes:


    • Carbonization: Material with carbon content is pyrolyzed at temperatures in the range 600–900 °C, usually in inert atmosphere with gases like argon or nitrogen


    • Activation/Oxidation: Raw material or carbonized material is exposed to oxidizing atmospheres (oxygen or steam) at temperatures above 250 °C, usually in the temperature range of 600–1200 °C.




  2. Chemical activation: Prior to carbonization, the raw material is impregnated with certain chemicals. The chemical is typically an acid, strong base,[1][2] or a salt[15] (phosphoric acid, potassium hydroxide, sodium hydroxide, calcium chloride, and zinc chloride 25%). Then, the raw material is carbonized at lower temperatures (450–900 °C). It is believed that the carbonization / activation step proceeds simultaneously with the chemical activation.[clarification needed] Chemical activation is preferred over physical activation owing to the lower temperatures and shorter time needed for activating material.



Classification


Activated carbons are complex products which are difficult to classify on the basis of their behaviour, surface characteristics and other fundamental criteria. However, some broad classification is made for general purpose based on their size, preparation methods, and industrial applications.



Powdered activated carbon


See also: Powdered activated carbon treatment



A micrograph of activated charcoal (R 1) under bright field illumination on a light microscope. Notice the fractal-like shape of the particles hinting at their enormous surface area. Each particle in this image, despite being only around 0.1 mm across, can have a surface area of several square centimeters. The entire image covers a region of approximately 1.1 by 0.7 mm, and the full resolution version is at a scale of 6.236 pixels/μm.


Normally, activated carbons (R 1) are made in particulate form as powders or fine granules less than 1.0 mm in size with an average diameter between 0.15 and 0.25 mm. Thus they present a large surface to volume ratio with a small diffusion distance.[clarification needed] Activated carbon (R 1) is defined as the activated carbon particles retained on a 50-mesh sieve (0.297 mm).


PAC material is finer material. PAC is made up of crushed or ground carbon particles, 95–100% of which will pass through a designated mesh sieve. The ASTM classifies particles passing through an 80-mesh sieve (0.177 mm) and smaller as PAC. It is not common to use PAC in a dedicated vessel, due to the high head loss that would occur. Instead, PAC is generally added directly to other process units, such as raw water intakes, rapid mix basins, clarifiers, and gravity filters.



Granular activated carbon




A micrograph of activated charcoal (GAC) under scanning electron microscope


Granular activated carbon (GAC) has a relatively larger particle size compared to powdered activated carbon and consequently, presents a smaller external surface. Diffusion of the adsorbate is thus an important factor. These carbons are suitable for adsorption of gases and vapors, because they diffuse rapidly. Granulated carbons are used for water treatment, deodorization and separation of components of flow system and is also used in rapid mix basins. GAC can be either in granular or extruded form. GAC is designated by sizes such as 8×20, 20×40, or 8×30 for liquid phase applications and 4×6, 4×8 or 4×10 for vapor phase applications. A 20×40 carbon is made of particles that will pass through a U.S. Standard Mesh Size No. 20 sieve (0.84 mm) (generally specified as 85% passing) but be retained on a U.S. Standard Mesh Size No. 40 sieve (0.42 mm) (generally specified as 95% retained). AWWA (1992) B604 uses the 50-mesh sieve (0.297 mm) as the minimum GAC size. The most popular aqueous phase carbons are the 12×40 and 8×30 sizes because they have a good balance of size, surface area, and head loss characteristics.



Extruded activated carbon


Extruded activated carbon (EAC) combines powdered activated carbon with a binder, which are fused together and extruded into a cylindrical shaped activated carbon block with diameters from 0.8 to 130 mm. These are mainly used for gas phase applications because of their low pressure drop, high mechanical strength and low dust content. Also sold as CTO filter (Chlorine, Taste, Odor).



Bead activated carbon (BAC)


Bead activated carbon (BAC) is made from petroleum pitch and supplied in diameters from approximately 0.35 to 0.80 mm. Similar to EAC, it is also noted for its low pressure drop, high mechanical strength and low dust content, but with a smaller grain size. Its spherical shape makes it preferred for fluidized bed applications such as water filtration.



Impregnated carbon


Porous carbons containing several types of inorganic impregnate such as iodine, silver, cations such as Al, Mn, Zn, Fe, Li, Ca have also been prepared for specific application in air pollution control especially in museums and galleries. Due to its antimicrobial and antiseptic properties, silver loaded activated carbon is used as an adsorbent for purification of domestic water. Drinking water can be obtained from natural water by treating the natural water with a mixture of activated carbon and Al(OH)3, a flocculating agent. Impregnated carbons are also used for the adsorption of Hydrogen Sulfide(H2S) and thiols. Adsorption rates for H2S as high as 50% by weight have been reported.



Polymer coated carbon


This is a process by which a porous carbon can be coated with a biocompatible polymer to give a smooth and permeable coat without blocking the pores. The resulting carbon is useful for hemoperfusion. Hemoperfusion is a treatment technique in which large volumes of the patient's blood are passed over an adsorbent substance in order to remove toxic substances from the blood.




Woven activated carbon cloth



Woven carbon


There is a technology of processing technical rayon fiber into activated carbon cloth for carbon filtering. Adsorption capacity of activated cloth is greater than that of activated charcoal (BET theory surface area: 500–1500 m2/g, pore volume: 0.3–0.8 cm3/g). Thanks to the different forms of activated material, it can be used in a wide range of applications (supercapacitors, odour-absorbers, CBRN defense industry etc.).



Properties


A gram of activated carbon can have a surface area in excess of 500 m2 (5,400 sq ft), with 3,000 m2 (32,000 sq ft) being readily achievable.[2][4][5] Carbon aerogels, while more expensive, have even higher surface areas, and are used in special applications.


Under an electron microscope, the high surface-area structures of activated carbon are revealed. Individual particles are intensely convoluted and display various kinds of porosity; there may be many areas where flat surfaces of graphite-like material run parallel to each other,[2] separated by only a few nanometers or so. These micropores provide superb conditions for adsorption to occur, since adsorbing material can interact with many surfaces simultaneously. Tests of adsorption behaviour are usually done with nitrogen gas at 77 K under high vacuum, but in everyday terms activated carbon is perfectly capable of producing the equivalent, by adsorption from its environment, liquid water from steam at 100 °C (212 °F) and a pressure of 1/10,000 of an atmosphere.


James Dewar, the scientist after whom the Dewar (vacuum flask) is named, spent much time studying activated carbon and published a paper regarding its adsorption capacity with regard to gases.[16] In this paper, he discovered that cooling the carbon to liquid nitrogen temperatures allowed it to adsorb significant quantities of numerous air gases, among others, that could then be recollected by simply allowing the carbon to warm again and that coconut based carbon was superior for the effect. He uses oxygen as an example, wherein the activated carbon would typically adsorb the atmospheric concentration (21%) under standard conditions, but release over 80% oxygen if the carbon was first cooled to low temperatures.


Physically, activated carbon binds materials by van der Waals force or London dispersion force.


Activated carbon does not bind well to certain chemicals, including alcohols, diols, strong acids and bases, metals and most inorganics, such as lithium, sodium, iron, lead, arsenic, fluorine, and boric acid.


Activated carbon adsorbs iodine very well. The iodine capacity, mg/g, (ASTM D28 Standard Method test) may be used as an indication of total surface area.


Carbon monoxide is not well adsorbed by activated carbon. This should be of particular concern to those using the material in filters for respirators, fume hoods or other gas control systems as the gas is undetectable to the human senses, toxic to metabolism and neurotoxic.


Substantial lists of the common industrial and agricultural gases adsorbed by activated carbon can be found online.[17]


Activated carbon can be used as a substrate for the application of various chemicals to improve the adsorptive capacity for some inorganic (and problematic organic) compounds such as hydrogen sulfide (H2S), ammonia (NH3), formaldehyde (HCOH), mercury (Hg) and radioactive iodine-131(131I). This property is known as chemisorption.



Iodine number


Many carbons preferentially adsorb small molecules. Iodine number is the most fundamental parameter used to characterize activated carbon performance.
It is a measure of activity level (higher number indicates higher degree of activation,[citation needed]) often reported in mg/g (typical range 500–1200 mg/g).
It is a measure of the micropore content of the activated carbon (0 to 20 Å, or up to 2 nm) by adsorption of iodine from solution.
It is equivalent to surface area of carbon between 900 and 1100 m2/g.
It is the standard measure for liquid-phase applications.


Iodine number is defined as the milligrams of iodine adsorbed by one gram of carbon when the iodine concentration in the residual filtrate is at a concentration of 0.02 normal (i.e. 0.02N). Basically, iodine number is a measure of the iodine adsorbed in the pores and, as such, is an indication of the pore volume available in the activated carbon of interest. Typically, water-treatment carbons have iodine numbers ranging from 600 to 1100. Frequently, this parameter is used to determine the degree of exhaustion of a carbon in use. However, this practice should be viewed with caution, as chemical interactions with the adsorbate may affect the iodine uptake, giving false results. Thus, the use of iodine number as a measure of the degree of exhaustion of a carbon bed can only be recommended if it has been shown to be free of chemical interactions with adsorbates and if an experimental correlation between iodine number and the degree of exhaustion has been determined for the particular application.



Molasses


Some carbons are more adept at adsorbing large molecules.
Molasses number or molasses efficiency is a measure of the mesopore content of the activated carbon (greater than 20 Å, or larger than 2 nm) by adsorption of molasses from solution.
A high molasses number indicates a high adsorption of big molecules (range 95–600). Caramel dp (decolorizing performance) is similar to molasses number. Molasses efficiency is reported as a percentage (range 40%–185%) and parallels molasses number (600 = 185%, 425 = 85%).
The European molasses number (range 525–110) is inversely related to the North American molasses number.


Molasses Number is a measure of the degree of decolorization of a standard molasses solution that has been diluted and standardized against standardized activated carbon. Due to the size of color bodies, the molasses number represents the potential pore volume available for larger adsorbing species. As all of the pore volume may not be available for adsorption in a particular waste water application, and as some of the adsorbate may enter smaller pores, it is not a good measure of the worth of a particular activated carbon for a specific application. Frequently, this parameter is useful in evaluating a series of active carbons for their rates of adsorption. Given two active carbons with similar pore volumes for adsorption, the one having the higher molasses number will usually have larger feeder pores resulting in more efficient transfer of adsorbate into the adsorption space.



Tannin


Tannins are a mixture of large and medium size molecules.
Carbons with a combination of macropores and mesopores adsorb tannins.
The ability of a carbon to adsorb tannins is reported in parts per million concentration (range 200 ppm–362 ppm).



Methylene blue


Some carbons have a mesopore (20 Å to 50 Å, or 2 to 5 nm) structure which adsorbs medium size molecules, such as the dye methylene blue.
Methylene blue adsorption is reported in g/100g (range 11–28 g/100g).



Dechlorination


Some carbons are evaluated based on the dechlorination half-life length, which measures the chlorine-removal efficiency of activated carbon. The dechlorination half-value length is the depth of carbon required to reduce the chlorine level of a flowing stream from 5 ppm to 3.5 ppm. A lower half-value length indicates superior performance.



Apparent density


The solid or skeletal density of activated carbons will typically range between 2000 and 2100 kg/m3 (125–130 lbs./cubic foot). However, a large part of an activated carbon sample will consist of air space between particles, and the actual or apparent density will therefore be lower, typically 400 to 500 kg/m3 (25–31 lbs./cubic foot).[18]


Higher density provides greater volume activity and normally indicates better-quality activated carbon.
ASTM D 2854 -09 (2014) is used to determine the apparent density of activated carbon.



Hardness/abrasion number


It is a measure of the activated carbon’s resistance to attrition.
It is an important indicator of activated carbon to maintain its physical integrity and withstand frictional forces. There are large differences in the hardness of activated carbons, depending on the raw material and activity levels.



Ash content


Ash reduces the overall activity of activated carbon and reduces the efficiency of reactivation.
The metal oxides (Fe2O3) can leach out of activated carbon resulting in discoloration. Acid/water-soluble ash content is more significant than total ash content. Soluble ash content can be very important for aquarists, as ferric oxide can promote algal growths. A carbon with a low soluble ash content should be used for marine, freshwater fish and reef tanks to avoid heavy metal poisoning and excess plant/algal growth.
Standard method D 2866-2011 is used to determine the ash content of activated carbon.



Carbon tetrachloride activity


Measurement of the porosity of an activated carbon by the adsorption of saturated carbon tetrachloride vapour.



Particle size distribution


The finer the particle size of an activated carbon, the better the access to the surface area and the faster the rate of adsorption kinetics. In vapour phase systems this needs to be considered against pressure drop, which will affect energy cost. Careful consideration of particle size distribution can provide significant operating benefits.
However, in the case of using activated carbon for adsorption of minerals such as gold, the particle size should be in the range of 3.35–1.4 millimetres (0.132–0.055 in). Activated carbon with particle size less than 1 mm would not be suitable for elution (the stripping of mineral from an activated carbon).



Modification of properties and reactivity


Acid-base, oxidation-reduction and specific adsorption characteristics are strongly dependent on the composition of the surface functional groups.[19]


The surface of conventional activated carbon is reactive, capable of oxidation by atmospheric oxygen and oxygen plasma[20][21][22][23][24][25][26][27] steam,[28][29][30] and also carbon dioxide[24] and ozone.[31][32][33]


Oxidation in the liquid phase is caused by a wide range of reagents (HNO3, H2O2, KMnO4).[34][35][36]


Through the formation of a large number of basic and acidic groups on the surface of oxidized carbon to sorption and other properties can differ significantly from the unmodified forms.[19]


Activated carbon can be nitrogenated by natural products or polymers[37][38] or processing of carbon with nitrogenating reagents.[39][40][41]


Activated carbon can interact with chlorine,[42][43]bromine[44] and fluorine.[45]


Surface of activated carbon, like other carbon materials can be fluoralkylated by treatment with (per)fluoropolyether peroxide[46] in a liquid phase, or with wide range of fluoroorganic substances by CVD-method.[47] Such materials combine high hydrophobicity and chemical stability with electrical and thermal conductivity and can be used as electrode material for supercapacitors.[48]


Sulfonic acid functional groups can be attached to activated carbon to give "starbons" which can be used to selectively catalyse the esterification of fatty acids.[49] Formation of such activated carbons from halogenated precursors gives a more effective catalyst which is thought to be a result of remaining halogens improving stability.[50] It is reported about synthesis of activated carbon with chemically grafted superacid sites –CF2SO3H.[51]


Some of the chemical properties of activated carbon have been attributed to presence of the surface active carbon double bond.[33][52]


The Polyani adsorption theory is a popular method for analyzing adsorption of various organic substances to their surface.



Examples of adsorption



Heterogeneous catalysis


The most commonly encountered form of chemisorption in industry, occurs when a solid catalyst interacts with a gaseous feedstock, the reactant/s. The adsorption of reactant/s to the catalyst surface creates a chemical bond, altering the electron density around the reactant molecule and allowing it to undergo reactions that would not normally be available to it.



Reactivation and regeneration




World's largest reactivation plant located in Feluy [fr], Belgium.




Activated carbon reactivation center in Roeselare, Belgium.


The reactivation or the regeneration of activated carbons involves restoring the adsorptive capacity of saturated activated carbon by desorbing adsorbed contaminants on the activated carbon surface.



Thermal reactivation


The most common regeneration technique employed in industrial processes is thermal reactivation.[53] The thermal regeneration process generally follows three steps:[54]



  • Adsorbent drying at approximately 105 °C (221 °F)

  • High temperature desorption and decomposition (500–900 °C (932–1,652 °F)) under an inert atmosphere

  • Residual organic gasification by a non-oxidising gas (steam or carbon dioxide) at elevated temperatures (800 °C (1,470 °F))


The heat treatment stage utilises the exothermic nature of adsorption and results in desorption, partial cracking and polymerization of the adsorbed organics. The final step aims to remove charred organic residue formed in the porous structure in the previous stage and re-expose the porous carbon structure regenerating its original surface characteristics. After treatment the adsorption column can be reused. Per adsorption-thermal regeneration cycle between 5–15 wt% of the carbon bed is burnt off resulting in a loss of adsorptive capacity.[55] Thermal regeneration is a high energy process due to the high required temperatures making it both an energetically and commercially expensive process.[54] Plants that rely on thermal regeneration of activated carbon have to be of a certain size before it is economically viable to have regeneration facilities onsite. As a result, it is common for smaller waste treatment sites to ship their activated carbon cores to specialised facilities for regeneration.[56]



Other regeneration techniques


Current concerns with the high energy/cost nature of thermal regeneration of activated carbon has encouraged research into alternative regeneration methods to reduce the environmental impact of such processes. Though several of the regeneration techniques cited have remained areas of purely academic research, some alternatives to thermal regeneration systems have been employed in industry. Current alternative regeneration methods are:



  • Chemical and solvent regeneration[57]

  • Microbial regeneration[58]


  • Electrochemical regeneration[59]

  • Ultrasonic regeneration[60]

  • Wet air oxidation[61]



See also



  • Biochar

  • Bamboo charcoal

  • Binchōtan

  • Bone char

  • Carbon filtering

  • Conjugated microporous polymer

  • Kværner-process

  • Onboard refueling vapor recovery

  • Carbocatalysis

  • Hydrogen storage



References





  1. ^ abcdefghi "Activated carbon monoliths for methane storage". Bulletin of the American Physical Society. 57 (1). 2012-03-01..mw-parser-output cite.citation{font-style:inherit}.mw-parser-output .citation q{quotes:"""""""'""'"}.mw-parser-output .citation .cs1-lock-free a{background:url("//upload.wikimedia.org/wikipedia/commons/thumb/6/65/Lock-green.svg/9px-Lock-green.svg.png")no-repeat;background-position:right .1em center}.mw-parser-output .citation .cs1-lock-limited a,.mw-parser-output .citation .cs1-lock-registration a{background:url("//upload.wikimedia.org/wikipedia/commons/thumb/d/d6/Lock-gray-alt-2.svg/9px-Lock-gray-alt-2.svg.png")no-repeat;background-position:right .1em center}.mw-parser-output .citation .cs1-lock-subscription a{background:url("//upload.wikimedia.org/wikipedia/commons/thumb/a/aa/Lock-red-alt-2.svg/9px-Lock-red-alt-2.svg.png")no-repeat;background-position:right .1em center}.mw-parser-output .cs1-subscription,.mw-parser-output .cs1-registration{color:#555}.mw-parser-output .cs1-subscription span,.mw-parser-output .cs1-registration span{border-bottom:1px dotted;cursor:help}.mw-parser-output .cs1-ws-icon a{background:url("//upload.wikimedia.org/wikipedia/commons/thumb/4/4c/Wikisource-logo.svg/12px-Wikisource-logo.svg.png")no-repeat;background-position:right .1em center}.mw-parser-output code.cs1-code{color:inherit;background:inherit;border:inherit;padding:inherit}.mw-parser-output .cs1-hidden-error{display:none;font-size:100%}.mw-parser-output .cs1-visible-error{font-size:100%}.mw-parser-output .cs1-maint{display:none;color:#33aa33;margin-left:0.3em}.mw-parser-output .cs1-subscription,.mw-parser-output .cs1-registration,.mw-parser-output .cs1-format{font-size:95%}.mw-parser-output .cs1-kern-left,.mw-parser-output .cs1-kern-wl-left{padding-left:0.2em}.mw-parser-output .cs1-kern-right,.mw-parser-output .cs1-kern-wl-right{padding-right:0.2em}


  2. ^ abcdefghijk "Adsorbed Methane Film Properties in Nanoporous Carbon Monoliths". Bulletin of the American Physical Society. 58 (1). 2013-03-20.


  3. ^ ""Properties of Activated Carbon", CPL Caron Link, accessed 2008-05-02". Archived from the original on 19 June 2012. Retrieved 13 October 2014.


  4. ^ ab Dillon, Edward C; Wilton, John H; Barlow, Jared C; Watson, William A (1989-05-01). "Large surface area activated charcoal and the inhibition of aspirin absorption". Annals of Emergency Medicine. 18 (5): 547–552. doi:10.1016/S0196-0644(89)80841-8.


  5. ^ ab P. J. Paul. "Value Added Products from Gasification – Activated Carbon" (PDF). Bangalore: The Combustion, Gasification and Propulsion Laboratory (CGPL) at the Indian Institute of Science (IISc).


  6. ^ "Charcoal, Activated". The American Society of Health-System Pharmacists. Retrieved 23 April 2014.


  7. ^ Elliott CG, Colby TV, Kelly TM, Hicks HG (1989). "Charcoal lung. Bronchiolitis obliterans after aspiration of activated charcoal". Chest. 96 (3): 672–4. doi:10.1378/chest.96.3.672. PMID 2766830.


  8. ^ EPA Alumni Association: Senior EPA officials discuss early implementation of the Safe Drinking Water Act of 1974, Video, Transcript (see pages 15-16).


  9. ^ "Industrial Water Treatment | High-Purity Water | Treatment Services". Culligan Industrial Water. Retrieved 2018-02-15.


  10. ^ Activated Charcoal Review Sheet, USDA Organic Materials Review, February 2002.


  11. ^ Activated Carbon Petition, USDA Organic Materials Review petition, Canadaigua Wine, May 2002.


  12. ^ "Alliance for Collaborative Research in Alternative Fuel Technology". All-craft.missouri.edu. Retrieved 2014-03-13.


  13. ^ Bourke, Marta (1989). "Activated Carbon for Mercury Removal". Archived from the original on 2013-08-03. Retrieved 2013-08-27.


  14. ^ Tim Flannery, Here On Earth: A New Beginning, Allen Lane (2011), p. 186.


  15. ^ J.Romanos; et al. (2012). "Nanospace engineering of KOH activated carbon". Nanotechnology. 23 (1): 015401. Bibcode:2012Nanot..23a5401R. doi:10.1088/0957-4484/23/1/015401.


  16. ^ The separation of the most volatile gases from air without liquefaction


  17. ^ "SentryAir". SentryAir. Retrieved 2014-03-13.


  18. ^ TIGG Corporation. Granular activated carbon selection Archived 2012-09-12 at the Wayback Machine. Published 2012-05-8, retrieved 2012-09-21.


  19. ^ ab Philippe Serp, José Luis Figueiredo, Carbon Materials for Catalysis, Wiley, – 2009, – 550 p.


  20. ^ Gómez-Serrano, V.; Piriz-Almeida, F. N.; Durán-Valle, C. J.; Pastor-Villegas, J. (1999). "Formation of oxygen structures by air activation. A study by FT-IR spectroscopy". Carbon. 37 (10): 1517–1528. doi:10.1016/S0008-6223(99)00025-1.


  21. ^ Machnikowski J.; Kaczmarska H.; Gerus-Piasecka I.; Diez M.A.; Alvarez R.; Garcia R. (2002). "Structural modification of coal-tar pitch fractions during mild oxidation – relevance to carbonization behavior". Carbon. 40 (11): 1937–1947. doi:10.1016/s0008-6223(02)00029-5.


  22. ^ Petrov N.; Budinova T.; Razvigorova M.; Ekinci E.; Yardim F.; Minkova V. (2000). "Preparation and characterization of carbon adsorbents from furfural". Carbon. 38 (15): 2069–2075. doi:10.1016/s0008-6223(00)00063-4.


  23. ^ Garcia A.B.; Martinez-Alonso A.; Leon C. A.; Tascon J.M.D. (1998). "Modification of the surface properties of an activated carbon by oxygen plasma treatment". Fuel. 77 (1): 613–624.


  24. ^ ab Saha B.; Tai M.H.; Streat M. (2001). "Study of activated carbon after oxidation and subsequent treatment characterization". Process safety and environmental protection. 79 (4): 211–217. doi:10.1205/095758201750362253.


  25. ^ Polovina M.; Babic B.; Kaluderovic B.; Dekanski A. (1997). "Surface characterization of oxidized activated carbon cloth". Carbon. 35 (8): 1047–1052. doi:10.1016/s0008-6223(97)00057-2.


  26. ^ Fanning P.E.; Vannice M.A. (1993). "A DRIFTS study of the formation of surface groups on carbon by oxidation". Carbon. 31 (5): 721–730. doi:10.1016/0008-6223(93)90009-y.


  27. ^ Youssef A.M.; Abdelbary E.M.; Samra S.E.; Dowidar A.M. (1991). "Surface-properties of carbons obtained from polyvinyl-chloride". Ind. J. Chem. A. 30 (10): 839–843.


  28. ^ Arriagada R.; Garcia R.; Molina-Sabio M.; Rodriguez-Reinoso F. (1997). "Effect of steam activation on the porosity and chemical nature of activated carbons from Eucalyptus globulus and peach stones". Microporous Mat. 8 (3–4): 123–130. doi:10.1016/s0927-6513(96)00078-8.


  29. ^ Molina-Sabio M.; Gonzalez M.T.; Rodriguez-Reinoso F.; Sepulveda-Escribano A. (1996). "Effect of steam and carbon dioxide activation in the micropore size distribution of activated carbon". Carbon. 34 (4): 505–509. doi:10.1016/0008-6223(96)00006-1.


  30. ^ Bradley RH, Sutherland I, Sheng E (1996). "Carbon surface: Area, porosity, chemistry, and energy". Journal of Colloid and Interface Science. 179 (2): 561–569. Bibcode:1996JCIS..179..561B. doi:10.1006/jcis.1996.0250.


  31. ^ Sutherland I.; Sheng E.; Braley R.H.; Freakley P.K. (1996). "Effects of ozone oxidation on carbon black surfaces". J. Mater. Sci. 31 (21): 5651–5655. Bibcode:1996JMatS..31.5651S. doi:10.1007/bf01160810.


  32. ^ Rivera-Utrilla J, Sanchez-Polo M (2002). "The role of dispersive and electrostatic interactions in the aqueous phase adsorption of naphthalenesulphonic acids on ozone-treated activated carbons". Carbon. 40 (14): 2685–2691. doi:10.1016/s0008-6223(02)00182-3.


  33. ^ ab Valdés, H.; Sánchez-Polo, M.; Rivera-Utrilla, J.; Zaror, C. A. (2002). "Effect of Ozone Treatment on Surface Properties of Activated Carbon". Langmuir. 18 (6): 2111–2116. doi:10.1021/la010920a.


  34. ^ Pradhan B.K.; Sandle N.K. (1999). "Effect of different oxidizing agent treatments on the surface properties of activated carbons". Carbon. 37 (8): 1323–1332. doi:10.1016/s0008-6223(98)00328-5.


  35. ^ Acedo-Ramos M.; Gomez-Serrano V.; Valenzuella-Calahorro C.; Lopez-Peinado A.J. (1993). "Oxydation of activated carbon in liquid phase. Study by FT-IR". Spectroscopy letters. 26 (6): 1117–1137. Bibcode:1993SpecL..26.1117A. doi:10.1080/00387019308011598.


  36. ^ Gomez-Serrano V.; Acedo-Ramos M.; Lopez-Peinado A.J.; Valenzuela-Calahorro C. (1991). "Stability towards heating and outgassing of activated carbon oxidized in the liquid-phase". Thermochimica Acta. 176: 129–140. doi:10.1016/0040-6031(91)80268-n.


  37. ^ Stőhr B.; Boehm H.P.; Schlőgl R. (1991). "Enhancement of the catalytic activity of activated carbons in oxidation reactions by termal treatment with ammonia or hydrogen cyanide and observation of a superoxide species as a possible intermediate". Carbon. 29 (6): 707–720. doi:10.1016/0008-6223(91)90006-5.


  38. ^ Biniak S.; Szymański G.; Siedlewski J.; Światkowski A. (1997). "The characterizaíion of activated carbons with oxygen and nitrogen surface groups". Carbon. 35 (12): 1799–1810. doi:10.1016/s0008-6223(97)00096-1.


  39. ^ Boudou J.P.; Chehimi M.; Broniek E.; Siemieniewska T.; Bimer J. (2003). "Adsorption of H2S or SO2 on an activated carbon cloth modified by ammonia treatment". Carbon. 41 (10): 1999–2007. doi:10.1016/s0008-6223(03)00210-0.


  40. ^ Sano H.; Ogawa H. (1975). "Preparation and application nitrogen containing active carbons". Osaka Kogyo Gijutsu Shirenjo. 26 (5): 2084–2086.


  41. ^ Radkevich, V. Z.; Senko, T. L.; Wilson, K.; Grishenko, L. M.; Zaderko, A. N.; Diyuk, V. Y. (2008). "The influence of surface functionalization of activated carbon on palladium dispersion and catalytic activity in hydrogen oxidation". Applied Catalysis A: General. 335 (2): 241–251. doi:10.1016/j.apcata.2007.11.029.


  42. ^ Evans, M. J. B.; Halliop, E.; Liang, S.; MacDonald, J. A. F. (1998). "The effect of chlorination on surface properties of activated carbon". Carbon. 36 (11): 1677–1682. doi:10.1016/S0008-6223(98)00165-1.


  43. ^ Papirer, E. N.; Lacroix, R.; Donnet, J. B.; Nansé, G. R.; Fioux, P. (1995). "XPS study of the halogenation of carbon black—Part 2. Chlorination". Carbon. 33: 63–72. doi:10.1016/0008-6223(94)00111-C.


  44. ^ Papirer, Eugène; Lacroix, Renaud; Donnet, Jean-Baptiste; Nanse, Gérard; Fioux, Philippe (1994). "XPS Study of the halogenation of carbon black-part 1. Bromination". Carbon. 32 (7): 1341–1358. doi:10.1016/0008-6223(94)90121-X.


  45. ^ Nansé, G.; Papirer, E.; Fioux, P.; Moguet, F.; Tressaud, A. (1997). "Fluorination of carbon blacks: An X-ray photoelectron spectroscopy study: III. Fluorination of different carbon blacks with gaseous fluorine at temperatures below 100 °C influence of the morphology, structure and physico-chemical characteristics of the carbon black on the fluorine fixation". Carbon. 35 (4): 515–528. doi:10.1016/S0008-6223(97)00003-1.


  46. ^ US8648217B2, "Modification of carbonaceous materials", issued 2008-08-04 


  47. ^ US10000382B2, "Method for carbon materials surface modification by the fluorocarbons and derivatives", issued 2015-11-03 


  48. ^ "Fluoroalkylated Nanoporous Carbons: Testing as a Supercapacitor Electrode". Applied Surface Science. 2018-11-20. doi:10.1016/j.apsusc.2018.11.141. ISSN 0169-4332.


  49. ^ Aldana-Pérez, A.; Lartundo-Rojas, L.; Gómez, R.; Niño-Gómez, M. E. (2012). "Sulfonic groups anchored on mesoporous carbon Starbons-300 and its use for the esterification of oleic acid". Fuel. 100: 128–138. doi:10.1016/j.fuel.2012.02.025.


  50. ^ Diyuk, V. E.; Zaderko, A. N.; Grishchenko, L. M.; Yatsymyrskiy, A. V.; Lisnyak, V. V. (2012). "Efficient carbon-based acid catalysts for the propan-2-ol dehydration". Catalysis Communications. 27: 33–37. doi:10.1016/j.catcom.2012.06.018.


  51. ^ "WO18194533 METHOD FOR CHEMICAL MODIFICATION OF FLUORINATED CARBONS WITH SULFUR-CONTAINING SUBSTANCE". patentscope.wipo.int. Retrieved 2018-11-24.


  52. ^ Budarin, V. L.; Clark, J. H.; Tavener, S. J.; Wilson, K. (2004). "Chemical reactions of double bonds in activated carbon: Microwave and bromination methods". Chemical Communications (23): 2736. doi:10.1039/B411222A.


  53. ^ Bagreev, A.; Rhaman, H.; Bandosz, T. J (2001). "Thermal regeneration of a spent activated carbon adsorbent previously used as hydrogen sulfide adsorbent". Carbon. 39 (9): 1319–1326. doi:10.1016/S0008-6223(00)00266-9.


  54. ^ ab Sabio, E.; Gonzalez, E.; Gonzalez, J. F.; Gonzalez-Garcia, C. M.; Ramiro, A.; Ganan, J (2004). "Thermal regeneration of activated carbon saturated with p-nitrophenol". Carbon. 42 (11): 2285–2293. doi:10.1016/j.carbon.2004.05.007.


  55. ^ Miguel GS, Lambert SD, Graham NJ (2001). "The regeneration of field spent granular activated carbons". Water Research. 35 (11): 2740–2748. doi:10.1016/S0043-1354(00)00549-2. PMID 11456174.


  56. ^ Alvarez PM, Beltrán FJ, Gómez-Serrano V, Jaramillo J, Rodríguez EM (2004). "Comparison between thermal and ozone regenerations of spent activated carbon exhausted with phenol". Water Research. 38 (8): 2155–2165. doi:10.1016/j.watres.2004.01.030. PMID 15087197.


  57. ^ Martin, R. J.; Wj, N (1997). "The repeated exhaustion and chemical regeneration of activated carbon". Water Research. 21 (8): 961–965. doi:10.1016/S0043-1354(87)80014-3.


  58. ^ Aizpuru A, Malhautier L, Roux JC, Fanlo JL (2003). "Biofiltration of a mixture of volatile organic compounds on granular activated carbon". Biotechnology and Bioengineering. 83 (4): 479–488. doi:10.1002/bit.10691. PMID 12800142.


  59. ^ Narbaitz RM, Karimi-Jashni A (2009). "Electrochemical regeneration of granular activated carbons loaded with phenol and natural organic matter". Environmental Technology. 30 (1): 27–36. doi:10.1080/09593330802422803. PMID 19213463.


  60. ^ Lim JL, Okada M (2005). "Regeneration of granular activated carbon using ultrasound". Ultrasonic-Sono-Chemistry. 12 (4): 277–285. doi:10.1016/j.ultsonch.2004.02.003. PMID 15501710.


  61. ^ Shende RV, Mahajani VV (2002). "Wet oxidative regeneration of activated carbon loaded with reactive dye". Waste Management. 22 (1): 73–83. doi:10.1016/S0956-053X(01)00022-8. PMID 11942707.




External links








  • "Imaging the atomic structure of activated carbon" – JOURNAL OF PHYSICS: CONDENSED MATTER


  • "How Does Activated Carbon Work?" at Slate


  • "Worshiping the False Idols of Wellness" on activated charcoal as a useless wellness practice at The New York Times












-

Popular posts from this blog

Lambaréné

Image
Place in Moyen-Ogooué, Gabon Lambaréné Street in Lambaréné Lambaréné Location in Gabon Coordinates: 0°41′18″S 10°13′55″E  /  0.68833°S 10.23194°E  / -0.68833; 10.23194 Coordinates: 0°41′18″S 10°13′55″E  /  0.68833°S 10.23194°E  / -0.68833; 10.23194 Country   Gabon Province Moyen-Ogooué Population (2013 census)  • Total 38,775 Lambaréné is a town and the capital of Moyen-Ogooué in Gabon. With a population of 38,775 as of 2013, it is located 75 kilometres south of the equator. Lambaréné is based in the Central African Rainforest at the river Ogooué. This river divides the city into 3 districts: Rive Gauche, Ile Lambaréné and Rive Droite. The Albert Schweitzer Hospital and the districts Adouma and Abongo are located on Rive Droite. The districts Atongowanga, Sahoty, Dakar, Grand Village, Château, Lalala and Bordamur build the Ile Lambaréné. The majority of the people in Lambaréné live in the district Isaac located on Rive Gauche. This distr
Read more

維納斯堡 (華盛頓州)

Image
body.skin-minerva .mw-parser-output table.infobox caption{text-align:center} 維納斯堡 Venersborg （英文） CDP Venersborg, Washington 維納斯堡位置圖 坐标： 45°46′58″N 122°27′43″W  /  45.7828°N 122.462°W  / 45.7828; -122.462 國家   美國 州 華盛頓州 郡 克拉克县 面积  •  总计 27.8 平方公里（10.7 平方英里）  • 陸地 27.8 平方公里（10.7 平方英里）  • 水域 0.0 平方公里（0.0 平方英里） 海拔 155 米（509 英尺） 人口 （2000年）  • 總計 3,274  • 密度 118.0/平方公里（305.6/平方英里） 时区 PST （UTC-8）  • 夏时制 PDT（UTC-7） FIPS碼 53-74585 [1] GNIS編號 1527695 [2] 維納斯堡 （ 英语： Venersborg ）是美国华盛顿州克拉克县的一個普查规定居民点（CDP），2000年美國人口普查時人口為2,085人。 最初為瑞典人聚居地。 參見 維納什堡 参考資料 ^ American FactFinder. United States Census Bureau. [ 2008-01-31 ] .   ^ US Board on Geographic Names. United States Geological Survey. 2007-10-25 [ 2008-01-31 ] .   查 论 编 克拉克县 行政區劃 郡治 ： 溫哥華 市 巴特爾格朗德 | 卡默斯 | 拉申特 | 里奇菲尔德 | 溫哥華 | 瓦休戈 | 林地市‡ 鎮 亞科爾特 CDP 安波伊 | 巴伯頓 | 布拉什普雷里 | 櫻桃樹叢區 |
Read more

Mononymous person

Image
Plato, the Greek philosopher, is universally known by a single name. A mononymous person is an individual who is known and addressed by a single name, or mononym. [a] [b] In some cases, that name has been selected by the individual, who may have originally been given a polynym ("multiple name"). In other cases, it has been determined by the custom of the country [c] or by some interested segment. In the case of historical figures, it may be the only one of the individual's names that has survived and is still known today. Contents 1 Antiquity 2 Medieval uses 2.1 Europe 2.2 The Americas 3 Post-medieval uses 3.1 France 3.2 Other Europe 3.3 North America 4 Royalty 5 Modern times 5.1 Mononym-normal 5.2 Asia 5.3 The West 6 Gallery 7 See also 8 Notes 9 References 10 Bibliography 11 External links Antiquity Narmer The structure of persons' names has varied across ti
Read more