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Sample records for activated carbon process

  1. ACTIVATED CARBON PROCESS FOR TREATMENT OF WASTEWATERS CONTAINING HEXAVALENT CHROMIUM

    EPA Science Inventory

    The removal of hexavalent chromium, Cr(VI), from dilute aqueous solution by an activated carbon process has been investigated. Two removal mechanisms were observed; hexavalent chromium species were removed by adsorption onto the interior carbon surface and/or through reduction to...

  2. APPRAISAL OF POWDERED ACTIVATED CARBON PROCESSES FOR MUNICIPAL WASTEWATER TREATMENT

    EPA Science Inventory

    Powdered activated carbon has been the subject of several developmental efforts directed towards producing improved methods for treating municipal wastewaters. Granular activated carbon has proven itself as an effective means of reducing dissolved organic contaminant levels, but ...

  3. Physicochemical and porosity characteristics of thermally regenerated activated carbon polluted with biological activated carbon process.

    PubMed

    Dong, Lihua; Liu, Wenjun; Jiang, Renfu; Wang, Zhansheng

    2014-11-01

    The characteristics of thermally regenerated activated carbon (AC) polluted with biological activated carbon (BAC) process were investigated. The results showed that the true micropore and sub-micropore volume, pH value, bulk density, and hardness of regenerated AC decreased compared to the virgin AC, but the total pore volume increased. XPS analysis displayed that the ash contents of Al, Si, and Ca in the regenerated AC respectively increased by 3.83%, 2.62% and 1.8%. FTIR spectrum showed that the surface functional groups of virgin and regenerated AC did not change significantly. Pore size distributions indicated that the AC regeneration process resulted in the decrease of micropore and macropore (D>10 μm) volume and the increase of mesopore and macropore (0.1 μmprocess. PMID:25203235

  4. ACTIVATED SLUDGE WITH POWDERED ACTIVATED CARBON TREATMENT OF A DYES AND PIGMENTS PROCESSING WASTEWATER

    EPA Science Inventory

    This paper discusses completed efforts in the treatment of dyes and pigments processing wastewater utilizing the activated sludge process (ASP) enhanced with powdered activated carbon (PAC). The independent variables of the study were solids retention time (SRT) and PAC dosage. T...

  5. Carbon activation process for increased surface accessibility in electrochemical capacitors

    DOEpatents

    Doughty, Daniel H. (Albuquerque, NM); Eisenmann, Erhard T. (Belpre, OH)

    2001-01-01

    A process for making carbon film or powder suitable for double capacitor electrodes having a capacitance of up to about 300 F/cm.sup.3 is disclosed. This is accomplished by treating in aqueous nitric acid for a period of about 5 to 15 minutes thin carbon films obtained by carbonizing carbon-containing polymeric material having a high degree of molecular directionality, such as polyimide film, then heating the treated carbon film in a non-oxidizing atmosphere at a non-graphitizing temperature of at least 350.degree. C. for about 20 minutes, and repeating alternately the nitric acid step and the heating step from 7 to 10 times. Capacitors made with this carbon may find uses ranging from electronic devices to electric vehicle applications.

  6. ACTIVATED CARBON PROCESS FOR THE TREATMENT OF CADMIUM(II)-CONTAINING WASTEWATERS

    EPA Science Inventory

    The removal of cadmium(II) from two synthetic cadmium plating wastewaters by an activated carbon adsorption process has been investigated. Among the 17 different types of activated carbon tested, it was found that the acidic activated carbons, namely Nuchar SA and Nuchar SN exhib...

  7. Process for producing an activated carbon adsorbent with integral heat transfer apparatus

    NASA Technical Reports Server (NTRS)

    Jones, Jack A. (Inventor); Yavrouian, Andre H. (Inventor)

    1996-01-01

    A process for producing an integral adsorbent-heat exchanger apparatus useful in ammonia refrigerant heat pump systems. In one embodiment, the process wets an activated carbon particles-solvent mixture with a binder-solvent mixture, presses the binder wetted activated carbon mixture on a metal tube surface and thereafter pyrolyzes the mixture to form a bonded activated carbon matrix adjoined to the tube surface. The integral apparatus can be easily and inexpensively produced by the process in large quantities.

  8. Ultrahigh surface area carbon from carbonated beverages. Combining self-templaing process and in situ activation

    SciTech Connect

    Zhang, Pengfei; Zhang, Zhiyong; Chen, Jihua; Dai, Sheng

    2015-05-11

    Ultrahigh surface area carbons (USACs, e.g., >2000 m2/g) are attracting tremendous attention due to their outstanding performance in energy-related applications. The state-of-art approaches to USACs involve templating or activation methods and all these techniques show certain drawbacks. In this work, a series of USACs with specific surface areas up to 3633 m2/g were prepared in two steps: hydrothermal carbonization (200 °C) of carbonated beverages (CBs) and further thermal treatment in nitrogen (600–1000 °C). The rich inner porosity is formed by a self-templated process during which acids and polyelectrolyte sodium salts in the beverage formulas make some contribution. This strategy covers various CBs such as Coca Cola®, Pepsi Cola®, Dr. Pepper®, andFanta® and it enables an acceptable product yield (based on sugars), for example: 21 wt% for carbon (2940 m2/g) from Coca Cola®. Being potential electrode materials for supercapacitors, those carbon materials possessed a good specific capacitance (57.2–185.7 F g-1) even at a scan rate of 1000 mV s-1. Thus, a simple and efficient strategy to USACs has been presented.

  9. Ultrahigh surface area carbon from carbonated beverages. Combining self-templaing process and in situ activation

    DOE PAGESBeta

    Zhang, Pengfei; Zhang, Zhiyong; Chen, Jihua; Dai, Sheng

    2015-05-11

    Ultrahigh surface area carbons (USACs, e.g., >2000 m2/g) are attracting tremendous attention due to their outstanding performance in energy-related applications. The state-of-art approaches to USACs involve templating or activation methods and all these techniques show certain drawbacks. In this work, a series of USACs with specific surface areas up to 3633 m2/g were prepared in two steps: hydrothermal carbonization (200 °C) of carbonated beverages (CBs) and further thermal treatment in nitrogen (600–1000 °C). The rich inner porosity is formed by a self-templated process during which acids and polyelectrolyte sodium salts in the beverage formulas make some contribution. This strategy coversmore » various CBs such as Coca Cola®, Pepsi Cola®, Dr. Pepper®, andFanta® and it enables an acceptable product yield (based on sugars), for example: 21 wt% for carbon (2940 m2/g) from Coca Cola®. Being potential electrode materials for supercapacitors, those carbon materials possessed a good specific capacitance (57.2–185.7 F g-1) even at a scan rate of 1000 mV s-1. Thus, a simple and efficient strategy to USACs has been presented.« less

  10. Influence of process parameters on the surface and chemical properties of activated carbon obtained from biochar by chemical activation.

    PubMed

    Ang?n, Dilek; Altintig, Esra; Kse, Tijen Ennil

    2013-11-01

    Activated carbons were produced from biochar obtained through pyrolysis of safflower seed press cake by chemical activation with zinc chloride. The influences of process variables such as the activation temperature and the impregnation ratio on textural and chemical-surface properties of the activated carbons were investigated. Also, the adsorptive properties of activated carbons were tested using methylene blue dye as the targeted adsorbate. The experimental data indicated that the adsorption isotherms are well described by the Langmuir equilibrium isotherm equation. The optimum conditions resulted in activated carbon with a monolayer adsorption capacity of 128.21 mg g(-1) and carbon content 76.29%, while the BET surface area and total pore volume corresponded to 801.5m(2)g(-1) and 0.393 cm(3)g(-1), respectively. This study demonstrated that high surface area activated carbons can be prepared from the chemical activation of biochar with zinc chloride as activating agents. PMID:24080293

  11. DEVELOPMENT OF THE WESTVACO ACTIVATED CARBON PROCESS FOR SOX RECOVERY AS ELEMENTAL SULFUR. VOLUME I

    EPA Science Inventory

    The report gives results of a demonstration (in a 20,000-cfh integral pilot plant) of an all-dry, fluidized-bed process, using activated carbon for recovering SO2 as elemental sulfur. Granular carbon was recycled continuously more than 20 times between contact with flue gas from ...

  12. DEVELOPMENT OF THE WESTVACO ACTIVATED CARBON PROCESS FOR SOX RECOVERY AS ELEMENTAL SULFUR. VOLUME II. APPENDIX

    EPA Science Inventory

    The report gives results of a demonstration (in a 20,000-cfh integral pilot plant) of an all-dry, fluidized-bed process, using activated carbon for recovering SO2 as elemental sulfur. Granular carbon was recycled continuously more than 20 times between contact with flue gas from ...

  13. Production of activated carbons from waste tire--process design and economical analysis.

    PubMed

    Ko, Danny C K; Mui, Edward L K; Lau, Ken S T; McKay, Gordon

    2004-01-01

    The process design and economic analysis of process plants to produce activated carbons from waste tires and coal have been performed. The potential range of products from each process has been considered, namely for waste tire--pyro-gas, active carbon, carbon black and pyro-oil; for coal--pyro-gas and active carbons. Sensitivity analyses have been carried out on the main process factors; these are product price, production capacity, total production cost, capital investment and the tipping fee. Net present values for the two plants at various discount factors have been determined and the internal rates of return have been determined as 27.4% and 18.9% for the waste tire plant and the coal plant, respectively. PMID:15504665

  14. PROCESS DESCRIPTION AND PRODUCT COST TO MANUFACTURE SUGARCANE BAGASSE-BASED GRANULAR ACTIVATED CARBON

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Process flow diagrams and manufacturing costs were developed to convert sugarcane bagasse to granular activated carbon. Unit operations in the conversion process consisted of milling, pelletization, pyrolysis/activation, washing with acid and water, and drying/screening/collecting of the final prod...

  15. Increasing the sorption activity of carbon adsorbents by electron-beam processing and fullerene microadditives

    NASA Astrophysics Data System (ADS)

    Myakin, S. V.; Nikonova, V. Yu.; Korsakov, V. G.; Samonin, V. V.

    2011-09-01

    The sorption capacity of activated carbon with respect to Cu2+ cations was found to be enhanced considerably upon its chemical modification with fullerenes and during its electron-beam processing. It was discovered that introducing fullerenes (20 ?g/g) into activated carbon leads to a change in the chemical composition of its surface, due to changes in the system of conjugated bonds in activated carbon leading to an increase in the content of Brnsted acid (p K a 0-5) and weakly base (p K a 8-11) sites capable of cation exchange on the material surface. We conclude that electron-beam processing (optimal dose, 25-50 kGy) facilitates the rearrangement of bonds on the surface of activated carbon, thereby increasing the number of Lewis base and Brnsted acid sites capable of adsorbing metal ions in accordance with the donor-acceptor and cation-exchange mechanism, respectively.

  16. Interactions of xanthines with activated carbon. I. Kinetics of the adsorption process

    NASA Astrophysics Data System (ADS)

    Navarrete Casas, R.; Garca Rodriguez, A.; Rey Bueno, F.; Espnola Lara, A.; Valenzuela Calahorro, C.; Navarrete Guijosa, A.

    2006-06-01

    Because of their pharmaceutical and industrial applications, we have studied the adsorption of xanthine derivates (caffeine and theophylline) by activated carbon. To this end, we examined kinetic, equilibrium and thermodynamic aspects of the process. This paper reports the kinetics results. The experimental results indicate that the process was first order in C and the overall process was assumed to involve a single, reversible adsorption-desorption process obeying a kinetic law postulated by us.

  17. Dye removal of activated carbons prepared from NaOH-pretreated rice husks by low-temperature solution-processed carbonization and H3PO4 activation.

    PubMed

    Chen, Yun; Zhai, Shang-Ru; Liu, Na; Song, Yu; An, Qing-Da; Song, Xiao-Wei

    2013-09-01

    A coupling of low-temperature sulfuric acid-assisted carbonization and H3PO4 activation was employed to convert NaOH-pretreated rice husks into activated carbons with extremely high surface area (2028 m(2) g(-1)) and integrated characteristics. The influences of the activation temperature and impregnation ratio on the surface area, pore volume of activated carbons were thoroughly investigated. The morphology and surface chemistry of activated carbons were characterized using N2 sorption, FTIR, XPS, SEM, TEM, etc. The adsorption capacity of resulting carbons obtained under optimum preparation conditions was systematically evaluated using methylene blue under various simulated conditions. The adsorption process can be well described by both Langmuir isotherm model and the pseudo-second order kinetics models; and the maximum monolayer capacity of methylene blue was ca. 578 mg g(-1). PMID:23892148

  18. Mechanistic investigation of industrial wastewater naphthenic acids removal using granular activated carbon (GAC) biofilm based processes.

    PubMed

    Islam, Md Shahinoor; Zhang, Yanyan; McPhedran, Kerry N; Liu, Yang; Gamal El-Din, Mohamed

    2016-01-15

    Naphthenic acids (NAs) found in oil sands process-affected waters (OSPW) have known environmental toxicity and are resistant to conventional wastewater treatments. The granular activated carbon (GAC) biofilm treatment process has been shown to effectively treat OSPW NAs via combined adsorption/biodegradation processes despite the lack of research investigating their individual contributions. Presently, the NAs removals due to the individual processes of adsorption and biodegradation in OSPW bioreactors were determined using sodium azide to inhibit biodegradation. For raw OSPW, after 28 days biodegradation and adsorption contributed 14% and 63% of NA removal, respectively. For ozonated OSPW, biodegradation removed 18% of NAs while adsorption reduced NAs by 73%. Microbial community 454-pyrosequencing of bioreactor matrices indicated the importance of biodegradation given the diverse carbon degrading families including Acidobacteriaceae, Ectothiorhodospiraceae, and Comamonadaceae. Overall, results highlight the ability to determine specific processes of NAs removals in the combined treatment process in the presence of diverse bacteria metabolic groups found in GAC bioreactors. PMID:26410699

  19. Carbon wastewater treatment process

    NASA Technical Reports Server (NTRS)

    Humphrey, M. F.; Simmons, G. M.; Dowler, W. L.

    1974-01-01

    A new powdered-carbon treatment process is being developed for the elimination of the present problems, associated with the disposal of biologically active sewage waste solids, and with water reuse. This counter-current flow process produces an activated carbon, which is obtained from the pyrolysis of the sewage solids, and utilizes this material to remove the adulterating materials from the water. Additional advantages of the process are the elimination of odors, the removal of heavy metals, and the potential for energy conservation.

  20. Polymer flotation and activated carbon adsorption treatment for in situ tar sand process water

    SciTech Connect

    McTernan, W.F.; Blanton, W.E.; Boardman, G.D.; Nolan, B.T.; Kocornik, D.J.

    1986-01-01

    Process waters collected during a Department of Energy's in situ tar sand extraction experiment near Vernal, Utah were treated by polymer assisted induced air flotation and activated carbon adsorption. The flotation process removed over 99 percent of the organic load as emulsified bitumen but did little to reduce residual toxicity in the effluents. Activated carbon adsorption was needed to remove the toxic materials from the waste stream. GC/MS analysis, using a modification of the EPA Method 625, yielded an estimated 2000 compounds in the untreated process water. Internal and recovery standards present at 10 ppm were totally obscured in the chromatogram. Flotation effluents contained 39 identified organic compounds; none of which was listed on EPA's hazardous chemicals list. Internal and recovery standards were immediately visible in the chromatogram. The GC/MS analysis was unable to determine the chemical basis for the toxic properties present.

  1. Production of granular activated carbon from food-processing wastes (walnut shells and jujube seeds) and its adsorptive properties.

    PubMed

    Bae, Wookeun; Kim, Jongho; Chung, Jinwook

    2014-08-01

    Commercial activated carbon is a highly effective absorbent that can be used to remove micropollutants from water. As a result, the demand for activated carbon is increasing. In this study, we investigated the optimum manufacturing conditions for producing activated carbon from ligneous wastes generated from food processing. Jujube seeds and walnut shells were selected as raw materials. Carbonization and steam activation were performed in a fixed-bed laboratory electric furnace. To obtain the highest iodine number, the optimum conditions for producing activated carbon from jujube seeds and walnut shells were 2 hr and 1.5 hr (carbonization at 700 degrees C) followed by 1 hr and 0.5 hr (activation at 1000 degrees C), respectively. The surface area and iodine number of activated carbon made from jujube seeds and walnut shells were 1,477 and 1,184 m2/g and 1,450 and 1,200 mg/g, respectively. A pore-distribution analysis revealed that most pores had a pore diameter within or around 30-40 angstroms, and adsorption capacity for surfactants was about 2 times larger than the commercial activated carbon, indicating that waste-based activated carbon can be used as alternative. Implications: Wastes discharged from agricultural and food industries results in a serious environmental problem. A method is proposed to convert food-processing wastes such as jujube seeds and walnut shells into high-grade granular activated carbon. Especially, the performance of jujube seeds as activated carbon is worthy of close attention. There is little research about the application ofjujube seeds. Also, when compared to two commercial carbons (Samchully and Calgon samples), the results show that it is possible to produce high-quality carbon, particularly from jujube seed, using a one-stage, 1,000 degrees C, steam pyrolysis. The preparation of activated carbon from food-processing wastes could increase economic return and reduce pollution. PMID:25185390

  2. Biological activated carbon process for treatment of potato processing wastewater for in-plant reuse. Technical completion report

    SciTech Connect

    Hung, Y.T.; Priebe, B.D.

    1981-10-01

    Like many other food processing industries, potato processing could create a serious pollution problem. An average-sized processing plant, producing french fries and dehydrated potatoes, can generate a waste load equivalent to a city of 200,000 people. Any discharge of wastes into these waters would immediately result in detrimental effects to the environment. In a plant processing 15,000 tons of potatoes per year, 60 million gallons of water are required. With proper treatment, a large percentage of the wastewater could be reclaimed and reused in the potato processing plant. The scope of the study includes the operation of completely mixed activated sludge (CMAS) reactors as secondary treatment, and anaerobic upflow continuous biological activated carbon (BAC) and biological sand columns as tertiary treatment for potato processing wastewaters.

  3. Effect of ozone on the performance of a hybrid ceramic membrane-biological activated carbon process.

    PubMed

    Guo, Jianning; Hu, Jiangyong; Tao, Yi; Zhu, Jia; Zhang, Xihui

    2014-04-01

    Two hybrid processes including ozonation-ceramic membrane-biological activated carbon (BAC) (Process A) and ceramic membrane-BAC (Process B) were compared to treat polluted raw water. The performance of hybrid processes was evaluated with the removal efficiencies of turbidity, ammonia and organic matter. The results indicated that more than 99% of particle count was removed by both hybrid processes and ozonation had no significant effect on its removal. BAC filtration greatly improved the removal of ammonia. Increasing the dissolved oxygen to 30.0 mg/L could lead to a removal of ammonia with concentrations as high as 7.80 mg/L and 8.69 mg/L for Processes A and B, respectively. The average removal efficiencies of total organic carbon and ultraviolet absorbance at 254 nm (UV254, a parameter indicating organic matter with aromatic structure) were 49% and 52% for Process A, 51% and 48% for Process B, respectively. Some organic matter was oxidized by ozone and this resulted in reduced membrane fouling and increased membrane flux by 25%-30%. However, pre-ozonation altered the components of the raw water and affected the microorganisms in the BAC, which may impact the removals of organic matter and nitrite negatively. PMID:25079408

  4. Dewatering Peat With Activated Carbon

    NASA Technical Reports Server (NTRS)

    Rohatgi, N. K.

    1984-01-01

    Proposed process produces enough gas and carbon to sustain itself. In proposed process peat slurry is dewatered to approximately 40 percent moisture content by mixing slurry with activated carbon and filtering with solid/liquid separation techniques.

  5. Protein Immobilization on Carbon Nanotubes Via a Two-Step Process of Diimide-Activated Amidation

    SciTech Connect

    Jiang, Kuiyang; Schadler, Linda S.; Siegel, Richard W.; Zhang, Xinjie; Zhang, Haifeng; Terrones, Mauricio

    2004-11-06

    Carbon nanotubes exhibit interesting electrical, structural and mechanical properties that make them highly promising nanoscale building blocks for the construction of novel functional materials. Many potential applications have been proposed, such as conductive and high-strength composites, field emission displays, fuel cells, sensors, and hydrogen storage media. In addition, biosensors for detecting abnormalities and bio-fuel cells for embedded devices are among the most exciting applications. In order to create the synergy between the biomolecules and nanotubes required to realize these applications, biomolecules, such as proteins and DNAs, must be connected to the carbon nanotubes. This connection can be non-covalent interaction or covalent bonding. There have been several reports on the immobilization of biomolecules on carbon nanotubes, and most of them use non-covalent interaction. The best stability, accessibility and selectivity, however, will be achieved through covalent bonding because of its capability to control the location of the biomolecule, improve stability, accessibility and selectivity and reduce leaching. In the present study, we report the covalent bonding of proteins to nitrogen-doped multiwalled carbon nanotubes (CNx MWNTs) via a two-step process of diimide-activated amidation between the carboxylic acid groups on CNx MWNTs and the amine groups on proteins.

  6. Active processes on a mixed clastic carbonate Brazilian shelf margin: Importance for hydrocarbon exploration in turbidites

    SciTech Connect

    Cainelli, C. )

    1991-03-01

    The search for subtle hydrocarbon accumulations in turbidite systems requires additional approaches for more successful exploration, particularly when direct recognition on seismic lines is difficult. This includes the determination and understanding of processes controlling sand distribution on the shelf and the mapping of sand pathways from the shelf to the slop/basin that can guide efforts to look for more favorable sites for turbidite sandstone deposition. The approach can be exemplified in the Sergipe-Alagoas basin, on the Brazillian Atlantic passive margin. The section analyzed is the Piacabucu Formation, a thick seaward prograding wedge composed of coastal sandstones and shelf edge carbonates on a narrow shelf and slope-basin shales with turbidite lenses. Waves and currents control the redistribution of sediments transported to the shelf by rivers. More wave energy is expended in ten hours in the San Francisco delta than in an entire year in the Mississippi delta. Such environment precludes deposition of mud on the shelf, but it stimulates the development of shelf edge carbonates. Rimed carbonates along the shelf break serve as a barrier for downslope movements of coarse-grained sediment, where turbidites are oil targets. The search for gaps in the carbonate barrier which can tap the behind-barrier sands is critical for sand-rich turbidite development. It is believed that canyons create these gaps and act as active turbidity current routes.

  7. The effect of processing conditions on microstructure of Pd-containing activated carbon fibers

    SciTech Connect

    Wu, Xianxian; Gallego, Nidia C; Contescu, Cristian I; Tekinalp, Halil; Bhat, Vinay V; Baker, Frederick S; Thies, Mark C

    2008-01-01

    Palladium-doped activated carbon fibers are being evaluated as candidate materials for enhanced hydrogen storage at near ambient conditions. Pd-doped fibers were spun using a Pd salt mixed with an isotropic pitch precursor. Experimental techniques such as in-situ X-ray analysis, thermogravimetric studies, scanning transmission electron microscopy and gas adsorption were employed to understand how processing conditions for the production of Pd-doped activated carbon fibers affect the microstructure, pore development, and dispersion of metal particles throughout the fibers. The results showed that PdO phase is present in the stabilized fibers and that this oxide phase is stable up to about 250 aC. The oxide phase transforms into Pd metal with increasing heat treatment temperature, going through the formation of an intermediate carbide phase. Sintering of Pd particles was observed with heat treatment at temperatures over 750 aC. It was also found that pore development during physical activation with CO2 was not significantly affected by the presence of Pd particles within the fibers.

  8. Ozone-biological activated carbon as a pretreatment process for reverse osmosis brine treatment and recovery.

    PubMed

    Lee, Lai Yoke; Ng, How Yong; Ong, Say Leong; Hu, Jiang Yong; Tao, Guihe; Kekre, Kiran; Viswanath, Balakrishnan; Lay, Winson; Seah, Harry

    2009-09-01

    Ozonation was used in this study to improve biodegradability of RO brine from water reclamation facilities. An ozone dosage ranging from 3 to 10 mg O(3)/L and contact times of 10 and 20 min in batch studies were found to increase the biodegradability (BOD(5)/TOC ratio) of the RO brine by 1.8-3.5 times. At the same time, total organic carbon (TOC) removal was in the range of 5.3-24.5%. The lab-scale ozone-biological activated carbon (BAC) at an ozone dosage of 6.0mg O(3)/L with 20-min contact time was able to achieve 3 times higher TOC removal compared to using BAC alone. Further processing with Capacitive Deionization (CDI) process was able to generate a product water with better water quality than the RO feed water, i.e., with more than 80% ions removal and a lower TOC concentration. The ozone-BAC pretreatment has the potential of reducing fouling in the CDI process. PMID:19580984

  9. Toxicity of carbon nanotubes to the activated sludge process - examination of extracellular polymeric substances

    NASA Astrophysics Data System (ADS)

    Thakor, Harshrajsinh

    This thesis examines the effects of two types of single walled carbon nanotubes, namely, long single walled carbon nanotubes (LSWCNTs) and functionalized long single walled carbon nanotubes (FLSWCNTs) on the respiratory activity of the activated sludge microbial communities by a respiration inhibition test. The effectiveness of the extracellular polymeric substances (EPS) in protecting the microbial communities within the activated sludge against the CNTs was determined by using both sheared and unsheared activated sludge. The results showed that CNTs were more toxic under the sheared condition compared to the unsheared condition. LSWCNTS were more toxic towards sheared activated sludge compared to unsheared activated sludge. In case of FLSWCNTs similar inhibition was observed for sheared and unsheared activated sludge and FLSWCNTs were more toxic than LSWCNTs in unsheared activated sludge.

  10. SYSTEMATIC SCANNING ELECTRON MICROSCOPY TECHNIQUE FOR EVALUATING COMBINED BIOLOIGCAL/GRANULAR ACTIVATED CARBON TREATMENT PROCESSES

    EPA Science Inventory

    A systematic scanning election microscope analytical technique has been developed to examine granular activated carbon used a a medium for biomass attachment in liquid waste treatment. The procedure allows for the objective monitoring, comparing, and trouble shooting of combined ...

  11. New Carbon Activation Process for Increased Surface Accessibility in Electrochemical Capacitors

    SciTech Connect

    Doughty, Daniel H.; Eisenmann, Erhard T.

    1999-03-16

    A process for making carbon film or powder suitable for double capacitor electrodes having a capacitance of up to about 300 F/cm{sup 3} is disclosed. This is accomplished by treating in aqueous nitric acid for a period of about 5 to 15 minutes thin carbon films obtained by carbonizing carbon-containing polymeric material having a high degree of molecular directionality, such as polyimide film, then heating the treated carbon film in a non-oxidizing atmosphere at a non-graphitizing temperature of at least 350 C for about 20 minutes, and repeating alternately the nitric acid step and the heating step from 7 to 10 times. Capacitors made with this carbon may find uses ranging from electronic devices to electric vehicle applications.

  12. Adsorption studies on wastewaters from cypermethrin manufacturing process using activated coconut shell carbon.

    PubMed

    Bhuvaneswari, K; Ravi Prasad, P; Sarma, P N

    2007-10-01

    Cypermethrin is a pyrethroid pesticide and is used in the control of a wide range of insects on crops like vegetables, cereals, maize etc. In the present study, the adsorption efficiency of coconut shell based activated carbon for the removal of color and organic matter from cypermethrin pesticide manufacturing industrial wastewater was investigated. Effect of carbon dosage, pH and contact time on the removal of COD was also studied. Equilibrium and kinetic studies were carried out and the data was fitted in Freundlich and Langmuir models. The study proved that activated coconut shell carbon (acc) is an efficient adsorbent for treatment of cypermethrin industrial wastewaters under study. PMID:18476373

  13. Treatment of coke-oven wastewater with the powdered activated carbon-contact stabilization activated sludge process. Final report

    SciTech Connect

    Suidan, M.T.; Deady, M.A.; Gee, C.S.

    1983-11-01

    The objective of the study was to determine optimum parameters for the operation of an innovative process train used in the treatment of coke-over wastewater. The treatment process train consisted of a contact-stabilization activated sludge system with powdered activated carbon (PAC) addition, followed by activated sludge nitrification, followed by denitrification in an anoxic filter. The control and operating parameters evaluated during the study were: (a) the average mixed-liquor PAC concentration maintained in the contact-stabilization system, (b) the solids retention time practiced in the contact-stabilization system, and (c) the hydraulic detention time maintained in the contact aeration tank. Three identical treatement process trains were constructed and employed in this study. The coke-oven wastewater used for this investigation was fed to the treatment units at 30% strength. The first part of the study was devoted to determining the interactions between the mixed liquor PAC concentration and the solids retention time in the contact-stabilization tanks. Results showed that optimum overall system performance is attainable when the highest sludge age (30 day) and highest mixed liquor PAC concentration were practiced. During the second phase of the study, all three systems were operated at a 30 day solids retention time while different detention times of 1, 2/3 and 1/3 day were evaluated in the contact tank. PAC addition rates were maintained at the former levels and, consequently, reduced contact times entailed higher mixed liquor carbon concentrations. Once again, the system receiving the highest PAC addition rate of PAC exhibited the best overall performance. This system exhibited no deterioration in process performance as a result of decreased contact detention time. 72 references, 41 figures, 24 tables.

  14. Removal of diclofenac by conventional drinking water treatment processes and granular activated carbon filtration.

    PubMed

    Rigobello, Eliane Sloboda; Dantas, Angela Di Bernardo; Di Bernardo, Luiz; Vieira, Eny Maria

    2013-06-01

    This study was carried out to evaluate the efficiency of conventional drinking water treatment processes with and without pre-oxidation with chlorine and chlorine dioxide and the use of granular activated carbon (GAC) filtration for the removal of diclofenac (DCF). Water treatment was performed using the Jar test with filters on a lab scale, employing nonchlorinated artesian well water prepared with aquatic humic substances to yield 20HU true color, kaolin turbidity of 70 NTU and 1mgL(-1) DCF. For the quantification of DCF in water samples, solid phase extraction and HPLC-DAD methods were developed and validated. There was no removal of DCF in coagulation with aluminum sulfate (3.47mgAlL(-1) and pH=6.5), flocculation, sedimentation and sand filtration. In the treatment with pre-oxidation and disinfection, DCF was partially removed, but the concentration of dissolved organic carbon (DOC) was unchanged and byproducts of DCF were observed. Chlorine dioxide was more effective than chorine in oxidizing DCF. In conclusion, the identification of DCF and DOC in finished water indicated the incomplete elimination of DCF through conventional treatments. Nevertheless, conventional drinking water treatment followed by GAC filtration was effective in removing DCF (⩾99.7%). In the oxidation with chlorine, three byproducts were tentatively identified, corresponding to a hydroxylation, aromatic substitution of one hydrogen by chlorine and a decarboxylation/hydroxylation. Oxidation with chlorine dioxide resulted in only one byproduct (hydroxylation). PMID:23540811

  15. GRANULAR ACTIVATED CARBON INSTALLATIONS

    EPA Science Inventory

    This paper presents a compilation and summary of design criteria, performance, and cost data from 22 operating municipal and industrial granular activated carbon (GAC) installations that treat water and wastewater or process food and beverage products. Guidance for using this inf...

  16. Performance of magnetic activated carbon composite as peroxymonosulfate activator and regenerable adsorbent via sulfate radical-mediated oxidation processes.

    PubMed

    Oh, Wen-Da; Lua, Shun-Kuang; Dong, Zhili; Lim, Teik-Thye

    2015-03-01

    Magnetic activated carbon composite (CuFe2O4/AC, MACC) was prepared by a co-precipitation-calcination method. The MACC consisted of porous micro-particle morphology with homogeneously distributed CuFe2O4 and possessed high magnetic saturation moment (8.1 emu g(-1)). The performance of MACC was evaluated as catalyst and regenerable adsorbent via peroxymonosulfate (PMS, Oxone()) activation for methylene blue (MB) removal. Optimum CuFe2O4/AC w/w ratio was 1:1.5 giving excellent performance and can be reused for at least 3 cycles. The presence of common inorganic ions, namely Cl(-) and NO3(-) did not exert significant influence on MB degradation but humic acid decreased the MB degradation rate. As a regenerable adsorbent, negligible difference in regeneration efficiency was observed when a higher Oxone() dosage was employed but a better efficiency was obtained at a lower MACC loading. The factors hindering complete MACC regeneration are MB adsorption irreversibility and AC surface modification by PMS making it less favorable for subsequent MB adsorption. With an additional mild heat treatment (150 C) after regeneration, 82% of the active sites were successfully regenerated. A kinetic model incorporating simultaneous first-order desorption, second-order adsorption and pseudo-first order degradation processes was numerically-solved to describe the rate of regeneration. The regeneration rate increased linearly with increasing Oxone():MACC ratio. The MACC could potentially serve as a catalyst for PMS activation and regenerable adsorbent. PMID:25463211

  17. ACTIVATED CARBON FROM BROILER LITTER: PROCESS DESCRIPTION AND COST OF PRODUCTION

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Animal manure continues to represent a significantly large and problematic portion of the U.S. agricultural waste generated yearly. Granular activated carbons made from pelletized poultry litter have been shown to adsorb various positively charged metal ions from laboratory prepared solutions. Bas...

  18. Modification process optimization, characterization and adsorption property of granular fir-based activated carbon

    NASA Astrophysics Data System (ADS)

    Chen, Congjin; Li, Xin; Tong, Zhangfa; Li, Yue; Li, Mingfei

    2014-10-01

    Granular fir-based activated carbon (GFAC) was modified with H2O2, and orthogonal array experimental design method was used to optimize the process. The properties of the original and modified GFAC were characterized by N2 adsorption-desorption isotherms, Brunauer-Emmett-Teller (BET) equation, Barett-Joyner-Halenda (BJH) equation, field emission scanning electron microscopy (FESEM), and Fourier transform infrared spectroscopy (FT-IR) analysis, etc. When 10.00 g of GFAC with particle size of 0.25-0.85 mm was modified by 150.0 ml of aqueous H2O2 solution, the optimized conditions were found to be as follows: aqueous H2O2 solution concentration 1.0 moll-1, modification temperature 30.0 C, modification time 4.0 h. Modified under the optimized conditions, decolonization of caramel, methylene blue adsorption, phenol adsorption and iodine number of the modified GFAC increased by 500.0%, 59.7%, 32.5%, and 15.1%, respectively. The original and optimally modified GFAC exhibited adsorption isotherms of hybrid Type I-IV isotherms with H4 hysteresis. BET surface area, micropore area, total pore volume, micropore volume, and microporosity of the modified GFAC increased by 7.33%, 11.25%, 3.89%, 14.23%, 9.91%, respectively. Whereas the average pore width decreased by 3.16%. In addition, the amount of surface oxygen groups (such as carbonyl or carboxyl) increased in the modified GFAC.

  19. Thermal removal of mercury in spent powdered activated carbon from TOXECON process

    SciTech Connect

    Okwadha, G.D.O.; Li, J.; Ramme, B.; Kollakowsky, D.; Michaud, D.

    2009-10-15

    This research developed and demonstrated a technology to liberate Hg adsorbed onto powdered activated carbon (PAC) by the TOXECON process using pilot-scale high temperature air slide (HTAS) and bench-scale thermogravimetric analyzer (TGA). The HTAS removed 65, 83, and 92% of Hg captured with PAC when ran at 900{sup o}F, 1,000{sup o}F, and 1,200 {sup o}F, respectively, while the TGA removed 46 and 100% of Hg at 800 {sup o}F and 900{sup o}F, respectively. However, addition of CuO-Fe{sub 2}O{sub 3} mixture and CuCl catalysts enhanced Hg removal and PAC regeneration at lower temperatures. CuO-Fe{sub 2}O{sub 3} mixture performed better than CuCl in PAC regeneration. Scanning electron microscopy images and energy dispersive X-ray analysis show no change in PAC particle aggregation or chemical composition. Thermally treated sorbents had higher surface area and pore volume than the untreated samples indicating regeneration. The optimum temperature for PAC regeneration in the HTAS was 1,000{sup o}F. At this temperature, the regenerated sorbent had sufficient adsorption capacity similar to its virgin counterpart at 33.9% loss on ignition. Consequently, the regenerated PAC may be recycled back into the system by blending it with virgin PAC.

  20. Visualization and Measurement of Adsorption/Desorption Process of Ethanol in Activated Carbon Adsorber

    NASA Astrophysics Data System (ADS)

    Asano, Hitoshi; Murata, Kenta; Takenaka, Nobuyuki; Saito, Yasushi

    Adsorption refrigerator is one of the efficient tools for waste heat recovery, because the system is driven by heat at relative low temperature. However, the coefficient of performance is low due to its batch operation and the heat capacity of the adsorber. In order to improve the performance, it is important to optimize the configuration to minimize the amount of driving heat, and to clarify adsorption/desorption phenomena in transient conditions. Neutron radiography was applied to visualize and measure the adsorption amount distribution in an adsorber. The visualization experiments had been performed at the neutron radiography facility of E-2 port of Kyoto University Research Reactor. Activated carbon and ethanol were used as the adsorbent and refrigerant. From the acquired radiographs, adsorption amount was quantitatively measured by applying the umbra method using a checkered neutron absorber with boron powder. Then, transient adsorption and desorption processes of a rectangular adsorber with 84 mm in width, 50 mm in height and 20 mm in depth were visualized. As the result, the effect of fins in the adsorbent layer on the adsorption amount distribution was clearly visualized.

  1. Pilot scale study and design of a granular activated carbon regeneration process using supercritical fluids

    SciTech Connect

    Tomasko, D.L.; Hay, K.J. ); Leman, G.W. ); Eckert, C.A. )

    1993-08-01

    A technology which has great potential for environmental control and waste remediation is contaminant removal and separation with supercritical fluids (SCF's) or supercritical fluid extraction (SFE). Pressure tuning of solvent power allows SCF processes to adapt to a wide variety of small batch oriented separations typified by environmental cleanup operations. The ability of supercritical CO[sub 2] to extract model contaminant compounds from GAC and subsequently drop out most of the contaminant in a liquid phase has been investigated in a pilot scale apparatus. Typical desorption profiles indicate an 85% removal of the compound from the carbon which allows for reuse. The desorption results have been interpreted with a generalized desorption-mass transfer model. The results of the pilot plant studies have been applied to the design of a fixed-site GAC regeneration unit consisting of a three-element desorber with two-stage flash separation. Optimization of the process centers around minimizing the cost of recycling the SCF through an efficient recompression scheme and cycle configuration in the desorber unit. An economic evaluation shows a processing cost of 10.6 cents/lb (23 cents/kg) GAC which compares favorably with thermal regeneration and incineration. This non-destructive process allows re-use of the GAC while maintaining a high adsorbate capacity, which reduces carbon replacement costs and significantly decreases the need for carbon disposal by landfill or incineration. 25 refs., 13 figs., 3 tabs.

  2. Carbon dioxide removal process

    DOEpatents

    Baker, Richard W.; Da Costa, Andre R.; Lokhandwala, Kaaeid A.

    2003-11-18

    A process and apparatus for separating carbon dioxide from gas, especially natural gas, that also contains C.sub.3+ hydrocarbons. The invention uses two or three membrane separation steps, optionally in conjunction with cooling/condensation under pressure, to yield a lighter, sweeter product natural gas stream, and/or a carbon dioxide stream of reinjection quality and/or a natural gas liquids (NGL) stream.

  3. Activated carbon from biomass

    NASA Astrophysics Data System (ADS)

    Manocha, S.; Manocha, L. M.; Joshi, Parth; Patel, Bhavesh; Dangi, Gaurav; Verma, Narendra

    2013-06-01

    Activated carbon are unique and versatile adsorbents having extended surface area, micro porous structure, universal adsorption effect, high adsorption capacity and high degree of surface reactivity. Activated carbons are synthesized from variety of materials. Most commonly used on a commercial scale are cellulosic based precursors such as peat, coal, lignite wood and coconut shell. Variation occurs in precursors in terms of structure and carbon content. Coir having very low bulk density and porous structure is found to be one of the valuable raw materials for the production of highly porous activated carbon and other important factor is its high carbon content. Exploration of good low cost and non conventional adsorbent may contribute to the sustainability of the environment and offer promising benefits for the commercial purpose in future. Carbonization of biomass was carried out in a horizontal muffle furnace. Both carbonization and activation were performed in inert nitrogen atmosphere in one step to enhance the surface area and to develop interconnecting porosity. The types of biomass as well as the activation conditions determine the properties and the yield of activated carbon. Activated carbon produced from biomass is cost effective as it is easily available as a waste biomass. Activated carbon produced by combination of chemical and physical activation has higher surface area of 2442 m2/gm compared to that produced by physical activation (1365 m2/gm).

  4. Nitrogen removal from coal gasification wastewater by activated carbon technologies combined with short-cut nitrogen removal process.

    PubMed

    Zhao, Qian; Han, Hongjun; Hou, Baolin; Zhuang, Haifeng; Jia, Shengyong; Fang, Fang

    2014-11-01

    A system combining granular activated carbon and powdered activated carbon technologies along with shortcut biological nitrogen removal (GAC-PACT-SBNR) was developed to enhance total nitrogen (TN) removal for anaerobically treated coal gasification wastewater with less need for external carbon resources. The TN removal efficiency in SBNR was significantly improved by introducing the effluent from the GAC process into SBNR during the anoxic stage, with removal percentage increasing from 43.8%-49.6% to 68.8%-75.8%. However, the TN removal rate decreased with the progressive deterioration of GAC adsorption. After adding activated sludge to the GAC compartment, the granular carbon had a longer service-life and the demand for external carbon resources became lower. Eventually, the TN removal rate in SBNR was almost constant at approx. 43.3%, as compared to approx. 20.0% before seeding with sludge. In addition, the production of some alkalinity during the denitrification resulted in a net savings in alkalinity requirements for the nitrification reaction and refractory chemical oxygen demand (COD) degradation by autotrophic bacteria in SBNR under oxic conditions. PACT showed excellent resilience to increasing organic loadings. The microbial community analysis revealed that the PACT had a greater variety of bacterial taxons and the dominant species associated with the three compartments were in good agreement with the removal of typical pollutants. The study demonstrated that pre-adsorption by the GAC-sludge process could be a technically and economically feasible method to enhance TN removal in coal gasification wastewater (CGW). PMID:25458677

  5. Supercritical Carbon Dioxide Extraction of Bioactive Compounds from Ampelopsis grossedentata Stems: Process Optimization and Antioxidant Activity

    PubMed Central

    Wang, Yuefei; Ying, Le; Sun, Da; Zhang, Shikang; Zhu, Yuejin; Xu, Ping

    2011-01-01

    Supercritical carbon dioxide (SC-CO2) extraction of bioactive compounds including flavonoids and phenolics from Ampelopsis grossedentata stems was carried out. Extraction parameters such as pressure, temperature, dynamic time and modifier, were optimized using an orthogonal array design of L9 (34), and antioxidant activities of the extracts were evaluated by 2,2-diphenyl-1-picrylhydrazyl (DPPH) free radical scavenging assay and ferrous ion chelating (FIC) assay. The best conditions obtained for SC-CO2 extraction of flavonoids was 250 bar, 40 °C, 50 min, and with a modifier of methanol/ethanol (1:3, v/v), and that for phenolics extraction was 250 bar, 40 °C, 50 min, and with a modifier of methanol/ethanol (1:1, v/v). Meantime, flavonoids and phenolics were found to be mainly responsible for the DPPH scavenging activity of the extracts, but not for the chelating activity on ferrous ion according to Pearson correlation analysis. Furthermore, several unreported flavonoids such as apigenin, vitexin, luteolin, etc., have been detected in the extracts from A. grossedentata stems. PMID:22072923

  6. Application studies of activated carbon derived from rice husks produced by chemical-thermal process--a review.

    PubMed

    Chen, Yue; Zhu, Yanchao; Wang, Zichen; Li, Ying; Wang, Lili; Ding, Lili; Gao, Xiaoyan; Ma, Yuejia; Guo, Yupeng

    2011-03-15

    The production of functional activated carbon materials starting from cheap natural precursors using environmentally friendly processes is a highly attractive subject in material chemistry today. Recently, much attention has been focused on the use of plant biomass to produce functional carbonaceous materials, encompassing economic, environmental and social issues. Besides the classical route to produce activated carbons from fossil materials, rice husk shows clear advantages in that it can generate a variety of cheap and sustainable carbonaceous materials with attractive nanostructure and functional patterns for a wide range of applications. From a comprehensive literature review, it was found that porous carbon that derived from rice husks, in addition to having wide availability, has fast kinetics and appreciable adsorption capacities too. Porous carbon materials also play a significant role in new applications such as catalytic supports, battery electrodes, capacitors, and gas storage. In this review, an extensive list of rice husks literature has been compiled. Conclusions have been drawn from the literature reviewed, and suggestions for future research are proposed. PMID:21353192

  7. Activated carbon material

    DOEpatents

    Evans, A. Gary

    1978-01-01

    Activated carbon particles for use as iodine trapping material are impregnated with a mixture of selected iodine and potassium compounds to improve the iodine retention properties of the carbon. The I/K ratio is maintained at less than about 1 and the pH is maintained at above about 8.0. The iodine retention of activated carbon previously treated with or coimpregnated with triethylenediamine can also be improved by this technique. Suitable flame retardants can be added to raise the ignition temperature of the carbon to acceptable standards.

  8. Treatment of gas industry wastes using the biological granular activated carbon fluidized bed reactor process. Annual report, August 1994

    SciTech Connect

    Hickey, R.; Wagner, D.; Sunday, A.; Heine, B.; Rajan, R.

    1994-08-01

    The Granular Activated Carbon-Fluidized Bed Reactor (GAC-FBR) system is a high rate process that combines the advantages of biological and physical-chemical treatment in a single unit operation. The process is particularly well-suited to treatment of contaminants present in water and wastewater at relatively low concentrations. Process economics indicate the GAC-FBR can be extremely cost-effective compared to aqueous phase GAC adsorption and air stripping followed by vapor phase control. Accordingly, three field trials are scheduled for the next 18 months; one at a manufactured gas plant site (PAHs), one at a gas dehydration site (BTEX), and one to treat a chlorinated solvent (TCE) at a government installation.

  9. Trade-off between carbon emission and effluent quality of activated sludge processes under seasonal variations of wastewater temperature and mean cell retention time.

    PubMed

    Guo, Jingbo; Fu, Xin; Andrés Baquero, G; Sobhani, Reza; Nolasco, Daniel A; Rosso, Diego

    2016-03-15

    Over the seasonal cycles, the mean cell retention time (MCRT) of the activated sludge process is varied to compensate the wastewater temperature variations. The effects of these variations on the carbon footprint (CFP) and effluent quality index (EQI) of a conventional activated sludge (CAS) process and a nitrification/denitrification (NDN) process were quantified. The carbon emission included both biogenic and non-biogenic carbon. Carbon emissions of wasted biosolids management were also addressed. Our results confirmed that the effluent quality indicated by EQI was not necessarily improved by increasing MCRT. Higher MCRT increased the carbon emission and reduced excess sludge production, which decreased the potential for biogas energy recovery. The NDN process was preferable to the CAS process from the perspective of effluent quality. This consideration extended to the whole plant CFP if the N2O emitted during NDN was limited ([N2O]<1% [NH4(+)]removed) as the carbon emission per unit effluent quality achieved by NDN process is less than that of the CAS process. By putting forward carbon emission intensity (γ) derived from CFP and EQI, our work provides a quantitative tool for decision makers evaluating process alternatives when there is a trade-off between carbon emission and effluent quality. PMID:26789371

  10. Activated carbon to the rescue

    SciTech Connect

    Sen, S.

    1996-03-01

    This article describes the response to pipeline spill of ethylene dichloride (EDC) on the property of an oil company. Activated carbon cleanup proceedure was used. During delivery, changeout, transport, storage, thermal reactivation, and return delivery to the site, the carbon never came into direct contact with operating personnel or the atmosphere. More than 10,000 tones of dredge soil and 50 million gallons of surface water were processed during the emergency response.

  11. Influence of the activating agent and the inert gas (type and flow) used in an activation process for the porosity development of carbon nanofibers.

    PubMed

    Jimnez, Vicente; Snchez, Paula; Valverde, Jos Luis; Romero, Amaya

    2009-08-15

    Carbon nanofibers (CNFs) were activated with different activating agents (KOH, KHCO(3) and K(2)CO(3)). The effects of different activations conditions, including type of protector gas (He, Ar and N(2)) and helium flow rate on the properties of activated carbon nanofibers were studied. The structural changes in activated CNFs were investigated using the following characterization techniques: N(2) adsorption isotherms at 77K, XRD, temperature-programmed desorption of hydrogen, TEM, TPO and elemental composition. The results showed that the surface area increased by a factor of 3.3, 2.0 and 1.8 referred to the parent CNFs after the treatment with KOH, K(2)CO(3) and KHCO(3), respectively. In addition, KOH generated a greater pore volume than the other activating agents; micropores were mainly generated during the process. Finally, different carrier gases were added during the activation in order to study their influence on the pore opening behavior of CNFs. It was found that the activation degree increased in the following order: Ar

  12. Carbon dioxide capture process with regenerable sorbents

    DOEpatents

    Pennline, Henry W.; Hoffman, James S.

    2002-05-14

    A process to remove carbon dioxide from a gas stream using a cross-flow, or a moving-bed reactor. In the reactor the gas contacts an active material that is an alkali-metal compound, such as an alkali-metal carbonate, alkali-metal oxide, or alkali-metal hydroxide; or in the alternative, an alkaline-earth metal compound, such as an alkaline-earth metal carbonate, alkaline-earth metal oxide, or alkaline-earth metal hydroxide. The active material can be used by itself or supported on a substrate of carbon, alumina, silica, titania or aluminosilicate. When the active material is an alkali-metal compound, the carbon-dioxide reacts with the metal compound to generate bicarbonate. When the active material is an alkaline-earth metal, the carbon dioxide reacts with the metal compound to generate carbonate. Spent sorbent containing the bicarbonate or carbonate is moved to a second reactor where it is heated or treated with a reducing agent such as, natural gas, methane, carbon monoxide hydrogen, or a synthesis gas comprising of a combination of carbon monoxide and hydrogen. The heat or reducing agent releases carbon dioxide gas and regenerates the active material for use as the sorbent material in the first reactor. New sorbent may be added to the regenerated sorbent prior to subsequent passes in the carbon dioxide removal reactor.

  13. Optimization of process variables by response surface methodology for malachite green dye removal using lime peel activated carbon

    NASA Astrophysics Data System (ADS)

    Ahmad, Mohd Azmier; Afandi, Nur Syahidah; Bello, Olugbenga Solomon

    2015-04-01

    This study investigates the adsorptive removal of malachite green (MG) dye from aqueous solutions using chemically modified lime-peel-based activated carbon (LPAC). The adsorbent prepared was characterized using FTIR, SEM, Proximate analysis and BET techniques, respectively. Central composite design (CCD) in response surface methodology (RSM) was used to optimize the adsorption process. The effects of three variables: activation temperature, activation time and chemical impregnation ratio (IR) using KOH and their effects on percentage of dye removal and LPAC yield were investigated. Based on CCD design, quadratic models and two factor interactions (2FI) were developed correlating the adsorption variables to the two responses. Analysis of variance (ANOVA) was used to judge the adequacy of the model. The optimum conditions of MG dye removal using LPAC are: activation temperature (796 °C), activation time (1.0 h) and impregnation ratio (2.6), respectively. The percentage of MG dye removal obtained was 94.68 % resulting in 17.88 % LPAC yield. The percentage of error between predicted and experimental results for the removal of MG dye is 0.4 %. Model prediction was in good agreement with experimental results and LPAC was found to be effective in removing MG dye from aqueous solution.

  14. Granular activated carbon for simultaneous adsorption and biodegradation of toxic oil sands process-affected water organic compounds.

    PubMed

    Islam, Md Shahinoor; Zhang, Yanyan; McPhedran, Kerry N; Liu, Yang; Gamal El-Din, Mohamed

    2015-04-01

    Naphthenic acids (NAs) released into oil sands process-affected water (OSPW) during bitumen processing in Northern Alberta are problematic for oil sands industries due to their toxicity in the environment and resistance to degradation during conventional wastewater treatment processes. Granular activated carbon (GAC) has shown to be an effective media in removing biopersistent organics from wastewater using a combination of adsorption and biodegradation removal mechanisms. A simultaneous GAC (0.4g GAC/L) adsorption and biodegradation (combined treatment) study was used for the treatment of raw and ozonated OSPW. After 28 days of batch treatment, classical and oxidized NAs removals for raw OSPW were 93.3% and 73.7%, and for ozonated OSPW were 96.2% and 77.1%, respectively. Synergetic effects of the combined treatment process were observed in removals of COD, the acid extractable fraction, and oxidized NAs, which indicated enhanced biodegradation and bioregeneration in GAC biofilms. A bacteria copy number >10(8) copies/g GAC on GAC surfaces was found using quantitative real time polymerase chain reaction after treatment for both raw and ozonated OSPW. A Microtox() acute toxicity test (Vibrio fischeri) showed effective toxicity removal (>95.3%) for the combined treatments. Therefore, the simultaneous GAC adsorption and biodegradation treatment process is a promising technology for the elimination of toxic OSPW NAs. PMID:25617868

  15. Statistical optimization of adsorption processes for removal of 2,4-dichlorophenol by activated carbon derived from oil palm empty fruit bunches.

    PubMed

    Alam, M Zahangir; Muyibi, Suleyman A; Toramae, Juria

    2007-01-01

    The adsorption capacity of activated carbon produced from oil palm empty fruit bunches through removal of 2,4-dichlorophenol from aqueous solution was carried out in the laboratory. The activated carbon was produced by thermal activation of activation time with 30 min at 800 degrees C. The adsorption process conditions were determined with the statistical optimization followed by central composite design. A developed polynomial model for operating conditions of adsorption process indicated that the optimum conditions for maximum adsorption of phenolic compound were: agitation rate of 100 r/min, contact time of 8 h, initial adsorbate concentration of 250 mg/L and pH 4. Adsorption isotherms were conducted to evaluate biosorption process. Langmuir isotherm was more favorable (R2 = 0.93) for removal of 2,4-dichlorophenol by the activated carbon rather than Freundlich isotherm (R2 = 0.88). PMID:17969639

  16. SIMULTANEOUS MECHANICAL AND HEAT ACTIVATION: A NEW ROUTE TO ENHANCE SERPENTINE CARBONATION REACTIVITY AND LOWER CO2 MINERAL SEQUESTRATION PROCESS COST

    SciTech Connect

    M.J. McKelvy; J. Diefenbacher; R. Nunez; R.W. Carpenter; A.V.G. Chizmeshya

    2005-01-01

    Coal can support a large fraction of global energy demands for centuries to come, if the environmental problems associated with CO{sub 2} emissions can be overcome. Unlike other candidate technologies, which propose long-term storage (e.g., ocean and geological sequestration), mineral sequestration permanently disposes of CO{sub 2} as geologically stable mineral carbonates. Only benign, naturally occurring materials are formed, eliminating long-term storage and liability issues. Serpentine carbonation is a leading mineral sequestration process candidate, which offers large scale, permanent sequestration. Deposits exceed those needed to carbonate all the CO{sub 2} that could be generated from global coal reserves, and mining and milling costs are reasonable ({approx}$4 to $5/ton). Carbonation is exothermic, providing exciting low-cost process potential. The remaining goal is to develop an economically viable process. An essential step in this development is increasing the carbonation reaction rate and degree of completion, without substantially impacting other process costs. Recently, the Albany Research Center (ARC) has accelerated serpentine carbonation, which occurs naturally over geological time, to near completion in less than an hour. While reaction rates for natural serpentine have been found to be too slow for practical application, both heat and mechanical (attrition grinding) pretreatment were found to substantially enhance carbonation reactivity. Unfortunately, these processes are too energy intensive to be cost-effective in their present form. In this project we explored the potential that utilizing power plant waste heat (e.g., available up to {approx}200-250 C) during mechanical activation (i.e., thermomechanical activation) offers to enhance serpentine mineral carbonation, while reducing pretreatment energy consumption and process cost. This project was carried out in collaboration with the Albany Research Center (ARC) to maximize the insight into the potential thermomechanical activation offers. Lizardite was selected as the model serpentine material for investigation, due to the relative structural simplicity of its lamellar structure when compared with the corrugated and spiral structures of antigorite and chrysotile, respectively. Hot-ground materials were prepared as a function of grinding temperature, time, and intensity. Carbonation reactivity was explored using the standard ARC serpentine carbonation test (155 C, 150 atm CO{sub 2}, and 1 hr). The product feedstock and carbonation materials were investigated via a battery of techniques, including X-ray powder diffraction, electron microscopy, thermogravimetric and differential thermal, BET, elemental, and infrared analysis. The incorporation of low-level heat with moderate mechanical activation (i.e., thermomechanical activation) was found to be able to substantially enhance serpentine carbonation reactivity in comparison with moderate mechanical activation alone. Increases in the extent of carbonation of over 70% have been observed in this feasibility study, indicating thermomechanical activation offers substantial potential to lower process cost. Investigations of the thermomechanically activated materials that formed indicate adding low-level heat during moderately intense lizardite mechanical activation promotes (1) energy absorption during activation, (2) structural disorder, and (3) dehydroxylation, as well as carbonation reactivity, with the level of energy absorption, structural disorder and dehydroxylation generally increasing with increasing activation temperature. Increasing activation temperatures were also associated with decreasing surface areas and water absorptive capacities for the activated product materials. The above decreases in surface area and water absorption capacity can be directly correlated with enhanced particle sintering during thermomechanical activation, as evidenced by electron microscopy observation. The level of induced structural disorder appears to be a key parameter in enhancing carbonation reactivity. However, particle sintering may contribute to reduced reactivity. The effectiveness of thermomechanical activation at enhancing carbonation reactivity appears to be a complicated function of a variety of process parameters, including grinding intensity, feedstock-to-media ratio, time, temperature, etc.

  17. Treatment of industrial process effluents and contaminated groundwater using the Biological Granular Activated Carbon-Fluidized Bed Reactor (GAC-FBR) process: Volume 1. Final report

    SciTech Connect

    Benovska, M.; Cook, J.; Groshko, V.; Heine, B.; Hohman, C.

    1996-09-30

    In 1992, Congress allocated funds for development of expertise in applied environmental bioremediation restoration technology including work on process integration, scale-up and demonstration of the Granular Activated Carbon-Fluidized Bed Reactor (GAC-FBR) process. Specific targets included the treatment of chlorinated solvents, nitrated compounds and aromatic hydrocarbons. The goal of this SERDP funded project was to conduct experimental work at the bench-scale through field demonstration using the GAC-FBR as the platform for degradation of these compounds of concern. The results are presented of a three-year program designed to test and demonstrate the GAC-FBR process for a number of problem wastewaters facing the US Armed Forces. Both laboratory-pilot and field demonstrations using small commercial scale GAC-FBR systems were conducted.

  18. Treatment of industrial process effluents and contaminated groundwater using the Biological Granular Activated Carbon-Fluidized Bed Reactor (GAC-FBR) process: Volume 2. Final report

    SciTech Connect

    Benovska, M.; Cook, J.; Groshko, V.; Heine, B.; Hohman, C.

    1996-09-30

    In 1992, Congress allocated funds for development of expertise in applied environmental bioremediation restoration technology including work on process integration, scale-up and demonstration of the Granular Activated Carbon-Fluidized Bed Reactor (GAC-FBR) process. Specific targets included the treatment of chlorinated solvents, nitrated compounds and aromatic hydrocarbons. The goal of this SERDP funded project was to conduct experimental work at the bench-scale through field demonstration using the GAC-FBR as the platform for degradation of these compounds of concern. The results are presented of a three-year program designed to test and demonstrate the GAC-FBR process for a number of problem wastewaters facing the US Armed Forces. Both laboratory-pilot and field demonstrations using small commercial scale GAC-FBR systems were conducted.

  19. The effect of activated carbon addition on membrane bioreactor processes for wastewater treatment and reclamation - A critical review.

    PubMed

    Skouteris, George; Saroj, Devendra; Melidis, Paraschos; Hai, Faisal I; Ouki, Sabèha

    2015-06-01

    This review concentrates on the effect of activated carbon (AC) addition to membrane bioreactors (MBRs) treating wastewaters. Use of AC-assisted MBRs combines adsorption, biodegradation and membrane filtration. This can lead to advanced removal of recalcitrant pollutants and mitigation of membrane fouling. The relative contribution of adsorption and biodegradation to overall removal achieved by an AC-assisted MBR process can vary, and "biological AC" may not fully develop due to competition of target pollutants with bulk organics in wastewater. Thus periodic replenishment of spent AC is necessary. Sludge retention time (SRT) governs the frequency of spent AC withdrawal and addition of fresh AC, and is an important parameter that significantly influences the performance of AC-assisted MBRs. Of utmost importance is AC dosage because AC overdose may aggravate membrane fouling, increase sludge viscosity, impair mass transfer and reduce sludge dewaterability. PMID:25801795

  20. Remove organics by activated carbon adsorption

    SciTech Connect

    Stenzel, M.H. )

    1993-04-01

    Activated carbon has a wide variety of applications in the chemical process industries (CPI), one of which is water and wastewater treatment. Activated carbon is especially effective at removing soluble organic compounds (SOCs) from both surface and groundwater sources. This article focuses on the use of granular activated carbon to remove specific compounds from water sources. It provides a methodology to evaluate adsorption, establish a process design, develop a system design, and estimate preliminary capital and operating costs.

  1. Partial degradation of levofloxacin for biodegradability improvement by electro-Fenton process using an activated carbon fiber felt cathode.

    PubMed

    Gong, Yuexiang; Li, Jiuyi; Zhang, Yanyu; Zhang, Meng; Tian, Xiujun; Wang, Aimin

    2016-03-01

    Solutions of 500mL 200mgL(-1) fluoroquinolone antibiotic levofloxacin (LEVO) have been degraded by anodic oxidation (AO), AO with electrogenerated H2O2 (AO-H2O2) and electro-Fenton (EF) processes using an activated carbon fiber (ACF) felt cathode from the point view of not only LEVO disappearance and mineralization, but also biodegradability enhancement. The LEVO decay by EF process followed a pseudo-first-order reaction with an apparent rate constant of 2.37×10(-2)min(-1), which is much higher than that of AO or AO-H2O2 processes. The LEVO mineralization also evidences the order EF>AO-H2O2>AO. The biodegradability (BOD5/COD) increased from 0 initially to 0.24, 0.09, and 0.03 for EF, AO-H2O2 and AO processes after 360min treatment, respectively. Effects of several parameters such as current density, initial pH and Fe(2+) concentration on the EF degradation have also been examined. Three carboxylic acids including oxalic, formic and acetic acid were detected, as well as the released inorganic ions NH4(+), NO3(-) and F(-). At last, an ultra-performance liquid chromatography coupled with time-of-flight mass spectrometry was used to identify about eight aromatic intermediates formed in 60min of EF treatment, and a plausible mineralization pathway for LEVO by EF treatment was proposed. PMID:26561756

  2. High-rate activated sludge system for carbon management - Evaluation of crucial process mechanisms and design parameters.

    PubMed

    Jimenez, Jose; Miller, Mark; Bott, Charles; Murthy, Sudhir; De Clippeleir, Haydee; Wett, Bernhard

    2015-12-15

    The high-rate activated sludge (HRAS) process is a technology suitable for the removal and redirection of organics from wastewater to energy generating processes in an efficient manner. A HRAS pilot plant was operated under controlled conditions resulting in concentrating the influent particulate, colloidal, and soluble COD to a waste solids stream with minimal energy input by maximizing sludge production, bacterial storage, and bioflocculation. The impact of important process parameters such as solids retention time (SRT), hydraulic residence time (HRT) and dissolved oxygen (DO) levels on the performance of a HRAS system was demonstrated in a pilot study. The results showed that maximum removal efficiencies of soluble COD were reached at a DO > 0.3 mg O2/L, SRT > 0.5 days and HRT > 15 min which indicates that minimizing the oxidation of the soluble COD in the high-rate activated sludge process is difficult. The study of DO, SRT and HRT exhibited high degree of impact on the colloidal and particulate COD removal. Thus, more attention should be focused on controlling the removal of these COD fractions. Colloidal COD removal plateaued at a DO > 0.7 mg O2/L, SRT > 1.5 days and HRT > 30 min, similar to particulate COD removal. Concurrent increase in extracellular polymers (EPS) production in the reactor and the association of particulate and colloidal material into sludge flocs (bioflocculation) indicated carbon capture by biomass. The SRT impacted the overall mass and energy balance of the high-rate process indicating that at low SRT conditions, lower COD mineralization or loss of COD content occurred. In addition, the lower SRT conditions resulted in higher sludge yields and higher COD content in the WAS. PMID:26260539

  3. Solvent-regenerated activated carbon

    SciTech Connect

    McLaughlin, H. )

    1988-07-01

    This report summarizes the results of a University/Industry research project, sponsored by the New York State Energy Research and Development Authority and Fluids Design Corporation. The research project studied the solvent regeneration of activated carbon. Activate carbon was used to remove trace organics from aqueous streams, then regenerated by desorbing the adsorbates with organic solvents. The project included a survey of the potential applications in New York State industries, fundamental research on the adsorption/desorption phenomena, and design of a full-scale process. The economics of the full-scale process were evaluated and compared to alternate available technologies. The result of this work is a versatile process with attractive economics. A wide range of adsorbates and solvents were found to be acceptable for this process. The design methodologies are developed and the techniques for evaluating a new application are delineated. 13 refs., 12 figs., 4 tabs.

  4. Experience in design and commissioning of activated carbon adsorbers - STEAG/a/c/t{sup {trademark}} process in European waste incineration plants

    SciTech Connect

    Brueggendick, H.

    1996-10-01

    STEAG has many experience with designing, engineering, commissioning and operating activated carbon processes for the removal of heavy metals, dioxins and furans from the flue gas of medical, hazardous and municipal waste incinerators and with cleaning industrial flue gases from an HCl production plant. The first medical waste incinerator with an activated carbon adsorber commenced commercial operation in 1991, with excellent results. In March 1992, the hazardous waste incineration plant for a flue gas volume of 77,000 m{sup 3}/h SC started operation. The 6 STEAG activated carbon units for volumes of 155,000 m{sup 3}/h SC each have been in operation at a municipal solid waste incinerator since 1993. Line 7 at the same location is now in the startup phase. Municipal solid waste incinerator with an hourly flue gas flow rate of 292,000 m{sup 3}/h SC and 4 x 168,000 m{sup 3}/h SC are currently under start operation. An NCl production plant equipped with a STEAG /a/c/t{trademark}. Process for dioxins and furans removal from flue gas has been in operation since June 1995. The process and the design data of these plants will be introduced in this paper and the most important design details will be discussed. Additionally to the activated carbon process fixed-bed technology - the activated carbon injection process and their efficiencies for the removal of dioxins, furans and heavy metals will be briefly described in this paper.

  5. Efficiency enhancement of solution-processed inverted organic solar cells with a carbon-nanotube-doped active layer

    NASA Astrophysics Data System (ADS)

    Lin, Wen-Kai; Su, Shui-Hsiang; Yeh, Meng-Cheng; Huang, Yang-Chan; Yokoyama, Meiso

    2016-01-01

    Solution-processed titanium-doped ZnO (TZO) is synthesized by the sol–gel method to be the electron-transporting layer (ETL) in an inverted organic solar cell (IOSC). Carbon nanotubes (CNTs) are doped into an active layer of poly(3-hexylthiophene):[6,6]-phenyl C 61 butyric acid methyl ester (P3HT:PCBM). The addition of CNTs in the P3HT:PCBM composite increases the conjugation length of P3HT:PCBM:CNTs, which simultaneously enhances the capacity of the composite to absorb solar energy radiation. Vanadium oxide (V2O5) was spin-coated onto the active layer to be a hole-transporting layer (HTL). The power conversion efficiency (PCE) results indicate that the V2O5 nanobelt structure possesses better phase separation and provides a more efficient surface area for the P3HT:PCBM:CNT active layer to increase photocurrent. The optimized IOSCs exhibited an open circuit voltage (Voc), a short-circuit current density (Jsc), a fill factor (FF), and a PCE of 0.55 V, 6.50 mA/cm2, 58.34%, and 2.20%, respectively, under simulated AM1.5G illumination of 100 mW/cm2.

  6. A compact process for treating oilfield wastewater by combining hydrolysis acidification, moving bed biofilm, ozonation and biologically activated carbon techniques.

    PubMed

    Zheng, Tao

    2016-05-01

    A lab-scale hybrid system integrating a hybrid hydrolysis acidification (HA) reactor, a moving bed biofilm reactor (MBBR) and an ozonation-biologically activated carbon (O3-BAC) unit was used in the treatment of heavy oil wastewater with high chemical oxygen demand (COD) and low biodegradability. The effects of hydraulic retention time and ozonation time were investigated. The results show that under the optimal conditions, the effluent concentrations of COD, oil and ammonia were 48, 1.3 and 3.5 mg/L, respectively, corresponding to total removal efficiencies of 95.8%, 98.9% and 94.4%, respectively. The effluent could meet the grade I as required by the national discharge standard of China. The HA process remarkably improved the biodegradability of the wastewater, while the MBBR process played an important role in degrading COD. The ozonation process further enhanced the biodegradability of the MBBR effluent, and finally, deep treatment was completed in the BAC reactor. This work demonstrates that the hybrid HA/MBBR/O3-BAC system has the potential to be used for the treatment of high-strength oilfield wastewater. PMID:26507807

  7. Adsorption characteristics of malachite green on activated carbon derived from rice husks produced by chemical-thermal process.

    PubMed

    Rahman, I A; Saad, B; Shaidan, S; Sya Rizal, E S

    2005-09-01

    Phosphoric acid (H(3)PO(4)) and sodium hydroxide (NaOH) treated rice husks, followed by carbonization in a flowing nitrogen were used to study the adsorption of malachite green (MG) in aqueous solution. The effect of adsorption on contact time, concentration of MG and adsorbent dosage of the samples treated or carbonized at different temperatures were investigated. The results reveal that the optimum carbonization temperature is 500 degrees C in order to obtain adsorption capacity that is comparable to the commercial activated carbon for the husks treated by H(3)PO(4). It is interesting to note that MG adsorbed preferably on carbon-rich than on silica rich-sites. It is found that the behaviour of H(3)PO(4) treated absorbent followed both the Langmuir and Freundlich models while NaOH treated best fitted to only the Langmuir model. PMID:15978990

  8. Modeling external carbon addition in biological nutrient removal processes with an extension of the international water association activated sludge model.

    PubMed

    Swinarski, M; Makinia, J; Stensel, H D; Czerwionka, K; Drewnowski, J

    2012-08-01

    The aim of this study was to expand the International Water Association Activated Sludge Model No. 2d (ASM2d) to account for a newly defined readily biodegradable substrate that can be consumed by polyphosphate-accumulating organisms (PAOs) under anoxic and aerobic conditions, but not under anaerobic conditions. The model change was to add a new substrate component and process terms for its use by PAOs and other heterotrophic bacteria under anoxic and aerobic conditions. The Gdansk (Poland) wastewater treatment plant (WWTP), which has a modified University of Cape Town (MUCT) process for nutrient removal, provided field data and mixed liquor for batch tests for model evaluation. The original ASM2d was first calibrated under dynamic conditions with the results of batch tests with settled wastewater and mixed liquor, in which nitrate-uptake rates, phosphorus-release rates, and anoxic phosphorus uptake rates were followed. Model validation was conducted with data from a 96-hour measurement campaign in the full-scale WWTP. The results of similar batch tests with ethanol and fusel oil as the external carbon sources were used to adjust kinetic and stoichiometric coefficients in the expanded ASM2d. Both models were compared based on their predictions of the effect of adding supplemental carbon to the anoxic zone of an MUCT process. In comparison with the ASM2d, the new model better predicted the anoxic behaviors of carbonaceous oxygen demand, nitrate-nitrogen (NO3-N), and phosphorous (PO4-P) in batch experiments with ethanol and fusel oil. However, when simulating ethanol addition to the anoxic zone of a full-scale biological nutrient removal facility, both models predicted similar effluent NO3-N concentrations (6.6 to 6.9 g N/m3). For the particular application, effective enhanced biological phosphorus removal was predicted by both models with external carbon addition but, for the new model, the effluent PO4-P concentration was approximately one-half of that found from ASM2d. On a PO4-P removal percentage basis, the difference was small, that is, 94.1 vs. 97.1%, respectively, for the ASM2d and expanded ASM2d. PMID:22953449

  9. RO brine treatment and recovery by biological activated carbon and capacitive deionization process.

    PubMed

    Tao, Guihe; Viswanath, Bala; Kekre, Kiran; Lee, Lai Yoke; Ng, How Yong; Ong, Say Leong; Seah, Harry

    2011-01-01

    The generation of brine solutions from dense membrane (reverse osmosis, RO or nanofiltration, NF) water reclamation systems has been increasing worldwide, and the lack of cost effective disposal options is becoming a critical water resources management issue. In Singapore, NEWater is the product of a multiple barrier water reclamation process from secondary treated domestic effluent using MF/UF-RO and UV technologies. The RO brine (concentrates) accounts for more than 20% of the total flow treated. To increase the water recovery and treat the RO brine, a CDI based process with BAC as pretreatment was tested. The results show that ion concentrations in CDI product were low except SiO2 when compared with RO feed water. CDI product was passed through a RO and the RO permeate was of better quality including low SiO2 as compared to NEWater quality. It could be beneficial to use a dedicated RO operated at optimum conditions with better performance to recover the water. BAC was able to achieve 15-27% TOC removal of RO brine. CDI had been tested at a water recovery ranging from 71.6 to 92.3%. CDI based RO brine treatment could improve overall water recovery of NEWater production over 90%. It was found that calcium phosphate scaling and organic fouling was the major cause of CDI pressure increase. Ozone disinfection and sodium bisulfite dosing were able to reduce CDI fouling rate. For sustainable operation of CDI organic fouling control and effective organic fouling cleaning should be further studied. PMID:22053461

  10. Geostationary Carbon Process Mapper (GCPM)

    NASA Technical Reports Server (NTRS)

    Key, Richard; Sander, Stanley; Eldering, Annmarie; Miller, Charles; Frankenberg, Christian; Natraj, Vijay; Rider, David; Blavier, Jean-Francois; Bekker, Dmitriy; Wu, Yen-Hung

    2012-01-01

    Geostationary Carbon Process Mapper (GCPM) is an earth science mission to measure key atmospheric trace gases related to climate change and human activity.Understanding of sources and sinks of CO2 is currently limited by frequency of observations and uncertainty in vertical transport. GCPM improves this situation by making simultaneous high resolution measurements of CO2, CH4, CF, and CO in near-IR, many times per day. GCPM is able to investigate processes with time scales of minutes to hours. CO2, CH4, CF, Co selected because their combination provides information needed to disentangle natural and anthropogenic sources/sinks. Quasi-continuous monitoring effectively eliminates atmospheric transport uncertainties from source/sink inversion modeling. will have one instrument (GeoFTS), hosted on a commercial communications satellite, planned for two years operation. GCPM will affordably advance the understanding of observed cycle variability improving future climate projections.

  11. Determining activated carbon performance

    SciTech Connect

    Naylor, W.F.; Rester, D.O.

    1995-07-01

    This article discusses the key elements involved in evaluating a system`s performance. Empty bed contact time (EBCT) is a term used to describe the length of time a liquid stream being treated is in contact with a granular activated carbon bed. The EBCT is the time required for a fluid to pass through the volume equivalent of the media bed, without the media being present. In a bed of granular activated carbon, the void volume or space between particles is usually about 45 percent. Therefore, the EBCT is about twice the true or actual time of contact between the fluid being treated and the GAC particles. The EBCT plays an important role in determining the effectiveness and longevity of granular activated carbon (GAC) used to treat liquids in a fixed-bed adsorber. Factors that influence and are influenced by EBCT, and their relationship to GAC performance in a treatment scheme include: adsorption, mass transfer zone, impurity concentration, adsorption affinity, flow rate and system design considerations.

  12. Photoconductivity of activated carbon fibers

    SciTech Connect

    Kuriyama, K.; Dresselhaus, M.S. )

    1990-08-01

    The photoconductivity is measured on a high-surface-area disordered carbon material, namely activated carbon fibers, to investigate their electronic properties. Measurements of decay time, recombination kinetics and temperature dependence of the photoconductivity generally reflect the electronic properties of a material. The material studied in this paper is a highly disordered carbon derived from a phenolic precursor, having a huge specific surface area of 1000--2000m{sup 2}/g. Our preliminary thermopower measurements suggest that this carbon material is a p-type semiconductor with an amorphous-like microstructure. The intrinsic electrical conductivity, on the order of 20S/cm at room temperature, increases with increasing temperature in the range 30--290K. In contrast with the intrinsic conductivity, the photoconductivity in vacuum decreases with increasing temperature. The recombination kinetics changes from a monomolecular process at room temperature to a biomolecular process at low temperatures. The observed decay time of the photoconductivity is {approx equal}0.3sec. The magnitude of the photoconductive signal was reduced by a factor of ten when the sample was exposed to air. The intrinsic carrier density and the activation energy for conduction are estimated to be {approx equal}10{sup 21}/cm{sup 3} and {approx equal}20meV, respectively. The majority of the induced photocarriers and of the intrinsic carriers are trapped, resulting in the long decay time of the photoconductivity and the positive temperature dependence of the conductivity. 54 refs., 11 figs., 3 tabs.

  13. Photoconductivity of Activated Carbon Fibers

    DOE R&D Accomplishments Database

    Kuriyama, K.; Dresselhaus, M. S.

    1990-08-01

    The photoconductivity is measured on a high-surface-area disordered carbon material, namely activated carbon fibers, to investigate their electronic properties. Measurements of decay time, recombination kinetics and temperature dependence of the photoconductivity generally reflect the electronic properties of a material. The material studied in this paper is a highly disordered carbon derived from a phenolic precursor, having a huge specific surface area of 1000--2000m{sup 2}/g. Our preliminary thermopower measurements suggest that this carbon material is a p-type semiconductor with an amorphous-like microstructure. The intrinsic electrical conductivity, on the order of 20S/cm at room temperature, increases with increasing temperature in the range 30--290K. In contrast with the intrinsic conductivity, the photoconductivity in vacuum decreases with increasing temperature. The recombination kinetics changes from a monomolecular process at room temperature to a biomolecular process at low temperatures. The observed decay time of the photoconductivity is {approx equal}0.3sec. The magnitude of the photoconductive signal was reduced by a factor of ten when the sample was exposed to air. The intrinsic carrier density and the activation energy for conduction are estimated to be {approx equal}10{sup 21}/cm{sup 3} and {approx equal}20meV, respectively. The majority of the induced photocarriers and of the intrinsic carriers are trapped, resulting in the long decay time of the photoconductivity and the positive temperature dependence of the conductivity.

  14. Nanostructural activated carbons for hydrogen storage

    NASA Astrophysics Data System (ADS)

    Li, Suoding

    A series of nanostructured activated carbons have been synthesized from poly(ether ether ketone) (PEEK), and its derivatives. These carbons, with surface area exceeding 3000 m2/g and with average pore diameters of ? 20 A, are proven to be superior hydrogen storage materials, with hydrogen storage capacities up to 5.5 wt% at 77 K and 45 atm. The porous texture of these carbons was controlled via optimizing three synthetic steps: thermo-oxidation of PEEK in air, pyrolysis or carbonization of the oxidized PEEK in an inert atmosphere, and activation of the pre-carbonized PEEK with metal hydroxide. Thermo-oxidation of PEEK and carbonization process were thoroughly studied. These processes have been investigated by MDSC, FTIR, TGA and Py-MS. The pyrolysis or carbonization of PEEK involves the degradation of PEEK chains in three stages. Carbon morphology, including crystallinity and porous texture, is readily controlled by adjusting carbonization temperature. Activation of PEEK carbons, using inorganic bases and other activation agents, produces microporous carbons having a very narrow pore size distribution and an average pore diameter of ? 20 A. The activation control parameters including activation agent, activation temperature, time and carbon morphology have been investigated extensively. High surface area activated carbon is obtained by activating a highly amorphous carbon with a high activation agent/carbon ratio at 800C. Theoretical calculations show that the pores with smaller diameter, especially smaller than 7 A, favor hydrogen adsorption. The experimental results confirm this fact and show that: (1) the hydrogen adsorption capacity per unit surface area at 77 K and 1 bar is larger in the smaller pores, (2) gravimetric hydrogen storage capacity (W(H2)) is directly proportional to the ultramicropore (< 7 A) volume; and (3) the volumetric hydrogen storage capacity is directly proportional to the volume fraction of ultramicropores in carbon. Hydrogen adsorption in activated carbons synthesized from PEEK and poly(ether imide) blends, poly(phenylene oxide), polybenzimidazole and lignin show similar trends. In addition, W( H2) progressively increases as surface area increases for the carbons with similar average pore diameters. Keywords. carbon, activated carbon, poly(ether ether ketone), poly(ether imide), poly(phenylene oxide), polybenzimidazole, lignin, gas adsorption, hydrogen storage

  15. Making Activated Carbon by Wet Pressurized Pyrolysis

    NASA Technical Reports Server (NTRS)

    Fisher, John W.; Pisharody, Suresh; Wignarajah, K.; Moran, Mark

    2006-01-01

    A wet pressurized pyrolysis (wet carbonization) process has been invented as a means of producing activated carbon from a wide variety of inedible biomass consisting principally of plant wastes. The principal intended use of this activated carbon is room-temperature adsorption of pollutant gases from cooled incinerator exhaust streams. Activated carbon is highly porous and has a large surface area. The surface area depends strongly on the raw material and the production process. Coconut shells and bituminous coal are the primary raw materials that, until now, were converted into activated carbon of commercially acceptable quality by use of traditional production processes that involve activation by use of steam or carbon dioxide. In the wet pressurized pyrolysis process, the plant material is subjected to high pressure and temperature in an aqueous medium in the absence of oxygen for a specified amount of time to break carbon-oxygen bonds in the organic material and modify the structure of the material to obtain large surface area. Plant materials that have been used in demonstrations of the process include inedible parts of wheat, rice, potato, soybean, and tomato plants. The raw plant material is ground and mixed with a specified proportion of water. The mixture is placed in a stirred autoclave, wherein it is pyrolized at a temperature between 450 and 590 F (approximately between 230 and 310 C) and a pressure between 1 and 1.4 kpsi (approximately between 7 and 10 MPa) for a time between 5 minutes and 1 hour. The solid fraction remaining after wet carbonization is dried, then activated at a temperature of 500 F (260 C) in nitrogen gas. The activated carbon thus produced is comparable to commercial activated carbon. It can be used to adsorb oxides of sulfur, oxides of nitrogen, and trace amounts of hydrocarbons, any or all of which can be present in flue gas. Alternatively, the dried solid fraction can be used, even without the activation treatment, to absorb oxides of nitrogen.

  16. Equilibrium uptake, sorption dynamics, process optimization, and column operations for the removal and recovery of malachite green from wastewater using activated carbon and activated slag

    SciTech Connect

    Gupta, V.K.; Srivastava, S.K.; Mohan, D.

    1997-06-01

    The waste slurry generated in fertilizer plants and slag (blast furnace waste) have been converted into low-cost adsorbents, activated carbon and activated slag, respectively, and these are utilized for the removal of malachite green (a basic dye) from wastewater. In the batch experiments, parameters studied include the effect of pH, sorbent dosage, adsorbate concentration, temperature, and contact time. Kinetic studies have been performed to have an idea of the mechanistic aspects and to obtain the thermodynamic parameters of the process. The uptake of the dye is greater on carbonaceous material than on activated slag. Sorption data have been correlated with both Langmuir and Freundlich adsorption models. The presence of anionic surfactants does not affect the uptake of dye significantly. The mass transfer kinetic approach has been applied for the determination of various parameters necessary for the designing of fixed-bed contactors. Chemical regeneration has been achieved with acetone in order to recover the loaded dye and restore the column to its original capacity without dismantling the same.

  17. Application of the biological granular activated carbon fluidized bed reactor process for gas industry waste treatment. Topical report, January 1991-December 1992

    SciTech Connect

    Wagner, D.; Sunday, A.; Hickey, R.F.

    1993-06-01

    The research and development work is focused on evaluating the applicability of using the biological granular activated carbon-fluidized bed reactor (GAC-FBR) for helping to solve gas industry waste treatment needs. The specific goals are to use and modify the GAC-FBR process, as needed, for (1) remediation of groundwater contaminated by gas industry operations, and (2) treatment of gas production and exploration waters.

  18. WASTE ACTIVATED SLUDGE PROCESSING

    EPA Science Inventory

    A study was made at pilot scale of a variety of processes for dewatering and stabilization of waste activated sludge from a pure oxygen activated sludge system. Processes evaluated included gravity thickening, dissolved air flotation thickening, basket centrifugation, scroll cent...

  19. Nanospace engineering of KOH activated carbon.

    PubMed

    Romanos, J; Beckner, M; Rash, T; Firlej, L; Kuchta, B; Yu, P; Suppes, G; Wexler, C; Pfeifer, P

    2012-01-13

    This paper demonstrates that nanospace engineering of KOH activated carbon is possible by controlling the degree of carbon consumption and metallic potassium intercalation into the carbon lattice during the activation process. High specific surface areas, porosities, sub-nanometer (<1 nm) and supra-nanometer (1-5 nm) pore volumes are quantitatively controlled by a combination of KOH concentration and activation temperature. The process typically leads to a bimodal pore size distribution, with a large, approximately constant number of sub-nanometer pores and a variable number of supra-nanometer pores. We show how to control the number of supra-nanometer pores in a manner not achieved previously by chemical activation. The chemical mechanism underlying this control is studied by following the evolution of elemental composition, specific surface area, porosity, and pore size distribution during KOH activation and preceding H(3)PO(4) activation. The oxygen, nitrogen, and hydrogen contents decrease during successive activation steps, creating a nanoporous carbon network with a porosity and surface area controllable for various applications, including gas storage. The formation of tunable sub-nanometer and supra-nanometer pores is validated by sub-critical nitrogen adsorption. Surface functional groups of KOH activated carbon are studied by microscopic infrared spectroscopy. PMID:22156024

  20. Process of making carbon-carbon composites

    NASA Technical Reports Server (NTRS)

    Withers, James C. (Inventor); Loutfy, Raouf O. (Inventor); Kowbel, Witold (Inventor); Bruce, Calvin (Inventor); Vaidyanathan, Ranji (Inventor)

    2000-01-01

    A carbon composite structure, for example, an automotive engine piston, is made by preparing a matrix including of a mixture of non crystalline carbon particulate soluble in an organic solvent and a binder that has a liquid phase. The non crystalline particulate also contains residual carbon hydrogen bonding. An uncured structure is formed by combining the matrix mixture, for example, carbon fibers such as graphite dispersed in the mixture and/or graphite cloth imbedded in the mixture. The uncured structure is cured by pyrolyzing it in an inert atmosphere such as argon. Advantageously, the graphite reinforcement material is whiskered prior to combining it with the matrix mixture by a novel method involving passing a gaseous metal suboxide over the graphite surface.

  1. Adsorption behavior of direct red 80 and congo red onto activated carbon/surfactant: Process optimization, kinetics and equilibrium

    NASA Astrophysics Data System (ADS)

    Cheng, Zhengjun; Zhang, Lei; Guo, Xiao; Jiang, Xiaohui; Li, Tian

    2015-02-01

    Adsorptions of congo red and direct red 80 onto activated carbon/surfactant from aqueous solution were optimized. The Box-Behnken design (BBD) has been employed to analyze the effects of concentration of surfactant, temperature, pH, and initial concentration of the dye in the adsorption capacity. Their corresponding experimental data could be evaluated excellently by second order polynomial regression models and the two models were also examined based on the analysis of variance and t test statistics, respectively. The optimum conditions were obtained as follows: Cs = 34.10 ?M, T = 50 C, pH = 3.5, and CCR = 160 mg/L for the congo red system, and Cs = 34.10 ?M, T = 50 C, pH = 6.1, and CDR80 = 110 mg/L for the direct red 80 system. And in these conditions, the measured experimental maximum adsorption capacities for the congo red and direct red 80 removals were 769.48 mg/g and 519.90 mg/g, which were consistent with their corresponding predicted values, with small relative errors of -2.81% and -0.67%, respectively. The adsorption equilibrium and kinetics for the two dye adsorptions onto AC/DDAC were also investigated. The experimental data were fitted by four isotherm models, and Langmuir model presented the best fit. The kinetic studies indicated that the kinetic data followed the pseudo-second-order model.

  2. Adsorption behavior of direct red 80 and congo red onto activated carbon/surfactant: process optimization, kinetics and equilibrium.

    PubMed

    Cheng, Zhengjun; Zhang, Lei; Guo, Xiao; Jiang, Xiaohui; Li, Tian

    2015-02-25

    Adsorptions of congo red and direct red 80 onto activated carbon/surfactant from aqueous solution were optimized. The Box-Behnken design (BBD) has been employed to analyze the effects of concentration of surfactant, temperature, pH, and initial concentration of the dye in the adsorption capacity. Their corresponding experimental data could be evaluated excellently by second order polynomial regression models and the two models were also examined based on the analysis of variance and t test statistics, respectively. The optimum conditions were obtained as follows: Cs=34.10 ?M, T=50C, pH=3.5, and CCR=160 mg/L for the congo red system, and Cs=34.10 ?M, T=50C, pH=6.1, and CDR80=110 mg/L for the direct red 80 system. And in these conditions, the measured experimental maximum adsorption capacities for the congo red and direct red 80 removals were 769.48 mg/g and 519.90 mg/g, which were consistent with their corresponding predicted values, with small relative errors of -2.81% and -0.67%, respectively. The adsorption equilibrium and kinetics for the two dye adsorptions onto AC/DDAC were also investigated. The experimental data were fitted by four isotherm models, and Langmuir model presented the best fit. The kinetic studies indicated that the kinetic data followed the pseudo-second-order model. PMID:25305604

  3. Optimization of Cu/activated carbon catalyst in low temperature selective catalytic reduction of NO process using response surface methodology.

    PubMed

    Amanpour, Javad; Salari, Dariush; Niaei, Aligholi; Mousavi, Seyed Mahdi; Panahi, Parvaneh Nakhostin

    2013-01-01

    Preparation of Cu/Activated Carbon (Cu/AC) catalyst was optimized for low temperature selective catalytic reduction of NO by using response surface methodology. A central composite design (CCD) was used to investigate the effects of three independent variables, namely pre-oxidization degree (HNO3%), Cu loading (wt.%) and calcination temperature on NO conversion efficiency. The CCD was consisted of 20 different preparation conditions of Cu/AC catalysts. The prepared catalysts were characterized by XRD and SEM techniques. Predicting NO conversion was carried out using a second order model obtained from designed experiments and statistical software Minitab 14. Regression and Pareto graphic analysis showed that all of the chosen parameters and some interactions were effective on the NO conversion. The optimal values were pre-oxidization in 10.2% HNO3, 6.1 wt.% Cu loading and 480C for calcination temperature. Under the optimum condition, NO conversion (94.3%) was in a good agreement with predicted value (96.12%). PMID:23485237

  4. Process for sequestering carbon dioxide and sulfur dioxide

    DOEpatents

    Maroto-Valer, M. Mercedes (State College, PA); Zhang, Yinzhi (State College, PA); Kuchta, Matthew E. (State College, PA); Andresen, John M. (State College, PA); Fauth, Dan J. (Pittsburgh, PA)

    2009-10-20

    A process for sequestering carbon dioxide, which includes reacting a silicate based material with an acid to form a suspension, and combining the suspension with carbon dioxide to create active carbonation of the silicate-based material, and thereafter producing a metal salt, silica and regenerating the acid in the liquid phase of the suspension.

  5. Antimicrobial Activity of Carbon-Based Nanoparticles

    PubMed Central

    Maleki Dizaj, Solmaz; Mennati, Afsaneh; Jafari, Samira; Khezri, Khadejeh; Adibkia, Khosro

    2015-01-01

    Due to the vast and inappropriate use of the antibiotics, microorganisms have begun to develop resistance to the commonly used antimicrobial agents. So therefore, development of the new and effective antimicrobial agents seems to be necessary. According to some recent reports, carbon-based nanomaterials such as fullerenes, carbon nanotubes (CNTs) (especially single-walled carbon nanotubes (SWCNTs)) and graphene oxide (GO) nanoparticles show potent antimicrobial properties. In present review, we have briefly summarized the antimicrobial activity of carbon-based nanoparticles together with their mechanism of action. Reviewed literature show that the size of carbon nanoparticles plays an important role in the inactivation of the microorganisms. As major mechanism, direct contact of microorganisms with carbon nanostructures seriously affects their cellular membrane integrity, metabolic processes and morphology. The antimicrobial activity of carbon-based nanostructures may interestingly be investigated in the near future owing to their high surface/volume ratio, large inner volume and other unique chemical and physical properties. In addition, application of functionalized carbon nanomaterials as carriers for the ordinary antibiotics possibly will decrease the associated resistance, enhance their bioavailability and provide their targeted delivery. PMID:25789215

  6. Treatment of coal-conversion wastewater with the powdered activated carbon-contact stabilization activated-sludge process. First semiannual technical progress report, August 1, 1980-January 31, 1981

    SciTech Connect

    Suidan, M.T.; Pirbazari, M.; Gee, C.S.; Deady, M.A.

    1981-01-01

    The treatment of coal conversion wastewaters has traditionally been accomplished through the use of the activated sludge process and its various modifications. General observations have been that phenol was degraded efficiently; however, very poor removal efficiencies of thiocyanate, cyanide, and ammonia were obtained. The addition of powdered activated carbon (PAC) to the activated sludge process has been reported to result in a number of distinct advantages. Generally, however, improving the effluent water quality beyond the capabilities of conventional biological treatment and enhancing the treatability of wastewaters that inhibit or toxify biological treatment systems are the primary objectives of utilizing PAC in secondary biological treatment. The focus of the present research project is to assess the effectiveness of the powdered activated carbon-contact stabilization activated sludge process in the treatment of a coking wastewater. The purpose of the contact tank in such a process will be to provide sufficient time for the adsorbable constituents of the coking wastewater to adsorb onto the PAC. The liquor leaving the contact tank is then clarified with the concentratrated underflow receiving treatment in the stabilization tank. After stabilization the sludge is returned to the contact tank. The clarifier supernatant is then nitrified in an activated sludge-type nitrification process and the nitrified effluent is subsequently denitrified in an anoxic filter.

  7. Effects of process parameters on hydrothermal carbonization

    NASA Astrophysics Data System (ADS)

    Uddin, Md. Helal

    In recent years there has been increased research activity in renewable energy, especially upgrading widely available lignicellulosic biomass, in a bid to counter the increasing environmental concerns related with the use of fossil fuels. Hydrothermal carbonization (HTC), also known as wet torrefaction or hot water pretreatment, is a process for pretreatment of diverse lignocellulosic biomass feedstocks, where biomass is treated under subcritical water conditions in short contact time to produce high-value products. The products of this process are: a solid mass characterized as biochar/biocoal/biocarbon, which is homogeneous, energy dense, and hydrophobic; a liquid stream composed of five and six carbon sugars, various organic acids, and 5-HMF; and a gaseous stream, mainly CO2. A number of process parameters are considered important for the extensive application of the HTC process. Primarily, reaction temperature determines the characteristics of the products. In the solid product, the oxygen carbon ratio decreases with increasing reaction temperature and as a result, HTC biochar has the similar characteristics to low rank coal. However, liquid and gaseous stream compositions are largely correlated with the residence time. Biomass particle size can also limit the reaction kinetics due to the mass transfer effect. Recycling of process water can help to minimize the utility consumption and reduce the waste treatment cost as a result of less environmental impact. Loblolly pine was treated in hot compressed water at 200 C, 230 C, and 260 C with 5:1 water:biomass mass ratio to investigate the effects of process parameters on HTC. The solid product were characterized by their mass yields, higher heating values (HHV), and equilibrium moisture content (EMC), while the liquid were characterized by their total organic carbon content and pH value.

  8. ENGINEERING BULLETIN: GRANULAR ACTIVATED CARBON TREATMENT

    EPA Science Inventory

    Granular activated carbon (GAC) treatment is a physicochemical process that removes a wide variety of contaminants by adsorbing them from liquid and gas streams [1, p. 6-3]. This treatment is most commonly used to separate organic contaminants from water or air; however, it can b...

  9. Preparation of activated carbons from bituminous coal pitches

    NASA Astrophysics Data System (ADS)

    Gaan, J.; Gonzlez-Garca, C. M.; Gonzlez, J. F.; Sabio, E.; Macas-Garca, A.; Daz-Dez, M. A.

    2004-11-01

    High-porosity carbons were prepared from bituminous coal pitches by combining chemical and physical activation. The chemical activation process consisted of potassium hydroxide impregnation followed by carbonization in nitrogen atmosphere. The effect of the KOH impregnation ratio on the surface area and pore volumes evolution of the carbons derived from mesophase pitch was studied. The optimum KOH:pitch ratio was fixed to realize a physical activation process in order to increase the textural parameters of the KOH-activated carbons. Physical activation was performed by carbonizing the KOH-activated carbons followed by gasifying with air. The influence of the carbonization temperature and the residence time of the gasification with air were explored to optimize those preparation parameters.

  10. Granular activated carbon: Design, operation and cost

    SciTech Connect

    Clark, R.M.; Lykins, B.W.

    1990-01-01

    A summary is presented of design, cost, and performance information on the application of application of granular activated carbon (GAC) in drinking water based on field-scale experience. A brief history of the development of regulations for control of synthetic organics in drinking water is presented. The use of GAC in other countries is discussed and various design concepts for the unit operations that make up the GAC process are explored. Included in the book are chapters that present information from field-scale research projects dealing with the performance of virgin and reactivated carbon; problems and limitations of carbon reactivation systems; and use of carbon for removing trihalomethanes, trihalomethane precursors, and synthetic organics. The last chapter provides cost equations and comparative cost studies for full-scale application of GAC.

  11. Granular activated carbon and biological activated carbon treatment of dissolved and sorbed polychlorinated biphenyls

    SciTech Connect

    Ghosh, U.; Weber, A.S.; Jensen, J.N.; Smith, J.R.

    1999-03-01

    The most widely practiced treatment method for polychlorinated biphenyls (PCBs) in aqueous wastes is activated carbon adsorption. However, the presence of particulates in aqueous wastes may affect treatment processes primarily designed to treat dissolved. PCBs because PCBs tend to partition strongly to solid surfaces. In this research, bench-scale studies were conducted to investigate the performance of granular activated carbon (GAC) and biological activated carbon (BAC) processes for treating aqueous wastes containing dissolved and sorbed PCBs. When all influent PCBs were dissolved, influent PCBs of approximately 175 {micro}g/L were removed to approximately 0.2 {micro}g/L in the BAC column, compared to approximately 0.8 {micro}g/L in the GAC column. A reduction in the extent of PCB removal was observed for both GAC and BAC processes when 10 mg/L of 0.5-{micro}m polystyrene particles were added to the influent. In the presence of influent particulates, PCB removal was significantly better in the BAC column and equaled 99% compared to 62% in the GAC column. Performance differences between the GAC and BAC columns were attributed to higher particulate capture efficiency of the biological film covering the activated carbon in the BAC column. Biological activated carbon columns thus seem to offer advantages to conventional GAC processes for aqueous wastes containing either dissolved or sorbed PCBs.

  12. Retinal Light Processing Using Carbon Nanotubes

    NASA Technical Reports Server (NTRS)

    Loftus, David J. (Inventor); Leng, Theodore (Inventor); Fishman, Harvey (Inventor)

    2004-01-01

    Method and system for processing light signals received by the eye of a human or other animal, where the eye may be compromised or non-functioning. Incident light is received at first and second pixels in a photodetector array and provides a pixel electrical signal representing the received light. Each of an array of carbon nanotube (CNT) towers is connected to a pixel, has a first tower end penetrating a retinal active layer of the animal and has a second tower end positioned to receive to receive and transport the pixel electrical signal to the retinal active layer. The CNT tower may be coated with a biologically active substance or chemically modified to promote neurite connections with the tower. The photoreceptor array can be provide with a signal altering mechanism that alters at least one of light intensity and wavelength intensity sensed by a first pixel relative to a second pixel, to correct for one or more selected eye problems.

  13. Enhanced carbon monoxide utilization in methanation process

    DOEpatents

    Elek, Louis F. (Peekskill, NY); Frost, Albert C. (Congers, NY)

    1984-01-01

    Carbon monoxide - containing gas streams are passed over a catalyst to deposit a surface layer of active surface carbon thereon essentially without the formation of inactive coke. The active carbon is subsequently reacted with steam or hydrogen to form methane. Surprisingly, hydrogen and water vapor present in the feed gas do not adversely affect CO utilization significantly, and such hydrogen actually results in a significant increase in CO utilization.

  14. Evaluation on simultaneous removal of particles and off-flavors using population balance for application of powdered activated carbon in dissolved air flotation process.

    PubMed

    Kwak, D H; Yoo, S J; Lee, E J; Lee, J W

    2010-01-01

    Most of the water treatment plants applying the DAF process are faced with off-flavors control problems. For simultaneous control of particles of impurities and dissolved organics that cause pungent taste and odor in water, an effective method would be the simple application of powdered activated carbon (PAC) in the DAF process. A series of experiments were carried out to explore the feasibility for simultaneous removal of kaolin particles and organic compounds that produce off-flavors (2-MIB and geosmin). In addition, the flotation efficiency of kaolin and PAC particles adsorbing organics in the DAF process was evaluated by employing the population balance theory. The removal efficiency of 2-MIB and geosmin under the treatment condition with kaolin particles for simultaneous treatment was lower than that of the individual treatment. The decrease in the removal efficiency was probably caused by 2-MIB and geosmin remaining in the PAC particle in the treated water of DAF after bubble flotation. Simulation results obtained by the population balance model indicate, that the initial collision-attachment efficiency of PAC particles was lower than that of kaolin particles. PMID:20107258

  15. Making Activated Carbon for Storing Gas

    NASA Technical Reports Server (NTRS)

    Wojtowicz, Marek A.; Serio, Michael A.; Suuberg, Eric M.

    2005-01-01

    Solid disks of microporous activated carbon, produced by a method that enables optimization of pore structure, have been investigated as means of storing gas (especially hydrogen for use as a fuel) at relatively low pressure through adsorption on pore surfaces. For hydrogen and other gases of practical interest, a narrow distribution of pore sizes <2 nm is preferable. The present method is a variant of a previously patented method of cyclic chemisorption and desorption in which a piece of carbon is alternately (1) heated to the lower of two elevated temperatures in air or other oxidizing gas, causing the formation of stable carbon/oxygen surface complexes; then (2) heated to the higher of the two elevated temperatures in flowing helium or other inert gas, causing the desorption of the surface complexes in the form of carbon monoxide. In the present method, pore structure is optimized partly by heating to a temperature of 1,100 C during carbonization. Another aspect of the method exploits the finding that for each gas-storage pressure, gas-storage capacity can be maximized by burning off a specific proportion (typically between 10 and 20 weight percent) of the carbon during the cyclic chemisorption/desorption process.

  16. Effect of granular activated carbon addition on the effluent properties and fouling potentials of membrane-coupled expanded granular sludge bed process.

    PubMed

    Ding, An; Liang, Heng; Qu, Fangshu; Bai, Langming; Li, Guibai; Ngo, Huu Hao; Guo, Wenshan

    2014-11-01

    To mitigate membrane fouling of membrane-coupled anaerobic process, granular activated carbon (GAC: 50 g/L) was added into an expanded granular sludge bed (EGSB). A short-term ultrafiltration test was investigated for analyzing membrane fouling potential and underlying fouling mechanisms. The results showed that adding GAC into the EGSB not only improved the COD removal efficiency, but also alleviated membrane fouling efficiently because GAC could help to reduce soluble microbial products, polysaccharides and proteins by 26.8%, 27.8% and 24.7%, respectively, compared with the control system. Furthermore, excitation emission matrix (EEM) fluorescence spectroscopy analysis revealed that GAC addition mainly reduced tryptophan protein-like, aromatic protein-like and fulvic-like substances. In addition, the resistance distribution analysis demonstrated that adding GAC primarily decreased the cake layer resistance by 53.5%. The classic filtration mode analysis showed that cake filtration was the major fouling mechanism for membrane-coupled EGSB process regardless of the GAC addition. PMID:25203232

  17. Activated, coal-based carbon foam

    DOEpatents

    Rogers, Darren Kenneth; Plucinski, Janusz Wladyslaw

    2004-12-21

    An ablation resistant, monolithic, activated, carbon foam produced by the activation of a coal-based carbon foam through the action of carbon dioxide, ozone or some similar oxidative agent that pits and/or partially oxidizes the carbon foam skeleton, thereby significantly increasing its overall surface area and concurrently increasing its filtering ability. Such activated carbon foams are suitable for application in virtually all areas where particulate or gel form activated carbon materials have been used. Such an activated carbon foam can be fabricated, i.e. sawed, machined and otherwise shaped to fit virtually any required filtering location by simple insertion and without the need for handling the "dirty" and friable particulate activated carbon foam materials of the prior art.

  18. Activated, coal-based carbon foam

    SciTech Connect

    Rogers, Darren Kenneth; Plucinski, Janusz Wladyslaw

    2009-06-09

    An ablation resistant, monolithic, activated, carbon foam produced by the activation of a coal-based carbon foam through the action of carbon dioxide, ozone or some similar oxidative agent that pits and/or partially oxidizes the carbon foam skeleton, thereby significantly increasing its overall surface area and concurrently increasing its filtering ability. Such activated carbon foams are suitable for application in virtually all areas where particulate or gel form activated carbon materials have been used. Such an activated carbon foam can be fabricated, i.e. sawed, machined and otherwise shaped to fit virtually any required filtering location by simple insertion and without the need for handling the "dirty" and friable particulate activated carbon foam materials of the prior art.

  19. Acoustical Evaluation of Carbonized and Activated Cotton Nonwovens

    Technology Transfer Automated Retrieval System (TEKTRAN)

    The process of manufacturing a carbonized and activated nonwoven made by cotton fiber was investigated in this paper. The study was focused on the acoustic application and nonwoven composites with cotton nonwoven as a base layer and glass fiber nonwoven, cotton nonwoven, and carbonized and activated...

  20. Mercury binding on activated carbon

    SciTech Connect

    Bihter Padak; Michael Brunetti; Amanda Lewis; Jennifer Wilcox

    2006-11-15

    Density functional theory has been employed for the modeling of activated carbon (AC) using a fused-benzene ring cluster approach. Oxygen functional groups have been investigated for their promotion of effective elemental mercury binding on AC surface sites. Lactone and carbonyl functional groups yield the highest mercury binding energies. Further, the addition of halogen atoms has been considered to the modeled surface, and has been found to increase the AC's mercury adsorption capacity. The mercury binding energies increase with the addition of the following halogen atoms, F {gt} Cl {gt} Br {gt} I, with the fluorine addition being the most promising halogen for increasing mercury adsorption.

  1. Engineering carbon materials from the hydrothermal carbonization process of biomass.

    PubMed

    Hu, Bo; Wang, Kan; Wu, Liheng; Yu, Shu-Hong; Antonietti, Markus; Titirici, Maria-Magdalena

    2010-02-16

    Energy shortage, environmental crisis, and developing customer demands have driven people to find facile, low-cost, environmentally friendly, and nontoxic routes to produce novel functional materials that can be commercialized in the near future. Amongst various techniques, the hydrothermal carbonization (HTC) process of biomass (either of isolated carbohydrates or crude plants) is a promising candidate for the synthesis of novel carbon-based materials with a wide variety of potential applications. In this Review, we will discuss various synthetic routes towards such novel carbon-based materials or composites via the HTC process of biomass. Furthermore, factors that influence the carbonization process will be analyzed and the special chemical/physical properties of the final products will be discussed. Despite the lack of a clear mechanism, these novel carbonaceous materials have already shown promising applications in many fields such as carbon fixation, water purification, fuel cell catalysis, energy storage, CO(2) sequestration, bioimaging, drug delivery, and gas sensors. Some of the most promising examples will also be discussed here, demonstrating that the HTC process can rationally design a rich family of carbonaceous and hybrid functional carbon materials with important applications in a sustainable fashion. PMID:20217791

  2. Abundance and diversity of ammonia-oxidizing archaea and bacteria on granular activated carbon and their fates during drinking water purification process.

    PubMed

    Niu, Jia; Kasuga, Ikuro; Kurisu, Futoshi; Furumai, Hiroaki; Shigeeda, Takaaki; Takahashi, Kazuhiko

    2016-01-01

    Ammonia is a precursor to trichloramine, which causes an undesirable chlorinous odor. Granular activated carbon (GAC) filtration is used to biologically oxidize ammonia during drinking water purification; however, little information is available regarding the abundance and diversity of ammonia-oxidizing archaea (AOA) and bacteria (AOB) associated with GAC. In addition, their sources and fates in water purification process remain unknown. In this study, six GAC samples were collected from five full-scale drinking water purification plants in Tokyo during summer and winter, and the abundance and community structure of AOA and AOB associated with GAC were studied in these two seasons. In summer, archaeal and bacterial amoA genes on GACs were present at 3.7נ10(5)-3.9נ10(8) gene copies/g-dry and 4.5נ10(6)-4.2נ10(8) gene copies/g-dry, respectively. In winter, archaeal amoA genes remained at the same level, while bacterial amoA genes decreased significantly for all GACs. No differences were observed in the community diversity of AOA and AOB from summer to winter. Phylogenetic analysis revealed high AOA diversity in group I.1a and group I.1b in raw water. Terminal-restriction fragment length polymorphism analysis of processed water samples revealed that AOA diversity decreased dramatically to only two OTUs in group I.1a after ozonation, which were identical to those detected on GAC. It suggests that ozonation plays an important role in determining AOA diversity on GAC. Further study on the cell-specific activity of AOA and AOB is necessary to understand their contributions to in situ nitrification performance. PMID:26463999

  3. Characterization of Activated Carbons from Oil-Palm Shell by CO2 Activation with No Holding Carbonization Temperature

    PubMed Central

    Herawan, S. G.; Hadi, M. S.; Ayob, Md. R.; Putra, A.

    2013-01-01

    Activated carbons can be produced from different precursors, including coals of different ranks, and lignocellulosic materials, by physical or chemical activation processes. The objective of this paper is to characterize oil-palm shells, as a biomass byproduct from palm-oil mills which were converted into activated carbons by nitrogen pyrolysis followed by CO2 activation. The effects of no holding peak pyrolysis temperature on the physical characteristics of the activated carbons are studied. The BET surface area of the activated carbon is investigated using N2 adsorption at 77?K with selected temperatures of 500, 600, and 700C. These pyrolysis conditions for preparing the activated carbons are found to yield higher BET surface area at a pyrolysis temperature of 700C compared to selected commercial activated carbon. The activated carbons thus result in well-developed porosities and predominantly microporosities. By using this activation method, significant improvement can be obtained in the surface characteristics of the activated carbons. Thus this study shows that the preparation time can be shortened while better results of activated carbon can be produced. PMID:23737721

  4. Characterization of activated carbons from oil-palm shell by CO2 activation with no holding carbonization temperature.

    PubMed

    Herawan, S G; Hadi, M S; Ayob, Md R; Putra, A

    2013-01-01

    Activated carbons can be produced from different precursors, including coals of different ranks, and lignocellulosic materials, by physical or chemical activation processes. The objective of this paper is to characterize oil-palm shells, as a biomass byproduct from palm-oil mills which were converted into activated carbons by nitrogen pyrolysis followed by CO2 activation. The effects of no holding peak pyrolysis temperature on the physical characteristics of the activated carbons are studied. The BET surface area of the activated carbon is investigated using N2 adsorption at 77 K with selected temperatures of 500, 600, and 700°C. These pyrolysis conditions for preparing the activated carbons are found to yield higher BET surface area at a pyrolysis temperature of 700°C compared to selected commercial activated carbon. The activated carbons thus result in well-developed porosities and predominantly microporosities. By using this activation method, significant improvement can be obtained in the surface characteristics of the activated carbons. Thus this study shows that the preparation time can be shortened while better results of activated carbon can be produced. PMID:23737721

  5. Carbon balance of anaerobic granulation process: carbon credit.

    PubMed

    Wong, Biing-Teo; Show, K Y; Lee, D J; Lai, J Y

    2009-03-01

    The concept of carbon credit arose out of increasing awareness of the need to reduce emissions of greenhouse gases to combat global warming which was formalized in the Kyoto protocol. In addition to contribution to sustainable development with energy recovery in the form of methane, carbon credits can be claimed by application of advanced anaerobic processes in wastewater treatment for reducing emissions of greenhouse gases. As anaerobic granular systems are capable of handling high organic loadings concomitant with high strength wastewater and short hydraulic retention time, they could render much more carbon credits than other conventional anaerobic systems. This study investigated the potential carbon credit derived from laboratory-scale upflow anaerobic sludge blanket (UASB) reactors based on a carbon balance analysis. Methane emission reduction could be calculated by calculating the difference of UASB reactors and open lagoon treatment systems. Based on the 2.5l bench-scale reactor, the total CH(4) emissions reduction was calculated as 29 kg CO(2)/year. On scaling up to a typical full-scale anaerobic digester, the total CH(4) emissions reduction could achieve 46,420 tons CO(2) reduction/year. The estimated carbon credits would amount to 278,500 US$ per year by assuming a carbon price of 6 US$ per metric ton CO(2) reduction. The analysis postulated that it is financially viable to invest in advanced anaerobic granular treatment system from the revenue generated from carbon credits. PMID:18990565

  6. Aqueous mercury adsorption by activated carbons.

    PubMed

    Hadi, Pejman; To, Ming-Ho; Hui, Chi-Wai; Lin, Carol Sze Ki; McKay, Gordon

    2015-04-15

    Due to serious public health threats resulting from mercury pollution and its rapid distribution in our food chain through the contamination of water bodies, stringent regulations have been enacted on mercury-laden wastewater discharge. Activated carbons have been widely used in the removal of mercuric ions from aqueous effluents. The surface and textural characteristics of activated carbons are the two decisive factors in their efficiency in mercury removal from wastewater. Herein, the structural properties and binding affinity of mercuric ions from effluents have been presented. Also, specific attention has been directed to the effect of sulfur-containing functional moieties on enhancing the mercury adsorption. It has been demonstrated that surface area, pore size, pore size distribution and surface functional groups should collectively be taken into consideration in designing the optimal mercury removal process. Moreover, the mercury adsorption mechanism has been addressed using equilibrium adsorption isotherm, thermodynamic and kinetic studies. Further recommendations have been proposed with the aim of increasing the mercury removal efficiency using carbon activation processes with lower energy input, while achieving similar or even higher efficiencies. PMID:25644627

  7. Next-Generation Pyrosequencing Analysis of Microbial Biofilm Communities on Granular Activated Carbon in Treatment of Oil Sands Process-Affected Water

    PubMed Central

    Islam, M. Shahinoor; Zhang, Yanyan; McPhedran, Kerry N.

    2015-01-01

    The development of biodegradation treatment processes for oil sands process-affected water (OSPW) has been progressing in recent years with the promising potential of biofilm reactors. Previously, the granular activated carbon (GAC) biofilm process was successfully employed for treatment of a large variety of recalcitrant organic compounds in domestic and industrial wastewaters. In this study, GAC biofilm microbial development and degradation efficiency were investigated for OSPW treatment by monitoring the biofilm growth on the GAC surface in raw and ozonated OSPW in batch bioreactors. The GAC biofilm community was characterized using a next-generation 16S rRNA gene pyrosequencing technique that revealed that the phylum Proteobacteria was dominant in both OSPW and biofilms, with further in-depth analysis showing higher abundances of Alpha- and Gammaproteobacteria sequences. Interestingly, many known polyaromatic hydrocarbon degraders, namely, Burkholderiales, Pseudomonadales, Bdellovibrionales, and Sphingomonadales, were observed in the GAC biofilm. Ozonation decreased the microbial diversity in planktonic OSPW but increased the microbial diversity in the GAC biofilms. Quantitative real-time PCR revealed similar bacterial gene copy numbers (>109 gene copies/g of GAC) for both raw and ozonated OSPW GAC biofilms. The observed rates of removal of naphthenic acids (NAs) over the 2-day experiments for the GAC biofilm treatments of raw and ozonated OSPW were 31% and 66%, respectively. Overall, a relatively low ozone dose (30 mg of O3/liter utilized) combined with GAC biofilm treatment significantly increased NA removal rates. The treatment of OSPW in bioreactors using GAC biofilms is a promising technology for the reduction of recalcitrant OSPW organic compounds. PMID:25841014

  8. Next-generation pyrosequencing analysis of microbial biofilm communities on granular activated carbon in treatment of oil sands process-affected water.

    PubMed

    Islam, M Shahinoor; Zhang, Yanyan; McPhedran, Kerry N; Liu, Yang; Gamal El-Din, Mohamed

    2015-06-15

    The development of biodegradation treatment processes for oil sands process-affected water (OSPW) has been progressing in recent years with the promising potential of biofilm reactors. Previously, the granular activated carbon (GAC) biofilm process was successfully employed for treatment of a large variety of recalcitrant organic compounds in domestic and industrial wastewaters. In this study, GAC biofilm microbial development and degradation efficiency were investigated for OSPW treatment by monitoring the biofilm growth on the GAC surface in raw and ozonated OSPW in batch bioreactors. The GAC biofilm community was characterized using a next-generation 16S rRNA gene pyrosequencing technique that revealed that the phylum Proteobacteria was dominant in both OSPW and biofilms, with further in-depth analysis showing higher abundances of Alpha- and Gammaproteobacteria sequences. Interestingly, many known polyaromatic hydrocarbon degraders, namely, Burkholderiales, Pseudomonadales, Bdellovibrionales, and Sphingomonadales, were observed in the GAC biofilm. Ozonation decreased the microbial diversity in planktonic OSPW but increased the microbial diversity in the GAC biofilms. Quantitative real-time PCR revealed similar bacterial gene copy numbers (>10(9) gene copies/g of GAC) for both raw and ozonated OSPW GAC biofilms. The observed rates of removal of naphthenic acids (NAs) over the 2-day experiments for the GAC biofilm treatments of raw and ozonated OSPW were 31% and 66%, respectively. Overall, a relatively low ozone dose (30 mg of O3/liter utilized) combined with GAC biofilm treatment significantly increased NA removal rates. The treatment of OSPW in bioreactors using GAC biofilms is a promising technology for the reduction of recalcitrant OSPW organic compounds. PMID:25841014

  9. DEVELOPMENT OF ACTIVATED CARBONS FROM COAL COMBUSTION BY-PRODUCTS

    SciTech Connect

    Harold H. Schobert; M. Mercedes Maroto-Valer; Zhe Lu

    2003-09-30

    The increasing role of coal as a source of energy in the 21st century will demand environmental and cost-effective strategies for the use of coal combustion by-products (CCBPs), mainly unburned carbon in fly ash. Unburned carbon is nowadays regarded as a waste product and its fate is mainly disposal, due to the present lack of efficient routes for its utilization. However, unburned carbon is a potential precursor for the production of adsorbent carbons, since it has gone through a devolatilization process while in the combustor, and therefore, only requires to be activated. Accordingly, the principal objective of this work was to characterize and utilize the unburned carbon in fly ash for the production of activated carbons. The unburned carbon samples were collected from different combustion systems, including pulverized utility boilers, a utility cyclone, a stoker, and a fluidized bed combustor. LOI (loss-on-ignition), proximate, ultimate, and petrographic analyses were conducted, and the surface areas of the samples were characterized by N2 adsorption isotherms at 77K. The LOIs of the unburned carbon samples varied between 21.79-84.52%. The proximate analyses showed that all the samples had very low moisture contents (0.17 to 3.39 wt %), while the volatile matter contents varied between 0.45 to 24.82 wt%. The elemental analyses show that all the unburned carbon samples consist mainly of carbon with very little hydrogen, nitrogen, sulfur and oxygen In addition, the potential use of unburned carbon as precursor for activated carbon (AC) was investigated. Activated carbons with specific surface area up to 1075m{sup 2}/g were produced from the unburned carbon. The porosity of the resultant activated carbons was related to the properties of the unburned carbon feedstock and the activation conditions used. It was found that not all the unburned carbon samples are equally suited for activation, and furthermore, their potential as activated carbons precursors could be inferred from their physical and chemical properties. The developed porosity of the activated carbon was a function of the oxygen content, porosity and H/C ratio of the parent unburned carbon feedstock. It was observed that extended activation times and high activation temperatures increased the porosity of the produced activated carbon at the expense of the solid yield. The development of activated carbon from unburned carbon in fly ash has been proven to be a success by this study in terms of the higher surface areas of the resultant activated carbons, which are comparable with commercial activated carbons. However, unburned carbon samples obtained from coal-fired power plants as by-product have high ash content, which is unwanted for the production of activated carbons. Therefore, the separation of unburned carbon from the fly ash is expected to be beneficial for the utilization of unburned carbon to produce activated carbons with low ash content.

  10. Process for making carbon foam

    DOEpatents

    Klett, James W. (Knoxville, TN)

    2000-01-01

    The process obviates the need for conventional oxidative stabilization. The process employs mesophase or isotropic pitch and a simplified process using a single mold. The foam has a relatively uniform distribution of pore sizes and a highly aligned graphic structure in the struts. The foam material can be made into a composite which is useful in high temperature sandwich panels for both thermal and structural applications.

  11. Preparation and characterization of activated carbon produced from pomegranate seeds by ZnCl 2 activation

    NASA Astrophysics Data System (ADS)

    Uar, Suat; Erdem, Murat; Tay, Turgay; Karagz, Selhan

    2009-08-01

    In this study, pomegranate seeds, a by-product of fruit juice industry, were used as precursor for the preparation of activated carbon by chemical activation with ZnCl 2. The influence of process variables such as the carbonization temperature and the impregnation ratio on textural and chemical-surface properties of the activated carbons was studied. When using the 2.0 impregnation ratio at the carbonization temperature of 600 C, the specific surface area of the resultant carbon is as high as 978.8 m 2 g -1. The results showed that the surface area and total pore volume of the activated carbons at the lowest impregnation ratio and the carbonization temperature were achieved as high as 709.4 m 2 g -1 and 0.329 cm 3 g -1. The surface area was strongly influenced by the impregnation ratio of activation reagent and the subsequent carbonization temperature.

  12. Adsorption of herbicides using activated carbons

    SciTech Connect

    Derbyshire, F.; Jagtoyan, M.; Lafferty, C.; Kimber, G.

    1996-10-01

    This work describes development of a series of novel activated carbon materials and their testing for possible water treatment applications by studying the adsorption of sodium pentachlorphenolate, PCP (a common herbicide/wood preservative). Although the application of activated carbons is an established technology for the treatment of public water supplies, there is a growing need for materials with higher selectivity and adsorptive capacities as well as high abrasion resistance. The materials that will be discussed include extruded wood-derived carbons with novel pore size distributions and high hardness, as well as activated carbon fiber composites. Comparisons will be made with commercial granular water treatment carbons.

  13. Active braze process

    SciTech Connect

    Levine, I.L.; Pike, R.A.

    1990-11-02

    Active metal bonding using Cusil (silver-copper) braze alloys is a well established method used at GE Neutron Devices (GEND) for bonding metal to metal, metal to ceramics, and ceramics to ceramics. However, there are many instances in which using a silver alloy for bonding is undesirable (e.g., in vacuum tube envelopes, or where sequential braze steps at different temperatures are required to complete an assembly). The Material and Processes Laboratory at GEND has discovered a new method of active brazing with non-silver alloys which has proved especially successful in ceramic-to-ceramic joints. This method has the added advantage of eliminating several steps which are required in conventional bonding techniques. 2 figs., 10 tabs.

  14. JPL Activated Carbon Treatment System (ACTS) for sewage

    NASA Technical Reports Server (NTRS)

    1976-01-01

    An Activated Carbon Treatment System (ACTS) was developed for sewage treatment and is being applied to a one-million gallon per day sewage treatment pilot plant in Orange County California. Activities reported include pyrolysis and activation of carbon-sewage sludge, and activated carbon treatment of sewage to meet ocean discharge standards. The ACTS Sewage treatment operations include carbon-sewage treatment, primary and secondary clarifiers, gravity (multi-media) filter, filter press dewatering, flash drying of carbon-sewage filter cake, and sludge pyrolysis and activation. Tests were conducted on a laboratory scale, 10,000 gallon per day demonstration plant and pilot test equipment. Preliminary economic studies are favorable to the ACTS process relative to activated sludge treatment for a 175,000,000 gallon per day sewage treatment plant.

  15. Adsorption of chlorophenols on granular activated carbon

    SciTech Connect

    Yang, M.

    1993-12-31

    Studies were undertaken of the adsorption of chlorinated phenols from aqueous solution on granular activated carbon (Filtrasorb-400, 30 x 40 mesh). Single-component equilibrium adsorption data on the eight compounds in two concentration ranges at pH 7.0 fit the Langmuir equation better than the Freundlich equation. The adsorptive capacities at pH 7.0 increase from pentachlorophenol to trichlorophenols and are fairly constant from trichlorophenols to monochlorophenols. The adsorption process was found to be exothermic for pentachlorophenol and 2,4,6-trichlorophenol, and endothermic for 2,4-dichlorophenol and 4-chlorophenol. Equilibrium measurements were also conducted for 2,4,5-trichlorophenol, 2,4-dichlorophenol, and 4-chlorophenol over a wide pH range. A surface complexation model was proposed to describe the effect of pH on adsorption equilibria of chlorophenols on activated carbon. The simulations of the model are in excellent agreement with the experimental data. Batch kinetics studies were conducted of the adsorption of chlorinated phenols on granular activated carbon. The results show that the surface reaction model best describes both the short-term and long-term kinetics, while the external film diffusion model describes the short-term kinetics data very well and the linear-driving-force approximation improved its performance for the long-term kinetics. Multicomponent adsorption equilibria of chlorophenols on granular activated carbon was investigated in the micromolar equilibrium concentration range. The Langmuir competitive and Ideal Adsorbed Solution (IAS) models were tested for their performance on the three binary systems of pentachlorophenol/2,4,6-trichlorophenol, 2,4,6-trichlorophenol/2,4-dichlorophenol, and 2,4-dichlorophenol/4-chlorophenol, and the tertiary system of 2,4,6-trichlorophenol/2,4-dichlorophenol/4-chlorophenol, and found to fail to predict the two-component adsorption equilibria of the former two binary systems and the tertiary system.

  16. SORPTION OF ELEMENTAL MERCURY BY ACTIVATED CARBONS

    EPA Science Inventory

    The mechanisms and rate of elemental mercury (HgO) capture by activated carbons have been studied using a bench-scale apparatus. Three types of activated carbons, two of which are thermally activated (PC-100 and FGD) and one with elemental sulfur (S) impregnated in it (HGR), were...

  17. Studies and characterisations of various activated carbons used for carbon/carbon supercapacitors

    NASA Astrophysics Data System (ADS)

    Gamby, J.; Taberna, P. L.; Simon, P.; Fauvarque, J. F.; Chesneau, M.

    Various activated carbons from the PICA Company have been tested in supercapacitor cells in order to compare their performances. The differences measured in terms of specific capacitance and cell resistance are presented. Porosity measurements made on activated carbon powders and electrode allowed a better understanding of the electrochemical behaviour of these activated carbons. In this way, the PICACTIF SC carbon was found to be an interesting active material for supercapacitors, with a specific capacitance as high as 125 F/g.

  18. Charcoal and activated carbon at elevated pressure

    SciTech Connect

    Antal, M.J. Jr.; Dai, Xiangfeng; Norberg, N.

    1995-12-01

    High quality charcoal has been produced with very high yields of 50% to 60% from macadamia nut and kukui nut shells and of 44% to 47% from Eucalyptus and Leucaena wood in a bench scale unit at elevated pressure on a 2 to 3 hour cycle, compared to commercial practice of 25% to 30% yield on a 7 to 12 day operating cycle. Neither air pollution nor tar is produced by the process. The effects of feedstock pretreatments with metal additives on charcoal yield are evaluated in this paper. Also, the influences of steam and air partial pressure and total pressure on yields of activated carbon from high yield charcoal are presented.

  19. Purification process for vertically aligned carbon nanofibers

    NASA Technical Reports Server (NTRS)

    Nguyen, Cattien V.; Delziet, Lance; Matthews, Kristopher; Chen, Bin; Meyyappan, M.

    2003-01-01

    Individual, free-standing, vertically aligned multiwall carbon nanotubes or nanofibers are ideal for sensor and electrode applications. Our plasma-enhanced chemical vapor deposition techniques for producing free-standing and vertically aligned carbon nanofibers use catalyst particles at the tip of the fiber. Here we present a simple purification process for the removal of iron catalyst particles at the tip of vertically aligned carbon nanofibers derived by plasma-enhanced chemical vapor deposition. The first step involves thermal oxidation in air, at temperatures of 200-400 degrees C, resulting in the physical swelling of the iron particles from the formation of iron oxide. Subsequently, the complete removal of the iron oxide particles is achieved with diluted acid (12% HCl). The purification process appears to be very efficient at removing all of the iron catalyst particles. Electron microscopy images and Raman spectroscopy data indicate that the purification process does not damage the graphitic structure of the nanotubes.

  20. A NOVEL APPROACH TO MINERAL CARBONATION: ENHANCING CARBONATION WHILE AVOIDING MINERAL PRETREATMENT PROCESS COST

    SciTech Connect

    Michael J. McKelvy; Andrew V.G. Chizmeshya; Kyle Squires; Ray W. Carpenter; Hamadallah Bearat

    2005-10-01

    Known fossil fuel reserves, especially coal, can support global energy demands for centuries to come, if the environmental problems associated with CO{sub 2} emissions can be overcome. Unlike other CO{sub 2} sequestration candidate technologies that propose long-term storage, mineral sequestration provides permanent disposal by forming geologically stable mineral carbonates. Carbonation of the widely occurring mineral olivine (e.g., forsterite, Mg{sub 2}SiO{sub 4}) is a large-scale sequestration process candidate for regional implementation, which converts CO{sub 2} into the environmentally benign mineral magnesite (MgCO{sub 3}). The primary goal is cost-competitive process development. As the process is exothermic, it inherently offers low-cost potential. Enhancing carbonation reactivity is key to economic viability. Recent studies at the U.S. DOE Albany Research Center have established that aqueous-solution carbonation using supercritical CO{sub 2} is a promising process; even without olivine activation, 30-50% carbonation has been achieved in an hour. Mechanical activation (e.g., attrition) has accelerated the carbonation process to an industrial timescale (i.e., near completion in less than an hour), at reduced pressure and temperature. However, the activation cost is too high to be economical and lower cost pretreatment options are needed. Herein, we report our first year progress in exploring a novel approach that offers the potential to substantially enhance carbonation reactivity while bypassing pretreatment activation. We have discovered that robust silica-rich passivating layers form on the olivine surface during carbonation. As carbonation proceeds, these passivating layers thicken, fracture and eventually exfoliate, exposing fresh olivine surfaces during rapidly-stirred/circulating carbonation. We are exploring the mechanisms that govern carbonation reactivity and the impact that (1) modeling/controlling the slurry fluid-flow conditions, (2) varying the aqueous ion species/size and concentration (e.g., Li{sup +}, Na{sup +}, K{sup +}, Rb{sup +}, Cl{sup -}, HCO{sub 3}{sup -}), and (3) incorporating select sonication offer to enhance exfoliation and carbonation. Thus far, we have succeeded in nearly doubling the extent of carbonation observed compared with the optimum procedure previously developed by the Albany Research Center. Aqueous carbonation reactivity was found to be a strong function of the ionic species present and their aqueous activities, as well as the slurry fluid flow conditions incorporated. Synergistic control of these parameters offers the potential for further improvements in carbonation reactivity. A new sonication exfoliation system incorporating a novel sealing system was developed to carry out the sonication studies. Our initial studies that incorporate controlled sonication have not yet lead to a significant improvement in the extent of carbonation observed. Year 2 studies will emphasize those approaches that offer the greatest potential to cost effectively enhance carbonation, as well as combined approaches that may further enhance carbonation. Mechanistic investigations indicate incongruent dissolution results in the observed silica-rich passivating layer formation. Observations of magnesite nanocrystals within the passivating layers that form indicate the layers can exhibit significant permeability to the key reactants present (e.g., Mg{sup 2+}, H{sup +}, H{sub 2}O, CO{sub 2}, and HCO{sub 3} -). Atomistic modeling supports the observation of robust passivating layers that retain significant permeability to the key reaction species involved. Studies in Year 2 will emphasize the impact that controlled aqueous speciation and activity and slurry-flow dynamics have on the mechanisms that control carbonation reactivity and the potential they offer to substantially reduce olivine mineral sequestration process cost.

  1. Carbon dioxide reduction by the Bosch process

    NASA Technical Reports Server (NTRS)

    Manning, M. P.; Reid, R. C.

    1975-01-01

    Prototype units for carrying out the reduction of carbon dioxide to elementary carbon have been built and operated successfully. In some cases, however, startup difficulties have been reported. Moreover, the recycle reactor product has been reported to contain only small amounts of water and undesirably high yields of methane. This paper presents the results of the first phase of an experimental study that was carried out to define the mechanisms occurring in the reduction process. Conclusions are drawn and possible modifications to the present recycle process are suggested.

  2. Modeling carbonizing process in fluidized bed

    NASA Astrophysics Data System (ADS)

    Szota, M.; Jasinski, J.

    2010-06-01

    This paper presents possibility of using neural networks model for designing carbonizing process in fluidized bed. This process is very complicated and difficult as multi-parameters changes are non linear and car drive cross structure is non homogeneous. This fact and lack of mathematical algorithms describing this process makes modeling properties of drives elements by traditional numerical methods difficult or even impossible. In this case it is possible to try using artificial neural network. Using neural networks for modeling carbonizing in fluidized bed is caused by several nets' features: non linear character, ability to generalize the results of calculations for data out of training set, no need for mathematical algorithms describing influence changes input parameters on modeling materials properties. The neural network structure is designed and special prepared by choosing input and output parameters of process. The method of learning and testing neural network, the way of limiting nets structure and minimizing learning and testing error are discussed. Such prepared neural network model, after putting expected values of car cross driving properties in output layer, can give answers to a lot of questions about running carbonizing process in fluidized bed. The practical implications of the neural network models are possibility of using they to build control system capable of on-line controlling running process and supporting engineering decision in real time. The originality of this research is different conception to obtain foreseen materials properties after carbonizing in fluidized bed. The specially prepared neural networks model could be a help for engineering decisions and may be used in designing carbonizing process in fluidized bed as well as in controlling changes of this process.

  3. Activated carbon fiber composite material and method of making

    DOEpatents

    Burchell, Timothy D. (Oak Ridge, TN); Weaver, Charles E. (Knoxville, TN); Chilcoat, Bill R. (Knoxville, TN); Derbyshire, Frank (Lexington, KY); Jagtoyen, Marit (Lexington, KY)

    2001-01-01

    An activated carbon fiber composite for separation and purification, or catalytic processing of fluids is described. The activated composite comprises carbon fibers rigidly bonded to form an open, permeable, rigid monolith capable of being formed to near-net-shape. Separation and purification of gases are effected by means of a controlled pore structure that is developed in the carbon fibers contained in the composite. The open, permeable structure allows the free flow of gases through the monolith accompanied by high rates of adsorption. By modification of the pore structure and bulk density the composite can be rendered suitable for applications such as gas storage, catalysis, and liquid phase processing.

  4. Activated carbon fiber composite material and method of making

    SciTech Connect

    Burchell, Timothy D.; Weaver, Charles E.; Chilcoat, Bill R.; Derbyshire, Frank; Jagtoyen, Marit

    2000-01-01

    An activated carbon fiber composite for separation and purification, or catalytic processing of fluids is described. The activated composite comprises carbon fibers rigidly bonded to form an open, permeable, rigid monolith capable of being formed to near-net-shape. Separation and purification of gases are effected by means of a controlled pore structure that is developed in the carbon fibers contained in the composite. The open, permeable structure allows the free flow of gases through the monolith accompanied by high rates of adsorption. By modification of the pore structure and bulk density the composite can be rendered suitable for applications such as gas storage, catalysis, and liquid phase processing.

  5. Accelerated adsorption with activated carbon fiber

    SciTech Connect

    Pimenov, A.V.; Lieberman, A.I.; Shmidt, J.L.; Cheh, H.Y.

    1995-09-01

    The properties of a new type of polyamphoteric activated carbon fiber (ACF) were investigated theoretically and experimentally. Results are compared with those from granular activated carbon (GAC) and ion-exchange resin (IER) materials. The adsorption rate of ACF was found to be two orders of magnitude higher than that of the GAC and one order of magnitude higher than that of the IER.

  6. Microbial carbon recycling: an underestimated process controlling soil carbon dynamics

    NASA Astrophysics Data System (ADS)

    Basler, A.; Dippold, M.; Helfrich, M.; Dyckmans, J.

    2015-07-01

    The mean residence times (MRT) of different compound classes of soil organic matter (SOM) do not match their inherent recalcitrance to decomposition. One reason for this is the stabilisation within the soil matrix, but recycling, i.e. the reuse of "old" organic material to form new biomass may also play a role as it uncouples the residence times of organic matter from the lifetime of discrete molecules in soil. We analysed soil sugar dynamics in a natural 30 years old labelling experiment after a~wheat-maize vegetation change to determine the extent of recycling and stabilisation in plant and microbial derived sugars: while plant derived sugars are only affected by stabilisation processes, microbial sugars may be subject to both, stabilisation and recycling. To disentangle the dynamics of soil sugars, we separated different density fractions (free particulate organic matter (fPOM), light occluded particulate organic matter (≤1.6 g cm-3; oPOM1.6), dense occluded particulate organic matter (≤2 g cm-3; oPOM2) and mineral-associated organic matter (>2 g cm-3; Mineral)) of a~silty loam under long term wheat and maize cultivation. The isotopic signature of sugars was measured by high pressure liquid chromatography coupled to isotope ratio mass spectrometry (HPLC/IRMS), after hydrolysis with 4 M Trifluoroacetic acid (TFA). While apparent mean residence times (MRT) of sugars were comparable to total organic carbon in the bulk soil and mineral fraction, the apparent MRT of sugars in the oPOM fractions were considerably lower than those of the total carbon of these fractions. This indicates that oPOM formation was fuelled by microbial activity feeding on new plant input. In the bulk soil, mean residence times of the mainly plant derived xylose (xyl) were significantly lower than those of mainly microbial derived sugars like galactose (gal), rhamnose (rha), fucose (fuc), indicating that recycling of organic matter is an important factor regulating organic matter dynamics in soil.

  7. Selecting activated carbon for water and wastewater treatability studies

    SciTech Connect

    Zhang, W.; Chang, Q.G.; Liu, W.D.; Li, B.J.; Jiang, W.X.; Fu, L.J.; Ying, W.C.

    2007-10-15

    A series of follow-up investigations were performed to produce data for improving the four-indicator carbon selection method that we developed to identify high-potential activated carbons effective for removing specific organic water pollutants. The carbon's pore structure and surface chemistry are dependent on the raw material and the activation process. Coconut carbons have relatively more small pores than large pores; coal and apricot nutshell/walnut shell fruit carbons have the desirable pore structures for removing adsorbates of all sizes. Chemical activation, excessive activation, and/or thermal reactivation enlarge small pores, resulting in reduced phenol number and higher tannic acid number. Activated carbon's phenol, iodine, methylene blue, and tannic acid numbers are convenient indicators of its surface area and pore volume of pore diameters < 10, 10-15, 15-28, and > 28 angstrom, respectively. The phenol number of a carbon is also a good indicator of its surface acidity of oxygen-containing organic functional groups that affect the adsorptive capacity for aromatic and other small polar organics. The tannic acid number is an indicator of carbon's capacity for large, high-molecular-weight natural organic precursors of disinfection by-products in water treatment. The experimental results for removing nitrobenzene, methyl-tert-butyl ether, 4,4-bisphenol, humic acid, and the organic constituents of a biologically treated coking-plant effluent have demonstrated the effectiveness of this capacity-indicator-based method of carbon selection.

  8. Reduction of bromate by granular activated carbon

    SciTech Connect

    Kirisits, M.J.; Snoeyink, V.L.; Kruithof, J.C.

    1998-07-01

    Ozonation of waters containing bromide can lead to the formation of bromate, a probable human carcinogen. Since bromate will be regulated at 10 {micro}g/L by the Stage 1 Disinfectants/Disinfection By-Products Rule, there is considerable interest in finding a suitable method of bromate reduction. Granular activated carbon (GAC) can be used to chemically reduce bromate to bromide, but interference from organic matter and anions present in natural water render this process inefficient. In an effort to improve bromate reduction by GAC, several modifications were made to the GAC filtration process. The use of a biologically active carbon (BAC) filter ahead of a fresh GAC filter with and without preozonation, to remove the biodegradable organic matter, did not substantially improve the bromate removal of the GAC filter. The use of the BAC filter for biological bromate reduction proved to be the most encouraging experiment. By lowering the dissolved oxygen in the influent to the BAC from 8.0 mg/L to 2.0 mg/L, the percent bromate removal increased from 42% to 61%.

  9. Oxygen reduction activity of carbon nitride supported on carbon nanotubes.

    PubMed

    Lyth, S M; Nabae, Y; Islam, N M; Kuroki, S; Kakimoto, M; Miyata, S

    2012-06-01

    Fuel cells offer an alternative to burning fossil fuels, but use platinum as a catalyst which is expensive and scarce. Cheap, alternative catalysts could enable fuel cells to become serious contenders in the green energy sector. One promising class of catalyst for electrochemical oxygen reduction is iron-containing, nanostructured, nitrogen-doped carbon. The catalytic activity of such N-doped carbons has improved vastly over the years bringing industrial applications ever closer. Stoichiometric carbon nitride powder has only been observed in recent years. It has nitrogen content up to 57% and as such is an extremely interesting material to work with. The electrochemical activity of carbon nitride has already been explored, confirming that iron is not a necessary ingredient for 4-electron oxygen reduction. Here, we synthesize carbon nitride on a carbon nanotube support and subject it to high temperature treatment in an effort to increase the surface area and conductivity. The results lend insight into the mechanism of oxygen reduction and show the potential for carbon nanotube-supported carbon nitride to be used as a catalyst to replace platinum in fuel cells. PMID:22905547

  10. Catalytic Growth of Macroscopic Carbon Nanofibers Bodies with Activated Carbon

    SciTech Connect

    Abdullah, N.; Muhammad, I. S.; Hamid, S. B. Abd.; Rinaldi, A.; Su, D. S.; Schlogl, R.

    2009-06-01

    Carbon-carbon composite of activated carbon and carbon nanofibers have been synthesized by growing Carbon nanofiber (CNF) on Palm shell-based Activated carbon (AC) with Ni catalyst. The composites are in an agglomerated shape due to the entanglement of the defective CNF between the AC particles forming a macroscopic body. The macroscopic size will allow the composite to be used as a stabile catalyst support and liquid adsorbent. The preparation of CNT/AC nanocarbon was initiated by pre-treating the activated carbon with nitric acid, followed by impregnation of 1 wt% loading of nickel (II) nitrate solutions in acetone. The catalyst precursor was calcined and reduced at 300 deg. C for an hour in each step. The catalytic growth of nanocarbon in C{sub 2}H{sub 4}/H{sub 2} was carried out at temperature of 550 deg. C for 2 hrs with different rotating angle in the fluidization system. SEM and N{sub 2} isotherms show the level of agglomeration which is a function of growth density and fluidization of the system. The effect of fluidization by rotating the reactor during growth with different speed give a significant impact on the agglomeration of the final CNF/AC composite and thus the amount of CNFs produced. The macrostructure body produced in this work of CNF/AC composite will have advantages in the adsorbent and catalyst support application, due to the mechanical and chemical properties of the material.

  11. Catalytic Growth of Macroscopic Carbon Nanofibers Bodies with Activated Carbon

    NASA Astrophysics Data System (ADS)

    Abdullah, N.; Rinaldi, A.; Muhammad, I. S.; Hamid, S. B. Abd.; Su, D. S.; Schlogl, R.

    2009-06-01

    Carbon-carbon composite of activated carbon and carbon nanofibers have been synthesized by growing Carbon nanofiber (CNF) on Palm shell-based Activated carbon (AC) with Ni catalyst. The composites are in an agglomerated shape due to the entanglement of the defective CNF between the AC particles forming a macroscopic body. The macroscopic size will allow the composite to be used as a stabile catalyst support and liquid adsorbent. The preparation of CNT/AC nanocarbon was initiated by pre-treating the activated carbon with nitric acid, followed by impregnation of 1 wt% loading of nickel (II) nitrate solutions in acetone. The catalyst precursor was calcined and reduced at 300 C for an hour in each step. The catalytic growth of nanocarbon in C2H4/H2 was carried out at temperature of 550 C for 2 hrs with different rotating angle in the fluidization system. SEM and N2 isotherms show the level of agglomeration which is a function of growth density and fluidization of the system. The effect of fluidization by rotating the reactor during growth with different speed give a significant impact on the agglomeration of the final CNF/AC composite and thus the amount of CNFs produced. The macrostructure body produced in this work of CNF/AC composite will have advantages in the adsorbent and catalyst support application, due to the mechanical and chemical properties of the material.

  12. Chemical activation of gasification carbon residue for phosphate removal

    NASA Astrophysics Data System (ADS)

    Kilpimaa, Sari; Runtti, Hanna; Lassi, Ulla; Kuokkanen, Toivo

    2012-05-01

    Recycling of waste materials provides an economical and environmentally significant method to reduce the amount of waste. Bioash formed in the gasification process possesses a notable amount of unburned carbon and therefore it can be called a carbon residue. After chemical activation carbon residue could be use to replace activated carbon for example in wastewater purification processes. The effect of chemical activation process variables such as chemical agents and contact time in the chemical activation process were investigated. This study also explored the effectiveness of the chemically activated carbon residue for the removal of phosphate from an aqueous solution. The experimental adsorption study was performed in a batch reactor and the influence of adsorption time, initial phosphate concentration and pH was studied. Due to the carbon residue's low cost and high adsorption capacity, this type of waste has the potential to be utilised for the cost-effective removal of phosphate from wastewaters. Potential adsorbents could be prepared from these carbonaceous by-products and used as an adsorbent for phosphate removal.

  13. Reprocessing of used tires into activated carbon and other products

    SciTech Connect

    Teng, H.; Serio, M.A.; Wojtowicz, M.A.; Bassilakis, R.; Solomon, P.R.

    1995-09-01

    Landfilling used tires which are generated each year in the US is increasingly becoming an unacceptable solution. A better approach, from an environmental and economic standpoint, is to thermally reprocess the tires into valuable products such as activated carbon, other solid carbon forms (carbon black, graphite, and carbon fibers), and liquid fuels. In this study, high surface area activated carbons (> 800 m{sup 2}/g solid product) were produced in relatively high yields by pyrolysis of tires at up to 900 C, followed by activation in CO{sub 2} at the same temperature. The surface areas of these materials are comparable with those of commercial activated carbons. The efficiency of the activation process (gain in specific surface area/loss in mass) was greatest (up to 138 m{sup 2}/g original tire) when large pieces of tire material were used ({approximately} 170 mg). Oxygen pretreatment of tires was found to enhance both the yield and the surface area of the carbon product. High-pressure treatment of tires at low temperatures (< 400 C) is an alternative approach if the recovery of carbon black or fuel oils is the primary objective.

  14. Thermocatalytic process for CO.sub.2-free production of hydrogen and carbon from hydrocarbons

    DOEpatents

    Muradov, Nazim Z.

    2011-08-23

    A novel process and apparatus are disclosed for sustainable CO.sub.2-free production of hydrogen and carbon by thermocatalytic decomposition (dissociation, pyrolysis, cracking) of hydrocarbon fuels over carbon-based catalysts in the absence of air and/or water. The apparatus and thermocatalytic process improve the activity and stability of carbon catalysts during the thermocatalytic process and produce both high purity hydrogen (at least, 99.0 volume %) and carbon, from any hydrocarbon fuel, including sulfurous fuels. In a preferred embodiment, production of hydrogen and carbon is achieved by both internal and external activation of carbon catalysts. Internal activation of carbon catalyst is accomplished by recycling of hydrogen-depleted gas containing unsaturated and aromatic hydrocarbons back to the reactor. External activation of the catalyst can be achieved via surface gasification with hot combustion gases during catalyst heating. The process and apparatus can be conveniently integrated with any type of fuel cell to generate electricity.

  15. Measured Enthalpies of Adsorption of Boron-Doped Activated Carbons

    NASA Astrophysics Data System (ADS)

    Beckner, M.; Romanos, J.; Dohnke, E.; Singh, A.; Schaeperkoetter, J.; Stalla, D.; Burress, J.; Jalisatgi, S.; Suppes, G.; Hawthorne, M. F.; Yu, P.; Wexler, C.; Pfeifer, P.

    2012-02-01

    There is significant interest in the properties of boron-doped activated carbons for their potential to improve hydrogen storage.ootnotetextMultiply Surface-Functionalized Nanoporous Carbon for Vehicular Hydrogen Storage, P. Pfeifer et al. DOE Hydrogen Program 2011 Annual Progress Report, IV.C.3, 444-449 (2011). Boron-doped activated carbons have been produced using a process involving the pyrolysis of decaborane (B10H14) and subsequent high-temperature annealing. In this talk, we will present a systematic study of the effect of different boron doping processes on the samples' structure, hydrogen sorption, and surface chemistry. Initial room temperature experiments show a 20% increase in the hydrogen excess adsorption per surface area compared to the undoped material. Experimental enthalpies of adsorption will be presented for comparison to theoretical predictions for boron-doped carbon materials. Additionally, results from a modified version of the doping process will be presented.

  16. A Novel Approach To Mineral Carbonation: Enhancing Carbonation While Avoiding Mineral Pretreatment Process Cost

    SciTech Connect

    Michael J. McKelvy; Andrew V. G. Chizmeshya; Kyle Squires; Ray W. Carpenter; Hamdallah Bearat

    2006-06-21

    Known fossil fuel reserves, especially coal, can support global energy demands for centuries to come, if the environmental problems associated with CO{sub 2} emissions can be overcome. Unlike other CO{sub 2} sequestration candidate technologies that propose long-term storage, mineral sequestration provides permanent disposal by forming geologically stable mineral carbonates. Carbonation of the widely occurring mineral olivine (e.g., forsterite, Mg{sub 2}SiO{sub 4}) is a large-scale sequestration process candidate for regional implementation, which converts CO{sub 2} into the environmentally benign mineral magnesite (MgCO{sub 3}). The primary goal is cost-competitive process development. As the process is exothermic, it inherently offers low-cost potential. Enhancing carbonation reactivity is key to economic viability. Recent studies at the U.S. DOE Albany Research Center have established that aqueous-solution carbonation using supercritical CO{sub 2} is a promising process; even without olivine activation, 30-50% carbonation has been achieved in an hour. Mechanical activation (e.g., attrition) has accelerated the carbonation process to an industrial timescale (i.e., near completion in less than an hour), at reduced pressure and temperature. However, the activation cost is too high to be economical and lower cost pretreatment options are needed. Herein, we report our second year progress in exploring a novel approach that offers the potential to substantially enhance carbonation reactivity while bypassing pretreatment activation. As our second year progress is intimately related to our earlier work, the report is presented in that context to provide better overall understanding of the progress made. We have discovered that robust silica-rich passivating layers form on the olivine surface during carbonation. As carbonation proceeds, these passivating layers thicken, fracture and eventually exfoliate, exposing fresh olivine surfaces during rapidly-stirred/circulating carbonation. We are exploring the mechanisms that govern carbonation reactivity and the impact that (i) modeling/controlling the slurry fluid-flow conditions, (ii) varying the aqueous ion species/size and concentration (e.g., Li{sup +}, Na{sup +}, K{sup +}, Rb{sup +}, Cl{sup -}, HCO{sub 3}{sup -}), and (iii) incorporating select sonication offer to enhance exfoliation and carbonation. We have succeeded in nearly doubling the extent of carbonation observed compared with the optimum procedure previously developed by the Albany Research Center. Aqueous carbonation reactivity was found to be a strong function of the ionic species present and their aqueous activities, as well as the slurry fluid flow conditions incorporated. High concentration sodium, potassium, and sodium/potassium bicarbonate aqueous solutions have been found to be the most effective solutions for enhancing aqueous olivine carbonation to date. Slurry-flow modeling using Fluent indicates that the slurry-flow dynamics are a strong function of particle size and mass, suggesting that controlling these parameters may offer substantial potential to enhance carbonation. Synergistic control of the slurry-flow and aqueous chemistry parameters offers further potential to improve carbonation reactivity, which is being investigated during the no-cost extension period. During the first project year we developed a new sonication exfoliation system with a novel sealing system to carry out the sonication studies. We also initiated(Abstract truncated).

  17. The Transport Properties of Activated Carbon Fibers

    DOE R&D Accomplishments Database

    di Vittorio, S. L.; Dresselhaus, M. S.; Endo, M.; Issi, J-P.; Piraux, L.

    1990-07-01

    The transport properties of activated isotropic pitch-based carbon fibers with surface area 1000 m{sup 2}/g have been investigated. We report preliminary results on the electrical conductivity, the magnetoresistance, the thermal conductivity and the thermopower of these fibers as a function of temperature. Comparisons are made to transport properties of other disordered carbons.

  18. ACTIVATED CARBON FROM LIGNITE FOR WATER TREATMENT

    SciTech Connect

    Edwin S. Olson; Daniel J. Stepan

    2000-07-01

    High concentrations of humate in surface water result in the formation of excess amounts of chlorinated byproducts during disinfection treatment. These precursors can be removed in water treatment prior to disinfection using powdered activated carbon. In the interest of developing a more cost-effective method for removal of humates in surface water, a comparison of the activities of carbons prepared from North Dakota lignites with those of commercial carbons was conducted. Previous studies indicated that a commercial carbon prepared from Texas lignite (Darco HDB) was superior to those prepared from bituminous coals for water treatment. That the high alkali content of North Dakota lignites would result in favorable adsorptive properties for the very large humate molecules was hypothesized, owing to the formation of larger pores during activation. Since no standard humate test has been previously developed, initial adsorption testing was performed using smaller dye molecules with various types of ionic character. With the cationic dye, methylene blue, a carbon prepared from a high-sodium lignite (HSKRC) adsorbed more dye than the Darco HDB. The carbon from the low-sodium lignite was much inferior. With another cationic dye, malachite green, the Darco HDB was slightly better. With anionic dyes, methyl red and azocarmine-B, the results for the HSKRC and Darco HDB were comparable. A humate test was developed using Aldrich humic acid. The HSKRC and the Darco HDB gave equally high adsorption capacities for the humate (138 mg/g), consistent with the similarities observed in earlier tests. A carbon prepared from a high-sodium lignite from a different mine showed an outstanding improvement (201 mg/g). The carbons prepared from the low-sodium lignites from both mines showed poor adsorption capacities for humate. Adsorption isotherms were performed for the set of activated carbons in the humate system. These exhibited a complex behavior interpreted as resulting from two types of sorption sites. The effect of pH on adsorption was investigated using buffered solutions. The sorption capacity decreased with increasing pH. A study of the effect of activation conditions on the adsorption capacity of the resulting carbon showed that steam activation at 750 C provides the optimum activity with the high-sodium char. An attempt to scale up the carbon production to the 2-kg scale failed to produce the same high activity that was obtained in the 100-g batch unit. Although this research demonstrated that a highly active carbon for water treatment can be produced from high-sodium lignites, much further work is needed to understand what methods and equipment will be needed for large-scale production of this carbon.

  19. Production and characterization of activated carbons from cereal grains

    SciTech Connect

    Venkatraman, A.; Walawender, W.P.; Fan, L.T.

    1996-12-31

    The term, activated carbon, is a generic name for a family of carbonaceous materials with well-developed porosities and consequently, large adsorptive capacities. Activated carbons are increasingly being consumed worldwide for environmental applications such as separation of volatiles from bulk gases and purification of water and waste-water streams. The global annual production is estimated to be around 300 million kilograms, with a rate of increase of 7% each year. Activated carbons can be prepared from a variety of raw materials. Approximately, 60% of the activated carbons generated in the United States is produced from coal; 20%, from coconut shells; and the remaining 20% from wood and other sources of biomass. The pore structure and properties of activated carbons are influenced by the nature of the starting material and the initial physical and chemical conditioning as well as the process conditions involved in its manufacture. The porous structures of charcoals and activated carbons obtained by the carbonization of kernels have been characterized.

  20. Improved Process for Fabricating Carbon Nanotube Probes

    NASA Technical Reports Server (NTRS)

    Stevens, R.; Nguyen, C.; Cassell, A.; Delzeit, L.; Meyyappan, M.; Han, Jie

    2003-01-01

    An improved process has been developed for the efficient fabrication of carbon nanotube probes for use in atomic-force microscopes (AFMs) and nanomanipulators. Relative to prior nanotube tip production processes, this process offers advantages in alignment of the nanotube on the cantilever and stability of the nanotube's attachment. A procedure has also been developed at Ames that effectively sharpens the multiwalled nanotube, which improves the resolution of the multiwalled nanotube probes and, combined with the greater stability of multiwalled nanotube probes, increases the effective resolution of these probes, making them comparable in resolution to single-walled carbon nanotube probes. The robust attachment derived from this improved fabrication method and the natural strength and resiliency of the nanotube itself produces an AFM probe with an extremely long imaging lifetime. In a longevity test, a nanotube tip imaged a silicon nitride surface for 15 hours without measurable loss of resolution. In contrast, the resolution of conventional silicon probes noticeably begins to degrade within minutes. These carbon nanotube probes have many possible applications in the semiconductor industry, particularly as devices are approaching the nanometer scale and new atomic layer deposition techniques necessitate a higher resolution characterization technique. Previously at Ames, the use of nanotube probes has been demonstrated for imaging photoresist patterns with high aspect ratio. In addition, these tips have been used to analyze Mars simulant dust grains, extremophile protein crystals, and DNA structure.

  1. Adsorption of herbicides using activated carbons

    SciTech Connect

    Derbyshire, F.; Jagtoyen, M.; Lafferty, C.; Kimber, G.

    1996-12-31

    This paper describes the results of research in which novel activated carbons have been examined for their efficacy in water treatment and, specifically, for the adsorption of a common herbicide and wood preservative, sodium pentachlorophenolate. To place this work in context, the introduction will discuss first some of the considerations of using activated carbons for water treatment, and then certain aspects of the authors research that has led to this particular topic.

  2. Granular activated-carbon treatment. Engineering bulletin

    SciTech Connect

    Not Available

    1991-10-01

    Granular activated carbon (GAC) treatment is a physicochemical process that removes a wide variety of contaminants by adsorbing them from liquid and gas streams. The treatment is most commonly used to separate organic contaminants from water or air; however, it can be used to remove a limited number of inorganic contaminants. In most cases, the contaminants are collected in concentrated form on the GAC, and further treatment is required. Site-specific treatability studies are generally necessary to document the applicability and potential performance of a GAC system. The bulletin provides information on the technology applicability, technology limitations, a technology description, the types of residuals produced, site requirements, latest performance data, status of the technology, and sources for further information.

  3. Breakthrough CO2 adsorption in bio-based activated carbons.

    PubMed

    Shahkarami, Sepideh; Azargohar, Ramin; Dalai, Ajay K; Soltan, Jafar

    2015-08-01

    In this work, the effects of different methods of activation on CO2 adsorption performance of activated carbon were studied. Activated carbons were prepared from biochar, obtained from fast pyrolysis of white wood, using three different activation methods of steam activation, CO2 activation and Potassium hydroxide (KOH) activation. CO2 adsorption behavior of the produced activated carbons was studied in a fixed-bed reactor set-up at atmospheric pressure, temperature range of 25-65C and inlet CO2 concentration range of 10-30mol% in He to determine the effects of the surface area, porosity and surface chemistry on adsorption capacity of the samples. Characterization of the micropore and mesopore texture was carried out using N2 and CO2 adsorption at 77 and 273K, respectively. Central composite design was used to evaluate the combined effects of temperature and concentration of CO2 on the adsorption behavior of the adsorbents. The KOH activated carbon with a total micropore volume of 0.62cm(3)/g and surface area of 1400m(2)/g had the highest CO2 adsorption capacity of 1.8mol/kg due to its microporous structure and high surface area under the optimized experimental conditions of 30mol% CO2 and 25C. The performance of the adsorbents in multi-cyclic adsorption process was also assessed and the adsorption capacity of KOH and CO2 activated carbons remained remarkably stable after 50cycles with low temperature (160C) regeneration. PMID:26257348

  4. Carbon formation and metal dusting in advanced coal gasification processes

    SciTech Connect

    DeVan, J.H.; Tortorelli, P.F.; Judkins, R.R.; Wright, I.G.

    1997-02-01

    The product gases generated by coal gasification systems contain high concentrations of CO and, characteristically, have relatively high carbon activities. Accordingly, carbon deposition and metal dusting can potentially degrade the operation of such gasifier systems. Therefore, the product gas compositions of eight representative gasifier systems were examined with respect to the carbon activity of the gases at temperatures ranging from 480 to 1,090 C. Phase stability calculations indicated that Fe{sub 3}C is stable only under very limited thermodynamic conditions and with certain kinetic assumptions and that FeO and Fe{sub 0.877}S tend to form instead of the carbide. As formation of Fe{sub 3}C is a necessary step in the metal dusting of steels, there are numerous gasifier environments where this type of carbon-related degradation will not occur, particularly under conditions associated with higher oxygen and sulfur activities. These calculations also indicated that the removal of H{sub 2}S by a hot-gas cleanup system may have less effect on the formation of Fe{sub 3}C in air-blown gasifier environments, where the iron oxide phase can exist and is unaffected by the removal of sulfur, than in oxygen-blown systems, where iron sulfide provides the only potential barrier to Fe{sub 3}C formation. Use of carbon- and/or low-alloy steels dictates that the process gas composition be such that Fe{sub 3}C cannot form if the potential for metal dusting is to be eliminated. Alternatively, process modifications could include the reintroduction of hydrogen sulfide, cooling the gas to perhaps as low as 400 C and/or steam injection. If higher-alloy steels are used, a hydrogen sulfide-free gas may be processed without concern about carbon deposition and metal dusting.

  5. Activated carbon for gas phase arsenic capture

    SciTech Connect

    Jadhav, R.; Gupta, H.; Misro, S.; Agnihotri, R.; Fan, L.S.

    1999-07-01

    Investigation of activated carbon as a multifunctional sorbent for trace metal capture is the focus of this study. In addition to mercury and halides, selenium and arsenic represent two of the most volatile trace species that remain in gas phase in substantial amounts. In this work, fundamental sorption characteristics of the activated carbon for arsenic removal from the gas phase are investigated. Activated carbons with different structural properties are studied for their usefulness in removing arsenic species from flue gas. Arsenic oxide (As{sub 2}O{sub 3}) is used as the source of arsenic. Preliminary sorption studies indicate that arsenic removal occurs by physical adsorption, with increased capture by carbons with higher surface areas.

  6. Microwave-assisted regeneration of activated carbon.

    PubMed

    Foo, K Y; Hameed, B H

    2012-09-01

    Microwave heating was used in the regeneration of methylene blue-loaded activated carbons produced from fibers (PFAC), empty fruit bunches (EFBAC) and shell (PSAC) of oil palm. The dye-loaded carbons were treated in a modified conventional microwave oven operated at 2450 MHz and irradiation time of 2, 3 and 5 min. The virgin properties of the origin and regenerated activated carbons were characterized by pore structural analysis and nitrogen adsorption isotherm. The surface chemistry was examined by zeta potential measurement and determination of surface acidity/basicity, while the adsorptive property was quantified using methylene blue (MB). Microwave irradiation preserved the pore structure, original active sites and adsorption capacity of the regenerated activated carbons. The carbon yield and the monolayer adsorption capacities for MB were maintained at 68.35-82.84% and 154.65-195.22 mg/g, even after five adsorption-regeneration cycles. The findings revealed the potential of microwave heating for regeneration of spent activated carbons. PMID:22728787

  7. A Novel Approach to Mineral Carbonation: Enhancing Carbonation While Avoiding Mineral Pretreatment Process Cost

    SciTech Connect

    Andrew V. G. Chizmeshya; Michael J. McKelvy; Kyle Squires; Ray W. Carpenter; Hamdallah Bearat

    2007-06-21

    Known fossil fuel reserves, especially coal, can support global energy demands for centuries to come, if the environmental problems associated with CO{sub 2} emissions can be overcome. Unlike other CO{sub 2} sequestration candidate technologies that propose long-term storage, mineral sequestration provides permanent disposal by forming geologically stable mineral carbonates. Carbonation of the widely occurring mineral olivine (e.g., forsterite, Mg{sub 2}SiO{sub 4}) is a large-scale sequestration process candidate for regional implementation, which converts CO{sub 2} into the environmentally benign mineral magnesite (MgCO{sub 3}). The primary goal is cost-competitive process development. As the process is exothermic, it inherently offers low-cost potential. Enhancing carbonation reactivity is key to economic viability. Recent studies at the U.S. DOE Albany Research Center have established that aqueous-solution carbonation using supercritical CO{sub 2} is a promising process; even without olivine activation, 30-50% carbonation has been achieved in an hour. Mechanical activation (e.g., attrition) has accelerated the carbonation process to an industrial timescale (i.e., near completion in less than an hour), at reduced pressure and temperature. However, the activation cost is too high to be economical and lower cost pretreatment options are needed. We have discovered that robust silica-rich passivating layers form on the olivine surface during carbonation. As carbonation proceeds, these passivating layers thicken, fracture and eventually exfoliate, exposing fresh olivine surfaces during rapidly-stirred/circulating carbonation. We are exploring the mechanisms that govern carbonation reactivity and the impact that (1) modeling/controlling the slurry fluid-flow conditions, (2) varying the aqueous ion species/size and concentration (e.g., Li+, Na+, K+, Rb+, Cl-, HCO{sub 3}{sup -}), and (3) incorporating select sonication offer to enhance exfoliation and carbonation. Thus far, we have succeeded in nearly doubling the extent of carbonation observed compared with the optimum procedure previously developed by the Albany Research Center. Aqueous carbonation reactivity was found to be a strong function of the ionic species present and their aqueous activities, as well as the slurry fluid flow conditions incorporated. High concentration sodium, potassium, and sodium/potassium bicarbonate aqueous solutions have been found to be the most effective solutions for enhancing aqueous olivine carbonation to date. Slurry-flow modeling using Fluent indicates that the slurry-flow dynamics are a strong function of particle size and mass, suggesting that controlling these parameters may offer substantial potential to enhance carbonation. During the first project year we developed a new sonication exfoliation apparatus with a novel sealing system to carry out the sonication studies. We also initiated investigations to explore the potential that sonication may offer to enhance carbonation reactivity. During the second project year, we extended our investigations of the effects of sonication on the extent of carbonation as a function of the following parameters: particle size distribution, the mass of solid reactant, volume fraction of aqueous solution present, sonication power, time, temperature, and CO{sub 2} pressure. To date, none of the conditions investigated have significantly enhanced carbonation. Mechanistic investigations of the stirred ({approx}1,500 rpm) aqueous olivine carbonation process indicate the carbonation process involves both incongruent magnesium dissolution and silica precipitation, which results in robust silica-rich passivating layer formation. Secondary ion mass spectrometry observation of H within the passivating layer that forms during static carbonation suggests 2H{sup +}/Mg{sup 2+} ion exchange is associated with incongruent dissolution. Apparently, H{sub 2}O forms at or near the olivine/passivating-layer interface during the process and diffuses out through the passivating layers during the carbonation reaction. This is also consistent with the observation that magnesite nanocrystals form within the passivating layers, further indicating the layers offer significant permeability to the key solution reaction species present during carbonation (e.g., Mg2+, H+, H{sub 2}O, CO{sub 2}, and HCO{sub 3}{sup -}). Cracking of the passivating layer surface during carbonation is routinely observed and can be related to the tensile stress associated with the dramatic volume decrease as olivine forms silica at the reaction surface. In our YEAR 2 studies we also demonstrated that the addition of quartz particles as an abrasive slurry component significantly enhanced carbonation, further substantiating the importance of particle-particle abrasion in enhancing passivating layer exfoliation and carbonation.

  8. JV Task 90 - Activated Carbon Production from North Dakota Lignite

    SciTech Connect

    Steven Benson; Charlene Crocker; Rokan Zaman; Mark Musich; Edwin Olson

    2008-03-31

    The Energy & Environmental Research Center (EERC) has pursued a research program for producing activated carbon from North Dakota lignite that can be competitive with commercial-grade activated carbon. As part of this effort, small-scale production of activated carbon was produced from Fort Union lignite. A conceptual design of a commercial activated carbon production plant was drawn, and a market assessment was performed to determine likely revenue streams for the produced carbon. Activated carbon was produced from lignite coal in both laboratory-scale fixed-bed reactors and in a small pilot-scale rotary kiln. The EERC was successfully able to upgrade the laboratory-scale activated carbon production system to a pilot-scale rotary kiln system. The activated carbon produced from North Dakota lignite was superior to commercial grade DARCO{reg_sign} FGD and Rheinbraun's HOK activated coke product with respect to iodine number. The iodine number of North Dakota lignite-derived activated carbon was between 600 and 800 mg I{sub 2}/g, whereas the iodine number of DARCO FGD was between 500 and 600 mg I{sub 2}/g, and the iodine number of Rheinbraun's HOK activated coke product was around 275 mg I{sub 2}/g. The EERC performed both bench-scale and pilot-scale mercury capture tests using the activated carbon made under various optimization process conditions. For comparison, the mercury capture capability of commercial DARCO FGD was also tested. The lab-scale apparatus is a thin fixed-bed mercury-screening system, which has been used by the EERC for many mercury capture screen tests. The pilot-scale systems included two combustion units, both equipped with an electrostatic precipitator (ESP). Activated carbons were also tested in a slipstream baghouse at a Texas power plant. The results indicated that the activated carbon produced from North Dakota lignite coal is capable of removing mercury from flue gas. The tests showed that activated carbon with the greatest iodine number was superior to commercial DARCO FGD for mercury capture. The results of the activated carbon market assessment indicate an existing market for water treatment and an emerging application for mercury control. That market will involve both existing and new coal-fired plants. It is expected that 20% of the existing coal-fired plants will implement activated carbon injection by 2015, representing about 200,000 tons of annual demand. The potential annual demand by new plants is even greater. In the mercury control market, two characteristics are going to dominate the customer's buying habit-performance and price. As continued demonstration testing of activated carbon injection at the various coal-fired power plants progresses, the importance of fuel type and plant configuration on the type of activated carbon best suited is being identified.

  9. Activated coconut shell charcoal carbon using chemical-physical activation

    NASA Astrophysics Data System (ADS)

    Budi, Esmar; Umiatin, Nasbey, Hadi; Bintoro, Ridho Akbar; Wulandari, Futri; Erlina

    2016-02-01

    The use of activated carbon from natural material such as coconut shell charcoal as metal absorbance of the wastewater is a new trend. The activation of coconut shell charcoal carbon by using chemical-physical activation has been investigated. Coconut shell was pyrolized in kiln at temperature about 75 - 150 °C for about 6 hours in producing charcoal. The charcoal as the sample was shieved into milimeter sized granule particle and chemically activated by immersing in various concentration of HCl, H3PO4, KOH and NaOH solutions. The samples then was physically activated using horizontal furnace at 400°C for 1 hours in argon gas environment with flow rate of 200 kg/m3. The surface morphology and carbon content of activated carbon were characterized by using SEM/EDS. The result shows that the pores of activated carbon are openned wider as the chemical activator concentration is increased due to an excessive chemical attack. However, the pores tend to be closed as further increasing in chemical activator concentration due to carbon collapsing.

  10. Adsorption of geosmin and 2-methylisoborneol onto powdered activated carbon at non-equilibrium conditions: influence of NOM and process modelling.

    PubMed

    Zoschke, Kristin; Engel, Christina; Brnick, Hilmar; Worch, Eckhard

    2011-10-01

    The adsorption of the taste and odour (T&O) compounds geosmin and 2-methylisoborneol (2-MIB) onto powdered activated carbon (PAC) has been studied under conditions which are typical for a drinking water treatment plant that uses reservoir water for drinking water production. The reservoir water as well as the pre-treated water (after flocculation) contains NOM that competes with the trace compounds for the adsorption sites on the carbon surface. Although the DOC concentrations in the reservoir water and in the pre-treated water were different, no differences in the competitive adsorption could be seen. By using two special characterisation methods for NOM (adsorption analysis, LC/OCD) it could be proved that flocculation removes only NOM fractions which are irrelevant for competitive adsorption. Different model approaches were applied to describe the competitive adsorption of the T&O compounds and NOM, the tracer model, the equivalent background compound model, and the simplified equivalent background compound model. All these models are equilibrium models but in practice the contact time in flow-through reactors is typically shorter than the time needed to establish the adsorption equilibrium. In this paper it is demonstrated that the established model approaches can be used to describe competitive adsorption of T&O compounds and NOM also under non-equilibrium conditions. The results of the model applications showed that in particular the simplified equivalent background compound model is a useful tool to determine the PAC dosage required to reduce the T&O compounds below the threshold concentration. PMID:21752419

  11. Long-term impact of land management in soil biological processes can be assessed by fingerprint of dissolved organic carbon and peroxidase activity in topsoil and subsoil

    NASA Astrophysics Data System (ADS)

    Hernandez-Soriano, Maria C.; Maclean, Jamie L.; Dalal, Ram C.; Menzies, Neal W.; Kopittke, Peter M.

    2015-04-01

    The dissolved organic carbon (DOC) is a highly dynamic pool, directly related to biological functions and to the stabilization of organic carbon (OC) through interaction with the mineral phase. Therefore, the characterization of the main components of DOC can be linked to the metabolic status of soil and the turnover of OC and provides a sensitive approach to evaluate the impact of land use on OC turnover in soils. Accordingly, the objective of this study was to derive relationships between DOC characteristics and biochemical activity in soils under contrasting land management. The soil solution was isolated from topsoil and subsoil for three soils (Vertisol, Ferralsol, Acrisol, World Reference Base 2014) collected from undisturbed areas and from a location(s) immediately adjacent which has a long history of agricultural, pasture or afforestation use (>20 years) by centrifugation at 4000 rpm (20 min, 25 °C. The fingerprint of DOC was obtained to identify OC functionalities by spectrofluorometric analyses and Excitation-Emission matrices (EEM) were obtained for all samples. The excitation wavelengths were increased from 250 to 400 nm in 5-nm steps for each excitation wavelength, and emission was detected from 250 to 500 nm in 0.5-nm steps and. Humification index (HIX), freshness index (FrI), fluorescence index (FI) and redox index (RI) were derived from the EEMs. Extracellular laccase activity was examined by monitoring the oxidation of 2,2'-azinobis-3-ethylbenzothiazoline-6-sulfonic acid (ABTS) at 420 nm. The EEMs revealed a depletion of the humic-like component (250activity was generally higher for topsoils collected from undisturbed areas for the three soils examined and a significant decrease in the enzyme activity was determined for soils collected from the corresponding adjacent crop land. The rate of ABTS oxidation varied for the different soils following the order Vertisol>Acrisol>Ferralsol and was always higher for the topsoils compared to the corresponding subsoils. Overall, results indicate that land management has a strong impact on soil biological activity. Importantly, such impact is directly linked to changes in the composition of soil OC, particularly the transformation of OC inputs into oxidized products that can contribute to OC build up in soil. For the first time, we have utilized DOC fingerprinting and extracellular laccase activity as complementary techniques to examine changes in OC speciation in soil solutions. This approach provides a suitable link between variations in biological functions and OC dynamics.

  12. Friction stir processing on carbon steel

    SciTech Connect

    Tarasov, Sergei Yu.; Melnikov, Alexander G.; Rubtsov, Valery E.

    2014-11-14

    Friction stir processing of medium carbon steel samples has been carried out using a milling machine and tools made of cemented tungsten carbide. Samples have been machined from 40 and 40X steels. The tools have been made in the shape of 5×5×1.5 mm and 3×3×1.5 mm tetrahedrons. The microstructure of stirred zone has been obtained using the smaller tool and consists of fine recrystallized 2-3 μm grains, whereas the larger tool has produced the 'onion-like' structures comprising hard quenched 'white' 500-600 MPa layers with 300-350 MPa interlayers of bainite needles. The mean values of wear intensity obtained after measuring the wear scar width were 0.02 mm/m and 0.001 mm/m for non-processed and processed samples, respectively.

  13. PYROGENIC ACTIVITY OF CARBON-FILTERED WATERS

    EPA Science Inventory

    The endotoxin content and pyrogenic response of granular activated carbon (GAC) filtered waters were studied. GAC-filtered secondary effluent from an activated sludge pilot plant contained free endotoxins in the range 6-250 micrograms/l yielding positive pyrogenic responses in 18...

  14. Converting Poultry Litter into Activated Carbon

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Disposal of animal manure is one of the biggest problems facing agriculture today. Now new technology has been designed to covert manure into environmentally friendly and highly valued activated carbon. When pelletized and activated under specific conditions, the litter becomes a highly porous mat...

  15. Carbon nanotube mass production: principles and processes.

    PubMed

    Zhang, Qiang; Huang, Jia-Qi; Zhao, Meng-Qiang; Qian, Wei-Zhong; Wei, Fei

    2011-07-18

    Our society requires new materials for a sustainable future, and carbon nanotubes (CNTs) are among the most important advanced materials. This Review describes the state-of-the-art of CNT synthesis, with a focus on their mass-production in industry. At the nanoscale, the production of CNTs involves the self-assembly of carbon atoms into a one-dimensional tubular structure. We describe how this synthesis can be achieved on the macroscopic scale in processes akin to the continuous tonne-scale mass production of chemical products in the modern chemical industry. Our overview includes discussions on processing methods for high-purity CNTs, and the handling of heat and mass transfer problems. Manufacturing strategies for agglomerated and aligned single-/multiwalled CNTs are used as examples of the engineering science of CNT production, which includes an understanding of their growth mechanism, agglomeration mechanism, reactor design, and process intensification. We aim to provide guidelines for the production and commercialization of CNTs. Although CNTs can now be produced on the tonne scale, knowledge of the growth mechanism at the atomic scale, the relationship between CNT structure and application, and scale-up of the production of CNTs with specific chirality are still inadequate. A multidisciplinary approach is a prerequisite for the sustainable development of the CNT industry. PMID:21732544

  16. Deposition of Magnetite Nanoparticles in Activated Carbons and Preparation of Magnetic Activated Carbons

    NASA Astrophysics Data System (ADS)

    Kahani, S. A.; Hamadanian, M.; Vandadi, O.

    2007-08-01

    Magnetic activated carbons (MACs) for gold recovery from alkaline cyanide solutions have been developed by mixing a magnetic precursor with a carbon source, and treating the mixture under controlled conditions. As would be expected, these activated carbons have high specific surface areas due to their microporous structure. In addition, the small particle size of the MACs produced allows rapid adsorption of gold in solution, and the magnetic character of these MACs enables recovery from suspension by magnetic separation.

  17. Process for making hollow carbon spheres

    DOEpatents

    Luhrs, Claudia C.; Phillips, Jonathan; Richard, Monique N.; Knapp, Angela Michelle

    2013-04-16

    A hollow carbon sphere having a carbon shell and an inner core is disclosed. The hollow carbon sphere has a total volume that is equal to a volume of the carbon shell plus an inner free volume within the carbon shell. The inner free volume is at least 25% of the total volume. In some instances, a nominal diameter of the hollow carbon sphere is between 10 and 180 nanometers.

  18. Composite electrodes of activated carbon derived from cassava peel and carbon nanotubes for supercapacitor applications

    NASA Astrophysics Data System (ADS)

    Taer, E.; Iwantono, Yulita, M.; Taslim, R.; Subagio, A.; Salomo, Deraman, M.

    2013-09-01

    In this paper, a composite electrode was prepared from a mixture of activated carbon derived from precarbonization of cassava peel (CP) and carbon nanotubes (CNTs). The activated carbon was produced by pyrolysis process using ZnCl2 as an activation agent. A N2 adsorption-desorption analysis for the sample indicated that the BET surface area of the activated carbon was 1336 m2 g-1. Difference percentage of CNTs of 0, 5, 10, 15 and 20% with 5% of PVDF binder were added into CP based activated carbon in order to fabricate the composite electrodes. The morphology and structure of the composite electrodes were investigated by scanning electron microscopy (SEM) and X-ray diffraction (XRD) techniques. The SEM image observed that the distribution of CNTs was homogeneous between carbon particles and the XRD pattern shown the amorphous structure of the sample. The electrodes were fabricated for supercapacitor cells with 316L stainless steel as current collector and 1 M sulfuric acid as electrolyte. An electrochemical characterization was performed by using an electrochemical impedance spectroscopy (EIS) method using a Solatron 1286 instrument and the addition of CNTs revealed to improve the resistant and capacitive properties of supercapacitor cell.

  19. A novel activated carbon for supercapacitors

    SciTech Connect

    Shen, Haijie; Liu, Enhui; Xiang, Xiaoxia; Huang, Zhengzheng; Tian, Yingying; Wu, Yuhu; Wu, Zhilian; Xie, Hui

    2012-03-15

    Highlights: Black-Right-Pointing-Pointer A novel activated carbon was prepared from phenol-melamine-formaldehyde resin. Black-Right-Pointing-Pointer The carbon has large surface area with microporous, and high heteroatom content. Black-Right-Pointing-Pointer Heteroatom-containing functional groups can improve the pseudo-capacitance. Black-Right-Pointing-Pointer Physical and chemical properties lead to the good electrochemical properties. -- Abstract: A novel activated carbon has been prepared by simple carbonization and activation of phenol-melamine-formaldehyde resin which is synthesized by the condensation polymerization method. The morphology, thermal stability, surface area, elemental composition and surface chemical composition of samples have been investigated by scanning electron microscope, thermogravimetry and differential thermal analysis, Brunauer-Emmett-Teller measurement, elemental analysis and X-ray photoelectron spectroscopy, respectively. Electrochemical properties have been studied by cyclic voltammograms, galvanostatic charge/discharge, and electrochemical impedance spectroscopy measurements in 6 mol L{sup -1} potassium hydroxide. The activated carbon shows good capacitive behavior and the specific capacitance is up to 210 F g{sup -1}, which indicates that it may be a promising candidate for supercapacitors.

  20. Photochemical processing of aqueous atmospheric brown carbon

    NASA Astrophysics Data System (ADS)

    Zhao, R.; Lee, A. K. Y.; Huang, L.; Li, X.; Yang, F.; Abbatt, J. P. D.

    2015-01-01

    Atmospheric Brown Carbon (BrC) is a collective term for light absorbing organic compounds in the atmosphere. While the identification of BrC and its formation mechanisms is currently a central effort in the community, little is known about the atmospheric removal processes of aerosol BrC. As a result, we report a series of laboratory studies of photochemical processing of BrC in the aqueous phase, by direct photolysis and OH oxidation. Solutions of ammonium sulfate mixed with glyoxal (GLYAS) or methylglyoxal (MGAS) are used as surrogates for a class of secondary BrC mediated by imine intermediates. Three nitrophenol species, namely 4-nitrophenol, 5-nitroguaiacol and 4-nitrocatechol, were investigated as a class of water soluble BrC originating from biomass burning. Photochemical processing induced significant changes in the absorptive properties of BrC. The imine-mediated BrC solutions exhibited rapid photo-bleaching with both direct photolysis and OH oxidation, with atmospheric half-lives of minutes to a few hours. The nitrophenol species exhibited photo-enhancement in the visible range during direct photolysis and the onset of OH oxidation, but rapid photo-bleaching was induced by further OH exposure on an atmospheric timescale of an hour or less. To illustrate atmospheric relevance of this work, we also performed direct photolysis experiments on water soluble organic carbon extracted from biofuel combustion samples and observed rapid changes in optical properties of these samples as well. Overall, these experiments indicate that atmospheric models need to incorporate representations of atmospheric processing of BrC species to accurately model their radiative impacts.

  1. Photochemical processing of aqueous atmospheric brown carbon

    NASA Astrophysics Data System (ADS)

    Zhao, R.; Lee, A. K. Y.; Huang, L.; Li, X.; Yang, F.; Abbatt, J. P. D.

    2015-06-01

    Atmospheric brown carbon (BrC) is a collective term for light absorbing organic compounds in the atmosphere. While the identification of BrC and its formation mechanisms is currently a central effort in the community, little is known about the atmospheric removal processes of aerosol BrC. As a result, we report on a series of laboratory studies of photochemical processing of BrC in the aqueous phase, by direct photolysis and OH oxidation. Solutions of ammonium sulfate mixed with glyoxal (GLYAS) or methylglyoxal (MGAS) are used as surrogates for a class of secondary BrC mediated by imine intermediates. Three nitrophenol species, namely 4-nitrophenol, 5-nitroguaiacol and 4-nitrocatechol, were investigated as a class of water-soluble BrC originating from biomass burning. Photochemical processing induced significant changes in the absorptive properties of BrC. The imine-mediated BrC solutions exhibited rapid photo-bleaching with both direct photolysis and OH oxidation, with atmospheric half-lives of minutes to a few hours. The nitrophenol species exhibited photo-enhancement in the visible range during direct photolysis and the onset of OH oxidation, but rapid photo-bleaching was induced by further OH exposure on an atmospheric timescale of an hour or less. To illustrate the atmospheric relevance of this work, we also performed direct photolysis experiments on water-soluble organic carbon extracted from biofuel combustion samples and observed rapid changes in the optical properties of these samples as well. Overall, these experiments indicate that atmospheric models need to incorporate representations of atmospheric processing of BrC species to accurately model their radiative impacts.

  2. Removal of phenol from aqueous solution using carbonized Terminalia chebula-activated carbon: process parametric optimization using conventional method and Taguchi's experimental design, adsorption kinetic, equilibrium and thermodynamic study

    NASA Astrophysics Data System (ADS)

    Khare, Prateek; Kumar, Arvind

    2012-12-01

    In the present paper, the phenol removal from wastewater was investigated using agri-based adsorbent: Terminalia chebula-activated carbon (TCAC) produced by carbonization of Terminalia chebula (TC) in air-controlled atmosphere at 600 C for 4 h. The surface area of TCAC was measured as 364 m2/g using BET method. The surface characteristic of TCAC was analyzed based on the value of point of zero charge. The effect of parameters such as TCAC dosage, pH, initial concentration of phenol, time of contact and temperature on the sorption of phenol by TCAC was investigated using conventional method and Taguchi experimental design. The total adsorption capacity of phenol was obtained as 36.77 mg/g using Langmuir model at the temperature of 30 C at pH = 5.5. The maximum removal of phenol (294.86 mg/g) was obtained using Taguchi's method. The equilibrium study of phenol on TCAC showed that experimental data fitted well to R-P model. The results also showed that kinetic data were followed more closely the pseudo-first-order model. The results of thermodynamic study showed that the adsorption of phenol on TCAC was spontaneous and an exothermic in nature.

  3. SUPERCRITICAL FLUID REGENERATION OF ACTIVATED CARBON FOR ADSORPTION OF PESTICIDES

    EPA Science Inventory

    The report describes the development of a new process for regenerating activated carbon, using supercritical CO2 as a desorbent. Supercritical CO2 in the range of 30-250 C and at pressures > 80 atm. is a good solvent for organics. A series of pesticides was tested for treatment b...

  4. Decolorization / deodorization of zein via activated carbons and molecular sieves

    Technology Transfer Automated Retrieval System (TEKTRAN)

    The objective is to evaluate a series of granular media consisting of activated carbons and molecular sieves in a batch process for the purpose of clarifying and removal of color and odor components from yellow zein dispersed in an aqueous alcohol medium. The major contributors of yellow zein is du...

  5. Adsorption of dissolved natural organic matter by modified activated carbons.

    PubMed

    Cheng, Wei; Dastgheib, Seyed A; Karanfil, Tanju

    2005-06-01

    Adsorption of dissolved natural organic matter (DOM) by virgin and modified granular activated carbons (GACs) was studied. DOM samples were obtained from two water treatment plants before (i.e., raw water) and after coagulation/flocculation/sedimentation processes (i.e., treated water). A granular activated carbon (GAC) was modified by high temperature helium or ammonia treatment, or iron impregnation followed by high temperature ammonia treatment. Two activated carbon fibers (ACFs) were also used, with no modification, to examine the effect of carbon porosity on DOM adsorption. Size exclusion chromatography (SEC) and specific ultraviolet absorbance (SUVA(254)) were employed to characterize the DOMs before and after adsorption. Iron-impregnated (HDFe) and ammonia-treated (HDN) activated carbons showed significantly higher DOM uptakes than the virgin GAC. The enhanced DOM uptake by HDFe was due to the presence of iron species on the carbon surface. The higher uptake of HDN was attributed to the enlarged carbon pores and basic surface created during ammonia treatment. The SEC and SUVA(254) results showed no specific selectivity in the removal of different DOM components as a result of carbon modification. The removal of DOM from both raw and treated waters was negligible by ACF10, having 96% of its surface area in pores smaller than 1 nm. Small molecular weight (MW) DOM components were preferentially removed by ACF20H, having 33% of its surface area in 1--3 nm pores. DOM components with MWs larger than 1600, 2000, and 2700 Da of Charleston raw, Charleston-treated, and Spartanburg-treated waters, respectively, were excluded from the pores of ACF20H. In contrast to carbon fibers, DOM components from entire MW range were removed from waters by virgin and modified GACs. PMID:15927230

  6. Comparison of nickel oxide and palladium nanoparticle loaded on activated carbon for efficient removal of methylene blue: kinetic and isotherm studies of removal process.

    PubMed

    Arabzadeh, S; Ghaedi, M; Ansari, A; Taghizadeh, F; Rajabi, M

    2015-02-01

    Palladium nanoparticles (Pd-NPs) and nickel oxide nanoparticles (NiO-NPs) were synthesized and loaded on activated carbon (AC). This novel material successfully used for the removal of methylene blue (MB) dye from aqueous medium. Full characterization of both material using X-ray diffraction, transmission electron microscopy, scanning electron microscopy and Brunauer-Emmet-Teller analyses for Pd-NP show their high surface area (>1340 m(2)/g) and low pore size (<20 ) and average particle size lower than 45 and for NiO-NP show their high surface area (>1316.1554 m(2)/g) and low pore size (<20 ) and average particle size lower than 46 in addition to high reactive atom and presence of various functional groups. These unique properties make them possible for efficient removal of MB. In batch experimental set-up, optimum conditions for maximum removal of MB by both adsorbents were attained following searching effect of variables such as central composite design. The Langmuir isotherm was found to be highly recommended for fitting the experimental equilibrium data. The kinetic of adsorption of MB on both adsorbents strongly can be fitted by a combination of pseudo-second order and intraparticle diffusion pathway. The experimental result achieved in this article shows the superiority of Pd-NP-AC for MB removal than NiO-NP-AC, so the maximum adsorption capacities of Pd-NP-AC and NiO-NP-AC were 555.5 mg/g and 588.2 mg/g, respectively. PMID:24845705

  7. Activated carbon monoliths for methane storage

    NASA Astrophysics Data System (ADS)

    Chada, Nagaraju; Romanos, Jimmy; Hilton, Ramsey; Suppes, Galen; Burress, Jacob; Pfeifer, Peter

    2012-02-01

    The use of adsorbent storage media for natural gas (methane) vehicles allows for the use of non-cylindrical tanks due to the decreased pressure at which the natural gas is stored. The use of carbon powder as a storage material allows for a high mass of methane stored for mass of sample, but at the cost of the tank volume. Densified carbon monoliths, however, allow for the mass of methane for volume of tank to be optimized. In this work, different activated carbon monoliths have been produced using a polymeric binder, with various synthesis parameters. The methane storage was studied using a home-built, dosing-type instrument. A monolith with optimal parameters has been fabricated. The gravimetric excess adsorption for the optimized monolith was found to be 161 g methane for kg carbon.

  8. Surface chemistry of carbon: activation of molecular oxygen

    NASA Astrophysics Data System (ADS)

    Atamny, F.; Blöcker, J.; Dübotzky, A.; Kurt, H.; Timpe, O.; Loose, G.; Mahdi, W.; Schlögl, R.

    Three different industrial carbon blacks were characterized in their surface chemistry with respect to their relative abilities to activate molecular oxygen. A variety of techniques was used including x-ray diffraction, gasification experiments, electron spectroscopy as XPS and UPS, helium ion scattering spectroscopy, thermal desorption spectroscopy and the catalytic oxidation of aqueous SO2 as a "chemical probe" for activated oxygen. The activation properties for molecular oxygen at high temperatures were probed by analysing the gasification characteristics in 5 vol % oxygen-inert gas mixtures; at low temperatures the activity in the oxidation of SO2 to sulfuric acid with molecular oxygen was taken as indicator. For this reaction the carbons had to be activated by ammonia treatment at elevated temperatures. Thermal desorption spectroscopy and valence band photoemission provided data for the identification of reaction intermediates in the activation process of oxygen. The important role of surface chemical anisotropy caused by vast differences in bulk crystal structure is pointed out. The results are discussed within a model of oxygen activation which assumes two types of surface sites differing in their π electron density. Sites, rich in π electrons are graphitic and can activate oxygen to the O2-2 species which is short-lived and can be accumulated in the carbon pores. Further activation involves dissociation of the peroxo group into O- species which finally react with the second sites with the formation of covalent carbon-oxygen bonds. The relative abundance of the low temperature reactive O2-2 species and the high temperature active O- species is on as-received carbons, low for the peroxo species, and can be enhanced considerably by modifying the abundance of graphitic surface patches on carbon black and by generating suitable porosity.

  9. Production Scale-Up or Activated Carbons for Ultracapacitors

    SciTech Connect

    Dr. Steven D. Dietz

    2007-01-10

    Transportation use accounts for 67% of the petroleum consumption in the US. Electric and hybrid vehicles are promising technologies for decreasing our dependence on petroleum, and this is the objective of the FreedomCAR & Vehicle Technologies Program. Inexpensive and efficient energy storage devices are needed for electric and hybrid vehicle to be economically viable, and ultracapacitors are a leading energy storage technology being investigated by the FreedomCAR program. The most important parameter in determining the power and energy density of a carbon-based ultracapacitor is the amount of surface area accessible to the electrolyte, which is primarily determined by the pore size distribution. The major problems with current carbons are that their pore size distribution is not optimized for liquid electrolytes and the best carbons are very expensive. TDA Research, Inc. (TDA) has developed methods to prepare porous carbons with tunable pore size distributions from inexpensive carbohydrate based precursors. The use of low-cost feedstocks and processing steps greatly lowers the production costs. During this project with the assistance of Maxwell Technologies, we found that an impurity was limiting the performance of our carbon and the major impurity found was sulfur. A new carbon with low sulfur content was made and found that the performance of the carbon was greatly improved. We also scaled-up the process to pre-production levels and we are currently able to produce 0.25 tons/year of activated carbon. We could easily double this amount by purchasing a second rotary kiln. More importantly, we are working with MeadWestvaco on a Joint Development Agreement to scale-up the process to produce hundreds of tons of high quality, inexpensive carbon per year based on our processes.

  10. Carboncarbon bond activation of cyclobutenones enabled by the addition of chiral organocatalyst to ketone

    PubMed Central

    Li, Bao-Sheng; Wang, Yuhuang; Jin, Zhichao; Zheng, Pengcheng; Ganguly, Rakesh; Chi, Yonggui Robin

    2015-01-01

    The activation of carboncarbon (CC) bonds is an effective strategy in building functional molecules. The CC bond activation is typically accomplished via metal catalysis, with which high levels of enantioselectivity are difficult to achieve due to high reactivity of metal catalysts and the metal-bound intermediates. It remains largely unexplored to use organocatalysis for CC bond activation. Here we describe an organocatalytic activation of CC bonds through the addition of an NHC to a ketone moiety that initiates a CC single bond cleavage as a key step to generate an NHC-bound intermediate for chemo- and stereo-selective reactions. This reaction constitutes an asymmetric functionalization of cyclobutenones using organocatalysts via a CC bond activation process. Structurally diverse and multicyclic compounds could be obtained with high optical purities via an atom and redox economic process. PMID:25652912

  11. Retreat of carbonate platforms: Response to tectonic processes

    SciTech Connect

    Mullins, H.T.; Andersen, B.; Gaylord, M.; Petruccione, J.L.; Wellner, R.W. ); Dolan, J. ); Breen, N. ); Melillo, A.J.; Jurgens, A.D. )

    1991-11-01

    A SeaMARC 2 and seismic reflection investigation of the deep-water margins of carbonate banks in the southeast Bahamas has documented the retreat of these isolated platforms since mid-Cretaceous time. This retreat is in sharp contrast to prograding carbonate platforms in the passive northwest Bahamas and provides an initial framework within which to view the response of carbonate platforms to tectonic processes. Processes of retreat include large-scale (50-60 km) step-back to platform margins during the mid-Cretaceous; tectonic subsidence and downfaulting during the late Tertiary; and large-scale collapse of platform margins, which may be an active process. Step-back during the mid-Cretaceous correlates with a global tectonic pulse of ocean-crust formation and relative sea-level rise; downfaulting may be a response to either late Tertiary lithospheric bending during subduction and/or block rotation along the North American-Caribbean plate boundary; and collapse may be related to earthquake shocks generated by active plate-tectonic collision between the southwest Bahamas and Hispaniola.

  12. Adsorption of naphthenic acids on high surface area activated carbons.

    PubMed

    Iranmanesh, Sobhan; Harding, Thomas; Abedi, Jalal; Seyedeyn-Azad, Fakhry; Layzell, David B

    2014-01-01

    In oil sands mining extraction, water is an essential component; however, the processed water becomes contaminated through contact with the bitumen at high temperature, and a portion of it cannot be recycled and ends up in tailing ponds. The removal of naphthenic acids (NAs) from tailing pond water is crucial, as they are corrosive and toxic and provide a substrate for microbial activity that can give rise to methane, which is a potent greenhouse gas. In this study, the conversion of sawdust into an activated carbon (AC) that could be used to remove NAs from tailings water was studied. After producing biochar from sawdust by a slow-pyrolysis process, the biochar was physically activated using carbon dioxide (CO2) over a range of temperatures or prior to producing biochar, and the sawdust was chemically activated using phosphoric acid (H3PO4). The physically activated carbon had a lower surface area per gram than the chemically activated carbon. The physically produced ACs had a lower surface area per gram than chemically produced AC. In the adsorption tests with NAs, up to 35mg of NAs was removed from the water per gram of AC. The chemically treated ACs showed better uptake, which can be attributed to its higher surface area and increased mesopore size when compared with the physically treated AC. Both the chemically produced and physically produced AC provided better uptake than the commercially AC. PMID:24766592

  13. Cyclic process for producing methane from carbon monoxide with heat removal

    DOEpatents

    Frost, Albert C. (Congers, NY); Yang, Chang-lee (Spring Valley, NY)

    1982-01-01

    Carbon monoxide-containing gas streams are converted to methane by a cyclic, essentially two-step process in which said carbon monoxide is disproportionated to form carbon dioxide and active surface carbon deposited on the surface of a catalyst, and said carbon is reacted with steam to form product methane and by-product carbon dioxide. The exothermic heat of reaction generated in each step is effectively removed during each complete cycle so as to avoid a build up of heat from cycle-to-cycle, with particularly advantageous techniques being employed for fixed bed, tubular and fluidized bed reactor operations.

  14. System and method for coproduction of activated carbon and steam/electricity

    DOEpatents

    Srinivasachar, Srivats; Benson, Steven; Crocker, Charlene; Mackenzie, Jill

    2011-07-19

    A system and method for producing activated carbon comprising carbonizing a solid carbonaceous material in a carbonization zone of an activated carbon production apparatus (ACPA) to yield a carbonized product and carbonization product gases, the carbonization zone comprising carbonaceous material inlet, char outlet and carbonization gas outlet; activating the carbonized product via activation with steam in an activation zone of the ACPA to yield activated carbon and activation product gases, the activation zone comprising activated carbon outlet, activation gas outlet, and activation steam inlet; and utilizing process gas comprising at least a portion of the carbonization product gases or a combustion product thereof; at least a portion of the activation product gases or a combustion product thereof; or a combination thereof in a solid fuel boiler system that burns a solid fuel boiler feed with air to produce boiler-produced steam and flue gas, the boiler upstream of an air heater within a steam/electricity generation plant, said boiler comprising a combustion zone, a boiler-produced steam outlet and at least one flue gas outlet.

  15. Preparation of activated carbons with mesopores by use of organometallics

    SciTech Connect

    Yamada, Yoshio; Yoshizawa, Noriko; Furuta, Takeshi

    1996-12-31

    Activated carbons are commercially produced by steam or CO{sub 2} activation of coal, coconut shell and so on. In general the carbons obtained give pores with a broad range of distribution. The objective of this study was to prepare activated carbons from coal by use of various organometallic compounds. The carbons were evaluated for pore size by nitrogen adsorption experiments.

  16. ACTIVATED CARBON TREATMENT OF KRAFT BLEACHING EFFLUENTS

    EPA Science Inventory

    The removal of color and organic contaminants by adsorption on activated carbon from the effluent of a kraft pulp bleaching plant was investigated in a pilot plant. The caustic bleach effluent, which contains 80% of the color from pulp bleaching, was decolorized successfully when...

  17. EPA'S RESEARCH PROGRAM IN GRANULAR ACTIVATED CARBON

    EPA Science Inventory

    Research into Granular Activated Carbon (GAC) for use in drinking water treatment has a long history in the Drinking Water Research Division and its predecessor organizations. tudies were conducted by the U.S. Public Health Service in the late fifties and early sixties to examine...

  18. USING POWDERED ACTIVATED CARBON: A CRITICAL REVIEW

    EPA Science Inventory

    Because the performance of powdered activated carbon (PAC) for uses other than taste and odor control is poorly documented, the purpose of this article is to critically review uses that have been reported (i.e., pesticides and herbicides, synthetic organic chemicals, and trihalom...

  19. Activity of lithium intercalated in carbon materials

    SciTech Connect

    Skundin, A.M.; Egorkina, O.Yu.

    1995-04-01

    The equilibrium potentials of carbonized cloth electrode are measured upon lithium intercalation from LiClO{sub 4} in different solvents. In all cases, the relationship between the activity of lithium intercalated and its concentration is described by the power function, whose exponent depends on the electrolyte nature.

  20. MODELING MERCURY CONTROL WITH POWDERED ACTIVATED CARBON

    EPA Science Inventory

    The paper presents a mathematical model of total mercury removed from the flue gas at coal-fired plants equipped with powdered activated carbon (PAC) injection for Mercury control. The developed algorithms account for mercury removal by both existing equipment and an added PAC in...

  1. Sorption of atrazine on conventional and surface modified activated carbons.

    PubMed

    Chingombe, P; Saha, B; Wakeman, R J

    2006-10-15

    The sorption of atrazine from water has been studied using a conventional activated carbon, F400, an annealed carbon sample, F400AN, and an aminated carbon sample, F400NH(2). Characterisation of the carbon samples showed that sample F400NH(2) had the highest proportion of micropores, but had the lowest values of point of zero charge (PZC) and iso-electric point (IEP). This was attributed to the existence of a high proportion of oxygen containing functional groups. Sorption data showed that sample F400AN was superior in the sorption of atrazine to samples F400 and F400NH(2). It was noted that pore size distribution alone was not the only contributing factor for the uptake of atrazine onto the activated carbons. The sorption data were fitted well using the Freundlich isotherm. The free energy change showed that sorption of atrazine on activated carbons is a spontaneous process. A pseudo-second order kinetic model was used for analysing the kinetic data, and it was concluded that adsorption of atrazine was controlled by a film diffusion mechanism. PMID:16870200

  2. Atypical Hydrogen Uptake on Chemically Activated, Ultramicroporous Carbon

    SciTech Connect

    Bhat, Vinay V; Contescu, Cristian I; Gallego, Nidia C; Baker, Frederick S

    2010-01-01

    Hydrogen adsorption at near-ambient temperatures on ultramicroporous carbon (UMC), derived through secondary chemical activation from a wood-based activated carbon was studied using volumetric and gravimetric methods. The results showed that physisorption is accompanied by a process of different nature that causes slow uptake at high pressures and hysteresis on desorption. In combination, this results in unusually high levels of hydrogen uptake at near-ambient temperatures and pressures (e.g. up to 0.8 wt % at 25 oC and 2 MPa). The heat of adsorption corresponding to the slow process leading to high uptake (17 20 kJ/mol) is higher than usually reported for carbon materials, but the adsorption kinetics is slow, and the isotherms exhibit pronounced hysteresis. These unusual properties were attributed to contributions from polarization-enhanced physisorption caused by traces of alkali metals residual from chemical activation. The results support the hypothesis that polarization-induced physisorption in high surface area carbons modified with traces of alkali metal ions is an alternate route for increasing the hydrogen storage capacity of carbon adsorbents.

  3. Activated carbon coated palygorskite as adsorbent by activation and its adsorption for methylene blue.

    PubMed

    Zhang, Xianlong; Cheng, Liping; Wu, Xueping; Tang, Yingzhao; Wu, Yucheng

    2015-07-01

    An activation process for developing the surface and porous structure of palygorskite/carbon (PG/C) nanocomposite using ZnCl2 as activating agent was investigated. The obtained activated PG/C was characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), field-emission scanning electron microscopy (SEM), and Brunauer-Emmett-Teller analysis (BET) techniques. The effects of activation conditions were examined, including activation temperature and impregnation ratio. With increased temperature and impregnation ratio, the collapse of the palygorskite crystal structure was found to accelerate and the carbon coated on the surface underwent further carbonization. XRD and SEM data confirmed that the palygorskite structure was destroyed and the carbon structure was developed during activation. The presence of the characteristic absorption peaks of CC and C-H vibrations in the FTIR spectra suggested the occurrence of aromatization. The BET surface area improved by more than 11-fold (1201 m2/g for activated PG/C vs. 106 m2/g for PG/C) after activation, and the material appeared to be mainly microporous. The maximum adsorption capacity of methylene blue onto the activated PG/C reached 351 mg/g. The activated PG/C demonstrated better compressive strength than activated carbon without palygorskite clay. PMID:26141882

  4. Preparation of activated carbons from macadamia nut shell and coconut shell by air activation

    SciTech Connect

    Tam, M.S.; Antal, M.J. Jr.

    1999-11-01

    A novel, three-step process for the production of high-quality activated carbons from macadamia nut shell and coconut shell charcoals is described. In this process the charcoal is (1) heated to a high temperature (carbonized), (2) oxidized in air following a stepwise heating program from low (ca. 450 K) to high (ca. 660 K) temperatures (oxygenated), and (3) heated again in an inert environment to a high temperature (activated). By use of this procedure, activated carbons with surface areas greater than 1,000 m{sub 2}/g are manufactured with an overall yield of 15% (based on the dry shell feed). Removal of carbon mass by the development of mesopores and macropores is largely responsible for increases in the surface area of the carbons above 600 m{sub 2}/g. Thus, the surface area per gram of activated carbon can be represented by an inverse function of the yield for burnoffs between 15 and 60%. These findings are supported by mass-transfer calculations and pore-size distribution measurements. A kinetic model for gasification of carbon by oxygen, which provides for an Eley-Rideal type reaction of a surface oxide with oxygen in air, fits the measured gasification rates reasonably well over the temperature range of 550--660 K.

  5. Carbon-based Supercapacitors Produced by Activation of Graphene

    SciTech Connect

    Y Zhu; S Murali; M Stoller; K Ganesh; W Cai; P Ferreira; A Pirkle; R Wallace; K Cychosz; et al.

    2011-12-31

    Supercapacitors, also called ultracapacitors or electrochemical capacitors, store electrical charge on high-surface-area conducting materials. Their widespread use is limited by their low energy storage density and relatively high effective series resistance. Using chemical activation of exfoliated graphite oxide, we synthesized a porous carbon with a Brunauer-Emmett-Teller surface area of up to 3100 square meters per gram, a high electrical conductivity, and a low oxygen and hydrogen content. This sp{sup 2}-bonded carbon has a continuous three-dimensional network of highly curved, atom-thick walls that form primarily 0.6- to 5-nanometer-width pores. Two-electrode supercapacitor cells constructed with this carbon yielded high values of gravimetric capacitance and energy density with organic and ionic liquid electrolytes. The processes used to make this carbon are readily scalable to industrial levels.

  6. Carbon-Based Supercapacitors Produced by Activation of Graphene

    SciTech Connect

    Zhu, Y.; Su, D.; Murali, S.; Stoller, M.D.; Ganesh, K.J.; Cai, W.; Ferreira, P.J.; Pirkle, A.; Wallace, R.M.; Cychosz, K.A., Thommes, M.; Stach, E.A.; Ruoff, R.S.

    2011-06-24

    Supercapacitors, also called ultracapacitors or electrochemical capacitors, store electrical charge on high-surface-area conducting materials. Their widespread use is limited by their low energy storage density and relatively high effective series resistance. Using chemical activation of exfoliated graphite oxide, we synthesized a porous carbon with a Brunauer-Emmett-Teller surface area of up to 3100 square meters per gram, a high electrical conductivity, and a low oxygen and hydrogen content. This sp{sup 2}-bonded carbon has a continuous three-dimensional network of highly curved, atom-thick walls that form primarily 0.6- to 5-nanometer-width pores. Two-electrode supercapacitor cells constructed with this carbon yielded high values of gravimetric capacitance and energy density with organic and ionic liquid electrolytes. The processes used to make this carbon are readily scalable to industrial levels.

  7. Pore structure of the activated coconut shell charcoal carbon

    NASA Astrophysics Data System (ADS)

    Budi, E.; Nasbey, H.; Yuniarti, B. D. P.; Nurmayatri, Y.; Fahdiana, J.; Budi, A. S.

    2014-09-01

    The development of activated carbon from coconut shell charcoal has been investigated by using physical method to determine the influence of activation parameters in term of temperature, argon gas pressure and time period on the pore structure of the activated carbon. The coconut shell charcoal was produced by pyrolisis process at temperature of about 75 - 150 °C for 6 hours. The charcoal was activated at various temperature (532, 700 and 868 °C), argon gas pressure (6.59, 15 and 23.4 kgf/cm2) and time period of (10, 60 and 120 minutes). The results showed that the pores size were reduced and distributed uniformly as the activation parameters are increased.

  8. The biomass derived activated carbon for supercapacitor

    NASA Astrophysics Data System (ADS)

    Senthilkumar, S. T.; Selvan, R. Kalai; Melo, J. S.

    2013-06-01

    In this work, the activated carbon was prepared from biowaste of Eichhornia crassipes by chemical activation method using KOH as the activating agent at various carbonization temperatures (600 C, 700 C and 800 C). The disordered nature, morphology and surface functional groups of ACs were examined by XRD, SEM and FT-IR. The electrochemical properties of AC electrodes were studied in 1M H2SO4 in the potential range of -0.2 to 0.8 V using cyclic voltammetry (CV), galvanostatic charge-discharge and electrochemical impedance spectroscopy (EIS) techniques in a three electrode system. Subsequently, the fabricated supercapacitor using AC electrode delivered the higher specific capacitance and energy density of 509 F/g at current density of 1 mA/cm2 and 17 Wh/kg at power density of 0.416 W/g.

  9. Double-walled carbon nanotube processing.

    PubMed

    Moore, Katherine E; Tune, Daniel D; Flavel, Benjamin S

    2015-05-27

    Single-walled carbon nanotubes (SWCNTs) have been the focus of intense research, and the body of literature continues to grow exponentially, despite more than two decades having passed since the first reports. As well as extensive studies of the fundamental properties, this has seen SWCNTs used in a plethora of applications as far ranging as microelectronics, energy storage, solar cells, and sensors, to cancer treatment, drug delivery, and neuronal interfaces. On the other hand, the properties and applications of double-walled carbon nanotubes (DWCNTs) have remained relatively under-explored. This is despite DWCNTs not only sharing many of the same unique characteristics of their single-walled counterparts, but also possessing an additional suite of potentially advantageous properties arising due to the presence of the second wall and the often complex inter-wall interactions that arise. For example, it is envisaged that the outer wall can be selectively functionalized whilst still leaving the inner wall in its pristine state and available for signal transduction. A similar situation arises in DWCNT field effect transistors (FETs), where the outer wall can provide a convenient degree of chemical shielding of the inner wall from the external environment, allowing the excellent transconductance properties of the pristine nanotubes to be more fully exploited. Additionally, DWCNTs should also offer unique opportunities to further the fundamental understanding of the inter-wall interactions within and between carbon nanotubes. However, the realization of these goals has so far been limited by the same challenge experienced by the SWCNT field until recent years, namely, the inherent heterogeneity of raw, as-produced DWCNT material. As such, there is now an emerging field of research regarding DWCNT processing that focuses on the preparation of material of defined length, diameter and electronic type, and which is rapidly building upon the experience gained by the broader SWCNT community. This review describes the background of the field, summarizing some relevant theory and the available synthesis and purification routes; then provides a thorough synopsis of the current state-of-the-art in DWCNT sorting methodologies, outlines contemporary challenges in the field, and discusses the outlook for various potential applications of the resulting material. PMID:25899061

  10. Effect of microwave heating on the regeneration of modified activated carbons saturated with phenol

    NASA Astrophysics Data System (ADS)

    Ondon, B. S.; Sun, B.; Yan, Z. Y.; Zhu, X. M.; liu, H.

    2014-12-01

    The purpose of this work was to investigate the effect of microwave irradiation on the regeneration of modified activated carbons (GAC/MW, GAC/Ni, and GAC/Cu). The untreated activated carbon (GAC pure) was used for blank experiment. Microwave heating was used for preparation and regeneration of the modified activated carbons. The effect of loading Ni2+ and Cu2+ ions on the activated carbon adsorption capacity was investigated. The results showed that the activated carbon loaded with Ni2+ has no significant effect on phenol adsorption, while the adsorption capacity of activated carbon loaded with Cu2+ significantly decreased. Microwave irradiation showed a positive effect on activated carbon adsorption capacity. Under optimal conditions, the results showed that there was no effect when changing temperature and pH. The effect of ions Ni2+ and Cu2+ loaded into activated carbon were also investigated. During the regeneration process, the activated carbon loaded with Ni2+ showed a strong microwave energy adsorption than the activated carbon loaded with Cu2+. The effect increasing Ni2+ quantity decreases the activated carbon regeneration efficiency. During the regeneration of activated carbons, the highest temperature was observed in the cases of GAC/Ni. During regeneration, the temperature increases when the quantity Ni2+ loaded increases. The regeneration efficiency of activated carbons reaches 98 % even after 10 times of regeneration cycles. After several regenerations, MW/GAC and GAC/Ni regeneration efficiency was high, while regeneration efficiency of GAC/Cu decreased considerably. GAC regeneration efficiency also decreased several cycles. During regeneration process, phenol was simply desorbed from activated carbons under microwave irradiation.

  11. Influence of process water quality on hydrothermal carbonization of cellulose.

    PubMed

    Lu, Xiaowei; Flora, Joseph R V; Berge, Nicole D

    2014-02-01

    Hydrothermal carbonization (HTC) is a thermal conversion process that has been shown to be environmentally and energetically advantageous for the conversion of wet feedstocks. Supplemental moisture, usually in the form of pure water, is added during carbonization to achieve feedstock submersion. To improve process sustainability, it is important to consider alternative supplemental moisture sources. Liquid waste streams may be ideal alternative liquid source candidates. Experiments were conducted to systematically evaluate how changes in pH, ionic strength, and organic carbon content of the initial process water influences cellulose carbonization. Results from the experiments conducted evaluating the influence of process water quality on carbonization indicate that changes in initial water quality do influence time-dependent carbonization product composition and yields. These results also suggest that using municipal and industrial wastewaters, with the exception of streams with high CaCl2 concentrations, may impart little influence on final carbonization products/yields. PMID:24398151

  12. Carbon dioxide coordination and activation by niobium oxide molecules.

    PubMed

    Zhou, Mingfei; Zhou, Zijian; Zhuang, Jia; Li, Zhen Hua; Fan, Kangnian; Zhao, Yanying; Zheng, Xuming

    2011-12-22

    Carbon dioxide coordination and activation by niobium oxide molecules were studied by matrix isolation infrared spectroscopy. It was found that the niobium monoxide molecule reacted with carbon dioxide to form the niobium dioxide carbonyl complex NbO(2)(?(1)-CO) spontaneously on annealing in solid neon. The observation of the spontaneous reaction is consistent with theoretical predictions that this carbon dioxide activation process is both thermodynamically exothermic and kinetically facile. In contrast, four niobium dioxide-carbon dioxide complexes exhibiting three different coordination modes of CO(2) were formed from the reactions between niobium dioxide and carbon dioxide, which proceeded with the initial formation of the ?(1)-O bound NbO(2)(?(1)-OCO) and NbO(2)(?(1)-OCO)(2) complexes on annealing. The NbO(2)(?(1)-OCO) complex rearranged to the ?(2)-O,O bound NbO(2)(?(2)-O(2)C) isomer under visible light irradiation, while the NbO(2)(?(1)-OCO)(2) complex isomerized to the NbO(2)(?(1)-OCO)(?(2)-OC)O structure involving an ?(2)-C,O ligand under IR excitation. In these niobium dioxide carbon dioxide complexes, the ?(1)-O coordinated CO(2) ligand serves as an electron donor, whereas both the ?(2)-C,O and ?(2)-O,O coordinated CO(2) ligands act as electron acceptors. PMID:22059436

  13. Nitrogen activated-carbon sorption compressor

    NASA Astrophysics Data System (ADS)

    Tzabar, Nir; Grossman, Gershon

    2012-06-01

    Joule-Thomson (JT) sorption cryocooling is the most mature technology for cooling from a normal Room-Temperature (RT) down to temperatures below 100 K in the absence of moving parts. Therefore, high reliability and no vibrations are attainable, in comparison with other cryocoolers. Nitrogen is usually used as the working fluid for cooling to temperatures between 80 and 100 K and activated carbons are the best adsorbent for this purpose. In this paper we present the development of a sorption compressor for nitrogen with a commercial Chemviron pelleted activated carbon. The development consists of sorption measurements that we performed for characterizing the adsorption of nitrogen on the selected adsorbent, and the compressor experimental results are compared with equilibrium condition analysis and numerical heat transfer analysis predictions

  14. A novel carbon-based process for flue gas cleanup

    SciTech Connect

    Not Available

    1991-10-01

    The objective of this project is to demonstrate the preliminary technical and economic feasibility of a novel carbon-based process for removal of at least 95% SO{sub 2} and at least 75% NO{sub x} from coal combustion flue gas. In the process, flue gas leaving the electrostatic precipitator (ESP) is passed through a trickle bed of activated carbon catalyst employing a periodic flush of low strength sulfuric acid. The SO{sub 2} is oxidized to SO{sub 3} and removed as medium strength sulfuric acid. The SO{sub 2}-free flue gas is then mixed with NH{sub 3}, and the NO{sub x} in the gas is subjected to selective catalytic reduction (SCR) to N{sub 2} over a fixed-bed of activated carbon catalyst. The project is being carried over 14 months (June 4, 1991 to July 31, 1992). The experimental work is divided between Research Triangle Institute (RTI) and the University of Waterloo (Waterloo). RTI will conduct the NO{sub x} removal studies, whereas Waterloo will conduct the SO{sub 2} removal studies. The ultimate goal of the project is to demonstrate that the process can reduce the cost of electricity by 20% over conventional SCR/flue gas desulfurization (FGD) processes. In the present quarter, a detailed project management plan was prepared describing the experimental set-up, work plan and test plan. The experimental equipment is being constructed and is nearly complete with shakedown experiments scheduled to begin on or about November 1, 1991. Also, a paper was prepared and presented for the Seventh Annual Contractor's Conference. The first set of experiments will be completed in the next quarter. 7 refs., 5 figs., 4 tabs.

  15. Processing methods, characteristics and adsorption behavior of tire derived carbons: a review.

    PubMed

    Saleh, Tawfik A; Gupta, Vinod Kumar

    2014-09-01

    The remarkable increase in the number of vehicles worldwide; and the lack of both technical and economical mechanisms of disposal make waste tires to be a serious source of pollution. One potential recycling process is pyrolysis followed by chemical activation process to produce porous activated carbons. Many researchers have recently proved the capability of such carbons as adsorbents to remove various types of pollutants including organic and inorganic species. This review attempts to compile relevant knowledge about the production methods of carbon from waste rubber tires. The effects of various process parameters including temperature and heating rate, on the pyrolysis stage; activation temperature and time, activation agent and activating gas are reviewed. This review highlights the use of waste-tires derived carbon to remove various types of pollutants like heavy metals, dye, pesticides and others from aqueous media. PMID:25001042

  16. Processing of Activated Core Components

    SciTech Connect

    Friske, A.; Gestermann, G.; Finkbeiner, R.

    2003-02-26

    Used activated components from the core of a NPP like control elements, water channels from a BWR, and others like in-core measurement devices need to be processed into waste forms suitable for interim storage, and for the final waste repository. Processing of the activated materials can be undertaken by underwater cutting and packaging or by cutting and high-pressure compaction in a hot cell. A hot cell is available in Germany as a joint investment between GNS and the Karlsruhe Research Center at the latter's site. Special transport equipment is available to transport the components ''as-is'' to the hot cell. Newly designed underwater processing equipment has been designed, constructed, and operated for the special application of NPP decommissioning. This equipment integrates an underwater cutting device with an 80 ton force underwater in-drum compactor.

  17. Fabrication of novel micro-nano carbonous composites based on self-made hollow activated carbon fibers

    NASA Astrophysics Data System (ADS)

    Kong, Yuxia; Qiu, Tingting; Qiu, Jun

    2013-01-01

    The hollow activated carbon fibers (HACF) were prepared by using commercial polypropylene hollow fiber (PPHF) as the template, and phenol-formaldehyde resin (PF) as carbon precursors. Final HACF was formed through the thermal decomposition and carbonization of PF at 700 C under the nitrogen atmosphere, and activation at 800 C with carbon dioxide as the activating agent, consecutively. Then, carbon nanotubes (CNTs) were grown by chemical vapor deposition (CVD) techniques using the as-grown porous HACF as substrate. The growth process was achieved by pyrolyzing ethanol steam at 700 C using nickel as catalyst. Finally, CNTs was grown successfully on the substrate, and a novel tree-like micro-nano carbonous structure CNTs/HACF was fabricated. The as-grown HACF and micro-nano CNTs/HACF were characterized by scanning electron microscope (SEM), transmission electron microscope (TEM), X-ray diffraction (XRD), and thermogravimetric analysis (TG), respectively. Moreover, the formation mechanisms were also discussed.

  18. Activated carbon from char obtained from vacuum pyrolysis of teak sawdust: pore structure development and characterization.

    PubMed

    Ismadji, S; Sudaryanto, Y; Hartono, S B; Setiawan, L E K; Ayucitra, A

    2005-08-01

    The preparation of activated carbon from vacuum pyrolysis char of teak sawdust was studied and the results are presented in this paper. The effects of process variables such as temperature and activation time on the pore structure of activated carbons were studied. The activated carbon prepared from char obtained by vacuum pyrolysis has higher surface area and pore volume than that from atmospheric pyrolysis char. The BET surface area and pore volume of activated carbon prepared from vacuum pyrolysis char were 1150 m2/g and 0.43 cm3/g, respectively. PMID:15792584

  19. Production of activated carbon from coconut shell char in a fluidized bed reactor

    SciTech Connect

    Sai, P.M.S.; Ahmed, J.; Krishnaiah, K.

    1997-09-01

    Activated carbon is produced from coconut shell char using steam or carbon dioxide as the reacting gas in a 100 mm diameter fluidized bed reactor. The effect of process parameters such as reaction time, fluidizing velocity, particle size, static bed height, temperature of activation, fluidizing medium, and solid raw material on activation is studied. The product is characterized by determination of iodine number and BET surface area. The product obtained in the fluidized bed reactor is much superior in quality to the activated carbons produced by conventional processes. Based on the experimental observations, the optimum values of process parameters are identified.

  20. Preparation and characterization of activated carbon from demineralized tyre char

    NASA Astrophysics Data System (ADS)

    Manocha, S.; Prasad, Guddu R.; Joshi, Parth.; Zala, Ranjitsingh S.; Gokhale, Siddharth S.; Manocha, L. M.

    2013-06-01

    Activated carbon is the most adsorbing material for industrial waste water treatment. For wider applications, the main consideration is to manufacture activated carbon from low cost precursors, which are easily available and cost effective. One such source is scrap tyres. Recently much effort has been devoted to the thermal degradation of tyres into gaseous and liquid hydrocarbons and solid char residue, all of which have the potential to be processed into valuable products. As for solid residue, char can be used either as low-grade reinforcing filler or as activated carbon. The product recovered by a typical pyrolysis of tyres are usually, 33-38 wt% pyrolytic char, 38-55 wt% oil and 10-30 wt% solid fractions. In the present work activated carbon was prepared from pyrolyzed tyre char (PC). Demineralization involves the dissolution of metal into acids i.e. HCl, HNO3 and H2SO4 and in base i.e. NaOH. Different concentration of acid and base were used. Sodium hydroxide showed maximum amount of metal oxide removal. Further the concentration of sodium hydroxide was varied from 1N to 6N. As the concentration of acid are increased demineralization increases. 6N Sodium hydroxide is found to be more effective demineralising agent of tyre char.

  1. REACTION OF ACTIVATED CARBON WITH AQUEOUS CHLORINE AND CHLORINE DIOXIDE

    EPA Science Inventory

    The objective of this research was to determine whether aqueous chlorine and chlorine dioxide react with activated carbon, or with compounds adsorbed on activated carbon, to produce compounds that would not form in the absence of activated carbon. The experimental conditions were...

  2. Less-costly activated carbon for sewage treatment

    NASA Technical Reports Server (NTRS)

    Ingham, J. D.; Kalvinskas, J. J.; Mueller, W. A.

    1977-01-01

    Lignite-aided sewage treatment is based on absorption of dissolved pollutants by activated carbon. Settling sludge is removed and dried into cakes that are pyrolyzed with lignites to yield activated carbon. Lignite is less expensive than activated carbon previously used to supplement pyrolysis yield.

  3. Hierarchically structured activated carbon for ultracapacitors

    NASA Astrophysics Data System (ADS)

    Kim, Mok-Hwa; Kim, Kwang-Bum; Park, Sun-Min; Roh, Kwang Chul

    2016-02-01

    To resolve the pore-associated bottleneck problem observed in the electrode materials used for ultracapacitors, which inhibits the transport of the electrolyte ions, we designed hierarchically structured activated carbon (HAC) by synthesizing a mesoporous silica template/carbon composite and chemically activating it to simultaneously remove the silica template and increase the pore volume. The resulting HAC had a well-designed, unique porous structure, which allowed for large interfaces for efficient electric double-layer formation. Given the unique characteristics of the HAC, we believe that the developed synthesis strategy provides important insights into the design and fabrication of hierarchical carbon nanostructures. The HAC, which had a specific surface area of 1,957 m2 g‑1, exhibited an extremely high specific capacitance of 157 F g‑1 (95 F cc‑1), as well as a high rate capability. This indicated that it had superior energy storage capability and was thus suitable for use in advanced ultracapacitors.

  4. Hierarchically structured activated carbon for ultracapacitors

    PubMed Central

    Kim, Mok-Hwa; Kim, Kwang-Bum; Park, Sun-Min; Roh, Kwang Chul

    2016-01-01

    To resolve the pore-associated bottleneck problem observed in the electrode materials used for ultracapacitors, which inhibits the transport of the electrolyte ions, we designed hierarchically structured activated carbon (HAC) by synthesizing a mesoporous silica template/carbon composite and chemically activating it to simultaneously remove the silica template and increase the pore volume. The resulting HAC had a well-designed, unique porous structure, which allowed for large interfaces for efficient electric double-layer formation. Given the unique characteristics of the HAC, we believe that the developed synthesis strategy provides important insights into the design and fabrication of hierarchical carbon nanostructures. The HAC, which had a specific surface area of 1,957 m2 g−1, exhibited an extremely high specific capacitance of 157 F g−1 (95 F cc−1), as well as a high rate capability. This indicated that it had superior energy storage capability and was thus suitable for use in advanced ultracapacitors. PMID:26878820

  5. Hierarchically structured activated carbon for ultracapacitors.

    PubMed

    Kim, Mok-Hwa; Kim, Kwang-Bum; Park, Sun-Min; Roh, Kwang Chul

    2016-01-01

    To resolve the pore-associated bottleneck problem observed in the electrode materials used for ultracapacitors, which inhibits the transport of the electrolyte ions, we designed hierarchically structured activated carbon (HAC) by synthesizing a mesoporous silica template/carbon composite and chemically activating it to simultaneously remove the silica template and increase the pore volume. The resulting HAC had a well-designed, unique porous structure, which allowed for large interfaces for efficient electric double-layer formation. Given the unique characteristics of the HAC, we believe that the developed synthesis strategy provides important insights into the design and fabrication of hierarchical carbon nanostructures. The HAC, which had a specific surface area of 1,957 m(2) g(-1), exhibited an extremely high specific capacitance of 157 F g(-1) (95 F cc(-1)), as well as a high rate capability. This indicated that it had superior energy storage capability and was thus suitable for use in advanced ultracapacitors. PMID:26878820

  6. Asphalt-derived high surface area activated porous carbons for carbon dioxide capture.

    PubMed

    Jalilov, Almaz S; Ruan, Gedeng; Hwang, Chih-Chau; Schipper, Desmond E; Tour, Josiah J; Li, Yilun; Fei, Huilong; Samuel, Errol L G; Tour, James M

    2015-01-21

    Research activity toward the development of new sorbents for carbon dioxide (CO2) capture have been increasing quickly. Despite the variety of existing materials with high surface areas and high CO2 uptake performances, the cost of the materials remains a dominant factor in slowing their industrial applications. Here we report preparation and CO2 uptake performance of microporous carbon materials synthesized from asphalt, a very inexpensive carbon source. Carbonization of asphalt with potassium hydroxide (KOH) at high temperatures (>600 C) yields porous carbon materials (A-PC) with high surface areas of up to 2780 m(2) g(-1) and high CO2 uptake performance of 21 mmol g(-1) or 93 wt % at 30 bar and 25 C. Furthermore, nitrogen doping and reduction with hydrogen yields active N-doped materials (A-NPC and A-rNPC) containing up to 9.3% nitrogen, making them nucleophilic porous carbons with further increase in the Brunauer-Emmett-Teller (BET) surface areas up to 2860 m(2) g(-1) for A-NPC and CO2 uptake to 26 mmol g(-1) or 114 wt % at 30 bar and 25 C for A-rNPC. This is the highest reported CO2 uptake among the family of the activated porous carbonaceous materials. Thus, the porous carbon materials from asphalt have excellent properties for reversibly capturing CO2 at the well-head during the extraction of natural gas, a naturally occurring high pressure source of CO2. Through a pressure swing sorption process, when the asphalt-derived material is returned to 1 bar, the CO2 is released, thereby rendering a reversible capture medium that is highly efficient yet very inexpensive. PMID:25531980

  7. Biomass-based palm shell activated carbon and palm shell carbon molecular sieve as gas separation adsorbents.

    PubMed

    Sethupathi, Sumathi; Bashir, Mohammed Jk; Akbar, Zinatizadeh Ali; Mohamed, Abdul Rahman

    2015-04-01

    Lignocellulosic biomass has been widely recognised as a potential low-cost source for the production of high added value materials and proved to be a good precursor for the production of activated carbons. One of such valuable biomasses used for the production of activated carbons is palm shell. Palm shell (endocarp) is an abundant by-product produced from the palm oil industries throughout tropical countries. Palm shell activated carbon and palm shell carbon molecular sieve has been widely applied in various environmental pollution control technologies, mainly owing to its high adsorption performance, well-developed porosity and low cost, leading to potential applications in gas-phase separation using adsorption processes. This mini-review represents a comprehensive overview of the palm shell activated carbon and palm shell carbon molecular sieve preparation method, physicochemical properties and feasibility of palm shell activated carbon and palm shell carbon molecular sieve in gas separation processes. Some of the limitations are outlined and suggestions for future improvements are pointed out. PMID:25804669

  8. Ultrasound-assisted synthesis and processing of carbon materials

    NASA Astrophysics Data System (ADS)

    Fortunato, Maria E.

    2011-12-01

    Part I: Porous carbons are of interest in many applications because of their high surface areas and other physicochemical properties, and much effort has been directed towards developing new methods for controlling the porosity of carbons. Ultrasonic spray pyrolysis (USP) is an aerosol method suitable for large-scale, continuous synthesis of materials. Ultrasound is used to create aerosol droplets of a precursor solution which serve as micron-sized spherical reactors for materials synthesis. This work presents a precursor system for the template-free USP synthesis of porous carbons using low-cost precursors that do not evolve or require hazardous chemicals: sucrose was used as the carbon source, and sodium carbonate, sodium bicarbonate, or sodium nitrate was added as a decomposition catalyst and porogen. The USP carbons had macroporous interiors and microporous shells with surface areas as high as 800 m2/g and a narrow pore size distribution. It was determined that the interior porosity was a result of the gas evolution from salt decomposition and not from the presence of a salt template. Porous carbon is frequently used as a catalyst support because it provides high surface area and it is chemically and physically stable under many anoxic reaction conditions. Typically, the preparation of supported catalysts requires multiple steps for carbonization and metal impregnation. In this work, iron-impregnated porous carbon microspheres (Fe-C) were prepared by a one-step USP process by incorporating both the carbon and metal sources into the precursor solution. Carbonization, pore formation, metal impregnation, and metal activation occurred simultaneously to produce Fe-C materials with surface areas as high as 800 m2/g and up to 10 wt% Fe incorporated as nanoparticles < 20 nm in diameter. Fe-C was used as a catalyst to reduce aqueous hexavalent chromium, which demonstrated the accessibility of the iron nanoparticles despite the fact that they are likely encapsulated in the porous carbon support. Part II: The effects of high intensity ultrasound arise from acoustic cavitation: the formation, growth, and collapse of bubbles in a liquid. Bubble collapse produces intense localized heating (˜5000 K), high pressures (˜300 atm), and enormous heating and cooling rates (>109 K/sec). In solid-liquid slurries, surface erosion and particle fracture occur due to the shockwaves and microjets formed from asymmetric bubble collapse at extended surfaces. The chemical and physical effects of ultrasound have been studied as an adjunct to the traditional chemical pretreatment of lignocellulosic biomass for ethanol production. Lignocellulosic biomass consists of cellulose, hemicellulose, and lignin. The surface effects of ultrasound were used in this work to increase the accessibility of the cellulose, which can be converted to glucose and then fermented into ethanol. The lignocellulosic biomass used in this work was Miscanthus x giganteus (Mxg) which was grown at the University of Illinois at Urbana-Champaign. The chemical effects of NaOH pretreatment on Mxg were enhanced by ultrasound: greater delignification and a significant increase in the amount of pores >5 nm were observed. ˜ 70% of the theoretical glucose yield was obtained by enzymatic saccharification of the ultrasound-assisted NaOH-pretreated Mxg; this is comparable to the yields that can be obtained by traditional alkaline pretreatments, but it was achieved in a shorter time and at a lower temperature. Because the apparatus used for laboratory studies is not a likely device for scale-up, the economics of ultrasound with regards to energy balance are not yet resolved.

  9. Transition metal-catalyzed process for addition of amines to carbon-carbon double bonds

    DOEpatents

    Hartwig, John F.; Kawatsura, Motoi; Loeber, Oliver

    2002-01-01

    The present invention is directed to a process for addition of amines to carbon-carbon double bonds in a substrate, comprising: reacting an amine with a compound containing at least one carbon-carbon double bond in the presence a transition metal catalyst under reaction conditions effective to form a product having a covalent bond between the amine and a carbon atom of the former carbon-carbon double bond. The transition metal catalyst comprises a Group 8 metal and a ligand containing one or more 2-electron donor atoms. The present invention is also directed to enantioselective reactions of amine compounds with compounds containing carbon-carbon double bonds, and a calorimetric assay to evaluate potential catalysts in these reactions.

  10. Activated carbon adsorption from a high TOC wastewater

    SciTech Connect

    Hird, K.B.; Kube, W.R.; Schobert, H.H.

    1980-01-01

    The ability of activated carbon to reduce total organic carbon in highly concentrated wastewaters from a coal gasification pilot plant was evaluated in laboratory batch and column tests. The wastewater initially contains over 5000 mg/l TOC, largely phenols and cresols, with numerous other organic species in much lower concentrations. The physical adsorption process is best explained by the Freundlich model, with the slope and intercept of the Freundlich isotherm comparable to data reported for treatment of refinery wastes. Carbon exhaustion rates and bed depth-service time curves are also comparable to refinery treatment data obtained from waters of lower TOC or COD. Laboratory-scale column tests reduced TOC from 5740 mg/l to 200 mg/l.

  11. Nitric acid vapor removal by activated, impregnated carbons

    SciTech Connect

    Wood, G.O.

    1996-12-31

    Laboratory and industrial workers can be exposed to vapors of nitric acid, especially in accidents, such as spills. Nitric acid can also be a product of incineration for energy production or waste (e.g., CW agent) disposal. Activated carbons containing impregnants for enhancing vapor and gas removal have been tested for effectiveness in removing vapors of nitric acid from air. The nitric acid vapor was generated from concentrated acid solutions and detected by trapping in a water bubbler for pH measurements. Both low and moderate relative humidity conditions were used. All carbons were effective at vapor contact times representative of air-purifying respirator use. One surprising observation was the desorption of low levels of ammonia from impregnated carbons. This was apparently due to residual ammonia from the impregnation processes.

  12. Production and characterization of activated carbons from cereal grains

    SciTech Connect

    Venkatraman, A.; Walawender, S.P.; Fan, L.T.

    1996-10-01

    The kernels of grain such as corn and hard red winter wheat were subjected to a two-stage pyrolytic process to generate relatively high yields of charcoals. The process involved carbonization of the kernels at low temperatures (250-325{degrees}C) followed by complete devolatilization of the resultant charcoals at around 750{degrees}C. The charcoals were subsequently activated physically with CO{sub 2} at 800{degrees}C to yield activated carbons. The total pore volumes and surface areas of the activated carbons were determined at various degree of activation by physisorption methods. The surface areas from the nitrogen BET method ranged from 500 to 1750 m{sup 2}/g, while the total pore volumes obtained from the volumes at saturation were in the interval from 0.3 to 0.7 cm{sup 3}/g. The fractal nature of the pore interfaces as well as the existence of different types of pores were investigated through small-angle x-ray scattering.

  13. Dark Carbon Fixation: An Important Process in Lake Sediments

    PubMed Central

    Santoro, Ana Lcia; Bastviken, David; Gudasz, Cristian; Tranvik, Lars; Enrich-Prast, Alex

    2013-01-01

    Close to redox boundaries, dark carbon fixation by chemoautotrophic bacteria may be a large contributor to overall carbon fixation. Still, little is known about the relative importance of this process in lake systems, in spite the potentially high chemoautotrophic potential of lake sediments. We compared rates of dark carbon fixation, bacterial production and oxygen consumption in sediments from four Swedish boreal and seven tropical Brazilian lakes. Rates were highly variable and dark carbon fixation amounted up to 80% of the total heterotrophic bacterial production. The results indicate that non-photosynthetic carbon fixation can represent a substantial contribution to bacterial biomass production, especially in sediments with low organic matter content. PMID:23776549

  14. New indicator for the evaluation of the wood carbonization process

    SciTech Connect

    Schenkel, Y.; Temmerman, M.; Belle, J.F. van; Vankerkove, R.

    1999-12-01

    Evaluation of the results of a carbonization process is usually carried out by means of indicators such as mass yield, energy yield, or balanced mass yield. However, these indicators have some limits or drawbacks. A new indicator, the reference mass yield, is defined, based on the results of a well-controlled laboratory experimentation. This reference mass yield combines the mass yield and the fixed carbon content of the charcoal. It is a constant independent of the fixed carbon content, hence of the carbonization temperature. Some carbonization results from the literature are evaluated by means of the reference mass yield.

  15. Process for biological material carbon-carbon bond formation

    DOEpatents

    Hollingsworth, Rawle I. (Haslett, MI); Jung, Seunho (Kuyngkido, KR); Mindock, Carol A. (Lansing, MI)

    1998-01-01

    A process for providing vicinal dimethyl long chain between alkyl groups of organic compounds is described. The process uses intact or disrupted cells of various species of bacteria, particularly Thermoanaerobacter sp., Sarcina sp. and Butyrivibrio sp. The process can be conducted in an aqueous reaction mixture at room temperatures.

  16. Process for biological material carbon-carbon bond formation

    DOEpatents

    Hollingsworth, R.I.; Jung, S.; Mindock, C.A.

    1998-12-22

    A process for providing vicinal dimethyl long chain between alkyl groups of organic compounds is described. The process uses intact or disrupted cells of various species of bacteria, particularly Thermoanaerobacter sp., Sarcina sp. and Butyrivibrio sp. The process can be conducted in an aqueous reaction mixture at room temperatures. 8 figs.

  17. Waste polyvinylchloride derived pitch as a precursor to develop carbon fibers and activated carbon fibers.

    PubMed

    Qiao, W M; Yoon, S H; Mochida, I; Yang, J H

    2007-01-01

    Polyvinylchloride (PVC) was successfully recycled through the solvent extraction from waste pipe with an extraction yield of ca. 86%. The extracted PVC was pyrolyzed by a two-stage process (260 and 410 degrees C) to obtain free-chlorine PVC based pitch through an effective removal of chlorine from PVC during the heat-treatment. As-prepared pitch (softening point: 220 degrees C) was spun, stabilized, carbonized into carbon fibers (CFs), and further activated into activated carbon fibers (ACFs) in a flow of CO2. As-prepared CFs show comparable mechanical properties to commercial CFs, whose maximum tensile strength and modulus are 862 MPa and 62 GPa, respectively. The resultant ACFs exhibit a high surface area of 1200 m2/g, narrow pore size distribution and a low oxygen content of 3%. The study provides an effective insight to recycle PVC from waste PVC and develop a carbon precursor for high performance carbon materials such as CFs and ACFs. PMID:17157493

  18. Vibration damping with active carbon fiber structures

    NASA Astrophysics Data System (ADS)

    Neugebauer, Reimund; Kunze, Holger; Riedel, Mathias; Roscher, Hans-Jrgen

    2007-04-01

    This paper presents a mechatronic strategy for active reduction of vibrations on machine tool struts or car shafts. The active structure is built from a carbon fiber composite with embedded piezofiber actuators that are composed of piezopatches based on the Macro Fiber Composite (MFC) technology, licensed by NASA and produced by Smart Material GmbH in Dresden, Germany. The structure of these actuators allows separate or selectively combined bending and torsion, meaning that both bending and torsion vibrations can be actively absorbed. Initial simulation work was done with a finite element model (ANSYS). This paper describes how state space models are generated out of a structure based on the finite element model and how controller codes are integrated into finite element models for transient analysis and the model-based control design. Finally, it showcases initial experimental findings and provides an outlook for damping multi-mode resonances with a parallel combination of resonant controllers.

  19. ERIM processing and analysis activities

    NASA Astrophysics Data System (ADS)

    Lyden, J. D.; Shuchman, R. A.; Wackerman, C. C.

    1991-05-01

    Several activities were conducted over the past year in support of the P-3/SAR system. Recall that the P-3/SAR is a three-frequency Synthetic Aperture Radar (SAR) which was developed at the Environmental Research Institute of Michigan (ERIM) and is housed in a Naval Air Development Center (NADC) P-3 aircraft. These activities include: quick-look optical and digital processing, near-term digital analysis, processor upgrades for non-conventional SAR modes, and deployment of a calibration array. Each of these activities were in support of a classified data collection experiment conducted in May/June 1990 by the P-3/SAR and are described below. In addition to the activities listed above, ERIM scientists also played a key role in both the design and execution of last year's test. Finally, this contract has supported the participation of an ERIM scientist on a advisory panel established by the Navy. These activities will also be described below in the document.

  20. High surface area active carbon from coal

    SciTech Connect

    Yan Zhenming; Wen Lixian; Wang Yulan; Wang Junjie; Ding Jieran

    1997-12-31

    Recently, more and more attention has been paid to environment problems. Active carbon (AC) has been developed rapidly due to its good adsorption properties. Now, various kinds of AC with different pore structure and chemical property could be made according to the requirements of industrial applications. In America, high surface area active carbon (HSAC) has been made from petroleum coke and coal. It has also been commercialized in Japan by Kansai Coke and Chemicals Company from petroleum coke named Maxsorb. This kind of AC possesses high surface area (above 3,000 m{sup 2}/g) and excellent adsorption capacity. So, it could be used in a high performance adsorption system as well as in conventional situations. For example, it could be used for a high efficient capacitor, high capacity fuel battery and adsorption/separation of CH{sub 4}. However, HSAC from coal hasn`t been well studied in China. In this paper, using coal as raw material and KOH as activating agent, HSAC with surface area in excess of 3,000 m{sup 2}/g was made. The pore width of this AC were in the micropore range with concentrated distribution. It has also low ash content.

  1. Carbonate Precipitation through Microbial Activities in Natural Environment, and Their Potential in Biotechnology: A Review.

    PubMed

    Zhu, Tingting; Dittrich, Maria

    2016-01-01

    Calcium carbonate represents a large portion of carbon reservoir and is used commercially for a variety of applications. Microbial carbonate precipitation, a by-product of microbial activities, plays an important metal coprecipitation and cementation role in natural systems. This natural process occurring in various geological settings can be mimicked and used for a number of biotechnologies, such as metal remediation, carbon sequestration, enhanced oil recovery, and construction restoration. In this study, different metabolic activities leading to calcium carbonate precipitation, their native environment, and potential applications and challenges are reviewed. PMID:26835451

  2. Carbonate Precipitation through Microbial Activities in Natural Environment, and Their Potential in Biotechnology: A Review

    PubMed Central

    Zhu, Tingting; Dittrich, Maria

    2016-01-01

    Calcium carbonate represents a large portion of carbon reservoir and is used commercially for a variety of applications. Microbial carbonate precipitation, a by-product of microbial activities, plays an important metal coprecipitation and cementation role in natural systems. This natural process occurring in various geological settings can be mimicked and used for a number of biotechnologies, such as metal remediation, carbon sequestration, enhanced oil recovery, and construction restoration. In this study, different metabolic activities leading to calcium carbonate precipitation, their native environment, and potential applications and challenges are reviewed. PMID:26835451

  3. Formation of continuous activated carbon fibers for barrier fabrics

    NASA Astrophysics Data System (ADS)

    Liang, Ying

    1997-08-01

    Commercial protective suits made of active carbon granules or nonwoven fabrics are heavy, have low moisture vapor transport rate, and are uncomfortable. Inherent problems due to construction of barrier fabrics lead to severe heat stress when worn for even short time in warm environments. One proposed method to eliminate these problems is to facilitate the construction of a fabric made of continuous activated carbon fibers (CACF). This study is directed toward investigating the possibility of developing CAFC from two precursors: aramid and fibrillated PAN fiber. It was shown in this study that Kevlar-29 fibers could be quickly carbonized and activated to CACF with high adsorptivity and relatively low weight loss. CACF with high surface area (>500 msp2/g) and reasonable tenacity (?1g/denier) were successfully prepared from Kevlar fibers through a three-step process: pretreatment, carbonization, and activation. X-ray diffraction, Fourier Transform Infrared Spectroscopy (FTIR), and thermal analysis were conducted to understand the evolution of physical and chemical properties during pretreatment. The influence of temperature, heating rate, and pyrolysis environment on the thermal behavior was determined by DSC and TGA/DTA and used as an indicator for optimizing the pyrolysis conditions. Surface analysis by nitrogen isotherms indicated that the resultant fibers had micropores and mesopores on the surface of CACF. This was also inferred by studies on the surface morphology through Scanning Electron Microscopy (SEM) and Scanning Tunneling Microscopy (STM). An investigation of the surface chemical structure by X-ray photoelectron spectroscopy (XPS) before and after activation and elemental analysis confirmed that adsorption of Kevlar based CACF mainly arises due to the physisorption instead of chemisorption. A multistep stabilization along with carbonization and activation was used to prepare active carbon fiber from fibrillated PAN fiber. The resultant fiber retained its fibrillar structure and provided a very high surface area, up to 1400 msp2/g, but was brittle. The characterization of the thermal behavior, mechanical properties, and surface structure of the pyrolyzed fiber at each processing step was also carried out by using various techniques, such as DSC and TGA, Instron, and SEM. These studies provide directions for preparation of CACF from novel precursors.

  4. Adsorbed natural gas storage with activated carbon

    SciTech Connect

    Sun, Jian; Brady, T.A.; Rood, M.J.

    1996-12-31

    Despite technical advances to reduce air pollution emissions, motor vehicles still account for 30 to 70% emissions of all urban air pollutants. The Clean Air Act Amendments of 1990 require 100 cities in the United States to reduce the amount of their smog within 5 to 15 years. Hence, auto emissions, the major cause of smog, must be reduced 30 to 60% by 1998. Natural gas con be combusted with less pollutant emissions. Adsorbed natural gas (ANG) uses adsorbents and operates with a low storage pressure which results in lower capital costs and maintenance. This paper describes the production of an activated carbon adsorbent produced from an Illinois coal for ANG.

  5. Activation of structural carbon fibres for potential applications in multifunctional structural supercapacitors.

    PubMed

    Qian, Hui; Diao, Hele; Shirshova, Natasha; Greenhalgh, Emile S; Steinke, Joachim G H; Shaffer, Milo S P; Bismarck, Alexander

    2013-04-01

    The feasibility of modifying conventional structural carbon fibres via activation has been studied to create fibres, which can be used simultaneously as electrode and reinforcement in structural composite supercapacitors. Both physical and chemical activation, including using steam, carbon dioxide, acid and potassium hydroxide, were conducted and the resulting fibre properties compared. It was proven that the chemical activation using potassium hydroxide is an effective method to prepare activated structural carbon fibres that possess both good electrochemical and mechanical properties. The optimal activation conditions, such as the loading of activating agent and the burn-off of carbon fibres, was identified and delivered a 100-fold increase in specific surface area and 50-fold improvement in specific electrochemical capacitance without any degradation of the fibre mechanical properties. The activation process was successfully scaled-up, showing good uniformity and reproducibility. These activated structural carbon fibres are promising candidates as reinforcement/electrodes for multifunctional structural energy storage devices. PMID:23312580

  6. Authigenic carbonates from active methane seeps offshore southwest Africa

    NASA Astrophysics Data System (ADS)

    Pierre, Catherine; Blanc-Valleron, Marie-Madeleine; Demange, Jérôme; Boudouma, Omar; Foucher, Jean-Paul; Pape, Thomas; Himmler, Tobias; Fekete, Noemi; Spiess, Volkhard

    2012-12-01

    The southwest African continental margin is well known for occurrences of active methane-rich fluid seeps associated with seafloor pockmarks at water depths ranging broadly from the shelf to the deep basins, as well as with high gas flares in the water column, gas hydrate accumulations, diagenetic carbonate crusts and highly diverse benthic faunal communities. During the M76/3a expedition of R/V METEOR in 2008, gravity cores recovered abundant authigenic carbonate concretions from three known pockmark sites—Hydrate Hole, Worm Hole, the Regab pockmark—and two sites newly discovered during that cruise, the so-called Deep Hole and Baboon Cluster. The carbonate concretions were commonly associated with seep-benthic macrofauna and occurred within sediments bearing shallow gas hydrates. This study presents selected results from a comprehensive analysis of the mineralogy and isotope geochemistry of diagenetic carbonates sampled at these five pockmark sites. The oxygen isotope stratigraphy obtained from three cores of 2-5 m length indicates a maximum age of about 60,000-80,000 years for these sediments. The authigenic carbonates comprise mostly magnesian calcite and aragonite, associated occasionally with dolomite. Their very low carbon isotopic compositions (-61.0 < δ13C ‰ V-PDB < -40.1) suggest anaerobic oxidation of methane (AOM) as the main process controlling carbonate precipitation. The oxygen isotopic signatures (+2.4 < δ18O ‰ V-PDB < +6.2) lie within the range in equilibrium under present-day/interglacial to glacial conditions of bottom seawater; alternatively, the most positive δ18O values might reflect the contribution of 18O-rich water from gas hydrate decomposition. The frequent occurrence of diagenetic gypsum crystals suggests that reduced sulphur (hydrogen sulphide, pyrite) from sub-seafloor sediments has been oxidized by oxygenated bottom water. The acidity released during this process can potentially induce the dissolution of carbonate, thereby providing enough Ca2+ ions for pore solutions to reach gypsum saturation; this is thought to be promoted by the bio-irrigation and burrowing activity of benthic fauna. The δ18O-δ13C patterns identified in the authigenic carbonates are interpreted to reflect variations in the rate of AOM during the last glacial-interglacial cycle, in turn controlled by variably strong methane fluxes through the pockmarks. These results complement the conclusions of Kasten et al. in this special issue, based on authigenic barite trends at the Hydrate Hole and Worm Hole pockmarks which were interpreted to reflect spatiotemporal variations in AOM related to subsurface gas hydrate formation-decomposition.

  7. Void forming pyrolytic carbon coating process

    DOEpatents

    Beatty, Ronald L. (Oak Ridge, TN); Cook, Jackie L. (Oak Ridge, TN)

    2000-01-01

    A pyrolytic carbon coated nuclear fuel particle and method of making it. The fuel particle has a core composed of a refractory compound of an actinide metal. The pyrolytic carbon coating surrounds the core so as to provide a void volume therebetween. The coating has an initial density of no greater than 1.45 grams/cm.sup.3 and an anisotropy factor than 3.0 and a final density upon heat treatment above about 2000.degree. C. of greater than 1.7 grams/cm.sup.3 and an anisotropy factor greater than 5.

  8. Treatment of industrial effluents using electron beam accelerator and adsorption with activated carbon: a comparative study

    NASA Astrophysics Data System (ADS)

    de Oliveira Sampa, Maria Helena; Rela, Paulo Roberto; Casas, Alexandre Las; Mori, Manoel Nunes; Duarte, Celina Lopes

    2004-09-01

    This paper presents preliminary results of a study that compares the use of electron beam processing and activated carbon adsorption to clean up a standardized organic aqueous solution and a real industrial effluent. The electron beam treatment was performed in a batch system using the IPEN's Electron Beam Accelerators from Radiation Dynamics Inc., Dynamitron 37.5 kW. The granular activated carbon removal treatment was performed using charcoal made from wood "pinus". If the adequate irradiation dose is delivered to the organic pollutant, it is possible to conclude for the studied compounds that the Electron Beam Process is similar to the activated carbon process in organic removal efficiency.

  9. ENTRAINED-FLOW ADSORPTION OF MERCURY USING ACTIVATED CARBON

    EPA Science Inventory

    Bench-scale experiments were conducted in a flow reactor to simulate entrained-flow capture of elemental mercury (Hg) by activated carbon. Adsorption of Hg by several commercial activated carbons was examined at different carbon-to-mercury (C:Hg) ratios (by weight) (600:1 - 29000...

  10. The regeneration of polluted activated carbon by radiation techniques

    NASA Astrophysics Data System (ADS)

    Minghong, Wu; Borong, Bao; Ruimin, Zhou; Jinliang, Zhu; Longxin, Hu

    1998-10-01

    In this paper, the regeneration of used activated carbon from monosodium glutamate factory was experimented using radiation and acid-alkali chemical cleaning method. Results showed that the activated carbon saturated with pollutants can be wash away easily by flushing with chemical solution prior irradiation. DSC was used to monitor the change of carbon adsorption

  11. Acid sorption regeneration process using carbon dioxide

    DOEpatents

    King, C. Judson (Kensington, CA); Husson, Scott M. (Anderson, SC)

    2001-01-01

    Carboxylic acids are sorbed from aqueous feedstocks onto a solid adsorbent in the presence of carbon dioxide under pressure. The acids are freed from the sorbent phase by a suitable regeneration method, one of which is treating them with an organic alkylamine solution thus forming an alkylamine-carboxylic acid complex which thermally decomposes to the desired carboxylic acid and the alkylamine.

  12. Processes for reducing NHS carbon footprint.

    PubMed

    2007-08-01

    NHS Trust boards face challenging targets for cutting carbon emissions from new and existing facilities. Spirax Sarco's Murdo Macdonald looks at the help available and some of the latest examples of good practice in steam systems for hospital heating and hot water. PMID:17847881

  13. Preparation of binderless activated carbon monolith from pre-carbonization rubber wood sawdust by controlling of carbonization and activation condition

    NASA Astrophysics Data System (ADS)

    Taer, E.; Deraman, M.; Taslim, R.; Iwantono

    2013-09-01

    Binderless activated carbon monolith (ACM) was prepared from pre-carbonized rubber wood sawdust (RWSD). The effect of the carbonization temperature (400, 500, 600, 700, 800 dan 900 °C) on porosity characteristic of the ACM have been studied. The optimum carbonization temperature for obtaining ACM with high surface area of 600 °C with CO2 activation at 800 °C for one hour. At this condition, the surface area as high as 733 m2 g-1 could be successfully obtained. By improved the activation temperature at 900 °C for 2.5 h, it was found that the surface area of 860 m2 g-1. For this condition, the ACM exhibit the specific capacitance of 90 F g-1. In addition the termogravimertic (TG)-differential termografimertic (DTG) and field emission scanning electron microscope (FESEM) measurement were also performed on the ACMs and the result has been studied. Finally, it was conclude that the high surface area of ACM from RWSD could be produced by proper selections of carbonization and activation condition.

  14. Adsorption of Safranin-T from wastewater using waste materials- activated carbon and activated rice husks.

    PubMed

    Gupta, Vinod K; Mittal, Alok; Jain, Rajeev; Mathur, Megha; Sikarwar, Shalini

    2006-11-01

    Textile effluents are major industrial polluters because of high color content, about 15% unfixed dyes and salts. The present paper is aimed to investigate and develop cheap adsorption methods for color removal from wastewater using waste materials activated carbon and activated rice husk-as adsorbents. The method was employed for the removal of Safranin-T and the influence of various factors such as adsorbent dose, adsorbate concentration, particle size, temperature, contact time, and pH was studied. The adsorption of the dye over both the adsorbents was found to follow Langmuir and Freundlich adsorption isotherm models. Based on these models, different useful thermodynamic parameters have been evaluated for both the adsorption processes. The adsorption of Safranin-T over activated carbon and activated rice husks follows first-order kinetics and the rate constants for the adsorption processes decrease with increase in temperature. PMID:16934282

  15. Plant diversity increases soil microbial activity and soil carbon storage.

    PubMed

    Lange, Markus; Eisenhauer, Nico; Sierra, Carlos A; Bessler, Holger; Engels, Christoph; Griffiths, Robert I; Mellado-Vzquez, Perla G; Malik, Ashish A; Roy, Jacques; Scheu, Stefan; Steinbeiss, Sibylle; Thomson, Bruce C; Trumbore, Susan E; Gleixner, Gerd

    2015-01-01

    Plant diversity strongly influences ecosystem functions and services, such as soil carbon storage. However, the mechanisms underlying the positive plant diversity effects on soil carbon storage are poorly understood. We explored this relationship using long-term data from a grassland biodiversity experiment (The Jena Experiment) and radiocarbon ((14)C) modelling. Here we show that higher plant diversity increases rhizosphere carbon inputs into the microbial community resulting in both increased microbial activity and carbon storage. Increases in soil carbon were related to the enhanced accumulation of recently fixed carbon in high-diversity plots, while plant diversity had less pronounced effects on the decomposition rate of existing carbon. The present study shows that elevated carbon storage at high plant diversity is a direct function of the soil microbial community, indicating that the increase in carbon storage is mainly limited by the integration of new carbon into soil and less by the decomposition of existing soil carbon. PMID:25848862

  16. REPEATED REDUCTIVE AND OXIDATIVE TREATMENTS ON GRANULAR ACTIVATED CARBON

    EPA Science Inventory

    Fenton oxidation and Fenton oxidation preceded by reduction solutions were applied to granular activated carbon (GAC) to chemically regenerate the adsorbent. No adsorbate was present on the GAC so physicochemical effects from chemically aggressive regeneration of the carbon coul...

  17. REACTIONS OF CHLORITE WITH ACTIVATED CARBON AND WITH VANILLIC ACID AND INDAN ADSORBED ON ACTIVATED CARBON

    EPA Science Inventory

    The reaction between chlorite (CO2(-1)) and vanillic acid, at pH 6.0 in the presence of granular activated carbon (GAC), yielded several reaction products identifiable by GC/MS; no products were found in the absence of GAC. Indan and ClO2 or ClO2(-1) reacted in aqueous solution a...

  18. Solution-Processable Carbon Nanoelectrodes for Single-Molecule Investigations.

    PubMed

    Zhu, Jingyuan; McMorrow, Joseph; Crespo-Otero, Rachel; Ao, Geyou; Zheng, Ming; Gillin, William P; Palma, Matteo

    2016-03-01

    Here we present a solution-based assembly method for producing molecular transport junctions employing metallic single-walled carbon nanotubes as nanoelectrodes. The molecular junction conductance of a series of oligophenyls was successfully measured, highlighting the potential of an all-carbon based approach for the fabrication of solution-processable single-molecule junctions for molecular electronics. PMID:26854787

  19. Processes of carbonate precipitation in modern microbial mats

    NASA Astrophysics Data System (ADS)

    Dupraz, Christophe; Reid, R. Pamela; Braissant, Olivier; Decho, Alan W.; Norman, R. Sean; Visscher, Pieter T.

    2009-10-01

    Microbial mats are ecosystems that arguably greatly affected the conditions of the biosphere on Earth through geological time. These laminated organosedimentary systems, which date back to > 3.4 Ga bp, are characterized by high metabolic rates, and coupled to this, rapid cycling of major elements on very small (mm-m) scales. The activity of the mat communities has changed Earth's redox conditions (i.e. oxidation state) through oxygen and hydrogen production. Interpretation of fossil microbial mats and their potential role in alteration of the Earth's geochemical environment is challenging because these mats are generally not well preserved. Preservation of microbial mats in the fossil record can be enhanced through carbonate precipitation, resulting in the formation of lithified mats, or microbialites. Several types of microbially-mediated mineralization can be distinguished, including biologically-induced and biologically influenced mineralization. Biologically-induced mineralization results from the interaction between biological activity and the environment. Biologically-influenced mineralization is defined as passive mineralization of organic matter (biogenic or abiogenic in origin), whose properties influence crystal morphology and composition. We propose to use the term organomineralization sensu lato as an umbrella term encompassing biologically influenced and biologically induced mineralization. Key components of organomineralization sensu lato are the "alkalinity" engine (microbial metabolism and environmental conditions impacting the calcium carbonate saturation index) and an organic matrix comprised of extracellular polymeric substances (EPS), which may provide a template for carbonate nucleation. Here we review the specific role of microbes and the EPS matrix in various mineralization processes and discuss examples of modern aquatic (freshwater, marine and hypersaline) and terrestrial microbialites.

  20. Process for Making Carbon-Carbon Turbocharger Housing Unit for Intermittent Combustion Engines

    NASA Technical Reports Server (NTRS)

    Northam, G. Burton (Inventor); Ransone, Philip O. (Inventor); Rivers, H. Kevin (Inventor)

    1999-01-01

    An improved. lightweight, turbine housing unit for an intermittent combustion reciprocating internal combustion engine turbocharger is prepared from a lay-up or molding of carbon-carbon composite materials in a single-piece or two-piece process. When compared to conventional steel or cast iron, the use of carbon-carbon composite materials in a turbine housing unit reduces the overall weight of the engine and reduces the heat energy loss used in the turbo-charging process. This reduction in heat energy loss and weight reduction provides for more efficient engine operation.

  1. Carbon dioxide sequestration by direct mineral carbonation: process mineralogy of feed and products

    SciTech Connect

    O'Connor, William K.; Dahlin, David C.; Rush, G.E.; Dahlin, Cheryl L.; Collins, W. Keith

    2001-01-01

    Direct mineral carbonation has been investigated as a process to convert gaseous CO2 into a geologically stable final form. The process utilizes a slurry of water, with bicarbonate and salt additions, mixed with a mineral reactant, such as olivine (Mg2SiO4) or serpentine [Mg3Si2O5(OH)4]. Carbon dioxide is dissolved into this slurry, resulting in dissolution of the mineral and precipitation of magnesium carbonate (MgCO3). Optimum results have been achieved using heat pretreated serpentine feed material and high partial pressure of CO2 (PCO2). Specific conditions include: 155?C; PCO2=185 atm; 15% solids. Under these conditions, 78% conversion of the silicate to the carbonate was achieved in 30 minutes. Process mineralogy has been utilized to characterize the feed and process products, and interpret the mineral dissolution and carbonate precipitation reaction paths.

  2. Merging allylic carbon-hydrogen and selective carbon-carbon bond activation

    NASA Astrophysics Data System (ADS)

    Masarwa, Ahmad; Didier, Dorian; Zabrodski, Tamar; Schinkel, Marvin; Ackermann, Lutz; Marek, Ilan

    2014-01-01

    Since the nineteenth century, many synthetic organic chemists have focused on developing new strategies to regio-, diastereo- and enantioselectively build carbon-carbon and carbon-heteroatom bonds in a predictable and efficient manner. Ideal syntheses should use the least number of synthetic steps, with few or no functional group transformations and by-products, and maximum atom efficiency. One potentially attractive method for the synthesis of molecular skeletons that are difficult to prepare would be through the selective activation of C-H and C-C bonds, instead of the conventional construction of new C-C bonds. Here we present an approach that exploits the multifold reactivity of easily accessible substrates with a single organometallic species to furnish complex molecular scaffolds through the merging of otherwise difficult transformations: allylic C-H and selective C-C bond activations. The resulting bifunctional nucleophilic species, all of which have an all-carbon quaternary stereogenic centre, can then be selectively derivatized by the addition of two different electrophiles to obtain more complex molecular architecture from these easily available starting materials.

  3. Gel and process for preventing carbon dioxide break through

    SciTech Connect

    Sandiford, B.B.; Zillmer, R.C.

    1987-06-16

    A process is described for retarding the flow of carbon dioxide in carbon dioxide break-through fingers in a subterranean formation, the process comprising: (a) introducing a gas selected from the group consisting of carbon dioxide and gases containing carbon dioxide into a subterranean deposit containing carbon dioxide break-through fingers; (b) after the carbon dioxide break-through fingers have sorbed a predetermined amount of the gas, stopping the flow of the gas into the subterranean formation, (c) after stopping the flow of the gas into the subterranean formation, introducing an effective amount of a gel-forming composition into the subterranean formation and into the carbon dioxide break-through fingers, the gel-forming composition being operable, when contacting carbon dioxide break-through fingers containing the brine which has absorbed substantial amounts of carbon dioxide to form a gel in the fingers which is operable for retarding the flow of the gas in the finger. The gel-forming composition comprises: i. an aqueous solution comprising a first substance selected from the group consisting of polyvinyl alcohols, polyvinyl alcohol copolymers, and mixtures thereof, and ii. an amount of a second substance selected from the group consisting of aldehydes, aldehyde generating substances, acetals, acetal generating substances, and mixtures thereof.

  4. Modeling of HiPco Process for Carbon Nanotube Production

    NASA Technical Reports Server (NTRS)

    Gokcen, T.; Dateo, C. E.; Meyyappan, M.; Colbert, D. T.; Smith, D. T.; Smith, K.; Smalley, R. E.; Arnold, James O. (Technical Monitor)

    2000-01-01

    High-pressure carbon monoxide (HiPco) reactor, developed at Rice University, is used to produce single-walled carbon nanotubes (SWNT) from gas-phase reactions of iron carbonyl and nickel carbonyl in carbon monoxide at high pressures (10 - 100 atm). Computational modeling is used to better understand the HiPco process. In the present model, decomposition of the precursor, metal cluster formation and growth, and carbon nanotube growth are addressed. Decomposition of precursor molecules is necessary to initiate metal cluster formation. The metal clusters serve as catalysts for carbon nanotube growth. Diameter of metal clusters and number of atoms in these clusters are some of the essential information for predicting carbon nanotube formation and growth, which is then modeled by Boudouard reaction (2CO ---> C(s) + CO2) with metal catalysts. The growth kinetic model is integrated with a two-dimensional axisymmetric reactor flow model to predict reactor performance.

  5. Activated Carbon Composites for Air Separation

    SciTech Connect

    Baker, Frederick S; Contescu, Cristian I; Tsouris, Costas; Burchell, Timothy D

    2011-09-01

    Coal-derived synthesis gas is a potential major source of hydrogen for fuel cells. Oxygen-blown coal gasification is an efficient approach to achieving the goal of producing hydrogen from coal, but a cost-effective means of enriching O2 concentration in air is required. A key objective of this project is to assess the utility of a system that exploits porous carbon materials and electrical swing adsorption to produce an O2-enriched air stream for coal gasification. As a complement to O2 and N2 adsorption measurements, CO2 was used as a more sensitive probe molecule for the characterization of molecular sieving effects. To further enhance the potential of activated carbon composite materials for air separation, work was implemented on incorporating a novel twist into the system; namely the addition of a magnetic field to influence O2 adsorption, which is accompanied by a transition between the paramagnetic and diamagnetic states. The preliminary findings in this respect are discussed.

  6. Process synthesis and optimization for the production of carbon nanostructures.

    PubMed

    Iyuke, S E; Mamvura, T A; Liu, K; Sibanda, V; Meyyappan, M; Varadan, V K

    2009-09-16

    A swirled fluidized bed chemical vapour deposition (SFCVD) reactor has been manufactured and optimized to produce carbon nanostructures on a continuous basis using in situ formation of floating catalyst particles by thermal decomposition of organometallic ferrocene. During the process optimization, carbon nanoballs were produced in the absence of a catalyst at temperatures higher than 1000 degrees C, while carbon nanofibres, single-walled carbon nanotubes, helical carbon nanotubes, multi-walled carbon nanotubes (MWCNTs) and carbon nanofibres (CNFs) were produced in the presence of a catalyst at lower temperatures of between 750 and 900 degrees C. The optimum conditions for producing carbon nanostructures were a temperature of 850 degrees C, acetylene flow rate of 100 ml min(-1), and acetylene gas was used as the carbon source. All carbon nanostructures produced have morphologies and diameters ranging from 15 to 200 nm and wall thicknesses between 0.5 and 0.8 nm. In comparison to the quantity of MWCNTs produced with other methods described in the literature, the SFCVD technique was superior to floating catalytic CVD (horizontal fixed bed) and microwave CVD but inferior to rotary tube CVD. PMID:19706958

  7. Surface modification, characterization and adsorptive properties of a coconut activated carbon

    NASA Astrophysics Data System (ADS)

    Lu, Xincheng; Jiang, Jianchun; Sun, Kang; Xie, Xinping; Hu, Yiming

    2012-08-01

    A coconut activated carbon was modified using chemical methods. Different concentration of nitric acid oxidation of the conventional sample produced samples with weakly acidic functional groups. The oxidized samples were characterized by scanning electron micrograph, nitrogen absorption-desorption, Fourier transform infra red spectroscopy, Bothem method, pH titration, adsorption capacity of sodium and formaldehyde, and the adsorption mechanism of activated carbons was investigated. The results showed that BET surface area and pore volume of activated carbons were decreased after oxidization process, while acidic functional groups were increased. The surface morphology of oxidized carbons looked clean and eroded which was caused by oxidization of nitric acid. The oxidized carbons showed high adsorption capacity of sodium and formaldehyde, and chemical properties of activated carbon played an important role in adsorption of metal ions and organic pollutants.

  8. Production of activated carbons from pyrolysis of waste tires impregnated with potassium hydroxide.

    PubMed

    Teng, H; Lin, Y C; Hsu, L Y

    2000-11-01

    Activated carbons were produced from waste tires using a chemical activation method. The carbon production process consisted of potassium hydroxide (KOH) impregnation followed by pyrolysis in N2 at 600-900 degrees C for 0-2 hr. The activation method can produce carbons with a surface area (SA) and total pore volume as high as 470 m2/g and 0.57 cm3/g, respectively. The influence of different parameters during chemical activation, such as pyrolysis temperature, holding time, and KOH/tire ratio, on the carbon yield and the surface characteristics was explored, and the optimum preparation conditions were recommended. The pore volume of the resulting carbons generally increases with the extent of carbon gasified by KOH and its derivatives, whereas the SA increases with degree of gasification to reach a maximum value, and then decreases upon further gasification. PMID:11111338

  9. Restricted dynamics of molecular hydrogen confined in activated carbon nanopores

    SciTech Connect

    Contescu, Cristian I; Saha, Dipendu; Gallego, Nidia C; Mamontov, Eugene; Kolesnikov, Alexander I; Bhat, Vinay V

    2012-01-01

    Quasi-elastic neutron scattering was used for characterization of dynamics of molecular hydrogen confined in narrow nanopores of two activated carbon materials: PFAC (derived from polyfurfuryl alcohol) and UMC (ultramicroporous carbon). Fast, but incomplete ortho-para conversion was observed at 10 K, suggesting that scattering originates from the fraction of unconverted ortho isomer which is rotation-hindered because of confinement in nanopores. Hydrogen molecules entrapped in narrow nanopores (<7 ) were immobile below 22-25 K. Mobility increased rapidly with temperature above this threshold, which is 8 K higher than the melting point of bulk hydrogen. Diffusion obeyed fixed-jump length mechanism, indistinguishable between 2D and 3D processes. Thermal activation of diffusion was characterized between ~22 and 37 K, and structure-dependent differences were found between the two carbons. Activation energy of diffusion was higher than that of bulk solid hydrogen. Classical notions of liquid and solid do not longer apply for H2 confined in narrow nanopores.

  10. Processing and properties of pitch-based carbon-carbon composites

    SciTech Connect

    Rand, B.; Appleyard, S.P.; Ahearn, C.

    1995-12-01

    The processing of carbon-carbon composites using a pitch matrix and a variety of fibres will be described. The importance of the fibre surface chemistry in controlling all the major properties of the composites will be described along with methods of modifying the fibre-matrix bonding and interphase structure. Interfacial behavior also controls the matrix microstructural characteristics and the location of pores and cracks formed during carbonization and graphitization. This will be explained in detail.

  11. Sodium to sodium carbonate conversion process

    DOEpatents

    Herrmann, S.D.

    1997-10-14

    A method is described for converting radioactive alkali metal into a low level disposable solid waste material. The radioactive alkali metal is atomized and introduced into an aqueous caustic solution having caustic present in the range of from about 20 wt % to about 70 wt % to convert the radioactive alkali metal to a radioactive alkali metal hydroxide. The aqueous caustic containing radioactive alkali metal hydroxide and CO{sub 2} are introduced into a thin film evaporator with the CO{sub 2} present in an amount greater than required to convert the alkali metal hydroxide to a radioactive alkali metal carbonate, and thereafter the radioactive alkali metal carbonate is separated from the thin film evaporator as a dry powder. Hydroxide solutions containing toxic metal hydroxide including one or more metal ions of Sb, As, Ba, Be, Cd, Cr, Pb, Hg, Ni, Se, Ag and Tl can be converted into a low level non-hazardous waste using the thin film evaporator of the invention. 3 figs.

  12. Sodium to sodium carbonate conversion process

    DOEpatents

    Herrmann, Steven D.

    1997-01-01

    A method of converting radioactive alkali metal into a low level disposable solid waste material. The radioactive alkali metal is atomized and introduced into an aqueous caustic solution having caustic present in the range of from about 20 wt % to about 70 wt % to convert the radioactive alkali metal to a radioactive alkali metal hydroxide. The aqueous caustic containing radioactive alkali metal hydroxide and CO.sub.2 are introduced into a thin film evaporator with the CO.sub.2 present in an amount greater than required to convert the alkali metal hydroxide to a radioactive alkali metal carbonate, and thereafter the radioactive alkali metal carbonate is separated from the thin film evaporator as a dry powder. Hydroxide solutions containing toxic metal hydroxide including one or more metal ions of Sb, As, Ba, Be, Cd, Cr, Pb, Hg, Ni, Se, Ag and T1 can be converted into a low level non-hazardous waste using the thin film evaporator of the invention.

  13. Processing and Characterization of Carbon Nanotube Composites

    NASA Technical Reports Server (NTRS)

    Can, Roberto J.; Grimsley, Brian W.; Czabaj, Michael W.; Siochi, Emilie J.; Hull, Brandon

    2014-01-01

    Recent advances in the synthesis of large-scale quantities of carbon nanotubes (CNT) have provided the opportunity to study the mechanical properties of polymer matrix composites using these novel materials as reinforcement. Nanocomp Technologies, Inc. currently supplies large sheets with dimensions up to 122 cm x 244 cm containing both single-wall and few-wall CNTs. The tubes are approximately 1 mm in length with diameters ranging from 8 to 12 nm. In the present study being conducted at NASA Langley Research Center (LaRC), single and multiple layers of CNT sheets were infused or coated with various polymer solutions that included commercial toughened-epoxies and bismaleimides, as well as a LaRC developed polyimide. The resulting CNT composites were tested in tension using a modified version of ASTM D882-12 to determine their strength and modulus values. The effects of solvent treatment and mechanical elongation/alignment of the CNT sheets on the tensile performance of the composite were determined. Thin composites (around 50 wt% CNT) fabricated from acetone condensed and elongated CNT sheets with either a BMI or polyimide resin solution exhibited specific tensile moduli approaching that of toughened epoxy/ IM7 carbon fiber unidirectional composites.

  14. Production of activated carbons from waste tyres for low temperature NOx control.

    PubMed

    Al-Rahbi, Amal S; Williams, Paul T

    2016-03-01

    Waste tyres were pyrolysed in a bench scale reactor and the product chars were chemically activated with alkali chemical agents, KOH, K2CO3, NaOH and Na2CO3 to produce waste tyre derived activated carbons. The activated carbon products were then examined in terms of their ability to adsorb NOx (NO) at low temperature (25°C) from a simulated industrial process flue gas. This study investigates the influence of surface area and porosity of the carbons produced with the different alkali chemical activating agents on NO capture from the simulated flue gas. The influence of varying the chemical activation conditions on the porous texture and corresponding NO removal from the flue gas was studied. The activated carbon sorbents were characterized in relation to BET surface area, micropore and mesopore volumes and chemical composition. The highest NO removal efficiency for the waste tyre derived activated carbons was ∼75% which was obtained with the adsorbent treated with KOH which correlated with both the highest BET surface area and largest micropore volume. In contrast, the waste tyre derived activated carbons prepared using K2CO3, NaOH and Na2CO3 alkali activating agents appeared to have little influence on NO removal from the flue gases. The results suggest problematic waste tyres, have the potential to be converted to activated carbons with NOx removal efficiency comparable with conventionally produced carbons. PMID:26856444

  15. Parallel Activation in Bilingual Phonological Processing

    ERIC Educational Resources Information Center

    Lee, Su-Yeon

    2011-01-01

    In bilingual language processing, the parallel activation hypothesis suggests that bilinguals activate their two languages simultaneously during language processing. Support for the parallel activation mainly comes from studies of lexical (word-form) processing, with relatively less attention to phonological (sound) processing. According to

  16. CYANIDE REMOVAL FROM REFINERY WASTEWATER USING POWDERED ACTIVATED CARBON

    EPA Science Inventory

    The objective of this project was to evaluate the removal of low level cyanide in petroleum refinery wastewater by the addition of powdered activated carbon and cupric chloride to an activated sludge unit. The activated carbon and cupric chloride act as a catalyst in the oxidatio...

  17. The reversibility of adsorption of gold cyanide on activated carbon

    NASA Astrophysics Data System (ADS)

    van Deventer, J. S. J.; van der Merwe, P. F.

    1993-06-01

    Much controversy exists about the mechanism by which gold cyanide adsorbs on activated carbon. It is not the purpose of this article to explain the exact adsorption mechanism but, rather, to investigate the factors affecting the reversibility of adsorbed gold cyanide. Whereas Au(CN){2/-} is soluble in water, AuCN and Au require the addition of cyanide to form Au(CN){2/-}. The reversibility of the adsorption of gold onto carbon is a function of the nature of the adsorbed gold and determines the need for cyanide in the elution process, which affects the operating costs of a carbon-in-pulp (CIP) plant. The fraction of adsorbed Au(CN){2/-} that will be decomposed to AuCN was found to be a function of the pH and temperature of the solution and the type of activated carbon used. It was observed that two different batches of carbon from the same manufacturer yielded widely different ratios of AuCN to Au(CN){2/-}, although their specifications did not differ much. These results were confirmed by Fourier transform infrared spectroscopy (FTIR) and X-ray photoelectron spectroscopy (XPS). A combination of low pH and high temperature, as is found in the hot acid wash step of an AARL elution, leads to the reduction of both Au(1) species to metallic gold, Au(0). The fraction of the adsorbed Au(CN){2/-} that is converted to AuCN or Au(0) no longer participates in the equilibrium between Au(CN){2/-} in solution and Au(CN){2/-} in the adsorbed phase. It was observed that the isotherm for desorption is higher than the isotherm for adsorption by a percentage which is, on average, equal to the percentage of Au(CN){2/-} converted to AuCN or Au(0).

  18. Detection of single ion channel activity with carbon nanotubes

    NASA Astrophysics Data System (ADS)

    Zhou, Weiwei; Wang, Yung Yu; Lim, Tae-Sun; Pham, Ted; Jain, Dheeraj; Burke, Peter J.

    2015-03-01

    Many processes in life are based on ion currents and membrane voltages controlled by a sophisticated and diverse family of membrane proteins (ion channels), which are comparable in size to the most advanced nanoelectronic components currently under development. Here we demonstrate an electrical assay of individual ion channel activity by measuring the dynamic opening and closing of the ion channel nanopores using single-walled carbon nanotubes (SWNTs). Two canonical dynamic ion channels (gramicidin A (gA) and alamethicin) and one static biological nanopore (?-hemolysin (?-HL)) were successfully incorporated into supported lipid bilayers (SLBs, an artificial cell membrane), which in turn were interfaced to the carbon nanotubes through a variety of polymer-cushion surface functionalization schemes. The ion channel current directly charges the quantum capacitance of a single nanotube in a network of purified semiconducting nanotubes. This work forms the foundation for a scalable, massively parallel architecture of 1d nanoelectronic devices interrogating electrophysiology at the single ion channel level.

  19. Phenol adsorption by activated carbon produced from spent coffee grounds.

    PubMed

    Castro, Cnthia S; Abreu, Anelise L; Silva, Carmen L T; Guerreiro, Mrio C

    2011-01-01

    The present work highlights the preparation of activated carbons (ACs) using spent coffee grounds, an agricultural residue, as carbon precursor and two different activating agents: water vapor (ACW) and K(2)CO(3) (ACK). These ACs presented the microporous nature and high surface area (620-950 m(2) g(-1)). The carbons, as well as a commercial activated carbon (CAC) used as reference, were evaluated as phenol adsorbent showing high adsorption capacity (?150 mg g(-1)). The investigation of the pH solution in the phenol adsorption was also performed. The different activating agents led to AC with distinct morphological properties, surface area and chemical composition, although similar phenol adsorption capacity was verified for both prepared carbons. The production of activated carbons from spent coffee grounds resulted in promising adsorbents for phenol removal while giving a noble destination to the residue. PMID:22105129

  20. Production of activated carbon from a new precursor: Molasses

    NASA Astrophysics Data System (ADS)

    Legrouri, K.; Ezzine, M.; Ichcho, S.; Hannache, H.; Denoyel, R.; Pailler, R.; Naslain, R.

    2005-03-01

    Activated carbon has been prepared from molasses, a natural precursor of vegetable origin resulting from the sugar industry in Morocco. The preparation of the activated carbon from the molasses has been carried out by impregnation of the precursor with sulfuric acid, followed by carbonization. The adsorption capacity, the BET surface area, and the pore volume of the activated carbon were determined. The micropore volume was assessed by Dubinin- Radushkevich (DR) equation. The activated materials are mainly microporous and show the type I isotherm of the Brunauer classification for nitrogen adsorption. The activation in steam yielded a carbon that contains both micropores and supermicropores. Analysis of the nitrogen isotherm by BET and DR methods established that most of obtained carbons are highly microporous, with high surface areas (? 1200 m2/g) and very low mesoporosity.

  1. Characterization of activated carbon prepared from chlorella-based algal residue.

    PubMed

    Chang, Yuan-Ming; Tsai, Wen-Tien; Li, Ming-Hsuan

    2015-05-01

    The chlorella-based microalgal residue (AR) was tested as a novel precursor for preparing activated carbons. A combined carbonization-activation process with flowing N2 and CO2 gases was used to prepare the carbon materials at the activation temperatures of 800-1000 C and the residence times of 0-30 min in this work. The elemental contents, pore properties and scanning electron microscopy (SEM) observations of the resulting activated carbons have been performed. The results showed that activation temperature may be the most important parameter for determining their pore properties. The maximal Brunauer-Emmett-Teller (BET) surface area and total pore volume of the resulting activated carbon, which was produced at the activation temperature of 950 C with the residence time of 30 min, were 840 m(2)/g and 0.46 cm(3)/g, respectively. More interestingly, the resulting activated carbons have significant nitrogen contents of 3.6-9.6 wt%, which make them lower carbon contents (i.e., 54.6-68.4 wt%) than those of commercial activated carbons. PMID:25451779

  2. Micro-scale investigation of carbonation process in partially serpentinized peridotites

    NASA Astrophysics Data System (ADS)

    Andreani, M.; Menez, B.; Delacour, A.; Pasini, V.; Auzende, A. L.; Brunelli, D.

    2012-04-01

    The carbonation of ultramafic rocks is, theoretically, the most efficient reaction to trap CO2 irreversibly in the form of solid carbonates, as predicted by equilibrium thermodynamic calculations. However, the success of industrial or natural carbonation in large ultramafic aquifers or oceanic ultramafic exposures does not only rely on the thermodynamic conditions of chemical reactions, but also on their feedback effects on the reactive surface area and on the local porosity and permeability. In addition, side processes like serpentinization, redox reactions, abiotic catalytic effects, and biological activity, can be expected in such complex natural system. Their occurrence and implications on carbon speciation and carbon transfers during hydrothermal alteration of oceanic peridotites have not been explored yet and requires detailed study of natural and/or experimental carbonation zones. We have combined petrographic and electron microscopy with SIMS, Raman and FTIR microspectroscopy on partially serpentinized peridotites drilled during the IODP leg 304 (30N, MAR) in order to characterize the mechanisms of peridotite carbonation at the fluid-mineral interface and identify the associated speciation of carbon (inorganic and organic carbon occurrences). We present first results on zones located close to talc-tremolite sheared veins in holes 1309B and D. Associations of carbonates, porous phyllosilicates and oxides are observed in close vicinity of relict olivines that underwent a previous stage of serpentinization. The olivine-carbonate interface is nanoporous which facilitates mass transfer between fluid and mineral. The phyllosilicate identified as saponite results from the metasomatic replacement, during the carbonation stage, of previously formed serpentine. These observations do not favour reaction-induced cracking but rather a transfer-controlled process in an open system. Among the submicrometric dark clusters widely-distributed in saponite and in serpentine, vibrational microspectroscopy reveals the presence of various types of organic compounds that tend to be located close to micrometric sulphides grains. Those results underline the microscale variability of carbon speciation within hydrothermally altered peridotites. The association of reduced carbon phases with the carbonation texture suggests that CO2 conversion may not be limited to solid carbonate formation in natural systems and that biological activity and/or abiotic CO2 reduction, possibly catalyzed by Ni-rich sulphides, can occur contemporaneously. This complex association of reactions has to be unravelled further to determine the respective contribution of abiotic versus biological processes and integrate them in carbon transfers modelling through the oceanic lithosphere.

  3. Fabrication and processing of high-strength densely packed carbon nanotube yarns without solution processes.

    PubMed

    Liu, Kai; Zhu, Feng; Liu, Liang; Sun, Yinghui; Fan, Shoushan; Jiang, Kaili

    2012-06-01

    Defects of carbon nanotubes, weak tube-tube interactions, and weak carbon nanotube joints are bottlenecks for obtaining high-strength carbon nanotube yarns. Some solution processes are usually required to overcome these drawbacks. Here we fabricate ultra-long and densely packed pure carbon nanotube yarns by a two-rotator twisting setup with the aid of some tensioning rods. The densely packed structure enhances the tube-tube interactions, thus making high tensile strengths of carbon nanotube yarns up to 1.6 GPa. We further use a sweeping laser to thermally treat as-produced yarns for recovering defects of carbon nanotubes and possibly welding carbon nanotube joints, which improves their Young's modulus by up to ?70%. The spinning and laser sweeping processes are solution-free and capable of being assembled together to produce high-strength yarns continuously as desired. PMID:22538869

  4. Development of carbon free diffusion layer for activated carbon air cathode of microbial fuel cells.

    PubMed

    Yang, Wulin; Kim, Kyoung-Yeol; Logan, Bruce E

    2015-12-01

    The fabrication of activated carbon air cathodes for larger-scale microbial fuel cells requires a diffusion layer (DL) that is highly resistant to water leakage, oxygen permeable, and made using inexpensive materials. A hydrophobic polyvinylidene fluoride (PVDF) membrane synthesized using a simple phase inversion process was examined as a low cost ($0.9/m(2)), carbon-free DL that prevented water leakage at high pressure heads compared to a polytetrafluoroethylene/carbon black DL ($11/m(2)). The power density produced with a PVDF (20%, w/v) DL membrane of 1400±7mW/m(2) was similar to that obtained using a wipe DL [cloth coated with poly(dimethylsiloxane)]. Water head tolerance reached 1.9m (∼19kPa) with no mesh supporter, and 2.1m (∼21kPa, maximum testing pressure) with a mesh supporter, compared to 0.2±0.05m for the wipe DL. The elimination of carbon black from the DL greatly simplified the fabrication procedure and further reduced overall cathode costs. PMID:26342345

  5. Metal doped carbon nanoneedles and effect of carbon organization with activity for hydrogen evolution reaction (HER).

    PubMed

    Araujo, Rafael A; Rubira, Adley F; Asefa, Tewodros; Silva, Rafael

    2016-02-10

    Cellulose nanowhiskers (CNW) from cotton, was prepared by acid hydrolysis and purified using a size selection process to obtain homogeneous samples with average particle size of 270nm and 85.5% crystallinity. Purified CNW was used as precursor to carbon nanoneedles (CNN) synthesis. The synthesis of CNN loaded with different metals dopants were carried out by a nanoreactor method and the obtained CNNs applied as electrocatalysts for hydrogen evolution reaction (HER). In the carbon nanoneedles synthesis, Ni, Cu, or Fe worked as graphitization catalyst and the metal were found present as dopants in the final material. The used metal appeared to have direct influence on the degree of organization of the particles and also in the surface density of polar groups. It was evaluated the influence of the graphitic organization on the general properties and nickel was found as the more appropriate metal since it leads to a more organized material and also to a high activity toward HER. PMID:26686184

  6. Rhodamine B removal with activated carbons obtained from lignocellulosic waste.

    PubMed

    da Silva Lacerda, Viviane; Lpez-Sotelo, Juan B; Correa-Guimares, Adriana; Hernndez-Navarro, Salvador; Snchez-Bscones, Mercedes; Navas-Gracia, Luis M; Martn-Ramos, Pablo; Martn-Gil, Jess

    2015-05-15

    By-products from the wax production process from carnauba palm (leaves), from the extraction of oil from macauba seeds (endocarp) and from pine nut production (shell) have been assessed for activated carbon production, using H3PO4 or CaCl2 for their chemical activation. The resulting activated charcoals have been thoroughly characterized by elemental and thermal analysis, X-ray diffraction, infrared spectroscopy, electron scanning microscopy and N2 adsorption behavior. Subsequently, their adsorption capacity for the removal of rhodamine B (RhB) from aqueous solutions has been evaluated by studying different parameters: contact time, pH, adsorbent dose, initial dye concentration and solution temperature. The adsorption of RhB followed Freundlich's model in all cases. Kinetic studies indicate that the pseudo-second order model can be used for describing the dynamics of the adsorption process. Thermodynamic parameters have also been evaluated, indicating its endothermic and spontaneous nature. Finally, a preliminary analysis of the impact of cellulose content in the carbon precursor materials has been conducted, by using a mixture of native cellulose with one of the lignocellulosic materials. PMID:25770964

  7. Synthesis of fluorescent carbon nanoparticles directly from active carbon via a one-step ultrasonic treatment

    SciTech Connect

    Li, Haitao; He, Xiaodie; Liu, Yang; Department of Chemistry, Northeast Normal University, Changchun 130024 ; Yu, Hang; Kang, Zhenhui; Department of Chemistry, Northeast Normal University, Changchun 130024 ; Lee, Shuit-Tong

    2011-01-15

    Water-soluble fluorescent carbon nanoparticles were synthesized directly from active carbon by a one-step hydrogen peroxide-assisted ultrasonic treatment. The carbon nanoparticles were characterized by transmission electron microscopy, optical fluorescent microscopy, fluorescent spectroscopy, Fourier transform infrared spectroscopy and ultraviolet-visible spectrophotometer. The results showed that the surface of carbon nanoparticles was rich of hydroxyl groups resulting in high hydrophilicity. The carbon nanoparticles could emit bright and colorful photoluminescence covering the entire visible-to-near infrared spectral range. Furthermore, these carbon nanoparticles also had excellent up-conversion fluorescent properties.

  8. Low Speed Carbon Deposition Process for Hermetic Optical Fibers

    SciTech Connect

    ABRAMCZYK,JAROSLAW; ARTHUR,SARA E. TALLANT,DAVID R.; HIKANSSON,ADAM S.; LINDHOLM,ERIC A.; LO,JIE

    1999-09-29

    For optical fibers used in adverse environments, a carbon coating is frequently deposited on the fiber surface to prevent water and hydrogen ingression that lead respectively to strength degradation through fatigue and hydrogen-induced attenuation. The deposition of a hermetic carbon coating onto an optical fiber during the draw process holds a particular challenge when thermally-cured specialty coatings are subsequently applied because of the slower drawing rate. In this paper, we report on our efforts to improve the low-speed carbon deposition process by altering the composition and concentration of hydrocarbon precursor gases. The resulting carbon layers have been analyzed for electrical resistance, Raman spectra, coating thickness, and surface roughness, then compared to strength data and dynamic fatigue behavior.

  9. Spectral Analysis of Laser Processing of Carbon Fiber Reinforced Plastics

    NASA Astrophysics Data System (ADS)

    Jarwitz, M.; Onuseit, V.; Weber, R.; Graf, T.

    Spectra of the optical process emissions of carbon fiber reinforced plastics (CFRP) processing with a continuous wave (cw) thin disk laser are recorded for a basic characterization of the ablation process. The observed line spectra show a characteristic spectral line at a wavelength of 588.95 nm that is found to be atomic sodium (Na I). No spectral lines of atomic or ionized carbon appear in the recorded spectra leading to the conclusion that only a small fraction of C-atoms is ionized.

  10. Carbon Nanotube Bonding Strength Enhancement Using Metal "Wicking" Process

    NASA Technical Reports Server (NTRS)

    Lamb, James L.; Dickie, Matthew R.; Kowalczyk, Robert S.; Liao, Anna; Bronikowski, Michael J.

    2012-01-01

    Carbon nanotubes grown from a surface typically have poor bonding strength at the interface. A process has been developed for adding a metal coat to the surface of carbon nano tubes (CNTs) through a wicking process, which could lead to an enhanced bonding strength at the interface. This process involves merging CNTs with indium as a bump-bonding enhancement. Classical capillary theory would not normally allow materials that do not wet carbon or graphite to be drawn into the spacings by capillary action because the contact angle is greater than 90 degrees. However, capillary action can be induced through JPL's ability to fabricate oriented CNT bundles to desired spacings, and through the use of deposition techniques and temperature to control the size and mobility of the liquid metal streams and associated reservoirs. A reflow and plasma cleaning process has also been developed and demonstrated to remove indium oxide, and to obtain smooth coatings on the CNT bundles.

  11. Activated Carbon Modified with Copper for Adsorption of Propanethiol

    PubMed Central

    Moreno-Pirajn, Juan Carlos; Tirano, Joaqun; Salamanca, Brisa; Giraldo, Liliana

    2010-01-01

    Activated carbons were characterized texturally and chemically before and after treatment, using surface area determination in the BET model, Boehm titration, TPR, DRX and immersion calorimetry. The adsorption capacity and the kinetics of sulphur compound removal were determined by gas chromatography. It was established that the propanethiol retention capacity is dependent on the number of oxygenated groups generated on the activated carbon surface and that activated carbon modified with CuO at 0.25 M shows the highest retention of propanethiol. Additionally is proposed a mechanism of decomposition of propenothiol with carbon-copper system. PMID:20479992

  12. Process for the production of carbon fibres from petroleum pitch

    SciTech Connect

    Fug, G.

    1984-02-14

    A method of producing carbon or graphite fibres from a pitch obtained from a steam cracking residue of a petroleum fraction which pitch has a b resin content of from 2 to 40% by weight, comprises spinning the pitch into fibres at a temperature higher than the softening point, the fibres being treated to render them infusible and then subjecting the fibres to carbonization by heating, followed by graphitization if desired, characterized in that the treatment to infusibilize the fibres is controlled such that the resin content of the fibres does not exceed 30% by weight. The invention includes carbon and graphite fibres produced by the process.

  13. Activated carbon/enhanced biological treatment of a complex groundwater

    SciTech Connect

    Pugh, L.B.; Rediske, R.R.; Rogers, D.R.; Peden, D.H.

    1996-12-31

    Impacted groundwater at the Ott/Story/Cordova Superfund site near Muskegon, Michigan contains a complex mixture of organic compounds and nitrogen. The remediation plan for the site calls for extraction and treatment of 4,600 cubic meters per day of groundwater, estimated to contain 1,500 mg/L of chemical oxygen demand (COD) and 80 mg/L of ammonia-nitrogen. Approximately 30% of the COD is comprised of a mixture of 50 Appendix IX compounds, including halogenated and aromatic orcanics. The remaining COD is contributed by an unidentified group of process intermediates and degradation products related to historical production at this former chemical production facility. The objectives for discharge of the treated Groundwater to a local surface water body included removal of known organic compounds and ammonia-nitrogen, as well as numerous unidentified compounds in the site groundwater. The purpose of this work was to evaluate the effectiveness of two activated carbon-enhanced biological treatment systems: granular activated Carbon/fluidized bed (GAC/FB) and powdered activated carbon treatment (PACT{reg_sign}) for achieving the expected standards for surface water discharge. GAC/FB and PACT were initially evaluated using laboratory-scale reactors. The GAC/FB reactor achieved consistent, high removals of all organic compounds; however, consistent nitrification could not be maintained. The two-stage PACT system achieved nearly complete removal of all organic compounds and ammonia. A 9.5-L/minute pilot system was subsequently operated at the site to provide additional performance information for the two-stage PACT process. Three of the most highly impacted site wells were used to supply groundwater to the pilot system. Excellent removal of all known and unknown organic compounds, and nearly complete nitrification was consistently achieved. As a result of the on-site pilot study, a two-stage PACT system is being implemented at the site.

  14. Process for derivatizing carbon nanotubes with diazonium species

    NASA Technical Reports Server (NTRS)

    Tour, James M. (Inventor); Bahr, Jeffrey L. (Inventor); Yang, Jiping (Inventor)

    2007-01-01

    The invention incorporates new processes for the chemical modification of carbon nanotubes. Such processes involve the derivatization of multi- and single-wall carbon nanotubes, including small diameter (ca. 0.7 nm) single-wall carbon nanotubes, with diazonium species. The method allows the chemical attachment of a variety of organic compounds to the side and ends of carbon nanotubes. These chemically modified nanotubes have applications in polymer composite materials, molecular electronic applications and sensor devices. The methods of derivatization include electrochemical induced reactions thermally induced reactions (via in-situ generation of diazonium compounds or pre-formed diazonium compounds), and photochemically induced reactions. The derivatization causes significant changes in the spectroscopic properties of the nanotubes. The estimated degree of functionality is ca. 1 out of every 20 to 30 carbons in a nanotube bearing a functionality moiety. Such electrochemical reduction processes can be adapted to apply site-selective chemical functionalization of nanotubes. Moreover, when modified with suitable chemical groups, the derivatized nanotubes are chemically compatible with a polymer matrix, allowing transfer of the properties of the nanotubes (such as, mechanical strength or electrical conductivity) to the properties of the composite material as a whole. Furthermore, when modified with suitable chemical groups, the groups can be polymerized to form a polymer that includes carbon nanotubes ##STR00001##.

  15. [Flue gas desulfurization by a novel biomass activated carbon].

    PubMed

    Liu, Jie-Ling; Tang, Zheng-Guang; Chen, Jie; Jiang, Wen-Ju; Jiang, Xia

    2013-04-01

    A novel biomass columnar activated carbon was prepared from walnut shell and pyrolusite was added as a catalyst. The activated carbon prepared was used for flue gas desulphurization in a fixed-bed reactor with 16 g of activated carbon. The impact of operating parameters such as SO2 inlet concentration, space velocity, bed temperature, moisture content and O2 concentration on the desulfurization efficiency of activated carbon was investigated. The results showed that both the breakthrough sulfur capacity and breakthrough time of activated carbon decreased with the increase of SO2 inlet concentration within the range of 0.1% -0.3%. The breakthrough sulfur capacity deceased with the increase of space velocity, with optimal space velocity of 600 h(-1). The optimal bed temperature was 80 degrees C, and the desulfurization efficiency can be reduced if the temperature continue to increase. The presence of moisture and oxygen greatly promoted the adsorption of SO2 onto the activated carbon. The best moisture content was 10%. When the oxygen concentrations were between 10% and 13%, the desulfurization performance of activated carbon was the highest. Under the optimal operating conditions, the sulfur capacity of activated carbon was 252 mg x g(-1), and the breakthrough time was up to 26 h when the SO2 inlet concentration was 0.2%. PMID:23798152

  16. A Magnesium-Activated Carbon Hybrid Capacitor

    SciTech Connect

    Yoo, HD; Shterenberg, I; Gofer, Y; Doe, RE; Fischer, CC; Ceder, G; Aurbach, D

    2013-12-11

    Prototype cells of hybrid capacitor were developed, comprising activated carbon (AC) cloth and magnesium (Mg) foil as the positive and negative electrodes, respectively. The electrolyte solution included ether solvent (TBF) and a magnesium organo-halo-aluminate complex 0.25 M Mg2Cl3+-Ph2AlCl2-. In this solution Mg can be deposited/dissolved reversibly for thousands of cycles with high reversibility (100% cycling efficiency). The main barrier for integrating porous AC electrodes with this electrolyte solution was the saturation of the pores with the large ions in the AC prior to reaching the potential limit. This is due to the existence of bulky Mg and Al based ionic complexes consisting Cl, alkyl or aryl (R), and THF ligands. This problem was resolved by adding 0.5 M of lithium chloride (LiCl), thus introducing smaller ionic species to the solution. This Mg hybrid capacitor system demonstrated a stable cycle performance for many thousands of cycles with a specific capacitance of 90 Fg(-1) for the AC positive electrodes along a potential range of 2.4 V. (C) 2014 The Electrochemical Society. All rights reserved.

  17. [Study on adsorption properties of organic vapor on activated carbons].

    PubMed

    Cai, Dao-Fei; Huang, Wei-Qiu; Wang, Dan-Li; Zhang, Lin; Yang, Guang

    2013-12-01

    Adsorption technology is widely used in oil vapor recovery, and adsorbents have decisive effect on separation. Three kinds of activated carbon (AC) were chosen to study their adsorption properties and adsorption energy, where n-hexane and n-heptane acted as adsorbate and adsorption experiments were conducted at 293.15 K. At the same time, regression formula of Logistic model was used to fit the throughout curves of active carbons. The results showed that: surface area and pore volume of activated carbon were the main factors affecting its adsorption properties; the adsorption behavior of n-hexane and n-heptane were corresponding to Langmuir adsorption isotherm model; adsorption energy of these three kinds of activated carbon became greater with increasing specific surface area. Fitting curve of Logistic model had high similarity with the experimental results, which could be used in the prediction of breakthrough curves of activated carbons. PMID:24640910

  18. Ozone Removal by Filters Containing Activated Carbon: A Pilot Study

    SciTech Connect

    Fisk, William; Spears, Mike; Sullivan, Douglas; Mendell, Mark

    2009-09-01

    This study evaluated the ozone removal performance of moderate-cost particle filters containing activated carbon when installed in a commercial building heating, ventilating, and air conditioning (HVAC) system. Filters containing 300 g of activated carbon per 0.09 m2 of filter face area were installed in two 'experimental' filter banks within an office building located in Sacramento, CA. The ozone removal performance of the filters was assessed through periodic measurements of ozone concentrations in the air upstream and downstream of the filters. Ozone concentrations were also measured upstream and downstream of a 'reference' filter bank containing filters without any activated carbon. The filter banks with prefilters containing activated carbon were removing 60percent to 70percent of the ozone 67 and 81 days after filter installation. In contrast, there was negligible ozone removal by the reference filter bank without activated carbon.

  19. Bromate removal from water by polypyrrole tailored activated carbon.

    PubMed

    Hong, Siqi; Deng, Shubo; Yao, Xiaolong; Wang, Bin; Wang, Yujue; Huang, Jun; Yu, Gang

    2016-04-01

    Bromate adsorption behavior and mechanism were examined on a novel adsorbent devised via depositing polypyrrole (Ppy) into the pores of nut shell-based activated carbon (NAC). This Ppy-tailored activated carbon (Ppy-NAC) hosted positively charged polypyrrole functionality that offered considerable sorption capacity for bromate. Specifically, the Ppy-NAC achieved a bromate loading of 62.5mg/g in the adsorption isotherm, 8.3 times higher than the pristine NAC. The adsorption isotherm data were fitted well by the Langmuir model, and the adsorption kinetics were described well by the pseudo-second-order equation. The occurrence of chloride ions in solution showed that Cl(-) exchanged with BrO3(-) during the adsorption process. The X-ray photoelectron spectroscopy (XPS) analysis and the detection of bromide in solution indicated that some of BrO3(-) were reduced to Br(-), and the produced bromide ions were released to the solution and adsorbed on the Ppy-NAC. The increase of oxygen-containing functional groups on Ppy-NAC after adsorption verified that the redox reaction occurred during the adsorption process. The mechanisms of bromate removal by the Ppy-NAC included ion exchange and reduction reaction of bromate on the Ppy-NAC surfaces. PMID:26771750

  20. Characterisation under static and dynamic conditions of commercial activated carbons for their use in wastewater plants

    NASA Astrophysics Data System (ADS)

    Sabio, E.; Zamora, F.; Gonzlez, J. F.; Garca, C. M. Gonzlez; Romn, S.; Al-Kassir, A.

    2006-06-01

    The use of activated carbon for removing organic contaminants in fixed beds is increasing. This is a dynamic process in which the kinetics plays an important role. The aim of this paper is to get more insight into adsorption of p-nitrophenol (PNP) in activated carbon under equilibrium and dynamic conditions. Five commercial activated carbons were studied. The analysis carried out were PNP adsorption isotherms in aqueous solution at 20 C, N 2 at 77 K isotherms, FT-IR and PNP adsorption under dynamic conditions. The results indicate that the external porous affinity toward the organic contaminants determines in large extent the adsorbents behaviour under dynamic conditions.

  1. Reduction of iron(III) ion by activated carbon fiber

    SciTech Connect

    Uchida, M.; Shinohara, O.; Ito, S.; Kawasaki, N.; Nakamura, T.; Tanada, S.

    2000-04-15

    The mechanisms of adsorption of iron(II) ion, iron(III) ion, and reduced iron(III) ion onto an activated carbon fiber and the ability of carbon fibers to reduce iron(III) ion were investigated on the basis of the amounts of iron ion adsorbed. The amount of iron(II) ion adsorbed onto the activated carbon fiber increased with increasing adsorption temperature. Iron(II) ion was more easily removed by the activated carbon fiber than iron(III) ion. Iron(III) ion was adsorbed onto the activated carbon fiber after being reduced to iron(II) ion. The reduction ability of A-20 was stronger than that of A-10 because the hydrophilic groups of A-20 were larger than those of A-10. It is concluded that the activated carbon fiber has a reduction effect on iron(III) ion and that the reduction effect of the activated carbon fiber depended on the number of hydrophilic groups on the activated carbon fiber.

  2. Fractal analysis of granular activated carbons using isotherm data

    SciTech Connect

    Khalili, N.R.; Pan, M.; Sandi, G.

    1997-08-01

    Utilization of adsorption on solid surfaces was exercised for the first time in 1785. Practical application of unactivated carbon filters, and powdered carbon were first demonstrated in the American water treatment plant, and a municipal treatment plant in New Jersey, in 1883 and 1930, respectively. The use of activated carbon became widespread in the next few decades. At present, adsorption on carbons has a wide spread application in water treatment and removal of taste, odor, removal of synthetic organic chemicals, color-forming organics, and desinfection by-products and their naturally occurring precursors. This paper presents an analysis of the surface fractal dimension and adsorption capacity of a group of carbons.

  3. Low density microcellular carbon or catalytically impregnated carbon foams and process for their preparation

    DOEpatents

    Hooper, R.W.; Pekala, R.W.

    1987-04-30

    Machinable and structurally stable, low density microcellular carbon, and catalytically impregnated carbon, foams, and process for their preparation, are provided. Pulverized sodium chloride is classified to improve particle size uniformity, and the classified particles may be further mixed with a catalyst material. The particles are cold pressed into a compact having internal pores, and then sintered. The sintered compact is immersed and then submerged in a phenolic polymer solution to uniformly fill the pores of the compact with phenolic polymer. The compact is then heated to pyrolyze the phenolic polymer into carbon in the form of a foam. Then the sodium chloride of the compact is leached away with water, and the remaining product is freeze dried to provide the carbon, or catalytically impregnated carbon, foam.

  4. Low density microcellular carbon or catalytically impregnated carbon foams and process for their prepartion

    DOEpatents

    Hopper, Robert W. (Danville, CA); Pekala, Richard W. (Pleasant Hill, CA)

    1988-01-01

    Machinable and structurally stable, low density microcellular carbon, and catalytically impregnated carbon, foams, and process for their preparation, are provided. Pulverized sodium chloride is classified to improve particle size uniformity, and the classified particles may be further mixed with a catalyst material. The particles are cold pressed into a compact having internal pores, and then sintered. The sintered compact is immersed and then submerged in a phenolic polymer solution to uniformly fill the pores of the compact with phenolic polymer. The compact is then heated to pyrolyze the phenolic polymer into carbon in the form of a foam. Then the sodium chloride of the compact is leached away with water, and the remaining product is freeze dried to provide the carbon, or catalytically impregnated carbon, foam.

  5. Low density microcellular carbon or catalytically impregnated carbon forms and process for their preparation

    DOEpatents

    Hopper, Robert W. (Danville, CA); Pekala, Richard W. (Pleasant Hill, CA)

    1989-01-01

    Machinable and structurally stable, low density microcellular carbon, and catalytically impregnated carbon, foams, and process for their preparation, are provided. Pulverized sodium chloride is classified to improve particle size uniformity, and the classified particles may be further mixed with a catalyst material. The particles are cold pressed into a compact having internal pores, and then sintered. The sintered compact is immersed and then submerged in a phenolic polymer solution to uniformly fill the pores of the compact with phenolic polymer. The compact is then heated to pyrolyze the phenolic polymer into carbon in the form of a foam. Then the sodium chloride of the compact is leached away with water, and the remaining product is freeze dried to provide the carbon, or catalytically impregnated carbon, foam.

  6. Optimization of production conditions for activated carbons from Tamarind wood by zinc chloride using response surface methodology.

    PubMed

    Sahu, J N; Acharya, Jyotikusum; Meikap, B C

    2010-03-01

    The low-cost activated carbon was prepared from Tamarind wood an agricultural waste material, by chemical activation with zinc chloride. Activated carbon adsorption is an effective means for reducing organic chemicals, chlorine, heavy metals and unpleasant tastes and odours in effluent or colored substances from gas or liquid streams. Central composite design (CCD) was applied to study the influence of activation temperature, chemical ratio of zinc chloride to Tamarind wood and activation time on the chemical activation process of Tamarind wood. Two quadratic models were developed for yield of activated carbon and adsorption of malachite green oxalate using Design-Expert software. The models were used to calculate the optimum operating conditions for production of activated carbon providing a compromise between yield and adsorption of the process. The yield (45.26 wt.%) and adsorption (99.9%) of the activated carbon produced at these operating conditions showed an excellent agreement with the amounts predicted by the models. PMID:19913410

  7. Carbonation of residual brines produced by ammonia-soda process

    NASA Astrophysics Data System (ADS)

    Filippova, I. V.; Piriou, P.; Filippov, L. O.; Yvon, J.; Grandjean, M.

    2013-03-01

    This work deals with the carbonation of residual brines produced during the manufacture of soda ash to avoid the unsuitable phase transformation during the land storage. The study resulted in a demonstration pilot, which showed the feasibility of such an approach and the possibility of his extension to an industrial scale. Carbonation of the residual brines is a promising process as it entirely transforms Ca(OH)2, "CaOHCl" and CSH into calcite, avoids the further phase evolution, allows to obtain a neutral pH which considerably reduce the land storage impact on environment and shorten by around 10 % the global CO2 emission of the ammonia-soda process.

  8. Iron-carbon compacts and process for making them

    SciTech Connect

    Sheinberg, H.

    2000-07-25

    The present invention includes iron-carbon compacts and a process for making them. The process includes preparing a slurry comprising iron powder, furfuryl alcohol, and a polymerization catalyst for initiating the polymerization of the furfuryl alcohol into a resin, and heating the slurry to convert the alcohol into the resin. The resulting mixture is pressed into a green body and heated to form the iron-carbon compact. The compact can be used as, or machined into, a magnetic flux concentrator for an induction heating apparatus.

  9. Iron-carbon compacts and process for making them

    SciTech Connect

    Sheinberg, Haskell

    2000-01-01

    The present invention includes iron-carbon compacts and a process for making them. The process includes preparing a slurry comprising iron powder, furfuryl alcohol, and a polymerization catalyst for initiating the polymerization of the furfuryl alcohol into a resin, and heating the slurry to convert the alcohol into the resin. The resulting mixture is pressed into a green body and heated to form the iron-carbon compact. The compact can be used as, or machined into, a magnetic flux concentrator for an induction heating apparatus.

  10. Method for reducing carbon formation in a thermal cracking process

    SciTech Connect

    Kukes, S.; Harris, J.R.; Porter, R.A.; Reed, L.E.

    1983-10-18

    The formation of carbon on metals exposed to hydrocarbons in a thermal cracking process is reduced by contacting such metals with a halogen containing silicon compound selected from the group consisting of halogen containing silanes, halogen containing disilanes, and halogen containing siloxanes. After the metals are contacted with the halogen containing silicon compound, the halogen containing silicon compound is converted to silicon dioxide to form a protective coating on the metals. This protective coating substantially reduces the formation of carbon on metals exposed to hydrocarbons in a thermal cracking process.

  11. Ozonation of naphthalenesulphonic acid in the aqueous phase in the presence of basic activated carbons.

    PubMed

    Rivera-Utrilla, J; Snchez-Polo, M

    2004-10-12

    The present study aimed to explore the possibility of increasing the purification efficacy of ozone in the removal of high-toxicity contaminants by using carbons of basic character and to analyze the mechanism involved in this process. These carbons were prepared by treating a commercial activated carbon (Witco, W) with ammonia (W-A), ammonium carbonate (W-C), or urea (W-U), under high pressure and temperature. The ammonia and carbonate treatments slightly increased the mesoporosity and, to a greater degree, the macroporosity of carbon W, whereas the urea treatment produced an increase in the porosity across the whole range of pore sizes. In addition, treatment of the activated carbon with these nitrogenating agents produced a marked change in the chemical nature of its surface. Thus, according to the pH of the point of zero charge (pHPZC) values obtained for each sample, carbon W was neutral (pHPZC = 7.12), but the treated carbons were basic, especially carbon W-U (pHPZC = 8.85). This basicity results from an increased concentration of basic oxygenated and nitrogenated surface functional groups, as confirmed by the results of elemental and XPS analyses. An increase in the degradation of 1,3,6-naphthalenetrisulfonic acid was observed when the activated carbon samples were added to the system. This degradation was especially enhanced in the presence of carbon W-U. The increased NTS degradation rate in the presence of the activated carbon is due to an increased concentration of highly reactive radicals in the system. When the catalytic activity of the activated carbon samples was related to their chemical and textural characteristics, it was found that: (i) The catalytic activity increased with an increase in the surface basicity. Interestingly, in the sample with greatest catalytic activity in NTS ozonation, carbon W-U, most of the nitrogenated surface groups introduced were pyrrol groups. These groups increase the electronic density of the basal plane of the activated carbon, thereby enhancing the reduction of ozone on the surface and the generation of highly reactive radicals in the system. (ii) The greater catalytic activity of carbon W-U may also be partly related to its greater surface area and higher volume of mesopores and macropores; these large pores facilitate access of the ozone to the surface active centers of the carbon, increasing its catalytic activity. The presence of the activated carbon samples during NTS ozonation also favored the removal of total organic carbon present in the solution, due to (a) transformation of organic matter into CO2 through the generation of highly reactive species catalyzed by the presence of the activated carbons (catalytic contribution) and (b) adsorption of NTS oxidation byproducts on the activated carbon (adsorptive contribution). The results obtained show that activated carbons treated with nitrogenating agents are very promising catalysts for application in the ozonation of aromatic compounds. PMID:15461509

  12. Morphology and formation process of diamond from glassy carbon

    NASA Astrophysics Data System (ADS)

    Miyamoto, Manabu; Akaishi, Minoru; Ohsawa, Toshikazu; Yamaoka, Shinobu; Fukunaga, Osamu

    1989-10-01

    Under static high pressure conditions in the presence of a catalyst metal, a diamond formation process was studied using glassy carbon as a starting source, which was prepared by pyrolysis of furfuryl alcohol resin. Above 1200 °C of the pyrolysis temperature, diamond formation was clearly observed in Ni, Fe, Co and their alloy catalysts. The hydrogen content in the starting carbon has a drastic effect on the diamond formation. The maximum content of the hydrogen in the glassy carbon had to be between 1200 and 2200 ppm to see diamond formation. In the Fe-rich catalyst, a characteristic needle-like diamond was formed due to the texture of the carbon source and the nature of the catalyst.

  13. The processing, properties, and structure of carbon fibers

    NASA Astrophysics Data System (ADS)

    Minus, Marilyn; Kumar, Satish

    2005-02-01

    This paper reviews the processing, properties, and structure of carbon fibers. Carbon fibers are derived from several precursors, with polyacrylonitrile being the predominant precursor used today. Carbon fibers have high strength (3 7 GPa), high modulus (200 500 GPa), compressive strength (1 3 GPa), shear modulus (10 15 GPa), and low density (1.75 2.00 g/cm3). Carbon fibers made from pitch can have modulus, thermal, and electrical conductivities as high as 900 GPa, 1,000 W/mK, and 106 S/m, respectively. These fibers have become a dominant material in the aerospace industry and their use in the automotive and other industries is growing as their cost continues to come down.

  14. Slip zone structure and processes in seismogenic carbonate faults

    NASA Astrophysics Data System (ADS)

    Bullock, R. J.; De Paola, N.

    2011-12-01

    High velocity rotary shear experiments performed at seismic slip velocities (>1 m/s) have shown that experimental faults are weak; with increasing displacement, friction coefficient values decrease from Byerlee's values (? = 0.6-0.85) to values of ~0.1. In carbonate rocks, experimental studies have shown that fault lubrication is due to the operation of multiple dynamic weakening mechanisms (e.g., flash heating, thermal pressurization, nanoparticle lubrication), which are thermally activated due to the frictional heat generated along localized slip surfaces during rapid slip. This study has set out to investigate whether evidence for the operation of these weakening mechanisms can be found in naturally occurring carbonate fault zones. Field studies were carried out on the active Gubbio fault zone (1984, Mw = 5.6) in the northern Apennines of Italy. Jurassic-Oligocene carbonates in the footwall are heavily deformed within a fault core of ~15 m thickness, which contains a number of very well exposed, highly localized principal slip surfaces (PSSs). Fault rocks are predominantly breccias and foliated cataclasites. Microstructural analyses of the PSSs reveal that slip is localized within very narrow principal slip zones (PSZs), ranging from 10-85 ?m in thickness, with sub-millimetre scale asperities. PSZs are composed of very fine-grained, orange-brown ultracataclasite gouge containing a high proportion of nano-sized particles. The ultracataclasite commonly displays a foliated texture and sub-micron scale zones of extreme shear localization. A broader slip zone, up to 1.5 mm wide and containing multiple slip surfaces, is associated with the most evolved PSSs; it is located on the opposite side of the PSS to the PSZ. Here, the host rock material is heavily fractured, abraded and altered, sometimes with an ultracataclasite matrix. The surrounding wall rock often appears to have a porous texture, and calcite crystals within the slip zone have altered rims with lobate textures, both of which may be indicative of thermally activated chemical reactions. Occasionally, mantled clasts are observed; these consist of a central, sub-rounded monomineralic clast of calcite, or a polymineralic clast of both calcite and clay particles, enclosed by a cortex of ultracataclasite. These are features which are thought to be a product of thermal pressurization processes operating in the slip zone. These microstructures are compared to those in experimentally deformed dolomite gouges, and the slip zone features are found to be strikingly similar. It is clear that as slip accumulates along PSSs, well-developed PSZs are formed with well-defined foliations and R- and Y-shears, indicating progressive localization of deformation. The similarities between the two sets of samples implies that the dynamic weakening mechanisms known to occur in experimental carbonate slip zones are indeed likely to be in operation in their naturally occurring counterparts. Specifically, slip localization in the fault core may be associated with frictional heating; slip zone roughness may be associated with flash heating; mantled clasts may be attributed to thermal pressurization; and nanoparticles may be associated with nanoparticle lubrication.

  15. Adsorption uptake of synthetic organic chemicals by carbon nanotubes and activated carbons

    NASA Astrophysics Data System (ADS)

    Brooks, A. J.; Lim, Hyung-nam; Kilduff, James E.

    2012-07-01

    Carbon nanotubes (CNTs) have shown great promise as high performance materials for adsorbing priority pollutants from water and wastewater. This study compared uptake of two contaminants of interest in drinking water treatment (atrazine and trichloroethylene) by nine different types of carbonaceous adsorbents: three different types of single walled carbon nanotubes (SWNTs), three different sized multi-walled nanotubes (MWNTs), two granular activated carbons (GACs) and a powdered activated carbon (PAC). On a mass basis, the activated carbons exhibited the highest uptake, followed by SWNTs and MWNTs. However, metallic impurities in SWNTs and multiple walls in MWNTs contribute to adsorbent mass but do not contribute commensurate adsorption sites. Therefore, when uptake was normalized by purity (carbon content) and surface area (instead of mass), the isotherms collapsed and much of the CNT data was comparable to the activated carbons, indicating that these two characteristics drive much of the observed differences between activated carbons and CNT materials. For the limited data set here, the Raman D:G ratio as a measure of disordered non-nanotube graphitic components was not a good predictor of adsorption from solution. Uptake of atrazine by MWNTs having a range of lengths and diameters was comparable and their Freundlich isotherms were statistically similar, and we found no impact of solution pH on the adsorption of either atrazine or trichloroethylene in the range of naturally occurring surface water (pH = 5.7-8.3). Experiments were performed using a suite of model aromatic compounds having a range of ?-electron energy to investigate the role of ?-? electron donor-acceptor interactions on organic compound uptake by SWNTs. For the compounds studied, hydrophobic interactions were the dominant mechanism in the uptake by both SWNTs and activated carbon. However, comparing the uptake of naphthalene and phenanthrene by activated carbon and SWNTs, size exclusion effects appear to be more pronounced with activated carbon materials, perhaps due to smaller pore sizes or larger adsorption surface areas in small pores.

  16. Preparation of activated carbon monolith by application of phenolic resins as carbon precursors

    NASA Astrophysics Data System (ADS)

    Sajad, Mehran; Kazemzad, Mahmood; Hosseinnia, Azarmidokht

    2014-04-01

    In the current work, activated carbon monoliths have been prepared by application of different phenolic hydrocarbons namely catechol and resorcinol as carbon precursors. For synthesis of carbon monolith, the precursors have been mixed with Genapol PF-10 as template and then polymerized in the presence of lysine as catalyst. Then the polymerized monolith carbonized in inert atmosphere at 700C and activated by water steam at 550C. It was found that resorcinol polymerization is easier than catechol and occurred at 90C while for polymerization of catechol elevated temperature of 120C at hydrothermal condition is necessary. The prepared activated carbon samples have been characterized by various analysis methods including scanning electron microscopy (SEM), surface area measurement, and transmission electron microscopy (TEM). The adsorptions of three different aromatic hydrocarbons by the prepared activated carbon samples have also been investigated by high performance liquid chromatography (HPLC) and UV-Vis spectroscopy. It was found that carbon monolith prepared by catechol as carbon precursor has higher adsorpability and strength in comparison with the other sample. The higher performance of carbon monolith prepared by catechol can be associated with its higher active sites in comparison with resorcinol.

  17. Grain-based activated carbons for natural gas storage.

    PubMed

    Zhang, Tengyan; Walawender, Walter P; Fan, L T

    2010-03-01

    Natural gas has emerged as a potential alternative to gasoline due to the increase in global energy demand and environmental concerns. An investigation was undertaken to explore the technical feasibility of implementing the adsorbed natural gas (ANG) storage in the fuel tanks of motor vehicles with activated carbons from biomass, e.g., sorghum and wheat. The grain-based activated carbons were prepared by chemical activation; the experimental parameters were varied to identify the optimum conditions. The porosity of the resultant activated carbons was evaluated through nitrogen adsorption; and the storage capacity, through methane adsorption. A comparative study was also carried out with commercial activated carbons from charcoal. The highest storage factor attained was 89 for compacted grain-based activated carbons from grain sorghum with a bulk density of 0.65 g/cm(3), and the highest storage factor attained is 106 for compacted commercial activated carbons (Calgon) with a bulk density of 0.70 g/cm(3). The storage factor was found to increase approximately linearly with increasing bulk density and to be independent of the extent of compaction. This implies that the grain-based activated carbons are the ideal candidates for the ANG storage. PMID:19945864

  18. Carbon cycle. Sunlight controls water column processing of carbon in arctic fresh waters.

    PubMed

    Cory, Rose M; Ward, Collin P; Crump, Byron C; Kling, George W

    2014-08-22

    Carbon in thawing permafrost soils may have global impacts on climate change; however, the factors that control its processing and fate are poorly understood. The dominant fate of dissolved organic carbon (DOC) released from soils to inland waters is either complete oxidation to CO2 or partial oxidation and river export to oceans. Although both processes are most often attributed to bacterial respiration, we found that photochemical oxidation exceeds rates of respiration and accounts for 70 to 95% of total DOC processed in the water column of arctic lakes and rivers. At the basin scale, photochemical processing of DOC is about one-third of the total CO2 released from surface waters and is thus an important component of the arctic carbon budget. PMID:25146289

  19. Carbon dioxide sequestration by direct mineral carbonation: process mineralogy of feed and products

    SciTech Connect

    O'Connor, William K.; Dahlin, David C.; Rush, G.E.; Dahlin, Cheryl L.; Collins, W. Keith

    2002-05-01

    Direct mineral carbonation was investigated as a process to convert gaseous CO[2] into a geologically stable final form. The process utilizes a slurry of water, with bicarbonate and salt additions, mixed with a mineral reactant, such as olivine (Mg[2]SiO[4]) or serpentine [Mg[3]Si[2]O[5](OH)[4

  20. PRODUCTION OF CARBON PRODUCTS USING A COAL EXTRACTION PROCESS

    SciTech Connect

    Dady Dadyburjor; Philip R. Biedler; Chong Chen; L. Mitchell Clendenin; Manoj Katakdaunde; Elliot B. Kennel; Nathan D. King; Liviu Magean; Peter G. Stansberry; Alfred H. Stiller; John W. Zondlo

    2004-08-31

    This Department of Energy National Energy Technology Laboratory sponsored project developed carbon products, using mildly hydrogenated solvents to extract the organic portion of coal to create synthetic pitches, cokes, carbon foam and carbon fibers. The focus of this effort was on development of lower cost solvents, milder hydrogenation conditions and improved yield in order to enable practical production of these products. This technology is needed because of the long-term decline in production of domestic feedstocks such as petroleum pitch and coal tar pitch. Currently, carbon products represents a market of roughly 5 million tons domestically, and 19 million tons worldwide. Carbon products are mainly derived from feedstocks such as petroleum pitch and coal tar pitch. The domestic supply of petroleum pitch is declining because of the rising price of liquid fuels, which has caused US refineries to maximize liquid fuel production. As a consequence, the long term trend has a decline in production of petroleum pitch over the past 20 years. The production of coal tar pitch, as in the case of petroleum pitch, has likewise declined significantly over the past two decades. Coal tar pitch is a byproduct of metallurgical grade coke (metcoke) production. In this industry, modern metcoke facilities are recycling coal tar as fuel in order to enhance energy efficiency and minimize environmental emissions. Metcoke production itself is dependent upon the production requirements for domestic steel. Hence, several metcoke ovens have been decommissioned over the past two decades and have not been replaced. As a consequence sources of coal tar are being taken off line and are not being replaced. The long-term trend is a reduction in coal tar pitch production. Thus import of feedstocks, mainly from Eastern Europe and China, is on the rise despite the relatively large transportation cost. To reverse this trend, a new process for producing carbon products is needed. The process must be economically competitive with current processes, and yet be environmentally friendly as well. The solvent extraction process developed uses mild hydrogenation of low cost oils to create powerful solvents that can dissolve the organic portion of coal. The insoluble portion, consisting mainly of mineral matter and fixed carbon, is removed via centrifugation or filtration, leaving a liquid solution of coal chemicals and solvent. This solution can be further refined via distillation to meet specifications for products such as synthetic pitches, cokes, carbon foam and fibers. The most economical process recycles 85% of the solvent, which itself is obtained as a low-cost byproduct from industrial processes such as coal tar or petroleum refining. Alternatively, processes have been developed that can recycle 100% of the solvent, avoiding any need for products derived from petroleum or coal tar.

  1. More About Arc-Welding Process for Making Carbon Nanotubes

    NASA Technical Reports Server (NTRS)

    Benavides, Jeanette M.; Leidecker, Henning

    2005-01-01

    High-quality batches of carbon nanotubes are produced at relatively low cost in a modified atmospheric-pressure electric-arc welding process that does not include the use of metal catalysts. What would normally be a welding rod and a weldment are replaced by an amorphous carbon anode rod and a wider, hollow graphite cathode rod. Both electrodes are water-cooled. The cathode is immersed in ice water to about 0.5 cm from the surface. The system is shielded from air by flowing helium during arcing. As the anode is consumed during arcing at 20 to 25 A, it is lowered to maintain it at an approximately constant distance above the cathode. The process causes carbon nanotubes to form on the lowest 5 cm of the anode. The arcing process is continued until the anode has been lowered to a specified height. The nanotube-containing material is then harvested. The additional information contained in the instant report consists mostly of illustrations of carbon nanotubes and a schematic diagram of the arc-welding setup, as modified for the production of carbon nanotubes.

  2. Comparison of adsorption characteristics for VOCs on acivated carbon and oxidized activated carbon

    SciTech Connect

    You, J.H.; Chiang, H.L.; Chiang, P.C. )

    1994-02-01

    In this investigation, the selected activated carbon is treated in NaOH solution or gas fluid with ozone from an ozone generator. FTIR, BET specific surface area and element analysis instruments were used to identify the difference in the chemical and physical characteristics between the activated carbon and oxidized activated carbon. The system of adsorption apparatus consists of a fixed adsorption column, quartz pan, electronic balance, and data acquisition system to measure the adsorption capacities and adsorption rates for VOCs under various operating conditions. VOCs n-hexane, methyl-ethyl-ketone, and benzene were selected to evaluate the effect of adsorption characterisitics on the activated carbon and oxidized activated carbon. The results of chemical analysis with the FTIR instrument indicate the adsorption bands and peaks measured at 1632 cm[sup [minus]1] on the oxidized activated carbons (AOHO[sub 3] and AO[sub 3]) are much stronger than on the activated carbon (AC). This shows that carbonyl (conjugated C=O) of the functional group is predominantly found to increase on the oxidized activated carbons (AO[sub 3] and AOHO[sub 3]). Significant changes were observed for BET-specific areas for AOHO[sub 3] and AO[sub 3] but the carbon contents of AOHO[sub 3] and AO[sub 3] decreases slightly. Moreover, the oxidized activated carbons showed greater affinity for polar adsorbate than did AC, and the overall effective mass transfer coefficients, k[sub D], of AO[sub 3] for various VOC adsorption were larger than those of AC and AOHO[sub 3]. 12 refs., 8 figs., 4 tabs.

  3. Hydrogen Adsorption on Activated Carbon an Carbon Nanotubes Using Volumetric Differential Pressure Technique

    SciTech Connect

    Sanip, S. M.; Saidin, M. A. R.; Aziz, M.; Ismail, A. F.

    2010-03-11

    A simple hydrogen adsorption measurement system utilizing the volumetric differential pressure technique has been designed, fabricated and calibrated. Hydrogen adsorption measurements have been carried out at temperatures 298 K and 77 K on activate carbon and carbon nanotubes with different surface areas. The adsorption data obtained will be helpful in understanding the adsorption property of the studied carbon materials using the fundamentals of adsorption theory. The principle of the system follows the Sievert-type method. The system measures a change in pressure between the reference cell, R1 and the sample cell S1, S2, S3 over a certain temperature range, R1, S1, S2, and S3 having known fixed volume. The sample temperatures will be monitored by thermocouple TC while the pressures in R1 an S1, S2, S3 will be measured using a digital pressure transducer. The maximum operating pressure of the pressure transducer is 20 bar and calibrated with an accuracy of +-0.01 bar. High purity hydrogen is being used in the system and the amount of samples for the study is between 1.0-2.0 grams. The system was calibrated using helium gas without any samples in S1, S2 an S3. This will provide a correction factor during the adsorption process providing an adsorption free reference point when using hydrogen gas resulting in a more accurate reading of the adsorption process by eliminating the errors caused by temperature expansion effects and other non-adsorption related phenomena. The ideal gas equation of state is applied to calculate the hydrogen adsorption capacity based on the differential pressure measurements. Activated carbon with a surface area of 644.87 m{sup 2}/g showed a larger amount of adsorption as compared to multiwalled nanotubes (commercial) with a surface area of 119.68 m{sup 2}/g. This study als indicated that there is a direct correlation between the amounts of hydrogen adsorbed an surface area of the carbon materials under the conditions studied and that the adsorption significant at 77 K.

  4. Belowground Carbon Cycling Processes at the Molecular Scale: An EMSL Science Theme Advisory Panel Workshop

    SciTech Connect

    Hess, Nancy J.; Brown, Gordon E.; Plata, Charity

    2014-02-21

    As part of the Belowground Carbon Cycling Processes at the Molecular Scale workshop, an EMSL Science Theme Advisory Panel meeting held in February 2013, attendees discussed critical biogeochemical processes that regulate carbon cycling in soil. The meeting attendees determined that as a national scientific user facility, EMSL can provide the tools and expertise needed to elucidate the molecular foundation that underlies mechanistic descriptions of biogeochemical processes that control carbon allocation and fluxes at the terrestrial/atmospheric interface in landscape and regional climate models. Consequently, the workshop's goal was to identify the science gaps that hinder either development of mechanistic description of critical processes or their accurate representation in climate models. In part, this report offers recommendations for future EMSL activities in this research area. The workshop was co-chaired by Dr. Nancy Hess (EMSL) and Dr. Gordon Brown (Stanford University).

  5. Immobilization of phenol in cement-based solidified/stabilized hazardous wastes using regenerated activated carbon: role of carbon.

    PubMed

    Arafat, H A; Hebatpuria, V M; Rho, H S; Pinto, N G; Bishop, P L; Buchanan, R C

    1999-12-31

    The use of regenerated activated carbon as an immobilizing additive for phenol in solidification/stabilization (S/S) processes was investigated. The adsorption capacity of regenerated carbon was compared to that of the virgin form and was found to be very close. The effects of pH and Ca(OH)(2) concentration within the S/S monolith on the adsorption process were also examined. Kinetic tests were performed to evaluate the adsorption of phenol on different forms of F400 carbon, including the regenerated form. Kinetic tests were performed in aqueous solutions as well as in liquid-sand mixtures. In both cases, it was found that phenol adsorption on F400 carbon was fairly fast. More than 60% of the equilibrium adsorption amount could be achieved within the first hour for aqueous solutions. For sand-solution kinetics, it was found that 1% carbon (based on dry sand weight) was capable of achieving more than 95% removal of the initial amount of phenol present in solution (1000 and 5000 ppm). Fourier transform infrared (FT-IR) spectroscopy and X-ray mapping tests indicated a homogenous mixing of the carbon into the cement matrix. The carbon was also found to enhance the hydration of cement, which was retarded by the existence of phenol. PMID:10631353

  6. Carbon processing in the Kolyma River Watershed and the role it plays in CO2 outgassing

    NASA Astrophysics Data System (ADS)

    Denfeld, B. A.; Frey, K. E.; Bulygina, E. B.; Drake, T.; Holmes, R. M.; Schade, J. D.; Sobczak, W. V.; Zimov, N.

    2010-12-01

    The Kolyma River watershed in Northeast Siberia is the largest watershed underlain by continuous permafrost, storing vast amounts of organic carbon and nutrients, which if thawed will become available to microbial processing or transport downstream. Understanding the internal hydrological processes and outgassing across large Arctic river watersheds is crucial if we are to better refine estimates of GHG emissions. Previous conceptual models treated waterways as simple pipes, transporting water from land to ocean without internal processing but current research makes it evident that we must acknowledge them as possible active processors. In July and August 2010, a survey spanning 260 km of the Kolyma River Watershed was conducted to examine the rates of carbon processing in a diverse set of subwatersheds. A total of 23 subwatersheds (eleven streams, and twelve rivers) and nine mainstem locations were sampled at which water samples were collected for measurements of partial pressure of Carbon dioxide (pCO2), dissolved organic carbon (DOC), chromophoric dissolved organic matter (CDOM) and biological oxygen demand (BOD). Spatially, pCO2 concentrations decrease along flowpaths from small streams to the Ocean with the greatest variation between small streams and large rivers. Measurements of DOC concentrations and bioavailability indicate small streams are higher in the total amount and lability of DOC compared to larger tributaries. The results of this study suggest the headwater streams in the Kolyma River watershed are actively processing carbon during the summer at a more significant rate compared to larger tributaries and the Kolyma mainstem. Understanding the relationship between watershed size and carbon processing is critical for predicting how future warming will likely impact the Arctic carbon cycle. This study is part of the Polaris Project, an NSF-funded undergraduate field program based out of the Northeast Science Station in Cherskiy, Northeast Siberia (www.thepolarisproject.org).

  7. DETERMINATION OF DIOXIN LEVELS IN CARBON REACTIVATION PROCESS EFFLUENT STREAMS

    EPA Science Inventory

    A preliminary study was performed to evaluate the potential formation and persistence of tetrachlorodibenzo-p-dioxins (TCDDs) and tetrachlorodibenzo furans (TCDFs) in the effluent streams of a fluidized bed system used for thermal reactivation of granular activated carbon (GAC) t...

  8. Characteristics and humidity control capacity of activated carbon from bamboo.

    PubMed

    Horikawa, Toshihide; Kitakaze, Yoshiyuki; Sekida, Tomoki; Hayashi, Jun'ichi; Katoh, Masahiro

    2010-06-01

    Activated carbons were prepared from bamboo by chemical activation with K2CO3 or physical activation with CO2. The structural and surface chemical characteristics of the activated carbons were determined by N2 adsorption-desorption and Boehm titration, respectively. The water vapor adsorption properties of the activated carbons with various pore structures (preparation conditions) were examined. The relationship between water vapor adsorption capacity and pore properties, and the humidity control capacity of the prepared activated carbons are also discussed. The water adsorption isotherms show a region of rapidly increasing uptake of water vapor, and the relative humidity corresponding to those regions was different according to the preparation conditions, especially activation temperature. Water vapor adsorption capacity was improved with larger pore volume and surface area, but the humidity control capacity in a certain specific humidity region differed greatly according to the relative humidity corresponding to the steeply rising regions of the isotherms. In the typical operating conditions of an adsorption heat pump, RH 10-35%, the bamboo-sourced activated carbon that was prepared at 873K by potassium carbonate activation with impregnation ratio 1.0 had the highest humidity control capacity. PMID:20133125

  9. INDUSTRIAL PROCESS PROFILES FOR ENVIRONMENTAL USE: CHAPTER 4. CARBON BLACK INDUSTRY

    EPA Science Inventory

    The catalog of Industrial Process Profiles for Environmental Use was developed as an aid in defining the environmental impacts of industrial activity in the United States Entries for each industry are in consistent format and form separate chapters of the study. The carbon black ...

  10. Process for reducing Ramsbottom Carbon Test of long residues

    SciTech Connect

    Eilers, J.; Stork, W.H.J.

    1984-07-17

    Process for the preparation of a heavy oil with a low Ramsbottom Carbon Test (RCT) from a long residue by (a) catalytic hydrotreatment for RCT reduction at such severity that the C/sub 4/- gas production per percentage RCT reduction is kept between defined limits, followed by (b) solvent deasphalting of the (vacuum or atmospheric) distillation residue of the hydrotreated product.

  11. Supercritical carbon dioxide process for pasteurization of fruit juices

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Supercritical carbon dioxide (SCCO2) nonthermal processing inactivates microorganisms in juices using non-toxic and non-reactive CO2. However, data is lacking on the inactivation of E. coli K12 and L. plantarum in apple cider using pilot plant scale SCCO2 equipment. For this study, pasteurized pres...

  12. TRIHALOMETHANE PRECURSOR REMOVAL BY THE MAGNESIUM CARBONATE PROCESS

    EPA Science Inventory

    A project was conducted to determine and improve the ability of the magnesium carbonate process to remove trihalomethane (THM) precursors in treated drinking water. The project was conducted at a drinking water treatment plant in Melbourne, FL, which had been developed and instal...

  13. ORGANIC CARBON REMOVAL BY ADVANCED WASTE WATER TREATMENT PROCESSES

    EPA Science Inventory

    Fourteen physical-chemical processes singularly or in combination were evaluated for their ability to remove dissolved organic carbon in the effluent of a wastewater reclamation facility treating secondary effluent. The objective of the study was to produce a product water with o...

  14. Process for preparation of pitch for producing carbon fiber

    SciTech Connect

    Seo, I.

    1981-01-06

    A process for preparing a pitch for carbon fiber by filtering a heavy pitch having a softening point of 150*-200* C. At a temperature of 250*-300* C. And further treating at the same temperature under reduced pressure.

  15. Liquid-phase adsorption of organic compounds by granular activated carbon and activated carbon fibers

    SciTech Connect

    Lin, S.H.; Hsu, F.M.

    1995-06-01

    Liquid-phase adsorption of organic compounds by granular activated carbon (GAC) and activated carbon fibers (ACFs) is investigated. Acetone, isopropyl alcohol (IPA), phenol, and tetrahydrofuran (THF) were employed as the model compounds for the present study. It is observed from the experimental results that adsorption of organic compounds by GAC and ACF is influenced by the BET (Brunauer-Emmett-Teller) surface area of adsorbent and the molecular weight, polarity, and solubility of the adsorbate. The adsorption characteristics of GAC and ACFs were found to differ rather significantly. In terms of the adsorption capacity of organic compounds, the time to reach equilibrium adsorption, and the time for complete desorption, ACFs have been observed to be considerably better than GAC. For the organic compounds tested here, the GAC adsorptions were shown to be represented well by the Langmuir isotherm while the ACF adsorption could be adequately described by the Langmuir or the Freundlich isotherm. Column adsorption tests indicated that the exhausted ACFs can be effectively regenerated by static in situ thermal desorption at 150 C, but the same regeneration conditions do not do as well for the exhausted GAC.

  16. Oxidative degradation of trichloroethylene adsorbed on active carbons: Use of microwave energy

    SciTech Connect

    Varma, R.; Nandi, S.P.

    1991-01-01

    Chlorinated hydrocarbon compounds (CHCl), such as chlorinated alkanes/alkenes, benzene and biphenyl etc, represent an important fraction of the industrial hazardous wastes produced. Trichloroethylene (TCE) can be removed from waste streams by adsorption on active carbons. The primary objective of the present work was to study the detoxification in air-stream of TCE adsorbed on different types of active carbons using in situ microwave heating. A secondary objective was to examine the regeneration of used carbons from the effects of repeated cyclic operations (adsorption- detoxification). The experimental study has shown that trichloroethylene adsorbed on active carbon can be oxidatively degradated in presence of microwave radiation. Energy can be transferred efficiently to the reaction sites without losing heat to the surrounding vessel. One of the decomposition product of trichloroethylene is free chlorine which is held very strongly on active carbon. Hydrochloric acid on the other hand seems to be less strongly held and appears in large concentration in the exit gas. Production of free chlorine can be avoided by using chlorohydrocarbon mixed with sufficient internal hydrogen. This is also expected to minimize the problem of carbon regeneration encountered in this study. The results obtained from studies on the oxidative degradation of TCE under microwave radiation are promising in a number of respects: (1) the detoxification of TCE adsorbed on active carbon can be conducted at moderate (<400{degree}C) temperatures, and (2) the used carbon bed can be regenerated. A patent on the process has been issued. 9 refs., 2 figs., 2 tabs.

  17. Relation Between the Adsorbed Quantity and the Immersion Enthalpy in Catechol Aqueous Solutions on Activated Carbons

    PubMed Central

    Moreno-Pirajn, Juan Carlos; Blanco, Diego; Giraldo, Liliana

    2012-01-01

    An activated carbon, CarbochemTMPS230, was modified by chemical and thermal treatment in flow of H2, in order to evaluate the influence of the activated carbon chemical characteristics in the adsorption of the catechol. The catechol adsorption in aqueous solution was studied along with the effect of the pH solution in the adsorption process of modified activated carbons and the variation of immersion enthalpy of activated carbons in the aqueous solutions of catechol. The interaction solid-solution is characterized by adsorption isotherms analysis, at 298 K and pH 7, 9 and 11 in order to evaluate the adsorption value above and below that of the catechol pKa. The adsorption capacity of carbons increases when the solution pH decreases. The retained amount increases slightly in the reduced carbon to maximum adsorption pH and diminishes in the oxidized carbon. Similar conclusions are obtained from the immersion enthalpies, whose values increase with the solute quantity retained. In granular activated carbon (CAG), the immersion enthalpies obtained are between 21.5 and 45.7 Jg?1 for catechol aqueous solutions in a range of 20 at 1500 mgL?1. PMID:22312237

  18. Preparation and electrochemical investigation of the cobalt hydroxide carbonate/activated carbon nanocomposite for supercapacitor applications

    NASA Astrophysics Data System (ADS)

    Masikhwa, Tshifhiwa M.; Dangbegnon, Julien K.; Bello, Abdulhakeem; Madito, Moshawe J.; Momodu, Damilola; Manyala, Ncholu

    2016-01-01

    Cobalt hydroxide carbonate/activated carbon (AC) composite was successfully synthesized by hydrothermal method. Morphological characterizations of cobalt hydroxide carbonate/AC composite were carried out by scanning electron microscopy (SEM) and transmission electron microscopy (TEM), and the results show that the cobalt hydroxide carbonate nanorods are well dispersed on the AC. Due to the synergistic effects arising from cobalt hydroxide carbonate nanorods and AC, the electrochemical performances of pure cobalt hydroxide carbonate material is significantly improved by the addition of AC. The composite shows a specific capacitance of 301.44 F g-1 at a current density of 1 A g-1 in 6 M KOH electrolyte and exhibits good cycling stability. Based on the above results, the cobalt hydroxide carbonate/AC composite shows a considerable promise as electrode for electrochemical applications.

  19. Activated carbon fibers and engineered forms from renewable resources

    DOEpatents

    Baker, Frederick S

    2013-02-19

    A method of producing activated carbon fibers (ACFs) includes the steps of providing a natural carbonaceous precursor fiber material, blending the carbonaceous precursor material with a chemical activation agent to form chemical agent-impregnated precursor fibers, spinning the chemical agent-impregnated precursor material into fibers, and thermally treating the chemical agent-impregnated precursor fibers. The carbonaceous precursor material is both carbonized and activated to form ACFs in a single step. The method produces ACFs exclusive of a step to isolate an intermediate carbon fiber.

  20. Activated carbon fibers and engineered forms from renewable resources

    DOEpatents

    Baker, Frederick S.

    2010-06-01

    A method of producing activated carbon fibers (ACFs) includes the steps of providing a natural carbonaceous precursor fiber material, blending the carbonaceous precursor material with a chemical activation agent to form chemical agent-impregnated precursor fibers, spinning the chemical agent-impregnated precursor material into fibers, and thermally treating the chemical agent-impregnated precursor fibers. The carbonaceous precursor material is both carbonized and activated to form ACFs in a single step. The method produces ACFs exclusive of a step to isolate an intermediate carbon fiber.

  1. Preparation of activated carbons from agricultural residues for pesticide adsorption.

    PubMed

    Ioannidou, Ourania A; Zabaniotou, Anastasia A; Stavropoulos, George G; Islam, Md Azharul; Albanis, Triantafyllos A

    2010-09-01

    Activated carbons (ACs) can be used not only for liquid but also for vapour phase applications, such as water treatment, deodorisation, gas purification and air treatment. In the present study, activated carbons produced from agricultural residues (olive kernel, corn cobs, rapeseed stalks and soya stalks) via physical steam activation were tested for the removal of Bromopropylate (BP) from water. For the characterization of the activated carbons ICP, SEM, FTIR and XRD analyses were performed. Adsorption kinetics and equilibrium isotherms were investigated for all biomass activated carbons in aqueous solutions. Experimental data of BP adsorption have fitted best to the pseudo 2nd-order kinetic model and Langmuir isotherm. The study resulted that corn cobs showed better adsorption capacity than the other biomass ACs. Comparison among ACs from biomass and commercial ones (F400 and Norit GL50) revealed that the first can be equally effective for the removal of BP from water with the latter. PMID:20598734

  2. Computer-Aided Process Model For Carbon/Phenolic Materials

    NASA Technical Reports Server (NTRS)

    Letson, Mischell A.; Bunker, Robert C.

    1996-01-01

    Computer program implements thermochemical model of processing of carbon-fiber/phenolic-matrix composite materials into molded parts of various sizes and shapes. Directed toward improving fabrication of rocket-engine-nozzle parts, also used to optimize fabrication of other structural components, and material-property parameters changed to apply to other materials. Reduces costs by reducing amount of laboratory trial and error needed to optimize curing processes and to predict properties of cured parts.

  3. Process modeling for carbon-phenolic nozzle materials

    NASA Technical Reports Server (NTRS)

    Letson, Mischell A.; Bunker, Robert C.; Remus, Walter M., III; Clinton, R. G.

    1989-01-01

    A thermochemical model based on the SINDA heat transfer program is developed for carbon-phenolic nozzle material processes. The model can be used to optimize cure cycles and to predict material properties based on the types of materials and the process by which these materials are used to make nozzle components. Chemical kinetic constants for Fiberite MX4926 were determined so that optimization of cure cycles for the current Space Shuttle Solid Rocket Motor nozzle rings can be determined.

  4. Characterization of activated carbon prepared from chicken waste and coal

    SciTech Connect

    Yan Zhang; Hong Cui; Riko Ozao; Yan Cao; Bobby I.-T. Chen; Chia-Wei Wang; Wei-Ping Pan

    2007-12-15

    Activated carbons (ACs) were prepared from chicken waste (CW) and coal (E-coal) blended at the ratios of 100:0, 80:20, 50:50, 20:80, and 0:100. The process included carbonization in flowing gaseous nitrogen (300 mL min{sup -1}) at ca. 430{sup o}C for 60 min and successive steam activation (0.1 mL min{sup -1} water injection with a flow of N{sub 2} at 100 mL min{sup -1}) at 650{sup o}C for 30 min. Chicken waste is low in sulfur content but is high in volatile matter (about 55 wt %), and ACs with higher specific surface area were more successfully obtained by mixing with coal. The specific surface area of the CW/Coal blend AC can be estimated by SSA{sub BET} = -65.8x{sup 2} + 158x + 168, where SSA{sub BET} is the specific surface area in m{sup 2} g{sup -1} as determined by the BET method using CO{sub 2} as the adsorbent, where x is the coal fraction by weight in the CW/coal blend ranging from 0.0 to 1.0 (e.g., x = 0.0 signifies the blend contains no coal and x = 1.0 signifies the blend consists of 100% coal). 26 refs., 7 figs., 3 tabs.

  5. Activated carbon passes tests for acid-gas cleanup

    SciTech Connect

    Harruff, L.G.; Bushkuhl, S.J.

    1996-06-24

    Use of activated carbon to remove hydrocarbon contaminants from the acid-gas feed to Claus sulfur-recovery units has been successfully pilot tested in Saudi Arabia. Pilot plant results are discussed here along with issues involved in scale-up to commercial size. Heavy hydrocarbons, particularly benzene, toluene, and xylene (BTX) have been linked to coke formation and catalyst deactivation in Claus converters. This deactivation results in reduced sulfur recovery and increased sulfur emissions from these plants. This clean-up process was proven to be capable of removing 95% of the BTX and other C{sub 6}+s from acid gas over a wide range of actual plant conditions. Following the adsorption step, the activated carbon was easily regenerated by use of low-pressure steam. A post-regeneration drying step using plant fuel gas also proved beneficial. The paper discusses feed contaminants, vapor-phase cleanup, testing design, test parameters and results, bed drying after regeneration, regeneration conditions, basic flow, system control, and full-scale installation.

  6. Microstructure and surface properties of lignocellulosic-based activated carbons

    NASA Astrophysics Data System (ADS)

    Gonzlez-Garca, P.; Centeno, T. A.; Urones-Garrote, E.; vila-Brande, D.; Otero-Daz, L. C.

    2013-01-01

    Low cost activated carbons have been produced via chemical activation, by using KOH at 700 C, from the bamboo species Guadua Angustifolia and Bambusa Vulgaris Striata and the residues from shells of the fruits of Castanea Sativa and Juglans Regia as carbon precursors. The scanning electron microscopy micrographs show the conservation of the precursor shape in the case of the Guadua Angustifolia and Bambusa Vulgaris Striata activated carbons. Transmission electron microscopy analyses reveal that these materials consist of carbon platelet-like particles with variable length and thickness, formed by highly disordered graphene-like layers with sp2 content ? 95% and average mass density of 1.65 g/cm3 (25% below standard graphite). Textural parameters indicate a high porosity development with surface areas ranging from 850 to 1100 m2/g and average pore width centered in the supermicropores range (1.3-1.8 nm). The electrochemical performance of the activated carbons shows specific capacitance values at low current density (1 mA/cm2) as high as 161 F/g in the Juglans Regia activated carbon, as a result of its textural parameters and the presence of pseudocapacitance derived from surface oxygenated acidic groups (mainly quinones and ethers) identified in this activated carbon.

  7. Hydrogen storage on activated carbon. Final report

    SciTech Connect

    Schwarz, J.A.

    1994-11-01

    The project studied factors that influence the ability of carbon to store hydrogen and developed techniques to enhance that ability in naturally occurring and factory-produced commercial carbon materials. During testing of enhanced materials, levels of hydrogen storage were achieved that compare well with conventional forms of energy storage, including lead-acid batteries, gasoline, and diesel fuel. Using the best materials, an electric car with a modern fuel cell to convert the hydrogen directly to electricity would have a range of over 1,000 miles. This assumes that the total allowable weight of the fuel cell and carbon/hydrogen storage system is no greater than the present weight of batteries in an existing electric vehicle. By comparison, gasoline cars generally are limited to about a 450-mile range, and battery-electric cars to 40 to 60 miles. The project also developed a new class of carbon materials, based on polymers and other organic compounds, in which the best hydrogen-storing factors discovered earlier were {open_quotes}molecularly engineered{close_quotes} into the new materials. It is believed that these new molecularly engineered materials are likely to exceed the performance of the naturally occurring and manufactured carbons seen earlier with respect to hydrogen storage.

  8. Activated carbon testing for the 200 area effluent treatment facility

    SciTech Connect

    Wagner, R.N.

    1997-01-17

    This report documents pilot and laboratory scale testing of activated carbon for use in the 200 Area Effluent Treatment Facility peroxide decomposer columns. Recommendations are made concerning column operating conditions and hardware design, the optimum type of carbon for use in the plant, and possible further studies.

  9. DESIGN AND CONSTRUCTION OF A MOBILE ACTIVATED CARBON REGENERATOR SYSTEM

    EPA Science Inventory

    Activated carbon adsorption has become a standard procedure for the cleanup of contaminated water streams. To facilitate such cleanup at hazardous waste and spill sites, mobile carbon adsorption units have been constructed and are now in use. Their primary drawback is the logisti...

  10. HARDWOOD-BASED GRANULAR ACTIVATED CARBON FOR METALS REMEDIATION

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Granular activated carbon is usually the adsorbent of choice for removing organic pollutants from air and water waste streams. Its ability to remove metal ions from aqueous media is considered secondary to its ability to remove organics. Only recently was a coal-based, commerical carbon (Minotaur,...

  11. SYNTHETIC ORGANIC CHEMICAL REMOVAL BY GRANULAR ACTIVATED CARBON

    EPA Science Inventory

    The paper is an overview of the adsorbability of synthetic organic chemicals (SOC) by granular activated carbon (GAC). The paper demonstrates the adsorbability by presenting data on the removal of SOCs and organic surrogates such as total organic carbon and total organic halide b...

  12. ELEMENTAL MERCURY CAPTURE BY ACTIVATED CARBON IN A FLOW REACTOR

    EPA Science Inventory


    The paper gives results of bench-scale experiments in a flow reactor to simulate the entrained-flow capture of elemental mercury (Hgo) using solid sorbents. Adsorption of Hgo by a lignite-based activated carbon (Calgon FGD) was examined at different carbon/mercury (C/Hg) rat...

  13. HARDWOOD-BASED GRANULAR ACTIVATED CARBON FOR METALS REMEDIATION

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Granular activated carbon is usually the adsorbent of choice for removing organic pollutants from air and water waste streams. Its ability to remove metal ions from aqueous media is considered secondary to its ability to remove organics. Only recently was a coal-based, commercial carbon (Minotaur) m...

  14. HARDWOOD-BASED GRANULAR ACTIVATED CARBON FOR METALS REMEDIATION

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Granular activated carbon is usually the adsorbent of choice for removing organic pollutants from air and water waste streams. Its ability to remove metal ions from aqueous media is considered secondary to its ability to remove organics. Only recently was a coal-based, commercial carbon (Minotaur, C...

  15. Effect of calcination on Co-impregnated active carbon

    SciTech Connect

    Bekyarova, E.; Mehandjiev, D. . Inst. of General and Inorganic Chemistry)

    1993-11-01

    Active carbon (AC) from apricot shells with known characteristics has been impregnated with a 9.88% Co(NO[sub 3])[sub 2] [center dot] 6H[sub 2]O solution. The samples are destroyed in air at 200, 300, 400, and 550 C. The processes accompanying the thermal treatment are studied by DTA. Two processes are established during calcination of Co-impregnated active carbon: (i) destruction of the support as a result of oxidation catalyzed by the impregnated cobalt and (ii) interaction of the active phase (Co[sub 3]O[sub 4]) with the support (AC), during which Co[sub 3]O[sub 4] is reduced to CoO and Co. The presence of Co[sub 3]O[sub 4], and CoO phases is proved by X-ray measurements, while that of metal Co is established by magnetic measurements. The porous structure changes are investigated by adsorption studies. The characterization of the samples is performed by physical adsorption of N[sub 2] (77.4 K) and CO[sub 2] (273 K). The poresize distribution curves are plotted over the range 0.4--10 nm by the methods of Pierce (for the mesopores) and Medek (for the micropores). The micropore volume is determined by two independent methods: t/F method and D-R plot. The results from adsorption studies indicate a decrease of S[sub BET], V[sub mi], and, especially, the supermicropores of the samples.

  16. Moisture processes accompanying convective activity

    NASA Technical Reports Server (NTRS)

    Sienkiewicz, M. E.; Scoggins, J. R.

    1982-01-01

    A moisture budget analysis was performed on data collected during the AVE 7 (May 2 to 3, 1978) and AVE-SESAME1 (April 10 to 11, 1979) experiments. Local rates-of-change of moisture were compared with average moisture divergence in the same time period. Results were presented as contoured plots in the horizontal and as vertical cross sections. These results were used to develop models of the distribution of moisture processes in the vicinity of convective areas in two layers representing lower and middle tropospheric conditions. Good correspondence was found between the residual term of the moisture budget and actual precipitation.

  17. Exploration of the Role of Heat Activation in Enhancing Serpentine Carbon Sequestration Reactions

    SciTech Connect

    McKelvy, M.J.; Chizmeshya, A.V.G.; Diefenbacher, J.; Bearat, H.; Wolf, G.

    2005-03-29

    As compared with other candidate carbon sequestration technologies, mineral carbonation offers the unique advantage of permanent disposal via geologically stable and environmentally benign carbonates. The primary challenge is the development of an economically viable process. Enhancing feedstock carbonation reactivity is key. Heat activation dramatically enhances aqueous serpentine carbonation reactivity. Although the present process is too expensive to implement, the materials characteristics and mechanisms that enhance carbonation are of keen interest for further reducing cost. Simultaneous thermogravimetric and differential thermal analysis (TGA/DTA) of the serpentine mineral lizardite was used to isolate a series of heat-activated materials as a function of residual hydroxide content at progressively higher temperatures. Their structure and composition are evaluated via TGA/DTA, X-ray powder diffraction (including phase analysis), and infrared analysis. The meta-serpentine materials that were observed to form ranged from those with longer range ordering, consistent with diffuse stage-2 like interlamellar order, to an amorphous component that preferentially forms at higher temperatures. The aqueous carbonation reaction process was investigated for representative materials via in situ synchrotron X-ray diffraction. Magnesite was observed to form directly at 15 MPa CO{sub 2} and at temperatures ranging from 100 to 125 C. Carbonation reactivity is generally correlated with the extent of meta-serpentine formation and structural disorder.

  18. Exploration of the role of heat activation in enhancing serpentine carbon sequestration reactions.

    PubMed

    McKelvy, Michael J; Chizmeshya, Andrew V G; Diefenbacher, Jason; Barat, Hamdallah; Wolf, George

    2004-12-15

    As compared with other candidate carbon sequestration technologies, mineral carbonation offers the unique advantage of permanent disposal via geologically stable and environmentally benign carbonates. The primary challenge is the development of an economically viable process. Enhancing feedstock carbonation reactivity is key. Heat activation dramatically enhances aqueous serpentine carbonation reactivity. Although the present process is too expensive to implement, the materials characteristics and mechanisms that enhance carbonation are of keen interest for further reducing cost. Simultaneous thermogravimetric and differential thermal analysis (TGA/DTA) of the serpentine mineral lizardite was used to isolate a series of heat-activated materials as a function of residual hydroxide content at progressively higher temperatures. Their structure and composition are evaluated via TGA/DTA, X-ray powder diffraction (including phase analysis), and infrared analysis. The meta-serpentine materials that were observed to form ranged from those with longer range ordering, consistent with diffuse stage-2 like interlamellar order, to an amorphous component that preferentially forms at higher temperatures. The aqueous carbonation reaction process was investigated for representative materials via in situ synchrotron X-ray diffraction. Magnesite was observed to form directly at 15 MPa CO2 and at temperatures ranging from 100 to 125 degrees C. Carbonation reactivity is generally correlated with the extent of meta-serpentine formation and structural disorder. PMID:15669355

  19. Discovery and elimination of dioxins from a carbon reactivation process

    SciTech Connect

    DeMarco, J.; Miller, R.

    1985-01-01

    In a project done to ensure an environmentally acceptable granular activated carbon (GAC) adsorption and reactivation system - to be sure that chlorinated dibenzo-p-dioxins (CDD's) and chlorinated dibenzo furans (CDF's) and combustion would not present problems - results from a GAC system receiving chlorinated water were compared with those receiving unchlorinated water. The studies described here are for exhausting GAC in a post-filtration carbon contactor and reactivating GAC in a fluid-bed reactivation system. Lower stack emissions of CDD's and CDF's are produced by reactivating GAC that had received unchlorinated water.

  20. Effect of some organic solvent-water mixtures composition on precipitated calcium carbonate in carbonation process

    NASA Astrophysics Data System (ADS)

    Konopacka-Łyskawa, Donata; Kościelska, Barbara; Karczewski, Jakub

    2015-05-01

    Precipitated calcium carbonate particles were obtained during carbonation of calcium hydroxide slurry with carbon dioxide. Aqueous solutions of isopropyl alcohol, n-butanol and glycerol were used as solvents. Concentration of organic additives in the reactive mixture was from 0% to 20% (vol). Precipitation process were performed in a stirred tank reactor equipped with gas distributor. Multimodal courses of particles size distribution were determined for produced CaCO3 particles. Calcium carbonate as calcite was precipitated in all experiments. The mean Sauter diameter of CaCO3 particles decreased when the concentration of all used organic additives increased. The amount of small particle fraction in the product increased with the increasing concentration of organic solvents. Similar physical properties of used liquid phase resulted in the similar characteristics of obtained particles.

  1. Autoclave processing of thick carbon-phenolic composites

    SciTech Connect

    Kang, H.S.; Kim, K.S.

    1995-12-31

    Aerospace applications of carbon-phenolics are primarily structures and preforms for carbon-carbon composites. Phenolic composites are usually compression molded under high pressure to achieve good consolidation, high density, and enhanced mechanical properties; but for the applications where continuous fiber reinforcement is necessary, vacuum bagging and cure in the autoclave or hydroclave is preferrable. The resols used for ablative applications generate condensation by-products, either water or methanol, which may volatilize inside a curing composite and expand to form bubbles. The resulting pores in cured composites may act as weak points in the matrix and trapped volatiles may also expand explosively under the intensive heating typical of ablative applications. With phenolic, however, it is impossible to remove all volatiles prior to cure because water and methanol are reaction products. Therefore, it is very important to control process parameters in order to suppress the volatiles during processing for a void free matrix. In this paper, a reliable autoclave process has been developed for large and thick carbon-phenolic. Foam sandwich structural composites for the application to a blast deflector have been identified through the various nondestructive and destructive tests.

  2. TESTING GUIDELINES FOR TECHNETIUM-99 ABSORPTION ON ACTIVATED CARBON

    SciTech Connect

    BYRNES ME

    2010-09-08

    CH2M HILL Plateau Remediation Company (CHPRC) is currently evaluating the potential use of activated carbon adsorption for removing technetium-99 from groundwater as a treatment method for the Hanford Site's 200 West Area groundwater pump-and-treat system. The current pump-and-treat system design will include an ion-exchange (IX) system for selective removal of technetium-99 from selected wells prior to subsequent treatment of the water in the central treatment system. The IX resin selected for technetium-99 removal is Purolite A530E. The resin service life is estimated to be approximately 66.85 days at the design technetium-99 loading rate, and the spent resin must be replaced because it cannot be regenerated. The resulting operating costs associated with resin replacement every 66.85 days are estimated at $0.98 million/year. Activated carbon pre-treatment is being evaluated as a potential cost-saving measure to offset the high operating costs associated with frequent IX resin replacement. This document is preceded by the Literature Survey of Technetium-99 Groundwater Pre-Treatment Option Using Granular Activated Carbon (SGW-43928), which identified and evaluated prior research related to technetium-99 adsorption on activated carbon. The survey also evaluated potential operating considerations for this treatment approach for the 200 West Area. The preliminary conclusions of the literature survey are as follows: (1) Activated carbon can be used to selectively remove technetium-99 from contaminated groundwater. (2) Technetium-99 adsorption onto activated carbon is expected to vary significantly based on carbon types and operating conditions. For the treatment approach to be viable at the Hanford Site, activated carbon must be capable of achieving a designated minimum technetium-99 uptake. (3) Certain radionuclides known to be present in 200 West Area groundwater are also likely to adsorb onto activated carbon. (4) Organic solvent contaminants of concern (COCs) will load heavily onto activated carbon and should be removed from groundwater upstream of the activated carbon pre-treatment system. Unless removed upstream, the adsorbed loadings of these organic constituents could exceed the land disposal criteria for carbon.

  3. Solution-processed soldering of carbon nanotubes for flexible electronics

    NASA Astrophysics Data System (ADS)

    Rao, K. D. M.; Radha, B.; Smith, K. C.; Fisher, T. S.; Kulkarni, G. U.

    2013-02-01

    We report a simple lithography-free, solution-based method of soldering of carbon nanotubes with Ohmic contacts, by taking specific examples of multi-walled carbon nanotubes (MWNTs). This is achieved by self-assembling a monolayer of soldering precursor, Pd2+ anchored to 1,10 decanedithiol, onto which MWNTs could be aligned across the gap electrodes via solvent evaporation. The nanosoldering was realized by thermal/electrical activation or by both in sequence. Electrical activation and the following step of washing ensure selective retention of MWNTs spanning across the gap electrodes. The soldered joints were robust enough to sustain strain caused during the bending of flexible substrates as well as during ultrasonication. The estimated temperature generated at the MWNT-Au interface using an electro-thermal model is 150?C, suggesting Joule heating as the primary mechanism of electrical activation. Further, the specific contact resistance is estimated from the transmission line model.

  4. Selection and preparation of activated carbon for fuel gas storage

    DOEpatents

    Schwarz, James A. (Fayetteville, NY); Noh, Joong S. (Syracuse, NY); Agarwal, Rajiv K. (Las Vegas, NV)

    1990-10-02

    Increasing the surface acidity of active carbons can lead to an increase in capacity for hydrogen adsorption. Increasing the surface basicity can facilitate methane adsorption. The treatment of carbons is most effective when the carbon source material is selected to have a low ash content i.e., below about 3%, and where the ash consists predominantly of alkali metals alkali earth, with only minimal amounts of transition metals and silicon. The carbon is washed in water or acid and then oxidized, e.g. in a stream of oxygen and an inert gas at an elevated temperature.

  5. Oxidation of Black Carbon by Biotic and Abiotic Processes

    SciTech Connect

    Cheng, Chih-hsin; Lehmann, Johannes C.; Thies, Janice E.; Burton, Sarah D.; Engelhard, Mark H.

    2006-11-01

    The objectives of this study were to quantify the relative importance of either biotic or abiotic oxidation of biomass-derived black carbon (BC) and to characterize the surface properties and charge characteristics of oxidized particulate BC. We incubated BC and BC-soil mixtures at two different temperatures (30 C and 70 C) with and without microbial inoculation, nutrient additions, or manure amendments for four months. Abiotic processes were more important for oxidation of BC than biotic processes during this short-term incubation, as inoculation with microorganisms did not change any of the measured parameters. Black C incubated at both 30 C and 70 C without microbial activity showed dramatic decreases in pH (in water) from 5.4 to 5.2 and 3.4, as well as increases in cation exchange capacity (CEC at pH 7) by 53% and 538% and in oxygen (O) contents by 4% and 38%, respectively. Boehm titration and Fourier transform infrared (FTIR) spectroscopy suggested that the formation of carboxylic functional groups was the reason for the enhanced CEC during oxidation. The analyses of BC surface properties by X-ray photoelectron spectroscopy (XPS) indicated that the oxidation of BC particles initiated on the surface. Incubation at 30 C only enhanced oxidation on particle surfaces, while oxidation during incubation at 70 C penetrated into the interior of particles. Such short-term oxidation of BC has great significance for the stability of BC in soils as well as for its effects on soil fertility and biogeochemistry.

  6. Get the most from activated-carbon systems

    SciTech Connect

    Boppart, S.

    1995-05-01

    Many manufacturing operations use organic solvents that evaporate in the course of their transportation, storage and use. Adsorption systems using activated carbon have long been used to recover these airborne solvents and other organic vapors. Adsorption systems are an economical way to reclaim solvents for reuse. They are also an effective way to comply with pollution-control regulations that govern volatile organic compounds (VOCs) in industrial exhaust streams, and vapors collected during soil and site remediations. For most air-pollution-control applications, carbon is activated by subjecting the starting material to controlled charring in a kiln, extruding it into pellets and activating it with steam at roughly 1,000 C. During activation, the carbon pellets develop an intricate pore structure, which may have a total internal surface area of up to 1,500 m{sup 2}/g. It is this internal pore structure that gives activated carbon its purifying capacity. To recover solvents adsorbed on the carbon, energy must be applied to overcome the solvents` attraction to the pore surface. This is most commonly done by applying heat, by means of steam, hot inert gas or direct heating. Desorption can also be carried out by changing the equilibrium conditions, by applying a vacuum or purging the adsorbates from the carbon pores using a gas stream. The solvent vapors coming off the carbon will be concentrated, and can be condensed and recovered as a liquid.

  7. Natural gas storage with activated carbon from a bituminous coal

    USGS Publications Warehouse

    Sun, Jielun; Rood, M.J.; Rostam-Abadi, M.; Lizzio, A.A.

    1996-01-01

    Granular activated carbons ( -20 + 100 mesh; 0.149-0.84 mm) were produced by physical activation and chemical activation with KOH from an Illinois bituminous coal (IBC-106) for natural gas storage. The products were characterized by BET surface area, micropore volume, bulk density, and methane adsorption capacities. Volumetric methane adsorption capacities (Vm/Vs) of some of the granular carbons produced by physical activation are about 70 cm3/cm3 which is comparable to that of BPL, a commercial activated carbon. Vm/Vs values above 100 cm3/cm3 are obtainable by grinding the granular products to - 325 mesh (<0.044 mm). The increase in Vm/Vs is due to the increase in bulk density of the carbons. Volumetric methane adsorption capacity increases with increasing pore surface area and micropore volume when normalizing with respect to sample bulk volume. Compared with steam-activated carbons, granular carbons produced by KOH activation have higher micropore volume and higher methane adsorption capacities (g/g). Their volumetric methane adsorption capacities are lower due to their lower bulk densities. Copyright ?? 1996 Elsevier Science Ltd.

  8. Quality of poultry litter-derived granular activated carbon.

    PubMed

    Qiu, Guannan; Guo, Mingxin

    2010-01-01

    Utilization of poultry litter as a source material for generating activated carbon is a value-added and environmentally beneficial approach to recycling organic waste. In this study, the overall quality of poultry litter-derived granular activated carbon was systematically evaluated based on its various physical and chemical properties. Granular activated carbon generated from pelletized poultry litter following a typical steam-activation procedure possessed numerous micropores in the matrix. The product exhibited a mean particle diameter of 2.59 mm, an apparent density of 0.45 g cm(-3), a ball-pan hardness of 91.0, an iodine number of 454 mg g(-1), and a BET surface area of 403 m(2) g(-1). It contained high ash, nitrogen, phosphorus contents and the trace elements Cu, Zn, and As. Most of the nutrients and toxic elements were solidified and solution-unextractable. In general, poultry litter-based activated carbon demonstrated overall quality comparable to that of low-grade commercial activated carbon derived from coconut shell and bituminous coal. It is promising to use poultry litter as a feedstock to manufacture activated carbon for wastewater treatment. PMID:19703765

  9. Carbon Nanotube Activities at NASA-Johnson Space Center

    NASA Technical Reports Server (NTRS)

    Arepalli, Sivaram

    2006-01-01

    Research activities on carbon nanotubes at NASA-Johnson Space Center include production, purification, characterization and their applications for human space flight. In-situ diagnostics during nanotube production by laser oven process include collection of spatial and temporal data of passive emission and laser induced fluorescence from C2, C3 and Nickel atoms in the plume. Details of the results from the "parametric study" of the pulsed laser ablation process indicate the effect of production parameters including temperature, buffer gas, flow rate, pressure, and laser fluence. Improvement of the purity by a variety of steps in the purification process is monitored by characterization techniques including SEM, TEM, Raman, UV-VIS-NIR and TGA. A recently established NASA-JSC protocol for SWCNT characterization is undergoing revision with feedback from nanotube community. Efforts at JSC over the past five years in composites have centered on structural polymednanotube systems. Recent activities broadened this focus to multifunctional materials, supercapacitors, fuel cells, regenerable CO2 absorbers, electromagnetic shielding, radiation dosimetry and thermal management systems of interest for human space flight. Preliminary tests indicate improvement of performance in most of these applications because of the large surface area as well as high electrical and thermal conductivity exhibited by SWCNTs.

  10. Sustainable Regeneration of Nanoparticle Enhanced Activated Carbon in Water

    EPA Science Inventory

    The regeneration and reuse of exhausted granular activated carbon (GAC) is an appropriate method for lowering operational and environmental costs. Advanced oxidation is a promising environmental friendly technique for GAC regeneration. The main objective of this research was to ...

  11. GRANULAR ACTIVATED CARBON ADSORPTION AND INFRARED REACTIVATION: A CASE STUDY

    EPA Science Inventory

    A study evaluated the effectiveness and cost of removing trace organic contaminants and surrogates from drinking water by granular activated carbon (GAC) adsorption. The effect of multiple reactivations of spent GAC was also evaluated. Results indicated that reactivated GAC eff...

  12. EVALUATION OF POWDERED ACTIVATED CARBON FOR REMOVAL OF TRACE ORGANICS AT NEW ORLEANS, LOUISIANA

    EPA Science Inventory

    This research effort studied the effect of powdered activated carbon on the removal of trace organics in the water treatment process at New Orleans, LA. The water treatment processes were modeled in bench scale reactors that allowed control of treatment variables. A series of exp...

  13. Chemical Reactions in the Processing of Mosi2 + Carbon Compacts

    NASA Technical Reports Server (NTRS)

    Jacobson, Nathan S.; Lee, Kang N.; Maloy, Stuart A.; Heuer, Arthur H.

    1993-01-01

    Hot-pressing of MoSi2 powders with carbon at high temperatures reduces the siliceous grain boundary phase in the resultant compact. The chemical reactions in this process were examined using the Knudsen cell technique. A 2.3 wt pct oxygen MoSi2 powder and a 0.59 wt pct oxygen MoSi2 powder, both with additions of 2 wt pct carbon, were examined. The reduction of the siliceous grain boundary phase was examined at 1350 K and the resultant P(SiO)/P(CO) ratios interpreted in terms of the SiO(g) and CO(g) isobars on the Si-C-O predominance diagram. The MoSi2 + carbon mixtures were then heated at the hot-pressing temperature of 2100 K. Large weight losses were observed and could be correlated with the formation of a low-melting eutectic and the formation and vaporization of SiC.

  14. Exposures to carbon dioxide in the poultry processing industry

    SciTech Connect

    Jacobs, D.E.; Smith, M.S.

    1988-12-01

    The use of dry ice has increased dramatically in poultry processing plants because of changes in the fast food industry. Concentrations of carbon dioxide in four such plants were measured and were found to exceed the Immediately Dangerous to Life and Health Level (50,000 ppm) inside holding coolers where ventilation is poor. In other areas, where dry ice is delivered to poultry packages, time-weighted average exposures can exceed the threshold limit value of 5000 ppm by substantial margins, even if local exhaust ventilation systems are present. Reports of adverse health effects from carbon dioxide exposure and various control measures are reviewed. Recommendations regarding sampling and analytical techniques also are presented. Operators of poultry plants where dry ice is used need to recognize the occupational hazards of exposure to carbon dioxide.

  15. Hydrogen Adsorption on Activated Carbon an Carbon Nanotubes Using Volumetric Differential Pressure Technique

    NASA Astrophysics Data System (ADS)

    Sanip, S. M.; Saidin, M. A. R.; Aziz, M.; Ismail, A. F.

    2010-03-01

    A simple hydrogen adsorption measurement system utilizing the volumetri differential pressure technique has been designed, fabricated and calibrated. Hydroge adsorption measurements have been carried out at temperatures 298 K and 77 K on activate carbon and carbon nanotubes with different surface areas. The adsorption data obtained will b helpful in understanding the adsorption property of the studied carbon materials using th fundamentals of adsorption theory. The principle of the system follows the Sievert-type metho The system measures a change in pressure between the reference cell, R1 and the sample cell S1, S2, S3 over a certain temperature range. R1, S1, S2, and S3 having known fixed volume The sample temperatures will be monitored by thermocouple TC while the pressures in R1 an S1, S2, S3 will be measured using a digital pressure transducer. The maximum operatin pressure of the pressure transducer is 20 bar and calibrated with an accuracy of ±0.01 bar. Hig purity hydrogen is being used in the system and the amount of samples for the study is betwee 1.0-2.0 grams. The system was calibrated using helium gas without any samples in S1, S2 an S3. This will provide a correction factor during the adsorption process providing an adsorption free reference point when using hydrogen gas resulting in a more accurate reading of th adsorption process by eliminating the errors caused by temperature expansion effects and oth non-adsorption related phenomena. The ideal gas equation of state is applied to calculate th hydrogen adsorption capacity based on the differential pressure measurements. Activated carbo with a surface area of 644.87 m2/g showed a larger amount of adsorption as compared to multiwalled nanotubes (commercial) with a surface area of 119.68 m2/g. This study als indicated that there is a direct correlation between the amounts of hydrogen adsorbed an surface area of the carbon materials under the conditions studied and that the adsorption significant at 77 K.

  16. Application of thermal analysis techniques in activated carbon production

    USGS Publications Warehouse

    Donnals, G.L.; DeBarr, J.A.; Rostam-Abadi, M.; Lizzio, A.A.; Brady, T.A.

    1996-01-01

    Thermal analysis techniques have been used at the ISGS as an aid in the development and characterization of carbon adsorbents. Promising adsorbents from fly ash, tires, and Illinois coals have been produced for various applications. Process conditions determined in the preparation of gram quantities of carbons were used as guides in the preparation of larger samples. TG techniques developed to characterize the carbon adsorbents included the measurement of the kinetics of SO2 adsorption, the performance of rapid proximate analyses, and the determination of equilibrium methane adsorption capacities. Thermal regeneration of carbons was assessed by TG to predict the life cycle of carbon adsorbents in different applications. TPD was used to determine the nature of surface functional groups and their effect on a carbon's adsorption properties.

  17. Adsorption of dichlorodifluoromethane, chlorodifluoromethane, and chloropentafluoroethane on activated carbon

    SciTech Connect

    Berlier, K.; Frere, M.; Bougard, J.

    1995-09-01

    The CFCs (chlorofluorocarbons) are used as working refrigerant fluids. Recent concerns of the effects of CFCs on the ozone layer requires the development of efficient recovery methods. One technique is to adsorb the fluids onto a porous medium such as silica gel or activated carbon. Isotherms and enthalpies of adsorption curves of dichlorodifluoromethane (R12), chlorodifluoromethane (R22), and chloropentafluoroethane (R115) on three different activated carbons have been obtained at 303 K and at pressures to 602 kPa.

  18. Preparation and characterization of activated carbon from sugarcane bagasse by physical activation with CO2 gas

    NASA Astrophysics Data System (ADS)

    Bachrun, Sutrisno; AyuRizka, Noni; Annisa, SolichaHidayat; Arif, Hidayat

    2016-01-01

    A series of experiments have been conducted to study the effects of different carbonization temperatures (400, 600, and 800oC) on characteristics of porosity in activated carbon derived from carbonized sugarcane bagassechar at activation temperature of 800oC. The results showed that the activated carbon derived from high carbonized temperature of sugarcane bagassechars had higher BET surface area, total volume, micropore volume and yield as compared to the activated carbon derived from low carbonized temperature. The BET surface area, total volume and micropore volume of activated carbon prepared from sugarcane bagassechars obtained at 800oC of carbonized temperature and activation time of 120 min were 661.46m2/g, 0.2455cm3/g and 0.1989cm3/g, respectively. The high carbonization temperature (800oC) generated a highly microporous carbonwith a Type-I nitrogen adsorption isotherm, while the low carbonization temperature (400 and 600oC) generated a mesoporous one with an intermediate between types I and IInitrogen adsorption isotherm.

  19. Carbon Nanotube Materials for Substrate Enhanced Control of Catalytic Activity

    SciTech Connect

    Heben, M.; Dillon, A. C.; Engtrakul, C.; Lee, S.-H.; Kelley, R. D.; Kini, A. M.

    2007-05-01

    Carbon SWNTs are attractive materials for supporting electrocatalysts. The properties of SWNTs are highly tunable and controlled by the nanotube's circumferential periodicity and their surface chemistry. These unique characteristics suggest that architectures constructed from these types of carbon support materials would exhibit interesting and useful properties. Here, we expect that the structure of the carbon nanotube support will play a major role in stabilizing metal electrocatalysts under extreme operating conditions and suppress both catalyst and support degradation. Furthermore, the chemical modification of the carbon nanotube surfaces can be expected to alter the interface between the catalyst and support, thus, enhancing the activity and utilization of the electrocatalysts. We plan to incorporate discrete reaction sites into the carbon nanotube lattice to create intimate electrical contacts with the catalyst particles to increase the metal catalyst activity and utilization. The work involves materials synthesis, design of electrode architectures on the nanoscale, control of the electronic, ionic, and mass fluxes, and use of advanced optical spectroscopy techniques.

  20. Synthesis of a high-yield activated carbon by air gasification of macadamia nut shell charcoal

    SciTech Connect

    Dai, X.; Antal, M.J. Jr.

    1999-09-01

    Macadamia nut shell charcoal was heated in an inert environment to temperatures above 1000 K (carbonized), reacted with oxygen (Po{sub 2} = 2.68--11.3 kPa) at temperatures between 525 and 586 K (oxygenated), and heated again in an inert environment to temperatures above 1000 K (activated) to produce an activated carbon. Carbons produced by this process possess surface areas and iodine numbers in the range of 400--550. Overall yields of these carbons (based on the dry, raw macadamia nut shell feed) ranged from 24 to 30 wt %. Under the conditions employed in this work, the rates of chemisorption and gasification were not mass transfer limited. Initially, the gasification reaction was first-order with respect to oxygen concentration but became independent of oxygen concentration as the surface sites of the carbon became saturated with oxygen.

  1. Stretchable carbon nanosprings production by a catalytic growth process.

    PubMed

    Vaudreuil, Sbastien; Bousmina, Mosto

    2009-08-01

    Due to their peculiar electromagnetic and mechanical properties, helical carbon nanotubes (HCNT) have important potential applications in micro and nanoelectromechanical fields where they can be used as springs, magnetic field detectors, electromagnets, inductors and actuators. We report here the synthesis of carbon nanosprings through a non-classical catalytic growth process using a nanoporous support, where the regular array of openings allows the control of the diameter and coil pitch of the nanosprings. Exposition of such carbon nanosprings to a laser beam beyond an energy threshold can induce a permanent deformation characterized by the decoiling of the spring. Such permanent deformation results from an internal stresses relief mechanism, where pentagon-heptagon defect pairs reverting back to hexagon rings reduce the curvature of the coiled nanotube. This is expected to have important potential therapeutic applications in which carbon nanosprings can be located specifically in artery channels to remove fatty substances. They can also be located within cancer cells through specific interactions, after which the cells would be destroyed through the use of a more energetic but not harmful laser light. Such energy application is expected to fragment HCNT into digestible carbon for assimilation by the human body. PMID:19928164

  2. Water vapor adsorption on activated carbon preadsorbed with naphtalene.

    PubMed

    Zimny, T; Finqueneisel, G; Cossarutto, L; Weber, J V

    2005-05-01

    The adsorption of water vapor on a microporous activated carbon derived from the carbonization of coconut shell has been studied. Preadsorption of naphthalene was used as a tool to determine the location and the influence of the primary adsorbing centers within the porous structure of active carbon. The adsorption was studied in the pressure range p/p0=0-0.95 in a static water vapor system, allowing the investigation of both kinetic and equilibrium experimental data. Modeling of the isotherms using the modified equation of Do and Do was applied to determine the effect of preadsorption on the mechanism of adsorption. PMID:15797395

  3. REMOVAL OF ORGANIC POLLUTANTS FROM SUBCRITICAL WATER WITH ACTIVATED CARBON

    SciTech Connect

    Steven B. Hawthorne; Arnaud J. Lagadec

    1999-08-01

    The Energy & Environmental Research Center (EERC) has demonstrated that controlling the temperature (and to a lesser extent, the pressure) of water can dramatically change its ability to extract organics and inorganics from matrices ranging from soils and sediments to waste sludges and coal. The dielectric constant of water can be changed from about 80 (a very polar solvent) to <5 (similar to a nonpolar organic solvent) by controlling the temperature (from ambient to about 400 C) and pressure (from about 5 to 350 bar). The EERC has shown that hazardous organic pollutants such as pesticides, PACS (polycyclic aromatic hydrocarbons), and PCBs (polychlorinated biphenyls) can be completely removed from soils, sludges, and sediments at temperatures (250 C) and pressures (<50 atm) that are much milder than typically used for supercritical water processes (temperature >374 C, pressure >221 atm). In addition, the process has been demonstrated to be particularly effective for samples containing very high levels of contaminants (e.g., part per thousand). Current projects include demonstrating the subcritical water remediation process at the pilot scale using an 8-liter system constructed under separate funding during 1997. To date, subcritical water has been shown to be an effective extraction fluid for removing a variety of organic pollutants from soils and sludges contaminated with fossil fuel products and waste products, including PACS from soil (e.g., town gas sites), refining catalysts, and petroleum tank bottom sludges; PCBs from soil and sediments; toxic gasoline components (e.g., benzene) from soil and waste sludge; and phenols from petroleum refinery sludges. The obvious need to clean the wastewater from subcritical water processes led to preliminary experiments with activated carbon placed in line after the extractor. Initial experiments were performed before and after cooling the extractant water (e.g., with water at 200 C and with water cooled to 25 C). Surprisingly, the ability of activated carbon to remove organics from the water is better at a high temperature than at room temperature. These initial results are opposite to those expected from chromatographic theory, since the solubility of the organics is about 100,000-fold higher in the hot water than in ambient water. At present, the physicochemical mechanism accounting for these results is unknown; however, it is possible that the lower surface tension and lower viscosity of subcritical water (compared to water at ambient conditions) greatly increases the available area of the carbon by several orders of magnitude. Regardless of the mechanism involved, the optimal use of activated carbon to clean the wastewater generated from subcritical water remediation will depend on obtaining a better understanding of the controlling parameters. While these investigations focused on the cleanup of wastewater generated from subcritical water remediation, the results also apply to cleanup of any wastewater contaminated with nonpolar and moderately polar organics such as wastewaters from coal and petroleum processing.

  4. Production of energy and activated carbon from agri-residue: sunflower seed example.

    PubMed

    Donaldson, Adam A; Kadakia, Parag; Gupta, Murlidhar; Zhang, Zisheng

    2012-09-01

    In this work, a biomass processing facility is designed and simulated for the annual conversion of 77 ktons of sunflower residue into electricity and activated carbon. The residue is initially pyrolized to produce low hydrocarbon gases (35 wt%), bio-oils (30 wt%), and char (35 wt%). The gases and bio-oils are separated and combusted to generate high pressure steam, electricity, and steam for conversion of char into activated carbon. Assuming 35% of the char's mass is lost during activation, the proposed process produces 15.6 ktons activated carbon and 5.5 ktons ash annually, while generating 10.2 MW of electricity. Economic analysis of the proposed facility yielded capital costs of $31.64 million, annual operating costs of $31.58 million, and a yearly gross revenue of $38.9 million. A discounted payback period of 6.1 years was determined for the current design, extending to 10 years if the facility were operated at 75% capacity. While the proposed process appears to be economically viable, profitability is highly sensitive to the selling price of electricity and activated carbon, highlighting the need for additional research into the pyrolysis reactor design, char/ash separation techniques, and the quality of activated carbon obtained using char from sunflower residue pyrolysis. PMID:21938425

  5. Benign reduction of carbon nanotube agglomerates using a supercritical carbon dioxide process

    NASA Astrophysics Data System (ADS)

    Quigley, John P.; Herrington, Kevin; Bortner, Michael; Baird, Donald G.

    2014-09-01

    A method was developed to deagglomerate commercially available multi-walled carbon nanotube (MWCNT) bundles while maintaining the carbon nanotube aspect ratio. The process utilizes the rapid expansion of a supercritical carbon dioxide/MWCNT mixture to separate large primary carbon nanotube agglomerates. High levels of deagglomeration of Baytubes® C 150 P and Nanocyl™ NC-7000 MWCNT bundles were observed on the macroscale and nanoscale, resulting in 30-fold and 50-fold decreases in bulk density, respectively, with median agglomerate sizes <8 μm in diameter. These results were obtained while retaining the aspect ratio of the as-received nanomaterial, irrespective of the MWCNT agglomerate morphology. It was found that a temperature and pressure of 40 °C and 7.86 MP resulted in maximum deagglomeration without damage to the MWCNTs. Thermodynamic principles were applied to describe the effect of processing variables on the efficiency of the deagglomeration. These results suggest that combining this process with a composite processing step, such as melt compounding, will result in nanocomposites with enhanced electrical properties.

  6. Process for preparing tapes from thermoplastic polymers and carbon fibers

    NASA Technical Reports Server (NTRS)

    Chung, Tai-Shung (Inventor); Furst, Howard (Inventor); Gurion, Zev (Inventor); McMahon, Paul E. (Inventor); Orwoll, Richard D. (Inventor); Palangio, Daniel (Inventor)

    1986-01-01

    The instant invention involves a process for use in preparing tapes or rovings, which are formed from a thermoplastic material used to impregnate longitudinally extended bundles of carbon fibers. The process involves the steps of (a) gas spreading a tow of carbon fibers; (b) feeding the spread tow into a crosshead die; (c) impregnating the tow in the die with a thermoplastic polymer; (d) withdrawing the impregnated tow from the die; and (e) gas cooling the impregnated tow with a jet of air. The crosshead die useful in the instant invention includes a horizontally extended, carbon fiber bundle inlet channel, means for providing melted polymer under pressure to the die, means for dividing the polymeric material flowing into the die into an upper flow channel and a lower flow channel disposed above and below the moving carbon fiber bundle, means for applying the thermoplastic material from both the upper and lower channels to the fiber bundle, and means for withdrawing the resulting tape from the die.

  7. Influence of the precursor metamorphism degree on preparation of nitrogen-enriched activated carbons by ammoxidation and chemical activation of coals

    SciTech Connect

    Piotr Nowicki; Robert Pietrzak; Helena Wachowska

    2009-04-15

    The paper presents results of a study on obtaining N-enriched active carbons from four hard coals with different degree of metamorphism. The starting materials were carbonized, activated with KOH, and ammoxidized by a mixture of ammonia and air at the ratio 1:3 at 300 and 350{sup o}C, at each stage of the active carbon production. The efficiency of ammoxidation was found to depend on the degree of metamorphism of the precursor, the stage of processing at which ammoxidation is performed, and the temperature of this process. Ammoxidation of the active carbon led to a decrease in their surface area and pore volume, whereas that performed both at the stage of the precursor and the carbonizate brought improvement of textural parameters of the active carbons obtained. The sequence of the carbonization, activation, and ammoxidation processes had a significant effect on the acid-base character of the active carbon samples obtained. The majority of the active carbons modified at the stage of precursor and carbonizate showed considerable prevalence of surface acidic groups, whereas the samples ammoxidized after activation showed an intermediate acidic-basic character of the surface. 25 refs., 4 figs., 9 tabs.

  8. Carbon-Carbon Bond Cleavage in Activation of the Prodrug Nabumetone

    PubMed Central

    Varfaj, Fatbardha; Zulkifli, Siti N. A.; Park, Hyoung-Goo; Challinor, Victoria L.; De Voss, James J.

    2014-01-01

    Carbon-carbon bond cleavage reactions are catalyzed by, among others, lanosterol 14-demethylase (CYP51), cholesterol side-chain cleavage enzyme (CYP11), sterol 17β-lyase (CYP17), and aromatase (CYP19). Because of the high substrate specificities of these enzymes and the complex nature of their substrates, these reactions have been difficult to characterize. A CYP1A2-catalyzed carbon-carbon bond cleavage reaction is required for conversion of the prodrug nabumetone to its active form, 6-methoxy-2-naphthylacetic acid (6-MNA). Despite worldwide use of nabumetone as an anti-inflammatory agent, the mechanism of its carbon-carbon bond cleavage reaction remains obscure. With the help of authentic synthetic standards, we report here that the reaction involves 3-hydroxylation, carbon-carbon cleavage to the aldehyde, and oxidation of the aldehyde to the acid, all catalyzed by CYP1A2 or, less effectively, by other P450 enzymes. The data indicate that the carbon-carbon bond cleavage is mediated by the ferric peroxo anion rather than the ferryl species in the P450 catalytic cycle. CYP1A2 also catalyzes O-demethylation and alcohol to ketone transformations of nabumetone and its analogs. PMID:24584631

  9. Catalytic ozonation of p-chlorobenzoic acid by activated carbon and nickel supported activated carbon prepared from petroleum coke.

    PubMed

    Li, Xukai; Zhang, Qiuyun; Tang, Lili; Lu, Ping; Sun, Fengqiang; Li, Laisheng

    2009-04-15

    The aim of this research was to investigate catalytic activity of petroleum coke, activated carbon (AC) prepared from this material, Ni supported catalyst on activated carbon (Ni/AC) in the ozonation of aqueous phase p-chlorobenzoic acid (p-CBA). Activated carbon and Ni/AC catalyst were characterized by XRD and SEM. The presence of petroleum coke did not improve the degradation of p-CBA compared to ozonation alone, but it was advantageous for p-CBA mineralization (total organic carbon, TOC, reduction), indicating the generation of highly oxidant species (*OH) in the medium. The presence of either activated carbon or Ni/AC considerably improves TOC removal during p-CBA ozonation. Ni/AC catalyst shows the better catalytic activity and stability based on five repeated tests during p-CBA ozonation. During the ozonation (50 mg/h ozone flow rate) of a 10 mg/L p-CBA (pH 4.31), it can be more mineralized in the presence of Ni/AC catalyst (5.0 g/L), TOC removal rate is over 60% in 60 min, 43% using activated carbon as catalyst, only 30% with ozonation alone. PMID:18667273

  10. The Formation of Carbon Nanofibers on Powdered Activated Carbon Impregnated with Nickel

    NASA Astrophysics Data System (ADS)

    Ahmed, Y. M.; Al-Mamun, A. A.; Muyibi, S. A.; Al-Khatib, M. F. R.; Jameel, A. T.; AlSaadi, M. A.

    2009-06-01

    In the present work, the production and characterization of carbon nanofibers (CNFs) composite is reported. Carbon nanofibers (CNF) were produced on powdered activated carbon PAC—impregnated with nickel—by Chemical Vapor Deposition (CVD) of a hydrocarbon in the presence of hydrogen at ˜780° C. The flow rates of carbon source and hydrogen were fixed. The CNFs were formed directly over the impregnated AC. Variable weight percentage ratios of the catalyst salt (Ni+2) were used for the impregnation (1, 3, 5, 7 and 9%, respectively). The product displays a relatively high surface area, essentially constituted by the external surface, and the absence of the bottled pores encountered with activated carbon. FSEM, TEM and TGA were used for the characterization of the product.

  11. Processing and thermal properties of filament wound carbon-carbon composites for impact shell application

    NASA Astrophysics Data System (ADS)

    Zee, Ralph; Romanoski, Glenn; Gale, H. Shyam; Wang, Hsin

    2001-02-01

    The performance and safety of the radioisotope power source depend in part on the thermal and impact properties of the materials used in the general purpose heat source (GPHS) through the use of an impact shell, thermal insulation and an aeroshell. Results from an earlier study indicate the importance of circumferential fibers to the mechanical properties of cylindrical filament wound carbon-carbon composites for the impact shell application. Based on this study, an investigation was initiated to determine the processing characteristics and the mechanical and thermal response of three filament wound configurations with different percentages of circumferential fibers: 50%, 66% and 80%. The performs were fabricated using a 3-D filament winding machine followed by five cycles of resin impregnation and carbonization. In this paper, the processing sequence and the resulting microstructures of the composites will be described. The thermal conductivity values of the composites as a function of fiber configuration and density will be discussed. These results will be compared with the fine-weave pierced-fabric (FWPF) material and carbon-bonded carbon-fiber insulation. Finally, the relevance of the new configurations for applications in the general purpose heat source (GPHS) will also be inferred. .

  12. Nonclassical activation of carbon monoxide by organoactinides

    SciTech Connect

    Marks, T.J.; Manriquez, J.M.; Fagan, P.J.; Day, V.W.; Day, C.S.; Vollmer, S.H.

    1980-01-01

    This article reviews recent results on the carbonylation chemistry of bis(pentamethylcyclopentadienyl) thorium and uranium hydrocarbyl and dialkylamide complexes. Facile migratory insertion of carbon monoxide into metal-carbon and metal-nitrogen bonds is observed. In several cases bihaptoacyl and bihaptocarbamoyl complexes were isolated and characterized by single crystal x-ray diffraction. The great strength of the metal-oxygen bonding in these species is evident in metrical and spectral data, as well as in the reaction chemistry, which is decidedly alkoxycarbene-like. In the case of the bis(pentamethylcyclopentadienyl) actinide dialkyls, the final carbonylation products are C-C coupled cis-1,2-enediolate complexes, while for the corresponding bis(dialkylamides), the products are bis(carbamoyl) species. Both types of compound have been characterized by x-ray diffraction. The carbon monoxide chemistry observed here may be of relevance to mechanistic discussions of catalytic CO reduction, especially that involving actinide oxide or actinide oxide supported catalysts.

  13. A sustainable route for the preparation of activated carbon and silica from rice husk ash.

    PubMed

    Liu, Yan; Guo, Yupeng; Zhu, Yanchao; An, Dongmin; Gao, Wei; Wang, Zhuo; Ma, Yuejia; Wang, Zichen

    2011-02-28

    An environmentally friendly and economically effective process to produce silica and activated carbon form rice husk ask simultaneously has been developed in this study. An extraction yield of silica of 72-98% was obtained and the particle size was 40-50 nm. The microstructures of the as-obtained silica powders were characterized by X-ray diffraction (XRD) and infrared spectra (IR). The surface area, iodine number and capacitance value of activated carbon could achieve 570 m(2)/g, 1708 mg/g, 180 F/g, respectively. In the whole synthetic procedure, the wastewater and the carbon dioxide were collected and reutilized. The recovery rate of sodium carbonate was achieved 92.25%. The process is inexpensive, sustainable, environmentally friendly and suitable for large-scale production. PMID:21194835

  14. Influence of surface properties on the mechanism of H2S removal by alkaline activated carbons.

    PubMed

    Yan, Rong; Chin, Terence; Ng, Yuen Ling; Duan, Huiqi; Liang, David Tee; Tay, Joo Hwa

    2004-01-01

    Alkaline activated carbons are widely used as adsorbents of hydrogen sulfide (H2S), one of the major odorous compounds arising from sewage treatment facilities. Although a number of studies have explored the effects of various parameters, mechanisms of H2S adsorption by alkaline carbons are not yet fully understood. The major difficulty seems to lie in the fact that little is known with certainty about the predominant reactions occurring on the carbon surface. In this study, the surface properties of alkaline activated carbons were systematically investigated to further exploit and better understand the mechanisms of H2S adsorption by alkaline activated carbons. Two commercially available alkaline activated carbons and their representative exhausted samples (8 samples collected at different height of the column after H2S breakthrough tests) were studied. The 8 portions of the exhausted carbon were used to represent the H2S/carbon reaction process. The surface properties of both the original and the exhausted carbons were characterized using the sorption of nitrogen (BET test), surface pH, Boehm titration, thermal and FTIR analysis. Porosity and surface area provide detailed information about the pore structure of the exhausted carbons with respect to the reaction extent facilitating the understanding of potential pore blockages. Results of Boehm titration and FTIR both demonstrate the significant effects of surface functional groups, and identification of oxidation products confirmed the different mechanisms involved with the two carbons. From the DTG curves of thermal analysis, two well-defined peaks representing two products of surface reactions (i.e., sulfur and sulfuric acid) were observed from the 8 exhausted portions with gradually changing patterns coinciding with the extent of the reaction. Surface pH values of the exhausted carbons show a clear trend of pH drop along the reaction extent, while pH around 2 was observed for the bottom of the bed indicating sulfuric acid as the predominant products. Although both carbons are coal-based and of KOH impregnated type, performances of different carbons differ significantly. A correlation is well established to link the reaction extent with various surface properties. In summary, not only the homogeneous alkali impregnation and physical porosity but also the carbon surface chemistry are significant factors influencing the performances of alkaline activated carbons as H2S adsorbents. PMID:14740753

  15. On the interest of carbon-coated plasma reactor for advanced gate stack etching processes

    SciTech Connect

    Ramos, R.; Cunge, G.; Joubert, O.

    2007-03-15

    In integrated circuit fabrication the most wide spread strategy to achieve acceptable wafer-to-wafer reproducibility of the gate stack etching process is to dry-clean the plasma reactor walls between each wafer processed. However, inherent exposure of the reactor walls to fluorine-based plasma leads to formation and accumulation of nonvolatile fluoride residues (such as AlF{sub x}) on reactor wall surfaces, which in turn leads to process drifts and metallic contamination of wafers. To prevent this while keeping an Al{sub 2}O{sub 3} reactor wall material, a coating strategy must be used, in which the reactor is coated by a protective layer between wafers. It was shown recently that deposition of carbon-rich coating on the reactor walls allows improvements of process reproducibility and reactor wall protection. The authors show that this strategy results in a higher ion-to-neutral flux ratio to the wafer when compared to other strategies (clean or SiOCl{sub x}-coated reactors) because the carbon walls load reactive radical densities while keeping the same ion current. As a result, the etching rates are generally smaller in a carbon-coated reactor, but a highly anisotropic etching profile can be achieved in silicon and metal gates, whose etching is strongly ion assisted. Furthermore, thanks to the low density of Cl atoms in the carbon-coated reactor, silicon etching can be achieved almost without sidewall passivation layers, allowing fine critical dimension control to be achieved. In addition, it is shown that although the O atom density is also smaller in the carbon-coated reactor, the selectivity toward ultrathin gate oxides is not reduced dramatically. Furthermore, during metal gate etching over high-k dielectric, the low level of parasitic oxygen in the carbon-coated reactor also allows one to minimize bulk silicon reoxidation through HfO{sub 2} high-k gate dielectric. It is then shown that the BCl{sub 3} etching process of the HfO{sub 2} high-k material is highly selective toward the substrate in the carbon-coated reactor, and the carbon-coating strategy thus allows minimizing the silicon recess of the active area of transistors. The authors eventually demonstrate that the carbon-coating strategy drastically reduces on-wafer metallic contamination. Finally, the consumption of carbon from the reactor during the etching process is discussed (and thus the amount of initial deposit that is required to protect the reactor walls) together with the best way of cleaning the reactor after a silicon etching process.

  16. Detection of single ion channel activity with carbon nanotubes

    PubMed Central

    Zhou, Weiwei; Wang, Yung Yu; Lim, Tae-Sun; Pham, Ted; Jain, Dheeraj; Burke, Peter J.

    2015-01-01

    Many processes in life are based on ion currents and membrane voltages controlled by a sophisticated and diverse family of membrane proteins (ion channels), which are comparable in size to the most advanced nanoelectronic components currently under development. Here we demonstrate an electrical assay of individual ion channel activity by measuring the dynamic opening and closing of the ion channel nanopores using single-walled carbon nanotubes (SWNTs). Two canonical dynamic ion channels (gramicidin A (gA) and alamethicin) and one static biological nanopore (?-hemolysin (?-HL)) were successfully incorporated into supported lipid bilayers (SLBs, an artificial cell membrane), which in turn were interfaced to the carbon nanotubes through a variety of polymer-cushion surface functionalization schemes. The ion channel current directly charges the quantum capacitance of a single nanotube in a network of purified semiconducting nanotubes. This work forms the foundation for a scalable, massively parallel architecture of 1d nanoelectronic devices interrogating electrophysiology at the single ion channel level. PMID:25778101

  17. DEVELOPMENT OF CONTINUOUS SOLVENT EXTRACTION PROCESSES FOR COAL DERIVED CARBON PRODUCTS

    SciTech Connect

    Elliot B. Kennel; Stephen P. Carpenter; Dady Dadyburjor; Manoj Katakdaunde; Liviu Magean; Peter G. Stansberry; Alfred H. Stiller; John W. Zondlo

    2005-06-08

    The purpose of this DOE-funded effort is to develop continuous processes for solvent extraction of coal for the production of carbon products. These carbon products include materials used in metals smelting, especially in the aluminum and steel industries, as well as porous carbon structural material referred to as ''carbon foam'' and carbon fibers. During this reporting period, efforts have focused on the development of continuous processes for hydrogenation as well as continuous production of carbon foam and coke.

  18. DEVELOPMENT OF CONTINUOUS SOLVENT EXTRACTION PROCESSES FOR COAL DERIVED CARBON PRODUCTS

    SciTech Connect

    Elliot B. Kennel; Stephen P. Carpenter; Dady Dadyburjor; Manoj Katakdaunde; Liviu Magean; Madhavi Nallani-Chakravartula; Peter G. Stansberry; Alfred H. Stiller; John W. Zondlo

    2006-03-27

    The purpose of this DOE-funded effort is to develop continuous processes for solvent extraction of coal for the production of carbon products. These carbon products include materials used in metals smelting, especially in the aluminum and steel industries, as well as porous carbon structural material referred to as ''carbon foam'' and carbon fibers. During this reporting period, efforts have focused on the development of continuous processes for hydrogenation as well as continuous production of carbon foam and coke.

  19. Activated carbon from pyrolysis of brewer's spent grain: Production and adsorption properties.

    PubMed

    Vanreppelen, Kenny; Vanderheyden, Sara; Kuppens, Tom; Schreurs, Sonja; Yperman, Jan; Carleer, Robert

    2014-06-20

    Brewer's spent grain is a low cost residue generated by the brewing industry. Its chemical composition (high nitrogen content 4.35 wt.%, fibres, etc.) makes it very useful for the production of added value in situ nitrogenised activated carbon. The composition of brewer's spent grain revealed high amounts of cellulose (20.8 wt.%), hemicellulose (48.78 wt.%) and lignin (11.3 wt.%). The fat, ethanol extractives and ash accounted for 8.17 wt.%, 4.7 wt.% and 3.2 wt.%, respectively. Different activated carbons were produced in a lab-scale pyrolysis/activation reactor by applying several heat and steam activation profiles on brewer's spent grain. Activated carbon yields from 16.1 to 23.6 wt.% with high N-contents (> 2 wt.%) were obtained. The efficiency of the prepared activated carbons for phenol adsorption was studied as a function of different parameters: pH, contact time and carbon dosage relative to two commercial activated carbons. The equilibrium isotherms were described by the non-linear Langmuir and Freundlich models, and the kinetic results were fitted using the pseudo-first-order model and the pseudo-second-order model. The feasibility of an activated carbon production facility (onsite and offsite) that processes brewer's spent grain for different input feeds is evaluated based on a techno-economic model for estimating the net present value. Even though the model assumptions start from a rather pessimistic scenario, encouraging results for a profitable production of activated carbon using brewer's spent grain are obtained. PMID:25012859

  20. Process for reducing Ramsbottom Carbon Test of short residues

    SciTech Connect

    Eilers, J.; Stork, H.J.

    1984-07-24

    In the preparation of a heavy oil with a low Ramsbottom Carbon Test (RCT) from a long residue by a two-stage process comprising catalytic hydrotreatment followed by solvent deasphalting and recycle of the asphalt to the first stage the catalytic hydrotreatment for RCT reduction in the first stage is carried out at such a severity that the C/sub 4/ - gas production per percent RCT reduction is kept between defined limits.

  1. Computational Tools for Accelerating Carbon Capture Process Development

    SciTech Connect

    Miller, David

    2013-01-01

    The goals of the work reported are: to develop new computational tools and models to enable industry to more rapidly develop and deploy new advanced energy technologies; to demonstrate the capabilities of the CCSI Toolset on non-proprietary case studies; and to deploy the CCSI Toolset to industry. Challenges of simulating carbon capture (and other) processes include: dealing with multiple scales (particle, device, and whole process scales); integration across scales; verification, validation, and uncertainty; and decision support. The tools cover: risk analysis and decision making; validated, high-fidelity CFD; high-resolution filtered sub-models; process design and optimization tools; advanced process control and dynamics; process models; basic data sub-models; and cross-cutting integration tools.

  2. Pedogenetic processes and carbon budgets in soils of Queretaro, Mexico

    NASA Astrophysics Data System (ADS)

    Garca Caldern, Norma Eugenia; Fuentes Romero, Elizabeth; Hernandez Silva, Gilberto

    2014-05-01

    Pedogenetic processes have been investigated in two different physiographic regions of the state of Quertaro in order to assess the carbon budget of soils, looking into the gains and losses of organic and inorganic carbon: In the mountain region of the natural reserve Sierra Gorda (SG) with soils developed on cretaceous argillites and shales under sub-humid temperate to semi-arid conditions, and in the Transmexican Volcanic Belt (TMVB) with soils developed on acid and intermediate igneous rocks under humid temperate climate in the highlands and semi-arid and subhumid subtropical conditions in the lowlands. The analyses of soil organic carbon (SOC) and soil inorganic carbon (SIC) of the SG region, including additional physical, chemical and mineralogical investigations were based on 103 topsoils in an area of 170 km2. The analyses in the TMVB region were based on the profiles of a soil toposequence from high mountainous positions down to the plains of the lowlands. The results show a SOC accumulation from temperate to semi-arid forest environments, based on processes of humification and clay formation including the influence of exchangeable Ca and the quantity and quality of clay minerals. The turnover rates of SOC and SIC depended largely on the rock parent materials, especially the presence of carbonate rocks. Moreover, we found that the SOC content and distribution was clearly depending on land use, decreasing from forests to agricultural land, such as pasture and cropping areas and were lowest under mining sites. The highest SIC pools were found in accumulation horizons of soils under semi-arid conditions. On all investigated sites SOC decreased the mobility of cations and especially that of heavy metals, such as As, Hg, Sb, Pb, and Cd.

  3. [Biogeochemical processes of the major ions and dissolved inorganic carbon in the Guijiang River].

    PubMed

    Tang, Wen-Kui; Tao, Zhen; Gao, Quan-Zhou; Mao, Hai-Ruo; Jiang, Guang-Hui; Jiao, Shu-Lin; Zheng, Xiong-Bo; Zhang, Qian-Zhu; Ma, Zan-Wen

    2014-06-01

    Within the drainage basin, information about natural processes and human activities can be recorded in the chemical composition of riverine water. The analysis of the Guijiang River, the first level tributary of the Xijiang River, demonstrated that the chemical composition of water in the Guijiang River was mainly influenced by the chemical weathering of carbonate rocks within the drainage basin, in which CO2 was the main erosion medium, and that the weathering of carbonate rock by H2SO4 had a remarkable impact on the water chemical composition in the Guijiang River. Precipitation, human activities, the weathering of carbonate rocks and silicate rocks accounted for 2.7%, 6.3%, 72.8% and 18.2% of the total dissolved load, respectively. The stable isotopic compositions of dissolved inorganic carbon (delta13C(DIC)) indicated that DIC in the Guijiang River had been assimilated by the phytoplankton in photosynthesis. The primary production of phytoplankton contributed to 22.3%-30.9% of particulate organic carbon (POC) in the Guijiang River, which implies that phytoplankton can transform DIC into POC by photosynthesis, and parts of POC will sink into the bottom of the river in transit, which leads into the formation of burial organic carbon. PMID:25158483

  4. Micromechanism of sulfurizing activated carbon and its ability to adsorb mercury

    NASA Astrophysics Data System (ADS)

    Wu, Guofang; Xu, Minren; Liu, Qingcai; Yang, Jian; Ma, Dongran; Lu, Cunfang; Lan, Yuanpei

    2013-11-01

    To eliminate mercury from coal-fired flue gas, sulfurization of carbons has been found to be the most inexpensive approach to solve the problem of environment contamination by mercury. This study focuses on improving the adsorption capacity of activate carbon loaded with elemental sulfur as an active phase and further use in the removal of mercury vapors from fuel gas. In this paper, equipment such as the scanning electron microscope, specific surface area test machine and fluorescence spectrophotometer are employed to study the ability of the S-loaded activated carbon. The results show that unmodified activate carbon has smooth hole surface and uneven distributed hole size. Pore walls of activate carbon modified became rougher and the hole size distribution is asymmetrical. Sulfur is uniformly distributed and is mainly bonded on the surface of the skeleton of activate carbon. In addition, a small amount of granular sulfur was loaded on the surface of the pore walls. Higher temperature creates smaller pore size and larger microporous volume. Improving the process temperature is conducive to the development of micropore and the distribution of sulfur, and a larger amount of small molecular weight sulfur are created, which is helpful in the removal of HgO through chemical adsorption. The optimum modification temperature and holding time is 550 C and 60 min, which creates the adsorbents of the max absorption capability of 1227.5 ?g Hg/g.

  5. Effect of combined activation on the preparation of high porous active carbons from granulated post-consumer polyethyleneterephthalate

    NASA Astrophysics Data System (ADS)

    Sych, N. V.; Kartel, N. T.; Tsyba, N. N.; Strelko, V. V.

    2006-09-01

    Activated carbons were prepared from granulated post-consumer PET by combined activation including heat treatment with sulphuric acid (chemical activation) followed by steam activation. The effect of activation time, temperature, impregnation coefficient in the activation process was studied in order to optimize those reception parameters. One of the most important parameter in combined activation of crushed PET was found to be impregnation coefficient. It was defined that the optimal impregnation coefficient is equal 28%. Activation temperature is another variability which has a significant effect on the pore volume evolution. The increasing of activation temperature enhances the surface area and pore volumes of active carbons. The yield of final product which composes of nearly 15% is the factor limited the activation temperature above 800 C. Textural characteristics of the samples were carried out by performing N 2 adsorption isotherm at -196 C. The obtained active carbons were mainly micro- and mesoporous and with BET apparent surface areas of up to 1030 m 2/g. The adsorption capacity on methylene blue reaches 1.0 mmol/g, the sorption activity on iodine comes to 77%.

  6. Complete reaction mechanisms of mercury oxidation on halogenated activated carbon.

    PubMed

    Rungnim, Chompoonut; Promarak, Vinich; Hannongbua, Supa; Kungwan, Nawee; Namuangruk, Supawadee

    2016-06-01

    The reaction mechanisms of mercury (Hg) adsorption and oxidation on halogenated activated carbon (AC) have been completely studied for the first time using density functional theory (DFT) method. Two different halogenated AC models, namely X-AC and X-AC-X (X=Cl, Br, I), were adopted. The results revealed that HgX is found to be stable-state on the AC edge since its further desorption from the AC as HgX, or further oxidation to HgX2, are energetically unfavorable. Remarkably, the halide type does not significantly affect the Hg adsorption energy but it strongly affects the activation energy barrier of HgX formation, which obviously increases in the order HgIBr-AC>Cl-AC. Thus, the study of the complete reaction mechanism is essential because the adsorption energy can not be used as a guideline for the rational material design in the halide impregnated AC systems. The activation energy is an important descriptor for the predictions of sorbent reactivity to the Hg oxidation process. PMID:26943019

  7. Engineering catalytic activity via ion beam bombardment of catalyst supports for vertically aligned carbon nanotube growth

    NASA Astrophysics Data System (ADS)

    Islam, A. E.; Nikolaev, P.; Amama, P. B.; Zakharov, D.; Sargent, G.; Saber, S.; Huffman, D.; Erford, M.; Semiatin, S. L.; Stach, E. A.; Maruyama, B.

    2015-09-01

    Carbon nanotube growth depends on the catalytic activity of metal nanoparticles on alumina or silica supports. The control on catalytic activity is generally achieved by variations in water concentration, carbon feed, and sample placement on a few types of alumina or silica catalyst supports obtained via thin film deposition. We have recently expanded the choice of catalyst supports by engineering inactive substrates like c-cut sapphire via ion beam bombardment. The deterministic control on the structure and chemistry of catalyst supports obtained by tuning the degree of beam-induced damage have enabled better regulation of the activity of Fe catalysts only in the ion beam bombarded areas and hence enabled controllable super growth of carbon nanotubes. A wide range of surface characterization techniques were used to monitor the catalytically active surface engineered via ion beam bombardment. The proposed method offers a versatile way to control carbon nanotube growth in patterned areas and also enhances the current understanding of the growth process. With the right choice of water concentration, carbon feed and sample placement, engineered catalyst supports may extend the carbon nanotube growth yield to a level that is even higher than the ones reported here, and thus offers promising applications of carbon nanotubes in electronics, heat exchanger, and energy storage.

  8. Engineering catalytic activity via ion beam bombardment of catalyst supports for vertically aligned carbon nanotube growth

    DOE PAGESBeta

    Islam, A. E.; Zakharov, D.; Stach, E. A.; Nikoleav, P.; Amama, P. B.; Sargent, G.; Saber, S.; Huffman, D.; Erford, M.; Semiatin, S. L.; et al

    2015-09-16

    Carbon nanotube growth depends on the catalytic activity of metal nanoparticles on alumina or silica supports. The control on catalytic activity is generally achieved by variations in water concentration, carbon feed, and sample placement on a few types of alumina or silica catalyst supports obtained via thin film deposition. We have recently expanded the choice of catalyst supports by engineering inactive substrates like c-cut sapphire via ion beam bombardment. The deterministic control on the structure and chemistry of catalyst supports obtained by tuning the degree of beam-induced damage have enabled better regulation of the activity of Fe catalysts only inmore » the ion beam bombarded areas and hence enabled controllable super growth of carbon nanotubes. A wide range of surface characterization techniques were used to monitor the catalytically active surface engineered via ion beam bombardment. The proposed method offers a versatile way to control carbon nanotube growth in patterned areas and also enhances the current understanding of the growth process. As a result, with the right choice of water concentration, carbon feed and sample placement, engineered catalyst supports may extend the carbon nanotube growth yield to a level that is even higher than the ones reported here, and thus offers promising applications of carbon nanotubes in electronics, heat exchanger, and energy storage.« less

  9. Engineering catalytic activity via ion beam bombardment of catalyst supports for vertically aligned carbon nanotube growth

    SciTech Connect

    Islam, A. E.; Zakharov, D.; Stach, E. A.; Nikoleav, P.; Amama, P. B.; Sargent, G.; Saber, S.; Huffman, D.; Erford, M.; Semiatin, S. L.; Maruyama, B.

    2015-09-16

    Carbon nanotube growth depends on the catalytic activity of metal nanoparticles on alumina or silica supports. The control on catalytic activity is generally achieved by variations in water concentration, carbon feed, and sample placement on a few types of alumina or silica catalyst supports obtained via thin film deposition. We have recently expanded the choice of catalyst supports by engineering inactive substrates like c-cut sapphire via ion beam bombardment. The deterministic control on the structure and chemistry of catalyst supports obtained by tuning the degree of beam-induced damage have enabled better regulation of the activity of Fe catalysts only in the ion beam bombarded areas and hence enabled controllable super growth of carbon nanotubes. A wide range of surface characterization techniques were used to monitor the catalytically active surface engineered via ion beam bombardment. The proposed method offers a versatile way to control carbon nanotube growth in patterned areas and also enhances the current understanding of the growth process. As a result, with the right choice of water concentration, carbon feed and sample placement, engineered catalyst supports may extend the carbon nanotube growth yield to a level that is even higher than the ones reported here, and thus offers promising applications of carbon nanotubes in electronics, heat exchanger, and energy storage.

  10. Interactions in the Geo-Biosphere: Processes of Carbonate Precipitation in Microbial Mats

    NASA Astrophysics Data System (ADS)

    Dupraz, C.; Visscher, P. T.

    2009-12-01

    Microbial communities are situated at the interface between the biosphere, the lithosphere and the hydrosphere. These microbes are key players in the global carbon cycle, where they influence the balance between the organic and inorganic carbon reservoirs. Microbial populations can be organized in microbial mats, which can be defined as organosedimentary biofilms that are dominated by cyanobacteria, and exhibit tight coupling of element cycles. Complex interactions between mat microbes and their surrounding environment can result in the precipitation of carbonate minerals. This process refers as organomineralization sensu lato' (Dupraz et al. in press), which differs from biomineralization (e.g., in shells and bones) by lacking genetic control on the mineral product. Organomineralization can be: (1) active, when microbial metabolic reactions are responsible for the precipitation (biologically-induced mineralization) or (2) passive, when mineralization within a microbial organic matrix is environmentally driven (e.g., through degassing or desiccation) (biologically-influenced mineralization). Studying microbe-mineral interactions is essential to many emerging fields of the biogeoscience, such as the study of life in extreme environments (e.g, deep biosphere), the origin of life, the search for traces of extraterrestrial life or the seek of new carbon sink. This research approach combines sedimentology, biogeochemistry and microbiology. Two tightly coupled components that control carbonate organomineralization s.l.: (1) the alkalinity engine and (2) the extracellular organic matter (EOM), which is ultimately the location of mineral nucleation. Carbonate alkalinity can be altered both by microbial metabolism and environmental factors. In microbial mats, the net accumulation of carbonate minerals often reflect the balance between metabolic activities that consume/produce CO2 and/or organic acids. For example, photosynthesis and sulfate reduction will increase carbonate alkalinity and the potential of precipitation, whereas aerobic respiration and sulfide oxidation will promote carbonate dissolution. The EOM is composed of two main carbon pools: the high molecular weight extracellular polymeric substances (EPS) and the low molecular weight organic carbon compounds (LMW-OC). Both pools play a critical role in carbonate precipitation by providing Ca2+ and CO32- as well as a nucleation template for mineral growth. EOM contains several negatively charged functional groups, which, depending on the pH, can be deprotonated (each group has unique pK value(s)) and, thus, bind cations. This binding capacity can deplete the surrounding environment of cations (e.g., Ca2+, Mg2+) and, thus, inhibits carbonate precipitation. Therefore, organomineralization is only possible if the inhibition potential is reduced through (1) oversaturation of the EOM binding capacity or (2) EOM degradation.

  11. Removal of congo red using activated carbon and its regeneration.

    PubMed

    Purkait, M K; Maiti, A; DasGupta, S; De, S

    2007-06-25

    Activated carbon is used for the removal of colored toxic congo red dye. The effects of different operating conditions like, initial dye concentration, contact time, pH and temperature are studied for adsorption of congo red by a known amount of activated carbon (1.0g/L) under stirred batch condition. The zero point of charge of the activated carbon is found about 6.6. About 90% dye is removed for initial concentration of 50 and 100mg/L, it is about 80% at pH 7.0. Maximum adsorption (about 100%) of dye is observed at pH 2.0 for the concentration range studied here. Freundlich isotherm is found to fit the equilibrium data more adequately. Pseudo second order kinetic model explain successfully the kinetic data. The surfactant enhanced carbon regeneration (SECR) technique using both cationic and anionic surfactants is adopted for the regeneration of spent carbon by desorbing the dye. A kinetic model for dye desorption from the commercial activated carbon (CAC) is also proposed. Anionic surfactants show better performance than the cationic ones. Efficiency of dye desorption using surfactants is also compared with the desorption using pH change. PMID:17178190

  12. Activated Carbon Composites for Air Separation

    SciTech Connect

    Contescu, Cristian I; Baker, Frederick S; Tsouris, Costas; McFarlane, Joanna

    2008-03-01

    In continuation of the development of composite materials for air separation based on molecular sieving properties and magnetic fields effects, several molecular sieve materials were tested in a flow system, and the effects of temperature, flow conditions, and magnetic fields were investigated. New carbon materials adsorbents, with and without pre-loaded super-paramagnetic nanoparticles of Fe3O4 were synthesized; all materials were packed in chromatographic type columns which were placed between the poles of a high intensity, water-cooled, magnet (1.5 Tesla). In order to verify the existence of magnetodesorption effect, separation tests were conducted by injecting controlled volumes of air in a flow of inert gas, while the magnetic field was switched on and off. Gas composition downstream the column was analyzed by gas chromatography and by mass spectrometry. Under the conditions employed, the tests confirmed that N2 - O2 separation occurred at various degrees, depending on material's intrinsic properties, temperature and flow rate. The effect of magnetic fields, reported previously for static conditions, was not confirmed in the flow system. The best separation was obtained for zeolite 13X at sub-ambient temperatures. Future directions for the project include evaluation of a combined system, comprising carbon and zeolite molecular sieves, and testing the effect of stronger magnetic fields produced by cryogenic magnets.

  13. Preparation of activated carbon from wet sludge by electrochemical-NaClO activation.

    PubMed

    Miao, Chen; Ye, Caihong; Zhu, Tianxing; Lou, Ziyang; Yuan, Haiping; Zhu, Nanwen

    2014-01-01

    Activated carbon (AC) from sludge is one potential solution for sewage sludge disposal, while the drying sludge is cost and time consuming for preparation. AC preparation from the wet sludge with electrochemical-NaClO activation was studied in this work. Three pretreatment processes, i.e. chemical activation, electrolysis and electrochemical-reagent reaction, were introduced to improve the sludge-derived AC properties, and the optimum dosage of reagent was tested from the 0.1:1 to 1:1 (mass rate, reagent:dried sludge). It was shown that the electrochemical-NaClO preparation is the best method under the test conditions, in which AC has the maximum Brunauer, Emmett and Teller area of 436 m/g at a mass ratio of 0.7. Extracellular polymeric substances in sludge can be disintegrated by electrochemical-NaClO pretreatment, with a disintegration degree of more than 45%. The percentage of carbon decreased from 34.16 to 8.81 after treated by electrochemical-NaClO activation. Fourier transform infrared spectra showed that a strong C-Cl stretching was formed in electrochemical-NaClO prepared AC. The maximum adsorption capacity of AC reaches 109 mg/g on MB adsorption experiment at pH 10 and can be repeated for three times with high removal efficiency after regeneration. PMID:25176302

  14. 40 CFR 458.40 - Applicability; description of the carbon black lamp process subcategory.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... carbon black lamp process subcategory. 458.40 Section 458.40 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) EFFLUENT GUIDELINES AND STANDARDS CARBON BLACK MANUFACTURING POINT SOURCE CATEGORY Carbon Black Lamp Process Subcategory 458.40 Applicability; description of the carbon black...

  15. 40 CFR 458.30 - Applicability; description of the carbon black channel process subcategory.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... carbon black channel process subcategory. 458.30 Section 458.30 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) EFFLUENT GUIDELINES AND STANDARDS CARBON BLACK MANUFACTURING POINT SOURCE CATEGORY Carbon Black Channel Process Subcategory 458.30 Applicability; description of the carbon...

  16. 40 CFR 458.40 - Applicability; description of the carbon black lamp process subcategory.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... carbon black lamp process subcategory. 458.40 Section 458.40 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) EFFLUENT GUIDELINES AND STANDARDS CARBON BLACK MANUFACTURING POINT SOURCE CATEGORY Carbon Black Lamp Process Subcategory 458.40 Applicability; description of the carbon black...

  17. 40 CFR 458.10 - Applicability; description of the carbon black furnace process subcategory.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... carbon black furnace process subcategory. 458.10 Section 458.10 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) EFFLUENT GUIDELINES AND STANDARDS CARBON BLACK MANUFACTURING POINT SOURCE CATEGORY Carbon Black Furnace Process Subcategory 458.10 Applicability; description of the carbon...

  18. 40 CFR 458.30 - Applicability; description of the carbon black channel process subcategory.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... carbon black channel process subcategory. 458.30 Section 458.30 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) EFFLUENT GUIDELINES AND STANDARDS CARBON BLACK MANUFACTURING POINT SOURCE CATEGORY Carbon Black Channel Process Subcategory 458.30 Applicability; description of the carbon...

  19. 40 CFR 458.10 - Applicability; description of the carbon black furnace process subcategory.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... carbon black furnace process subcategory. 458.10 Section 458.10 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) EFFLUENT GUIDELINES AND STANDARDS CARBON BLACK MANUFACTURING POINT SOURCE CATEGORY Carbon Black Furnace Process Subcategory 458.10 Applicability; description of the carbon...

  20. Potential application of activated carbon from maize tassel for the removal of heavy metals in water

    NASA Astrophysics Data System (ADS)

    Olorundare, O. F.; Krause, R. W. M.; Okonkwo, J. O.; Mamba, B. B.

    Water-pollution problems worldwide have led to an acute shortage of clean and pure water for both domestic and human consumption. Various technologies and techniques are available for water treatment which includes the use of activated carbon. In this study activated carbons used for the removal of lead (II) ions from water samples were prepared from maize tassels (an agricultural waste residue) which were modified using physical and chemical activation. In the physical activation CO2 was used as the activating agent, while in chemical activation H3PO4 with an impregnation ratio ranging from 1 to 4 was employed. The maize tassel was pyrolysed at different temperatures ranging from 300 C to 700 C in an inert atmosphere for a period of 60 min and activated at 700 C for 30 min. The effects of activation temperature, impregnation ratio and duration were examined. The resultant modified tassels were characterised by measuring their particle-size distribution, porosities, pore volume, and pore-size distribution using scanning electron microscopy (SEM). The activated carbon produced by chemical activation had the highest BET surface area ranging from 623 m2 g-1 to 1 262 m2 g-1. The surface chemistry characteristics of the modified tassels were determined by FT-IR spectroscopy and Boehms titration method. The experimental data proved that properties of activated carbon depend on final temperature of the process, impregnation ratio and duration of the treatment at final temperature. The adsorption studies showed that chemically prepared activated carbon performed better than physically prepared activated carbon.

  1. Porous texture evolution in Nomex-derived activated carbon fibers.

    PubMed

    Villar-Rodil, S; Denoyel, R; Rouquerol, J; Martínez-Alonso, A; Tascón, J M D

    2002-08-01

    In the present work, the textural evolution of a series of activated carbon fibers with increasing burn-off degree, prepared by the pyrolysis and steam activation of Nomex aramid fibers, is followed by measurements of physical adsorption of N(2) (77 K) and CO(2) (273 K) and immersion calorimetry into different liquids (dichloromethane, benzene, cyclohexane). The immersion calorimetry results are discussed in depth, paying special attention to the choice of the reference material. The activated carbon fibers studied possess an essentially homogeneous microporous texture, which suggests that these materials may be applied in gas separation, either directly or with additional CVD treatment. PMID:16290775

  2. Regeneration of granular activated carbon using hydrothermal technology

    SciTech Connect

    Sufnarski, M.D.

    1999-05-01

    The economic feasibility of using granular activated carbon (GAC) to remove organic contaminants from industrial and municipal wastewater is contingent upon its reuse during multiple adsorption-regeneration cycles. The most common process for the regeneration of GAC is the thermal method. Drawbacks associated with thermal regeneration include a 5--10% loss of carbon due to oxidation and attrition, a decrease in adsorption capacity, and high energy costs. The purpose of this study was to investigate the regeneration of GAC using hydrothermal technology. Phenol contaminated and non-contaminated GAC samples were regenerated using supercritical water (411 deg C and 26.2 MPa) with dissolved oxygen concentrations of 0 mg/L, 5 mg/L, and 100 mg/L. For comparative purposes, GAC was regenerated using subcritical water (300 deg C and 12.4 MPa) with a dissolved oxygen concentration of 5 mg/L. Regenerated GAC samples were evaluated in terms of adsorption capacity, BET surface area, pore volume, and average pore size. After four adsorption-regeneration cycles, using supercritical water (SCW) regeneration, the average adsorption capacity of regenerated GAC was found to be 90% of that of virgin GAC. Although a slightly higher adsorption capacity was achieved for regeneration with degassed water, the overall impact of dissolved oxygen was insignificant. The high adsorption capacity achieved for SCW was not observed for subcritical water regeneration. After four adsorption-regeneration cycles, only 67% of the original adsorption capacity was restored. The better results observed for SCW, as compared to subcritical water, were related to two factors. First, the higher regeneration temperatures of SCW resulted in increased thermal desorption. Second, the increased solubility of organic compounds and enhanced mass transfer rates in SCW resulted in a more efficient extraction process.

  3. FENTON-DRIVEN REGENERATION OF GRANULAR ACTIVATED CARBON: A TECHNOLOGY OVERVIEW

    EPA Science Inventory

    A Fenton-driven mechanism for regenerating spent granular activated carbon (GAC) involves the combined, synergistic use of two reliable and well established treatment technologies - adsorption onto activated carbon and Fenton oxidation. During carbon adsorption treatment, enviro...

  4. 40 CFR 60.1820 - How do I monitor the injection rate of activated carbon?

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... activated carbon? If your municipal waste combustion unit uses activated carbon to control dioxins/furans or... dioxins/furans and mercury stack test, determine the average carbon feed rate in kilograms (or pounds)...

  5. Treatment of activated carbon to enhance catalytic activity for reduction of nitric oxide with ammonia

    SciTech Connect

    Ku, B.J.; Rhee, H.K. . Dept. of Chemical Engineering); Lee, J.K.; Park, D. )

    1994-11-01

    Catalytic activity of activated carbon treated with various techniques was examined in a fixed bed reactor for the reduction of nitric oxide with ammonia at 150 C. Activated carbon derived from coconut shell impregnated with an aqueous solution of ammonium sulfate, further treated with sulfuric acid, dried at 120 C, and then heated in an inert gas stream at 400 C, showed the highest catalytic activity within the range of experimental conditions. The enhancement of catalytic activity of modified activated carbon could be attributed to the increase in the amount of oxygen function groups which increased the adsorption site for ammonia. Catalytic activity of activated carbons depended on the surface area and the oxygen content as well.

  6. TOXIC SUBSTANCE REMOVAL IN ACTIVATED SLUDGE AND PAC (POWDERED ACTIVATED CARBON) TREATMENT SYSTEMS

    EPA Science Inventory

    The effectiveness of adding powdered activated carbon to activated sludge systems was evaluated for enhanced removal of specific toxic organic compounds. Nine organic compounds encompassing a range of solubility, volatility, biodegradability, and adsorptive properties were studie...

  7. Copper-Carbon and Aluminum-Carbon Composites Fabricated by Powder Metallurgy Processes

    NASA Astrophysics Data System (ADS)

    Silvain, Jean-François; Veillère, Amélie; Lu, Yongfeng

    2014-07-01

    The increase in both power and packing densities in power electronic devices has led to an increase in the market demand for effective heat-dissipating materials, with high thermal conductivity and thermal- expansion coefficient compatible with chip materials still ensuring the reliability of the power modules. In this context, metal matrix composites: carbon fibers and diamond-reinforced copper and aluminum matrix composites among them are considered very promising as a next generation of thermal-management materials in power electronic packages. These composites exhibit enhanced thermal properties compared to pure copper combined with lower density. This article presents the fabrication techniques of copper/carbon fibers and copper/diamond and aluminum/carbon fibers composite films by powder metallurgy and hot pressing. The thermal analyses clearly indicate that interfacial treatments are required in these composites to achieve high thermomechanical properties. Interfaces (through novel chemical and processing methods), when selected carefully and processed properly will form the right chemical/mechanical link between metal and carbon, enhancing all the desired thermal properties while minimizing the deleterious effect.

  8. Adsorption isotherms for chlorinated phenols on activated carbons

    SciTech Connect

    Colella, L.S.; Armenante, P.M.; Kafkewitz, D.; Allen, S.J.; Balkasundaram, V.

    1998-07-01

    The adsorption of 12 mono-, di-, and trichlorophenols from aqueous solutions on different activated carbons was studied. Distilled water and a minimal salt medium solution previously used in biotreatment studies with anaerobic organisms were used as solvents. A commercially available wood-based activated carbon (Chemviron carbon) and a lignite-based carbon produced at Queen`s University were used as the adsorbents. The Chemviron carbon was used in both granular and powder forms. The adsorption data for each chlorophenol were regressed using the Freundlich equation. The fit was generally satisfactory, especially since the range of chlorophenol concentrations tested in this work extended over 6 orders of magnitude. The exponents of the chlorophenol concentration term in the Freundlich equations were found to be in the relatively narrow range 0.127--0207. Therefore an attempt was made to regress all the data for all chlorophenols using a single isotherm, and a cumulative Freundlich isotherm was obtained. The Chemviron carbon was found to have a higher adsorbing capacity than the lignite-based carbon. The presence of additional inorganic solutes in the aqueous phase was found to have a negligible influence on adsorption.

  9. Carbon dioxide-activated carbons from almond tree pruning: Preparation and characterization

    NASA Astrophysics Data System (ADS)

    Gañán, J.; González, J. F.; González-García, C. M.; Ramiro, A.; Sabio, E.; Román, S.

    2006-06-01

    Activated carbons were prepared from almond tree pruning by non-catalytic and catalytic gasification with carbon dioxide and their surface characteristics were investigated. In both series a two-stage activation procedure (pyrolysis at 800 °C in nitrogen atmosphere, followed by carbon dioxide activation) was used for the production of activated samples. In non-catalytic gasification, the effect of the temperature (650-800 °C for 1 h) and the reaction time (1-12 h at 650 °C) on the surface characteristics of the prepared samples was investigated. Carbons were characterized by means of nitrogen adsorption isotherms at 77 K. The textural parameters of the carbons present a linear relation with the conversion degree until a value of approximately 40%, when they come independent from both parameters studied. The highest surface area obtained for this series was 840 m 2 g -1. In the catalytic gasification the effect of the addition of one catalyst (K and Co) and the gasification time (2-4 h) on the surface and porosity development of the carbons was also studied. At the same conditions, Co leads to higher conversion values than K but this last gives a better porosity development.

  10. Removal of Lead (II) Ions from Aqueous Solutions onto Activated Carbon Derived from Waste Biomass

    PubMed Central

    Erdem, Murat; Ucar, Suat; Karagz, Selhan; Tay, Turgay

    2013-01-01

    The removal of lead (II) ions from aqueous solutions was carried out using an activated carbon prepared from a waste biomass. The effects of various parameters such as pH, contact time, initial concentration of lead (II) ions, and temperature on the adsorption process were investigated. Energy Dispersive X-Ray Spectroscopy (EDS) analysis after adsorption reveals the accumulation of lead (II) ions onto activated carbon. The Langmuir and Freundlich isotherm models were applied to analyze equilibrium data. The maximum monolayer adsorption capacity of activated carbon was found to be 476.2?mg?g?1. The kinetic data were evaluated and the pseudo-second-order equation provided the best correlation. Thermodynamic parameters suggest that the adsorption process is endothermic and spontaneous. PMID:23853528

  11. Biofuel intercropping effects on soil carbon and microbial activity.

    PubMed

    Strickland, Michael S; Leggett, Zakiya H; Sucre, Eric B; Bradford, Mark A

    2015-01-01

    Biofuels will help meet rising demands for energy and, ideally, limit climate change associated with carbon losses from the biosphere to atmosphere. Biofuel management must therefore maximize energy production and maintain ecosystem carbon stocks. Increasingly, there is interest in intercropping biofuels with other crops, partly because biofuel production on arable land might reduce availability and increase the price of food. One intercropping approach involves growing biofuel grasses in forest plantations. Grasses differ from trees in both their organic inputs to soils and microbial associations. These differences are associated with losses of soil carbon when grasses become abundant in forests. We investigated how intercropping switchgrass (Panicum virgalum), a major candidate for cellulosic biomass production, in loblolly pine (Pinus taeda) plantations affects soil carbon, nitrogen, and microbial dynamics. Our design involved four treatments: two pine management regimes where harvest residues (i.e., biomass) were left in place or removed, and two switchgrass regimes where the grass was grown with pine under the same two biomass scenarios (left or removed). Soil variables were measured in four 1-ha replicate plots in the first and second year following switchgrass planting. Under switchgrass intercropping, pools of mineralizable and particulate organic matter carbon were 42% and 33% lower, respectively. These declines translated into a 21% decrease in total soil carbon in the upper 15 cm of the soil profile, during early stand development. The switchgrass effect, however, was isolated to the interbed region where switchgrass is planted. In these regions, switchgrass-induced reductions in soil carbon pools with 29%, 43%, and 24% declines in mineralizable, particulate, and total soil carbon, respectively. Our results support the idea that grass inputs to forests can prime the activity of soil organic carbon degrading microbes, leading to net reductions in stocks of soil carbon. Active microbial biomass, however, is higher under switchgrass, and this microbial biomass is a dominant precursor of soil carbon formation. Future studies need to investigate soil carbon dynamics throughout the lifetime of intercropping rotations to evaluate whether increases in microbial biomass can offset initial declines in soil carbon, and hence, maintain ecosystem carbon stocks. PMID:26255363

  12. Microbial activity promotes carbon storage in temperate soils

    NASA Astrophysics Data System (ADS)

    Lange, Markus; Eisenhauer, Nico; Sierra, Carlos; Gleixner, Gerd

    2014-05-01

    Soils are one of the most important carbon sink and sources. Soils contain up to 3/4 of all terrestrial carbon. Beside physical aspects of soil properties (e.g. soil moisture and texture) plants play an important role in carbon sequestration. The positive effect of plant diversity on carbon storage is already known, though the underlying mechanisms remain still unclear. In the frame of the Jena Experiment, a long term biodiversity experiment, we are able to identify these processes. Nine years after an land use change from an arable field to managed grassland the mean soil carbon concentrations increased towards the concentrations of permanent meadows. The increase was positively linked to a plant diversity gradient. High diverse plant communities produce more biomass, which in turn results in higher amounts of litter inputs. The plant litter is transferred to the soil organic matter by the soil microbial community. However, higher plant diversity also causes changes in micro-climatic condition. For instance, more diverse plant communities have a more dense vegetation structure, which reduced the evaporation of soils surface and thus, increases soil moisture in the top layer. Higher inputs and higher soil moisture lead to an enlarged respiration of the soil microbial community. Most interestingly, the carbon storage in the Jena Experiment was much more related to microbial respiration than to plant root inputs. Moreover, using radiocarbon, we found a significant younger carbon age in soils of more diverse plant communities than in soils of lower diversity, indicating that more fresh carbon is integrated into the carbon pool. Putting these findings together, we could show, that the positive link between plant diversity and carbon storage is due to a higher microbial decomposition of plant litter, pointing out that carbon storage in soils is a function of the microbial community.

  13. A comparison of the electrochemical behavior of carbon aerogels and activated carbon fiber cloths

    SciTech Connect

    Tran, T.D.; Alviso, C.T.; Hulsey, S.S.; Nielsen, J.K.; Pekala, R.W.

    1996-05-10

    Electrochemical capacitative behavior of carbon aerogels and commercial carbon fiber cloths was studied in 5M KOH, 3M sulfuric acid, and 0.5M tetrethylammonium tetrafluoroborate/propylene carbonate electrolytes. The resorcinol-formaldehyde based carbon aerogels with a range of denisty (0.2-0.85 g/cc) have open-cell structures with ultrafine pore sizes (5-50 nm), high surface area (400-700 m{sup 2}/g), and a solid matrix composed of interconnected particles or fibers with characteristic diameters of 10 nm. The commercial fiber cloths in the density range 0.2-04g/cc have high surface areas (1000-2500 m{sup 2}/g). The volumetric capacitances of high-density aerogels are shown to be comparable to or exceeding those from activated carbon fibers. Electrochemical behavior of these materials in various electrolytes is compared and related to their physical properties.

  14. Optimizing a Laser Process for Making Carbon Nanotubes

    NASA Technical Reports Server (NTRS)

    Arepalli, Sivaram; Nikolaev, Pavel; Holmes, William

    2010-01-01

    A systematic experimental study has been performed to determine the effects of each of the operating conditions in a double-pulse laser ablation process that is used to produce single-wall carbon nanotubes (SWCNTs). The comprehensive data compiled in this study have been analyzed to recommend conditions for optimizing the process and scaling up the process for mass production. The double-pulse laser ablation process for making SWCNTs was developed by Rice University researchers. Of all currently known nanotube-synthesizing processes (arc and chemical vapor deposition), this process yields the greatest proportion of SWCNTs in the product material. The aforementioned process conditions are important for optimizing the production of SWCNTs and scaling up production. Reports of previous research (mostly at Rice University) toward optimization of process conditions mention effects of oven temperature and briefly mention effects of flow conditions, but no systematic, comprehensive study of the effects of process conditions was done prior to the study described here. This was a parametric study, in which several production runs were carried out, changing one operating condition for each run. The study involved variation of a total of nine parameters: the sequence of the laser pulses, pulse-separation time, laser pulse energy density, buffer gas (helium or nitrogen instead of argon), oven temperature, pressure, flow speed, inner diameter of the flow tube, and flow-tube material.

  15. Oxidative Process for Cutting Single-Walled Carbon Nanotubes

    NASA Astrophysics Data System (ADS)

    Shaver, Jonah

    2005-03-01

    Cut single-walled carbon nanotubes (SWNTs) are needed for many applications. An efficient way to produce bulk amounts of cut SWNTs is a two step process consisting of sidewall damage and oxidative exploitation. In these experiments sidewall damage is introduced by ozonation in a perfluoropolyether (PFPE) while monitoring the degree of functionalization with in-situ Raman spectroscopy. Use of PFPE allows for a high degree of sidewall functionalization at room temperature, mainly in the form of epoxides. These damaged SWNTs are exposed to piranha (4:1 96%H2SO4:H2O2) for one hour and then quenched. The piranha exposed samples are then functionalized with alkyl groups and spin cast on mica for length analysis. The cut samples are found to have significantly shorter lengths while maintaining a relatively high carbon yield.

  16. Carbonate Beaches: A Balance Between Biological and Physical Processes

    NASA Astrophysics Data System (ADS)

    Nairn, R.; Risk, M.

    2004-12-01

    Carbonate beaches are a unique example of the interaction between biological processes, creating the sediments, and physical processes, moving and often removing the sediments. On the sediment supply side, carbonate sediments are born, not made. They exist in dynamic equilibrium between production and destruction. Following the creation of carbonate sediment in coral reef and lagoon environments, the sediments are moved shoreward to the beach, transport along the shore and sometimes, eventually lost offshore, often as the result of tropical storms. Comprehensive studies of the balance between the supply and loss of carbonate sediments and beach dynamics have been completed for the islands of Mauritius and Barbados. Field studies and remote sensing (Compact Airborne Spectrometry Imaging) have been applied to develop carbonate sediment production rates for a range of reef and lagoon conditions. Using GIS, these production rates have been integrated to determine sediment supply rates for different segments of the coastline. 1-D and 2-D models of waves, hydrodynamics, sediment transport and morphodynamics were set-up and tested against observed beach response to storm events or a sequence of storm events. These complex deterministic models are not suitable for application over periods of decades. However, it was possible to characterize storm events by the extent of sand loss, and relate this to key descriptive factors for groups of storm events, thereby encapsulating the erosion response. A long-term predictive tool for evaluating beach erosion and accretion response, over a period of several decades, was developed by combining the supply rates for carbonate sediment and the encapsulated representation of the loss rates through physical processes. The ability of this predictive tool was successfully tested against observed long term beach evolution along sections of the coast in Barbados and Mauritius using air photo analysis in GIS for shoreline change over periods of 40 years. The long-term predictive tool for carbonate beach evolution provided valuable support to developing coastal zone management policy and actions to preserve the beaches in their natural form, minimizing the need for artificial nourishment of the beaches. Many models of sediment movement on shorelines are derived from clastic examples, and fit carbonate coastlines only with difficulty. We have combined field surveys of benthic biota, estimates of sediment production from skeletal growth and bioerosion, and sediment destruction by comminution and dissolution with dynamic models of sediment movement in the littoral zone, achieving improved understanding of coastal processes of erosion and deposition. Mauritius is fringed by shallow lagoons, often with luxuriant stands of Acropora. The offshore region is exhumed Pleistocene-all the sediment on the beaches comes from the lagoons. From surveys of coral cover, and estimates of sediment production from reef, sand and hardground areas, we produced dynamic models that faithfully hindcast shoreline dynamics for decades, and allowed identification of regions especially vulnerable to erosion. On the south coast of Barbados, one of the main issues in stabilising and rehabilitation the coastline is the balance between sediment from longshore drift and local sources. By identifying localised areas of characteristic sediment-producers (e.g., the foraminiferan Homotrema rubrum, the green alga Halimeda), we were able to determine the balance between proximal and distal sediment sources. The resulting model hindcasts the coastline through all the major hurricanes of the past 30 years.

  17. Electron beam processing of carbon fibre reinforced braided composites

    NASA Astrophysics Data System (ADS)

    Zsigmond, B.; Halsz, L.; Czvikovszky, T.

    2003-06-01

    The possibility of producing a new type carbon fibre reinforced composite profile has been examined by applying braiding, a well-known process of textile technology. Pipe and hollow profile composite products can be manufactured this way by applying Electron Beam curing. The fabric-like braided reinforcing structure was manufactured out of Hungarian-made carbon fibre roving of 48,000 elementary fibres. The mutual irradiation of the system impregnated with epoxy-acrylate oligomer by 8 MeV EB resulted in better mechanical properties then conventional chemical curing. Owing to its low density and high specific strength this new composite product can possibly be applied in dynamically loaded structures e.g. in the automotive industry.

  18. Sorption and stability of mercury on activated carbon for emission control.

    PubMed

    Graydon, John W; Zhang, Xinzhi; Kirk, Donald W; Jia, Charles Q

    2009-09-15

    A leading strategy for control of mercury emissions from combustion processes involves removal of elemental mercury from the flue gas by injection of activated carbon sorbent. After particulate capture and disposal in a landfill, it is critical that the captured mercury remains permanently sequestered in the sorbent. The environmental stability of sorbed mercury was determined on two commercial, activated carbons, one impregnated using gaseous sulfur, and on two activated carbons that were impregnated with sulfur by reaction with SO(2). After loading with mercury vapor using a static technique, the stability of the sorbed mercury was characterized by two leaching methods. The standard toxicity characteristic leaching procedure showed leachate concentrations well below the limit of 0.2mg/L for all activated carbons. The nature of the sorbed mercury was further characterized by a sequential extraction scheme that was specifically optimized to distinguish clearly among the highly stable phases of mercury. This analysis revealed that there are two forms in which mercury is sequestered. In the sorbent that was impregnated by gaseous sulfur at a relatively low temperature, the mercury is present predominantly as HgS. In the other three sorbents, including two impregnated using SO(2), the mercury is predominantly present in the elemental form, physisorbed and chemisorbed to thiophene groups on the carbon surface. Both forms of binding are sufficiently stable to provide permanent sequestration of mercury in activated carbon sorbents after disposal. PMID:19327890

  19. Annealing effect on the particle size and chemical composition of activated carbon obtained from vacuum furnace of teak sawdust

    NASA Astrophysics Data System (ADS)

    Armynah, B.; Tahir, D.; Jaya, N.

    2014-09-01

    Activated carbon was produced from sawdust by using physical method in a high temperature vacuum furnace without additional chemical. Fast pyrolysis process was carried out prior in fluidized a bed furnace to produce char before activation process. Experiments were conducted to investigate the influence of various process parameters such as particle size, activation temperature and activation time on the quality of the activated carbon. In addition, the chemical composition studies were done by using x-ray fluorescence (XRF) spectroscopy. The crystallite sizes were calculated by using Scherer equation based on x-ray diffraction (XRD) spectroscopy data. The pyrolysis temperature and time were varied from 600°C to 900°C and from 3 hours to 6 hours, respectively. The particle size of activated carbon was increase with increasing temperature. The composition and crystallite size of the prepared activated carbon was compared with the non-activated carbon. The results indicated that the teak sawdust carbon could be employed as a low cost alternative to produce commercial activated carbon.

  20. Annealing effect on the particle size and chemical composition of activated carbon obtained from vacuum furnace of teak sawdust

    SciTech Connect

    Armynah, B. Tahir, D. Jaya, N.

    2014-09-25

    Activated carbon was produced from sawdust by using physical method in a high temperature vacuum furnace without additional chemical. Fast pyrolysis process was carried out prior in fluidized a bed furnace to produce char before activation process. Experiments were conducted to investigate the influence of various process parameters such as particle size, activation temperature and activation time on the quality of the activated carbon. In addition, the chemical composition studies were done by using x-ray fluorescence (XRF) spectroscopy. The crystallite sizes were calculated by using Scherer equation based on x-ray diffraction (XRD) spectroscopy data. The pyrolysis temperature and time were varied from 600°C to 900°C and from 3 hours to 6 hours, respectively. The particle size of activated carbon was increase with increasing temperature. The composition and crystallite size of the prepared activated carbon was compared with the non-activated carbon. The results indicated that the teak sawdust carbon could be employed as a low cost alternative to produce commercial activated carbon.

  1. Silicate Carbonation Processes in Water-Bearing Supercritical CO2 Fluids: Implications for Geologic Carbon Sequestration

    NASA Astrophysics Data System (ADS)

    Miller, Q. R.; Schaef, T.; Thompson, C.; Loring, J. S.; Windisch, C. F.; Bowden, M. E.; Arey, B. W.; McGrail, P.

    2012-12-01

    Global climate change is viewed by many as an anthropogenic phenomenon that could be mitigated through a combination of conservation efforts, alternative energy sources, and the development of technologies capable of reducing carbon dioxide (CO2) emissions. Continued increases of atmospheric CO2 concentrations are projected over the next decade, due to developing nations and growing populations. One economically favorable option for managing CO2 involves subsurface storage in deep basalt formations. The silicate minerals and glassy mesostasis basalt components act as metal cation sources, reacting with the CO2 to form carbonate minerals. Most prior work on mineral reactivity in geologic carbon sequestration settings involves only aqueous dominated reactions. However, in most sequestration scenarios, injected CO2 will reside as a buoyant fluid in contact with the sealing formation (caprock) and slowly become water bearing. Comparatively little laboratory research has been conducted on reactions occurring between minerals in the host rock and the wet scCO2. In this work, we studied the carbonation of wollastonite [CaSiO3] exposed to variably wet supercritical CO2 (scCO2) at a range of temperatures (50, 55 and 70 °C) and pressures (90,120 and 160 bar) in order to gain insight into reaction processes. Mineral transformation reactions were followed by two novel in situ high pressure techniques, including x-ray diffraction that tracked the rate and extents of wollastonite conversion to calcite. Increased dissolved water concentrations in the scCO2 resulted in increased carbonation approaching ~50 wt. %. Development of thin water films on the mineral surface were directly observed with infrared (IR) spectroscopy and indirectly with 18O isotopic labeling techniques (Raman spectroscopy). The thin water films were determined to be critical for facilitating carbonation processes in wet scCO2. Even in extreme low water conditions, the IR technique detected the formation of amorphous silica. Unlike the thick (<10 μm) passivating silica layers observed in the reacted samples from fully water saturated scCO2 experiments, images obtained from a focused ion beam sectioned sample indicted these coatings were chemically wollastonite but structurally amorphous. In addition, evidence of an intermediate hydrated amorphous calcium carbonate forming under these conditions further emphasize the importance of understanding geochemical processes occurring in water-bearing scCO2 fluids.

  2. Ammonia modification of activated carbon to enhance carbon dioxide adsorption: Effect of pre-oxidation

    NASA Astrophysics Data System (ADS)

    Shafeeyan, Mohammad Saleh; Daud, Wan Mohd Ashri Wan; Houshmand, Amirhossein; Arami-Niya, Arash

    2011-02-01

    A commercial granular activated carbon (GAC) was subjected to thermal treatment with ammonia for obtaining an efficient carbon dioxide (CO2) adsorbent. In general, CO2 adsorption capacity of activated carbon can be increased by introduction of basic nitrogen functionalities onto the carbon surface. In this work, the effect of oxygen surface groups before introduction of basic nitrogen functionalities to the carbon surface on CO2 adsorption capacity was investigated. For this purpose two different approaches of ammonia treatment without preliminary oxidation and amination of oxidized samples were studied. Modified carbons were characterized by elemental analysis and Fourier Transform Infrared spectroscopy (FT-IR) to study the impact of changes in surface chemistry and formation of specific surface groups on adsorption properties. The texture of the samples was characterized by conducting N2 adsorption/desorption at -196 C. CO2 capture performance of the samples was investigated using a thermogravimetric analysis (TGA). It was found that in both modification techniques, the presence of nitrogen functionalities on carbon surface generally increased the CO2 adsorption capacity. The results indicated that oxidation followed by high temperature ammonia treatment (800 C) considerably enhanced the CO2 uptake at higher temperatures.

  3. Dye adsorption of mesoporous activated carbons produced from NaOH-pretreated rice husks.

    PubMed

    Lin, Long; Zhai, Shang-Ru; Xiao, Zuo-Yi; Song, Yu; An, Qing-Da; Song, Xiao-Wei

    2013-05-01

    In continuation of previous work on utilizing rice husks, this study aimed to prepare mesoporous activated carbons using residues of sodium hydroxide-pretreated RHs, and then examine their dye adsorption performance. The influences of the activation temperature and activation time on the surface area, pore volume, and pore radius of the activated carbon were investigated based on nitrogen adsorption/desorption isotherms and transmission electron microscopy. The adsorptive behavior of the mesoporous activated carbons obtained under optimum preparation conditions was evaluated using methyleneblue as the model adsorbate. The adsorption kinetics was studied by pseudo-first-and pseudo-second-order models, and the adsorption isotherms were studied by Langmuir and Freundlich models. The pseudo-second-order model and Langmuir isotherm were found to fit well the adsorption characteristics of the as-prepared mesoporous activated carbons. Thermodynamic data of the adsorption process were also obtained to elucidate the adsorption thermo-chemistry between the activated carbons produced from NaOH-pretreated RHs and MB molecules. PMID:23567714

  4. Improved Bioethanol Production Using Activated Carbon-treated Acid Hydrolysate from Corn Hull in Pachysolen tannophilus

    PubMed Central

    Seo, Hyeon-Beom; Kim, Seungseop; Lee, Hyeon-Yong

    2009-01-01

    To optimally convert corn hull, a byproduct from corn processing, into bioethanol using Pachysolen tannophlius, we investigated the optimal conditions for hydrolysis and removal of toxic substances in the hydrolysate via activated carbon treatment as well as the effects of this detoxification process on the kinetic parameters of bioethanol production. Maximum monosaccharide concentrations were obtained in hydrolysates in which 20 g of corn hull was hydrolyzed in 4% (v/v) H2SO4. Activated carbon treatment removed 92.3% of phenolic compounds from the hydrolysate. When untreated hydrolysate was used, the monosaccharides were not completely consumed, even at 480 h of culture. When activated carbon-treated hydrolysate was used, the monosaccharides were mostly consumed at 192 h of culture. In particular, when activated carbon-treated hydrolysate was used, bioethanol productivity (P) and specific bioethanol production rate (Qp) were 2.4 times and 3.4 times greater, respectively, compared to untreated hydrolysate. This was due to sustained bioethanol production during the period of xylose/arabinose utilization, which occurred only when activated carbon-treated hydrolysate was used. PMID:23983522

  5. Carbon Sequestration and Peat Accretion Processes in Peatland Systems: A North-South Comparison

    NASA Astrophysics Data System (ADS)

    Richardson, C. J.; Wang, H.; Bridgham, S. D.

    2012-12-01

    Millions of hectares of peatlands exist in the U.S. and Canada but few comparisons have been made on the process controlling peat accretion, carbon sequestration and GHG losses across latitudinal gradients. Historic threats to carbon sequestration for these areas have been drainage and conversion to agriculture and forestry, which promotes the decomposition of the organic matter in the soil, leading to accelerated soil subsidence, severe carbon losses, and accelerated transport of C and nutrients to adjoining ecosystems. A more recent and insidious threat to the survival of peatlands worldwide is the increased temperature and drought conditions projected for many areas of global peatlands (IPCC 2007). A comparison of carbon sequestration rates and controlling processes for southeastern shrub bogs, the Florida Everglades and selected peatlands of the northern US and Canada under current climatic conditions reveals several major differences in controlling factors and rates of sequestration and carbon flux. Numerous studies have shown that drought or drainage can unlock historically stored carbon, thus releasing more CO2 ¬ and dissolved organic carbon (Blodau et al. 2004; Furukawa et al. 2005; Von Arnold et al. 2005; Hirano et al. 2007), and such effects might last for decades (Fenner & Freeman 2011). The main driver of this process is the O2 introduced by drought or drainage, which will increase the activity of phenol oxidase, then accelerate the decomposition of phenol compounds, which is generally considered the "enzymatic latch" for carbon storage in peatlands (Freeman et al. 2001). However, our recent studies in southeastern peatlands along the coast of North Carolina have found that drought or drainage does not affect CO2 emission in some southern peatlands where the initial water level is below the ground surface (unsaturated peats), as polyphenol increases rather than decreases. Our results suggest that additional controlling factors, rather than anoxia exist in unsaturated peats, allowing them to accumulate carbon, and resist decomposition and CO2 losses. The importance of native phenolic producing plant species and substrate quality are key controlling factors. Our study offers new evidence that frequently occurring summer drought or climate-induced moderate drought will not increase the loss of stored carbon in unsaturated peatlands. These findings have important ramifications concerning carbon storage and losses in peatlands under future climate change predictions.

  6. A General Methodology for Evaluation of Carbon Sequestration Activities and Carbon Credits

    SciTech Connect

    Klasson, KT

    2002-12-23

    A general methodology was developed for evaluation of carbon sequestration technologies. In this document, we provide a method that is quantitative, but is structured to give qualitative comparisons despite changes in detailed method parameters, i.e., it does not matter what ''grade'' a sequestration technology gets but a ''better'' technology should receive a better grade. To meet these objectives, we developed and elaborate on the following concepts: (1) All resources used in a sequestration activity should be reviewed by estimating the amount of greenhouse gas emissions for which they historically are responsible. We have done this by introducing a quantifier we term Full-Cycle Carbon Emissions, which is tied to the resource. (2) The future fate of sequestered carbon should be included in technology evaluations. We have addressed this by introducing a variable called Time-adjusted Value of Carbon Sequestration to weigh potential future releases of carbon, escaping the sequestered form. (3) The Figure of Merit of a sequestration technology should address the entire life-cycle of an activity. The figures of merit we have developed relate the investment made (carbon release during the construction phase) to the life-time sequestration capacity of the activity. To account for carbon flows that occur during different times of an activity we incorporate the Time Value of Carbon Flows. The methodology we have developed can be expanded to include financial, social, and long-term environmental aspects of a sequestration technology implementation. It does not rely on global atmospheric modeling efforts but is consistent with these efforts and could be combined with them.

  7. Focused-electron-beam-induced processing (FEBIP) for emerging applications in carbon nanoelectronics

    NASA Astrophysics Data System (ADS)

    Fedorov, Andrei G.; Kim, Songkil; Henry, Mathias; Kulkarni, Dhaval; Tsukruk, Vladimir V.

    2014-12-01

    Focused-electron-beam-induced processing (FEBIP), a resist-free additive nanomanufacturing technique, is an actively researched method for "direct-write" processing of a wide range of structural and functional nanomaterials, with high degree of spatial and time-domain control. This article attempts to critically assess the FEBIP capabilities and unique value proposition in the context of processing of electronics materials, with a particular emphasis on emerging carbon (i.e., based on graphene and carbon nanotubes) devices and interconnect structures. One of the major hurdles in advancing the carbon-based electronic materials and device fabrication is a disjoint nature of various processing steps involved in making a functional device from the precursor graphene/CNT materials. Not only this multi-step sequence severely limits the throughput and increases the cost, but also dramatically reduces the processing reproducibility and negatively impacts the quality because of possible between-the-step contamination, especially for impurity-susceptible materials such as graphene. The FEBIP provides a unique opportunity to address many challenges of carbon nanoelectronics, especially when it is employed as part of an integrated processing environment based on multiple "beams" of energetic particles, including electrons, photons, and molecules. This avenue is promising from the applications' prospective, as such a multi-functional (electron/photon/molecule beam) enables one to define shapes (patterning), form structures (deposition/etching), and modify (cleaning/doping/annealing) properties with locally resolved control on nanoscale using the same tool without ever changing the processing environment. It thus will have a direct positive impact on enhancing functionality, improving quality and reducing fabrication costs for electronic devices, based on both conventional CMOS and emerging carbon (CNT/graphene) materials.

  8. Improved granular activated carbon for the stabilization of wastewater pH

    SciTech Connect

    1996-10-01

    Many times the start up of granular activated carbon adsorption systems for the control of organic contaminants in wastewater cm exhibit unacceptable increases in the adscurber effluent pH. Experience shows that the duration of the pH increase ranges from several hours to several days, during which time several hundred bed volumes of water can be discharged with a pH in excess of 9. Laboratory studies have identified the cause of the pH rise as an interaction between the naturally occurring anions and protons ar the water and the carbon surface. The interaction can be described as an ion exchange type of phenomenon, in which the carbon surface sorbs the anions and corresponding hydronium ions from the water. Capacities of the carbon for the anions range from 2 to 9 mg/g GAC, depending upon the water characteristics, the carbon type, the nature of the anion and its influent concentration. These studies have shown de the anion sorption and resulting pH increase is independent of the raw material used for die activated carbon production, e.g. bituminous or sub-bituminous coal, peat, wood or coconut. Also, the pH excursions occur with virgin, reactivated, and acid washed granular carbons. Current pH control technologies focus on adjustment of wastewater pH prior to discharge or recycle of the initial effluent water until the pH increase abates. However, improved water pH control options have been realized by altering the carbon surface rather than the water chemistry. The change to the carbon surface is accomplished through a controlled oxidation process. This process provides a more acidic carbon surface with a reduced affinity for the anions in the waste water. As a result, the pH excursions above 9 are eliminated and the initial effluent from the adsorption system can be discharged without further treatment.

  9. Assessing the carbon balance of circumpolar Arctic tundra using remote sensing and process modeling.

    PubMed

    Sitch, Stephen; McGuire, A David; Kimball, John; Gedney, Nicola; Gamon, John; Engstrom, Ryan; Wolf, Annett; Zhuang, Qianlai; Clein, Joy; McDonald, Kyle C

    2007-01-01

    This paper reviews the current status of using remote sensing and process-based modeling approaches to assess the contemporary and future circumpolar carbon balance of Arctic tundra, including the exchange of both carbon dioxide and methane with the atmosphere. Analyses based on remote sensing approaches that use a 20-year data record of satellite data indicate that tundra is greening in the Arctic, suggesting an increase in photosynthetic activity and net primary production. Modeling studies generally simulate a small net carbon sink for the distribution of Arctic tundra, a result that is within the uncertainty range of field-based estimates of net carbon exchange. Applications of process-based approaches for scenarios of future climate change generally indicate net carbon sequestration in Arctic tundra as enhanced vegetation production exceeds simulated increases in decomposition. However, methane emissions are likely to increase dramatically, in response to rising soil temperatures, over the next century. Key uncertainties in the response of Arctic ecosystems to climate change include uncertainties in future fire regimes and uncertainties relating to changes in the soil environment. These include the response of soil decomposition and respiration to warming and deepening of the soil active layer, uncertainties in precipitation and potential soil drying, and distribution of wetlands. While there are numerous uncertainties in the projections of process-based models, they generally indicate that Arctic tundra will be a small sink for carbon over the next century and that methane emissions will increase considerably, which implies that exchange of greenhouse gases between the atmosphere and Arctic tundra ecosystems is likely to contribute to climate warming. PMID:17479847

  10. Modified Activated Carbon to be Used in Clinical Applications

    NASA Astrophysics Data System (ADS)

    Fernando, M. S.; de Silva, W. R. M.; de Silva, K. M. N.

    2014-11-01

    In this study a novel nano composite of hydroxyapatite nano particles impregnated activated carbon (C-HAp), which was synthesized in our own method, was used in iron adsorption studies. The study was conducted in order to investigate the potential of using C-HAp nanocomposite to be used in clinical detoxifications such as acute iron toxicity where the use of Activated carbon (GAC) is not very effective. Adsorption studies were conducted for synthetic solutions of Fe2+, Fe3+ and iron syrup using GAC, C-HAp and neat HAp as adsorbents. According to the results C-HAp nano composite showed improved properties than GAC in adsorbing Fe2+, Fe3+ and also Fe ions in iron syrup solutions. Thus the results of the in-vitro studies of iron adsorption studies indicated the potential of using C-HAp as an alternative to activated carbon in such clinical applications.

  11. Chars pyrolyzed from oil palm wastes for activated carbon preparation

    SciTech Connect

    Lua, A.C.; Guo, J.

    1999-01-01

    Chars pyrolyzed from extracted oil palm fibers for the preparation of activated carbons were studied. The effects of pyrolysis temperature and hold time on density, porosity, yield, BET and micropore surface areas, total pore volume, and pore size distributions of chars were investigated. The optimum conditions for pyrolysis were found to be at a pyrolysis temperature of 850 C for a hold time of 3.5 h. Scanning electron micrographs of the char surfaces verified the presence of porosities. The experimental results showed that it was feasible to produce chars with high BET and micropore surface areas from extracted oil palm fibers. The resulting chars will be subjected to steam or carbon dioxide activation to prepare activated carbons for use as gas adsorbents for air pollution control.

  12. Impact of sulfur oxides on mercury capture by activated carbon

    SciTech Connect

    Albert A. Presto; Evan J. Granite

    2007-09-15

    Recent field tests of mercury removal with activated carbon injection (ACI) have revealed that mercury capture is limited in flue gases containing high concentrations of sulfur oxides (SOx). In order to gain a more complete understanding of the impact of SOx on ACI, mercury capture was tested under varying conditions of SO{sub 2} and SO{sub 3} concentrations using a packed bed reactor and simulated flue gas (SFG). The final mercury content of the activated carbons is independent of the SO{sub 2} concentration in the SFG, but the presence of SO{sub 3} inhibits mercury capture even at the lowest concentration tested (20 ppm). The mercury removal capacity decreases as the sulfur content of the used activated carbons increases from 1 to 10%. In one extreme case, an activated carbon with 10% sulfur, prepared by H{sub 2}SO{sub 4} impregnation, shows almost no mercury capacity. The results suggest that mercury and sulfur oxides are in competition for the same binding sites on the carbon surface. 30 refs., 3 figs., 2 tabs.

  13. Laser Processing of Carbon Nanotube Transparent Conducting Films

    NASA Astrophysics Data System (ADS)

    Mann, Andrew

    Transparent conducting films, or TCFs, are 2D electrical conductors with the ability to transmit light. Because of this, they are used in many popular electronics including smart phones, tablets, solar panels, and televisions. The most common material used as a TCF is indium tin oxide, or ITO. Although ITO has great electrical and optical characteristics, it is expensive, brittle, and difficult to pattern. These limitations have led researchers toward other materials for the next generation of displays and touch panels. The most promising material for next generation TCFs is carbon nanotubes, or CNTs. CNTs are cylindrical tubes of carbon no more than a few atoms thick. They have different electrical and optical properties depending on their atomic structure, and are extremely strong. As an electrode, they conduct electricity through an array of randomly dispersed tubes. The array is highly transparent because of gaps between the tubes, and size and optical properties of the CNTs. Many research groups have tried making CNT TCFs with opto-electric properties similar to ITO but have difficultly achieving high conductivity. This is partly attributed to impurities from fabrication and a mix of different tube types, but is mainly caused by low junction conductivity. In functionalized nanotubes, junction conductivity is impaired by covalently bonded molecules added to the sidewalls of the tubes. The addition of this molecule, known as functionalization, is designed to facilitate CNT dispersion in a solvent by adding properties of the molecule to the CNTs. While necessary for a good solution, functionalization decreases the conductivity in the CNT array by creating defects in the tube's structures and preventing direct inter-carbon bonding. This research investigates removing the functional coating (after tube deposition) by laser processing. Laser light is able to preferentially heat the CNTs because of their optical and electrical properties. Through local conduction, the relatively weak functional molecules are thermally decomposed. This restores the pristine CNT structure and allows carbon to carbon bonds to form; thereby significantly improving the junction and sheet conductivity. Laser processing is performed without damaging the TCF substrate (usually glass or PET) because laser light is not absorbed by the substrate and conduction from the CNTs is limited. In addition to removing the functional coating, laser light improves the electrical conductivity by purifying the CNT array. The purity is improved through the ablation of defective tubes and amorphous carbon in the CNT film.[1] Using higher laser power, it is possible to locally remove the CNTs. Selective laser removal of the CNTs is a dry process that can be used to pattern the electrode. This is a much simpler and less expensive patterning technique than wet acid etching used for ITO. In summary, laser processing of CNT TCFs is shown to improve the electrical conductivity by defunctionalizing the CNTs. In addition, laser exposure increases purity by removing defects and can be used to pattern the electrode. These advances make CNTs more competitive as an alternative for ITO which has both cost and performance limitations. [1] T. Ueda, S. K. (2008). Effect of laser irradiation on carbon nanotube films for NOx gas sensor. Surface & Coatings Technology, 202, 5325--5328.

  14. Production of activated carbon and its catalytic application for oxidation of hydrogen sulphide

    NASA Astrophysics Data System (ADS)

    Azargohar, Ramin

    Hydrogen sulphide is an environmentally hazardous gas which is present in many gas streams associated with oil and gas industry. Oxidation of H 2S to sulphur in air produces no bulky or waste material and requires no further purification. Activated carbon is known as a catalyst for this reaction. In this research, a coal-based precursor (luscar char) and a biomass-based precursor (biochar) were used for production of activated carbons by two common methods of activation: physical and chemical activation in which steam and potassium hydroxide (KOH), respectively, were used. Experiments were designed by the statistical central composite design method. Two models were developed for the BET surface area and reaction yield of each activation process. These models showed the effects of operating conditions, such as activation temperature, mass ratio of activating agent to precursor, activation time, and nitrogen flowrate on the BET surface area and reaction yield for each activation method for each precursor. The optimum operating conditions were calculated using these models to produce activated carbons with relatively large BET surface area (> 500 m2/g) and high reaction yield (> 50 wt %). The BET surface area and reaction yield for activated carbons produced at optimum operating conditions showed maximum 7 and 7.4% difference, respectively, comparing to the values predicted by models. The activated carbons produced at optimum operating conditions were used as the base catalysts for the direct oxidation of 1 mol % hydrogen sulphide in nitrogen to sulphur at the temperature range of 160-205°C and pressure of 700 kPa. Originally activated carbons showed a good potential for oxidation of hydrogen sulphide by their selectivity for sulphur product and low amount of sulphur dioxide production. To improve the performance of steam-activated carbons, the catalysts were modified by acid-treatment followed by thermal desorption. This method increased the break-through times for coal-based and biomass-based catalysts to 115 and 141 minutes, respectively. The average amounts of sulphur dioxide produced during the reaction time were 0.14 and 0.03% (as % of hydrogen sulphide fed to the reactor) for modified activated carbons prepared from biochar and luscar char, respectively. The effects of porous structure, surface chemistry, and ash content on the performances of these activated carbon catalysts were investigated for the direct oxidation reaction of hydrogen sulphide. The acid-treatment followed by thermal desorption of activated carbons developed the porosity which produced more surface area for active sites and in addition, provided more space for sulphur product storage resulting in higher life time for catalyst. Boehm titration and temperature program desorption showed that the modification method increased basic character of carbon surface after thermal desorption in comparison to acid-treated sample. In addition, the effects of impregnating agents (potassium iodide and manganese nitrate) and two solvents for impregnation process were studied on the performance of the activated carbon catalysts for the direct oxidation of H2S to sulphur. Sulphur L-edge X-ray near edge structure (XANES) showed that the elemental sulphur was the dominant sulphur species in the product. The kinetic study for oxidation reaction of H2S over LusAC-O-D(650) was performed for temperature range of 160-190°C, oxygen to hydrogen sulphide molar ratio of 1-3, and H2S concentration of 6000-10000 ppm at 200 kPa. The values of activation energy were 26.6 and 29.3 kJ.gmol-1 for Eley-Rideal and Langmuir-Hinshelwood mechanisms, respectively.

  15. Gasification characteristics of an activated carbon catalyst during the decomposition of hazardous waste material in supercritical water

    SciTech Connect

    Matsumura, Yukihiko; Nuessle, F.W.; Antal, M.J. Jr.

    1996-12-31

    Recently, carbonaceous materials including activated carbon were proven to be effective catalysts for hazardous waste gasification in supercritical water. Using coconut shell activated carbon catalyst, complete decomposition of industrial organic wastes including methanol and acetic acid was achieved. During this process, the total mass of the activated carbon catalyst changes by two competing processes: a decrease in weight via gasification of the carbon by supercritical water, or an increase in weight by deposition of carbonaceous materials generated by incomplete gasification of the biomass feedstocks. The deposition of carbonaceous materials does not occur when complete gasification is realized. Gasification of the activated carbon in supercritical water is often favored, resulting in changes in the quality and quantity of the catalyst. To thoroughly understand the hazardous waste decomposition process, a more complete understanding of the behavior of activated carbon in pure supercritical water is needed. The gasification rate of carbon by water vapor at subcritical pressures was studied in relation to coal gasification and generating activated carbon.

  16. Litter contribution to soil organic carbon in the agriculture abandons processes

    NASA Astrophysics Data System (ADS)

    Novara, Agata; Francaviglia, Dario; La Mantia, tommaso; Gristina, Luciano; La Bella, Salvatore; Tuttolomondo, Teresa

    2015-04-01

    Mechanisms of litter decomposition, translocation and stabilization into soil layers are fundamental processes in ecosystem functioning as it regulates the cycle of soil organic matter (SOM), CO2 emission into the atmosphere, carbon sequestration into the soil. In this study, it was investigated the contribution of litters of different stages of Mediterranean secondary succession on Carbon sequestration, analyzing the role of earthworms on translocation of SOM into soil profile. For this purpose δ13C difference between meadow C4-C soil and C3-C litter were used in a field experiment. Four undisturbed litters of different stages of succession were collected (45, 70, 100 and 120 since agriculture abandon) and placed on the top of isolated soil cores. The litter contribution to C stock was affected by plant species and increased with the age of the stage of secondary succession. The soil organic carbon after 1 year since litter position increased up to 40% in comparison to no litter treatment in soil with litter of 120 years since abandon. The new carbon derived from C3-litter was decomposed and transferred into soil profile thanks to earthworms and dissolved organic carbon leaching. After 1 years the carbon increase attributed to earthworm activity ranged from 6% to 13% in soil under litter in field abandoned since 120 and 45 years, respectively.

  17. Litter contribution to soil organic carbon in the agriculture abandons processes

    NASA Astrophysics Data System (ADS)

    Novara, A.; Rühl, J.; La Mantia, T.; Gristina, L.; La Bella, S.; Tuttolomondo, T.

    2015-02-01

    Mechanisms of litter decomposition, translocation and stabilization into soil layers are fundamental processes in ecosystem functioning as it regulates the cycle of soil organic matter (SOM), CO2 emission into the atmosphere, carbon sequestration into the soil. In this study, it was investigated the contribution of litters of different stages of Mediterranean secondary succession on Carbon sequestration, analyzing the role of earthworms on translocation of SOM into soil profile. For this purpose δ13C difference between meadow C4-Csoil and C3-Clitter were used in a field experiment. Four undisturbed litters of different stages of succession were collected (45, 70, 100 and 120 since agriculture abandon) and placed on the top of isolated soil cores. The litter contribution to C stock was affected by plant species and increased with the age of the stage of secondary succession. The soil organic carbon after 1 year since litter position increased up to 40% in comparison to no litter treatment in soil with litter of 120 years since abandon. The new carbon derived from C3-litter was decomposed and transferred into soil profile thanks to earthworms and dissolved organic carbon leaching. After 1 years the carbon increase attributed to earthworm activity ranged from 6 to 13% in soil under litter in field abandoned since 120 and 45 years, respectively.

  18. 40 CFR 458.20 - Applicability: description of the carbon black thermal process subcategory.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... carbon black thermal process subcategory. 458.20 Section 458.20 Protection of Environment ENVIRONMENTAL... SOURCE CATEGORY Carbon Black Thermal Process Subcategory § 458.20 Applicability: description of the carbon black thermal process subcategory. The provisions of this subpart are applicable to...

  19. 40 CFR 458.20 - Applicability: description of the carbon black thermal process subcategory.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... carbon black thermal process subcategory. 458.20 Section 458.20 Protection of Environment ENVIRONMENTAL... SOURCE CATEGORY Carbon Black Thermal Process Subcategory § 458.20 Applicability: description of the carbon black thermal process subcategory. The provisions of this subpart are applicable to...

  20. 40 CFR 458.20 - Applicability: description of the carbon black thermal process subcategory.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... carbon black thermal process subcategory. 458.20 Section 458.20 Protection of Environment ENVIRONMENTAL... CATEGORY Carbon Black Thermal Process Subcategory § 458.20 Applicability: description of the carbon black thermal process subcategory. The provisions of this subpart are applicable to discharges resulting...

  1. 40 CFR 458.20 - Applicability: description of the carbon black thermal process subcategory.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... carbon black thermal process subcategory. 458.20 Section 458.20 Protection of Environment ENVIRONMENTAL... SOURCE CATEGORY Carbon Black Thermal Process Subcategory § 458.20 Applicability: description of the carbon black thermal process subcategory. The provisions of this subpart are applicable to...

  2. 40 CFR 458.20 - Applicability: description of the carbon black thermal process subcategory.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... carbon black thermal process subcategory. 458.20 Section 458.20 Protection of Environment ENVIRONMENTAL... CATEGORY Carbon Black Thermal Process Subcategory § 458.20 Applicability: description of the carbon black thermal process subcategory. The provisions of this subpart are applicable to discharges resulting...

  3. Self-organisation Processes In The Carbon ARC For Nanosynthis

    SciTech Connect

    Ng, J.; Raitses, Yefgeny

    2014-02-02

    The atmospheric pressure carbon arc in inert gases such as helium is an important method for the production of nanomaterials. It has recently been shown that the formation of the carbon deposit on the cathode from gaseous carbon plays a crucial role in the operation of the arc, reaching the high temperatures necessary for thermionic emission to take place even with low melting point cathodes. Based on observed ablation and deposition rates, we explore the implications of deposit formation on the energy balance at the cathode surface, and show how the operation of the arc is self-organised process. Our results suggest that the can arc operate in two di erent regimes, one of which has an important contribution from latent heat to the cathode energy balance. This regime is characterised by the enhanced ablation rate, which may be favourable for high yield synthesis of nanomaterials. The second regime has a small and approximately constant ablation rate with a negligible contribution from latent heat.

  4. Self-organisation Processes In The Carbon ARC For Nanosynthis

    SciTech Connect

    Ng, Jonathan; Raitses, Yevgeny

    2014-02-26

    The atmospheric pressure carbon arc in inert gases such as helium is an important method for the production of nanomaterials. It has recently been shown that the formation of the carbon deposit on the cathode from gaseous carbon plays a crucial role in the operation of the arc, reaching the high temperatures necessary for thermionic emission to take place even with low melting point cathodes. Based on observed ablation and deposition rates, we explore the implications of deposit formation on the energy balance at the cathode surface, and show how the operation of the arc is self-organised process. Our results suggest that the can arc operate in two di erent regimes, one of which has an important contribution from latent heat to the cathode energy balance. This regime is characterised by the enhanced ablation rate, which may be favourable for high yield synthesis of nanomaterials. The second regime has a small and approximately constant ablation rate with a negligible contribution from latent heat.

  5. Material processing with hydrogen and carbon monoxide on Mars

    NASA Technical Reports Server (NTRS)

    Hepp, Aloysius F.; Linne, Diane L.; Landis, Geoffrey A.

    1991-01-01

    Several novel proposals are examined for propellant production from carbon dioxide and monoxide and hydrogen. Potential uses were also examined of CO as a fuel or as a reducing agent in metal oxide processing as obtained or further reduced to carbon. Hydrogen can be reacted with CO to produce a wide variety of hydrocarbons, alcohols, and other organic compounds. Methanol, produced by Fischer-Tropsch chemistry may be useful as a fuel; it is easy to store and handle because it is a liquid at Mars temperatures. The reduction of CO2 to hydrocarbons such as methane or acetylene can be accomplished with hydrocarbons. Carbon monoxide and hydrogen require cryogenic temperatures for storage as liquid. Noncryogenic storage of hydrogen may be accomplished using hydrocarbons, inorganic hydrides, or metal hydrides. Noncryogenic storage of CO may be accomplished in the form of iron carbonyl (FE(CO)5) or other metal carbonyls. Low hydrogen content fuels such as acetylene (C2H2) may be effective propellants with low requirements for earth derived resources. The impact on manned Mars missions of alternative propellant production and utilization is discussed.

  6. Automatic Control of Arc Process for Making Carbon Nanotubes

    NASA Technical Reports Server (NTRS)

    Scott, Carl D.; Pulumbarit, Robert B.; Victor, Joe

    2004-01-01

    An automatic-control system has been devised for a process in which carbon nanotubes are produced in an arc between a catalyst-filled carbon anode and a graphite cathode. The control system includes a motor-driven screw that adjusts the distance between the electrodes. The system also includes a bridge circuit that puts out a voltage proportional to the difference between (1) the actual value of potential drop across the arc and (2) a reference value between 38 and 40 V (corresponding to a current of about 100 A) at which the yield of carbon nanotubes is maximized. Utilizing the fact that the potential drop across the arc increases with the interelectrode gap, the output of the bridge circuit is fed to a motor-control circuit that causes the motor to move the anode toward or away from the cathode if the actual potential drop is more or less, respectively, than the reference potential. Thus, the system regulates the interelectrode gap to maintain the optimum potential drop. The system also includes circuitry that records the potential drop across the arc and the relative position of the anode holder as function of time.

  7. Material processing with hydrogen and carbon monoxide on Mars

    NASA Technical Reports Server (NTRS)

    Hepp, Aloysius F.; Landis, Geoffrey A.; Linne, Diane L.

    1991-01-01

    Several novel proposals are examined for propellant production from carbon dioxide and monoxide and hydrogen. Potential uses were also examined of CO as a fuel or as a reducing agent in metal oxide processing as obtained or further reduced to carbon. Hydrogen can be reacted with CO to produce a wide variety of hydrocarbons, alcohols, and other organic compounds. Methanol, produced by Fischer-Tropsch chemistry may be useful as a fuel; it is easy to store and handle because it is a liquid at Mars temperatures. The reduction of CO2 to hydrocarbons such as methane or acetylene can be accomplished with hydrogen. Carbon monoxide and hydrogen require cryogenic temperatures for storage as liquids. Noncryogenic storage of hydrogen may be accomplished using hydrocarbons, inorganic hydrides, or metal hydrides. Noncryogenic storage of CO may be accomplished in the form of iron carbonyl (FE(CO)5) or other metal carbonyls. Low hydrogen content fuels such as acetylene (C2H2) may be effective propellants with low requirements for earth derived resources. The impact on manned Mars missions of alternative propellant production and utilization is discussed.

  8. Improved granular activated carbon for the stabilization of wastewater PH

    SciTech Connect

    Farmer, R.W.; Dussert, B.W.; Kovacic, S.L.

    1996-12-31

    Laboratory studies have identified the cause of the pH rise, which occurs during water treatment with activated carbon, as an interaction between the naturally occurring anions and protons in the water and the carbon surface. The interaction can be described as an ion exchange type of phenomenon, in which the carbon surface sorbs the anions and corresponding hydronium ions from the water. These studies have shown that the anion sorption and resulting pH increase is independent of the raw material used for the activated carbon production, e.g. bituminous or subbituminous coal, peat, wood or coconut. Also, the pH excursions occur with virgin, reactivated, and acid washed granular carbons. Current pH control technologies focus on adjustment of the wastewater pH prior to discharge or recycle of the initial effluent water until the pH increase abates. However, improved water pH control options have been realized by altering the carbon surface through controlled oxidation rather than the water chemistry or extended preprocessing at the treatment site.

  9. Removal of benzocaine from water by filtration with activated carbon

    USGS Publications Warehouse

    Howe, G.E.; Bills, T.D.; Marking, L.L.

    1990-01-01

    Benzocaine is a promising candidate for registration with the U.S. Food and Drug Administration for use as an anesthetic in fish culture, management, and research. A method for the removal of benzocaine from hatchery effluents could speed registration of this drug by eliminating requirements for data on its residues, tolerances, detoxification, and environmental hazards. Carbon filtration effectively removes many organic compounds from water. This study tested the effectiveness of three types of activated carbon for removing benzocaine from water by column filtration under controlled laboratory conditions. An adsorptive capacity was calculated for each type of activated carbon. Filtrasorb 400 (12 x 40 mesh; U.S. standard sieve series) showed the greatest capacity for benzocaine adsorption (76.12 mg benzocaine/g carbon); Filtrasorb 300 (8 x 30 mesh) ranked next (31.93 mg/g); and Filtrasorb 816 (8 x 16 mesh) absorbed the least (1.0 mg/g). Increased adsorptive capacity was associated with smaller carbon particle size; however, smaller particle size also impeded column flow. Carbon filtration is a practical means for removing benzocaine from treated water.

  10. Continuous flow thermal desorption of VOC's from activated carbon

    SciTech Connect

    Klobucar, J.M.; Pilat, M.J. )

    1992-02-01

    A countercurrent thermal VOC desorber apparatus with 0.43 to 0.67 lb/hr activated carbon flow and 0.43 to 0.49 scfm purge air flow provided 26.6 to 77.7% VOC desorption efficiency over the 62 to 199 F operating range. The VOC concentration of the carbon was measured at the carbon inlet, outlet, and two intermediate points in the desorber by thermogravimetric analysis. Inlet adsorbent carbon VOC concentrations ranged from 0.23 to 0.44 grams VOC/gram carbon. The VOC concentration of the purge air was measured at the purge air outlet and two points within the desorber by GC-FID. The VOC concentration of the outlet purge air ranged from 14,627 to 44,209 ppm. The VOC concentrations measured in the activated carbon and in the purge air provided the operating line data for plotting on an X-Y diagram and together with the equilibrium isotherms resulted in mass transfer coefficients K{sub g}a in the 472 to 864 lb/ft{sup 3} hr range.

  11. Friction stir processing on high carbon steel U12

    NASA Astrophysics Data System (ADS)

    Tarasov, S. Yu.; Melnikov, A. G.; Rubtsov, V. E.

    2015-10-01

    Friction stir processing (FSP) of high carbon steel (U12) samples has been carried out using a milling machine and tools made of cemented tungsten carbide. The FSP tool has been made in the shape of 5×5×1.5 mm. The microstructural characterization of obtained stir zone and heat affected zone has been carried out. Microhardness at the level of 700 MPa has been obtained in the stir zone with microstructure consisting of large grains and cementitte network. This high-level of microhardness is explained by bainitic reaction developing from decarburization of austenitic grains during cementite network formation.

  12. Mechanisms of Carbon Nanotube Production by Laser Ablation Process

    NASA Technical Reports Server (NTRS)

    Scott, Carl D.; Arepalli, Sivaram; Nikolaev, Pavel; Smalley, Richard E.; Nocholson, Leonard S. (Technical Monitor)

    2000-01-01

    We will present possible mechanisms for nanotube production by laser oven process. Spectral emission of excited species during laser ablation of a composite graphite target is compared with that of laser irradiated C60 vapor. The similarities in the transient and spectral data suggest that fullerenes are intermediate precursors for nanotube formation. The confinement of the ablation products by means of a 25-mm diameter tube placed upstream of the target seems to improve the production and purity of nanotubes. Repeated laser pulses vaporize the amorphous/graphitic carbon and possibly catalyst particles, and dissociate fullerenes yielding additional feedstock for SWNT growth.

  13. ON-SITE PRODUCTION OF ACTIVATED CARBON FROM KRAFT BLACK LIQUOR

    EPA Science Inventory

    A pilot plant was designed and constructed to produce char via the St. Regis hydropyrolysis kraft chemical recovery process and to produce activated carbon from the char. This report includes discussion of laboratory and prepilot work, the pilot plant, and presents operating resu...

  14. Activated carbon: Utilization excluding industrial waste treatment. (Latest citations from the Compendex database). Published Search

    SciTech Connect

    Not Available

    1993-06-01

    The bibliography contains citations concerning the commercial use and theoretical studies of activated carbon. Topics include performance evaluations in water treatment processes, preparation and regeneration techniques, materials recovery, and pore structure studies. Adsorption characteristics for specific materials are discussed. Studies pertaining specifically to industrial waste treatment are excluded. (Contains 250 citations and includes a subject term index and title list.)

  15. IRON OPTIMIZATION FOR FENTON-DRIVEN OXIDATION OF MTBE-SPENT GRANULAR ACTIVATED CARBON

    EPA Science Inventory

    Fenton-driven chemical regeneration of granular activated carbon (GAC) is accomplished through the addition of H2O2 and iron (Fe) to spent GAC. The overall objective of this treatment process is to transform target contaminants into less toxic byproducts, re-establish the sorpti...

  16. EFFECTIVENESS OF ACTIVATED CARBON FOR REMOVAL OF TOXIC AND/OR CARCINOGENIC COMPOUNDS FROM WATER SUPPLIES

    EPA Science Inventory

    This research addressed quantification of the performance of fixed-bed granular activated carbon processes for treatment of public water supplies. It included evaluation of the adsorption of selected toxic and/or carcinogenic trace compounds of man-related origin, including carbo...

  17. PRODUCTION OF GRANULAR ACTIVATED CARBONS FROM PIG MANURE FOR METAL IONS ADSORPTION

    Technology Transfer Automated Retrieval System (TEKTRAN)

    The current method of processing pig waste involves diluting it into large lagoons, which carries both environmental and human health risks. Alternatives to pig waste disposal are its reuse into value added products. This study produces activated carbons from swine manure and characterizes them in...

  18. Avoiding Carbon Bed Hot Spots in Thermal Process Off-Gas Systems

    SciTech Connect

    Nick Soelberg; Joe Enneking

    2011-05-01

    Mercury has had various uses in nuclear fuel reprocessing and other nuclear processes, and so is often present in radioactive and mixed (radioactive and hazardous) wastes. Test programs performed in recent years have shown that mercury in off-gas streams from processes that treat radioactive wastes can be controlled using fixed beds of activated sulfur-impregnated carbon, to levels low enough to comply with air emission regulations such as the Hazardous Waste Combustor (HWC) Maximum Achievable Control Technology (MACT) standards. Carbon bed hot spots or fires have occurred several times during these tests, and also during a remediation of tanks that contained mixed waste. Hot spots occur when localized areas in a carbon bed become heated to temperatures where oxidation occurs. This heating typically occurs due to heat of absoption of gas species onto the carbon, but it can also be caused through external means such as external heaters used to heat the carbon bed vessel. Hot spots, if not promptly mitigated, can grow into bed fires. Carbon bed hot spots and fires must be avoided in processes that treat radioactive and mixed waste. Hot spots are detected by (a) monitoring in-bed and bed outlet gas temperatures, and (b) more important, monitoring of bed outlet gas CO concentrations. Hot spots are mitigated by (a) designing for appropriate in-bed gas velocity, for avoiding gas flow maldistribution, and for sufficient but not excessive bed depth, (b) appropriate monitoring and control of gas and bed temperatures and compositions, and (c) prompt implementation of corrective actions if bed hot spots are detected. Corrective actions must be implemented quickly if bed hot spots are detected, using a graded approach and sequence starting with corrective actions that are simple, quick, cause the least impact to the process, and are easiest to recover from.

  19. Effect of silicate modulus and metakaolin incorporation on the carbonation of alkali silicate-activated slags

    SciTech Connect

    Bernal, Susan A.; Mejia de Gutierrez, Ruby; Provis, John L.; Rose, Volker

    2010-06-15

    Accelerated carbonation is induced in pastes and mortars produced from alkali silicate-activated granulated blast furnace slag (GBFS)-metakaolin (MK) blends, by exposure to CO{sub 2}-rich gas atmospheres. Uncarbonated specimens show compressive strengths of up to 63 MPa after 28 days of curing when GBFS is used as the sole binder, and this decreases by 40-50% upon complete carbonation. The final strength of carbonated samples is largely independent of the extent of metakaolin incorporation up to 20%. Increasing the metakaolin content of the binder leads to a reduction in mechanical strength, more rapid carbonation, and an increase in capillary sorptivity. A higher susceptibility to carbonation is identified when activation is carried out with a lower solution modulus (SiO{sub 2}/Na{sub 2}O ratio) in metakaolin-free samples, but this trend is reversed when metakaolin is added due to the formation of secondary aluminosilicate phases. High-energy synchrotron X-ray diffractometry of uncarbonated paste samples shows that the main reaction products in alkali-activated GBFS/MK blends are C-S-H gels, and aluminosilicates with a zeolitic (gismondine) structure. The main crystalline carbonation products are calcite in all samples and trona only in samples containing no metakaolin, with carbonation taking place in the C-S-H gels of all samples, and involving the free Na{sup +} present in the pore solution of the metakaolin-free samples. Samples containing metakaolin do not appear to have the same availability of Na{sup +} for carbonation, indicating that this is more effectively bound in the presence of a secondary aluminosilicate gel phase. It is clear that claims of exceptional carbonation resistance in alkali-activated binders are not universally true, but by developing a fuller mechanistic understanding of this process, it will certainly be possible to improve performance in this area.

  20. Process analysis of CO{sub 2} capture from flue gas using carbonation/calcination cycles

    SciTech Connect

    Li, Z.S.; Cai, N.S.; Croiset, E.

    2008-07-15

    Process analysis of CO{sub 2} capture from flue gas using Ca-based carbonation/calcination cycles is presented here. A carbonation/calcination system is composed essentially of two reactors (an absorber and a regenerator) with Ca-based sorbent circulating between the two reactors (assumed here as fluidized beds). CO{sub 2} is, therefore, transferred from the absorber to the regenerator. Because of the endothermicity of the calcination reaction, a certain amount of coal is burned with pure oxygen in the regenerator. Detailed mass balance, heat balance and cost of electricity and CO{sub 2} mitigation for the carbonation/calcination cycles with three Ca-based sorbents in dual fluidized beds were calculated and analyzed to study the effect of the Ca-based sorbent activity decay on CO{sub 2} capture from flue gas. The three sorbents considered were: limestone, dolomite and CaO/Ca{sub 12}Al{sub 14}O{sub 33} (75/25 wt %) sorbent. All results, including the amount of coal and oxygen required, are presented with respect to the difference in calcium oxide conversion between the absorber and the regenerator, which is an important design parameter. Finally, costs of electricity and CO{sub 2} mitigation costs using carbonation/calcination cycles for the three sorbents were estimated. The results indicate that the economics of the carbonation/calcination process compare favorably with competing technologies for capturing CO{sub 2}.

  1. Removing lead in drinking water with activated carbon

    SciTech Connect

    Taylor, R.M.; Kuennen, R.W. )

    1994-02-01

    A point-of-use (POU) granular activated carbon (GAC) fixed bed adsorber (FBA) was evaluated for reduction of soluble and insoluble lead from drinking water. Some of the factors which affect lead removal by GAC were evaluated, such as carbon type, solution pH, and a limited amount of work on competitive interactions. The design criteria for lead reduction by a POU device are also addressed. Minicolumns were used to evaluate the capacity of carbon for lead under a variety of conditions. The importance of surface chemistry of the carbon and the relationship with the pH of the water for lead reduction was demonstrated. Results indicate that a properly designed POU-GAC-FBA can reduce lead in drinking water to below the EPA action level of 15 ppb while being tested under a variety of conditions as specified under the National Sanitation Foundation (NSF) International Standard 53 test protocol. 37 refs., 9 figs., 1 tab.

  2. Activated carbon adsorption of trichloroethylene (TCE) vapor stripped from TCE-contaminated water.

    PubMed

    Miyake, Yusaku; Sakoda, Akiyoshi; Yamanashi, Hiroaki; Kaneda, Hirotaka; Suzuki, Motoyuki

    2003-04-01

    Ground water contaminated with trichloroethylene (TCE) used in electronic, electric, dry cleaning and the like industries is often treated by air-stripping. In this treatment process, TCE in its vapor form is stripped from ground water by air stream and sometimes emitted into the atmosphere without any additional treatments. Activated carbon adsorption is one of the practical and useful processes for recovering the TCE vapor from the exhaust air stream. However, adsorption of the TCE vapor from the stripping air stream onto activated carbons is not so simple as that from dry air, since in the exhaust air stream the TCE vapor coexists with water vapor with relatively high concentrations. The understanding of the adsorption characteristics of the TCE vapor to be adsorbed on activated carbon in the water vapor-coexisting system is essential for successfully designing and operating the TCE recovery process. In this work, the adsorption equilibrium relations of the TCE vapor adsorption on activated carbons were elucidated as a function of various relative humidity. Activated carbon fibers (ACFs) were used as model activated carbon. The adsorption equilibrium relations were studied by the column adsorption method. The adsorption isotherms of TCE vapor adsorbed on sample ACFs were successfully correlated by the Dubinin-Radushkevich equation for both cases with and without coexistent water vapor. No effects of coexistent water vapor were found on the limiting adsorption volume. However, the adsorption characteristic energy was significantly reduced by the coexistence of water vapor and its reduction was successfully correlated with the equilibrium amount of water vapor adsorbed under the dynamic condition. PMID:12697228

  3. Tc-99 Adsorption on Selected Activated Carbons - Batch Testing Results

    SciTech Connect

    Mattigod, Shas V.; Wellman, Dawn M.; Golovich, Elizabeth C.; Cordova, Elsa A.; Smith, Ronald M.

    2010-12-01

    CH2M HILL Plateau Remediation Company (CHPRC) is currently developing a 200-West Area groundwater pump-and-treat system as the remedial action selected under the Comprehensive Environmental Response, Compensation, and Liability Act Record of Decision for Operable Unit (OU) 200-ZP-1. This report documents the results of treatability tests Pacific Northwest National Laboratory researchers conducted to quantify the ability of selected activated carbon products (or carbons) to adsorb technetium-99 (Tc-99) from 200-West Area groundwater. The Tc-99 adsorption performance of seven activated carbons (J177601 Calgon Fitrasorb 400, J177606 Siemens AC1230AWC, J177609 Carbon Resources CR-1240-AW, J177611 General Carbon GC20X50, J177612 Norit GAC830, J177613 Norit GAC830, and J177617 Nucon LW1230) were evaluated using water from well 299-W19-36. Four of the best performing carbons (J177606 Siemens AC1230AWC, J177609 Carbon Resources CR-1240-AW, J177611 General Carbon GC20X50, and J177613 Norit GAC830) were selected for batch isotherm testing. The batch isotherm tests on four of the selected carbons indicated that under lower nitrate concentration conditions (382 mg/L), Kd values ranged from 6,000 to 20,000 mL/g. In comparison. Under higher nitrate (750 mg/L) conditions, there was a measureable decrease in Tc-99 adsorption with Kd values ranging from 3,000 to 7,000 mL/g. The adsorption data fit both the Langmuir and the Freundlich equations. Supplemental tests were conducted using the two carbons that demonstrated the highest adsorption capacity to resolve the issue of the best fit isotherm. These tests indicated that Langmuir isotherms provided the best fit for Tc-99 adsorption under low nitrate concentration conditions. At the design basis concentration of Tc 0.865 µg/L(14,700 pCi/L), the predicted Kd values from using Langmuir isotherm constants were 5,980 mL/g and 6,870 mL/g for for the two carbons. These Kd values did not meet the target Kd value of 9,000 mL/g. Tests conducted to ascertain the effects of changing pH showed that at pH values of 6.5 and 7.5, no significant differences existed in Tc-adsorption performance for three of the carbons, but the fourth carbon performed better at pH 7.5. When the pH was increased to 8.5, a slight decline in performance was observed for all carbons. Tests conducted to ascertain the temperature effect on Tc-99 adsorption indicated that at 21 ºC, 27 ºC, and 32 ºC there were no significant differences in Tc-99 adsorption for three of the carbons. The fourth carbon showed a noticeable decline in Tc-99 adsorption performance with increasing temperature. The presence of volatile organic compounds (VOCs) in the source water did not significantly affect Tc-99 adsorption on either of two carbons tested. Technetium-99 adsorption differed by less than 15% with or without VOCs present in the test water, indicating that Tc-99 adsorption would not be significantly affected if VOCs were removed from the water prior to contact with carbon.

  4. Sunlight Controls Water Column Processing of Carbon in Arctic Freshwaters

    NASA Astrophysics Data System (ADS)

    Cory, R. M.; Ward, C. P.; Crump, B. C.; Kling, G. W.

    2014-12-01

    Carbon (C) in thawing permafrost soils may have global impacts on climate change, yet controls on its processing and fate are poorly understood. The dominant fate of dissolved organic C (DOC) released from soils to inland waters is either complete oxidation to CO2 or partial oxidation and river export to oceans. Both processes are most often attributed to bacterial respiration, but we recently showed that photochemical oxidation exceeds rates of respiration and accounts for 70-95% of total DOC processed in the water column of arctic lakes and rivers. While the overall dominance of photochemical processing in streams and lakes remained, the fate of DOC varied consistently by water type. In small streams DOC was mainly mineralized by sunlight to CO2, while in lakes the main fate of DOC was partial photo-oxidation. Large rivers were intermediate between these end members, and photo-mineralization to CO2 was about equal to or less than partial photo-oxidation. We suggest this pattern is a result of light-exposure history, where DOC leached from soils into headwater streams has little prior light exposure and is labile to complete photo-oxidation, but as light exposure increases moving downstream and into lakes with longer residence times the DOC photo-lability declines. Thus as easily photo-mineralized moieties are removed, DOC fate shifts toward partial photo-oxidation and downstream export in rivers and lakes. At the basin scale, photochemical processing of DOC is about one third of the total CO2 released from surface waters, and is thus an important, newly measured component of the Arctic C budget. We also suggest that these photochemical transformations of DOC will occur in any shallow surface water, and could be important for better understanding inland water carbon cycling.

  5. Removal of steroid estrogens from wastewater using granular activated carbon: comparison between virgin and reactivated carbon.

    PubMed

    Rowsell, Victoria Francesca; Pang, Dawn Sok Cheng; Tsafou, Foteini; Voulvoulis, Nikolaos

    2009-04-01

    This research was set up in response to new European legislation to identify cost-effective treatment for removal of steroid estrogens from effluent. This study aimed to compare estrogen removal of two types of granular activated carbon: virgin (F400) and reactivated (C401) carbon. Rapid, small-scale column tests were conducted with a total bed volume of 24.9 cm3 over three columns, and analysis was carried out using high-performance liquid chromatography. Results demonstrated that C401 performed more efficiently with greater than or equal to 81% estrogen removal in wastewater compared to F400 which produced greater than or equal to 65% estrogen removal. Estrogen removal can be affected by competitive adsorption from natural organic matter present in wastewater. In addition, the physical properties of each carbon had the potential to influence adsorption differently, thus resulting in the observed varied adsorption capability of the two carbons. PMID:19445328

  6. Can iron-making and steelmaking slag products be used to sequester CO2? Passive weathering and active carbonation experiments.

    NASA Astrophysics Data System (ADS)

    Worrall, Fred; Dobrzański, Andrew

    2015-04-01

    The high calcium content of iron and steel-making slags has been highlighted as providing a suitable feedstock material and medium with which to sequester CO2 into geologically stable carbonate phases. Optimisation of the natural carbonation process provides the potential for increasing the degree of carbonation above that possible via passive weathering. This study has assessed the baseline passive carbonation potential of several different slag products (graded steel slag aggregate, pellite, GBFS) within the climate of the northern UK. This baseline was then used as a comparison to the carbonation values achieved by the same products when actively reacted in a CO2-rich environment. The active carbonation phase of the project involved a factorial experimental study of materials reacted at 1MPa/10MPa CO2 pressure and 25˚C/125˚C. This study has shown: 1) That active carbonation of these products can successfully sequester additional CO2. 2) Carbonation potential in general is highly dependent upon grain size within material types, 3) There is a material-dependant cost-benefit issue when using different active carbonation conditions as well as the choice to use active vs. passive carbonation. The median sequestration potential of the slag products in this study is equivalent to the total emissions from 910 people from the UK; the CO2 emissions from 10000 tonnes of cement production; or 340000 tonnes of steel production.

  7. A novel carbon-based process for flue-gas cleanup. Final report

    SciTech Connect

    Gangwal, S.K.; Howe, G.B.; McMichael, W.J.; Spivey, J.J.

    1993-10-01

    A low-temperature process employing activated carbon-based catalysts and operating downstream of the electrostatic precipitator (ESP) was evaluated jointly by Research Triangle Institute (RTI) and the University of Waterloo (Waterloo). The RTI-Waterloo process was projected to be capable of removing more than 95% SO{sub 2} and 75% NO{sub x }from coal combustion flue gas. In the process, the flue gas leaving the ESP is first cooled to approximately 100{degree}C. The SO{sub 2} is then catalytically oxidized to SO{sub 3} which is removed as medium-strength sulfuric acid in a series of periodically flushed trickle-bed reactors containing an activated carbon-based catalyst. The SO{sub 2}-free gas is then reheated to approximately 150{degree}C and NH{sub 3} is injected into the gas stream. It is then passed over a fixed bed of another activated carbon-based catalyst to reduce the NO{sub x} to N{sub 2} and H{sub 2}O. The clean flue gas is then vented to the stack. The feasibility of the process has been demonstrated in laboratory-scale experiments using simulated flue gas. Catalysts have been identified that gave the required performance for SO{sub 2} and NO{sub x} removal with <25 ppM NH{sub 3} slip. Potential for producing up to 10 N sulfuric acid by periodically flushing the SO{sub 2} removal reactor and further concentration to industrial strength 93.17% sulfuric acid was also demonstrated. Using the results of the experimental work, an engineering evaluation was conducted. Cost for the RTI-Waterloo process was competitive with conventional selective catalytic reduction (SCR) -- flue gas desulfurization (FGD) process and other emerging combined SO{sub 2}/NO{sub x} removal processes.

  8. Process-based interpretation of tracer tests in carbonate aquifers.

    PubMed

    Birk, Steffen; Geyer, Tobias; Liedl, Rudolf; Sauter, Martin

    2005-01-01

    A tracer test in a carbonate aquifer is analyzed using the method of moments and two analytical advection-dispersion models (ADMs) as well as a numerical model. The numerical model is a coupled continuum-pipe flow and transport model that accounts for two different flow components in karstified carbonate aquifers, i.e., rapid and often turbulent conduit flow and Darcian flow in the fissured porous rock. All techniques employed provide reasonable fits to the tracer breakthrough curve (TBC) measured at a spring. The resulting parameter estimates are compared to investigate how each conceptual model of flow and transport processes that forms the basis of the analyses affects the interpretation of the tracer test. Numerical modeling results suggest that the method of moments and the analytical ADMs tend to overestimate the conduit volume because part of the water discharged at the spring is wrongly attributed to the conduit system if flow in the fissured porous rock is ignored. In addition, numerical modeling suggests that mixing of the two flow components accounts for part of the dispersion apparent in the measured TBC, while the remaining part can be attributed to Taylor dispersion. These processes, however, cannot reasonably explain the tail of the TBC. Instead, retention in immobile-fluid regions as included in a nonequilibrium ADM provides a possible explanation. PMID:15882329

  9. Reversible Storage of Hydrogen and Natural Gas in Nanospace-Engineered Activated Carbons

    NASA Astrophysics Data System (ADS)

    Romanos, Jimmy; Beckner, Matt; Rash, Tyler; Yu, Ping; Suppes, Galen; Pfeifer, Peter

    2012-02-01

    An overview is given of the development of advanced nanoporous carbons as storage materials for natural gas (methane) and molecular hydrogen in on-board fuel tanks for next-generation clean automobiles. High specific surface areas, porosities, and sub-nm/supra-nm pore volumes are quantitatively selected by controlling the degree of carbon consumption and metallic potassium intercalation into the carbon lattice during the activation process. Tunable bimodal pore-size distributions of sub-nm and supra-nm pores are established by subcritical nitrogen adsorption. Optimal pore structures for gravimetric and volumetric gas storage, respectively, are presented. Methane and hydrogen adsorption isotherms up to 250 bar on monolithic and powdered activated carbons are reported and validated, using several gravimetric and volumetric instruments. Current best gravimetric and volumetric storage capacities are: 256 g CH4/kg carbon and 132 g CH4/liter carbon at 293 K and 35 bar; 26, 44, and 107 g H2/kg carbon at 303, 194, and 77 K respectively and 100 bar. Adsorbed film density, specific surface area, and binding energy are analyzed separately using the Clausius-Clapeyron equation, Langmuir model, and lattice gas models.

  10. Adsorption of cadmium ions on oxygen surface sites in activated carbon

    SciTech Connect

    Jia, Y.F.; Thomas, K.M.

    2000-02-08

    Various types of oxygen functional groups were introduced onto the surface of coconut shell derived activated carbon by oxidation using nitric acid. Fourier-transform infrared spectroscopy (FTIR), temperature-programmed desorption (TPD), and selective neutralization were used to characterize the surface oxygen functional groups. The oxidized carbons were also heat treated to provide a suite of carbons where the oxygen functional groups of various thermal stabilities were varied progressively. The adsorption of cadmium ions was enhanced dramatically by oxidation of the carbon. The ratio of released protons to adsorbed cadmium ions on oxidized carbon was approximately 2, indicating cation exchange was involved in the process of adsorption. Na{sup +} exchange studies with the oxidized carbon gave a similar ratio. After heat treatment of the oxidized carbons to remove oxygen functional groups, the ratio of H{sup +} released to Cd{sup 2+} adsorbed and the adsorption capacity decreased significantly. Both reversible and irreversible processes were involved in cadmium ion adsorption with reversible adsorption having higher enthalpy. The irreversible adsorption resulted from cation exchange with carboxylic acid groups, whereas the reversible adsorption probably involved physisorption of the partially hydrated cadmium ion.

  11. 40 CFR 60.1820 - How do I monitor the injection rate of activated carbon?

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... activated carbon? 60.1820 Section 60.1820 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY... activated carbon? If your municipal waste combustion unit uses activated carbon to control dioxins/furans or mercury emissions, you must meet three requirements: (a) Select a carbon injection system...

  12. Saltwater intrusion into tidal freshwater marshes alters the biogeochemical processing of organic carbon

    NASA Astrophysics Data System (ADS)

    Neubauer, S. C.; Franklin, R. B.; Berrier, D. J.

    2013-12-01

    Environmental perturbations in wetlands affect the integrated plant-microbial-soil system, causing biogeochemical responses that can manifest at local to global scales. The objective of this study was to determine how saltwater intrusion affects carbon mineralization and greenhouse gas production in coastal wetlands. Working with tidal freshwater marsh soils that had experienced ~ 3.5 yr of in situ saltwater additions, we quantified changes in soil properties, measured extracellular enzyme activity associated with organic matter breakdown, and determined potential rates of anaerobic carbon dioxide (CO2) and methane (CH4) production. Soils from the field plots treated with brackish water had lower carbon content and higher C : N ratios than soils from freshwater plots, indicating that saltwater intrusion reduced carbon availability and increased organic matter recalcitrance. This was reflected in reduced activities of enzymes associated with the hydrolysis of cellulose and the oxidation of lignin, leading to reduced rates of soil CO2 and CH4 production. The effects of long-term saltwater additions contrasted with the effects of short-term exposure to brackish water during three-day laboratory incubations, which increased rates of CO2 production but lowered rates of CH4 production. Collectively, our data suggest that the long-term effect of saltwater intrusion on soil CO2 production is indirect, mediated through the effects of elevated salinity on the quantity and quality of autochthonous organic matter inputs to the soil. In contrast, salinity, organic matter content, and enzyme activities directly influence CH4 production. Our analyses demonstrate that saltwater intrusion into tidal freshwater marshes affects the entire process of carbon mineralization, from the availability of organic carbon through its terminal metabolism to CO2 and/or CH4, and illustrate that long-term shifts in biogeochemical functioning are not necessarily consistent with short-term disturbance-type responses.

  13. Saltwater intrusion into tidal freshwater marshes alters the biogeochemical processing of organic carbon

    NASA Astrophysics Data System (ADS)

    Neubauer, S. C.; Franklin, R. B.; Berrier, D. J.

    2013-07-01

    Environmental perturbations in wetlands affect the integrated plant-microbial-soil system, causing biogeochemical responses that can manifest at local to global scales. The objective of this study was to determine how saltwater intrusion affects carbon mineralization and greenhouse gas production in coastal wetlands. Working with tidal freshwater marsh soils that had experienced roughly 3.5 yr of in situ saltwater additions, we quantified changes in soil properties, measured extracellular enzyme activity associated with organic matter breakdown, and determined potential rates of anaerobic carbon dioxide (CO2) and methane (CH4) production. Soils from the field plots treated with brackish water had lower carbon content and higher C : N ratios than soils from freshwater plots, indicating that saltwater intrusion reduced carbon availability and increased organic matter recalcitrance. This was reflected in reduced activities of enzymes associated with the hydrolysis of cellulose and the oxidation of lignin, leading to reduced rates of soil CO2 and CH4 production. The effects of long-term saltwater additions contrasted with the effects of short-term exposure to brackish water during three-day laboratory incubations, which increased rates of CO2 production but lowered rates of CH4 production. Collectively, our data suggest that the long-term effect of saltwater intrusion on soil CO2 production is indirect, mediated through the effects of elevated salinity on the quantity and quality of autochthonous organic matter inputs to the soil. In contrast, salinity, organic matter content, and enzyme activities directly influence CH4 production. Our analyses demonstrate that saltwater intrusion into tidal freshwater marshes affects the entire process of carbon mineralization, from the availability of organic carbon through its terminal metabolism to CO2 and/or CH4, and illustrate that long-term shifts in biogeochemical functioning are not necessarily consistent with short-term disturbance-type responses.

  14. Adsorption of ethanol onto activated carbon: Modeling and consequent interpretations based on statistical physics treatment

    NASA Astrophysics Data System (ADS)

    Bouzid, Mohamed; Sellaoui, Lotfi; Khalfaoui, Mohamed; Belmabrouk, Hafedh; Lamine, Abdelmottaleb Ben

    2016-02-01

    In this work, we studied the adsorption of ethanol on three types of activated carbon, namely parent Maxsorb III and two chemically modified activated carbons (H2-Maxsorb III and KOH-H2-Maxsorb III). This investigation has been conducted on the basis of the grand canonical formalism in statistical physics and on simplified assumptions. This led to three parameter equations describing the adsorption of ethanol onto the three types of activated carbon. There was a good correlation between experimental data and results obtained by the new proposed equation. The parameters characterizing the adsorption isotherm were the number of adsorbed molecules (s) per site n, the density of the receptor sites per unit mass of the adsorbent Nm, and the energetic parameter p1/2. They were estimated for the studied systems by a non linear least square regression. The results show that the ethanol molecules were adsorbed in perpendicular (or non parallel) position to the adsorbent surface. The magnitude of the calculated adsorption energies reveals that ethanol is physisorbed onto activated carbon. Both van der Waals and hydrogen interactions were involved in the adsorption process. The calculated values of the specific surface AS, proved that the three types of activated carbon have a highly microporous surface.

  15. Chemically and biologically modified activated carbon sorbents for the removal of lead ions from aqueous media.

    PubMed

    Mahmoud, Mohamed E; Abdel-Fattah, Tarek M; Osman, Maher M; Ahmed, Somia B

    2012-01-01

    A method is described for hybridization of the adsorption and biosorption characteristics of chemically treated commercial activated carbon and baker's yeast, respectively, for the formation of environmental friendly multifunctional sorbents. Activated carbon was loaded with baker's yeast after acid-base treatment. Scanning Electron Microscopy (SEM) and Fourier Transform Infrared (FTIR) Spectroscopy were used to characterize these sorbents. Moreover, the sorption capabilities for lead (II) ions were evaluated. A value of 90 ?mol g(-1) was identified as the maximum sorption capacity of activated carbon. Acid-base treatment of activated carbon was found to double the sorption capacity (140-180 ?mol g(-1)). Immobilization of baker's yeast on the surface of activated carbon sorbents was found to further improve the sorption capacity efficiency of lead to 360, 510 and 560 ?mol g(-1), respectively. Several important factors such as pH, contact time, sorbent dose, lead concentration and interfering ions were examined. Lead sorption process was studied and evaluated by several adsorption isotherms and found to follow the Langmuir and BET models. The potential applications of various chemically and biologically modified sorbents and biosorbents for removal of lead from real water matrices were also investigated via multistage micro-column technique and the results referred to excellent recovery values of lead (95.0-99.0 3.0-5.0 %). PMID:22217091

  16. Acoustical Evaluation of Carbonized and Activated Cotton Nonwovens

    Technology Transfer Automated Retrieval System (TEKTRAN)

    An activated carbon fiber nonwoven (ACF) was manufactured from cotton nonowoven fabric. For the ACF acoustical application, a nonwoven composite of ACF with cotton nonwoven as a base layer was developed. Also produced were the composites of the cotton nonwoven base layer with a layer of glass fiber ...

  17. GAC (GRANULAR ACTIVATED CARBON) TREATMENT COSTS: A SENSITIVITY ANALYSIS

    EPA Science Inventory

    Although admittedly effective for removing organic compounds, concerns have been raised about the cost of using GAC for treating drinking water. This paper is devoted to the discussion of the cost of granular activated carbon for removing organic compounds from drinking water. Ac...

  18. EVALUATION OF PROCEDURES TO DESORB BACTERIA FROM GRANULAR ACTIVATED CARBON

    EPA Science Inventory

    Physical, chemical, and enzymatic means for the desorption of micro-organisms from granular activated carbon (GAC) were assessed. Data indicate that homogenization at 16,000 rpm for 3 min at 4 C with a mixture of peptone (0.01%), Zwittergent 3-12 ( times 10 to the minus 6 power M...

  19. 78 FR 13894 - Certain Activated Carbon From China

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-03-01

    ... From the Federal Register Online via the Government Publishing Office INTERNATIONAL TRADE COMMISSION Certain Activated Carbon From China Determination On the basis of the record \\1\\ developed in the subject five-year review, the United States International Trade Commission (Commission) determines, pursuant to section 751(c) of the Tariff Act...

  20. Activated carbon injection - a mercury control success story

    SciTech Connect

    2008-07-01

    Almost 100 full-scale activated carbon injection (ACI) systems have been ordered by US electric utilities. These systems have the potential to remove over 90% of the mercury in flue, at a cost below $10,000 per pound of mercury removal. Field trials of ACI systems arm outlined. 1 fig.

  1. POWDERED ACTIVATED CARBON ADSORPTION ISOTHERMS FOR SELECTED TANNERY EFFLUENTS

    EPA Science Inventory

    Two raw untreated tanning effluents were initially tested for the removal of COD, BOD, TOC, total and specific phenols, oil and grease, and total chromium, using the following six individual powdered activated carbons (PAC): ICI-HDC, ICI-HDH, Nuchar SA-15, Amoco PX-21, Norit FQA,...

  2. Sulfur tolerant molten carbonate fuel cell anode and process

    DOEpatents

    Remick, Robert J. (Naperville, IL)

    1990-01-01

    Molten carbonate fuel cell anodes incorporating a sulfur tolerant carbon monoxide to hydrogen water-gas-shift catalyst provide in situ conversion of carbon monoxide to hydrogen for improved fuel cell operation using fuel gas mixtures of over about 10 volume percent carbon monoxide and up to about 10 ppm hydrogen sulfide.

  3. Self-organization processes at active interfaces

    NASA Astrophysics Data System (ADS)

    Alonso, S.; Chen, H.-Y.; Br, M.; Mikhailov, A. S.

    2010-12-01

    Four examples for active processes at interfaces are studied and reveal complex pattern formation phenomena including complex defect dynamics, standing waves and turbulence, bistability and domain formation and Turing patterns. The examples studied range from active Langmuir monolayers to thin films with floating molecular machines and biomembranes with active proteins. It is shown that linear stability analysis and numerical simulations of the resulting continuum model equations allow to qualitatively reproduce previous experimental observation in some cases and offer intriguing predictions for future investigations in the laboratory.

  4. Ammonia-Activated Mesoporous Carbon Membranes for Gas Separations

    SciTech Connect

    Mahurin, Shannon Mark; Lee, Jeseung; Wang, Xiqing; Dai, Sheng

    2011-01-01

    Porous carbon membranes, which generally show improved chemical and thermal stability compared to polymer membranes, have been used in gas separations for many years. In this work, we show that the post-synthesis ammonia treatment of porous carbon at elevated temperature can improve the permeance and selectivity of these membranes for the separation of carbon dioxide and hydrocarbons from permanent gases. Hierarchically structured porous carbon membranes were exposed to ammonia gas at temperatures ranging from 850 C to 950 C for up to 10 min and the N{sub 2}, CO{sub 2}, and C{sub 3}H{sub 6} permeances were measured for these different membranes. Higher treatment temperatures and longer exposure times resulted in higher gas permeance values. In addition, CO{sub 2}/N{sub 2} and C{sub 3}H{sub 6}/N{sub 2} selectivities increased by a factor of 2 as the treatment temperature and time increased up to a temperature and time of 900 C, 10 min. Higher temperatures showed increased permeance but decreased selectivity indicating excess pore activation. Nitrogen adsorption measurements show that the ammonia treatment increased the porosity of the membrane while elemental analysis revealed the presence of nitrogen-containing surface functionalities in the treated carbon membranes. Thus, ammonia treatment at high temperature provides a controlled method to introduce both added microporosity and surface functionality to enhance gas separations performance of porous carbon membranes.

  5. Techniques for tritium recovery from carbon flakes and dust at the JET active gas handling system

    SciTech Connect

    Gruenhagen, S.; Perevezentsev, A.; Brennan, P. D.; Camp, P.; Knipe, S.; Miller, A.; Yorkshades, J.

    2008-07-15

    Detritiation of highly tritium contaminated carbon and metal material used as first wall armour is a key issue for fusion machines like JET and ITER. Re-deposited carbon and hydrogen in the form of flakes and dust can lead to a build-up of the tritium inventory and therefore this material must be removed and processed. The high tritium concentration of the flake and dust material collected from the JET vacuum vessel makes it unsuitable for direct waste disposal without detritiation. A dedicated facility to process the tritiated carbon flake material and recover the tritium has been designed and built. In several test runs active material was successfully processed and de-tritiated in the new facility. Samples containing only carbon and hydrogen isotopes have been completely oxidized without any residue. Samples containing metallic impurities, e.g. beryllium, require longer processing times, adjusted processing parameters and yield an oxide residue. The detritiation factor was 2x10{sup 4}. In order to simulate in-vessel and ex-vessel detritiation techniques, the detritiation of a carbon flake sample by isotopic exchange in a hydrogen atmosphere was investigated. 2.8% of tritium was recovered by this means. (authors)

  6. Immobilization of Hg(II) in water with polysulfide-rubber (PSR) polymer-coated activated carbon.

    PubMed

    Kim, Eun-Ah; Seyfferth, Angelia L; Fendorf, Scott; Luthy, Richard G

    2011-01-01

    An effective mercury removal method using polymer-coated activated carbon was studied for possible use in water treatment. In order to increase the affinity of activated carbon for mercury, a sulfur-rich compound, polysulfide-rubber (PSR) polymer, was effectively coated onto the activated carbon. The polymer was synthesized by condensation polymerization between sodium tetrasulfide and 1,2-dichloroethane in water. PSR-mercury interactions and Hg-S bonding were elucidated from x-ray photoelectron spectroscopy, and Fourier transform infra-red spectroscopy analyses. The sulfur loading levels were controlled by the polymer dose during the coating process and the total surface area of the activated carbon was maintained for the sulfur loading less than 2 wt%. Sorption kinetic studies showed that PSR-coated activated carbon facilitates fast reaction by providing a greater reactive surface area than PSR alone. High sulfur loading on activated carbon enhanced mercury adsorption contributing to a three orders of magnitude reduction in mercury concentration. ?-X-ray absorption near edge spectroscopic analyses of the mercury bound to activated carbon and to PSR on activated carbon suggests the chemical bond with mercury on the surface is a combination of Hg-Cl and Hg-S interaction. The pH effect on mercury removal and adsorption isotherm results indicate competition between protons and mercury for binding to sulfur at low pH. PMID:20965542

  7. Transcription Factor Arabidopsis Activating Factor1 Integrates Carbon Starvation Responses with Trehalose Metabolism1[OPEN

    PubMed Central

    Garapati, Prashanth; Feil, Regina; Lunn, John Edward; Van Dijck, Patrick; Balazadeh, Salma; Mueller-Roeber, Bernd

    2015-01-01

    Plants respond to low carbon supply by massive reprogramming of the transcriptome and metabolome. We show here that the carbon starvation-induced NAC (for NO APICAL MERISTEM/ARABIDOPSIS TRANSCRIPTION ACTIVATION FACTOR/CUP-SHAPED COTYLEDON) transcription factor Arabidopsis (Arabidopsis thaliana) Transcription Activation Factor1 (ATAF1) plays an important role in this physiological process. We identified TREHALASE1, the only trehalase-encoding gene in Arabidopsis, as a direct downstream target of ATAF1. Overexpression of ATAF1 activates TREHALASE1 expression and leads to reduced trehalose-6-phosphate levels and a sugar starvation metabolome. In accordance with changes in expression of starch biosynthesis- and breakdown-related genes, starch levels are generally reduced in ATAF1 overexpressors but elevated in ataf1 knockout plants. At the global transcriptome level, genes affected by ATAF1 are broadly associated with energy and carbon starvation responses. Furthermore, transcriptional responses triggered by ATAF1 largely overlap with expression patterns observed in plants starved for carbon or energy supply. Collectively, our data highlight the existence of a positively acting feedforward loop between ATAF1 expression, which is induced by carbon starvation, and the depletion of cellular carbon/energy pools that is triggered by the transcriptional regulation of downstream gene regulatory networks by ATAF1. PMID:26149570

  8. Mini-review: green sustainable processes using supercritical fluid carbon dioxide.

    PubMed

    Ramsey, Edward; Sun, Qiubai; Zhang, Zhiqiang; Zhang, Chongmin; Gou, Wei

    2009-01-01

    Environmentally benign carbon dioxide offers significant potential in its supercritical fluid phase to replace current reliance on a range of hazardous, relatively expensive and environmentally damaging organic solvents that are used on an extensive global basis. The unique combination of the physical properties of supercritical fluids are being exploited and further researched to continue the development and establishment of high efficiency, compact plant to provide energy and water efficient manufacturing processes. This mini-review is focused on the use and potential applications of supercritical fluid carbon dioxide for a selected range of key and emerging industrial processes as a sustainable alternative to totally eliminate or greatly reduce the requirement of numerous conventional organic solvents. Examples of the industries include: chemical extraction and purification, synthetic chemical reactions including polymerization and inorganic catalytic processes. Biochemical reactions involving enzymes, particle size engineering, textile dyeing and advanced material manufacture provide further illustrations of vital industrial activities where supercritical fluid technology processes are being implemented or developed. Some aspects relating to the economics of sustainable supercritical fluid carbon dioxide processes are also considered. PMID:19803072

  9. Removal of hexavalent chromium from groundwater by granular activated carbon

    SciTech Connect

    Han, I.; Schlautman, M.A.; Batchelor, B.

    2000-02-01

    Removal of hexavalent chromium, Cr(VI), from an artificial groundwater by two commercially available granular activated carbons (GACs) was investigated in batch and continuous-flow column studies. Experimental parameters examined included solution pH, presence of dissolved oxygen (DO), and GAC pretreatment with reducing agents. As solution pH increased from 4 to 7.5, the amount of Cr(VI) removed by both GACs decreased significantly. Removal of DO from experimental systems enhanced GAC performance, but pretreatment of the GACs with reductants (ferrous iron or dithionite) did not improve Cr(VI) removal. Equilibration with 0.01 M dibasic potassium phosphate [to extract adsorbed Cr(VI)] followed by a wash with 0.02 N sulfuric acid [to remove precipitated-sorbed Cr(III)] proved to be a viable method to regenerate carbons whose Cr(VI) removal capacities were exhausted. Performance of regenerated carbons exceeded that of virgin carbons, primarily because of the favorable adsorption of Cr(VI) at low pH values and the reduction of Cr(VI) to Cr(III) on acidic GAC surfaces. The presence of Cr(III) in acid wash solutions provides direct evidence that Cr(VI) is reduced to Cr(III) in GAC systems under relatively acidic conditions. Granular activated carbon performance during five complete cycles was consistently high, which suggests that such a system will be able to function over many operation cycles without deleterious effects.

  10. Adsorption and biodegradation of high explosives on granular activated carbon

    SciTech Connect

    Morley, M.C.; Shammas, S.; Speitel, G.E. Jr.

    1999-07-01

    Adsorption to granular activated carbon (GAC) is an effective method for removing high explosives (HE) compounds from water, but no permanent treatment is achieved. An off-line bioregeneration system, which combines adsorption and biodegradation, is being developed to reduce GAC usage rates and destroy RDX and HMX. Desorption is often the limiting mass transfer mechanism in bioregeneration systems; thus, two cosolvents, four surfactants, and two cyclodextrins were considered for improving desorption of RDX and HMX. In batch experiments, about 3% of the adsorbed RDX was desorbed over 11 days using buggered water as the desorption fluid. In comparison, about 96% of the RDX was extracted from the GAC by acetonitrile. Ethanol and methanol were both effective in desorbing RDX and HMX. Sodium dodecyl sulfate (SDS), an anionic surfactant, desorbed 56.4% of the RDX at a concentration of 500 mg SDS/L. Cyclodextrins were marginally more effective than water. Continuous operation of a sequencing batch reactor (SBR) has effectively treated both contaminants. In an SBR that was operated with 4-day cycles for 72 days, mixed cultures consistently reduced RDX concentrations from 1 mg/L to non-detectable levels and HMX from 0.6 mg/L to 0.4 mg/L over each cycle. When removal from groundwater by adsorption is combined with enhanced desorption and subsequent biological treatment, the overall process is expected to effectively increase the GAC service life and provide a permanent treatment method for RDX and HMX.

  11. Effect of ?-irradiation on the structure of activated carbons produced from Turkish Elbistan lignite

    NASA Astrophysics Data System (ADS)

    Erin, Demet; Eken, Mahmut; Aktas, Zeki; etinkaya, Sevil; Sakintuna, Billur; Yrm, Yuda

    2005-08-01

    The results of the treatment of activated carbons prepared from Turkish Elbistan lignite with ?-irradiation from a 60Co source are presented and associated volatilization of surface material of the activated carbon as a means to obtain a physical modification of the material is discussed in terms of changes in surface area, free radical concentrations and structural changes determined with FTIR and solid-state 13C NMR spectroscopical methods. BET areas of irradiated samples are measured to be greater than those of non-irradiated samples; this might be considered as an indication to some loss of material from the surface by ?-irradiation. ?-Irradiation caused remarkable erosion on the surface with the loss of some carbonaceous matter by probable bond cleavage reactions. As the activation temperature was raised, both of the carbon content and the intensities of the carbon functionalities decreased in the 13C NMR spectra. The observation of symmetric shapes in the ESR spectra might be considered as an indication to the delocalization of the electrons over the graphite-like microcrystallites present in the active carbons. The broadening of the ESR signals in the present work might be both due to the effect of oxygen during the measurements in lower activation temperatures and the enhanced effect of the presence of Fe 3+ ion in the form of pyrites in the mineral matter the lignite used. Increase of the relative intensities of free radicals with activation temperature may be indicative of some molecular cracking leading to organic radicals. Irradiation of the activated carbon samples seemed to increase the peak widths and g-values. g-value of 2.003 was due to semiquinone-type free radical which was probably created in oxidation reaction during activation processes.

  12. Bimodal activated carbons derived from resorcinol-formaldehyde cryogels

    NASA Astrophysics Data System (ADS)

    Szczurek, Andrzej; Amaral-Labat, Gisele; Fierro, Vanessa; Pizzi, Antonio; Celzard, Alain

    2011-06-01

    Resorcinol-formaldehyde cryogels prepared at different dilution ratios have been activated with phosphoric acid at 450 °C and compared with their carbonaceous counterparts obtained by pyrolysis at 900 °C. Whereas the latter were, as expected, highly mesoporous carbons, the former cryogels had very different pore textures. Highly diluted cryogels allowed preparation of microporous materials with high surface areas, but activation of initially dense cryogels led to almost non-porous carbons, with much lower surface areas than those obtained by pyrolysis. The optimal acid concentration for activation, corresponding to stoichiometry between molecules of acid and hydroxyl groups, was 2 M l-1, and the acid-cryogel contact time also had an optimal value. Such optimization allowed us to achieve surface areas and micropore volumes among the highest ever obtained by activation with H3PO4, close to 2200 m2 g-1 and 0.7 cm3 g-1, respectively. Activation of diluted cryogels with a lower acid concentration of 1.2 M l-1 led to authentic bimodal activated carbons, having a surface area as high as 1780 m2 g-1 and 0.6 cm3 g-1 of microporous volume easily accessible through a widely developed macroporosity.

  13. Large-area compliant tactile sensors using printed carbon nanotube active-matrix backplanes.

    PubMed

    Yeom, Chiseon; Chen, Kevin; Kiriya, Daisuke; Yu, Zhibin; Cho, Gyoujin; Javey, Ali

    2015-03-01

    A 20 20 pixel pressure sensor array based on a printed active-matrix single-wall carbon-nanotube thin-film transistor backplane is presented. Using a gravure printing process that is compatible with fully printed large-area roll-to-roll processing, a 97% device yield is obtained on the 400-transistor backplane. As a proof of concept, pressure sensors are integrated to map the applied tactile pressure across the array. PMID:25640804

  14. Processing of Color Words Activates Color Representations

    ERIC Educational Resources Information Center

    Richter, Tobias; Zwaan, Rolf A.

    2009-01-01

    Two experiments were conducted to investigate whether color representations are routinely activated when color words are processed. Congruency effects of colors and color words were observed in both directions. Lexical decisions on color words were faster when preceding colors matched the color named by the word. Color-discrimination responses

  15. Enhancement of ORR catalytic activity by multiple heteroatom-doped carbon materials.

    PubMed

    Kim, Dae-wook; Li, Oi Lun; Saito, Nagahiro

    2015-01-01

    Heteroatom-doped carbon matrices have been attracting significant attention due to their superior electrochemical stability, light weight and low cost. Hence, in this study, various types of heteroatom, including single dopants of N, B and P and multiple dopants of B-N and P-N with a carbon matrix were synthesized by an innovative method named the solution plasma process. The heteroatom was doped into the carbon matrix during the discharge process by continuous dissociation and recombination of precursors. The chemical bonding structure, ORR activity and electrochemical performance were compared in detail for each single dopant and multiple dopants. According to the Raman spectra, the carbon structures were deformed by the doped heteroatoms in the carbon matrix. In comparison with N-doped structures (NCNS), the ORR potential of PN-doped structures (PNCNS) was positively shifted from -0.27 V to -0.24 V. It was observed that doping with N decreased the bonding between P and C in the matrix. The multiple doping induced additional active sites for ORR which further enhanced ORR activity and stability. Therefore, PNCNS is a promising metal-free catalyst for ORR at the cathode in a fuel cell. PMID:25406572

  16. Esterase activity of carbonic anhydrases serves as surrogate for selecting antibodies blocking hydratase activity.

    PubMed

    Uda, Narasimha Rao; Seibert, Volker; Stenner-Liewen, Frank; Mller, Philipp; Herzig, Petra; Gondi, Gabor; Zeidler, Reinhard; van Dijk, Marc; Zippelius, Alfred; Renner, Christoph

    2015-12-01

    Carbonic anhydrase 9 (CA9) and carbonic anhydrase 12 (CA12) were proposed as potential targets for cancer therapy more than 20 years ago. However, to date, there are only very few antibodies that have been described to specifically target CA9 and CA12 and also block the enzymatic activity of their targets. One of the early stage bottlenecks in identifying CA9- and CA12-inhibiting antibodies has been the lack of a high-throughput screening system that would allow for rapid assessment of inhibition of the targeted carbon dioxide hydratase activity of carbonic anhydrases. In this study, we show that measuring the esterase activity of carbonic anhydrase offers a robust and inexpensive screening method for identifying antibody candidates that block both hydratase and esterase activities of carbonic anhydrase's. To our knowledge, this is the first implementation of a facile surrogate-screening assay to identify potential therapeutic antibodies that block the clinically relevant hydratase activity of carbonic anhydrases. PMID:25775095

  17. Structural analysis of water and carbon tetrachloride adsorbed in activated carbon fibres.

    PubMed

    Sliwi?ska-Bartkowiak, Ma?gorzata; Drozdowski, Henryk; Kempi?ski, Mateusz; Ja?d?ewska, Monika; Long, Yun; Palmer, Jeremy C; Gubbins, Keith E

    2012-05-21

    We report X-ray diffraction studies of water and carbon tetrachloride adsorbed in nanoporous activated carbon fibres. The fibres are built of turbostratic nanoparticles separated by quasi two-dimensional voids, forming narrow slit-shaped pores. In order to determine the structure of water within the pores and its influence on the fibres' structure, mean interatomic and intermolecular distances have been estimated from the positions of the maxima of the normalized angular distribution functions obtained by X-ray diffraction. We observe a cluster arrangement of the water molecules, as well as significant changes in the interlayer distance of the carbon nanoparticles upon adsorption of both water and carbon tetrachloride. The results suggest that very high pressures arise within the pores, as has been observed in molecular simulations, and this may give rise to the large change in electronic properties of the fibres after adsorption of guest molecules. The in-pore pressure normal to the pore walls is estimated from the experimental data, and is found to be positive and of the order 4000 bar. Molecular simulation results for the normal pressure component are presented for both water and carbon tetrachloride in carbon slit pores, and are in general agreement with the experiments. For both fluids the normal pressure is an oscillating function of pore width. PMID:22491317

  18. 40 CFR 62.15275 - How do I monitor the injection rate of activated carbon?

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... carbon? If your municipal waste combustion unit uses activated carbon to control dioxins/furans or... dioxins/furans and mercury stack test, determine the average carbon feed rate in kilograms (or pounds)...

  19. PERFORMANCE OF ACTIVATED SLUDGE-POWDERED ACTIVATED CARBON-WET AIR REGENERATION SYSTEMS

    EPA Science Inventory

    The investigation summarized in this report was undertaken to evaluate the performance of powdered activated carbon (PAC) technology used in conjuntion with wet air regeneration (WAR) at municipal wastewater treatment plants. xcessive ash concentrations accumulated in the mixed l...

  20. PERFORMANCE OF ACTIVATED SLUDGE-POWDERED ACTIVATED CARBON-WET AIR REGENERATION SYSTEMS

    EPA Science Inventory

    The investigation summarized in the report was undertaken to evaluate the performance of powdered activated carbon (PAC) technology used in conjunction with wet air regeneration (WAR) at municipal wastewater treatment plants. Excessive ash concentrations accumulated in the mixed ...