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Sample records for activated carbon surface

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

    Energy Technology Data Exchange (ETDEWEB)

    Gonzalez-Garcia, P., E-mail: pegonzal@quim.ucm.es [Departamento de Quimica Inorganica, Facultad de Ciencias Quimicas, Universidad Complutense, E-28040, Madrid (Spain); Centeno, T.A. [Instituto Nacional del Carbon-CSIC, Apartado 73, E-33080 Oviedo (Spain); Urones-Garrote, E. [Centro Nacional de Microscopia Electronica, Universidad Complutense, E-28040, Madrid (Spain); Avila-Brande, D.; Otero-Diaz, L.C. [Departamento de Quimica Inorganica, Facultad de Ciencias Quimicas, Universidad Complutense, E-28040, Madrid (Spain)

    2013-01-15

    Highlights: Black-Right-Pointing-Pointer Activated carbons were produced by KOH activation at 700 Degree-Sign C. Black-Right-Pointing-Pointer The observed nanostructure consists of highly disordered graphene-like layers with sp{sup 2} bond content Almost-Equal-To 95%. Black-Right-Pointing-Pointer Textural parameters show high surface area ( Almost-Equal-To 1000 m{sup 2}/g) and pore width of 1.3-1.8 nm. Black-Right-Pointing-Pointer Specific capacitance reaches values as high as 161 F/g. - Abstract: Low cost activated carbons have been produced via chemical activation, by using KOH at 700 Degree-Sign 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 sp{sup 2} content Almost-Equal-To 95% and average mass density of 1.65 g/cm{sup 3} (25% below standard graphite). Textural parameters indicate a high porosity development with surface areas ranging from 850 to 1100 m{sup 2}/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/cm{sup 2}) 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.

  2. Ozonation of benzothiazole saturated-activated carbons: Influence of carbon chemical surface properties

    Energy Technology Data Exchange (ETDEWEB)

    Valdes, H. [Facultad de Ingenieria, Universidad Catolica de la Santisima Concepcion, Caupolican 491, Concepcion (Chile)]. E-mail: hvaldes@ucsc.cl; Zaror, C.A. [Departamento de Ingenieria Quimica (F. Ingenieria), Universidad de Concepcion, Correo 3, Casilla 160-C, Concepcion (Chile)

    2006-09-21

    The combined or sequential use of ozone and activated carbon to treat toxic effluents has increased in recent years. However, little is known about the influence of carbon surface active sites on ozonation of organic adsorbed pollutants. This paper presents experimental results on the effect of metal oxides and oxygenated surface groups on gaseous ozonation of spent activated carbons. Benzothiazole (BT) was selected as a target organic compound in this study due to its environmental concern. Activated carbons with different chemical surface composition were prepared from a Filtrasorb-400 activated carbon. Pre-treatment included: ozonation, demineralisation, and deoxygenation of activated carbon. Ozonation experiments of BT saturated-activated carbons were conducted in a fixed bed reactor loaded with 2 g of carbon samples. The reactor was fed with an O{sub 2}/O{sub 3} gas mixture (2 dm{sup 3}/min, 5 g O{sub 3}/h), for a given exposure time, in the range 10-120 min, at 298 K and 1 atm. Results show that extended gaseous ozonation of activated carbon saturated with BT led to the effective destruction of the adsorbate by oxidation reactions. Oxidation of BT adsorbed on activated carbon seemed to occur via both direct reaction with ozone molecules, and by oxygen radical species generated by catalytic ozone decomposition on metallic surface sites.

  3. Surface functional groups and redox property of modified activated carbons

    Institute of Scientific and Technical Information of China (English)

    Zhang Xianglan; Deng Shengfu; Liu Qiong; Zhang Yan; Cheng Lei

    2011-01-01

    A series of activated carbons (ACs) were prepared using HNO3, H2O2 and steam as activation agents with the aim to introduce functional groups to carbon surface in the ACs preparation process. The effects of concentration of activation agent, activation time on the surface functional groups and redox property of ACs were characterized by Temperature Program Desorption (TPD) and Cyclic Voitammetry (CV). Results showed that lactone groups of ACs activated by HNO3 increase with activation time, and the carboxyl groups increase with the concentration of HNO3. Carbonyl/quinine groups of ACs activated by H2O2 increase with the activation time and the concentration of H2O2, although the acidic groups decrease with the concentration of H2O2. The redox property reflected by CV at 0 and 0.5 V is different with any kinds of oxygen functional groups characterized by TPD, but it is consistent with the SO2 catalytic oxidization/oxidation properties indicated by TPR.

  4. Covalent organic polymer functionalization of activated carbon surfaces through acyl chloride for environmental clean-up

    DEFF Research Database (Denmark)

    Mines, Paul D.; Thirion, Damien; Uthuppu, Basil;

    2017-01-01

    Nanoporous networks of covalent organic polymers (COPs) are successfully grafted on the surfaces of activated carbons, through a series of surface modification techniques, including acyl chloride formation by thionyl chloride. Hybrid composites of activated carbon functionalized with COPs exhibit...

  5. Effects of Surface Treatment of Activated Carbon on Its Surface and Cr(VI) Adsorption Characteristics

    Energy Technology Data Exchange (ETDEWEB)

    Park, Soo Jin; Jang, Yu Sin [Advanced Materials Division., Korea Research Institute of Chimical Technology, Taejon (Korea)

    2001-04-01

    In this work, the effect of surface treatments on activated carbons (ACs) has been studied in the context of gas and liquid adsorption behaviors. The chemical solutions used in this experiment were 35% sodium hydroxide, and these were used for the acidic and basic treatments, respectively. The surface properties have been determined by pH, acid-base values, and FT-IR. The adsorption isotherms of Cr(VI) ion on activated carbons have been studied with the 5 mg/l concentration at ambient temperature. N{sub 2} adsorption isotherm characteristics, which include the specific surface area, micro pore volume, and microporosity, were determined by BET and Boer's-plot methods. In case of the acidic treatment of activated carbons, it was observed that the adsorption of Cr(VI) ion was more effective due to the increase acid value (or acidic functional group) of activated carbon surfaces. However, the basic treatment on activated carbons was caused no significant effects, probably due to the decreased specific surface area and total pore volume. 27 refs., 7 figs., 4 tabs.

  6. A REVIEW OF OXYGEN-CONTAINING SURFACE GROUPS AND SURFACE MODIFICATION OF ACTIVATED CARBON

    Institute of Scientific and Technical Information of China (English)

    WU Yongwen; LI Zhong; XI Hongxia; XIA Qibin

    2004-01-01

    This review focused on the recent reports related to the function, characterization and modification of oxygen-containing surface groups of activated carbon (AC). The Oxygen-containing surface groups were briefly described, and the most frequently used techniques for characterization of the oxygen-containing surface groups on ACs were also briefly stated. A detailed discussion of the effects of the oxygen-containing surface groups on the adsorptive capacity of AC was given. The recent progresses in modification of the oxygen-containing surface groups of AC were also reviewed.

  7. High surface area activated carbon prepared from cassava peel by chemical activation.

    Science.gov (United States)

    Sudaryanto, Y; Hartono, S B; Irawaty, W; Hindarso, H; Ismadji, S

    2006-03-01

    Cassava is one of the most important commodities in Indonesia, an agricultural country. Cassava is one of the primary foods in our country and usually used for traditional food, cake, etc. Cassava peel is an agricultural waste from the food and starch processing industries. In this study, this solid waste was used as the precursor for activated carbon preparation. The preparation process consisted of potassium hydroxide impregnation at different impregnation ratio followed by carbonization at 450-750 degrees C for 1-3 h. The results revealed that activation time gives no significant effect on the pore structure of activated carbon produced, however, the pore characteristic of carbon changes significantly with impregnation ratio and carbonization temperature. The maximum surface area and pore volume were obtained at impregnation ratio 5:2 and carbonization temperature 750 degrees C.

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

    Science.gov (United States)

    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.

  9. Activity of catalase adsorbed to carbon nanotubes: effects of carbon nanotube surface properties.

    Science.gov (United States)

    Zhang, Chengdong; Luo, Shuiming; Chen, Wei

    2013-09-15

    Nanomaterials have been studied widely as the supporting materials for enzyme immobilization. However, the interactions between enzymes and carbon nanotubes (CNT) with different morphologies and surface functionalities may vary, hence influencing activities of the immobilized enzyme. To date how the adsorption mechanisms affect the activities of immobilized enzyme is not well understood. In this study the adsorption of catalase (CAT) on pristine single-walled carbon nanotubes (SWNT), oxidized single-walled carbon nanotubes (O-SWNT), and multi-walled carbon nanotubes (MWNT) was investigated. The adsorbed enzyme activities decreased in the order of O-SWNT>SWNT>MWNT. Fourier transforms infrared spectroscopy (FTIR) and circular dichrois (CD) analyses reveal more significant loss of α-helix and β-sheet of MWNT-adsorbed than SWNT-adsorbed CAT. The difference in enzyme activities between MWNT-adsorbed and SWNT-adsorbed CAT indicates that the curvature of surface plays an important role in the activity of immobilized enzyme. Interestingly, an increase of β-sheet content was observed for CAT adsorbed to O-SWNT. This is likely because as opposed to SWNT and MWNT, O-SWNT binds CAT largely via hydrogen bonding and such interaction allows the CAT molecule to maintain the rigidity of enzyme structure and thus the biological function.

  10. Surface properties of activated carbon from different raw materials

    Institute of Scientific and Technical Information of China (English)

    Zhang XiangLan; Zhang Yan; Liu Qiong; Zhou Wei

    2012-01-01

    Activated carbons (ACs) with different surface properties were prepared from different raw materials.N2 adsorption,pH value,Boehm titration,Temperature-programmed reduction (TPR) and FTIR were employed to characterize the pore structure and surface chemical properties of the ACs.The results show that AC from bituminous coal (AC-B) has more meso-pores,higher pH value,more carboxylic groups and basic site than ACs from coconut shell and hawthorn(AC-C,AC-H).Oxygen in the mixture gas has great effect on SO2 catalytic oxidation/oxidation ability of AC-B.In the absence of oxygen,the adsorbed SO2 on AC-B is 0.16 mmol/g and the conversion ratio of adsorbed SO2 to SO3 is 22,07%; while in the presence of oxygen,the adsorbed amount of SO2 is 0.42 mmol/g,and all of the adsorbed SO2 was totally converted to SO3.This feature of AC-B is consistent with its higher pH value,basic site and the reaction ability with H2 from TPR.The conversion ratios of SO2 absorbed on both AC-C and AC-H were 100%,respectively.

  11. Surface modification of activated carbon for enhanced adsorption of perfluoroalkyl acids from aqueous solutions.

    Science.gov (United States)

    Zhi, Yue; Liu, Jinxia

    2016-02-01

    The objective of the research was to examine the effect of increasing carbon surface basicity on uptake of perfluorooctane sulfonic (PFOS) and carboxylic acids (PFOA) by activated carbon. Granular activated carbons made from coal, coconut shell, wood, and phenolic-polymer-based activated carbon fibers were modified through high-temperature and ammonia gas treatments to facilitate systematical evaluation of the impact of basicity of different origins. Comparison of adsorption isotherms and adsorption distribution coefficients showed that the ammonia gas treatment was more effective than the high-temperature treatment in enhancing surface basicity. The resultant higher point of zero charges and total basicity (measured by total HCl uptake) correlated with improved adsorption affinity for PFOS and PFOA. The effectiveness of surface modification to enhance adsorption varied with carbon raw material. Wood-based carbons and activated carbon fibers showed enhancement by one to three orders of magnitudes while other materials could experience reduction in adsorption towards either PFOS or PFOA.

  12. Surface heterogeneity effects of activated carbons on the kinetics of paracetamol removal from aqueous solution

    Science.gov (United States)

    Ruiz, B.; Cabrita, I.; Mestre, A. S.; Parra, J. B.; Pires, J.; Carvalho, A. P.; Ania, C. O.

    2010-06-01

    The removal of a compound with therapeutic activity (paracetamol) from aqueous solutions using chemically modified activated carbons has been investigated. The chemical nature of the activated carbon material was modified by wet oxidation, so as to study the effect of the carbon surface chemistry and composition on the removal of paracetamol. The surface heterogeneity of the carbon created upon oxidation was found to be a determinant in the adsorption capability of the modified adsorbents, as well as in the rate of paracetamol removal. The experimental kinetic data were fitted to the pseudo-second order and intraparticle diffusion models. The parameters obtained were linked to the textural and chemical features of the activated carbons. After oxidation the wettability of the carbon is enhanced, which favors the transfer of paracetamol molecules to the carbon pores (smaller boundary layer thickness). At the same time the overall adsorption rate and removal efficiency are reduced in the oxidized carbon due to the competitive effect of water molecules.

  13. Textural, surface, thermal and sorption properties of the functionalized activated carbons and carbon nanotubes

    Directory of Open Access Journals (Sweden)

    Nowicki Piotr

    2015-12-01

    Full Text Available Two series of functionalised carbonaceous adsorbents were prepared by means of oxidation and nitrogenation of commercially available activated carbon and multi-walled carbon nanotubes. The effect of nitrogen and oxygen incorporation on the textural, surface, thermal and sorption properties of the adsorbents prepared was tested. The materials were characterized by elemental analysis, low-temperature nitrogen sorption, thermogravimetric study and determination of the surface oxygen groups content. Sorptive properties of the materials obtained were characterized by the adsorption of methylene and alkali blue 6B as well as copper(II ions. The final products were nitrogen- and oxygen-enriched mesoporous adsorbents of medium-developed surface area, showing highly diverse N and O-heteroatom contents and acidic-basic character of the surface. The results obtained in our study have proved that through a suitable choice of the modification procedure of commercial adsorbents it is possible to produce materials with high sorption capacity towards organic dyes as well as copper(II ions.

  14. THE EFFECT OF ACTIVATED CARBON SURFACE MOISTURE ON LOW TEMPERATURE MERCURY ADSORPTION

    Science.gov (United States)

    Experiments with elemental mercury (Hg0) adsorption by activated carbons were performed using a bench-scale fixed-bed reactor at room temperature (27 degrees C) to determine the role of surface moisture in capturing Hg0. A bituminous-coal-based activated carbon (BPL) and an activ...

  15. Preparation, Surface and Pore Structure of High Surface Area Activated Carbon Fibers from Bamboo by Steam Activation

    Directory of Open Access Journals (Sweden)

    Xiaojun Ma

    2014-06-01

    Full Text Available High surface area activated carbon fibers (ACF have been prepared from bamboo by steam activation after liquefaction and curing. The influences of activation temperature on the microstructure, surface area and porosity were investigated. The results showed that ACF from bamboo at 850 °C have the maximum iodine and methylene blue adsorption values. Aside from the graphitic carbon, phenolic and carbonyl groups were the predominant functions on the surface of activated carbon fiber from bamboo. The prepared ACF from bamboo were found to be mainly type I of isotherm, but the mesoporosity presented an increasing trend after 700 °C. The surface area and micropore volume of samples, which were determined by application of the Brunauer-Emmett-Teller (BET and t-plot methods, were as high as 2024 m2/g and 0.569 cm3/g, respectively. It was also found that the higher activation temperature produced the more ordered microcrystalline structure of ACF from bamboo.

  16. Effect of activation agents on the surface chemical properties and desulphurization performance of activated carbon

    Institute of Scientific and Technical Information of China (English)

    2010-01-01

    Flue gas pollution is a serious environmental problem that needs to be solved for the sustainable development of China.The surface chemical properties of carbon have great influence on its desulphurization performance.A series of activated carbons (ACs) were prepared using HNO3,H2O2,NH3·H2O and steam as activation agents with the aim to introduce functional groups to carbon surface in the ACs preparation process.The ACs were physically and chemically characterized by iodine and SO2 adsorption,ultimate analysis,Boehm titration,and temperature-programmed reduction (TPR).Results showed that the iodine number and desulphurization capacity of NH3·H2O activated carbon (AC-NH3) increase with both activation time,and its desulphurization capacity also increases with the concentration of activation agent.However,HNO3 activated carbon (AC-HNO3) and H2O2 activated carbon (AC-H2O2) exhibit more complex behavior.Only their iodine numbers increase monotonously with activation time.Compared with steam activated AC (AC-H2O),the nitrogen content increases 0.232% in AC-NH3 and 0.077% in AC-HNO3.The amount of total basic site on AC-HNO3 is 0.19 mmol·g-1 higher than that on AC-H2O.H2O2 activation introduces an additional 0.08 mmol·g-1 carboxyl groups to AC surface than that introduced by steam activation.The desulphurization capacity of ACs in simulate flue gas desulphurization decreases as follows: AC-NH3 > AC-HNO3 > AC-H2O2 > AC-H2O.This sequence is in accord with the SO2 catalytic oxidation/oxidation ratio in the absence of oxygen and the oxidation property reflected by TPR.In the presence of oxygen,all adsorbed SO2 on ACs can be oxidized into SO3.The desulphurization capacity increases differently according to the activation agents;the desulphurization capacity of AC-NH3 and AC-HNO3 improves by 4.8 times,yet AC-H2O increases only by 2.62 as compared with the desulphurization of corresponding ACs in absence of oxygen.

  17. Surface and Adsorption Properties of Activated Carbon Fabric Prepared from Cellulosic Polymer: Mixed Activation Method

    Energy Technology Data Exchange (ETDEWEB)

    Bhati, Surendra; Mahur, J. S.; Choubey, O. N. [Barkatullah Univ., Bhopal (India); Dixit, Mahur Savita [Maulana Azad National Institute of Technology, Bhopla (India)

    2013-02-15

    In this study, activated carbon fabric was prepared from a cellulose-based polymer (viscose rayon) via a combination of physical and chemical activation (mixed activation) processes by means of CO{sub 2} as a gasifying agent and surface and adsorption properties were evaluated. Experiments were performed to investigate the consequence of activation temperature (750, 800, 850 and 925 .deg. C), activation time (15, 30, 45 and 60 minutes) and CO{sub 2} flow rate (100, 200, 300 and 400 mL/min) on the surface and adsorption properties of ACF. The nitrogen adsorption isotherm at 77 K was measured and used for the determination of surface area, total pore volume, micropore volume, mesopore volume and pore size distribution using BET, t-plot, DR, BJH and DFT methods, respectively. It was observed that BET surface area and TPV increase with rising activation temperature and time due to the formation of new pores and the alteration of micropores into mesopores. It was also found that activation temperature dominantly affects the surface properties of ACF. The adsorption of iodine and CCl{sub 4} onto ACF was investigated and both were found to correlate with surface area.

  18. Influence of anodic surface treatment of activated carbon on adsorption and ion exchange properties

    Energy Technology Data Exchange (ETDEWEB)

    Park, S.J.; Kim, K.D.

    1999-10-01

    The effect of anodic surface treatment of activated carbon on adsorption and ion exchange characteristics was investigated in the condition of 35 wt% NaOH electrolyte for 60 s. The acid and base values were determined by a titration technique, and surface and pore structures were studied in terms of BET volumetric measurement with N{sub 2} adsorption. The ion exchange capacity of the anodized activated carbons was characterized by a dry weight capacity technique. It was observed that an increase in current intensity leads to an increase in the surface functional groups of activated carbons, resulting in increasing pH, acid-base values, and anion-cation exchange capacities, without significant change of surface and pore structures (i.e., specific surface area, total pore volume, micropore volume, and average pore diameter). Also, anodically treated activated carbons are more effectively evaluated on the base value or cation exchange capacity than on the oppose properties in this electrolytic system.

  19. IMPORTANCE OF ACTIVATED CARBON'S OXYGEN SURFACE FUNCTIONAL GROUPS ON ELEMENTAL MERCURY ADSORPTION

    Science.gov (United States)

    The effect of varying physical and chemical properties of activated carbons on adsorption of elemental mercury [Hg(0)] was studied by treating two activated carbons to modify their surface functional groups and pore structures. Heat treatment (1200 K) in nitrogen (N2), air oxidat...

  20. Importance of surface chemical properties in catalytic ozonation of benzothiazole promoted by activated carbon

    Energy Technology Data Exchange (ETDEWEB)

    Valdes, H.; Zaror, C.A. [Chemical Eng. Dept., Univ. of Concepcion, Concepcion (Chile)

    2003-07-01

    The combined use of ozone and activated carbon to treat toxic effluents has increased in recent years. Activated carbon has been shown to enhance ozone oxidation of organic compounds. However, little is known about the influence of carbon surface active sites on ozonation of organic pollutants. This paper presents experimental results on the effect of metal oxides and oxygenated surface groups on such reaction. Benzothiazole (BT) was selected as a target organic compound in this study due its environmental concern. Activated carbons with different surface chemical composition were prepared from a filtrasorb-400 activated carbon. Pre-treatment included ozonation, demineralisation and deoxygenation of activated carbon. BT degradation experiments were conducted in a fixed bed reactor loaded with 2 g of carbon samples. The reactor was fed with an O{sub 2}/O{sub 3} mixture (2 dm{sup 3}/min, 5 g O{sub 3}/h), for a given exposure time, in the range 10-120 min, at 298 K and 1 atm. The results suggest that high electron density from the carbon basal planes and surface metal oxides are primarily responsible for increase in the overall BT oxidation rate; whereas high surface concentration of electron withdrawing groups such as carboxylic acids, and carboxylic anhydrides retarded the overall BT oxidation rate. (orig.)

  1. [Surface characteristics of alkali modified activated carbon and the adsorption capacity of methane].

    Science.gov (United States)

    Zhang, Meng-Zhu; Li, Lin; Liu, Jun-Xin; Sun, Yong-Jun; Li, Guo-Bin

    2013-01-01

    Coconut shell based activated carbon was modified by alkali with different concentrations. The surface structures of tested carbons were observed and analyzed by SEM and BET methods. Boehm's titration and SEM/EDS methods were applied to assay the functional groups and elements on the carbon surface. The adsorption of methane on tested carbons was investigated and adsorption behavior was described by the adsorption isotherms. Results showed that surface area and pore volume of modified carbon increased and surface oxygen groups decreased as the concentration of the alkali used increased, with no obvious change in pore size. When concentration of alkali was higher than 3.3 mol x L(-1), the specific surface area and pore volume of modified carbon was larger than that of original carbon. Methane adsorption capacity of alkali modified carbon increased 24%. Enlargement of surface area and pore volume, reduction of surface oxygen groups will benefit to enhance the methane adsorption ability on activated carbon. Adsorption behavior of methane followed the Langmuir isotherm and the adsorption coefficient was 163.7 m3 x mg(-1).

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

    Science.gov (United States)

    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.

  3. A simple and highly effective process for the preparation of activated carbons with high surface area

    Energy Technology Data Exchange (ETDEWEB)

    Li Ying, E-mail: liyingjlu@163.com [College of Chemistry, Jilin University, Changchun 130012 (China); Ding Xuefeng; Guo Yupeng; Wang Lili; Rong Chunguang; Qu Yuning; Ma Xiaoyu [College of Chemistry, Jilin University, Changchun 130012 (China); Wang Zichen, E-mail: wangzc@jlu.edu.cn [College of Chemistry, Jilin University, Changchun 130012 (China)

    2011-06-15

    Highlights: {yields} High surface area activated carbon can be prepared by rice husk H{sub 3}PO{sub 4} without pretreatment. {yields} The characteristics of the activated carbon were greatly influenced by post-processing method. {yields} The lower SiO{sub 2} content of the activated carbons, the higher pore volume the carbons had. {yields} Some silica in rice husk reacted with H{sub 3}PO{sub 4} to form SiP{sub 2}O{sub 7} which could be removed by post-process. - Abstract: Activated carbons with high surface area were prepared by phosphoric acid as activation agent and rice husks as precursors. It was found that the characteristics of the activated carbons were influenced not only by the preparation but also by the post-processing method. The high surface area of the activated carbons was prepared under the optimum condition (50% H{sub 3}PO{sub 4} with impregnation ratio of 5:1, activation temperature of 500 deg. C, activation time of 0.5 h, wash water temperature of 100 deg. C). SiO{sub 2} content could affect the surface area of activated carbons, either. The lower SiO{sub 2} content of the activated carbons, the higher pore volume the carbons had. The SiO{sub 2} content was 11.2% when used the optimum condition. The explanation was that silicon element in rice husks reacted with H{sub 3}PO{sub 4} to form silicon phosphate (SiP{sub 2}O{sub 7}), and it could be proved further by X-ray diffraction analysis, SiP{sub 2}O{sub 7} could be removed by post-process.

  4. Influence of chemical agents on the surface area and porosity of active carbon hollow fibers

    Directory of Open Access Journals (Sweden)

    LJILJANA M. KLJAJEVIĆ

    2011-09-01

    Full Text Available Active carbon hollow fibers were prepared from regenerated polysulfone hollow fibers by chemical activation using: disodium hydrogen phosphate 2-hydrate, disodium tetraborate 10-hydrate, hydrogen peroxide, and diammonium hydrogen phosphate. After chemical activation fibers were carbonized in an inert atmosphere. The specific surface area and porosity of obtained carbons were studied by nitrogen adsorption–desorption isotherms at 77 K, while the structures were examined with scanning electron microscopy and X-ray diffraction. The activation process increases these adsorption properties of fibers being more pronounced for active carbon fibers obtained with disodium tetraborate 10-hydrate and hydrogen peroxide as activator. The obtained active hollow carbons are microporous with different pore size distribution. Chemical activation with phosphates produces active carbon material with small surface area but with both mesopores and micropores. X-ray diffraction shows that besides turbostratic structure typical for carbon materials, there are some peaks which indicate some intermediate reaction products when sodium salts were used as activating agent. Based on data from the electrochemical measurements the activity and porosity of the active fibers depend strongly on the oxidizing agent applied.

  5. Porous structure and surface chemistry of phosphoric acid activated carbon from corncob

    Energy Technology Data Exchange (ETDEWEB)

    Sych, N.V.; Trofymenko, S.I.; Poddubnaya, O.I.; Tsyba, M.M. [Institute for Sorption and Endoecology Problems, National Academy of Sciences of Ukraine, 13 General Naumov St., 03164 Kyiv (Ukraine); Sapsay, V.I.; Klymchuk, D.O. [M.G. Kholodny Institute of Botany, National Academy of Sciences of Ukraine, 2 Tereshchenkivska St., 01601 Kyiv (Ukraine); Puziy, A.M., E-mail: alexander.puziy@ispe.kiev.ua [Institute for Sorption and Endoecology Problems, National Academy of Sciences of Ukraine, 13 General Naumov St., 03164 Kyiv (Ukraine)

    2012-11-15

    Highlights: Black-Right-Pointing-Pointer Phosphoric acid activation results in formation of carbons with acidic surface groups. Black-Right-Pointing-Pointer Maximum amount of surface groups is introduced at impregnation ratio 1.25. Black-Right-Pointing-Pointer Phosphoric acid activated carbons show high capacity to copper. Black-Right-Pointing-Pointer Phosphoric acid activated carbons are predominantly microporous. Black-Right-Pointing-Pointer Maximum surface area and pore volume achieved at impregnation ratio 1.0. - Abstract: Active carbons have been prepared from corncob using chemical activation with phosphoric acid at 400 Degree-Sign C using varied ratio of impregnation (RI). Porous structure of carbons was characterized by nitrogen adsorption and scanning electron microscopy. Surface chemistry was studied by IR and potentiometric titration method. It has been shown that porosity development was peaked at RI = 1.0 (S{sub BET} = 2081 m{sup 2}/g, V{sub tot} = 1.1 cm{sup 3}/g), while maximum amount of acid surface groups was observed at RI = 1.25. Acid surface groups of phosphoric acid activated carbons from corncob includes phosphate and strongly acidic carboxylic (pK = 2.0-2.6), weakly acidic carboxylic (pK = 4.7-5.0), enol/lactone (pK = 6.7-7.4; 8.8-9.4) and phenol (pK = 10.1-10.7). Corncob derived carbons showed high adsorption capacity to copper, especially at low pH. Maximum adsorption of methylene blue and iodine was observed for carbon with most developed porosity (RI = 1.0).

  6. Adsorption of atrazine on hemp stem-based activated carbons with different surface chemistry

    OpenAIRE

    Lupul, Iwona; Yperman, Jan; Carleer, Robert; Gryglewicz, Grazyna

    2015-01-01

    Surface-modified hemp stem-based activated carbons (HACs) were prepared and used for the adsorption of atrazine from aqueous solution, and their adsorption performance was examined. A series of HACs were prepared by potassium hydroxide activation of hemp stems, followed by subsequent modification by thermal annealing, oxidation with nitric acid and amination. The resultant HACs differed in surface chemistry, while possessing similar porous structure. The surface group characteristics were exa...

  7. Effect of surface modification of activated carbon on its adsorption capacity for NH3

    Institute of Scientific and Technical Information of China (English)

    SHAN Xiao-mei; ZHU Shu-quan; ZHANG Wen-hui

    2008-01-01

    To investigate the effects of carbon surface characteristics on NH3 adsorption, coal-based and coconut shell activated carbons were modified by treatment with oxidants. The surface properties of the carbons were characterized by low temperature nitrogen sorption, by Boehm's titrations and by XPS techniques. NH3 adsorption isotherms of the original and the modified carbons were determined. The results show that the carbons were oxidized by HNO3 and (NH4)2S2O8, and that there was an increase in oxygen containing functional groups on the surface. However, the pore-size distribution of the coal-based carbons was changed after KMnO4 treatment. It was found that the NH3 adsorption capacity of the modified carbons was enhanced and that the most pronounced enhancement results from (NH4)2S2O8 oxidation. Under our experimental conditions, the capacity is positively corrected to the number of surface functional groups containing oxygen, and to the number of micro-pores. Furthermore, an empirical model of the relationship between NH3 adsorption and multiple factors on the carbon surface was fit using a complex regression method.

  8. Impact of carbon on the surface and activity of silica-carbon supported copper catalysts for reduction of nitrogen oxides

    Science.gov (United States)

    Spassova, I.; Stoeva, N.; Nickolov, R.; Atanasova, G.; Khristova, M.

    2016-04-01

    Composite catalysts, prepared by one or more active components supported on a support are of interest because of the possible interaction between the catalytic components and the support materials. The supports of combined hydrophilic-hydrophobic type may influence how these materials maintain an active phase and as a result a possible cooperation between active components and the support material could occur and affects the catalytic behavior. Silica-carbon nanocomposites were prepared by sol-gel, using different in specific surface areas and porous texture carbon materials. Catalysts were obtained after copper deposition on these composites. The nanocomposites and the catalysts were characterized by nitrogen adsorption, TG, XRD, TEM- HRTEM, H2-TPR, and XPS. The nature of the carbon predetermines the composite's texture. The IEPs of carbon materials and silica is a force of composites formation and determines the respective distribution of the silica and carbon components on the surface of the composites. Copper deposition over the investigated silica-carbon composites leads to formation of active phases in which copper is in different oxidation states. The reduction of NO with CO proceeds by different paths on different catalysts due to the textural differences of the composites, maintaining different surface composition and oxidation states of copper.

  9. Mesopore control of high surface area NaOH-activated carbon.

    Science.gov (United States)

    Tseng, Ru-Ling

    2006-11-15

    Activated carbon with BET surface areas in a narrow range from 2318 to 2474 m2/g was made by soaking the char made from corncob in a concentrated NaOH solution at NaOH/char ratios from 3 to 6; the mesopore volumes of the activated carbon were significantly changed from 21 to 58%. The relationships between pore properties (Sp, Vpore, Vmicro/Vpore, Dp) and NaOH dosage were investigated. Comparisons between the methods of NaOH and KOH activation revealed that NaOH activation can suitably control the mesopore specific volume of the activated carbon. Elemental analysis revealed that the H/C and O/C values of the activated carbons of NaOH/char ratios from 3 to 6 were significantly lower. SEM observation of surface hole variation of the activated carbon ascertained that the reaction process was inner pore etching. Based on the above three measurements and experimental investigations, the assumption made by previous researchers, namely that NaOH and KOH produce similar results, was challenged. Furthermore, the adsorption kinetics was used to investigate the adsorption rate of an Elovich equation to determine the relationships between the adsorption behavior on larger molecules (dyes) and smaller molecules (phenols) and the pore structure of the activated carbon.

  10. Surface characterization of electrodeposited silver on activated carbon for bactericidal purposes.

    Science.gov (United States)

    Ortiz-Ibarra, Hector; Casillas, Norberto; Soto, Victor; Barcena-Soto, Maximiliano; Torres-Vitela, Refugio; de la Cruz, Wencel; Gómez-Salazar, Sergio

    2007-10-15

    The use of an electrochemical reactor operated under different flow conditions to deposit silver from aqueous AgNO(3) solutions and tartaric acid as an organic additive on a commercial activated carbon with ultimate bactericidal applications in water purification processes is presented. The characterization of carbon/silver samples was studied by BET, FTIR, X-ray diffraction, XPS, and SEM techniques. The bactericidal activity of the carbon/silver samples was tested on drinking water samples inoculated with E. coli. A reduction of carbon surface area was detected and was caused by increased amounts of silver deposited on carbon samples. Adherent silver deposits were obtained on the carbon/silver samples. X-ray diffraction studies of carbon with electrodeposited silver showed two different preferential deposition planes, [111] and [220]. The FTIR results confirm the presence of carboxyl, phenolic, quinone, and ether surface groups. The XPS results suggest the formation of Ag(2)O and AgO surface species and confirm the reduction of silver to the metallic form. Antimicrobial activity toward E. coli indicated reductions by up to 7 orders of magnitude in the log CFU/mL in just 10 min contact time and for silver contents of 2.47 wt%.

  11. Surface modification of coconut shell based activated carbon for the improvement of hydrophobic VOC removal.

    Science.gov (United States)

    Li, Lin; Liu, Suqin; Liu, Junxin

    2011-08-30

    In this study, coconut shell based carbons were chemically treated by ammonia, sodium hydroxide, nitric acid, sulphuric acid, and phosphoric acid to determine suitable modification for improving adsorption ability of hydrophobic volatile organic compounds (VOCs) on granular activated carbons (GAC). The saturated adsorption capacities of o-xylene, a hydrophobic volatile organic compound, were measured and adsorption effects of the original and modified activated carbons were compared. Results showed that GAC modified by alkalis had better o-xylene adsorption capacity. Uptake amount was enhanced by 26.5% and reduced by 21.6% after modification by NH(3)H(2)O and H(2)SO(4), respectively. Compared with the original, GAC modified by acid had less adsorption capacity. Both SEM/EDAX and BET were used to identify the structural characteristics of the tested GAC, while IR spectroscopy and Boehm's titration were applied to analysis the surface functional groups. Relationships between physicochemical characteristics of GAC and their adsorption performances demonstrated that o-xylene adsorption capacity was related to surface area, pore volume, and functional groups of the GAC surface. Removing surface oxygen groups, which constitute the source of surface acidity, and reducing hydrophilic carbon surface favors adsorption capacity of hydrophobic VOCs on carbons. The performances of modified GACs were also investigated in the purification of gases containing complex components (o-xylene and steam) in the stream.

  12. Adsorption and destruction of PCDD/Fs using surface-functionalized activated carbons.

    Science.gov (United States)

    Atkinson, J D; Hung, P C; Zhang, Z; Chang, M B; Yan, Z; Rood, M J

    2015-01-01

    Activated carbon adsorbs polychlorinated dibenzo-p-dioxins and -furans (PCDD/Fs) from gas streams but can simultaneously generate PCDD/Fs via de novo synthesis, increasing an already serious disposal problem for the spent sorbent. To increase activated carbon's PCDD/F sorption capacity and lifetime while reducing the impact of hazardous waste, it is beneficial to develop carbon-based sorbents that simultaneously destroy PCDD/Fs while adsorbing the toxic chemicals from gas streams. In this work, hydrogen-treated and surface-functionalized (i.e., oxygen, bromine, nitrogen, and sulfur) activated carbons are tested in a bench-scale reactor as adsorbents for PCDD/Fs. All tested carbons adsorb PCDD/F efficiently, with international toxic equivalent removal efficiencies exceeding 99% and mass removal efficiencies exceeding 98% for all but one tested material. Hydrogen-treated materials caused negligible destruction and possible generation of PCDD/Fs, with total mass balances between 100% and 107%. All tested surface-functionalized carbons, regardless of functionality, destroyed PCDD/Fs, with total mass balances between 73% and 96%. Free radicals on the carbon surface provided by different functional groups may contribute to PCDD/F destruction, as has been hypothesized in the literature. Surface-functionalized materials preferentially destroyed higher-order (more chlorine) congeners, supporting a dechlorination mechanism as opposed to oxidation. Carbons impregnated with sulfur are particularly effective at destroying PCDD/Fs, with destruction efficiency improving with increasing sulfur content to as high as 27%. This is relevant because sulfur-treated carbons are used for mercury adsorption, increasing the possibility of multi-pollutant control.

  13. Effect of Activating Agent on the Preparation of Bamboo-Based High Surface Area Activated Carbon by Microwave Heating

    Science.gov (United States)

    Xia, Hongying; Wu, Jian; Srinivasakannan, Chandrasekar; Peng, Jinhui; Zhang, Libo

    2016-06-01

    The present work attempts to convert bamboo into a high surface area activated carbon via microwave heating. Different chemical activating agents such as KOH, NaOH, K2CO3 and Na2CO3 were utilized to identify a most suitable activating agent. Among the activating agents tested KOH was found to generate carbon with the highest porosity and surface area. The effect of KOH/C ratio on the porous nature of the activated carbon has been assessed. An optimal KOH/C ratio of 4 was identified, beyond which the surface area as well as the pore volume were found to decrease. At the optimized KOH/C ratio the surface area and the pore volume were estimated to be 3,441 m2/g and 2.093 ml/g, respectively, with the significant proportion of which being microporous (62.3%). Activated carbon prepared under the optimum conditions was further characterized using Fourier transform infrared spectroscopy (FTIR) and scanning electron microscope (SEM). Activated carbons with so high surface area and pore volume are very rarely reported, which could be owed to the nature of the precursor and the optimal conditions of mixture ratio adopted in the present work.

  14. Magnetic susceptibility of oxygen adsorbed on the surface of spherical and fibrous activated carbon.

    Directory of Open Access Journals (Sweden)

    Kiyoshi Kawamura

    2009-02-01

    Full Text Available The magnetic susceptibilities of oxygen adsorbed on the surface of bead-shaped activated carbon and activated carbon fibers were evaluated as a function of temperature between 4.2 K and 300 K, and found to exhibit a sharp peak at around 50 K. This implies that the adsorbed oxygen molecules form an antiferromagnetic state. The relation between the susceptibility and the adsorbed mass suggest that the thickness of the adsorbed oxygen is thin enough to consider a two-dimensional structure for bead–shaped activated carbon and carbon fibers across the fiber axis but thick enough to regard it as three-dimensional along the fiber axis. The result is discussed with reference to the study on one-dimensional oxygen array.

  15. Dye adsorption onto activated carbons from tyre rubber waste using surface coverage analysis.

    Science.gov (United States)

    Mui, Edward L K; Cheung, W H; Valix, Marjorie; McKay, Gordon

    2010-07-15

    Two types of activated carbons from tyre char (with or without sulphuric acid treatment) were produced via carbon dioxide activation with BET surface areas in the range 59-1118 m(2)/g. Other characterisation tests include micropore and mesopore surface areas and volumes, pH, and elemental compositions, particularly heteroatoms such as nitrogen and sulphur. They were correlated to the adsorption capacity which were in the range of 0.45-0.71 mmol/g (untreated) and 0.62-0.84 mmol/g (acid-treated) for Acid Blue 25. In the case of larger-sized molecules like Acid Yellow 117, capacities were in the range of 0.23-0.42 mmol/g (untreated) and 0.29-0.40 mmol/g (acid-treated). Some tyre carbons exhibit a more superior performance than a microporous, commercial activated carbon (Calgon F400). By modelling the dye adsorption equilibrium data, the Redlich-Peterson isotherm is adopted as it has the lowest SSE. Based on the surface coverage analysis, a novel molecular orientation modelling of adsorbed dyes has been proposed and correlated with surface area and surface charge. For the acid dyes used in this study, molecules were likely to be adsorbed by the mesopore areas.

  16. Surface characteristics and antibacterial activity of a silver-doped carbon monolith

    Directory of Open Access Journals (Sweden)

    Marija Vukčević et al

    2008-01-01

    Full Text Available A carbon monolith with a silver coating was prepared and its antimicrobial behaviour in a flow system was examined. The functional groups on the surface of the carbon monolith were determined by temperature-programmed desorption and Boehm's method, and the point of zero charge was determined by mass titration. The specific surface area was examined by N2 adsorption using the Brunauer, Emmett and Teller (BET method. As a test for the surface activity, the deposition of silver from an aqueous solution of a silver salt was used. The morphology and structure of the silver coatings were characterized by scanning electron microscopy and x-ray diffraction. The resistance to the attrition of the silver deposited on the carbon monolith was tested. The antimicrobial activity of the carbon monolith with a silver coating was determined using standard microbiological methods. Carbon monolith samples with a silver coating showed good antimicrobial activity against Escherichia coli, Staphylococcus aureus and Candida albicans, and are therefore suitable for water purification, particularly as personal disposable water filters with a limited capacity.

  17. Tailoring activated carbon by surface chemical modification with O, S, and N containing molecules

    Directory of Open Access Journals (Sweden)

    Rachel RibeiroVieira Azzi Rios

    2003-06-01

    Full Text Available In this work the surface of activated carbon was chemically modified in order to introduce O, S and N containing groups. The activated carbon surface was selectively oxidized with concentrated HNO3 under controlled conditions. Characterization by thermogravimetric analyses, infrared spectroscopy and NaOH titration suggested the formation of mainly -COOH and small amounts of -OH groups, with concentration of approximately 4.10(21 groups/g of carbon. These -COOH functionalized carbons showed high adsorption capacity for metal cations in aqueous solution in the following order: Pb+2>Cu+2>Ni+2 >Cd+2~Co+2>Ca+2 , suggesting a cation exchange mechanism via a surface complex [COO-M+2]. These -COOHsurf groups can be reacted with SOCl2 to produce a surface acylchloride group, -COCl. This surface -COCl group proved to be a very reactive and versatile intermediate for the grafting of different S and N containing molecules onto the carbon surface, such as 1,2-ethaneditiol (EDT-, HSCH2CH2SH 1,7-dimercapto-4-thioheptane (DMTH-HSCH2CH2CH2SCH2CH 2CH2SH or 1,2-ethylenediamine (EDA- NH2CH2CH2NH2 and triethyltetraamine, TEA (H2NCH2CH2NHCH2CH 2NHCH2CH2 NH2. The characterization of these materials was carried out by TG, IR and TPDMS (Temperature Programmed Decomposition Mass Spectrometry experiments suggesting the formation of thioesther and amide surface groups, i.e. -COSR and -CONHR, with yields of approximately 50 and 75% for the reaction with DME and EDA, respectively. Preliminary adsorption experiments showed that these materials can efficiently remove metals such as Pb+2, Cu+2 and Ni+2 from aqueous medium.

  18. Surface Properties and Catalytic Performance of Activated Carbon Fibers Supported TiO2 Photocatalyst

    Science.gov (United States)

    Yang, Huifen; Fu, Pingfeng

    Activated carbon fibers supported TiO2 photocatalyst (TiO2/ACF) in felt-form was successfully prepared with a dip-coating process using organic silicon modified acrylate copolymer as a binder followed by calcination at 500°C in a stream of Ar gas. The photocatalyst was characterized by SEM, XRD, XPS, FTIR, and BET surface area. Most of carbon fibers were coated with uniformly distributed TiO2 clusters of nearly 100 nm. The loaded TiO2 layer was particulate for the organic binder in the compact film was carbonized. According to XPS and FTIR analysis, amorphous silica in carbon grains was synthesized after carbonizing organic silicon groups, and the Ti-O-Si bond was formed between the interface of loaded TiO2 and silica. Additionally, the space between adjacent carbon fibers still remained unfilled after TiO2 coating, into which both UV light and polluted solutions could penetrate to form a three-dimensional environment for photocatalytic reactions. While loaded TiO2 amount increased to 456 mg TiO2/1 g ACF, the TiO2/ACF catalyst showed its highest photocatalytic activity, and this activity only dropped about 10% after 12 successive runs, exhibiting its high fixing stability of coated TiO2.

  19. SURFACE PROPERTIES AND CATALYTIC PERFORMANCE OF ACTIVATED CARBON FIBERS SUPPORTED TiO2 PHOTOCATALYST

    OpenAIRE

    HUIFEN YANG; PINGFENG FU

    2008-01-01

    Activated carbon fibers supported TiO2 photocatalyst (TiO2/ACF) in felt-form was successfully prepared with a dip-coating process using organic silicon modified acrylate copolymer as a binder followed by calcination at 500°C in a stream of Ar gas. The photocatalyst was characterized by SEM, XRD, XPS, FTIR, and BET surface area. Most of carbon fibers were coated with uniformly distributed TiO2 clusters of nearly 100 nm. The loaded TiO2 layer was particulate for the organic binder in the compac...

  20. Energy storage on ultrahigh surface area activated carbon fibers derived from PMIA.

    Science.gov (United States)

    Castro-Muñiz, Alberto; Suárez-García, Fabián; Martínez-Alonso, Amelia; Tascón, Juan M D; Kyotani, Takashi

    2013-08-01

    High-performance carbon materials for energy storage applications have been obtained by using poly(m-phenylene isophthalamide), PMIA, as a precursor through the chemical activation of the carbonized aramid fiber by using KOH. The yield of the process of activation was remarkably high (25-40 wt%), resulting in activated carbon fibers (ACFs) with ultrahigh surface areas, over 3000 m(2) g(-1) , and pore volumes exceeding 1.50 cm(3) g(-1) , keeping intact the fibrous morphology. The porous structure and the surface chemical properties could easily be controlled through the conditions of activation. The PMIA-derived ACFs were tested in two types of energy storage applications. At -196 °C and 1 bar, H2 uptake values of approximately 3 t% were obtained, which, in combination with the textural properties, rendered it a good candidate for H2 adsorption at high pressure and temperature. The performance of the ACFs as electrodes for electrochemical supercapacitors was also investigated. Specific capacitance values between 297 and 531 g(-1) at 50 mA g(-1) were obtained in aqueous electrolyte (1 H2 SO4 ), showing different behaviors depending on the surface chemical properties.

  1. Utilization of zinc chloride for surface modification of activated carbon derived from Jatropha curcas L. for absorbent material.

    Science.gov (United States)

    Pratumpong, P; Toommee, S

    2016-12-01

    The objective of this research is to produce the low-cost activated carbon from Jatropha curcas L. by chemical activation using zinc chloride ZnCl2. The effects of the impregnation ratio on the surface and chemical properties of activated carbon were investigated. The impregnation ratio was selected at the range of 1:1-10:1 for investigation. The optimum conditions resulted in an activated carbon with a carbon content of 80% wt, while the specific surface area evaluated using nitrogen adsorption isotherm corresponds to 600 m(2)/g.

  2. Preparation and Characterization of High Surface Area Activated Carbon Fibers from Lignin

    Directory of Open Access Journals (Sweden)

    Jian Lin

    2016-10-01

    Full Text Available Activated carbon fibers (ACFs were successfully prepared from softwood lignin, which was isolated with polyethylene glycol 400 (PEG-400 as a solvolysis reagent, by water steam activation. The pore characterization and adsorption property of ACFs were investigated. The results showed that all the ACFs with more micropores exhibited high specific surface area and total pore volume which increased with the activation time prolonging; the highest ones were around 3100 m2/g and 1.5 mL/g, respectively. The specific surface area and total pore volume were much larger than those of other types of lignin-based ACFs and activated charcoal. Besides, with increasing activation time, the amount of graphitic carbon, which was the main compound on the surface of ACFs, decreased, while the amount of functional groups containing C–O slightly increased. In addition, the adsorption capacity of ACFs for methylene blue was highly increased as the activation time increased. Accordingly, lignin isolated with PEG is a promising precursor for ACF production.

  3. Porous carbon with a large surface area and an ultrahigh carbon purity via templating carbonization coupling with KOH activation as excellent supercapacitor electrode materials

    Science.gov (United States)

    Sun, Fei; Gao, Jihui; Liu, Xin; Pi, Xinxin; Yang, Yuqi; Wu, Shaohua

    2016-11-01

    Large surface area and good structural stability, for porous carbons, are two crucial requirements to enable the constructed supercapacitors with high capacitance and long cycling lifespan. Herein, we successfully prepare porous carbon with a large surface area (3175 m2 g-1) and an ultrahigh carbon purity (carbon atom ratio of 98.25%) via templating carbonization coupling with KOH activation. As-synthesized MTC-KOH exhibits excellent performances as supercapacitor electrode materials in terms of high specific capacitance and ultrahigh cycling stability. In a three electrode system, MTC-KOH delivers a high capacitance of 275 F g-1 at 0.5 A g-1 and still 120 F g-1 at a high rate of 30 A g-1. There is almost no capacitance decay even after 10,000 cycles, demonstrating outstanding cycling stability. In comparison, pre-activated MTC with a hierarchical pore structure shows a better rate capability than microporous MTC-KOH. Moreover, the constructed symmetric supercapacitor using MTC-KOH can achieve high energy densities of 8.68 Wh kg-1 and 4.03 Wh kg-1 with the corresponding power densities of 108 W kg-1 and 6.49 kW kg-1, respectively. Our work provides a simple design strategy to prepare highly porous carbons with high carbon purity for supercapacitors application.

  4. Activated carbon fibers with a high content of surface functional groups by phosphoric acid activation of PPTA.

    Science.gov (United States)

    Castro-Muñiz, Alberto; Suárez-García, Fabián; Martínez-Alonso, Amelia; Tascón, Juan M D

    2011-09-01

    Activated carbon fibers (ACFs) were prepared by chemical activation of poly(p-phenylene terephthalamide (PPTA) with phosphoric acid, with a particular focus on the effects of impregnation ratio and carbonization temperature on both surface chemistry and porous texture. Thermogravimetric studies of the pyrolysis of PPTA impregnated with different amounts of phosphoric acid indicated that this reagent has a strong influence on the thermal degradation of the polymer, lowering the decomposition temperature and increasing the carbon yield. As concerns surface chemistry, TPD and chemical analysis results indicated that the addition of phosphoric acid increases the concentration of oxygenated surface groups, with a maximum at an impregnation ratio of 100 wt.%. The resulting materials present uncommon properties, namely a large amount of oxygen- and phosphorus-containing surface groups and a high nitrogen content. Porosity development following H(3)PO(4) activation was very significant, with values close to 1700 m(2)/g and 0.80 cm(3)/g being reached for the BET surface area and total pore volume, respectively. The pore size distributions remained confined to the micropore and narrow mesopore (<10 nm) range.

  5. SILICA SURFACED CARBON FIBERS.

    Science.gov (United States)

    carbon fibers . Several economical and simple processes were developed for obtaining research quantities of silica surfaced carbon filaments. Vat dipping processes were utilized to deposit an oxide such as silica onto the surface and into the micropores of available carbon or graphite base fibers. High performance composite materials were prepared with the surface treated carbon fibers and various resin matrices. The ablative characteristics of these composites were very promising and exhibited fewer limitations than either silica or...treated

  6. Effects of steam activation on the pore structure and surface chemistry of activated carbon derived from bamboo waste

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Yan-Juan [School of Chemical Engineering, Xiangtan University, Xiangtan 411105 (China); Institute of Urban Environment, Chinese Academy of Sciences, Xiamen 36102 (China); Xing, Zhen-Jiao [Institute of Urban Environment, Chinese Academy of Sciences, Xiamen 36102 (China); Duan, Zheng-Kang [School of Chemical Engineering, Xiangtan University, Xiangtan 411105 (China); Meng Li [Institute of Urban Environment, Chinese Academy of Sciences, Xiamen 36102 (China); Wang, Yin, E-mail: yinwang@iue.ac.cn [Institute of Urban Environment, Chinese Academy of Sciences, Xiamen 36102 (China)

    2014-10-01

    The effects of steam activation on the pore structure evolution and surface chemistry of activated carbon (AC) obtained from bamboo waste were investigated. Nitrogen adsorption–desorption isotherms revealed that higher steam activation temperatures and/or times promoted the creation of new micropores and widened the existing micropores, consequently decreasing the surface area and total pore volume. Optimum conditions included an activation temperature of 850 °C, activation time of 120 min, and steam flush generated from deionized water of 0.2 cm{sup 3} min{sup −1}. Under these conditions, AC with a BET surface area of 1210 m{sup 2} g{sup −1} and total pore volume of 0.542 cm{sup −3} g{sup −1}was obtained. Changes in surface chemistry were determined through Boehm titration, pH measurement, Fourier transform infrared spectroscopy (FTIR), and X-ray photoelectron spectroscopy (XPS). Results revealed the presence of a large number of basic groups on the surface of the pyrolyzed char and AC. Steam activation did not affect the species of oxygen-containing groups but changed the contents of these species when compared with pyrolyzed char. Scanning electron microscopy was used to observe the surface morphology of the products. AC obtained under optimum conditions showed a monolayer adsorption capacity of 330 mg g{sup −1} for methylene blue (MB), which demonstrates its excellent potential for MB adsorption applications.

  7. Effects of steam activation on the pore structure and surface chemistry of activated carbon derived from bamboo waste

    Science.gov (United States)

    Zhang, Yan-Juan; Xing, Zhen-Jiao; Duan, Zheng-Kang; Li, Meng; Wang, Yin

    2014-10-01

    The effects of steam activation on the pore structure evolution and surface chemistry of activated carbon (AC) obtained from bamboo waste were investigated. Nitrogen adsorption-desorption isotherms revealed that higher steam activation temperatures and/or times promoted the creation of new micropores and widened the existing micropores, consequently decreasing the surface area and total pore volume. Optimum conditions included an activation temperature of 850 °C, activation time of 120 min, and steam flush generated from deionized water of 0.2 cm3 min-1. Under these conditions, AC with a BET surface area of 1210 m2 g-1 and total pore volume of 0.542 cm-3 g-1was obtained. Changes in surface chemistry were determined through Boehm titration, pH measurement, Fourier transform infrared spectroscopy (FTIR), and X-ray photoelectron spectroscopy (XPS). Results revealed the presence of a large number of basic groups on the surface of the pyrolyzed char and AC. Steam activation did not affect the species of oxygen-containing groups but changed the contents of these species when compared with pyrolyzed char. Scanning electron microscopy was used to observe the surface morphology of the products. AC obtained under optimum conditions showed a monolayer adsorption capacity of 330 mg g-1 for methylene blue (MB), which demonstrates its excellent potential for MB adsorption applications.

  8. Effect of surface property of activated carbon on adsorption of nitrate ion.

    Science.gov (United States)

    Iida, Tatsuya; Amano, Yoshimasa; Machida, Motoi; Imazeki, Fumio

    2013-01-01

    In this study, the removal of acidic functional groups and introduction of basic groups/sites on activated carbons (ACs) by outgassing and ammonia gas treatment were respectively carried out to enhance the nitrate ion adsorption in aqueous solution. Then, the relationships between nitrate ion adsorption and solution pH as well as surface charge of AC were investigated to understand the basic mechanisms of nitrate ion adsorption by AC. The result showed that the nitrate ion adsorption depended on the equilibrium solution pH (pHe) and the adsorption amount was promoted with decreasing pHe. The ACs treated by outgassing and ammonia gas treatment showed larger amount of nitrate ion adsorption than that by untreated AC. These results indicated that, since basic groups/sites could adsorb protons in the solution, the AC surface would be charged positively, and that the nitrate ion would be electrically interacted with positively charged carbon surface. Accordingly, it was concluded that basic groups/sites on the surface of AC could promote nitrate ion adsorption.

  9. Mechano-activated surface modification of calcium carbonate in wet stirred mill and its properties

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    Surface modification of calcium carbonate particles using sodium stearate(SDS) as a modification agent incorporated with the simultaneous wet ultra-fine grinding in the laboratory stirred mill was investigated. The physical properties and application properties of modified calcium carbonate were measured and evaluated. The action mechanism between SDS and calcium carbonate in the modification was studied by infrared spectrometry(IR) and X-ray photoelectron energy spectroscopy(XPS). The results indicate that the crushing mechanic force intensity can obviously influence the modification effect of calcium carbonate because of mechano-chemical effect. The hydrophilic surface of calcium carbonate is turned into hydrophobic after modification. The properties of polyethylene(PE) filled by modified calcium carbonate powder is markedly improved. And the adsorption of SDS could occur by chemical reaction with calcium carbonate surface.

  10. Surface functional characteristics (C, O, S) of waste tire-derived carbon black before and after steam activation.

    Science.gov (United States)

    Lin, Hsun-Yu; Chen, Wei-Chin; Yuan, Chung-Shin; Hung, Chung-Hsuang

    2008-01-01

    The effects of steam activation on the surface functional characteristics of waste tire-derived carbon black were investigated. Two carbon-based materials, powdered carbon black (PCB) and PCB-derived powdered activated carbon (PCB-PAC), were selected for this study. A stainless steel tubular oven was used to activate the PCB at an activation temperature of 900 degrees C and 1 atm using steam as an activating reagent. X-ray photoelectron spectroscopy (XPS) was adopted to measure the surface composition and chemical structure of carbon surface. Various elemental spectra (C, O, and S) of each carbon sample were further deconvoluted by peak synthesis. Results showed that the surfaces of PCB and PCB-PAC consisted mainly of C-C and C-O. The PCB-PAC surface had a higher percentage of oxygenated functional groups (C=O and O-C=O) than PCB. The O1s spectra show that the oxygen detected on the PCB surface was mainly bonded to carbon (C-O), whereas the oxygen on the PCB-PAC surface could be bonded to hydrogen (O-H) and carbon (C-O). Sulfur on the surface of PCB consisted of 58.9 wt% zinc sulfide (ZnS) and 41.1 wt% S=C=S, whereas that on the surfaces of PCB-PAC consisted mainly of S=C=S. Furthermore, the increase of oxygen content from 9.6% (PCB) to 11.9% (PCB-PAC) resulted in the increase of the pH values of PCB-PAC after steam activation.

  11. p-Chlorophenol adsorption on activated carbons with basic surface properties

    Science.gov (United States)

    Lorenc-Grabowska, Ewa; Gryglewicz, Grażyna; Machnikowski, Jacek

    2010-05-01

    The adsorption of p-chlorophenol (PCP) from aqueous solution on activated carbons (ACs) with basic surface properties has been studied. The ACs were prepared by two methods. The first method was based on the modification of a commercial CWZ AC by high temperature treatment in an atmosphere of ammonia, nitrogen and hydrogen. The second approach comprised the carbonization followed by activation of N-enriched polymers and coal tar pitch using CO 2 and steam as activation agent. The resultant ACs were characterized in terms of porous structure, elemental composition and surface chemistry (pH PZC, acid/base titration, XPS). The adsorption of PCP was carried out from an aqueous solution in static conditions. Equilibrium adsorption isotherm was of L2 type for polymer-based ACs, whereas L3-type isotherm was observed for CWZ ACs series. The Langmuir monolayer adsorption capacity was related to the porous structure and the amount of basic sites. A good correlation was found between the adsorption capacity and the volume of micropores with a width < 1.4 nm for polymer-based ACs. Higher nitrogen content, including that in basic form, did not correspond to the enhanced adsorption of PCP from aqueous solution. The competitive effect of water molecule adsorption on the PCP uptake is discussed.

  12. Control of Surface Functional Groups on Pertechntate Sorption on Activated Carbon

    Energy Technology Data Exchange (ETDEWEB)

    Y. Wang; H. Gao; R. Yeredla; H. Xu; M. Abrecht; G.D. Stasio

    2006-07-05

    {sup 99}Tc is highly soluble and poorly adsorbed by natural materials under oxidizing conditions, thus being of particular concern for radioactive waste disposal. Activated carbon can potentially be used as an adsorbent for removing Tc from aqueous solutions. We have tested six commercial activated carbon materials for their capabilities for sorption of pertechnetate (TcO{sub 4}{sup -}). The tested materials can be grouped into two distinct types: Type I materials have high sorption capabilities with the distribution coefficients (K{sub d}) varying from 9.5 x 10{sup 5} to 3.2 x 10{sup 3} mL/g as the pH changes from 4.5 to 9.5, whereas type II materials have relatively low sorption capabilities with K{sub d} remaining more or less constant (1.1 x 10{sup 3} - 1.8 x 10{sup 3} mL/g) over a similar pH range. The difference in sorption behavior between the two types of materials is attributed to the distribution of surface functional groups. The predominant surface groups are identified to be carboxylic and phenolic groups. The carboxylic group can be further divided into three subgroups A, B, and C in the order of increasing acidity. The high sorption capabilities of type I materials are found to be caused by the presence of a large fraction of carboxylic subgroups A and B, while the low sorption capabilities of type II materials are due to the exclusive presence of phenolic and carboxylic subgroup C. Therefore, the performance of activated carbon for removing TcO{sub 4}{sup -} can be improved by enhancing the formation of carboxylic subgroups A and B during material processing.

  13. Ozone treatment of coal- and coffee grounds-based active carbons: Water vapor adsorption and surface fractal micropores

    Energy Technology Data Exchange (ETDEWEB)

    Tsunoda, Ryoichi; Ozawa, Takayoshi; Ando, Junichi [Kanagawa Industrial Technology Research Inst., Ebina, Kanagawa (Japan)

    1998-09-15

    Characteristics of the adsorption iostherms of water vapor on active carbons from coal and coffee grounds and those ozonized ones from the surface fractal dimension analysis are discussed. The upswing of the adsorption isotherms in the low relative pressure of coffee grounds-based active carbon, of which isotherms were not scarcely affected on ozonization, was attributed to the adsorption of water molecules on the metallic oxides playing the role of oxygen-surface complexes, which formed the corrugated surfaces on the basal planes of micropore walls with the surface fractal dimension D{sub s} > 2. On the other hand, coal-based active carbon with D{sub s} < 2, which indicated the flat surfaces of micropore walls, showed little effect on the upswing even on ozonization, even though the adsorption amounts of water vapor were increased in the low relative pressure.

  14. Role of surface chemistry in modified ACF (activated carbon fiber)-catalyzed peroxymonosulfate oxidation

    Science.gov (United States)

    Yang, Shiying; Li, Lei; Xiao, Tuo; Zheng, Di; Zhang, Yitao

    2016-10-01

    A commercial activated carbon fiber (ACF-0) was modified by three different methods: nitration treatment (ACF-N), heat treatment (ACF-H) and heat treatment after nitration (ACF-NH), and the effects of textural and chemical properties on the ability of the metal-free ACF-catalyzed peroxymonosulfate (PMS) oxidation of Reactive Black 5 (RB5), an azo dye being difficultly adsorbed onto ACF, in aqueous solution were investigated in this work. Surface density of functional groups, surface area changes, surface morphology and the chemical state inside ACF samples were characterized by Boehm titration, N2 adsorption, scanning electron microscopy in couple with energy dispersive spectroscopy (SEM-EDS) and X-ray photoelectron spectroscopy (XPS), respectively. XPS spectra deconvolution was applied to figure out the importance of surface nitrogen-containing function groups. We found that π-π, pyridine and amine have promoting effect on the catalytic oxidation while the -NO2 has inhibitory effect on the ACF/PMS systems for RB5 destroy. Sustainability and renewability of the typical ACF-NH for catalytic oxidation of RB5 were also discussed in detail. Information about our conclusions are useful to control and improve the performance of ACF-catalyzed PMS oxidation for organic pollutants in wastewater treatment.

  15. Preparation of activated carbon with high surface area for high-capacity methane storage

    Institute of Scientific and Technical Information of China (English)

    Bingsi Liua; Wenshuo Wanga; Na Wanga; Peter Chak Tong Aub

    2014-01-01

    Activated carbon (AC) was fabricated from corncob, which is cheap and abundant. Experimental parameters such as particle size of corncob, KOH/char weight ratio, and activation temperature and time were optimized to generate AC, which shows high methane sorption capacity. AC has high specific surface area (3227 m2/g), with pore volume and pore size distribution equal to 1.829 cm3/g and ca. 1.7-2.2 nm, respectively. Under the condition of 2◦C and less than 7.8 MPa, methane sorption in the presence of water (Rw=1.4) was as high as 43.7 wt%methane per unit mass of dry AC. The result is significantly higher than those of coconut-derived AC (32 wt%) and ordered mesoporous carbon (41.2 wt%, Rw=4.07) under the same condition. The physical properties and amorphous chaotic structure of AC were characterized by N2 adsorption isotherms, XRD, SEM and HRTEM. Hence, the corncob-derived AC can be considered as a competitive methane-storage material for vehicles, which are run by natural gas.

  16. Effect of temperature and time on microstructure and surface functional groups of activated carbon fibers prepared from liquefied wood

    Directory of Open Access Journals (Sweden)

    Wenjing Liu

    2012-11-01

    Full Text Available Activated carbon fibers were prepared from liquefied wood through stream activation. The effects of activation temperature and time on the microstructure and surface functional groups of the liquefied wood activated carbon fibers (LWACFs were studied using analysis of burning behavior, X-ray diffraction, nitrogen adsorption-desorption isotherms, X-ray photoelectron spectroscopy, and SEM. The results showed that the burn-off value of the LWACFs increased gradually with the increase in temperature or time. All the LWACFs were far from being structurally graphitized, and in general, as temperature or time increased, the degree of graphitization and thickness of crystal structure increased. In addition, the LWACFs possessed rich micropores, and their specific surface area, pore volume, micropore size, and mesopore quantity were directly related to the activation temperature or time. The maximum specific surface area was found to be 2641 m2/g. The fractal dimension values of all samples were close to 3, indicating that their surfaces were very rough. Furthermore, with an increase in temperature or time, the elemental content of carbon increased, while that of oxygen decreased. Meanwhile, as the temperature or time increased, the relative content of graphitic carbon decreased, whereas that of carbon bonded to oxygen-containing functions increased. The surface of samples prepared at higher temperature or with longer time formed a considerable amount of holes.

  17. Preparation of activated carbon with low ash content and high specific surface area from coal in the presence of KOH

    Institute of Scientific and Technical Information of China (English)

    XIE Qiang(解强); CHEN Qing-ru(陈清如); GONG Guo-zhuo(宫国卓); ZHANG Xiang-lan(张香兰); XU De-ping(许德平)

    2003-01-01

    An activated carbon with ash content less than 10% and specific surface area more than 1 600 m2/g was prepared from coal and the effect of K-containing compounds in preparation of coal-based activated carbon was investigated in detail in this paper. KOH was used in co-carbonization with coal, changes in graphitic crystallites in chars derived from carbonization of coal with and without KOH were analyzed by X-ray diffraction (XRD) technique, activation rates of chars with different contents of K-containing compounds were deduced, and resulting activated carbons were characterized by nitrogen adsorption isotherms at 77 K and iodine numbers. The results showed that the addition of KOH to the coal before carbonization can realize the intensive removal of inorganic matters from chars under mild conditions, especially the efficient removal of dispersive quartz, an extremely difficult separated mineral component in other processes else. Apart from this, KOH demonstrates a favorable effect in control over coal carbonization with the goal to form nongraphitizable isotropic carbon precursor, which is a necessary prerequisite for the formation and development of micro pores. However, the K-containing compounds such as K2CO3 and K2O remaining in chars after carbonization catalyze the reaction between carbon and steam in activation, which leads to the formation of macro pores. In the end an innovative method, in which KOH is added to coal before carbonization and K-containing compounds are removed by acid washing after carbonization, was proposed for the synthesis of quality coal-based activated carbon.

  18. Role of surface chemistry in modified ACF (activated carbon fiber)-catalyzed peroxymonosulfate oxidation

    Energy Technology Data Exchange (ETDEWEB)

    Yang, Shiying, E-mail: ysy@ouc.edu.cn [Key Laboratory of Marine Environment and Ecology, Ministry of Education, Qingdao 266100 (China); College of Environmental Science and Engineering, Ocean University of China, Qingdao 266100 (China); Shandong Provincial Key Laboratory of Marine Environment and Geological Engineering (MEGE), Qingdao 266100 (China); Li, Lei [College of Environmental Science and Engineering, Ocean University of China, Qingdao 266100 (China); Xiao, Tuo [College of Environmental Science and Engineering, Ocean University of China, Qingdao 266100 (China); China City Environment Protection Engineering Limited Company, Wuhan 430071 (China); Zheng, Di; Zhang, Yitao [College of Environmental Science and Engineering, Ocean University of China, Qingdao 266100 (China)

    2016-10-15

    Highlights: • ACF can efficiently activate peroxymonosulfate to degrade organic pollutants. • Basic functional groups may mainly increase the adsorption capacity of ACF. • C1, N1, N2 have promoting effect on the ACF catalyzed PMS oxidation. • Modification by heat after nitric acid is also a way of ACF regeneration. - Abstract: A commercial activated carbon fiber (ACF-0) was modified by three different methods: nitration treatment (ACF-N), heat treatment (ACF-H) and heat treatment after nitration (ACF-NH), and the effects of textural and chemical properties on the ability of the metal-free ACF-catalyzed peroxymonosulfate (PMS) oxidation of Reactive Black 5 (RB5), an azo dye being difficultly adsorbed onto ACF, in aqueous solution were investigated in this work. Surface density of functional groups, surface area changes, surface morphology and the chemical state inside ACF samples were characterized by Boehm titration, N{sub 2} adsorption, scanning electron microscopy in couple with energy dispersive spectroscopy (SEM-EDS) and X-ray photoelectron spectroscopy (XPS), respectively. XPS spectra deconvolution was applied to figure out the importance of surface nitrogen-containing function groups. We found that π-π, pyridine and amine have promoting effect on the catalytic oxidation while the −NO{sub 2} has inhibitory effect on the ACF/PMS systems for RB5 destroy. Sustainability and renewability of the typical ACF-NH for catalytic oxidation of RB5 were also discussed in detail. Information about our conclusions are useful to control and improve the performance of ACF-catalyzed PMS oxidation for organic pollutants in wastewater treatment.

  19. Gas-phase formaldehyde adsorption isotherm studies on activated carbon: correlations of adsorption capacity to surface functional group density.

    Science.gov (United States)

    Carter, Ellison M; Katz, Lynn E; Speitel, Gerald E; Ramirez, David

    2011-08-01

    Formaldehyde (HCHO) adsorption isotherms were developed for the first time on three activated carbons representing one activated carbon fiber (ACF) cloth, one all-purpose granular activated carbon (GAC), and one GAC commercially promoted for gas-phase HCHO removal. The three activated carbons were evaluated for HCHO removal in the low-ppm(v) range and for water vapor adsorption from relative pressures of 0.1-0.9 at 26 °C where, according to the IUPAC isotherm classification system, the adsorption isotherms observed exhibited Type V behavior. A Type V adsorption isotherm model recently proposed by Qi and LeVan (Q-L) was selected to model the observed adsorption behavior because it reduces to a finite, nonzero limit at low partial pressures and it describes the entire range of adsorption considered in this study. The Q-L model was applied to a polar organic adsorbate to fit HCHO adsorption isotherms for the three activated carbons. The physical and chemical characteristics of the activated carbon surfaces were characterized using nitrogen adsorption isotherms, X-ray photoelectron spectroscopy (XPS), and Boehm titrations. At low concentrations, HCHO adsorption capacity was most strongly related to the density of basic surface functional groups (SFGs), while water vapor adsorption was most strongly influenced by the density of acidic SFGs.

  20. Optimization of Orange G dye adsorption by activated carbon of Thespesia populnea pods using response surface methodology.

    Science.gov (United States)

    Arulkumar, M; Sathishkumar, P; Palvannan, T

    2011-02-15

    Thespesia populnea is a large tree found in the tropical regions and coastal forests of India. Its pods were used as a raw material for the preparation of activated carbon. The prepared activated carbon was used for the adsorptive removal of Orange G dye from aqueous system. The effects of various parameters such as agitation time, initial dye concentration and adsorbent dosage were studied using response surface methodology (RSM). RSM results show that 0.54 g of activated carbon was required for the maximum adsorption of Orange G dye (17.6 mg L(-1)) within a time period of 4.03 h. Adsorption data were modeled using Freundlich and Langmuir adsorption isotherms. The adsorption of Orange G dye by activated carbon obeyed both Fruendlich and Langmuir isotherm. Adsorption kinetic data were tested using pseudo-zero, first, second-order and intraparticle diffusion models. Kinetic studies revealed that the adsorption followed pseudo-second-order reaction with regard to the intraparticle diffusion. FTIR spectral result indicated all the functional group except primary amines (3417 cm(-1)) and CN (1618 cm(-1)) were involved in the adsorption process. XRD data showed that Orange G dye adsorbed activated carbon might not induce the bulk phase changes. SEM results showed that the surface of the activated carbon was turned from dark to light color after dye adsorption.

  1. Modification of Activated Carbon by Means of Microwave Heating and Its Effects on the Pore Texture and Surface Chemistry

    Directory of Open Access Journals (Sweden)

    Bing Li

    2013-02-01

    Full Text Available Two kinds of typical Activated Carbons (coal based AC and coconut shell based AC were modified in a flow of N0 gas has been carried out using a microwave device operating at 2450 MHz and different input power, instead of a conventional furnace. The samples were analyzed by means of low temperatureN0 adsorption, elemental analysis and Boehm titration. The results show that microwave heating is an effective means of activated carbon modification. The temperature of activated carbon increases rapidly under microwave heating and then gradual increase to a quasi-stationary temperature. The pore texture of activated carbon changes slightly after microwave treatment and the two activated carbons still keep rich pore structure. The oxygen functional groups decompose and evolve with the form of CO and CO2. This in turn gives rise to a significant decrease in oxygen content. These changes of oxygen contents increase as the microwave input power increases. During microwave treatment, a gradual decrease in the surface acidic functional groups is observed. More important, with the removal of the surface acidic groups, the number of the basic group increased gradually, the activated carbon with oxygen functional groups become basic properties material.

  2. Modification of Activated Carbon by Means of Microwave Heating and Its Effects on the Pore Texture and Surface Chemistry

    Directory of Open Access Journals (Sweden)

    Liqiang Zhang

    2013-02-01

    Full Text Available Two kinds of typical activated carbons (coal based AC and coconut shell based AC were modified in a flow of N2 gas has been carried out using a microwave device operating at 2450 MHz and different input power, instead of a conventional furnace. The samples were analyzed by means of low temperature N2 adsorption, elemental analysis and Boehm titration. The results show that microwave heating is an effective means of activated carbon modification. The temperature of activated carbon increases rapidly under microwave heating and then gradual increase to a quasi-stationary temperature. The pore texture of activated carbon changes slightly after microwave treatment and the two activated carbons still keep rich pore structure. The oxygen functional groups decompose and evolve with the form of CO and CO2. This in turn gives rise to a significant decrease in oxygen content. These changes of oxygen contents increase as the microwave input power increases. During microwave treatment, a gradual decrease in the surface acidic functional groups is observed. More important, with the removal of the surface acidic groups, the number of the basic group increased gradually, the activated carbon with oxygen functional groups become basic properties material.

  3. Single-Walled Carbon Nanotube Surface Control of Complement Recognition and Activation

    DEFF Research Database (Denmark)

    Andersen, Alina Joukainen; Robinson, Joshua T.; Dai, Hongjie

    2013-01-01

    Carbon nanotubes (CNTs) are receiving considerable attention in site-specific drug and nucleic acid delivery, photodynamic therapy, and photoacoustic molecular imaging. Despite these advances, nanotubes may activate the complement system (an integral part of innate immunity), which can induce...

  4. Modification of granular activated carbon surface by chitosan coating for geosmin removal: sorption performances.

    Science.gov (United States)

    Vinitnantharat, S; Rattanasirisophon, W; Ishibashi, Y

    2007-01-01

    This study presents the results of the sorption performances for geosmin removal by sorption onto granular activated carbons (GAC) manufactured from different raw materials of coconut shell and bituminous coal. The surface of GAC was modified by chitosan coating. The 90% deacetylated chitosan flakes were used for coating on GAC with the GAC: chitosan ratio of 5:1. The surface of GAC was characterised by scanning electron microscope (SEM) analysis, Fourier transform infrared spectroscopy and measurement of the pH solution of GAC samples. The sorption of geosmin onto the chitosan for both uncoated and coated GACs could be described by the Freundlich adsorption model. Data revealed that the sequence of Freundlich constant (K(F)) was chitosan coated bitominous coal (CB) > uncoated bituminous coal (UB) > chitos approximately equal to an coated coconut shell (CC) approximately equal to uncoated coconut shell (UC). The bituminous coal based GAC with chitosan coating had a maximum capacity of 23.57 microg/g which was approximately two-fold of uncoated bituminous coal based GAC. Two simplified kinetic models, pseudo-first order and pseudo-second order, were tested to investigate the sorption mechanisms. It was found that the intraparticle diffusion was a rate controlling step for the sorption and followed the pseudo-second order equation.

  5. Direct Electrochemical Reaction of Horseradish Peroxidase Immobilized on the Surface of Active Carbon Powders

    Institute of Scientific and Technical Information of China (English)

    Dong Mei SUN; Chen Xin CAI; Wei XING; Tian Hong LU

    2004-01-01

    It is reported for the first time that horseradish peroxidase(HRP)immobilized on the active carbon can undergo a direct quasi-reversible electrochemical reaction. In addition,the immobilized HRP showed the stable bioelectrocatalytic activity for the reduction of H2O2.

  6. Activated carbon enhanced ozonation of oxalate attributed to HO oxidation in bulk solution and surface oxidation: effect of activated carbon dosage and pH.

    Science.gov (United States)

    Xing, Linlin; Xie, Yongbing; Minakata, Daisuke; Cao, Hongbin; Xiao, Jiadong; Zhang, Yi; Crittenden, John C

    2014-10-01

    Ozonation of oxalate in aqueous phase was performed with a commercial activated carbon (AC) in this work. The effect of AC dosage and solution pH on the contribution of hydroxyl radicals (HO) in bulk solution and oxidation on the AC surface to the removal of oxalate was studied. We found that the removal of oxalate was reduced by tert-butyl alcohol (tBA) with low dosages of AC, while it was hardly affected by tBA when the AC dosage was greater than 0.3g/L. tBA also inhibited ozone decomposition when the AC dosage was no more than 0.05g/L, but it did not work when the AC dosage was no less than 0.1g/L. These observations indicate that HO in bulk solution and oxidation on the AC surface both contribute to the removal of oxalate. HO oxidation in bulk solution is significant when the dosage of AC is low, whereas surface oxidation is dominant when the dosage of AC is high. The oxalate removal decreased with increasing pH of the solution with an AC dosage of 0.5g/L. The degradation of oxalate occurs mainly through surface oxidation in acid and neutral solution, but through HO oxidation in basic bulk solution. A mechanism involving both HO oxidation in bulk solution and surface oxidation was proposed for AC enhanced ozonation of oxalate.

  7. Importance of surface diffusivities in pesticide adsorption kinetics onto granular versus powdered activated carbon: experimental determination and modeling.

    Science.gov (United States)

    Baup, S; Wolbert, D; Laplanche, A

    2002-10-01

    Three pesticides (atrazine, bromoxynil and diuron) and two granular activated carbons are involved in equilibrium and kinetic adsorption experiments. Equilibrium is represented by Freundlich isotherm law and kinetic is described by the Homogeneous Surface Diffusion Model, based on external mass transfer and intraparticle surface diffusion. Equilibrium and long-term experiments are conducted to compare Powdered Activated Carbon and Granular Activated Carbon. These first investigations show that crushing GAC into PAC improves the accessibility of the adsorption sites without increasing the number of these sites. In a second part, kinetics experiments are carried out using a Differential Column Batch Reactor. Thanks to this experimental device, the external mass transfer coefficient k(f) is calculated from empirical correlation and the effect of external mass transfer on adsorption is likely to be minimized. In order to obtain the intraparticle surface diffusion coefficient D. for these pesticides, comparisons between experimental kinetic data and simulations are conducted and the best agreement leads to the Ds coefficient. This procedure appears to be an efficient way to acquire surface diffusion coefficients for the adsorption of pesticides onto GAC. Finally it points out the role of surface diffusivity in the adsorption rate. As a matter of fact, even if the amount of the target-compound that could be potentially adsorbed is really important, its surface diffusion coefficient may be small, so that its adsorption may not have enough contact time to be totally achieved.

  8. Specific Surface versus Electrochemically Active Area of the Carbon/Polypyrrole Capacitor: Correlation of Ion Dynamics Studied by an Electrochemical Quartz Crystal Microbalance with BET Surface.

    Science.gov (United States)

    Mosch, Heike L K S; Akintola, Oluseun; Plass, Winfried; Höppener, Stephanie; Schubert, Ulrich S; Ignaszak, Anna

    2016-05-10

    Carbon/polypyrrole (PPy) composites are promising electrode materials for energy storage applications such as lightweight capacitors. Although these materials are composed of relatively inexpensive components, there is a gap of knowledge regarding the correlation between surface, porosity, ion exchange dynamics, and the interplay of the double layer capacitance and pseudocapacitance. In this work we evaluate the specific surface area analyzed by the BET method and the area accessible for ions using electrochemical quartz-crystal microbalance (EQCM) for SWCNT/PPy and carbon black Vulcan XC72-R/PPy composites. The study revealed that the polymer has significant influence on the pore size of the composites. Although the BET surface is low for the polypyrrole, the electrode mass change and thus the electrochemical area are large for the polymer-containing electrodes. This indicates that multiple redox active centers in the charged polymer chain are good ion scavengers. Also, for the composite electrodes, the effective charge storage occurs at the polypyrrole-carbon junctions, which are easy to design/multiply by a proper carbon-to-polymer weight ratio. The specific BET surface and electrochemically accessible surface area are both important parameters in calculation of the electrode capacitance. SWCNTs/PPy showed the highest capacitances normalized to the BET and electrochemical surface as compared to the polymer-carbon black. TEM imaging revealed very homogeneous distribution of the nanosized polymer particles onto the CNTs, which facilitates the synergistic effect of the double layer capacitance (CNTs) and pseudocapacitance (polymer). The trend in the electrode mass change in correlation with the capacitance suggest additional effects such as a solvent co-insertion into the polymer and the contribution of the charge associated with the redox activity of oxygen-containing functional groups on the carbon surface.

  9. High surface area carbon and process for its production

    Science.gov (United States)

    Romanos, Jimmy; Burress, Jacob; Pfeifer, Peter; Rash, Tyler; Shah, Parag; Suppes, Galen

    2016-12-13

    Activated carbon materials and methods of producing and using activated carbon materials are provided. In particular, biomass-derived activated carbon materials and processes of producing the activated carbon materials with prespecified surface areas and pore size distributions are provided. Activated carbon materials with preselected high specific surface areas, porosities, sub-nm (carbon consumption and metallic potassium intercalation into the carbon lattice during the activation process.

  10. Effects of Temperature and Pore Structure on High Surface Area-Activated Carbon Obtained from Peanut Shells.

    Science.gov (United States)

    Kalpana, D; Lee, Y S

    2016-03-01

    Activated carbon was synthesized from peanut shells by treating with H3PO4 with an intention to enhance the surface area and to find its electrochemical performance in EDLC as electrode material. The powdered peanut shells were pyrolyzed at three different temperatures namely 300 degrees C, 600 degrees C and 800 degrees C respectively. The structural and surface properties of the pyrolyzed carbon materials were studied using N2 adsorption/desorption, Raman, TEM and SEM analysis. There has been remarkable increase in the surface area of the carbon pyrolyzed at 600 degrees C due to the effect of pore generations. The surface area of the 600 degrees C pyrolyzed sample was found to be 1629 m2/g. The electrochemical properties of all the samples were evaluated by cyclic voltammetry, impedance spectroscopy, and galvanostatic charge-discharge tests. The system showed excellent cycleability and a maximum specific capacitance of 291 Fg(-1) was obtained in a 0.1 M H2SO4 electrolyte solution. The effects of the various properties of the activated carbon on the EDLC performance are discussed.

  11. Influence of activated carbon surface acidity on adsorption of heavy metal ions and aromatics from aqueous solution

    Energy Technology Data Exchange (ETDEWEB)

    Sato, Sanae; Yoshihara, Kazuya; Moriyama, Koji [Faculty of Engineering, Chiba University, Yayoi-cho 1-33, Inage-ku, Chiba 263-8522 (Japan); Machida, Motoi [Graduate School of Engineering, Chiba University, Yayoi-cho 1-33, Inage-ku, Chiba 263-8522 (Japan)], E-mail: machida@faculty.chiba-u.jp; Tatsumoto, Hideki [Graduate School of Engineering, Chiba University, Yayoi-cho 1-33, Inage-ku, Chiba 263-8522 (Japan)

    2007-08-15

    Adsorption of toxic heavy metal ions and aromatic compounds onto activated carbons of various amount of surface C-O complexes were examined to study the optimum surface conditions for adsorption in aqueous phase. Cadmium(II) and zinc(II) were used as heavy metal ions, and phenol and nitrobenzene as aromatic compounds, respectively. Activated carbon was de-ashed followed by oxidation with nitric acid, and then it was stepwise out-gassed in helium flow up to 1273 K to gradually remove C-O complexes introduced by the oxidation. The oxidized activated carbon exhibited superior adsorption for heavy metal ions but poor performance for aromatic compounds. Both heavy metal ions and aromatics can be removed to much extent by the out-gassed activated carbon at 1273 K. Removing C-O complexes, the adsorption mechanisms would be switched from ion exchange to C{pi}-cation interaction for the heavy metals adsorption, and from some kind of oxygen-aromatics interaction to {pi}-{pi} dispersion for the aromatics.

  12. Adsorption of Carbon Dioxide on Activated Carbon

    Institute of Scientific and Technical Information of China (English)

    Bo Guo; Liping Chang; Kechang Xie

    2006-01-01

    The adsorption of CO2 on a raw activated carbon A and three modified activated carbon samples B, C, and D at temperatures ranging from 303 to 333 K and the thermodynamics of adsorption have been investigated using a vacuum adsorption apparatus in order to obtain more information about the effect of CO2 on removal of organic sulfur-containing compounds in industrial gases. The active ingredients impregnated in the carbon samples show significant influence on the adsorption for CO2 and its volumes adsorbed on modified carbon samples B, C, and D are all larger than that on the raw carbon sample A. On the other hand, the physical parameters such as surface area, pore volume, and micropore volume of carbon samples show no influence on the adsorbed amount of CO2. The Dubinin-Radushkevich (D-R) equation was the best model for fitting the adsorption data on carbon samples A and B, while the Freundlich equation was the best fit for the adsorption on carbon samples C and D. The isosteric heats of adsorption on carbon samples A, B, C, and D derived from the adsorption isotherms using the Clapeyron equation decreased slightly increasing surface loading. The heat of adsorption lay between 10.5 and 28.4 kJ/mol, with the carbon sample D having the highest value at all surface coverages that were studied. The observed entropy change associated with the adsorption for the carbon samples A, B, and C (above the surface coverage of 7 ml/g) was lower than the theoretical value for mobile adsorption. However, it was higher than the theoretical value for mobile adsorption but lower than the theoretical value for localized adsorption for carbon sample D.

  13. Optimum BET surface areas for activated carbon produced from textile sewage sludges and its application as dye removal.

    Science.gov (United States)

    Kacan, Erdal

    2016-01-15

    The purpose of this experimental study is to determine optimum preparation conditions for activated carbons obtained from textile sewage sludge (TSS) for removal of dyes from aqueous solutions. The textile sewage sludge activated carbon (TSSAC) was prepared by chemical activation with potassium hydroxide using Response Surface Methodology (RSM). The most influential factor on each experimental design responses was identified via ANNOVA analysis. Based on the central composite design (CCD), quadratic model was developed to correlate the preparation variables for one response which is the Brunauer-Emmelt-Teller (BET) surface area. RSM based on a three-variable CCD was used to determine the effect of pyrolyzed temperature (400-700 °C), carbonization time (45-180 min) and KOH: weight of TSS (wt%) impregnation ratio (0.5:1-1.5:1) on BET surface area. According to the results, pyrolyzed temperature and impregnation ratio were found as the significant factors for maximizing the BET surface area. The major effect which influences the BET surface area was found as pyrolyzed temperature. Both carbonization time and impregnation ratio of KOH had no significant effect. The optimum conditions for preparing TSSAC, based on response surface and contour plots, were found as follows: pyrolyzed temperature 700 °C, carbonization time of 45 min and chemical impregnation ratio of 0.5. The maximum and optimum BET surface area of TSSAC were found as 336 m(2)/g and 310.62 m(2)/g, respectively. Synozol Blue reactive (RSB) and Setapers Yellow-Brown (P2RFL) industrial textile dyes adsorption capacities were investigated. As expected the TSSAC which has the biggest BET surface area (336 m(2)/g) adsorbed dye best. The maximum (RSB) and (P2RFL) uptake capacities were found as 8.5383 mg/g and 5.4 mg/g, respectively. The results of this study indicated the applicability of TSSAC for removing industrial dyes from aqueous solution.

  14. TiO{sub 2} activation by using activated carbon as a support. Part I. Surface characterisation and decantability study

    Energy Technology Data Exchange (ETDEWEB)

    Arana, J.; Dona-Rodriguez, J.M.; Tello Rendon, E.; Garriga i Cabo, C.; Gonzalez-Diaz, O.; Herrera-Melian, J.A.; Perez-Pena, J. [Photocatalysis and Electrochemical Laboratory, Parque Cientifico y Tecnologico, University of Las Palmas de Gran Canaria, E-35017 Las Palmas de Gran Canaria, Gran Canaria (Spain); Colon, G.; Navio, J.A. [Instituto de Ciencia de Materiales de Sevilla, Centro Mixto CSIC-Universidad de Sevilla, Americo Vespucio s/n. 41092, Sevilla (Spain)

    2003-08-20

    In the present work, the effect of mixing TiO{sub 2} with different portions of activated carbon (AC) has been studied. Transmission electron microscopy (TEM), scanning electron micrograph (SEM), laser scattering, FTIR and UV spectrophotometric analysis have shown changes of some of the TiO{sub 2} physico-chemical characteristics in catalysts containing an AC concentration lower than 15% in weight. Changes in the catalyst colour, the vibration bands of the hydroxylic groups from FTIR studies and the UV absorption spectrum have been observed. It seems that these changes correspond with TiO{sub 2} acid-base changes. SEM and TEM studies show a perfect TiO{sub 2} particles distribution on the AC surface in catalysts with lower AC contents, that also yields a homogeneous particle size distribution. One of the most interesting features of the resulting catalysts is their fast decantability in comparison with that of TiO{sub 2}. This way one of the most important drawbacks of photocatalysis, the catalyst separation from the solution, may be overcome.The present study shows that the AC not only exerts a synergistic effect when is combined with TiO{sub 2} as some authors suggest, but it also modifies the catalyst characteristics.

  15. Effects of textural and surface characteristics of microporous activated carbons on the methane adsorption capacity at high pressures

    Energy Technology Data Exchange (ETDEWEB)

    Bastos-Neto, M. [Grupo de Pesquisas em Separacoes por Adsorcao (GPSA), Departamento de Engenharia Quimica, Universidade Federal do Ceara, Campus Universitario do Pici, Bl 709 60455-760 Fortaleza, CE (Brazil); Canabrava, D.V. [Grupo de Pesquisas em Separacoes por Adsorcao (GPSA), Departamento de Engenharia Quimica, Universidade Federal do Ceara, Campus Universitario do Pici, Bl 709 60455-760 Fortaleza, CE (Brazil); Torres, A.E.B. [Grupo de Pesquisas em Separacoes por Adsorcao (GPSA), Departamento de Engenharia Quimica, Universidade Federal do Ceara, Campus Universitario do Pici, Bl 709 60455-760 Fortaleza, CE (Brazil); Rodriguez-Castellon, E. [Departamento de Quimica Inorganica, Cristalografia y Mineralogia (Unidad Asociada al ICP-CSIC), Facultad de Ciencias, Universidad de Malaga, 29071 Malaga (Spain); Jimenez-Lopez, A. [Departamento de Quimica Inorganica, Cristalografia y Mineralogia (Unidad Asociada al ICP-CSIC), Facultad de Ciencias, Universidad de Malaga, 29071 Malaga (Spain); Azevedo, D.C.S. [Grupo de Pesquisas em Separacoes por Adsorcao (GPSA), Departamento de Engenharia Quimica, Universidade Federal do Ceara, Campus Universitario do Pici, Bl 709 60455-760 Fortaleza, CE (Brazil)]. E-mail: diana@gpsa.ufc.br; Cavalcante, C.L. [Grupo de Pesquisas em Separacoes por Adsorcao (GPSA), Departamento de Engenharia Quimica, Universidade Federal do Ceara, Campus Universitario do Pici, Bl 709 60455-760 Fortaleza, CE (Brazil)

    2007-04-30

    The objective of this study is to relate textural and surface characteristics of selected microporous activated carbons to their methane storage capacity. In this work, a magnetic suspension balance (Rubotherm, Germany) was used to measure methane adsorption isotherms of several activated carbon samples. Textural characteristics were assessed by nitrogen adsorption on a regular surface area analyzer (Autosorb-MP, by Quantachrome, USA). N{sub 2} adsorption was analysed by conventional models (BET, DR, HK) and by Monte Carlo molecular simulations. Elemental and surface analyses were performed by X-ray photoelectronic spectroscopy (XPS) for the selected samples. A comparative analysis was then carried out with the purpose of defining some correlation among the variables under study. For the system under study, pore size distribution and micropore volume seem to be a determining factor as long as the solid surface is perfectly hydrophobic. It was concluded that the textural parameters per se do not unequivocally determine natural gas storage capacities. Surface chemistry and methane adsorption equilibria must be taken into account in the decision-making process of choosing an adsorbent for gas storage.

  16. Preparation of oil palm empty fruit bunch-based activated carbon for removal of 2,4,6-trichlorophenol: Optimization using response surface methodology

    Energy Technology Data Exchange (ETDEWEB)

    Hameed, B.H., E-mail: chbassim@eng.usm.my [School of Chemical Engineering, Engineering Campus, Universiti Sains Malaysia, 14300 Nibong Tebal, Penang (Malaysia); Tan, I.A.W.; Ahmad, A.L. [School of Chemical Engineering, Engineering Campus, Universiti Sains Malaysia, 14300 Nibong Tebal, Penang (Malaysia)

    2009-05-30

    The effects of three preparation variables: CO{sub 2} activation temperature, CO{sub 2} activation time and KOH:char impregnation ratio (IR) on the 2,4,6-trichlorophenol (2,4,6-TCP) uptake and carbon yield of the activated carbon prepared from oil palm empty fruit bunch (EFB) were investigated. Based on the central composite design, two quadratic models were developed to correlate the three preparation variables to the two responses. The activated carbon preparation conditions were optimized using response surface methodology by maximizing both the 2,4,6-TCP uptake and activated carbon yield within the ranges studied. The optimum conditions for preparing activated carbon from EFB for adsorption of 2,4,6-TCP were found as follows: CO{sub 2} activation temperature of 814 deg. C, CO{sub 2} activation time of 1.9 h and IR of 2.8, which resulted in 168.89 mg/g of 2,4,6-TCP uptake and 17.96% of activated carbon yield. The experimental results obtained agreed satisfactorily with the model predictions. The activated carbon prepared under optimum conditions was mesoporous with BET surface area of 1141 m{sup 2}/g, total pore volume of 0.6 cm{sup 3}/g and average pore diameter of 2.5 nm. The surface morphology and functional groups of the activated carbon were respectively determined from the scanning electron microscopy and Fourier transform infrared analysis.

  17. Preparation of oil palm empty fruit bunch-based activated carbon for removal of 2,4,6-trichlorophenol: optimization using response surface methodology.

    Science.gov (United States)

    Hameed, B H; Tan, I A W; Ahmad, A L

    2009-05-30

    The effects of three preparation variables: CO(2) activation temperature, CO(2) activation time and KOH:char impregnation ratio (IR) on the 2,4,6-trichlorophenol (2,4,6-TCP) uptake and carbon yield of the activated carbon prepared from oil palm empty fruit bunch (EFB) were investigated. Based on the central composite design, two quadratic models were developed to correlate the three preparation variables to the two responses. The activated carbon preparation conditions were optimized using response surface methodology by maximizing both the 2,4,6-TCP uptake and activated carbon yield within the ranges studied. The optimum conditions for preparing activated carbon from EFB for adsorption of 2,4,6-TCP were found as follows: CO(2) activation temperature of 814 degrees C, CO(2) activation time of 1.9h and IR of 2.8, which resulted in 168.89 mg/g of 2,4,6-TCP uptake and 17.96% of activated carbon yield. The experimental results obtained agreed satisfactorily with the model predictions. The activated carbon prepared under optimum conditions was mesoporous with BET surface area of 1141 m(2)/g, total pore volume of 0.6 cm(3)/g and average pore diameter of 2.5 nm. The surface morphology and functional groups of the activated carbon were respectively determined from the scanning electron microscopy and Fourier transform infrared analysis.

  18. Adsorption of a Textile Dye on Commercial Activated Carbon: A Simple Experiment to Explore the Role of Surface Chemistry and Ionic Strength

    Science.gov (United States)

    Martins, Angela; Nunes, Nelson

    2015-01-01

    In this study, an adsorption experiment is proposed using commercial activated carbon as adsorbent and a textile azo dye, Mordant Blue-9, as adsorbate. The surface chemistry of the activated carbon is changed through a simple oxidation treatment and the ionic strength of the dye solution is also modified, simulating distinct conditions of water…

  19. Powder Activated Carbon Pretreatment of a Microfiltration Membrane for the Treatment of Surface Water

    Directory of Open Access Journals (Sweden)

    Yali Song

    2015-09-01

    Full Text Available This study focused on the effect of powder activated carbon (PAC adsorption on microfiltration (MF membrane performance. The results showed that PAC pretreatment offered high organic matter removal rates for both dissolved organic carbon (DOC and ultraviolet absorbance at 254 nm (UV254 during 10–200 mg/L PAC dosage. The removal efficiencies of organic matter by MF membrane filtration decreased with the increase of organic matter removal rate by PAC adsorption. PAC mainly removed organic matter of about 3 kDa molecular weight (MW. MF membrane maintained more than 5 kDa MW organic matter on the membrane after PAC adsorption. The results of membrane filtration indicated that PAC pretreatment slightly promoted membrane flux, regardless of PAC dosage. It seems that the organic matter fouling membrane was concentrated in more than 3 kDa MW. PAC removed markedly less than 3 kDa MW organic matter and had less effect on more than 3 kDa organic matter. Thus, PAC cannot reduce membrane fouling.

  20. Powder Activated Carbon Pretreatment of a Microfiltration Membrane for the Treatment of Surface Water.

    Science.gov (United States)

    Song, Yali; Dong, Bingzhi; Gao, Naiyun; Ma, Xiaoyan

    2015-09-10

    This study focused on the effect of powder activated carbon (PAC) adsorption on microfiltration (MF) membrane performance. The results showed that PAC pretreatment offered high organic matter removal rates for both dissolved organic carbon (DOC) and ultraviolet absorbance at 254 nm (UV254) during 10-200 mg/L PAC dosage. The removal efficiencies of organic matter by MF membrane filtration decreased with the increase of organic matter removal rate by PAC adsorption. PAC mainly removed organic matter of about 3 kDa molecular weight (MW). MF membrane maintained more than 5 kDa MW organic matter on the membrane after PAC adsorption. The results of membrane filtration indicated that PAC pretreatment slightly promoted membrane flux, regardless of PAC dosage. It seems that the organic matter fouling membrane was concentrated in more than 3 kDa MW. PAC removed markedly less than 3 kDa MW organic matter and had less effect on more than 3 kDa organic matter. Thus, PAC cannot reduce membrane fouling.

  1. In vitro platelet activation, aggregation and platelet-granulocyte complex formation induced by surface modified single-walled carbon nanotubes.

    Science.gov (United States)

    Fent, János; Bihari, Péter; Vippola, Minnamari; Sarlin, Essi; Lakatos, Susan

    2015-08-01

    Surface modification of single-walled carbon nanotubes (SWCNTs) such as carboxylation, amidation, hydroxylation and pegylation is used to reduce the nanotube toxicity and render them more suitable for biomedical applications than their pristine counterparts. Toxicity can be manifested in platelet activation as it has been shown for SWCNTs. However, the effect of various surface modifications on the platelet activating potential of SWCNTs has not been tested yet. In vitro platelet activation (CD62P) as well as the platelet-granulocyte complex formation (CD15/CD41 double positivity) in human whole blood were measured by flow cytometry in the presence of 0.1mg/ml of pristine or various surface modified SWCNTs. The effect of various SWCNTs was tested by whole blood impedance aggregometry, too. All tested SWCNTs but the hydroxylated ones activate platelets and promote platelet-granulocyte complex formation in vitro. Carboxylated, pegylated and pristine SWCNTs induce whole blood aggregation as well. Although pegylation is preferred from biomedical point of view, among the samples tested by us pegylated SWCNTs induced far the most prominent activation and a well detectable aggregation of platelets in whole blood.

  2. ACTIVATION ENERGY OF DESORPTION OF DIBENZOFURAN ON ACTIVATED CARBONS

    Institute of Scientific and Technical Information of China (English)

    LI Xiang; LI Zhong; XI Hongxia; LUO Lingai

    2004-01-01

    Three kinds of commercial activated carbons, such as Norit RB1, Monolith and Chemviron activated carbons, were used as adsorbents for adsorption of dibenzofuran. The average pore size and specific surface area of these activated carbons were measured. Temperature Programmed Desorption (TPD) experiments were conducted to measure the TPD curves of dibenzofuran on the activated carbons, and then the activation energy for desorption of dibenzofuran on the activated carbons was estimated. The results showed that the Chemviron and the Norit RB1 activated carbon maintained higher specific surface area and larger micropore pore volume in comparison with the Monolith activated carbon, and the activation energy for the desorption of dibenzofuran on these two activated carbons was higher than that on the Monolith activated carbon. The smaller the pore of the activated carbon was, the higher the activated energy of dibenzofuran desorption was.

  3. Effect of Polarity of Activated Carbon Surface, Solvent and Adsorbate on Adsorption of Aromatic Compounds from Liquid Phase.

    Science.gov (United States)

    Goto, Tatsuru; Amano, Yoshimasa; Machida, Motoi; Imazeki, Fumio

    2015-01-01

    In this study, introduction of acidic functional groups onto a carbon surface and their removal were carried out through two oxidation methods and outgassing to investigate the adsorption mechanism of aromatic compounds which have different polarity (benzene and nitrobenzene). Adsorption experiments for these aromatics in aqueous solution and n-hexane solution were conducted in order to obtain the adsorption isotherms for commercial activated carbon (BAC) as a starting material, its two types of oxidized BAC samples (OXs), and their outgassed samples at 900 °C (OGs). Adsorption and desorption kinetics of nitrobenzene for the BAC, OXs and OGs in aqueous solution were also examined. The results showed that the adsorption of benzene molecules was significantly hindered by abundant acidic functional groups in aqueous solution, whereas the adsorbed amount of nitrobenzene on OXs gradually increased as the solution concentration increased, indicating that nitrobenzene can adsorb favourably on a hydrophilic surface due to its high dipole moment, in contrast to benzene. In n-hexane solution, it was difficult for benzene to adsorb on any sample owing to the high affinity between benzene and n-hexane solvent. On the other hand, adsorbed amounts of nitrobenzene on OXs were larger than those of OGs in n-hexane solution, implying that nitrobenzene can adsorb two adsorption sites, graphene layers and surface acidic functional groups. The observed adsorption and desorption rate constants of nitrobenzene on the OXs were lower than those on the BAC due to disturbance of diffusion by the acidic functional groups.

  4. Adsorption of gaseous hydrocarbons on activated carbon: characteristic kinetic curve. [Includes effect of surface migration on kinetics

    Energy Technology Data Exchange (ETDEWEB)

    Costa, E.; Calleja, G.; Domingo, F.

    1985-06-01

    The internal diffusion coefficients, D /sub i/ , of pure methane, ethane and ethylene as well as some of their binary and ternary mixtures, have been calculated at 20/sup 0/C for solid particles of a commercial activated carbon. It has been observed that the contribution of the surface migration mechanism to the global mass transfer process inside the adsorbent particles can be as much as 70-80%. Values for the surface migration coefficient D /sub s/ have also been calculated from the relation D /sub i/ = D /sub g/ + KD /sub s/ , where K is a dimensionless mean slope factor. Values found for both coefficients are of the same order of magnitude as those reported in the literature for similar systems. All the values for the internal diffusion coefficients of these pure components and their mixtures fit into a single correlation curve, the characteristic kinetic curve of the adsorbent.

  5. Modification of Activated Carbon by Means of Microwave Heating and Its Effects on the Pore Texture and Surface Chemistry

    OpenAIRE

    2013-01-01

    Two kinds of typical activated carbons (coal based AC and coconut shell based AC) were modified in a flow of N2 gas has been carried out using a microwave device operating at 2450 MHz and different input power, instead of a conventional furnace. The samples were analyzed by means of low temperature N2 adsorption, elemental analysis and Boehm titration. The results show that microwave heating is an effective means of activated carbon modification. The temperature of activated carbon increases ...

  6. Preparation, surface characteristics, and electrochemical double-layer capacitance of KOH-activated carbon aerogels and their O- and N-doped derivatives

    Science.gov (United States)

    Zapata-Benabithe, Zulamita; Carrasco-Marín, Francisco; Moreno-Castilla, Carlos

    2012-12-01

    Carbon aerogels are obtained by carbonizing organic aerogels prepared by polycondensation reaction of resorcinol or pyrocatechol with formaldehyde. They are KOH-activated at two KOH/carbon ratios to increase pore volume and surface area. Selected samples are also surface-treated to introduce oxygen and nitrogen functionalities. The objectives are to investigate the effect of porosity and surface functionalities on the electrochemical capacitance of the carbon and activated carbon aerogels. Samples are characterized by N2 and CO2 adsorption at -196 and 0 °C, respectively, immersion calorimetry, temperature-programmed desorption, and X-ray photoelectron spectroscopy in order to determine their surface area, porosity, and surface chemistry. Two series of samples are obtained: one micro-mesoporous and the other basically microporous. A surface area up to 1935 m2 g-1 was obtained after KOH activation. Electrochemical double-layer capacitance was studied by cyclovoltammetry and chronopotentiometry with a three-electrode cell, using Ag/AgCl as reference electrode. Gravimetric capacitance at 0.125 A g-1 is related to N2 adsorption-measured micropore volume and mean size and to particle density. The highest gravimetric capacitance, 220 F g-1, is obtained with two O- and N-doped samples. Volumetric capacitance of 123 F cm-3, double the value generally needed for applications in small-volume systems, is obtained with a largely microporous oxygen-doped activated carbon aerogel.

  7. High surface area carbon and process for its production

    Energy Technology Data Exchange (ETDEWEB)

    Romanos, Jimmy; Burress, Jacob; Pfeifer, Peter; Rash, Tyler; Shah, Parag; Suppes, Galen

    2016-12-13

    Activated carbon materials and methods of producing and using activated carbon materials are provided. In particular, biomass-derived activated carbon materials and processes of producing the activated carbon materials with prespecified surface areas and pore size distributions are provided. Activated carbon materials with preselected high specific surface areas, porosities, sub-nm (<1 nm) pore volumes, and supra-nm (1-5 nm) pore volumes may be achieved by controlling the degree of carbon consumption and metallic potassium intercalation into the carbon lattice during the activation process.

  8. Theoretical study of γ-hexachlorocyclohexane and β-hexachlorocyclohexane isomers interaction with surface groups of activated carbon model.

    Science.gov (United States)

    Enriquez-Victorero, Carlos; Hernández-Valdés, Daniel; Montero-Alejo, Ana Lilian; Durimel, Axelle; Gaspard, Sarra; Jáuregui-Haza, Ulises

    2014-06-01

    Activated carbon (AC) is employed in drinking water purification without almost any knowledge about the adsorption mechanism of persistent organic pollutants (POPs) onto it. Hexachlorocyclohexane (HCH) is an organochlorinated contaminant present in water and soils of banana crops production zones of the Caribbean. The most relevant isomers of HCH are γ-HCH and β-HCH, both with great environmental persistence. A theoretical study of the influence of AC surface groups (SGs) on HCH adsorption is done in order to help to understand the process and may lead to improve the AC selection process. A simplified AC model consisting of naphthalene with a functional group was used to assess the influence of SGs over the adsorption process. The Multiple Minima Hypersurface (MMH) methodology was employed to study γ-HCH and β-HCH interactions with different AC SGs (hydroxyl and carboxyl) under different hydration and pH conditions. The results obtained showed that association of HCH with SGs preferentially occurs between the axial protons of HCH and SG's oxygen atom, and the most favorable interactions occurring with charged SGs. An increase in carboxylic SGs content is proposed to enhance HCH adsorption onto AC under neutral pH conditions. Finally, this work presents an inexpensive computer aided methodology for preselecting activated carbon SGs content for the removal of a given compound.

  9. A Study on the Surface Structures of Viscose-based Activated Carbon Fiber by FT-IR Spectroscopy and XPS

    Institute of Scientific and Technical Information of China (English)

    黄强; 黄永秋; 潘鼎

    2004-01-01

    Using viscose fiber (VF) as starting material and common steam as activating agent, formation of oxygen structures in activated carbon fiber is investigated. In the preparation of samples, VF was first heated at temperatures between 450℃ and 900℃ in N2 artmosphere. Then, in a successive activation stage, the product carbonized at 600℃ was activated in steam at 450 - 900℃ for 30 min, and at 600℃for 5- 30 min. The other carbonization products were activated at 600 and 900℃ for 30 min respectively. The products activated at 900℃ were then activated at 450℃ for 30 min again. The starting material, carbonized products and all activation products were examined by FT-IR spectroscopy and some products were examined by X-ray photoelectron spectroscope (XPS). And the yields of the carbonized and activated products were calculated. By analysing these spectra, the amount of oxygen-containing functional groups of the activated products attained under various activation time, various activation temperature and various previous carbonization temperature was determined.

  10. Influence of the pore structure and surface chemical properties of activated carbon on the adsorption of mercury from aqueous solutions.

    Science.gov (United States)

    Lu, Xincheng; Jiang, Jianchun; Sun, Kang; Wang, Jinbiao; Zhang, Yanping

    2014-01-15

    Reactivation and chemical modification were used to obtain modified activated carbons with different pore structure and surface chemical properties. The samples were characterized by nitrogen absorption-desorption, Fourier transform infrared spectroscopy and the Bothem method. Using mercury chloride as the target pollutant, the Hg(2+) adsorption ability of samples was investigated. The results show that the Hg(2+) adsorption capacity of samples increased significantly with increases in micropores and acidic functional groups and that the adsorption process was exothermic. Different models and thermodynamic parameters were evaluated to establish the mechanisms. It was concluded that the adsorption occurred through a monolayer mechanism by a two-speed process involving both rapid adsorption and slow adsorption. The adsorption rate was determined by chemical reaction.

  11. Amphoteric surface active agents

    Directory of Open Access Journals (Sweden)

    Eissa, A.M. F.

    1995-10-01

    Full Text Available 2-[trimethyl ammonium, triethyl ammonium, pyridinium and 2-amino pyridinium] alkanoates, four series of surface active agents containing carbon chain C12, C14, C16 and C18carbon atoms, were prepared. Their structures were characterized by microanalysis, infrared (IR and nuclear magnetic resonance (NMR. Surface and interfacial tension, Krafft point, wetting time, emulsification power, foaming height and critical micelle concentration (cmc were determined and a comparative study was made between their chemical structure and surface active properties. Antimicrobial activity of these surfactants was also determined.

    Se prepararon cuatro series de agentes tensioactivos del tipo 2-[trimetil amonio, trietil amonio, piridinio y 2-amino piridinio] alcanoatos, que contienen cadenas carbonadas con C12, C14, C16 y C18 átomos de carbono.
    Se determinaron la tensión superficial e interfacial, el punto de Krafft, el tiempo humectante, el poder de emulsionamiento, la altura espumante y la concentración critica de miscela (cmc y se hizo un estudio comparativo entre la estructura química y sus propiedades tensioactivas. Se determinó también la actividad antimicrobiana de estos tensioactivos. Estas estructuras se caracterizaron por microanálisis, infrarrojo (IR y resonancia magnética nuclear (RMN.

  12. Equilibrium and column adsorption studies of 2,4-dinitroanisole (DNAN) on surface modified granular activated carbons.

    Science.gov (United States)

    Boddu, V M; Abburi, K; Fredricksen, A J; Maloney, S W; Damavarapu, R

    2009-02-01

    2,4-Dinitroanisole (DNAN) is used as a component extensively in the development of insensitive munitions. This may result in release of DNAN into the environment. Here, the results are reported of a study on the removal characteristics of DNAN through adsorption on granular activated carbon (GAC), chitosan coated granular activated carbon (CGAC), acid treated granular activated carbon (AGAC) and alkali treated granular activated carbon (BGAC) under equilibrium and column flow conditions. The effect of pH, contact time, concentration of DNAN, and presence of electrolytes on the uptake of DNAN by the adsorbents was investigated. The equilibrium data were fitted to different types of adsorption isotherms. The data were further analysed on the basis of Lagergren first-order, pseudo second-order and intraparticle diffusion kinetic models. Breakthrough curves were obtained based on column flow results. All the adsorbents were capable of removing about 99% of DNAN from aqueous media, except CGAC which adsorbed about 87% of DNAN.

  13. Complement activation by PEG-functionalized multi-walled carbon nanotubes is independent of PEG molecular mass and surface density

    DEFF Research Database (Denmark)

    Andersen, Alina Joukainen; Windschiegl, Barbara; Ilbasmis-Tamer, Sibel

    2013-01-01

    Carboxylated (4%) multi-walled carbon nanotubes were covalently functionalized with poly(ethylene glycol)1000 (PEG1000), PEG1500 and PEG4000 with a PEG loading of approximately 11% in all cases. PEG loading generated non-uniform and heterogeneous higher surface structures and increased nanotube...... eliminated. Our observations address the difficulty in making carbon nanotubes more compatible with innate immunity through covalent PEG functionalization as well as double PEGylation strategies. From the Clinical EditorComplement-mediated toxicity is a major limiting factor in certain nanomedicine...... applications. This study clarifies that PEGylation of carbon nanotubes is unlikely to address this complication....

  14. Luminescent Surface Quaternized Carbon Dots

    KAUST Repository

    Bourlinos, Athanasios B.

    2012-01-10

    Thermal oxidation of a salt precursor made from the acid base combination of tris(hydroxymethyl)aminomethane and betaine hydrochloride results in light-emitting surface quaternized carbon dots that are water-dispersible, display anion exchange properties, and exhibit uniform size/surface charge. © 2011 American Chemical Society.

  15. Theoretical study of chlordecone and surface groups interaction in an activated carbon model under acidic and neutral conditions.

    Science.gov (United States)

    Gamboa-Carballo, Juan José; Melchor-Rodríguez, Kenia; Hernández-Valdés, Daniel; Enriquez-Victorero, Carlos; Montero-Alejo, Ana Lilian; Gaspard, Sarra; Jáuregui-Haza, Ulises Javier

    2016-04-01

    Activated carbons (ACs) are widely used in the purification of drinking water without almost any knowledge about the adsorption mechanisms of the persistent organic pollutants. Chlordecone (CLD, Kepone) is an organochlorinated synthetic compound that has been used mainly as agricultural insecticide. CLD has been identified and listed as a persistent organic pollutant by the Stockholm Convention. The selection of the best suited AC for this type of contaminants is mainly an empirical and costly process. A theoretical study of the influence of AC surface groups (SGs) on CLD adsorption is done in order to help understanding the process. This may provide a first selection criteria for the preparation of AC with suitable surface properties. A model of AC consisting of a seven membered ring graphene sheet (coronene) with a functional group on the edge was used to evaluate the influence of the SGs over the adsorption. Multiple Minima Hypersurface methodology (MMH) coupled with PM7 semiempirical Hamiltonian was employed in order to study the interactions of the chlordecone with SGs (hydroxyl and carboxyl) at acidic and neutral pH and different hydration conditions. Selected structures were re-optimized using CAM-B3LYP to achieve a well-defined electron density to characterize the interactions by the Quantum Theory of Atoms in Molecules approach. The deprotonated form of surface carboxyl and hydroxyl groups of AC models show the strongest interactions, suggesting a chemical adsorption. An increase in carboxylic SGs content is proposed to enhance CLD adsorption onto AC at neutral pH conditions.

  16. Studies of activated carbon and carbon black for supercapacitor applications

    Energy Technology Data Exchange (ETDEWEB)

    Richner, R.; Mueller, S.; Koetz, R.; Wokaun, A. [Paul Scherrer Inst. (PSI), Villigen (Switzerland)

    1999-08-01

    Carbon Black and activated carbon materials providing high surface areas and a distinct pore distribution are prime materials for supercapacitor applications at frequencies < 0.5 Hz. A number of these materials were tested for their specific capacitance, surface and pore size distribution. High capacitance electrodes were manufactured on the laboratory scale with attention to ease of processability. (author) 1 fig., 1 ref.

  17. Influence of the Surface and Structural Characteristics of Activated Carbons on Adsorptive Removal of Halo-Olefinic Impurities from 1,1,1,3,3-Pentafluoropropane

    Institute of Scientific and Technical Information of China (English)

    Bo Zhang; Chuang Zhang; Mingquan Wei

    2014-01-01

    abstract Halo-olefinic impurities in 1,1,1,3,3-pentafluoropropane (HFC-245fa) product used as blowing agents, etc. could damage the human body and must be removed. Activated carbon was treated by HCl, HNO3 and NaOH, respec-tively. The adsorptive performance of unmodified and modified activated carbons for the removal of a low con-tent of 1-chloro-3,3,3-trifluoro-1-propene (HCFC-1233zd), 1,3,3,3-tetrafluoro-1-propene (HFC-1234ze), 1-chloro-1,3,3,3-tetrafluoro-1-propene (HFC-1224zb) and 2-chloro-1,3,3,3-tetrafluoro-1-propene (HFC-1224xe) halo-olefins in the 1,1,1,3,3-pentafluoropropane (HFC-245fa) product was investigated. These halo-olefinic im-purities could be substantially removed from the HFC-245fa product via the adsorption over activated carbon when the adsorption temperature was under 333 K, which can be attributed to theπ-πdispersion interactions between the halo-olefins and carbon graphite layer. The basic surface groups of activated carbon could catalyze the decomposition of HFC-245fa to form HFC-1234ze. However, the significant increase in the amount of surface acidic groups of activated carbon led to a distinct decrease of adsorption capacity due to the reduction in the mi-cropore volume of adsorbent and a decrease in the strength of theπ-πdispersive interactions between halo-olefin molecules and carbon basal. The breakthrough time of halo-olefinic impurities on activated carbon in-creased with the increase of molecular mass and the decrease of molecular symmetry.

  18. Influence of surface oxygenated groups on the formation of active Cu species and the catalytic activity of Cu/AC catalyst for the synthesis of dimethyl carbonate

    Science.gov (United States)

    Zhang, Guoqiang; Li, Zhong; Zheng, Huayan; Hao, Zhiqiang; Wang, Xia; Wang, Jiajun

    2016-12-01

    Activated carbon (AC) supported Cu catalysts are employed to study the influence of surface oxygenated groups on the formation of active Cu species and the catalytic activity of Cu/AC catalyst for oxidative carbonylation of methanol to dimethyl carbonate (DMC). The AC supports are thermal treated under different temperatures in order to adjust the levels of surface oxygenated groups. The AC supports are characterized by BET, TPD-MS and XRD, and the Cu/AC catalysts are characterized by BET, XRD, TEM, XPS, AAS, CH3OH-TPD and N2O chemisorption. The results show that as the treatment temperature is below 800 °C, the BET surface area of the corresponding AC supports are nearly unchanged and close to that of the original AC (1529.6 m2/g). But as the thermal treatment temperature is elevated from 1000 to 1600 °C, the BET surface area of AC supports gradually decreases from 1407.6 to 972.2 m2/g. After loading of Cu, the BET surface area of copper catalysts is in the range of 834.4 to 1545.3 m2/g, which is slightly less than that of the respective supports. When AC is thermal treated at 400 and 600 °C, the unstable carboxylic acid and anhydrides groups are selectively removed, which has weakened the mobility and agglomeration of Cu species during the calcination process, and thus improve the Cu species dispersion over AC support. But as the treatment temperature is elevated from 600 °C to 1200 °C, the Cu species dispersion begins to decline suggesting further removal of stable surface oxygenated groups is unfavorable for Cu species dispersion. Moreover, higher thermal treatment temperature (above 1200 °C) promotes the graphitization degree of AC and leds to the decrease of Cu loading on AC support. Meanwhile, the removal of surface oxygenated groups by thermal treatment is conducive to the formation of more π-sites, and thus promote the reduction of Cu2+ to Cu+ and Cu0 as active centers. The specific surface area of (Cu+ + Cu0) is improved by thermal treatment of AC

  19. Preparation of activate carbon with high specific surface area from beer lees by chemical activation with KOH; Suisankakariumu wo mochiita yakuhin fukatsuho ni yoru birukasu karano kohihyoumenseki kasseitan no seizo

    Energy Technology Data Exchange (ETDEWEB)

    Hayashi, J.; Kubo, A.; Furukawa, A.; Muroyama, K. [Kansai University, Osaka (Japan). Dept. of Chemical Engineering

    2000-03-10

    Activated carbons with high specific surface area were prepared from beer lees by chemical activation with KOH. We examined the influence of the preparation conditions, such as temperature and impregnation ratio, on the pore structure of the prepared activated carbon. The specific surface area increased with an increase in carbonization temperature up to 800 degree C and decreased at 900 degree C because of excess activation. It reached a maximum value at the impregnation ratio of 2.0. The activated carbon, which was prepared at the carbonization temperature of 800 degree C and at the impregnation ratio of 2.0, had very high specific surface area of 2,440 m{sup 2}/g. It was found that KOH worked effectively as the activating reagent in two temperature ranges, below 500 degree C and above 600 degree C. The amount of benzene and acetone adsorbed on the prepared activated carbon were much larger than that on the commercial activated carbons. (author)

  20. Simulations of phenol adsorption on activated carbon and carbon black

    OpenAIRE

    Prosenjak, Claudia; Valente Nabais, Joao; Laginhas, Carlos; Carrott, Peter; Carrott, Manuela

    2010-01-01

    We use grand canonical Monte Carlo and molecular dynamics simulations to study the adsorption of phenol on carbon materials. Activated carbon is modelled by pore size distributions based on DFT methods; carbon black is represented by a single carbon slab with varying percentages of surface atoms removed. GCMC results for the adsorption from the corresponding gas phase gave reasonable agreement with experimental adsorption results. MD simulations, that studied the influence of the presence of ...

  1. PROGRESS ON ACTIVATED CARBON FIBERS

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    Activated carbon fiber is one kind of important adsorption materials. These novel fibrousadsorbents have high specific surface areas or abundant functional groups, which make them havegreater adsorption/desorption rates and larger adsorption capacities than other adsorbents. They canbe prepared as bundle, paper, cloth and felt to meet various technical requirement. They also showreduction property. In this paper the latest progress on the studies of the preparation and adsorptionproperties of activated carbon fibers is reviewed. The application of these materials in drinking waterpurification, environmental control, resource recovery, chemical industry, and in medicine and healthcare is also presented.

  2. Activated, coal-based carbon foam

    Energy Technology Data Exchange (ETDEWEB)

    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.

  3. Activated, coal-based carbon foam

    Energy Technology Data Exchange (ETDEWEB)

    Rogers, Darren Kenneth [Wheeling, WV; Plucinski, Janusz Wladyslaw [Glen Dale, WV

    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.

  4. Surface-active proteins from Fusarium spp. and their role in gushing in carbonated beverages

    OpenAIRE

    Lutterschmid, Georg

    2011-01-01

    Gushing is the spontaneous over-foaming of bottled carbonated beverages, particularly of beer. Due to its negative economical and image-damaging consequences it is of great interest for the beverage industry. To clarify the molecular causes of malt-related gushing, five surface-active proteins from filamentous fungi and from barley were heterologously expressed in Pichia pastoris. The proteins were isolated and their gushing-inducing activity was determined. The protein FcHyd5p was identified...

  5. Mesoporous magnetic activated carbon: Effect of preparation route on texture and surface properties and on effect for Reactive Black 5 adsorption.

    Science.gov (United States)

    Giannakoudakis, Dimitrios; Saroyan, Hayarpi; Lazaridis, Nikolaos; Deliyanni, Eleni

    2016-04-01

    Mesoporous magnetic activated carbon: Effect of preparation route on texture and surface properties and on effect for Reactive Black 5 adsorption. Dimitrios Giannakoudakis1, Hayarpi Saroyan2, Nikolaos Lazaridis2, Eleni Deliyanni2 1 City College of New York, Chemistry Department, 160 Convent Avenue, New York, United States 2 Laboratory of General and oInorganic Chemical Technology, Department of Chemistry, Aristotle University of Thessaloniki, GR-541 24 Thessaloniki, Greece In this study, the effect of preparation route of a mesoporous magnetic activated carbon on Reactive Black 5 (RB5) adsorption was investigated. The synthesis of the magnetic activated carbon was achieved both with (i) impregnation method (Bmi), and (ii) co-precipitation with two precipitation agents: NaOH (Bm) and NH4OH (Bma). After synthesis, the full characterization with various techniques (SEM, FTIR, XRD, DTA, DTG, VSM) was achieved in order to testify the effect of the preparation route on its textural and surface properties. It was shown that after the precipitation method the prepared carbon presented a collapsed texture and small magnetic properties. Effects of initial solution pH, effect of temperature, adsorption isotherms and kinetics were investigated in order to conclude about the aforementioned effect of the preparation method on dye adsorption performance of the magnetic carbons. The adsorption evaluation of the magnetic activated carbon presented higher adsorption capacity of Bmi carbon (350 mg/g) and lower of Bm (150 mg/g). Equilibrium experiments are also performed studying the effect of contact time (pseudo-first and -second order equations) and temperature (isotherms at 25, 45 and 65 °C fitted to Langmuir and Freundlich model). A full thermodynamic evaluation was carried out, calculating the parameters of enthalpy, free energy and entropy (ΔHο, ΔGο and ΔSο). The characterization with various techniques revealed the possible interactions/forces of dye-composite system.

  6. Nanostructure of Poly(Acrylic Acid) Adsorption Layer on the Surface of Activated Carbon Obtained from Residue After Supercritical Extraction of Hops

    Science.gov (United States)

    Wiśniewska, M.; Nosal-Wiercińska, A.; Ostolska, I.; Sternik, D.; Nowicki, P.; Pietrzak, R.; Bazan-Wozniak, A.; Goncharuk, O.

    2017-01-01

    The nanostructure of poly(acrylic acid) (PAA) adsorption layer on the surface of mesoporous-activated carbon HPA obtained by physical activation of residue after supercritical extraction of hops was characterized. This characterization has been done based on the analysis of determination of adsorbed polymer amount, surface charge density, and zeta potential of solid particles (without and in the PAA presence). The SEM, thermogravimetric, FTIR, and MS techniques have allowed one to examine the solid surface morphology and specify different kinds of HPA surface groups. The effects of solution pH, as well as polymer molecular weight and concentration, were studied. The obtained results indicated that the highest adsorption on the activated carbon surface was exhibited by PAA with lower molecular weight (i.e., 2000 Da) at pH 3. Under such conditions, polymeric adsorption layer is composed of nanosized PAA coils (slightly negatively charged) which are densely packed on the positive surface of HPA. Additionally, the adsorption of polymeric macromolecules into solid pores is possible.

  7. Carbon Nanomaterials: Surface Structure and Morphology

    Science.gov (United States)

    Mansurov, Z. A.; Shabanova, T. A.; Mofa, N. N.; Glagolev, V. A.

    2014-09-01

    We propose a classification of individual nanoparticles on the basis of the form of the surface and the internal architectural packing for investigations carried out with the help of transmission electron microscopy. The investigated samples contain individual nanoparticles of seven kinds in different ratios: rounded, tubular, fibrous, fi lm, "veil," "active" particles and "particles with regular geometric contours." The classification was made on the basis of an analysis of the results of investigations of the surfaces and internal architectural packing of carbon particles obtained in different physiochemical processes (carbonization, carburizing, arc discharge, mechanochemical treatment, plasma chemistry, and in carbon-containing fl ames). For the source materials, we used waste of farming products and widely distributed mineral raw materials.

  8. Effects of Microporosity and Surface Chemistry on Separation Performances of N-Containing Pitch-Based Activated Carbons for CO2/N2 Binary Mixture

    Science.gov (United States)

    Lee, Min-Sang; Park, Mira; Kim, Hak Yong; Park, Soo-Jin

    2016-01-01

    In this study, N-containing pitch-based activated carbons (NPCs) were prepared using petroleum pitch with a low softening point and melamine with a high nitrogen content. The major advantage of the preparation method is that it enables variations in chemical structures and textural properties by steam activation at high temperatures. The adequate micropore structures, appropriate chemical modifications, and high adsorption enthalpies of NPCs are favorable for CO2 adsorption onto carbon surfaces. Furthermore, the structure generates a considerable gas/N-containing carbon interfacial area, and provides selective access to CO2 molecules over N2 molecules by offering an increased number of active sites on the carbon surfaces. The highest CO2/N2 selectivity, i.e., 47.5, and CO2 adsorption capacity for a CO2/N2 (0.15:0.85) binary gas mixture, i.e., 5.30 wt%, were attained at 298 K. The NPCs also gave reversible and durable CO2-capturing performances. All the results suggest that NPCs are promising CO2 sorbents, which can meet the challenges of current CO2 capture and separation techniques. PMID:26987683

  9. Effects of Microporosity and Surface Chemistry on Separation Performances of N-Containing Pitch-Based Activated Carbons for CO2/N2 Binary Mixture

    Science.gov (United States)

    Lee, Min-Sang; Park, Mira; Kim, Hak Yong; Park, Soo-Jin

    2016-03-01

    In this study, N-containing pitch-based activated carbons (NPCs) were prepared using petroleum pitch with a low softening point and melamine with a high nitrogen content. The major advantage of the preparation method is that it enables variations in chemical structures and textural properties by steam activation at high temperatures. The adequate micropore structures, appropriate chemical modifications, and high adsorption enthalpies of NPCs are favorable for CO2 adsorption onto carbon surfaces. Furthermore, the structure generates a considerable gas/N-containing carbon interfacial area, and provides selective access to CO2 molecules over N2 molecules by offering an increased number of active sites on the carbon surfaces. The highest CO2/N2 selectivity, i.e., 47.5, and CO2 adsorption capacity for a CO2/N2 (0.15:0.85) binary gas mixture, i.e., 5.30 wt%, were attained at 298 K. The NPCs also gave reversible and durable CO2-capturing performances. All the results suggest that NPCs are promising CO2 sorbents, which can meet the challenges of current CO2 capture and separation techniques.

  10. Methane adsorption on activated carbon

    OpenAIRE

    Perl, Andras; Koopman, Folkert; Jansen, Peter; Rooij, Marietta de; Gemert, Wim van

    2014-01-01

    Methane storage in adsorbed form is a promising way to effectively and safely store fuel for vehicular transportation or for any other potential application. In a solid adsorbent, nanometer wide pores can trap methane by van der Waals forces as high density fluid at low pressure and room temperature. This provides the suitable technology to replace bulky and expensive cylindrical compressed natural gas tanks. Activated carbons with large surface area and high porosity are particularly suitabl...

  11. Photoconductivity of Activated Carbon Fibers

    Science.gov (United States)

    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.

  12. Surface Active Components: Review

    Directory of Open Access Journals (Sweden)

    Z. Shafiei

    2014-03-01

    Full Text Available Biosurfactant or surface active components are produced by many different microorganisms. Biosurfactants are amphiphilic molecules with both hydrophilic and hydrophobic (generally hydrocarbon moieties that partition preferentially a within the interface between fluid phases with some other degrees of polarity and hydrogen bonding including oil/water or air/water interfaces. These properties render surfactants able to reducing surface and interfacial tension and forming microemulsion where hydrocarbons can solubilize in water or where water can solubilize in hydrocarbons, the majority of surfactants have gained importance in the fields of enhanced oil recovery, environmental bioremediation, food processing and pharmaceuticals. However, large-scale production of these molecules has not been realized as a result of low yields in production processes and high recovery and purification costs. This review article represents a classification of biosurfactant in addition to their microbial origin and effect of some nutrition and environmental factor for high production of biosurfactant. The nitrogen, carbon sources and environmental factors can make a difference key to the regulating biosurfactants synthesis Fascination with microbial surfactants have been steadily increasing recently because of advantages over the chemical surfactants for example environmentally friendly nature, lower toxicity, higher biodegradability, higher selectivity and specific gravity at extreme temperature, pH and salinity. For this reason the demand of biosurfactant are increasing day by day.

  13. High concentration powdered activated carbon-membrane bioreactor (PAC-MBR) for slightly polluted surface water treatment at low temperature.

    Science.gov (United States)

    Ma, Cong; Yu, Shuili; Shi, Wenxin; Tian, Wende; Heijman, S G J; Rietveld, L C

    2012-06-01

    In this study, different concentrations of PAC combined with MBR were carried out to treat slightly polluted surface water (SPSW) at low temperature (10°C). Effects of PAC on the efficiencies of operation, treatment, and the performance of the process were investigated. It was found that the effluent quality, performance efficiency, resistance of shock load were all enhanced and chemical irreversible membrane fouling was reduced with increasing dosage of PAC in MBR. Only when the concentration of PAC which acted as biological carriers was high enough (i.g., 50 g/L), nitrification without initial inoculation in the filtration tank could start within 19 days and be completed within 35 days at 10°C. Fifty grams per liter PAC was the optimal dosage in MBR for stable and extended operation. Under this condition, mean removal efficiencies of ammonia nitrogen (NH(3)-N), dissolved organic carbon (DOC) and UV(254) were 93%, 75%, and 85%, respectively.

  14. Catalytic activity of carbons for methane decomposition reaction

    Energy Technology Data Exchange (ETDEWEB)

    Muradov, Nazim; Smith, Franklyn; T-Raissi, Ali [Florida Solar Energy Center, University of Central Florida, 1679 Clearlake Road, Cocoa, FL 32922 (United States)

    2005-05-15

    Catalytic decomposition of methane is an environmentally attractive approach to CO{sub 2}-free production of hydrogen. The objective of this work is to evaluate catalytic activity of a wide range of carbon materials for methane decomposition reaction and determine major factors governing their activity. It was demonstrated that the catalytic activity of carbon materials for methane decomposition is mostly determined by their structural and surface properties. Kinetics of methane decomposition reaction over disordered (amorphous) carbons such as carbon black and activated carbon were determined. The mechanism of carbon-catalyzed methane decomposition reaction and the nature of active sites on the carbon surface are discussed in this paper.

  15. Characteristics of Nonafluorobutyl Methyl Ether (NFE) Adsorption onto Activated Carbon Fibers and Different-Size-Activated Carbon Particles.

    Science.gov (United States)

    Tanada; Kawasaki; Nakamura; Araki; Tachibana

    2000-08-15

    The characteristics of adsorption of 1,1,1,2,2,3,3,4,4-nonafluorobutyl methyl ether (NFE), a chlorofluorocarbon (CFC) replacement, onto six different activated carbon; preparations (three activated carbon fibers and three different-sized activated carbon particles) were investigated to evaluate the interaction between activated carbon surfaces and NFE. The amount of NFE adsorbed onto the three activated carbon fibers increased with increasing specific surface area and pore volume. The amount of NFE adsorbed onto the three different-sized-activated carbon particles increased with an increase in the particle diameter of the granular activated carbon. The differential heat of the NFE adsorption onto three activated carbon fibers depended on the porosity structure of the activated carbon fibers. The adsorption rate of NFE was also investigated in order to evaluate the efficiency of NFE recovery by the activated carbon surface. The Sameshima equation was used to obtain the isotherms of NFE adsorption onto the activated carbon fibers and different-sized-activated carbon particles. The rate constant k for NFE adsorption onto activated carbon fibers was larger for increased specific surface area and pore volume. The rate of NFE adsorption on activated carbons of three different particle sizes decreased with increasing particle diameter at a low initial pressure. The adsorption isotherms of NFE for the six activated carbons conformed to the Dubinin-Radushkevich equation; the constants BE(0) (the affinity between adsorbate and adsorbent) and W(0) (the adsorption capacity) were calculated. These results indicated that the interaction between the activated carbon and NFE was larger with the smaller specific surface area of the activated carbon fibers and with the smaller particle diameter of the different-sized-activated carbon particles. The degree of packing of NFE in the pores of the activated carbon fibers was greater than that in the pores of the granular activated

  16. Progress in the Characterization of the Surface Species in Activated Carbons by means of INS Spectroscopy Coupled with Detailed DFT Calculations

    Directory of Open Access Journals (Sweden)

    Andrea Piovano

    2015-01-01

    Full Text Available Activated carbons are materials with relevance in different industrial applications. Due to the inherent complexity and heterogeneity of their structures, an easy assignment of the species present on their surface has a challenging result. Only recently, with the possibility to collect well-resolved inelastic neutron spectra and to simulate by DFT methods more or less extended graphitic clusters, this task is starting to become feasible. Here we report our investigation on a steam activated carbon and we show that different vibrations in the region of out-of-plane C-H bending modes are specifically connected to hydrogen terminations belonging to extended and regular borders or to short and defective ones. Furthermore, simulations including heteroatoms such as oxygen allowed us to point out spectral regions with a contribution from carboxyl species.

  17. The Adsorption Mechanism of Modified Activated Carbon on Phenol

    OpenAIRE

    Lin J. Q.; Yang S. E.; Duan J. M.; Wu J.J.; Jin L. Y.; Lin J. M.; Deng Q. L.

    2016-01-01

    Modified activated carbon was prepared by thermal treatment at high temperature under nitrogen flow. The surface properties of the activated carbon were characterized by Boehm titration, BET and point of zero charge determination. The adsorption mechanism of phenol on modified activated carbon was explained and the adsorption capacity of modified activated carbon for phenol when compared to plain activated carbon was evaluated through the analysis of adsorption isotherms, thermodynamic and ki...

  18. The Transport Properties of Activated Carbon Fibers

    Science.gov (United States)

    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.

  19. Petrographic evaluation of xylite activated carbon

    Energy Technology Data Exchange (ETDEWEB)

    Predeanu, G. [Metallurgical Research Institute, Department of Raw Materials, Mehadia St. 39, Sector 6, 060543 Bucharest (Romania); Panaitescu, C. [University POLITEHNICA Bucharest, Faculty of Industrial Chemistry, Fuel Laboratory, Polizu St. 1, Sector 1, 011061, Bucharest (Romania)

    2007-08-01

    Xylites are promising materials for activated carbon manufacturing due to their low rank, low inorganic content, and structural characteristics similar to the strong consistence of wood. These are similar to the classical adsorbents used for waste water purification, and available and profitable in the long term. This study has been undertaken to provide by means of petrographic data, new information on the porous structure development in chars during direct heating carbonization and physical activation. The xylite petrographic composition is very important, mainly due to the existence of structured wooden material - textinite with round and elongated cells - that influences the development of the structure and texture during carbonization and activation. The charcoal microstructure reveals some interesting aspects about the carbonization process with regard to evolution, efficiency and pore development. In the xylite activated carbon, the adsorption surface development by means of the highly porous system depends on the type of petrographical components, raw material grain size, and carbonization parameters. (author)

  20. Impacto del tratamiento con ozono sobre las propiedades superficiales del carbón activado Impact of ozone treatment on activated carbon surface properties

    Directory of Open Access Journals (Sweden)

    Héctor Valdés

    2011-08-01

    Full Text Available El uso conjunto de ozono y carbón activado para tratar efluentes tóxicos ha sido demostrado recientemente. Sin embargo, existen dudas acerca del efecto del ozono sobre las propiedades del carbón activado. En este artículo se presentan resultados sobre la modificación de las propiedades superficiales de un carbón activado comercial por la acción del ozono durante diferentes tiempos de exposición. Las propiedades químicas superficiales del carbón activado fueron evaluadas utilizando las técnicas de neutralización selectiva, desorción térmica programada (DTP y el pH del punto de carga cero. Las características texturales fueron evaluadas mediante microscopía electrónica de barrido. El área superficial aparente, el volumen de microporos y mesoporos fueron obtenidos a partir de las isotermas de adsorción de nitrógeno a 77 K. Las propiedades adsortivas fueron caracterizadas por el índice de adsorción de azul de metileno. Los resultados demuestran que los grupos superficiales oxigenados presentes en el carbón activado se modifican producto del tratamiento con el ozono. A mayores dosis de ozono, el carbón sufre mayor oxidación y se incrementan los grupos ácidos en especial los grupos carboxílicos, mientras que el pH de punto de carga cero disminuye. El área BET, así como el volumen de microporos disminuyen al igual que el poder de adsorción de azul de metileno.The combined use of ozone and activated carbon has recently started to be developed for the treatment of toxic effluents. However, the effect of ozone on the properties of activated carbon is not fully elucidated. A study was undertaken of modifications of the surface properties of a commercial activated carbon produced by its ozonation during different time periods. Surface chemistry of the activated carbon samples was characterized by of selective neutralization, temperature-programmed desorption, and pH of the point of zero charge. Surface area and volume of

  1. Making Activated Carbon by Wet Pressurized Pyrolysis

    Science.gov (United States)

    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

  2. Carbon fiber resin matrix interphase: effect of carbon fiber surface treatment on composite performance

    Energy Technology Data Exchange (ETDEWEB)

    Lehmann, S.; Megerdigian, C.; Papalia, R.

    1985-04-01

    Carbon fibers are supplied by various manufacturers with a predetermined level of surface treatment and matrix compatible sizings. Surface treatment of the carbon fiber increases the active oxygen content, the polarity and the total free surface energy of the fiber surface. This study is directed toward determining the effect of varying carbon fiber surface treatment on the composite performance of thermoset matrix resins. The effect of varying fiber surface treatment on performance of a promising proprietary sizing is also presented. 6 references, 11 figures.

  3. Application of optimized large surface area date stone (Phoenix dactylifera ) activated carbon for rhodamin B removal from aqueous solution: Box-Behnken design approach.

    Science.gov (United States)

    Danish, Mohammed; Khanday, Waheed Ahmad; Hashim, Rokiah; Sulaiman, Nurul Syuhada Binti; Akhtar, Mohammad Nishat; Nizami, Maniruddin

    2017-02-03

    Box-Behnken model of response surface methodology was used to study the effect of adsorption process parameters for Rhodamine B (RhB) removal from aqueous solution through optimized large surface area date stone activated carbon. The set experiments with three input parameters such as time (10-600min), adsorbent dosage (0.5-10g/L) and temperature (25-50°C) were considered for statistical significance. The adequate relation was found between the input variables and response (removal percentage of RhB) and Fisher values (F- values) along with P-values suggesting the significance of various term coefficients. At an optimum adsorbent dose of 0.53g/L, time 593min and temperature 46.20°C, the adsorption capacity of 210mg/g was attained with maximum desirability. The negative values of Gibb(')s free energy (ΔG) predicted spontaneity and feasibility of adsorption; whereas, positive Enthalpy change (ΔH) confirmed endothermic adsorption of RhB onto optimized large surface area date stone activated carbons (OLSADS-AC). The adsorption data were found to be the best fit on the Langmuir model supporting monolayer type of adsorption of RhB with maximum monolayer layer adsorption capacity of 196.08mg/g.

  4. Minimizing activated carbons production cost

    Energy Technology Data Exchange (ETDEWEB)

    Stavropoulos, G.G.; Zabaniotou, A.A. [Department of Chemical Engineering, Aristotle University of Thessaloniki, Univ. P. O. Box 1520, 54006, Thessaloniki (Greece)

    2009-07-15

    A detailed economic evaluation of activated carbons production process from various raw materials is undertaken using the conventional economic indices (ROI, POT, and NPV). The fundamental factors that affect production cost were taken into account. It is concluded that for an attractive investment in activated carbons production one should select the raw material with the highest product yield, adopt a chemical activation production scheme and should base product price on product-surface area (or more generally on product adsorption capacity for the adsorbate in consideration). A raw material that well meets the above-mentioned criteria is petroleum coke but others are also promising (charcoals, and carbon black). Production cost then can be optimized by determining its minimum value of cost that results from the intercept between the curves of plant capacity and raw material cost - if any. Taking into account the complexity of such a techno-economic analysis, a useful suggestion could be to start the evaluations from a plant capacity corresponding to the break-even point, i. e. the capacity at which income equals production cost. (author)

  5. Nanospace engineering of KOH activated carbon.

    Science.gov (United States)

    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 (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.

  6. Design of activated carbon/activated carbon asymmetric capacitors

    Directory of Open Access Journals (Sweden)

    Isabel ePiñeiro-Prado

    2016-03-01

    Full Text Available Supercapacitors are energy storage devices that offer a high power density and a low energy density in comparison with batteries. Their limited energy density can be overcome by using asymmetric configuration in mass electrodes, where each electrode works within their maximum available potential window, rendering the maximum voltage output of the system. Such asymmetric capacitors must be optimized through careful electrochemical characterization of the electrodes for accurate determination of the capacitance and the potential stability limits. The results of the characterization are then used for optimizing mass ratio of the electrodes from the balance of stored charge. The reliability of the design largely depends on the approach taken for the electrochemical characterization. Therefore, the performance could be lower than expected and even the system could break down, if a well thought out procedure is not followed.In this work, a procedure for the development of asymmetric supercapacitors based on activated carbons is detailed. Three activated carbon materials with different textural properties and surface chemistry have been systematically characterized in neutral aqueous electrolyte. The asymmetric configuration of the masses of both electrodes in the supercapacitor has allowed to cover a higher potential window, resulting in an increase of the energy density of the three devices studied when compared with the symmetric systems, and an improved cycle life.

  7. Surface State of Carbon Fibers Modified by Electrochemical Oxidation

    Institute of Scientific and Technical Information of China (English)

    Yunxia GUO; Jie LIU; Jieying LIANG

    2005-01-01

    Surface of polyacrylonitrile (PAN)-based carbon fibers was modified by electrochemical oxidation. The modification effect on carbon fibers surface was explored using atomic force microscopy (AFM), X-ray photoelectron spectroscopy (XPS) and X-ray diffraction (XRD). Results showed that on the modified surface of carbon fibers, the carbon contents decreased by 9.7% and the oxygen and nitrogen contents increased by 53.8% and 7.5 times, respectively. The surface roughness and the hydroxyl and carbonyl contents also increased. The surface orientation index was reduced by 1.5%which decreased tensile strength of carbon fibers by 8.1%, and the microcrystalline dimension also decreased which increased the active sites of carbon fiber surface by 78%. The physical and chemical properties of carbon fibers surface were modified through the electrochemical oxidative method, which improved the cohesiveness between the fibers and resin matrix and increased the interlaminar shear strength (ILSS) of carbon fibers reinforced epoxy composite (CFRP) over 20%.

  8. The influence of pore size and surface area of activated carbons on the performance of ionic liquid based supercapacitors.

    Science.gov (United States)

    Pohlmann, Sebastian; Lobato, Belén; Centeno, Teresa A; Balducci, Andrea

    2013-10-28

    This study analyses and compares the behaviour of 5 commercial porous carbons in the ionic liquid N-butyl-N-methylpyrrolidinium bis(trifluoromethanesulfonyl)imide (PYR14TFSI) and its mixture with propylene carbonate (PC) as electrolytes. The results of this investigation show that the existence of a distribution of pore sizes and/or constrictions at the entrance of the pores leads to significant changes in the specific capacitance of the investigated materials. The use of PYR14TFSI as an electrolyte has a positive effect on the EDLC energy storage, but its high viscosity limits the power density. The mixture 50 : 50 wt% propylene carbonate-PYR14TFSI provides high operative voltage as well as low viscosity and thus notably enhances EDLC operation.

  9. Optimization of preparation conditions for activated carbon from palm oil fronds using response surface methodology on removal of pesticides from aqueous solution

    Directory of Open Access Journals (Sweden)

    J.M. Salman

    2014-01-01

    Full Text Available Palm oil fronds were used to prepare activated carbon using the physiochemical activation method, which consisted of potassium hydroxide (KOH treatment and carbon dioxide (CO2 gasification. The effects of variable parameters activation temperature, activation time and chemical impregnation ratios (KOH: char by weight on the preparation of the activated carbon and for the removal of pesticides: bentazon, carbofuran and 2,4-Dichlorophenoxyacetic acid (2,4-D were investigated. Based on the central composite design (CCD, two factor interaction (2FI and quadratic models were respectively employed to correlate the effect of variable parameters on the preparation of activated carbon used for the removal of pesticides with carbon yield. From the analysis of variance (ANOVA, the most influential factor on each experimental design response was identified. The optimum conditions for preparing the activated carbon from oil palm fronds were found as follows: activation temperature of 750 °C, activation time of 2 h and chemical impregnation ratio of 2.38. The percentage error between predicted and experimental results for the removal of bentazon, carbofuran and 2,4-D were 8.2, 1.3 and 9.2%, respectively and for the yield of the palm oil frond activated carbon was 5.6.

  10. Preparation of mesoporous activated carbon from palm-date pits: optimization study on removal of bentazon, carbofuran, and 2,4-D using response surface methodology.

    Science.gov (United States)

    Salman, J M; Abid, F M

    2013-01-01

    Palm-date pits were used to prepare activated carbon by physiochemical activation method, which consisted of potassium hydroxide (KOH) treatment and carbon dioxide (CO(2)) gasification. The effects of variable parameters, activation temperature, activation time and chemical impregnation ratios (KOH: char by weight) on the preparation of activated carbon and for removal of pesticides: bentazon, carbofuran and 2,4-dichlorophenoxyacetic acid (2,4-D) were investigated. Based on the central composite design (CCD), two factor interaction (2FI) and quadratic models were respectively employed to correlate the effect of variable parameters on the preparation of activated carbon used for removal of pesticides with carbon yield. From the analysis of variance (ANOVA), the most influential factor on each experimental design response was identified. The optimum conditions for preparing activated carbon from palm-date pits were found to be: activation temperature of 850 °C, activation time of 3 h and chemical impregnation ratio of 3.75, which resulted in an activated carbon yield of 19.5% and bentazon, carbofuran, and 2,4-D removal of 84, 83, and 93%, respectively.

  11. Surface modification and functionalization of nanostructured carbons

    Directory of Open Access Journals (Sweden)

    A. Stanishevsky

    2009-12-01

    Full Text Available Purpose: Nanostructured carbon nanomaterials (e.g., nanocrystalline diamond films and particles, carbon nanotubes, carbon onions, fullerenes, etc. are being extensively explored for numerous biomedical applications in surgical implants, therapy, drug delivery, and biosensoring due to their interesting physical, chemical, and biological properties. Such applications of carbon nanomaterials often require specific surface functionality to be introduced for better integration of these materials with physiological environment. In the last decade, substantial progress has been made in the development of controllable surface modification methods and in the introduction of different functional groups on the surface of carbon nanomaterials.Design/methodology/approach: This paper briefly overviews the surface modification and functionalization approaches for various carbon nanomaterials, and it focuses on the plasma modification and functionalization of nanocrystalline diamond films, diamond nanoparticles, and carbon nanospheres. The results on the surface characterization using FTIR and XPS techniques, and the preliminary studies of cellular response to these modified carbon nanomaterials are presented and discussed.Findings: The results of surface modification of NCD films, detonation nanodiamonds, and carbon nanospheres, demonstrate the flexibility of nanocarbons to attain various surface functionality that can be adjusted for specific applications. It has been shown that neither of tested nanocarbon materials was cytotoxic in this study, although the attachement and proliferation of various cells was strongly affected by the specific type of surface functionalization.Research limitations/implications: At the present, it is not clear to what degree the available surface sites on NCD films or carbon nanoparticles can be occupied with functional groups. Furthermore, while there is clear selectivity of cellular response to H, O, and F surface

  12. ACTIVATED CARBON FROM LIGNITE FOR WATER TREATMENT

    Energy Technology Data Exchange (ETDEWEB)

    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

  13. An X-ray photoelectron spectroscopy study of surface changes on brominated and sulfur-treated activated carbon sorbents during mercury capture: performance of pellet versus fiber sorbents.

    Science.gov (United States)

    Saha, Arindom; Abram, David N; Kuhl, Kendra P; Paradis, Jennifer; Crawford, Jenni L; Sasmaz, Erdem; Chang, Ramsay; Jaramillo, Thomas F; Wilcox, Jennifer

    2013-12-03

    This work explores surface changes and the Hg capture performance of brominated activated carbon (AC) pellets, sulfur-treated AC pellets, and sulfur-treated AC fibers upon exposure to simulated Powder River Basin-fired flue gas. Hg breakthrough curves yielded specific Hg capture amounts by means of the breakthrough shapes and times for the three samples. The brominated AC pellets showed a sharp breakthrough after 170-180 h and a capacity of 585 μg of Hg/g, the sulfur-treated AC pellets exhibited a gradual breakthrough after 80-90 h and a capacity of 661 μg of Hg/g, and the sulfur-treated AC fibers showed no breakthrough even after 1400 h, exhibiting a capacity of >9700 μg of Hg/g. X-ray photoelectron spectroscopy was used to analyze sorbent surfaces before and after testing to show important changes in quantification and oxidation states of surface Br, N, and S after exposure to the simulated flue gas. For the brominated and sulfur-treated AC pellet samples, the amount of surface-bound Br and reduced sulfur groups decreased upon Hg capture testing, while the level of weaker Hg-binding surface S(VI) and N species (perhaps as NH4(+)) increased significantly. A high initial concentration of strong Hg-binding reduced sulfur groups on the surface of the sulfur-treated AC fiber is likely responsible for this sorbent's minimal accumulation of S(VI) species during exposure to the simulated flue gas and is linked to its superior Hg capture performance compared to that of the brominated and sulfur-treated AC pellet samples.

  14. Hydrogen isotherms in palladium loaded carbon nanotubes and activated carbons

    Energy Technology Data Exchange (ETDEWEB)

    Martinez, M. T.; Anson, A.; Lafuente, E.; Urriolabeitia, E.; Navarro, R.; Benito, A. M.; Maser, W. K.

    2005-07-01

    Session 5a In order to increase the hydrogen sorption capacity of carbon materials, a sample of single-wall carbon nanotubes (SWNTs) and the activated carbon MAXSORB have been loaded with palladium nanoparticles. While carbon materials adsorb hydrogen due to physical interactions, palladium can capture hydrogen into the bulk structure or chemically react to form hydrides. Experiental SWNTs have been synthesized in an electric arc reactor, using Ni and Y as catalysts in a 660 mbar He atmosphere. MAXSORB is a commercial activated carbon obtained from petroleum coke through a chemical treatment with KOH. Palladium has been deposited over the carbon support by means of a reflux method in a solution of an organometallic complex. Different samples have been prepared depending on the weight ratio (Carbon material / Pd) in the original reactants. The effectiveness of the deposition method has been examined by means of X-ray diffraction (XRD), induction coupled plasma spectrometry (ICPS) and transmission electron microscopy (TEM). The volumetric system Autosorb-1 from Quantachrome Instruments has been used to obtain the nitrogen adsorption isotherms at 77 K for all the materials. The hydrogen isotherms at 77 K and room temperature and up to 800 torr have also been obtained in the Autosorb-1. The BET specific surface area and the micropore volume have been calculated from the nitrogen adsorption data. High pressure hydrogen isotherms up to 90 bar have been carried out at room temperature in a VTI system provided with a Rubotherm microbalance. (Author)

  15. Investigation of the Changes in Surface Area and FT-IR Spectra of Activated Carbons Obtained from Hazelnut Shells by Physicochemical Treatment Methods

    Directory of Open Access Journals (Sweden)

    Aziz Şencan

    2015-01-01

    Full Text Available In this study, raw hazelnut shells were used to obtain charcoal by pyrolysis at 250°C. The obtained material was subjected to physical, chemical, and physicochemical treatment methods to obtain activated carbons (ACs. Effect of the treatment procedures was determined by measuring the surface area of the produced ACs. In addition, changes in the functional groups of the obtained ACs during these treatments were determined with the Fourier transform infrared spectroscopy (FT-IR. To determine the most effective chemical agent, the charcoal samples were examined for Pb(II adsorption from aqueous solutions under different pH conditions of 4 to 6. According to the results, the most effective chemical agent was determined as Ca(OCl2. Effect of microwave and ultrasound treatments was also examined during Pb(II adsorption by the chemically treated AC. The results showed that chemical treatment with Ca(OCl2, microwave treatment for 5 minutes, ultrasound treatment for 20 minutes, and pyrolysis at 700°C together were the most suitable combination enhancing the surface area of the adsorbent. This combination increased the surface area and the adsorption capacity of the adsorbent by 202 and 4.76 times, respectively, when compared to those of the raw hazelnut shell.

  16. Separating proteins with activated carbon.

    Science.gov (United States)

    Stone, Matthew T; Kozlov, Mikhail

    2014-07-15

    Activated carbon is applied to separate proteins based on differences in their size and effective charge. Three guidelines are suggested for the efficient separation of proteins with activated carbon. (1) Activated carbon can be used to efficiently remove smaller proteinaceous impurities from larger proteins. (2) Smaller proteinaceous impurities are most efficiently removed at a solution pH close to the impurity's isoelectric point, where they have a minimal effective charge. (3) The most efficient recovery of a small protein from activated carbon occurs at a solution pH further away from the protein's isoelectric point, where it is strongly charged. Studies measuring the binding capacities of individual polymers and proteins were used to develop these three guidelines, and they were then applied to the separation of several different protein mixtures. The ability of activated carbon to separate proteins was demonstrated to be broadly applicable with three different types of activated carbon by both static treatment and by flowing through a packed column of activated carbon.

  17. Preparation of nitrogen-doped cotton stalk microporous activated carbon fiber electrodes with different surface area from hexamethylenetetramine-modified cotton stalk for electrochemical degradation of methylene blue

    Science.gov (United States)

    Li, Kunquan; Rong, Zhang; Li, Ye; Li, Cheng; Zheng, Zheng

    Cotton-stalk activated carbon fibers (CSCFs) with controllable micropore area and nitrogen content were prepared as an efficient electrode from hexamethylenetetramine-modified cotton stalk by steam/ammonia activation. The influence of microporous area, nitrogen content, voltage and initial concentration on the electrical degradation efficiency of methylene blue (MB) was evaluated by using CSCFs as anode. Results showed that the CSCF electrodes exhibited excellent MB electrochemical degradation ability including decolorization and COD removal. Increasing micropore surface area and nitrogen content of CSCF anode leaded to a corresponding increase in MB removal. The prepared CSCF-800-15-N, which has highest N content but lowest microporous area, attained the best degradation effect with 97% MB decolorization ratio for 5 mg/L MB at 12 V in 4 h, implying the doped nitrogen played a prominent role in improving the electrochemical degradation ability. The electrical degradation reaction was well described by first-order kinetics model. Overall, the aforesaid findings suggested that the nitrogen-doped CSCFs were potential electrode materials, and their electrical degradation abilities could be effectively enhanced by controlling the nitrogen content and micropore surface area.

  18. Carbon Surface Modification for Enhanced Corrosion Resistance

    Science.gov (United States)

    2008-01-01

    2 R. Rayne,1 and R.A. Bayles1 1Chemistry Division 2SAIC Introduction: Case hardening by carburization has long been recognized to produce wear... carburization technique has been developed for intro- ducing carbon into stainless steel surfaces without formation of carbides.1,2 This surface modification...Michal, F. Ernst, H. Kahn, Y. Cao, F. Oba, N. Agarwal, and A.H. Heuer, “Carbon Supersaturation due to Paraequilibrium Carburization : Stainless

  19. A novel activated carbon for supercapacitors

    Energy Technology Data Exchange (ETDEWEB)

    Shen, Haijie [Key Laboratory of Environmentally Friendly Chemistry and Applications of Ministry of Education, College of Chemistry, Xiangtan University, Hunan 411105 (China); Liu, Enhui, E-mail: liuenhui99@sina.com.cn [Key Laboratory of Environmentally Friendly Chemistry and Applications of Ministry of Education, College of Chemistry, Xiangtan University, Hunan 411105 (China); Xiang, Xiaoxia; Huang, Zhengzheng; Tian, Yingying; Wu, Yuhu; Wu, Zhilian; Xie, Hui [Key Laboratory of Environmentally Friendly Chemistry and Applications of Ministry of Education, College of Chemistry, Xiangtan University, Hunan 411105 (China)

    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. Preparation and characterization of activated carbon from waste biomass.

    Science.gov (United States)

    Tay, Turgay; Ucar, Suat; Karagöz, Selhan

    2009-06-15

    Lignocellulosic materials are good and cheap precursors for the production of activated carbon. In this study, activated carbons were prepared from the pyrolysis of soybean oil cake at 600 and 800 degrees C by chemical activation with K(2)CO(3) and KOH. The influence of temperature and type of chemical reagents on the porosity development was investigated and discussed. K(2)CO(3) was found more effective than KOH as a chemical reagent under identical conditions in terms of both porosity development and yields of the activated carbons. The maximum surface area (1352.86 m(2)g(-1)) was obtained at 800 degrees C with K(2)CO(3) activation which lies in the range of commercial activated carbons. Elemental analyses of the activated carbons indicate insignificant sulphur content for all activated carbons. The ash and sulphur contents of the activated carbons obtained with chemical activation by K(2)CO(3) were lower than those by chemical activation with KOH.

  1. Review of the Technology of Surface Modification of Activated Carbon%活性炭表面化学改性技术的研究进展与展望

    Institute of Scientific and Technical Information of China (English)

    孙倩; 方琴; 陈玉婷; 田青青; 吴光前

    2012-01-01

    活性炭表面官能团和杂原子的数量与种类是影响活性炭吸附性能的重要因素。国内外研究表明,通过对活性炭进行表面改性可以显著改善活性炭对特定物质的吸附性能。文章简要介绍了活性炭的物理和化学性质,并从活性炭材料的表面化学性质方面论述了近年来国内外在活性炭材料改性方面的研究进展,最后提出了活性炭表面改性技术的发展方向和趋势。%The functional groups,heteroatoms and chemical compounds on the surface of activated carbons are important factors to determine their adsorption capacity.The adsorption properties of activated carbons can be improved through the surface modification.In the paper,the physical and chemical properties of activated carbon were briefly discussed,and the new progresses in studies on surface chemical modification of activated carbon used as absorbent were reviewed,and the future development of surface modification technology of activated carbons was also suggested at the end of the paper.

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

    Science.gov (United States)

    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.

  3. Production and characterization of granular activated carbon from activated sludge

    Directory of Open Access Journals (Sweden)

    Z. Al-Qodah

    2009-03-01

    Full Text Available In this study, activated sludge was used as a precursor to prepare activated carbon using sulfuric acid as a chemical activation agent. The effect of preparation conditions on the produced activated carbon characteristics as an adsorbent was investigated. The results indicate that the produced activated carbon has a highly porous structure and a specific surface area of 580 m²/g. The FT-IR analysis depicts the presence of a variety of functional groups which explain its improved adsorption behavior against pesticides. The XRD analysis reveals that the produced activated carbon has low content of inorganic constituents compared with the precursor. The adsorption isotherm data were fitted to three adsorption isotherm models and found to closely fit the BET model with R² equal 0.948 at pH 3, indicating a multilayer of pesticide adsorption. The maximum loading capacity of the produced activated carbon was 110 mg pesticides/g adsorbent and was obtained at this pH value. This maximum loading was found experimentally to steeply decrease as the solution pH increases. The obtained results show that activated sludge is a promising low cost precursor for the production of activated carbon.

  4. Methane Adsorption Study Using Activated Carbon Fiber and Coal Based Activated Carbon

    Institute of Scientific and Technical Information of China (English)

    Guo Deyong; Li Fei; Liu Wenge

    2013-01-01

    Inlfuence of ammonium salt treatment and alkali treatment of the coal based activated carbon (AC) and activated carbon ifber (ACF) adsorbents on methane adsorption capacity was studied via high-pressure adsorption experiment. Sur-face functional groups and pore structure of two types of adsorbents were characterized by the application of infrared ab-sorption spectroscopy (IR) and low temperature liquid nitrogen adsorption method. The results show that both ammonium salt treatment and alkali treatment have obvious effect on changing BET, pore volume as well as pore size distribution of adsorbents; and methane adsorption capacity of the activated carbon ifber is the maximum after the ammonium salt treatment.

  5. Antimicrobial Activity of Carbon-Based Nanoparticles

    Directory of Open Access Journals (Sweden)

    Solmaz Maleki Dizaj

    2015-03-01

    Full Text Available 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.

  6. Influence of activated carbon porosity and surface oxygen functionalities' presence on adsorption of acetonitrile as a simple polar volatile organic compound.

    Science.gov (United States)

    Furmaniak, Sylwester

    2015-01-01

    Based on series of porous carbon models, systematic Monte Carlo studies on the adsorption of acetonitrile (as a simple representative of polar volatile organic compounds) were performed. The influence of porosity and chemical composition of the carbon surface on CH3CN adsorption was studied and it was shown that both the factors influenced the adsorption mechanism. A decrease in the pore size and the introduction of oxygen surface groups led to a rise in adsorption energy and to an increase in the filling of accessible volume in the low-pressure part of the isotherm. However, from a practical point of view, it is easier to increase the adsorption by introducing polar groups on the carbon surface than by modifying the porosity.

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

    Science.gov (United States)

    Uçar, Suat; Erdem, Murat; Tay, Turgay; Karagöz, 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.

  8. Thermal modification of activated carbon surface chemistry improves its capacity as redox mediator for azo dye reduction

    OpenAIRE

    Pereira, Luciana; Pereira, Ricardo; Pereira, M. F. R.; Van der Zee, F. P.; Cervantes, F. J.; Alves, M.M.

    2010-01-01

    The surface chemistry of a commercial AC (AC0) was selectively modified, without changing significantly its textural properties, by chemical oxidation with HNO3 (ACHNO3 ) and O2 (ACO2 ), and thermal treatments under H2 (ACH2) or N2 (ACN2 ) flow. The effect of modified AC on anaerobic chemical dye reduction was assayed with sulphide at different pH values 5, 7 and 9. Four dyes were tested: Acid Orange 7, Reactive Red 2, Mordant Yellow 10 and Direct Blue 71. Batch experiments with l...

  9. CARBON SEQUESTRATION SURFACE MINE LANDS

    Energy Technology Data Exchange (ETDEWEB)

    Donald H. Graves; Christopher Barton; Richard Sweigard; Richard Warner

    2003-07-24

    Over 160 acres of tree seedlings were planted during the last quarter. This quarter marked the beginning of the installation of new instrumentation and the inspection and calibration of previously installed recording devices. Sampling systems were initiated to quantify initial seedling success as well as height measurements. Nursery seedlings have been inoculated to produce mycorrhizal treated stock for 2004 spring plantings to determine the effects on carbon sequestration. All planting areas in western Kentucky have been sampled with the recording cone penetrometer and the nuclear density gauge to measure soil density.

  10. Preparation and application of active gangue's carbon black

    Institute of Scientific and Technical Information of China (English)

    ZHANG Xiang-lin; ZHANG Yi-dong

    2007-01-01

    After three-stage pulverization, dry-distillated activation and coupling agent surface modification, the kaolinite-typed gangue of Sichuan Hongni Coal Mine(SHCM) can be manufactured into activated gangue's carbon black. Its surface area is >25 m2/g, and possesses carbon black's carbon framework and structure. It can be used as strengthening agent of high polymer material such as rubber.

  11. Adsorption characteristics of activated carbon hollow fibers

    OpenAIRE

    2009-01-01

    Carbon hollow fibers were prepared with regenerated cellulose or polysulfone hollow fibers by chemical activation using sodium phosphate dibasic followed by the carbonization process. The activation process increases the adsorption properties of fibers which is more prominent for active carbone fibers obtained from the cellulose precursor. Chemical activation with sodium phosphate dibasic produces an active carbon material with both mesopores and micropores.

  12. Surface plasma functionalization influences macrophage behavior on carbon nanowalls

    Energy Technology Data Exchange (ETDEWEB)

    Ion, Raluca [University of Bucharest, Department of Biochemistry and Molecular Biology, 91-95 Spl. Independentei, 050095 Bucharest (Romania); Vizireanu, Sorin [National Institute for Laser, Plasma and Radiation Physics, 409 Atomistilor, PO Box MG-36, 077125, Magurele, Bucharest (Romania); Stancu, Claudia Elena [National Institute for Laser, Plasma and Radiation Physics, 409 Atomistilor, PO Box MG-36, 077125, Magurele, Bucharest (Romania); Leibniz Institute for Plasma Science and Technology (INP Greifswald), Felix-Hausdorff-Str. 2, 17489 Greifswald (Germany); Luculescu, Catalin [National Institute for Laser, Plasma and Radiation Physics, 409 Atomistilor, PO Box MG-36, 077125, Magurele, Bucharest (Romania); Cimpean, Anisoara, E-mail: anisoara.cimpean@bio.unibuc.ro [University of Bucharest, Department of Biochemistry and Molecular Biology, 91-95 Spl. Independentei, 050095 Bucharest (Romania); Dinescu, Gheorghe [National Institute for Laser, Plasma and Radiation Physics, 409 Atomistilor, PO Box MG-36, 077125, Magurele, Bucharest (Romania)

    2015-03-01

    The surfaces of carbon nanowall samples as scaffolds for tissue engineering applications were treated with oxygen or nitrogen plasma to improve their wettability and to functionalize their surfaces with different functional groups. X-ray photoelectron spectroscopy and water contact angle results illustrated the effective conversion of the carbon nanowall surfaces from hydrophobic to hydrophilic and the incorporation of various amounts of carbon, oxygen and nitrogen functional groups during the treatments. The early inflammatory responses elicited by un-treated and modified carbon nanowall surfaces were investigated by quantifying tumor necrosis factor-alpha and macrophage inflammatory protein-1 alpha released by attached RAW 264.7 macrophage cells. Scanning electron microscopy and fluorescence studies were employed to investigate the changes in macrophage morphology and adhesive properties, while MTT assay was used to quantify cell proliferation. All samples sustained macrophage adhesion and growth. In addition, nitrogen plasma treatment was more beneficial for cell adhesion in comparison with un-modified carbon nanowall surfaces. Instead, oxygen plasma functionalization led to increased macrophage adhesion and spreading suggesting a more activated phenotype, confirmed by elevated cytokine release. Thus, our findings showed that the chemical surface alterations which occur as a result of plasma treatment, independent of surface wettability, affect macrophage response in vitro. - Highlights: • N{sub 2} and O{sub 2} plasma treatments alter the CNW surface chemistry and wettability. • Cells seeded on CNW scaffolds are viable and metabolically active. • Surface functional groups, independent of surface wettability, affect cell response. • O{sub 2} plasma treatment of CNW leads to a more activated macrophage phenotype.

  13. Volumetric and superficial characterization of carbon activated; Caracterizacion volumetrica y superficial de carbon activado

    Energy Technology Data Exchange (ETDEWEB)

    Carrera G, L.M.; Garcia S, I.; Jimenez B, J.; Solache R, M.; Lopez M, B.; Bulbulian G, S.; Olguin G, M.T. [Departamento de Quimica, Gerencia de Ciencias Basicas, Instituto Nacional de Investigaciones Nucleares, A.P. 18-1027, 11801 Mexico D.F. (Mexico)

    2000-07-01

    The activated carbon is the resultant material of the calcination process of natural carbonated materials as coconut shells or olive little bones. It is an excellent adsorbent of diluted substances, so much in colloidal form, as in particles form. Those substances are attracted and retained by the carbon surface. In this work is make the volumetric and superficial characterization of activated carbon treated thermically (300 Centigrade) in function of the grain size average. (Author)

  14. Method for in-situ cleaning of carbon contaminated surfaces

    Science.gov (United States)

    Klebanoff, Leonard E.; Grunow, Philip; Graham, Jr., Samuel

    2006-12-12

    Activated gaseous species generated adjacent a carbon contaminated surface affords in-situ cleaning. A device for removing carbon contamination from a surface of the substrate includes (a) a housing defining a vacuum chamber in which the substrate is located; (b) a source of gaseous species; and (c) a source of electrons that are emitted to activate the gaseous species into activated gaseous species. The source of electrons preferably includes (i) a filament made of a material that generates thermionic electron emissions; (ii) a source of energy that is connected to the filament; and (iii) an electrode to which the emitted electrons are attracted. The device is particularly suited for photolithography systems with optic surfaces, e.g., mirrors, that are otherwise inaccessible unless the system is dismantled. A method of removing carbon contaminants from a substrate surface that is housed within a vacuum chamber is also disclosed. The method employs activated gaseous species that react with the carbon contaminants to form carbon containing gaseous byproducts.

  15. Stability and effects of carbon-induced surface reconstructions in cobalt Fischer-Tropsch synthesis

    Science.gov (United States)

    Ciobîcă, I. M.; van Helden, P.; van Santen, R. A.

    2016-11-01

    This computational study of carbon induced reconstruction of Co surfaces demonstrates that surface reconstruction is stable in the presence of a hydrogen at low coverage. These reconstructions can create new sites that allow for low activation energy CO dissociation. Carbon induced surface reconstruction of the edge of the FCC-Co(221) step surface will result in highly reactive step-edge sites. Such sites also provide a low activation energy for carbon to diffuse into the subsurface layer of cobalt.

  16. Superhydrophobic activated carbon-coated sponges for separation and absorption.

    Science.gov (United States)

    Sun, Hanxue; Li, An; Zhu, Zhaoqi; Liang, Weidong; Zhao, Xinhong; La, Peiqing; Deng, Weiqiao

    2013-06-01

    Highly porous activated carbon with a large surface area and pore volume was synthesized by KOH activation using commercially available activated carbon as a precursor. By modification with polydimethylsiloxane (PDMS), highly porous activated carbon showed superhydrophobicity with a water contact angle of 163.6°. The changes in wettability of PDMS- treated highly porous activated carbon were attributed to the deposition of a low-surface-energy silicon coating onto activated carbon (confirmed by X-ray photoelectron spectroscopy), which had microporous characteristics (confirmed by XRD, SEM, and TEM analyses). Using an easy dip-coating method, superhydrophobic activated carbon-coated sponges were also fabricated; those exhibited excellent absorption selectivity for the removal of a wide range of organics and oils from water, and also recyclability, thus showing great potential as efficient absorbents for the large-scale removal of organic contaminants or oil spills from water.

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

    Directory of Open Access Journals (Sweden)

    S. G. Herawan

    2013-01-01

    Full Text Available 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.

  18. Biomass derived graphene-like activated and non-activated porous carbon for advanced supercapacitors

    Indian Academy of Sciences (India)

    KASINATH OJHA; BHARAT KUMAR; ASHOK K GANGULI

    2017-03-01

    Graphene-like activated and non-activated carbon nanostructures were synthesized from various natural sources like sugar, rice husk and jute. These carbon nanostructures were characterized using SEM, FTIR and Raman spectroscopy, surface area and thermogravimetric analysis. The electrochemical studies of these carbon materials confirm their promising characteristics for supercapacitor applications. Activated carbon nanostructures exhibit higher specific capacitance compared to that of non-activated carbons (non-Ac sugar).The activated carbon (Ac-jute) exhibits maximum specific capacitance of 476 F/g at an applied current density of 0.2 A/g which is much higher than that of graphene oxide (GO).

  19. ACTIVATED CARBON (CHARCOAL OBTAINING . APPLICATION

    Directory of Open Access Journals (Sweden)

    Florin CIOFU

    2015-05-01

    Full Text Available The activated carbon is a microporous sorbent with a very large adsorption area that can reach in some cases even 1500sqm / gram. Activated carbon is produced from any organic material with high carbon content: coal, wood, peat or moor coal, coconut shells. The granular activated charcoal is most commonly produced by grinding the raw material, adding a suitable binder to provide the desired hardness and shape. Enabling coal is a complete process through which the raw material is fully exposed to temperatures between 600-900 degrees C, in the absence of oxygen, usually in a domestic atmosphere as gases such as nitrogen or argon; as material that results from this process is exposed in an atmosphere of oxygen and steam at a temperature in the interval from 600 - 1200 degrees C.

  20. Experimental design based response surface methodology optimization of ultrasonic assisted adsorption of safaranin O by tin sulfide nanoparticle loaded on activated carbon

    Science.gov (United States)

    Roosta, M.; Ghaedi, M.; Daneshfar, A.; Sahraei, R.

    2014-03-01

    In this research, the adsorption rate of safranine O (SO) onto tin sulfide nanoparticle loaded on activated carbon (SnS-NPAC) was accelerated by the ultrasound. SnS-NP-AC was characterized by different techniques such as SEM, XRD and UV-Vis measurements. The present results confirm that the ultrasound assisted adsorption method has remarkable ability to improve the adsorption efficiency. The influence of parameters such as the sonication time, adsorbent dosage, pH and initial SO concentration was examined and evaluated by central composite design (CCD) combined with response surface methodology (RSM) and desirability function (DF). Conducting adsorption experiments at optimal conditions set as 4 min of sonication time, 0.024 g of adsorbent, pH 7 and 18 mg L-1 SO make admit to achieve high removal percentage (98%) and high adsorption capacity (50.25 mg g-1). A good agreement between experimental and predicted data in this study was observed. The experimental equilibrium data fitting to Langmuir, Freundlich, Tempkin and Dubinin-Radushkevich models show that the Langmuir model is a good and suitable model for evaluation and the actual behavior of adsorption. Kinetic evaluation of experimental data showed that the adsorption processes followed well pseudo-second-order and intraparticle diffusion models.

  1. Experimental design based response surface methodology optimization of ultrasonic assisted adsorption of safaranin O by tin sulfide nanoparticle loaded on activated carbon.

    Science.gov (United States)

    Roosta, M; Ghaedi, M; Daneshfar, A; Sahraei, R

    2014-03-25

    In this research, the adsorption rate of safranine O (SO) onto tin sulfide nanoparticle loaded on activated carbon (SnS-NPAC) was accelerated by the ultrasound. SnS-NP-AC was characterized by different techniques such as SEM, XRD and UV-Vis measurements. The present results confirm that the ultrasound assisted adsorption method has remarkable ability to improve the adsorption efficiency. The influence of parameters such as the sonication time, adsorbent dosage, pH and initial SO concentration was examined and evaluated by central composite design (CCD) combined with response surface methodology (RSM) and desirability function (DF). Conducting adsorption experiments at optimal conditions set as 4 min of sonication time, 0.024 g of adsorbent, pH 7 and 18 mg L(-1) SO make admit to achieve high removal percentage (98%) and high adsorption capacity (50.25 mg g(-)(1)). A good agreement between experimental and predicted data in this study was observed. The experimental equilibrium data fitting to Langmuir, Freundlich, Tempkin and Dubinin-Radushkevich models show that the Langmuir model is a good and suitable model for evaluation and the actual behavior of adsorption. Kinetic evaluation of experimental data showed that the adsorption processes followed well pseudo-second-order and intraparticle diffusion models.

  2. Removal of Cr(VI) from low-temperature micro-polluted surface water by tannic acid immobilized powdered activated carbon.

    Science.gov (United States)

    Li, Weiguang; Gong, Xujin; Li, Xin; Zhang, Duoying; Gong, Hainan

    2012-06-01

    In this study, food-grade tannic acid-immobilized powdered activated carbon (TA-PAC) was prepared, and adsorption of Cr(VI) (0.500 mg/L) onto TA-PAC as a function of pH, contact time, adsorption capacities and adsorption isotherms at 280 K was investigated. The results indicated that the immobilization process introduced abundant acid functional groups. The adsorption capacity of TA-PAC was found to be pH-dependent, and the optimal pH value was found to be 4.0. The equilibrium time was 240 min for TA-PAC. Adsorption data for total chromium were modeled using both two-parameter and three-parameter isotherm models. Freundlich and linear forms of three-parameter models yielded the best results for all of the data. Desorption studies of immobilized material suggested that the immobilization of food-grade tannic acid is steady. The adsorption mechanism of Cr(VI) on TA-PAC was assumed to be a comprehensive process consisting of surface reduction of Cr(VI), esterification between catechol and chromate, and ion exchange.

  3. High surface area, high permeability carbon monoliths

    Energy Technology Data Exchange (ETDEWEB)

    Lagasse, R.R.; Schroeder, J.L. [Sandia National Labs., Albuquerque, NM (United States). Organic Materials Processing Dept.

    1994-12-31

    The goal of this work is to prepare carbon monoliths having precisely tailored pore size distribution. Prior studies have demonstrated that poly(acrylonitrile) can be processed into a precursor having tailored macropore structure. Since the macropores were preserved during pyrolysis, this synthetic process provided a route to porous carbon having macropores with size =0.1 to 10{mu}m. No micropores of size <2 nm could be detected in the carbon, however, by nitrogen adsorption. In the present work, the authors have processed a different polymer, poly(vinylidene chloride) into a macroporous precursor, Pyrolysis produced carbon monoliths having macropores derived from the polymer precursor as well as extensive microporosity produced during the pyrolysis of the polymer. One of these carbons had BET surface area of 1,050 m{sup 2}/g and about 1.2 cc/g total pore volume, with about 1/3 of the total pore volume in micropores and the remainder in 1{mu}m macropores. No mesopores in the intermediate size range could be detected by nitrogen adsorption. Carbon materials having high surface area as well as micron size pores have potential applications as electrodes for double layer supercapacitors containing liquid electrolyte, or as efficient media for performing chemical separations.

  4. In vitro adsorption study of fluoxetine in activated carbons and activated carbon fibres

    Energy Technology Data Exchange (ETDEWEB)

    Nabais, J.M. Valente; Mouquinho, A.; Galacho, C.; Carrott, P.J.M.; Ribeiro Carrott, M.M.L. [Centro de Quimica de Evora e Departamento de Quimica da Universidade de Evora, Rua Romao Ramalho no. 59, 7000-671 Evora (Portugal)

    2008-05-15

    We study the in vitro adsorption of fluoxetine hydrochloride by different adsorbents in simulated gastric and intestinal fluid, pH 1.2 and 7.5, respectively. The tested materials were two commercial activated carbons, carbomix and maxsorb MSC30, one activated carbon fibre produced in our laboratory and also three MCM-41 samples, also produced by us. Selected samples were modified by liquid phase oxidation and thermal treatment in order to change the surface chemistry without significant modifications to the porous characteristics. The fluoxetine adsorption follows the Langmuir model. The calculated Q{sub 0} values range from 54 to 1112 mg/g. A different adsorption mechanism was found for the adsorption of fluoxetine in activated carbon fibres and activated carbons. In the first case the most relevant factors are the molecular sieving effect and the dispersive interactions whereas in the activated carbons the mechanism seams to be based on the electrostatic interactions between the fluoxetine molecules and the charged carbon surface. Despite the different behaviours most of the materials tested have potential for treating potential fluoxetine intoxications. (author)

  5. Carbon Sequestration on Surface Mine Lands

    Energy Technology Data Exchange (ETDEWEB)

    Donald H. Graves; Christopher Barton; Richard Sweigard; Richard Warner

    2005-10-02

    During this quarter a general forest monitoring program was conducted to measure treatment effects on above ground and below ground carbon C and Nitrogen (N) pools for the tree planting areas. Detailed studies to address specific questions pertaining to Carbon cycling was initiated with the development of plots to examine the influence of mycorrhizae, spoil chemical and mineralogical properties, and use of amendment on forest establishment and carbon sequestration. Efforts continued during this period to examine decomposition and heterotrophic respiration on C cycling in the reforestation plots. Projected climate change resulting from elevated atmospheric carbon dioxide has given rise to various strategies to sequester carbon in various terrestrial ecosystems. Reclaimed surface mine soils present one such potential carbon sink where traditional reclamation objectives can complement carbon sequestration. New plantings required the modification and design and installation on monitoring equipment. Maintenance and data monitoring on past and present installations are a continuing operation. The Department of Mining Engineering continued the collection of penetration resistance, penetration depth, and bulk density on both old and new treatment areas. Data processing and analysis is in process for these variables. Project scientists and graduate students continue to present results at scientific meetings, tours and field days presentations of the research areas are being conducted on a request basis.

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

    Science.gov (United States)

    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.

  7. Science Letters: Nitrogen doping of activated carbon loading Fe2O3 and activity in carbon-nitric oxide reaction

    Institute of Scientific and Technical Information of China (English)

    WAN Xian-kai; ZOU Xue-quan; SHI Hui-xiang; WANG Da-hui

    2007-01-01

    Nitrogen doping of activated carbon loading Fe2O3 was performed by annealing in ammonia, and the activity of the modified carbon for NO reduction was studied in the presence of oxygen. Results show that Fe2O3 enhances the amount of surface oxygen complexes and facilitates nitrogen incorporation in the carbon, especially in the form of pyridinic nitrogen. The modified carbon shows excellent activity for NO reduction in the low temperature regime (<500 ℃) because of the cooperative effect of Fe2O3 and the surface nitrogen species.

  8. High activity carbon sorbents for mercury capture

    Energy Technology Data Exchange (ETDEWEB)

    George G. Stavropoulos; Irene S. Diamantopoulou; George E. Skodras; George P. Sakellaropoulos [Aristotle University of Thessaloniki, Thessaloniki (Greece). Chemical Process Engineering Laboratory

    2006-07-01

    High efficiency activated carbons have been prepared for removing mercury from gas streams. Starting materials used were petroleum coke, lignite, charcoal and olive seed waste, and were chemically activated with KOH. Produced adsorbents were primarily characterized for their porosity by N{sub 2} adsorption at 77K. Their mercury retention capacity was characterized based on the breakthrough curves. Compared with typical commercial carbons, they have exhibited considerably enhanced mercury adsorption capacity. An attempt has been made to correlate mercury entrapment and pore structure. It has been shown that physical surface area is increased during activation in contrast to the mercury adsorption capacity that initially increases and tends to decrease at latter stages. Desorption of active sites may be responsible for this behavior. 10 refs., 3 figs., 1 tab.

  9. Fractal analysis of granular activated carbons using isotherm data

    Energy Technology Data Exchange (ETDEWEB)

    Khalili, N.R.; Pan, M. [Illinois Institute of Technology, Chicago, IL (United States). Dept. of Chemical and Environmental Engineering; Sandi, G. [Argonne National Lab., IL (United States)

    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.

  10. The Adsorption Mechanism of Modified Activated Carbon on Phenol

    Directory of Open Access Journals (Sweden)

    Lin J. Q.

    2016-01-01

    Full Text Available Modified activated carbon was prepared by thermal treatment at high temperature under nitrogen flow. The surface properties of the activated carbon were characterized by Boehm titration, BET and point of zero charge determination. The adsorption mechanism of phenol on modified activated carbon was explained and the adsorption capacity of modified activated carbon for phenol when compared to plain activated carbon was evaluated through the analysis of adsorption isotherms, thermodynamic and kinetic properties. Results shows that after modification the surface alkaline property and pHpzc value of the activated carbon increase and the surface oxygen-containing functional groups decrease. The adsorption processes of the plain and modified carbon fit with Langmuir isotherm equation well, and the maximum adsorption capacity increase from 123.46, 111.11, 103.09mg/g to 192.31, 178.57, 163,93mg/g under 15, 25 and 35°C after modification, respectively. Thermodynamic parameters show that the adsorption of phenol on activated carbon is a spontaneously exothermic process of entropy reduction, implying that the adsorption is a physical adsorption. The adsorption of phenol on activated carbon follows the pseudo-second-order kinetics (R2>0.99. The optimum pH of adsorption is 6~8.

  11. Aqueous mercury adsorption by activated carbons.

    Science.gov (United States)

    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.

  12. Simultaneous ultrasound-assisted ternary adsorption of dyes onto copper-doped zinc sulfide nanoparticles loaded on activated carbon: Optimization by response surface methodology

    Science.gov (United States)

    Asfaram, Arash; Ghaedi, Mehrorang; Hajati, Shaaker; Goudarzi, Alireza; Bazrafshan, Ali Akbar

    2015-06-01

    The simultaneous and competitive ultrasound-assisted removal of Auramine-O (AO), Erythrosine (Er) and Methylene Blue (MB) from aqueous solutions were rapidly performed onto copper-doped zinc sulfide nanoparticles loaded on activated carbon (ZnS:Cu-NP-AC). ZnS:Cu nanoparticles were studied by FESEM, XRD and TEM. First, the effect of pH was optimized in a one-at-a-time procedure. Then the dependency of dyes removal percentage in their ternary solution on the level and magnitude of variables such as sonication time, initial dyes concentrations and adsorbent dosage was fully investigated and optimized by central composite design (CCD) under response surface methodology (RSM) as well as by regarding desirability function (DF) as a good and general criterion. The good agreement found between experimental and predicted values supports and confirms the suitability of the present model to predict adsorption state. The applied ultrasound strongly enhanced mass transfer process and subsequently performance. Hence, a small amount of the adsorbent (0.04 g) was capable to remove high percentage of dyes, i.e. 100%, 99.6% and 100% for MB, AO and Er, respectively, in very short time (2.5 min). The experimental equilibrium data fitting to Langmuir, Freundlich, Temkin and Dubinin-Radushkevich models showed that the Langmuir model applies well for the evaluation and description of the actual behavior of adsorption. The small amount of proposed adsorbent (0.015 g) was applicable for successful removal of dyes (RE > 99.0%) in short time (2.5 min) with high adsorption capacity in single component system (123.5 mg g-1 for MB, 123 mg g-1 for AO and 84.5 mg g-1 for Er). Kinetics evaluation of experiments at various time intervals reveals that adsorption processes can be well predicated and fitted by pseudo-second-order and Elovich models.

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

    Energy Technology Data Exchange (ETDEWEB)

    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

  14. OXIDATION AND CHARACTERIZATION OF ACTIVE CARBON AG-5

    Directory of Open Access Journals (Sweden)

    Tatiana Goreacioc

    2015-06-01

    Full Text Available The surface chemistry of the commercial active carbon AG-5 has been modified by oxidation with concentrated nitric acid. The structural changes caused by oxidative treatment were estimated on the basis of nitrogen adsorption-desorption isotherms and thermal analysis. Boehm titration method and infrared spectral analysis have been used in order to evaluate surface chemistry characteristics of active carbon samples. After oxidation process the amount of total acidic groups on oxidized active carbon surface (AG-5ox increases by about 6 times in comparison with unmodified sample (AG-5. The concentration of the acidic groups on the oxidized active carbon surface (AG-5ox was in the following order: strong acidic >>> weak acidic > phenolic.

  15. Liquid surface model for carbon nanotube energetics

    DEFF Research Database (Denmark)

    Solov'yov, Ilia; Mathew, Maneesh; Solov'yov, Andrey V.;

    2008-01-01

    an important insight in the energetics and stability of nanotubes of different chirality and might be important for the understanding of nanotube growth process. For the computations we use empirical Brenner and Tersoff potentials and discuss their applicability to the study of carbon nanotubes. From......In the present paper we developed a model for calculating the energy of single-wall carbon nanotubes of arbitrary chirality. This model, which we call as the liquid surface model, predicts the energy of a nanotube with relative error less than 1% once its chirality and the total number of atoms...... are known. The parameters of the liquid surface model and its potential applications are discussed. The model has been suggested for open end and capped nanotubes. The influence of the catalytic nanoparticle, atop which nanotubes grow, on the nanotube stability is also discussed. The suggested model gives...

  16. Adsorption of ciprofloxacin on surface-modified carbon materials.

    Science.gov (United States)

    Carabineiro, S A C; Thavorn-Amornsri, T; Pereira, M F R; Figueiredo, J L

    2011-10-01

    The adsorption capacity of ciprofloxacin (CPX) was determined on three types of carbon-based materials: activated carbon (commercial sample), carbon nanotubes (commercial multi-walled carbon nanotubes) and carbon xerogel (prepared by the resorcinol/formaldehyde approach at pH 6.0). These materials were used as received/prepared and functionalised through oxidation with nitric acid. The oxidised materials were then heat treated under inert atmosphere (N2) at different temperatures (between 350 and 900°C). The obtained samples were characterised by adsorption of N2 at -196 °C, determination of the point of zero charge and by temperature programmed desorption. High adsorption capacities ranging from approximately 60 to 300 mgCPxgC(-1) were obtained (for oxidised carbon xerogel, and oxidised thermally treated activated carbon Norit ROX 8.0, respectively). In general, it was found that the nitric acid treatment of samples has a detrimental effect in adsorption capacity, whereas thermal treatments, especially at 900 °C after oxidation, enhance adsorption performance. This is due to the positive effect of the surface basicity. The kinetic curves obtained were fitted using 1st or 2nd order models, and the Langmuir and Freundlich models were used to describe the equilibrium isotherms obtained. The 2nd order and the Langmuir models, respectively, were shown to present the best fittings.

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

    Science.gov (United States)

    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.

  18. Highly porous activated carbons prepared from carbon rich Mongolian anthracite by direct NaOH activation

    Science.gov (United States)

    Byamba-Ochir, Narandalai; Shim, Wang Geun; Balathanigaimani, M. S.; Moon, Hee

    2016-08-01

    Highly porous activated carbons (ACs) were prepared from Mongolian raw anthracite (MRA) using sodium hydroxide as an activation agent by varying the mass ratio (powdered MRA/NaOH) as well as the mixing method of chemical agent and powdered MRA. The specific BET surface area and total pore volume of the prepared MRA-based activated carbons (MACs) are in the range of 816-2063 m2/g and of 0.55-1.61 cm3/g, respectively. The pore size distribution of MACs show that most of the pores are in the range from large micropores to small mesopores and their distribution can be controlled by the mass ratio and mixing method of the activating agent. As expected from the intrinsic property of the MRA, the highly graphitic surface morphology of prepared carbons was confirmed from Raman spectra and transmission electron microscopy (TEM) studies. Furthermore the FTIR and XPS results reveal that the preparation of MACs with hydrophobic in nature is highly possible by controlling the mixing conditions of activating agent and powdered MRA. Based on all the results, it is suggested that the prepared MACs could be used for many specific applications, requiring high surface area, optimal pore size distribution, proper surface hydrophobicity as well as strong physical strength.

  19. Surface Carbonization of Mo-La2O3 Cathode

    Institute of Scientific and Technical Information of China (English)

    1999-01-01

    The carbonized structures of Mo-La2O3 cathode specimens have been investigated by means of FE SEM and XRD, respectively. The substructure of carbonized layer in the Mo-La2O3 cathode has been found for the first time. The results showed that the carbonized layer with uniform Mo2C was helpful to emission,while the demixing carbonized layer with a compact MoC outside layer was harmful to emission. The uniform Mo2C layer consists of coarse particles with lots of grain boundary crevices as well as holes arranging perpendic ular to the wire axle and up to surface, which was beneficial to the migration of activated rare-earth in activa tion and operating.

  20. Al current collector surface treatment and carbon nano tubes influences on Carbon / Carbon super-capacitors performances

    Energy Technology Data Exchange (ETDEWEB)

    Portet, C.; Taberna, P.L.; Simon, P. [Universite Paul Sabatier, CIRIMAT-LCMIE, 31 - Toulouse (France)

    2004-07-01

    Performances of 4 cm{sup 2} carbon/carbon super-capacitors cells using Al current collectors foils in organic electrolyte are presented; the improvement of electrode material has been investigated. In a first part, a surface treatment of the Al current collector is proposed in order to improve contact surface between the current collector and the active material leading to an internal resistance decrease. The process consists in an etching of the Al foil and is followed by a carbonaceous sol-gel deposit. Galvano-static cycling and Electrochemical Impedance Spectroscopy measurements of super-capacitors all assembled with treated Al foil were tested over 10,000 cycles: an ESR of 0.5 {omega} cm{sup 2} and a capacitance of 95 F g{sup -1} of activated carbon are obtained and performances remain stable during cycling. The second part is devoted to the study of Carbon Nano Tubes (CNTs) adding into the active material on the performances of super-capacitors. A content of 15% of CNTs appears to be the best composition; the ESR is 0.4 {omega} cm{sup 2} (20% lowered as compared to a cell using activated carbon based electrode) and the capacitance remain high 93 F g{sup -1} of carbonaceous active material. (authors)

  1. Enhanced adsorption of humic acids on ordered mesoporous carbon compared with microporous activated carbon.

    Science.gov (United States)

    Liu, Fengling; Xu, Zhaoyi; Wan, Haiqin; Wan, Yuqiu; Zheng, Shourong; Zhu, Dongqiang

    2011-04-01

    Humic acids are ubiquitous in surface and underground waters and may pose potential risk to human health when present in drinking water sources. In this study, ordered mesoporous carbon was synthesized by means of a hard template method and further characterized by X-ray diffraction, N2 adsorption, transition electron microscopy, elemental analysis, and zeta-potential measurement. Batch experiments were conducted to evaluate adsorption of two humic acids from coal and soil, respectively, on the synthesized carbon. For comparison, a commercial microporous activated carbon and nonporous graphite were included as additional adsorbents; moreover, phenol was adopted as a small probe adsorbate. Pore size distribution characterization showed that the synthesized carbon had ordered mesoporous structure, whereas the activated carbon was composed mainly of micropores with a much broader pore size distribution. Accordingly, adsorption of the two humic acids was substantially lower on the activated carbon than on the synthesized carbon, because of the size-exclusion effect. In contrast, the synthesized carbon and activated carbon showed comparable adsorption for phenol when the size-exclusion effect was not in operation. Additionally, we verified by size-exclusion chromatography studies that the synthesized carbon exhibited greater adsorption for the large humic acid fraction than the activated carbon. The pH dependence of adsorption on the three carbonaceous adsorbents was also compared between the two test humic acids. The findings highlight the potential of using ordered mesoporous carbon as a superior adsorbent for the removal of humic acids.

  2. Surface analysis of carbon black waste materials from tire residues

    Science.gov (United States)

    Lee, W. H.; Kim, J. Y.; Ko, Y. K.; Reucroft, P. J.; Zondlo, J. W.

    1999-03-01

    X-ray photoelectron spectroscopy (XPS) has been used to obtain surface chemical state information on two carbon black waste materials in terms of the surface element distribution/concentration and chemical structure. Small amounts of sulfur in the form of CS 2 were detected on the surface (less than 1.7 mass %). C-H/C-C was the major carbon functional component on the surface of carbon black samples but other functional forms of carbon were also present such as CO and C-O. The surface of the carbon black obtained from a hydropyrolysis process was highly oxidized primarily in the form of carbon based oxygen groups. On the other hand, surface oxygen atoms on the surface of the carbon black obtained from a pyrolysis process in the absence of H 2 were in the form of both metal oxides and carbon based oxygen groups.

  3. Interaction between Palladium Nanoparticles and Surface-Modified Carbon Nanotubes: Role of Surface Functionalities

    DEFF Research Database (Denmark)

    Zhang, Bingsen; Shao, Lidong; Zhang, Wei;

    2014-01-01

    It is crucial to accurately describe the interaction between the surface functionality and the supported metal catalyst because it directly determines the activity and selectivity of a catalytic reaction. It is, however, challenging with a metal-carbon catalytic system owing to the ultrafine feat...

  4. A low-temperature synthesis of electrochemical active Pt nanoparticles and thin films by atomic layer deposition on Si(111) and glassy carbon surfaces

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Rui [Joint Center for Artificial Photosynthesis, California Institute of Technology, Pasadena, CA 91125 (United States); Han, Lihao [Joint Center for Artificial Photosynthesis, California Institute of Technology, Pasadena, CA 91125 (United States); Photovoltaic Materials and Devices (PVMD) Laboratory, Delft University of Technology, P.O. Box 5031, GA Delft 2600 (Netherlands); Huang, Zhuangqun; Ferrer, Ivonne M. [Joint Center for Artificial Photosynthesis, California Institute of Technology, Pasadena, CA 91125 (United States); Division of Chemistry and Chemical Engineering, California Institute of Technology, 210 Noyes Laboratory 127-72, Pasadena, CA 91125 (United States); Smets, Arno H.M.; Zeman, Miro [Photovoltaic Materials and Devices (PVMD) Laboratory, Delft University of Technology, P.O. Box 5031, GA Delft 2600 (Netherlands); Brunschwig, Bruce S., E-mail: bsb@caltech.edu [Beckman Institute, California Institute of Technology, Pasadena, CA 91125 (United States); Lewis, Nathan S., E-mail: nslewis@caltech.edu [Joint Center for Artificial Photosynthesis, California Institute of Technology, Pasadena, CA 91125 (United States); Beckman Institute, California Institute of Technology, Pasadena, CA 91125 (United States); Division of Chemistry and Chemical Engineering, California Institute of Technology, 210 Noyes Laboratory 127-72, Pasadena, CA 91125 (United States); Kavli Nanoscience Institute, California Institute of Technology, Pasadena, CA 91125 (United States)

    2015-07-01

    Atomic layer deposition (ALD) was used to deposit nanoparticles and thin films of Pt onto etched p-type Si(111) wafers and glassy carbon discs. Using precursors of MeCpPtMe{sub 3} and ozone and a temperature window of 200–300 °C, the growth rate was 80–110 pm/cycle. X-ray photoelectron spectroscopy (XPS), atomic force microscopy (AFM), and scanning electron microscopy (SEM) were used to analyze the composition, structure, morphology, and thickness of the ALD-grown Pt nanoparticle films. The catalytic activity of the ALD-grown Pt for the hydrogen evolution reaction was shown to be equivalent to that of e-beam evaporated Pt on glassy carbon electrode. - Highlights: • Pure Pt films were grown by atomic layer deposition (ALD) using MeCpPtMe3 and ozone. • ALD-grown Pt thin films had high growth rates of 110 pm/cycle. • ALD-grown Pt films were electrocatalytic for hydrogen evolution from water. • Electrocatalytic activity of the ALD Pt films was equivalent to e-beam deposited Pt. • No carbon species were detected in the ALD-grown Pt films.

  5. Interaction forces between waterborne bacteria and activated carbon particles

    NARCIS (Netherlands)

    Busscher, Henk J.; Dijkstra, Rene J. B.; Langworthy, Don E.; Collias, Dimitris I.; Bjorkquist, David W.; Mitchell, Michael D.; Van der Mei, Henny C.

    2008-01-01

    Activated carbons remove waterborne bacteria from potable water systems through attractive Lifshitz-van der Waals forces despite electrostatic repulsion between negatively charged cells and carbon surfaces. In this paper we quantify the interaction forces between bacteria with negatively and positiv

  6. Iron cycling at corroding carbon steel surfaces.

    Science.gov (United States)

    Lee, Jason S; McBeth, Joyce M; Ray, Richard I; Little, Brenda J; Emerson, David

    2013-01-01

    Surfaces of carbon steel (CS) exposed to mixed cultures of iron-oxidizing bacteria (FeOB) and dissimilatory iron-reducing bacteria (FeRB) in seawater media under aerobic conditions were rougher than surfaces of CS exposed to pure cultures of either type of microorganism. The roughened surface, demonstrated by profilometry, is an indication of loss of metal from the surface. In the presence of CS, aerobically grown FeOB produced tight, twisted helical stalks encrusted with iron oxides. When CS was exposed anaerobically in the presence of FeRB, some surface oxides were removed. However, when the same FeOB and FeRB were grown together in an aerobic medium, FeOB stalks were less encrusted with iron oxides and appeared less tightly coiled. These observations suggest that iron oxides on the stalks were reduced and solubilized by the FeRB. Roughened surfaces of CS and denuded stalks were replicated with culture combinations of different species of FeOB and FeRB under three experimental conditions. Measurements of electrochemical polarization resistance established different rates of corrosion of CS in aerobic and anaerobic media, but could not differentiate rate differences between sterile controls and inoculated exposures for a given bulk concentration of dissolved oxygen. Similarly, total iron in the electrolyte could not be used to differentiate treatments. The experiments demonstrate the potential for iron cycling (oxidation and reduction) on corroding CS in aerobic seawater media.

  7. INFLUENCIA DE LA COMPOSICIÓN QUÍMICA SUPERFICIAL DEL CARBÓN ACTIVADO EN LA ADSORCIÓN DE BENZOTIAZOLES INFLUENCE OF ACTIVATED CARBON CHEMICAL SURFACE COMPOSITION ON THE ADSORPTION OF BENZOTHIAZOLES

    Directory of Open Access Journals (Sweden)

    Héctor Valdés

    2010-04-01

    Full Text Available Los benzotiazoles están esparcidos en el ambiente debido a su gran variedad de aplicaciones. Dentro de ellos, el benzotiazol (BT, el 2-hidroxibenzotiazol (OHBT, y el 2-metilbenzotiazol (MeBT son conocidos como agentes tóxicos y poco biodegradables. La adsorción con carbón activado se plantea como una opción atractiva para la remoción de estos contaminantes. Sin embargo, existen dudas acerca del efecto de las propiedades químicas superficiales del carbón activado sobre la capacidad de adsorción de estos compuestos. Para el estudio se utilizó carbón activado granular Filtrasorb-400 modificado con el objetivo de obtener carbones con diferentes propiedades químicas superficiales. Las series de carbones activados fueron obtenidas por pretratamiento por desoxigenación y por oxidación con ozono a diferentes tiempos de contacto. El incremento en la concentración de los grupos oxigenados superficiales produce una disminución en la capacidad de adsorción de los tres contaminantes ensayados. Los resultados sugieren que el mecanismo de adsorción transcurre principalmente a través de las interacciones de dispersión π-π entre los electrones del plano basal del carbón y el anillo aromático de los benzotiazoles. A valores de pH mayores al valor del pH de carga cero de la superficie del carbón activado (pH PZC, la capacidad de adsorción del carbón activado disminuye debido a la aparición de interacciones electrostáticas repulsivas entre los grupos superficiales oxigenados ionizados y las moléculas ionizadas de los benzotiazoles.Benzothiazoles, such as benzothiazole (BT, 2-hydroxybenzothiazole (OHBT, and 2-methylbenzothiazole (MeBT are toxic and poorly biodegradable organic compounds, frequently present in wastewater from rubber related applications. Activated carbon adsorption has been identified as an attractive treatment to removing those contaminants. This paper presents experimental results on the effect of chemical surface

  8. Riemann Surfaces of Carbon as Graphene Nanosolenoids.

    Science.gov (United States)

    Xu, Fangbo; Yu, Henry; Sadrzadeh, Arta; Yakobson, Boris I

    2016-01-13

    Traditional inductors in modern electronics consume excessive areas in the integrated circuits. Carbon nanostructures can offer efficient alternatives if the recognized high electrical conductivity of graphene can be properly organized in space to yield a current-generated magnetic field that is both strong and confined. Here we report on an extraordinary inductor nanostructure naturally occurring as a screw dislocation in graphitic carbons. Its elegant helicoid topology, resembling a Riemann surface, ensures full covalent connectivity of all graphene layers, joined in a single layer wound around the dislocation line. If voltage is applied, electrical currents flow helically and thus give rise to a very large (∼1 T at normal operational voltage) magnetic field and bring about superior (per mass or volume) inductance, both owing to unique winding density. Such a solenoid of small diameter behaves as a quantum conductor whose current distribution between the core and exterior varies with applied voltage, resulting in nonlinear inductance.

  9. High surface area silicon carbide-coated carbon aerogel

    Science.gov (United States)

    Worsley, Marcus A; Kuntz, Joshua D; Baumann, Theodore F; Satcher, Jr, Joe H

    2014-01-14

    A metal oxide-carbon composite includes a carbon aerogel with an oxide overcoat. The metal oxide-carbon composite is made by providing a carbon aerogel, immersing the carbon aerogel in a metal oxide sol under a vacuum, raising the carbon aerogel with the metal oxide sol to atmospheric pressure, curing the carbon aerogel with the metal oxide sol at room temperature, and drying the carbon aerogel with the metal oxide sol to produce the metal oxide-carbon composite. The step of providing a carbon aerogel can provide an activated carbon aerogel or provide a carbon aerogel with carbon nanotubes that make the carbon aerogel mechanically robust. Carbon aerogels can be coated with sol-gel silica and the silica can be converted to silicone carbide, improved the thermal stability of the carbon aerogel.

  10. Microscopic Study of Carbon Surfaces Interacting with High Carbon Ferromanganese Slag

    Science.gov (United States)

    Safarian, Jafar; Kolbeinsen, Leiv

    2015-02-01

    The interaction of carbon materials with molten slags occurs in many pyro-metallurgical processes. In the production of high carbon ferromanganese in submerged arc furnace, the carbothermic reduction of MnO-containing silicate slags yields the metal product. In order to study the interaction of carbon with MnO-containing slags, sessile drop wettability technique is employed in this study to reduce MnO from a molten slag drop by carbon substrates. The interfacial area on the carbon substrate before and after reaction with slag is studied by scanning electron microscope. It is indicated that no Mn metal particles are found at the interface through the reduction of the MnO slag. Moreover, the reduction of MnO occurs through the contribution of Boudouard reaction and it causes carbon consumption in particular active sites at the interface, which generate carbon degradation and open pore growth at the interface. It is shown that the slag is fragmented to many micro-droplets at the reaction interface, potentially due to the effect on the interfacial energies of a provisional liquid Mn thin film. The rapid reduction of these slag micro-droplets affects the carbon surface with making deep micro-pores. A mechanism for the formation of slag micro-droplets is proposed, which is based on the formation of provisional micro thin films of liquid Mn at the interface.

  11. Surface chemistry of carbon dioxide revisited

    Science.gov (United States)

    Taifan, William; Boily, Jean-François; Baltrusaitis, Jonas

    2016-12-01

    This review discusses modern developments in CO2 surface chemistry by focusing on the work published since the original review by H.J. Freund and M.W. Roberts two decades ago (Surface Science Reports 25 (1996) 225-273). It includes relevant fundamentals pertaining to the topics covered in that earlier review, such as conventional metal and metal oxide surfaces and CO2 interactions thereon. While UHV spectroscopy has routinely been applied for CO2 gas-solid interface analysis, the present work goes further by describing surface-CO2 interactions under elevated CO2 pressure on non-oxide surfaces, such as zeolites, sulfides, carbides and nitrides. Furthermore, it describes additional salient in situ techniques relevant to the resolution of the interfacial chemistry of CO2, notably infrared spectroscopy and state-of-the-art theoretical methods, currently used in the resolution of solid and soluble carbonate species in liquid-water vapor, liquid-solid and liquid-liquid interfaces. These techniques are directly relevant to fundamental, natural and technological settings, such as heterogeneous and environmental catalysis and CO2 sequestration.

  12. Evidence for Carbonate Surface Complexation during Forsterite Carbonation in Wet Supercritical Carbon Dioxide

    Energy Technology Data Exchange (ETDEWEB)

    Loring, John S.; Chen, Jeffrey; Benezeth Ep Gisquet, Pascale; Qafoku, Odeta; Ilton, Eugene S.; Washton, Nancy M.; Thompson, Christopher J.; Martin, Paul F.; McGrail, B. Peter; Rosso, Kevin M.; Felmy, Andrew R.; Schaef, Herbert T.

    2015-07-14

    Continental flood basalts are attractive formations for geologic sequestration of carbon dioxide because of their reactive divalent-cation containing silicates, such as forsterite (Mg2SiO4), suitable for long-term trapping of CO2 mineralized as metal carbonates. The goal of this study was to investigate at a molecular level the carbonation products formed during the reaction of forsterite with supercritical CO2 (scCO2) as a function of the concentration of H2O adsorbed to the forsterite surface. Experiments were performed at 50 °C and 90 bar using an in situ IR titration capability, and post-reaction samples were examined by ex situ techniques, including SEM, XPS, FIB-TEM, TGA-MS, and MAS-NMR. Carbonation products and reaction extents varied greatly with adsorbed H2O. We show for the first time evidence of Mg-carbonate surface complexation under wet scCO2 conditions. Carbonate is found to be coordinated to Mg at the forsterite surface in a predominately bidentate fashion at adsorbed H2O concentrations below 27 µmol/m2. Above this concentration and up to 76 µmol/m2, monodentate coordinated complexes become dominant. Beyond a threshold adsorbed H2O concentration of 76 µmol/m2, crystalline carbonates continuously precipitate as magnesite, and the particles that form are hundreds of times larger than the estimated thicknesses of the adsorbed water films of about 7 to 15 Å. At an applied level, these results suggest that mineral carbonation in scCO2 dominated fluids near the wellbore and adjacent to caprocks will be insignificant and limited to surface complexation, unless adsorbed H2O concentrations are high enough to promote crystalline carbonate formation. At a fundamental level, the surface complexes and their dependence on adsorbed H2O concentration give insights regarding forsterite dissolution processes and magnesite nucleation and growth.

  13. Grafting of activated carbon cloths for selective adsorption

    Science.gov (United States)

    Gineys, M.; Benoit, R.; Cohaut, N.; Béguin, F.; Delpeux-Ouldriane, S.

    2016-05-01

    Chemical functionalization of an activated carbon cloth with 3-aminophthalic acid and 4-aminobenzoic acid groups by the in situ formation of the corresponding diazonium salt in aqueous acidic solution is reported. The nature and amount of selected functions on an activated carbon surface, in particular the grafted density, were determined by potentiometric titration, elemental analysis and X-ray photoelectron spectroscopy (XPS). The nanotextural properties of the modified carbon were explored by gas adsorption. Functionalized activated carbon cloth was obtained at a discrete grafting level while preserving interesting textural properties and a large porous volume. Finally, the grafting homogeneity of the carbon surface and the nature of the chemical bonding were investigated using Time-of-Flight Secondary Ion Mass Spectrometry (ToF-SIMS) technique.

  14. The synthesis of Ag nanoparticles and loading it on activated carbon as a novel adsorbent for removing methyl orange by using surface response methodology

    Directory of Open Access Journals (Sweden)

    S. Javad Hosseini

    2014-12-01

    Full Text Available After synthesizing Ag nanoparticles and loading onto activated carbon (from olive stone, the adsorption of methyl orange (MO onto the prepared nanoparticles was studied. In this connection, the effect of experimental parameters such as pH range, reagent concentration, contact time, dosage amount of adsorbent and so on, on the adsorption process were studied. The experimental results were analyzed upon various kinetic models such as pseudo first order reaction, pseudo second order reaction, Elovich model, intraparticle diffusion model and various adsorption isotherms such as Langmuir isotherm, Freundlich isotherm and Temkin isotherm.

  15. Activated carbon from leather shaving wastes and its application in removal of toxic materials.

    Science.gov (United States)

    Kantarli, Ismail Cem; Yanik, Jale

    2010-07-15

    In this study, utilization of a solid waste as raw material for activated carbon production was investigated. For this purpose, activated carbons were produced from chromium and vegetable tanned leather shaving wastes by physical and chemical activation methods. A detailed analysis of the surface properties of the activated carbons including acidity, total surface area, extent of microporosity and mesoporosity was presented. The activated carbon produced from vegetable tanned leather shaving waste produced has a higher surface area and micropore volume than the activated carbon produced from chromium tanned leather shaving waste. The potential application of activated carbons obtained from vegetable tanned shavings as adsorbent for removal of water pollutants have been checked for phenol, methylene blue, and Cr(VI). Adsorption capacities of activated carbons were found to be comparable to that of activated carbons derived from biomass.

  16. Effects of Elevation on Surface Layer Soil Active Organic Carbon Content in Shennongjia Nature Reserve%海拔对神农架表层土壤活性有机碳含量的影响

    Institute of Scientific and Technical Information of China (English)

    卢慧; 丛静; 薛亚东; 杨敬元; 陈克龙; 李迪强; 张于光

    2014-01-01

    In this study,five typical vegetation types were selected along the elevational gradient in Shennongjia Nature Reserve,including shrubs, coniferous forest, mixed forest between coniferous and deciduous broad-leaved forest, deciduous broad-leaved forest,and evergreen broad-leaved forest. The content of soil organic carbon ( SOC ) ,water dissolved organic carbon ( WDOC ) ,labile organic carbon ( LOC ) ,and microbial biomass carbon ( MBC ) and their allocation proportions to SOC were analyzed. Furthermore,the Pearson relationship was analyzed between soil active organic carbon and plant diversity or soil physiochemical properties. The results showed that the soil organic carbon in the surface layer increased with the elevation increased, except for the deciduous broad-leaved forest. Distribution characteristics of MBC and LOC content along elevation gradient were obvious,but WDOC content was independent of the elevation gradient. The contents of the three kinds of active organic carbon in different elevational gradients were in the order of: LOC>MBC >WDOC. The allocation ratios of MBC,LOC and WDOC to SOC did not significantly alter with elevational gradient. Pearson relationship showed that SOC and MBC had a significant negative correlation with the diversity of trees and shrubs (P < 0. 05),while LOC and WDOC content had no significant correlation with plant diversity. In addition,SOC and MBC were significantly positively correlated with the content of soil moisture,total nitrogen,available nitrogen,total phosphorus and total sulfur (P<0. 01). LOC had a significant and positive correlation with the content of soil moisture,total nitrogen,available nitrogen and total sulfur (P <0. 01). There was a significant correlation between LOC and total phosphorus ( P<0 . 05 ) . The results revealed that these factors had a dominating impact on SOC,LOC and MBC. WDOC content had no obvious correlation with soil factors.

  17. Preparation of activated carbons from Chinese coal and hydrolysis lignin

    Energy Technology Data Exchange (ETDEWEB)

    Zou, Y.; Han, B.X. [Tuskegee University, Tuskegee, AL (USA). School of Engineering, Dept. of Chemical Engineering

    2001-07-01

    Activated carbons from Chinese coal and Chinese hydrolysis lignin have been prepared by chemical activation with potassium hydroxide. The following aspects of these activated materials have been analyzed: raw material; pre-treatment of raw material; activation agent, activation temperature and time, acid the activation agent/raw material ratio. Activated carbons with BET specific surface areas of the order of 2400-2600 m{sup 2}/g which exhibited substantial microporosity, a total pore volume of over 1.30 cm{sup 3}/g and a Methylene Blue adsorption capacity of over 440 mg/g were obtained.

  18. Creation of surface defects on carbon nanofibers by steam treatment

    Institute of Scientific and Technical Information of China (English)

    Zhengfeng; Shao; Min; Pang; Wei; Xia; Martin; Muhler; Changhai; Liang

    2013-01-01

    A direct strategy for the creation of defects on carbon nanofibers (CNFs) has been developed by steam treatment.Nitrogen physisorption,XRD,Raman spectra,SEM and TEM analyses proved the existence of the new defects on CNFs.BET surface area of CNFs after steam treatment was enhanced from 20 to 378 m2/g.Pd catalysts supported on CNFs were also prepared by colloidal deposition method.The different activity of Pd/CNFs catalysts in the partial hydrogenation of phenylacetylene further demonstrated the diverse surfaces of CNFs could be formed by steam treatment.

  19. Apparatus and process for the surface treatment of carbon fibers

    Energy Technology Data Exchange (ETDEWEB)

    Paulauskas, Felix Leonard; Ozcan, Soydan; Naskar, Amit K.

    2016-05-17

    A method for surface treating a carbon-containing material in which carbon-containing material is reacted with decomposing ozone in a reactor (e.g., a hollow tube reactor), wherein a concentration of ozone is maintained throughout the reactor by appropriate selection of at least processing temperature, gas stream flow rate, reactor dimensions, ozone concentration entering the reactor, and position of one or more ozone inlets (ports) in the reactor, wherein the method produces a surface-oxidized carbon or carbon-containing material, preferably having a surface atomic oxygen content of at least 15%. The resulting surface-oxidized carbon material and solid composites made therefrom are also described.

  20. Adsorption of aromatic compounds by carbonaceous adsorbents: a comparative study on granular activated carbon, activated carbon fiber, and carbon nanotubes.

    Science.gov (United States)

    Zhang, Shujuan; Shao, Ting; Kose, H Selcen; Karanfil, Tanju

    2010-08-15

    Adsorption of three aromatic organic compounds (AOCs) by four types of carbonaceous adsorbents [a granular activated carbon (HD4000), an activated carbon fiber (ACF10), two single-walled carbon nanotubes (SWNT, SWNT-HT), and a multiwalled carbon nanotube (MWNT)] with different structural characteristics but similar surface polarities was examined in aqueous solutions. Isotherm results demonstrated the importance of molecular sieving and micropore effects in the adsorption of AOCs by carbonaceous porous adsorbents. In the absence of the molecular sieving effect, a linear relationship was found between the adsorption capacities of AOCs and the surface areas of adsorbents, independent of the type of adsorbent. On the other hand, the pore volume occupancies of the adsorbents followed the order of ACF10 > HD4000 > SWNT > MWNT, indicating that the availability of adsorption site was related to the pore size distributions of the adsorbents. ACF10 and HD4000 with higher microporous volumes exhibited higher adsorption affinities to low molecular weight AOCs than SWNT and MWNT with higher mesopore and macropore volumes. Due to their larger pore sizes, SWNTs and MWNTs are expected to be more efficient in adsorption of large size molecules. Removal of surface oxygen-containing functional groups from the SWNT enhanced adsorption of AOCs.

  1. Carbon Sequestration on Surface Mine Lands

    Energy Technology Data Exchange (ETDEWEB)

    Donald H. Graves; Christopher Barton; Bon Jun Koo; Richard Sweigard; Richard Warner

    2004-11-30

    The first quarter of 2004 was dedicated to tree planting activities in two locations in Kentucky. During the first year of this project there was not available mine land to plant in the Hazard area, so 107 acres were planted in the Martin County mine location. This year 120 acres were planted in the Hazard area to compensate for the prior year and an additional 57 acres were planted on Peabody properties in western Kentucky. Additional sets of special plots were established on each of these areas that contained 4800 seedlings each for carbon sequestration demonstrations. Plantings were also conducted to continue compaction and water quality studies on the newly established areas as well as continual measurements of the first year's plantings. Total plantings on this project now amount to 357 acres containing 245,960 seedlings. During the second quarter of this year monitoring systems were established for all the new research areas. Weather data pertinent to the research as well as hydrology and water quality monitoring continues to be conducted on all areas. Studies established to assess specific questions pertaining to carbon flux and the invasion of the vegetation by small mammals are being quantified. Experimental practices initiated with this research project will eventually allow for the planting on long steep slopes with loose grading systems and allow mountain top removal areas to be constructed with loose spoil with no grading of the final layers of rooting material when establishing trees for the final land use designation. Monitoring systems have been installed to measure treatment effects on both above and below ground carbon and nitrogen pools in the planting areas. Soil and tissue samples were collected from both years planting and analyses were conducted in the laboratory. Examination of decomposition and heterotropic respiration on carbon cycling in the reforestation plots continued during the reporting period. Entire planted trees were

  2. Evidence for Carbonate Surface Complexation during Forsterite Carbonation in Wet Supercritical Carbon Dioxide

    Energy Technology Data Exchange (ETDEWEB)

    Loring, John S.; Chen, Jeffrey; Benezeth, Pascale; Qafoku, Odeta; Ilton, Eugene S.; Washton, Nancy M.; Thompson, Christopher J.; Martin, Paul F.; McGrail, B. Peter; Rosso, Kevin M.; Felmy, Andrew R.; Schaef, Herbert T.

    2015-06-16

    Continental flood basalts are attractive formations for geologic sequestration of carbon dioxide because of their reactive divalent-cation containing silicates, such as forsterite (Mg2SiO4), suitable for long-term trapping of CO2 mineralized as metal carbonates. The goal of this study was to investigate at a molecular level the carbonation products formed during the reaction of forsterite with supercritical CO2 (scCO2) as a function of the concentration of H2O adsorbed to the forsterite surface. Experiments were performed at 50 °C and 90 bar using an in situ IR titration capability, and post-reaction samples were examined by ex situ techniques, including SEM, XPS, FIB-TEM, TGA-MS, and MAS-NMR. Carbonation products and reaction extents varied greatly with adsorbed H2O. We show for the first time evidence of Mg-carbonate surface complexation under wet scCO2 conditions. Carbonate is found to be coordinated to Mg at the forsterite surface in a predominately bidentate fashion at adsorbed H2O concentrations below 27 µmol/m2. Above this concentration and up to 76 µmol/m2, monodentate coordinated complexes become dominant. Beyond a threshold adsorbed H2O concentration of 76 µmol/m2, crystalline carbonates continuously precipitate as magnesite, and the particles that form are hundreds of times larger than the estimated thicknesses of the adsorbed water films of about 7 to 15 Å. At an applied level, the implication of these results is that mineral trapping in scCO2 dominated fluids will be insignificant and limited to surface complexation unless adsorbed H2O concentrations are high enough to promote crystalline carbonate formation. At a fundamental level, the surface complexes and their dependence on adsorbed H2O concentration give insights regarding forsterite dissolution processes and magnesite nucleation and growth.

  3. Microbial Surfaces and their Effects on Carbonate Mineralization

    Science.gov (United States)

    Cappuccio, J. A.; Pillar, V. D.; Lui, G. V.; Ajo-Franklin, C.

    2011-12-01

    Geologic carbon dioxide sequestration, the underground storage of carbon dioxide (CO2), will be an essential component of climate change mitigation. Carbonate minerals are a promising form of stable CO2 storage, but their geologic formation is slow. Many microbes can increase the rate of carbonate mineral formation; however the mechanisms of such mineralization are largely unknown. Hypothesized mechanisms include metabolic processes that alter pH and supersaturation, as well as cell surface properties that induce mineral nucleation. This work systematically investigates these mechanisms by allowing calcium carbonate (CaCO3) to form in the presence or absence of microbes with various surfaces features included Escherichia coli, Synechocystis sp. PCC 6803, Caulobacter vibrioides, and Lysinibacilllus sphaericus. Surprisingly, formation of stable crystalline CaCO3 was accelerated by the presence of all microbes relative to abiotic solutions. This rate acceleration also occurred for metabolically inactive bacteria, indicating that metabolic activity was not the operating mechanism. Rather, since the CaCO3 crystals increased in number as the cell density increased, these results indicate that many bacterial species accelerate the nucleation of CaCO3 crystals. To understand the role of specific biomolecules on nucleation, we used genetic mutants with altered lipopolysaccharides (LPS) and crystalline surface layer proteins (S-layers). Bacterial surface charge and cation binding was assessed using zeta potential measurements and correlated to the bacterial surface chemistry and biomineralization experiments with varying Ca2+ concentrations. From these results, we postulate that the S-layer surfaces can selectively attract Ca2+ ions, serving as nucleation sites for CaCO3, thereby accelerating crystal formation. These observations provide substantive evidence for a non-specific nucleation mechanism, and stress the importance of microbes, even dead ones, on the rate of

  4. ADSORPTION OF STRONTIUM IONS FROM WATER ON MODIFIED ACTIVATED CARBONS

    Directory of Open Access Journals (Sweden)

    Mihai Ciobanu

    2016-12-01

    Full Text Available Adsorption of strontium ions from aqueous solutions on active carbons CAN-7 and oxidized CAN-8 has been studied. It has been found that allure of the adsorption isotherms for both studied active carbons are practically identical. Studies have shown that the adsorption isotherms for strontium ions from aqueous solutions are well described by the Langmuir and Dubinin-Radushkevich equations, respectively. The surface heterogeneity of activated carbons CAN-7 and oxidized CAN-8 has been assessed by using Freundlich equation.

  5. Impact of sulfur oxides on mercury capture by activated carbon.

    Science.gov (United States)

    Presto, Albert A; Granite, Evan J

    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 ACl, mercury capture was tested under varying conditions of SO2 and SO3 concentrations using a packed bed reactor and simulated flue gas (SFG). The final mercury content of the activated carbons is independent of the SO2 concentration in the SFG, but the presence of SO3 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 H2SO4 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.

  6. Microbial Enzyme Activity and Carbon Cycling in Grassland Soil Fractions

    Science.gov (United States)

    Allison, S. D.; Jastrow, J. D.

    2004-12-01

    Extracellular enzymes are necessary to degrade complex organic compounds present in soils. Using physical fractionation procedures, we tested whether old soil carbon is spatially isolated from degradative enzymes across a prairie restoration chronosequence in Illinois, USA. We found that carbon-degrading enzymes were abundant in all soil fractions, including macroaggregates, microaggregates, and the clay fraction, which contains carbon with a mean residence time of ~200 years. The activities of two cellulose-degrading enzymes and a chitin-degrading enzyme were 2-10 times greater in organic matter fractions than in bulk soil, consistent with the rapid turnover of these fractions. Polyphenol oxidase activity was 3 times greater in the clay fraction than in the bulk soil, despite very slow carbon turnover in this fraction. Changes in enzyme activity across the restoration chronosequence were small once adjusted for increases in soil carbon concentration, although polyphenol oxidase activity per unit carbon declined by 50% in native prairie versus cultivated soil. These results are consistent with a `two-pool' model of enzyme and carbon turnover in grassland soils. In light organic matter fractions, enzyme production and carbon turnover both occur rapidly. However, in mineral-dominated fractions, both enzymes and their carbon substrates are immobilized on mineral surfaces, leading to slow turnover. Soil carbon accumulation in the clay fraction and across the prairie restoration chronosequence probably reflects increasing physical isolation of enzymes and substrates on the molecular scale, rather than the micron to millimeter scale.

  7. Production of activated carbon from rice husk Vietnam

    Science.gov (United States)

    Korobochkin, V. V.; Tu, N. V.; Hieu, N. M.

    2016-09-01

    This work is dedicated to the production of activated carbon from rice husk from Delta of the Red River in Viet Nam. At the first stage, carbonization of a rice husk was carried out to obtain material containing 43.1% carbon and 25 % silica with a specific surface area of 51.5 m2/g. After separating of silica (the second stage), the specific surface area of the product increased to 204 m2/g and the silica content decreased to 1.23% by weight as well. The most important stage in the formation of the porous structure of the material is the activation. The products with the high specific surface area in the range of 800-1345 m2/g were obtained by activation of carbonized product with water vapour or carbon dioxide at temperatures of 700 °C and 850 °C, with varying the flow rate of the activating agent and activation time. The best results were achieved by activation of carbon material with water vapour at the flow rate of 0.08 dm3/min per 500 g of material and the temperature of 850 °C.

  8. Production of activated carbon from peanut hill using phosphoric acid and microwave activation

    Directory of Open Access Journals (Sweden)

    Weerawat Clowutimon

    2015-06-01

    Full Text Available The optimum conditions for preparing activated carbon from peanut hulls by phosphoric acid and microwave activation were studied. Factors investigated in this study were temperature of carbonization at 300, 350, 400 and 450๐ C, and time of carbonization at 30, 60 and 90 minutes. The optimum yield was observed that carbonization temperature of 400๐ C and time at 60 minutes, respectively. The yield of charcoal was 39% and the f ix carbon was 69%. Then the charcoal was activated by phosphoric acid and microwave irradiation, respectively. The effect of the weight per volume ratios of charcoal to activating acid (1:1, 1:2 and 2:1(W/V, microwave power at (activated 300, 500 and 700 watts, and activated time (30, 60 and 90 seconds were studied. The results showed that the optimum conditions for activating peanut charcoal were 1:2 (W/V charcoal per activating acid, microwave power 700 watts for 90 seconds. The results yielding maximum surface area by BET method was 303.1 m2 /g and pore volume was 0.140 cm3 /g. An efficiency of maximum iodine adsorption was 418 mg iodine/g activated carbon. Comparing the adsorption efficiency of non- irradiated and irradiated activated carbon, the efficiency of irradiated activated carbon improved up to 31%, due to its larger surface area and pore volume.

  9. CARBON SEQUESTRATION ON SURFACE MINE LANDS

    Energy Technology Data Exchange (ETDEWEB)

    Donald H. Graves; Christopher Barton; Richard Sweigard; Richard Warner

    2004-08-02

    The April-June 2004 quarter was dedicated to the establishment of monitoring systems for all the new research areas. Hydrology and water quality monitoring continues to be conducted on all areas as does weather data pertinent to the research. Studies assessing specific questions pertaining to carbon flux has been established and the invasion of the vegetation by small mammals is being quantified. The approval of two experimental practices associated with this research by the United States Office of Surface Mining was a major accomplishment during this period of time. These experimental practices will eventually allow for tree planting on long steep slopes with loose grading systems and for the use of loose dumped spoil on mountain top removal areas with no grading in the final layer of rooting material for tree establishment.

  10. Effect of preparation method on the surface characteristics and activity of the Pd/OMS-2 catalysts for the oxidation of carbon monoxide, toluene, and ethyl acetate

    Science.gov (United States)

    Liu, Lisha; Song, Yong; Fu, Zhidan; Ye, Qing; Cheng, Shuiyuan; Kang, Tianfang; Dai, Hongxing

    2017-02-01

    The cryptomelane-type manganese oxide octahedral molecular sieve (OMS-2)-supported Pd (0.5 wt% Pd/OMS-2-DP, 0.5 wt% Pd/OMS-2-PI, and 0.5 wt% Pd/OMS-2-EX) catalysts were prepared by the deposition-precipitation, pre-incorporation, and ion-exchanging strategies, respectively. It is shown that the preparation method exerted an important effect on the physicochemical property of the sample. Among the OMS-2-supported Pd catalysts, 0.5 wt% Pd/OMS-2-DP possessed the highest surface (Mn2+ + Mn3+)/Mn4+ atomic ratio and the highest surface Pd loading and acid sites. The 0.5 wt% Pd/OMS-2 catalysts outperformed the Pd-free counterpart, among which 0.5 wt% Pd/OMS-2-DP presented the best catalytic activity (T50% and T90% were 25 and 55 °C for CO oxidation, 240 and 285 °C for toluene oxidation, and 160 and 200 °C for ethyl acetate oxidation, respectively). We believe that the high Pd surface loading, high surface atomic ratio of (Mn2+ + Mn3+)/Mn4+, and good low-temperature reducibility, good oxygen mobility, and high acidity were responsible for the excellent performance of the 0.5 wt% Pd/OMS-2-DP catalyst.

  11. Active Free Surface Density Maps

    Science.gov (United States)

    Çelen, S.

    2016-10-01

    Percolation problems were occupied to many physical problems after their establishment in 1957 by Broadbent and Hammersley. They can be used to solve complex systems such as bone remodeling. Volume fraction method was adopted to set some algorithms in the literature. However, different rate of osteoporosis could be observed for different microstructures which have the same mass density, mechanical stimuli, hormonal stimuli and nutrition. Thus it was emphasized that the bone might have identical porosity with different specific surfaces. Active free surface density of bone refers the used total area for its effective free surface. The purpose of this manuscript is to consolidate a mathematical approach which can be called as “active free surface density maps” for different surface patterns and derive their formulations. Active free surface density ratios were calculated for different Archimedean lattice models according to Helmholtz free energy and they were compared with their site and bond percolation thresholds from the background studies to derive their potential probability for bone remodeling.

  12. CCN activation of pure and coated carbon black particles.

    Science.gov (United States)

    Dusek, U; Reischl, G P; Hitzenberger, R

    2006-02-15

    The CCN (cloud condensation nucleus) activation of pure and coated carbon black particles was investigated using the University of Vienna cloud condensation nuclei counter (Giebl, H.; Berner, A.; Reischl, G.; Puxbaum, H.; Kasper-Giebl, A.; Hitzenberger, R. J. Aerosol Sci. 2002, 33, 1623-1634). The particles were produced by nebulizing an aqueous suspension of carbon black in a Collison atomizer. The activation of pure carbon black particles was found to require higher supersaturations than predicted by calculations representing the particles as insoluble, wettable spheres with mobility equivalent diameter. To test whether this effect is an artifact due to heating of the light-absorbing carbon black particles in the laser beam, experiments at different laser powers were conducted. No systematic dependence of the activation of pure carbon black particles on laser power was observed. The observations could be modeled using spherical particles and an effective contact angle of 4-6 degrees of water at their surface. The addition of a small amount of NaCl to the carbon black particles (by adding 5% by mass NaCl to the carbon black suspension) greatly enhanced their CCN efficiency. The measured CCN efficiencies were consistent with Kohler theory for particles consisting of insoluble and hygroscopic material. However, coating the carbon black particles with hexadecanol (a typical film-forming compound with one hydrophobic and one hydrophilic end) efficiently suppressed the CCN activation of the carbon black particles.

  13. Evidence for Carbonate Surface Complexation during Forsterite Carbonation in Wet Supercritical Carbon Dioxide.

    Science.gov (United States)

    Loring, John S; Chen, Jeffrey; Bénézeth, Pascale; Qafoku, Odeta; Ilton, Eugene S; Washton, Nancy M; Thompson, Christopher J; Martin, Paul F; McGrail, B Peter; Rosso, Kevin M; Felmy, Andrew R; Schaef, Herbert T

    2015-07-14

    Continental flood basalts are attractive formations for geologic sequestration of carbon dioxide because of their reactive divalent-cation containing silicates, such as forsterite (Mg2SiO4), suitable for long-term trapping of CO2 mineralized as metal carbonates. The goal of this study was to investigate at a molecular level the carbonation products formed during the reaction of forsterite with supercritical CO2 (scCO2) as a function of the concentration of H2O adsorbed to the forsterite surface. Experiments were performed at 50 °C and 90 bar using an in situ IR titration capability, and postreaction samples were examined by ex situ techniques, including scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), focused ion beam transmission electron microscopy (FIB-TEM), thermal gravimetric analysis mass spectrometry (TGA-MS), and magic angle spinning nuclear magnetic resonance (MAS NMR). Carbonation products and reaction extents varied greatly with adsorbed H2O. We show for the first time evidence of Mg-carbonate surface complexation under wet scCO2 conditions. Carbonate is found to be coordinated to Mg at the forsterite surface in a predominately bidentate fashion at adsorbed H2O concentrations below 27 μmol/m(2). Above this concentration and up to 76 μmol/m(2), monodentate coordinated complexes become dominant. Beyond a threshold adsorbed H2O concentration of 76 μmol/m(2), crystalline carbonates continuously precipitate as magnesite, and the particles that form are hundreds of times larger than the estimated thicknesses of the adsorbed water films of about 7 to 15 Å. At an applied level, these results suggest that mineral carbonation in scCO2 dominated fluids near the wellbore and adjacent to caprocks will be insignificant and limited to surface complexation, unless adsorbed H2O concentrations are high enough to promote crystalline carbonate formation. At a fundamental level, the surface complexes and their dependence on adsorbed H2O

  14. Comparison of toluene adsorption among granular activated carbon and different types of activated carbon fibers (ACFs).

    Science.gov (United States)

    Balanay, Jo Anne G; Crawford, Shaun A; Lungu, Claudiu T

    2011-10-01

    Activated carbon fiber (ACF) has been demonstrated to be a good adsorbent for the removal of organic vapors in air. Some ACF has a comparable or larger surface area and higher adsorption capacity when compared with granular activated carbon (GAC) commonly used in respiratory protection devices. ACF is an attractive alternative adsorbent to GAC because of its ease of handling, light weight, and decreasing cost. ACF may offer the potential for short-term respiratory protection for first responders and emergency personnel. This study compares the critical bed depths and adsorption capacities for toluene among GAC and ACF of different forms and surface areas. GAC and ACF in cloth (ACFC) and felt (ACFF) forms were challenged in stainless steel chambers with a constant concentration of 500 ppm toluene via conditioned air at 25°C, 50% RH, and constant airflow (7 L/min). Breakthrough data were obtained for each adsorbent using gas chromatography with flame ionization detector. Surface areas of each adsorbent were determined using a physisorption analyzer. Results showed that the critical bed depth of GAC is 275% higher than the average of ACFC but is 55% lower than the average of ACFF. Adsorption capacity of GAC (with a nominal surface area of 1800 m(2)/g) at 50% breakthrough is 25% higher than the average of ACF with surface area of 1000 m(2)/g, while the rest of ACF with surface area of 1500 m(2)/g and higher have 40% higher adsorption capacities than GAC. ACFC with higher surface area has the smallest critical bed depth and highest adsorption capacity, which makes it a good adsorbent for thinner and lighter respirators. We concluded that ACF has great potential for application in respiratory protection considering its higher adsorption capacity and lower critical bed depth in addition to its advantages over GAC, particularly for ACF with higher surface area.

  15. Research on microstructure and surface morphology of sulfur-loading active carbon%载硫活性炭微观结构和表面形态研究

    Institute of Scientific and Technical Information of China (English)

    鹿存房; 刘清才; 高威; 董凌燕

    2009-01-01

    Hg can react with sulfur to form HgS which is stable.To remove mercury in fuel gas from coal combustion plant.sulfur content in active carbon was increased by thermal deposition in this work.SEM,BET,TGA and other measurement methods were used to characterize the effect on surface morphology,sulfur distribution and specific surface.The experimental results showed that thermal deposition was effective in increasing sulfur content in active carbon:most sulfur was adhered on the carbon chain and little was on the wall of pore;specific surface was decreased though deposition and it increased with temperature increase;binding between carbonand sulfur molecular was increased.%为了增强活性炭脱除燃煤电厂烟气中汞的能力,利用汞和硫可以生成稳定的HgS的性质,研究了通过热沉淀增加了活性炭中的硫含量的改性方法,并以SEM、BET、TGA等方法,研究了改性对活性炭表面形貌、硫在活性炭中的分布、活性炭比表面积等性能的影响.结果表明,热沉淀改性方法可以增加活性炭中的硫含量;硫粘附在活性炭的炭链上量较多,孔壁较少;改性工艺降低了活性炭的比表面积,且改性活性炭的比表面积随着温度的升高而增大;载硫后,活性炭中元素硫和炭的结合被增强.

  16. Multiwalled Carbon Nanotube Deposition on Model Environmental Surfaces

    Science.gov (United States)

    Deposition of multiwalled carbon nanotubes (MWNTs) on model environmental surfaces was investigated using a quartz crystal microbalance with dissipation monitoring (QCM-D). Deposition behaviors of MWNTs on positively and negatively charged surfaces were in good agreement with Der...

  17. CARBON SEQUESTRATION OF SURFACE MINE LANDS

    Energy Technology Data Exchange (ETDEWEB)

    Donald H. Graves; Christopher Barton; Richard Sweigard; Richard Warner

    2004-05-19

    The January-March 2004 Quarter was dedicated to tree planting activities in two locations in Kentucky. During year one of this project there was no available mine land to plant in the Hazard area so 107 acres were planted in the Martin county mine location. This year 120 acres was planted in the Hazard area to compensate for the prior year and an additional 57 acres was planted on Peabody properties in western Kentucky. An additional set of special plots were established on each of these areas that contained 4800 seedlings each for special carbon sequestration determinations. Plantings were also conducted to continue compaction and water quality studies on two newly established areas as well as confirmed measurements on the first years plantings. Total plantings on this project now amount to 357 acres containing 245,960 tree seedlings.

  18. The Analysis of Activated Carbon Regeneration Technologies

    Institute of Scientific and Technical Information of China (English)

    姚芳

    2014-01-01

    A series of methods for activated carbon regeneration were briefly introduced.Such as thermal regeneration,chemical regeneration,biochemical regeneration,and newly supercritical fluid regeneration, electrochemical regeneration,light-catalyzed regeneration,and microwave radiation method,and the developing trend of activated carbon regeneration was predicted.

  19. Relation between interfacial energy and adsorption of organic micropollutants onto activated carbon

    KAUST Repository

    De Ridder, David J.

    2013-03-01

    The adsorption efficacy of 16 pharmaceuticals on six different activated carbons is correlated to the thermodynamic work of adhesion, which was derived following the surface tension component approach. Immersion calorimetry was used to determine the surface tension components of activated carbon, while contact angle measurements on compressed plates were used to determine these for solutes. We found that the acid-base surface tension components of activated carbon correlated to the activated carbon oxygen content. Solute-water interaction correlated well to their solubility, although four solutes deviated from the trend. In the interaction between solute and activated carbon, van der Waals interactions were dominant and explained 65-94% of the total interaction energy, depending on the hydrophobicity of the activated carbon and solute. A reasonable relationship (r2 > 70) was found between the calculated work of adhesion and the experimentally determined activated carbon loading. © 2012 Elsevier Ltd. All rights reserved.

  20. Production of activated carbon from TCR char

    Science.gov (United States)

    Stenzel, Fabian; Heberlein, Markus; Klinner, Tobias; Hornung, Andreas

    2016-04-01

    The utilization of char for adsorptive purposes is known since the 18th century. At that time the char was made of wood or bones and used for decoloration of fluids. In the 20th century the production of activated carbon in an industrial scale was started. The today's raw materials for activated carbon production are hard coal, peat, wood or coconut shells. All these materials entail costs especially the latter. Thus, the utilization of carbon rich residues (biomass) is an interesting economic opportunity because it is available for no costs or even can create income. The char is produced by thermo-catalytic reforming (TCR®). This process is a combination of an intermediate pyrolysis and subsequently a reforming step. During the pyrolysis step the material is decomposed in a vapor and a solid carbon enriched phase. In the second step the vapor and the solid phase get in an intensive contact and the quality of both materials is improved via the reforming process. Subsequently, the condensables are precipitated from the vapor phase and a permanent gas as well as oil is obtained. Both are suitable for heat and power production which is a clear advantage of the TCR® process. The obtained biochar from the TCR® process has special properties. This material has a very low hydrogen and oxygen content. Its stability is comparable to hard coal or anthracite. Therefore it consists almost only of carbon and ash. The latter depends from input material. Furthermore the surface structure and area can be influenced during the reforming step. Depending from temperature and residence time the number of micro pores and the surface area can be increased. Preliminary investigations with methylene blue solution have shown that a TCR® char made of digestate from anaerobic digestion has adsorptive properties. The decoloration of the solution was achieved. A further influencing factor of the adsorption performance is the particle size. Based on the results of the preliminary tests a

  1. Adsorption of Remazol Black B dye on Activated Carbon Felt

    Directory of Open Access Journals (Sweden)

    Donnaperna Lucio

    2008-11-01

    Full Text Available The adsorption of Remazol Black B (anionic dye on a microporous activated carbon felt is investigated from its aqueous solution. The surface chemistry of activated carbon is studied using X-ray microanalysis, "Boehm" titrations and pH of PZC measurements which indicates that the surface oxygenated groups are mainly acidic in nature. The kinetics of Remazol Black B adsorption is observed to be pH dependent and governed by the diffusion of the dye molecules. The experimental data can be explained by "intra-particle diffusion model". For Remazol Black B, the Khan model is best suited to simulate the adsorption isotherms.

  2. Characterization of Microporous Activated Carbon Electrodes for Electric Double-layer Capacitors

    Institute of Scientific and Technical Information of China (English)

    MENG Qing-han; LIU Ling; SONG Huai-he

    2004-01-01

    Activated carbons (ACs) with a wide range of surface areas were made from petroleum coke by means of KOH activation. The electrochemical characterization was carried out for several activated carbons used as polariz able electrodes of electric double-layer capacitors (EDLCs) in an aqueous electrolytic solution. The porous structures and electrochemical double-layer capacitance of the activated carbons were investigated by virtue of nitrogen gas adsorption and constant current cycling(CCC) methods. The relationship among the surface area, pore volume of the activated carbons and specific double-layer capacitance was discussed. It was found that the specific capacitance of ACs increased linearly with the increase of surface area. The presence of mesopores in the activated carbons with very high surface area(>2000 m2/g) was not very effective for them to be used as EDLCs. The influence of chemical characteristics of the activated carbons on the double layer formation could be considered to be negligible.

  3. Improvement of carbon fiber surface properties using electron beam irradiation

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    Carbon fiber-reinforced advance composites have been used for struetural applications, mainly on account of their mechanical properties. The main factor for a good mechanical performance of carbon fiber-reinforced composite is the interfacial interaction between its components, which are carbon fiber and polymeric matrix. The aim of this study is to improve the surface properties of the carbon fiber using ionizing radiation from an electron beam to obtain better adhesion properties in the resultant composite. EB radiation was applied on the carbon fiber itself before preparing test specimens for the mechanical tests. Experimental results showed that EB irradiation improved the tensile strength of carbon fiber samples. The maximum value in tensile strength was reached using doses of about 250kGy. After breakage, the morphology aspect of the tensile specimens prepared with irradiated and non-irradiated carbon fibers were evaluated. SEM micrographs showed modifications on the carbon fiber surface.

  4. Enhanced Capacitive Characteristics of Activated Carbon by Secondary Activation

    Institute of Scientific and Technical Information of China (English)

    YANG Hui; LU Tian-hong; Yoshio Masaki

    2004-01-01

    The effect of the improvement of commercial activated carbon(AC) on its specific capacitance and high rate capability of double layer(dl) charging/discharging process has been studied. The improvement of AC was carried out via a secondary activation under steam in the presence of catalyst NiCl2, and the suitable condition was found to be a heat treatment at about 875 ℃ for 1 h. Under those conditions, the discharge specific capacitance of the improved AC increases up to 53.67 F/g, showing an increase of about 25% as compared with that of as-received AC. The good rectangular-shaped voltammograms and A.C. impedance spectra prove that the high rate capability of the capacitor made of the improved AC is enhanced significantly. The capacitance resistance(RC) time constant of the capacitor containing the improved AC is 1.74 s, which is much lower than that of the one containing as-received AC(an RC value of 4. 73 s). It is noted that both kinds of AC samples show a similar specific surface area and pore size distribution, but some changes have taken place in the carbon surface groups, especially a decrease in the concentration of surface carbonyl groups after the improvement, which have been verified by means of X-photoelectron spectroscopy. Accordingly, it is suggested that the decrease in the concentration of surface carbonyl groups for the improved AC is beneficial to the organic electrolyte ion penetrating into the pores, thus leading to the increase in both the specific capacitance and high rate capability of the supercapacitor.

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

    Science.gov (United States)

    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.

  6. Release of Crude Oil from Silica and Calcium Carbonate Surfaces

    DEFF Research Database (Denmark)

    Liu, Xiaoyan; Yan, Wei; Stenby, Erling Halfdan;

    2016-01-01

    Adsorption and desorption of a North Sea crude oil to silica and calcium carbonate surfaces were studied by a quartz crystal microbalance, while the bare surfaces and adsorbed oil layers were characterized by atomic force microscopy and contact angle measurements. Water contact angles were measured...... on the bare surfaces, surfaces with an adsorbed oil layer, and surfaces after being exposed to aqueous salt solutions. This showed that the silica surface became more hydrophobic after oil adsorption, while the wettability of the calcium carbonate surface was not significantly changed by adsorption of an oil...... layer. A surface energy component analysis based on the acid base theory showed that oil adsorption on the surfaces depends upon apolar, acidic, and basic oil components of the crude oil and that the adsorbed oil components differ for adsorption to silica and calcium carbonate. Desorption of the crude...

  7. [Raman spectra of PAN-based carbon fibers during surface treatment].

    Science.gov (United States)

    Cao, Wei-wei; Zhu, Bo; Jing, Min; Wang, Cheng-guo

    2008-12-01

    Laser Raman spectroscopy was employed to characterize the microstructure changes of PAN based carbon fibers among different surface treatments, and the characteristics of first-order Raman spectra of carbon fibers during surface treatment were investigated in the present paper. The results show that the variety of carbon fibers' phase structures can be represented by Raman spectroscopy parameters, such as the Raman frequency shifts of main D and G bands, FWHMs and additive bands' area ratios at the positions of different Raman frequency shifts. During different surface treatment, some changes in the first-order Raman spectroscopy parameters of PAN based carbon fibers were observed, the Raman frequency shifts of D and G bands moved toward higher wavenumber, and the values of R(I(D)/I(G)) also improved, which can be used to measure the graphite crystallite size of carbon fiber. It is suggested that the graphite microstructure of carbon fibers is decomposed during surface treatment, the crystallite size is reduced, and the activity of the graphite crystallite boundary is improved. Moreover, the full-widths at half maximum (FWHM) of D and G bands both decrease, which can give information on the order of graphite microstructure and the quantity of defects in carbon fibers, and the relative bands' areas of A and D" bands also decrease, which can be attributed to the structure of amorphous carbon or some kinds of organic functional groups in carbon fibers. These differences among the spectra demonstrate that the structure of amorphous carbon in carbon fibers is easier to oxidize or decompose than multilayer graphite structure, so the relative proportion of amorphous carbon decreases during surface treatment. The conclusions obtained by Raman spectra are basically in agreement with the improvement of apparent crystallization degrees of carbon fibers during surface treatment, which were calculated by X-ray diffraction method. So the variety rules of carbon fibers' phase

  8. Carbon Sequestration on Surface Mine Lands

    Energy Technology Data Exchange (ETDEWEB)

    Donald Graves; Christopher Barton; Richard Sweigard; Richard Warner; Carmen Agouridis

    2006-03-31

    Since the implementation of the federal Surface Mining Control and Reclamation Act of 1977 (SMCRA) in May of 1978, many opportunities have been lost for the reforestation of surface mines in the eastern United States. Research has shown that excessive compaction of spoil material in the backfilling and grading process is the biggest impediment to the establishment of productive forests as a post-mining land use (Ashby, 1998, Burger et al., 1994, Graves et al., 2000). Stability of mine sites was a prominent concern among regulators and mine operators in the years immediately following the implementation of SMCRA. These concerns resulted in the highly compacted, flatly graded, and consequently unproductive spoils of the early post-SMCRA era. However, there is nothing in the regulations that requires mine sites to be overly compacted as long as stability is achieved. It has been cultural barriers and not regulatory barriers that have contributed to the failure of reforestation efforts under the federal law over the past 27 years. Efforts to change the perception that the federal law and regulations impede effective reforestation techniques and interfere with bond release must be implemented. Demonstration of techniques that lead to the successful reforestation of surface mines is one such method that can be used to change perceptions and protect the forest ecosystems that were indigenous to these areas prior to mining. The University of Kentucky initiated a large-scale reforestation effort to address regulatory and cultural impediments to forest reclamation in 2003. During the three years of this project 383,000 trees were planted on over 556 acres in different physiographic areas of Kentucky (Table 1, Figure 1). Species used for the project were similar to those that existed on the sites before mining was initiated (Table 2). A monitoring program was undertaken to evaluate growth and survival of the planted species as a function of spoil characteristics and

  9. Characterization of activated carbon produced from urban organic waste

    Directory of Open Access Journals (Sweden)

    Abdul Gani Haji

    2013-10-01

    Full Text Available The difficulties to decompose organic waste can be handled naturally by pyrolisis so it can  decomposes quickly that produces charcoal as the product. This study aims to investigate the characteristics of activated carbon from urban organic waste. Charcoal results of pyrolysis of organic waste activated with KOH 1.0 M at a temperature of 700 and 800oC for 60 to 120 minutes. Characteristics of activated carbon were identified by Furrier Transform Infra Red (FTIR, Scanning Electron Microscopy (SEM, and X-Ray Diffraction (XRD. However, their quality is determined yield, moisture content, ash, fly substances, fixed carbon, and the power of adsorption of iodine and benzene. The identified functional groups on activated carbon, such as OH (3448,5-3436,9 cm-1, and C=O (1639,4 cm-1. In general, the degree and distance between the layers of active carbon crystallites produced activation in all treatments showed no significant difference. The pattern of activated carbon surface topography structure shows that the greater the pore formation in accordance with the temperature increase the more activation time needed. The yield of activated carbon obtained ranged from 72.04 to 82.75%. The results of characterization properties of activated carbon was obtained from 1.11 to 5.41% water, 13.68 to 17.27% substance fly, 20.36 to 26.59% ash, and 56.14 to 62.31% of fixed carbon . Absorption of activated carbon was good enough at 800oC and 120 minutes of activation time, that was equal to 409.52 mg/g of iodine and 14.03% of benzene. Activated carbon produced has less good quality, because only the water content and flying substances that meet the standards.Doi: 10.12777/ijse.5.2.89-94 [How to cite this article: Haji, A.G., Pari, G., Nazar, M., and Habibati.  (2013. Characterization of activated carbon produced from urban organic waste . International Journal of Science and Engineering, 5(2,89-94. Doi: 10.12777/ijse.5.2.89-94

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

    Science.gov (United States)

    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 25-65°C and inlet CO2 concentration range of 10-30 mol% 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 273 K, 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 0.62 cm(3)/g and surface area of 1400 m(2)/g had the highest CO2 adsorption capacity of 1.8 mol/kg due to its microporous structure and high surface area under the optimized experimental conditions of 30 mol% CO2 and 25°C. 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 50 cycles with low temperature (160°C) regeneration.

  11. Iron oxide nanoparticles embedded in activated carbons prepared from hydrothermally treated waste biomass.

    Science.gov (United States)

    Hao, Wenming; Björkman, Eva; Yun, Yifeng; Lilliestråle, Malte; Hedin, Niklas

    2014-03-01

    Particles of iron oxide (Fe3O4 ; 20–40 nm) were embedded within activated carbons during the activation of hydrothermally carbonized (HTC) biomasses in a flow of CO2. Four different HTC biomass samples (horse manure, grass cuttings, beer production waste, and biosludge) were used as precursors for the activated carbons. Nanoparticles of iron oxide formed from iron catalyst included in the HTC biomasses. After systematic optimization, the activated carbons had specific surface areas of about 800 m2g1. The pore size distributions of the activated carbons depended strongly on the degree of carbonization of the precursors. Activated carbons prepared from highly carbonized precursors had mainly micropores, whereas those prepared from less carbonized precursors contained mainly mesopores. Given the strong magnetism of the activated carbon–nano-Fe3O4 composites, they could be particularly useful for water purification.

  12. CARBON SEQUESTRATION ON SURFACE MINE LANDS

    Energy Technology Data Exchange (ETDEWEB)

    Donald H. Graves; Christopher Barton; Richard Sweigard; Richard Warner

    2005-02-25

    The October-December Quarter was dedicated to analyzing the first two years tree planting activities and evaluation of the results. This included the analyses of the species success at each of the sites and quantifying the data for future year determination of research levels. Additional detailed studies have been planned to further quantify total carbon storage accumulation on the research areas. At least 124 acres of new plantings will be established in 2005 to bring the total to 500 acres or more in the study area across the state of Kentucky. During the first 2 years of activities, 172,000 tree seedlings were planted on 257 acres in eastern Kentucky and 77,520 seedlings were planted on 119 acres in western Kentucky. The quantities of each species was discussed in the first Annual Report. A monitoring program was implemented to measure treatment effects on above and below ground C and nitrogen (N) pools and fluxes. A sampling strategy was devised that will allow for statistical comparisons of the various species within planting conditions and sites. Seedling heights and diameters are measured for initial status and re-measured on an annual basis. Leaves were harvested and leaf area measurements were performed. They were then dried and weighed and analyzed for C and N. Whole trees were removed to determine biomass levels and to evaluate C and N levels in all components of the trees. Clip plots were taken to determine herbaceous production and litter was collected in baskets and gathered each month to quantify C & N levels. Soil samples were collected to determine the chemical and mineralogical characterization of each area. The physical attributes of the soils are also being determined to provide information on the relative level of compaction. Hydrology and water quality monitoring is being conducted on all areas. Weather data is also being recorded that measures precipitation values, temperature, relative humidity wind speed and direction and solar radiation

  13. The performance of supercapacitor electrodes developed from chemically activated carbon produced from waste tea

    Science.gov (United States)

    Inal, I. Isil Gurten; Holmes, Stuart M.; Banford, Anthony; Aktas, Zeki

    2015-12-01

    Highly microporous and mesoporous activated carbons were produced from waste tea for application as supercapacitor electrodes, utilising a chemical activation method involving treatment with either K2CO3 or H3PO4. The area, pore structure characteristics and surface functionality of the activated carbons were evaluated to investigate the influence on electrochemical performance. The performance of the activated carbons as supercapacitor electrodes was tested by cyclic voltammetry (CV), impedance spectroscopy (EIS) and galvanostatic charge-discharge (GCD) measurements, in an aqueous electrolyte. The results showed that the pore structure and type of the activated carbon have significant impact on the supercapacitor performance. Both waste tea-based activated carbon electrodes showed good cyclic stability. However, despite its lower specific surface area the highly microporous activated carbon produced with K2CO3, exhibited much better capacitive performance than that of the mesoporous activated carbon produced with H3PO4.

  14. Influence of adhesion to activated carbon particles on the viability of waterborne pathogenic bacteria under flow

    NARCIS (Netherlands)

    van der Mei, Henny C.; Atema-Smit, Jelly; Jager, Debbie; Langworthy, Don E.; Collias, Dimitris I.; Mitchell, Michael D.; Busscher, Henk J.

    2008-01-01

    In rural areas around the world, people often rely on water filtration plants using activated carbon particles for safe water supply. Depending on the carbon surface, adhering microorganisms die or grow to form a biofilm. Assays to assess the efficacy of activated carbons in bacterial removal do not

  15. Quality of poultry litter-derived granular activated carbon.

    Science.gov (United States)

    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.

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

    Science.gov (United States)

    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.

  17. 活性炭表面性质对染料废水生化出水深度净化效果的影响%Effects of the surface properties of activated carbon on the advanced purification of the effluent of biochemical treatment from dye wastewater

    Institute of Scientific and Technical Information of China (English)

    冯玥; 王密灵; 柳欢欢; 陈泉源

    2013-01-01

    The adsorptive effects of different kinds of activated carbon on actual wastewater are greatly different.The biochemical effluent from a large-scale dyestuff production plant has been studied by activated carbon adsorption.The adsorptive efflcacies of activated carbon with different surface properties are compared.The relationship between the adsorptive efficacy of biochemical effluent from dye wastewater and the activated carbon functional group,adsorption indexes,specific surface area are discussed.The results show that activated carbon adsorption is not only related to the specific surface area of activated carbon,but also is closely related to porous structure.The soluble organisms of biochemical effluent from dye wastewater and the activated carbon surface alkaline functional group can be adsorbed on activate carbon surface via hydrogen bond and electrostatic interaction.%不同种类活性炭对实际废水的吸附效果差异很大,由此对某大型染料生产厂的染料废水生化出水进行了活性炭吸附实验研究,对具有不同表面性质的活性炭的吸附效果进行了比较,探讨了染料废水生化出水吸附效果与活性炭表面官能团、吸附指标、比表面积之间的关系.结果表明,活性炭的吸附作用不仅与活性炭比表面积有关,还与孔结构有密切关系;染料废水生化出水中的溶解性有机物与活性炭表面碱基团可通过氢键、静电作用在活性炭表面吸附.

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

    Science.gov (United States)

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

    2012-07-27

    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 π-electron energy to investigate the role of π-π 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

  19. Adsorption Properties of Lignin-derived Activated Carbon Fibers (LACF)

    Energy Technology Data Exchange (ETDEWEB)

    Contescu, Cristian I. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Gallego, Nidia C. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Thibaud-Erkey, Catherine [United Technologies Research Center (UTRC), East Hartford, CT (United States); Karra, Reddy [United Technologies Research Center (UTRC), East Hartford, CT (United States)

    2016-04-01

    The object of this CRADA project between Oak Ridge National Laboratory (ORNL) and United Technologies Research Center (UTRC) is the characterization of lignin-derived activated carbon fibers (LACF) and determination of their adsorption properties for volatile organic compounds (VOC). Carbon fibers from lignin raw materials were manufactured at Oak Ridge National Laboratory (ORNL) using the technology previously developed at ORNL. These fibers were physically activated at ORNL using various activation conditions, and their surface area and pore-size distribution were characterized by gas adsorption. Based on these properties, ORNL did down-select five differently activated LACF materials that were delivered to UTRC for measurement of VOC adsorption properties. UTRC used standard techniques based on breakthrough curves to measure and determine the adsorption properties of indoor air pollutants (IAP) - namely formaldehyde and carbon dioxide - and to verify the extent of saturated fiber regenerability by thermal treatments. The results are summarized as follows: (1) ORNL demonstrated that physical activation of lignin-derived carbon fibers can be tailored to obtain LACF with surface areas and pore size distributions matching the properties of activated carbon fibers obtained from more expensive, fossil-fuel precursors; (2) UTRC investigated the LACF potential for use in air cleaning applications currently pursued by UTRC, such as building ventilation, and demonstrated their regenerability for CO2 and formaldehyde, (3) Both partners agree that LACF have potential for possible use in air cleaning applications.

  20. Effect of surface modification on carbon fiber and its reinforced phenolic matrix composite

    Science.gov (United States)

    Yuan, Hua; Wang, Chengguo; Zhang, Shan; Lin, Xue

    2012-10-01

    In this work, polyacrylonitrile (PAN)-based carbon fiber were chemically modified with H2SO4, KClO3 and silane coupling agent (γ-aminopropyltriethoxysilane, APS), and carbon fiber reinforced phenolic matrix composites were prepared. The structural and surface characteristics of the carbon fiber were investigated by scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), laser Raman scattering (LRS) and Fourier transform infrared spectroscopy (FTIR). Single fiber mechanical properties, specific surface area, composite impact properties and interfacial shear strength (ILSS) were researched to indicate the effects of surface modification on fibers and the interaction between modified fiber surface and phenolic matrix. The results showed that carbon fiber surface modification by oxidation and APS can strengthen fiber surface chemical activity and enlarge the fiber surface area as well as its roughness. When carbon fiber (CF) is oxidized treatment, the oxygen content as well as the O/C ratio will be obviously increased. Oxygen functional groups increase with oxidation time increasing. Carbon fiber treated with APS will make Csbnd Osbnd R content increase and Osbnd Cdbnd O content decrease due to surface reaction. Proper treatment of carbon fiber with acid and silane coupling agent prove an effective way to increase the interfacial adhesion and improve the mechanical and outdoor performance of the resulting fiber/resin composites.

  1. XPS of nitrogen-containing functional groups on activated carbon

    NARCIS (Netherlands)

    Jansen, R.J.J.; Bekkum, van H.

    1995-01-01

    XPS is used to study the binding energy of the Cls, Nls and Ols photoelectrons of surface groups on several nitrogen-containing activated carbons. Specific binding energies are assigned to amide (399.9 eV). lactam and imidc (399.7 eV). pyridine (398.7 eV), pyrrole (400.7 eV), alkylamine. secondary a

  2. Role of activated carbon on micropollutans degradation by different radiation processes

    Directory of Open Access Journals (Sweden)

    Inmaculada Velo Gala

    2015-04-01

    Full Text Available The objective of this study was to analyse the influence of the presence of activated carbon on radiation processes. The triiodinated contrast medium diatrizoate was chosen as the contaminant model. We selected four commercial activated carbons and sixteen gamma radiation-modified carbons derived from these. The different advanced oxidation/reduction processes that have been studied were improved through the addition of activated carbon in the UV light and gamma radiating processes. In the UV/activated carbon process, the synergic activity of the activated carbon is enhanced in the samples with higher percentages of surface oxygen, ester/anhydride groups and carbon atoms with sp2 hybridization. Band gap determination of activated carbons revealed that they behave as semiconductor materials and, therefore, as photoactive materials in the presence of UV radiation, given that all band gap values are <4 eV. We also observed that the gamma radiation treatment reduces the band gap values of the activated carbons and that, in a single series of commercial carbons, lower band gap values correspond to higher contaminant removal rate values. We observed that the activity of the reutilized activated carbons is similar to that of the original carbons. Based on these results, we proposed that the activated carbon acts as a photocatalyst, promoting electrons of the valence band to the conduction band and increasing the generation of HO• radicals in the medium. Similarly, there was a synergic effect made by the presence of activated carbon in gamma radiation system, which favours pollutant removal. This synergic effect is independent of the textural but not the chemical characteristics of the activated carbon, observing a higher synergic activity for carbons with a higher surface content of oxygen, specifically quinone groups. We highlight that the synergic effect of the activated carbon requires adsorbent–adsorbate electrostatic interaction and is absent

  3. Activation of Carbon Dioxide and Synthesis of Propylene Carbonate

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    Cycloaddition of carbon dioxide and propylene oxide to propylene carbonate catalyzed by tetra-tert-butyl metal phthalocyanine in the presence of tributylamine (TBA) shows higher yield than catalyzed by unsubstituted metal phthalocyanine. Comparing different catalysts of diverse metals, (t-Bu)4PcMg is more active than (t-Bu)4PcFe. But (t-Bu)4PcCo and (t-Bu)4PcNi only have low catalytic activities towards the reaction. Moreover, the yield will increase as the temperature increases.

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

    Science.gov (United States)

    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.

  5. Bimodal activated carbons derived from resorcinol-formaldehyde cryogels

    Energy Technology Data Exchange (ETDEWEB)

    Szczurek, Andrzej; Amaral-Labat, Gisele; Fierro, Vanessa; Celzard, Alain [Institut Jean Lamour-UMR CNRS 7198, CNRS-Nancy-Universite-UPV-Metz, Departement Chimie et Physique des Solides et des Surfaces. ENSTIB, 27 rue Philippe Seguin, BP 1041, 88051 Epinal cedex 9 (France); Pizzi, Antonio, E-mail: Alain.Celzard@enstib.uhp-nancy.fr [ENSTIB-LERMAB, Nancy-Universite, 27 rue Philippe Seguin, BP1041, 88051 Epinal cedex 9 (France)

    2011-06-15

    Resorcinol-formaldehyde cryogels prepared at different dilution ratios have been activated with phosphoric acid at 450 deg. C and compared with their carbonaceous counterparts obtained by pyrolysis at 900 deg. 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{sup -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 H{sub 3}PO{sub 4}, close to 2200 m{sup 2} g{sup -1} and 0.7 cm{sup 3} g{sup -1}, respectively. Activation of diluted cryogels with a lower acid concentration of 1.2 M l{sup -1} led to authentic bimodal activated carbons, having a surface area as high as 1780 m{sup 2} g{sup -1} and 0.6 cm{sup 3} g{sup -1} of microporous volume easily accessible through a widely developed macroporosity.

  6. Granular Activated Carbon Performance Capability and Availability.

    Science.gov (United States)

    1983-06-01

    Kinetics of Activated Carbon Adsorption Journal of Water Polution 47(4) Aoril 1975 Control Federation 4-t9 Wnitna) G Aoalied Polarography for...proposed models for kinetics of adsorption of pink water organics by activated carbon. Both models are basically similar in nature and propose that...include formulation of a complete model of the pink water system based upon existing data. This model would then serve to reduce the amount of

  7. CARBON SEQUESTRATION ON SURFACE MINE LANDS

    Energy Technology Data Exchange (ETDEWEB)

    Donald H. Graves; Christopher Barton; Richard Sweigard; Richard Warner

    2004-11-30

    A monitoring program to measure treatment effects on above ground, and below ground carbon and nitrogen pools for the planting areas is being conducted. The collection of soil and tissue samples from both the 2003 and 2004 plantings is complete and are currently being processed in the laboratory. Detailed studies have been initiated to address specific questions pertaining to carbon cycling. Examinations of decomposition and heterotropic respiration on carbon cycling in the reforestation plots were continued during this reporting period. A whole-tree harvesting method was employed to evaluate carbon accumulation as a function of time on the mined site. The trees were extracted from the sites and separated into the following components: foliage, stems, branches, and roots.

  8. PREPARATION OF MESOPOROUS CARBON BY CARBON DIOXIDE ACTIVATION WITH CATALYST

    Institute of Scientific and Technical Information of China (English)

    W.Z.Shen; A.H.Lu; J.T.Zheng

    2002-01-01

    A mesoporous activated carbon (AC) can be successfully prepared by catalytic activa-tion with carbon dioxide. For iron oxide as catalyst, there were two regions of mesoporesize distribution, i.e. 2-5nm and 30-70nm. When copper oxide or magnesium oxidecoexisted with iron oxide as composite catalyst, the content of pores with sizes of 2-5nm was decreased, while the pores with 30 70nm were increased significantly. Forcomparison, AC reactivated by carbon dioxide directly was also investigated. It wasshown that the size of mesopores of the resulting AC concentrated in 2-5nm with lessvolume. The adsorption of Congo red was tested to evaluate the property of the result-ing AC. Furthermore, the factors affecting pore size distribution and the possibility ofmesopore formation were discussed.

  9. Proton catalysis with active carbons and partially pyrolyzed carbonaceous materials

    Institute of Scientific and Technical Information of China (English)

    V. V. Strelko; S. S. Stavitskaya; Yu. I. Gorlov

    2014-01-01

    The development of environmentally friendly solid acid catalysts is a priority task. Highly oxidized activated carbon and their ion-substituted (saline) forms are effective proton transfer catalysts in esterification, hydrolysis, and dehydration, and thus are promising candidates as solid acid cata-lysts. Computations by the ab initio method indicated the cause for the enchanced acidity of the carboxylic groups attached to the surface of highly oxidized carbon. The synthesis of phosphorilated carbon was considered, and the proton transfer reactions catalyzed by them in recent studies were analyzed. The development of an amorphous carbon acid catalyst comprising polycyclic carbonaceous (graphene) sheets with-SO3H,-COOH and phenolic type OH-groups was carried out. These new catalysts were synthesized by partial pyrolysis and subsequent sulfonation of carbohydrates, polymers, and other organic compounds. Their high catalytic activities in proton transfere reactions including the processing of bio-based raw materials was demonsrated.

  10. Adsorption of triton X100 and potassium hydrogen phthalate on granular activated carbon from date pits

    Energy Technology Data Exchange (ETDEWEB)

    Merzougui, Z.; Nedjah, S.; Azoudj, Y.; Addoun, F. [Laboratoire d' etude physic-chimique des materiaux et application a l' environnement, Faculte de Chimie, USTHB (Algeria)], E-mail: zmerzougi@yahoo.fr

    2011-07-01

    Activated carbons, thanks to their versatility, are being used in the water treatment sector to absorb pollutants. Several factors influence the adsorption capacity of activated carbon and the aim of this study was to assess the effects of the porous texture and chemical nature of activated carbons on the adsorption of triton X100 and potassium hydrogen phthalate. Activated carbons used in this study were prepared from date pits with ZnCl2, KOH and H3PO4 by carbonization without adjuvant and adsorption of triton X100 and potassium hydrogen phthalate was conducted at 298K. Results showed that activated carbons prepared from date pits have a great potential for removing organic and inorganic pollutants from water and that the adsorption potential depends on the degree of activation of the activated carbons and on the compounds to absorb. This study highlighted that an increase of the carbon surface area and porosity results in a better adsorption capacity.

  11. ESTIMATION OF ACTIVATED ENERGY OF DESORPTION OF n—HEXANE ON ACTIVATED CARBONS BY PTD TECHNIQUE

    Institute of Scientific and Technical Information of China (English)

    LIZhong; WANGHongjuan; 等

    2001-01-01

    In this paper,six kinds of activated carbons such as Ag+-activated carbon,Cu2+activated carbon,Fe3+-activated carbon,activated carbon,Ba2+-activated carbon and Ca2+activated carbon were prepared.The model for estimating activated energy of desorption was established.Temperature-programmed desorption(TPD)experiments were conducted to measure the TPD curves of n-hexanol and then estimate the activation energy for desorption of n-hexanol on the activated carbons.Results showed that the activation energy for the desorption of n-hexanol on the Ag+-activated carbon,the Cu2+-activated carbon and the Fe3+-activated carbon were higher than those of n-hexanol on the activated carbon,the Ca2+-activated carbon and the Ba2+-activated carbon.

  12. ESTIMATION OF ACTIVATED ENERGY OF DESORPTION OF n-HEXANE ON ACTIVATED CARBONS BY TPD TECHNIQUE

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    In this paper, six kinds of activated carbons such as Ag+-activated carbon, Cu2+-activated carbon, Fe3+- activated carbon, activated carbon, Ba2+- activated carbon and Ca2+-activated carbon were prepared. The model for estimating activated energy of desorption was established. Temperature-programmed desorption (TPD) experiments were conducted to measure the TPD curves of n-hexanol and then estimate the activation energy for desorption of n-hexanol on the activated carbons. Results showed that the activation energy for the desorption of n-hexanol on the Ag+- activated carbon, the Cu2+- activated carbon and the Fe3+- activated carbon were higher than those of n-hexanol on the activated carbon, the Ca2+- activated carbon and the Ba2+- activated carbon.

  13. Effect of activated carbon and electrolyte on properties of supercapacitor

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    Effect of activated carbon and electrolyte on electrochemical properties of organic supercapacitor was investigated. The results show that specific surface area and mesoporosity of activated carbon influence specific capacitance. If specific surface area is larger and mesoporosity is higher, the specific capacitance will become bigger. Specific surface area influences resistance of carbon electrode and consequently influences power property and pore size distribution. If specific surface area is smaller and mesoporosity is higher, the power property will become better. Ash influences leakage current and electrochemical cycling stability. If ash content is lower, the performance will become better. The properties of supercapacitor highly depend on the electrolyte. The compatibility of electrolyte and activated carbon is a determining factor of supercapacitor's working voltage. LiPF6/(EC+EMC+DMC) is inappropriate for double layer capacitor. MeEt3NPF4/PC has higher specific capacitance than EtnNPFn/PC because methyl's electronegativity value is lower than ethyl and MeEt3N+ has more positive charges and stronger polarizability than Et4N+ when an ethyl is substituted by methyl.

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

    Science.gov (United States)

    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.

  15. Synthesis of High-Surface-Area Nitrogen-Doped Porous Carbon Microflowers and Their Efficient Carbon Dioxide Capture Performance.

    Science.gov (United States)

    Li, Yao; Cao, Minhua

    2015-07-01

    Sustainable carbon materials have received particular attention in CO2 capture and storage owing to their abundant pore structures and controllable pore parameters. Here, we report high-surface-area hierarchically porous N-doped carbon microflowers, which were assembled from porous nanosheets by a three-step route: soft-template-assisted self-assembly, thermal decomposition, and KOH activation. The hydrazine hydrate used in our experiment serves as not only a nitrogen source, but also a structure-directing agent. The activation process was carried out under low (KOH/carbon=2), mild (KOH/carbon=4) and severe (KOH/carbon=6) activation conditions. The mild activated N-doped carbon microflowers (A-NCF-4) have a hierarchically porous structure, high specific surface area (2309 m(2)  g(-1)), desirable micropore size below 1 nm, and importantly large micropore volume (0.95 cm(3)  g(-1)). The remarkably high CO2 adsorption capacities of 6.52 and 19.32 mmol g(-1) were achieved with this sample at 0 °C (273 K) and two pressures, 1 bar and 20 bar, respectively. Furthermore, this sample also exhibits excellent stability during cyclic operations and good separation selectivity for CO2 over N2.

  16. ACTIVATED CARBONS FROM VEGETAL RAW MATERIALS TO SOLVE ENVIRONMENTAL PROBLEMS

    Directory of Open Access Journals (Sweden)

    Viktor Mukhin

    2014-06-01

    Full Text Available Technologies for active carbons obtaining from vegetable byproducts such as straw, nut shells, fruit stones, sawdust, hydrolysis products of corn cobs and sunflower husks have been developed. The physico-chemical characteristics, structural parameters and sorption characteristics of obtained active carbons were determined. The ability of carbonaceous adsorbents for detoxification of soil against pesticides, purification of surface waters and for removal of organic pollutants from wastewaters has been evaluated. The obtained results reveal the effectiveness of their use in a number of environmental technologies.

  17. Enhanced mercuric chloride adsorption onto sulfur-modified activated carbons derived from waste tires.

    Science.gov (United States)

    Yuan, Chung-Shin; Wang, Guangzhi; Xue, Sheng-Han; Ie, Iau-Ren; Jen, Yi-Hsiu; Tsai, Hsieh-Hung; Chen, Wei-Jin

    2012-07-01

    A number of activated carbons derived from waste tires were further impregnated by gaseous elemental sulfur at temperatures of 400 and 650 degrees C, with a carbon and sulfur mass ratio of 1:3. The capabilities of sulfur diffusing into the micropores of the activated carbons were significantly different between 400 and 650 degrees C, resulting in obvious dissimilarities in the sulfur content of the activated carbons. The sulfur-impregnated activated carbons were examined for the adsorptive capacity of gas-phase mercuric chloride (HgC1) by thermogravimetric analysis (TGA). The analytical precision of TGA was up to 10(-6) g at the inlet HgCl2 concentrations of 100, 300, and 500 microg/m3, for an adsorption time of 3 hr and an adsorption temperature of 150 degrees C, simulating the flue gas emitted from municipal solid waste (MSW) incinerators. Experimental results showed that sulfur modification can slightly reduce the specific surface area of activated carbons. High-surface-area activated carbons after sulfur modification had abundant mesopores and micropores, whereas low-surface-area activated carbons had abundant macropores and mesopores. Sulfur molecules were evenly distributed on the surface of the inner pores after sulfur modification, and the sulfur content of the activated carbons increased from 2-2.5% to 5-11%. After sulfur modification, the adsorptive capacity of HgCl2 for high-surface-area sulfurized activated carbons reached 1.557 mg/g (22 times higher than the virgin activated carbons). The injection of activated carbons was followed by fabric filtration, which is commonly used to remove HgCl2 from MSW incinerators. The residence time of activated carbons collected in the fabric filter is commonly about 1 hr, but the time required to achieve equilibrium is less than 10 min. Consequently, it is worthwhile to compare the adsorption rates of HgCl2 in the time intervals of < 10 and 10-60 min.

  18. Atmospheric pressure plasma surface modification of carbon fibres

    DEFF Research Database (Denmark)

    Kusano, Yukihiro; Løgstrup Andersen, Tom; Michelsen, Poul

    2008-01-01

    Carbon fibres are continuously treated with dielectric barrier discharge plasma at atmospheric pressure in various gas conditions for adhesion improvement in mind. An x-ray photoelectron spectroscopic analysis indicated that oxygen is effectively introduced onto the carbon fibre surfaces by He, He...

  19. EFFECT OF SURFACE CHEMISTRY OF ACTIVATED CARBON ON ITS EQUILIBRIUM ADSORPTION CAPACITY FOR CO2%活性炭表面化学性质对二氧化碳吸附平衡的影响

    Institute of Scientific and Technical Information of China (English)

    张睿; 周贝; 段晓佳; 胡子君; 李俊宁; 金鸣林

    2011-01-01

    把氢氧化钾活化的石油焦基活性炭进行浓硫酸氧化,并对氧化物进行热处理,得到不同氧含量的活性炭,并用氮气物理吸附和XPS对活性炭的孔及其表面化学官能团进行了表征.研究了二氧化碳在不同氧含量活性炭上的吸附平衡容量随温度的变化以及氧含量对于二氧化碳吸附容量的影响.结果表明:在25℃~175℃和0.001 MPa~1.5 MPa的范围内,二氧化碳在活性炭上的吸附可以用Langmuir方程很好地描述,饱和覆盖度和黏附系数均随温度的升高而下降,吸附热随活性炭的氧化和热处理变化很小.随活性炭O/C比的增加,饱和覆盖度下降,而黏附系数增加.适合二氧化碳吸附的活性炭应具有适中的O/C比,O/C比太大和太小均不利于二氧化碳的吸附.%Activated carbon from petroleum coke by KOH activation was oxidized by concentrated sulfuric acid at 170 ℃ for 3 h, followed by heat treatment under protection of nitrogen at 450 and 750 'C for 3 h. The as-activated carbon, oxidized activated carbon and heat-treated carbon with different oxygen contents were characterized by nitrogen adsorption and X-ray photo-electron spectroscopy, and their adsorptive capacities for CO2 at 25 °C to 175 'C and 10 mbar to 15 000 mbar were investigated. It was found that their BET surface areas and pore size distributions were similar while their surface oxygen contents were different depending on the oxidation and heat treatment conditions. The adsorptive capacities for CO2 in the experimental conditions can be well fitted by Langmuir equation. The monolayer capacity and sticking coefficient decreased with adsorption temperature and the heat of adsorption changed little with the oxidation or heat treatment. The monolayer capacity decreased and sticking coefficient increased with O/C atom ratios. Suitable activated carbon should have a moderate O/C ratio for a better adsorption forCO2.

  20. Investigating effectiveness of activated carbons of natural sources on various supercapacitors

    Science.gov (United States)

    Faisal, Md. Shahnewaz Sabit; Rahman, Muhammad M.; Asmatulu, Ramazan

    2016-04-01

    Activated carbon can be produced from natural sources, such as pistachio and acorn shells, which can be an inexpensive and sustainable sources of natural wastes for the energy storage devices, such as supercapacitors. The carbonaceous materials used in this study were carbonized at the temperatures of 700°C and 900°C after the stabilization process at 240°C for two hours. These shells showed approximately 60% carbon yield. Carbonized nutshells were chemically activated using1wt% potassium hydroxide (KOH). Activated carbon powders with polyvinylidene fluoride (PVdF) were used to construct carbon electrodes. A 1M of tetraethylammonium tetrafluoroborate (TEABF4) and propylene carbonate (PC) were used as electrolytes. Electrochemical techniques, such as cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS) were used for the characterization of the supercapacitors. Scanning electron microscopy (SEM) was used to inspect the surface texture of the activated carbons. Activated pistachio shells carbonized at 700°C showed more porous surface texture than those carbonized at 900°C. Effects of the carbonization temperatures were studied for their electrochemical characteristics. The shells carbonized at 700°C showed better electrochemical characteristics compared to those carbonized at 900°C. The test results provided about 27,083 μF/g specific capacitance at a scan rate of 10mV/s. This study showed promising results for using these activated carbons produced from the natural wastes for supercapacitor applications.

  1. ADSORPTION OF DYES ON ACTIVATED CARBON FIBERS

    Institute of Scientific and Technical Information of China (English)

    ChenShuixia; WuChangqing; 等

    1998-01-01

    The adsorption behavior of dyes on a variety of sisal based activated carbon fibers (SACF) has been studied in this paper. The results show that this kind of ACF has excellent adsorption capacities for some organic (dye) molecules.SACF can remove nearly all methylene blue,crystal violet,bromophenol blue and Eriochrome blue black R from water after static adsorption for 24h. at 30℃. The adsorption amounts can reach more than 400mg/g when adding 50 mg SACF into 50 ml dye solution.Under the same conditions,the adsorption amounts of xylenol orange fluorescein and Eriochrome black T wree lower.On the other hand,the adsorption amounts change along with the characteristics of adsorbents.The SACFs activated above 840℃,which have higher specific surface areas and wider pore radii,have higher adsorption amounts for the dyes.The researching results also show that the adsorption rates of dyes onto SACFs decrease by the order of methylene blue,Eriochrome blue black R and crystal violet.

  2. A kinetic model for describing effect of the external surface concentration of TiO2 on the reactivity of egg-shell activated carbon supported TiO2 photocatalyst

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    The porous support supported TiO2 is considered to be the promising photocatalyst due to the fact that it is easily recovered from water and has high capacity to mineralize pollutants. Obviously, the expected structure of this kind of photocatalyst is egg-shell, that is, TiO2 is mainly on the external surface of the porous support. The reactivity of the supported photocatalyst strongly depends on the concentration of TiO2 on the external surface of the porous support. In this study, a kinetic model was developed to describe the effect of the external surface concentration of TiO2 (CESC) on the reactivity of egg-shell activated carbon (AC) supported TiO2 photocatalysts. It was found that the obtained model precisely described the effect of CESC, on the reactivity of TiO2/AC photocatalysts. This study can be used to deeply understand the performance of TiO2/AC catalysts and to provide valuable information on designing efficient supported TiO2 photocatalysts.

  3. Production and Characterization of Activated Carbon from Çanakkale-Çan Lignite by KOH and ZnCl2 Activation

    Directory of Open Access Journals (Sweden)

    Filiz Karacan

    2014-01-01

    Full Text Available Activated carbon was produced from Çanakkale-Çan lignite using potassium hydroxide (KOH and zinc chloride (ZnCl2 as activating agent. The influence of carbonization temperatures (500-900 0C and different chemical reagents (KOH and ZnCl2 on the pore development and the yield of the prepared activated carbon were investigated. The resultant activated carbons were characterized in terms of the yield, BET surface area, pore volumes, micropore and mesopore fraction. Results showed that increasing the carbonization temperature, the yield decreased, while surface area and micro-porosity increased. Maximum surface area was about 1092 m2/g at 900 0C with KOH activation and carbonization duration of 1 h. The surface area of char obtained from carbonization of lignite sample without impregnation by chemical reagent was 157 m2/g at 900 0C. From these data, it has been showed that in order to produce activated carbons with high surface area and porosity, thermal activation (without impregnation itself is not sufficient. The prepared activated carbon was compared with commercial activated carbon. Surface area and micropore fraction of activated carbons obtained from both KOH and ZnCl2 activation much larger than those of the commercial activated carbon.

  4. Activated carbon derived from carbon residue from biomass gasification and its application for dye adsorption: Kinetics, isotherms and thermodynamic studies.

    Science.gov (United States)

    Maneerung, Thawatchai; Liew, Johan; Dai, Yanjun; Kawi, Sibudjing; Chong, Clive; Wang, Chi-Hwa

    2016-01-01

    In this work, activated carbon (AC) as an effective and low-cost adsorbent was successfully prepared from carbon residue (or char, one of the by-products from woody biomass gasification) via physical activation. The surface area of char was significantly increased from 172.24 to 776.46m(2)/g after steam activation at 900°C. The obtained activated carbons were then employed for the adsorption of dye (Rhodamine B) and it was found that activated carbon obtained from steam activation exhibited the highest adsorption capability, which is mainly attributed to the higher surface area and the abundance of hydroxyl (-OH) and carboxyl (-COOH) groups on the activated carbon surface. Moreover, it was also found that the adsorption capability significantly increased under the basic condition, which can be attributed to the increased electrostatic interaction between the deprotonated (negatively charged) activated carbon and dye molecules. Furthermore, the equilibrium data were fitted into different adsorption isotherms and found to fit well with Langmuir model (indicating that dye molecules form monolayer coverage on activated carbon) with a maximum monolayer adsorption capability of 189.83mg/g, whereas the adsorption kinetics followed the pseudo-second-order kinetics.

  5. Highly active catalyst for vinyl acetate synthesis by modified activated carbon

    Institute of Scientific and Technical Information of China (English)

    Chun Yan Hou; Liang Rong Feng; Fa Li Qiu

    2009-01-01

    A new zinc acetate catalyst which was prepared from modified activated carbon exhibited extreme activity towards the synthesis of vinyl acetate. The activated carbon was modified by nitric acid, vitriol and peroxyacetic acid (PAA). The effect on specific area, structure, pH and surface acidity groups of carriers by modification was discussed. Amount of carbonyl and carboxyl groups in activated carbon was increased by peroxyacetic acid treatment. The productivity of the new catalyst was 14.58% higher than that of catalyst prepared using untreated activated carbon. The relationship between amount of carbonyl and carboxyl groups (m) and catalyst productivity (P) was P = 1.83 + 2.26 x 10-3e3.17m. Reaction mechanism was proposed.

  6. Studies on Supercapacitor Electrode Material from Activated Lignin-Derived Mesoporous Carbon

    Energy Technology Data Exchange (ETDEWEB)

    Saha, Dipendu [ORNL; Li, Yunchao [ORNL; Bi, Zhonghe [ORNL; Chen, Jihua [ORNL; Keum, Jong Kahk [ORNL; Hensley, Dale K [ORNL; Grappe, Hippolyte A. [Oak Ridge Institute for Science and Education (ORISE); Meyer III, Harry M [ORNL; Dai, Sheng [ORNL; Paranthaman, Mariappan Parans [ORNL; Naskar, Amit K [ORNL

    2014-01-01

    We synthesized mesoporous carbon from pre-cross-linked lignin gel impregnated with a surfactant as the pore-forming agent, and then activated the carbon through physical and chemical methods to obtain activated mesoporous carbon. The activated mesoporous carbons exhibited 1.5- to 6-fold increases in porosity with a maximum BET specific surface area of 1148 m2/g and a pore volume of 1.0 cm3/g. Slow physical activation helped retain dominant mesoporosity; however, aggressive chemical activation caused some loss of the mesopore volume fraction. Plots of cyclic voltammetric data with the capacitor electrode made from these carbons showed an almost rectangular curve depicting the behavior of ideal double-layer capacitance. Although the pristine mesoporous carbon exhibited the same range of surface-area-based capacitance as that of other known carbon-based supercapacitors, activation decreased the surface-area-based specific capacitance and increased the gravimetric-specific capacitance of the mesoporous carbons. Surface activation lowered bulk density and electrical conductivity. Warburg impedance as a vertical tail in the lower frequency domain of Nyquist plots supported good supercapacitor behavior for the activated mesoporous carbons. Our work demonstrated that biomass-derived mesoporous carbon materials continue to show potential for use in specific electrochemical applications.

  7. Influence of coal preoxidation on the porosity of the activated carbons with steam activation

    Energy Technology Data Exchange (ETDEWEB)

    Zhu, Yuwen; Gao, Jihui; Sun, Fei; Li, Yang; Wu, Shaohua; Qin, Yukun [Harbin Institute of Technology, Harbin (China). School of Energy Science and Engineering

    2013-07-01

    Activated carbons have been prepared from a low ash content anthracite preoxidized in air to different degrees. Steam has been used as activating agent to prepare different burn-off samples. The preoxidation effect on the physico-chemical characteristics of the resulting chars and activated carbons were comparatively studied. The surface area and porosity of sample was studied by N{sub 2} adsorption at 77 0A0;K. The results show that introduced oxygen in coal structure had a great influence on the carbonization and subsequent activation process. The carbonization of oxidized coal exhibited a broader volatile evolution with respect to temperature, and the resulting chars had a larger microporosity. The porosity of the char is a primary foundation to develop more microporosity upon activation. Activation of char from oxidized coal facilitated development of small scale micropore, however, the micropore widening was also observed at high burn-offs. Compared with development of supermicropore, the evolution of mesoporosity is hindered strongly by preoxidation treatment. The quantity of basic surface sites in activated carbons increased with an increase in oxidation degree, while the quantity of acidic sites appeared equivalent. It seemed that the amount of surface groups and the microporosity mainly developed in a parallel way.

  8. Ferrous ion oxidation by Thiobacillus ferrooxidans immobilized on activated carbon

    Institute of Scientific and Technical Information of China (English)

    ZHOU Ji-kui; QIN Wen-qing; NIU Yin-jian; LI Hua-xia

    2006-01-01

    The immobilization of Thiobacillus ferrooxidans on the activated carbon particles as support matrix was investigated. Cycling batch operation results in the complete oxidation of ferrous iron in 8 d when the modified 9 K medium is set to flow through the mini-bioreactor at a rate of 0.104 L/h at 25 ℃. The oxidation rate of ferrous iron with immobilized T. ferrooxidans is 9.38 g/(L·h). The results show that the immobilization of T. ferrooxidans on activated carbon can improve the rate of oxidation of ferrous iron. The SEM images show that a build-up of cells of T. ferrooxidans and iron precipitates is formed on the surface of activated carbon particles.

  9. Converting Poultry Litter into Activated Carbon

    Science.gov (United States)

    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...

  10. Reprogramming cellular signaling machinery using surface-modified carbon nanotubes.

    Science.gov (United States)

    Zhang, Yi; Wu, Ling; Jiang, Cuijuan; Yan, Bing

    2015-03-16

    Nanoparticles, such as carbon nanotubes (CNTs), interact with cells and are easily internalized, causing various perturbations to cell functions. The mechanisms involved in such perturbations are investigated by a systematic approach that utilizes modified CNTs and various chemical-biological assays. Three modes of actions are (1) CNTs bind to different cell surface receptors and perturb different cell signaling pathways; (2) CNTs bind to a receptor with different affinity and, therefore, strengthen or weaken signals; (3) CNTs enter cells and bind to soluble signaling proteins involved in a signaling pathway. Understanding of such mechanisms not only clarifies how CNTs cause cytotoxicity but also demonstrates a useful method to modulate biological/toxicological activities of CNTs for their various industrial, biomedical, and consumer applications.

  11. Stability of Carbon Incorpoated Semipolar GaN(1101) Surface

    Science.gov (United States)

    Akiyama, Toru; Nakamura, Kohji; Ito, Tomonori

    2011-08-01

    The structural stability of carbon incorporated GaN(1101) surfaces is theoretically investigated by performing first-principles pseudopotential calculations. The calculated surface formation energies taking account of the metal organic vapor phase epitaxy conditions demonstrate that several carbon incorporated surfaces are stabilized depending on the growth conditions. Using surface phase diagrams, which are obtained by comparing the calculated adsorption energy with vapor-phase chemical potentials, we find that the semipolar surface forms NH2 and CH2 below ˜1660 K while the polar GaN(0001) surface with CH3 is stabilized below ˜1550 K. This difference could be one of possible explanations for p-type doping on the semipolar GaN(1101) surface.

  12. Heterologous expression of the hydrophobin FcHyd5p from Fusarium culmorum in Pichia pastoris and evaluation of its surface activity and contribution to gushing of carbonated beverages.

    Science.gov (United States)

    Stübner, Matthias; Lutterschmid, Georg; Vogel, Rudi F; Niessen, Ludwig

    2010-06-30

    The class II hydrophobin FcHyd5p from Fusarium culmorum was heterologously expressed by Pichia pastoris. Transcription of the recombinant gene was confirmed by RT-PCR and expression of FcHyd5p was demonstrated using SDS-PAGE and immuno-staining with 6 x His-tag antibodies. FcHyd5p was purified and concentrated by dialysis, isoelectric focussing and the use of ultra filtration. It was demonstrated that FcHyd5p is able to change the hydrophopic properties of surfaces rendering them wettable after coating with the supernatant of recombinant P. pastoris cultures. Furthermore, due to its surface activity, FcHyd5p was able to stabilise air bubbles in aqueous solutions. The supernatant of a culture medium containing a FcHyd5p producing P. pastoris clone remained turbid for 24h and the foam stable for more than 72 h after the treatment with a homogeniser, whereas the liquid of the wild type strain clarified after 10 min and the foam disintegrated after 2h. Finally it was demonstrated, that FcHyd5p can induce spontaneous overfoaming of carbonated liquids, referred to as gushing. Addition of 2 mg freeze-dried culture supernatant from a FcHyd5p producing P. pastoris clone resulted in a lost volume of 252 ml +/- 20 per 500 ml of beer (50%) and 179 ml +/- 7 per 330 ml of carbonated water (54%), respectively. Neither untreated beer/water, nor beer/water treated with freeze-dried culture supernatant from the wild type strain showed any gushing. Furthermore, addition of 215 microg highly purified FcHyd5p resulted in a lost volume of 77 ml +/- 40 per 500 ml beer (15%).

  13. Activation and Micropore Structure Determination of Activated Carbon-Fiber Composites

    Energy Technology Data Exchange (ETDEWEB)

    Jagtoyen, M.; Derbyshire, F.

    1999-04-23

    Previous work focused on the production of carbon fiber composites and subsequently activating them to induce adsorbent properties. One problem related to this approach is the difficulty of uniformly activating large composites. In order to overcome this problem, composites have been made from pre-activated fibers. The loss of surface area upon forming the composites after activation of the fibers was investigated. The electrical resistivity and strength of these composites were compared to those made by activation after forming. It was found that the surface area is reduced by about 35% by forming the composite from pre-activated fibers. However, the properties of the activated sample are very uniform: the variation in surface area is less than {+-}0.5%. So, although the surface area is somewhat reduced, it is believed that making composites from pre-activated fibers could be useful in applications where the BET surface area is not required to be very high. The strength of the composites produced from pre-activated fibers is lower than for composites activated after forming when the carbon burnoff is below 45%. For higher burnoffs, the strength of composites made with pre-activated fibers is as good or better. In both cases, there is a dramatic decrease in strength when the fiber:binder ratio is reduced below 4:1. The electrical resistivity is slightly higher for composites made from pre-activated fibers than for composites that are activated after forming, other parameters being constant (P-200 fibers, similar carbon burnoffs). For both types of composite the resistivity was also found to increase with carbon burnoff. This is attributed to breakage of the fiber causing shorter conductive paths. The electrical resistivity also increases when the binder content is lowered, which suggests that there are fewer solid contact points between the fibers.

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

    Science.gov (United States)

    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 μm

  15. Comparison on pore development of activated carbon produced by chemical and physical activation from palm empty fruit bunch

    Science.gov (United States)

    Hidayat, A.; Sutrisno, B.

    2016-11-01

    It is well-known that activated carbon is considered to be the general adsorbent due to the large range of applications. Numerous works are being continuously published concerning its use as adsorbent for: treatment of potable water; purification of air; retention of toxins by respirators; removal of organic and inorganic pollutants from flue gases and industrial waste gases and water; recuperation of solvents and hydrocarbons volatilized from petroleum derivatives; catalysis; separation of gas mixtures (molecularsieve activated carbons); storage of natural gas and hydrogen; energy storage in supercapacitors; recovery of gold, silver and othernoble metals; etc. This work presents producing activated carbons from palm empty fruit bunch using both physical activation with CO2 and chemical activation with KOH. The resultant activated carbons were characterized by measuring their porosities and pore size distributions. A comparison of the textural characteristics and surface chemistry of the activated carbon from palm empty fruit bunch by the CO2 and the KOH activation leads to the following findings: An activated carbon by the CO2 activation under the optimum conditions has a BET surface area of 717 m2/g, while that by the KOH activation has a BET surface area of 613 m2/g. The CO2 activation generated a highly microporous carbon (92%) with a Type-I isotherm, while the KOH activation generated a mesoporous one (70%) with a type-IV isotherm, the pore volumes are 0.2135 and 0.7426 cm3.g-1 respectively. The average pore size of the activated carbons is 2.72 and 2.56 nm for KOH activation and CO2 activation, respectively. The FT-IR spectra indicated significant variation in the surface functional groups are quite different for the KOH activated and CO2 activated carbons.

  16. Studies on adsorptive desulfurization by activated carbon

    Energy Technology Data Exchange (ETDEWEB)

    Rakesh Kumar, D.; Srivastava, Vimal Chandra [Department of Chemical Engineering, Indian Institute of Technology Roorkee, Roorkee, Uttarakhand (India)

    2012-05-15

    Sulfur removal using adsorption requires a proper process parametric study to determine its optimal performance characteristics. In this study, response surface methodology was employed for sulfur removal from model oil (dibenzothiophene; DBT dissolved in iso-octane) using commercial activated carbon (CAC) as an adsorbent. Experiments were carried out as per central composite design with four input parameters such as initial concentration (C{sub 0}: 100-900 mg/L), adsorbent dosage (m: 2-22 g/L), time of adsorption (t: 15-735 min), and temperature (T: 10-50 C). Regression analysis showed good fit of the experimental data to the second-order polynomial model with coefficient of determination R{sup 2}-value of 0.9390 and Fisher F-value of 16.5. The highest removal of sulfur by CAC was obtained with m = 20 g/L, t = 6 h, and T = 30 C. (Copyright copyright 2012 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  17. Understanding the Effects of Surface Chemistry and Microstructure on the Activity and Stability of Pt Electrocatalysts on Non-Carbon Supports

    Energy Technology Data Exchange (ETDEWEB)

    Mustain, William [Univ. of Conneticut, Storrs, CT (United States)

    2015-02-12

    The objective of this project is to elucidate the effects of the chemical composition and microstructure of the electrocatalyst support on the activity, stability and utilization of supported Pt clusters.

  18. Carbon nanotube oscillator surface profiling device and method of use

    Science.gov (United States)

    Popescu, Adrian; Woods, Lilia M.; Bondarev, Igor V.

    2011-11-15

    The proposed device is based on a carbon nanotube oscillator consisting of a finite length outer stationary nanotube and a finite length inner oscillating nanotube. Its main function is to measure changes in the characteristics of the motion of the carbon nanotube oscillating near a sample surface, and profile the roughness of this surface. The device operates in a non-contact mode, thus it can be virtually non-wear and non-fatigued system. It is an alternative to the existing atomic force microscope (AFM) tips used to scan surfaces to determine their roughness.

  19. Scaling and Removal of Calcium Carbonate on Electroless Plating Surface

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    The scaling process of calcium carbonate on a low-energy heat transfer surface-electroless plating surface was investigated in a simulated cooling water system. Owing to the very low surface energy, the electroless plating surface exhibited less scaling susceptibility. A longer induction period and a lower scaling rate were obtained on the low-energy surface compared to copper surface under identical conditions. The calcite particles obtained on the electroless plating surface during the induction period were larger in size than those on copper surface because fewer crystals formed and grew at the same time on the low-energy surface. With increasing surface temperature, the induction period reduced and the scaling rate increased for the low-energy surface. When initial surface temperature was fixed, an increase in fluid velocity would reduce the induction period and increase the scaling rate due to the diffusion effect. However, when the heat flux was fixed, an increase in fluid velocity would decrease the surface temperature, and lead to a longer induction period and a lower scaling rate. The removal experiments of calcium carbonate scale indicated that during post induction period, the detachment was not obvious, while during the induction period, apparent removal of crystal particles was obtained on the electroless plating surface owing to the weak adhesion force. The more frequently the transient high hydrodynamic force acted, the more the detached crystal particles were.

  20. Preparation of functionalized and metal-impregnated activated carbon by a single-step activation method

    Science.gov (United States)

    Dastgheib, Seyed A.; Ren, Jianli; Rostam-Abadi, Massoud; Chang, Ramsay

    2014-01-01

    A rapid method to prepare functionalized and metal-impregnated activated carbon from coal is described in this paper. A mixture of ferric chloride and a sub-bituminous coal was used to demonstrate simultaneous coal activation, chlorine functionalization, and iron/iron oxides impregnation in the resulting porous carbon products. The FeCl3 concentration in the mixture, the method to prepare the FeCl3-coal mixture (solid mixing or liquid impregnation), and activation atmosphere and temperature impacted the surface area and porosity development, Cl functionalization, and iron species impregnation and dispersion in the carbon products. Samples activated in nitrogen or a simulated flue gas at 600 or 1000 °C for 1-2 min had surface areas up to ∼800 m2/g, bulk iron contents up to 18 wt%, and surface chlorine contents up to 27 wt%. Potential catalytic and adsorption application of the carbon materials was explored in catalytic wet air oxidation (CWAO) of phenol and adsorption of ionic mercury from aqueous solutions. Results indicated that impregnated activated carbons outperformed their non-impregnated counterparts in both the CWAO and adsorption tests.

  1. CARBON SEQUESTRATION ON SURFACE MINE LANDS

    Energy Technology Data Exchange (ETDEWEB)

    Donald H. Graves; Christopher Barton; Richard Sweigard; Richard Warner

    2005-06-22

    An area planted in 2004 on Bent Mountain in Pike County was shifted to the Department of Energy project to centralize an area to become a demonstration site. An additional 98.3 acres were planted on Peabody lands in western Kentucky and Bent Mountain to bring the total area under study by this project to 556.5 acres as indicated in Table 2. Major efforts this quarter include the implementation of new plots that will examine the influence of differing geologic material on tree growth and survival, water quality and quantity and carbon sequestration. Normal monitoring and maintenance was conducted and additional instrumentation was installed to monitor the new areas planted.

  2. Sulfurized activated carbon for high energy density supercapacitors

    Science.gov (United States)

    Huang, Yunxia; Candelaria, Stephanie L.; Li, Yanwei; Li, Zhimin; Tian, Jianjun; Zhang, Lili; Cao, Guozhong

    2014-04-01

    Sulfurized activated carbon (SAC), made by coating the pore surface with thiophenic sulfur functional groups from the pyrolysis of sulfur flakes, were characterized and tested for supercapacitor applications. From X-ray photoelectron spectroscopy (XPS), the sulfur content in the SAC was found to be 2.7 at%. Electrochemical properties from potentiostatic and galvanostatic measurements, and electrochemical impedance spectroscopy (EIS) were used to evaluate the effect of sulfur on porous carbon electrodes. The SAC electrode exhibits better conductivity, and an obvious increase in specific capacitance that is almost 40% higher than plain activated carbons (ACs) electrode at a high current density of 1.4 A g-1. The proposed mechanism for improved conductivity and capacitive performance due to the sulfur functional groups on ACs will be discussed.

  3. Use of cyclic voltammetry and electrochemical impedance spectroscopy for determination of active surface area of modified carbon-based electrodes; Uso da voltametria ciclica e da espectroscopia de impedancia eletroquimica na determinacao da area superficial ativa de eletrodos modificados a base de carbono

    Energy Technology Data Exchange (ETDEWEB)

    Souza, Leticia Lopes de

    2011-07-01

    Carbon-based electrodes as well the ion exchange electrodes among others have been applied mainly in the treatment of industrial effluents and radioactive wastes. Carbon is also used in fuel cells as substrate for the electrocatalysts, having high surface area which surpasses its geometric area. The knowledge of the total active area is important for the determination of operating conditions of an electrochemical cell with respect to the currents to be applied (current density). In this study it was used two techniques to determine the electrochemical active surface area of glassy carbon, electrodes and ion exchange electrodes: cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS). The experiments were carried out with KNO{sub 3} 0.1 mol.L{sup -1} solutions in a three-electrode electrochemical cell: carbon-based working electrode, platinum auxiliary electrode and Ag/AgCl reference electrode. The glassy carbon and porous carbon electrodes with geometric areas of 3.14 x 10{sup -2} and 2.83 X 10{sup -1} cm{sup 2}, respectively, were used. The ion exchange electrode was prepared by mixing graphite, carbon, ion exchange resin and a binder, and this mixture was applied in three layers on carbon felt, using a geometric area of 1.0 cm{sup 2} during the experiments. The capacitance (Cd) of the materials was determined by EIS using Bode diagrams. The value of 172 {mu}F.cm{sup -2} found for the glassy carbon is consistent with the literature data ({approx} 200 {mu}F.cm'-{sup 2}). By VC, varying the scan rate from 0.2 to 2.0 mV.s-1, the capacitance CdS (S = active surface area) in the region of the electric double layer (EDL) of each material was determined. By EIS, the values of C{sub d}, 3.0 x 10{sup -5} {mu}F.cm'-{sup 2} and 11 x 10{sup 3} {mu}F.cm-2, were found for the porous carbon and ion exchange electrodes, respectively, which allowed the determination of active surface areas as 3.73 x 106 cm{sup 2} and 4.72 cm{sup 2}. To sum up, the

  4. Investigation into the surface active groups of coal

    Institute of Scientific and Technical Information of China (English)

    XU Jing-cai; XUE Han-ling; Deng Jun; Wen Hu; ZHANG Xing-hai

    2001-01-01

    The oxidation heat of coal is the direct reason leading to coal spontaneous combustion.When coal is exposed in oxygen atmosphere, the physical adsorption and chemisorption happened, and then which resulting chemical reaction followed heat between coal and oxygen. Owing to the complexity and uncertain of molecular structure of coal, it was only reduced that bridge bonds, side chains and O2-containing functional groups in coal may be prone to oxidation in last year, but not to deeply investigate into the structures and the type of the active radicals. In this paper, according to the last achievements in coal structure research, the hypomethylether bond,hypoalkyl bond of α-carbon atom with hydroxyl and α-carbon atom with hypomethy side chain and hypomettyl bonds linking up two aromatic hydrocarbon in bridge bonds, and methoxy, aldehyde and alkyls of α-carbon atom with hydroxy in side bonds are inferred to be free radical easily to lead to oxidize coal under the ambient temperature and pressure. The order from strong to week of oxide activation of the seven surface active groups is aldehyde side chains, hypomethylether bonds, hypoalkyl bonds of α-carbon atom with hydroxyl, hypoalkyl bonds of α-carbon atom with hypomethyl, hypomethyl bonds linking up two aromatic hydrocarbon, methoxy, alkyls side chains of α-carbon atom with hydroxyl. Because of the two unsaturated molecular tracks of C2, unpaired eleotron clouds of the part of surface active groups of coal enter molecular tracks of O2 to lead to chemisorb on the conjugate effect and induced effect of surface active groups, and then chemical reaction followed heat happens in them. On the basis of change of bond energy, weighted average method is adopted to count the reactionheat value of each mol CO, CO2 and H2O. The property of coal spontaneous combustion is different for the different number and oxidability of the active structure in the coal resulting in the different oxidation heat.

  5. Activated carbon derived from marine Posidonia Oceanica for electric energy storage

    Directory of Open Access Journals (Sweden)

    N. Boukmouche

    2014-07-01

    Full Text Available In this paper, the synthesis and characterization of activated carbon from marine Posidonia Oceanica were studied. The activated carbon was prepared by a simple process namely pyrolysis under inert atmosphere. The activated carbon can be used as electrodes for supercapacitor devices. X-ray diffraction result revealed a polycrystalline graphitic structure. While scanning electron microscope investigation showed a layered structure with micropores. The EDS analysis showed that the activated carbon contains the carbon element in high atomic percentage. Electrochemical impedance spectroscopy revealed a capacitive behavior (electrostatic phenomena. The specific capacity per unit area of the electrochemical double layer of activated carbon electrode in sulfuric acid electrolyte was 3.16 F cm−2. Cyclic voltammetry and galvanostatic chronopotentiometry demonstrated that the electrode has excellent electrochemical reversibility. It has been found that the surface capacitance was strongly related to the specific surface area and pore size.

  6. The uptake of ethyl iodide on black carbon surface

    Institute of Scientific and Technical Information of China (English)

    YIN Shi; WANG WeiGang; GE MaoFa

    2008-01-01

    The importance of the iodine chemistry in the atmosphere has been demonstrated by recent observations. The uptake of ethyl iodine on black carbon surface was investigated at 298 K for the first time. Degussa FW2 (an amorphous black carbon comprising medium oxides) was used as black carbon sample. Black carbon surface was found to be deactivated in reaction with C2H5I, and the uptake coefficient (γ) was dependent on the time of exposure. The value of (2.3±0.9)×10-2 was determined for the initial uptake coefficient (γ0). The result suggests that the heterogeneous loss of C2H5I on carbonaceous aerosols may be important under the atmospheric conditions.

  7. Constraining surface carbon fluxes using in situ measurements of carbonyl sulfide and carbon dioxide

    Science.gov (United States)

    Berkelhammer, M.; Asaf, D.; Still, C.; Montzka, S.; Noone, D.; Gupta, M.; Provencal, R.; Chen, H.; Yakir, D.

    2014-02-01

    Understanding the processes that control the terrestrial exchange of carbon is critical for assessing atmospheric CO2 budgets. Carbonyl sulfide (COS) is taken up by vegetation during photosynthesis following a pathway that mirrors CO2 but has a small or nonexistent emission component, providing a possible tracer for gross primary production. Field measurements of COS and CO2 mixing ratios were made in forest, senescent grassland, and riparian ecosystems using a laser absorption spectrometer installed in a mobile trailer. Measurements of leaf fluxes with a branch-bag gas-exchange system were made across species from 10 genera of trees, and soil fluxes were measured with a flow-through chamber. These data show (1) the existence of a narrow normalized daytime uptake ratio of COS to CO2 across vascular plant species of 1.7, providing critical information for the application of COS to estimate photosynthetic CO2 fluxes and (2) a temperature-dependent normalized uptake ratio of COS to CO2 from soils. Significant nighttime uptake of COS was observed in broad-leafed species and revealed active stomatal opening prior to sunrise. Continuous high-resolution joint measurements of COS and CO2 concentrations in the boundary layer are used here alongside the flux measurements to partition the influence that leaf and soil fluxes and entrainment of air from above have on the surface carbon budget. The results provide a number of critical constraints on the processes that control surface COS exchange, which can be used to diagnose the robustness of global models that are beginning to use COS to constrain terrestrial carbon exchange.

  8. Activated Carbon, Carbon Nanofiber and Carbon Nanotube Supported Molybdenum Carbide Catalysts for the Hydrodeoxygenation of Guaiacol

    Directory of Open Access Journals (Sweden)

    Eduardo Santillan-Jimenez

    2015-03-01

    Full Text Available Molybdenum carbide was supported on three types of carbon support—activated carbon; multi-walled carbon nanotubes; and carbon nanofibers—using ammonium molybdate and molybdic acid as Mo precursors. The use of activated carbon as support afforded an X-ray amorphous Mo phase, whereas crystalline molybdenum carbide phases were obtained on carbon nanofibers and, in some cases, on carbon nanotubes. When the resulting catalysts were tested in the hydrodeoxygenation (HDO of guaiacol in dodecane, catechol and phenol were obtained as the main products, although in some instances significant amounts of cyclohexane were produced. The observation of catechol in all reaction mixtures suggests that guaiacol was converted into phenol via sequential demethylation and HDO, although the simultaneous occurrence of a direct demethoxylation pathway cannot be discounted. Catalysts based on carbon nanofibers generally afforded the highest yields of phenol; notably, the only crystalline phase detected in these samples was Mo2C or Mo2C-ζ, suggesting that crystalline Mo2C is particularly selective to phenol. At 350 °C, carbon nanofiber supported Mo2C afforded near quantitative guaiacol conversion, the selectivity to phenol approaching 50%. When guaiacol HDO was performed in the presence of acetic acid and furfural, guaiacol conversion decreased, although the selectivity to both catechol and phenol was increased.

  9. Activated carbon from vetiver roots: gas and liquid adsorption studies.

    Science.gov (United States)

    Gaspard, S; Altenor, S; Dawson, E A; Barnes, P A; Ouensanga, A

    2007-06-01

    Large quantities of lignocellulosic residues result from the industrial production of essential oil from vetiver grass (Vetiveria zizanioides) roots. These residues could be used for the production of activated carbon. The yield of char obtained after vetiver roots pyrolysis follows an equation recently developed [A. Ouensanga, L. Largitte, M.A. Arsene, The dependence of char yield on the amounts of components in precursors for pyrolysed tropical fruit stones and seeds, Micropor. Mesopor. Mater. 59 (2003) 85-91]. The N(2) adsorption isotherm follows either the Freundlich law K(F)P(alpha) which is the small alpha equation limit of a Weibull shaped isotherm or the classical BET isotherm. The surface area of the activated carbons are determined using the BET method. The K(F) value is proportional to the BET surface area. The alpha value increases slightly when the burn-off increases and also when there is a clear increase in the micropore distribution width.

  10. Selection of pecan shell based activated carbons for removal of organic and inorganic impurities from simulated well-water

    Science.gov (United States)

    Activated carbons are a byproduct from pyrolysis and have value as a purifying agent. The effectiveness of activated carbons is dependent on feedstock selection and pyrolysis conditions that modify its surface properties. Therefore, pecan shell-based activated carbons (PSACs) were prepared by soakin...

  11. Activation and micropore structure of carbon-fiber composites

    Energy Technology Data Exchange (ETDEWEB)

    Jagtoyen, M.; Derbyshire, F.; Kimber, G. [Univ. of Kentucky, Lexington, KY (United States). Center for Applied Energy Research

    1997-12-01

    Rigid, high surface area activated carbon fiber composites have been produced with high permeabilities for environmental applications in gas and water purification. The project involves a collaboration between the Oak Ridge National Laboratory (ORNL) and the Center for Applied Energy Research (CAER), University of Kentucky. The main focus of recent work has been to find a satisfactory means to uniformly activate large samples of carbon fiber composites to produce controlled pore structures. Processes have been developed using activation in steam and CO{sub 2}, and a less conventional method involving oxygen chemisorption and subsequent heat treatment. Another objective has been to explore applications for the activated composites in environmental applications related to fossil energy production.

  12. PREPARATION AND CHARACTERIZATION OF POLYMER-BASED SPHERICAL ACTIVATED CARBONS

    Institute of Scientific and Technical Information of China (English)

    Zhao-lian Zhu; Ai-min Li; Ming-fang Xia; Jin-nan Wan; Quan-xing Zhang

    2008-01-01

    A series of spherical activated carbons(SACs)with different pore structures were prepared from chloromethylated polydivinylbenzene by ZnCl2 activation.The effects of activation temperature and retention time on the yield and textural properties of the resulting SACs were studied.All the SACs are generated with high yield of above 65% and exhibit relatively high mesopore fraction(me%) of 35.7%-43.6% compared with conventional activated carbons.The sample zlc28 prepared at 800℃ for 2 h has the largest BET surface area of 891m2g-1 and pore volume of 0.489 cm3g-1,SEM and XRD analyses of zlc28 verify the presence of developed porous structure composed of disordered micrographite stacking with large amounts of interspaces in the order of nanometers.

  13. The Effect of Anodic Surface Treatment on the Oxidation of Catechols at Ultrasmall Carbon Ring Electrodes

    Science.gov (United States)

    1991-07-09

    selectivity. A model of the surface formed following anodic oxidation is consistent with previous models involving both surface cleanliness and carbon...involving both surface cleanliness and carbon structure orientation. 2 INTRODUCTION Because of the vast electroanalytical utility of carbon electrodes...of the electron transfer rate following treatment are a function of the surface cleanliness and the orientation of the carbon structure

  14. Effect of textural property of coconut shell-based activated carbon on desorption activation energy of benzothiophene

    Institute of Scientific and Technical Information of China (English)

    Moxin YU; Zhong LI; Hongxia XI; Qibin XIA; Shuwen WANG

    2008-01-01

    In this work,the effect of the textural property of activated carbons on desorption activation energy and adsorption capacity for benzothiophene (BT) was investi-gated.BET surface areas and the textural parameters of three kinds of the activated carbons,namely SY-6,SY-13 and SY-19,were measured with an ASAP 2010 instru-ment.The desorption activation energies of BT on the activated carbons were determined by temperature-pro-grammed desorption (TPD).Static adsorption experi-ments were carried out to determine the isotherms of BT on the activated carbons.The influence of the textural property of the activated carbons on desorption activa-tion energy and the adsorption capacity for BT was dis-cussed.Results showed that the BET surface areas of the activated carbons,SY-6,SY-13 and SY-19 were 1106,diameters were 1.96,2.58 and 2.16 nm,respectively.The TPD results indicated that the desorption activation energy of BT on the activated carbons,SY-6,SY-19 and SY-13 were 58.84,53.02 and 42.57 KJ/mol,respectively.The isotherms showed that the amount of BT adsorbed on the activated carbons followed the order of SY-6 > SY-19 > SY-13.The smaller the average pore diameter of the activated carbon,the stronger its adsorption for BT and the higher the activation energy required for BT desorp-tion on its surface.The Freundlich adsorption isotherm model can be properly used to formulate the adsorption behavior of BT on the activated carbons.

  15. PREPARATION OF ACTIVATED CARBON FIBER AND THEIR XENON ADSORPTION PROPERTIES (Ⅲ)-ADSORPTION ON MODIFIED ACTIVATED CARBON FIBER

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    Structures of a series of activated carbon fibers were modified by impregnating them withorganic and inorganic materials such as Methylene blue(Mb)、 p-nitrophenol (PNP)、 NaCl or byoxidizing with KMnO4 or HNO3. The influence of pore filling or chemical treatment on their xenonadsorption properties was studied. The experimental results show that Mb and PNP filling ofactivated carbon fibers result in the decrease of xenon adsorption capacities of these treated ACFs,which is due to the decrease of their surface area and micro-pore volume. However, the adsorptioncapacity increases greatly with oxidizing treatment of activated carbon fibers by 7mol/L HNO3.

  16. The adsorption of pharmaceutically active compounds from aqueous solutions onto activated carbons.

    Science.gov (United States)

    Rakić, Vesna; Rac, Vladislav; Krmar, Marija; Otman, Otman; Auroux, Aline

    2015-01-23

    In this study, the adsorption of pharmaceutically active compounds - salicylic acid, acetylsalicylic acid, atenolol and diclofenac-Na onto activated carbons has been studied. Three different commercial activated carbons, possessing ∼650, 900 or 1500m(2)g(-1) surface areas were used as solid adsorbents. These materials were fully characterized - their textural, surface features and points of zero charge have been determined. The adsorption was studied from aqueous solutions at 303K using batch adsorption experiments and titration microcalorimetry, which was employed in order to obtain the heats evolved as a result of adsorption. The maximal adsorption capacities of investigated solids for all target pharmaceuticals are in the range of 10(-4)molg(-1). The obtained maximal retention capacities are correlated with the textural properties of applied activated carbon. The roles of acid/base features of activated carbons and of molecular structures of adsorbate molecules have been discussed. The obtained results enabled to estimate the possibility to use the activated carbons in the removal of pharmaceuticals by adsorption.

  17. Water and Carbon Dioxide Adsorption at Olivine Surfaces

    Energy Technology Data Exchange (ETDEWEB)

    Kerisit, Sebastien N.; Bylaska, Eric J.; Felmy, Andrew R.

    2013-11-14

    Plane-wave density functional theory (DFT) calculations were performed to simulate water and carbon dioxide adsorption at the (010) surface of five olivine minerals, namely, forsterite (Mg2SiO4), calcio-olivine (Ca2SiO4), tephroite (Mn2SiO4), fayalite (Fe2SiO4), and Co-olivine (Co2SiO4). Adsorption energies per water molecule obtained from energy minimizations varied from -78 kJ mol-1 for fayalite to -128 kJ mol-1 for calcio-olivine at sub-monolayer coverage and became less exothermic as coverage increased. In contrast, carbon dioxide adsorption energies at sub-monolayer coverage ranged from -20 kJ mol-1 for fayalite to -59 kJ mol-1 for calcio-olivine. Therefore, the DFT calculations show a strong driving force for carbon dioxide displacement by water at the surface of all olivine minerals in a competitive adsorption scenario. Additionally, adsorption energies for both water and carbon dioxide were found to be more exothermic for the alkaline-earth (AE) olivines than for the transition-metal (TM) olivines and to not correlate with the solvation enthalpies of the corresponding divalent cations. However, a correlation was obtained with the charge of the surface divalent cation indicating that the more ionic character of the AE cations in the olivine structure relative to the TM cations leads to greater interactions with adsorbed water and carbon dioxide molecules at the surface and thus more exothermic adsorption energies for the AE olivines. For calcio-olivine, which exhibits the highest divalent cation charge of the five olivines, ab initio molecular dynamics simulations showed that this effect leads both water and carbon dioxide to react with the surface and form hydroxyl groups and a carbonate-like species, respectively.

  18. Comparison of adsorption behavior of PCDD/Fs on carbon nanotubes and activated carbons in a bench-scale dioxin generating system.

    Science.gov (United States)

    Zhou, Xujian; Li, Xiaodong; Xu, Shuaixi; Zhao, Xiyuan; Ni, Mingjiang; Cen, Kefa

    2015-07-01

    Porous carbon-based materials are commonly used to remove various organic and inorganic pollutants from gaseous and liquid effluents and products. In this study, the adsorption of dioxins on both activated carbons and multi-walled carbon nanotube was internally compared, via series of bench scale experiments. A laboratory-scale dioxin generator was applied to generate PCDD/Fs with constant concentration (8.3 ng I-TEQ/Nm(3)). The results confirm that high-chlorinated congeners are more easily adsorbed on both activated carbons and carbon nanotubes than low-chlorinated congeners. Carbon nanotubes also achieved higher adsorption efficiency than activated carbons even though they have smaller BET-surface. Carbon nanotubes reached the total removal efficiency over 86.8 % to be compared with removal efficiencies of only 70.0 and 54.2 % for the two other activated carbons tested. In addition, because of different adsorption mechanisms, the removal efficiencies of carbon nanotubes dropped more slowly with time than was the case for activated carbons. It could be attributed to the abundant mesopores distributed in the surface of carbon nanotubes. They enhanced the pore filled process of dioxin molecules during adsorption. In addition, strong interactions between the two benzene rings of dioxin molecules and the hexagonal arrays of carbon atoms in the surface make carbon nanotubes have bigger adsorption capacity.

  19. Surface bioactivity of plasma implanted silicon and amorphous carbon

    Institute of Scientific and Technical Information of China (English)

    Paul K CHU

    2004-01-01

    Plasma immersion ion implantation and deposition (PⅢ&D) has been shown to be an effective technique to enhance the surface bioactivity of materials. In this paper, recent progress made in our laboratory on plasma surface modification single-crystal silicon and amorphous carbon is reviewed. Silicon is the most important material in the integrated circuit industry but its surface biocompatibility has not been investigated in details. We have recently performed hydrogen PⅢ into silicon and observed the biomimetic growth of apatite on its surface in simulated body fluid. Diamond-like carbon (DLC) is widely used in the industry due to its excellent mechanical properties and chemical inertness. The use of this material in biomedical engineering has also attracted much attention. It has been observed in our laboratory that doping DLC with nitrogen by means of PⅢ can improve the surface blood compatibility. The properties as well as in vitro biological test results will be discussed in this article.

  20. Pesticide removal by combined ozonation and granular activated carbon filtration

    OpenAIRE

    Orlandini, E.

    1999-01-01

    Since the seventies, new water treatment processes have been introduced in the production of drinking water from surface water. Their major aim was to adequately cope with the disinfection of this water, and/or with the removal of pesticides and other organic micropollutants from it. This research focused on Biological Activated Carbon (BAC) filtration, which is a combination of ozonation and GAC filtration. Its general goal was identification and understanding of the mechanisms that underlie...

  1. SURFACE MORPHOLOGY OF CARBON FIBER POLYMER COMPOSITES AFTER LASER STRUCTURING

    Energy Technology Data Exchange (ETDEWEB)

    Sabau, Adrian S [ORNL; Chen, Jian [ORNL; Jones, Jonaaron F. [University of Tennessee (UT); Alexandra, Hackett [University of Tennessee (UT); Jellison Jr, Gerald Earle [ORNL; Daniel, Claus [ORNL; Warren, Charles David [ORNL; Rehkopf, Jackie D. [Plasan Carbon Composites

    2015-01-01

    The increasing use of Carbon Fiber Polymer Composite (CFPC) as a lightweight material in automotive and aerospace industries requires the control of surface morphology. In this study, the composites surface was prepared by ablating the resin in the top fiber layer of the composite using an Nd:YAG laser. The CFPC specimens with T700S carbon fiber and Prepreg - T83 resin (epoxy) were supplied by Plasan Carbon Composites, Inc. as 4 ply thick, 0/90o plaques. The effect of laser fluence, scanning speed, and wavelength was investigated to remove resin without an excessive damage of the fibers. In addition, resin ablation due to the power variation created by a laser interference technique is presented. Optical property measurements, optical micrographs, 3D imaging, and high-resolution optical profiler images were used to study the effect of the laser processing on the surface morphology.

  2. DLVO interactions of carbon nanotubes with isotropic planar surfaces.

    Science.gov (United States)

    Wu, Lei; Gao, Bin; Tian, Yuan; Muñoz-Carpena, Rafael; Zigler, Kirk J

    2013-03-26

    Knowledge of the interaction between carbon nanotubes (CNTs) and planar surfaces is essential to optimizing CNT applications as well as reducing their environmental impact. In this work, the surface element integration (SEI) technique was coupled with the DLVO theory to determine the orientation-dependent interaction energy between a single-walled carbon nanotube (SWNT) and an infinite isotropic planar surface. For the first time, an analytical formula was developed to describe accurately the interaction between not only pristine but also surface-charged CNTs and planar surfaces with arbitrary rotational angles. Compared to other methods, the new analytical formulas were either more convenient or more accurate in describing the interaction between CNTs and planar surfaces, especially with respect to arbitrary angles. The results revealed the complex dependences of both force and torque between SWNTs and planar surfaces on the separation distances and rotational angles. With minor modifications, the analytical formulas derived for SWNTs can also be applied to multiwalled carbon nanotubes (MWNTs). The new analytical expressions presented in this work can be used as a robust tool to describe the DLVO interaction between CNTs and planar surfaces under various conditions and thus to assist in the design and application of CNT-based products.

  3. Structural Characterization and Property Study on the Activated Alumina-activated Carbon Composite Material

    Institute of Scientific and Technical Information of China (English)

    CHEN Yan-Qing; WU Ren-Ping; YE Xian-Feng

    2012-01-01

    AlCl3,NH3·H2O,HNO3 and activated carbon were used as raw materials to prepare one new type of activated alumina-activated carbon composite material.The influence of heat treatment conditions on the structure and property of this material was discussed;The microstructures of the composite material were characterized by XRD,SEM,BET techniques;and its formaldehyde adsorption characteristic was also tested.The results showed that the optimal heat treatment temperature of the activated alumina-activated carbon composite material was 450 ℃,iodine adsorption value was 441.40 mg/g,compressive strength was 44 N,specific surface area was 360.07 m2/g,average pore size was 2.91 nm,and pore volume was 0.26 m3/g.According to the BET pore size distribution diagram,the composite material has dual-pore size distribution structure,the micro-pore distributes in the range of 0.6-1.7 nm,and the meso-pore in the range of 3.0-8.0 nm.The formaldehyde adsorption effect of the activated alumina-activated carbon composite material was excellent,much better than that of the pure activated carbon or activated alumina,and its saturated adsorption capacity was 284.19 mg/g.

  4. DEVELOPMENT OF A CL-IMPREGNATED ACTIVATED CARBON FOR ENTRAINED-FLOW CAPTURE OF ELEMENTAL MERCURY

    Science.gov (United States)

    Efforts to discern the role of an activated carbon's surface functional groups on the adsorption of elemental mercury [Hg(0)] and mercuric chloride demonstrated that chlorine (Cl) impregnation of a virgin activated carbon using dilute solutions of hydrogen chloride leads to incre...

  5. EFFECT OF MOISTURE ON ADSORPTION OF ELEMENTAL MERCURY BY ACTIVATED CARBON

    Science.gov (United States)

    The paper discusses experiments using activated carbon to capture elemental mercury (Hgo), and a bench-scale dixed-bed reactor and a flow reactor to determine the role of surface moisture in Hgo adsorption. Three activated-carbon samples, with different pore structure and ash co...

  6. CHARACTERIZATION OF ACTIVATED CARBONS' PHYSICAL AND CHEMICAL PROPERTIES IN RELATION TO THEIR MERCURY ADSORPTION

    Science.gov (United States)

    The paper gives results of a characterization of the physical and chemical properties of the activated carbons used for elemental mercury (Hgo) adsorption, in order to understand the role of oxygen surface functional groups on the mechanism of Hgo adsorption by activated carbons....

  7. Studies on supercapacitor electrode material from activated lignin-derived mesoporous carbon.

    Science.gov (United States)

    Saha, Dipendu; Li, Yunchao; Bi, Zhonghe; Chen, Jihua; Keum, Jong K; Hensley, Dale K; Grappe, Hippolyte A; Meyer, Harry M; Dai, Sheng; Paranthaman, M Parans; Naskar, A K

    2014-01-28

    We synthesized mesoporous carbon from pre-cross-linked lignin gel impregnated with a surfactant as the pore-forming agent and then activated the carbon through physical and chemical methods to obtain activated mesoporous carbon. The activated mesoporous carbons exhibited 1.5- to 6-fold increases in porosity with a maximum Brunauer-Emmett-Teller (BET) specific surface area of 1148 m(2)/g and a pore volume of 1.0 cm(3)/g. Both physical and chemical activation enhanced the mesoporosity along with significant microporosity. Plots of cyclic voltammetric data with the capacitor electrode made from these carbons showed an almost rectangular curve depicting the behavior of ideal double-layer capacitance. Although the pristine mesoporous carbon exhibited a range of surface-area-based capacitance similar to that of other known carbon-based supercapacitors, activation decreased the surface-area-based specific capacitance and enhanced the gravimetric specific capacitance of the mesoporous carbons. A vertical tail in the lower-frequency domain of the Nyquist plot provided additional evidence of good supercapacitor behavior for the activated mesoporous carbons. We have modeled the equivalent circuit of the Nyquist plot with the help of two constant phase elements (CPE). Our work demonstrated that biomass-derived mesoporous carbon materials continue to show potential for use in specific electrochemical applications.

  8. Study on electroactive and electrocatalytic surfaces of single walled carbon nanotube-modified electrodes

    Energy Technology Data Exchange (ETDEWEB)

    Salinas-Torres, David [Departamento de Quimica Fisica and Instituto Universitario de Materiales de Alicante, Universidad de Alicante, Apdo. de Correos 99, E-03080 Alicante (Spain); Huerta, Francisco [Departamento de Ingenieria Textil y Papelera, Universidad Politecnica de Valencia, Plaza Ferrandiz y Carbonell, 1. E-03801 Alcoy (Spain); Montilla, Francisco, E-mail: francisco.montilla@ua.e [Departamento de Quimica Fisica and Instituto Universitario de Materiales de Alicante, Universidad de Alicante, Apdo. de Correos 99, E-03080 Alicante (Spain); Morallon, Emilia [Departamento de Quimica Fisica and Instituto Universitario de Materiales de Alicante, Universidad de Alicante, Apdo. de Correos 99, E-03080 Alicante (Spain)

    2011-02-01

    An investigation of the electrocatalysis of single-walled carbon nanotubes modified electrodes has been performed in this work. Nanotube-modified electrodes present a surface area much higher than the bare glassy carbon surfaces as determined by capacitance measurements. Several redox probes were selected for checking the reactivity of specific sites at the carbon nanotube surface. The presence of carbon nanotubes on the electrode improves the kinetics for all the reactions studied compared with the bare glassy carbon electrode with variations of the heterogeneous electron transfer rate constant up to 5 orders of magnitude. The most important effects are observed for the benzoquinone/hydroquinone and ferrocene/ferricinium redox couples, which show a remarkable improvement of their electron transfer kinetics on SWCNT-modified electrodes, probably due to strong {pi}-{pi} interaction between the organic molecules and the walls of the carbon nanotubes. For many of the reactions studied, less than 1% of the nanotube-modified electrode surface is transferring charge to species in solution. This result suggests that only nanotube tips are active sites for the electron transfer in such cases. On the contrary, the electroactive surface for the reactions of ferrocene and quinone is higher indicating that the electron transfer is produced also from the nanotube walls.

  9. A highly permeable and enhanced surface area carbon-cloth electrode for vanadium redox flow batteries

    Science.gov (United States)

    Zhou, X. L.; Zhao, T. S.; Zeng, Y. K.; An, L.; Wei, L.

    2016-10-01

    In this work, a high-performance porous electrode, made of KOH-activated carbon-cloth, is developed for vanadium redox flow batteries (VRFBs). The macro-scale porous structure in the carbon cloth formed by weaving the carbon fibers in an ordered manner offers a low tortuosity (∼1.1) and a broad pore distribution from 5 μm to 100 μm, rendering the electrode a high hydraulic permeability and high effective ionic conductivity, which are beneficial for the electrolyte flow and ion transport through the porous electrode. The use of KOH activation method to create nano-scale pores on the carbon-fiber surfaces leads to a significant increase in the surface area for redox reactions from 2.39 m2 g-1 to 15.4 m2 g-1. The battery assembled with the present electrode delivers an energy efficiency of 80.1% and an electrolyte utilization of 74.6% at a current density of 400 mA cm-2, as opposed to an electrolyte utilization of 61.1% achieved by using a conventional carbon-paper electrode. Such a high performance is mainly attributed to the combination of the excellent mass/ion transport properties and the high surface area rendered by the present electrode. It is suggested that the KOH-activated carbon-cloth electrode is a promising candidate in redox flow batteries.

  10. Activated carbon derived from waste coffee grounds for stable methane storage.

    Science.gov (United States)

    Kemp, K Christian; Baek, Seung Bin; Lee, Wang-Geun; Meyyappan, M; Kim, Kwang S

    2015-09-25

    An activated carbon material derived from waste coffee grounds is shown to be an effective and stable medium for methane storage. The sample activated at 900 °C displays a surface area of 1040.3 m(2) g(-1) and a micropore volume of 0.574 cm(3) g(-1) and exhibits a stable CH4 adsorption capacity of ∼4.2 mmol g(-1) at 3.0 MPa and a temperature range of 298 ± 10 K. The same material exhibits an impressive hydrogen storage capacity of 1.75 wt% as well at 77 K and 100 kPa. Here, we also propose a mechanism for the formation of activated carbon from spent coffee grounds. At low temperatures, the material has two distinct types with low and high surface areas; however, activation at elevated temperatures drives off the low surface area carbon, leaving behind the porous high surface area activated carbon.

  11. Decolorization of sugar syrups using commercial and sugar beet pulp based activated carbons.

    Science.gov (United States)

    Mudoga, H L; Yucel, H; Kincal, N S

    2008-06-01

    Sugar syrup decolorization was studied using two commercial and eight beet pulp based activated carbons. In an attempt to relate decolorizing performances to other characteristics, surface areas, pore volumes, bulk densities and ash contents of the carbons in the powdered form; pH and electrical conductivities of their suspensions and their color adsorption properties from iodine and molasses solution were determined. The color removal capabilities of all carbons were measured at 1/100 (w/w) dosage, and isotherms were determined on better samples. The two commercial activated carbons showed different decolorization efficiencies; which could be related to their physical and chemical properties. The decolorization efficiency of beet pulp carbon prepared at 750 degrees C and activated for 5h using CO2 was much better than the others and close to the better one of the commercial activated carbons used. It is evident that beet pulp is an inexpensive potential precursor for activated carbons for use in sugar refining.

  12. Influence of KOH activation techniques on pore structure and electrochemical property of carbon electrode materials

    Institute of Scientific and Technical Information of China (English)

    LI Jing; LI Jie; LAI Yan-qing; SONG Hai-sheng; ZHANG Zhi-an; LIU Ye-xiang

    2006-01-01

    Taking the selection of coal-tar pitch as precursor and KOH as activated agent, the activated carbon electrode material was fabricated for supercapacitor. The surface area and the pore structure of activated carbon were analyzed by Nitro adsorption method. The electrochemical properties of the activated carbons were determined using two-electrode capacitors in 6 mol/L KOH aqueous electrolytes. The influences of activated temperature and mass ratio ofKOH to C on the pore structure and electrochemical property of porous activated carbon were investigated in detail. The reasons for the changes of pore structure and electrochemical performance of activated carbon prepared under different conditions were also discussed theoretically. The results indicate that the maximum specific capacitance of 240 F/g can be obtained in alkaline medium, and the surface area, the pore structure and the specific capacitance of activated carbon depend on the treatment methods; the capacitance variation of activated carbon cannot be interpreted only by the change of surface area and pore structure, the lattice order and the electrolyte wetting effect of the activated carbon should also be taken into account.

  13. Electrochemical characteristics of activated carbon nanofiber electrodes for supercapacitors

    Energy Technology Data Exchange (ETDEWEB)

    Seo, Min-Kang [Dept. of Chemistry, Inha University, 253, Nam-gu, Incheon 402-751 (Korea, Republic of); Park, Soo-Jin [Dept. of Chemistry, Inha University, 253, Nam-gu, Incheon 402-751 (Korea, Republic of)], E-mail: sjpark@inha.ac.kr

    2009-08-25

    In this work, poly(amide imide) solutions in dimethylformamide were electrospun into webs consisting of 350 nm ultrafine nanofibers. These nanofiber webs were used to produce activated carbon nanofibers (ACNFs), through stabilization and carbonisation-activation processes. Experimental results indicated that ACNFs activated at 800 deg. C afforded the highest specific surface area but low mesopore volume. The high specific surface area, mainly due to the micropores, introduced maximum specific capacitance at low current density (150 F g{sup -1} at 10 mA g{sup -1}). Elevating the volume fraction of mesopores gave maximum specific capacitance at high current density (100 F g{sup -1} at 1000 mA g{sup -1}), which could be explained on the basis of ion mobility in the pores. Thus, the capacitance of the supercapacitors was strongly dependent on the specific surface area and micro- or mesopore volume of the ACNFs.

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

    Science.gov (United States)

    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.

  15. Surface characterization of silver and palladium modified glassy carbon

    Indian Academy of Sciences (India)

    Aleksandra A Perić-Grujić; Olivera M Nešković; Miomir V Veljković; Zoran V Laušević; Mila D Laušević

    2007-12-01

    In this work, the influence of silver and palladium on the surface of undoped, boron doped and phosphorus doped glassy carbon has been studied. The silver and palladium concentrations in solution, after metal deposition, were measured by atomic absorption spectrophotometer. The morphology of metal coatings was characterized by scanning electron microscopy. In order to investigate the nature and thermal stability of surface oxygen groups, temperature-programmed desorption method combined with mass spectrometric analyses, was performed. The results obtained have shown that silver and palladium spontaneously deposit from their salt solutions at the surface of glassy carbon samples. Silver deposits have dendrite structure, whilst palladium forms separate clusters. The highest amount of both silver and palladium deposits at the surface of sample containing the highest quantity of surface oxide complexes. It has been concluded that carboxyl groups and structure defects are responsible for metal reduction. Calculated desorption energies have shown that the surface modification by metal deposition leads to the formation of more stable surface of undoped and doped glassy carbon samples.

  16. Production Scale-Up or Activated Carbons for Ultracapacitors

    Energy Technology Data Exchange (ETDEWEB)

    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.

  17. Computational Chemistry Approach to Interpret the Crystal Violet Adsorption on Golbasi Lignite Activated Carbon

    Science.gov (United States)

    Depci, Tolga; Sarikaya, Musa; Prisbrey, Keith A.; Yucel, Aysegul

    2016-10-01

    In this paper, adsorption mechanism of Crystal Violet (CV) dye from the aqueous solution on the activated carbon prepared from Golbasi lignite was explained and interpreted by a computational chemistry approach and experimental studies. Molecular dynamic simulations and Ab initio frontier orbital analysis indicated relatively high energy and electron transfer processes during adsorption, and molecular dynamics simulations showed CV dye molecules moving around on the activated carbon surface after adsorption, facilitating penetration into cracks and pores. The experimental results supported to molecular dynamic simulation and showed that the monolayer coverage occurred on the activated carbon surface and each CV dye ion had equal sorption activation energy.

  18. Carbon nanofibers grafted on activated carbon as an electrode in high-power supercapacitors.

    Science.gov (United States)

    Gryglewicz, Grażyna; Śliwak, Agata; Béguin, François

    2013-08-01

    A hybrid electrode material for high-power supercapacitors was fabricated by grafting carbon nanofibers (CNFs) onto the surface of powdered activated carbon (AC) through catalytic chemical vapor deposition (CCVD). A uniform thin layer of disentangled CNFs with a herringbone structure was deposited on the carbon surface through the decomposition of propane at 450 °C over an AC-supported nickel catalyst. CNF coating was controlled by the reaction time and the nickel content. The superior CNF/AC composite displays excellent electrochemical performance in a 0.5 mol L(-1) solution of K2 SO4 due to its unique structure. At a high scan rate (100 mV s(-1) ) and current loading (20 A g(-1) ), the capacitance values were three- and fourfold higher than those for classical AC/carbon black composites. Owing to this feature, a high energy of 10 Wh kg(-1) was obtained over a wide power range in neutral medium at a voltage of 0.8 V. The significant enhancement of charge propagation is attributed to the presence of herringbone CNFs, which facilitate the diffusion of ions in the electrode and play the role of electronic bridges between AC particles. An in situ coating of AC with short CNFs (below 200 nm) is a very attractive method for producing the next generation of carbon composite materials with a high power performance in supercapacitors working in neutral medium.

  19. Systematic Analysis of Carbon Dioxide Activation of Waste Tire by Factorial Design

    Institute of Scientific and Technical Information of China (English)

    P.P.M. Fung; W.H-Cheung; G. McKay

    2012-01-01

    In this study, waste tire was used as raw material for the production of activated carbons through pyrolysis. 'Fire char was first produced by carbomzation at 550℃ under nitrogen. A two tactortal design was used to optimize the production of activated carbon from tire char. The effects of several factors controlling the activation process, such as temperature (.830-930℃), time (2-6h) and percentage ot carbon dioxide (70%-100%) were investigated. The production was described mathematically as a function of these three factors. First order modeling equations were developed for surface area, yield and mesopore volume. It was concluded that the yield, BET surface area and mesopore volume of activated carbon were most sensitive to activation temperature and time while percentage of carbon dioxide in the activation gas was a less significant factor.

  20. Adsorption characteristics of acetone, chloroform and acetonitrile on sludge-derived adsorbent, commercial granular activated carbon and activated carbon fibers.

    Science.gov (United States)

    Tsai, Jiun-Horng; Chiang, Hsiu-Mei; Huang, Guan-Yinag; Chiang, Hung-Lung

    2008-06-15

    The adsorption characteristics of chloroform, acetone, and acetonitrile on commercial activated carbon (C1), two types of activated carbon fibers (F1 and F2), and sludge adsorbent (S1) was investigated. The chloroform influent concentration ranged from 90 to 7800 ppm and the acetone concentration from 80 to 6900 ppm; the sequence of the adsorption capacity of chloroform and acetone on adsorbents was F2>F1 approximately C1 approximately S1. The adsorption capacity of acetonitrile ranged from 4 to 100 mg/g, corresponding to the influent range from 43 to 2700 ppm for C1, S1, and F1. The acetonitrile adsorption capacity of F2 was approximately 20% higher than that of the other adsorbents at temperaturescarbon fibers is higher than that of the other adsorbents due to their smaller fiber diameter and higher surface area. The micropore diffusion coefficient of VOC on activated carbon and sludge adsorbent was approximately 10(-4) cm2 s(-1). The diffusion coefficient of VOC on carbon fibers ranged from 10(-8) to 10(-7) cm2 s(-1). The small carbon fiber pore size corresponds to a smaller diffusion coefficient.

  1. Effects of microwave heating on porous structure of regenerated powdered activated carbon used in xylose.

    Science.gov (United States)

    Li, Wei; Wang, Xinying; Peng, Jinhui

    2014-01-01

    The regeneration of spent powdered activated carbons used in xylose decolourization by microwave heating was investigated. Effects of microwave power and microwave heating time on the adsorption capacity of regenerated activated carbons were evaluated. The optimum conditions obtained are as follows: microwave power 800W; microwave heating time 30min. Regenerated activated carbon in this work has high adsorption capacities for the amount of methylene blue of 16 cm3/0.1 g and the iodine number of 1000.06mg/g. The specific surface areas of fresh commercial activated carbon, spent carbon and regenerated activated carbon were calculated according to the Brunauer, Emmett and Teller method, and the pore-size distributions of these carbons were characterized by non-local density functional theory (NLDFT). The results show that the specific surface area and the total pore volume of regenerated activated carbon are 1064 m2/g and 1.181 mL/g, respectively, indicating the feasibility of regeneration of spent powdered activated carbon used in xylose decolourization by microwave heating. The results of surface fractal dimensions also confirm the results of isotherms and NLDFT.

  2. Voltammetric Response of Epinephrine at Carbon Nanotube Modified Glassy Carbon Electrode and Activated Glassy Carbon Electrode

    Institute of Scientific and Technical Information of China (English)

    WANG Juan; TANG Ping; ZHAO Fa-qiong; ZENG Bai-zhao

    2005-01-01

    The electrochemical behavior of epinephrine at activated glassy carbon electrode and carbon nanotube-coated glassy carbon electrode was studied. Epinephrine could exhibit an anodic peak at about 0.2 V (vs. SCE) at bare glassy carbon electrode, but it was very small.However, when the electrode was activated at certain potential (i. e. 1.9V) or modified with carbon nanotube, the peak became more sensitive,resulting from the increase in electrode area in addition to the electrostatic attraction. Under the selected conditions, the anodic peak current was linear to epinephrine concentration in the range of 3.3 × 10-7-1.1 × 10-5mol/L at activated glassy carbon electrode and in the range of 1.0 × 10-6-5.0 × 10-5 mol/L at carbon nanotube-coated electrode. The correlation coefficients were 0. 998 and 0. 997, respectively. The determination limit was 1.0 × 10-7 mol/L. The two electrodes have been successfully applied for the determination of epinephrine in adrenaline hydrochloride injection with recovery of 95%-104%.

  3. Cooperative redox activation for carbon dioxide conversion

    Science.gov (United States)

    Lian, Zhong; Nielsen, Dennis U.; Lindhardt, Anders T.; Daasbjerg, Kim; Skrydstrup, Troels

    2016-12-01

    A longstanding challenge in production chemistry is the development of catalytic methods for the transformation of carbon dioxide into useful chemicals. Silane and borane promoted reductions can be fined-tuned to provide a number of C1-building blocks under mild conditions, but these approaches are limited because of the production of stoichiometric waste compounds. Here we report on the conversion of CO2 with diaryldisilanes, which through cooperative redox activation generate carbon monoxide and a diaryldisiloxane that actively participate in a palladium-catalysed carbonylative Hiyama-Denmark coupling for the synthesis of an array of pharmaceutically relevant diarylketones. Thus the disilane reagent not only serves as the oxygen abstracting agent from CO2, but the silicon-containing `waste', produced through oxygen insertion into the Si-Si bond, participates as a reagent for the transmetalation step in the carbonylative coupling. Hence this concept of cooperative redox activation opens up for new avenues in the conversion of CO2.

  4. Surface characteristics of carbon fibers modified by direct oxyfluorination.

    Science.gov (United States)

    Seo, Min-Kang; Park, Soo-Jin

    2009-02-01

    The effect of oxyfluorinated conditions on the surface characteristics of carbon fibers was investigated. Infrared (IR) spectroscopy results indicated that the oxyfluorinated carbon fibers showed carboxyl/ester groups (CO) at 1632 cm(-1) and hydroxyl groups (OH) at 3450 cm(-1) and had a higher OH peak intensity than that of the fluorinated ones. X-ray photoelectron spectroscopy (XPS) results for the fibers also showed that oxyfluorination introduced a much higher oxygen concentration onto the fiber surfaces than fluorination with F(2) only. Additionally, contact-angle results showed that the surface was better wetted by following oxyfluorination and that the polarity of the surface was increased by increasing the oxyfluorination temperature.

  5. Modeling of hydrogen adsorption on activated carbon and SWNT nanotubes

    Energy Technology Data Exchange (ETDEWEB)

    Benard, P.; Chahine, R. [Quebec Univ., Hydrogen Research Institute, Trois Rivieres, PQ (Canada)

    1999-12-01

    The physical properties of hydrogen adsorption on activated carbon over a temperature range of 77 to 273 degrees K and pressure range 0 to 6 MPa are discussed. Results show that for the hydrogen/activated carbon system over a wide temperature and pressure range the Langmuir model is adequate, however, at low temperatures and high pressures a new approach is required, one that takes into account excess adsorption and adsorbate-adsorbate interactions. Under these conditions the Ono-Kondo approach is more appropriate. The adsorption properties of hydrogen on single-walled nanotubes (SWNT) were also studied using the Stan and Cole potential to account for the effect of the cylindrical geometry of the nanotubes on the adsorption properties. Comparison of the adsorption properties of activated carbon and SWNTs showed that the larger specific surfaces on activated carbon can lead to larger adsorption effects at higher pressures, even though the adsorption energy is smaller. SWNTs are effective only at low pressures. 5 refs., 3 figs.

  6. Metal-loaded polystyrene-based activated carbons as DBT removal media via reactive adsorption

    OpenAIRE

    2006-01-01

    [EN] To improve the desulfurization capability of activated carbons, new metal-loaded carbon-based sorbents containing sodium, cobalt, copper, and silver highly dispersed within the carbon matrix were prepared and tested at room temperature for dibenzothiophene (DBT) adsorption. The content of metals can be controlled by selective washing. The new adsorbents showed good adsorption capacities and selectivity towards DBT. The metals incorporated to the surface act not only as active sites for s...

  7. Corn stalks char from fast pyrolysis as precursor material for preparation of activated carbon in fluidized bed reactor.

    Science.gov (United States)

    Wang, Zhiqi; Wu, Jingli; He, Tao; Wu, Jinhu

    2014-09-01

    Corn stalks char from fast pyrolysis was activated by physical and chemical activation process in a fluidized bed reactor. The structure and morphology of the carbons were characterized by N2 adsorption and SEM. Effects of activation time and activation agents on the structure of activation carbon were investigated. The physically activated carbons with CO2 have BET specific surface area up to 880 m(2)/g, and exhibit microporous structure. The chemically activated carbons with H3PO4 have BET specific surface area up to 600 m(2)/g, and exhibit mesoporous structure. The surface morphology shows that physically activated carbons exhibit fibrous like structure in nature with long ridges, resembling parallel lines. Whereas chemically activated carbons have cross-interconnected smooth open pores without the fibrous like structure.

  8. Application of response surface methodology (RSM) for optimisation of COD, NH3-N and 2,4-DCP removal from recycled paper wastewater in a pilot-scale granular activated carbon sequencing batch biofilm reactor (GAC-SBBR).

    Science.gov (United States)

    Muhamad, Mohd Hafizuddin; Sheikh Abdullah, Siti Rozaimah; Mohamad, Abu Bakar; Abdul Rahman, Rakmi; Hasan Kadhum, Abdul Amir

    2013-05-30

    In this study, the potential of a pilot-scale granular activated carbon sequencing batch biofilm reactor (GAC-SBBR) for removing chemical oxygen demand (COD), ammoniacal nitrogen (NH3-N) and 2,4-dichlorophenol (2,4-DCP) from recycled paper wastewater was assessed. For this purpose, the response surface methodology (RSM) was employed, using a central composite face-centred design (CCFD), to optimise three of the most important operating variables, i.e., hydraulic retention time (HRT), aeration rate (AR) and influent feed concentration (IFC), in the pilot-scale GAC-SBBR process for recycled paper wastewater treatment. Quadratic models were developed for the response variables, i.e., COD, NH3-N and 2,4-DCP removal, based on the high value (>0.9) of the coefficient of determination (R(2)) obtained from the analysis of variance (ANOVA). The optimal conditions were established at 750 mg COD/L IFC, 3.2 m(3)/min AR and 1 day HRT, corresponding to predicted COD, NH3-N and 2,4-DCP removal percentages of 94.8, 100 and 80.9%, respectively.

  9. Production of activated carbon from a new precursor molasses by activation with sulphuric acid.

    Science.gov (United States)

    Legrouri, K; Khouya, E; Ezzine, M; Hannache, H; Denoyel, R; Pallier, R; Naslain, R

    2005-02-14

    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 sulphuric acid, followed by carbonisation at varying conditions (temperature and gas coverage) in order to optimize preparation parameters. The influence of activation conditions was investigated by determination of adsorption capacity of methylene blue and iodine, the BET surface area, and the pore volume of the activated carbon were determined while the micropore volume was determined by the Dubinin-Radushkevich (DR) equation. The activated materials are mainly microporous and reveal the type I isotherm of the Brunauer classification for nitrogen adsorption. The activated carbons properties in this study were found for activation of the mixture (molasses/sulphuric acid) in steam at 750 degrees C. The samples obtained in this condition were highly microporous, with high surface area (> or =1200 m2/g) and the maximum adsorption capacity of methylene blue and iodine were 435 and 1430 mg/g, respectively.

  10. Pharmaceutical and biomedical applications of surface engineered carbon nanotubes.

    Science.gov (United States)

    Mehra, Neelesh Kumar; Jain, Keerti; Jain, Narendra Kumar

    2015-06-01

    Surface engineered carbon nanotubes (CNTs) are attracting recent attention of scientists owing to their vivid biomedical and pharmaceutical applications. The focus of this review is to highlight the important role of surface engineered CNTs in the highly challenging but rewarding area of nanotechnology. The major strength of this review lies in highlighting the exciting applications of CNTs to boost the research efforts, which unfortunately are otherwise scattered in the literature making the reading non-coherent and non-homogeneous.

  11. Synthesis, chemical modification, and surface assembly of carbon nanowires

    Energy Technology Data Exchange (ETDEWEB)

    Amma, A.; St. Angelo, S.K.; Mallouk, T.E. [Department of Chemistry, The Pennsylvania State University, University Park, PA 16802 (United States); Razavi, B.; Mayer, T.S. [Electrical Engineering, The Pennsylvania State University, University Park, PA 16802 (United States)

    2003-05-01

    Carbon nanotubules and nanowires were synthesized by pyrolysis of polymer precursors in the pores of alumina membranes. The nanowires were released by dissolving the membranes, and were then made hydrophobic or hydrophilic by chemical surface derivatization. These nanowires could be placed into lithographically defined wells on surfaces by means of electrostatic interactions with monolayers at the bottoms of the wells. (Abstract Copyright [2003], Wiley Periodicals, Inc.)

  12. A comparative study of carbon dioxide adsorption on multi-walled carbon nanotubes versus activated charcoal

    Science.gov (United States)

    Khalili, S.; Ghoreyshi, A. A.; Jahanshahi, M.; Davoodi, M.

    2012-09-01

    In this study, the quilibrium adsorption of CO2 on activated charcoal and multi-walled carbon nanotube (MWCNT) were experimentally investigated at temperature range of 298-318 K and pressures up to 40 bars. The maximum storage capacity for both materials was obtained at lowest temperature and highest pressure under study. The amount of CO2 adsorbed on MWCNT is 2 times higher than that of activated Charcoal whereas the specific surface area of activated carbon is aboute 2 times higher than MWNT. The experimental data of CO2 adsorption have been analyzed using different model isotherms such as the Freundlich and Langmuir. Heat of adsorption evaluated from a set of isotherms based on the Clausius-Clapeyron equation indicated physical nature of adsorption mechanism.

  13. Molten carbonate fuel cell cathodes. Improvement of the electrocatalytic activity

    Energy Technology Data Exchange (ETDEWEB)

    Escudero, M.J.; Daza, L. [Dpto. Energia, CIEMAT, Av. Complutense 22, 28040 Madrid (Spain); Rodrigo, T. [Instituto de Catalisis y Petroleoquimica, CSIC, Campus Cantoblanco, 28049 Madrid (Spain)

    2005-10-30

    The purpose of this work is to improve the electrocatalytic activity of Li-Ni mixed oxides by the addition of rare earth oxides (cerium or lanthanum). The influence of cerium and lanthanum on the electrocatalytic activity of these compounds was investigated by means of electrochemical impedance spectroscopy (EIS). The stability of these compounds was studied in a mixture of 62% lithium carbonate and 38% potassium carbonate at high temperature under an atmosphere rich in carbon dioxide to accelerate their dissolution. The morphology and the crystalline structure of the samples were not affected by the incorporation of cerium or lanthanum. The samples impregnated with CeO{sub 2} or La{sub 2}O{sub 3} showed lower resistance to charger-transfer processes than the sample without earth rare oxides. Both cerium and lanthanum improved the charger-transfer processes for oxygen reduction in an atmosphere rich in carbon dioxide. The reason may be due to cerium oxide acting as oxygen donor, and lanthanum oxide capturing CO{sub 2}, and the partial pressure of carbon dioxide on the surface of electrode.

  14. Activated carbon from flash pyrolysis of eucalyptus residue

    Directory of Open Access Journals (Sweden)

    Grima-Olmedo C

    2016-09-01

    Full Text Available Forestry waste (eucalyptus sp was converted into activated carbon by initial flash pyrolysis followed carbonization and CO2 activation. These residues were obtained from a pilot plant in Spain that produces biofuel, the biochar represented 10–15% in weight. It was observed that the highest activation was achieved at a temperature of 800 °C, the specific surface increased with time but, on the contrary, high loss of matter was observed. At 600 °C, although there was an important increase of the specific surface and the volume of micropores, at this temperature it was observed that the activation time was not an influential parameter. Finally, at 400 °C it was observed that the activation process was not very significant. Assessing the average pore diameter it was found that the lowest value corresponded to the activation temperature of 600 °C, which indicated the development of microporosity. When the activation temperature increases up to 800 °C the pore diameter increased developing mesoporosity.

  15. Activated carbon from flash pyrolysis of eucalyptus residue.

    Science.gov (United States)

    Grima-Olmedo, C; Ramírez-Gómez, Á; Gómez-Limón, D; Clemente-Jul, C

    2016-09-01

    Forestry waste (eucalyptus sp) was converted into activated carbon by initial flash pyrolysis followed carbonization and CO2 activation. These residues were obtained from a pilot plant in Spain that produces biofuel, the biochar represented 10-15% in weight. It was observed that the highest activation was achieved at a temperature of 800 °C, the specific surface increased with time but, on the contrary, high loss of matter was observed. At 600 °C, although there was an important increase of the specific surface and the volume of micropores, at this temperature it was observed that the activation time was not an influential parameter. Finally, at 400 °C it was observed that the activation process was not very significant. Assessing the average pore diameter it was found that the lowest value corresponded to the activation temperature of 600 °C, which indicated the development of microporosity. When the activation temperature increases up to 800 °C the pore diameter increased developing mesoporosity.

  16. Enhancing the capacitances of electric double layer capacitors based on carbon nanotube electrodes by carbon dioxide activation and acid oxidization

    Institute of Scientific and Technical Information of China (English)

    2010-01-01

    Polarizable electrodes of electric double layer capacitors(EDLCs) were made from carbon nanotubes(CNTs).Effect of carbon dioxide activation together with acid oxidation for the electrodes on the characteristics and performances of electrodes and EDLCs was studied.Carbon dioxide activation changed the microstructure of the electrodes,increased the effective surface area of CNTs and optimized the distribution of apertures of the electrodes.Acid oxidization modified the surface characteristics of CNTs.Based on the polarizable electrodes treated by carbon dioxide activation and acid oxidization,the performances of EDLCs were greatly enhanced.The specific capacitance of the electrodes with organic electrolyte was increased from 21.8 F/g to 60.4 F/g.

  17. Surface modification of commercial tin coatings by carbon ion implantation

    Energy Technology Data Exchange (ETDEWEB)

    Liu, L.J.; Sood, D.K.; Manory, R.R. [Royal Melbourne Inst. of Tech., VIC (Australia)

    1993-12-31

    Commercial TiN coatings of about 2 {mu}m thickness on high speed steel substrates were implanted at room temperature with 95 keV carbon ions at nominal doses between 1 x 10{sup 17} - 8x10{sup 17} ions cm{sup -2}. Carbon ion implantation induced a significant improvement in ultramicrohardness, friction coefficient and wear properties. The surface microhardness increases monotonically by up to 115% until a critical dose is reached. Beyond this dose the hardness decreases, but remains higher than that of unimplanted sample. A lower friction coefficient and a longer transition period towards a steady state condition were obtained by carbon ion implantation. The changes in tribomechanical properties are discussed in terms of radiation damage and possible formation of a second phase rich in carbon. 6 refs., 3 figs.

  18. CARBON SEQUESTRATION ON SURFACE MINE LANDS

    Energy Technology Data Exchange (ETDEWEB)

    Donald H. Graves; Christopher Barton; Richard Sweigard; Richard Warner

    2003-10-30

    The 2002-2003 Department of Energy plantings amounted to 164 acres containing 111,520 tree seedlings in eastern and western Kentucky. Data gathered on these trees included an inventory to determine survival of all planted species. A sub-sample of seedlings was selected to assess the height and diameter of individual species of seedlings established. Additional efforts involved collection of soil sample and litter samples, analysis of herbaceous ground cover from vegetation clip plots and leaf area on each tree species, and development of tissue collections. All areas were sampled for penetration resistance, penetration depth (or depth to refusal), and bulk density at various depths. Rain fall events and flow rates were recorded. The water quality of runoff samples involved the determination of total and settleable solids and particle size distribution. A study was initiated that will focus on the colonization of small mammals from forest edges to various areas located on reclaimed surface mines. This effort will provide a better understanding of the role small mammals and birds have in the establishment of plant communities on mine lands that will be useful in developing and improving reclamation techniques.

  19. Highly porous activated carbons from resource-recovered Leucaena leucocephala wood as capacitive deionization electrodes.

    Science.gov (United States)

    Hou, Chia-Hung; Liu, Nei-Ling; Hsi, Hsing-Cheng

    2015-12-01

    Highly porous activated carbons were resource-recovered from Leucaena leucocephala (Lam.) de Wit. wood through combined chemical and physical activation (i.e., KOH etching followed by CO2 activation). This invasive species, which has severely damaged the ecological economics of Taiwan, was used as the precursor for producing high-quality carbonaceous electrodes for capacitive deionization (CDI). Carbonization and activation conditions strongly influenced the structure of chars and activated carbons. The total surface area and pore volume of activated carbons increased with increasing KOH/char ratio and activation time. Overgasification induced a substantial amount of mesopores in the activated carbons. In addition, the electrochemical properties and CDI electrosorptive performance of the activated carbons were evaluated; cyclic voltammetry and galvanostatic charge/discharge measurements revealed a typical capacitive behavior and electrical double layer formation, confirming ion electrosorption in the porous structure. The activated-carbon electrode, which possessed high surface area and both mesopores and micropores, exhibited improved capacitor characteristics and high electrosorptive performance. Highly porous activated carbons derived from waste L. leucocephala were demonstrated to be suitable CDI electrode materials.

  20. Activated carbons prepared from refuse derived fuel and their gold adsorption characteristics.

    Science.gov (United States)

    Buah, William K; Williams, Paul T

    2010-02-01

    Activated carbons produced from refuse derived fuel (RDF), which had been prepared from municipal solid waste have been characterized and evaluated for their potential for gold adsorption from gold chloride solution. Pyrolysis of the RDF produced a char, which was then activated via steam gasification to produce activated carbons. Steam gasification of the char at 900 degrees C for 3 h yielded 73 wt% activated carbon. The derived activated carbon had a surface area of 500 m2 g(-1) and a total pore volume of 0.19 cm3 g(-1). The gold adsorption capacity of the activated carbon was 32.1 mg Au g(-1) of carbon when contacted with an acidified gold chloride solution. The gold adsorption capacity was comparable to that of a commercial activated carbon tested under the same conditions and was well in the range of values of activated carbons used in the gold industry. Demineralization of the RDF activated carbon in a 5 M HCl solution resulted in enhancement of its textural properties but a reduction in the gold adsorption rate, indicating that the metal content of the RDF activated carbon influenced its gold adsorption rate.

  1. Bioactive carbon-PEEK composites prepared by chemical surface treatment.

    Science.gov (United States)

    Miyazaki, Toshiki; Matsunami, Chisato; Shirosaki, Yuki

    2017-01-01

    Polyetheretherketone (PEEK) has attracted much attention as an artificial intervertebral spacer for spinal reconstruction. Furthermore, PEEK plastic reinforced with carbon fiber has twice the bending strength of pure PEEK. However, the PEEK-based materials do not show ability for direct bone bonding, i.e., bioactivity. Although several trials have been conducted for enabling PEEK with bioactivity, few studies have reported on bioactive surface modification of carbon-PEEK composites. In the present study, we attempted the preparation of bioactive carbon-PEEK composites by chemical treatments with H2SO4 and CaCl2. Bioactivity was evaluated by in vitro apatite formation in simulated body fluid (SBF). The apatite formation on the carbon-PEEK composite was compared with that of pure PEEK. Both pure PEEK and carbon-PEEK composite formed the apatite in SBF when they were treated with H2SO4 and CaCl2; the latter showed higher apatite-forming ability than the former. It is conjectured that many functional groups able to induce the apatite nucleation, such as sulfo and carboxyl groups, are incorporated into the dispersed carbon phase in the carbon-PEEK composites.

  2. Controllable Deposition of Alloy Clusters or Nanoparticles Catalysts on Carbon Surfaces

    Energy Technology Data Exchange (ETDEWEB)

    Sasaki, K.; Ando, Y.; Su, D.; Adzic, R.

    2011-08-15

    We describe a simple method for controllably depositing Pt-Ru alloy nanoparticles on carbon surfaces that is mediated by Pb or Cu adlayers undergoing underpotential deposition and stripping during Pt and Ru codeposition at diffusion-limiting currents. The amount of surface Pt atoms deposited largely reflects the number of potential cycles causing the deposition and stripping of the metal adlayer at underpotentials, the metal species used as a mediator, and the scan rate of the potential cycles. We employed electrochemical methanol oxidation to gain information on the catalyst's activities. The catalysts with large amounts of surface Pt atoms have relatively high methanol-oxidation activity. Catalysts prepared using this method enhance methanol-oxidation activity per electrode surface area, while maintaining catalytic activity per surface Pt atom; thus, the amount of Pt is reduced in comparison with conventional methanol-oxidation catalysts. The method is suitable for efficient synthesizing various bimetallic catalysts.

  3. Adsorption of naphthalene from aqueous solution on activated carbons obtained from bean pods.

    Science.gov (United States)

    Cabal, Belen; Budinova, Temenuzhka; Ania, Conchi O; Tsyntsarski, Boyko; Parra, José B; Petrova, Bilyana

    2009-01-30

    The preparation of activated carbons from bean pods waste by chemical (K(2)CO(3)) and physical (water vapor) activation was investigated. The carbon prepared by chemical activation presented a more developed porous structure (surface area 1580 m(2) g(-1) and pore volume 0.809 cm(3) g(-1)) than the one obtained by water vapor activation (258 m(2) g(-1) and 0.206 cm(3) g(-1)). These carbons were explored as adsorbents for the adsorption of naphthalene from water solutions at low concentration and room temperature and their properties are compared with those of commercial activated carbons. Naphthalene adsorption on the carbons obtained from agricultural waste was stronger than that of carbon adsorbents reported in the literature. This seems to be due to the presence of large amounts of basic groups on the bean-pod-based carbons. The adsorption capacity evaluated from Freundlich equation was found to depend on both the textural and chemical properties of the carbons. Naphthalene uptake on biomass-derived carbons was 300 and 85 mg g(-1) for the carbon prepared by chemical and physical activation, respectively. Moreover, when the uptake is normalized per unit area of adsorbent, the least porous carbon displays enhanced naphthalene removal. The results suggest an important role of the carbon composition including mineral matter in naphthalene retention. This issue remains under investigation.

  4. Effect of the nature the carbon precursor on the physico-chemical characteristics of the resulting activated carbon materials

    Energy Technology Data Exchange (ETDEWEB)

    Jimenez, Vicente, E-mail: vicente.jimenez@uclm.es [Facultad de Ciencias Quimicas, Departamento de Ingenieria Quimica, Universidad de Castilla-La Mancha, 13071 Ciudad Real (Spain); Sanchez, Paula; Valverde, Jose Luis [Facultad de Ciencias Quimicas, Departamento de Ingenieria Quimica, Universidad de Castilla-La Mancha, 13071 Ciudad Real (Spain); Romero, Amaya [Escuela Tecnica Agricola, Departamento de Ingenieria Quimica, Universidad de Castilla-La Mancha, 13071 Ciudad Real (Spain)

    2010-11-01

    Carbon materials, including amorphous carbon, graphite, carbon nanospheres (CNSs) and different types of carbon nanofibers (CNFs) [platelet, herringbone and ribbon], were chemically activated using KOH. The pore structure of carbon materials was analyzed using N{sub 2}/77 K adsorption isotherms. The presence of oxygen groups was analyzed by temperature programmed desorption in He and acid-base titration. The structural order of the materials was studied by X-ray diffraction and temperature programmed oxidation. The morphology and diameter distribution of CNFs and CNSs were characterized by transmission electron microscopy. The materials were also characterized by temperature-desorption programmed of H{sub 2} and elemental composition. The ways in which the different structures were activated are described, showing the type of pores generated. Relationships between carbon yield, removed carbon, activation degree and graphitic character were also examined. The oxygen content in the form of oxygen-containing surface groups increased after the activation giving qualitative information about them. The average diameter of both CNFs and CNSs was decreased after the activation process as consequence of the changes produced on the material surface.

  5. Analysis of the Interaction of Pulsed Laser with Nanoporous Activated Carbon Cloth

    Institute of Scientific and Technical Information of China (English)

    B.V. Kalucljerovic; M.S. Trtica; B.B. Radak; J.M. Stasic; S.S. Krstic Musovic; V.M. Dodevski

    2011-01-01

    Interaction of pulsed transversely excited atmospheric (TEA) CO2-1aser radiation at 10.6 μm with nanoporous activated carbon cloth was investigated. Activated carbon cloth of different adsorption characteristics was used. Activated carbon cloth modifications were initiated by laser pulse intensities from 0.5 to 28 MW/cm^2, depending on the cloth adsorption characteristics. CO2 laser radiation was effectively absorbed by the used activated carbon cloth and largely converted into thermal energy. The type of modification depended on laser power density, number of pulses, but mostly on material characteristics such as specific surface area. The higher the surface area of activated carbon cloth, the higher the damage threshold.

  6. Enhanced capacitive properties of commercial activated carbon by re-activation in molten carbonates

    Science.gov (United States)

    Lu, Beihu; Xiao, Zuoan; Zhu, Hua; Xiao, Wei; Wu, Wenlong; Wang, Dihua

    2015-12-01

    Simple, affordable and green methods to improve capacitive properties of commercial activated carbon (AC) are intriguing since ACs possess a predominant role in the commercial supercapacitor market. Herein, we report a green reactivation of commercial ACs by soaking ACs in molten Na2CO3-K2CO3 (equal in mass ratios) at 850 °C combining the merits of both physical and chemical activation strategies. The mechanism of molten carbonate treatment and structure-capacitive activity correlations of the ACs are rationalized. Characterizations show that the molten carbonate treatment increases the electrical conductivity of AC without compromising its porosity and wettability of electrolytes. Electrochemical tests show the treated AC exhibited higher specific capacitance, enhanced high-rate capability and excellent cycle performance, promising its practical application in supercapacitors. The present study confirms that the molten carbonate reactivation is a green and effective method to enhance capacitive properties of ACs.

  7. Proximate analysis for determination of micropores in granulated activated carbon

    Energy Technology Data Exchange (ETDEWEB)

    Berman, Ya. G.; Nikolaev, V.B.; Shepelev, A.N.

    1987-02-01

    A method is discussed for determining the specific micropore volume of granulated activated carbon used for water treatment in Soviet coking plants. Toluene molecules with a diameter of 0.67 nm are sorbed by activated carbon with micropore diameter ranging from 0.7 to 1.4 nm. Therefore, sorptive properties of activated carbon in relation to toluene supply information on micropore volume in carbon. A formula which describes this relation is derived. The method for determining micropore volume on the basis of toluene adsorption was tested using 8 types of activated carbon produced from coal and petroleum. Types of activated carbon characterized by the highest adsorption were selected. 1 ref.

  8. Characterization and restoration of performance of {open_quotes}aged{close_quotes} radioiodine removing activated carbons

    Energy Technology Data Exchange (ETDEWEB)

    Freeman, W.P. [NUCON International, Inc., Columbus, OH (United States)

    1997-08-01

    The degradation of radioiodine removal performance for impregnated activated carbons because of ageing is well established. However, the causes for this degradation remain unclear. One theory is that this reduction in performance from the ageing process results from an oxidation of the surface of the carbon. Radioiodine removing activated carbons that failed radioiodine removal tests showed an oxidized surface that had become hydrophilic compared with new carbons. We attempted to restore the performance of these {open_quotes}failed{close_quotes} carbons with a combination of thermal and chemical treatment. The results of these investigations are presented and discussed with the view of extending the life of radioiodine removing activated carbons. 4 refs., 2 tabs.

  9. Loss Mechanism and Loss Rate of Zinc Acetate from the Surface of the Activated Carbon in the Reaction Process%醋酸锌自催化剂表面上的流失机理和流失速度

    Institute of Scientific and Technical Information of China (English)

    孙培勤; 乌云高娃; 刘大壮

    2001-01-01

    In the reaction process of synthesizing vinyl acetate,the loss of the active species Zn(OAc)2 from the surface of activated carbon results from Zn(OAc)2 sublimating of gas phase and the blocking inside micropores with condensation products.The sublimation mechanism is that the reaction product vinyl acetate acts with Zn(OAc)2 to produce a volatilizable complex,then sublimates to gas phase.The overall loss ratio(LR) can be described as the equation LR=1-exp(-kvt),which is extensive application of the sublimation rate equation,where v is the flow rate of gas stream,t is reaction time,and k is loss rate constant.%乙炔和醋酸合成醋酸乙烯的反应过程中,催化剂的失活,是由催化剂中的醋酸锌Zn (OAc)2从活性炭表面上升华到气相中以及被凝聚物堵在微孔内部而引起的.升华机理是反应产物与Zn (OAc)2作用生成挥发性络合物再升华到气相中去.总流失速度可用LR=1-exp (-kvt)来描述,这是升华速度方程式的应用推广.式中v为气流速度,t为反应时间,k为速度常数.

  10. [Adsorption of perfluorooctanesulfonate (PFOS) onto modified activated carbons].

    Science.gov (United States)

    Tong, Xi-Zhen; Shi, Bao-You; Xie, Yue; Wang, Dong-Sheng

    2012-09-01

    Modified coal and coconut shell based powdered activated carbons (PACs) were prepared by FeCl3 and medium power microwave treatment, respectively. Batch experiments were carried out to evaluate the characteristics of adsorption equilibrium and kinetics of perfluorooctanesulfonate (PFOS) onto original and modified PACs. Based on pore structure and surface functional groups characterization, the adsorption behaviors of modified and original PACs were compared. The competitive adsorption of humic acid (HA) and PFOS on original and modified coconut shell PACs were also investigated. Results showed that both Fe3+ and medium power microwave treatments changed the pore structure and surface functional groups of coal and coconut shell PACs, but the changing effects were different. The adsorption of PFOS on two modified coconut shell-based PACs was significantly improved. While the adsorption of modified coal-based activated carbons declined. The adsorption kinetics of PFOS onto original and modified coconut shell-based activated carbons were the same, and the time of reaching adsorption equilibrium was about 6 hours. In the presence of HA, the adsorption of PFOS by modified PAC was reduced but still higher than that of the original.

  11. Femtosecond laser-induced surface structures on carbon fibers.

    Science.gov (United States)

    Sajzew, Roman; Schröder, Jan; Kunz, Clemens; Engel, Sebastian; Müller, Frank A; Gräf, Stephan

    2015-12-15

    The influence of different polarization states during the generation of periodic nanostructures on the surface of carbon fibers was investigated using a femtosecond laser with a pulse duration τ=300  fs, a wavelength λ=1025  nm, and a peak fluence F=4  J/cm². It was shown that linear polarization results in a well-aligned periodic pattern with different orders of magnitude concerning their period and an alignment parallel and perpendicular to fiber direction, respectively. For circular polarization, both types of uniform laser-induced periodic surface structures (LIPSS) patterns appear simultaneously with different dominance in dependence on the position at the fiber surface. Their orientation was explained by the polarization-dependent absorptivity and the geometrical anisotropy of the carbon fibers.

  12. Wetting and Non-Wetting Models of Black Carbon Activation

    Science.gov (United States)

    Henson, B. F.; Laura, S.

    2006-12-01

    We present the results of recent modeling studies on the activation of black carbon (BC) aerosol to form cloud condensation nuclei (CCN). We use a model of BC activation based on a general modification of the Koehler equation for insoluble activation in which we introduce a term based on the activity of water adsorbed on the particle surface. We parameterize the model using the free energy of adsorption, a parameter directly comparable to laboratory measurements of water adsorption on carbon. Although the model of the water- surface interaction is general, the form of the activation equation that results depends upon a further model of the distribution of water on the particle. One possible model involves the symmetric growth of a water shell around the isoluble particle core (wetting). This model predicts upper and lower bounding curves for the activation supersaturation given by the range of water interaction energies from hydrophobic to hydrophilic which are in agreement with a large body of recent activation data. The resulting activation diameters are from 3 to 10 times smaller than activation of soluble particles of identical dry diameter. Another possible model involves an exluded liquid droplet growing in contact with the particle (non-wetting). The geometry of this model much more resembles classic assumptions of heterogeneous nucleation theory. This model can yield extremely high activation supersaturation as a function of diameter, as has been observed in some experiments, and enables calculations in agreement with some of these results. We discuss these two geometrical models of water growth, the different behaviors predicted by the resulting activation equation, and the means to determine which model of growth is appropriate for a given BC particle characterized by either water interaction energy or morphology. These simple models enable an efficient and physically reasonable means to calculate the activation of BC aerosol to form CCN based upon a

  13. YAG laser welding with surface activating flux

    Institute of Scientific and Technical Information of China (English)

    樊丁; 张瑞华; 田中学; 中田一博; 牛尾诚夫

    2003-01-01

    YAG laser welding with surface activating flux has been investigated, and the influencing factors and mechanism are discussed. The results show that both surface activating flux and surface active element S have fantastic effects on the YAG laser weld shape, that is to obviously increase the weld penetration and D/W ratio in various welding conditions. The mechanism is thought to be the change of weld pool surface tension temperature coefficient, thus, the change of fluid flow pattern in weld pool due to the flux.

  14. Activated carbon treatment of municipal solid waste incineration flue gas.

    Science.gov (United States)

    Lu, Shengyong; Ji, Ya; Buekens, Alfons; Ma, Zengyi; Jin, Yuqi; Li, Xiaodong; Yan, Jianhua

    2013-02-01

    Activated carbon injection is widely used to control dioxins and mercury emissions. Surprisingly little attention has been paid to its modelling. This paper proposes an expansion of the classical Everaerts-Baeyens model, introducing the expression of fraction of free adsorption sites, f (s), and asserting the significant contribution of fly ash to dioxins removal. Moreover, the model monitors dioxins partitioning between vapour and particulate phase, as well as removal efficiency for each congener separately. The effects of the principal parameters affecting adsorption are analysed according to a semi-analytical, semi-empirical model. These parameters include temperature, contact time during entrained-flow, characteristics (grain-size, pore structure, specific surface area) and dosage of activated carbon, lignite cokes or mineral adsorbent, fly ash characteristics and concentration, and type of incinerator plant.

  15. Composite supercapacitor electrodes made of activated carbon/PEDOT:PSS and activated carbon/doped PEDOT

    Indian Academy of Sciences (India)

    T S Sonia; P A Mini; R Nandhini; Kalluri Sujith; Balakrishnan Avinash; S V Nair; K R V Subramanian

    2013-08-01

    In this paper, we report on the high electrical storage capacity of composite electrodes made from nanoscale activated carbon combined with either poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) or PEDOT doped with multiple dopants such as ammonium persulfate (APS) and dimethyl sulfoxide (DMSO). The composites were fabricated by electropolymerization of the conducting polymers (PEDOT:PSS, doped PEDOT) onto the nanoscale activated carbon backbone, wherein the nanoscale activated carbon was produced by ball-milling followed by chemical and thermal treatments. Activated carbon/PEDOT:PSS yielded capacitance values of 640 F g-1 and 26mF cm-2, while activated carbon/doped PEDOT yielded capacitances of 1183 F g-1 and 42 mF cm-2 at 10 mV s-1. This is more than five times the storage capacity previously reported for activated carbon–PEDOT composites. Further, use of multiple dopants in PEDOT improved the storage performance of the composite electrode well over that of PEDOT:PSS. The composite electrodes were characterized for their electrochemical behaviour, structural and morphological details and electronic conductivity and showed promise as high-performance energy storage systems.

  16. Absorption and adsorption of methane and carbon dioxide in hard coal and active carbon

    Energy Technology Data Exchange (ETDEWEB)

    Milewska-Duda, J.; Duda, J.; Nodzenski, A.; Lakatos, J. [Stanislaw Staszic University of Mining and Metallurgy, Krakow (Poland). Faculty of Fuels and Energy

    2000-07-01

    The paper shows what can be deduced on sorption mechanisms in hard coals and active carbon by using a theoretical model of sorption of small molecules in elastic submicroporous materials. This multiple sorption model (MSM) describes both adsorption and absorption phenomena. Basic assumptions and formulae of the MSM are presented. The computations were performed for isotherms of CO{sub 2} and CH{sub 4} at elevated pressures on three coal samples of different rank and on an active carbon. Nonideality of the sorbates is handled by an original state equation providing consistent information on fugacity and cohesion energy corresponding to a given molar volume of sorbate molecules in the sorption system. Surface structure of the studied coals and energetic parameters of the systems determined with MSM are compared to those obtained by using BET and Dubinin-Radushkievitch equations.

  17. 78 FR 13894 - Certain Activated Carbon From China

    Science.gov (United States)

    2013-03-01

    ... COMMISSION Certain Activated Carbon From China Determination On the basis of the record \\1\\ developed in the... antidumping duty order on certain activated carbon from China would be likely to lead to continuation or... USITC Publication 4381 (February 2013), entitled Certain Activated Carbon from China: Investigation...

  18. Nickel catalysts supported on MgO with different specific surface area for carbon dioxide reforming of methane

    Institute of Scientific and Technical Information of China (English)

    Luming; Zhang; Lin; Li; Yuhua; Zhang; Yanxi; Zhao; Jinlin; Li

    2014-01-01

    In this paper, three kinds of MgO with different specific surface area were prepared, and their effects on the catalytic performance of nickel catalysts for the carbon dioxide reforming of methane were investigated. The results showed that MgO support with the higher specific surface area led to the higher dispersion of the active metal, which resulted in the higher initial activity. On the other hand, the specific surface area of MgO materials might not be the dominant factor for the basicity of support to chemisorb and activate CO2, which was another important factor for the performance of catalysts. Herein, Ni/MgO(CA) catalyst with proper specific surface area and strong ability to activate CO2exhibited stable catalytic property and the carbon species deposited on the Ni/MgO(CA) catalyst after 10 h of reaction at 650 ?C were mainly activated carbon species.

  19. Activated carbons from potato peels: The role of activation agent and carbonization temperature of biomass on their use as sorbents for bisphenol A uptake from aqueous solutions

    Science.gov (United States)

    Arampatzidou, An; Deliyanni, Eleni A.

    2015-04-01

    Activated carbons prepared from potato peels, a solid waste by product, and activated with different activating chemicals, have been studied for the adsorption of an endocrine disruptor (Bisphenol-A) from aqueous solutions. The potato peels biomass was activated with phosphoric acid, KOH and ZnCl2. The different activating chemicals were tested in order the better activation agent to be found. The carbons were carbonized by pyrolysis, in one step procedure, at three different temperatures in order the role of the temperature of carbonization to be pointed out. The porous texture and the surface chemistry of the prepared activated carbons were characterized by Nitrogen adsorption (BET), Scanning Electron Microscope (SEM), thermal analysis (DTA) and Fourier Transform Infrared Spectroscopy (FTIR). Batch experiments were performed to investigate the effect of pH, the adsorbent dose, the initial bisphenol A concentration and temperature. Equilibrium adsorption data were analyzed by Langmuir and Freundlich isotherms. The thermodynamic parameters such as the change of enthalpy (ΔH0), entropy (ΔS0) and Gibb's free energy (ΔG0) of adsorption systems were also evaluated. The adsorption capacity calculated from the Langmuir isotherm was found to be 450 mg g-1 at an initial pH 3 at 25 °C for the phosphoric acid activated carbon, that make the activated carbon a promising adsorbent material.

  20. Removal of carbon contaminations by RF plasma generated reactive species and subsequent effects on optical surface

    Energy Technology Data Exchange (ETDEWEB)

    Yadav, P. K., E-mail: praveenyadav@rrcat.gov.in; Rai, S. K.; Modi, M. H.; Nayak, M.; Lodha, G. S. [Indus Synchrotron Utilization Division, Raja Ramanna Centre for Advanced Technology, Indore-452013 (India); Kumar, M.; Chakera, J. A.; Naik, P. A. [Laser Plasma Laboratory, Laser Plasma Division, Raja Ramanna Centre for Advanced Technology, Indore-452013 (India)

    2015-06-24

    Carbon contamination on optical elements is a serious issue in synchrotron beam lines for several decades. The basic mechanism of carbon deposition on optics and cleaning strategies are not fully understood. Carbon growth mechanism and optimized cleaning procedures are worldwide under development stage. Optimized RF plasma cleaning is considered an active remedy for the same. In present study carbon contaminated optical test surfaces (carbon capped tungsten thin film) are exposed for 30 minutes to four different gases, rf plasma at constant power and constant dynamic pressure. Structural characterization (thickness, roughness and density) of virgin samples and plasma exposed samples was done by soft x-ray (λ=80 Å) reflectivity measurements at Indus-1 reflectivity beam line. Different gas plasma removes carbon with different rate (0.4 to 0.65 nm /min). A thin layer 2 to 9 nm of different roughness and density is observed at the top surface of tungsten film. Ar gas plasma is found more suitable for cleaning of tungsten surface.

  1. Following the Interstellar History of Carbon: From the Interiors of Stars to the Surfaces of Planets

    Science.gov (United States)

    Ziurys, L. M.; Halfen, D. T.; Geppert, W.; Aikawa, Y.

    2016-12-01

    The chemical history of carbon is traced from its origin in stellar nucleosynthesis to its delivery to planet surfaces. The molecular carriers of this element are examined at each stage in the cycling of interstellar organic material and their eventual incorporation into solar system bodies. The connection between the various interstellar carbon reservoirs is also examined. Carbon has two stellar sources: supernova explosions and mass loss from evolved stars. In the latter case, the carbon is dredged up from the interior and then ejected into a circumstellar envelope, where a rich and unusual C-based chemistry occurs. This molecular material is eventually released into the general interstellar medium through planetary nebulae. It is first incorporated into diffuse clouds, where carbon is found in polyatomic molecules such as H2CO, HCN, HNC, c-C3H2, and even C60+. These objects then collapse into dense clouds, the sites of star and planet formation. Such clouds foster an active organic chemistry, producing compounds with a wide range of functional groups with both gas-phase and surface mechanisms. As stars and planets form, the chemical composition is altered by increasing stellar radiation, as well as possibly by reactions in the presolar nebula. Some molecular, carbon-rich material remains pristine, however, encapsulated in comets, meteorites, and interplanetary dust particles, and is delivered to planet surfaces.

  2. Characterization and Properties of Nanostructured Surface Layer in a Low Carbon Steel Subjected to Surface Mechanical Attrition

    Institute of Scientific and Technical Information of China (English)

    2003-01-01

    A nanostructured surface layer was synthesized on a Iow carbon steel by using surface mechanical attrition (SMA)technique. The refined microstructure of the surface layer was characterized by means of different techniques,and the hardness variation along the depth was examined. Experimental results show that the microstructure isinhomogeneous along the depth. In the region from top surface to about 40μm deep, the grain size increases fromabout 10 nm to 100 nm. In the adjacent region of about 40~80μm depth, the grain size increases from about 100nm to 1000 nm. The grain refinement can be associated with the activity of dislocations. After the SMA treatment,the hardness of the surface layer is enhanced significantly compared with that of the original sample, which canprimarily be attributed to the grain refinement.

  3. Adsorption of non-ionic surfactants on hydrophobic and hydrophilic carbon surfaces.

    Science.gov (United States)

    Soria-Sánchez, M; Maroto-Valiente, A; Guerrero-Ruiz, A; Nevskaia, D M

    2010-03-01

    The adsorption from aqueous solutions of a series of non-ionic surfactants (TX-114, TX-100, TX-165 and TX-305, where the ethoxylation degree is increasing in the series) on a non-microporous carbon surface, that is a high surface area graphite (GT), and on a mainly microporous activated carbon (NT) has been comparatively studied. Also the initially hydrophobic GT and NT surfaces have been modified by oxidation treatments in order to achieve partially hydrophilic carbon materials (GTox and NTox samples). The adsorption results reveal that for GT sample below the critical micellar concentrations (cmc) of surfactants practically the whole surface is covered by monomers. For NT there are steric hindrance limitations, so the surfactant molecules are adsorbed only on micropores of sizes larger than 8A. When oxygen surface groups are introduced on the carbonaceous surfaces, the adsorption behaviour is again different for both materials. Thus, for GTox the adsorbed amounts below the cmc decrease probably due to withdrawal effect of the oxygen surface groups. On the contrary, the adsorbed amounts above the cmc slightly increase with regard to bare graphite, possibly due to an improved formation of micelles. In the case of NTox the adsorbed uptakes below and above cmc increase remarkably in comparison with NT sample, which can be explained by some specific interactions of the surfactants molecules with oxygen surface groups inside the micropores.

  4. Adsorption of aromatic compounds from the biodegradation of azo dyes on activated carbon

    Science.gov (United States)

    Faria, P. C. C.; Órfão, J. J. M.; Figueiredo, J. L.; Pereira, M. F. R.

    2008-03-01

    The adsorption of three selected aromatic compounds (aniline, sulfanilic acid and benzenesulfonic acid) on activated carbons with different surface chemical properties was investigated at different solution pH. A fairly basic commercial activated carbon was modified by means of chemical treatment with HNO 3, yielding an acid activated carbon. The textural properties of this sample were not significantly changed after the oxidation treatment. Equilibrium isotherms of the selected compounds on the mentioned samples were obtained and the results were discussed in relation to their surface chemistry. The influence of electrostatic and dispersive interactions involved in the uptake of the compounds studied was evaluated. The Freundlich model was used to fit the experimental data. Higher uptakes are attained when the compounds are present in their molecular form. In general, adsorption was disfavoured by the introduction of oxygen-containing groups on the surface of the activated carbon.

  5. Surface characterization and orientation interaction between diamond- like carbon layer structure and dimeric liquid crystals

    Science.gov (United States)

    Naradikian, H.; Petrov, M.; Katranchev, B.; Milenov, T.; Tinchev, S.

    2017-01-01

    Diamond-like carbon (DLC) and amorphous carbon films are very promising type of semiconductor materials. Depending on the hybridization sp2/sp3 ratio, the material’s band gap varies between 0.8 and 3 eV. Moreover carbon films possess different interesting for practice properties: comparable to the Silicon, Diamond like structure has 22-time better thermal conductivity etc. Here we present one type of implementation of such type nanostructure. That is one attempt for orientation of dimeric LC by using of pre-deposited DLC layer with different ratio of sp2/sp3 hybridized carbon content. It could be expected a pronounced π1-π2interaction between s and p orbital levels on the surface and the dimeric ring of LC. We present comparison of surface anchoring strengths of both orientation inter-surfaces DLC/dimeric LC and single wall carbon nanotubes (SWCNT)/dimeric LC. The mechanism of interaction of dimeric LC and activated surfaces with DLC or SWCNT will be discussed. In both cases we have π-π interaction, which in combination with hydrogen bonding, typical for the dimeric LCs, influence the LC alignment. The Raman spectroscopy data evidenced the presence of charge transfer between contacting hexagonal rings of DLC and the C = O groups of the LC molecules.

  6. An activated microporous carbon prepared from phenol-melamine-formaldehyde resin for lithium ion battery anode

    Energy Technology Data Exchange (ETDEWEB)

    Zhu, Yinhai; Xiang, Xiaoxia [Key Laboratory of Environmentally Friendly Chemistry and Applications of Ministry of Education, College of Chemistry, Xiangtan University, Hunan 411105 (China); Liu, Enhui, E-mail: liuenhui99@sina.com.cn [Key Laboratory of Environmentally Friendly Chemistry and Applications of Ministry of Education, College of Chemistry, Xiangtan University, Hunan 411105 (China); Wu, Yuhu; Xie, Hui; Wu, Zhilian; Tian, Yingying [Key Laboratory of Environmentally Friendly Chemistry and Applications of Ministry of Education, College of Chemistry, Xiangtan University, Hunan 411105 (China)

    2012-08-15

    Highlights: ► Microporous carbon was prepared by chemical activation of phenol-melamine-formaldehyde resin. ► Activation leads to high surface area, well-developed micropores. ► Micropores lead to strong intercalation between carbon and lithium ion. ► Large surface area promotes to improve the lithium storage capacity. -- Abstract: Microporous carbon anode materials were prepared from phenol-melamine-formaldehyde resin by ZnCl{sub 2} and KOH activation. The physicochemical properties of the obtained carbon materials were characterized by scanning electron microscope, X-ray diffraction, Brunauer–Emmett–Teller, and elemental analysis. The electrochemical properties of the microporous carbon as anode materials in lithium ion secondary batteries were evaluated. At a current density of 100 mA g{sup −1}, the carbon without activation shows a first discharge capacity of 515 mAh g{sup −1}. After activation, the capacity improved obviously. The first discharge capacity of the carbon prepared by ZnCl{sub 2} and KOH activation was 1010 and 2085 mAh g{sup −1}, respectively. The reversible capacity of the carbon prepared by KOH activation was still as high as 717 mAh g{sup −1} after 20 cycles, which was much better than that activated by ZnCl{sub 2}. These results demonstrated that it may be a promising candidate as an anode material for lithium ion secondary batteries.

  7. Influence of deposited CNTs on the surface of carbon fiber by ultrasonically assisted electrophoretic deposition

    Science.gov (United States)

    Jiang, J. J.; Liu, F.; Deng, C.; Fang, L. C.; Li, D. J.

    2015-07-01

    The surface property of carbon fiber directly affects the interface performance between carbon fiber and matrix. To improve the surface property of carbon fiber, we proposed a simple method to prepare carbon nanotubes /carbon fiber hybrid fiber via ultrasonically assisted electrophoretic deposition (EPD). Surface morphologies and surface functional group of carbon fibers were examined by atomic force microscopy (AFM), scanning electron microscopy (SEM) and fourier transform infrared spectrometer (FTIR), respectively. The results show that the deposition of carbon nanotubes changed the surface morphologies of carbon fibers and introduced polar groups (C=O and C-O) to carbon fiber surface. Comparing the results with EPD-only, ultrasonically assisted EPD increased the uniformity of carbon nanotubes coatings whereas only sparse and not uniformly deposition formed without ultrasonic.

  8. Effects of Surface-modification of Carbon Black on the Characteristics of Polymerized Toner

    Energy Technology Data Exchange (ETDEWEB)

    Lee, Eun Ho; Kim, Dae Su [Chungbuk National University, Cheongju (Korea, Republic of)

    2013-10-15

    Carbon black was surface-modified to prepare styrene-based suspension polymerized toner with excellent carbon black dispersibility inside toner particles. Carbon black was oxidized first to introduce hydroxyl groups on the surfaces, then esterification between the hydroxyl groups and carboxyl groups of organic acids (oleic acid, palmitic acid, acrylic acid) was followed to obtain organically surface-modified carbon black. The surface-modification of carbon black was confirmed by FTIR. Apparent carbon black dispersibility in the monomer mixture of the binder resin was tested and the particle size of dispersed carbon black was measured by particle size analyzer. Optical micrographs showed that carbon black dispersibility inside toner particles was improved considerably when the carbon black surface-modified with oleic acid was used. The polymerized toner prepared with the carbon black surface-modified with oleic acid showed ideal particle size and size distribution as a toner.

  9. An operando surface enhanced Raman spectroscopy (SERS) study of carbon deposition on SOFC anodes.

    Science.gov (United States)

    Li, Xiaxi; Liu, Mingfei; Lee, Jung-pil; Ding, Dong; Bottomley, Lawrence A; Park, Soojin; Liu, Meilin

    2015-09-07

    Thermally robust and chemically inert Ag@SiO2 nanoprobes are employed to provide the surface enhanced Raman scattering (SERS) effect for an in situ/operando study of the early stage of carbon deposition on nickel-based solid oxide fuel cell (SOFC) anodes. The enhanced sensitivity to carbon enables the detection of different stages of coking, offering insights into intrinsic coking tolerance of material surfaces. Application of a thin coating of gadolinium doped ceria (GDC) enhances the resistance to coking of nickel surfaces. The electrochemically active Ni-YSZ interface appears to be more active for hydrocarbon reforming, resulting in the accumulation of different hydrocarbon molecules, which can be readily removed upon the application of an anodic current. Operando SERS is a powerful tool for the mechanistic study of coking in SOFC systems. It is also applicable to the study of other catalytic and electrochemical processes in a wide range of conditions.

  10. Polymer surface modification and characterization of particulate calcium carbonate fillers

    Energy Technology Data Exchange (ETDEWEB)

    Shui Miao

    2003-12-30

    The efficacy of the surface treatment of particulate fillers depends on the chemical character of the components, on the method and conditions of the treatment, and on the amount of the treating agent. Here, the ultra-fine calcium carbonate is surface treated with 1, 2, 3 and 4 wt.% polyacrylic acid (PAA) synthesized by ourselves, which has strong ionic interaction and is an efficient surface modifier. The PAA coated filler is submitted to the measurement of the surface bonded amount, bonding efficacy, X-ray photoelectron spectroscopy (XPS) and inverse gas chromatography. Maximum efficacy is expected at the monolayer coverage of the surface, which is about 0.6 wt.% according to the calculation based on the way they are aligned and is basically in agreement with the 'substrate overlayer' model based on the mole ratio of C{sup 286} and C{sup 290} taking no account of the possible underestimation because of the inaccuracy or because of the CH{sub x} contamination present originally on the CaCO{sub 3}. The initial decrease of the mole ratio of C{sup 290}/O and C{sup 290}/Ca with the surface bonded PAA may indicate that the bonding interaction between the polymer and the filler surface is the leaving of one molecular carbon dioxide. The IGC measurement shows that there is a considerable surface tension falling in the case of the PAA modified filler compared with the reference. An abnormal high surface energy in the case of filler treated with 4% PAA is observed.

  11. On the formation and bonding of a surface carbonate on Ni(100)

    Science.gov (United States)

    Behm, R. J.; Brundle, C. R.

    1991-09-01

    The formation, stability, adsorption geometry and electronic structure of a surface carbonate on Ni(100) have been investigated by photoemission (XPS, UPS) and temperature-programmed reaction (TPR). The core level binding energies of 531.2 eV for 0(1s) and 289.0 eV for C(1s) are comparable to those of bulk carbonates. The He(II) spectrum of the carbonate valence levels is not well defined because of the coexisting adsorbed and oxidic oxygen. The angular dependence of the carbonate core level intensities is characteristic of the carbonate being present as an overlayer species rather than a thicker surface phase. The XPS data and isotope labelled TPR experiments indicate the oxygen atoms of the carbonate to be electronically and chemically equivalent, and on this basis we favor a structure in which the carbonate is attached to the metal via all three oxygen atoms. This is supported by comparision with the core level binding energies of HCOO ab and chemisorbed CO 2,ad, which are similarly attached to the surface. From the core level angular behavior, the close similarity of core level binding energies and available vibrational spectroscopic data, a (nearly) planar geometry of the CO 3,ad on Ni(100) is concluded, which is comparable to the planar bulk carbonate anion and the planar carbonate species on Ag(110). The activation barrier for decomposition is estimated from the observed maximum in TPR at 420 K to be 25 ± 2 kcal/mol. CO 2 does not accumulate on the clean or O ad-precovered Ni(100) surface at 130 K. The stabilized, chemisorbed CO 2,ad species often observed on other metal surfaces therefore does not play a critical role for carbonate formation on Ni(100). Also a mechanism involving the disproportionation of a CO 2… CO 2,ad- dimer anion can be ruled out from TPR data. The evidence of the experiments discussed in this paper suggests that the carbonate is predominantly formed by reaction of CO 2,ad with a less stable, defect (disordered) O ad species rather

  12. Effect of Activated Carbon as a Support on Metal Dispersion and Activity of Ruthenium Catalyst for Ammonia Synthesis

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    Ten kinds of activated carbon from different raw materials were used as supports to prepare ruthenium catalysts. N2 physisorption and CO chemisorption were carried out to investigate the pore size distribution and the ruthenium dispersion of the catalysts. It was found that the Ru dispersion of the catalyst was closely related to not only the texture of carbon support but also the purity of activated carbon. The activities of a series of the carbon-supported barium-promoted Ru catalysts for ammonia synthesis were measured at 425 ℃, 10.0 MPa and 10 000 h-1. The result shows that the same raw material activated carbon, with a high purity, high surface area, large pore volume and reasonable pore size distribution might disperse ruthenium and promoter sufficiently, which activated carbon as support, could be used to manufacture ruthenium catalyst with a high activity for ammonia synthesis. The different raw material activated carbon as the support would greatly influence the catalytic properties of the ruthenium catalyst for ammonia synthesis. For example, with coconut shell carbon(AC1) as the support, the ammonia concentration in the effluent was 13.17% over 4%Ru-BaO/AC1 catalyst, while with the desulfurized coal carbon(AC10) as the support, that in the effluent was only 1.37% over 4%Ru-BaO/AC10 catalyst.

  13. Characteristic and mercury adsorption of activated carbon produced by CO2 of chicken waste

    Institute of Scientific and Technical Information of China (English)

    HUANG Yaji; JIN Baosheng; ZHONG Zhaoping; ZHONG Wenqi; XIAO Rui

    2008-01-01

    Preparation of activated carbon from chicken waste is a promising way to produce a useful adsorbent for Hg removal.A three-stage activation process (drying at 200℃,pyrolysis in N2 atmosphere,followed by CO2 activation) was used for the production of activated samples.The effects of carbonization temperature (400-600 ℃),activation temperature (700-900 ℃),and activation time (1-2.5 h) on the physicochemieal properties (weight-loss and BET surface) of the prepared carbon were investigated.Adsorptive removal of mercury from real flue gas onto activated carbon has been studied.The activated carbon from chicken waste has the same mercury capacity as commercial activated carbon (Darco LH) (HgV:38.7% vs.53.5%,HgO:50.5% vs.68.8%),although its surface area is around 10 times smaller,89.5 m2/g vs.862 m2/g.The low cost activated carbon can be produced from chicken waste,and the procedure is suitable.

  14. Orthophosphoric Acid Activated Babul Seed Carbon as an Adsorbent for the Removal of Methylene Blue

    Directory of Open Access Journals (Sweden)

    M. Sujatha

    2008-01-01

    Full Text Available An Experimental and theoretical study has been conducted on the adsorption of methylene blue dye using activated carbon prepared from babul seed by chemical activation with orthophosphoric acid. BET surface area of the activated carbon was determined as 1060 m2/g. Adsorption kinetics, equilibrium and thermodynamics were investigated as a function of initial dye concentration, temperature and pH. First order Lagergren, pseudo-second order and Elovich kinetic models were used to test the adsorption kinetics. Results were analyzed by the Langmuir, Freundlich and Temkin isotherm models. Based on regression coefficient, the equilibrium data found fitted well to the Langmuir equilibrium model than other models. The characteristics of the prepared activated carbon were found comparable to the commercial activated carbon. It is found that the babul seed activated carbon is very effective for the removal of colouring matter.

  15. Improved Composites Using Crosslinked, Surface-Modified Carbon Nanotube Materials

    Science.gov (United States)

    Baker, James Stewart

    2014-01-01

    Individual carbon nanotubes (CNTs) exhibit exceptional tensile strength and stiffness; however, these properties have not translated well to the macroscopic scale. Premature failure of bulk CNT materials under tensile loading occurs due to the relatively weak frictional forces between adjacent CNTs, leading to poor load transfer through the material. When used in polymer matrix composites (PMCs), the weak nanotube-matrix interaction leads to the CNTs providing less than optimal reinforcement.Our group is examining the use of covalent crosslinking and surface modification as a means to improve the tensile properties of PMCs containing carbon nanotubes. Sheet material comprised of unaligned multi-walled carbon nanotubes (MWCNT) was used as a drop-in replacement for carbon fiber in the composites. A variety of post-processing methods have been examined for covalently crosslinking the CNTs to overcome the weak inter-nanotube shear interactions, resulting in improved tensile strength and modulus for the bulk sheet material. Residual functional groups from the crosslinking chemistry may have the added benefit of improving the nanotube-matrix interaction. Composites prepared using these crosslinked, surface-modified nanotube sheet materials exhibit superior tensile properties to composites using the as received CNT sheet material.

  16. Ocean Surface Carbon Dioxide Fugacity Observed from Space

    Science.gov (United States)

    Liu, W. Timothy; Xie, Xiaosu

    2014-01-01

    We have developed and validated a statistical model to estimate the fugacity (or partial pressure) of carbon dioxide (CO2) at sea surface (pCO2sea) from space-based observations of sea surface temperature (SST), chlorophyll, and salinity. More than a quarter million in situ measurements coincident with satellite data were compiled to train and validate the model. We have produced and made accessible 9 years (2002-2010) of the pCO2sea at 0.5 degree resolutions daily over the global ocean. The results help to identify uncertainties in current JPL Carbon Monitoring System (CMS) model-based and bottom-up estimates over the ocean. The utility of the data to reveal multi-year and regional variability of the fugacity in relation to prevalent oceanic parameters is demonstrated.

  17. Physical and chemical properties and adsorption type of activated carbon prepared from plum kernels by NaOH activation.

    Science.gov (United States)

    Tseng, Ru-Ling

    2007-08-25

    Activated carbon was prepared from plum kernels by NaOH activation at six different NaOH/char ratios. The physical properties including the BET surface area, the total pore volume, the micropore ratio, the pore diameter, the burn-off, and the scanning electron microscope (SEM) observation as well as the chemical properties, namely elemental analysis and temperature programmed desorption (TPD), were measured. The results revealed a two-stage activation process: stage 1 activated carbons were obtained at NaOH/char ratios of 0-1, surface pyrolysis being the main reaction; stage 2 activated carbons were obtained at NaOH/char ratios of 2-4, etching and swelling being the main reactions. The physical properties of stage 2 activated carbons were similar, and specific area was from 1478 to 1887m(2)g(-1). The results of reaction mechanism of NaOH activation revealed that it was apparently because of the loss ratio of elements C, H, and O in the activated carbon, and the variations in the surface functional groups and the physical properties. The adsorption of the above activated carbons on phenol and three kinds of dyes (MB, BB1, and AB74) were used for an isotherm equilibrium adsorption study. The data fitted the Langmuir isotherm equation. Various kinds of adsorbents showed different adsorption types; separation factor (R(L)) was used to determine the level of favorability of the adsorption type. In this work, activated carbons prepared by NaOH activation were evaluated in terms of their physical properties, chemical properties, and adsorption type; and activated carbon PKN2 was found to have most application potential.

  18. Physical and chemical properties and adsorption type of activated carbon prepared from plum kernels by NaOH activation

    Energy Technology Data Exchange (ETDEWEB)

    Tseng, R.-L. [Department of Safety, Health and Environmental Engineering, National United University, Miao-Li 360, Taiwan (China)]. E-mail: trl@nuu.edu.tw

    2007-08-25

    Activated carbon was prepared from plum kernels by NaOH activation at six different NaOH/char ratios. The physical properties including the BET surface area, the total pore volume, the micropore ratio, the pore diameter, the burn-off, and the scanning electron microscope (SEM) observation as well as the chemical properties, namely elemental analysis and temperature programmed desorption (TPD), were measured. The results revealed a two-stage activation process: stage 1 activated carbons were obtained at NaOH/char ratios of 0-1, surface pyrolysis being the main reaction; stage 2 activated carbons were obtained at NaOH/char ratios of 2-4, etching and swelling being the main reactions. The physical properties of stage 2 activated carbons were similar, and specific area was from 1478 to 1887 m{sup 2} g{sup -1}. The results of reaction mechanism of NaOH activation revealed that it was apparently because of the loss ratio of elements C, H, and O in the activated carbon, and the variations in the surface functional groups and the physical properties. The adsorption of the above activated carbons on phenol and three kinds of dyes (MB, BB1, and AB74) were used for an isotherm equilibrium adsorption study. The data fitted the Langmuir isotherm equation. Various kinds of adsorbents showed different adsorption types; separation factor (R {sub L}) was used to determine the level of favorability of the adsorption type. In this work, activated carbons prepared by NaOH activation were evaluated in terms of their physical properties, chemical properties, and adsorption type; and activated carbon PKN2 was found to have most application potential.

  19. Natural variability in the surface ocean carbonate ion concentration

    Directory of Open Access Journals (Sweden)

    N. S. Lovenduski

    2015-11-01

    Full Text Available We investigate variability in the surface ocean carbonate ion concentration ([CO32−] on the basis of a~long control simulation with an Earth System Model. The simulation is run with a prescribed, pre-industrial atmospheric CO2 concentration for 1000 years, permitting investigation of natural [CO32−] variability on interannual to multi-decadal timescales. We find high interannual variability in surface [CO32−] in the tropical Pacific and at the boundaries between the subtropical and subpolar gyres in the Northern Hemisphere, and relatively low interannual variability in the centers of the subtropical gyres and in the Southern Ocean. Statistical analysis of modeled [CO32−] variance and autocorrelation suggests that significant anthropogenic trends in the saturation state of aragonite (Ωaragonite are already or nearly detectable at the sustained, open-ocean time series sites, whereas several decades of observations are required to detect anthropogenic trends in Ωaragonite in the tropical Pacific, North Pacific, and North Atlantic. The detection timescale for anthropogenic trends in pH is shorter than that for Ωaragonite, due to smaller noise-to-signal ratios and lower autocorrelation in pH. In the tropical Pacific, the leading mode of surface [CO32−] variability is primarily driven by variations in the vertical advection of dissolved inorganic carbon (DIC in association with El Niño–Southern Oscillation. In the North Pacific, surface [CO32−] variability is caused by circulation-driven variations in surface DIC and strongly correlated with the Pacific Decadal Oscillation, with peak spectral power at 20–30-year periods. North Atlantic [CO32−] variability is also driven by variations in surface DIC, and exhibits weak correlations with both the North Atlantic Oscillation and the Atlantic Multidecadal Oscillation. As the scientific community seeks to detect the anthropogenic influence on ocean carbonate chemistry, these results

  20. Activated Carbon-Fly Ash-Nanometal Oxide Composite Materials: Preparation, Characterization, and Tributyltin Removal Efficiency

    Directory of Open Access Journals (Sweden)

    Olushola S. Ayanda

    2013-01-01

    Full Text Available The physicochemical properties, nature, and morphology of composite materials involving activated carbon, fly ash, nFe3O4, nSiO2, and nZnO were investigated and compared. Nature and morphology characterizations were carried out by means of scanning electron and transmission electron microscopy, X-ray diffraction, and Fourier transform infrared spectroscopy. Other physicochemical characterizations undertaken were CNH analysis, ash content, pH, point of zero charge, and surface area and porosity determination by BET. Experimental results obtained revealed that activated carbon, nSiO2, activated carbon-fly ash, activated carbon-fly ash-nFe3O4, activated carbon-fly ash-nSiO2, and activated carbon-fly ash-nZnO composite materials exhibited net negative charge on their surfaces while fly ash, nFe3O4, and nZnO possessed net positive charge on their surfaces. Relatively higher removal efficiency (>99% of TBT was obtained for all the composite materials compared to their respective precursors except for activated carbon. These composite materials therefore offer great potential for the remediation of TBT in wastewaters.

  1. Modeling high adsorption capacity and kinetics of organic macromolecules on super-powdered activated carbon.

    Science.gov (United States)

    Matsui, Yoshihiko; Ando, Naoya; Yoshida, Tomoaki; Kurotobi, Ryuji; Matsushita, Taku; Ohno, Koichi

    2011-02-01

    The capacity to adsorb natural organic matter (NOM) and polystyrene sulfonates (PSSs) on small particle-size activated carbon (super-powdered activated carbon, SPAC) is higher than that on larger particle-size activated carbon (powdered-activated carbon, PAC). Increased adsorption capacity is likely attributable to the larger external surface area because the NOM and PSS molecules do not completely penetrate the adsorbent particle; they preferentially adsorb near the outer surface of the particle. In this study, we propose a new isotherm equation, the Shell Adsorption Model (SAM), to explain the higher adsorption capacity on smaller adsorbent particles and to describe quantitatively adsorption isotherms of activated carbons of different particle sizes: PAC and SPAC. The SAM was verified with the experimental data of PSS adsorption kinetics as well as equilibrium. SAM successfully characterized PSS adsorption isotherm data for SPACs and PAC simultaneously with the same model parameters. When SAM was incorporated into an adsorption kinetic model, kinetic decay curves for PSSs adsorbing onto activated carbons of different particle sizes could be simultaneously described with a single kinetics parameter value. On the other hand, when SAM was not incorporated into such an adsorption kinetic model and instead isotherms were described by the Freundlich model, the kinetic decay curves were not well described. The success of the SAM further supports the adsorption mechanism of PSSs preferentially adsorbing near the outer surface of activated carbon particles.

  2. Modification of the dentin surface by using carbon nanotubes.

    OpenAIRE

    Akasaka, Tsukasa; Nakata, Keiko; Uo, Motohiro; WATARI, Fumio

    2009-01-01

    Recent studies have shown that carbon nanotubes (CNTs) can be used as biomedical materials because of their unique properties. CNTs effect nucleation of hydroxyapatite, because of which considerable interest has been generated regarding the use of CNTs in dentistry. However, there are only a few reports on the use of CNTs as dental materials. In this study, we investigated the changes induced in the surfaces of tooth slices by the application of a coating of CNTs by observing CNT-coated tooth...

  3. Electric arc surfacing on low carbon steel: Structure and properties

    Science.gov (United States)

    Ivanov, Yurii; Gromov, Victor; Kormyshev, Vasilii; Konovalov, Sergey; Kapralov, Evgenii; Semin, Alexander

    2016-11-01

    By the methods of modern materials science, the structure-phase state and microhardness distribution along the cross-section of single and double coatings surfaced on martensite low carbon steel by alloy powder-cored wire were studied. It was established that the increased mechanical properties of surfaced layer are determined by the sub-micro and nanodispersed martensite structure formation, containing iron borides forming the eutectic of lamellar form. The plates of Fe2B are formed mainly in the eutectic of a single-surfaced layer, while FeB is formed in a double-surfaced layer. The existence of bend extinction contours indicating the internal stress fields formation at the boundaries of Fe borides-α-Fe phases were revealed.

  4. Hierarchical porous carbon with ultrahigh surface area from corn leaf for high-performance supercapacitors application

    Science.gov (United States)

    Yang, Xiaoqing; Li, Chengfei; Chen, Yue

    2017-02-01

    A new class of hierarchical porous carbon (HPC) with ultrahigh surface area is successfully fabricated by carefully selecting biomass carbon precursors and activation reagent, through which corn leaf (CL) with natural well-defined macropore channels is used as the carbon precursor, and H3PO4 is used as the active agent by virtue of its pore-widening effect. The as-prepared CL-based HPC (CLHPC) with a H3PO4/semi-carbonized CL mass ratio of 2 (CLHPC-2) demonstrates the highest specific surface area of 2507 m2 g-1 donated by 28.3% of micropore and 71.6% of mesopore, while maintaining the channel-like macroporous structure derived from the well-defined natural structure in CL. The combination of the hierarchical porous structure and ultrahigh surface area enables rapid electrolyte diffusion and sufficient active sites for charge accumulation. As a result, CLHPC-2 exhibits excellent electrochemical performance, such as high specific capacitance of 230 F g-1 at the current density of 0.1 A g-1, excellent high-rate capability (retention of 91% from 0.1 to 5 A g-1), and good cycling stability (99% capacitance retention after 10 000 cycles).

  5. Charcoal and activated carbon at elevated pressure

    Energy Technology Data Exchange (ETDEWEB)

    Antal, M.J. Jr.; Dai, Xiangfeng; Norberg, N. [Univ. of Hawaii at Manoa, Honolulu, HI (United States)] [and others

    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.

  6. Effect of samarium on methanation resistance of activated carbon supported ruthenium catalyst for ammonia synthesis

    Institute of Scientific and Technical Information of China (English)

    周春晖; 祝一锋; 刘化章

    2010-01-01

    The effects of samarium(Sm) on carbon-methanation and catalytic activity of the Ba-Ru-K/AC (active carbon) catalyst for ammonia synthesis were investigated. The addition of samarium improved significantly the activity and stability of the catalyst. The results of temperature-programmed desorption (H2-TPD) and in-situ-TPSR FTIR indicated that samarium impeded the adsorption of hydrogen on the catalyst surface, thus leading to the high catalytic activity and resistance to carbon-methanation. XRD patterns reve...

  7. Preparation and hydrogen storage capacity of highly porous activated carbon materials derived from polythiophene

    OpenAIRE

    2011-01-01

    [EN] Highly porous carbons have been successfully synthesized by chemical activation of polythiophene with KOH. The activation process was performed under relatively mild activation conditions, i. e., a KOH/polymer weight ratio of 2 and reaction temperatures in the 600–850 °C range. The porous carbons thus obtained possess very large surface areas, up to 3000 m2/g, and pore volumes of up to 1.75 cm3/g. The pore size distribution of these carbons can be tuned via modification of the activation...

  8. Adsorption onto fibrous activated carbon: applications to water treatment

    Energy Technology Data Exchange (ETDEWEB)

    Le Cloirec, P.; Brasquet, C.; Subrenat, E. [Ecole des Mines de Nantes, Nantes (France)

    1997-03-01

    The adsorption of polluted waters is performed by activated carbon fibers (ACF). This new material is characterized by scanning electron microscopy. BET surface areas and pore volumes are determined. Adsorption of natural organics (humic substances) and micropollutants (aromatic compounds such as benzene and toluene) is carried out in a batch or dynamic reactor. Classical models are applied and kinetic constants calculated. The results show that the performance of ACF is significantly higher than that of granular activated carbon (GAC) in terms of adsorption velocity and selectivity for micropollutants. These higher performances are due to some ACF physical properties, such as their high BET surface area and micropore volume. Moreover, the micropores are directly connected on the external surface area of fibers, which allows smaller mass transfer resistance. In a dynamic reactor, the breakthrough curves obtained with ACF beds are particularly steep, suggesting a smaller mass transfer resistance than that of GAC. The adsorption zone in an ACF bed is about 3.5 mm and is not really dependent on the water flow rate within the studied range. 25 refs., 14 figs., 6 tabs.

  9. 花生壳活性炭的表征,表面改性及吸附脱除水中Pb2+离子%Peanut Shell Activated Carbon: Characterization, Surface Modification and Adsorption of Pb2+ from Aqueous Solution

    Institute of Scientific and Technical Information of China (English)

    徐涛; 刘晓勤

    2008-01-01

    Metal ion contamination of drinking water and waste water, especially with heavy metal ion such as lead, is a serious and ongoing problem. In this work, activated carbon prepared from peanut shell (PAC) was used for the removal of Pb2+ from aqueous solution. The impacts of the Pb2+ adsorption capacities of the acid-modified carbons oxidized with HNO3 were also investigated. The surface functional groups of PAC were confirmed by Fourier transform infrared (FTIR) spectroscopy, X-ray photoelectron spectroscopy (XPS), Boehm titration. The textural properties (surface area, total pore volume) were evaluated from the nitrogen adsorption isotherm at 77K. The experimental results presented indicated that the adsorption data fitted better with the Langmuir adsorption model. A comparative study with a commercial granular activated carbon (GAC) showed that PAC was 10.3 times more efficient compared to GAC based on Langmuir maximum adsorption capacity. Further analysis results by the Langmuir equation showed that HNO3 [20% (by mass)] modified PAC has larger adsorption capacity of Pb2+ from aqueous solution (as much as 35.5mg.g1). The adsorption capacity enhancement ascribed to pore widening, increased cation-exchange capacity by oxygen groups, and the promoted hydrophilicity of the carbon surface.

  10. Adsorption onto fluidized powdered activated carbon flocs-pACF.

    Science.gov (United States)

    Serpa, Ana Lídia; Schneider, Ivo André H; Rubio, Jorge

    2005-02-01

    This work presents a new adsorption technique where the adsorbent (powdered activated carbon-PAC) is in the form of suspended flocs formed with water-soluble polymer flocculants. Thus, the adsorption of a typical dye, methylene blue (MB), was studied onto polyacrylamide flocs of PAC (PACF) in a fluidized bed reactor. The technique is based on the fact that the adsorption capacity of PAC does not decrease after flocculation because the adsorbed polymer occupies only a few surface sites, in the form of trains, loops, and tails. Moreover, the adsorption was found to proceed through a rapid mass transfer of MB to the adsorbing PAC flocs, in the same extent as onto PAC. Because of the rapid settling characteristics of the aggregates formed, the two phase separations, loaded PAC and solution, become easier. Thus, the technique offers the advantages of conducting simultaneously both adsorption and solid/liquid separation all in one single stage. Results obtained showed that high MB removal values can be attained in a fluidized bed reactor (>90%) and that PACF presents a much higher adsorption capacity (breakthrough points) than granulated activated carbon (GAC) in the same adsorbing bed. It is believed that this technique highly broadens the potential of the use of powdered activated carbon or other similar ultrafine adsorbents.

  11. ENTRAINED-FLOW ADSORPTION OF MERCURY USING ACTIVATED CARBON

    Science.gov (United States)

    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...

  12. Activated-Carbon Sorbent With Integral Heat-Transfer Device

    Science.gov (United States)

    Jones, Jack A.; Yavrouian, Andre

    1996-01-01

    Prototype adsorption device used, for example, in adsorption heat pump, to store natural gas to power automobile, or to separate components of fluid mixtures. Device includes activated carbon held together by binder and molded into finned heat-transfer device providing rapid heating or cooling to enable rapid adsorption or desorption of fluids. Concepts of design and fabrication of device equally valid for such other highly thermally conductive devices as copper-finned tubes, and for such other high-surface-area sorbents as zeolites or silicates.

  13. Activated carbon adsorption for chromium treatment and recovery; Adsorbimento di cromo su carboni attivi a scopo di recupero e decontaminazione

    Energy Technology Data Exchange (ETDEWEB)

    Baroncelli, F.; Castelli, S.; De Francesco, M. [ENEA, Casaccia (Italy). Area Energia e Innovazione

    1994-05-01

    The capability of actived carbon systems to adsorb chromium from wastewater of galvanic industry is valued. Batch tests and column tests are carried out with good results. An activated carbon with acidic surface oxides can adsorb both chromate and chromium (III); chromate is reduced in situ and then adsorbed as chromium (III). Chromium can be desorbed from carbon by an acid or basic treatment obtaining respectively chromium (III) or chromate solutions. Carbon can be regenerated many times without evident signs of deterioration.

  14. Immobilization of Active Bacteriophages on Polyhydroxyalkanoate Surfaces.

    Science.gov (United States)

    Wang, Chanchan; Sauvageau, Dominic; Elias, Anastasia

    2016-01-20

    A rapid, efficient technique for the attachment of bacteriophages (phages) onto polyhydroxyalkanoate (PHA) surfaces has been developed and compared to three reported methods for phage immobilization. Polymer surfaces were modified to facilitate phage attachment using (1) plasma treatment alone, (2) plasma treatment followed by activation by 1-ethyl-3-(3-(dimethylamino)propyl)carbodiimide hydrochloride (EDC) and N-hydroxysulfosuccinimide (sulfo-NHS), (3) plasma-initiated acrylic acid grafting, or (4) plasma-initiated acrylic acid grafting with activation by EDC and sulfo-NHS. The impact of each method on the surface chemistry of PHA was investigated using contact angle analysis and X-ray photoelectron spectroscopy. Each of the four treatments was shown to result in both increased hydrophilicity and in the modification of the surface functional groups. Modified surfaces were immersed in suspensions of phage T4 for immobilization. The highest level of phage binding was observed for the surfaces modified by plasma treatment alone. The change in chemical bond states observed for surfaces that underwent plasma treatment is suspected to be the cause of the increased binding of active phages. Plasma-treated surfaces were further analyzed through phage-staining and fluorescence microscopy to assess the surface density of immobilized phages and their capacity to capture hosts. The infective capability of attached phages was confirmed by exposing the phage-immobilized surfaces to the host bacteria Escherichia coli in both plaque and infection dynamic assays. Plasma-treated surfaces with immobilized phages displayed higher infectivity than surfaces treated with other methods; in fact, the equivalent initial multiplicity of infection was 2 orders of magnitude greater than with other methods. Control samples - prepared by immersing polymer surfaces in phage suspensions (without prior plasma treatment) - did not show any bacterial growth inhibition, suggesting they did not bind

  15. Characterization of a surface modified carbon cryogel and a carbon supported Pt catalyst

    Directory of Open Access Journals (Sweden)

    BILJANA M. BABIĆ

    2007-08-01

    Full Text Available A carbon cryogel, synthesized by carbonization of a resorcinol/formaldehyde cryogel and oxidized in nitric acid, was used as catalyst support for Pt nano-particles. The Pt/C catalyst was prepared by a modified polyol synthesis method in an ethylene glycol (EG solution. Characterization by nitrogen adsorption showed that the carbon cryogel support and the Pt/C catalyst were mesoporous materials with high specific surface areas (SBET > 400 m2 g-1 and large mesoporous volumes. X-Ray diffraction of the catalyst demonstrated the successful reduction of the Pt precursor to metallic form. TEM Images of the Pt/C catalyst and Pt particle size distribution showed that the mean Pt particle size was about 3.3 nm. Cyclic voltammetry (CV experiments at various scan rates (from 2 to 200 mV s-1 were performed in 0.5 mol dm-3 HClO4 solution. The large capacitance of the oxidized carbon cryogel electrode, which arises from a combination of the double-layer capacitance and pseudocapacitance, associated with the participation of surface redox-type reactions was demonstrated. For the oxidized carbon cryogel, the total specific capacitance determined by 1/C vs. ν0.5 extrapolation method was found to be 386 F g-1. The hydrogen oxidation reaction at the investigated Pt/C catalyst proceeded as an electrochemically reversible, two-electron direct discharge reaction.

  16. On the photoactivity of S-doped nanoporous carbons:Importance of surface chemistry and porosity

    Institute of Scientific and Technical Information of China (English)

    Teresa J. Bandosz; Mykola Seredych

    2014-01-01

    This minireview summarizes our recent findings on the photoactivity of S-doped nanoporous car-bons. The materials were either synthesized from the sulfur-containing polymers or obtained by heat treatment of commercial carbon with hydrogen sulfide. Their surface was extensively charac-terized from the points of view of its surface chemistry, porosity, morphology, and electronic prop-erties. The carbons showed enhanced activity towards oxidation of arsine and removal of diben-zothiophenes from model diesel fuel. The latter were oxidized to various oxygen containing inter-mediates and the cleavage of C-C bonds in aromatic ring was detected when carbon with adsorbed species was exposed to UV or visible light. Irradiation resulted in generation of photocurrent in a broad range of wavelength. The presence of sulfur led to the reduction of oxygen and contributed to an increased capacitive performance. We link these effects to the presence of reduced sulfur in the small pores which enhances the dispersive interactions via inducing a positive charge to carbon atoms, to sulfur in oxygenated forms which contribute to Faradaic reactions and increase the polar interactions, and to the hydrophobicity of a surface in small pores where oxygen can be reduced by excited electrons from chromophoric-like sulfur containing groups.

  17. Activated Carbon Fibers For Gas Storage

    Energy Technology Data Exchange (ETDEWEB)

    Burchell, Timothy D [ORNL; Contescu, Cristian I [ORNL; Gallego, Nidia C [ORNL

    2017-01-01

    The advantages of Activated Carbon Fibers (ACF) over Granular Activated Carbon (GAC) are reviewed and their relationship to ACF structure and texture are discussed. These advantages make ACF very attractive for gas storage applications. Both adsorbed natural gas (ANG) and hydrogen gas adsorption performance are discussed. The predicted and actual structure and performance of lignin-derived ACF is reviewed. The manufacture and performance of ACF derived monolith for potential automotive natural gas (NG) storage applications is reported Future trends for ACF for gas storage are considered to be positive. The recent improvements in NG extraction coupled with the widespread availability of NG wells means a relatively inexpensive and abundant NG supply in the foreseeable future. This has rekindled interest in NG powered vehicles. The advantages and benefit of ANG compared to compressed NG offer the promise of accelerated use of ANG as a commuter vehicle fuel. It is to be hoped the current cost hurdle of ACF can be overcome opening ANG applications that take advantage of the favorable properties of ACF versus GAC. Lastly, suggestions are made regarding the direction of future work.

  18. Flame retardant polypropylene nanocomposites reinforced with surface treated carbon nanotubes

    Science.gov (United States)

    Guleria, Abhishant

    Polypropylene nanocomposites are prepared by reinforcing carbon nanotubes by ex-situ solution mixing method. Interfacial dispersion of carbon nanotubes in polypropylene have been improved by surface modification of CNTs and adding surfactants. Polypropylene nanocomposites fabrication was done after treating CNTs. Firstly, oxidation of CNTs followed by silanization for addition of functionalized groups on the surface of CNTs. Maleic anhydride grafted PPs were used as surfactants. Maleic anhydrides with two different molecular weights were LAMPP and HMAPP. Successful oxidation of CNTs by nitric acid and functionalized CNTs by 3-Aminopropyltriethoxysilane was confirmed by attenuated total reflection-Fourier transform infrared spectroscopy (ATR-FTIR) with evidence of absorption peak at 1700 and 1100-1000 cm-1. Scanning electron microscopy (SEM) micrographs revealed that the CNTs dispersion quality was improved by directly adding LMAPP/HMAPP into PP/CNTs system and the PP-CNTs adhesion was enhanced through both the CNTs surface treatment and the addition of surfactant. Thermal gravimetric analysis (TGA) revealed an enhanced thermal stability in the PP/CNTs and PP/CNTs/MAPP. Differential scanning calorimetry (DSC) characterization demonstrated that the crystalline temperature, fusion heat and crystalline fraction of hosting PP were decreased with the introduction of CNTs and surface treated CNTs; however, melting temperature was only slightly changed. Melting rheological behaviors including complex viscosity, storage modulus, and loss modulus indicated significant changes in the PP/MAPP/CNTs system before and after functionalization of CNTs, and the mechanism were also discussed in details.

  19. Surface modification of multiwall carbon nanotubes by sulfonitric treatment

    Science.gov (United States)

    Gómez, Sofía; Rendtorff, Nicolás M.; Aglietti, Esteban F.; Sakka, Yoshio; Suárez, Gustavo

    2016-08-01

    Carbon nanotubes are widely used for electronic, mechanical, and optical devices due to their unique structural and quantum characteristics. The species generated by oxidation on the surface of these materials permit binding new reaction chains, which improves the dispersibility, processing and compatibility with other materials. Even though different acid treatments and applications of these CNT have been reported, relatively few research studies have focused on the relationship between the acid treatment and the formation of nanodefects, specific oxidized species or CNT surface defects. In this work, multiwall carbon nanotube (MWCNT) oxidation at 90 °C was characterized in order to determine the acid treatment effect on the surface. It was found that oxidized species are already present in MWCNT without an acid treatment, but there are not enough to cause water-based dispersion. The species were identified and quantified by infrared spectroscopy and X-ray photoelectron spectroscopy. Also, transmission electron microscopy observations showed not only modifications of the oxidized species, but also morphological damage on the surfaces of MWCNT after being subjected to the acid treatment. This effect was also confirmed by Raman spectroscopy. The acid treatment generates higher oxidized species, decreasing the zeta potential in the whole pH range.

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

    Science.gov (United States)

    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.

  1. Characterization and Methanol Adsorption of Walnut-shell Activated Carbon Prepared by KOH Activation

    Institute of Scientific and Technical Information of China (English)

    YU Qiongfen; LI Ming; JI Xu; QIU Yu; ZHU Yuntao; LENG Congbin

    2016-01-01

    Walnut-shell activated carbons (WSACs) were prepared by the KOH chemical activation. The effects of carbonization temperature, activation temperature, and ratio of KOH to chars on the pore development of WSACs were investigated. Fourier transform infrared spectroscopy (FTIR), X-ray powder diffraction (XRD), and scanning electron microscopy (SEM) were employed to characterize the microstructure and morphology of WSACs. Methanol adsorption performance onto the optimal WSAC and the coal-based AC were also investigated. The results show that the optimal preparation conditions are a carbonization temperature of 700℃, an activation temperature of 700℃, and a mass ratio of 3. The BET surface area, the micropore volume, and the micropore volume percentage of the optimal WASC are 1636 m2/g, 0.641 cm3/g and 81.97%, respectively. There are a lot of micropores and a certain amount of meso- and macropores. The characteristics of the amorphous state are identified. The results show that the optimal WSAC is favorable for methanol adsorption. The equilibrium adsorption capacity of the optimal WSAC is 248.02mg/g. It is shown that the equilibrium adsorption capacity of the optimal WSAC is almost equivalent to that of the common activated carbon. Therefore the optimal WSAC could be a potential adsorbent for the solar energy adsorption refrigeration cycle.

  2. Metal-Free Counter Electrode for Efficient Dye-Sensitized Solar Cells through High Surface Area and Large Porous Carbon

    Directory of Open Access Journals (Sweden)

    Pavuluri Srinivasu

    2011-01-01

    Full Text Available Highly efficient, large mesoporous carbon is fabricated as a metal-free counter electrode for dye-sensitized solar cells. The mesoporous carbon shows very high energy conversion efficiency of 7.1% compared with activated carbon. The mesoporous carbon is prepared and characterized by nitrogen adsorption, scanning electron microscopy (SEM, and transmission electron microscopy (TEM. The nitrogen adsorption data reveals that the material possesses BET specific surface area ca.1300 m2/g and pore diameter 4.4 nm. Hexagonal rod-like morphology and ordered pore structure of mesoporous carbon are confirmed by electron microscopy data. The better performance of this carbon material is greatly benefited from its ordered interconnected mesoporous structure and high surface area.

  3. Physical and chemical properties of selected agricultural byproduct-based activated carbons and their ability to adsorb geosmin.

    Science.gov (United States)

    Ng, Chilton; Losso, Jack N; Marshall, Wayne E; Rao, Ramu M

    2002-09-01

    The objectives of this study were to evaluate selected physical and chemical properties of agricultural byproduct-based activated carbons made from pecan shells and sugarcane bagasse, and compare those properties to a commercial coal-based activated carbon as well as to compare the adsorption efficiency of these carbons for geosmin. Comparison of the physical and chemical properties of pecan shell- and bagasse-based carbons to the commercial carbon, Calgon Filtrasorb 400, showed that pecan shell carbon, but not the bagasse carbon, compared favorably to Filtrasorb 400, especially in terms of surface area, bulk density, ash and attrition. A carbon dosage study done in a model system showed the amount of geosmin adsorbed to be greater for Filtrasorb 400 and the bagasse-based carbon at low carbon concentrations than for the pecan shell carbons, but geosmin adsorption was similar in all carbons at higher carbon dosages. Application of the Freundlich isotherm model to the adsorption data showed that carbons made by steam activation of pecan shells or sugarcane bagasse had geosmin adsorption characteristics most like those of the commercial carbon. In terms of physical, chemical and adsorptive properties, steam-activated pecan shell carbon most resembled the commercial carbon and has the potential to replace Filtrasorb 400 in applications involving removal of geosmin from aqueous environments.

  4. Activated carbon fiber for heterogeneous activation of persulfate: implication for the decolorization of azo dye.

    Science.gov (United States)

    Chen, Jiabin; Hong, Wei; Huang, Tianyin; Zhang, Liming; Li, Wenwei; Wang, Ying

    2016-09-01

    Activated carbon fiber (ACF) was used as a green catalyst to activate persulfate (PS) for oxidative decolorization of azo dye. ACF demonstrated a higher activity than activated carbon (AC) to activate PS to decolorize Orange G (OG). The decolorization efficiency of OG increased as ACF loading, PS dosage, and temperature increased. OG decolorization followed a pseudo first-order kinetics, and the activation energy was 40.902 kJ/mol. pH had no apparent effect on OG decolorization. Radical quenching experiments with various radical scavengers (e.g., alcohols, phenol) showed that radical-induced decolorization of OG took place on the surface of ACF, and both SO4 (·-) and HO· were responsible for OG decolorization. The impact of inorganic salts was also evaluated because they are important compositions of dye wastewater. Cl(-) and SO4 (2-) exhibited a promoting effect on OG decolorization, and the accelerating rate increased with elevating dosage of ions. Addition of Cl(-) and SO4 (2-) could increase the adsorption of OG on ACF surface, thus favorable for OG decolorization caused by the surface-bound SO4 (·-) and HO·. Conversely, HCO3 (-) and humic acid (HA) slightly inhibited OG decolorization. The azo band and naphthalene ring on OG were remarkably destructed to other intermediates and finally mineralized to CO2 and H2O.

  5. Experimental study on adsorption kinetics of activated carbon/R134a and activated carbon/R507A pairs

    Energy Technology Data Exchange (ETDEWEB)

    Habib, Khairul; Koyama, Shigeru [Interdisciplinary Graduate School of Engineering Sciences, Kyushu University, 6-1 Kasuga-koen, Kasuga-shi, Fukuoka 816-8580 (Japan); Saha, Bidyut B. [Mechanical Engineering Department, Kyushu University, 744 Motooka, Fukuoka-shi, Fukuoka 819-0395 (Japan); Rahman, Kazi A.; Chakraborty, Anutosh; Ng, Kim Choon [Mechanical Engineering Department, National University of Singapore, 10 Kent Ridge Crescent (Singapore)

    2010-06-15

    The objective of this article is to evaluate adsorption kinetics of R134a and R507A on pitch based activated carbon experimentally by a constant volume variable pressure method at different adsorption temperatures ranging from 20 to 60 C. These data are useful for the design of adsorption cooling and refrigeration systems and are unavailable in the literature. Data obtained from the kinetic studies were analyzed with various kinetic models and the Fickian diffusion model is found to be the most suitable overall. Guided by the experimental measurements, the surface diffusion is also estimated and is found that it follows the classical Arrhenius law within the experimental range. (author)

  6. A synthesis method for cobalt doped carbon aerogels with high surface area and their hydrogen storage properties

    Energy Technology Data Exchange (ETDEWEB)

    Tian, H.Y.; Buckley, C.E. [Department of Imaging and Applied Physics, Curtin University of Technology, GPO Box U 1987, Perth 6845, WA (Australia); CSIRO National Hydrogen Materials Alliance, CSIRO Energy Centre, 10 Murray Dwyer Circuit, Steel River Estate, Mayfield West, NSW 2304 (Australia); Sheppard, D.A.; Paskevicius, M. [Department of Imaging and Applied Physics, Curtin University of Technology, GPO Box U 1987, Perth 6845, WA (Australia); Hanna, N. [CSIRO Process Science and Engineering, Waterford, WA (Australia)

    2010-12-15

    Carbon aerogels doped with nanoscaled Co particles were prepared by first coating activated carbon aerogels using a wet-thin layer coating process. The resulting metal-doped carbon aerogels had a higher surface area ({proportional_to}1667 m{sup 2} g{sup -1}) and larger micropore volume ({proportional_to}0.6 cm{sup 3} g{sup -1}) than metal-doped carbon aerogels synthesised using other methods suggesting their usefulness in catalytic applications. The hydrogen adsorption behaviour of cobalt doped carbon aerogel was evaluated, displaying a high {proportional_to}4.38 wt.% H{sub 2} uptake under 4.6 MPa at -196 C. The hydrogen uptake capacity with respect to unit surface area was greater than for pure carbon aerogel and resulted in {proportional_to}1.3 H{sub 2} (wt. %) per 500 m{sup 2} g{sup -1}. However, the total hydrogen uptake was slightly reduced as compared to pure carbon aerogel due to a small reduction in surface area associated with cobalt doping. The improved adsorption per unit surface area suggests that there is a stronger interaction between the hydrogen molecules and the cobalt doped carbon aerogel than for pure carbon aerogel. (author)

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

    Science.gov (United States)

    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.

  8. Laser alloying of the plain carbon steel surface layer

    Directory of Open Access Journals (Sweden)

    A. Radziszewska

    2008-07-01

    Full Text Available As an example of the types of features observed after laser alloying, the addition of Ta to mild carbon steel is described. The system is of interest because such alloying is beneficial in improving surface related properties. The paper describes the microstructure and properties (phase and chemical composition, microhardness of the laser alloyed surface layer. In the investigation the optical microscope, the scanning electron microscope (SEM, chemical (EDS microanalysis composition and microhardness testing methods have been used. Specimens of 0,17 %C plain steel were coated with Ta powder layers. The paints containing organic components were used as the binders during deposition of Ta powder layers on the sample surface. The thickness of Ta deposited layers amounted to 0,16 mm. The specimens were then swept through high power (of nominal power 2,5 kW CW CO2 laser radiation at different speeds.The surface alloyed layers varied in microstructure consisted of fiber like Ta2C + γ eutectics, chemical composition and microhardness. The EDS analyses revealed the enrichment of tantalum in the laser alloyed zone (LAZ. The changes of process parameters had an influence on the hardness of alloyed surface layers: by increasing scanning velocity (from 12 mm/s to 20 mm/s and decreasing laser power (from 1,8 kW to 1,35 kW, the hardness diminished. The wear tests were also carried out which showed that laser alloying of plain carbon steel surface layer led to improvement of their wear resistance.

  9. Surface modification of multiwall carbon nanotubes by sulfonitric treatment

    Energy Technology Data Exchange (ETDEWEB)

    Gómez, Sofía, E-mail: sofiagomez@cetmic.unlp.edu.ar [Centro de Tecnología de Recursos Minerales y Cerámica (CETMIC), Camino Centenario y 506, C.C.49, M.B. Gonnet B1897ZCA (Argentina); Rendtorff, Nicolás M., E-mail: rendtorff@cetmic.unlp.edu.ar [Centro de Tecnología de Recursos Minerales y Cerámica (CETMIC), Camino Centenario y 506, C.C.49, M.B. Gonnet B1897ZCA (Argentina); Departamento de Química, Facultad de Ciencias Exactas—UNLP, Calle 115 y 47, La Plata 1900 (Argentina); Aglietti, Esteban F., E-mail: eaglietti@cetmic.unlp.edu.ar [Centro de Tecnología de Recursos Minerales y Cerámica (CETMIC), Camino Centenario y 506, C.C.49, M.B. Gonnet B1897ZCA (Argentina); Departamento de Química, Facultad de Ciencias Exactas—UNLP, Calle 115 y 47, La Plata 1900 (Argentina); Sakka, Yoshio, E-mail: SAKKA.Yoshio@nims.go.jp [National Institute for Materials Science, Tsukuba, Ibaraki 305-0047 (Japan); Suárez, Gustavo, E-mail: gsuarez@cetmic.unlp.edu.ar [Centro de Tecnología de Recursos Minerales y Cerámica (CETMIC), Camino Centenario y 506, C.C.49, M.B. Gonnet B1897ZCA (Argentina); Departamento de Química, Facultad de Ciencias Exactas—UNLP, Calle 115 y 47, La Plata 1900 (Argentina)

    2016-08-30

    Highlights: • After the acid treatment highly increase the amount carbonyl and carboxylic groups. • The oxidation of MWCNT generates a high negative charge of it in all the pH range. • It could achieve a good dispersion of the MWCNT in water-based suspension. • There is morphological damage on the surfaces of MWCNT after the acid treatment. • Some surface defects but no shortening were observed by TEM images. - Abstract: Carbon nanotubes are widely used for electronic, mechanical, and optical devices due to their unique structural and quantum characteristics. The species generated by oxidation on the surface of these materials permit binding new reaction chains, which improves the dispersibility, processing and compatibility with other materials. Even though different acid treatments and applications of these CNT have been reported, relatively few research studies have focused on the relationship between the acid treatment and the formation of nanodefects, specific oxidized species or CNT surface defects. In this work, multiwall carbon nanotube (MWCNT) oxidation at 90 °C was characterized in order to determine the acid treatment effect on the surface. It was found that oxidized species are already present in MWCNT without an acid treatment, but there are not enough to cause water-based dispersion. The species were identified and quantified by infrared spectroscopy and X-ray photoelectron spectroscopy. Also, transmission electron microscopy observations showed not only modifications of the oxidized species, but also morphological damage on the surfaces of MWCNT after being subjected to the acid treatment. This effect was also confirmed by Raman spectroscopy. The acid treatment generates higher oxidized species, decreasing the zeta potential in the whole pH range.

  10. Coordinated surface activities in Variovorax paradoxus EPS

    Directory of Open Access Journals (Sweden)

    Gregory Glenn A

    2009-06-01

    Full Text Available Abstract Background Variovorax paradoxus is an aerobic soil bacterium frequently associated with important biodegradative processes in nature. Our group has cultivated a mucoid strain of Variovorax paradoxus for study as a model of bacterial development and response to environmental conditions. Colonies of this organism vary widely in appearance depending on agar plate type. Results Surface motility was observed on minimal defined agar plates with 0.5% agarose, similar in nature to swarming motility identified in Pseudomonas aeruginosa PAO1. We examined this motility under several culture conditions, including inhibition of flagellar motility using Congo Red. We demonstrated that the presence of a wetting agent, mineral, and nutrient content of the media altered the swarming phenotype. We also demonstrated that the wetting agent reduces the surface tension of the agar. We were able to directly observe the presence of the wetting agent in the presence and absence of Congo Red, and found that incubation in a humidified chamber inhibited the production of wetting agent, and also slowed the progression of the swarming colony. We observed that swarming was related to both carbon and nitrogen sources, as well as mineral salts base. The phosphate concentration of the mineral base was critical for growth and swarming on glucose, but not succinate. Swarming on other carbon sources was generally only observed using M9 salts mineral base. Rapid swarming was observed on malic acid, d-sorbitol, casamino acids, and succinate. Swarming at a lower but still detectable rate was observed on glucose and sucrose, with weak swarming on maltose. Nitrogen source tests using succinate as carbon source demonstrated two distinct forms of swarming, with very different macroscopic swarm characteristics. Rapid swarming was observed when ammonium ion was provided as nitrogen source, as well as when histidine, tryptophan, or glycine was provided. Slower swarming was observed

  11. Coupling template nanocasting and self-activation for fabrication of nanoporous carbon

    Science.gov (United States)

    Kong, Lingjun; Liu, Mingxiang; Diao, Zenghui; Chen, Diyun; Chang, Xiangyang; Xiong, Ya

    2016-11-01

    Hierarchical nanoporous carbon (NPC) with great surface area and developed pore size distribution has been intently concerned. Herein, we report a facile method coupling template nanocasting and self-activation to fabricate nanoporous carbon with continuous micro, meso and macro pores, in which CaCO3 acted as template and activation reagent while the flour was the carbon precursor. Effects of mass ratio of CaCO3 to flour and carbonized temperature on the pore structures of NPC were investigated by nitrogen adsorption-desorption isotherms and SEM analysis. Another kind of carbon was prepared by directly mixed powder CaCO3 with flour carbonized at 800 °C (NPC-p) to comparatively investigate the pore fabricating mechanism. Results shown that carbonized at 800 °C was favorable to fabricate the continuous macro, meso and micro pores. The resulted NPC in a mass ratio of 1 to 2 had the considerable SBET and VT of 575.4 m2/g and 0.704 cm3/g, respectively. Only surface activation was observed for NPC-p. Nanocasting of the powder CaCO3 contributed to fabricate macropores and the CO2 activation contributed to meso- and micropores. Coupling activation and nanocasting effect due to the decomposition of CaCO3 template into CO2 and CaO was ascribed to synthesize the nanoporous carbon.

  12. Effects of carbon fiber surface characteristics on interfacial bonding of epoxy resin composite subjected to hygrothermal treatments

    Science.gov (United States)

    Li, Min; Liu, Hongxin; Gu, Yizhuo; Li, Yanxia; Zhang, Zuoguang

    2014-01-01

    The changes of interfacial bonding of three types of carbon fibers/epoxy resin composite as well as their corresponding desized carbon fiber composites subjecting to hygrothermal conditions were investigated by means of single fiber fragmentation test. The interfacial fracture energy was obtained to evaluate the interfacial bonding before and after boiling water aging. The surface characteristics of the studied carbon fiber were characterized using X-ray photoelectron spectroscopy. The effects of activated carbon atoms and silicon element at carbon fiber surface on the interfacial hygrothermal resistance were further discussed. The results show that the three carbon fiber composites with the same resin matrix possess different hygrothermal resistances of interface and the interfacial fracture energy after water aging can not recovery to the level of raw dry sample (irreversible changes) for the carbon fiber composites containing silicon. Furthermore, the activated carbon atoms have little impact on the interfacial hygrothermal resistance. The irreversible variations of interfacial bonding and the differences among different carbon fiber composites are attributed to the silicon element on the carbon fiber bodies, which might result in hydrolyzation in boiling water treatment and degrade interfacial hygrothermal resistance.

  13. Next Generation Structural Composite Using Surface Grown Carbon Nanotubes

    Science.gov (United States)

    2012-10-01

    Marwan  Al‐Haik (Virginia Tech, Mechanical Engineering)  3‐ Claudi Luhrs (Co‐PI, UNM, Mechanical Engineering)  4‐ Hamid Garmestani (Georgia Tech, Mechanical...Taha  Army  Office  of  Research  Award:  DURIP:  High  Velocity  Impact  Equipment, May 2010.  5. Dr  Marwan   Al‐Haik  and  Dr. Mahmoud  Reda  Taha...Chavez.   Honor Undergraduate Thesis, Growth of carbon nanotubes/nanofibers on the  surface  of  carbon  fibers.  Advisor  Marwan   Al‐Haik  May  2009

  14. Salinity Effect on Ocean Surface Carbon Dioxide Fugacity

    Science.gov (United States)

    Xie, X.; Liu, W. T.

    2015-12-01

    Sea surface salinity (SSS) measured by Aquarius and the Soil Moisture Ocean Salinity (SMOS) over global ocean is used to characterize the change of the partial pressure of carbon dioxide at sea (pCO2sea). A statistical model on satellite retrieval of pCO2sea is used to examine the relation between the two parameters over two selected regions. One is the tropical western Atlantic, where hydrological forcing by Amazon River discharge causes major changes, and the other is the equatorial eastern Pacific, where ocean thermodynamics is more important. In both regions, pCO2sea tracks SSS closely in seasonal and year-to-year changes. In the Pacific, tropical instability wave is a major factor in the high frequency changes of both parameters. The manifestations of this relation in ocean-atmosphere carbon dioxide exchange and ocean acidification are explored.

  15. Surface diffusion of a carbon adatom on charged SWCNT

    Science.gov (United States)

    Han, Longtao; Krstic, Predrag; Kaganovich, Igor

    2016-09-01

    Diffusion of a carbon adatom on SWCNT could be a mechanism for a CNT growth in a volume plasma, supplementing its growth from a transition metal catalyst nanoparticle. However, being embedded in plasma, the nanotube can charge by the plasma particles irradiation, in particular by electrons. Using Density Functional Theory, Nudged Elastic Band and Kinetic Monte Carlo methods we find (1) equilibrium sites, (2) adsorption energies, (3) potential barriers, (4) vibrational frequencies and (5) most probable pathways for diffusion of the adatom on external surfaces of SWCNTs of (5,5), (10,0) and (10,5) chirality, as function of its charge. The metal (5,5) SWCNT can support a fast diffusion of the carbon adatom, which is accelerated by the presence of the SWCNT negative charge. Reduced model of SWCNT growth is proposed. This work was supported by the U.S. Department of Energy, Office of Science, Basic Energy Sciences, Materials Sciences and Engineering Division.

  16. Activation of interfacial enzymes at membrane surfaces

    DEFF Research Database (Denmark)

    Mouritsen, Ole G.; Andresen, Thomas Lars; Halperin, Avi;

    2006-01-01

    A host of water-soluble enzymes are active at membrane surfaces and in association with membranes. Some of these enzymes are involved in signalling and in modification and remodelling of the membranes. A special class of enzymes, the phospholipases, and in particular secretory phospholipase A2 (s......PLA2), are only activated at the interface between water and membrane surfaces, where they lead to a break-down of the lipid molecules into lysolipids and free fatty acids. The activation is critically dependent on the physical properties of the lipid-membrane substrate. A topical review is given...

  17. Air Oxidation of Activated Carbon to Synthesize a Biomimetic Catalyst for Hydrolysis of Cellulose.

    Science.gov (United States)

    Shrotri, Abhijit; Kobayashi, Hirokazu; Fukuoka, Atsushi

    2016-06-01

    Oxygenated carbon catalyzes the hydrolysis of cellulose present in lignocellulosic biomass by utilizing the weakly acidic functional groups on its surface. Here we report the synthesis of a biomimetic carbon catalyst by simple and economical air-oxidation of a commercially available activated carbon. Air- oxidation at 450-500 °C introduced 2000-2400 μmol g(-1) of oxygenated functional groups on the material with minor changes in the textural properties. Selectivity towards the formation of carboxylic groups on the catalyst surface increased with the increase in oxidation temperature. The degree of oxidation on carbon catalyst was found to be proportional to its activity for hydrolysis of cellulose. The hydrolysis of eucalyptus in the presence of carbon oxidized at 475 °C afforded glucose yield of 77 % and xylose yield of 67 %.

  18. Thermal analysis of activated carbons modified with silver metavanadate

    Energy Technology Data Exchange (ETDEWEB)

    Goscianska, Joanna; Nowicki, Piotr; Nowak, Izabela [Faculty of Chemistry, Adam Mickiewicz University in Poznan, Grunwaldzka 6, 60-780 Poznan (Poland); Pietrzak, Robert, E-mail: pietrob@amu.edu.pl [Faculty of Chemistry, Adam Mickiewicz University in Poznan, Grunwaldzka 6, 60-780 Poznan (Poland)

    2012-08-10

    Highlights: Black-Right-Pointing-Pointer Preparation of the activated carbons from waste materials as new supports for AgVO{sub 3}. Black-Right-Pointing-Pointer Decomposition of AgVO{sub 3} to V{sub 2}O{sub 5} and Ag{sup 0} for the samples 1 and 3 wt.% Ag-V is observed. Black-Right-Pointing-Pointer Samples containing 5 wt.% Ag-V decompose to vanadyl species as intermediate compounds. - Abstract: The effect of silver metavanadate doping on physicochemical properties and thermal behaviour of the activated carbons obtained from waste materials was investigated. The carbonaceous supports were subjected to carbonisation at 400 or 600 Degree-Sign C. The samples carbonised at 600 Degree-Sign C have much more developed surface area and porous structure than the analogous samples obtained at 400 Degree-Sign C. Impregnation of activated carbons with silver metavanadate leads to a decrease in their surface area and pore volume. According to thermal analysis (TG, DTG) in the samples containing 1 and 3 wt.% of silver metavanadate, AgVO{sub 3} is fully decomposed to do vanadium oxide and Ag, with no intermediate products, while in the samples containing 5 wt.% AgVO{sub 3}, this salt is decomposed to vanadyl species as intermediate compounds at 350 Degree-Sign C before the formation of V{sub 2}O{sub 5} at 500 Degree-Sign C. Moreover, in all samples impregnated with silver metavanadate the nanoparticles of silver undergo crystallisation leading to reduction of Ag{sup +} ions from the vanadium salt to Ag{sup 0}.

  19. Modified granular activated carbon: A carrier for the recovery of nickel ions from aqueous wastes

    Energy Technology Data Exchange (ETDEWEB)

    Satapathy, D.; Natarajan, G.S.; Sen, R. [Central Fuel Research Inst., Nagpur (India)

    2004-07-01

    Granular Activated Carbon (GAC) is widely used for the removal and recovery of toxic pollutants including metals because of its low cost and high affinity towards the scavenging of metal ions. Activated carbon derived from bituminous coal is preferred for wastewater treatment due to its considerable hardness, a characteristic needed to keep down handling losses during re-activation. Commercial grade bituminous coal based carbon, viz. Filtrasorb (F-400), was used in the present work. The scavenging of precious metals such as nickel onto GAC was studied and a possible attempt made to recover the adsorbed Ni{sup 2+} ions through the use of some suitable leaching processes. As part of the study, the role of complexing agents on the surface of the carbon was also investigated. The use of organic complexing agents such as oxine and 2-methyloxine in the recovery process was found to be promising. In addition, the surface of the carbon was modified with suitable oxidising agents that proved to be more effective than chelating agents. Several attempts were made to optimise the recovery of metal ions by carrying out experiments with oxidising agents in order to obtain maximum recovery from the minimum quantity of carbon. Experiments with nitric acid indicated that not only was the carbon surface modified but such modification also helped in carbon regeneration.

  20. Active micromixer using surface acoustic wave streaming

    Science.gov (United States)

    Branch; Darren W. , Meyer; Grant D. , Craighead; Harold G.

    2011-05-17

    An active micromixer uses a surface acoustic wave, preferably a Rayleigh wave, propagating on a piezoelectric substrate to induce acoustic streaming in a fluid in a microfluidic channel. The surface acoustic wave can be generated by applying an RF excitation signal to at least one interdigital transducer on the piezoelectric substrate. The active micromixer can rapidly mix quiescent fluids or laminar streams in low Reynolds number flows. The active micromixer has no moving parts (other than the SAW transducer) and is, therefore, more reliable, less damaging to sensitive fluids, and less susceptible to fouling and channel clogging than other types of active and passive micromixers. The active micromixer is adaptable to a wide range of geometries, can be easily fabricated, and can be integrated in a microfluidic system, reducing dead volume. Finally, the active micromixer has on-demand on/off mixing capability and can be operated at low power.

  1. Activated Carbon Composites for Air Separation

    Energy Technology Data Exchange (ETDEWEB)

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

    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.

  2. PREPARATION OF MICROWAVE ABSORBING NICKEL-BASED ACTIVATED CARBON BY ELECTROLESS PLATING WITH PALLADIUM-FREE ACTIVATION

    Directory of Open Access Journals (Sweden)

    Boyang Jia

    2010-08-01

    Full Text Available Nickel-based activated carbon was prepared from coconut shell activated carbon by electroless plating with palladium-free activation. The materials were characterized by scanning electron microscopy (SEM, X-ray energy dispersion spectroscopy (EDS, vibrating sample magnetometry (VSM, and vector network analyzer, respectively. The results show that the surface of the activated carbon was covered by a Ni-P coating, which was uniform, compact, and continuous and had an obvious metallic sheen. The content of P and Ni was 2.73% and 97.27% in the coating. Compared with the untreated activated carbon, the real permeability μ′ and imaginary permeability μ″ of Ni-based activated carbon became greater, whereas the real permittivity ε′ and imaginary permittivity ε″ became smaller. Also, the plated activated carbon was magnetic, making it suitable for some special applications. In general, the method reported here might be a feasible procedure to coat activated carbon with other magnetic metals, which may find application in various areas.

  3. Activated carbon fibers with a high heteroatom content by chemical activation of PBO with phosphoric acid.

    Science.gov (United States)

    Vázquez-Santos, M B; Suárez-García, F; Martínez-Alonso, A; Tascón, J M D

    2012-04-03

    The preparation of activated carbon fibers (ACFs) by phosphoric acid activation of poly(p-phenylene benzobisoxazole) (PBO) fibers was studied, with particular attention to the effects of impregnation ratio and carbonization temperature on porous texture. Phosphoric acid has a strong effect on PBO degradation, lowering the temperature range at which the decomposition takes place and changing the number of mass loss steps. Chemical analysis results indicated that activation with phosphoric acid increases the concentration of oxygenated surface groups; the resulting materials also exhibiting high nitrogen content. ACFs are obtained with extremely high yields; they have well-developed porosity restricted to the micropore and narrow mesopore range and with a significant concentration of phosphorus incorporated homogeneously in the form of functional groups. An increase in the impregnation ratio leads to increases in both pore volume and pore size, maximum values of surface area (1250 m(2)/g) and total pore volume (0.67 cm(3)/g) being attained at the highest impregnation ratio (210 wt % H(3)PO(4)) and lowest activation temperature (650 °C) used; the corresponding yield was as large as 83 wt %. The obtained surface areas and pore volumes were higher than those achieved in previous works by physical activation with CO(2) of PBO chars.

  4. FLUORIDE SORPTION USING MORRINGA INDICA-BASED ACTIVATED CARBON

    Directory of Open Access Journals (Sweden)

    G. Karthikeyan, S. Siva Ilango

    2007-01-01

    Full Text Available Batch adsorption experiments using activated carbon prepared from Morringa Indica bark were conducted to remove fluoride from aqueous solution. A minimum contact time of 25 min was required for optimum fluoride removal. The influence of adsorbent, dose, pH, co-ions (cations and anions on fluoride removal by the activated carbon has been experimentally verified. The adsorption of fluoride was studied at 30 C, 40 C and 50 C. The kinetics of adsorption and adsorption isotherms at different temperatures were studied. The fluoride adsorption obeyed both Langmuir and Freundlich isotherms and followed a pseudo first order kinetic model. The thermodynamic studies revealed that the fluoride adsorption by Morringa Indica is an endothermic process indicating an increase in sorption rate at higher temperatures. The negative values of G indicate the spontaneity of adsorption. SEM and XRD studies confirmed the surface morphological characteristics of the adsorbent and the deposition of fluoride on the surface of the material.

  5. Cellulose: A review as natural, modified and activated carbon adsorbent.

    Science.gov (United States)

    Suhas; Gupta, V K; Carrott, P J M; Singh, Randhir; Chaudhary, Monika; Kushwaha, Sarita

    2016-09-01

    Cellulose is a biodegradable, renewable, non-meltable polymer which is insoluble in most solvents due to hydrogen bonding and crystallinity. Natural cellulose shows lower adsorption capacity as compared to modified cellulose and its capacity can be enhanced by modification usually by chemicals. This review focuses on the utilization of cellulose as an adsorbent in natural/modified form or as a precursor for activated carbon (AC) for adsorbing substances from water. The literature revealed that cellulose can be a promising precursor for production of activated carbon with appreciable surface area (∼1300m(2)g(-1)) and total pore volume (∼0.6cm(3)g(-1)) and the surface area and pore volume varies with the cellulose content. Finally, the purpose of review is to report a few controversies and unresolved questions concerning the preparation/properties of ACs from cellulose and to make aware to readers that there is still considerable scope for future development, characterization and utilization of ACs from cellulose.

  6. Reuse performance of granular-activated carbon and activated carbon fiber in catalyzed peroxymonosulfate oxidation.

    Science.gov (United States)

    Yang, Shiying; Li, Lei; Xiao, Tuo; Zhang, Jun; Shao, Xueting

    2017-03-01

    Recently, activated carbon was investigated as an efficient heterogeneous metal-free catalyst to directly activate peroxymonosulfate (PMS) for degradation of organic compounds. In this paper, the reuse performance and the possible deactivation reasons of granular-activated carbon (GAC) and activated carbon fiber (ACF) in PMS activation were investigated. As results indicated, the reusability of GAC, especially in the presence of high PMS dosage, was relatively superior to ACF in catalyzed PMS oxidation of Acid Orange 7 (AO7), which is much more easily adsorbed by ACF than by GAC. Pre-oxidation experiments were studied and it was demonstrated that PMS oxidation on ACF would retard ACF's deactivation to a big extent. After pre-adsorption with AO7, the catalytic ability of both GAC and ACF evidently diminished. However, when methanol was employed to extract the AO7-spent ACF, the catalytic ability could recover quite a bit. GAC and ACF could also effectively catalyze PMS to degrade Reactive Black 5 (RB5), which is very difficult to be adsorbed even by ACF, but both GAC and ACF have poor reuse performance for RB5 degradation. The original organic compounds or intermediate products adsorbed by GAC or ACF would be possibly responsible for the deactivation.

  7. Carbon nanotube growth activated by quantum-confined silicon nanocrystals

    Science.gov (United States)

    Mariotti, D.; Švrček, V.; Mathur, A.; Dickinson, C.; Matsubara, K.; Kondo, M.

    2013-03-01

    We report on the use of silicon nanocrystals (Si-ncs) to activate nucleation and growth of carbon nanotubes (CNTs) without using any metal catalyst. Si-ncs with different surface characteristics have been exposed to the same CH4 low-pressure plasma treatment producing quite different results. Specifically, Si-ncs prepared by laser ablation in water have contributed to the formation of micrometre-sized silicon spherical particles. On the other hand, Si-ncs prepared by electrochemical etching did not induce any specific growth while the third type of Si-ncs, prepared by electrochemical etching and treated by a laser fragmentation process, induced the growth of multi-walled CNTs. The different outcomes of the same plasma process are attributed to the diverse surface features presented by the Si-ncs.

  8. The Deposition of Gold Nanoparticles Onto Activated Carbon

    Directory of Open Access Journals (Sweden)

    Jaworski W.

    2014-10-01

    Full Text Available This work reports the results of spectrophotometric, dynamic light scattering (DLS and microscopic (SEM studies of the gold nanoparticles (AuNPs deposition on activated carbon (AC surface modified with primary (ethanolamine and secondary (diethylenetriamine and triethylenetetramine amines. It was found that this method is efficient for deposition of AuNPs from aqueous solution. However, nanoparticles change their morphology depending on the kind of amine used in experiments. On the AC surface modified with ethanolamine, the uniform spherical AuNPs were formed. In case of diethylenetriamine and triethylenetetramine application, the agglomerates of AuNPs are present. The diameter of individual AuNPs did not exceed 15 nm and was bigger as compared with the diameter of particles present in precursor solution (ca. 10 nm.

  9. Effects of thermal activation conditions on the microstructure regulation of corncob-derived activated carbon for hydrogen storage

    Institute of Scientific and Technical Information of China (English)

    Dabin Wang; Zhen Geng; Cunman Zhang; Xiangyang Zhou; Xupeng Liu

    2014-01-01

    Activated carbons derived from corncob (CACs) were prepared by pyrolysis carbonization and KOH activation. Through modifying activation conditions, samples with large pore volume and ultrahigh BET specific surface area could be obtained. The sample achieved the highest hydrogen uptake capacity of 5.80 wt%at 40 bar and -196◦C. The as-obtained samples were characterized by N2-sorption, transmission electron microscopy (TEM) and scanning electron microscopy (SEM). Besides, thermogravimetric analysis was also employed to investigate the activation behavior of CACs. Detailed investigation on the activation parameters reveals that moderate activation temperature and heating rate are favorable for preparing CACs with high surface area, large pore volume and optimal pore size distribution. Meanwhile, the micropore volume between 0.65 nm and 0.85 nm along with BET surface area and total pore volume has great effects on hydrogen uptake capacities. The present results indicate that CACs are the most promising materials for hydrogen storage application.

  10. STUDY PORE CHARACTERIZATION OF γ-ALUMINA – ACTIVATED CARBON COMPOSITE MADE OF CASSAVA PEELS (Manihot esculenta Cranz

    Directory of Open Access Journals (Sweden)

    Hartini Hartini

    2015-12-01

    Full Text Available A composite of γ-alumina and activated carbon made of cassava peels was studied in terms of its pore structures and its properties. The objective of this study was to determine the interaction and structure, as well as the character and pore size of γ-alumina – activated carbon composite. Carbon made of cassava peels was activated by H2SO4 and its activities were tested according to the Indonesian Industrial Standards (SII. The addition of activated carbon into γ-alumina made in variations of 10, 20, 30, 40 and 50 % w/w, of the total weight of 10 grams. The composite of γ-alumina - activated carbon was characterized by FTIR, SAA (Surface Area Analyzer, XRD, and determination of Hysteresis Loop composites. The greater addition of activated carbon to γ-alumina causes intermolecular interactions between –O-H groups form rehydrated hydrogen bonds in the composite is greater. The structure of γ-alumina in the composites remain intact although the percentage of activated carbon in composite is large. The total pore volume and surface area using the BET method of the composite decreases with increasing activated carbon percentage. The greater addition of activated carbon to γ-alumina causes size of mesoporous composites decreased with the characteristic of a composite formed is closer to the activated carbon.

  11. Tungsten carbide modified high surface area carbon as fuel cell catalyst support

    Science.gov (United States)

    Shao, Minhua; Merzougui, Belabbes; Shoemaker, Krista; Stolar, Laura; Protsailo, Lesia; Mellinger, Zachary J.; Hsu, Irene J.; Chen, Jingguang G.

    Phase pure WC nanoparticles were synthesized on high surface area carbon black (800 m 2 g -1) by a temperature programmed reaction (TPR) method. The particle size of WC can be controlled under 30 nm with a relatively high coverage on the carbon surface. The electrochemical testing results demonstrated that the corrosion resistance of carbon black was improved by 2-fold with a surface modification by phase pure WC particles. However, the WC itself showed some dissolution under potential cycling. Based on the X-ray diffraction (XRD) and inductively coupled plasma (ICP) analysis, most of the WC on the surface was lost or transformed to oxides after 5000 potential cycles in the potential range of 0.65-1.2 V. The Pt catalyst supported on WC/C showed a slightly better ORR activity than that of Pt/C, with the Pt activity loss rate for Pt/WC/C being slightly slower compared to that of Pt/C. The performance and decay rate of Pt/WC/C were also evaluated in a fuel cell.

  12. Development of Formaldehyde Adsorption using Modified Activated Carbon – A Review

    Directory of Open Access Journals (Sweden)

    W.D.P Rengga

    2012-11-01

    Full Text Available Gas storage is a technology developed with an adsorptive storage method, in which gases are stored as adsorbed components on the certain adsorbent. Formaldehyde is one of the major indoor gaseous pollutants. Depending on its concentration, formaldehyde may cause minor disorder symptoms to a serious injury. Some of the successful applications of technology for the removal of formaldehyde have been reported. However, this paper presents an overview of several studies on the elimination of formaldehyde that has been done by adsorption method because of its simplicity. The adsorption method does not require high energy and the adsorbent used can be obtained from inexpensive materials. Most researchers used activated carbon as an adsorbent for removal of formaldehyde because of its high adsorption capacity. Activated carbons can be produced from many materials such as coals, woods, or agricultural waste. Some of them were prepared by specific activation methods to improve the surface area. Some researchers also used modified activated carbon by adding specific additive to improve its performance in attracting formaldehyde molecules. Proposed modification methods on activation and additive impregnated carbon are thus discussed in this paper for future development and improvement of formaldehyde adsorption on activated carbon. Specifically, a waste agricultural product is chosen for activated carbon raw material because it is renewable and gives an added value to the materials. The study indicates that the performance of the adsorption of formaldehyde might be improved by using modified activated carbon. Bamboo seems to be the most appropriate raw materials to produce activated carbon combined with applying chemical activation method and addition of metal oxidative catalysts such as Cu or Ag in nano size particles. Bamboo activated carbon can be developed in addition to the capture of formaldehyde as well as the storage of adsorptive hydrogen gas that

  13. Natural variability in the surface ocean carbonate ion concentration

    Directory of Open Access Journals (Sweden)

    N. S. Lovenduski

    2015-08-01

    Full Text Available We investigate variability in the surface ocean carbonate ion concentration ([CO32−] on the basis of a long control simulation with a fully-coupled Earth System Model. The simulation is run with a prescribed, pre-industrial atmospheric CO2 concentration for 1000 years, permitting investigation of natural [CO32−] variability on interannual to multi-decadal timescales. We find high interannual variability in surface [CO32−] in the tropical Pacific and at the boundaries between the subtropical and subpolar gyres in the Northern Hemisphere, and relatively low interannual variability in the centers of the subtropical gyres and in the Southern Ocean. Statistical analysis of modeled [CO32−] variance and autocorrelation suggests that significant anthropogenic trends in the saturation state of aragonite (Ωaragonite are already or nearly detectable at the sustained, open-ocean timeseries sites, whereas several decades of observations are required to detect anthropogenic trends in Ωaragonite in the tropical Pacific, North Pacific, and North Atlantic. The detection timescale for anthropogenic trends in pH is shorter than that for Ωaragonite, due to smaller noise-to-signal ratios and lower autocorrelation in pH. In the tropical Pacific, the leading mode of surface [CO32−] variability is primarily driven by variations in the vertical advection of dissolved inorganic carbon (DIC in association with El Niño–Southern Oscillation. In the North Pacific, surface [CO32−] variability is caused by circulation-driven variations in surface DIC and strongly correlated with the Pacific Decadal Oscillation, with peak spectral power at 20–30 year periods. North Atlantic [CO32−] variability is also driven by variations in surface DIC, and exhibits weak correlations with both the North Atlantic Oscillation and the Atlantic Multidecadal Oscillation. As the scientific community seeks to detect the anthropogenic influence on ocean carbonate chemistry, these

  14. Porous carbon nitride nanosheets for enhanced photocatalytic activities

    Science.gov (United States)

    Hong, Jindui; Yin, Shengming; Pan, Yunxiang; Han, Jianyu; Zhou, Tianhua; Xu, Rong

    2014-11-01

    Porous carbon nitride nanosheets (PCNs) have been prepared for the first time by a simple liquid exfoliation method via probe sonication. These mesoporous nanosheets of around 5 nm in thickness combine several advantages including high surface area, enhanced light absorption and excellent water dispersity. It can be used as a versatile support for co-catalyst loading for photocatalytic dye degradation and water reduction. With 3.8 wt% Co3O4 loaded, PCNs can achieve more efficient photocatalytic degradation of Rhodamine B, compared with non-porous C3N4 nanosheets (CNs), bulk porous C3N4 (PCN) and bulk nonporous C3N4 (CN). With 1.0 wt% Pt loaded, CNs and PCN exhibit 7-8 times enhancement in H2 evolution than CN. Remarkably, PCNs with both porous and nanosheet-like features achieve 26 times higher activity in H2 evolution than CN. These significant improvements in photocatalytic activities can be attributed to the high surface area as well as better electron mobility of the two-dimensional nanostructure.Porous carbon nitride nanosheets (PCNs) have been prepared for the first time by a simple liquid exfoliation method via probe sonication. These mesoporous nanosheets of around 5 nm in thickness combine several advantages including high surface area, enhanced light absorption and excellent water dispersity. It can be used as a versatile support for co-catalyst loading for photocatalytic dye degradation and water reduction. With 3.8 wt% Co3O4 loaded, PCNs can achieve more efficient photocatalytic degradation of Rhodamine B, compared with non-porous C3N4 nanosheets (CNs), bulk porous C3N4 (PCN) and bulk nonporous C3N4 (CN). With 1.0 wt% Pt loaded, CNs and PCN exhibit 7-8 times enhancement in H2 evolution than CN. Remarkably, PCNs with both porous and nanosheet-like features achieve 26 times higher activity in H2 evolution than CN. These significant improvements in photocatalytic activities can be attributed to the high surface area as well as better electron mobility of

  15. Preparation and adsorption performances of mesopore-enriched bamboo activated carbon

    Institute of Scientific and Technical Information of China (English)

    Yuxin WANG; Congmin LIU; Yaping ZHOU

    2008-01-01

    Activated carbon with high specific surface area and considerable mesopores was prepared from bam-boo scraps by phosphoric acid activation. The effect of activation conditions was studied. Under the conditions of impregnating bamboo with 80% H3PO4 at 80℃ for 9 days and activation at 500℃ for 4 h, the prepared acti-vated carbon had the highest mesopore volume of 0.67 cm3/g, a specific surface area of 1567 m2/g, and the mesopore ratio reached 47.18%. The study on adsorption isotherms of CH4, CO2, N2 and O2on the activated carbon were carried out at 298 K. The considerable difference in the adsorption capacity between CO2 and the other gases was observed, which would be of interest for the adsorp-tive separation/purification of gaseous CO2 from its mix-tures, especially from mixtures with N2 and/or O2.

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

    Science.gov (United States)

    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

  17. Adsorption of phenol and reactive dye from aqueous solution on activated carbons derived from solid wastes.

    Science.gov (United States)

    Nakagawa, Kyuya; Namba, Akio; Mukai, Shin R; Tamon, Hajime; Ariyadejwanich, Pisit; Tanthapanichakoon, Wiwut

    2004-04-01

    Activated carbons were produced from several solid wastes, namely, waste PET, waste tires, refuse derived fuel and wastes generated during lactic acid fermentation from garbage. Activated carbons having various pore size distributions were obtained by the conventional steam-activation method and via the pre-treatment method (i.e., mixture of raw materials with a metal salt, carbonization and acid treatment prior to steam-activation) that was proposed by the authors. The liquid-phase adsorption characteristics of organic compounds from aqueous solution on the activated carbons were determined to confirm the applicability of these carbons, where phenol and a reactive dye, Black5, were employed as representative adsorbates. The hydrophobic surface of the carbons prepared was also confirmed by water vapor adsorption. The characteristics of a typical commercial activated carbon were also measured and compared. It was found that the activated carbons with plentiful mesopores prepared from PET and waste tires had quite high adsorption capacity for large molecules. Therefore they are useful for wastewater treatment, especially, for removal of bulky adsorbates.

  18. THE ROLE OF ACTIVATED CARBON IN SOLVING ECOLOGICAL PROBLEMS

    Directory of Open Access Journals (Sweden)

    V. M. Mukhin

    2008-06-01

    Full Text Available The authors present a brief analysis of the current global situation concerning the utilization of activated carbon in various fields. The article presents data concerning the synthesis and adsorption and structure properties of new activated carbons, used for solving ecological problems. The authors investigated the newly obtained activated carbons in comparison with several AC marks known in the world. It has been shown that currently synthesized AC are competitive with foreign marks.

  19. Carbon Nanofibers (CNFs) Surface Modification to Fabricate Carbon Nanofibers_Nanopaper Integrated Polymer Composite Material.

    Science.gov (United States)

    Jiang, Jianjun; Zhao, Ziwei; Deng, Chao; Liu, Fa; Li, Dejia; Fang, Liangchao; Zhang, Dan; Castro Jose M; Chen, Feng; Lee, L James

    2016-06-01

    Carbon Nanofibers (CNFs) have shown great potential to improve the physical and mechanical properties of conventional Fiber Reinforced Polymer Composites (FRPCs) surface. Excellent dispersion CNFs into water or polymer matrix was very crucial to get good quality CNFs enhanced FRPCs. Because of the hydrophobic properties of CNFs, we apply the reversible switching principles to transfer the hydrophobic surface into hydrophilic surface by growing polyaniline nanograss on the surface of CNFs which was carried out in hydrochloric acid condition. Incorporating CNFs into FRPCs as a surface layer named CNFs Nanopaper to increase the erosion resistance and electrical conductivity in this research which was very important in the wind energy field. In order to get high quality dispersed CNFs suspension, a sonication unit was used to detangle and uniform disperse the functionalized CNFs. A filter with vacuum pressure used to filter the suspension of CNFs onto Carbon veil to make CNFs Nanopaper. Vacuum Aided Resin Transfer Modeling (VARTM) process was used to fabricate Nano-enhanced FRPCs samples. In order to characterize the mechanical properties, three point bending experiment was measured. The flexural strength capacity and deformation resistance and behavior were compared and analyzed. In this paper, we discussed the methods used and provided experimental parameter and experimental results.

  20. Preparation of a MFI zeolite coating on activated carbon

    NARCIS (Netherlands)

    Vaart, van der R.; Bosch, H.; Keizer, K.; Reith, T.

    1997-01-01

    A new and simple method for the preparation of MFI zeolite coated activated carbon is presented. Suitable nucleation sites for the growth of zeolites were introduced to the carbon by adding hydrophilic montmorillonite clay to the carbon substrate. A gas tight MFI zeolite coating was obtained on this

  1. Role of black carbon electrical conductivity in mediating hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX) transformation on carbon surfaces by sulfides.

    Science.gov (United States)

    Xu, Wenqing; Pignatello, Joseph J; Mitch, William A

    2013-07-01

    Recent research has demonstrated that black carbons catalyze the transformation of a range of nitrated explosives sorbed to the carbon surfaces in the presence of sulfides. Although surface oxygenated functional groups, particularly quinones, and electrical conductivity have both been hypothesized to promote these reactions, the importance of these properties has not been tested. In this work, the importance of electrical conductivity was addressed by producing chars of increasing electrical conductivity via pyrolysis of wood shavings at increasing temperature. The reactivity of chars with respect to transformation of the explosive RDX in the presence of sulfides correlated with electrical conductivity. Oxygenated functional groups were apparently not involved, as demonstrated by the elimination of reactivity of an activated carbon after ozone treatment or sorption of model quinones to the activated carbon surface. Although RDX transformation correlated with char electrical conductivity, no RDX transformation was observed when RDX was physically separated from sulfides but electrically connected through an electrochemical cell. RDX transformation occurred in the presence of a surface-associated sulfur species. The correlation with char electrical conductivity suggests that sulfides are oxidized on carbon surfaces to products that serve as potent nucleophiles promoting RDX transformation.

  2. Activated carbon from thermo-compressed wood and other lignocellulosic precursors

    Directory of Open Access Journals (Sweden)

    Capart, R.

    2007-05-01

    Full Text Available The effects of thermo-compression on the physical properties such as bulk density, mass yield, surface area, and also adsorption capacity of activated carbon were studied. The activated carbon samples were prepared from thermo-compressed and virgin fir-wood by two methods, a physical activation with CO2 and a chemical activation with KOH. A preliminary thermo-compression method seems an easy way to confer to a tender wood a bulk density almost three times larger than its initial density. Thermo-compression increased yield regardless of the mode of activation. The physical activation caused structural alteration, which enhanced the enlargement of micropores and even their degradation, leading to the formation of mesopores. Chemical activation conferred to activated carbon a heterogeneous and exclusively microporous nature. Moreover, when coupled to chemical activation, thermo-compression resulted in a satisfactory yield (23%, a high surface area (>1700 m2.g-1, and a good adsorption capacity for two model pollutants in aqueous solution: methylene blue and phenol. Activated carbon prepared from thermo-compressed wood exhibited a higher adsorption capacity for both the pollutants than did a commercial activated carbon.

  3. Immobilization of carbon nanotubes and metallophthalocyanines on conductive surfaces by electrochemical means for electroanalytical purposes

    Energy Technology Data Exchange (ETDEWEB)

    Porras Gutierrez, A.; Gutierrez Granados, S. [Centre national de la recherche scientifique, Paris (France). Unite de Pharmacologie Chimique et Genetique; Guanajuato Univ. Guanajuato (Mexico). Inst. de Investigaciones Cientificas; Richard, C.; Griveau, S.; Bedioui, F. [Centre national de la recherche scientifique, Paris (France). Unite de Pharmacologie Chimique et Genetique; Zagal, J.H. [Santiago Univ. de Chile, Santiago (Chile)

    2008-07-01

    Carbon nanotubes (CNT) have been touted as viable candidates for the design of new electrode materials because of their high conductivity and high specific surface area. This study explored the use of electrochemical methods to immobilize single walled carbon nanotubes (SWCNT) on glassy carbon (GC) in a stable and controlled fashion. Two electrochemical routes were investigated to get the stable immobilization of nanotubes, notably (1) electropolymerization of conducting polymers in presence of SWCNT, and (2) the electrochemical grafting of diazonium salts in presence of SWCNT. The objective was to obtain chemically and mechanically stable composite GC/SWCNT electrodes. The electrochemical performances and reactivity of the electrodes were analyzed by voltammetry and by scanning electrochemical microscopy. The optimized immobilization methods were then applied to the conception of electrocatalysts hybrids, by co-immobilization of nanotubes with well-known redox catalyst metallocomplexes for activation of the electro-oxidation of biologically relevant thiol. The study showed that the nanocomposite material based on the combined use of metallophthalocynines, functionalized SWCNTs and electropolymerizable matrices enables the assembly of highly stable electrodes with better electrocatalytic oxidation of thiols. This fast procedure to modify glassy carbon (GC) electrode using commercially available cobalt phthalocyanine (CoPc) and tetrasulfonated nickel phthalocyanine (NiTSPc), oxidized single walled carbon nanotubes SWCNT and electropolymerized polypyrrole or diazonium derivatives. It was concluded that the electrodes are highly stable and the tailored hybrid surfaces improves electron transfer. 4 refs.

  4. Nano surface generation of grinding process using carbon nano tubes

    Indian Academy of Sciences (India)

    S Prabhu; B K Vinayagam

    2010-12-01

    Nano surface finish has become an important parameter in the semiconductor, optical, electrical and mechanical industries. The materials used in these industries are classified as difficult to machine materials such as ceramics, glasses and silicon wafers. Machining of these materials up to nano accuracy is a great challenge in the manufacturing industry. Finishing of micro components such as micro-moulds, micro-lenses and micro-holes need different processing techniques. Conventional finishing methods used so far become almost impossible or cumbersome. In this paper, a nano material especially multi wall carbon nano tube is used in the machining process like grinding to improve the surface characteristics from micro to nano level.

  5. Bionanohybrid based on bioplastic and surface-functionalized carbon nanotubes.

    Science.gov (United States)

    Singh, Ravina; Ray, Suprakas Sinha

    2010-12-01

    A bionanohybrid consisting of biodegradable/biocompatible poly(butylene succinate) (PBS) and surface-oxidized carbon nanotubes (o-CNTs) was prepared via melt-mixing method. The inherent properties of PBS were concurrently improved by the incorporation of a small amount of o-CNTs. For example, at room temperature, elongation at break increased from approximately 21.2% for pure PBS to approximately 55.1% for the nanohybrid and an increase of about approximately 150% in the value of toughness with moderate improvement in tensile modulus and strength. The dynamic mechanical properties of PBS also increased significantly after nanocomposite formation with o-CNTs. Electron microscopy and Raman spectroscopy were used to investigate the mechanical properties and improvement mechanism of surface-functionalized o-CNTs containing PBS nanohybrid.

  6. Hydrogenation of ortho-nitrochlorobenzene on activated carbon supported platinum catalysts

    Institute of Scientific and Technical Information of China (English)

    JIANG Cheng-jun; YIN Hong; CHEN Zhi-rong

    2005-01-01

    Platinum/carbon catalyst is one of the most important catalysts in hydrogenation of ortho-nitrochlorobenzene to 2,2'-dichlorohydrazobenzene. The preparation process and the supports of catalysts are studied in this paper. Raw materials and preparation procedure of the activated carbon have great influences on the compositions and surface structure of platinum/carbon catalysts. Platinum catalysts supported on activated carbon with high purity, high surface area, large pore volume and appropriate pore structure usually exhibit higher activities for hydrogenation of ortho-nitrochlorobenzene to 2,2'-dichlorohydrazobenzene.The catalyst prepared from H2PtCl6 with pH=3 shows greater catalytic performance than those prepared under other conditions.

  7. A novel method for production of activated carbon from waste tea by chemical activation with microwave energy

    Energy Technology Data Exchange (ETDEWEB)

    Emine Yagmur; Meryem Ozmak; Zeki Aktas [Ankara University, Ankara (Turkey). Faculty of Engineering

    2008-11-15

    This study presents the production of activated carbon from waste tea. Activated carbons were prepared by phosphoric acid activation with and without microwave treatment and carbonisation of the waste tea under nitrogen atmosphere at various temperatures and different phosphoric acid/precursor impregnation ratios. The surface properties of the activated carbons were investigated by elemental analysis, BET surface area, SEM, FTIR. Prior to heat treatment conducted in a furnace, the mixture of the waste tea and H{sub 3}PO{sub 4} was treated with microwave heating. The maximum BET surface area was 1157 m{sup 2}/g for the sample treated with microwave energy and then carbonised at 350{sup o}C. In case of application of conventional method, the BET surface area of the resultant material was 928.8 m{sup 2}/g using the same precursor and conditions. According to the Dubinin-Radushkevich (DR) method the micropore surface area for the sample treated with microwave energy was higher than the sample obtained from the conventional method. Results show that microwave heating reasonably influenced the micropore surface area of the samples as well as the BET surface area. The samples activated were also characterised in terms of the cumulative pore and micropore volumes according to the BJH, DR and t-methods, respectively. 35 refs., 6 figs., 4 tabs.

  8. [Effects of different fertilizer application on soil active organic carbon].

    Science.gov (United States)

    Zhang, Rui; Zhang, Gui-Long; Ji, Yan-Yan; Li, Gang; Chang, Hong; Yang, Dian-Lin

    2013-01-01

    The variation characteristics of the content and components of soil active organic carbon under different fertilizer application were investigated in samples of calcareous fluvo-aquic soil from a field experiment growing winter wheat and summer maize in rotation in the North China Plain. The results showed that RF (recommended fertilization), CF (conventional fertilization) and NPK (mineral fertilizer alone) significantly increased the content of soil dissolved organic carbon and easily oxidized organic carbon by 24.92-38.63 mg x kg(-1) and 0.94-0.58 mg x kg(-1) respectively compared to CK (unfertilized control). The soil dissolved organic carbon content under OM (organic manure) increased greater than those under NPK and single fertilization, soil easily oxidized organic carbon content under OM and NPK increased greater than that under single chemical fertilization. OM and NPK showed no significant role in promoting the soil microbial biomass carbon, but combined application of OM and NPK significantly increased the soil microbial biomass carbon content by 36.06% and 20.69%, respectively. Soil easily oxidized organic carbon, dissolved organic carbon and microbial biomass carbon accounted for 8.41% - 14.83%, 0.47% - 0.70% and 0.89% - 1.20% of the total organic carbon (TOC), respectively. According to the results, the fertilizer application significantly increased the proportion of soil dissolved organic carbon and easily oxidized organic carbon, but there was no significant difference in the increasing extent of dissolved organic carbon. The RF and CF increased the proportion of soil easily oxidized organic carbon greater than OM or NPK, and significantly increased the proportion of microbial biomass carbon. OM or RF had no significant effect on the proportion of microbial biomass carbon. Therefore, in the field experiment, appropriate application of organic manure and chemical fertilizers played an important role for the increase of soil active organic carbon

  9. Potential of jackfruit peel as precursor for activated carbon prepared by microwave induced NaOH activation.

    Science.gov (United States)

    Foo, K Y; Hameed, B H

    2012-05-01

    The feasibility of preparing activated carbon (JPAC) from jackfruit peel, an industrial residue abundantly available from food manufacturing plants via microwave-assisted NaOH activation was explored. The influences of chemical impregnation ratio, microwave power and radiation time on the properties of activated carbon were investigated. JPAC was examined by pore structural analysis, scanning electron microscopy, Fourier transform infrared spectroscopy, nitrogen adsorption isotherm, elemental analysis, surface acidity/basicity and zeta potential measurements. The adsorptive behavior of JPAC was quantified using methylene blue as model dye compound. The best conditions resulted in JPAC with a monolayer adsorption capacity of 400.06 mg/g and carbon yield of 80.82%. The adsorption data was best fitted to the pseudo-second-order equation, while the adsorption mechanism was well described by the intraparticle diffusion model. The findings revealed the versatility of jackfruit peels as good precursor for preparation of high quality activated carbon.

  10. Copper on activated carbon for catalytic wet air oxidation

    Directory of Open Access Journals (Sweden)

    Nora Dolores Martínez

    2009-03-01

    Full Text Available Textile industry is an important source of water contamination. Some of the organic contaminants cannot be eliminated by nature in a reasonable period. Heterogeneous catalytic wet air oxidation is one of the most effective methods to purify wastewater with organic contaminants. In this work, catalysts based on copper supported on activated carbon were synthesized. The activated carbons were obtained from industrial wastes (apricot core and grape stalk of San Juan, Argentina. These were impregnated with a copper salt and thermically treated in an inert atmosphere. Analysis of specific surface, pore volume, p zc, acidity, basicity and XRD patterns were made in order to characterize the catalysts. The catalytic activity was tested in the oxidation of methylene blue (MB and polyvinyl alcohol (PVA in aqueous phase with pure oxygen. Reaction tests were carried out in a Parr batch reactor at different temperatures, with a 0.2 MPa partial pressure of oxygen. The amount of unconverted organics was measured by spectrophotometry. Higher temperatures were necessary for the degradation of PVA compared to those for methylene blue.

  11. Efficient L-lactic acid fermentation by the mold Rhizopus oryzae using activated carbon

    Energy Technology Data Exchange (ETDEWEB)

    Koide, M.; Hirata, M.; Gaw, M.; Takanashi, H.; Hano, T. [Oita Univ, Oita (Japan). Dept. of Applied Chemistry

    2004-11-01

    Batch fermentations of Rhizopus oryzae AHU 6537 in medium containing granular activated carbon from coal, powder activated carbon from coal or granular activated carbon from coconut were carried out in an airlift bioreactor. As a result, fermentation broths were decolorized by activated carbon, and clearer fermentation broths were obtained than in fermentation without activated carbon. With activated carbon from coal, the cells formed smaller pellets than in fermentation without activated carbon, and fermentation performance was improved. Productivity was further improved by increasing the amount of activated carbon from coal. Therefore, the productivity of lactic acid fermentation could be improved by selecting a suitable activated carbon and by controlling the amount of activated carbon.

  12. [Preparation, characterization and adsorption performance of mesoporous activated carbon with acidic groups].

    Science.gov (United States)

    Li, Kun-Quan; Li, Ye; Zheng, Zheng; Zhang, Yu-Xuan

    2013-06-01

    Mesoporous activated carbons containing acidic groups were prepared with cotton stalk based fiber as raw materials and H3PO4 as activating agent by one step carbonization method. Effects of impregnation ratio, carbonization temperature and heat preservation time on the yield, elemental composition, oxygen-containing acid functional groups and adsorptive capacity of activated carbon were studied. The adsorption capacity of the prepared activated carbon AC-01 for p-nitroaniline and Pb(II) was studied, and the adsorption mechanism was also suggested according to the equilibrium experimental results. The maximum yield of activated carbons prepared from cotton stalk fiber reached 35.5% when the maximum mesoporous volume and BET surface area were 1.39 cm3 x g(-1) and 1 731 m2 x g(-1), respectively. The activated carbon AC-01 prepared under a H3 PO4/precursor ratio of 3:2 and activated at 900 degrees C for 90 min had a total pore volume of 1.02 cm3 x g(-1), a micoporous ratio of 31%, and a mesoporous ratio of 65%. The pore diameter of the mesoporous activated carbon was mainly distributed in the range of 2-5 nm. The Langmuir maximum adsorption capacities of Pb(II) and p-nitroaniline on cotton stalk fiber activated carbon were 123 mg x g(-1) and 427 mg x g(-1), respectively, which were both higher than those for commercial activated carbon fiber ACF-CK. The equilibrium adsorption experimental data showed that mesopore and oxygen-containing acid functional groups played an important role in the adsorption.

  13. Activated carbon is an electron-conducting amphoteric ion adsorbent

    CERN Document Server

    Biesheuvel, P M

    2015-01-01

    Electrodes composed of activated carbon (AC) particles can desalinate water by ion electrosorption. To describe ion electrosorption mathematically, accurate models are required for the structure of the electrical double layers (EDLs) that form within electrically charged AC micropores. To account for salt adsorption also in uncharged ACs, an "attraction term" was introduced in modified Donnan models for the EDL structure in ACs. Here it will be shown how instead of using an attraction term, chemical information of the surface structure of the carbon-water interface in ACs can be used to construct an alternative EDL model for ACs. This EDL model assumes that ACs contain both acidic groups, for instance due to carboxylic functionalities, and basic groups, due to the adsorption of protons to the carbon basal planes. As will be shown, this "amphoteric Donnan" model accurately describes various data sets for ion electrosorption in ACs, for solutions of NaCl, of CaCl2, and mixtures thereof, as function of the exter...

  14. Adsorption of methyl orange using activated carbon prepared from lignin by ZnCl2 treatment

    Science.gov (United States)

    Mahmoudi, K.; Hamdi, N.; Kriaa, A.; Srasra, E.

    2012-08-01

    Lignocellulosic materials are good and cheap precursors for the production of activated carbon. In this study, activated carbons were prepared from the lignin at different temperatures (200 to 500°C) by ZnCl2. The effects influencing the surface area of the resulting activated carbon are activation temperature, activation time and impregnation ratio. The optimum condition, are found an impregnation ratio of 2, an activation temperature of 450°C, and an activation time of 2 h. The results showed that the surface area and micropores volume of activated carbon at the experimental conditions are achieved to 587 and 0.23 cm3 g-1, respectively. The adsorption behavior of methyl orange dye from aqueous solution onto activated lignin was investigated as a function of equilibrium time, pH and concentration. The Langmuir and Freundlich adsorption models were applied to describe the equilibrium isotherms. A maximum adsorption capacity of 300 mg g-1 of methyl orange by activated carbon was achieved.

  15. Quantitative Analysis on Carbon Migration in Double-Glow Discharge Plasma Surface Alloying Process

    Institute of Scientific and Technical Information of China (English)

    ZHANGZhen-xia; WANGCong-zeng; ZHANGWen-quan; SUXue-kuan

    2004-01-01

    Carbon migration is of great significance in double-glow discharge plasma surface alloying process, but literature of quantitative analysis about carbon migration is relatively scarce. In this paper differential equations of the carbon and metal concentration distribution were established. By means of differential equations carbon migration was described and a numerical solution was acquired. The computational results fit the experiment results quite well.

  16. Tailoring the Surface Chemistry of Zeolite Templated Carbon by Electrochemical Methods

    Directory of Open Access Journals (Sweden)

    R. Berenguer

    2013-01-01

    Full Text Available One option to optimize carbon materials forsupercapacitor applications is the generation ofsurface functional groups that contribute to thepseudocapacitance without losing the designedphysical properties. This requires suitablefunctionalization techniques able to selectivelyintroduce a given amount of electroactive oxygengroups. In this work, the influence of the chemical andelectrochemical oxidation methods, on the chemicaland physical properties of a zeolite templated carbon(ZTC, as a model carbon material, have beenstudied and compared. Although both oxidationmethods generally produce a loss of the originalZTC physical properties with increasing amount ofoxidation, the electrochemical method shows muchbetter controllability and, unlike chemical treatments,enables the generation of a large number of oxygengroups (O = 11000- 3300 μmol/g, with a higherproportion of active functionalities, while retaining ahigh surface area (ranging between 1900-3500 m2/g,a high microporosity and an ordered 3-D structure.

  17. Carbon dioxide chemistry on the surface of Titan

    Science.gov (United States)

    Hodyss, Robert; Piao, Sophie; Malaska, Michael; Cable, Morgan

    2016-10-01

    Titan possesses many of the basic elements of habitability, including a rich organic chemistry. However, the thick atmosphere of Titan shields the surface from radiation, which makes the incorporation of oxygen into organic compounds difficult, due to a reducing environment and low temperatures that slow chemical reactions. These obstacles may be overcome by impacts or cryovolcanic heating of ice, which would mix organics with liquid water and allow chemical reactions that can incorporate oxygen. However, reactions involving oxygen can occur on Titan without invoking such unusual conditions. We show that the reaction of carbon dioxide with amines can lead to oxygenated organics at Titan's surface without the need for external energy input, via the carbamation reaction: R-NH2 + CO2 → R-NH-COOH. Using a combination of micro-Raman spectroscopy and UHV FTIR spectroscopy, we examine the reaction products and kinetics of the carbamation reaction for a variety of primary and secondary amines. We have observed carbamic acid formation in mixtures of methylamine, ethylamine and dibutylamine with CO2 at cryogenic temperatures. This indicates that both primary and secondary amines can undergo carbamation at low temperatures. Reaction was observed with methylamine as low as 40 K, and with ethylamine at 100 K, demonstrating that carbamation is fast at Titan surface temperatures. We will present data on the kinetics of the carbamation reaction for a variety of amines, as well as estimates of the quantity of carbamic acids that may be produced on Titan's surface and in the atmosphere.

  18. Understanding the effect of steps, strain, poisons, and alloying: Methane activation on Ni surfaces

    DEFF Research Database (Denmark)

    Abild-Pedersen, Frank; Greeley, Jeffrey Philip; Nørskov, Jens Kehlet

    2005-01-01

    It is shown that a single parameter characterizing the electronic structure of a transition metal surface, the d-band center (epsilon(d)), can be used to provide a unified description of a range of phenomena in heterogeneous catalysis. Using methane activation on Ni surfaces as an example, we show...... that variations in epsilon(d) can be used to quantitatively describe variations in the activation energy when the surface structure is changed, when the coverage of carbon is changed, when the surface is strained, when the surface is alloyed, and when the surface is poisoned by sulfur. The d-band center is...

  19. Adsorption of direct dye onto activated carbon prepared from areca nut pod--an agricultural waste.

    Science.gov (United States)

    Gopalswami, P; Sivakumar, N; Ponnuswamy, S; Venkateswaren, V; Kavitha, G

    2010-10-01

    Activated carbons are made from various agricultural wastes by physical and chemical activation. The preparation of activated carbon from agricultural waste could increase economic return and also provides an excellent method for the solid waste disposal thereby reduce pollution. Areca nut pod, which is an agricultural waste, has been used as a raw material to produce activated carbon (AAC) by four different methods. The adsorption of Direct blue dye used in textile industry on the porous areca nut pod activated carbon was investigated. The activated carbon AAC has an average surface area of 502 m2/g. CAC, the commercial reference was mainly micro porous with a surface area of 1026 m2/g .The study investigated the removal of direct dye from simulated water. The effects of adsorbent dosage, initial dye concentration, pH and contact time were studied. The results showed that as the amount of the adsorbent was increased, the percentage of dye removal increased accordingly. The results indicate that AAC could be employed as low-cost alternative to commercial activated carbon in wastewater treatment for the removal of acid dyes.

  20. Surface Chemistry and Tribology of Copper Surfaces in Carbon Dioxide and Water Vapor Environments

    Science.gov (United States)

    2011-02-23

    progress). Simultaneous XAS and cyclic voltammetry of Cu in bicarbonate solutions under potentiostatic control at the Berkeley Synchrotron facility (Figure...bicarbonate ions that mimic the conditions of the wet brush-rotor contact. Electrochemical control of the surface by cyclic voltammetry makes it...the electrochemical modifications of Cu under potentiostat control and solution pH 3) Determine the loss of mass of Cu when in carbonate containing

  1. Production of Biologically Activated Carbon from Orange Peel and Landfill Leachate Subsequent Treatment Technology

    Directory of Open Access Journals (Sweden)

    Zhigang Xie

    2014-01-01

    Full Text Available In order to improve adsorption of macromolecular contaminants and promote the growth of microorganisms, active carbon for biological wastewater treatment or follow-up processing requires abundant mesopore and good biophile ability. In this experiment, biophile mesopore active carbon is produced in one-step activation with orange peel as raw material, and zinc chloride as activator, and the adsorption characteristics of orange peel active carbon is studied by static adsorption method. BET specific surface area and pore volume reached 1477 m2/g and 2.090 m3/g, respectively. The surface functional groups were examined by Fourier transform infrared spectroscopy (FT-IR. The surface of the as-prepared activated carbon contained hydroxyl group, carbonyl group, and methoxy group. The analysis based on X-ray diffraction spectrogram (XRD and three-dimensional fluorescence spectrum indicated that the as-prepared activated carbon, with smaller microcrystalline diameter and microcrystalline thickness and enhanced reactivity, exhibited enhanced adsorption performance. This research has a deep influence in effectively controlling water pollution, improving area water quality, easing orange peel waste pollution, and promoting coordinated development among society, economy, and environment.

  2. EFFECT OF MOLECULAR OXYGEN ON ADSORPTIVE CAPACITY AND EXTRACTION EFFICIENCY OF GRANULATED ACTIVATED CARBON FOR THREE ORTHO-SUBSTITUTED PHENOLS

    Science.gov (United States)

    Adsorptive capacity of activated carbon for several organic compounds was found to be strongly influenced by the presence of molecular oxygen. This influence is manifested by the polymerization of adsorbate on the surface of activated carbon. As a result, GAC exhibits much high...

  3. Surface and sub-surface degradation of unidirectional carbon fiber reinforced epoxy composites under dry and wet reciprocating sliding

    OpenAIRE

    Dhieb, H.; Buijnsters, J.G.; Eddoumy, F.; Vázquez, Luis; Celis, J. P.

    2013-01-01

    The role of water on the sub-surface degradation of unidirectional carbon fiber reinforced epoxy composite is examined. The correlation between the debonding of carbon fibers at the fiber-epoxy interface, and the wear behavior of the carbon fiber composite are discussed based on an in-depth analysis of the worn surfaces. We demonstrate that a reciprocating sliding performed along an anti-parallel direction to the fiber orientation under dry conditions results in a large degradation by debondi...

  4. Surface modification of oil fly ash and its application in selective capturing of carbon dioxide

    Science.gov (United States)

    Yaumi, Ali L.; Hussien, Ibnelwaleed A.; Shawabkeh, Reyad A.

    2013-02-01

    Oil fly ash from power generation plants was activated with 30% NH4OH and used for selective adsorption of carbon dioxide from CO2/N2 mixture. The treated samples were characterized for their surface area, morphology, crystalline phase, chemical composition and surface functional groups. Energy dispersive X-ray analysis showed an increase in the carbon contents from 45 to 73 wt% as a result of leaching out metal oxides. XRD proved that chemical activation of ash resulted in diminishing of major crystalline phases of zeolite, and other alumino-silicates leaving only quartz and mullite. BET analysis showed an increase in surface area from 59 to 318 m2/g after chemical activation and the pore volume increased from 0.0368 to 0.679 cm3/g. This increase in pore volume is supported by the results of SEM, where more micropores were opened with well-defined particle sizes and porous structure. The TGA of the treated fly ash showed stability at higher temperature as the weight loss decreased with increasing temperature. For treated ash, the FTIR displayed new peaks of amine functional group. The treated ash was used for the removal of CO2 from CO2/N2 mixture and the maximum adsorption/capturing capacity was found to be 240 mg/g. This capacity increases with increase in initial gas concentration, inlet flow rate and temperature suggesting the endothermic nature of the interaction between the gas molecules and the surface of the ash.

  5. Preparation of porous bio-char and activated carbon from rice husk by leaching ash and chemical activation.

    Science.gov (United States)

    Ahiduzzaman, Md; Sadrul Islam, A K M

    2016-01-01

    Preparation porous bio-char and activated carbon from rice husk char study has been conducted in this study. Rice husk char contains high amount silica that retards the porousness of bio-char. Porousness of rice husk char could be enhanced by removing the silica from char and applying heat at high temperature. Furthermore, the char is activated by using chemical activation under high temperature. In this study no inert media is used. The study is conducted at low oxygen environment by applying biomass for consuming oxygen inside reactor and double crucible method (one crucible inside another) is applied to prevent intrusion of oxygen into the char. The study results shows that porous carbon is prepared successfully without using any inert media. The adsorption capacity of material increased due to removal of silica and due to the activation with zinc chloride compared to using raw rice husk char. The surface area of porous carbon and activated carbon are found to be 28, 331 and 645 m(2) g(-1) for raw rice husk char, silica removed rice husk char and zinc chloride activated rice husk char, respectively. It is concluded from this study that porous bio-char and activated carbon could be prepared in normal environmental conditions instead of inert media. This study shows a method and possibility of activated carbon from agro-waste, and it could be scaled up for commercial production.

  6. Preparation and characterization of activated carbon from sunflower seed oil residue via microwave assisted K2CO3 activation.

    Science.gov (United States)

    Foo, K Y; Hameed, B H

    2011-10-01

    Sunflower seed oil residue, a by-product of sunflower seed oil refining, was utilized as a feedstock for preparation of activated carbon (SSHAC) via microwave induced K(2)CO(3) chemical activation. SSHAC was characterized by Fourier transform infrared spectroscopy, nitrogen adsorption-desorption and elemental analysis. Surface acidity/basicity was examined with acid-base titration, while the adsorptive properties of SSHAC were quantified using methylene blue (MB) and acid blue 15 (AB). The monolayer adsorption capacities of MB and AB were 473.44 and 430.37 mg/g, while the Brunauer-Emmett-Teller surface area, Langmuir surface area and total pore volume were 1411.55 m(2)/g, 2137.72 m(2)/g and 0.836 cm(3)/g, respectively. The findings revealed the potential to prepare high surface area activated carbon from sunflower seed oil residue by microwave irradiation.

  7. Ion-assisted precursor dissociation and surface diffusion: Enabling rapid, low-temperature growth of carbon nanofibers

    Science.gov (United States)

    Denysenko, I.; Ostrikov, K.

    2007-06-01

    Growth kinetics of carbon nanofibers in a hydrocarbon plasma is studied. In addition to gas-phase and surface processes common to chemical vapor deposition, the model includes (unique to plasma-exposed catalyst surfaces) ion-induced dissociation of hydrocarbons, interaction of adsorbed species with incoming hydrogen atoms, and dissociation of hydrocarbon ions. It is shown that at low, nanodevice-friendly process temperatures the nanofibers grow via surface diffusion of carbon adatoms produced on the catalyst particle via ion-induced dissociation of a hydrocarbon precursor. These results explain a lower activation energy of nanofiber growth in a plasma and can be used for the synthesis of other nanoassemblies.

  8. Effects of surface treating methods of high-strength carbon fibers on interfacial properties of epoxy resin matrix composite

    Energy Technology Data Exchange (ETDEWEB)

    Ma, Quansheng; Gu, Yizhuo, E-mail: benniegu@buaa.edu.cn; Li, Min; Wang, Shaokai; Zhang, Zuoguang

    2016-08-30

    Highlights: • Effects of surface treating on T700 grade high strength carbon fiber were discussed. • The fiber surface roughness, surface energy and chemical properties are analyzed. • The surface treating significantly affect the properties of carbon fiber. • The composite with electrolysis and sizing-fiber has the highest mechanical properties. - Abstract: This paper aims to study the effects of surface treating methods, including electrolysis of anodic oxidation, sizing and heat treatment at 200 °C, on physical and chemical properties of T700 grade high-strength carbon fiber GQ4522. The fiber surface roughness, surface energy and chemical properties were analyzed for different treated carbon fibers, using atom force microscopy, contact angle, Fourier transformed infrared and X-ray photoelectron spectroscopy, respectively. The results show that the adopted surface treating methods significantly affect surface roughness, surface energy and active chemical groups of the studied carbon fibers. Electrolysis and sizing can increase the roughness, surface energy and chemical groups on surface, while heat treatment leads to decreases in surface energy and chemical groups due to chemical reaction of sizing. Then, unidirectional epoxy 5228 matrix composite laminates were prepared using different treated GQ4522 fibers, and interlaminar shear strength and flexural property were measured. It is revealed that the composite using electrolysis and sizing-fiber has the strongest interfacial bonding strength, indicating the important roles of the two treating processes on interfacial adhesion. Moreover, the composite using heat-treating fiber has lower mechanical properties, which is attributed to the decrease of chemical bonding between fiber surface and matrix after high temperature treatment of fiber.

  9. Electron beam induced surface activation of oxide surfaces for nanofabrication

    Energy Technology Data Exchange (ETDEWEB)

    Vollnhals, Florian; Seiler, Steffen; Walz, Marie-Madeleine; Steinrueck, Hans-Peter; Marbach, Hubertus [Lehrstuhl fuer Physikalische Chemie II and Interdisciplinary Center for Molecular Materials (ICMM), Friedrich-Alexander-Universitaet Erlangen-Nuernberg, Erlangen (Germany); Woolcot, Tom; Thornton, Geoff [London Centre for Nanotechnology and Department of Chemistry, University College London (United Kingdom)

    2012-07-01

    The controlled fabrication of structures on the nanoscale is a major challenge in science and engineering. Direct-write techniques like Electron Beam Induced Deposition (EBID) were shown to be suitable tools in this context. Recently, Electron Beam Induced Surface Activation (EBISA) has been introduced as a new focused electron beam technique. In EBISA, a surface, e.g. SiO{sub 2}, is irradiated by a focused electron beam, resulting in an activation of the exposed area. The activated area can then react and decompose precursor gases like iron pentacarbonyl, Fe(CO){sub 5}. This leads to a primary deposit, which continues to grow autocatalytically as long as Fe(CO){sub 5} is supplied, resulting in pure (> 90 % at.), crystalline iron nanostructures. We expand the use of this concept by exploring EBISA to produce metallic nanostructures on TiO{sub 2}(110) in UHV; atomistic insight into the process is obtained via Scanning Tunneling Microscopy (STM) and chemical insight via Auger Electron Spectroscopy (AES).

  10. Comparison of capacitive behavior of activated carbons with different pore structures in aqueous and nonaqueous systems

    Institute of Scientific and Technical Information of China (English)

    ZHOU Shao-yun; LI Xin-hai; WANG Zhi-xing; GUO Hua-jun; PENG Wen-jie

    2008-01-01

    The pore structures of two activated carbons from sawdust with KOH activation and coconut-shell with steam activation for supercapacitor were analyzed by N2 adsorption method. The electrochemical properties of both activated carbons in 6mol/L KOH solution and 1mol/L Et4NPF4/PC were compared, and the effect of pore structure on the capacitance was investigated by cyclic voltammetry, AC impedance and charge-discharge measurements. The results indicate that the capacitance mainly depends on effective surface area, but the power property mainly depends on mesoporosity. At low specific current (1A/g), the maximum specific capacitances of 276.3F/g in aqueous system and 123.9F/g in nonaqueous system can be obtained from sawdust activated carbon with a larger surface area of 1808m2/g, but at a high specific current, the specific capacitance of coconut-shell activated carbon with a higher mesoporosity of 75.1% is more excellent. Activated carbon by KOH activation is fitter for aqueous system and that by steam activation is fitter for nonaqueous system.

  11. Adsorption Studies of Chromium(VI) on Activated Carbon Derived from Mangifera indica (Mango) Seed Shell

    Science.gov (United States)

    Mise, Shashikant; Patil, Trupti Nagendra

    2015-09-01

    The removal of chromium(VI) from synthetic sample by adsorption on activated carbon prepared from Mangifera indica (mango) seed shell have been carried out at room temperature 32 ± 1 °C. The removal of chromium(VI) from synthetic sample by adsorption on two types of activated carbon, physical activation and chemical activation (Calcium chloride and Sodium chloride), Impregnation Ratio's (IR) 0.25, 0.50, 0.75 for optimum time, optimum dosages and variation of pH were studied. It is observed that contact time differs for different carbons i.e. for physically and chemically activated carbons. The contact time decreases for chemically activated carbon compared to the physically activated carbon. It was observed that as dosage increases the adsorption increased along with the increase in impregnation ratio. It was also noted that as I.R. increases the surface area of Mangifera indica shell carbon increased. These dosage data were considered in the construction of isotherms and it was found that adsorption obeys Freundlich Isotherm and does not obey Langmuir Isotherm. The maximum removal of chromium (VI) was obtained in highly acidic medium at a pH of 1.50.

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

    Science.gov (United States)

    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%.

  13. Indoor Air Contaminant Adsorption By Palm Shell Activated Carbon Filter – A Proposed Study

    Directory of Open Access Journals (Sweden)

    Leman A.M

    2016-01-01

    Full Text Available Indoor air contaminant is a public issue. High Volatile Organic Compound (VOC, Carbon monoxide (CO, Carbon dioxide (CO2, and particulate matter is becoming main issue that needs to solve. Therefore, this study focus on improving indoor air quality by using activated carbon (AC for Ventilation and Air-Conditioning (VAC. It investigated because AC is widely explored but developing AC as a filter for VAC is not developed yet. The AC prepared by physical and chemical activation process and combination both of process and it was activated by H3PO4 and NaOH. Characterization and analysis process are consists of water content, ash content, bulk density, adsorption capacity, iodine number and indoor air filtering analysis. Treated activated carbon potential in achieving higher surface area of the structure to the range of 950 to 1150 m2/g for gas phase application. The higher surface area will adsorb more air pollution. Maintained properties of activated carbon such as hardness, density, pore, extractable ash, particle size (12 by 40 mesh and pH are becoming the main concern in achieving high quality of activated carbon.

  14. Electrocatalytic oxidation of dopamine, ascorbic acid and uric acid at poly­2,6­diaminopyridine on the surface of carbon nanotubes/gc electrodes

    OpenAIRE

    Kamyabi,Mohammad Ali; Shafiee,Mohammad Ali

    2012-01-01

    The preparation and application of poly-(2,6-diaminopyridine) on the surface of a glassy carbon electrode (GCE) modified with multi-walled carbon nanotubes (CNTs) are reported. Cyclic voltammetry was used for both the electrochemical synthesis and characterization of the polymers deposited on GCE. The modified electrode shows a synergic effect of the electrocatalytic properties and high active surface area of both the conducting polymer and carbon nanotubes, giving rise to a remarkable improv...

  15. Mechanotransductive surfaces for reversible biocatalysis activation

    Science.gov (United States)

    Mertz, Damien; Vogt, Cédric; Hemmerlé, Joseph; Mutterer, Jérôme; Ball, Vincent; Voegel, Jean-Claude; Schaaf, Pierre; Lavalle, Philippe

    2009-09-01

    Fibronectin, like other proteins involved in mechanotransduction, has the ability to exhibit recognition sites under mechanical stretch. Such cryptic sites are buried inside the protein structure in the native fold and become exposed under an applied force, thereby activating specific signalling pathways. Here, we report the design of new active polymeric nanoassembled surfaces that show some similarities to these cryptic sites. These nanoassemblies consist of a first polyelectrolyte multilayer stratum loaded with enzymes and capped with a second polyelectrolyte multilayer acting as a mechanically sensitive nanobarrier. The biocatalytic activity of the film is switched on/off reversibly by mechanical stretching, which exposes enzymes through the capping barrier, similarly to mechanisms involved in proteins during mechanotransduction. This first example of a new class of biologically inspired surfaces should have great potential in the design of various devices aimed to trigger and modulate chemical reactions by mechanical action with applications in the field of microfluidic devices or mechanically controlled biopatches for example.

  16. Biomimetic surface modification of polyurethane with phospholipids grafted carbon nanotubes.

    Science.gov (United States)

    Tan, Dongsheng; Liu, Liuxu; Li, Zhen; Fu, Qiang

    2015-08-01

    To improve blood compatibility of polyurethane (PU), phospholipids grafted carbon nanotubes (CNTs) were prepared through zwitterion-mediated cycloaddition reaction and amide condensation, and then were added to the PU as fillers via solution mixing to form biomimetic surface. The properties of phospholipids grafted CNTs (CNT-PC) were investigated by thermal gravimetric analysis (TGA), X-ray photoelectron spectroscopy (XPS) and proton nuclear magnetic resonance ((1) H NMR). The results indicated that the phospholipids were grafted onto CNTs in high efficiency, and the hydrophilicity and dispersibility of the modified CNTs were improved effectively. The structures and properties of composites containing CNT-PC were investigated by optical microscope, XPS, and water contact angles. The results indicated that phospholipids were enriched on the surface with addition of 0.1 wt % of CNT-PC, which significantly reduced protein adsorption and platelet adhesion. The method of carrying phospholipids on the nanofiller to modify polymers has provided a promising way of constructing biomimetic phospholipid membrane on the surface to improve blood compatibility.

  17. Modification of the dentin surface by using carbon nanotubes.

    Science.gov (United States)

    Akasaka, Tsukasa; Nakata, Keiko; Uo, Motohiro; Watari, Fumio

    2009-01-01

    Recent studies have shown that carbon nanotubes (CNTs) can be used as biomedical materials because of their unique properties. CNTs effect nucleation of hydroxyapatite, because of which considerable interest has been generated regarding the use of CNTs in dentistry. However, there are only a few reports on the use of CNTs as dental materials. In this study, we investigated the changes induced in the surfaces of tooth slices by the application of a coating of CNTs by observing CNT-coated tooth slices both macroscopically as well as under a scanning electron microscope. Further, we investigated the effect of CNT coating on the tensile bond strength of dentin adhesives. CNTs adhered easily to the tooth surfaces when tooth slices were suspended in a CNT-dispersed solution. Interestingly, it was observed that CNTs selectively adhered to the surfaces of dentin and cementum, possibly by adhering to their exposed collagen fibers. In addition, the CNT coating did not affect the tensile bond strength of dentin adhesives. These results indicate that coating of the teeth with CNTs can be a possible application of CNTs as dental materials.

  18. A Magnesium-Activated Carbon Hybrid Capacitor

    Energy Technology Data Exchange (ETDEWEB)

    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.

  19. Microporous activated carbons prepared from palm shell by thermal activation and their application to sulfur dioxide adsorption.

    Science.gov (United States)

    Guo, Jia; Lua, Aik Chong

    2002-07-15

    Textural characterization of activated carbons prepared from palm shell by thermal activation with carbon dioxide (CO(2)) gas is reported in this paper. Palm shell (endocarp) is an abundant agricultural solid waste from palm-oil processing mills in many tropical countries such as Malaysia, Indonesia, and Thailand. The effects of activation temperature on the textural properties of the palm-shell activated carbons, namely specific surface area (BET method), porosity, and microporosity, were investigated. The activated carbons prepared from palm shell possessed well-developed porosity, predominantly microporosity, leading to potential applications in gas-phase adsorption for air pollution control. Static and dynamic adsorption tests for sulfur dioxide (SO(2)), a common gaseous pollutant, were carried out in a thermogravimetric analyzer and a packed column configuration respectively. The effects of adsorption temperature, adsorbate inlet concentration, and adsorbate superficial velocity on the adsorptive performance of the prepared activated carbons were studied. The palm-shell activated carbon was found to have substantial capability for the adsorption of SO(2), comparable to those of some commercial products and an adsorbent derived from another biomass.

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

    Energy Technology Data Exchange (ETDEWEB)

    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 con