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Sample records for activated carbon prepared

  1. Preparation of activated carbon from a renewable agricultural ...

    African Journals Online (AJOL)

    STORAGESEVER

    2010-05-10

    May 10, 2010 ... Preparation of activated carbon from a renewable agricultural ... fuel-wood because household energy requirements are met with multiple ..... for activated carbon production - A review. Renewable & Sustainable. Energy ...

  2. Activated Carbon Preparation and Modification for Adsorption

    Science.gov (United States)

    Cao, Yuhe

    . The adsorption capacities of these active carbon samples were almost three times that of zeolite. However, the un-modified active carbon had the highest adsorption capacity for butanol vapor (259.6 mg g-1), compared to 222.4 mg g-1 after 10% H2O2 hydrothermal treatment. Both modified and un-modified active carbon can be easily regenerated for repeatable adsorption by heating to 150 °C. Therefore, surface oxygen groups significantly reduced the adsorption capacity of active carbons for butanol vapor. In addition, original active carbon and AC samples modified by nitric acid hydrothermal modification were assessed for their ability to adsorb butanol vapor. The specific surface area and oxygen-containing functional groups of AC were tested before and after modification. The adsorption capacity of unmodified AC samples were the highest. Hydrothermal oxidation of AC with HNO3 increased the surface oxygen content, Brunauer-Emmett-Teller (BET) surface area, micropore, mesopore and total pore volume of AC. Although the pore structure and specific surface area were greatly improved after hydrothermal oxidization with 4 M HNO3, the increased oxygen on the surface of AC decreased the dynamic adsorption capacity. In order to get high adsorption capacity adsorbents, we used corn stalk as precursor to fabricate porous carbon. ACs were prepared through chemical activation of biochar from whole corn stalk (WCS) and corn stalk pith (CSP) at varying temperatures using potassium hydroxide as the activating agent. ACs were characterized via pore structural analysis and scanning electron microscopy (SEM). These adsorbents were then assessed for their adsorption capacity for butanol vapor. It was found that WCS activated at 900 °C for 1 h (WCS-900) had optimal butanol adsorption characteristics. The BET surface area and total pore volume of the WCS-900 were 2330 m2 g-1 and 1.29 cm3 g-1, respectively. The dynamic adsorption capacity of butanol vapor was 410.0 mg g-1, a 185.1 % increase

  3. 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.

  4. 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.

  5. 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

  6. 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.

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

    Energy Technology Data Exchange (ETDEWEB)

    Byamba-Ochir, Narandalai [School of Chemical Engineering, Chonnam National University, 77 Yongbong-Ro, Gwangju 61186 (Korea, Republic of); Shim, Wang Geun [Department of Polymer Science and Engineering, Sunchon National University, 255 Jungang-Ro, Suncheon, Jeollanam-Do 57922 (Korea, Republic of); Balathanigaimani, M.S., E-mail: msbala@rgipt.ac.in [Department of Chemical Engineering, Rajiv Gandhi Institute of Petroleum Technology, Ratapur Chowk, Rae Bareli, 229316 Uttar Pradesh (India); Moon, Hee, E-mail: hmoon@jnu.ac.kr [School of Chemical Engineering, Chonnam National University, 77 Yongbong-Ro, Gwangju 61186 (Korea, Republic of)

    2016-08-30

    Highlights: • Highly porous carbon materials from Mongolian anthracite by chemical activation. • Cheaper and eco-friendly activation process has been employed. • Activated carbons with graphitic structure and energetically heterogeneous surface. • Surface hydrophobicity and porosity of the activated carbons can be controlled. - Abstract: 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 m{sup 2}/g and of 0.55–1.61 cm{sup 3}/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.

  8. Preparation of Paper Containing Activated Carbon.

    Science.gov (United States)

    1984-06-01

    development of charcoal paper. RESUME On a obtenu du papier contenant du charbon actif en dispersant du charbon r~duit en poudre et en versant des agents de...sa capaciti d’adsorption et de ritention du charbon . Ce papier pourrait servir d𔄀crans dans une salle de contr~le de contamination pour le balayage...contenant du charbon . "l-ii:: . ---:.-o * *** * *. .. t C Cd. .. . . . . . . . . . . . . . . . . . . . . . . . . . . 1 S 2 INTRODUCTION . Activated

  9. Urea adsorption by activated carbon prepared from palm kernel shell

    Science.gov (United States)

    Ooi, Chee-Heong; Sim, Yoke-Leng; Yeoh, Fei-Yee

    2017-07-01

    Dialysis treatment is crucial for patients suffer from renal failure. The dialysis system removes the uremic toxin to a safe level in a patient's body. One of the major limitations of the current hemodialysis system is the capability to efficiently remove uremic toxins from patient's body. Nanoporous materials can be applied to improve the treatment. Palm kernel shell (PKS) biomass generated from palm oil mills can be utilized to prepare high quality nanoporous activated carbon (AC) and applied for urea adsorption in the dialysis system. In this study, AC was prepared from PKS via different carbonization temperatures and followed by carbon dioxide gas activation processes. The physical and chemical properties of the samples were studied. The results show that the porous AC with BET surface areas ranging from 541 to 622 m2g-1 and with total pore volumes varying from 0.254 to 0.297 cm3g-1, are formed with different carbonization temperatures. The equilibrium constant for urea adsorption by AC samples carbonized at 400, 500 and 600 °C are 0.091, 0.287 and 0.334, respectively. The increase of carbonization temperatures from 400 to 600 °C resulted in the increase in urea adsorption by AC predominantly due to increase in surface area. The present study reveals the feasibility of preparing AC with good porosity from PKS and potentially applied in urea adsorption application.

  10. 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.

  11. 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.

  12. Preparation and Characterization of Activated Carbon from Palm Kernel Shell

    Science.gov (United States)

    Andas, J.; Rahman, M. L. A.; Yahya, M. S. M.

    2017-08-01

    In this study, a high quality of activated carbon (AC) was successfully synthesized from palm kernel shell (PKS) via single step KOH activation. Several optimal conditions such as impregnation ratio and activation temperature were investigated. The prepared activated carbon under the optimum condition of impregnation ratio (1:1.5 raw/KOH) and activation temperature (800 °C) was characterized using Na2S2O3 volumetric method, CHNS/O analysis and Scanning Electron Microscope (SEM). Na2S2O3 volumetric showed an iodine number of 994.83 mgg-1 with yield % of 8.931 %. CHNS/O analysis verified an increase in C content for KOH-AC (61.10 %) in comparison to the raw PKS (47.28 %). Well-formation of porous structure was evidenced through SEM for KOH-AC. From this study, it showed a successful conversion of agricultural waste into value added porous material under benign condition.

  13. Preparation and characterization of activated carbons from rice ...

    African Journals Online (AJOL)

    atmosphere followed by activation using CO2 gas at various temperatures and ... available carbons, such as coal and coconut shells (Anon 1992). The ash ... extraction of the chemical from the carbonized char an activated carbon is obtained.

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

    Science.gov (United States)

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

    2013-06-01

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

  15. 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.

  16. Preparation, characterization, and dye removal study of activated carbon prepared from palm kernel shell.

    Science.gov (United States)

    García, Juan Rafael; Sedran, Ulises; Zaini, Muhammad Abbas Ahmad; Zakaria, Zainul Akmar

    2017-04-08

    Palm oil mill wastes (palm kernel shell (PKS)) were used to prepare activated carbons, which were tested in the removal of colorants from water. The adsorbents were prepared by 1-h impregnation of PKS with ZnCl2 as the activating agent (PKS:ZnCl2 mass ratios of 1:1 and 2:1), followed by carbonization in autogenous atmosphere at 500 and 550 °C during 1 h. The characterization of the activated carbons included textural properties (porosity), surface chemistry (functional groups), and surface morphology. The dye removal performance of the different activated carbons was investigated by means of the uptake of methylene blue (MB) in solutions with various initial concentrations (25-400 mg/L of MB) at 30 °C, using a 0.05-g carbon/50-mL solution relationship. The sample prepared with 1:1 PKS:ZnCl2 and carbonized at 550 °C showed the highest MB adsorption capacity (maximum uptake at the equilibrium, q max = 225.3 mg MB / g adsorbent), resulting from its elevated specific surface area (BET, 1058 m(2)/g) and microporosity (micropore surface area, 721 m(2)/g). The kinetic experiments showed that removals over 90% of the equilibrium adsorptions were achieved after 4-h contact time in all the cases. The study showed that palm oil mill waste biomass could be used in the preparation of adsorbents efficient in the removal of colorants in wastewaters.

  17. 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.

  18. 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.

  19. 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.

  20. Activated Carbon Prepared in a Novel Gas Fired Static Bed ...

    African Journals Online (AJOL)

    Michael O. Mensah

    2015-12-02

    Dec 2, 2015 ... The reactor is fabricated using stainless steel plates of 4 mm ... is introduced into the reaction chamber. The ... reaction of carbon with the activating agent. A number ..... organic liquids, characterisation of the organic fraction of.

  1. Preparation of TiO2-activated carbon complex membranes and their photoelectrocatalytic activity

    Institute of Scientific and Technical Information of China (English)

    尤宏; 姚杰; 孙丽欣; 王强

    2003-01-01

    The experimental process of preparing TiO2-activated carbon complex membranes with activated carbon powder as main carrier, PTFE as binder and wire netting as matrix is described in detail, and both photo-catalysis and photo-electro-catalysis are measured to study the properties of complex membranes. Experimental results show that the photo-catalytic activity of the membranes is high and stable in the process of treating Rhodamine-B; the application of an electric field accelerates the speed of photo-catalysis, and the efficiency of photo-catalysis is increased 2.5 times when the applied voltage is 0.8 V; and the degradation of Rhodamine-B follows the dynamics of first order reaction. It is concluded from the discussion of experimental results that the preparation process of TiO2-activated carbon complex membranes is a simple low-cost process suitable for large scale application.

  2. Preparation of creating active carbon from cigarette filter waste using microwave-induced KOH activation

    Science.gov (United States)

    Hamzah, Yanuar; Umar, Lazuardi

    2017-05-01

    For the first time, cigarette filter waste, which is an environmental hazardous material, is used as basic material prepared for creating activated carbon (AC) via KOH chemical activation using a microwave input power of 630 W and irradiation time of 20 minutes. Active carbon was characterized by TGA, x-ray diffraction, scanning electron microscopy, energy dispersive x-ray, nitrogen adsorption-desorption, and absorption of methylene blue (MB). The results of x-ray diffraction showed that active carbon has a semi-crystalline structure with peaks of 2θ of 22.87° and 43.70°. Active carbon microstructure analysis showed that the layer height (Lc ) is inversely proportional to the width of the layer (La ), and the distance between the two layers is d002 and d100 , which depends significantly on the ratio of AC: KOH. It was found that the optimum BET surface area and adsorption capacity for MB were 328.13 m2 / g and 88.76 m2 / g, respectively. The results revealed the potential to prepare activated carbon from cigarette filter waste using microwave irradiation.

  3. 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.

  4. Adsorption of dyes onto activated carbon prepared from olive stones

    Institute of Scientific and Technical Information of China (English)

    Souad NAJAR-SOUISSI; Abdelmottaleb OUEDERNI; Abdelhamid RATEL

    2005-01-01

    Activated carbon was produced from olive stones(OSAC) by a physical process in two steps. The adsorption character of this activated carbon was tested on three colour dyes molecules in aqueous solution: Methylene blue(MB), Rhodamine B(RB) and Congo Red(CR). The adsorption equilibrium was studied through isotherms construction at 30℃, which were well described by Langmuir model.The adsorption capacity on the OSAC was estimated to be 303 mg/g, 217 mg/g and 167 mg/g respectively for MB, RB and CR. This activated carbon has a similar adsorption properties to that of commercial ones and show the same adsorption performances. The adsorption kinetics of the MB molecule in aqueous solution at different initial concentrations by OSAC was also studied. Kinetic experiments were well fitted by a simple intra-particle diffusion model. The measured kinetics constant was influenced by the initial concentration and we found the following correlation: Kid = 1.55 C00.51 .

  5. PREPARATION OF ACTIVATED CARBON FIBERS AND THEIR XENON ADSORPTION PROPERTIES (Ⅰ)-PREPARATION AND PORE STRUCTURE CHARACTERIZATION

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    A series of sisal based activated carbon fibers were prepared with steam activation attemperature from 750 ℃ to 900 ℃. Their pore structures were characterized through their nitrogenadsorption isotherms at 77K using different theories. The results showed that t-plot method andDR-plot method could suitably be used to characterize the mesopore structure and the multi-stagedistribution of pore size of activated carbon fibers. It also showed that the pore size widens with theincrease of activation temperature.

  6. 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.

  7. 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.

  8. Preparation of activated carbon from wet sludge by electrochemical-NaClO activation.

    Science.gov (United States)

    Miao, Chen; Ye, Caihong; Zhu, Tianxing; Lou, Ziyang; Yuan, Haiping; Zhu, Nanwen

    2014-01-01

    Activated carbon (AC) from sludge is one potential solution for sewage sludge disposal, while the drying sludge is cost and time consuming for preparation. AC preparation from the wet sludge with electrochemical-NaClO activation was studied in this work. Three pretreatment processes, i.e. chemical activation, electrolysis and electrochemical-reagent reaction, were introduced to improve the sludge-derived AC properties, and the optimum dosage of reagent was tested from the 0.1:1 to 1:1 (mass rate, reagent:dried sludge). It was shown that the electrochemical-NaClO preparation is the best method under the test conditions, in which AC has the maximum Brunauer, Emmett and Teller area of 436 m²/g at a mass ratio of 0.7. Extracellular polymeric substances in sludge can be disintegrated by electrochemical-NaClO pretreatment, with a disintegration degree of more than 45%. The percentage of carbon decreased from 34.16 to 8.81 after treated by electrochemical-NaClO activation. Fourier transform infrared spectra showed that a strong C-Cl stretching was formed in electrochemical-NaClO prepared AC. The maximum adsorption capacity of AC reaches 109 mg/g on MB adsorption experiment at pH 10 and can be repeated for three times with high removal efficiency after regeneration.

  9. Characterization of activated carbon prepared by phosphoric acid activation of olive stones

    Directory of Open Access Journals (Sweden)

    S.M. Yakout

    2016-11-01

    Full Text Available The effects of activating agent concentration on the pore structure and surface chemistry of activated carbons derived from olive stone with chemical activation method using phosphoric acid as the activating agent were studied. Mass changes associated with the impregnation, carbonization and washing processes were measured. With H3PO4 dilute solutions (60, 70, and 80 wt% H3PO4, the loading of substance on CS increases with concentration. The concentration of the H3PO4 solution seems to control the processes of impregnation, carbonization and washing in the preparation of AC from olive stones by H3PO4 chemical activation. ACs have been characterized from the results obtained by N2 adsorption at 77 K. Moreover, the fractal dimension (D has been calculated in order to determine the AC surface roughness degree. Optimal textural properties of ACs have been obtained by chemical activation with H3PO4 80 wt.%. The BET surface areas and total pore volumes of the carbons produced at H3PO4 80 wt.% are 1218 m2/g and 0.6 cm3/g, respectively.

  10. Adsorption of SO2 on bituminous coal char and activated carbon fiber prepared from phenol formaldehyde

    Science.gov (United States)

    DeBarr, Joseph A.; Lizzio, Anthony A.; Daley, Michael A.

    1996-01-01

    Carbon-based materials are used commercially to remove SO2 from coal combustion flue gases. Historically, these materials have consisted of granular activated carbons prepared from lignite or bituminous coal. Recent studies have reported that activated carbon fibers (ACFs) may have potential in this application due to their relatively high SO2 adsorption capacity. In this paper, a comparison of SO2 adsorption for both coal-based carbons and ACFs is presented, as well as ideas on carbon properties that may influence SO2 adsorption

  11. Preparation of palladium loaded carbon nanotubes and activated carbons for hydrogen sorption

    Energy Technology Data Exchange (ETDEWEB)

    Anson, A. [Instituto de Carboquimica, CSIC, Miguel Luesma Castan, 4, 50018 Zaragoza (Spain)]. E-mail: aanson@ualberta.ca; Lafuente, E. [Instituto de Carboquimica, CSIC, Miguel Luesma Castan, 4, 50018 Zaragoza (Spain); Urriolabeitia, E. [Departamento de Quimica Inorganica, Universidad de Zaragoza, 50009 Zaragoza (Spain); Navarro, R. [Departamento de Quimica Inorganica, Universidad de Zaragoza, 50009 Zaragoza (Spain); Benito, A.M. [Instituto de Carboquimica, CSIC, Miguel Luesma Castan, 4, 50018 Zaragoza (Spain); Maser, W.K. [Instituto de Carboquimica, CSIC, Miguel Luesma Castan, 4, 50018 Zaragoza (Spain); Martinez, M.T. [Instituto de Carboquimica, CSIC, Miguel Luesma Castan, 4, 50018 Zaragoza (Spain)

    2007-06-14

    Single wall carbon nanotubes (SWNTs) and MAXSORB activated carbon have been used as the support of palladium nanoparticles. The preparation of the palladium loaded carbon materials has been done by direct reaction between the support and a Pd (0) compound, either Pd{sub 2}(dba){sub 3}.CHCl{sub 3} or Pd(PPh{sub 3}){sub 4}. The efficiency of the loading reaction has been much better when Pd{sub 2}(dba){sub 3}.CHCl{sub 3} has been chosen as the Pd source, reaching high palladium loadings (up to ca. 45 wt.%) with relatively small particle size (5-10 nm for SWNTs and 30-40 nm for MAXSORB). The hydrogen isotherms of the palladium loaded materials present a steep increase at very low pressures. The H/Pd atomic ratio of the samples has been found to be dependent on the Pd precursor, being higher in the case of Pd{sub 2}(dba){sub 3}.CHCl{sub 3}. Several samples have achieved H/Pd ratios higher than the value for bulk Pd (H/Pd {approx} 0.6-0.7). Maximum hydrogen sorption at room temperature in the palladium loaded samples has been found to be of 0.5 wt.% at atmospheric pressure. Oxidative treatments on the substrate before the palladium loading have diminished the efficiency of the loading reaction, the hydrogen adsorption, and the H/Pd atomic ratio.

  12. 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.

  13. [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.

  14. Preparation and characterization of activated carbon fiber (ACF) from cotton woven waste

    Energy Technology Data Exchange (ETDEWEB)

    Jieying Zheng,; Zhao, Quanlin; Ye, Zhengfang, E-mail: zhengfangye@163.com

    2014-04-01

    Highlights: • Cotton woven waste can be recycled as precursor to produce activated carbon fiber. • The optimum carbonization and activation temperature are 700 °C and 800 °C. • The prepared ACF is in the form of fiber, with the surface area of 789 m{sup 2}/g. • The prepared ACF can be used to remove over 80% of COD from oilfield wastewater. - Abstract: In this study, the activated carbon fibers (ACFs) were prepared using cotton woven waste as precursor. The cotton woven waste was first partly dissolved by 80% phosphoric acid and then was pre-soaked in 7.5% diammonium hydrogen phosphate solution. Finally, carbonization and activation were proceeded to get ACF. The optimum preparation conditions, including carbonization temperature, carbonization time, activation temperature and activation time, were chosen by orthogonal design. Nitrogen adsorption/desorption test was conducted to characterize the prepared ACF's pore structure. Fourier transform infrared spectroscopy (FTIR) analysis, X-ray photoelectron spectroscopy (XPS) and environmental scanning electron microscope (ESEM) were employed to characterize its chemical properties and morphology. Adsorption of oilfield wastewater was used to evaluate its adsorption properties. The results show that the prepared ACF is in the form of fiber, with the sectional diameters of 11.7 × 2.6 μm and the surface area of 789 m{sup 2}/g. XPS results show that carbon concentration of the prepared ACF is higher than that of the commercial ACF. When the prepared ACF dosage is 6 g/L, over 80% of COD and over 70% of chrominance can be removed after 24 h of adsorption at 18 °C.

  15. 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.

  16. 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.

  17. PREPARATION OF ACTIVATED CARBON FROM SILK COTTON WOOD AND COCONUT SHELL BY PYROLISIS WITH CERAMIC FURNACE

    Directory of Open Access Journals (Sweden)

    Winarto Haryadi

    2010-06-01

    Full Text Available Preparation of activated carbon from silk cotton wood and coconut shell has been done. Carbon was made by pyrolysis process in the Muchalal furnace with 3000 watt electric power. The electric power was increased gradually from 1000, 2000 and then 3000 watt with interval 2 hours during 7 hours. Carbon was activated in Muchalal furnace with 4000 watt electric power during 2 hours and flowed with nitrogen gas. Product of the activated carbon was compared to standart product with several analysis including the surface area, acetic acid adsorption, iod adsorption and vapour adsorption. The results of analysis showed that surface area for silk cotton wood carbon, coconut shell carbon, and E.Merck product were 288.8072 m2/g, 222.9387 m2/g and 610.5543 m2/g, respectively. Acetic acid adsorption for silk cotton wood carbon, coconut shell carbon, and standart product were 157.391 mg/g, 132.791 mg/g, and 186.911 mg/g, respectively. Iodine adsorption for cotton wood carbon, coconut shell carbon, and standart product were 251.685 mg/g, 207.270 mg/g and 310.905 mg/g, respectively. Vapour adsorption for cotton wood carbon, coconut shell carbon and standart product were 12%, 4%,and 14%., respectively Key words : Activated carbon, pyrolysis, Muchalal furnace

  18. PREPARATION OF ACTIVATED CARBON FROM TWO CHINESE ANTHRACITES IN THE PRESENCE OF OXIDATIVE ADDITIVES

    Institute of Scientific and Technical Information of China (English)

    张双全; 何维军; 王祖讷

    1998-01-01

    This paper broke with the conventional ways of oxidizing and catalyzing. It researcheda new way to prepare activated carbon from anthracites which employed oxidative additives. Itinvestigated the effects of the additive on adsorption and activation rate of the resultant activatedcarbon. The results showed that the new additives not only improved the adsorptivity but alsoincreased the activation rate greatly, which is able to decrease the preparation cost.

  19. 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.

  20. Preparation of activated carbons and their adsorption properties for greenhouse gases: CH4 and CO2

    Institute of Scientific and Technical Information of China (English)

    Hao Yang; Maochu Gong; Yaoqiang Chen

    2011-01-01

    Three kinds of activated carbons were prepared using coconut-shells as carbon precursors and characterized by XRD,FT-IR and texture property test.The results indicate that the prepared activated carbons were mainly amorphous and only a few impurity groups were adsorbed on their surfaces.The texture property test reveals that the activated carbons displayed different texture properties,especially the micropore size distribution.The adsorption capacities of the activated carbons were investigated by adsorbing CH4,CO2,N2 and O2 at 25 ℃ in the pressure range of 0-200 kPa.The results reveal that all the activated carbons had high CO2 adsorption capacity,one of which had the highest CO2 adsorption value of 2.55 mmol/g at 200 kPa.And the highest adsorption capacity for CH4 of the activated carbons can reach 1.93 mmol/g at 200 kPa.In the pressure range of 0-200 kPa,the adsorption capacities for N2 and O2 were increased linearly with the change of pressure and K-AC is an excellent adsorbent towards the adsorption separation of greenhouse gases.

  1. Preparation of activated carbon from sorghum pith and its structural and electrochemical properties

    Energy Technology Data Exchange (ETDEWEB)

    Senthilkumar, S.T.; Senthilkumar, B. [Solid State Ionics and Energy Devices Laboratory, Department of Physics, Bharathiar University, Coimbatore 641046 (India); Balaji, S. [Materials Laboratory, Thiagarajar Advanced Research Center, Thiagarajar College of Engineering, Madurai 625015 (India); Sanjeeviraja, C. [Department of Physics, Alagappa University, Karaikudi 630003 (India); Kalai Selvan, R., E-mail: selvankram@buc.edu.in [Solid State Ionics and Energy Devices Laboratory, Department of Physics, Bharathiar University, Coimbatore 641046 (India)

    2011-03-15

    Research highlights: {yields} Sorghum pith as the cost effective raw material for activated carbon preparation. {yields} Physicochemical method/KOH activation for preparation of activated carbon is inexpensive. {yields} Activated carbon having lower surface area surprisingly delivered a higher specific capacitance. {yields} Treated at 500 {sup o}C activated carbon exceeds maximum specific capacitances of 320.6 F/g at 10 mV/s. -- Abstract: The cost effective activated carbon (AC) has been prepared from sorghum pith by NaOH activation at various temperatures, including 300 {sup o}C (AC1), 400 {sup o}C (AC2) and 500 {sup o}C (AC3) for the electrodes in electric double layer capacitor (EDLC) applications. The amorphous nature of the samples has been observed from X-ray diffraction and Raman spectral studies. Subsequently, the surface functional groups, surface morphology, pore diameter and specific surface area have been identified through FT-IR, SEM, histogram and N{sub 2} adsorption/desorption isotherm methods. The electrochemical characterization of AC electrodes has been examined using cyclic voltammetry technique in the potential range of -0.1-1.2 V in 1.0 M H{sub 2}SO{sub 4} electrolyte at different scan rates (10, 20, 30, 40, 50 and 100 mV/s). The maximum specific capacitances of 320.6 F/g at 10 mV/s and 222.1 F/g at 100 mV/s have been obtained for AC3 electrode when compared with AC1 and AC2 electrodes. Based on the characterization studies, it has been inferred that the activated carbon prepared from sorghum pith may be one of the innovative carbon electrode materials for EDLC applications.

  2. Preparation and Characterization of Activated Carbon from Coconut Shell – Doped Tio2 in Water Solution

    Directory of Open Access Journals (Sweden)

    Maulidiyah

    2015-12-01

    Full Text Available The objective of the study was to prepare the activated carbon material doped TiO2-P25 (P25in order to determine the interaction occured in the water medium. The method was to prepare the activated carbon from coconut shell which had been cleaned, pyrolyzed, sievedthen followed by physical activation using a thermal process. Preparation of P25 was to form structures of anatase crystals in the furnace at temperature of 500°C for 3 hours. Both materials were mixed using distilled water until sol-gel was formed. Results of characterization using SEM showed that there is interaction between the activated carbon and P25inserted in the pores of the carbon, while SEM-EDX showed the composition of carbon, titanium and oxide are 46.9%; 27.5% and 25.6%, respectively. Data from XRD showed the formation of peaks from P25 anatase crystals and the carbon. It was supported by data of Flourier Transform Infra Red (FTIR which showed the bonds of –OH; C-H; C=C; COand the O-Ti-O.

  3. Preparation and characterizations of activated carbon monolith from rubber wood and its effect on supercapacitor performances

    Science.gov (United States)

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

    2016-02-01

    Preparation of activated carbon monolith (ACM) from rubber wood was investigated. Two kind of preparation method were carried out by pre-carbonized of rubber wood saw dust and rubber wood material as it is naturally. The samples were prepared with pelletizing method and small cutting of rubber wood in cross sectional method. Both of samples were characterized by physical and electrochemical technique. The physical properties such as morphology and porosity were investigated. The electrochemical properties of both samples such as equivalent series resistances (ESR) and specific capacitances were also compared. In conclusion, this study showed that both of different preparation method would propose a simple method of ACM electrode preparation technique for supercapacitor applications.

  4. Preparation of activated carbon by microwave heating of langsat (Lansium domesticum) empty fruit bunch waste.

    Science.gov (United States)

    Foo, K Y; Hameed, B H

    2012-07-01

    The feasibility of langsat empty fruit bunch waste for preparation of activated carbon (EFBLAC) by microwave-induced activation was explored. Activation with NaOH at the IR ratio of 1.25, microwave power of 600 W for 6 min produced EFBLAC with a carbon yield of 81.31% and adsorption uptake for MB of 302.48 mg/g. Pore structural analysis, scanning electron microscopy and Fourier transform infrared spectroscopy demonstrated the physical and chemical characteristics of EFBLAC. Equilibrium data were best described by the Langmuir isotherm, with a monolayer adsorption capacity of 402.06 mg/g, and the adsorption kinetics was well fitted to the pseudo-second-order equation. The findings revealed the potential to prepare high quality activated carbon from langsat empty fruit bunch waste by microwave irradiation.

  5. PREPARATION AND THEIR ANTIBACTERIAL ACTIVITY OF ACTIVATED CARBON FIBER CONTAINING SILVER

    Institute of Scientific and Technical Information of China (English)

    CHENShuixia; LUOYing; 等

    2000-01-01

    Several kinds of activated carbon fiber(ACF),Granule Activated carbon(AC) containing silver ion or fine silver particle(Ag-ACF/AC) have been prepared by soaking ACF or AC in the salt solution of silver.Ag,AgCl and AgI compounds have been loaded onto the fibers:The stucture of the fibers was measured by scanning electron microscopy(SEM) and power X-ray diffraction(XRD),THe Ag content in the fiber was obtained by an Atomic absorption spectroscopy(AAS),The Ag+ content in water after the antibacterial test was measured by an Inductively Coupled plasma(ICP) emission spectroscopy.Antibacterial test was carried out against Escherichia coli(E.coli) and Staphylococcus aureus(S.aureus).The results show that Ag-ACF/AC have strong antibacterial activity against E.Coli and S.aureus.After dealt with ACF/AC loading Ag,AgCl,AgI,no E.coli and S.aureus alive in solution can be detected.The analysis of Agcontent in water after antibacterial test showed that the content of Ag meet the quality requirement of the National Potable Water Standrd,It is indicated that ACF/AC-Ag in this experiment would be a safe antibacterial agent.

  6. Chemical study of extracted rockrose and of chars and activated carbons prepared at different temperatures

    Energy Technology Data Exchange (ETDEWEB)

    Pastor-Villegas, J.; Gomez-Serrano, V.; Duran-Valle, C.J.; Higes-Rolando, F.J. [Departamento de Quimica Inorganica, Universidad de Extremadura, Badajoz (Spain)

    1999-04-01

    This paper discusses the chemical composition and chemical structure of rockrose (Cistus ladaniferus L.) extracted into petroleum ether and resulting chars as well as activated carbons. The isothermal temperature of carbonization of extracted rockrose (Jex) in N{sub 2} ranged between 600 and 1000C. The char (C{sub Jex}-600) employed in the preparation of activated carbons was prepared by treatment of Jex at 30-600C. This char was heated in N{sub 2} before activation, which was carried out in CO{sub 2} or steam at 700-950C to 40% burn-off. Chemical analyses, Fourier transform infrared spectroscopy, thermogravimetry and X-ray diffraction techniques have been applied. The extraction does not exert a significant influence on the organic chemical structure of raw material. In ash prepared at 600C from Jex (ash content 1.29%), the major elements are Ca, K, Mg and P; calcite is the main component. When this ash is heated at 950C, lime is the main component. The chars and activated carbons contain carbon-carbon double bonds and ether structures; C{sub Jex}-600 also contains carbonyl groups. The ether groups decrease with the temperature increase. The analyses of chars and activated carbons show an ash content close to 6-8%, and calcite as the main component. The presence of whewellite, CaC{sub 2}O{sub 4}{center_dot}H{sub 2}O, indicates that the pyrolysis is delayed in the preparation of C{sub Jex}-600, that a partial calcium-carboxylate association occurs, and that hydration takes place during storage period. The mineral matter of the activated carbons prepared at 700C depends on the activating agent: calcite is the only component identified using CO{sub 2}, whereas lime, portlandite and vaterite are also identified using steam. At higher temperatures, the mineral matter is practically independent of the activating agent. Probably, CaO transforms into Ca(OH){sub 2} and CaCO{sub 3} during the char and activated carbon storage periods

  7. 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.

  8. Adsorption-desorption characteristics of phenol and reactive dyes from aqueous solution on mesoporous activated carbon prepared from waste tires.

    Science.gov (United States)

    Tanthapanichakoon, W; Ariyadejwanich, P; Japthong, P; Nakagawa, K; Mukai, S R; Tamon, H

    2005-04-01

    Liquid-phase adsorption-desorption characteristics and ethanol regeneration efficiency of an activated carbon prepared from waste tires and a commercial activated carbon were investigated. Water vapor adsorption experiments reveal that both activated carbons showed hydrophobic surface characteristics. Adsorption experiments reveal that the prepared activated carbon possessed comparable phenol adsorption capacity as the commercial one but clearly larger adsorption capacity of two reactive dyes, Black 5 and Red 31. It was ascertained that the prepared activated carbon exhibited less irreversible adsorption of phenol and the two dyes than its commercial counterpart. Moreover, ethanol regeneration efficiency of the prepared AC saturated with either dye was higher than that of the commercial AC. Because of its superior liquid-phase adsorption-desorption characteristics as well as higher ethanol regeneration efficiency, the prepared activated carbon is more suitable for wastewater treatment, especially for adsorbing similarly bulky adsorbates.

  9. STUDIES ON THE PREPARATION OF ZINC-CONTAINING ACTIVATED CARBON FIBERS AND THEIR ANTIBACTERIAL ACTIVITY

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    Several kinds of activated carbon fibers, using sisal fiber as precursors, were preparedwith steam activation or with ZnCl2 activation. Zinc or its compounds were dispersed in them. Theantibacterial activities of these activated carbon fibers were determined and compared. The researchresults showed that these sisal based activated carbon fibers supporting zinc have strongerantibacterial activity against Escherichia coli and S. aureus. The antibacterial activity is related tothe precursors, the pyrolysis temperature, and the zinc content. In addition, small quantity of silversupported on zinc-containing ACFs will greatly enhance the antibacterial activity of ACFs.

  10. Preparation and Electrochemistry of Hydrous Ruthenium Oxide/Active Carbon Electrode materials for Supercapacitor

    Institute of Scientific and Technical Information of China (English)

    Zhang; Jianrong

    2001-01-01

    In this paper, we reported a new method to directly prepare the amorphous hydrous ruthenium oxide/active carbon powders. The relationship between the specific capacitance and ruthenium content in powders was studied in detail. Physical properties of the powders such as crystallinity、 particle size, and electrochemical characteristics of electrodes were reported along with the capacitor performance.  ……

  11. Preparation and Electrochemistry of Hydrous Ruthenium Oxide/Active Carbon Electrode materials for Supercapacitor

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    @@ In this paper, we reported a new method to directly prepare the amorphous hydrous ruthenium oxide/active carbon powders. The relationship between the specific capacitance and ruthenium content in powders was studied in detail. Physical properties of the powders such as crystallinity、 particle size, and electrochemical characteristics of electrodes were reported along with the capacitor performance.

  12. Adsorption studies of methylene blue and phenol onto vetiver roots activated carbon prepared by chemical activation

    Energy Technology Data Exchange (ETDEWEB)

    Altenor, Sandro [COVACHIMM, EA 3592 Universite des Antilles et de la Guyane, BP 250, 97157 Pointe a Pitre Cedex, Guadeloupe (France); LAQUE, Universite Quisqueya d' Haiti, Port-au-Prince (Haiti); Carene, Betty [COVACHIMM, EA 3592 Universite des Antilles et de la Guyane, BP 250, 97157 Pointe a Pitre Cedex, Guadeloupe (France); Emmanuel, Evens [LAQUE, Universite Quisqueya d' Haiti, Port-au-Prince (Haiti); Lambert, Jacques; Ehrhardt, Jean-Jacques [Laboratoire de Chimie Physique et Microbiologie pour l' Environnement, UMR 7564 CNRS-Nancy Universities, 405 rue de Vandoeuvre, F 54600 Villers-les-Nancy Cedex (France); Gaspard, Sarra, E-mail: sgaspard@univ-ag.fr [COVACHIMM, EA 3592 Universite des Antilles et de la Guyane, BP 250, 97157 Pointe a Pitre Cedex, Guadeloupe (France)

    2009-06-15

    Vetiver roots have been utilized for the preparation of activated carbon (AC) by chemical activation with different impregnation ratios of phosphoric acid, X{sub P} (g H{sub 3}PO{sub 4}/g precursor): 0.5:1; 1:1 and 1.5:1. Textural characterization, determined by nitrogen adsorption at 77 K shows that mixed microporous and mesoporous structures activated carbons (ACs) with high surface area (>1000 m{sup 2}/g) and high pore volume (up to 1.19 cm{sup 3}/g) can be obtained. The surface chemical properties of these ACs were investigated by X-ray photoelectron spectroscopy (XPS) and Boehm titration. Their textural and chemical characteristics were compared to those of an AC sample obtained by steam activation of vetiver roots. Classical molecules used for characterizing liquid phase adsorption, phenol and methylene blue (MB), were used. Adsorption kinetics of MB and phenol have been studied using commonly used kinetic models, i.e., the pseudo-first-order model, the pseudo-second-order model, the intraparticle diffusion model and as well the fractal, BWS (Brouers, Weron and Sotolongo) kinetic equation. The correlation coefficients (R{sup 2}) and the normalized standard deviation {Delta}q (%) were determined showing globally, that the recently derived fractal kinetic equation could best describe the adsorption kinetics for the adsorbates tested here, indicating a complex adsorption mechanism. The experimental adsorption isotherms of these molecules on the activated carbon were as well analysed using four isotherms: the classical Freundlich, Langmuir, Redlich-Peterson equations, but as well the newly published deformed Weibull Brouers-Sotolongo isotherm. The results obtained from the application of the equations show that the best fits were achieved with the Brouers-Sotolongo equation and with the Redlich-Peterson equation. Influence of surface functional groups towards MB adsorption is as well studied using various ACs prepared from vetiver roots and sugar cane bagasse

  13. Adsorption studies of methylene blue and phenol onto vetiver roots activated carbon prepared by chemical activation.

    Science.gov (United States)

    Altenor, Sandro; Carene, Betty; Emmanuel, Evens; Lambert, Jacques; Ehrhardt, Jean-Jacques; Gaspard, Sarra

    2009-06-15

    Vetiver roots have been utilized for the preparation of activated carbon (AC) by chemical activation with different impregnation ratios of phosphoric acid, X(P) (gH(3)PO(4)/g precursor): 0.5:1; 1:1 and 1.5:1. Textural characterization, determined by nitrogen adsorption at 77K shows that mixed microporous and mesoporous structures activated carbons (ACs) with high surface area (>1000 m(2)/g) and high pore volume (up to 1.19 cm(3)/g) can be obtained. The surface chemical properties of these ACs were investigated by X-ray photoelectron spectroscopy (XPS) and Boehm titration. Their textural and chemical characteristics were compared to those of an AC sample obtained by steam activation of vetiver roots. Classical molecules used for characterizing liquid phase adsorption, phenol and methylene blue (MB), were used. Adsorption kinetics of MB and phenol have been studied using commonly used kinetic models, i.e., the pseudo-first-order model, the pseudo-second-order model, the intraparticle diffusion model and as well the fractal, BWS (Brouers, Weron and Sotolongo) kinetic equation. The correlation coefficients (R(2)) and the normalized standard deviation Deltaq (%) were determined showing globally, that the recently derived fractal kinetic equation could best describe the adsorption kinetics for the adsorbates tested here, indicating a complex adsorption mechanism. The experimental adsorption isotherms of these molecules on the activated carbon were as well analysed using four isotherms: the classical Freundlich, Langmuir, Redlich-Peterson equations, but as well the newly published deformed Weibull Brouers-Sotolongo isotherm. The results obtained from the application of the equations show that the best fits were achieved with the Brouers-Sotolongo equation and with the Redlich-Peterson equation. Influence of surface functional groups towards MB adsorption is as well studied using various ACs prepared from vetiver roots and sugar cane bagasse. Opposite effects governing MB

  14. Preparation of activated carbon from waste plastics polyethylene terephthalate as adsorbent in natural gas storage

    Science.gov (United States)

    Yuliusman; Nasruddin; Sanal, A.; Bernama, A.; Haris, F.; Ramadhan, I. T.

    2017-02-01

    The main problem is the process of natural gas storage and distribution, because in normal conditions of natural gas in the gas phase causes the storage capacity be small and efficient to use. The technology is commonly used Compressed Natural Gas (CNG) and Liquefied Natural Gas (LNG). The weakness of this technology safety level is low because the requirement for high-pressure CNG (250 bar) and LNG requires a low temperature (-161°C). It takes innovation in the storage of natural gas using the technology ANG (Adsorbed Natural Gas) with activated carbon as an adsorbent, causing natural gas can be stored in a low pressure of about 34.5. In this research, preparation of activated carbon using waste plastic polyethylene terephthalate (PET). PET plastic waste is a good raw material for making activated carbon because of its availability and the price is a lot cheaper. Besides plastic PET has the appropriate characteristics as activated carbon raw material required for the storage of natural gas because the material is hard and has a high carbon content of about 62.5% wt. The process of making activated carbon done is carbonized at a temperature of 400 ° C and physical activation using CO2 gas at a temperature of 975 ° C. The parameters varied in the activation process is the flow rate of carbon dioxide and activation time. The results obtained in the carbonization process yield of 21.47%, while the yield on the activation process by 62%. At the optimum process conditions, the CO2 flow rate of 200 ml/min and the activation time of 240 minutes, the value % burn off amounted to 86.69% and a surface area of 1591.72 m2/g.

  15. Removal of organic dyes using Cr-containing activated carbon prepared from leather waste.

    Science.gov (United States)

    Oliveira, Luiz C A; Coura, Camila Van Zanten; Guimarães, Iara R; Gonçalves, Maraisa

    2011-09-15

    In this work, hydrogen peroxide decomposition and oxidation of organics in aqueous medium were studied in the presence of activated carbon prepared from wet blue leather waste. The wet blue leather waste, after controlled pyrolysis under CO(2) flow, was transformed into chromium-containing activated carbons. The carbon with Cr showed high microporous surface area (up to 889 m(2)g(-1)). Moreover, the obtained carbon was impregnated with nanoparticles of chromium oxide from the wet blue leather. The chromium oxide was nanodispersed on the activated carbon, and the particle size increased with the activation time. It is proposed that these chromium species on the carbon can activate H(2)O(2) to generate HO radicals, which can lead to two competitive reactions, i.e. the hydrogen peroxide decomposition or the oxidation of organics in water. In fact, in this work we observed that activated carbon obtained from leather waste presented high removal of methylene blue dye combining the adsorption and oxidation processes.

  16. Preparation of Bamboo Chars and Bamboo Activated Carbons to Remove Color and COD from Ink Wastewater.

    Science.gov (United States)

    Hata, Motohide; Amano, Yoshimasa; Thiravetyan, Paitip; Machida, Motoi

    2016-01-01

    Bamboo chars and bamboo activated carbons prepared by steam activation were applied for ink wastewater treatment. Bamboo char at 800 °C was the best for the removal of color and chemical oxygen demand (COD) from ink wastewater compared to bamboo chars at 300 to 700 °C due to higher surface area and mesopore volume. Bamboo activated carbon at 600 °C (S600) was the best compared to bamboo activated carbon at 800 °C (S800), although S800 had larger surface area (1108 m(2)/g) than S600 (734 m(2)/g). S600 had higher mesopore volume (0.20 cm(3)/g) than S800 (0.16 cm(3)/g) and therefore achieved higher color and COD removal. All bamboo activated carbons showed higher color and COD removal efficiency than commercial activated carbon. In addition, S600 had the superior adsorption capacity for methylene blue (0.89 mmol/g). Therefore, bamboo is a suitable material to prepare adsorbents for removal of organic pollutants.

  17. Activated carbons prepared from wood particleboard wastes: characterisation and phenol adsorption capacities.

    Science.gov (United States)

    Girods, P; Dufour, A; Fierro, V; Rogaume, Y; Rogaume, C; Zoulalian, A; Celzard, A

    2009-07-15

    The problems of valorisation of particleboard wastes on one hand, and contamination of aqueous effluents by phenolic compounds on the other hand, are simultaneously considered in this work. Preparation of activated carbons from a two steps thermo-chemical process, formerly designed for generating combustible gases, is suggested. The resultant carbonaceous residue is activated with steam at 800 degrees C. Depending on the preparation conditions, surface areas within the range 800-1300 m(2)/g are obtained, close to that of a commercial activated carbon (CAC) specially designed for water treatment and used as a reference material. The present work shows that particleboard waste-derived activated carbons (WAC) are efficient adsorbents for the removal of phenol from aqueous solutions, with maximum measured capacities close to 500 mg/g. However, most of times, the adsorption capacities are slightly lower than that of the commercial material in the same conditions, i.e., at equilibrium phenol concentrations below 300 ppm. Given the extremely low cost of activated carbons prepared from particleboard waste, it should not be a problem to use it in somewhat higher amounts than what is required with a more expensive commercial material. Phenol adsorption isotherms at 298 K were correctly fitted by various equations modelling type I and type II isotherms for CAC and WAC, respectively. Phenol adsorption isotherms of type II were justified by a 3-stages adsorption mechanism.

  18. 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.

  19. 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.

  20. Study on preparation of Luffa activated carbon and its adsorption of metal ions

    Science.gov (United States)

    Zhai, Kuilu; Li, Zichao; Li, Qun

    2017-03-01

    In this paper, loofah was used as raw material and alkali and hydrogen peroxide were used to pre-oxidize. The activated carbon was activated by zinc chloride, and the activated carbon was used to desorb the heavy metal ions nickel and copper. The removal efficiency of heavy metal ions was studied under different conditions. The effects of retinervus Luffae Fructus active carbon adsorption of metal ions on process conditions, including metal ion concentration, reaction temperature, loofah activated carbon types and activated carbon dosage. In the present study, in different strain rate on the loofah sponge material compression tests in a wide range of density from 24 to 64 kg cubic meters. Luffa fibers and followed by carbonization to prepare MCAC KOH activation. MCAC has dense in parallel channels 10 mm in diameter and 4 - 0.3 - 1 mm wall thickness, which is inherited from the native structure of Luffa. Micro and middle holes are formed on the inner surface of the channel wall to form a hierarchical porous structure.

  1. 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.

  2. Characterization of mesoporous carbon prepared from date stems by H3PO4 chemical activation

    Science.gov (United States)

    Hadoun, H.; Sadaoui, Z.; Souami, N.; Sahel, D.; Toumert, I.

    2013-09-01

    The present work was focused on the determination of texture, morphology, crystanillity and oxygenated surface groups characteristics of an activated carbon prepared from date stems. Chemical activation of this precursor at different temperatures (450, 550 and 650 °C) was adopted using phosphoric acid as dehydrating agent at (2/1) impregnation ratio. Fourier transform infrared spectroscopy study was carried out to identify surface groups in date stems activated carbons. The microscopic structure was examined by nitrogen adsorption at 77 K. The interlayer spacing (d200 and d100), stack height (Lc), stack width (La) and effective dimension L of the turbostratic crystallites (microcrystallite) in the date stems activated carbons were estimated from X-ray diffraction data (XRD). Results yielded a surface area, SBET, and total pore volume of 682, 1455, 1319 m2/g and 0,343, 1,045 and 0.735 cm3/g, for the carbon prepared at 450, 550 and 650 °C, respectively. Scanning electron microscopy exhibits a highly developed porosity which is in good agreement with the porous texture derived from gas adsorption data and these results confirm that the activated carbon is dominated by network of slit-shaped mesopores morphology and in some cases by varied micropores morphologies.

  3. 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.

  4. 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.

  5. Adsorption of cadmium from aqueous solutions on sulfurized activated carbon prepared from nut shells.

    Science.gov (United States)

    Fouladi Tajar, Amir; Kaghazchi, Tahereh; Soleimani, Mansooreh

    2009-06-15

    Low-cost activated carbon, derived from nut shells, and its modified sample have been used as replacements for the current expensive methods of removing cadmium from aqueous solutions and waste waters. Adsorption of cadmium onto four kinds of activated carbons has been studied; prepared activated carbon (PAC), commercial activated carbon (CAC), and the sulfurized ones (SPAC & SCAC). The activated carbon has been derived, characterized, treated with sulfur and then utilized for the removal of Cd(2+). Sulfurizing agent (SO(2) gas) was successfully used in adsorbents' modification process at the ambient temperature. Samples were then characterized and tested as adsorbents of cadmium. Effect of some parameters such as contact time, initial concentration and pH were examined. With increasing pH, the adsorption of cadmium ions was increased and maximum removal, 92.4% for SPAC, was observed in pH>8.0 (C(0)=100mg/L). The H-type adsorption isotherms, obtained for the adsorbents, indicated a favorable process. Adsorption data on both prepared and commercial activated carbon, before and after sulfurization, followed both the Frendlich and Langmuir models. They were better fitted by Frendlich isotherm as compared to Langmuir. The maximum adsorption capacities were 90.09, 104.17, 126.58 and 142.86 mg/g for CAC, PAC, SCAC and SPAC, respectively. Accordingly, surface modification of activated carbons using SO(2) greatly enhanced cadmium removal. The reversibility of the process has been studied in a qualitative manner and it shows that the spent SPAC can be effectively regenerated for further use easily.

  6. Phenol adsorption onto powdered and granular activated carbon, prepared from Eucalyptus wood.

    Science.gov (United States)

    Tancredi, Nestor; Medero, Natalia; Möller, Fabiana; Píriz, Javier; Plada, Carina; Cordero, Tomás

    2004-11-15

    Eucalyptus grandis sawdust, a major waste from the growing Uruguayan wood industry, was used in previous work to prepare powdered activated carbon (PAC). In the present work, granular activated carbon (GAC) was prepared by mixing PAC, carboxymethyl cellulose as a binder, and kaolin as reinforcer. Ultimate analysis and surface characterization of GAC and PAC were performed. Phenol adsorption was used as a way to compare the characteristics of different PAC and GAC preparations. Kinetics and isotherms of the different GAC and PAC were performed in a shaking bath at 100 rpm and 298 K. Phenol concentrations were determined by UV spectroscopy. Some kinetics parameters were calculated; from kinetics results, external resistance to mass transfer from the bulk liquid can be neglected as the controlling step. Isotherms were fitted to Langmuir and Freundlich models, and corresponding parameters were determined. Maximum phenol uptakes for all carbons were determined and correlated with carbon characteristics. Thermogravimertic analysis (TGA) determinations were performed in order to study adsorption characteristics and conditions for GAC regeneration after its use. The results showed that phenol is preferentially physisorbed on the carbon of the granules, though some chemisorption was detected. No adsorption was detected in the kaolin-carboxymethyl cellulose mixture.

  7. Studies on adsorption of mercury from aqueous solution on activated carbons prepared from walnut shell.

    Science.gov (United States)

    Zabihi, M; Haghighi Asl, A; Ahmadpour, A

    2010-02-15

    The adsorption ability of a powdered activated carbons (PAC) derived from walnut shell was investigated in an attempt to produce more economic and effective sorbents for the control of Hg(II) ion from industrial liquid streams. Carbonaceous sorbents derived from local walnut shell, were prepared by chemical activation methods using ZnCl(2) as activating reagents. Adsorption of Hg(II) from aqueous solutions was carried out under different experimental conditions by varying treatment time, metal ion concentration, pH and solution temperature. It was shown that Hg(II) uptake decreases with increasing pH of the solution. The proper choice of preparation conditions were resulted in microporous activated carbons with different BET surface areas of 780 (Carbon A, 1:0.5 ZnCl(2)) and 803 (Carbon B, 1:1 ZnCl(2))m(2)/g BET surface area. The monolayer adsorption capacity of these particular adsorbents were obtained as 151.5 and 100.9 mg/g for carbons A and B, respectively. It was determined that Hg(II) adsorption follows both Langmuir and Freundlich isotherms as well as pseudo-second-order kinetics.

  8. Preparation, characterization and phenol adsorption capacity of activated carbons from African beech wood sawdust

    Directory of Open Access Journals (Sweden)

    N.T. Abdel-Ghani

    2016-05-01

    Full Text Available In the present study, different activated carbons were prepared from carbonized African beech wood sawdust by potassium hydroxide activation. The activated carbons were characterized by brunauer–emmett–teller, scanning electron microscope, fourier transform infrared spectroscopy, and thermogravimetric analyzer. The phenol adsorption capacity of the prepared carbons was evaluated. The different factors affecting phenol’s removal were studied including: contact time, solution pH and initial phenol concentration. The optimum phenol removal was obtained after a contact time of 300 min. and at an initial phenol solution pH 7. The maximum removal percentages were determined at 5mg/l initial phenol concentration as 79, 93, 94 and 98% for AC0, AC1, AC2 and AC3; respectively. The adsorption of phenol on African beech sawdust activated carbons was found to follow the Lagergren first order kinetics and the intraparticle diffusion mechanism gave a good fit to the experimental data. The isothermal models applied fitted the experimental data in the order: Langmuir> Dubinin–Radushkevich> Freundlich and Temkin.

  9. Microstructure of polyacrylonitrile-based activated carbon fibers prepared from solvent-free coagulation process

    Directory of Open Access Journals (Sweden)

    Norhaniza Yusof

    2016-02-01

    Full Text Available Polyacrylonitrile precursor fibers prepared using a solvent-free coagulation process were stabilized, carbonized, and physically activated by carbon dioxide into activated carbon fibers (ACFs. The activation temperature varied from 600 to 900 °C while the activation time was 1 h. Atomic force microscopy was used to observe the surface morphology, as well as the surface roughness of the ACFs. Higher pyrolysis temperature formed rougher surfaces, and increased the pore sizes. Meanwhile, Fourier transform infrared spectroscopy revealed more conversion of oxygen containing functional groups to carbonaceous materials as the activation temperature increased. Moreover, the microstructure properties were thoroughly characterized by the X-ray photoelectron spectroscopy (XPS and X-ray diffraction (XRD studies. XRD analysis showed that the activation of the ACFs shrank the ordered structure, reducing the D-spacing from 0.358 to 0.347 nm for the fibers prepared at activation temperatures of 600 to 900 °C. Meanwhile, XPS analysis concluded that that the oxygen containing functional groups were still retained even at high activation temperatures while the nitrogen containing functional groups were reduced during the high temperature activation in the CO2 atmosphere.

  10. Elimination of textile dyes using activated carbons prepared from vegetable residues and their characterization.

    Science.gov (United States)

    Peláez-Cid, Alejandra-Alicia; Herrera-González, Ana-María; Salazar-Villanueva, Martín; Bautista-Hernández, Alejandro

    2016-10-01

    In this study, three mesoporous activated carbons prepared from vegetable residues were used to remove acid, basic, and direct dyes from aqueous solutions, and reactive and vat dyes from textile wastewater. Granular carbons obtained by chemical activation at 673 K with phosphoric acid from prickly pear peels (CarTunaQ), broccoli stems (CarBrocQ), and white sapote seeds (CarZapQ) were highly efficient for the removal of dyes. Adsorption equilibrium studies were carried out in batch systems and treated with Langmuir and Freundlich isotherms. The maximum adsorption capacities calculated from the Langmuir isotherms ranged between 131.6 and 312.5 mg/g for acid dyes, and between 277.8 and 500.0 mg/g for basic dyes at 303 K. Our objective in this paper was to show that vegetable wastes can serve as precursors for activated carbons that can be used for the adsorption of dyes. Specifically CarBrocQ was the best carbon produced for the removal of textile dyes. The color removal of dyes present in textile wastewaters was compared with that of a commercial powdered carbon, and it was found that the carbons produced using waste material reached similar efficiency levels. Carbon samples were characterized by bulk density, point of zero charge, thermogravimetric analysis, elemental analysis, Fourier transform infrared spectroscopy, scanning electron microscopy, methylene blue adsorption isotherms at 303 K, and nitrogen adsorption isotherms at 77 K (SBET). The results show that the activated carbons possess a large specific surface area (1025-1177 m(2)/g) and high total pore volume (1.06-2.16 cm(3)/g) with average pore size diameters between 4.1 and 8.4 nm. Desorption and regeneration tests were made to test the viability of reusing the activated carbons. Copyright © 2016 Elsevier Ltd. All rights reserved.

  11. Preparation of the sludge activated carbon with domestic sludge mixed agricultural straw

    Science.gov (United States)

    Wang, Laifu; Wang, Yan; Lian, Jingyan

    2017-01-01

    Urban sewage sludge with complicated composition produce largely each year, pollution problem and resource utilization has increasingly become the focus of attention. Sewage sludge is utilized to prepare adsorbent that is a new type method. Agricultural stalks was added to material (urban sewage sludge) and activator (ZnCl2), calcined under the condition of no inert gas, and obtained domestic sludge activated carbon. The properties were measured by iodine adsorption value and BET, discussed influence factors of sludge activated carbon preparation, including activator concentration, solid-liquid ratio, calcific temperature and calcific time. The best process condition of orthogonal experiment had explored that activated time is 10 minutes, calcific temperature is 350°C, the activator concentration ZnCl2 is 3 mol/L and the mixing ratio of raw materials and activator is approximately 1:5. The iodine adsorption value and the optimal BET of as-obtained domestic sludge activated carbon is 445.06 mg/g, 525.31m2/g, respectively.

  12. Study on the preparation of straw activated carbon and its phenol adsorption properties

    Science.gov (United States)

    Chen, Liping

    2017-01-01

    Using sunflower straw as raw materials to manufacture straw activated carbon-modified by phosphoric acidand adsorption isotherm of phenol on straw activated carbon was studied in a batch reactor. The physical properties of the prepared straw activated carbons were characterized by scanning electron microscopy. The effect of various parameters, adsorbent dose, pH and temperature, were studied on optimum conditions. The results have shown that the absorbent was efficient, the removal ratio of phenol up to 99.36% with an adsorbent dosage of 16 g·L-1, a pH of 6.0-8.0, at 25 °C. The experimental adsorption data fitted reasonably well to the Langmuir isotherm, the maximum adsorption capacity was 109.89 mg/g. The process of adsorption is a exothermic process.

  13. Preparation and Properties of Paraffin/TiO2/Active-carbon Composite Phase Change Materials

    Directory of Open Access Journals (Sweden)

    HAO Yong-gan

    2016-11-01

    Full Text Available A novel composite phase change materials (PCMs of paraffin/TiO2/active-carbon was prepared by a microemulsion method, where paraffin acted as a PCM and titanium dioxide (TiO2 as matrix material, and a small amount of active carbon was added to improve the thermal conductivity. The compositions, morphology and thermal properties of the paraffin/TiO2/active-carbon composite PCMs were characterized by XRD, SEM, TGA and DSC respectively. The shape stability during phase change process of this composite was also tested. The results show that paraffin is well encapsulated by TiO2 matrix, and thus exhibiting excellent shape-stabilized phase change feature. Besides, this composite PCM also presents superhydrophobic property. Therefore, these multifunctional features will endow PCMs with important application potential in energy efficient buildings.

  14. Preparation and performance of photocatalytic regenerationable activated carbon prepared via sol-gel TiO2

    Institute of Scientific and Technical Information of China (English)

    LIU Shou-xin; SUN Cheng-lin

    2006-01-01

    Preparation ofphotocatalytic regenerationable activated carbon (AC) is the key step for the practical application of in situ regeneration of exhausted AC. A novel photocatalytic regenerationable AC was prepared by sol-gel TiO2 in this work. The adsorption and regeneration performance of TiO2/AC were evaluated using phenol as model compound. Scanning electron microscope (SEM)and nitrogen (77 K) adsorption isotherm were used to determine the surface area, pore structure and the distribution of TiO2. The results showed that with the increase of TiO2 loading, adsorption capacity of TiO2/AC decreased and the regeneration efficiency increased. The photocatalytic regenerationable AC with suitable TiO2 loading (2 wt%) exhibited suitable adsorption capacity and regeneration efficiency. TiO2 located mainly in the entrance of macro-pore of carbon. The prepared TiO2/AC exhibited similar surface structure and pore structure with material carbon.

  15. 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.

  16. 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.

  17. Preparation and characterization of activated carbon fiber (ACF) from cotton woven waste

    Science.gov (United States)

    Zheng, Jieying; Zhao, Quanlin; Ye, Zhengfang

    2014-04-01

    In this study, the activated carbon fibers (ACFs) were prepared using cotton woven waste as precursor. The cotton woven waste was first partly dissolved by 80% phosphoric acid and then was pre-soaked in 7.5% diammonium hydrogen phosphate solution. Finally, carbonization and activation were proceeded to get ACF. The optimum preparation conditions, including carbonization temperature, carbonization time, activation temperature and activation time, were chosen by orthogonal design. Nitrogen adsorption/desorption test was conducted to characterize the prepared ACF's pore structure. Fourier transform infrared spectroscopy (FTIR) analysis, X-ray photoelectron spectroscopy (XPS) and environmental scanning electron microscope (ESEM) were employed to characterize its chemical properties and morphology. Adsorption of oilfield wastewater was used to evaluate its adsorption properties. The results show that the prepared ACF is in the form of fiber, with the sectional diameters of 11.7 × 2.6 μm and the surface area of 789 m2/g. XPS results show that carbon concentration of the prepared ACF is higher than that of the commercial ACF. When the prepared ACF dosage is 6 g/L, over 80% of COD and over 70% of chrominance can be removed after 24 h of adsorption at 18 °C. We demonstrated the catalytic growth of m-axial InxGa1-xN (0.10 ≤ x ≤ 0.17) nanocolumn arrays with high crystallinity on silicon substrates using metal-organic chemical vapor deposition with trimethylindium (TMIn), triethylgallium (TEGa), and ammonia as precursors. The high quality of InGaN nanocolumns (NCs) were believed to be due to the utilization of TEGa that achieved less carbon impurities and offered more comparable vapor pressure with that of TMIn at low temperature. In addition, these NCs were grown in non-polar m-axis, which the internal electric field of the InGaN that often deteriorates the device performances might be able to be eliminated. Furthermore, the bandgap of this InGaN can be modulated from

  18. The Adsorption Efficiency of Chemically Prepared Activated Carbon from Cola Nut Shells by on Methylene Blue

    OpenAIRE

    Julius Ndi Nsami; Joseph Ketcha Mbadcam

    2013-01-01

    The adsorption of methylene blue from aqueous solution onto activated carbon prepared from cola nut shell has been investigated under batch mode. The influence of major parameters governing the efficiency of the process such as, solution pH, sorbent dose, initial concentration, and contact time on the removal process was investigated. The time-dependent experimental studies showed that the adsorption quantity of methylene blue increases with initial concentration and decreasing adsorbent dosa...

  19. 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.

  20. Preparation of manganese dioxide loaded activated carbon adsorbents and their desulfurization performance

    Science.gov (United States)

    Zhang, Jiaojing; Wang, Guojian; Wang, Wenyi; Song, Hua; Wang, Lu

    2016-12-01

    Manganese dioxide loaded activated carbon adsorbents (MnO2/AC) were prepared and characterized by N2 adsorption-desorption, BET method, X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), Fourier transform infrared spectrometry (FT-IR) and scanning electron microscopy (SEM). Effects of preparation conditions and adsorption conditions on desulfurization performance of the adsorbents were studied in a fixed-bed adsorption apparatus. Experimental results show that the surface area and pore volume of MnO2/AC decreased compared with the unmodified activated carbon, but the adsorption capacity to H2S was improved greatly. A suitable H2S removal activity was obtained with manganese dioxide to activated carbon ratio of 1.1: 1 and the calcination temperature of 250°C. At the adsorption temperature of 40°C and gas flow rate of 20 mL/min, the H2S saturation capacity and H2S removal rate reached up to 713.25 mg/g and 89.9%, respectively.

  1. Photocatalytic properties of TiO2 bonded active carbon composites prepared by SOL-GEL

    Institute of Scientific and Technical Information of China (English)

    李佑稷; 李效东; 李君文; 尹静

    2004-01-01

    Photocatalyst of TiO2 bonded active carbon (TiO2/AC), was prepared via sol-gel method from a mixture of TiO2 sol with active carbon. Post heat treatment was performed at 250 ℃ for 2 h in air and then kept at 400 ℃ to 600 ℃ under a flow of nitrogen for 2 h. The TiO2/AC composites obtained were characterized by SEM, XRD, UV-vis and BET. The photocatalytic activities of the TiO2/AC composites were studied in comparison with TiO2, AC,P-25 and a mixture of TiO2 and AC, respectively. The Ramnant rate of Rhodamine B absorbed by the active carbon is found to be almost 70% and the remnant rates of the Rhodamine B decolorized by TiO2 and the mixture of TiO2 and the active carbon are 30% and 25%, respectively. However, nearly complete removal of Rhodamine B is observed for a TiO2/AC composite after 200 min under UV irradiation, which will take the P-25 commercial product 5 h. Therefore, the TiO2/AC composite is much more effective in decolorization of aqueous Rhodamine B. In addition, the composite can be easily separated from solutions.

  2. Recent developments in the preparation and regeneration of activated carbons by microwaves.

    Science.gov (United States)

    Yuen, Foo Keng; Hameed, B H

    2009-07-30

    To date, microwave energy has been widely developed and applied to almost every field of chemistry. In many cases, microwave technology has proven to remarkably reducing costs, accelerating reaction rates, improving yields and selectively activating. This paper presents a state of art review of microwave technology, its background studies, fundamental chemistry and industrial applications. With the renaissance of activated carbon, there has been a steadily growing interest in this research field. The review provides a summary on recent development in preparation and regeneration of activated carbons. The key advance of introducing microwave energy has been highlighted relative to conventional methods. Moreover, the major drawbacks, challenges with its future expectation are presented and discussed. Conclusively, microwave energy is predicted to be a potentially viable and powerful replacement for fuel technology in various areas, while its progress represents an expanding field in the area of adsorption science.

  3. Preparation of activated carbon from corn cob and its adsorption behavior on Cr(VI) removal.

    Science.gov (United States)

    Tang, Shuxiong; Chen, Yao; Xie, Ruzhen; Jiang, Wenju; Jiang, Yanxin

    2016-01-01

    Operation experiments were conducted to optimize the preparation of activated carbons from corn cob. The Cr(VI) adsorption capacity of the produced activated carbons was also evaluated. The impact of the adsorbent dosage, contact time, initial solution pH and temperature was studied. The results showed that the produced corn cob activated carbon had a good Cr(VI) adsorptive capacity; the theoretical maximum adsorption was 34.48 mg g(-1) at 298 K. The Brunauer-Emmett-Teller and iodine adsorption value of the produced activated carbon could be 924.9 m(2) g(-1) and 1,188 mg g(-1), respectively. Under the initial Cr(VI) concentration of 10 mg L(-1) and the original solution pH of 5.8, an adsorption equilibrium was reached after 4 h, and Cr(VI) removal rate was from 78.9 to 100% with an adsorbent's dosage increased from 0.5 to 0.7 g L(-1). The kinetics and equilibrium data agreed well with the pseudo-second-order kinetics model and the Langmuir isotherm model. The equilibrium adsorption capacity improved with the increment of the temperature.

  4. The use of piassava fibers (Attalea funifera) in the preparation of activated carbon.

    Science.gov (United States)

    Avelar, Fabiana Ferreira; Bianchi, Maria Lúcia; Gonçalves, Maraisa; da Mota, Estella Gaspar

    2010-06-01

    The piassava fiber, residue of the broom industry, was used as precursor for the preparation of activated carbons (AC). AC were prepared by chemical activation with zinc chloride (AC ZnCl(2)) or phosphoric acid (AC H(3)PO(4)) and by physical activation with carbon dioxide (AC CO(2)) or water vapor (AC H(2)O). These materials were characterized by adsorption/desorption of N(2) to determine the BET areas, elemental analysis (CHN), thermogravimetric analysis (TG, DTA) and scanning electron microscopy (SEM). The carbons were tested with respect to their adsorption capacity of methylene blue, reactive red, phenol and metallic ions (Cr(+6), Cu(+2) and Zn(+2)). AC ZnCl(2) presented the highest surface area (1190 m(2)g(-1)) and AC H(3)PO(4), the largest pore volume (0.543 cm(3)g(-1)). AC ZnCl(2) was more efficient in the adsorption of methylene blue, Cr(+6) and Cu(+2) ions. AC H(2)O was the better adsorbent for phenol, while AC CO(2) was better for Zn(+2) ions.

  5. Phenol Adsorption on Nitrogen-enriched Activated Carbon Prepared from Bamboo Residues

    Directory of Open Access Journals (Sweden)

    Ji Zhang

    2013-12-01

    Full Text Available Nitrogen-enriched activated carbons prepared from bamboo residues were characterized by means of BET, XPS, and elemental analysis. Then adsorption experiments were carried out to study the effects of various physicochemical parameters such as contact time, temperature, pH, and initial concentration. Adsorption equilibrium was achieved within 120 min at a phenol concentration of 250 mg/L. When the pH was 4 and 0.1 g of the carbon absorbent and 100 mL of phenol solution at 250 mg/L were used, the phenol adsorption of the ACs with melamine and urea modifications were 219.09 mg/g and 214.45 mg/g, respectively. Both were greater than the capacity of unmodified AC, which was 163.82 mg/g. The Langmuir isotherm adsorption equation well described the experimental adsorption isotherms. The adsorption kinetics was well explained by pseudo-second-order kinetics rather than the pseudo-first-order. In conclusion, the nitrogen-enriched activated carbon proposed as adsorbents of the phenol wastewater were shown to be effective, which also means that bamboo residues have promise as activated carbon precursors for liquid phase adsorbents for environmental protection.

  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. 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.

  8. Characterizing o- and p-nitrophenols adsorption onto innovative activated carbon prepared from date pits.

    Science.gov (United States)

    Altaher, Hossam; Dietrich, Andrea M

    2014-01-01

    The production and performance of activated carbon prepared from date pits was investigated. Date pits are an abundant local waste product in many countries; converting them to a commercial product would increase the sustainability of this fruit crop. The date pit activated carbon was shown to have similar characteristics of pore size and surface functional groups as other commercial carbons. Batch experiments were conducted with o- and p-nitrophenol to evaluate the performance of this carbon. Results were analyzed according to Langmuir, Freundlich, and Dubinin-Radushkevich adsorption isotherms. The adsorption capacity of o-nitrophenol was 142.9 mg/g while that of p-nitrophenol was 108.7 mg/g. The adsorption process was physical in nature. The position of the -NO(2) group in the benzene ring has a considerable effect on the adsorption capacity and rate of uptake. The kinetic results showed that a pseudo second-order model appropriately describes the experimental data. The analysis of kinetic data revealed that the mechanism of adsorption is complex with both liquid film diffusion and intraparticle diffusion contributing to adsorption of both adsorbates.

  9. 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.

  10. Optimization of Preparation Program for Biomass Based Porous Active Carbon by Response Surface Methodology Based on Adsorptive Property

    Directory of Open Access Journals (Sweden)

    ZHANG Hao

    2017-06-01

    Full Text Available With waste walnut shell as raw material, biomass based porous active carbon was made by microwave oven method. The effects of microwave power, activation time and mass fraction of phosphoric acid on adsorptive property of biomass based porous active carbon in the process of physical activation of active carbon precursor were studied by response surface method and numerical simulation method, the preparation plan of biomass based porous active carbon was optimized, and the optimal biomass based porous active carbon property was characterized. The results show that three factors affect the adsorptive property of biomass based porous active carbon, but the effect of microwave power is obviously more significant than that of mass fraction of phosphoric acid, and the effect of mass fraction of phosphoric acid is more significant than that of activation time. The optimized preparation conditions are:microwave power is 746W, activation time is 11.2min and mass fraction of phosphoric acid is 85.9% in the process of physical activation of activated carbon precursor by microwave heating method. For the optimal biomass based porous active carbon, the adsorption value of iodine is 1074.57mg/g, adsorption value of methylene blue is 294.4mL/g and gain rate is 52.1%.

  11. Effect of Activation Temperature and Heating Duration on Physical Characteristics of Activated Carbon Prepared from Agriculture Waste

    Directory of Open Access Journals (Sweden)

    Tham Yee Jun

    2010-01-01

    Full Text Available This study was conducted to determine the physical characteristics of activated carbon prepared from durian shell in varied heating durations from 10 min to 30 min and activation temperatures of 400C and 500C. Durian shells have been characterized in term of ultimate and proximate analysis, chemical composition and thermal behaviour with a view to be used as activated carbon precursor. Durian shell activated carbon was prepared by impregnating 10g of sample in 10% (v/v concentration of phosphoric acid for 24 h, followed by carbonization at 400C and 500C with different heating durations under nitrogen atmosphere. The results showed that various treatment conditions affect the percentage of yield, BET surface area, micropore volume, and average pore diameter. The highest surface area (SBET 1024 m2/g was obtained at 500C and 20 min of heating duration with 63% of yield and 0.21 cm3/g micropore volume.

  12. Microscopic and mesoscopic structural features of an activated carbon sample, prepared from sorghum via activation by phosphoric acid

    Energy Technology Data Exchange (ETDEWEB)

    Temleitner, László [SPring-8, JASRI, 1-1-1 Kouto, Sayo-cho, Sayo-gun, Hyogo 679-5198 (Japan); Pusztai, László, E-mail: pusztai.laszlo@wigner.mta.hu [Institute for Solid State Physics and Optics, Wigner Research Centre for Physics, Hungarian Academy of Sciences, P.O. Box 49, H-1525 Budapest (Hungary); Rubio-Arroyo, Manuel F.; Aguilar-López, Sergio [Instituto de Quimica, UNAM, Circuito Exterior S/N, Ciudad Universitaria, Coyoacán, México D.F. 04510 (Mexico); Klimova, Tatiana [Facultad de Quimica, UNAM, Edif. E, Ciudad Universitaria, Coyoacán, México D.F. 04510 (Mexico); Pizio, Orest [Instituto de Quimica, UNAM, Circuito Exterior S/N, Ciudad Universitaria, Coyoacán, México D.F. 04510 (Mexico)

    2012-12-15

    Graphical abstract: Display Omitted Highlights: ► Preparation of a new activated carbon sample from sorghum. ► Characterization by adsorption/desorption methods. ► Determination of the structure by synchrotron X-ray diffraction. ► The sample is amorphous and contains distorted graphene fragments. ► A characteristic nanoscale distance is established from the radial distribution function. -- Abstract: An acidic chemical activation procedure has been used for preparing activated carbon with a surface area exceeding 1000 m{sup 2}/g from sorghum. In order to reveal structural features, synchrotron X-ray diffraction measurements have been performed. The structure of the material has been characterized by the total scattering structure factor and the radial distribution function describing short-range arrangement of atoms at distances of the order of a few atomic diameters as well as correlations at a longer scale, of the order of nanometers. The atomic arrangement has been found to be consistent with that of amorphous graphite-like carbon. As far as the mesoscopic structure is concerned, the presence of a characteristic distance is suggested on the basis of the clear nanometer scale oscillations of the radial distribution function, which distance may be assigned as the mesopore size in the material. It is suggested that the approach devized here may later be applied routinely for other activated carbon samples, too, for characterizing atomic and nanoscale order simultaneously.

  13. Preparation of Ammonia Adsorbent by Carbonizing and Activating Mixture of Biomass Material and Hygroscopic Salt

    Institute of Scientific and Technical Information of China (English)

    LONG Zhen; BU Xianbiao; LU Zhenneng; LI Huashan; MA Weibin

    2015-01-01

    We put forward a new and ingenious method for the preparation of a new adsorbent by soaking, carbonizing and activating the mixture of hygroscopic salt and biomass material. The new adsorbent has high porosity, uniform distribution and high content of CaCl2, and exhibits high adsorption performance. The ammonia uptake and specific cooling power (SCP) at 5 min adsorption time can reach as high as 0.19 g•g-1 and 793.9 W•kg-1, respectively. The concept of utilizing the biomass materials and hygroscopic salts as raw materials for the preparation of adsorbents is of practical interest with respect to the potential quantity of biomass materials around the world, indicating that there would be a new market for biomass materials.

  14. TEXTURAL AND CHEMICAL CHARACTERISATION OF ACTIVATED CARBONS PREPARED FROM RICE HUSK (ORYZA SATIVA USING A TWO- STAGE ACTIVATION PROCESS

    Directory of Open Access Journals (Sweden)

    JOSEPH G. COLLIN

    2008-12-01

    Full Text Available Activated carbons from agro-industrial wastes; rice husk; were prepared by physical and chemical activation using phosphoric acid as the dehydrating agent. A two-stage activation process method was used; with semi-carbonisation stage at 200oC for 15 minutes as the first stage followed by an activation stage at 500oC for 45 minutes as the second stage. The precursor material with the impregnation agent was exposed straightaway to semi-carbonization and activation temperature unlike the specific temperature progression as reported in the literature. All experiments were conducted in a laboratory scale muffle furnace under static conditions in a self generated atmosphere covering process parameters such as impregnation ratios. We found that by using this method, the AC5 had the highest iodine number and methylene blue adsorption capacity which was 506.6 mg/g and 319.0 mg/g respectively.

  15. 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.

  16. 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.

  17. Preparation of sulfurized powdered activated carbon from waste tires using an innovative compositive impregnation process.

    Science.gov (United States)

    Yuan, Chung-Shin; Lin, Hsun-Yu; Wu, Chun-Hsin; Liu, Ming-Han; Hung, Chung-Hsuang

    2004-07-01

    The objective of this study is to develop an innovative compositive impregnation process for preparing sulfurized powdered activated carbon (PAC) from waste tires. An experimental apparatus, including a pyrolysis and activation system and a sulfur (S) impregnation system, was designed and applied to produce sulfurized PAC with a high specific surface area. Experimental tests involved the pyrolysis, activation, and sulfurization of waste tires. Waste-tire-derived PAC (WPAC) was initially produced in the pyrolysis and activation system. Experimental results indicated that the Brunauer-Emmett-Teller (BET) surface area of WPAC increased, and the average pore radius of WPAC decreased, as water feed rate and activation time increased. In this study, a conventional direct impregnation process was used to prepare the sulfurized PAC by impregnating WPAC with sodium sulfide (Na2S) solution. Furthermore, an innovative compositive impregnation process was developed and then compared with the conventional direct impregnation process. Experimental results showed that the compositive impregnation process produced the sulfurized WPAC with high BET surface area and a high S content. A maximum BET surface area of 886 m2/g and the S content of 2.61% by mass were obtained at 900 degrees C and at the S feed ratio of 2160 mg Na2S/g C. However, the direct impregnation process led to a BET surface area of sulfurized WPAC that decreased significantly as the S content increased.

  18. Preparation and characterization of activated carbons from impregnation pitch by ZnCl 2

    Science.gov (United States)

    Gañán-Gómez, J.; Macías-García, A.; Díaz-Díez, M. A.; González-García, C.; Sabio-Rey, E.

    2006-06-01

    Using an impregnation pitch from bituminous coal tar (OP) supplied by Industrias Químicas del Nalon Company as raw material, two phases (isotropic and anisotropic) have been obtained. The latter was used as precursor for the preparation of activated carbons. First, a chemical activation process was carried out with ZnCl 2 as activating agent. The process was conducted at different concentrations and temperatures and by means of impregnation with solid zinc chloride. Optimal values were obtained for samples prepared by using a ZnCl 2:pitch ratio equal to 3:1 (sample AZn3). Next, this sample was thermally treated at two different temperatures, i.e., 700 and 800 °C. A lose of specific surface area, microporosity and mesoporosity was observed with respect to sample AZn3, such a lose being more remarkable as temperature increased. Moreover, impregnation of the anisotropic phase of the original pitch with an aqueous solution of ZnCl 2 followed by thermal treatment resulted in a poorly developed surface area and porous texture, probably due to the presence of Zn complexes, which interfere with the activation process.

  19. Preparation of biochar by simultaneous carbonization, magnetization and activation for norfloxacin removal in water.

    Science.gov (United States)

    Wang, Bo; Jiang, Yan-Song; Li, Fa-Yun; Yang, Deng-Yue

    2017-06-01

    Activated magnetic biochar (AMB) was prepared with corn stalks, reed stalks, and willow branches by simultaneous carbonization, magnetization, and activation, and used for norfloxacin removal in water. The exploration results showed that the zeta potential was positively charged at pH 2-10. These prepared activated magnetic biochars have a large specific surface area (>700m(2)·g(-1)) and pore volume (>0.3cm(3)·g(-1)). The quasi-second-order kinetic adsorption equation could better describe the adsorption of NOR on AMB. The Langmuir isotherm showed the better fitting results on AMB. The AMB showed the strong adsorption of NOR, and the saturated adsorption capacity of corn activated magnetic biochar was the highest, 7.6249mg·g(-1). The adsorption of NOR on AMB was a spontaneous endothermic process. The effect of pH on the adsorption behaviors of NOR on AMB was not obvious, and AMB had a good adsorption effect on NOR in a wide pH range. Copyright © 2017 Elsevier Ltd. All rights reserved.

  20. Activated carbon fibers/poly(lactic-co-glycolic) acid composite scaffolds: preparation and characterizations.

    Science.gov (United States)

    Shi, Yanni; Han, Hao; Quan, Haiyu; Zang, Yongju; Wang, Ning; Ren, Guizhi; Xing, Melcolm; Wu, Qilin

    2014-10-01

    The present work is a first trial to introduce activated carbon fibers (ACF) with high adsorption capacity into poly(lactic-co-glycolic) acid (PLGA), resulting in a novel kind of scaffolds for tissue engineering applications. ACF, prepared via high-temperature processing of carbon fibers, are considered to possess bioactivity and biocompatibility. The ACF/PLGA composite scaffolds are prepared by solvent casting/particulate leaching method. Increments in both pore quantity and quality over the surface of ACF as well as a robust combination between ACF and PLGA matrix are observed via scanning electron microscopy (SEM). The high adsorption capacity of ACF is confirmed by methylene blue solution absorbency test. The surfaces of ACF are affiliated with many hydrophilic groups and characterized by Fourier transform infrared spectroscopy. Furthermore, the SEM images show that cells possess a favorable spreading morphology on the ACF/PLGA scaffolds. Besides, vivo experiments are also carried out to evaluate the histocompatibility of the composite scaffolds. The results show that ACF have the potential to become one of the most promising materials in biological fields.

  1. Activated carbon fibers/poly(lactic-co-glycolic) acid composite scaffolds: Preparation and characterizations

    Energy Technology Data Exchange (ETDEWEB)

    Shi, Yanni [State Key Laboratory for Modification of Chemical Fibers and Polymer Materials, Donghua University, Shanghai 201620 (China); College of Materials Science and Engineering, Donghua University, Shanghai 201620 (China); Han, Hao [College of Materials Science and Engineering, Donghua University, Shanghai 201620 (China); Bayer Material Science China Co., Ltd, Shanghai 200120 (China); Quan, Haiyu; Zang, Yongju; Wang, Ning; Ren, Guizhi [College of Materials Science and Engineering, Donghua University, Shanghai 201620 (China); Xing, Melcolm [Department of Mechanical Engineering, Faculty of Engineering and Department of Biochemistry and Genetics, Faculty of Medicine P.I., Manitoba Institute of Child Health, University of Manitoba, Winnipeg, Manitoba (Canada); Wu, Qilin, E-mail: wql@dhu.edu.cn [State Key Laboratory for Modification of Chemical Fibers and Polymer Materials, Donghua University, Shanghai 201620 (China); College of Materials Science and Engineering, Donghua University, Shanghai 201620 (China)

    2014-10-01

    The present work is a first trial to introduce activated carbon fibers (ACF) with high adsorption capacity into poly(lactic-co-glycolic) acid (PLGA), resulting in a novel kind of scaffolds for tissue engineering applications. ACF, prepared via high-temperature processing of carbon fibers, are considered to possess bioactivity and biocompatibility. The ACF/PLGA composite scaffolds are prepared by solvent casting/particulate leaching method. Increments in both pore quantity and quality over the surface of ACF as well as a robust combination between ACF and PLGA matrix are observed via scanning electron microscopy (SEM). The high adsorption capacity of ACF is confirmed by methylene blue solution absorbency test. The surfaces of ACF are affiliated with many hydrophilic groups and characterized by Fourier transform infrared spectroscopy. Furthermore, the SEM images show that cells possess a favorable spreading morphology on the ACF/PLGA scaffolds. Besides, vivo experiments are also carried out to evaluate the histocompatibility of the composite scaffolds. The results show that ACF have the potential to become one of the most promising materials in biological fields. - Highlights: • ACF with strong adsorption capacity and porous structure for enhanced surface area • The incorporation of ACF promoting the porosity of composite scaffolds • The composite scaffolds having no side effect on cell adhesion and proliferation • The composite scaffolds presenting good biocompatibility in vivo.

  2. Preparation and Characterization of Impregnated Commercial Rice Husks Activated Carbon with Piperazine for Carbon Dioxide (CO2) Capture

    Science.gov (United States)

    Masoum Raman, S. N.; Ismail, N. A.; Jamari, S. S.

    2017-06-01

    Development of effective materials for carbon dioxide (CO2) capture technology is a fundamental importance to reduce CO2 emissions. This work establishes the addition of amine functional group on the surface of activated carbon to further improve the adsorption capacity of CO2. Rice husks activated carbon were modified using wet impregnation method by introducing piperazine onto the activated carbon surfaces at different concentrations and mixture ratios. These modified activated carbons were characterized by using X-Ray Diffraction (XRD), Brunauer, Emmett and Teller (BET), Fourier Transform Infrared Spectroscopy (FTIR) and Field Emission Scanning Electron Microscopy (FESEM). The results from XRD analysis show the presence of polyethylene butane at diffraction angles of 21.8° and 36.2° for modified activated carbon with increasing intensity corresponding to increase in piperazine concentration. BET results found the surface area and pore volume of non-impregnated activated carbon to be 126.69 m2/g and 0.081 cm3/g respectively, while the modified activated carbons with 4M of piperazine have lower surface area and pore volume which is 6.77 m2/g and 0.015 cm3/g respectively. At 10M concentration, the surface area and pore volume are the lowest which is 4.48 m2/g and 0.0065 cm3/g respectively. These results indicate the piperazine being filled inside the activated carbon pores thus, lowering the surface area and pore volume of the activated carbon. From the FTIR analysis, the presence of peaks at 3312 cm-1 and 1636 cm-1 proved the existence of reaction between carboxyl groups on the activated carbon surfaces with piperazine. The surface morphology of activated carbon can be clearly seen through FESEM analysis. The modified activated carbon contains fewer pores than non-modified activated carbon as the pores have been covered with piperazine.

  3. Mesoporous activated coconut shell-derived hydrochar prepared via hydrothermal carbonization-NaOH activation for methylene blue adsorption.

    Science.gov (United States)

    Islam, Md Azharul; Ahmed, M J; Khanday, W A; Asif, M; Hameed, B H

    2017-12-01

    Mesoporous activated carbon was prepared using a hydrochar derived from coconut shell waste through hydrothermal carbonization and NaOH chemical activation process (COSHTC). Three sets of activated carbons were obtained with different hydrochar:NaOH impregnation ratios (1:1, 1:2, and 1:3). Among these ratios, 1:3 (COSHTC3) exhibited the optimum adsorption for methylene blue (MB). COSHTC3 adsorbed MB with an initial concentration of 25-250 mg/L at pH 3-11 and 30 °C. The adsorption isotherm of MB on COSHTC3 demonstrated that Langmuir isotherm could be better applied at a maximum monolayer adsorption capacity of 200.01 mg/g at 30 °C. The data was well fitted to the pseudo-second-order (PSO) kinetic model. These results show that the COSHTC3 prepared from low-cost agricultural waste (coconut shell) with average pore diameter 28.6 Å and surface area 876.14 m(2)/g acts as a better adsorbent for removal of cationic dyes and could pave the way for more low-cost adsorbents for dye removal. Copyright © 2017 Elsevier Ltd. All rights reserved.

  4. Optically active substituted polyacetylene@carbon nanotube hybrids: Preparation, characterization and infrared emissivity property study

    Energy Technology Data Exchange (ETDEWEB)

    Bu, Xiaohai; Zhou, Yuming, E-mail: ymzhou@seu.edu.cn; Zhang, Tao; Wang, Yongjuan; Zhang, Zewu; He, Man

    2014-08-15

    Optically active substituted polyacetylene@multiwalled carbon nanotubes (SPA@MWCNTs) nanohybrids were fabricated by wrapping helical SPA copolymers onto the surface of modified nanotubes through ester bonding linkage. SPA copolymer based on chiral phenylalanine and serine was pre-polymerized by a rhodium zwitterion catalyst in THF, and evidently proved to possess strong optical activity and adopt a predominately one-handed helical conformation. Various characterizations including Fourier transform infrared spectroscopy (FT-IR), X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD), and transmission electron microscopy (TEM) demonstrated that the SPA had been covalently grafted onto the nanotubes without destroying their original graphite structure. The wrapped SPA was found to exhibit an enhancement in thermal stability and still maintained considerable optical activity after grafting. The infrared emissivity property of the nanohybrids at 8–14 μm was investigated in addition. The results indicated that the SPA@MWCNTs hybrid matrix could possess a much lower infrared emissivity value (ε=0.707) than raw MWCNTs, which might be due to synergistic effect of the unique helical conformation of optically active SPA and strengthened interfacial interaction between the organic polymers and inorganic nanoparticles. - Graphical abstract: Optically active SPA@MWCNTs nanohybrids with low infrared emissivity. - Highlights: • Synthesis of optically active SPA copolymer derived from serine and phenylalanine. • Preparation and characterization of optically active SPA@MWCNTs nanohybrids. • Application study of the SPA@MWCNTs nanohybrids (ε=0.707) in lowering the infrared emissivity.

  5. A Study on Recycling of Spent Mushroom Substrate to Prepare Chars and Activated Carbon

    Directory of Open Access Journals (Sweden)

    Yuhui Ma

    2014-05-01

    Full Text Available Chars were obtained from spent mushroom substrate (SMS via pyrolysis. It was found that as the pyrolysis temperature increased from 400 to 700 °C, the char yield decreased from 45.10 to 33.79 wt.% and the higher heating value increased from 17.32 to 22.72 MJ/kg. The largest BET surface area (13 m2/g was created at 500 °C. Hydrogen atoms were continuously lost during pyrolysis, whereas oxygen atoms were difficult to eliminate. Whewellite, calcite, lime, and quartz were the minerals in the chars, and their forms and crystallinity changed with changing pyrolysis temperature. Activated carbon with a BET surface area of 1023 m2/g and a total pore volume of 0.595 cm3/g was obtained from the char prepared at 500 °C. Its characteristics were studied by N2-adsorption, Fourier transform infrared spectroscopy (FTIR, and X-ray diffraction (XRD. The pyrolysis and KOH-activation processes were investigated by thermogravimetric analysis (TGA. The results showed that the pyrolysis of SMS occurred primarily between 217 and 375 °C and that the energies needed for the pyrolysis reactions were relatively low due to the prior mushroom cultivation. Furthermore, lignin was incompletely decomposed in the char prepared at 500 °C, and KOH suppressed tar evolution and reduced the energy needed to decompose the residual lignin during activation.

  6. 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.

  7. Preparation and Adsorption Performances of Phragmites australis Activated Carbon with High Acidity

    Directory of Open Access Journals (Sweden)

    FU Cheng-kai

    2017-03-01

    Full Text Available For removal of heavy metals from wastewater and recycling the wetland plants, the present study investigated the viability of using silage of Phragmites australis (PA to prepare activated carbons (ACs with high acidity. BET surface area, porous texture and surface functional characteristics of ACs were analyzed by N2 adsorption/desorption, elemental analysis and Boehm titration method. ACs presented well-developed micro-porosity and favorable surface acidity. The sorption equilibrium data for Ni (Ⅱ and Cd (Ⅱ sorption onto ACs were analyzed by the Langmuir and Freundlich models. The Langmuir model was fitted well to the adsorption behavior. The properties of high surface acidity promoted the adsorption of heavy metals by the silage-treated ACs and the chemical sorption played the key role in the sorption process.

  8. Efficacy evaluation of activated carbon prepared from date stones in cyanide adsorption from synthetic wastewater

    Directory of Open Access Journals (Sweden)

    Bahman Ramavandi

    2013-02-01

    Results: The maximum adsorption capacity of 50.21 mg/g corresponded with Langmuir model. Kinetic evaluation indicated that the adsorption of cyanide ions by the adsorbent clearly followed the pseudo-second order rate reaction. The absorption was pH dependent and the maximum adsorption was done by solutions having pH 9. At an optimum pH 9, over 97% removal of 100 mg/L cyanide was attained for an adsorbent dose of 1.25 g/L during a 40 min contact time. Conclusion: Activated carbon prepared from date stones is an efficient and low-cost adsorbent for removing of different concentrations of cyanide from water and wastewater.

  9. Chemical and structural evaluation of activated carbon prepared from jute sticks for Brilliant Green dye removal from aqueous solution.

    Science.gov (United States)

    Asadullah, Mohammad; Asaduzzaman, Mohammad; Kabir, Mohammad Shajahan; Mostofa, Mohammad Golam; Miyazawa, Tomohisa

    2010-02-15

    Activated carbons have been prepared from jute sticks by chemical activation using ZnCl(2) and physical activation using steam for the removal of Brilliant Green dye from aqueous solution. The activated carbons and charcoal prepared from jute sticks were characterized by evaluating the surface chemistry, structural features and surface morphology. The maximum BET surface area was obtained to be 2304 m(2)/g for chemical activated carbon (ACC) while it is 730 and 80 m(2)/g for steam activated carbon (ACS) and charcoal, respectively. The FT-IR spectra exhibited that the pyrolysis and steam activation of jute sticks resulted in the release of aliphatic and O-containing functional groups by thermal effect. However, the release of functional groups is the effect of chemical reaction in the ZnCl(2) activation process. A honeycomb-type carbon structure in ACC was formed as observed on SEM images. Although charcoal and ACC were prepared at 500 degrees C the ACC exhibited much lower Raman sensitivity due to the formation of condensed aromatic ring systems. Due to high surface area and high porous structure with abundance of functional groups, the ACC adsorbed dye molecules with much higher efficiency than those of ACS and charcoal.

  10. Adsorption of Lead (II) from aqueous solutions onto activated carbon prepared from Algerian dates stones of Phoenix dactylifera.L (Ghars variety) by H3PO4 activation

    OpenAIRE

    N. Chaouch; M. R. Ouahrani; S. E. Laouini

    2014-01-01

    Currently water pollution constitutes a great challenge, and activated carbon is a common adsorbent used to remove lead contaminants. Unfortunately, it is a non selective process. The main object of this study was the use of an activated carbon prepared from nuts of dates Algerian origin to remove this metal. The adsorption measurement of lead on activated carbon showed a real potential for removing this metal contaminants waste. The result showed also that the determination of lead remained ...

  11. Preparation of Nano-Porous Activated Carbon Aerogel Using a Single-Step Activation Method for Use as High-Power EDLC Electrode in Organic Electrolyte.

    Science.gov (United States)

    Kwon, Soon Hyung; Kim, Bum-Soo; Kim, Sang-Gil; Lee, Byung-Jun; Kim, Myung-Soo; Jung, Ji Chul

    2016-05-01

    Carbon aerogel was chemically activated with KOH using two different activation methods (conventional activation method and single-step activation method) to yield the nano-porous activated carbon aerogel. Both nano-porous activated carbon aerogels exhibited a better capacitive behavior than carbon aerogel in organic electrolyte. However, a drastic decrease in the specific capacitance with increasing current density was observed in the ACA_C (activated carbon aerogel prepared by a conventional activation method), which is a general tendency of carbon electrode for EDLC in organic electrolyte. Interestingly, the specific capacitance of ACA_S electrode (activated carbon aerogel prepared by a single-step activation method) decreased slowly with increasing current density and its CV curve maintained a rectangular shape well even at a high scan rate of 500 mV/s. The enhanced electrochemical performance of ACA_S at a high current density was attributed to its low ionic resistance caused by the well-developed pore structure with appropriate pore size for easy moving of organic electrolyte ion. Therefore, it can be concluded that single-step activation method could be one of the efficient methods for preparation of nano-porous activated carbon aerogel electrode for high-power EDLC in organic electrolyte.

  12. Microwave-assisted preparation and adsorption performance of activated carbon from biodiesel industry solid reside: influence of operational parameters.

    Science.gov (United States)

    Foo, K Y; Hameed, B H

    2012-01-01

    Preparation of activated carbon has been attempted using KOH as activating agent by microwave heating from biodiesel industry solid residue, oil palm empty fruit bunch (EFBAC). The significance of chemical impregnation ratio (IR), microwave power and activation time on the properties of activated carbon were investigated. The optimum condition has been identified at the IR of 1.0, microwave power of 600 W and activation time of 7 min. EFBAC was characterized by scanning electron microscopy, Fourier transform infrared spectroscopy and nitrogen adsorption isotherm. The surface chemistry was examined by zeta potential measurement, determination of surface acidity/basicity, while the adsorptive property was quantified using methylene blue as dye model compound. The optimum conditions resulted in activated carbon with a monolayer adsorption capacity of 395.30 mg/g and carbon yield of 73.78%, while the BET surface area and total pore volume were corresponding to 1372 m2/g and 0.76 cm3/g, respectively.

  13. Preparation of iron oxide-impregnated spherical granular activated carbon-carbon composite and its photocatalytic removal of methylene blue in the presence of oxalic acid.

    Science.gov (United States)

    Kadirova, Zukhra C; Hojamberdiev, Mirabbos; Katsumata, Ken-Ichi; Isobe, Toshihiro; Matsushita, Nobuhiro; Nakajima, Akira; Sharipov, Khasan; Okada, Kiyoshi

    2014-01-01

    The spherical granular activated carbon-carbon composites (GAC-Fe) with different iron oxide contents (Fe mass% = 0.6-10) were prepared by a pore volume impregnation method. The X-ray diffraction (XRD), scanning electron microscopy (SEM), and N2-adsorption results confirm the presence of amorphous iron oxide, pyrolytic carbon, and graphitized globular carbon nanoparticles covered with amorphous carbon in the CAG-Fe. The rate of photodegradation of methylene blue (MB) in aqueous solution under UV light in the presence of oxalic acid correlates with porosity of the prepared materials. The total MB removal includes the combination of adsorption and photodegradation without the addition of H2O2. The results of total organic carbon (TOC) analysis reveal that the decolorization of MB in aqueous solution containing oxalic acid corresponds to the decomposition of organic compounds to CO2 and H2O.

  14. Removal of phenol by powdered activated carbon prepared from coal gasification tar residue.

    Science.gov (United States)

    Wang, Xiong-Lei; Shen, Jun; Niu, Yan-Xia; Wang, Yu-Gao; Liu, Gang; Sheng, Qing-Tao

    2017-04-10

    Coal gasification tar residue (CGTR) is a kind of environmentally hazardous byproduct generated in fixed-bed coal gasification process. The CGTR extracted by ethyl acetate was used to prepare powdered activated carbon (PAC), which is applied later for adsorption of phenol. The results showed that the PAC prepared under optimum conditions had enormous mesoporous structure, and the iodine number reached 2030.11 mg/g, with a specific surface area of 1981 m(2)/g and a total pore volume of 0.92 ml/g. Especially, without loading other substances, the PAC, having a strong magnetism, can be easily separated after it adsorbs phenol. The adsorption of phenol by PAC was studied as functions of contact time, temperature, PAC dosage, solution concentration and pH. The results showed a fast adsorption speed and a high adsorption capacity of PAC. The adsorption process was exothermic and conformed to the Freundlich models. The adsorption kinetics fitted better to the pseudo-second-order model. These results show that CGTR can be used as a potential adsorbent of phenols in wastewater.

  15. Activated carbon prepared from coffee pulp: potential adsorbent of organic contaminants in aqueous solution.

    Science.gov (United States)

    Gonçalves, Maraisa; Guerreiro, Mário César; Ramos, Paulize Honorato; de Oliveira, Luiz Carlos Alves; Sapag, Karim

    2013-01-01

    The processing of coffee beans generates large amounts of solid and liquid residues. The solid residues (pulp, husk and parchment) represent a serious environmental problem and do not have an adequate disposal mechanism. In this work, activated carbons (ACs) for adsorption of organic compounds were prepared from coffee pulp by controlled temperature at different pulp/Na2HPO4 ratios (4:1, 2:1, 5:4 and 1:1). The N2 adsorption/desorption isotherms showed ACs with high quantities of mesopores and micropores and specific surface areas of 140, 150, 450 and 440 m(2)g(-1) for AC 4:1, AC 2:1, AC 5:4 and AC 1:1, respectively. The prepared material AC 5:4 showed a higher removal capacity of the organic contaminants methylene blue (MB), direct red (DR) and phenol than did a Merck AC. The maximum capacities for this AC are approximately 150, 120 and 120 mg g(-1) for MB, DR and phenol, respectively. Thus, a good adsorbent was obtained from coffee pulp, an abundant Brazilian residue.

  16. Role of Ni(NO3)2 in the preparation of a magnetic coal-based activated carbon

    Institute of Scientific and Technical Information of China (English)

    Zhang Jun; Xie Qiang; Liu Juan; Yang Mingshun; Yao Xing

    2011-01-01

    The role of Ni(NO3)2 in the preparation of a magnetic activated carbon is reported in this paper.Magnetic coal-based activated carbons (MCAC) were prepared from Taixi anthracite with low ash content in the presence of Ni(NO3)2.The MCAC materials were characterized by a vibrating sample magnetometer (VSM),X-ray diffraction (XRD),a scanning electric microscope (SEM),and by N2 adsorption.The cylindrical precursors and derived char were also subjected to thermogravimetric analysis to compare their behavior of weight losses during carbonization.The results show that MCAC has a larger surface area (1074 m2/g) and a higher pore volume (0.5792 cm3/g) with enhanced mesopore ratio (by about 10%).It also has a high saturation magnetization (1.6749 emu/g) and low coercivity (43.26 Oe),which allows the material to be magnetically separated.The MCAC is easily magnetized because the nickel salt is converted into Ni during carbonization and activation.Metallic Ni has a strong magnetism on account of electrostatic interaction.Added Ni(NO3)2 catalyzes the carbonization and activation process by accelerating burn off of the carbon,which contributes to the development of mesopores and macropores in the activated carbon.

  17. Preparation of activated carbon from Tunisian olive-waste cakes and its application for adsorption of heavy metal ions

    Energy Technology Data Exchange (ETDEWEB)

    Baccar, R. [Laboratoire Eau Energie Environnement, Ecole Nationale d' Ingenieurs de Sfax, BP W 3038 Sfax (Tunisia)], E-mail: rym.baccar@tunet.tn; Bouzid, J. [Laboratoire Eau Energie Environnement, Ecole Nationale d' Ingenieurs de Sfax, BP W 3038 Sfax (Tunisia)], E-mail: jalel.bouzid@tunet.tn; Feki, M. [Unite de Recherche de Chimie Industrielle et Materiaux, Ecole Nationale d' Ingenieurs de Sfax, BP W 3038 Sfax (Tunisia)], E-mail: mongi.feki@yahoo.fr; Montiel, A. [Laboratoire Eau Energie Environnement, Ecole Nationale d' Ingenieurs de Sfax, BP W 3038 Sfax (Tunisia)], E-mail: montiel.antoine@free.fr

    2009-03-15

    The present work explored the use of Tunisian olive-waste cakes, a by-product of the manufacture process of olive oil in mills, as a potential feedstock for the preparation of activated carbon. Chemical activation of this precursor, using phosphoric acid as dehydrating agent, was adopted. To optimize the preparation method, the effect of the main process parameters (such as acid concentration, impregnation ratio, temperature of pyrolysis step) on the performances of the obtained activated carbons (expressed in terms of iodine and methylene blue numbers and specific surface area) was studied. The optimal activated carbon was fully characterized considering its adsorption properties as well as its chemical structure and morphology. To enhance the adsorption capacity of this carbon for heavy metals, a modification of the chemical characteristics of the sorbent surface was performed, using KMnO{sub 4} as oxidant. The efficiency of this treatment was evaluated considering the adsorption of Cu{sup 2+} ions as a model for metallic species. Column adsorption tests showed the high capacity of the activated carbon to reduce KMnO{sub 4} into insoluble manganese (IV) oxide (MnO{sub 2}) which impregnated the sorbent surface. The results indicated also that copper uptake capacity was enhanced by a factor of up to 3 for the permanganate-treated activated carbon.

  18. 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...

  19. Preparation of sludge-based activated carbon and its application in dye wastewater treatment.

    Science.gov (United States)

    Wang, Xiaoning; Zhu, Nanwen; Yin, Bingkui

    2008-05-01

    A novel activation process was adopted to produce highly porous activated carbon from cyclic activated sludge in secondary precipitator in municipal wastewater treatment plant for dye removal from colored wastewater. The physical properties of activated carbon produced with the activation of 3M KOH solution in the atmosphere of steam were investigated. Adsorption removal of a dye, Acid Brilliant Scarlet GR, from aqueous solution onto the sludge-based activated carbon was studied under varying conditions of adsorption time, initial concentration, carbon dosage and pH. Adsorption equilibrium was obtained in 15 min for the dye initial concentration of 300 mg/L. Initial pH of solution had an insignificant impact on the dye removal. Results indicated that 99.7% coloration and 99.6% total organic carbon (TOC) were removed after 15 min adsorption in the synthetic solution of Acid Brilliant Scarlet GR with initial concentration of 300 mg/L of the dye and 20 g/L activated carbon. The Langmuir and Freundlich equilibrium isotherm models fitted the adsorption data well with R(2)=0.996 and 0.912, respectively. Accordingly, it is concluded that the procedure of developing activated carbon used in this study could be effective and practical for utilizing in dye wastewater treatment.

  20. Removal of phenol by activated carbons prepared from palm oil mill effluent sludge

    Institute of Scientific and Technical Information of China (English)

    Md. Zahangir ALAM; Suleyman A. MUYIBI; Mariatul F.MANSOR; Radziah WAHID

    2006-01-01

    The study was attempted to produce activated carbons from palm oil mill effluent (POME) sludge. The adsorption capacity of the activated carbons produced was evaluated in aqueous solution of phenol. Two types of activation were followed, namely,thermal activation at 300, 500 and 800℃, and physical activation at 150℃ (boiling treatment). A control (raw POME sludge) was used to compare the adsorption capacity of the activated carbons produced. The results indicated that the activation temperature of 800℃showed maximum absorption capacity by the activated carbon (POME 800) in aqueous solution of phenol. Batch adsorption studies showed an equilibrium time of 6 h for the activated carbon of POME 800. It was observed that the adsorption capacity was higher at lower values of pH (2-3) and higher value of initial concentration of phenol (200-300 mg/L). The equilibrium data were fitted by the Langmuir and Freundlich adsorption isotherms. The adsorption of phenol onto the activated carbon POME 800 was studied in terms of pseudo- first and second order kinetics to predict the rate constant and equilibrium capacity with the effect of initial phenol concentrations. The rate of adsorption was found to be better correlation for the pseudo-second order kinetics compared to the first order kinetics.

  1. Preparation,Electrochemical Behavior and Electrocatalytic Activity of a Copper Hexacyanoferrate Modified Ceramic Carbon Electrode

    Institute of Scientific and Technical Information of China (English)

    YU,Hao; ZHENG,Jian-Bin

    2007-01-01

    A copper hexacyanoferrate modified ceramic carbon electrode(CuHCF/CCE)had been prepared by two-step sol-gel technique and characterized using electrochemical methods.The resulting modified electrode showed a pair of well-defined surface waves in the potential range of 0.40 to 1.0 V with the formal potential of 0.682 V (vs.SCE)in 0.050 mol·dm-3 HOAc-NaOAc buffer containing 0.30 mol·dm-3 KCI.The charge transfer coefficient (α) and charge transfer rate constant(Ks)for the modified electrode were calculated.The electrocatalytic activity of this modified electrode to hydrazine was also investigated,and chronoamperometry was exploited to conveniently determine the diffusion coefficient(D)of hydrazine in solution and the catalytic rate constant(Kcat).Finally,hydrazine was determined with amperometry using the resulting modified electrode.The calibration plot for hydrazine determination was linear in 3.0×10-6-7.5×10-4 mol·dm-3 with the detection limit of 8.0×10-7 mol·dm-3.This modified electrode had some advantages over the modified film electrodes constructed by the conventional methods,such as renewable surface,good long-term stability,excellent catalytic activity and short response time to hydrazine.

  2. Preparation of diethylene glycol monomethyl ether monolaurate catalyzed by active carbon supported KF/CaO.

    Science.gov (United States)

    Lou, Shengfeng; Jia, Lihua; Guo, Xiangfeng; Wu, Ping; Gao, Lianbing; Wang, Jianjun

    2015-01-01

    Diethylene glycol monomethyl ether monolaurate (DGMEML) was synthesized via the reaction of diethylene glycol monomethyl ether (DGME) with methyl laurate (ML) by a new solid base catalyst of KF/CaO/AC, which was prepared by impregnation method using active carbon as carrier. The catalysts were characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), scanning electron microscopy (SEM), nitrogen physisorption-desorption and Hammett indicator methods; the effect of the mole ratio of KF to CaO, DGME to ML molar ratio, amount of catalyst, reaction time and temperature on the yield of DGMEML were studied; and the relationship between the structure of the catalyst and the yield of DGMEML was investigated. The formed KCaF3 and K2O were acting as the main active components in the catalytic transesterification; the highest yield of 96.3 % was obtained as KF-to-CaO molar ratio of 2.0, DGME to ML molar ratio of 4.0, catalyst amount of 5 wt%, and reaction time of 30 min at 75 °C; and the catalyst displayed good stability in the transesterification.

  3. Preparation of a specific bamboo based activated carbon and its application for ciprofloxacin removal.

    Science.gov (United States)

    Wang, Y X; Ngo, H H; Guo, W S

    2015-11-15

    The studied bamboo based activated carbon (BbAC) with high specific surface area (SSA) and high micro pore volume was prepared from bamboo scraps by the combined activation of H3PO4 and K2CO3. The BbAC was characterized based on the N2 adsorption isotherm at 77K. The results showed that the SSA and pore volume of BbAC increased with increasing impregnation ratio and reached maxima at the impregnation ratio of 3:1 at 750°C. Under these optimal conditions, the BbAC obtained could have a maximum SSA of 2237 m(2)/g and a maximum total pore volume of 1.23 cm(3)/g with the micro pore ratio of more than 90%. The adsorption performance of ciprofloxacin (CIP) on the BbAC was determined at 298 K. The Langmuir and Freundlich models were employed to describe the adsorption equilibrium and the kinetic data were fitted by pseudo first-order and pseudo second-order kinetic models. The results showed that the Langmuir model and the pseudo second-order kinetic model presented better fittings for the adsorption equilibrium and kinetics data, respectively. The maximum adsorption amount of CIP (613 mg/g) on the BbAC was much higher than the report in the literature. Conclusively, the BbAC could be a promising adsorption material for CIP removal from water. Copyright © 2015 Elsevier B.V. All rights reserved.

  4. 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.

  5. Preparing electrochemical active hierarchically porous carbons for detecting nitrite in drinkable water

    KAUST Repository

    Ding, Baojun

    2016-01-13

    A class of hierarchically porous carbons were prepared by a facile dual-templating approach. The obtained samples were characterized by scanning electron microscopy, X-ray diffraction, Raman spectroscopy, Brunaner-Emmett-Teller measurement and electrochemical work station, respectively. The porous carbons could possess large specific surface area, interconnected pore structures, high conductivity and graphitizing degree. The resulting materials were used to prepare integrated modified electrodes. Based on the experimental results, the as-prepared hierarchically porous graphite (HPG) modified electrode showed the best electroactive performances toward the detection of nitrite with a detection limit of 8.1 × 10-3 mM. This HPG electrode was also repeatable and stable for 6 weeks. Moreover, this electrode was used for the determination of nitrite in drinkable water, and had acceptable recoveries. © The Royal Society of Chemistry 2016.

  6. Simple preparation of tungsten supported carbon nanoreactors for specific applications: Adsorption, catalysis and electrochemical activity

    Energy Technology Data Exchange (ETDEWEB)

    Mayani, Vishal J.; Mayani, Suranjana V.; Kim, Sang Wook, E-mail: swkim@dongguk.ac.kr

    2015-08-01

    Graphical abstract: - Highlights: • Tungsten carbon composites have shown great recognition in catalysis and electrochemistry. • W-carbon composites are prepared by template replication and W-doping on carbon cage. • Nanocomposites offer enormous assurance as adsorbent, electrode and heterogeneous catalyst. - Abstract: Porous carbon supported tungsten carbide nanoreactors, two sizes (∼25 and 170 nm), were designed using economical petroleum pitch residue followed by tungsten (W) doping. X-ray diffractions showed both carbon tungsten composites (CTC-25 and CTC-170) contained tungsten subcarbide (W{sub 2}C) and monocarbide (WC) as the major and minor crystalline phases, respectively. The present study provides a multiple perspective of carbon tungsten composites (CTCs) for methanol oxidation (as an electrode), adsorption (as an adsorbent) and degradation (as a solid catalyst) of methylene blue (MB). The operational electrodes were designed from both CTCs and used as a catalyst in an electrocatalysis process. The electrocatalysts exhibited high and stable catalytic performance (CTCE-25 > CTCE-170) in methanol electro-oxidation. The newly synthesized W-doped carbon nanoreactors were used successfully as an adsorbent for MB and a heterogeneous catalyst for MB oxidation. Ordered CTC-25 and CTC-170 exhibited dynamic MB adsorption within 15 min and complete oxidation of MB in 25–40 min. A synergetic effect between tungsten carbide and the carbon cage framework was noted.

  7. Preparation and evaluation of coal-derived activated carbons for removal of mercury vapor from simulated coal combustion flue fases

    Science.gov (United States)

    Hsi, H.-C.; Chen, S.; Rostam-Abadi, M.; Rood, M.J.; Richardson, C.F.; Carey, T.R.; Chang, R.

    1998-01-01

    Coal-derived activated carbons (CDACs) were tested for their suitability in removing trace amounts of vapor-phase mercury from simulated flue gases generated by coal combustion. CDACs were prepared in bench-scale and pilot-scale fluidized-bed reactors with a three-step process, including coal preoxidation, carbonization, and then steam activation. CDACs from high-organicsulfur Illinois coals had a greater equilibrium Hg0 adsorption capacity than activated carbons prepared from a low-organic-sulfur Illinois coal. When a low-organic-sulfur CDAC was impregnated with elemental sulfur at 600 ??C, its equilibrium Hg0 adsorption capacity was comparable to the adsorption capacity of the activated carbon prepared from the high-organicsulfur coal. X-ray diffraction and sulfur K-edge X-ray absorption near-edge structure examinations showed that the sulfur in the CDACs was mainly in organic forms. These results suggested that a portion of the inherent organic sulfur in the starting coal, which remained in the CDACs, played an important role in adsorption of Hg0. Besides organic sulfur, the BET surface area and micropore area of the CDACs also influenced Hg0 adsorption capacity. The HgCl2 adsorption capacity was not as dependent on the surface area and concentration of sulfur in the CDACs as was adsorption of Hg0. The properties and mercury adsorption capacities of the CDACs were compared with those obtained for commercial Darco FGD carbon.

  8. Preparation of Activated Carbon from Palm Shells Using KOH and ZnCl2 as the Activating Agent

    Science.gov (United States)

    Yuliusman; Nasruddin; Afdhol, M. K.; Amiliana, R. A.; Hanafi, A.

    2017-07-01

    Palm shell is a potential source of raw materials for the produce of activated carbon as biosorbent for quite large numbers. The purpose of this study is to produce activated carbon qualified Indonesian Industrial Standard (SNI), which will be used as biosorbent to purify the impurities in the off gas petroleum refinery products. Stages of manufacture of activated carbon include carbonization, activation of chemistry and physics. Carbonization of activated carbon is done at a temperature of 400°C followed by chemical activation with active agent KOH and ZnCl2. Then the physical activation is done by flowing N2 gas for 1 hour at 850°C and followed by gas flow through the CO2 for 1 hour at 850°C. Research results indicate that activation of the active agent KOH produce activated carbon is better than using the active agent ZnCl2. The use of KOH as an active agent to produce activated carbon with a water content of 13.6%, ash content of 9.4%, iodine number of 884 mg/g and a surface area of 1115 m2/g. While the use of ZnCl2 as the active agent to produce activated carbon with a water content of 14.5%, total ash content of 9.0%, iodine number 648 mg/g and a surface area of 743 m2/g.

  9. Preparation of activated carbon from dried pods of Prosopis cineraria with zinc chloride activation for the removal of phenol.

    Science.gov (United States)

    Nath, Kaushik; Panchani, Suresh; Bhakhar, M S; Chatrola, Sandip

    2013-06-01

    Utilization of agrowaste materials for the production of activated carbon, as an excellent adsorbent with large surface area, is well established industrially, for dephenolation of wastewater. In the present work, dried pods of Prosopis cineraria-a novel and low-cost agrowaste material-were used to prepare activated carbons by zinc chloride activation. Batch adsorption experiments were carried out to study the effects of various physicochemical parameters such as initial phenol concentration, adsorbent dose, initial solution pH, and temperature. Pseudo-first-order second-order and diffusion kinetic models were used to identify the possible mechanisms of such adsorption process. The Langmuir and Freundlich equations were used to analyze the adsorption equilibrium. Maximum removal efficiency of 86 % was obtained with 25 mg L(-1) of initial phenol concentration. The favorable pH for maximum phenol adsorption was 4.0. Freundlich equation represented the adsorption equilibrium data more ideally than the Langmuir. The maximum adsorption capacity obtained was 78.32 mg g(-1) at a temperature of 30 °C and 25 mg L(-1) initial phenol concentration. The adsorption was spontaneous and endothermic. The pseudo-second-order model, an indication of chemisorption mechanism, fitted the experimental data better than the pseudo-first-order Lagergren model. Regeneration of spent activated carbon was carried out using Pseudomonas putida MTCC 2252 as the phenol-degrading microorganism. Maximum regeneration up to 57.5 % was recorded, when loaded phenol concentration was 25 mg L(-1). The data obtained in this study would be useful in designing and fabricating an efficient treatment plant for phenol-rich effluents.

  10. The Adsorption Efficiency of Chemically Prepared Activated Carbon from Cola Nut Shells by on Methylene Blue

    Directory of Open Access Journals (Sweden)

    Julius Ndi Nsami

    2013-01-01

    Full Text Available The adsorption of methylene blue from aqueous solution onto activated carbon prepared from cola nut shell has been investigated under batch mode. The influence of major parameters governing the efficiency of the process such as, solution pH, sorbent dose, initial concentration, and contact time on the removal process was investigated. The time-dependent experimental studies showed that the adsorption quantity of methylene blue increases with initial concentration and decreasing adsorbent dosage. The equilibrium time of 180 min was observed and maximum adsorption was favoured at pH 3.5. The dye removal using 0.1 g of adsorbent was more than 90%. This dosage (0.1 g was considered as the optimum dosage to remove methylene blue from aqueous solutions. The equilibrium adsorption data were analyzed by the Freundlich, Langmuir adsorption isotherm models. The kinetics of methylene blue solution was discussed by pseudo-first-order, pseudo-second-order, and Elovich models. The adsorption process follows the Elovich rate kinetic model, having a correlation coefficient in the range between 0.9811 and 1.

  11. Preparation of mesoporous carbon from fructose using zinc-based activators

    Directory of Open Access Journals (Sweden)

    Tutik Setianingsih

    2015-07-01

    Full Text Available Mesoporous carbons were synthesized from fructose using activators of zinc silicate (ZS, zinc borate (ZB, and zinc borosilicate (ZBS. The synthesis involves 3 steps, including caramelization of sugar, carbonization of caramel, and washing of carbon to separate the activator from the carbon. The solid products were characterized by N2 gas adsorption-desorption, X-ray diffraction, FTIR spectrophotometry, and Transmission Electron Microscopy. The pore characterizations of the carbons indicate that in ZBS system, ZB may have the role as mesopore size controller, whereas silica component may improve porosity created by ZB without changing the size. This role of ZB may be connected to it’s performance as catalyst of caramelization and it’s crystalinity, as supported by measurement of caramel intermediete and characterization of the activators with X-ray diffraction. The infrared spectra confirms that the carbons’s surfaces have C=O, C-O, and O-H functional groups. The XRD patterns of the carbons show that all activators create the turbotratic carbons.

  12. Characterization of mesoporous carbon prepared from date stems by H{sub 3}PO{sub 4} chemical activation

    Energy Technology Data Exchange (ETDEWEB)

    Hadoun, H., E-mail: hhadoun@hotmail.com [Nuclear Research Center, 2 Bd Frantz Fanon, Algiers (Algeria); Laboratory of Reaction Genius, Mechanical and Processes Genius Faculty, University of Sciences and Technology Houari – Boumediene, BP n°32, El alia, bab ezzouar, 16111 Algiers (Algeria); Sadaoui, Z. [Laboratory of Reaction Genius, Mechanical and Processes Genius Faculty, University of Sciences and Technology Houari – Boumediene, BP n°32, El alia, bab ezzouar, 16111 Algiers (Algeria); Souami, N.; Sahel, D.; Toumert, I. [Nuclear Research Center, 2 Bd Frantz Fanon, Algiers (Algeria)

    2013-09-01

    The present work was focused on the determination of texture, morphology, crystanillity and oxygenated surface groups characteristics of an activated carbon prepared from date stems. Chemical activation of this precursor at different temperatures (450, 550 and 650 °C) was adopted using phosphoric acid as dehydrating agent at (2/1) impregnation ratio. Fourier transform infrared spectroscopy study was carried out to identify surface groups in date stems activated carbons. The microscopic structure was examined by nitrogen adsorption at 77 K. The interlayer spacing (d{sub 200} and d{sub 100}), stack height (L{sub c}), stack width (L{sub a}) and effective dimension L of the turbostratic crystallites (microcrystallite) in the date stems activated carbons were estimated from X-ray diffraction data (XRD). Results yielded a surface area, S{sub BET}, and total pore volume of 682, 1455, 1319 m{sup 2}/g and 0,343, 1,045 and 0.735 cm{sup 3}/g, for the carbon prepared at 450, 550 and 650 °C, respectively. Scanning electron microscopy exhibits a highly developed porosity which is in good agreement with the porous texture derived from gas adsorption data and these results confirm that the activated carbon is dominated by network of slit-shaped mesopores morphology and in some cases by varied micropores morphologies.

  13. 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.

  14. Preparation and characterization of activated carbon from castor de-oiled cake

    Directory of Open Access Journals (Sweden)

    Viviana M. Ospina-Guarín

    2014-01-01

    Full Text Available Biomass residues have been used to produce activated carbons. On this process, the activation method and the raw composition determine the properties as porosity and surface area of the charcoal. After the extraction of castor oil, there is a solid byproduct (cake of low added value, which was used in the production of activated carbon to add value to this waste. For this purpose two traditional methods were used, first, physical activation using as activating agents steam, CO2 and mixture of both, and additionally chemical activation using K2CO3 as the activating agent. Some activated carbons were characterized using N2 adsorption isotherms, BET surface areas varied between 255.98 (m2/g and 1218.43 (m2/g. By SEM and EDS analysis was possible to observe that materials obtained by the two types of activation are principally amorphous and morphological characteristics of the carbon obtained by physical activation are very different from those obtained by chemical activation. Finally, through impregnation of inorganic phases of Ni and Mo was revealed that the high dispersion characteristics, these carbonaceous materials will have potential to be used as catalyst support.

  15. Preparation and CO conversion activity of ceria nanotubes by carbon nanotubes templating method

    Institute of Scientific and Technical Information of China (English)

    FANG Jianhui; CAO Zhiyuan; ZHANG Dengsong; SHEN Xia; DING Weizhong; SHI Liyi

    2008-01-01

    Ceria nanotubes with high CO conversion activity by means of carbon nanotubes as removable templates in the simple liquid phase process were fabricated under moderate conditions. The pristine CNTs were first pretreated by refluxing in a 30% nitric acid solution at 140 °C for 24 h, then dispersed in an ethanolic Ce(NO3)3·6H2O solution with ultrasonic radiation at room temperature for 1 h. Under vigorous stirring, NaOH solution was added drop by drop into the above ethanolic solution until the pH value was 10. The product was collected and repeatedly washed with ethanol and on drying at 60 °C, the CeO2/CNT composites were obtained. Then, the as-prepared composites were heated at 450 °C in an air atmosphere for 30 min to remove CNTs. The ceria nanotubes were characterized by X-Ray Diffraction (XRD), Transmission Electron Microscopy (TEM), and X-Ray Photoelectron Spectrum (XPS). The results showed that the ceria nanotubes were polycrystalline face-centered cubic phase and were composed of lots of dense ceria nanoparticles. The diameter of ceria nanotubes was about 40-50 nm. Catalytic activity of the product for CO oxidation was carried out at the region of 30-300 °C in a U-shaped quartz reactor with feeding about 0.15 g of the catalyst, which was loaded on Al2O3 carrier. The inlet gas composition was 1.0% CO and 28% O2 with N2 as balance, and the rate of flow was kept at 40 ml/min. The catalytic products were analyzed by gas chromatography. The as-prepared CeO2 nanotubes showed higher CO oxidation activity, which indicated that the morphology of ceria products affected the catalytic performance. The ceria nanotubes supported on Al2O3 demonstrated that conversion temperature for CO oxidation to CO2 was lower than that for bulk catalysts.

  16. A comparative investigation on adsorption performances of mesoporous activated carbon prepared from waste rubber tire and activated carbon for a hazardous azo dye--Acid Blue 113.

    Science.gov (United States)

    Gupta, V K; Gupta, Bina; Rastogi, Arshi; Agarwal, Shilpi; Nayak, Arunima

    2011-02-15

    A mesoporous carbon developed from waste tire rubber, characterized by chemical analysis, FTIR, and SEM studies, was used as an adsorbent for the removal and recovery of a hazardous azo dye, Acid Blue 113. Surface area, porosity, and density were determined. The adsorption of the dye over the prepared adsorbent and a commercial activated carbon was achieved under different pH, adsorbate concentration, sieve size, adsorbent dosage, contact time and temperature conditions. Langmuir and Freundlich adsorption isotherm models were applied and thermodynamic parameters were calculated. Kinetic studies indicated that the adsorption process follow first order kinetics and particle diffusion mechanisms are operative. By percolating the dye solution through fixed-bed columns the bulk removal of the Acid Blue 113 was carried out and necessary parameters were determined to find out the percentage saturation of both the columns. Recovery of the dye was made by eluting 0.1 M NaOH through the column.

  17. Characterization and ciprofloxacin adsorption properties of activated carbons prepared from biomass wastes by H3PO4 activation.

    Science.gov (United States)

    Sun, Yuanyuan; Li, Hong; Li, Guangci; Gao, Baoyu; Yue, Qinyan; Li, Xuebing

    2016-10-01

    As biomass wastes, Arundo donax Linn and pomelo peel were used as precursors for activated carbons (ALAC and PPAC) preparation by phosphoric acid activation. The pore structure and surface acidic functional groups of both carbons were characterized by nitrogen adsorption/desorption experiment, NH3-temperature-programmed desorption (NH3-TPD) and Fourier transform infrared spectroscopy (FTIR). A batch of experiments was carried out to investigate the adsorption performances of ciprofloxacin under different conditions. Results showed that PPAC exhibited larger surface area (1252m(2)/g) and larger portion of mesoporous, while ALAC was typical of microporous materials. Results from NH3-TPD suggested that ALAC was characteristic of more acidic functional group than PPAC. The maximum monolayer adsorption capability was 244mg/g for ALAC and 400mg/L for PPAC. Kinetics studies showed intra-particle diffusion was not the unique rate-controlling step. Boundary layer resistance existed between adsorbent and adsorbate. Copyright © 2016 Elsevier Ltd. All rights reserved.

  18. Synthesis of nitrogen doped microporous carbons prepared by activation-free method and their high electrochemical performance

    Energy Technology Data Exchange (ETDEWEB)

    Kim, Ki-Seok [Department of Chemistry, Inha University, Incheon 402-751 (Korea, Republic of); Park, Soo-Jin, E-mail: sjpark@inha.ac.kr [Department of Chemistry, Inha University, Incheon 402-751 (Korea, Republic of)

    2011-11-30

    Graphical abstract: This describes the increase of specific capacitance in hybrid electrodes as a function of melamine content. Display Omitted Highlights: > For N-enriched hybrid carbons, co-precursors, PVDF/melamine composites, were used. > Microporous carbons were formed by only carbonization without chemical activation. > The nitrogen content of microporous carbons was controlled by melamine content. > N-doped carbons showed higher specific capacitance compared to microporous carbons. > It was attributed to the easy electron transfer and pseudocapacitance. - Abstract: Nitrogen-doped microporous carbons (N-MCs) were prepared by the carbonization of the polyvinylidene fluoride (PVDF)/melamine mixture without chemical activation. The electrochemical performance of the N-MCs was investigated as a function of PVDF/melamine ratio. It was found that, without additional activation, the N-MCs had a high specific surface area (greater than 560 m{sup 2}/g) because of the micropore formation by the release of fluorine groups. In addition, although the specific surface area decreased, nitrogen groups were increased with increasing melamine content, leading to an enhanced electrochemical performance. Indeed, the N-MCs showed a better electrochemical performance than that of microporous carbons (MCs) prepared by PVDF alone, and the highest specific capacitance (310 F/g) was obtained at a current density of 0.5 A/g, as compared to a value of 248 F/g for MCs. These results indicate that the microporous features of N-MC lead to feasible ion transfer during charge/discharge duration and the presence of nitrogen groups as strong electron donor on the N-MC electrode in electrolyte could provide a pseudocapacitance by the redox reaction.

  19. Adsorption of Reactive Blue 171 from Aqueous Solution using Low Cost Activated Carbon Prepared from Agricultural Solid Waste: Albizia amara

    Directory of Open Access Journals (Sweden)

    K. Anitha

    2015-07-01

    Full Text Available The adsorption of Reactive Blue 171 (Reactive Dye from aqueous solution using activated carbon prepared from Albizia amara pod shell waste as an adsorbent have been carried out. The experimental adsorption data fitted reasonably well to Langmuir and Freundlich adsorption isotherms. Kinetic parameters as a function of Initial dye concentration have been calculated and the kinetic data were substituted in Pseudo First Order, Elovich and Pseudo Second order equations. A probable explanation is offered to account for the results of kinetic study. The thermodynamic parameter enthalpy change (∆H suggests the exothermic nature of absorption of Reactive Blue 171 onto activated Albizia amara pod shell waste carbon.

  20. PREPARATION OF ACTIVATED CARBON FIBER AND THEIR XENON ADSORPTION PROPERTIES (Ⅱ)-XENON ADSORPTION PROPERTIES

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    The adsorption of xenon from air has an interest in the monitoring of nuclear explosion oraccident, or in the treatment of nuclear waste gas. In this paper, the pore structure of several series ofactivated carbon fibers has been characterized. The adsorption properties of xenon on theseactivated carbon fibers under different temperatures have been studied in details. The results showthat the xenon adsorption amount on activated carbon fibers do not increase with specific surfacearea of adsorbents, but are closely related to their pore size distribution. Pores whose radius equal toor narrow than 0.4nm would be more advantageous to the adsorption of xenon.

  1. Preparation and characterisation of raw chars and physically activated carbons derived from marine Posidonia oceanica (L.) fibres

    Energy Technology Data Exchange (ETDEWEB)

    Ncibi, M.C., E-mail: ncibi_mc@yahoo.com [Laboratoire de chimie, Institut Superieur Agronomique, Chott Meriem 4042, Sousse (Tunisia); Unite de Recherche ' Chimie Appliquee et Environnement' , EPAM Sousse 4000 (Tunisia); Laboratoire COVACHIMM, EA 3592 Universite des Antilles et de la Guyane, BP 250, 97157 Pointe a Pitre Cedex, Guadeloupe (France); Jeanne-Rose, V. [Laboratoire COVACHIMM, EA 3592 Universite des Antilles et de la Guyane, BP 250, 97157 Pointe a Pitre Cedex, Guadeloupe (France); Mahjoub, B. [Laboratoire de chimie, Institut Superieur Agronomique, Chott Meriem 4042, Sousse (Tunisia); Unite de Recherche ' Chimie Appliquee et Environnement' , EPAM Sousse 4000 (Tunisia); Jean-Marius, C. [Laboratoire COVACHIMM, EA 3592 Universite des Antilles et de la Guyane, BP 250, 97157 Pointe a Pitre Cedex, Guadeloupe (France); Lambert, J.; Ehrhardt, J.J. [Laboratoire de Chimie Physique et Microbiologie pour l' Environnement, UMR 7564 CNRS, Universites de Nancy, 405, rue de Vandoeuvre, F 56600 Villers-les-Nancy cedex (France); Bercion, Y. [Groupe de Technologie des Surfaces et Interfaces (GTSI), EA 2432, Faculte des Sciences Exactes et Naturelles, Universite des Antilles et de la Guyane, BP 250, 97157 Pointe a Pitre Cedex, Guadeloupe (France); Seffen, M. [Laboratoire de chimie, Institut Superieur Agronomique, Chott Meriem 4042, Sousse (Tunisia); Unite de Recherche ' Chimie Appliquee et Environnement' , EPAM Sousse 4000 (Tunisia); Gaspard, S. [Laboratoire COVACHIMM, EA 3592 Universite des Antilles et de la Guyane, BP 250, 97157 Pointe a Pitre Cedex, Guadeloupe (France)

    2009-06-15

    Industrial valorisation of low cost and renewable biomass as raw precursor of activated carbon for environmental applications is an interesting alternative to costly commercial activated carbons. In this study, the possible use of Mediterranean, Posidonia oceanica fibrous biomass, as a precursor for chars and physically activated carbons, is investigated. Firstly, the raw marine material was chemically and biochemically characterised throughout dry-basis elemental, X-ray photoelectron spectroscopy (XPS) and scanning electron microscopy (SEM) analysis. Then, several P. oceanica chars were prepared and characterised under different pyrolysis times and temperatures. In addition, physically activated carbons (PACs) were produced via water steam flow under various activation periods. The results showed that the pyrolysis induces the creation of pores at different levels with respect to the involved temperature. Thereafter, the physical activation tends to enhance the development of the porous structure. In that issue, the performed Brunauer-Emmett-Teller (BET) and Barrett-Joiner-Halenda (BJH) analysis revealed that the prepared PACs have a mainly mesoporous inner morphology with a varying fraction of micropores.

  2. Activated Carbon Prepared From Orange Peels Coated With Titanium Oxide Nanoparticles: Characterization and Applications in the Decomposition of Nox

    Directory of Open Access Journals (Sweden)

    Liliana Giraldo

    2014-06-01

    Full Text Available In this work, we report the degradation of NOx using two catalysts prepared by coating activated carbon from orange peels with TiO2. This study compared the performance of TiO2-coated catalysts prepared by CVD (AC1/TiO2 and the sol-gel method (AC2/TiO2. The catalysts were characterized by X-ray diffraction, BET surface area and TEM. The photocatalytic activity was measured by studying the degradation of NOx in the vapor phase. The results show that the catalyst synthesized by the CVD method was more efficient in the decomposition of NOx. TEM and XRD revealed the presence of a mixture of the anatase and rutile phases, which favors the NOx decomposition process. Nitrogen isotherms showed that coating the nanoparticles with titanium oxide did not significantly change the surface area of the original activated carbon.

  3. 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.

  4. 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.

  5. Biosorption Studies for the Removal of Malachite Green from its Aqueous Solution by Activated Carbon Prepared from Cassava Peel

    Directory of Open Access Journals (Sweden)

    C. Parvathi

    2011-01-01

    Full Text Available The association of dyes with health related problems is not a new phenomenon. The effectiveness of carbon adsorption for dye removal from textile effluent has made it an ideal alternative to other expensive treatment methods. The preparation of activated carbon from agricultural waste could increase economic return and reduce pollution. Cassava peel has been used as a raw material to produce activated carbon. The study investigates the removal of malachite green dye from its aqueous solution. The effects of condition such as adsorbent dosage, initial dye concentration, pH and contact time were studied. The adsorption capacity was demonstrated as a function of time for malachite green from aqueous solution by the prepared activated carbon. The results showed that as the amount of the adsorbent was increased, the percentage of dye removal increased accordingly. Higher adsorption percentages were observed at lower concentrations of malachite green dye. Silver nitrate treated cassava peel showed a better performance compared to Sulphuric acid treated and raw carbons, thus making it an interesting option for dye removal textile effluent.

  6. Adsorption of Crystal Violet on Activated Carbon Prepared from Coal Flotation Concentrate

    Science.gov (United States)

    Aydogmus, Ramazan; Depci, Tolga; Sarikaya, Musa; Riza Kul, Ali; Onal, Yunus

    2016-10-01

    The objective of this study is firstly to investigate the floatability properties of Zilan- Van coal after microwave irradiation and secondly to produce activated carbon from flotation concentrate in order to remove Crystal Violet (CV) from waste water. The flotation experiments showed that microwave heating at 0.9 kW power level for 60 sec exposure time enhanced the hydrophobicity and increased the flotation yield. The activated carbon with remarkable surface area (696 m2/g) was produced from the flotation concentrate and used to adsorb CV from aqueous solution in a batch reactor at different temperature. The adsorption properties of CV onto the activated carbon are discussed in terms of the adsorption isotherms (Langmuir and Freundlich) and found that the experimental results best fitted by the Langmuir model.

  7. Separation of Tetramethyl Ammonium Hydroxide in Waste Water with Ion Exchange Using Activated Carbon Prepared by Bamboo

    Science.gov (United States)

    Yamaguchi, Ayako; Nishihama, Syouhei; Yoshizuka, Kazuharu

    Activated carbon is prepared by bamboo for the selective recovery of tetramethyl ammonium hydroxide (TMAH), contained in waste water from semiconductive industry, at the end of pipe of the plant. The adsorption ability of the activated carbon from bamboo (BAC) is comparable to the commercial activated carbons. The adsorption of TMAH with BAC in batchwise system increases with increase in pH value of the aqueous solution, and the effective adsorption and elution yield is also obtained in column system. Quantitative adsorption-elution processing can be achieved with the present BAC, and thus indicating the BAC is effective material as the adsorbent of TMAH at the end of pipe of the plant.

  8. Characterization and Properties of Activated Carbon Prepared from Tamarind Seeds by KOH Activation for Fe(III) Adsorption from Aqueous Solution.

    Science.gov (United States)

    Mopoung, Sumrit; Moonsri, Phansiri; Palas, Wanwimon; Khumpai, Sataporn

    2015-01-01

    This research studies the characterization of activated carbon from tamarind seed with KOH activation. The effects of 0.5 : 1-1.5 : 1 KOH : tamarind seed charcoal ratios and 500-700°C activation temperatures were studied. FTIR, SEM-EDS, XRD, and BET were used to characterize tamarind seed and the activated carbon prepared from them. Proximate analysis, percent yield, iodine number, methylene blue number, and preliminary test of Fe(III) adsorption were also studied. Fe(III) adsorption was carried out by 30 mL column with 5-20 ppm Fe(III) initial concentrations. The percent yield of activated carbon prepared from tamarind seed with KOH activation decreased with increasing activation temperature and impregnation ratios, which were in the range from 54.09 to 82.03 wt%. The surface functional groups of activated carbon are O-H, C=O, C-O, -CO3, C-H, and Si-H. The XRD result showed high crystallinity coming from a potassium compound in the activated carbon. The main elements found in the activated carbon by EDS are C, O, Si, and K. The results of iodine and methylene blue adsorption indicate that the pore size of the activated carbon is mostly in the range of mesopore and macropore. The average BET pore size and BET surface area of activated carbon are 67.9764 Å and 2.7167 m(2)/g, respectively. Finally, the tamarind seed based activated carbon produced with 500°C activation temperature and 1.0 : 1 KOH : tamarind seed charcoal ratio was used for Fe(III) adsorption test. It was shown that Fe(III) was adsorbed in alkaline conditions and adsorption increased with increasing Fe(III) initial concentration from 5 to 20 ppm with capacity adsorption of 0.0069-0.019 mg/g.

  9. Removal of fluoride by thermally activated carbon prepared from neem (Azadirachta indica) and kikar (Acacia arabica) leaves.

    Science.gov (United States)

    Kumar, Sunil; Gupta, Asha; Yadav, J P

    2008-03-01

    The present investigation deals with fluoride removal from aqueous solution by thermally activated neem (Azadirachta indica) leaves carbon (ANC) and thermally activated kikar (Acacia arabica) leaves carbon (AKC) adsorbents. In this study neem leaves carbon and kikar leaves carbon prepared by heating the leaves at 400 degrees C in electric furnace was found to be useful for the removal of fluoride. The adsorbents of 0.3 mm and 1.0 mm sizes of neem and kikar leaves carbon was prepared by standard sieve. Batch experiments done to see the fluoride removal properties from synthetic solution of 5 ppm to study the influence of pH, adsorbent dose and contact time on adsorption efficiency The optimum pH was found to be 6 for both adsorbents. The optimum dose was found to be 0.5g/100 ml forANC (activated neem leaves carbon) and 0.7g/100 ml forAKC (activated kikar leaves carbon). The optimum time was found to be one hour for both the adsorbent. It was also found that adsorbent size of 0.3 mm was more efficient than the 1.0 mm size. The adsorption process obeyed Freundlich adsorption isotherm. The straight line of log (qe-q) vs time at ambient temperature indicated the validity of langergren equation consequently first order nature of the process involved in the present study. Results indicate that besides intraparticle diffusion there maybe other processes controlling the rate which may be operating simultaneously. All optimized conditions were applied for removal of fluoride from four natural water samples.

  10. PREPARATION OF TiO2 PHOTOCATALYST ANCHORED ON ACTIVATED CARBON FIBERS AND ITS PHOTODEGRADATION OF METHYLENE BLUE

    Institute of Scientific and Technical Information of China (English)

    Pingfeng Fu; Yong Luan; Xuegang Dai

    2004-01-01

    TiO2 particulate photocatalyst anchored on activated carbon fibers (ACFs) was prepared by a molecular adsorption-deposition method. The TiO2 particles deposited on the carbon fibers formed a coating of about 100 nm in thickness. The photocatalyst prepared was characterized by means of SEM, EDS, XRD and UV-vis adsorption spectroscopy. Anatase-type TiO2 was uniquely developed, and the micrographic structure of ACFs was not damaged during preparation. The roomy space between adjacent carbon fibers could allow UV-light to penetrate into the felt-form photocatalyst to a certain depth, so that a three dimensional environment was formed for the photocatalytic reaction.Such TiO2/ACFs photocatalyst exhibited its photocatalytic reactivity in photodegradation of concentrated methylene blue(MB) solutions. The MB molecules in the bulk solutions was supposed to be condensed around TiO2 particles by adsorption by ACFs. Therefore, the photocatalyst possesses the combined effect of adsorption by activated carbon fibers and photocatalytic reactivity of anatase-type TiO2 on MB photodegradation.

  11. Fast and efficient adsorption of methylene green 5 on activated carbon prepared from new chemical activation method.

    Science.gov (United States)

    Tran, Hai Nguyen; You, Sheng-Jie; Chao, Huan-Ping

    2017-03-01

    Activated carbon (AC) was synthesized from golden shower (GS) through a new chemical activation process. The three-stage process comprised (1) hydrothermal carbonization of GS to produce hydrochar, (2) pyrolysis of hydrochar to produce biochar, and (3) subsequent chemical activation of biochar with K2CO3 to obtain GSHBAC. The traditional synthesis processes (i.e., one-stage and two-stage) were also examined for comparison. In the one-stage process, GS that was impregnated with K2CO3 was directly pyrolyzed (GSAC), and the two-stage process consisted of (1) pyrolytic or hydrothermal carbonization to produce biochar or hydrochar and (2) subsequent chemical activation was defined as GSBAC and GSHAC, respectively. The synthesized ACs were characterized by scanning electron microscope, Brunauer-Emmett-Teller (BET) surface area analysis, Fourier transform infrared spectrometry, point zero charge, and Boehm titration. The adsorption results demonstrated that the MG5 adsorption process was not remarkably affected by neither the solution pH (2.0-10) nor ionic strength (0-0.5 M NaCl). Kinetic studies showed that the adsorption equilibrium was quickly established, with a low activation energy required for adsorption (Ea; 3.30-27.8 kJ/mol), and the ACs removed 50-73% of the MG5 concentration from solution within 01 min. Desorption studies confirmed the adsorption was irreversible. Thermodynamic experiments suggested that the MG5 adsorption was spontaneous (-ΔG°) and endothermic (+ΔH°), and increased the randomness (+ΔS°) in the system. Although the specific surface areas of the ACs followed the order GSAC (1,413) > GSHAC (1,238) > GSHBAC (903) > GSBAC (812 m(2)/g), the maximum adsorption capacities determined from the Langmuir model (Q(o)max) at 30 °C exhibited the following order: GSHBAC (531) > GSAC (344) > GSHAC (332) > GSBAC (253 mg/g). Oxygenation of the ACs' surface through a hydrothermal process with acrylic acid resulted in a decrease in MG5

  12. ADSORPTION PROPERTIES OF NICKEL-BASED MAGNETIC ACTIVATED CARBON PREPARED BY PD-FREE ELECTROLESS PLATING

    Directory of Open Access Journals (Sweden)

    Boyang Jia

    2011-02-01

    Full Text Available Nickel-based magnetic activated carbon was synthesized from coconut shell activated carbon by electroless plating with palladium-free activation. The effect of plating solution volume on metallic ratio and adsorption capacity were evaluated. The effect of metallic ratio on specific area, pore volume, and magnetic properties were investigated. The morphologies of activated carbon before and after plating were observed by SEM, and the composition of the layer was analyzed by EDS analysis. The results showed that the metallic ratio was increased with the increase of the plating solution volume. The magnetic activated carbon showed high adsorption capacity for methylene blue and a high iodine number. Those values reached 142.5 mg/g and 1035 mg/g, respectively. The specific area and pore volume decreased from 943 m2/g to 859 m2/g and 0.462 ml/g to 0.417 ml/g, respectively. And the layer was more compact and continuous when the metallic ratio reached 16.37 wt.%. In the layer, there was about 97 wt.% nickel and 3 wt.% phosphorus, which indicates that the layer was a low-phosphorus one. At the same time, magnetism was enhanced, making the product suitable for some special applications.

  13. Preparation of activated carbons from Iris tectorum employing ferric nitrate as dopant for removal of tetracycline from aqueous solutions.

    Science.gov (United States)

    Li, Gang; Zhang, Dongsheng; Wang, Man; Huang, Ji; Huang, Lihui

    2013-12-01

    Ferric nitrate was employed to modify activated carbon prepared from Iris tectorum during H₃PO₄ activation and ability of prepared activated carbon for removal of tetracycline (TC) was investigated. The properties of the activated carbon samples with or without ferric nitrate, ITAC-Fe and ITAC, were measured by scanning electron microscopy (SEM), N₂ adsorption/desorption isotherms, Fourier transform infrared spectroscopy (FTIR) and Boehm's titration. The results showed that mixing with iron increased the BET surface area, total pore volume and the adsorption capacity as compared to the original carbon. FTIR and Boehm's titration suggested that ITAC-Fe was characteristic of more acidic functional groups than ITAC. Adsorption of TC on both samples exhibited a strong pH-dependent behavior and adsorption capacity reduced rapidly with the increasing solution pH. The adsorption kinetics agreed well with the pseudo-second-order model and the adsorption isotherms data were well described by Langmuir model with the maximum adsorption capacity of 625.022 mg/g for ITAC and 769.231 mg/g for ITAC-Fe. The present work suggested that ITAC-Fe could be used to remove tetracycline effectively from aqueous solutions.

  14. Pyrolysis polygeneration of pine nut shell: Quality of pyrolysis products and study on the preparation of activated carbon from biochar.

    Science.gov (United States)

    Chen, Dengyu; Chen, Xiaojuan; Sun, Jun; Zheng, Zhongcheng; Fu, Kexin

    2016-09-01

    A lab-scale pyrolysis reactor was utilized to investigate the effect of pyrolysis temperature (300-700°C) on the yield, quality, and energy distribution of products issued from the pyrolysis polygeneration of pine nut shells. Afterward, activated carbon was prepared from biochar using the steam activation method. Pyrolysis temperatures ranging from 500 to 600°C were found to be optimal in inducing products with improved properties, such as higher heating values of non-condensable gas, lower water content and elevated heating values of bio-oil, and substantial fixed carbon content and greater specific surface area of biochar. In addition, it was noticed that the activation conditions had a significant effect on the yield and adsorption performance of the activated carbon. As a result, activated carbon with elevated specific surface area reaching 1057.8m(2)/g was obtained at the optimal conditions of 850°C activation temperature, 80min activation time, and 1.5 steam/biochar ratio.

  15. Treatment of semi-aerobic landfill leachate using durian peel-based activated carbon adsorption- Optimization of preparation conditions

    Directory of Open Access Journals (Sweden)

    Mohamad Anuar Kamaruddin, Mohd Suffian Yusoff, Mohd Azmier Ahmad

    2012-01-01

    Full Text Available The treatability of semi-aerobic landfill leachate parameters using durian peel-based activated carbon (DPAC was investigated. An ideal experimental design was conducted based on central composite design (CCD using response surface methodology to evaluate individual and interactive effects of operational variables namely activation temperature, activation time and carbon dioxide (CO2 flow rate on treatment performance in terms of chemical oxygen demand (COD and colour removal efficiencies. The DPAC was prepared using physical activation method which consists of CO2 gasification. The adsorptions of COD and colour were described by Langmuir and Freundlich isotherm models. Based on the CCD, quadratic model was developed to correlate preparation variables to the two responses. The optimum DPAC preparation conditions were obtained using 800 °C activation temperature, 2.1 h activation time and 68.68 ml/s of CO2 flow rate. From the experimental work, the maximum removal of COD and colour obtained were 41.98 and 39.86%, respectively.

  16. Treatment of semi-aerobic landfill leachate using durian peel-based activated carbon adsorption- Optimization of preparation conditions

    Energy Technology Data Exchange (ETDEWEB)

    Kamaruddin, Mohamad Anuar; Yusoff, Mohd Suffian [School of Civil Engineering, Engineering Campus, Universiti Sains Malaysia, 14300 Nibong Tebal, Penang (Malaysia); Ahmad, Mohd Azmier [School of Chemical Engineering, Engineering Campus, Universiti Sains Malaysia, 14300 Nibong Tebal, Penang (Malaysia)

    2012-07-01

    The treatability of semi-aerobic landfill leachate parameters using durian peel-based activated carbon (DPAC) was investigated. An ideal experimental design was conducted based on central composite design (CCD) using response surface methodology to evaluate individual and interactive effects of operational variables namely activation temperature, activation time and carbon dioxide (CO2) flow rate on treatment performance in terms of chemical oxygen demand (COD) and colour removal efficiencies. The DPAC was prepared using physical activation method which consists of CO2 gasification. The adsorptions of COD and colour were described by Langmuir and Freundlich isotherm models. Based on the CCD, quadratic model was developed to correlate preparation variables to the two responses. The optimum DPAC preparation conditions were obtained using 800 C activation temperature, 2.1 h activation time and 68.68 ml/s of CO2 flow rate. From the experimental work, the maximum removal of COD and colour obtained were 41.98 and 39.86%, respectively.

  17. Characterization and Properties of Activated Carbon Prepared from Tamarind Seeds by KOH Activation for Fe(III) Adsorption from Aqueous Solution

    OpenAIRE

    Sumrit Mopoung; Phansiri Moonsri; Wanwimon Palas; Sataporn Khumpai

    2015-01-01

    This research studies the characterization of activated carbon from tamarind seed with KOH activation. The effects of 0.5 : 1–1.5 : 1 KOH : tamarind seed charcoal ratios and 500–700°C activation temperatures were studied. FTIR, SEM-EDS, XRD, and BET were used to characterize tamarind seed and the activated carbon prepared from them. Proximate analysis, percent yield, iodine number, methylene blue number, and preliminary test of Fe(III) adsorption were also studied. Fe(III) adsorption was carr...

  18. Preparing to Capture Carbon

    National Research Council Canada - National Science Library

    Daniel P. Schrag

    2007-01-01

    .... Scientific and economic challenges still exist, but none are serious enough to suggest that carbon capture and storage will not work at the scale required to offset trillions of tons of carbon...

  19. Adsorption of U(VI) ions from aqueous solutions by activated carbon prepared from Antep pistachio (Pistacia vera L.) shells

    Energy Technology Data Exchange (ETDEWEB)

    Donat, Ramazan [Pamukkale Univ., Denizli (Turkey). Dept. of Chemistry; Erden, Kadriye Esen [Pamukkale Univ., Kinikli-Denizli (Turkey). Denizli Vocational School of Technical Sciences

    2017-08-01

    Antep pistachio (Pistacia vera L.) shells an abundant and low cost natural resource in Turkey was used to prepare activated carbon by physiochemical activation and carbon dioxide (CO{sub 2}) atmosphere as the activating agents at 700 C for 2 h. The adsorption equilibrium of U(VI) from aqueous solutions on such carbon has been studied using a batch system. The parameters that affect the U(VI) adsorption, such as particle size of adsorbent, contact time, of pH of the solution, and temperature, have been investigated and conditions have also been optimized. The equilibrium data for U(VI) ions' adsorption onto activated carbon well fitted to the Langmuir equation, with a maximum monolayer adsorption capacity of 8.68 mg/g, The Freundlich and Dubinin-Radushkevich (D-R) isotherms have been applied and the data correlated well with Freundlich model and that the adsorption is physical in nature (E{sub a}=15.46 kJ/mol). Thermodynamic parameters [ΔH{sub s}=11.33 kJ/mol, ΔS=0.084 kJ/molK, ΔG (293.15 K)=-13.29 kJ/mol] showed the endothermic heat of adsorption and the feasibility of the process.

  20. Preparation of nanoporous activated carbon and its application as nano adsorbent for CO{sub 2} storage

    Energy Technology Data Exchange (ETDEWEB)

    Rashidi, Ali Morad; Kazemi, Davood; Izadi, Nosrat; Pourkhalil, Mahnaz; Jorsaraei, Abbas; Lotfi, Roghayeh [Research Institute of Petroleum Industry, Tehran (Iran, Islamic Republic of); Ganji, Enseyeh [Research Institute of Petroleum Industry, Tehran (Iran, Islamic Republic of)

    2016-02-15

    Nanoporous activated carbons, as adsorbent for CO{sub 2} storage, were prepared from walnut shells via two chemical processes including phosphoric acid treatment and KOH activation at high temperature. Specific surface area and porosities were controlled by KOH concentration and activation temperature. The obtained adsorbents were characterized by N2 adsorption at 77.3 K. Their carbon dioxide adsorption capacities were measured at different pressures at 290 K by using volumetric adsorption equipment. The KOH-treated nanoporous carbons typically led to the production of high specific surface areas and high micropore volumes and showed better performance for CO{sub 2} adsorptions. The maximum experimental value for adsorption capacity happened when pressure increased from 5 to 10 bar (1.861- 2.873mmol·g{sup -1}). It was found that in order to improve the highest capacity of CO{sub 2} adsorption for KOH-modified carbon (9.830-18.208mmol·g{sup -1}), a KOH: C weight ratio of 3.5 and activation temperature of 973 K were more suitable for pore development and micro-mesopore volume enhancement.

  1. Performance of Electric Double Layer Capacitors using Active Carbons Prepared from Petroleum Coke by KOH and Vapor Re-Etching

    Institute of Scientific and Technical Information of China (English)

    2003-01-01

    The electrochemical storage of energy in a special kind of active carbon materials used as capacitor electrodes isconsidered. Pet roleum coke was used for preparation of carbons with different porosities by KOH and vapor etchingwith catalysis of FeCl3 in turn. Carbon electrodes were fabricated and used as electrodes of double layer capacitors.Nitrogen adsorption was used to characterize the porous structure of the carbons. The electrochemical performanceof the capacitors in 6 mol/L KOH was investigated with constant current charge and discharge experiments. Aspecific capacitance larger than 160 F/g was achieved with an electrode composed of 75% active carbon with aspecific surface area of 1180 m2/g and 20% graphite as conductive agent. Evaluation of capacitor performance wasconducted by different techniques, e.g. voltammetry and impedance spectroscopy. Characteristics of the capacitorwere also discussed. A hybrid power source consisting of nickel- hydrogen and double layer capacitor was demonstratedby powering successfully a simulated power load encountered in communication equipment.

  2. A comparative investigation on adsorption performances of mesoporous activated carbon prepared from waste rubber tire and activated carbon for a hazardous azo dye-Acid Blue 113

    Energy Technology Data Exchange (ETDEWEB)

    Gupta, V.K., E-mail: vinodfcy@iitr.ernet.in [Department of Chemistry, Indian Institute of Technology Roorkee, Roorkee 247667 (India); Chemistry Department, King Fahd University of Petroleum and Minerals, Dhahran 31261 (Saudi Arabia); Gupta, Bina [Department of Chemistry, Indian Institute of Technology Roorkee, Roorkee 247667 (India); Rastogi, Arshi [Chemistry Department, K.L.D.A.V.(P.G.) College, Roorkee (India); Agarwal, Shilpi [School of Studies in Chemistry, Jiwaji University, Gwalior, MP (India); Nayak, Arunima [Department of Chemistry, Indian Institute of Technology Roorkee, Roorkee 247667 (India)

    2011-02-15

    Research highlights: {yields} The system is cheap, efficient and fast for the removal of dyes from waters. {yields} Higher adsorption capacity is due to higher mesoporous volume of the adsorbent. {yields} The rate determining step of the adsorption process is particle diffusion. - Abstract: A mesoporous carbon developed from waste tire rubber, characterized by chemical analysis, FTIR, and SEM studies, was used as an adsorbent for the removal and recovery of a hazardous azo dye, Acid Blue 113. Surface area, porosity, and density were determined. The adsorption of the dye over the prepared adsorbent and a commercial activated carbon was achieved under different pH, adsorbate concentration, sieve size, adsorbent dosage, contact time and temperature conditions. Langmuir and Freundlich adsorption isotherm models were applied and thermodynamic parameters were calculated. Kinetic studies indicated that the adsorption process follow first order kinetics and particle diffusion mechanisms are operative. By percolating the dye solution through fixed-bed columns the bulk removal of the Acid Blue 113 was carried out and necessary parameters were determined to find out the percentage saturation of both the columns. Recovery of the dye was made by eluting 0.1 M NaOH through the column.

  3. Titania modified activated carbon prepared from sugarcane bagasse: adsorption and photocatalytic degradation of methylene blue under visible light irradiation.

    Science.gov (United States)

    El-Salamony, R A; Amdeha, E; Ghoneim, S A; Badawy, N A; Salem, K M; Al-Sabagh, A M

    2017-03-01

    Activated carbon (AC), prepared from sugarcane bagasse waste through a low-temperature chemical carbonization treatment, was used as a support for nano-TiO2. TiO2 supported on AC (xTiO2-AC) catalysts (x = 10, 20, 50, and 70 wt.%) were prepared through a mechano-mixing method. The photocatalysts were characterized by Raman, X-ray diffraction analysis, FTIR, SBET, field emission scanning electron microscope, and optical technique. The adsorption and photo-activity of the prepared catalysts (xTiO2-AC) were evaluated using methylene blue (MB) dye. The photocatalytic degradation of MB was evaluated under UVC irradiation and visible light. The degradation percentage of the 100 ppm MB at neutral pH using 20TiO2-AC reaches 96 and 91 after 180 min under visible light and UV irradiation, respectively. In other words, these catalysts are more active under visible light than under UV light irradiation, opening the possibility of using solar light for this application.

  4. Textural and chemical characterization of activated carbon prepared from shell of african palm (Elaeis guineensis by chemical activation with CaCl2 and MgCl2

    Directory of Open Access Journals (Sweden)

    Sergio Acevedo

    2015-09-01

    Full Text Available Activated carbons through chemical activation of African palm shells (Elaeis guineensis with magnesium chloride and calcium chloride solutions at different concentrations were obtained. The prepared materials were characterized textural and chemically. The results show that activated carbons with higher values of surface area and pore volume are obtained when solutions with lower concentrations of the activating agent are used. The obtained activated carbons have surface areas and pore volumes with values between 10 and 501 m2 /g and 0.01 and 0.29 cm3 /g respectively. Immersion enthalpies values of solids in water were between -14.3 and -32.8 J/g and benzene between -13.9 and -38.6 J/g. Total acidity and basicity of the activated carbons had values between 23 and 262 μmol/g 123 and 1724 μmol/g respectively. pH at the point of zero charge was also determined with values between 4.08 and 9.92 for set of activated carbons . The results show that activation with CaCl2 and MgCl2 salts produce activated carbons with pores in the range of mesopores for facilitate entry of the adsorbate into the materials.

  5. Preparation and characterization activated carbon from rice husk and oil palm empty fruit bunches for removal of Zn2+ in aqueous solution

    Science.gov (United States)

    Ismail, Nur Enzati Afwana; Taha, Mohd F.; Ramli, Anita

    2016-11-01

    The ability of activated carbon prepared from rice husk (RH), oil palm empty fruit bunches (EFB) and mixture (Mix) activated carbon in adsorption of Zinc (Zn2+) from aqueous solution was investigated. The Mix activated carbon has prepared from mixture of RH and EFB activated carbon with weight ratio (1:1) The RH and EFB activated carbon were produced by using sodium hydroxide (NaOH) as a dehydrating agent in chemical activation process.EFB activated carbon showed excellent efficiency in removing Zn2+ with their percentage removal up to 100% even at low adsorbent dosage. The study also showed that the adsorption of Zn2+ by EFB, RH and Mix activated carbon is dependent on the adsorbent dosage and initial metal concentration. The adsorption isotherms of the Zn2+ of EFB, RH and Mix activated carbon were determined and compared with Langmuir and Freundlich models. It was showed that Langmuir model was more favorable for RH and Mix activated carbon with correlation coefficient (R2) value is 0.9958 and 0.9847. In contrast, EFB activated carbon was more favorable to the Freundlich and Langmuir model with correlation coefficient (R2) are 0.9967 and 0.9967

  6. Preparation and Characterization of Nano-TiO2 Loaded Bamboo-based Activated Carbon Fibers by H2O Activation

    OpenAIRE

    Dongna Li; Xiaojun Ma; Xinyan Liu; Lili Yu

    2013-01-01

    As the support for loading TiO2, bamboo-based activated carbon fibers (BACFs) were obtained from Phyllostachys pubescens Mazel after liquefaction using phenol, melt-spinning, curing carbonization, and H2O activation. TiO2/BACFs were prepared by the sol–gel method and characterized by SEM, XRD, FTIR, and XPS. Anatase TiO2 film with high photocatalytic activity was formed on the surface of BACFs, and the average crystallite size of the TiO2 film was 17 to 30 nm. The characteristic absorbance pe...

  7. Preparation of polyacrylnitrile (PAN)/ Manganese oxide based activated carbon nanofibers (ACNFs) for adsorption of Cadmium (II) from aqueous solution

    Science.gov (United States)

    Abdullah, N.; Yusof, N.; Jaafar, J.; Ismail, AF; Che Othman, F. E.; Hasbullah, H.; Salleh, W. N. W.; Misdan, N.

    2016-06-01

    In this work, activated carbon nanofibers (ACNFs) from precursor polyacrylnitrile (PAN) and manganese oxide (MnO2) were prepared via electrospinning process. The electrospun PAN/MnO2-based ACNFs were characterised in term of its morphological structure and specific surface area using SEM and BET analysis respectively. The comparative adsorption study of cadmium (II) ions from aqueous solution between the neat ACNFs, composite ACNFs and commercial granular activated carbon was also conducted. SEM analysis illustrated that composite ACNFs have more compact fibers with presence of MnO2 beads with smaller fiber diameter of 437.2 nm as compared to the neat ACNFs which is 575.5 nm. BET analysis elucidated specific surface area of ACNFs/MnO2 to be 67 m2/g. Under adsorption study, it was found out that Cd (II) removal by ACNFs/MnO2 was the highest (97%) followed by neat ACNFs (96%) and GAC (74%).

  8. Advances in preparation of modified activated carbon and its applications in the removal of chromium (VI) from aqueous solutions

    Science.gov (United States)

    Deng, Z. L.; Liang, M. N.; Li, H. H.; Zhu, Z. J.

    2016-08-01

    The wastewater in which Cr(VI) is not fully treated has drawn environment researchers’ attention increasingly, due to its environmental pollution and harms to human health. Thus a high efficiency of modified activated carbon (MAC) to remove Cr(VI) has become one of the hot topics among environmental material research. This paper introduces the modification methods from the physical structure features and chemical properties of the activated carbon (AC) surface. At the same time, it briefly analyses the chemical characteristics of Cr(VI) in aqueous solutions, and on the basis of the aforementioned introduces the modification methods of the surface chemical characteristics of AC, such as: oxidation modification, reduction modification, loaded metal modification, and microwave modification. Combining studies on removing Cr(VI) from aqueous solutions by MAC in recent years, this paper anticipates the new trends of preparing MAC and the points in absorption research, offering some suggestions for future studies.

  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. 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.

  12. Adsorption of bentazon on activated carbon prepared from Lawsonia inermis wood: Equilibrium, kinetic and thermodynamic studies

    Directory of Open Access Journals (Sweden)

    Abdessalem Omri

    2016-11-01

    Full Text Available The adsorption of bentazon onto Lawsonia inermis wood-based activated carbon (LWAC was carried out in this work. The effects of different reaction parameters such as the initial bentazon concentration, contact time, activated carbon dosage, stirring rate, temperature and pH on bentazon adsorption were investigated in a batch process mode. Equilibrium data were analyzed by the Langmuir, Freundlich and Temkin isotherm model. Langmuir isotherm provided the best fit to the equilibrium data with maximum adsorption capacity of 169.49 mg/g at 20 °C. Adsorption kinetic was found to follow the pseudo-second-order kinetic model. The mechanism of the adsorption process was determined from the intraparticle diffusion model. The calculated thermodynamic parameters such as ΔG°, ΔH° and ΔS° showed that the adsorption of bentazon onto LWAC was feasible, spontaneous and exothermic at 20–40 °C. Desorption of the used LWAC was studied using ethanol as solvent and a percent desorption efficiency of bentazon equalizes 73.8% was obtained after three cycles.

  13. Preparation of sewage sludge based activated carbon by using Fenton's reagent and their use in 2-naphthol adsorption.

    Science.gov (United States)

    Gu, Lin; Wang, Yachen; Zhu, Nanwen; Zhang, Daofang; Huang, Shouqiang; Yuan, Haiping; Lou, Ziyang; Wang, Miaolin

    2013-10-01

    In this study, Fenton's reagents (H2O2/Fe(2+)) are used to activate raw sewage sludge for the preparation of the sludge based activated carbon. The effect of the amount of hydrogen peroxide addition on carbon's chemical composition, texture properties, surface chemistry and morphology are investigated. Choosing an appropriate H2O2 dosage (5 v%) (equivalent to 70.7 mM/(g VS)), it is possible to obtain a comparatively highly porous materials with SBET and the total pore volume being 321 m(2)/g and 0.414 cm(3)/g, respectively. Continuously increasing the oxidant ratio resulted in a decreased SBET value. Further adsorption experiments by using 2-naphthol as model pollutant revealed that the adoption followed a pseudo-second-order kinetics better than pseudo-first-order. The calculated adsorption capacity is 111.9 mg/g on the carbon with 5% H2O2 pretreatment while this value is just 51.5mg/g on carbons without any pretreatment.

  14. Spent coffee grounds-based activated carbon preparation for sequestering of malachite green

    Science.gov (United States)

    Lim, Jun-Wei; Lam, Keat-Ying; Bashir, Mohammed J. K.; Yeong, Yin-Fong; Lam, Man-Kee; Ho, Yeek-Chia

    2016-11-01

    The key of reported work was to optimize the fabricating factors of spent coffee grounds-based activated carbon (SCG-bAC) used to sequester Malachite Green (MG) form aqueous solution via adsorption process. The fabricating factors of impregnation ratio with ortho-phosphoric acid, activation temperature and activation time were simultaneously optimized by central composite design (CCD) of response surface methodology (RSM) targeting on maximum removal of MG. At the optimum condition, 96.3% of MG was successfully removed by SCG-bAC at the impregnation ratio with ortho-phosphoric acid of 0.50, activation temperature of 554°C and activation time of 31.4 min. Statistical model that could predict the MG removal percentage was also derived and had been statistically confirmed to be significant. Subsequently, the MG adsorption equilibrium data was found well-fitted to Langmuir isotherm model, indicating the predominance of monolayer adsorption of MG on SCG-bAC surface. To conclude, the findings from the this study unveil the potential of spent coffee grounds as an alternative precursor in fabricating low-cost AC for the treatment of wastewater loaded with MG pollutant.

  15. Preparation and Characterization of Activated Carbon from Iraqi Khestawy Date Palm

    Directory of Open Access Journals (Sweden)

    Falah H. Hussein

    2015-01-01

    Full Text Available This work includes a synthesis of three types of the activated carbon (AC from three different positions from the same Iraqi Khestawy date palm. These three positions are the palm fronds (AC1, the date palm seeds (AC2, and the palm fiber (AC3. These three types of AC were synthesized by a physiochemical activation method using the same activator which was H3PO4. These materials were investigated using different techniques such as Fourier transform infrared spectroscopy (FTIR and scanning electron microscopy (SEM. The adsorption activity of the synthesized AC samples was investigated by following the removal of both Bismarck brown G (BBG and reactive yellow dye 145 (RY145. Both the kinetics of adsorption and the removal percentage of these dyes were investigated from the batch tests in this study. Different reaction parameters and conditions for adsorption processes were investigated. Also an investigation of both Langmuir and Freundlich adsorption isotherms was considered. The different physical properties of these materials were undertaken such as the point zero charges of the synthesized samples (PZCs, the percentage of humidity, and the adsorption capacity also being investigated. The activity of these materials in the removal of BBG from the aqueous solution was as follows: AC1>AC2>AC3.

  16. Preparation and Characteristics of Activated Carbon from Wood Bark and Its Use for Adsorption of Cu (II

    Directory of Open Access Journals (Sweden)

    Jiahui ZHANG

    2014-12-01

    Full Text Available In this study, wood bark activated carbon (bark activated carbon, BAC were prepared by the method of steam activation at the activation temperature of 700 °C and 800 °C. The pore structures of BAC samples obtained were analysed via means of low temperature nitrogen adsorption. Iodine adsorption value and Cu (II ions adsorption capacity were also investigated. The results indicated that micropores and mesopores were abundant in BACs, which indicated a better adsorption effect in iodine and Cu (II ions adsorption capacities than wood bark carbon. The efficiency for the removal of Cu (II ions were carried out as a function of contact time. The optimal dosage of Cu (II ions by BAC700 and BAC800 samples is 5 g/L with an optimal time of 30 min. The kinetic studies of BACs revealed a better correlation with the Lagergren pseudo-second order model. DOI: http://dx.doi.org/10.5755/j01.ms.20.4.6400

  17. Characterization and Properties of Activated Carbon Prepared from Tamarind Seeds by KOH Activation for Fe(III Adsorption from Aqueous Solution

    Directory of Open Access Journals (Sweden)

    Sumrit Mopoung

    2015-01-01

    Full Text Available This research studies the characterization of activated carbon from tamarind seed with KOH activation. The effects of 0.5 : 1–1.5 : 1 KOH : tamarind seed charcoal ratios and 500–700°C activation temperatures were studied. FTIR, SEM-EDS, XRD, and BET were used to characterize tamarind seed and the activated carbon prepared from them. Proximate analysis, percent yield, iodine number, methylene blue number, and preliminary test of Fe(III adsorption were also studied. Fe(III adsorption was carried out by 30 mL column with 5–20 ppm Fe(III initial concentrations. The percent yield of activated carbon prepared from tamarind seed with KOH activation decreased with increasing activation temperature and impregnation ratios, which were in the range from 54.09 to 82.03 wt%. The surface functional groups of activated carbon are O–H, C=O, C–O, –CO3, C–H, and Si–H. The XRD result showed high crystallinity coming from a potassium compound in the activated carbon. The main elements found in the activated carbon by EDS are C, O, Si, and K. The results of iodine and methylene blue adsorption indicate that the pore size of the activated carbon is mostly in the range of mesopore and macropore. The average BET pore size and BET surface area of activated carbon are 67.9764 Å and 2.7167 m2/g, respectively. Finally, the tamarind seed based activated carbon produced with 500°C activation temperature and 1.0 : 1 KOH : tamarind seed charcoal ratio was used for Fe(III adsorption test. It was shown that Fe(III was adsorbed in alkaline conditions and adsorption increased with increasing Fe(III initial concentration from 5 to 20 ppm with capacity adsorption of 0.0069–0.019 mg/g.

  18. Kinetics and equilibrium adsorption study of lead(II) onto activated carbon prepared from coconut shell.

    Science.gov (United States)

    Sekar, M; Sakthi, V; Rengaraj, S

    2004-11-15

    Removal of lead from aqueous solutions by adsorption onto coconut-shell carbon was investigated. Batch adsorption experiments were performed to find out the effective lead removal at different metal ion concentrations. Adsorption of Pb2+ ion was strongly affected by pH. The coconut-shell carbon (CSC) exhibited the highest lead adsorption capacity at pH 4.5. Isotherms for the adsorption of lead on CSC were developed and the equilibrium data fitted well to the Langmuir, Freundlich, and Tempkin isotherm models. At pH 4.5, the maximum lead adsorption capacity of CSC estimated with the Langmuir model was 26.50 mg g(-1) adsorbent. Energy of activation (Ea) and thermodynamic parameters such as DeltaG, DeltaH, and DeltaS were evaluated by applying the Arrhenius and van't Hoff equations. The thermodynamics of Pb(II) on CSC indicates the spontaneous and endothermic nature of adsorption. Quantitative desorption of Pb(II) from CSC was found to be 75% which facilitates the sorption of metal by ion exchange.

  19. Preparation, characterization, and photocatalytic activity of La-doped TiO2 supported on activated carbon at the decomposition of methylene orange

    Science.gov (United States)

    Xing, Jun; Sun, Xiaogang; Qiu, Jingping

    2015-06-01

    A composite photocatalyst (La/TiO2/AC) has been prepared by supporting photoactive La-doped TiO2 (La/TiO2) on activated carbon (AC) via hydrolysis of tetrabutyl titanate (Ti(OC4H9)4) with La(NO3)3 · 6H2O and Ti(OC4H9)4 as precursors in the presence of activated carbon. The prepared photocatalysts were characterized by BET surface area, scanning electron microscopy (SEM), X-ray diffraction (XRD) and UV-vis absorption spectroscopy. The photocatalytic activities of the obtained photocatalysts under UV light are estimated by measuring the degradation rate of methylene orange in aqueous solution. The effect of La-doped content on the photocatalytic activity was studied and the result revealed that 0.2 mol % La/TiO2/AC exhibited highest photoactivity. In addition, the recyclability of the prepared photocatalyst was also confirmed, the photocatalytic activity of La/TiO2/AC remains about 86.5% of its activity as-prepared after being used four times. The photocatalyst therefore may be used as effective catalyst in photooxidation reactions and potentially applied for the treatment of water contaminated by organic pollutants.

  20. A comprehensive review on removal of arsenic using activated carbon prepared from easily available waste materials.

    Science.gov (United States)

    Mondal, Monoj Kumar; Garg, Ravi

    2017-05-01

    Arsenic contamination in water bodies is a serious problem and causes various health problems due to which US Environment Protection Agency (USEPA) set its maximum permissible limit of 10 ppb. The present review article starts with the removal of toxic arsenic using adsorbents prepared from easily available waste materials. Adsorbent either commercial or low-cost adsorbent can be used for arsenic removal but recent research was focused on the low-cost adsorbent. Preparation and activation of various adsorbents were discussed. Adsorption capacities, surface area, thermodynamic, and kinetics data of various adsorbents for As(III) and As(V) removal were compiled. Desorption followed by regeneration and reuse of adsorbents is an important step in adsorption and leads to economical process. Various desorbing and regenerating agents were discussed for arsenic decontamination from the adsorbent surface. Strong acids, bases, and salts are the main desorbing agents. Disposal of arsenic-contaminated adsorbent and arsenic waste was also a big problem because of the toxic and leaching effect of arsenic. So, arsenic waste was disposed of by proper stabilization/solidification (S/S) technique by mixing it in Portland cement, iron, ash, etc. to reduce the leaching effect.

  1. Adsorption of Lead (II from aqueous solutions onto activated carbon prepared from Algerian dates stones of Phoenix dactylifera.L (Ghars variety by H3PO4 activation

    Directory of Open Access Journals (Sweden)

    N. Chaouch

    2014-09-01

    Full Text Available Currently water pollution constitutes a great challenge, and activated carbon is a common adsorbent used to remove lead contaminants. Unfortunately, it is a non selective process. The main object of this study was the use of an activated carbon prepared from nuts of dates Algerian origin to remove this metal. The adsorption measurement of lead on activated carbon showed a real potential for removing this metal contaminants waste. The result showed also that the determination of lead remained dependent on some parameters such as pH, time contact, temperature and initial concentrations of metal. Adsorption data followed Freundlich model, they were better fitted by Langmuir isotherm as compared to Freundlich.

  2. Preparation of iron-impregnated granular activated carbon for arsenic removal from drinking water.

    Science.gov (United States)

    Chang, Qigang; Lin, Wei; Ying, Wei-chi

    2010-12-15

    Granular activated carbon (GAC) was impregnated with iron through a new multi-step procedure using ferrous chloride as the precursor for removing arsenic from drinking water. Scanning electron microscopy (SEM) and energy dispersive X-ray spectroscopy (EDS) analysis demonstrated that the impregnated iron was distributed evenly on the internal surface of the GAC. Impregnated iron formed nano-size particles, and existed in both crystalline (akaganeite) and amorphous iron forms. Iron-impregnated GACs (Fe-GACs) were treated with sodium hydroxide to stabilize iron in GAC and impregnated iron was found very stable at the common pH range in water treatments. Synthetic arsenate-contaminated drinking water was used in isotherm tests to evaluate arsenic adsorption capacities and iron use efficiencies of Fe-GACs with iron contents ranging from 1.64% to 12.13% (by weight). Nonlinear regression was used to obtain unbiased estimates of Langmuir model parameters. The arsenic adsorption capacity of Fe-GAC increased significantly with impregnated iron up to 4.22% and then decreased with more impregnated iron. Fe-GACs synthesized in this study exhibited higher affinity for arsenate as compared with references in literature and shows great potential for real implementations.

  3. Effective removal of tetracycline from aqueous solution using activated carbon prepared from tomato (Lycopersicon esculentum Mill.) industrial processing waste.

    Science.gov (United States)

    Sayğılı, Hasan; Güzel, Fuat

    2016-09-01

    Activated carbon (TAC) prepared under optimized conditions with ZnCl2 activation from a new precursor; tomato industrial processing waste (TW), was applied as an adsorbent to remove tetracycline (TC) from aqueous solution. The factors (TAC dosage, initial TC concentration, contact time, ionic strength and solution temperature) affecting the adsorption process were examined at natural pH (5.7) of TAC-TC system in aqueous solution. Kinetic data was found to be best complied by the pseudo-second order model. The isotherm analysis indicated that the equilibrium data could be represented by the Langmuir model. The maximum adsorption capacity was identified as 500.0mgg(-1) at 308K.

  4. Preparation of activated carbons from coffee husks utilizing FeCl3 and ZnCl2 as activating agents.

    Science.gov (United States)

    Oliveira, Luiz C A; Pereira, Elaine; Guimaraes, Iara R; Vallone, Andrea; Pereira, Márcio; Mesquita, João P; Sapag, Karim

    2009-06-15

    Ferric chloride was used as a new activating agent, to obtain activated carbons (AC) from agro industrial waste (coffee husks). This material was compared with two samples from the same raw material: one of them activated by using the classical activating agent, zinc chloride, and the other, activated with a mixture of the two mentioned activating agents in the same mass proportion. The carbonaceous materials obtained after the activation process showed high specific surface areas (BET), with values higher than 900 m(2)g(-1). It is interesting to observe that the activation with FeCl(3) produces smaller pores compared to the activation with ZnCl(2). An important fact to emphasize in the use of FeCl(3) as activating agent is the activation temperature at 280 degrees C, which is clearly below to the temperature commonly employed for chemical or physical activation, as described in the bibliography. All the studied materials showed different behaviors in the adsorption of methylene blue dye and phenol from aqueous solutions.

  5. An efficient visible-light photocatalyst prepared by modifying AgBr particles with a small amount of activated carbon

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Desong, E-mail: dswang06@126.com; Zhao, Mangmang; Luo, Qingzhi; Yin, Rong; An, Jing; Li, Xueyan

    2016-04-15

    Highlights: • An efficient visible-light photocatalyst was prepared by modifying AgBr particles. • A small amount of activated carbon was used to modify AgBr particles. • The modified AgBr exhibited improved visible-light photocatalytic performances. - Abstract: An efficient visible-light photocatalyst was successfully prepared by modifying AgBr particles with a small amount of activated carbon (AC) via a simple chemical precipitation approach. The AC/AgBr composite was characterized by X-ray diffraction, X-ray photoelectron spectroscopy, scanning electron microscopy, UV–vis diffuse reflection spectroscopy, photoluminescence spectroscopy, electrochemical impedance spectroscopy. The photocatalytic performances of the AC/AgBr composite were investigated by evaluating photodegradation of methyl orange (MO) and phenol under visible light irradiation, and the effects of the AC content in the composite, concentrations of AC/AgBr composite and MO, carrier scavengers on MO photodegradation rate were systematically investigated. The results indicated that the modification of AC can hardly change the crystalline and crystal size of AgBr particles, while significantly improve their specific surface areas, visible-light absorption and separation efficiency of photogenerated electron–hole pairs. Compared with pure AgBr, the AC/AgBr composite exhibited drastically enhanced visible-light photocatalytic activity and stability. The photogenerated electrons and holes, hydroxyl radicals are responsible to the photodegradation of organic pollutants, and the photogenerated holes are the main active species. On the basis of the results and the properties of AC and AgBr, the visible-light photocatalytic mechanism of the AC/AgBr composite was discussed.

  6. 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.

  7. Preparation and Characterization of Three-dimensional Photocatalyst-TiO2 Particulate Film Immobilized on Activated Carbon Fibers

    Institute of Scientific and Technical Information of China (English)

    傅平丰; 栾勇; 戴学刚; 张建强; 张安华

    2006-01-01

    A novel three-dimensional photocatalyst, TiO2 particulate film immobilized on activated carbon fibers (TiO2/ACFs),was prepared by liquid phase deposittion. The photocatalyst was characterized by SEM, XRD, BET surface area and photodegradation of methylene blue solution. TiO2 particulate film, with a thickness of nearly 200 nm and grain sizes of 30~50 nm, was deposited on almost each carbon fiber. The inner space between adjacent fibers remained as unmodified ACFs,therefore, both UV illumination and polluted solutions were allowed to pass through the felt-form photocatalyst to form a three-dimensional environment for photocatalytic reactions. With BET surface areas of 400~600 m2/g, the TiO2/ACFs exhibited an enhanced adsorption of pollutants for photocatalysis. Comparative degradations indicated that photocatalytic activity of the TiO2/ACFs was slightly higher than that of Degussa P-25 TiO2. Two special properties, the three-dimensional structure and combined effects of ACFs' adsorption and titania's photodegradation, made contribution to high photocatalytic activity. Additionally, the TiO2/ACFs exhibited high stability and potentially application for practical usage.

  8. Catalytic activity vs. size correlation in platinum catalysts of PEM fuel cells prepared on carbon black by different methods

    Energy Technology Data Exchange (ETDEWEB)

    Nores-Pondal, F.J.; Granada, M.; Corti, H.R. [Departamento de Fisica de la Materia Condensada, Centro Atomico Constituyentes, Comision Nacional de Energia Atomica (CNEA), General Paz 1499, 1650 San Martin, Buenos Aires (Argentina); Vilella, I.M.J.; de Miguel, S.R.; Scelza, O.A. [Instituto de Investigaciones en Catalisis y Petroquimica (INCAPE), Facultad de Ingenieria Quimica (Universidad Nacional del Litoral) - CONICET, Santiago del Estero 2654, 3000 Santa Fe (Argentina); Troiani, H. [Departamento de Fisica, Centro Atomico Bariloche, Comision Nacional de Energia Atomica (CNEA), Av. Bustillo 9500, 8400 San Carlos de Bariloche (Argentina)

    2009-10-15

    In this work nanoparticulated platinum catalysts have been prepared on carbon Vulcan XC-72 using three methods starting with chloroplatinic acid as a precursor: (i) formic acid as a reductor agent; (ii) impregnation method followed by reduction in hydrogen atmosphere at moderated temperature; and (iii) microwave-assisted reduction in ethylene glycol. The catalytic and size studies were also performed on a commercial Pt catalyst (E-Tek, De Nora). The characterization of the particle size and distribution was performed by means of transmission electron microscopy (TEM) and X-ray diffraction (XRD). The characterizations of the catalytic and electrocatalytic properties of the catalysts were determined by studying the cyclohexane dehydrogenation reaction (CHD) and the behavior under cyclic voltammetry (CV) in sulfuric acid solutions. The measured electrochemical activity, along with the hydrogen chemisorption of the catalysts allows the estimation of effective particle sizes, which are much larger than those measured by TEM and XRD. The catalysts prepared by reduction with formic acid and ethylene glycol (microwave-assisted) show electrochemical activities very close to those of the commercial catalyst, and are almost insensitive to the Pt dispersion or Pt particle size. The chemical activity in CHD correlates well with the metallic dispersion determined by hydrogen chemisorption, indicating similar accesibility of H{sub 2} and cyclohexane to the catalyst surface. (author)

  9. Porosity Evolution of Activated Carbon Fiber Prepared from Liquefied Wood. Part I: Water Steam Activation at 650 to 800 °C

    Directory of Open Access Journals (Sweden)

    Zhi Jin

    2014-03-01

    Full Text Available Activated carbon fiber is known as an excellent adsorbent material due to its well-developed pore structure. In this work, the porosity evolution of activated carbon fiber prepared from phenol liquefied wood with water steam activation at 650 to 800 °C for 20 to 260 min was examined by physical adsorption of N2 at -196 °C. By the series of activation processes, the specific surface area and pore volume were increased with the increase of activation time, most significantly by activation at 750 °C for 20 to 180 min and by activation at 800 °C for 20 to 260 min. The microporosity was gently and progressively developed with increasing activation time at 650 to 700 °C, while it was sharply developed at the early stage of activations at 750 to 800 °C, and then tended to almost stabilize. The mesoporosity was well developed only by activation at 800 °C for longer than 100 min. The pore size distributions were principally ultramicropores (0.5 - 0.7 nm during activations at 650 to 700 °C. By activations at 750 to 800 °C, the supermicropores (0.7 to 2.0 nm as well as mesopores (2 to 4 nm became progressively more important as the activation time was increased.

  10. Carbons prepared from Spartina alterniflora and its anaerobically digested residue by H3PO4 activation: characterization and adsorption of cadmium from aqueous solutions.

    Science.gov (United States)

    Wang, Zhengfang; Nie, Er; Li, Jihua; Zhao, Yongjun; Luo, Xingzhang; Zheng, Zheng

    2011-04-15

    Two series of activated carbons were prepared from Spartina alterniflora and from its anaerobically digested residue by H(3)PO(4) activation at various process conditions, and used as adsorbents for the removal of cadmium (II) in aqueous solutions. The surface areas and pore volumes of carbons were derived from adsorption isotherms (N(2) at 77K). The surface chemistry of carbons was investigated by infrared spectroscopy. Comparison study indicated that physicochemical properties of the activated carbons were strongly dependent not only on activation conditions but also on biopolymer contents of precursors. Several isotherm models were investigated and the adsorption isotherm data were best represented by the Langmuir isotherm model, with a maximum monolayer adsorption capacity of 47.85 mg/g at 25 °C. The results showed that the activated carbon produced from S. alterniflora could be employed as a promising adsorbent for removing cadmium (II) from aqueous solutions.

  11. Removal of malachite green from aqueous solution by activated carbon prepared from the epicarp of Ricinus communis by adsorption.

    Science.gov (United States)

    Santhi, T; Manonmani, S; Smitha, T

    2010-07-15

    The use of low-cost, locally available, highly efficient and eco-friendly adsorbents has been investigated as an ideal alternative to the current expensive methods of removing dyes from wastewater. This study investigates the potential use of activated carbon prepared from the epicarp of Ricinus communis for the removal of malachite green (MG) dye from simulated wastewater. The effects of different system variables, adsorbent dosage, initial dye concentration, pH and contact time were investigated and optimal experimental conditions were ascertained. The results showed that as the amount of the adsorbent increased, the percentage of dye removal increased accordingly. Optimum pH value for dye adsorption was 7.0. Maximum dye was sequestered within 50 min of the start of every experiment. The adsorption of malachite green followed the pseudo-second-order rate equation and fits the Langmuir, Freundlich, Dubinin-Radushkevich (D-R) and Tempkin equations well. The maximum removal of MG was obtained at pH 7 as 99.04% for adsorbent dose of 1 g 50 mL(-1) and 25 mg L(-1) initial dye concentration at room temperature. Activated carbon developed from R. communis can be an attractive option for dye removal from diluted industrial effluents since test reaction made on simulated dyeing wastewater showed better removal percentage of MG. 2010 Elsevier B.V. All rights reserved.

  12. Air-cathode preparation with activated carbon as catalyst, PTFE as binder and nickel foam as current collector for microbial fuel cells.

    Science.gov (United States)

    Cheng, Shaoan; Wu, Jiancheng

    2013-08-01

    A cathode is a critical factor that limits the practical application of microbial fuel cells (MFCs) in terms of cost and power generation. To develop a cost-effective cathode, we investigate a cathode preparation technique using nickel foam as a current collector, activated carbon as a catalyst and PTFE as a binder. The effects of the type and loading of conductive carbon, the type and loading of activated carbon, and PTFE loading on cathode performance are systematically studied by linear sweep voltammetry (LSV). The nickel foam cathode MFC produces a power density of 1190±50 mW m(-2), comparable with 1320 mW m(-2) from a typical carbon cloth Pt cathode MFC. However, the cost of a nickel foam activated carbon cathode is 1/30 of that of carbon cloth Pt cathode. The results indicate that a nickel foam cathode could be used in scaling up the MFC system.

  13. Adsorption of dissolved Reactive red dye from aqueous phase onto activated carbon prepared from agricultural waste.

    Science.gov (United States)

    Senthilkumaar, S; Kalaamani, P; Porkodi, K; Varadarajan, P R; Subburaam, C V

    2006-09-01

    The adsorption of Reactive red dye (RR) onto Coconut tree flower carbon (CFC) and Jute fibre carbon (JFC) from aqueous solution was investigated. Adsorption studies were carried out at different initial dye concentrations, initial solution pH and adsorbent doses. The kinetic studies were also conducted; the adsorption of Reactive red onto CFC and JFC followed pseudosecond-order rate equation. The effective diffusion coefficient was evaluated to establish the film diffusion mechanism. Quantitative removal of Reactive red dye was achieved at strongly acidic conditions for both the carbons studied. The adsorption isotherm data were fitted well to Langmuir isotherm and the adsorption capacity were found to be 181.9 and 200 mg/g for CFC and JFC, respectively. The overall rate of dye adsorption appeared to be controlled by chemisorption, in this case in accordance with poor desorption studies.

  14. Preparation of Pinewood- and Wheat Straw-based Activated Carbon via a Microwave-assisted Potassium Hydroxide Treatment and an Analysis of the Effects of the Microwave Activation Conditions

    Directory of Open Access Journals (Sweden)

    Haiyan Mao

    2014-12-01

    Full Text Available This study explored the effect of activated carbon preparation conditions on their adsorption performance. Pinewood and wheat straw were used as source materials to prepare activated carbon via a fast activation process using KOH and microwave heating. The iodine numbers and carbon yields were determined to evaluate the adsorption properties of the activated carbon. The effects of various KOH/char mass ratios, particle sizes, humidity levels, and microwave heating times on the physical characteristics of the activated carbon were investigated. The iodine number and yield and SEM images were used to characterize the activated carbon. Small particle sizes, the presence of humidity in the purge gas, and high KOH/char ratios resulted in higher iodine numbers. The best activated carbons were obtained using a KOH/char ratio of 3.0, a microwave power of 600 W, a radiation time of 30 min, and a particle size of 0.1 to 0.42 mm in a humid environment; these carbons showed iodine numbers of 2208 mg/g (pinewood activated carbon and 1420 mg/g (wheat straw activated carbon, with carbon yields of 73% and 52%, respectively. Longer microwave heating times increased the iodine number. The iodine numbers and yields of the pinewood activated carbons were much higher than those of their wheat straw counterparts.

  15. The effect of activated carbon support surface modification on characteristics of carbon nanospheres prepared by deposition precipitation of Fe-catalyst

    Science.gov (United States)

    Kristianto, H.; Arie, A. A.; Susanti, R. F.; Halim, M.; Lee, J. K.

    2016-11-01

    In this study the effect of activated carbon support modification to synthesis of CNSs was observed. Modification of activated carbon was done by using nitric acid. The effect of modification was analyzed from its FTIR spectra. The Fe catalysts were deposited on to the support by using urea deposition precipitation method at various initial catalysts concentration. CNSs was synthesized by utilizing cooking palm oil as renewable carbon source, and pyrolized at 700°C for 1 hour under nitrogen atmosphere. The products obtained then analyzed using SEM-EDS, TEM, XRD, and Raman spectroscopy. The modification of activated carbon support had increased the oxygen functional group. This increase resulted on increase of metal catalysts deposited on activated carbon surface. Peak of C (100) was observed, while ID/IG of samples were obtained around 0.9, which is commonly obtained for CNSs. High catalysts loading on modified activated carbon support caused decomposition of CNSs and formation carbon onion.

  16. Batch and fixed-bed adsorption of tartrazine azo-dye onto activated carbon prepared from apricot stones

    Science.gov (United States)

    Albroomi, H. I.; Elsayed, M. A.; Baraka, A.; Abdelmaged, M. A.

    2017-07-01

    This work describes the potential of utilizing prepared activated carbon from apricot stones as an efficient adsorbent material for tartrazine (TZ) azo-dye removal in a batch and dynamic adsorption system. The results revealed that activated carbons with well-developed surface area (774 m2/g) and pore volume (1.26 cm3/g) can be manufactured from apricot stones by H3PO4 activation. In batch experiments, effects of the parameters such as initial dye concentration and temperature on the removal of the dye were studied. Equilibrium was achieved in 120 min. Adsorption capacity was found to be dependent on the initial concentration of dye solution, and maximum adsorption was found to be 76 mg/g at 100 mg/L of TZ. The adsorption capacity at equilibrium ( q e) increased from 22.6 to 76 mg/g with an increase in the initial dye concentrations from 25 to 100 mg/L. The thermodynamic parameters such as change in free energy (Δ G 0), enthalpy (Δ H 0) and entropy (Δ S 0) were determined and the positive value of (Δ H) 78.1 (K J mol-1) revealed that adsorption efficiency increased with an increase in the process temperature. In fixed-bed column experiments, the effect of selected operating parameters such as bed depth, flow rate and initial dye concentration on the adsorption capacity was evaluated. Increase in bed height of adsorption columns leads to an extension of breakthrough point as well as the exhaustion time of adsorbent. However, the maximum adsorption capacities decrease with increases of flow rate. The breakthrough data fitted well to bed depth service time and Thomas models with high coefficient of determination, R 2 ≥ 94.

  17. Batch and fixed-bed adsorption of tartrazine azo-dye onto activated carbon prepared from apricot stones

    Science.gov (United States)

    Albroomi, H. I.; Elsayed, M. A.; Baraka, A.; Abdelmaged, M. A.

    2016-02-01

    This work describes the potential of utilizing prepared activated carbon from apricot stones as an efficient adsorbent material for tartrazine (TZ) azo-dye removal in a batch and dynamic adsorption system. The results revealed that activated carbons with well-developed surface area (774 m2/g) and pore volume (1.26 cm3/g) can be manufactured from apricot stones by H3PO4 activation. In batch experiments, effects of the parameters such as initial dye concentration and temperature on the removal of the dye were studied. Equilibrium was achieved in 120 min. Adsorption capacity was found to be dependent on the initial concentration of dye solution, and maximum adsorption was found to be 76 mg/g at 100 mg/L of TZ. The adsorption capacity at equilibrium (q e) increased from 22.6 to 76 mg/g with an increase in the initial dye concentrations from 25 to 100 mg/L. The thermodynamic parameters such as change in free energy (ΔG 0), enthalpy (ΔH 0) and entropy (ΔS 0) were determined and the positive value of (ΔH) 78.1 (K J mol-1) revealed that adsorption efficiency increased with an increase in the process temperature. In fixed-bed column experiments, the effect of selected operating parameters such as bed depth, flow rate and initial dye concentration on the adsorption capacity was evaluated. Increase in bed height of adsorption columns leads to an extension of breakthrough point as well as the exhaustion time of adsorbent. However, the maximum adsorption capacities decrease with increases of flow rate. The breakthrough data fitted well to bed depth service time and Thomas models with high coefficient of determination, R 2 ≥ 94.

  18. 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.

  19. Silver nanoparticles-loaded activated carbon fibers using chitosan as binding agent: Preparation, mechanism, and their antibacterial activity

    Science.gov (United States)

    Tang, Chengli; Hu, Dongmei; Cao, Qianqian; Yan, Wei; Xing, Bo

    2017-02-01

    The effective and strong adherence of silver nanoparticles (AgNPs) to the substrate surface is pivotal to the practical application of those AgNPs-modified materials. In this work, AgNPs were synthesized through a green and facile hydrothermal method. Chitosan was introduced as the binding agent for the effective loading of AgNPs on activated carbon fibers (ACF) surface to fabricate the antibacterial material. Apart from conventional instrumental characterizations, i. e., scanning electron microscope (SEM), X-ray diffraction (XRD), Fourier Transform Infrared Spectroscopy (FT-IR), zeta potential and Brunauer-Emmett-Teller (BET) surface area measurement, molecular dynamics simulation method was also applied to explore the loading mechanism of AgNPs on the ACF surface. The AgNPs-loaded ACF material showed outstanding antibacterial activity for S. aureus and E. coli. The combination of experimental and theoretical calculation results proved chitosan to be a promising binding agent for the fabrication of AgNPs-loaded ACF material with excellent antibacterial activity.

  20. Preparation of N-doped ultramicropore-containing active carbons from waste soybean dreg by one-step carbonization/activation%炭活化一步法制备豆渣基极微孔活性炭

    Institute of Scientific and Technical Information of China (English)

    李大伟; 田原宇; 郝俊辉; 田斌; 李俊花; 车远军

    2015-01-01

    So far, some studies have been conducted on preparation of nitrogen-doped (N-doped) active carbon from N-containing biomasses using alkalis as activators. In these studies, the commonly used preparation method was activation with alkali after biomass carbonization. Compared with this method, the one-step carbonization/activation method was simple and apt to reduce energy consumption, but its application in the preparation of N-doped active carbon was not investigated. In this research, N-doped active carbon with ultramicropores was prepared from waste soybean dreg using K2CO3 as activator via one-step carbonization/activation technology. The effects of activation temperature on chemical composition, pore structure, and low-pressure CO2 adsorption performances of the active carbon were investigated. To prepare active carbon, waste soybean dreg with particle size of 0.15-0.90 mm was impregnated with K2CO3 aqueous solution at K2CO3/dreg dry-basis weight ratio of 2:1, and after mixing uniformly, the mixture was sealed and kept for 4 h. Then, it was dried in an oven at 110℃ till constant weight was achieved. Subsequently, the dried mixture was heated to 500-650℃ at an average heating rate of 6℃/minand then kept for 75 min. Afterwards, the heated mixture was washed with distilled water until the pH value reached about neutral, and then dried at 110℃ for 12 h to produce active carbon. The obtained samples were subsequently characterized; pore structure and CO2 adsorption performance were measured with volumetric adsorption analyzers, elemental composition was measured with an elemental analyzer, surface chemistry was measured with an X-ray photoelectron spectroscopy, and surface morphology was measured with a scanning electron microscope (SEM) and a transmission electron microscope (TEM). To gain an insight into the mechanism of pore formation, the soybean dreg and K2CO3-impregnated soybean dreg were pyrolyzed and analyzed using a thermogravimetric analyzer

  1. Preparation of ultrafine magnetic biochar and activated carbon for pharmaceutical adsorption and subsequent degradation by ball milling

    Science.gov (United States)

    Shan, Danna; Deng, Shubo; Zhao, Tianning; Wang, Bin; Wang, Yujue; Huang, Jun; Yu, Gang; Winglee, Judy; Wiesner, Mark R.

    2017-01-01

    Ball milling was used to prepare two ultrafine magnetic biochar/Fe3O4 and activated carbon (AC)/Fe3O4 hybrid materials targeted for use in pharmaceutical removal by adsorption and mechanochemical degradation of pharmaceutical compounds. Both hybrid adsorbents prepared after 2 hours milling exhibited high removal of carbamazepine (CBZ), and were easily separated magnetically. These adsorbents exhibited fast adsorption of CBZ and tetracycline (TC) in the initial 1 hour. The biochar/Fe3O4 had a maximum adsorption capacity of 62.7 mg/g for CBZ and 94.2 mg/g for TC, while values obtained for AC/Fe3O4 were 135.1 mg/g for CBZ and 45.3 mg/g for TC respectively when data were fitted using the Langmuir expression. Solution pH values slightly affected the sorption of TC on the adsorbents, while CBZ sorption was almost pH-independent. The spent adsorbents with adsorbed CBZ and TC were milled to degrade the adsorbed pollutants. The adsorbed TC itself was over 97% degraded after 3 hours of milling, while about half of adsorbed CBZ were remained. The addition of quartz sand was found to improve the mechanochemical degradation of CBZ on biochar/Fe3O4, and its degradation percent was up to 98.4% at the dose of 0.3 g quarts sand/g adsorbent. This research provided an easy method to prepare ultrafine magnetic adsorbents for the effective removal of typical pharmaceuticals from water or wastewater and degrade them using ball milling. PMID:26685062

  2. Preparation of ultrafine magnetic biochar and activated carbon for pharmaceutical adsorption and subsequent degradation by ball milling.

    Science.gov (United States)

    Shan, Danna; Deng, Shubo; Zhao, Tianning; Wang, Bin; Wang, Yujue; Huang, Jun; Yu, Gang; Winglee, Judy; Wiesner, Mark R

    2016-03-15

    Ball milling was used to prepare two ultrafine magnetic biochar/Fe3O4 and activated carbon (AC)/Fe3O4 hybrid materials targeted for use in pharmaceutical removal by adsorption and mechanochemical degradation of pharmaceutical compounds. Both hybrid adsorbents prepared after 2h milling exhibited high removal of carbamazepine (CBZ), and were easily separated magnetically. These adsorbents exhibited fast adsorption of CBZ and tetracycline (TC) in the initial 1h. The biochar/Fe3O4 had a maximum adsorption capacity of 62.7mg/g for CBZ and 94.2mg/g for TC, while values obtained for AC/Fe3O4 were 135.1mg/g for CBZ and 45.3mg/g for TC respectively when data were fitted using the Langmuir expression. Solution pH values slightly affected the sorption of TC on the adsorbents, while CBZ sorption was almost pH-independent. The spent adsorbents with adsorbed CBZ and TC were milled to degrade the adsorbed pollutants. The adsorbed TC itself was over 97% degraded after 3h of milling, while about half of adsorbed CBZ were remained. The addition of quartz sand was found to improve the mechanochemical degradation of CBZ on biochar/Fe3O4, and its degradation percent was up to 98.4% at the dose of 0.3g quarts sand/g adsorbent. This research provided an easy method to prepare ultrafine magnetic adsorbents for the effective removal of typical pharmaceuticals from water or wastewater and degrade them using ball milling.

  3. Preparation of hollow spherical carbon nanocages

    Energy Technology Data Exchange (ETDEWEB)

    Tsai, C.-K.; Kang, H. Y.; Hong, C.-I; Huang, C.-H.; Chang, F.-C.; Wang, H. Paul, E-mail: wanghp@mail.ncku.edu.tw [National Cheng Kung University, Department of Environmental Engineering, Taiwan (China)

    2012-12-15

    This study presents a new and simple method for the synthesis of hollow carbon spheres possessing nanocage sizes of 7.1, 14, and 20 nm in diameter. The core-shell (i.e., Cu-C) nanoparticles prepared by carbonization of the Cu{sup 2+}-cyclodextrin (CD) complexes at 573 K for 2 h was etched with HCl (6N) to yield the hollow carbon spheres. The carbon-shell of the hollow carbon nanospheres, which consisted of mainly diamond-like and graphite carbons, is not perturbed during etching. In addition to the nanocages, the hollow carbon nanospheres also possess micropores with an opening of 0.45 nm, allowing small molecules to diffuse in and out through the carbon-shell. Many elements (such as Zn{sup 2+} or Cu{sup 2+}) can therefore be filled into the nanocages of the hollow carbon nanospheres. With these unique properties, for instance, designable active species such as Cu and ZnO encapsulated in the carbon-shell can act as Cu-ZnO-C yolk-shell nanoreactors which are found very effective in the catalytic decomposition of methanol.

  4. 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.

  5. Removal of malachite green from aqueous solution by activated carbon prepared from the Annona squmosa seed by adsorption

    Directory of Open Access Journals (Sweden)

    T. Santhi

    2010-12-01

    Full Text Available The use of low -cost, locally available, highly efficient and eco-friendly adsorbents has been investigated as an ideal alternative to the current expensive methods of removing dyes from wastewater. This study investigates the potential use of activated carbon prepared from the Annona squmosa seed for the removal of malachite green (MG dye from simulated wastewater. The effects of different system variables, adsorbent dosage, initial dye concentration, pH and contact time were investigated and optimal experimental conditions were ascertained. The results showed that as the amount of the adsorbent is increased, the percentage of dye removal increase accordingly. Optimum pH value for dye adsorption was 7.0. Maximum dye was sequestered within 50 min from the start of every experiment. The adsorption of malachite green followed the pseudo-second –order rate equation and fits the Langmuir, Freundlich, Dubinin-Radushekevich (D-R and Tempkin equations well. The maximum removal of MG was obtained at pH 7 as 86.11% for adsorbent dose of 0.2 g/ 50 mL and 25 mg L -1 initial dye concentration at room temperature. Furthermore, adsorption kinetics of MG was studied and the rate of adsorption was found to conform to pseudo-second –order kinetics with a good correlation (R2 > 0.99 with intraparticle diffusion as one of the rate determining steps. Activated carbon developed from the Annona squmosa seed can be an attractive option for dye removal from diluted industrial effluents since test reaction made on simulated dyeing wastewater showed better removal percentage of MG.

  6. REMOVAL OF METHYLENE BLUE FROM AQUEOUS SOLUTION BY ACTIVATED CARBON PREPARED FROM THE PEEL OF CUCUMIS SATIVA FRUIT BY ADSORPTION

    Directory of Open Access Journals (Sweden)

    Manonmani Subbian

    2010-02-01

    Full Text Available The use of low-cost, locally available, highly efficient, and eco-friendly adsorbents has been investigated as an ideal alternative to the current expensive methods of removing dyes from wastewater. This study investigates the potential use of activated carbon prepared from the peel of Cucumis sativa fruit for the removal of methylene blue (MB dye from simulated wastewater. The effects of different system variables, adsorbent dosage, initial dye concentration, pH, and contact time were investigated, and optimal experimental conditions were ascertained. The results showed that as the amount of the adsorbent increased, the percentage of dye removal increased accordingly. The optimum pH for dye adsorption was 6.0. Maximum dye was sequestered within 50 min of the start of each experiment. The adsorption of methylene blue followed the pseudo-second-order rate equation and fit the Langmuir, Freundlich, Dubinin-Radushekevich (D-R, and Tempkin equations well. Maximum removal of MB was obtained at pH 6 as 99.79% for adsorbent doses of 0.6 g/ 50 mL and 25 mg/L initial dye concentrations at room temperature. The maximum adsorption capacity obtained from the Langmuir equation was 46.73 mg g-1. The rate of adsorption was found to conform to pseudo-second-order kinetics with a good correlation (R2 > 0.9677 with intraparticle diffusion as one of the rate-determining steps. Activated carbon developed from the peel of Cucumis sativa fruit can be an attractive option for dye removal from wastewater.

  7. 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)

  8. Effect of Pre-oxidation on the Properties of Crushed Bituminous Coal and Activated Carbon Prepared Therefrom

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    The influence of a pre-oxidation process on the chemical properties of crushed bituminous coal and on adsorption properties of the subsequently formed char and activated carbon is discussed in this paper.Datong bituminous coal samples sized 6 mm were oxidized at different temperatures and for different times and then carbonized and activated by steam to obtain activated carbons.A Uniform Design method was used to arrange the experiments, IR and adsorption experiments were used to characterize these oxidized coals, chars and activated carbon samples.The results show that the carboxyl group disappeared and α-CH2 groups joined to alkenes decreased dramatically but the carbonyl group clearly increased in the coal sample oxidized at 543 K; The chemical composition of coal samples oxidized at lower temperature is different from that of coal oxidized at 543 K.Oxidizing coal samples at higher temperatures for a short time or at lower temperatures for a longer time resulted in activated carbon samples that tended toward the same adsorption properties: Iodine number 1100 mg/g and Methylene blue value 252 mg/g.The yield of activated carbon obtained from the pre-oxidized coal is 10% higher than the yield from parent coal but the activated carbons have the same adsorption properties.

  9. Preparation of TiO2/Activated Carbon Composites for Photocatalytic Degradation of RhB under UV Light Irradiation

    Directory of Open Access Journals (Sweden)

    Baolin Xing

    2016-01-01

    Full Text Available Photocatalysts comprising nanosized TiO2 particles on activated carbon (AC were prepared by a sol-gel method. The TiO2/AC composites were characterized by X-ray diffraction (XRD, thermogravimetric (TG analysis, nitrogen adsorption, scanning electron microscope (SEM, transmission electron microscope (TEM, and energy dispersive X-ray (EDX. Their photocatalytic activities were studied through the degradation of Rhodamine B (RhB in photocatalytic reactor at room temperature under ultraviolet (UV light irradiation and the effect of loading cycles of TiO2 on the structural properties and photocatalytic activity of TiO2/AC composites was also investigated. The results indicate that the anatase TiO2 particles with a crystal size of 10–20 nm can be deposited homogeneously on the AC surface under calcination at 500°C. The loading cycle plays an important role in controlling the loading amount of TiO2 and morphological structure and photocatalytic activity of TiO2/AC composites. The porosity parameters of these composite photocatalysts such as specific surface area and total pore volume decrease whereas the loading amount of TiO2 increases. The TiO2/AC composite synthesized at 2 loading cycles exhibits a high photocatalytic activity in terms of the loading amount of TiO2 and as high as 93.2% removal rate for RhB from the 400 mL solution at initial concentration of 2 × 10−5 mol/L under UV light irradiation.

  10. Preparation and characterization of activated carbon from the char produced in the thermolysis of granulated scrap tyres.

    Science.gov (United States)

    López, F A; Centeno, T A; Rodríguez, O; Alguacil, E J

    2013-05-01

    The char produced in the thermolysis of granulated scrap tyres has few market outlets, reducing the economic viability of the thermolytic process. This paper reports the potential of this char as a low-cost precursor of porous carbons. The tyre-derived char was demineralized in either alkaline or acidic media to reduce its ash, zinc, sulfur, and silica contents. The lowest impurity content was achieved with an HNO3/H2O treatment. The resulting demineralized char was then subjected to activation by KOH or CO2. The Brunauer-Emmett-Teller (BET)-specific surface area of the activated carbon produced by the KOH treatment was 242 m2/g, whereas that of the CO2-activated carbon was 720 m2/g. The textural properties of the latter product were similar to those of some commercial activated carbons. The use of tyre-derived char as a precursor of porous carbons could render the thermolytic treatment of scrap tyres more economically attractive. Char produced in thermolysis of granulated scrap tyres has a few market outlets; in this paper an alternative for its use is presented. The char was converted into activated carbon with textural properties similar to those of some commercial activated carbons. This process could render the thermolytic treatment of scrap tyres more economically attractive.

  11. Utilization of various agricultural wastes for activated carbon preparation and application for the removal of dyes and metal ions from aqueous solutions.

    Science.gov (United States)

    Kadirvelu, K; Kavipriya, M; Karthika, C; Radhika, M; Vennilamani, N; Pattabhi, S

    2003-03-01

    Activated carbons were prepared from the agricultural solid wastes, silk cotton hull, coconut tree sawdust, sago waste, maize cob and banana pith and used to eliminate heavy metals and dyes from aqueous solution. Adsorption of all dyes and metal ions required a very short time and gave quantitative removal. Experimental results show all carbons were effective for the removal of pollutants from water. Since all agricultural solid wastes used in this investigation are freely, abundantly and locally available, the resulting carbons are expected to be economically viable for wastewater treatment.

  12. 脱汞载硫活性炭的制备及表征%Preparation and Characterization of Sulfur-loaded Activated Carbon for Mercury Removal

    Institute of Scientific and Technical Information of China (English)

    范莉莉; 刘晓玲; 刘霞

    2016-01-01

    In this paper, the preparation of sulfur-loaded activated carbon was studied,Taixi Coal Based-Activated Carbon used as the carrier. Some factors were discussed such as the carbon tetrachloride adsorption, S/C and dipping time on the influence of amount of sulfur. Meantime the structure of the prepared carrier was characterized by BET. The results showed that:when the carbon tetrachloride adsorption value was 60%, S/C was 14%, and the time was 24h, the sulfur content of the prepared activated carbon was 10.89%, and the solvent recovery rate was 90%.%本文以太西煤基活性炭为载体,研究了载硫活性炭的制备工艺,并探讨了四氯化碳吸附值、S/C和浸渍时间对载硫量的影响,同时采用BET表征对制备的载硫体的结构进行了表征。结果表明:当四氯化碳吸附值为60%,S/C为14%,浸渍时间为24h时,所制备的载硫活性炭载硫量最高为10.89%,且溶剂回收率高达90%。

  13. Preparation and Characterization of Nano-TiO2 Loaded Bamboo-based Activated Carbon Fibers by H2O Activation

    Directory of Open Access Journals (Sweden)

    Dongna Li

    2013-12-01

    Full Text Available As the support for loading TiO2, bamboo-based activated carbon fibers (BACFs were obtained from Phyllostachys pubescens Mazel after liquefaction using phenol, melt-spinning, curing carbonization, and H2O activation. TiO2/BACFs were prepared by the sol–gel method and characterized by SEM, XRD, FTIR, and XPS. Anatase TiO2 film with high photocatalytic activity was formed on the surface of BACFs, and the average crystallite size of the TiO2 film was 17 to 30 nm. The characteristic absorbance peaks of anatase TiO2 were observed at 1402 and 541 to 605 cm-1 on the infrared spectrum of TiO2/BACFs. The surface of TiO2/BACFs was mainly comprised of C–C, C–O, C=O, and Ti-O bonds. With increased calcination temperature, the contents of element Ti and Ti-O bonds of lattice oxygen on the surface of TiO2/BACFs increased and then decreased. The degradation rate of TiO2/BACFs for methylene blue (MB solution reached more than 98% after 7 h of UV illumination.

  14. Adsorption Studies of Coconut Shell Carbons Prepared by KOH Activation for Removal of Lead(II From Aqueous Solutions

    Directory of Open Access Journals (Sweden)

    Chengwen Song

    2013-12-01

    Full Text Available Removal of Pb2+ from aqueous solutions using coconut shell carbons produced by KOH activation is performed in this paper. Morphology and pore structure characteristic of coconut shell carbons are analyzed by SEM and nitrogen adsorption techniques. Effects of adsorbent concentration, agitation time and initial ion concentration on the adsorption behavior are investigated, and adsorption isotherm and kinetics on coconut shell carbons are also studied. The results show that high weight ratio of KOH/sample is favorable to produce rich porous structure. The resultant coconut shell carbons with a high specific surface area of 1135 m2/g is obtained and demonstrates good adsorption potential on removal of Pb2+ from aqueous solutions. Adsorption data fit well with Freundlich and Halsey isotherms. The kinetic studies indicate that adsorption behavior can be described by pseudo-second-order kinetic model, which also follows external diffusion and intra-particle diffusion in the adsorption process.

  15. 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.

  16. Preparation and textural characterisation of activated carbon from vine shoots ( Vitis vinifera) by H 3PO 4—Chemical activation

    Science.gov (United States)

    Corcho-Corral, B.; Olivares-Marín, M.; Fernández-González, C.; Gómez-Serrano, V.; Macías-García, A.

    2006-06-01

    An abundant and low-cost agricultural waste as vine shoots ( Vitis vinifera) (VS), which is generated by the annual pruning of vineyards, has been used as raw material in the preparation of powder activated carbon (AC) by the method of chemical activation with phosphoric acid. After size reduction, VS were impregnated for 2 h with 60 wt.% H 3PO 4 solution at room temperature, 50 and 85 °C. The three impregnated products were carbonised at 400 °C. The product impregnated at 50 °C was heated either first at 150-250 °C and then at 400 °C or simply at 350-550 °C in N 2 atmosphere. The time of isothermal treatment after each dynamic heating was 2 h. The carbons were texturally characterised by gas adsorption (N 2, -196 °C), mercury porosimetry, and density measurements. FT-IR spectroscopy was also applied. Better developments of surface area and microporosity are obtained when the impregnation of VS with the H 3PO 4 solution is effected at 50 °C and for the products heated isothermally at 200 and 450 °C. The mesopore volume is also usually higher for the products impregnated and heated at intermediate temperatures.

  17. Study on preparation of water hyacinth-based activated carbon for pulp and paper mill wastewater treatment.

    Science.gov (United States)

    Boonpoke, Anusorn

    2015-09-01

    Mulberry pulp and paper mills produce high chemical- and organic matter containing waste water in Thailand. Many of the mills are not equipped with wastewater treatment unit; their untreated effluent is directly discharged into recipient water resources. The effluent constituents are well recognized as acute and chronic pollutants that are hazardous to the environment. The present study aimed to investigate the utilization of an activated carbon from a low-cost material and to examine its adsorption performance using batch and fixed-bed adsorption. Water hyacinth was used as a raw material for activated carbon production via a chemical activation method. The results showed that water hyacinth-based activated carbon (WHAC) provided a high surface area of 912-1,066 m2g(-1) and exhibited micropore structure. Based on the Freundlich fit, the maximum adsorption capacity of COD and color was 4.52 mgg(-1) and 13.57 Pt-Cog(-1), respectively. The fixed bed adsorption provided maximum removal efficiency of 91.70 and 92.62% for COD and color, respectively. A continuous adsorption data agreed well with the Thomas kinetic model. In summary, water hyacinth can be used as a low-cost material for activated carbon production with high removal efficiency of COD and color for pulp and paper mill wastewater treatment.

  18. Mesoporous-activated carbon prepared from chitosan flakes via single-step sodium hydroxide activation for the adsorption of methylene blue.

    Science.gov (United States)

    Marrakchi, F; Ahmed, M J; Khanday, W A; Asif, M; Hameed, B H

    2017-05-01

    In this work, mesoporous-activated carbon (CSAC) was prepared from chitosan flakes (CS) via single-step sodium hydroxide activation for the adsorption of methylene blue (MB). CSAC was prepared using different impregnation ratios of NaOH:CS (1:1, 2:1, 3:1, and 4:1) at 800°C for 90min. The adsorption performance of CSAC was evaluated for MB at different adsorption variables, such MB initial concentrations (25-400mg/L), solution pH (3-11), and temperature (30-50°C). The adsorption isotherm data of CSAC-MB were well fitted to Langmuir model with a maximum adsorption capacity 143.53mg/g at 50°C. Best representation of kinetic data was obtained by the pseudo-second order model. CSAC exhibited excellent adsorption uptake for MB and can potentially be used for other cationic dyes. Copyright © 2017 Elsevier B.V. All rights reserved.

  19. Preparation of Co-Mo catalyst using activated carbon produced from egg shell and SiO2 as support – A hydrogenation study

    Directory of Open Access Journals (Sweden)

    Adeniyi Sunday Ogunlaja

    2010-12-01

    Full Text Available The preparation of a series of cobalt-molybdenum (Co-Mo catalysts supported on SiO2 and carbonized egg shells were investigated using standard procedures; the catalysts were further calcined at the 500 oC temperature to generate the internally consistent set, and the metal atoms content were varied in a regular manner. The ratio 1:4 (Co2+: Mo6+ by weight was employed for the various catalysts prepared. The carbonized egg shells were divided into two parts: the first part was leached with HNO3, as the other one was not leached. Activity tests were run using these catalysts containing leached and unleached carbon for the hydrogenation of methyl orange; the changes in absorbance regarding the unhydrogenated methyl orange at a wavelength of 460 nm were respectively 0.07 and 0.067 when the catalyst containing the leached carbonized egg shell (catalyst A and the catalyst containing the unleached activated carbon (catalyst B were used for the hydrogenation reaction. This confirms that catalyst A is more efficient in hydrogenating methyl orange than catalyst B.

  20. Preparation of nitrogen-doped graphene/activated carbon composite papers to enhance energy storage in supercapacitors

    Science.gov (United States)

    Li, Yong-feng; Liu, Yan-zhen; Liang, Yu; Guo, Xiao-hui; Chen, Cheng-meng

    2017-09-01

    This report presents a facile and effective method to synthesize freestanding nitrogen-doped reduced graphene oxide (rGO)/activated carbon (AC) composite papers for supercapacitors by a method combining vacuum filtration with post-annealing in NH3 atmosphere. The effect of activated carbon contents on the microstructure and capacitive behavior of the resulting composite papers before and after the annealing was investigated by X-ray diffraction, scanning electron microscopy, and Raman and X-ray photoelectron spectroscopy. Results show that the composite paper with a 30% activated carbon loading has a high nitrogen content of 14.6 at% and superior capacitive performance (308 F/g, 1 A/g) to the other composite papers with various activated carbon loadings. Nitrogen was doped and GO reduced during the annealing. The rGO nanosheets acted as a framework, and the AC particles served as spacers to avoid agglomeration of graphene sheets. The high capacitance of the composite paper is ascribed to the electric double-layer behavior and the reversible redox reactions of the nitrogen and oxygen groups. The entire process is simple, environmental friendly and easily scalable for mass production.

  1. The differences of electrochemical performance between the purchased lead carbonate and the prepared lead carbonate

    Institute of Scientific and Technical Information of China (English)

    包有富

    2005-01-01

    The differences of electrochemistry performance between the purchased lead carbonate and the prepared lead carbonate were studied by the methods of cycle voltammogram, electrochemical impedance spectroscope (EIS), constant current discharge, thermal gravimetric analysis, and scan electron microscope (SEM) etc. in the paper. It was showed that the reacting activity of the prepared lead carbonate was higher than that of the purchased lead carbonate. And several points of view were concluded as follows. (1) The prepared lead carbonate contains chemical structure water, but the purchased lead carbonate doesn't contain chemical structure water. (2) The main chemical substance in the purchased lead carbonate powder is PbCO3, while the one in the prepared lead carbonate is smaller than that of the pur-chased lead carbonate.

  2. Kinetic, equilibrium and thermodynamic studies of synthetic dye removal using pomegranate peel activated carbon prepared by microwave-induced KOH activation

    Directory of Open Access Journals (Sweden)

    Mohd Azmier Ahmad

    2014-08-01

    Full Text Available Pomegranate peel was converted into activated carbon using microwave induced and KOH activation techniques. The prepared activated carbon (PPAC was characterized using FTIR, TGA, SEM, and nitrogen-adsorption surface area (BET. BET measurements gave remarkable increase in both the surface area (941.02 m2/g and total pore volume (0.470 cm3/g. Various operational parameters such as pH, initial dye concentration, contact time and solution temperature in batch systems were investigated on the use of PPAC in the adsorption of remazol brilliant blue reactive (RBBR dye. At pH 2, the optimum dye removal was 94.36%. The amount of dye removed was dependent on initial dye concentration and solution temperature. Adsorption kinetics was found to follow pseudo-second-order kinetic model. Experimental data were analyzed using eight model equations: Langmuir, Freundlich, Temkin, Dubinin–Radushkevich, Radke Prausnite, Sips, Viet–Sladek and Brouers – Sotolongo isotherms and it was found that the Freundlich isotherm model fitted the adsorption data most with the highest correlation (R2≥0.99 and lowest normalized standard deviation, ∆qe. Both intra-particle and film diffusion governed the adsorption process. Thermodynamic parameters, such as standard Gibbs free energy (∆G0, standard enthalpy (∆H0, standard entropy (∆S0, and the activation energy (Ea were calculated. The adsorption of RBBR dye onto PPAC was found to be spontaneous and exothermic in nature. This study shows that the adsorption follows physisorption mechanism.

  3. The influence of oxidation with nitric acid on the preparation and properties of active carbon enriched in nitrogen

    Energy Technology Data Exchange (ETDEWEB)

    Pietrzak, Robert [Laboratory of Coal Chemistry and Technology, Faculty of Chemistry, Adam Mickiewicz University, Grunwaldzka 6, 60-780 Poznan (Poland)], E-mail: pietrob@amu.edu.pl; Nowicki, Piotr; Wachowska, Helena [Laboratory of Coal Chemistry and Technology, Faculty of Chemistry, Adam Mickiewicz University, Grunwaldzka 6, 60-780 Poznan (Poland)

    2009-01-01

    The effect of oxidation by 20% nitric acid on the properties and performance of active carbons enriched with nitrogen by means of the reaction with urea in the presence of air has been studied. The study has been made on demineralised orthocoking coal and the carbonisates obtained from it at 600 or 700 deg. C, subjected to the processes of nitrogenation, oxidation and activation with KOH in different sequences. The amount of nitrogen introduced into the carbon with the aid of urea has been found to depend on the stage at which the process of nitrogenation was performed. The process of oxidation of the demineralised coal and the active carbon obtained from the former has been found to favour nitrogen introduction into the carbon structure. In the process of nitrogenation of the carbonisates the amount of nitrogen introduced has inversely depended on the temperature of carbonisation. The modifications of the processes permitted obtaining materials of different textural parameters, different acid-base character of the surface and different iodine sorption capacity.

  4. TiO2 Immobilized on Manihot Carbon: Optimal Preparation and Evaluation of Its Activity in the Decomposition of Indigo Carmine

    Directory of Open Access Journals (Sweden)

    Cynthia M. Antonio-Cisneros

    2015-01-01

    Full Text Available Applications of carbon-TiO2 materials have attracted attention in nanotechnology due to their synergic effects. We report the immobilization of TiO2 on carbon prepared from residues of the plant Manihot, commercial TiO2 and glycerol. The objective was to obtain a moderate loading of the anatase phase by preserving the carbonaceous external surface and micropores of the composite. Two preparation methods were compared, including mixing dry precursors and immobilization using a glycerol slurry. The evaluation of the micropore blocking was performed using nitrogen adsorption isotherms. The results indicated that it was possible to use Manihot residues and glycerol to prepare an anatase-containing material with a basic surface and a significant SBET value. The activities of the prepared materials were tested in a decomposition assay of indigo carmine. The TiO2/carbon eliminated nearly 100% of the dye under UV irradiation using the optimal conditions found by a Taguchi L4 orthogonal array considering the specific surface, temperature and initial concentration. The reaction was monitored by UV-Vis spectrophotometry and LC-ESI-(Qq-TOF-MS, enabling the identification of some intermediates. No isatin-5-sulfonic acid was detected after a 60 min photocatalytic reaction, and three sulfonated aromatic amines, including 4-amino-3-hydroxybenzenesulfonic acid, 2-(2-amino-5-sulfophenyl-2-oxoacetic acid and 2-amino-5-sulfobenzoic acid, were present in the reaction mixture.

  5. TiO2 immobilized on Manihot carbon: optimal preparation and evaluation of its activity in the decomposition of indigo carmine.

    Science.gov (United States)

    Antonio-Cisneros, Cynthia M; Dávila-Jiménez, Martín M; Elizalde-González, María P; García-Díaz, Esmeralda

    2015-01-12

    Applications of carbon-TiO2 materials have attracted attention in nanotechnology due to their synergic effects. We report the immobilization of TiO2 on carbon prepared from residues of the plant Manihot, commercial TiO2 and glycerol. The objective was to obtain a moderate loading of the anatase phase by preserving the carbonaceous external surface and micropores of the composite. Two preparation methods were compared, including mixing dry precursors and immobilization using a glycerol slurry. The evaluation of the micropore blocking was performed using nitrogen adsorption isotherms. The results indicated that it was possible to use Manihot residues and glycerol to prepare an anatase-containing material with a basic surface and a significant SBET value. The activities of the prepared materials were tested in a decomposition assay of indigo carmine. The TiO2/carbon eliminated nearly 100% of the dye under UV irradiation using the optimal conditions found by a Taguchi L4 orthogonal array considering the specific surface, temperature and initial concentration. The reaction was monitored by UV-Vis spectrophotometry and LC-ESI-(Qq)-TOF-MS, enabling the identification of some intermediates. No isatin-5-sulfonic acid was detected after a 60 min photocatalytic reaction, and three sulfonated aromatic amines, including 4-amino-3-hydroxybenzenesulfonic acid, 2-(2-amino-5-sulfophenyl)-2-oxoacetic acid and 2-amino-5-sulfobenzoic acid, were present in the reaction mixture.

  6. Supercapacitor performances of activated carbon fiber webs prepared by electrospinning of PMDA-ODA poly(amic acid) solutions

    Energy Technology Data Exchange (ETDEWEB)

    Chan Kim; Lee, Wan Jin; Yang, Kep Seung [Chonnam National Univ., Gwangju (Korea). Faculty of Applied Chemical Engineering; Choi, Yeong Og [Korea Inst. of Industrial Technology, ChonAn (Korea). Technical Textile Research Team

    2004-11-30

    The poly(amic acid) (PAA) solution was successfully electrospun at voltages between 13 and 15 kV, forming yellow webs of fibers with diameters of 2-3 {mu}m. The PAA web was then imidized with yield of about 81%. The imidized webs were carbonized in the temperature range from 700 to 1000 {sup o}C under a nitrogen atmosphere with yields greater than or equal to 53%. The flexible carbonized fiber web with the amorphous structure and the relatively high electrical conductivity of 2.5 S/cm at 1000 {sup o}C appears to be a good candidate material for the electrode of electrical double layer capacitors (EDLCs). The carbonized webs were activated under steam in the temperature range of 650-850 {sup o}C resulting surface specific surface area of 940-2100 m{sup 2}/g. The activated carbonized webs were tested electrochemically for the performances as electrodes of EDLC in 30 wt.% KOH aqueous solution. The specific capacitance was 175 F/g even at a high current density of 1000 mA/g. (Author)

  7. High-valued Utilization of China Fir Sawdust Extracted Essential Oil: Preparation of Granular Activated Carbons for n-Butane Adsorption

    Institute of Scientific and Technical Information of China (English)

    ZHU Guang-zhen; DENG Xian-lun; LIU Xiao-min

    2011-01-01

    [Objective] The aim was to study on the high-valued utilization of China Fir sawdust extracted essential oil. [Method] In the field of fir essential oil extraction, the processed China fir sawdust was used to prepare low-valued products. The high-valued utilization of China fir sawdust extracted essential oil (CFSEEO), namely as a precursor to prepare granular activated carbons (GACs), was attempted. The materials were characterized by ultimate analysis, SEM and XRD. [Rusult] A butane working capacity (BWC) of 14.3 g/100 ml was obtained by using the GACs with apparent density of 0.25 g/ml. It was available to introduce the technology of extracting essential oil from the China fir sawdust (CFS) in the industrial production process of activated carbons with high BWC (12.0 -16.5 g/100 ml) and high surface area (2 000 -2 630m2/g) using phosphoric acid based on previous studies of the authors. [Conclusion] The resulting carbon prepared with the raw materials containing lower moisture exhibited a better property on n-butane adsorption.

  8. A simple preparation of carbon doped porous Bi{sub 2}O{sub 3} with enhanced visible-light photocatalytic activity

    Energy Technology Data Exchange (ETDEWEB)

    Dai, Gaopeng, E-mail: dgp2000@126.com [Department of Chemical Engineering and Food Science, Hubei University of Arts and Science, Xiangyang 441053 (China); Hubei Key Laboratory of Low Dimensional Optoelectronic Materials and Devices, Xiangyang 441053 (China); Liu, Suqin [Department of Chemical Engineering and Food Science, Hubei University of Arts and Science, Xiangyang 441053 (China); Hubei Key Laboratory of Low Dimensional Optoelectronic Materials and Devices, Xiangyang 441053 (China); Liang, Ying [Department of Chemical Engineering and Food Science, Hubei University of Arts and Science, Xiangyang 441053 (China)

    2014-09-01

    Graphical abstract: Carbon doped bismuth oxide with a porous structure was prepared by calcination of bismuth nitrate in glycol solution. The as-prepared samples show enhanced visible-light photocatalytic activity. - Highlights: • C-doped Bi{sub 2}O{sub 3} with a porous structure is obtained by a simply calcination of Bi(NO{sub 3}){sub 3} in glycol. • The C-doped Bi{sub 2}O{sub 3} exhibited much higher photocatalytic activity than the pure Bi{sub 2}O{sub 3}. • Carbon was incorporated into the lattice of Bi{sub 2}O{sub 3} lattice. - Abstract: Carbon doped bismuth oxide (Bi{sub 2}O{sub 3}) with a porous structure is obtained by a simply calcination of bismuth nitrate pentahydrate (Bi(NO{sub 3}){sub 3}⋅5H{sub 2}O) in glycol solution. The as-prepared samples were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), and UV–Vis absorption spectroscopy. The photocatalytic activity was evaluated by the photocatalytic degradation of methyl orange (MO) in an aqueous solution under visible-light radiation (λ > 420 nm). The results show that carbon was incorporated into the lattice of Bi{sub 2}O{sub 3}. The absorption intensity of C-doped Bi{sub 2}O{sub 3} increases in the region of 450–530 nm and the absorption edge has an obvious shift to long wavelength. The C-doped Bi{sub 2}O{sub 3} exhibited much higher photocatalytic activity than the pure one due to the synergetic effects of the porous structure and the improved absorption in the visible-light region.

  9. Equilibrium, Kinetics, and Thermodynamics of Remazol Brilliant Blue R Dye Adsorption onto Activated Carbon Prepared from Pinang Frond

    OpenAIRE

    Mohd Azhar Ahmad; Safarudin Gazali Herawan; Ahmad Anas Yusof

    2014-01-01

    The adsorption of remazol brilliant blue R (RBBR) dye on pinang frond based activated carbon (PF-AC) was investigated in a batch process. The effects of initial dye concentration, contact time, solution temperature, and solution pH were evaluated. The adsorption equilibrium and kinetic were found to follow Freundlich isotherm models and pseudo-second-order kinetic model, respectively. The mechanism of the adsorption process was found from the intraparticle diffusion model. Result from adsorpt...

  10. Evaluation of removal efficiency of heavy metals by low-cost activated carbon prepared from African palm fruit

    Science.gov (United States)

    Abdulrazak, Sani; Hussaini, K.; Sani, H. M.

    2016-09-01

    This study details the removal of heavy metals; Cadmium, Copper, Nickel, and Lead from wastewater effluent using an activated carbon produced from African palm fruit. The effluent was obtained from Old Panteka market; a metal scrap Market located in Kaduna State, Nigeria, which has several components that constitute high level of pollution in the environment. The effect of temperature and contact time on the removal of these heavy metals using the activated carbon produced was investigated. The activated carbon showed a significant ability in removing heavy metals; Cadmium, Copper, Nickel, and Lead from the wastewater. Higher percentage removal was observed at a temperature of 80 °C (93.23 ± 0.035, 96.71 ± 0.097, 92.01 ± 0.018, and 95.42 ± 0.067 % for Cadmium, Copper, Nickel, and Lead, respectively) and at an optimum contact time of 60 min (99.235 ± 0.148, 96.711 ± 0.083, 95.34 ± 0.015, and 97.750 ± 0.166 % for Cadmium, Copper, Nickel, and Lead, respectively) after which the percentage removal decreases. This work, therefore, suggests that African palm fruit can be successfully applied to solve this environmental pollution.

  11. Preparation of flat carbon support films

    NARCIS (Netherlands)

    Koning, RI; Oostergetel, GT; Brisson, A

    2003-01-01

    Wrinkling of carbon support films is known to limit the resolution of electron microscopy images of protein two-dimensional crystals. The origin of carbon wrinkling during preparation of the support films was investigated by reflected light microscopy. We observed that carbon films go through severa

  12. 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.

  13. Study on Preparation of Formed Activated Carbon from Bagasse%甘蔗渣制备板状成型活性炭的研究

    Institute of Scientific and Technical Information of China (English)

    张承龙; 白建峰; 孙可伟

    2011-01-01

    Formed activated carbon block was prepared using powdered activated carbon prepared from bagasse with phosphoric acid activation.The influence of various preparation parameters such as the type binders and the amount of the binders was investigated.The test results showed that the iodine value of quantity adsorption and volume adsorption of formed activated carbon block decreased as ratio of binder increased,the penetration rate of formed activated carbon block decreased with increasing ratio of binder when using carboxymethylcellulose as binder,and the penetration rate first decreased a little,then increased with increasing ratio of binder when using polyvinyl alcohol as binder.The adsorption behavior of formed activated carbon block binded by carboxymethylcellulose was better;the iodine value of quantity adsorption and volume adsorption was 418.8211 mg/cm^3 on 10% of carboxymethylcellulose.%以磷酸活化法所制得的甘蔗渣粉状活性炭为原料,研究不同粘接剂种类、粘接剂添加量对板状成型活性炭性能的影响。结果表明:板状成型活性炭的体积吸附量及质量吸附量随着粘结剂添加量的增加而减小;渗透速率随着羧甲基纤维素添加量的增加而减小,随着聚乙烯醇素添加量的增加先是呈略微下降而后增加;以羧甲基纤维素为粘接剂制得的板状成型活性炭的性能较好,当羧甲基纤维素的添加量为10%时,其体积碘吸附量为418.82 mg/cm^3。

  14. Preparation, Characterization, and In Vitro and Vivo Antitumor Activity of Oridonin-Conjugated Multiwalled Carbon Nanotubes Functionalized with Carboxylic Group

    Directory of Open Access Journals (Sweden)

    Chuanjin Wang

    2016-01-01

    Full Text Available Carbon nanotubes have shown great potential in tumor therapy. Oridonin (ORI is a poorly water-soluble diterpenoid compound (C20H28O6 used in the treatment of esophageal and hepatic carcinoma for decades. For the purpose of enhancing the antitumor potency and reducing cytotoxicity of ORI, multiwalled carbon nanotubes functionalized with carboxylic group (MWCNTs-COOH were used as ORI carrier. ORI was noncovalently encapsulated into (or onto the functionalized carbon nanotubes (MWCNTs-ORI. The obtained MWCNTs-ORI has been characterized. The ORI loading efficiency in MWCNTs-COOH carrier was studied to be about 82.6% (w/w. In vitro cytotoxicity assay on MWCNTs-ORI gave IC50 of 7.29±0.5 μg/mL and ORI-F gave IC50 of 14.5±1.4 μg/mL. The antitumor effect studies in vivo showed that MWCNTs-ORI improved antitumor activity of ORI in comparison with ORI-F. The tumor inhibition ratio for MWCNTs-ORI (1.68×10-2 g·Kg−1·d−1 was 86.4%, higher than that of ORI-F (1.68×10-2 g·Kg−1·d−1 which was 39.2%. This can greatly improve the pharmaceutical efficiency and reduce potential side effects.

  15. Preparation of highly porous binderless activated carbon electrodes from fibres of oil palm empty fruit bunches for application in supercapacitors.

    Science.gov (United States)

    Farma, R; Deraman, M; Awitdrus, A; Talib, I A; Taer, E; Basri, N H; Manjunatha, J G; Ishak, M M; Dollah, B N M; Hashmi, S A

    2013-03-01

    Fibres from oil palm empty fruit bunches, generated in large quantities by palm oil mills, were processed into self-adhesive carbon grains (SACG). Untreated and KOH-treated SACG were converted without binder into green monolith prior to N2-carbonisation and CO2-activation to produce highly porous binderless carbon monolith electrodes for supercapacitor applications. Characterisation of the pore structure of the electrodes revealed a significant advantage from combining the chemical and physical activation processes. The electrochemical measurements of the supercapacitor cells fabricated using these electrodes, using cyclic voltammetry, electrochemical impedance spectroscopy and galvanostatic charge-discharge techniques consistently found that approximately 3h of activation time, achieved via a multi-step heating profile, produced electrodes with a high surface area of 1704m(2)g(-1) and a total pore volume of 0.889cm(3)g(-1), corresponding to high values for the specific capacitance, specific energy and specific power of 150Fg(-1), 4.297Whkg(-1) and 173Wkg(-1), respectively.

  16. Preparation and photocatalytic activity of TiO2-coated granular activated carbon composites by a molecular adsorption-deposition method

    Institute of Scientific and Technical Information of China (English)

    2008-01-01

    TiO2 nanoparticle-coated granular activated carbon (GAC) composite photocatalysts (CPs) were suc-cessfully prepared by a molecular adsorption-deposition (MAD) method. The CPs were detected by scanning electron microscopy (SEM), X-ray diffraction (XRD), X-ray Photoelectron Spectroscopy (XPS), BET surface area and UV-Vis adsorption spectroscopy, and their photoactivity was evaluated by methyl orange (MO) photodegradation. The results show that small-sized TiO2 nanoparticles were dispersed well, deposited on the surface of GAC, and showed slight blue shift in comparison with pure TiO2. With the increase in TiO2 content, the CPs showed band gaps in lower energy, smaller surface areas and the higher content of Ti3+ ions. Compared with pure TiO2 and others CPs samples, CPs-382 sample showed the highest photoactivity due to the optimum TiO2 content and surface area besides the synergic effect of photocatalytic degradation of TiO2 and adsorptive property of GAC. In addition, the CPs could be very easily reclaimed, recycled and reused for methyl orange removal while high photoactivity is pre-served.

  17. Preparation and photocatalytic activity of TiO2-coated granular activated carbon composites by a molecular adsorption-deposition method

    Institute of Scientific and Technical Information of China (English)

    LI Youdi; LI Jing; MA MingYuan; OUYANG YuZhu; YAN WenBin

    2008-01-01

    TiO2 nanoparUcle-coated granular activated carbon (GAC) composite photocatalysts (CPs) were suc-cessfully prepared by a molecular adsorption-deposition (MAD) method. The CPs were detected by scanning electron microscopy (SEM), X-ray diffraction (XRD), X-ray Photoelectron Spectroscopy (XPS), BET surface area and UV-Vis adsorption spectroscopy, and their photoactivity was evaluated by methyl orange (MO) photodegradation. The results show that small-sized TiO2 nanoparticles were dispersed well, deposited on the surface of GAC, and showed slight blue shift in comparison with pure TiO2. With the increase in TiO2 content, the CPs showed band gaps in lower energy, smaller surface areas and the higher content of Ti3+ ions. Compared with pure TiO2 and others CPs samples, CPs-382 sample showed the highest photoactivity due to the optimum TiO2 content and surface area besides the synergic effect of photocatslytic degradation of TiO2 and adsorptive property of GAC. In addition, the CPs could be very easily reclaimed, recycled and reused for methyl orange removal while high photoactivity is pre-served.

  18. Carbon membranes precursor, preparation, and funtionalization

    NARCIS (Netherlands)

    Barsema, Jonathan Nathaniel

    2004-01-01

    In this thesis we study the preparation of Carbon Molecular Sieve (CMS) membranes for the separation of gases. The gases are separated based on their size difference and affinity for the membrane material.

  19. Two kinds of composite films: Graphene oxide/carbon nanotube film and graphene oxide/activated carbon film via a self-assemble preparation process

    Science.gov (United States)

    Zou, Li-feng; Ma, Nan; Sun, Mei; Ji, Tian-hao

    2014-11-01

    Two kinds of free-standing composite films, including graphene oxide and activated carbon film as well as graphene oxide and carbon nanotube film, were fabricated through a simple suspension mixing and then natural deposition process. The films were characterized by various measurement techniques in detail. The results show that the composite films without any treatment almost still remain the original properties of the corresponding precursors, and exhibit loose structure, which can be easily broken in water; whereas after treated at 200 °C in air, the films become relatively more dense, and even if immersed into concentrated strong alkali or acid for five days, they still keep the film-morphologies, but regretfully, they show obvious brittleness and slight hydrophilicity. As soon as the treated films are performed in high concentrated strong alkali for about one day, their brittleness and wettability can be improved and became good flexibility and complete hydrophilicity.

  20. Preparation, electrochemical behavior and electrocatalytic activity of chlorogenic acid multi-wall carbon nanotubes as a hydroxylamine sensor

    Energy Technology Data Exchange (ETDEWEB)

    Zare, Hamid R., E-mail: hrzare@yazduni.ac.ir; Nasirizadeh, Navid; Ajamain, Hamideh; Sahragard, Ali

    2011-07-20

    Electrochemical characteristics of an electrodeposited chlorogenic acid film on multi-wall carbon nanotubes glassy carbon electrode (CGA-MWCNT-GCE) and its role as a sensor for electrocatalytic oxidation of hydroxylamine are described. Cyclic voltammograms of the CGA-MWCNT-GCE indicate a pair of well-defined and nearly reversible redox couple with the surface confined characteristics at a wide pH range of 2.0-12.0. The charge transfer coefficient, {alpha}, and the charge transfer rate constant, k{sub s}, of CGA adsorbed on MWCNT were calculated 0.48 and 44 {+-} 2 s{sup -1} respectively. The CGA-MWCNT-GCE shows a dramatic increase in the peak current and/or a decrease in the overvoltage of hydroxylamine electrooxidation in comparison with that seen at a CGA modified GCE, MWCNT modified GCE and activated GCE. The kinetic parameters of electron transfer coefficient, {alpha}, the heterogeneous electron transfer rate constant, k', and exchange current, i{sub 0}, for oxidation of hydroxylamine at the modified electrode surface were determined using cyclic voltammetry. Four linear calibration ranges and high repeatability with relative standard deviation of 4.6%, for a series of four successive measurements in 17.7 {mu}M hydroxylamine, are obtained at the CGA-MWCNT-GCE using an amperometric method. Finally, the modified electrode was successfully used for determination of spiked hydroxylamine in two water samples.

  1. Application of least squares support vector regression and linear multiple regression for modeling removal of methyl orange onto tin oxide nanoparticles loaded on activated carbon and activated carbon prepared from Pistacia atlantica wood.

    Science.gov (United States)

    Ghaedi, M; Rahimi, Mahmoud Reza; Ghaedi, A M; Tyagi, Inderjeet; Agarwal, Shilpi; Gupta, Vinod Kumar

    2016-01-01

    Two novel and eco friendly adsorbents namely tin oxide nanoparticles loaded on activated carbon (SnO2-NP-AC) and activated carbon prepared from wood tree Pistacia atlantica (AC-PAW) were used for the rapid removal and fast adsorption of methyl orange (MO) from the aqueous phase. The dependency of MO removal with various adsorption influential parameters was well modeled and optimized using multiple linear regressions (MLR) and least squares support vector regression (LSSVR). The optimal parameters for the LSSVR model were found based on γ value of 0.76 and σ(2) of 0.15. For testing the data set, the mean square error (MSE) values of 0.0010 and the coefficient of determination (R(2)) values of 0.976 were obtained for LSSVR model, and the MSE value of 0.0037 and the R(2) value of 0.897 were obtained for the MLR model. The adsorption equilibrium and kinetic data was found to be well fitted and in good agreement with Langmuir isotherm model and second-order equation and intra-particle diffusion models respectively. The small amount of the proposed SnO2-NP-AC and AC-PAW (0.015 g and 0.08 g) is applicable for successful rapid removal of methyl orange (>95%). The maximum adsorption capacity for SnO2-NP-AC and AC-PAW was 250 mg g(-1) and 125 mg g(-1) respectively.

  2. Preparation of gold- and chlorine-impregnated bead-type activated carbon for a mercury sorbent trap.

    Science.gov (United States)

    Song, Young Cheol; Lee, Tai Gyu

    2016-12-01

    This study aimed to develop a mercury (Hg) adsorption trap, which can be used to measure the concentration of elemental Hg in emissions from a Hg discharge facility, and evaluate its adsorption efficiency. The Hg spiking efficiency was compared by impregnating metallic and halogen materials that have high affinity for Hg into activated carbon (AC) to determine an accurate spiking method for Hg on AC. The Hg spiking efficiency was compared according to the type and content of the impregnated substances. AC impregnated with Cl and Au had a 15-20% higher Hg spiking efficiency compared to virgin AC. For Au impregnation at weight ratios of 0-20 wt% of adsorbent, spiking efficiencies of over 97% were observed under certain conditions. The Hg adsorption properties of the above adsorbent were determined experimentally, and the results were used to test the adsorption performance of Hg adsorption traps.

  3. Comparison of ultrasonic with stirrer performance for removal of sunset yellow (SY) by activated carbon prepared from wood of orange tree: Artificial neural network modeling

    Science.gov (United States)

    Ghaedi, A. M.; Ghaedi, M.; Karami, P.

    2015-03-01

    The present work focused on the removal of sunset yellow (SY) dye from aqueous solution by ultrasound-assisted adsorption and stirrer by activated carbon prepared from wood of an orange tree. Also, the artificial neural network (ANN) model was used for predicting removal (%) of SY dye based on experimental data. In this study a green approach was described for the synthesis of activated carbon prepared from wood of an orange tree and usability of it for the removal of sunset yellow. This material was characterized using scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The impact of variables, including initial dye concentration (mg/L), pH, adsorbent dosage (g), sonication time (min) and temperature (°C) on SY removal were studied. Fitting the experimental equilibrium data of different isotherm models such as Langmuir, Freundlich, Temkin and Dubinin-Radushkevich models display the suitability and applicability of the Langmuir model. Analysis of experimental adsorption data by different kinetic models including pseudo-first and second order, Elovich and intraparticle diffusion models indicate the applicability of the second-order equation model. The adsorbent (0.5 g) is applicable for successful removal of SY (>98%) in short time (10 min) under ultrasound condition.

  4. Comparison of ultrasonic with stirrer performance for removal of sunset yellow (SY) by activated carbon prepared from wood of orange tree: artificial neural network modeling.

    Science.gov (United States)

    Ghaedi, A M; Ghaedi, M; Karami, P

    2015-03-05

    The present work focused on the removal of sunset yellow (SY) dye from aqueous solution by ultrasound-assisted adsorption and stirrer by activated carbon prepared from wood of an orange tree. Also, the artificial neural network (ANN) model was used for predicting removal (%) of SY dye based on experimental data. In this study a green approach was described for the synthesis of activated carbon prepared from wood of an orange tree and usability of it for the removal of sunset yellow. This material was characterized using scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The impact of variables, including initial dye concentration (mg/L), pH, adsorbent dosage (g), sonication time (min) and temperature (°C) on SY removal were studied. Fitting the experimental equilibrium data of different isotherm models such as Langmuir, Freundlich, Temkin and Dubinin-Radushkevich models display the suitability and applicability of the Langmuir model. Analysis of experimental adsorption data by different kinetic models including pseudo-first and second order, Elovich and intraparticle diffusion models indicate the applicability of the second-order equation model. The adsorbent (0.5g) is applicable for successful removal of SY (>98%) in short time (10min) under ultrasound condition. Copyright © 2014 Elsevier B.V. All rights reserved.

  5. Preparation and Characterization of the Activated Carbon-Nylon Beads: Novel Material for In Situ Microbe Sampler and Microcosm Experiment in Groundwater Environment

    Science.gov (United States)

    Liu, J.; Liu, H.

    2015-12-01

    The organic pollution of groundwater is a widespread problem in the word. It is significant to study the microbial community especially related to organic contaminant biodegradation and their variation with groundwater environment parameters, so as to evaluate the biodegradability of the organic contaminants and then make a right decision for bioremediation. One of good ways for this study is to build a microcosm in groundwater containing target contaminant, where microbes especially relating to biodegradation will grow in the microcosm and be collected for analysis. This research aims to prepare a novel material for in situ microbe sampler and microcosm experiment in groundwater environment. The novel material, namely, the activated carbon-nylon (AC-N) beads, was prepared using activated carbon and nylon as main raw materials. The material consists of 3-4mm diameter spherical beads (Fig.1A and Fig.2 A) which have an internal surface area greater than 500 m2 g-1. FT-IR spectra (Fig.3) indicated the composition of activated carbon and nylon due to the variation of the peaks at the near 1627 cm-1and 1558 -1538 cm-1 before and after complex reaction. The equilibrium adsorption capacity of benzene on the beads was 16.76 mg/g at the initial concentration of 100 mg/L. The adsorption kinetics was found to follow the pseudo-second-order kinetic model (Fig.4). The mechanism of the adsorption process was determined from the intraparticle diffusion model. Camera and SEM images (Fig.1 B and Fig.2 A and B) showed that the beads had an open and channel pore structures, the microbes might enter into and grow up in the beads (Fig.1 C and Fig.2 C). All these results showed that the AC-N beads could form the in situ microcosm of organic pollutants and microbes, which provided a promising prospect for assessing the biodegradability of the organic pollutants by intrinsic microbes in the groundwater.

  6. Effect of HNO{sub 3} treatment on the SO{sub 2} adsorption capacity of activated carbon prepared from Chinese low-rank coal

    Energy Technology Data Exchange (ETDEWEB)

    Hang Wenhui; Wang ling; Li Shurong [China Coal Research Institute, Beijing (China)

    1999-11-01

    SO{sub 2} removal from flue gas by activated carbon and HNO{sub 3} treated activated carbon from Chinese low-rank coal was studied. SO{sub 2} adsorption on activated carbon is mainly chemisorption. There was shown to be a correlation between adsorption capacity and the number of active sites on the carbon surface. HNO{sub 3} treatment transforms C-H bonds in activated carbon into active sites, for removal of SO{sub 2}. 2 figs., 2 tabs.

  7. Preparation of composite electroheat carbon film

    Institute of Scientific and Technical Information of China (English)

    XIA Jin-tong; TU Chuan-jun; LI Yan; HU Li-min; DENG Jiu-hua

    2005-01-01

    A kind of conductive and heating unit, which can reach a high surface electroheat temperature at a low voltage, was developed in view of the traditional electroheat coating which has a low surface electroheat temperature and an insufficient heat resistance of its binder. The coating molded electroheat carbon film(CMECF) was prepared by carbonizing the coating which was prepared by adding modified resin into flake graphite and carbon fiber, coating molded onto the surface of the heat resisting matrix after dried, while the hot pressing molded electroheat thick carbon film(HPMETCF) was prepared by carbonizing the bodies whose powders were hot pressing molded directly.The surface and inner microstructure of the carbon film was characterized and analyzed by SEM and DSC/TG, while electroheat property was tested by voltage-current volume resistivity tester and electrical parameter tester. The results show that, close-packed carbon network configuration is formed within the composite electroheat carbon film film after anti-oxidizable treatment reaches a higher surface electroheat temperature than that of the existing electroheat coatings at a low voltage, and has excellent electroheat property, high thermal efficiency as well as stable physicochemical property. It is found that, at room temperature(19± 2 ℃) and 22 V for 5 min, the surface electroheat temperature of the self-produced CMECF (mfiller/mresin = 1. 8/1) reaches 112 ℃ while HPMETCF (mfiller/mresin = 3. 6/1) reaches 265 ℃.

  8. Synthesis, characterization and performance in arsenic removal of iron-doped activated carbons prepared by impregnation with Fe(III) and Fe(II).

    Science.gov (United States)

    Muñiz, G; Fierro, V; Celzard, A; Furdin, G; Gonzalez-Sánchez, G; Ballinas, M L

    2009-06-15

    Arsenic removal from natural well water from the state of Chihuahua (Mexico) is investigated by adsorption using a commercial activated carbon (AC). The latter is used as such, or after oxidation by several chemicals in aqueous solution: nitric acid, hydrogen peroxide, and ammonium persulphate. Raw and oxidised activated carbons are fully characterised (elementary analysis, surface chemistry, pore texture parameters, pH(ZC), and TEM observation). Adsorption of As is measured in the aforementioned water, containing ca. 300 ppb of arsenic: removal of As is poor with the raw AC, and only the most oxidised carbons exhibit higher performances. By contrast, iron-doped ACs are much more efficient for that purpose, though their As uptake strongly depends on their preparation conditions: a number of samples were synthesised by impregnation of raw and oxidised ACs with HCl aqueous solutions of either FeCl(3) or FeCl(2) at various concentrations and various pH. It is shown that iron(II) chloride is better for obtaining high iron contents in the resultant ACs (up to 8.34 wt.%), leading to high As uptake, close to 0.036 mg As/g C. In these conditions, 100% of the As initially present in the natural well water is removed, as soon as the Fe content of the adsorbent is higher than 2 wt.%.

  9. Synthesis, characterization and performance in arsenic removal of iron-doped activated carbons prepared by impregnation with Fe(III) and Fe(II)

    Energy Technology Data Exchange (ETDEWEB)

    Muniz, G. [Laboratoire de Chimie du Solide Mineral, Nancy-Universite, UMR CNRS 7555, BP 239, 54506 Vandoeuvre-les Nancy (France); Facultad de Ciencias Quimicas, Universidad Autonoma de Chihuahua, Circuito Universitario S/N, Chihuahua (Mexico); Fierro, V., E-mail: Vanessa.Fierro@lcsm-uhp.nancy.fr [Laboratoire de Chimie du Solide Mineral, Nancy-Universite, UMR CNRS 7555, BP 239, 54506 Vandoeuvre-les Nancy (France); Celzard, A. [Laboratoire de Chimie du Solide Mineral, UMR CNRS 7555, Nancy-Universite, ENSTIB, 27 rue du Merle Blanc, BP 1041, 88051 Epinal Cedex 9 (France); Furdin, G. [Laboratoire de Chimie du Solide Mineral, Nancy-Universite, UMR CNRS 7555, BP 239, 54506 Vandoeuvre-les Nancy (France); Gonzalez-Sanchez, G. [Centro de Investigacion en Materiales Avanzados (CIMAV) Miguel de Cervantes 120, Compl. Ind. Chih., 31109 Chihuahua (Mexico); Ballinas, M.L. [Facultad de Ciencias Quimicas, Universidad Autonoma de Chihuahua, Circuito Universitario S/N, Chihuahua (Mexico)

    2009-06-15

    Arsenic removal from natural well water from the state of Chihuahua (Mexico) is investigated by adsorption using a commercial activated carbon (AC). The latter is used as such, or after oxidation by several chemicals in aqueous solution: nitric acid, hydrogen peroxide, and ammonium persulphate. Raw and oxidised activated carbons are fully characterised (elementary analysis, surface chemistry, pore texture parameters, pH{sub ZC}, and TEM observation). Adsorption of As is measured in the aforementioned water, containing ca. 300 ppb of arsenic: removal of As is poor with the raw AC, and only the most oxidised carbons exhibit higher performances. By contrast, iron-doped ACs are much more efficient for that purpose, though their As uptake strongly depends on their preparation conditions: a number of samples were synthesised by impregnation of raw and oxidised ACs with HCl aqueous solutions of either FeCl{sub 3} or FeCl{sub 2} at various concentrations and various pH. It is shown that iron(II) chloride is better for obtaining high iron contents in the resultant ACs (up to 8.34 wt.%), leading to high As uptake, close to 0.036 mg As/g C. In these conditions, 100% of the As initially present in the natural well water is removed, as soon as the Fe content of the adsorbent is higher than 2 wt.%.

  10. Optimization of Preparation of Hazelnut Shell Activated Carbon and Characterization%榛子壳活性炭的制备工艺优化及表征

    Institute of Scientific and Technical Information of China (English)

    房丹丹; 吕春茂; 孟宪军; 张炜佳; 邓晓雨

    2016-01-01

    The preparation of activated carbon of hazelnut shell and characterization were studied. Activated carbon was prepared from waste hazelnut shell through phosphoric acid activation. To optimize the preparation process of phosphoric acid concentration, activation temperature, activation time and solid-to-liquid ratio, the response surface methodology was adopted on the basis of single factor experiment. The results showed that the optimum conditions were determined as follows: phosphoric acid concentration of 48.5%, activation temperature of 494℃, activation time of 117min and solid to liquid ratio of 1:2. Under these conditions, the iodine value of activated carbon was 1029 mg•g-1. The surface characteristics of activated carbon were examined by scanning electron microscope (SEM), Fourier transform infrared spectroscopy (FT-IR) and BET specific surface area analyzer etc. The specific surface area was 1364.00m2•g-1,the average pore size was 3.17nm, and the total pore volume was 1.08cm3•g-1. Activated carbon of hazelnut shell has good adsorption effect, can be used as a kind of environmental friendly low-cost adsorbent.%为研究榛子壳活性炭的制备工艺和活性炭表征,以农林果壳废弃物榛子壳作为原料,采用磷酸浸渍活化法制备活性炭。在单因素试验基础上,运用响应面法对活性炭制备工艺中磷酸质量分数、活化温度、活化时间、料液比等各影响因素进行优化。结果表明:在磷酸质量分数为48.5%、活化温度为494℃、活化时间为117min、料液比为1:2条件下,活性炭的碘吸附值为1029mg•g-1。采用扫描式电子显微镜(SEM)、傅里叶红外光谱(FT-IR)、比表面积及孔径分布分析仪等方法对优化条件下制备的活性炭进行表征,活性炭的比表面积可达到1364.00m2•g-1,平均孔径为3.17nm,总孔容为1.08cm3•g-1,表明榛子壳活性炭具有较好的吸附效果,可作为一种环保型低成本吸附剂。

  11. Preparation of activated carbon from carbonized rice husk by ozone activation for Cr(VI) removal%炭化米糠经臭氧活化制备活性炭及其去除Cr(VI)离子

    Institute of Scientific and Technical Information of China (English)

    Sivaraju Sugashini

    2015-01-01

    以臭氧为活化剂,炭化的米糠为原料制备出活性炭。采用氮吸附、SEM-EDAX 和FT-IR对样品进行表征。活性炭的比表面积由活化前的20 m2/g增加到380 m2/g。在臭氧活化过程中,吸附在炭材料上的二氧化硅变疏松,从而导致碳逸出。臭氧同时以氧分子和原子形式存在于炭表面。氧原子,作为强氧化剂,将炭表面氧化成酸性官能团如羧基、酮基和酚基。采用该活性炭吸附Cr (VI)离子,Cr (VI)离子的最大去除率(94%)的条件为:pH值2.0、浓度100 mg/L、吸附量0.2 g,时间2.5 h及转速300 r/min。采用吸附平衡和动力学模型探讨吸附机理,结果表明,吸附等温线符合Freundlich方程,吸附速率符合准二级动力学方程。吸附是自发的放热反应,可能与NaOH脱落而恢复Cr和碳有关。%Activated carbon ( AC) was prepared from carbonized rice husks using ozone as an activating agent. The AC was char-acterized by nitrogen adsorption, SEM-EDAX and FT-IR. The Brunauer-Emmett-Teller surface area of the carbons was increased from 20 to 380 m2/g by the activation. It was observed that the silica attached to the carbonaceous material is loosened, leading to a release of carbon during the ozone activation. Ozone exists as both molecular and atomic oxygen on the surface of carbon. Atomic oxygen, as a powerful oxidizing agent, oxidizes the carbon surface into acidic functional groups such as carboxylic, ketonic and phenolic. The rice husk AC was used for the adsorption of Cr (VI) ions. A maximum removal percentage (94%) of Cr (VI) ions was obtained for a 100 mg/L aqueous solution at the optimized conditions of pH value of 2. 0, adsorbent dosage of 0. 2 g, time of 2. 5 h and stirring speed of 300 r/min. Adsorption equilibrium and kinetic models were used to investigate the adsorption mecha-nism. It was found that the adsorption isotherms were well fitted by the Freundlich equation. The adsorption rate follows pseudo sec-ond order kinetics

  12. Co-pyrolysis behaviour and kinetic of two typical solid wastes in China and characterisation of activated carbon prepared from pyrolytic char.

    Science.gov (United States)

    Ma, Yuhui; Niu, Ruxuan; Wang, Xiaona; Wang, Qunhui; Wang, Xiaoqiang; Sun, Xiaohong

    2014-11-01

    This is the first study on the co-pyrolysis of spent substrate of Pleurotus ostreatus and coal tar pitch, and the activated carbon prepared from the pyrolytic char. Thermogravimetry (TG) analysis was carried out taking spent substrate, coal tar pitch and spent substrate-coal tar pitch mixture. The activation energies of pyrolysis reactions were obtained via the Flynn-Wall-Ozawa and Kissinger-Akahira-Sunose methods. The kinetic models were determined by the master-plots method. The activated carbons were characterised by N2-adsorption, Fourier transform infrared spectroscopy and X-ray diffraction. Experimental results demonstrated a synergistic effect happened during co-pyrolysis, which was characterised by a decreased maximum decomposition rate and an enhanced char yield. The average activation energies of the pyrolysis reactions of spent substrate, coal tar pitch and the mixture were 115.94, 72.92 and 94.38 kJ mol(-1) for the Flynn-Wall-Ozawa method, and 112.17, 65.62 and 89.91 kJ mol(-1) for the Kissinger-Akahira-Sunose method. The reaction model functions were f(α) = (1-α)(3.42), (1-α)(1.72) and (1-α)(3.07) for spent substrate, coal tar pitch and the mixture, respectively. The mixture char-derived activated carbon had a Brunauer-Emmett-Teller surface area up to 1337 m(2) g(-1) and a total pore volume of 0.680 cm(3) g(-1). Mixing spent substrate with coal tar pitch led to the creation of more micropores and a higher surface area compared with the single spent substrate and coal tar pitch char. Also, the mixture char-derived activated carbon had a higher proportion of aromatic stacking. This study provides a reference for the utilisation of spent substrate and coal tar pitch via co-pyrolysis, and their pyrolytic char as a promising precursor of activated carbon.

  13. Study on Preparation Mechanism of Activated Carbon by Phosphoric Acid Activation%磷酸法制备活性炭活化机理研究

    Institute of Scientific and Technical Information of China (English)

    朱光真; 邓先伦

    2011-01-01

    [目的]研究磷酸法制备活性炭的活化机理.[方法]将磷酸浸渍后的木质纤维素类原料经稀酸水解后提取还原糖,研究还原糖含量与相应工艺条件下制备的活性炭产品孔性能之间的关系.[结果]在该试验条件下,还原糖含量与活性炭产品孔性能基本呈正相关,而在浓硫酸添加量较高时,呈反相关,可能是由于浓硫酸的过度催化导致形成更小分子量的低聚糖,对较大拓扑结构的形成不利,反而会降低比表面积和孔的发展.[结论]为活性炭生产提供一定的理论指导.%[Objective] To study the preparation mechanism of activated carbon (AC) National EngineeingLab for Biomass Chemical Utilization; Keylab on Forese chemical Engineening,SAF;Key Lab of Biomass Energy and Material,Jiangsu Proinmce,by phosphoric acid activation. [ Method] Reducing sugar was extracted through dilute acid hydrolysis of lignocellulosic materials impregnated with phosphoric acid and the relationship between reducing sugar content and pore texture of corresponding AC was explored. [ Result] Within experimental conditions,there was a positive correlation between the reducing sugar content and pore texture of corresponding AC,while a negative correlation was seen under high dose of concentrated sulfuric acid,oligosaccharides with lower molecule size,which were produced due to the excessive hydrolysis of higher concentrated sulfuric acid content,were unfavorable to form larger topological structure and on the contrary prevented the development of specific surface area and pore of AC. [Conclusion] The study provided theoretical direction for the industrial production of AC.

  14. Carbon particle induced foaming of molten sucrose for the preparation of carbon foams

    Energy Technology Data Exchange (ETDEWEB)

    Narasimman, R.; Vijayan, Sujith; Prabhakaran, K., E-mail: kp2952002@gmail.com

    2014-11-15

    Graphical abstract: - Highlights: • An easy method for the preparation of carbon foam from sucrose is presented. • Wood derived activated carbon particles are used to stabilize the molten sucrose foam. • The carbon foams show relatively good mechanical strength. • The carbon foams show excellent CO{sub 2} adsorption and oil absorption properties. • The process could be scaled up for the preparation of large foam bodies. - Abstract: Activated carbon powder was used as a foaming and foam setting agent for the preparation of carbon foams with a hierarchical pore structure from molten sucrose. The rheological measurements revealed the interruption of intermolecular hydrogen bonding in molten sucrose by the carbon particles. The carbon particles stabilized the bubbles in molten sucrose by adsorbing on the molten sucrose–gas interface. The carbon foams obtained at the activated carbon powder to sucrose weight ratios in the range of 0–0.25 had a compressive strength in the range of 1.35–0.31 MPa. The produced carbon foams adsorb 2.59–3.04 mmol/g of CO{sub 2} at 760 mmHg at 273 K and absorb oil from oil–water mixtures and surfactant stabilized oil-in-water emulsions with very good selectivity and recyclability.

  15. Removal of fluoride from drinking water using aluminum hydroxide coated activated carbon prepared from bark of Morinda tinctoria

    Science.gov (United States)

    Amalraj, Augustine; Pius, Anitha

    2016-10-01

    The aim of this study is to design and develop a novel cost effective method for fluoride removal, applicable to rural areas of developing countries. Adsorption is widely considered as one of the appropriate technologies for water defluoridation. This study investigates the feasibility of using low-cost biomass based activated carbon from the bark of Morinda tinctoria coated with aluminum hydroxide (AHAC) for water defluoridation, at neutral pH range. Characterization of AHAC was done through IR, SEM with EDAX studies before and after fluoride treatment. The fluoride adsorption capacity of AHAC as a function of contact time, pH and initial fluoride concentration was investigated. The role of co-existing interfering ions also was studied. The isotherm and kinetic models were used to understand the nature of the fluoride adsorption onto AHAC. Freundlich isotherm and intra-particle diffusion were the best-fitting models for the adsorption of fluoride on AHAC. Fluoride adsorption kinetics well fitted with pseudo-second order model. The results showed excellent fluoride adsorption capacity was found to be 26.03 mg g-1 at neutral pH.

  16. Preparation of amino-modified active carbon cartridges and their use in the extraction of quercetin from Oldenlandia diffusa.

    Science.gov (United States)

    Zhu, Tao; Row, Kyung Ho

    2011-12-05

    Polyethyleneimine (PEI) and ethylenediamine (EDA) as modifiers were bonded on active carbon (AC) surface for specific selective extraction of quercetin from Oldenlandia diffusa. The characteristics of the modified AC materials that were obtained were investigated by field emission-scanning electron microscopy (FE-SEM) and Fourier transform infrared spectrometer (FT-IR). The interactions between quercetin and the AC materials were investigated by fitting the static adsorption data to four linear and nonlinear adsorption isotherm models. Of these four models, the Langmuir-Freundlich adsorption isotherm was proved the best for investigating quercetin on AC materials. Scatchard analysis was used to evaluate the binding properties of the AC materials for quercetin. Solvent extraction and solid-phase extraction (SPE) were optimized, and the effect of the mobile phase pH was investigated to improve the performance for the separation of quercetin on high performance liquid chromatography (HPLC). The results from the validation of the proposed analytical method demonstrated that the EDA-modified AC was the most suitable SPE cartridge for the purification of quercetin from O. diffusa. Copyright © 2011 Elsevier B.V. All rights reserved.

  17. Study on Preparation of Activated Carbon Fiber Based on Biomass%生物质海绵基活性炭纤维制备研究

    Institute of Scientific and Technical Information of China (English)

    肖信彤; 余云祥; 徐思; 夏世斌

    2012-01-01

    The preparation of activated carbon fiber based on luffa sponge fibers (LSF-ACFs) was studied. Orthogonal test had been employed to analyse the function of (NH4)2HPO4 as the activating agent. The process included pretreat-ment, pre-oxidation and activation. Scanning electron microscopy (SEM) was applied to characterize its morphology. Nitrogen adsorption-desorption isotherms were applied to characterize its surface pore texture. The reseach results indicated that the BET surface area of LSF-ACF prepared in experiments presented the biggest of 812. 7 m2/g. abundant micro-pores were observed, and the pore volume reached 0. 390 cm3/g. The activated carbon fibers produced from luffa sponge fibers showed a promising application prospect.%采用正交试验方法,以生物质海绵-丝瓜络纤维为原料、(NH4)2HPO4作为活化剂制备活性炭纤维(ACF).制备过程包括预处理、预氧化、高温活化.采用扫描电镜(SEM)对制备的活性炭纤维结构进行表征分析.通过N2吸附-脱附等温曲线对其表面孔结构进行研究.结果表明:制备的丝瓜络海绵基活性炭纤维比表面积达到812.7m2/g,孔隙结构主要为微孔结构,孔体积可达0.390cm3/g,在环保等领域具备良好的应用前景.

  18. Preparation of double-walled carbon nanotubes

    Institute of Scientific and Technical Information of China (English)

    JIANG Bin; WEI Jinquan; CI Lijie; WU Dehai

    2004-01-01

    Double-walled carbon nanotubes were prepared using the floating chemical vapor deposition with methane as carbon source and adding small amount of sulfur into the ferrocene catalyst. The optimized technological parameters are: the reaction temperature is 1200℃; the catalyst vapor temperature is 80℃; the flow rate of argon is 2000 SCCM; the flow rate of methane is 5 SCCM. The purified DWNTs under these optimized technological parameters have high purity above 90 wt%.

  19. 玉米秸秆制备活性炭的吸附性能研究%Experiment on Adsorption Performance of Activated Carbon Prepared by Corn Straws

    Institute of Scientific and Technical Information of China (English)

    刘恩海; 刘圣勇; 王长忠; 潘嘉信; 赵坤正; 徐云婷; 苏之勇

    2016-01-01

    Objective] To study the adsorption performance of activated carbon prepared by corn straws.[ Methods] Activated carbon pre-pared by corn straws was taken as research object, adsorption performance simulation test equipment was set up, and the static weight method was used to measure the activated carbon adsorption capacity of methanol.Also, adsorption bed structure, adsorption bed containing different particle size carbon particle, activated carbon supplemented with different amounts of graphite powder and modified activated carbon adsorption performance impact on the system were studied.[Results] For the bed material containing the same kinds of carbon adsorption samples at the same temperature, the new adsorption bed A adsorption performance was significantly better than for bed B whose structure is not transformed;when it reached the same absorption capacity 0.22 g/g, bed A will absorb five minutes earlier;in the comparison test of different size and the same diameter of the activated carbon bed, for adsorption at the same temperature, the adsorption performance was significantly better than containing the same diameter, and achieved the same adsorption capacity 0.22 g/g, the adsorption was implemented 16 minutes ahead of time;add proper amount of activated carbon graphite in the bed can enhance thermal conductivity and strengthen adsorption properties;the op-timum dosage was 20% of total activated carbon; in the modified activated carbon test, after a weak acid solution soak charcoal, it can en-hance the adsorption performance, compared to the control group, the absorption was completed 3 minutes ahead of time when reaching 87. 1% of the balanced adsorption capacity.[Conclusion] This study is expected to provide reference for optimizing structural design of absorption bed and absorption type refrigeration system.%[目的]研究玉米秸秆制备活性炭的吸附性能。[方法]以玉米秸秆制备的粒状活性炭为研究对象,搭建了吸附性能模

  20. 磷酸活化法黄麻杆活性炭的制备及表征%Preparation and Characterization of Jute Stick-Based Activated Carbon

    Institute of Scientific and Technical Information of China (English)

    刘其霞; 何丽芬; 高强

    2012-01-01

    以黄麻杆为原料,采用磷酸活化法制备活性炭,通过正交试验探讨了磷酸浓度、活化温度、活化时间对活性炭得率和吸附性能的影响,确立了最佳制备工艺,即:磷酸浓度2mol/L、活化温度400℃、活化时间1h.实验结果表明:在最佳工艺条件下制得的黄麻杆活性炭得率为4,2.93%,碘吸附值为1059.26mg/g,亚甲基蓝吸附值为353.10mg/g,比表面积为1779.4m㎡/g,总孔容为0.960m3/g,平均孔径为2.16nm,呈现出高中孔率结构.%Jute stick-based activated carbon are prepared by using jute sticks as raw materials and phosphoric acid as activating agent. The effects of several main factors such as concentration of activating agent, activation temperature and activation time on the yield and adsorption properties of active carbon are investigated via orthogonal experiments. Results show that the optimum conditions are phosphoric acid concentration of 2 mol/L, activation temperature of 400 ~C and activation time of 1 h. The yield is 42.93%, the iodine adsorption value and methylene blue adsorption value of the activated carbon are 1 059.26 mg/g and 353.10 mg/g, respectively. The specific surface area is 1 779.4 ㎡/g, the total pore volume is 0.960 m3/g and the average pore size is 2.16 nm, showing highly mesoporous structures.

  1. Preparation of Carbon Nanosheets at Room Temperature.

    Science.gov (United States)

    Schrettl, Stephen; Schulte, Bjoern; Stefaniu, Cristina; Oliveira, Joana; Brezesinski, Gerald; Frauenrath, Holger

    2016-03-08

    Amphiphilic molecules equipped with a reactive, carbon-rich "oligoyne" segment consisting of conjugated carbon-carbon triple bonds self-assemble into defined aggregates in aqueous media and at the air-water interface. In the aggregated state, the oligoynes can then be carbonized under mild conditions while preserving the morphology and the embedded chemical functionalization. This novel approach provides direct access to functionalized carbon nanomaterials. In this article, we present a synthetic approach that allows us to prepare hexayne carboxylate amphiphiles as carbon-rich siblings of typical fatty acid esters through a series of repeated bromination and Negishi-type cross-coupling reactions. The obtained compounds are designed to self-assemble into monolayers at the air-water interface, and we show how this can be achieved in a Langmuir trough. Thus, compression of the molecules at the air-water interface triggers the film formation and leads to a densely packed layer of the molecules. The complete carbonization of the films at the air-water interface is then accomplished by cross-linking of the hexayne layer at room temperature, using UV irradiation as a mild external stimulus. The changes in the layer during this process can be monitored with the help of infrared reflection-absorption spectroscopy and Brewster angle microscopy. Moreover, a transfer of the carbonized films onto solid substrates by the Langmuir-Blodgett technique has enabled us to prove that they were carbon nanosheets with lateral dimensions on the order of centimeters.

  2. 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.

  3. High efficient preparation of carbon nanotube-grafted carbon fibers with the improved tensile strength

    Science.gov (United States)

    Fan, Wenxin; Wang, Yanxiang; Wang, Chengguo; Chen, Jiqiang; Wang, Qifen; Yuan, Yan; Niu, Fangxu

    2016-02-01

    An innovative technique has been developed to obtain the uniform catalyst coating on continuously moving carbon fibers. Carbon nanotube (CNT)-grafted carbon fibers with significantly improved tensile strength have been succeeded to produce by using chemical vapor deposition (CVD) when compared to the tensile strength of untreated carbon fibers. The critical requirements for preparation of CNT-grafted carbon fibers with high tensile strength have been found, mainly including (i) the obtainment of uniform coating of catalyst particles with small particle size, (ii) the low catalyst-induced and mechano-chemical degradation of carbon fibers, and (iii) the high catalyst activity which could facilitate the healing and strengthening of carbon fibers during the growth of CNTs. The optimum growth temperature was found to be about 500 °C, and the optimum catalyst is Ni due to its highest activity, there is a pronounced increase of 10% in tensile strength of carbon fibers after CNT growth at 500 °C by using Ni catalyst. Based on the observation from HRTEM images, a healing and crosslink model of neighboring carbon crystals by CNTs has been formulated to reveal the main reason that causes an increase in tensile strength of carbon fibers after the growth of CNTs. Such results have provided the theoretical and experimental foundation for the large-scale preparation of CNT-grafted carbon fibers with the improved tensile strength, significantly promoting the development of CNT-grafted carbon fiber reinforced polymer composites.

  4. Methods for preparation of carbon nanotubes

    Energy Technology Data Exchange (ETDEWEB)

    Rakov, Eduard G [D.I. Mendeleev Russian University of Chemical Technology, Moscow (Russian Federation)

    2000-01-31

    The most important methods of synthesis and purification of carbon nanotubes, a new form of material, are described. The prospects for increasing the scale of preparation processes and for more extensive application of nanotubes are evaluated. The bibliography includes 282 references.

  5. Preparation and structure characterization of activated carbon from cotton stalk%棉杆活性炭的制备及其结构表征

    Institute of Scientific and Technical Information of China (English)

    李风娟; 李铁虎; 周岭; 安静; 秦翠兰

    2016-01-01

    以棉花秸秆为原料,ZnCl2与AlCl3组成的熔盐为活化剂,采用化学活化法制备活性炭。利用正交实验探讨了熔盐与原料比例、ZnCl2与AlCl3的比例、浸渍时间、活化温度、保温时间对制备的活性炭收率和碘吸附性能的影响,得到了熔盐活化法制备棉杆活性炭的最佳工艺条件:熔盐与棉杆比例为1.5∶1、熔盐中ZnCl2与AlCl3比例为9∶1、浸渍时间16 h、活化温度650℃、保温时间90 min,在此工艺条件下制备的活性炭的收率为23.06%,碘吸附值为708.32 mg/g;采用SEM和XED对制备的活性炭进行表征,结果表明:活性炭的表面分布了发达的、大小形状不一样的孔洞,且活性炭内部是由类石墨结构组成的,但石墨微晶层片排列比较紊乱,石墨化程度不高。%Activated carbon was prepared by molten salt of ZnCl2 and AlCl3 using cotton stalk as raw material. The effects of the ratio of molten salt to cotton stalk, the ratio of ZnCl2 to AlCl3, impregnation time, activation temperature and holding time on the yield and iodine adsorption property of activated carbon were evaluated via orthogonal array design. It indicated that the optimum process was as follows:the ratio of molten salt to cotton stalk of 1.5∶1, the ratio of ZnCl2 to AlCl3 is 9∶1, impregnation time of 16 h, activation temperature of 650℃, and holding time of 90 min. Under the process condition, the yield of activated carbon is 23.06%, and the io-dine adsorption value is 708.32 mg/g. Activated carbon was characterized by SEM and XRD. The results show that there are devel-oped holes with different size and shape on the surface of the activated carbon. And the activated carbon is made up of graphite-like structure, but the microcrystalline layer of graphite is disordered, and graphitization degree is not high.

  6. 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.

  7. 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.

  8. Preparation of highly developed mesoporous activated carbon fiber from liquefied wood using wood charcoal as additive and its adsorption of methylene blue from solution.

    Science.gov (United States)

    Ma, Xiaojun; Zhang, Fan; Zhu, Junyan; Yu, Lili; Liu, Xinyan

    2014-07-01

    Activated carbon fiber (C-WACF) with super high surface area and well-developed small mesopores were prepared by liquefied wood and uses wood charcoal (WC) as additive. The characterization and properties of C-WACF were investigated by XRD, XPS and N2 adsorption. Results showed the pore development was significant at temperatures >750°C, and reached a maximum BET surface area (2604.7 m(2)/g) and total pore volume (1.433 cm(3)/g) at 850°C, of which 86.8% was from the contribution of the small mesopores of 2-4 nm. It was also found that the mesopore volume and methylene blue adsorption of C-WACF were highly increased as the temperature increases from 750 to 850°C. Additionally, the reduction of graphitic layers, the obvious changes of functional groups and the more unstable carbons on the surface of C-WACF, which played important roles in the formation of mesopores, were also observed.

  9. Porosity Evolution of Activated Carbon Fiber Prepared from Liquefied Wood. Part II: Water Steam Activation from 850 to 950 °C

    Directory of Open Access Journals (Sweden)

    Zhi Jin

    2014-09-01

    Full Text Available To acquire activated carbon fiber from phenol-liquefied wood (PLWACF with better developed pore structure and a high proportion of mesoporosity, the porosity evolution of PLWACF activated at temperatures from 850 to 950 °C by water steam was detected by the physical adsorption of N2 at -196 °C. Results showed that the pore structure was well developed by prolonging the activation time at 850 to 910 °C, and it was easy to obtain PLWACF having exceptionally high surface area (larger than 2560 m2 g-1. However, PLWACF with a specific surface area larger than 3000 m2 g-1 could only be obtained in the late activation stages from 850 to 880 °C. Using this activation process, the mesoporosity was remarkably developed. The mesopore proportion drastically increased with an increase in activation temperature or time, reaching a maximum of 49.5%. The pore size distribution widened as the activation time increased and appeared to accelerate with the use of a higher activation temperature. The mesopore size distribution was enlarged from 2.8 to 5.8 nm.

  10. Preparation and properties of pitch carbon based supercapacitor

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    Using the mesophase pitch as precursor, KOH and CO2 as activated agents, the activated carbon electrode material was fabricated by physical-chemical combined activated technique for supercapacitor. The influence of activated process on the pore structure of activated carbon was analyzed and 14 F supercapacitor with working voltage of 2.5 V was prepared. The charge and discharge behaviors, the properties of cyclic voltammetry, specific capacitance, equivalent serials resistance (ESR), cycle properties, and temperature properties of prepared supercapacitor were examined. The cyclic voltammetry curve results indicate that the carbon based supercapacitor using the self-made activated carbon as electrode materials shows the desired capacitance properties. In 1 mol/L Et4NBFVAN electrolyte, the capacitance and ESR of the supercapacitor are 14.7 F and 60 mΩ, respectively. The specific capacitance of activated carbon electrode materials is 99.6 F/g; its energy density can reach 2.96 W·h/kg under the large current discharge condition. There is no obvious capacitance decay that can be observed after 5000 cycles. The leakage current is below 0.2 mA after keeping the voltage at 2.5 V for 1 h. Meanwhile, the supercapacitor shows desired temperature property; it can be operated normally in the temperature ranging from -40 ℃ to 70 ℃.

  11. Fibrous TiO2 prepared by chemical vapor deposition using activated carbon fibers as template via adsorption, hydrolysis and calcinations

    Institute of Scientific and Technical Information of China (English)

    Hui-na YANG; Li-fen LIU; Feng-lin YANG; Jimmy C. YU

    2008-01-01

    TiO2 fibers were prepared via alternatively introducing water vapor and Ti precursor carried by Ne to an APCVD (chemical vapor deposition under atmospheric pressure) reactor at <200 ℃. Activated carbon fibers (ACFs) were used as templates for deposition and later removed by calcinations. The obtained catalysts were characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), Brtmauer, Emmett and Teller (BET) and X-ray diffraction (XRD) analysisThe pores within TiO2 fibers included micro-range and meso-range, e.g., 7 nm, and the specific surface areas for TiO2 fibers were 141 m2/g and 148 m2/g for samples deposited at 100 ℃ and 200 ℃ (using ACF1700 as template), respectively. The deposition temperature significantly influenced TiO2 morphology. The special advantages of this technique for preparing porous nano-material include no consumption of organic solvent in the process and easy control of deposition conditions and speeds.

  12. The preparation, properties and application of carbon fibers for SPME.

    Science.gov (United States)

    Gierak, A; Seredych, M; Bartnicki, A

    2006-07-15

    The conditions of preparation of new types of carbon fibers for solid phase micro extraction (SPME) prepared by methylene chloride pyrolysis (at 600 degrees C) on the quartz fiber (100 microm) as well as by supporting synthetic active carbon (prepared especially for this purposes) supported in a special epoxide-acrylic polymer is described. The properties of such carbon fibers for SPME were defined by determination of the partition coefficient of the tested substances (i.e., benzene, toluene, xylenes, trichloromethane and tetrachloromethane) and by the microscopic investigations with the application of the optical and scanning electron microscope. The obtained carbon SPME fibers were applied to the analysis of some volatile organic compounds from its aqueous matrix. During chromatographic GC test, at the investigated SPME carbon fibers, we obtained different but mostly high partition coefficients for the determined compounds (Kfs from 120 for trichloromethane up to 11,500 for tetrachloromethane). Owing to the high partition coefficients of the studied substances obtained on carbon fibers, it was possible to do the analysis of organic substances occurring in trace amounts in different matrices. In this paper, we present the analysis of BTX contents in the petrol analyzed with the application carbonized with CH(2)Cl(2) SPME fiber (C1NM) and a headspace over the petrol sample (concentration of each BTX approximately g/dm(3)).

  13. Adsorption of 2,4-dichlorophenoxyacetic acid by mesoporous activated carbon prepared from H3PO4-activated langsat empty fruit bunch.

    Science.gov (United States)

    Njoku, V O; Islam, Md Azharul; Asif, M; Hameed, B H

    2015-05-01

    The removal of toxic herbicide from wastewater is challenging due to the availability of suitable adsorbents. The Langsat empty fruit bunch is an agricultural waste and was used in this study as a cheap precursor to produce activated carbon for the adsorption of herbicide 2,4-dichlorophenoxyacetic acid (2,4-D) at different initial concentrations ranging from 50 to 400 mg/L. The produced Langsat empty fruit bunch activated carbon (LEFBAC) was mesoporous and had high surface area of 1065.65 m(2)/g with different active functional groups. The effect of shaking time, temperature and pH on 2,4-D removal were investigated using the batch technique. The adsorption capacity of 2,4-D by LEFBAC was decreased with increase in pH of solution whereas adsorption capacity increased with temperature. The adsorption data was well described by Langmuir isotherm followed by removal capacity of 261.2 mg/g at 30 °C. The results from this work showed that LEFBAC can be used as outstanding material for anionic herbicide uptake from wastewater.

  14. 活性炭及工艺参数对所制固体活性炭性能的影响%PREPARATION OF ACTIVATED CARBON FORM II. ROLES OF ACTIVATED CARBONS ON THE STRENGTH OF ACTIVATED CARBON FORM USING A THERMOPLASTIC POLYMER AS BINDER

    Institute of Scientific and Technical Information of China (English)

    乔文明; 光来要三; 持田力; 堀雄一; 前田岳志

    2001-01-01

    以煤焦油基活性炭(TAC)和椰子壳活性炭(CAC)为原料,以聚乙烯醇缩丁醛(PVB)为粘接剂,以邻苯二甲酸二丁酯(DBP)为增塑剂,通过混合、成型、硬化及炭化处理,最终制得固体活性炭。详细地考查了工艺条件(如强度、收率、收缩率、比表面积等)的影响。研究结果表明:对于椰子壳活性炭来说,制备高强度(>5000kPa)的固体活性炭是困难的,其主要原因在于椰子壳活性炭比煤焦油基活性炭含有更少的表面官能团(-COOH,-OH等),而这些官能团可能增强PVB在活性炭表面的粘接,并且参与粘接剂的氧化硬化,硬化的粘接剂在炭化过程中在活性炭颗粒间形成炭桥或者枝状结构而粘接这些颗粒。因此,为了制备高强度的固体活性炭,椰子壳活性炭的表面改性是必要的。%Activated carbon/polymer derived carbon form for capacitor electrode was prepared from coconut shell activated carbon (CAC) through mixing, moulding, curing and carbonizing using polyvinylbutyral resin (PVB) as the binder, dibutylphthalate (DBP) as a plastisizing agent. The strength of CAC form was found always poor and difficult to be above 5000kPa which was easily obtained with tar based activated carbon (TAC) in a previous paper. Severer curing conditions and cross-linking agent failed to improve the strength. Higher pressure of moulding was effective to increase the strength, and 500MPa or more pressure is required to achieve 5000kPa. IR and TPD demonstrated that CAC carried much less oxygen functional groups, especially CO2 evolving and low temperature CO evolving groups than TAC. Such surface oxygen functional groups on the activated carbon may adhere to PVB on the carbon surface and may participate in the oxidative curing of the polymer to bind the grains through the carbon bridges after the carbonization. Surface modification of activated carbon is suggested to obtain high strength of its carbonized form

  15. Effect of precursor and preparation method on manganese based activated carbon sorbents for removing H2S from hot coal gas.

    Science.gov (United States)

    Wang, Jiancheng; Qiu, Biao; Han, Lina; Feng, Gang; Hu, Yongfeng; Chang, Liping; Bao, Weiren

    2012-04-30

    Activated carbon (AC) supported manganese oxide sorbents were prepared by the supercritical water impregnation (SCWI) using two different precursor of Mn(NO(3))(2) (SCW(N)) and Mn(Ac)(2)·4H(2)O (SCW(A)). Their capacities of removing H(2)S from coal gas were evaluated and compared to the sorbents prepared by the pore volume impregnation (PVI) method. The structure and composition of different sorbents were characterized by XRD, SEM, TEM, XPS and XANES techniques. It is found that the precursor of active component plays the crucial role and SCW(N) sorbents show much better sulfidation performance than the SCW(A) sorbents. This is because the Mn(3)O(4) active phase of the SCW(N) sorbents are well dispersed on the AC support, while the Mn(2)SiO(4)-like species in the SCW(A) sorbent can be formed and seriously aggregated. The SCW(N) sorbents with 2.80% and 5.60% manganese are favorable for the sulfidation reaction, since the Mn species are better dispersed on the SCW(N) sorbents than those on the PV(N) sorbents and results in the better sulfidation performance of the SCW(N) sorbents. As the Mn content increases to 11.20%, the metal oxide particles on AC supports aggregate seriously, which leads to poorer sulfidation performance of the SCW(N)11.20% sorbents than that of the PV(N)11.20% sorbents. Copyright © 2012 Elsevier B.V. All rights reserved.

  16. 磷酸法竹质活性炭的制备及其二次活化处理的研究%Phosphoric Acid Method Preparation of Bamboo Activated Carbon and Its' Secondary Activation

    Institute of Scientific and Technical Information of China (English)

    赵小红; 蒋云姣

    2013-01-01

    Bamboo waste was made into activated carbon by phosphoric acid activation method, and then the modified activated carbon was preparated with cobalt oxide which was from nitric acid cobalt' s high temperature decomposition. The results of the study showed that; The optimum preparing conditions of activated carbon were as follows; phosphoric acid concentration was 80% , impregnated than for 6: 17 (g/g) , activation time of 2. 5 h, activation temperature of 550 ℃ and obtained activated carbon' s decolorization ability of methylene blue solution was 650 mL/g. The optimum conditions of the modification of activated carbon were as follows: impregnation ratio of 1.5:5 g/mL , mass fraction of cobalt nitrate aqueous was 1.5%, modification time was 90 min and calcined at 400 ℃ for 3 h. The modified activated carbon' s decolorization ability of methylene blue solution was 1 150 mL/g, increased by 76. 92% comparing with the unmodified products.%通过磷酸活化法将毛竹废料制备成活性炭,再利用硝酸钴高温分解的氧化钴来对其二次活化改性.考察了其制备和改性工艺.研究确定活性炭的最佳制备条件为:磷酸浓度80%,浸渍比为6:17 g/g,活化时间为2.5h,活化温度为550℃,产品对亚甲基蓝溶液的脱色力值为650 mL/g.活性炭的适宜改性条件为:用质量分数为7.5%的硝酸钴水溶液按1.5:5 g/mL浸渍比浸渍改性90 min,并在400℃焙烧3h.产品对亚甲基蓝溶液的脱色力值为1 150 mL/g,与未改性产品相比较,提高了76.92%.

  17. Preference of multi-walled carbon nanotube (MWCNT) to single-walled carbon nanotube (SWCNT) and activated carbon for preparing silica nanohybrid pickering emulsion for chemical enhanced oil recovery (C-EOR)

    Science.gov (United States)

    AfzaliTabar, M.; Alaei, M.; Ranjineh Khojasteh, R.; Motiee, F.; Rashidi, A. M.

    2017-01-01

    The aim of this research was to determine the best nano hybrid that can be used as a Pickering emulsion Chemical Enhanced Oil Recovery (C-EOR). Therefore, we have prepared different carbon structures nano hybrids with SiO2 nano particles with different weight percent using sol-gel method. The as-prepared nano materials were characterized with X-Ray Diffraction (XRD), Field Emission Scanning Electron Microscopy (FE-SEM) and Thermal Gravimetric Analysis (TGA). Pickering emulsions of these nanohybrids were prepared at pH=7 in ambient temperature and with distilled water. Stability of the mentioned Pickering emulsions was controlled for one month. Emulsion phase morphology was investigated using optical microscopic imaging. Evaluation results demonstrated that the best sample is the 70% MWCNT/SiO2 nanohybrid. Stability of the selected nanohybrid (70% MWCNT/SiO2 nanohybrid) was investigated by alteration of salinity, pH and temperature. Results showed that the mentioned Pickering emulsion has very good stability at 0.1%, 1% salinity, moderate and high temperature (25 °C and 90 °C) and neutral and alkaline pH (7, 10) that is suitable for the oil reservoirs conditions. The effect of the related nano fluid on the wettability of carbonate rock was investigated by measuring the contact angle and interfacial tension. Results show that the nanofluid could significantly change the wettability of the carbonate rock from oil wet to water wet and can decrease the interfacial tension. Therefore, the 70% MWCNT/SiO2 nanohybrid Pickering emulsion can be used for Chemical Enhanced Oil Recovery (C-EOR).

  18. 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...

  19. Self-activated Carex Meyeriana Kunth-based Porous Carbon Prepared by Direct Carbonization and Its Electrochemical Properties%自活化乌拉草基多孔碳的制备和电化学性质

    Institute of Scientific and Technical Information of China (English)

    王昀; 贲腾; 裘式纶

    2016-01-01

    Porous carbon material UlaC-950-HF( Ula stands for Carex meyeriana Kunth, C is short for carbo-nized, 950 is the optimized temperature, and HF is the etchant) was prepared through direct carbonization of Carex meyeriana Kunth after necessary impurity removal. The precursor self-activated in the process of pyroly-sis. The electrochemical measurements of the UlaC-950-HF sample and several other carbonized biomass-based porous carbon materials were carried out. The results revealed that the capacitance of UlaC-950-HF was 113 F/g. In addition, the electrode showed excellent cycling stability as its specific capacitance decreased only by 4 F/g after 4000 voltammetry cycles, showing its potential of being applied in the supercapacitor electrode material.%以乌拉草为原料,采用直接碳化方法,通过热解过程中前驱体自活化(即利用自身包含的活化剂实现分子内的化学活化),并经过必要的除杂过程制备了多孔碳材料UlaC-950-HF.测试了该多孔碳的电化学性质,并与以几种常见的生物质为原料制备的多孔碳材料及商用活性炭的电化学性质进行对比.结果表明,乌拉草基多孔碳材料UlaC-950-HF的电容值为113 F/g,经过4000次循环后,材料的电容值仅降低了4 F/g,显示出用作超级电容器电极材料的潜力.

  20. Preparation of tamarind fruit seed activated carbon by microwave heating for the adsorptive treatment of landfill leachate: A laboratory column evaluation.

    Science.gov (United States)

    Foo, K Y; Lee, L K; Hameed, B H

    2013-04-01

    The preparation of tamarind fruit seed granular activated carbon (TSAC) by microwave induced chemical activation for the adsorptive treatment of semi-aerobic landfill leachate has been attempted. The chemical and physical properties of TSAC were examined. A series of column tests were performed to determine the breakthrough characteristics, by varying the operational parameters, hydraulic loading rate (5-20 mL/min) and adsorbent bed height (15-21 cm). Ammonical nitrogen and chemical oxygen demand (COD), which provide a prerequisite insight into the prediction of leachate quality was quantified. Results illustrated an encouraging performance for the adsorptive removal of ammonical nitrogen and COD, with the highest bed capacity of 84.69 and 55.09 mg/g respectively, at the hydraulic loading rate of 5 mL/min and adsorbent bed height of 21 cm. The dynamic adsorption behavior was satisfactory described by the Thomas and Yoon-Nelson models. The findings demonstrated the applicability of TSAC for the adsorptive treatment of landfill leachate.

  1. Mesoporous activated carbons with metal-oxide particles prepared from Morwell coal; Morwell tan wo genryo to shita kinzoku sankabutsu tanji kasseitan no saiko kozo

    Energy Technology Data Exchange (ETDEWEB)

    Yoshizawa, N.; Yamada, Y.; Shiraishi, M. [National Institute for Resources and Environment, Tsukuba (Japan); Kojima, S.; Tamai, H.; Yasuda, H. [Hiroshima University, Hiroshima (Japan). Faculty of Engineering

    1996-10-28

    The metal dependence of mesoporous activated carbons with various metal acetylacetonate (acac) particles prepared from Morwell coal was studied. In experiment, the mixture of Morwell coal and acac metal complexes were dissipated into tetrahydrofuran, and after agitation in Ar atmosphere, the solvent was removed by vacuum distillation. Coal specimens with Fe(acac)3, Ni(acac)2 and Co(acac)2 as acac complexes were activated by exchanging flow gas with water vapor after heat treatment in N2 gas flow at 900{degree}C. The pore sizes of the specimens were obtained from N2 adsorption isotherms by BET method and BJH method. Conditions of pores and metals in the specimens were examined by XRD measurement and TEM observation. The relation between the above conditions and pore characteristics obtained from adsorption experiment was also examined. As a result, the difference in mesopore ratio between the specimens and blank specimens was larger in the order of Fe, Co and Ni, and the effect of added metal complexes was also larger in this order. 3 refs., 3 figs., 3 tabs.

  2. Synthesis and Characterization of Iron-impregnated Pre-oxidized Activated Carbon Prepared by Microwave Radiation for As(V) Removal from Water

    Science.gov (United States)

    Yurum, Yuda; Yurum, Alp; Ozlem Kocabas, Zuleyha; Semiat, Raphael

    2013-04-01

    One of the most efficient ways to treat water is probably by adsorption and catalytic oxidation. Surely, for such a process to be economical, the catalyst and the adsorber should have a high catalytic activity and adsorption capacity, and be inexpensive. One of these materials is iron oxide, which is studied and used in areas like catalysis and environmental applications. It is known that synthesizing iron oxides in nano size enhances the catalytic activity. Pre-oxidized activated carbons impregnated with iron-based nanoparticles are prepared in a single step under hydrothermal conditions with microwave radiation. The hydrothermal treatment provides an important advantage by forming fine particles that can easily impregnate deep in to the porous support by the help of water. Their efficiency for the removal of As(V) from water was compared with the pure pre-oxidized activated carbon and iron oxide nanoparticles impregnated without microwave radiation. The synthesized nanomaterials with different iron oxide loadings were characterized by x-ray diffraction (XRD), scanning electron microscopy (SEM), and Brunauer-Emmett-Teller (BET) surface area analyzer. Iron loadings were calculated using flame atomic absorbance. Microwave radiation provided much faster iron impregnation on the active carbon surface. At the first stage of microwave radiation iron oxide impregnation is low but after 6 minutes, iron oxide nanoparticles of 100 nm size started to cover the surface homogeneously. Further treatment with microwave increased the size of particles and the amount of surface coverage. Additionally, with microwave hydrothermal treatment, relatively higher iron oxide loadings were achieved within 10 minutes. From the XRD characterization it was seen that at the first stage of radiation, iron deposited in the form of β-FeOOH, but after the first stage the structure became Fe2O3. While radiation increased the surface area of the material during the first stages, at the last stage

  3. 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

  4. Preparation and Adsorptive Property of Mangosteen Activated Carbon%山竹壳活性炭的制备与吸附性能研究

    Institute of Scientific and Technical Information of China (English)

    谈梦仙; 洪孝挺; 吕向红

    2016-01-01

    Activated carbons with different alkali/carbon ratios were prepared using the mangosteen skin. The sur-face and structural properties of samples were analyzed with SEM and BET. The specific surface area of the best one reached up to 2 961. 53 m2/g. Then the adsorption isotherms for rhodamine B and Pb2+, adsorption isotherm fit-ted two common models, Freundlich and Langmuir models were studied. The results show that adsorption isotherm to rhodamine B is best fitted with the Langmuir model, while Pb2+ is both fitted with the Freundlich and Langmuir mod-els. The adsorption capacities towards rhodamine B and Pb2+ reached to 1 222. 18 mg/g, 107. 07 mg/g, respectively.%以山竹壳为原料,采用氢氧化钾活化法制备了不同碱炭比的活性炭,通过扫描电子显微镜( SEM)和比表面积( BET)等对活性炭进行了物理性质表征.最优活性炭的比表面积高达2961.53 m2/g.对其进行罗丹明B和铅离子的吸附实验,并进行Langmuir和Freundlich吸附模型拟合,结果表明,山竹壳活性炭对罗丹明B的吸附更符合Lang-muir吸附等温模型,而铅离子的吸附符合2种吸附模型.另外,该活性炭对罗丹明B和铅离子的饱和吸附量分别达到1222.18 mg/g和107.07 mg/g.

  5. Preparation and Characterization of Calcium Carbonate Nanoparticles

    Science.gov (United States)

    Hassim, Aqilah; Rachmawati, Heni

    2010-10-01

    Taking calcium supplements can reduce the risk of developing osteoporosis, but they are not readily absorbed in the gastrointestinal tract. Nanotechnology is expected to resolve this problem. In this study, we prepared and characterized calcium carbonate nanoparticle to improve the solubility by using bottom-up method. The experiment was done by titrating calcium chloride with sodium carbonate with the addition of polyvinylpyrrolidone (PVP) as stabilizer, using ultra-turrax. Various concentrations of calcium chloride and sodium carbonate as well as various speed of stirring were used to prepare the calcium carbonate nanoparticles. Evaluations studied were including particle size, polydispersity index (PI) and zeta potential with particle analyzer, surface morphology with scanning electron microscope, and saturated solubility. In addition, to test the ability of PVP to prevent particles growth, short stability study was performed by storing nano CaCO3 suspension at room temperature for 2 weeks. Results show that using 8000 rpm speed of stirring, the particle size tends to be bigger with the range of 500-600 nm (PI between 0.2-0.4) whereas with stirring speed of 4000 rpm, the particle size tends to be smaller with 300-400 nm (PI between 0.2-0.4). Stirring speed of 6000 rpm produced particle size within the range of 400-500 nm (PI between 0.2-0.4). SEM photograph shows that particles are monodisperse confirming that particles were physically stable without any agglomeration within 2 weeks storage. Taken together, nano CaCO3 is successfully prepared by bottom-up method and PVP is a good stabilizer to prevent the particle growth.

  6. Preparation of Microporous Activated Carbon from Raw Coconut Shell by Two-step Procedure%两步法制备椰壳基微孔活性炭

    Institute of Scientific and Technical Information of China (English)

    苏伟; 周理; 周亚平

    2006-01-01

    A novel two-step procedure was used to manufacture microporous activated carbon from raw coconut shell. In this process, the raw coconut shell was (1) heated in an inert environment to temperatures between 450℃ and 850℃, and reacted with oxygen ( po2 = 1.1 -5.3kPa) for some time, and (2) heated again in inert environment to activation temperature(850℃) to produce an activated carbon. Activated carbons with specific surface area greater than 700m2.g-1 were manufactured with a yield between 24% and 28%. It was shown that the carbon had a narrow distribution of pore size, possibly less than lnm, which was calculated by a simple method based on local density function theory.

  7. Preparation of low cost activated carbon from Myrtus communis and pomegranate and their efficient application for removal of Congo red from aqueous solution.

    Science.gov (United States)

    Ghaedi, Mehrorang; Tavallali, Hossein; Sharifi, Mahdi; Kokhdan, Syamak Nasiri; Asghari, Alireza

    2012-02-01

    In this research, the potential applicability of activated carbon prepared from Myrtus communis (AC-MC) and pomegranate (AC-PG) as useful adsorbents for the removal of Congo red (CR) from aqueous solutions in batch method was investigated. The effects of pH, contact time, agitation time and amount of adsorbents on removal percentage of Congo red on both adsorbents were examined. Increase in pH up to 6 for AC-MC and pH 7 for AC-PG increase the adsorption percentage (capacity) and reach equilibrium within 30 min of contact time. Fitting the experimental data to conventional isotherm models like Freundlich, Langmuir, Tempkin and Dubinin-Radushkevich show that the experimental data fitted very well to the Freundlich isotherm for AC-MC and Langmuir isotherm for AC-PG. Fitting the experimental data to different kinetic models such as pseudo first-order, pseudo second-order, Elovich and intraparticle diffusion mechanism showed the applicability of a pseudo second-order with involvement of intraparticle diffusion model for interpretation of experimental data for both adsorbents. The adsorption capacity of AC-PG and AC-MC for the removal of CR was found to be 19.231 and 10 mg g(-1). These results clearly indicate the efficiency of adsorbents as a low cost adsorbent for treatment of wastewater containing CR.

  8. Preparation of low cost activated carbon from Myrtus communis and pomegranate and their efficient application for removal of Congo red from aqueous solution

    Science.gov (United States)

    Ghaedi, Mehrorang; Tavallali, Hossein; Sharifi, Mahdi; Kokhdan, Syamak Nasiri; Asghari, Alireza

    2012-02-01

    In this research, the potential applicability of activated carbon prepared from Myrtus communis (AC-MC) and pomegranate (AC-PG) as useful adsorbents for the removal of Congo red (CR) from aqueous solutions in batch method was investigated. The effects of pH, contact time, agitation time and amount of adsorbents on removal percentage of Congo red on both adsorbents were examined. Increase in pH up to 6 for AC-MC and pH 7 for AC-PG increase the adsorption percentage (capacity) and reach equilibrium within 30 min of contact time. Fitting the experimental data to conventional isotherm models like Freundlich, Langmuir, Tempkin and Dubinin-Radushkevich show that the experimental data fitted very well to the Freundlich isotherm for AC-MC and Langmuir isotherm for AC-PG. Fitting the experimental data to different kinetic models such as pseudo first-order, pseudo second-order, Elovich and intraparticle diffusion mechanism showed the applicability of a pseudo second-order with involvement of intraparticle diffusion model for interpretation of experimental data for both adsorbents. The adsorption capacity of AC-PG and AC-MC for the removal of CR was found to be 19.231 and 10 mg g -1. These results clearly indicate the efficiency of adsorbents as a low cost adsorbent for treatment of wastewater containing CR.

  9. A Comparative Study on Equilibrium Adsorption of Dyes on Adsorbents Prepared from Coastal Plant, C. equisetifolia Seeds via Green Modification and Activated Carbon

    Directory of Open Access Journals (Sweden)

    Jaafar Jazulhafiz Jefri

    2016-01-01

    Full Text Available Eco-friendly adsorbents were prepared from coastal plant, C. equisetifolia seeds treated with β-cyclodextrin (Rhusorbent for the removal of dyes. The study was carried out to determine the effectiveness of Rhusorbent to remove common dyes such as malachite green (MG and neutral red (NR dyes from aqueous solutions in batch experiments. The commercial activated carbon (AC was also used in this equilibrium absorption study which includes the effect of adsorbent dosage, initial dye concentration and contact time. The percentage of MG dye removal of about 92.4% and 88.4% was achieved for both Rhusorbent and AC respectively at concentration of 60mg/L and 0.4g absorbent. The equilibrium adsorption of about 91.1% and 79.1% was achieved for both Rhusorbent and AC respectively involving NR dye. The scanning electron micrographs of Rhusorbent show uneven and rough surface prompting evidence for the effective adsorption of MG and NR dyes on the surface of adsorbents. For both adsorption studies, Langmuir and Freundlich isotherm models fitted well the adsorption data involving both Rhusorbent and AC. C. equisetifolia seeds are a potential source for bio-inspired adsorbents for the removal of MG and NR dyes.

  10. Preparation and Characterization of Mn/N Co-Doped TiO2 Loaded on Wood-Based Activated Carbon Fiber and Its Visible Light Photodegradation

    Directory of Open Access Journals (Sweden)

    Xiaojun Ma

    2015-09-01

    Full Text Available Using MnSO4·H2O as manganese source and urea as nitrogen source, Mn/N co-doped TiO2 loaded on wood-based activated carbon fiber (Mn/Ti-N-WACF was prepared by sol–gel method. Mn/Ti-N-WACF with different Mn doping contents was characterized by scanning electron microscopy, X-ray diffraction (XRD and X-ray photoelectron spectroscopies (XPS, and ultraviolet-visible spectrophotometer. Results showed that the loading rate of TiO2 in Mn/Ti-N-WACF was improved by Mn/N co-doping. After calcination at 450 °C, the degree of crystallinity of TiO2 was reduced due to Mn/N co-doption in the resulting Mn/Ti-N-WACF samples, but the TiO2 crystal phase was not changed. XPS spectra revealed that some Ti4+ ions from the TiO2 lattice of Mn/Ti-N-WACF system were substituted by doped Mn. Moreover, new bonds formed within N–Ti–N and Ti–N–O because of the doped N that substituted some oxygen atoms in the TiO2 lattice. Notably, the degradation rate of methylene blue for Mn/Ti-N-WACF was improved because of the co-doped Mn/N under visible-light irradiation.

  11. Facile preparation of magnetic separable powdered-activated-carbon/Ni adsorbent and its application in removal of perfluorooctane sulfonate (PFOS) from aqueous solution.

    Science.gov (United States)

    Liang, Xuanqi; Gondal, Mohammed A; Chang, Xiaofeng; Yamani, Zain H; Li, Nianwu; Lu, Hongling; Ji, Guangbin

    2011-01-01

    The main aim of this study was to synthesize magnetic separable Nickel/powdered activated carbon (Ni/PAC) and its application as an adsorbent for removal of PFOS from aqueous solution. In this work, the synthesized adsorbent using simple method was characterized by using X-ray diffractionometer (XRD), surface area and pore size analyzer, vibrating sample magnetometer (VSM), and high resolution transmission electron microscope (HRTEM). The surface area, pore volume and pore size of synthesized PAC was 1521.8 m(2)g(-1), 0.96 cm(3)g(-1), 2.54 nm, respectively. Different kinetic models: the pseudo-first-order model, the pseudo-second-order model, and three adsorption isotherms--Langmuir, Freundlich and Temkin--were applied to study the sorption kinetics and isothermal behavior of PFOS onto the surface of an as-prepared adsorbent. The rate constant using the pseudo-second-order model for removal of 150 ppm PFOS was estimated as 8.82×10(-5) and 1.64×10(-4) for PAC and 40% Ni/PAC, respectively. Our results demonstrated that the composite adsorbents exhibited a clear magnetic hysteretic behavior, indicating the potential practical application in magnetic separation of adsorbents from aqueous solution phase as well.

  12. The removal of endocrine disrupting compounds, pharmaceutically activated compounds and cyanobacterial toxins during drinking water preparation using activated carbon--a review.

    Science.gov (United States)

    Delgado, Luis F; Charles, Philippe; Glucina, Karl; Morlay, Catherine

    2012-10-01

    This paper provides a review of recent scientific research on the removal by activated carbon (AC) in drinking water (DW) treatment of 1) two classes of currently unregulated trace level contaminants with potential chronic toxicity-pharmaceutically activate compounds (PhACs) and endocrine disrupting compounds (EDCs); 2) cyanobacterial toxins (CyBTs), which are a group of highly toxic and regulated compounds (as microcystin-LR); and 3) the above mentioned compounds by the hybrid system powdered AC/membrane filtration. The influence of solute and AC properties, as well as the competitive effect from background natural organic matter on the adsorption of such trace contaminants, are also considered. In addition, a number of adsorption isotherm parameters reported for PhACs, EDCs and CyBTs are presented herein. AC adsorption has proven to be an effective removal process for such trace contaminants without generating transformation products. This process appears to be a crucial step in order to minimize PhACs, EDCs and CyBTs in finished DW, hence calling for further studies on AC adsorption removal of these compounds. Finally, a priority chart of PhACs and EDCs warranting further study for the removal by AC adsorption is proposed based on the compounds' structural characteristics and their low removal by AC compared to the other compounds.

  13. Preparation of TiO2/activated carbon with Fe ions doping photocatalyst and its application to photocatalytic degradation of reactive brilliant red K2G

    Institute of Scientific and Technical Information of China (English)

    LI YouJi; LI Jing; MA MingYuan; OUYANG YuZhu; YAN WenBin

    2009-01-01

    Titanium dioxide coated on activated carbon(AC)with Fe ions doping(Fe-TiO2/AC)composite was prepared by an improved sol-gel method.The photocatalytic activities were tested by photocatalytic degradation of reactive brilliant red K2G in solution.The results show that in comparison with the agglomeration of pure TiO2,the TiO2 nanoparticles are well dispersed in the AC matrix,of which sizes are decreased with Fe ions doping.Additionally,the iron species on TiO2 of composite are Fe2O3 and FeO,which do not affect the crystalline structures of TiO2 nanopanicles.The AC matrix and iron doping content influence the fluorescence intensity of composite due to their effects on recombination prob ability of hole-electron paire.Compared with TiO2,0.3%Fe-TiO2,TiO2/AC,0.5% Fe-TiO2/AC and 0.1% Fe-TiO2/AC,the 0.3%Fe-TiO2/AC shows the highest photoactivity with the complete mineralization of K2G for finite time due to the optimum Fe ions content and AC matrix.Furthermore,the kinetic constant(K=0.0229 min-1)of 0.3% Fe-TiO2/AC composite is more than the sum of both TiO2/AC(0.0154 min-1)and 0.3% Fe-TiO2(0.0057 min-1)because coexistence of the AC end Fe ions has an enlarging effect on improving the photoactivity of TiO2.

  14. Preparation of TiO2/activated carbon with Fe ions doping photocatalyst and its application to photocatalytic degradation of reactive brilliant red K2G

    Institute of Scientific and Technical Information of China (English)

    2009-01-01

    Titanium dioxide coated on activated carbon(AC) with Fe ions doping(Fe-TiO2/AC) composite was prepared by an improved sol-gel method.The photocatalytic activities were tested by photocatalytic degradation of reactive brilliant red K2G in solution.The results show that in comparison with the agglomeration of pure TiO2,the TiO2 nanoparticles are well dispersed in the AC matrix,of which sizes are decreased with Fe ions doping.Additionally,the iron species on TiO2 of composite are Fe2O3 and FeO,which do not affect the crystalline structures of TiO2 nanoparticles.The AC matrix and iron doping content influence the fluorescence intensity of composite due to their effects on recombination probability of hole-electron pairs.Compared with TiO2,0.3% Fe-TiO2,TiO2/AC,0.5% Fe-TiO2/AC and 0.1% Fe-TiO2/AC,the 0.3% Fe-TiO2/AC shows the highest photoactivity with the complete mineralization of K2G for finite time due to the optimum Fe ions content and AC matrix.Furthermore,the kinetic constant(k=0.0229 min-1) of 0.3% Fe-TiO2/AC composite is more than the sum of both TiO2/AC(0.0154 min-1) and 0.3% Fe-TiO2(0.0057 min-1) because coexistence of the AC and Fe ions has an enlarging effect on improving the photoactivity of TiO2.

  15. Carbon paper supported Pt/Au catalysts prepared via Cu underpotential deposition-redox replacement and investigation of their electrocatalytic activity for methanol oxidation and oxygen reduction reactions

    Energy Technology Data Exchange (ETDEWEB)

    Khosravi, Mohsen; Amini, Mohammad K. [Chemistry Department, University of Isfahan, Isfahan 81744-73441 (Iran)

    2010-10-15

    Through a simple and rapid method, carbon papers (CPs) were coated with Au and the resulting Au/CP substrates were used for the preparation of Pt/Au/CP by Cu underpotential deposition (Cu UPD) and redox replacement technique. A series of Pt{sub n}/Au/CP catalysts (where n = number of UPD-redox replacement cycles) were synthesized and their electrochemical properties for methanol oxidation reaction (MOR), and oxygen reduction reaction (ORR) were investigated by electrochemical measurements. The Pt{sub n}/Au/CP electrodes show higher electrocatalytic activity and enhanced poison tolerance for the MOR as compared to a commercial Pt/C on CP (Pt/C/CP). The highest mass specific activity and Pt utilization efficiency for MOR was observed on Pt{sub 1}/Au/CP with a thickness close to a monatomic Pt layer. Chronoamperometric tests in methanol solution revealed that Pt{sub n}/Au/CPs have much higher CO tolerance compared to Pt/C/CP. Among the Pt{sub n}/Au/CPs, CO tolerance decreases with increasing the amount of deposited Pt, indicating that the exposed Au atoms in close proximity to Pt plays a positive role against CO poisoning. Compared with the Pt/C/CP, all the Pt{sub n}/Au/CP electrodes show more positive onset potentials and lower overpotentials for ORR. For instance, the onset potential of ORR is 150 mV more positive and the overpotential is {proportional_to}140 mV lower on Pt{sub 4}/Au/CP with respect to Pt/C/CP. (author)

  16. The effects of autohydrolysis pretreatment on the structural characteristics, adsorptive and catalytic properties of the activated carbon prepared from Eucommia ulmoides Oliver based on a biorefinery process.

    Science.gov (United States)

    Zhu, Ming-Qiang; Wang, Zhi-Wen; Wen, Jia-Long; Qiu, Ling; Zhu, Ya-Hong; Su, Yin-Quan; Wei, Qin; Sun, Run-Cang

    2017-05-01

    Eucommia ulmoides Oliver (EU) wood was consecutively treated by autohydrolysis pretreatment and chemical carbonization post-treatment based on a biorefinery process. Results showed that the optimal condition of the autohydrolysis pretreatment and carbonization process yielded 10.37kg xylooligosaccharides (XOS), 1.39kg degraded hemicellulosic products, 17.29kg other degraded products from hemicelluloses and 40.72kg activated carbon (SBET of 1534.06m(2)/g) from the 100kg raw materials. Simultaneously, 29.14kg gas products generated from the optimum integrated process was significantly lower than that from the direct carbonization process (68.84kg). Besides, the optimal activated carbon (AC170-1.0) also showed a moderate catalytic activity and high stability for hydrogen production by catalytic methane decomposition. Overall, the data presented indicated that the integrated process is an eco-friendly and efficient process to produce XOS and activated carbon, which is beneficial for value-added and industrial application of EU wood. Copyright © 2017 Elsevier Ltd. All rights reserved.

  17. Metal-carbon nanocomposites based on activated IR pyrolized polyacrylonitrile

    Energy Technology Data Exchange (ETDEWEB)

    Efimov, Mikhail N.; Zhilyaeva, Natalya A.; Vasilyev, Andrey A.; Muratov, Dmitriy G.; Zemtsov, Lev M.; Karpacheva, Galina P. [A.V. Topchiev Institute of Petrochemical Synthesis RAS, Leninskiy Prospekt 29, 119991 Moscow Russia (Russian Federation)

    2016-05-18

    In this paper we report about new approach to preparation of metal-carbon nanocomposites based on activated carbon. Polyacrylonitrile is suggested as a precursor for Co, Pd and Ru nanoparticles carbon support which is prepared under IR pyrolysis conditions of a precursor. The first part of the paper is devoted to study activated carbon structural characteristics dependence on activation conditions. In the second part the effect of type of metal introduced in precursor on metal-carbon nanocomposite structural characteristics is shown. Prepared AC and nanocomposite samples are characterized by BET, TEM, SEM and X-ray diffraction.

  18. Kinetics and mechanism studies of p-nitroaniline adsorption on activated carbon fibers prepared from cotton stalk by NH4H2PO4 activation and subsequent gasification with steam.

    Science.gov (United States)

    Li, Kunquan; Li, Ye; Zheng, Zheng

    2010-06-15

    Activated carbon fibers (ACFs) were prepared for the removal of p-nitroaniline (PNA) from cotton stalk by chemical activation with NH(4)H(2)PO(4) and subsequent physical activation with steam. Surface properties of the prepared ACFs were performed using nitrogen adsorption, FTIR spectroscopy and SEM. The influence of contact time, solution temperature and surface property on PNA adsorption onto the prepared ACFs was investigated by conducting a series of batch adsorption experiments. The kinetic rates at different temperatures were modeled by using the Lagergren-first-order, pseudo-second-order, Morris's intraparticle diffusion and Boyd's film-diffusion models, respectively. It was found that the maximum adsorption of PNA on the ACFs was more than 510 mg/L, and over 60% adsorption occurred in first 25 min. The effect of temperature on the adsorption was related to the contacting time and the micropore structure of the adsorbents. And the increase of micropore surface area favored the adsorption process. Kinetic rates fitted the pseudo-second-order model very well. The pore diffusion played an important role in the entire adsorption period, and intraparticle diffusion was the rate-limiting step in the beginning 20 min. The Freundlich model provided a better data fitting as compared with the Langmuir model. The surface micrograph of the ACF after adsorption showed a distinct roughness with oval patterns. The results revealed that the adsorption was in part with multimolecular layers of coverage.

  19. 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.

  20. Preparation and Application of Fluorescent Carbon Dots

    Directory of Open Access Journals (Sweden)

    Jun Zuo

    2015-01-01

    Full Text Available Fluorescent carbon dots (CDs are a novel type of fluorescent nanomaterials, which not only possess the specific quantum confinement effects of nanomaterials due to the small size of nanomaterials, but also have good biocompatibility and high fluorescence. Meanwhile, fluorescence CDs overcome the shortcomings of high toxicity of traditional nanomaterials. Moreover, the preparation procedure of fluorescent CDs is simple and easy. Therefore, fluorescent CDs have great potential applied in photocatalysis, biochemical sensing, bioimaging, drug delivery, and other related areas. In this paper, recent hot researches on fluorescent CDs are reviewed and some problems in the progress of fluorescent CDs are also summarized. At last, a future outlook in this direction is presented.

  1. Ultrasonic preparation of nano-nickel/activated carbon composite using spent electroless nickel plating bath and application in degradation of 2,6-dichlorophenol.

    Science.gov (United States)

    Su, Jingyu; Jin, Guanping; Li, Changyong; Zhu, Xiaohui; Dou, Yan; Li, Yong; Wang, Xin; Wang, Kunwei; Gu, Qianqian

    2014-11-01

    Ni was effectively recovered from spent electroless nickel (EN) plating baths by forming a nano-nickel coated activated carbon composite. With the aid of ultrasonication, melamine-formaldehyde-tetraoxalyl-ethylenediamine chelating resins were grafted on activated carbon (MFT/AC). PdCl2 sol was adsorbed on MFT/AC, which was then immersed in spent electroless nickel plating bath; then nano-nickel could be reduced by ascorbic acid to form a nano-nickel coating on the activated carbon composite (Ni/AC) in situ. The materials present were carefully examined by Fourier transform infrared spectroscopy, X-ray diffraction, field emission scanning electron microscopy, X-ray photoelectron spectroscopy and electrochemistry techniques. The resins were well distributed on the inside and outside surfaces of activated carbon with a size of 120 ± 30 nm in MFT/AC, and a great deal of nano-nickel particles were evenly deposited with a size of 3.8 ± 1.1 nm in Ni/MFT. Moreover, Ni/AC was successfully used as a catalyst for ultrasonic degradation of 2,6-dichlorophenol.

  2. 不同方法制备碳载金催化剂对臭氧的催化分解%Catalytic Activity of Au Supported on Activated Carbon Catalyst Preparing with Different Methods for Ozone Decomposition

    Institute of Scientific and Technical Information of China (English)

    张博; 徐九华; 李宏煦; 史蕊

    2011-01-01

    采用浸渍法和溶胶负载法制备以改性活性碳为载体以纳米金为活性组分的催化剂,通过BET,SEM和XPS表征制备方法对催化剂比表面积、孔隙结构、表面形貌及表面元素组成的影响,测试催化剂在室温下对低浓度臭氧的催化分解性能.结果显示,在室温,相对湿度为45±5%,空速为96000h(-1).臭氧初始浓度为50mg/m3,气体与催化剂的接触时间为0.04s的条件下,在1200min时采用浸渍法制备的催化剂对臭氧的分解率为85%,而溶胶负载法制备的催化剂此时对臭氧的分解效率仍在94%以上.采用溶胶负载法制备的催化剂纳米金颗粒粒径更小、更均匀,在催化剂表面的覆盖率更大是其催化活性更高的主要原因.%The catalysts of nano-particle Au supported by modified activated carbon are prepared with the methods of impregnation and sol-immobilized, and characterized by BET, SEM and XPS to consider the influence of preparation method to its specific surface area, pore structure, surface topography and composition.The catalytic activity for low-level ozone decomposition at ambient temperature of the catalysts is evaluated.The results show that under the condition of 50mg/m3 ozone in air, space velocity 96000 h-1, relative humidity 45 ±5% , contact time 0.04s and ambient temperature, the ozone removal ratio with the catalyst prepared by impregnation method is at 85% within 1200min, however, the ozone removal ratio with the catalyst by sol-immobilized method could be maintained above 94%.This is due to the reason that the supported gold nanoparticles in the catalyst prepared with sol-immobilized method are much smaller and more uniformly dispersed on the activated carbon, exhibit the higher fraction of coverage.

  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. 城市污泥添加软锰矿制备活性炭的研究%Study on Preparation of Activated Carbon from Pyrolusite-added Sewage Sludge

    Institute of Scientific and Technical Information of China (English)

    谭显东; 陈红燕; 羊依金; 徐成华; 刘建英; 钱志勇

    2011-01-01

    以城市污泥为原料,添加适量的软锰矿,采用氯化锌活化法制备活性炭.采用BET、SEM、FT-IR、O2-TPO、XRD、TGA等方法对其结构和性能进行了表征,并分析了软锰矿对活性炭制备过程的影响.研究结果表明,在实验条件下,城市污泥添加软锰矿制备的活性炭比表面积为354.198 m2/g,总孔体积为0.809 6 cm3/g,微孔体积为0.159 cm3/g,平均孔半径为4.6 nm,碘吸附值为558.05 mg/g.上述性能参数相较于纯污泥制备的活性碳都有较大程度的提高.在使用添加了软锰矿的城市污泥制备活性炭的过程巾软锰矿催化了污泥中有机质的分解,同时也为新生炭提供了更多的骨架,促进了积炭反应,有助于形成孔隙发达的微晶结构.%Activated carbon was prepared from pyrolusite-added sewage sludge by ZnCl2 activation method.Its structure and performance were characterized by BET, SEM, FT - IR, XRD, O2 - TPO and TGA, and the impact of pyrolusite to the preparation of activated carbon was analyzed.The result showed that the specific surface area, total pore volume, micro-pore volume, average pore radius and iodine adsorption of activated carbon from pyrolusite-added sewage sludge can reach 354.198 m2/g, 0.809 6 cm3/g, 0.159 cm3/g, 4.6 nm and 558.05 mg/g, respectively, much more than that of activated carbon from sewage sludge.Pyrolusite catalyzed the decomposition of organic matters in the sewage sludge, which provided more framework for the new generated carbon, facilitated the carbon deposit and contributed to the formation ofmicrocrystalline structure simultaneously in the preparation of activated carbon from pyrolusite-added sewage sludge.

  5. Study of ciprofloxacin adsorption and regeneration of activated carbon prepared from Enteromorpha prolifera impregnated with H3PO4 and sodium benzenesulfonate.

    Science.gov (United States)

    Wang, Man; Li, Gang; Huang, Lihui; Xue, Jing; Liu, Quan; Bao, Nan; Huang, Ji

    2017-05-01

    Activated carbons were derived from Enteromorpha prolifera immersed in H3PO4 solution or the H3PO4 solution mixed with sodium benzenesulfonate (SBS), producing AC and AC-SBS. NaOH solution was employed in regeneration of ciprofloxacin (CIP)-loaded AC and AC-SBS to obtain RAC and RAC-SBS. The properties of the original and regenerated activated carbons were characterized by thermo-gravimetric analysis (TGA), scanning electron microscopy (SEM), N2 adsorption/desorption isotherms and Fourier transform infrared spectroscopy (FTIR). Batched adsorption studies were carried out to compare CIP adsorption behaviors of the four carbons. The results suggested that the four samples exhibited higher proportions of mesopores and similar functional groups. Although AC displayed much higher specific surface area (SBET) (1045.79m(2)/g) than AC-SBS (738.03m(2)/g), its CIP adsorption capacity was much less than AC-SBS. The maximum adsorption capacity for AC, AC-SBS, RAC and RAC-SBS were found to be 250mg/g, 286mg/g, 233mg/g and 256mg/g, respectively, with the isotherms adhering to Langmuir isotherm model. The electrostatic attraction and cation exchange between CIP and the four carbons were the dominant adsorption mechanisms. Moreover, the thermodynamic parameters represented that the adsorption process had been confirmed to be a spontaneous and endothermic reaction. Copyright © 2017. Published by Elsevier Inc.

  6. Novel preparation of carbon-TiO{sub 2} composites

    Energy Technology Data Exchange (ETDEWEB)

    Elizalde-González, María P., E-mail: maria.elizalde.uap.mx@gmail.com; García-Díaz, Esmeralda; Sabinas-Hernández, Sergio A.

    2013-12-15

    Highlights: • Glycerol and TiOSO{sub 4}·xH{sub 2}O produced a carbon-anatase precursor in a one-step sol–gel reaction. • Ultrasound irradiation led to the formation of crystalline TiO{sub 2} prior to thermal treatment. • Carbon and TiO{sub 2} nanocrystals developed larger specific surface in composites. • Large band gap (3.6 eV) in TiO{sub 2} was obtained. • Benzenesulfonic acid identified by LC–MS among decomposition reaction intermediates of the dye Acid Orange 7. -- Abstract: Carbon-TiO{sub 2} sulfated composites were obtained from TiOSO{sub 4}·xH{sub 2}O and glycerol as the TiO{sub 2} and carbon sources, respectively. The precursor xerogels were prepared in a one-step ultrasonic-assisted sol–gel reaction, followed by thermal treatment at 400 °C under a nitrogen atmosphere to produce carbon-TiO{sub 2} sulfated composites. XRD, micro-Raman, SEM, and TEM studies showed that the composites consisted of nanocrystalline clusters of TiO{sub 2} and carbon. Ultrasonication in glycerol promoted the crystallinity of the xerogel precursors prior to thermal treatment. X-ray powder diffraction and Raman spectroscopy studies confirmed that glycerol also facilitated the formation of small crystallites. The band gaps of carbon-TiO{sub 2} composites with two different carbon loadings were found to be 3.06 eV and 2.69 eV. By contrast, the band gap of TiO{sub 2} prepared by our method was 3.53 eV. Calcination of the precursors led to an unusual increase in the specific surface and porosity of the composites compared to TiO{sub 2}. The photocatalytic activities of the prepared composites were tested in a decomposition assay of Acid Orange 7. The reaction was monitored by UV–vis spectrophotometry and by LC-ESI-(Qq)-TOF-MS-DAD. Some intermediate species were identified by LC-ESI-QTOF-MS.

  7. Activated carbon preparation with pore nanosized from biomass precursors; Preparacao de carvoes ativados com poros de dimensoes nanometricas a partir de precursores de biomassa

    Energy Technology Data Exchange (ETDEWEB)

    Capobianco, Gino [Universidade Estadual de Campinas (UNICAMP), SP (Brazil). Fac. de Engenharia Mecanica. Dept. de Planejamento de Sistemas Energeticos; Coutinho, Aparecido dos Reis [Universidade Metodista de Piracicaba, SP (Brazil). Lab. de Materiais Carbonosos; Luengo, Carlos Alberto [Universidade Estadual de Campinas (UNICAMP), SP (Brazil). Inst. de Fisica Gleb Wataghin. Grupo Combustiveis Alternativos

    2004-07-01

    Here are reported preliminary tests using pinnus wood, mesocarpo of green coconut and macadamia shell. They are carbonized and later physically activated with CO{sub 2} or chemically with ZnCl{sub 2}. The resulting activated carbons (AC) are characterized with scanning electronic microscopy, the BET method for determination of the specific surface area-ASE, real density-DR, helium picnometry among others. The results indicate macadamia shell originates better AC, with average micropores in the range of 1,2-1,6 nm, apparent density of 1,08 g/cm{sup 3}, and ASE-BET 1400m{sup 2}/g. Then, these AC have the possibility to be applied in NG storage. (author)

  8. 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

  9. 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)

  10. Effect of Different Activation Methods on the Pore Structure of Activated Carbons Prepared from Pistachio Shells%不同活化方法对开心果壳活性炭的孔结构影响

    Institute of Scientific and Technical Information of China (English)

    陈虹霖; 宋磊

    2014-01-01

    以开心果壳为原料制备活性炭,通过在-196℃下测定活性炭的氮气吸附等温线,探讨 ZnCl2法、KCl法以及ZnCl2?KCl?H2 O联合活化法对活性炭孔结构的影响.研究表明:ZnCl2法制备的开心果果壳活性炭以微孔为主,采用40%ZnCl2溶液浸渍,在500℃下活化1.5 h后得到的活性炭的比表面积为630 m2·g-1;单独KCl活化法不能起到较好的活化效果;对于ZnCl2活化法和KCl活化法,增加水蒸气活化都能增强活化效果,尤其对KCl活化的增强效果最为明显,使其比表面积增大近9倍,但其孔结构仍是微孔为主;ZnCl2?KCl? H2 O联合活化法能有效增加活性炭的中孔,采用40%ZnCl2和6%KCl溶液浸渍,在900℃下活化1.5 h后得到的活性炭的中孔添加量为0.10 cm3·g-1,比表面为740 m2·g-1,中孔孔径集中在4 nm.%Activated carbons were prepared from Pistachio nut shells by using ZnCl2 ,KCl and ZnCl2?KCl?H2 O as activa-ting agents separately,and were tested at-1 9 6 ℃ to obtain the N2 adsorption isotherms to get the pore structure proper-ties.It showed that the pore structure of ZnCl2?activated carbons was mainly micropore,and the max BET area of the ac-tivated carbons was 630 m2 ·g-1 when impregnated with 40% ZnCl2 and activated at 500 ℃ for 1.5 h.While using KCl as activating agent alone,it could be hardly to obtain good activation effect.The activation effect was improved by intro-ducing vapor as the activating gas by using ZnCl2 and KCl as activating agent,which played a much more important played a much more important role on formation of new pores,especially for the method of KCl,and its BET area increased by a-bout 9 times,and the pore structure was mainly micropore.Mesopore was effectivlely donated by using ZnCl2?KCl?H2 O as a mixed activating agent.Under the condition of impregnating with 40% ZnCl2 and 6% KCl,the BET area of the acti-vated carbons was 740 m2 ·g-1 ,as well as the

  11. 不同生物质发酵残渣及泥煤制备活性炭比较研究%Comparison of Activated Carbon Prepared from Different Fermentation of Biomass Residues and Peat

    Institute of Scientific and Technical Information of China (English)

    刘彦涛; 吉骊; 周自圆; 蒋建新; 朱莉伟

    2016-01-01

    近年来,农林废弃物进行资源再利用越来越受到重视,本研究进行了不同生物质发酵残渣及泥煤制备活性炭的比较。组分分析表明,不同生物质发酵残渣及泥煤的组分存在显著差异。在所制备的活性炭中,以糠醛渣为原料、900℃条件下、KOH作为活化剂制得活性炭具有最大比表面积,其值超过2200 m2/g;吸附脱附等温曲线也表明该条件下制备的活性炭具有发达的微孔结构。未分离蛋白玉米秸秆发酵残渣制备活性炭的比表面积随活化温度的升高而升高。%In recent years, more and more attention has been paid to the utilization of biomass. The present study used different biomass feedstock fermentation residue and peat for preparation of activated carbon. Component analysis showed that there were significant differences between the different components of the fermentation of biomass residues and peat. The largest specific surface area of activated carbon was obtained using furfural residue as raw material, at 900 ℃, KOH as activator. Under the above conditions, adsorption desorption isotherm curves also showed that the activated carbon produced an extremely well-developed microporous structure. The specific surface area of activated carbon prepared from corn straw fermentation residue increased with the increase of the activation temperature.

  12. Preparation of free-standing high quality mesoporous carbon membranes

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Xiqing [ORNL; Liang, Chengdu [ORNL; Dai, Sheng [ORNL; Mahurin, Shannon Mark [ORNL; Zhu, Qing [ORNL

    2010-01-01

    Flat-sheet mesoporous carbon membranes with uniform pore size (e.g., 6.4 nm) and controllable thickness were prepared by pyrolysis of polymeric composite films, which were formed by self-assembly of phenolic resin and block copolymer under acidic conditions. Hexamethylenetetramine was selected as a solid cross-linker to control the rheology of polymeric carbon precursors so that the flat-sheet polymeric films could undergo carbonization without deformation, ensuring the preparation of mesoporous carbon membranes on a large scale with high quality. Gas transport properties through these mesoporous carbon membranes are also reported.

  13. Preparation of Crystallized Carbon Nitride Based on Microwave Plasma CVD

    National Research Council Canada - National Science Library

    Masatoshi INOUE; Yukihiro SAKAMOTO; Matsufumi TAKAYA

    2010-01-01

    ... on. To obtain this material, generally CH4 is used as a carbon source. Therefore, to make clear the effects of the reaction gas on the preparation of carbon nitride, we tried to use C2H4 as a carbon source instead of CH4...

  14. PREPARATION OF CARBON NANOFIBERS BY POLYMER BLEND TECHNIQUE

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    The polymer blend technique is a novel method to produced carbon nanofibers. In this paper, we have prepared fine carbon fibers and porous carbon materials by this technique, and we will discuss the experiment results by means of SEM, TGA, Element Analysis, etc.

  15. Preparation of carbon monoliths from orange peel for NOx retention

    Directory of Open Access Journals (Sweden)

    Liliana Giraldo

    2014-12-01

    Full Text Available A series of monoliths are prepared from orange peels and chemically activated with H3PO4, KOH, ZnCl2, and water vapor without a binder. The monoliths were characterized by N2 adsorption-desorption isotherms at 77 K, Boehm titrations and XPS. Thereafter, monoliths were tested for their ability to establish NOx retention. The results show that the retention capacities of NOx were a function of the textural properties and chemistries. The carbons synthesized with ZnCl2 and KOH retained similar amounts of NOx.

  16. Facile preparation of hierarchically porous carbon using diatomite as both template and catalyst and methylene blue adsorption of carbon products.

    Science.gov (United States)

    Liu, Dong; Yuan, Peng; Tan, Daoyong; Liu, Hongmei; Wang, Tong; Fan, Mingde; Zhu, Jianxi; He, Hongping

    2012-12-15

    Hierarchically porous carbons were prepared using a facile preparation method in which diatomite was utilized as both template and catalyst. The porous structures of the carbon products and their formation mechanisms were investigated. The macroporosity and microporosity of the diatomite-templated carbons were derived from replication of diatom shell and structure-reconfiguration of the carbon film, respectively. The macroporosity of carbons was strongly dependent on the original morphology of the diatomite template. The macroporous structure composed of carbon plates connected by the pillar- and tube-like macropores resulted from the replication of the central and edge pores of the diatom shells with disk-shaped morphology, respectively. And another macroporous carbon tubes were also replicated from canoe-shaped diatom shells. The acidity of diatomite dramatically affected the porosity of the carbons, more acid sites of diatomite template resulted in higher surface area and pore volume of the carbon products. The diatomite-templated carbons exhibited higher adsorption capacity for methylene blue than the commercial activated carbon (CAC), although the specific surface area was much smaller than that of CAC, due to the hierarchical porosity of diatomite-templated carbons. And the carbons were readily reclaimed and regenerated. Copyright © 2012 Elsevier Inc. All rights reserved.

  17. A new method of preparing single-walled carbon nanotubes

    Indian Academy of Sciences (India)

    S R C Vivekchand; A Govindaraj

    2003-10-01

    A novel method of purification for single-walled carbon nanotubes, prepared by an arc-discharge method, is described. The method involves a combination of acid washing followed by high temperature hydrogen treatment to remove the metal nanoparticles and amorphous carbon present in the as-synthesized singlewalled carbon nanotubes. The purified single-walled carbon nanotubes have been characterised by low-angle X-ray diffraction, electron microscopy, thermo-gravimetric analysis and Raman spectroscopy.

  18. A new method of preparing single-walled carbon nanotubes

    OpenAIRE

    Vivekchang, SRC; Govindaraj, A.

    2003-01-01

    A novel method of purification for single-walled carbon nanotubes, prepared by an arc-discharge method, is described. The method involves a combination of acid washing followed by high temperature hydrogen treatment to remove the metal nanoparticles and amorphous carbon present in the as-synthesized single-walled carbon nanotubes. The purified single-walled carbon nanotubes have been characterised by low-angle X-ray diffraction, electron microscopy, thermo-gravimetric analysis and Raman spect...

  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. Preparação de carvão ativado em baixas temperaturas de carbonização a partir de rejeitos de café: utilização de FeCl3 como agente ativante Preparation of activated carbon at low carbonization temperatures: utilization of FeCl3 as an alternative activating agent

    Directory of Open Access Journals (Sweden)

    Elaine Pereira

    2008-01-01

    Full Text Available Ferric chloride as a new activating agent was used to obtain activated carbons from agroindustrial waste. This material was prepared at three temperatures of pyrolysis, 200, 280 and 400 ºC. The carbonaceous materials obtained after the activation processes showed high specific surface areas (BET, with values higher than 900 m² g-1. The materials showed different behaviors in the adsorption of methylene blue dye and reactive red textile dye in water solutions. An important fact in the use of FeCl3 as an activating agent is that the activation temperature is at 280 ºC, well below of those commonly employed in chemical or physical activations described in the literature.

  1. 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.

  2. Preparation of sulfur-loaded activated carbons for removing gaseous elemental mercury%高温载硫活性炭的制备及脱汞能力研究

    Institute of Scientific and Technical Information of China (English)

    颜甜; 左宋林; 赵昕; 张宏阳; 施荫锐; 荀永葆

    2012-01-01

    研究了载硫温度、硫炭比(简称S/C),吸附温度等因素对载硫活性炭的硫含量、脱汞能力以及硫损失的影响,探讨载硫活性炭制备的工艺条件优化.结果表明,不同载硫温度下制备的载硫活性炭的气态Hg0吸附能力远强于原料活性炭;载硫温度不同时,负载到活性炭孔隙或表面上的硫的形态不同,导致了脱汞能力的差异,较合适的载硫温度为350℃:S/C为5%(质量分数,下同)时,随着吸附温度的升高,载硫活性炭的气态Hgo吸附量降低;在一定的载硫温度下,原料中S/C越高时,制备的载硫活性炭的硫含量越高、气态Hgo吸附能力越强,但其硫损失率也越高,从实际的使用效果来看,较合适的S/C为10%.%Series of sulfur-loaded activated carbons were prepared for removing gaseous elemental mercury from simulated flue gas. The effects of sulfur loading temperature, sulfur and carbon ratio (S/C), and adsorption temperature on the sulfur-loaded activated carbons were investigated from 3 aspects of sulfur loading quantity, mercury adsorption capacity and sulfur stability. Results showed that the mercury removal ability of sulfur loaded activated carbon was much higher than raw activated carbon) the form of sulfur that loading on the surface or pore of activated carbon was different under different loading temperature, the best temperature for sulfur loading was 350 V. When the S/C was 5% (mass ratio), mercury capture ability of the activated carbons was decreased with increasing the adsorption temperature. Under the same loading temperature, higher sulfur loading content would promote mercury capture ability but also increase the sulfur loss, and the optimal S/C was 10%.

  3. 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.

  4. Preparation of U-Shape Carbon Stripper Foil

    Institute of Scientific and Technical Information of China (English)

    ZHANG; Rong; FAN; Qi-wen; DU; Ying-hui

    2012-01-01

    <正>In an experiment for the Beijing Radioactive Ion-beam Facility, the self-supportting U-shape carbon foils are strongly required to serve as the stripper foils. The preparation procedures are as following. First, the carbon foils with thickness of about 60 μg/cm2 were deposited by the CAA (Controlled AC Arc-discharge) method onto the glass slides coated with betaine-saccharose as releasing agent. The parameters in preparation are listed in Table 1.

  5. 磷酸法制备山楂籽粉末活性炭技术的研究%The Research on the Activated Carbon Preparation Technology from Hawthorn Seeds by the Method of Phosphoric Acid

    Institute of Scientific and Technical Information of China (English)

    王蕾; 李贤宇; 朱传合

    2015-01-01

    In this paper, the activated carbon preparation technology from hawthorn seeds was investigated. Firstly, the related factors that can influence the preparation of activated carbon were run. According to the Single-factor experiment, the optimal condition was established using Plackett-Burman design and Box-Benhnken design. The final result indicated that the best condition was impregnated time 37.3 h, L/P 1∶1.1, the density of phosphoric acid 72.8%, carbonized time1.6 h, carbonized temperature 500℃, the product yield and methylene blue decolorization were 41.11%, 14 mL, respectively.%运用响应面法对磷酸浸泡制备山楂籽粉末活性炭的工艺条件进行了优化。采用单因素试验、Plackett-Burman设计及Box-Behnken设计,确定了山楂籽粉末活性炭最佳制备条件:浸泡时间37.3 h、固液比1∶1.1(1 g山楂籽粉末∶1.1 mL磷酸)、磷酸浓度72.8%、碳化时间1.6 h,炭化温度500℃。该条件下山楂籽活粉末性炭的产率为41.11%,亚甲基蓝的吸附值为14 mL。

  6. Method for the preparation of carbon fiber from polyolefin fiber precursor, and carbon fibers made thereby

    Energy Technology Data Exchange (ETDEWEB)

    Naskar, Amit Kumar; Hunt, Marcus Andrew; Saito, Tomonori

    2015-08-04

    Methods for the preparation of carbon fiber from polyolefin fiber precursor, wherein the polyolefin fiber precursor is partially sulfonated and then carbonized to produce carbon fiber. Methods for producing hollow carbon fibers, wherein the hollow core is circular- or complex-shaped, are also described. Methods for producing carbon fibers possessing a circular- or complex-shaped outer surface, which may be solid or hollow, are also described.

  7. Preparation of array of long carbon nanotubes and fibers therefrom

    Science.gov (United States)

    Arendt, Paul N.; DePaula, Ramond F.; Zhu, Yuntian T.; Usov, Igor O.

    2015-11-19

    An array of carbon nanotubes is prepared by exposing a catalyst structure to a carbon nanotube precursor. Embodiment catalyst structures include one or more trenches, channels, or a combination of trenches and channels. A system for preparing the array includes a heated surface for heating the catalyst structure and a cooling portion that cools gas above the catalyst structure. The system heats the catalyst structure so that the interaction between the precursor and the catalyst structure results in the formation of an array of carbon nanotubes on the catalyst structure, and cools the gas near the catalyst structure and also cools any carbon nanotubes that form on the catalyst structure to prevent or at least minimize the formation of amorphous carbon. Arrays thus formed may be used for spinning fibers of carbon nanotubes.

  8. Enhancement of the analytical properties and catalytic activity of a nickel hexacyanoferrate modified carbon ceramic electrode prepared by two-step sol-gel technique: application to amperometric detection of hydrazine and hydroxyl amine.

    Science.gov (United States)

    Salimi, Abdollah; Abdi, Kamaleddin

    2004-05-28

    The electroless sol-gel technique was used for the construction of nickel hexacyanoferrat (NiHCF) modified carbon composite electrodes (CCEs).This involves two steps: formation of a carbon ceramic electrode fabricated by nickel powder and then immersing the electrode into a sodium- hexacyanoferate solution for the immobilization of NiHCF films. The cyclic voltammety of the resulting modified CCEs prepared under optimum conditions, shows a well defined surface redox couple due to the [Ni(II)Fe(III/II)(CN)(6)](-2/-1) system. The effect of different alkali metal cations in supporting electrolyte on the behavior of the modified electrode were studied. The charge transfer coefficient (alpha) and charge transfer rate constant (k(s)) for modified films were calculated. Hydrazine and hydroxylamine have been chosen as a model to elucidate the electocatalytic ability and analytical parameters of NiHCF modified CCE prepared by one and two-step sol-gel techniques and these compounds determined amperometically at the surface of modified electrodes. The latter shows a good electocatalytic activity towards the oxidation of hydrazine and hydroxylamine in the pH range 3-8 in comparison with CCEs modified by homogeneous mixture of graphite powder, Ni(NO(3))(2) and Na(2)[Fe(CN)(6)], (one-step sol-gel technique). Furthermore, the catalytic rate constant, linear dynamic range, limit of detection, and sensitivity for hydrazine and hydroxylamine detections were evaluated and compared with CCEs prepared with one-step sol-gel method. The modified CCEs containing NiHCF shows good repeatability, short response time, t 90%<3s, long term stability (3 months) and excellent catalytic activity. Furthermore, the method of preparation is rapid and simple and the modified electrodes are renewed by simple mechanical polishing and immersing in [Na(3)Fe(CN](6)] solution.

  9. Preparation of Electrically Conductive Polystyrene/Carbon Nanofiber Nanocomposite Films

    Science.gov (United States)

    Sun, Luyi; O'Reilly, Jonathan Y.; Tien, Chi-Wei; Sue, Hung-Jue

    2008-01-01

    A simple and effective approach to prepare conductive polystyrene/carbon nanofiber (PS/CNF) nanocomposite films via a solution dispersion method is presented. Inexpensive CNF, which has a structure similar to multi-walled carbon nanotubes, is chosen as a nanofiller in this experiment to achieve conductivity in PS films. A good dispersion is…

  10. Method for the preparation of ferrous low carbon porous material

    Energy Technology Data Exchange (ETDEWEB)

    Miller, Curtis Jack

    2014-05-27

    A method for preparing a porous metal article using a powder metallurgy forming process is provided which eliminates the conventional steps associated with removing residual carbon. The method uses a feedstock that includes a ferrous metal powder and a polycarbonate binder. The polycarbonate binder can be removed by thermal decomposition after the metal article is formed without leaving a carbon residue.

  11. Method for the preparation of ferrous low carbon porous material

    Science.gov (United States)

    Miller, Curtis Jack

    2014-05-27

    A method for preparing a porous metal article using a powder metallurgy forming process is provided which eliminates the conventional steps associated with removing residual carbon. The method uses a feedstock that includes a ferrous metal powder and a polycarbonate binder. The polycarbonate binder can be removed by thermal decomposition after the metal article is formed without leaving a carbon residue.

  12. Processes for preparing carbon fibers using gaseous sulfur trioxide

    Energy Technology Data Exchange (ETDEWEB)

    Barton, Bryan E.; Lysenko, Zenon; Bernius, Mark T.; Hukkanen, Eric J.

    2016-01-05

    Disclosed herein are processes for preparing carbonized polymers, such as carbon fibers, comprising: sulfonating a polymer with a sulfonating agent that comprises SO.sub.3 gas to form a sulfonated polymer; treating the sulfonated polymer with a heated solvent, wherein the temperature of said solvent is at least 95.degree. C.; and carbonizing the resulting product by heating it to a temperature of 500-3000.degree. C.

  13. 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.

  14. Preparation, characterization and performance of a novel visible light responsive spherical activated carbon-supported and Er3+:YFeO3-doped TiO2 photocatalyst.

    Science.gov (United States)

    Hou, Dianxun; Feng, Liang; Zhang, Jianbin; Dong, Shuangshi; Zhou, Dandan; Lim, Teik-Thye

    2012-01-15

    A novel spherical activated carbon (SAC) supported and Er(3+):YFeO(3)-doped TiO(2) visible-light responsive photocatalyst (Er(3+):YFeO(3)/TiO(2)-SAC) was synthesized by a modified sol-gel method with ultrasonic dispersion. It was characterized by scanning electron microscope (SEM), energy dispersive X-ray spectroscope (EDS), powder X-ray diffractometer (XRD) and UV-vis diffuse reflectance spectrophotometer (DRS). The photocatalytic activity of Er(3+):YFeO(3)/TiO(2)-SAC was evaluated for degradation of methyl orange (MO) under visible light irradiation. The effects of calcination temperature and irradiation time on its photocatalytic activity were examined. The experimental results indicated that Er(3+):YFeO(3) could function as an upconversion luminescence agent, enabling photocatalytic degradation of MO by TiO(2) under visible light. The Er(3+):YFeO(3)/TiO(2) calcinated at 700°C showed the highest photocatalytic capability compared to those calcinated at other temperatures. The photocatalytic degradation of MO followed the Langmuir-Hinshelwood kinetic model. Although the photocatalyst showed a good physical stability and could tolerate a shear force up to 25 × 10(-3)N/g, its photocatalytic activity decreased over a four-cycle of reuse in concentrated MO solution, indicating that the decreased activity was ascribed to the fouling of catalyst surface by MO during the degradation process. However, the fouled Er(3+):YFeO(3)/TiO(2)-SAC could be regenerated through water rinsing-calcination or acid rinsing-calcination treatment.

  15. Discussion on Coal-base Carbonaceous Material and Activated Carbon Preparation and Properties%煤基碳质反应剂与活性炭的制备和性能

    Institute of Scientific and Technical Information of China (English)

    李晋萍

    2013-01-01

    利用先锋褐煤为原料制备碳质反应剂,采用湿法工艺脱硫除铁,解决了木炭来源对生态所造成的破坏。控制一定的酸度、浓度和液固比,利用水蒸汽活化法制备标准的活性炭。在使用了特制的添加剂后,随着活化温度的升高,各种添加剂成分具有一定的协同作用,使活化时间延长,符合产品质量的要求,提高活化温度使所需活性炭的强度。通过脱硫除杂后工业实验表明,利用活性炭的吸附性或者催化性,能够将其运用于广泛的工业领域,是今后发展特异用途很重要一点。充分利用和开发活性炭的用途,具有重要的社会、经济以及环保效益。%The use of Xianfeng brown coal as raw material to prepare carbonaceous material by wet process of FGD, iron, solves the charcoal sources caused damage to the ecology. Control of acidity, concentration and ratio of liquid to solid, using steam method for preparation of activated carbon standard. In the use of special additives, along with the activation temperature, various additive components has a synergistic effect, so the activation time, meet the requirement of product quality, improve the activation temperature so that the required activated carbon intensity. Through the desulfurization after impurity removal from industrial experiments, the use of activated carbon adsorption or catalysis, can be applied to a wide range of industries, is the future development of specific use is very important. Make full use of and develop the use of activated carbon, has important social, economic and environmental benefits.

  16. 氮硫双掺杂活性炭材料的制备和电容性能%Preparation and Supercapacitive Performance of N, S Co-Doped Activated Carbon Materials

    Institute of Scientific and Technical Information of China (English)

    李朝辉; 李仕蛟; 周晋; 朱婷婷; 沈红龙; 禚淑萍

    2015-01-01

    In this work, N, S co-doped microporous carbon materials were successful y prepared using human hair and sucrose as carbon precursors via a two-step method that combined hydrothermal treatment and post-KOH activation. The morphology, pore texture, and surface chemical properties of the activated carbon materials were investigated by scanning electron microscopy, transmission electron microscopy, N2 adsorption/desorption, X-ray photoelectron spectroscopy, energy dispersive spectroscopy, and Fourier transform infrared spectroscopy. The electrochemical capacitive behavior of the prepared carbons was systematical y studied in 6 mol∙L-1 KOH electrolyte. The maximum specific surface area of the prepared carbons was found to be 1849.4 m2∙g-1 with a porosity that mainly consisted of micropores. Nitrogen and sulfur contents varied from 1.6%to 2.5%and from 0.2%to 0.5%(atomic fraction (x)), respectively. The synergistic-positive effect of N, O, and S-containing groups caused the prepared carbons to exhibit a large pseudo-capacitance. High specific capacitances of up to 200 F∙g-1 at 0.2 A∙g-1 were observed, response to an energy density of 6.9 Wh∙kg-1. At a power density of 10000 W∙kg-1, the energy density was found to be 4.1 Wh∙kg-1. The present work highlights the significance of this new strategy to prepare N, S co-doped carbon materials from renewable biomass.%以头发和蔗糖为原料,通过水热碳化和KOH活化两步法制备了氮硫双掺杂微孔炭材料.利用扫描电子显微镜,透射电子显微镜,氮气吸脱附,X射线光电子能谱,电子能谱和傅里叶交换红外光谱等手段系统表征了所制备活性炭材料的微观形貌,孔隙结构和表面化学性质.并在6 mol∙L-1 KOH溶液中研究了所制备活性炭材料的电容性能.氮气吸脱附测试表明,所制备活性炭材料的比表面积最高可达1849.4 m2∙g-1,孔道以微孔为主.所制备活性炭材料氮元素含量为1.6%-2.5%(原子

  17. Preparation of arrays of long carbon nanotubes using catalyst structure

    Energy Technology Data Exchange (ETDEWEB)

    Zhu, Yuntian T.; Arendt, Paul; Li, Qingwen; Zhang, Xiefie

    2016-03-22

    A structure for preparing an substantially aligned array of carbon nanotubes include a substrate having a first side and a second side, a buffer layer on the first side of the substrate, a catalyst on the buffer layer, and a plurality of channels through the structure for allowing a gaseous carbon source to enter the substrate at the second side and flow through the structure to the catalyst. After preparing the array, a fiber of carbon nanotubes may be spun from the array. Prior to spinning, the array can be immersed in a polymer solution. After spinning, the polymer can be cured.

  18. 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.

  19. 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.

  20. 磷酸活化草浆黑液木质素制备活性炭的研究%Preparation of Activated Carbon from Straw Black Liquor Lignin Impregnated by Phosphoric Acid

    Institute of Scientific and Technical Information of China (English)

    闫伟; 张艳; 杨建华; 鲁金明; 王金渠

    2011-01-01

    用磷酸活化草浆造纸黑液木质素制备活性炭.探讨了磷酸在木质素活化过程中的作用,研究了磷料比、活化温度、活化时间对所制活性炭的比表面积和对正丁烷吸附量的影响.结果表明,草浆造纸黑液木质素是一种优良的制备活性炭的原料,磷酸不仅是脱水剂,而且还是活化过程的保护剂.活性炭制备条件为:磷料比值2.5,活化温度450℃,活化时间60~70 min,制得活性炭的BET比表面积达1772 m2/g,吸附等温线介于Ⅰ型和Ⅱ型之间,正丁烷吸附量为485 mg/g.%Activated carbon was prepared from straw black liquor lignin using phosphoric add as aclivation agenl. The function of phosphoric acid in activation process was discussed, and effects of reaction conditions such as ratio of activation reagent to maleri-al, the temperature and the activation time were investigated. The results showed (hat the lignin of straw black liquor was a good material for preparing activated carbon. Phosphoric acid acts as both [he dehydrating agent and the protective agent during the activation process. The optimum conditions are as follows;activation reagent lo material ratio 2. 5 , activation temperature 450 % , and activation lime 60-70 min. Under these conditions, the BET surface of the carbon is up to 1772 m2/g, and the adsorption isotherm is between the type I and type II with adsorption capacity of n-butane 485 mg/g.

  1. Preparation of perlite-based carbon dioxide absorbent.

    Science.gov (United States)

    He, H; Wu, L; Zhu, J; Yu, B

    1994-02-01

    A new highly efficient carbon dioxide absorbent consisting of sodium hydroxide, expanded perlite and acid-base indicator was prepared. The absorption efficiency, absorption capacity, flow resistance and color indication for the absorbent were tested and compared with some commercial products. The absorbent can reduce the carbon dioxide content in gases to 3.3 ppb (v/v) and absorbs not less than 35% of its weight of carbon dioxide. Besides its large capacity and sharp color indication, the absorbent has an outstanding advantage of small flow resistance in comparison with other commercial carbon dioxide absorbents. Applications in gas analysis and purification were also investigated.

  2. Preparation of porous carbon sphere from waste sugar solution for electric double-layer capacitor

    Science.gov (United States)

    Hao, Zhi-Qiang; Cao, Jing-Pei; Wu, Yan; Zhao, Xiao-Yan; Zhuang, Qi-Qi; Wang, Xing-Yong; Wei, Xian-Yong

    2017-09-01

    Waste sugar solution (WSS), which contains abundant 2-keto-L-gulonic acid, is harmful to the environment if discharged directly. For value-added utilization of the waste resource, a novel process is developed for preparation of porous carbon spheres by hydrothermal carbonization (HTC) of WSS followed by KOH activation. Additionally, the possible preparation mechanism of carbon spheres is proposed. The effects of hydrothermal and activation parameters on the properties of the carbon sphere are also investigated. The carbon sphere is applied to electric double-layer capacitor and its electrochemical performance is studied. These results show that the carbon sphere obtained by HTC at 180 °C for 12 h with the WSS/deionized water volume ratio of 2/3 possess the highest specific capacitance under identical activation conditions. The specific capacitance of the carbon spheres can reach 296.1 F g-1 at a current density of 40 mA g-1. Besides, excellent cycle life and good capacitance retention (89.6%) are observed at 1.5 A g-1 after 5000 cycles. This study not only provides a facile and potential method for the WSS treatment, but also achieves the high value-added recycling of WSS for the preparation of porous carbon spheres with superior electrochemical properties.

  3. Preparation of carbon molecular sieve membranes by KOH activation for gas separation%KOH活化法制备气体分离用炭分子筛膜

    Institute of Scientific and Technical Information of China (English)

    张小勇; 刘锐; 胡浩权; 郑明东

    2012-01-01

    选用KOH为活化剂,利用化学活化法制备炭分子筛膜,考察在热塑性酚醛树脂(PFNR)涂膜液中添加不同质量分数的KOH对炭分子筛膜的影响.结果表明,在炭化过程中,KOH的加入可促进炭分子筛膜孔径的均匀分布,使炭分子筛膜具有发达的孔隙结构.当KOH在PFNR中的添加量从0%增加到4%时,H2的渗透速率由23.68×10-10 mol·m-2·s-1·pa-1提高到28.6×10-10 mol·m-2·s-1·Pa-1;但H2/N2和H2/CH4的分离系数明显下降,分别从471.3下降到147.5、540下降到270.CO2/CH4和O2/N2的分离系数只有轻微下降.%Carbon molecular sieve membranes were prepared by the pyrolysis of a mixture containing phenolic novolac resin and KOH. The effects of KOH on the properties of the membranes were investigated. Results showed that membranes with homogeneous pore size distributions and high gas permeation rates can be obtained by controlling the amount of KOH . Their H2 gas permeability increased from 23.68×10-10to28.6×10-10 mol·m-2·s-1·Pa-1and H2/N2 and H/CH4 selectivity decreased from 471.3 to 147.5 and 540 to 270 respectively, while the CO2/CH4 and O2/N, selectivity changed little with increasing KOH content in the coating solution from 0 to 4 mass% .

  4. 2,4-D adsorption to biochars: effect of preparation conditions on equilibrium adsorption capacity and comparison with commercial activated carbon literature data.

    Science.gov (United States)

    Kearns, J P; Wellborn, L S; Summers, R S; Knappe, D R U

    2014-10-01

    Batch isotherm experiments were conducted with chars to study adsorption of the herbicide 2,4-dichlorophenoxyacetic acid (2,4-D). Chars generated from corncobs, bamboo and wood chips in a laboratory pyrolyzer at 400-700 °C were compared with traditional kiln charcoals collected from villages in S/SE Asia and with activated carbons (ACs). 2,4-D uptake by laboratory chars obtained from bamboo and wood chips after 14 h of pyrolysis at 700 °C, from wood chips after 96 h of pyrolysis at 600 °C, and one of the field-collected chars (basudha) was comparable to ACs. H:C and O:C ratios declined with pyrolysis temperature and duration while surface area increased to >500 m(2)/g. Increasing pyrolysis intensity by increasing temperature and/or duration of heating was found to positively influence adsorption capacity yield (mg(2,4-D/g(feedstock))) over the range of conditions studied. Economic analysis showed that high temperature chars can be a cost-effective alternative to ACs for water treatment applications.

  5. Enhanced Photocatalytic Activity of C-TiO2 Thin Films Prepared by Magnetron Sputtering and Post-carbon Ion Implantation

    Institute of Scientific and Technical Information of China (English)

    LUO Shengyun; YAN Bingxi; CAO Minjian; SHEN Jie

    2015-01-01

    TiO2 thin films were fabricated by RF magnetron sputtering on titanium substrates and then implanted with different amounts of carbon. The microstructure, valence states and optical characteristics of each sample were investigated by X-ray diffraction, X-ray photoelectron spectroscopy and UV-vis diffuse reflection spectroscopy. Photoelectric property was evaluated under visible light using a xenon lamp as illuminant. The experimental results indicate that the implanting carbon concentration has a significant influence on film’s micro structure and element valence states. The dominant valence states of carbon vary as carbon content increases. Carbon ion implantation remarkably enhances the current density and photocatalytic capability of TiO2 thin films. The optimized implanting content is 9.83×1017 ion/cm2, which gives rise to a 150%increased photocurrent and degradation rate.

  6. Preparation and Characterization of Carbon Filaments

    Science.gov (United States)

    1991-04-01

    catalysts gave straight filaments, while the use of nickel and other catalysts resulted in a variety of vermicular forms of filaments. Ferrocene, (C5H5)2Fe...vapor deposition of carbon filaments is presented along with a theory for the vermicular growth of filaments on quartz substrates. I U I I I I I I...one hour. The experimental details of the matrix and results are discussed, also theories for the role of hydrogen and the vermicular growth of

  7. Numerical analysis of the influence of the impregnation ratio on the microporous structure formation of activated carbons, prepared by chemical activation of waste biomass with phosphoric(V) acid

    Science.gov (United States)

    Kwiatkowski, Mirosław; Kalderis, Dimitrios; Diamadopoulos, Evan

    2017-06-01

    This paper presents the results of the application of new mathematical adsorption models with the unique numerical fast multivariate identification procedure as the tool for analysing the influence of the impregnation ratio i.e. activator to the raw material mass ratio on the microporous structure development of the activated carbons, obtained from sugarcane bagasse and rice husk by chemical activation with phosphoric(V) acid.

  8. 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.

  9. 活性炭负载镍锌铁氧体的制备及电磁性能研究%Preparation and electromagnetism property of activated carbon loaded with Ni-Zn ferrite

    Institute of Scientific and Technical Information of China (English)

    安玉良; 李杰; 袁霞; 隋宏超

    2014-01-01

    以柠檬酸为络合剂制备镍锌铁氧体溶胶,以活性炭为基体负载 Ni-Zn 铁氧体,再通过焙烧制备出形态和结构理想的活性炭/镍锌铁氧体复合材料;详细地考察烧结温度、煅烧气氛及活性炭与铁氧体的配比等工艺参数对复合材料的形态和结构的影响;分别采用X射线衍射(XRD)和扫描电镜(SEM)对制备出的复合材料进行形貌、结构表征分析.采用波导法在8.2~12.4 GHz波段对活性炭负载纳米镍锌铁氧体复合材料进行电磁参数测试,结果表明所制备活性炭负载镍锌铁氧体复合材料具有较高的电、磁损耗角正切值,其吸波性能较好.%The Ni-Zn ferrite sol was synthesized with citric acid as complexing reagent,and the ferrite and activa-ted carbon composite gel was obtained by vaporization treatment,then the activated carbon loaded with Ni-Zn ferrite composite was prepared by calcination treatment of the gel.The effect of process parameters such as the sintering temperature,sintering gas and ratio of carbon/ferrite on the morphology and structure of composite were studied in detail,in which the morphology,structure and compose of composite were characterized by scanning electron microscopy (SEM)and elements X-ray diffraction (XRD).Furthermore,the complex permit-tivity and permeability of the as-prepared composites were characterized in the frequency ranges of 8.2-12.4 GHz by the wave-guide method on the vector network analyzer,in which the higher electrical and magnetic loss tan-gent values of the activated carbon loaded with Ni-Zn ferrite composite were obtained.

  10. Preparation of spherical cobalt carbonate powder with high tap density

    Institute of Scientific and Technical Information of China (English)

    XIAO Jin; WANG Jian-feng; LIU Yong-dong; LI Jie; LIU Ye-xiang

    2006-01-01

    Spherical cobalt carbonate with high tap density, good crystallization and uniform particle size was prepared by controlled chemical crystal method using cobalt chloride and ammonium bicarbonate as cobalt source and precipitator. The effects of pH value and reaction time on crystallization and physical properties of cobalt carbonate were studied. The results show that the key factors influencing the preparation process of spherical cobalt carbonate with high tap density and good crystallization are how to control pH value (7.25 ± 0.05) and keep some reaction time (about 10 h). Co4O3 was prepared by sintering spherical morphology CoCO3 samples at varied temperatures. The results show that as the decomposition temperature increases, the as-obtained Co4O3 products with porous structure transform into polyhedral structure with glazed surface, and simultaneously the cobalt content and tap density increase. However, the specific surface area shows a trend of decrease.

  11. Preparation of carbon-free TEM microgrids by metal sputtering.

    Science.gov (United States)

    Janbroers, S; de Kruijff, T R; Xu, Q; Kooyman, P J; Zandbergen, H W

    2009-08-01

    A new method for preparing carbon-free, temperature-stable Transmission Electron Microscope (TEM) grids is presented. An 80% Au/20% Pd metal film is deposited onto a 'holey' microgrid carbon supported on standard mixed-mesh Au TEM grids. Subsequently, the carbon film is selectively removed using plasma cleaning. In this way, an all-metal TEM film is made containing the 'same' microgrid as the original carbon film. Although electron transparency of the foil is reduced significantly, the open areas for TEM inspection of material over these areas are maintained. The metal foil can be prepared with various thicknesses and ensures good electrical conductivity. The new Au/Pd grids are stable to at least 775K under vacuum conditions.

  12. Preparation of Carbon Nanotubes from Methane on Ni/Cu/A1 Catalyst

    Institute of Scientific and Technical Information of China (English)

    Renzhong Wei; Fengyi Li; Yan Ju

    2005-01-01

    A series of Ni/Cu/Al catalyst samples were prepared by the co-precipitation method. Carbon nanotubes with large inner diameters are successfully synthesized from methane on Ni/Cu/Al catalyst by adding sodium carbonate. The effects of the copper content and amounts of sodium carbonate on the morphology and microstructures of carbon nanotubes were investigated by CO adsorption and TEM technique. The experimental results showed that copper can influence both the catalytic activity and catalyst life. Best result was obtained when the copper content was 15%. Addition of sodium carbonate favors the formation of carbon nanotubes with large inner diameters. The growth mechanism of carbon nanotubes with large inner diameter is discussed.

  13. 海绵状活性炭/有机复合多孔材料的制备及其吸油性能%Preparation and oil absorption performance of sponge-like activated carbon/organic composites

    Institute of Scientific and Technical Information of China (English)

    马伟; 徐赛男; 陈克; 郭玉强; 赵峰惠; 陈永

    2015-01-01

    针对活性炭粉末和活性炭块体在吸油除污过程中,易沉积到水中,不利于吸附漂浮在水面上的油膜,同时难以回收再利用的问题. 首先对椰壳活性炭改性,以提高其吸油性能;再通过聚乙烯醇与甲醛聚合反应,并经发泡致孔,制备出可循环使用﹑具有三维网络孔结构的活性炭/有机复合材料. 通过正交实验方案设计,考察水﹑活性炭﹑稀硫酸(9%)﹑甲醛溶液(40%)﹑可溶性淀粉的量及反应温度对所制多孔复合材料吸附油水混合体系效果的影响. 相对于粉末活性炭和块体活性炭,所制柔性复合材料密度小(0.1977g/cm3),在使用过程中可以完全漂浮在水面上,有利于吸附漂浮的油膜,方便回收再利用.所制的多孔复合材料呈海绵状,具有丰富发达的多级孔结构,在最佳工艺条件下油吸附量达到活性炭的1. 5倍左右.%Activated carbons in powder and monolithic form easily form sediments in water, leading to the failure to adsorb an oil film on the water surface. To solve these problems, coconut shell activated carbons were modified to increase their oil-absorption ability and a 3D sponge-like activated carbon/organic composite was then prepared through polymerization of polyvinyl alcohol with formalin in the presence of a foaming agent and the modified activated carbon. The effects of the amounts of water, activated car-bon, dilute sulfuric acid (9%) and formaldehyde solution (40%), and reaction temperature on the oil adsorption performance of the composites were investigated. The composites had a hierarchical porous structure and floated on the water surface due to their low density (about 0. 197 7 g/cm3). A composite prepared under optimal conditions can adsorb approximately 1. 5 times as much oil as the original activated carbon. Its robust and flexible properties make it suitable for recycling during use.

  14. Use of sawdust Eucalyptus sp. in the preparation of activated carbons Utilização de serragem de Eucalyptus sp. na preparação de carvões ativados

    Directory of Open Access Journals (Sweden)

    Gabriela Martucci Couto

    2012-02-01

    Full Text Available Wood sawdust is a solid residue, generated in the timber industry, which is of no profitable use and can cause serious environmental problems if disposed inadequately. The aim of this study was to use the eucalyptus sawdust in the preparation of activated carbons AC and test them as adsorbents of methylene blue (MB and phenol, representative pollutants from aqueous effluents of various industries. The eucalyptus sawdust was characterized by instrumental analysis such as elementary analysis (CHNS-O, thermogravimetric analysis (TGA, infrared spectroscopy (FTIR and scanning electron microscopy (SEM. The activated carbons were prepared by physical activation with carbon dioxide AC_CO2, (10º C min-1, 850º C, 1h and by chemical activation with potassium carbonate AC_K2CO3 (10º C min-1, 850º C, 3h. The AC_CO2 and AC_K2CO3 were characterized by CHN-O, TGA, FTIR, N2 adsorption/desorption (BET to evaluate the specific surface area and SEM. The resulting activated carbons were tested for their ability to adsorb MB and phenol in water. The activated carbons produced in this work were predominantly microporous and showed specific surface area of about 535 m² g-1. The AC_K2CO3 was more effective in the adsorption of MB (81 mg g-1 and phenol (330 mg g-1 than AC_CO2 (32 mg g-1 and 172 mg g-1, respectively, for MB and phenol.A serragem é um resíduo sólido, gerado na indústria madeireira, que não tem uso rentável e pode causar sérios problemas ambientais quando disposta inadequadamente. Neste estudo, objetivou-se utilizar a serragem de eucalipto na preparação de carvões ativados (AC e testá-los como adsorventes do corante azul de metileno (MB e fenol; moléculas que representam poluentes de efluentes industriais. A serragem de eucalipto foi caracterizada por análises instrumentais, tais como: análise elementar (CHNS-O, análise termogravimétrica (TGA, espectroscopia na região do infravermelho (FTIR e microscopia eletrônica de varredura (SEM

  15. Preparation of supported electrocatalyst comprising multiwalled carbon nanotubes

    Science.gov (United States)

    Wu, Gang; Zelenay, Piotr

    2013-08-27

    A process for preparing a durable non-precious metal oxygen reduction electrocatalyst involves heat treatment of a ball-milled mixture of polyaniline and multiwalled carbon nanotubes in the presence of a Fe species. The catalyst is more durable than catalysts that use carbon black supports. Performance degradation was minimal or absent after 500 hours of operation at constant cell voltage of 0.40 V.

  16. 新型胺化介孔炭的制备及其对Pb(II)的吸附%Preparation of amine-modified mesoporous activated carbon and its adsorption of lead (II) from aqueous solution

    Institute of Scientific and Technical Information of China (English)

    李坤权; 杨美蓉; 王燕锦; 贾佳祺; 郑正

    2014-01-01

    Biomass-based mesoporous carbons were prepared from bagasse by microwave assisted H3PO4 activation. Polyamine groups were modified on the prepared carbon channels’ surfaces by nitric acid oxidation followed by reaction with ethylenediamine. The influence of initial concentration, temperature, carbon dose on the adsorption capacity, characteristic and thermodynamics of Pb (II) on the modified mesoporous carbon was investigated. The results showed that nitrogen-containing groups such as amido and imido group were successfully grafted on the surface of mesoporous carbon. The introduction of nitrogen-containing polyamine groups greatly enhanced the separation of Pb (II) from aqueous solution. The Langmuir Pb (II) adsorption capacity on the polyamine-modified carbon reached nearly 180mg/g, which was 1.5times of that on the untreated mesoporous carbon. The removal rate of Pb (II) from aqueous solution was significantly improved on the polyamine-modified carbon. Almost 100%of Pb (II) was adsorbed on the modified carbon with Pb (II) initial concentration less than 60mg/L. The adsorption amount of Pb (II) was increased with increasing temperature. The adsorption behavior and thermodynamic data suggested that the polyamine-modified material had a heterogeneous surface energy distribution, the adsorption was a spontaneous endothermic process, and chemical reaction could be involved and play an important role.%采用微波辅助磷酸活化制备了高中孔率蔗渣基介孔炭,并通过硝酸氧化和乙二胺聚合在其孔道内修饰了含氮多胺基团,探索了溶液浓度、温度、吸附剂剂量等对改性介孔炭的Pb(II)吸附性能、行为和热力学特性的影响.结果表明,蔗渣基介孔炭较宽的孔道结构可通过乙二胺缩水聚合反应在其表面接枝酰胺、仲胺等含氮基团;胺化改性增强化了介孔炭对水溶液中Pb(II)的固定作用,改性后介孔炭对Pb(II)的吸附量高达180mg/g,是改性前介孔炭的1.5倍;

  17. Influence of different carbon monolith preparation parameters on pesticide adsorption

    Directory of Open Access Journals (Sweden)

    Vukčević Marija

    2013-01-01

    Full Text Available The capacity of carbon monolith for pesticide removal from water, and the mechanism of pesticide interaction with carbon surface were examined. Different carbon monolith samples were obtained by varying the carbonization and activation parameters. In order to examine the role of surface oxygen groups in pesticide adsorption, carbon monolith surface was functionalized by chemical treatment in HNO3, H2O2 and KOH. The surface properties of the obtained samples were investigated by BET surface area, pore size distribution and temperature-programmed desorption. Adsorption of pesticides from aqueous solution onto activated carbon monolith samples was studied by using five pesticides belonging to different chemical groups (acetamiprid, dimethoate, nicosulfuron, carbofuran and atrazine. Presented results show that higher temperature of carbonization and the amount of activating agent allow obtaining microporous carbon monolith with higher amount of surface functional groups. Adsorption properties of the activated carbon monolith were more readily affected by the amount of the surface functional groups than by specific surface area. Results obtained by carbon monolith functionalisation showed that π-π interactions were the main force for adsorption of pesticides with aromatic structure, while acidic groups play an important role in adsorption of pesticides with no aromatic ring in the chemical structure.

  18. 沥青/树脂基活性炭的制备及其吸脱附性能研究%Preparation and adsorption/desorption properties of pitch/resin based activated carbon

    Institute of Scientific and Technical Information of China (English)

    杨斌; 郑军; 王成扬

    2013-01-01

    By mechanical mixing,pitch/resin-based activated carbon was prepared from high soft pointing coal-tar pitch and Novolac-phenolic resin which showed high specific surface area,short adsorption/desorption time and high mechanical strength.In this experiment,optical microscopy,N2 adsorption/desorption isotherms,transmission electron microscope and static benzene adsorption/desorption experiments were chosen to characterize the changes for different pitch/resin-based granules.The results showed that pitch-based activated carbon took shorter adsorption/desorption time and phenolic resin-based activated carbon embraced higher static adsorption capacitors and mechanical strength.What's more,the pitch/resin-based activated carbon combines the advantages of the pitch-based activated carbon and phenolic resin-based activated carbon at the same time.For activated carbon CP/PF-50/50,the mechanism strength and static benzene capacitor reached 6.5 N and 472 mg/g,respectively,and only need 60 min for desorption process.The reason for this change may be caused by the thermal stress between pitch and phenolic resin during the pyrolysis which leads to form a large number of new pores.%以高软化点煤沥青、热塑性酚醛树脂为原料,在机械混合条件下,制备出比表面积大、吸脱附时间短、机械强度高的沥青/树脂基活性炭.通过偏光显微镜(OM)、N2物理吸脱附、TEM及苯的静态吸脱附实验对不同复合比沥青/树脂基复合颗粒进行对比研究.实验结果表明:沥青基活性炭吸脱附时间短,酚醛树脂基活性炭的静态饱和吸附值大、机械强度高;而沥青/树脂基活性炭则兼具沥青基活性炭与酚醛树脂基活性炭的优点,在机械强度为6.5 N(CP/PF-50/50)、静态苯吸附值达到472 mg/g时,仅需60 min进行脱附.结构及性质变化的原因在于:两种前躯体分子结构的不同导致两者在高温煅烧过程中由于所受热应力的不同而产生一定程度的界面剥

  19. 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.

  20. Preparation and Characterization of a Calcium Carbonate Aerogel

    Directory of Open Access Journals (Sweden)

    Johann Plank

    2009-01-01

    Full Text Available We report on a facile method for the preparation of a calcium carbonate aerogel consisting of aggregated secondary vaterite particles with an approximate average diameter of 50 nm. It was synthesized via a sol-gel process by reacting calcium oxide with carbon dioxide in methanol and subsequent supercritical drying of the alcogel with carbon dioxide. The resulting monolith was opaque, brittle and had overall dimensions of 6×2×1 cm. It was characterized by X-ray powder diffraction, nitrogen adsorption method (BET, and scanning electron microscopy.

  1. Preparation and Electrochemical Properties of Silver Doped Hollow Carbon Nanofibers

    Directory of Open Access Journals (Sweden)

    LI Fu

    2016-11-01

    Full Text Available Silver doped PAN-based hollow carbon nanofibers were prepared combining co-electrospinning with in situ reduction technique subsequently heat treatment to improve the electrochemical performances of carbon based supercapacitor electrodes. The morphology, structure and electrochemical performances of the resulted nanofiber were studied. The results show that the silver nanoparticles can be doped on the surface of hollow carbon nanofibers and the addition of silver favors the improvement of the electrochemical performances, exhibiting the enhanced reversibility of electrode reaction and the capacitance and the reduced charge transfer impedance.

  2. 污泥活性炭的制备及对甲苯吸附性能研究%Preparation of Sludge-based Activated Carbon and Adsorptive Properties of Toluene

    Institute of Scientific and Technical Information of China (English)

    苏欣; 黄学敏; 曹利; 杨全

    2012-01-01

    以城市污水厂脱水污泥为原料,采用ZnCl2化学活化法,通过添加适量锯末(SAC-W)或椰壳(SAC-C)制备出不同污泥活性炭,其比表面积分别为450.3 m2/g和539.4 m2/g,比纯污泥活性炭的比表面积增加了31.63%和57.67%.将污泥活性炭和选用的煤质活性炭(CAC)用于甲苯动态吸附实验,研究不同活性炭的吸附性能.结果表明,在相同的甲苯初始浓度下,平衡吸附量大小顺序为SAC-C>CAC>SAC-W,污泥活性炭表现较好的吸附性能.对污泥活性炭进行理化性能分析,发现中孔和化学吸附作用对吸附量增加有一定贡献.污泥活性炭的吸附平衡与Langmuir方程拟合较好,相关系数R2为0.995.%With dewatered sludge from municipal wastewater plant as raw material, sludge-based activated carbon was prepared by chemical activation of ZnCl2 through mixing with appropriately additive wood (SAC-W) or coconut husk (SAC-C) whose BET surface areas were as high as 450.3 m2/g and 539.4 m2/g, increasing by 31.63% and 57.67% respectively comparing with that of pure sludge activated carbon. Using dynamic adsorption experiments, adsorptive properties for toluene was compared with commercial activated carbon (CAC). Results indicated that the order of adsorption capacities from high to low were as SAC-C, CAC, SAC-W at the same initial concentration of toluene. SAC has strong adsorption for toluene. The physicochemical properties of SACs were analyzed, and it showed that mesoporous structure and surface chemistry of sludge activated carbon play key role on the removal of toluene. Langmuir equilibrium isotherm model fits better adsorption data with coefficient of 0.995.

  3. [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%.

  4. 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.

  5. Preparation of porous carbon particle with shell/core structure

    Directory of Open Access Journals (Sweden)

    2007-05-01

    Full Text Available Porous carbon particles with a shell/core structure have been prepared successfully by controlled precipitation of the polymer from droplets of oil-in-water emulsion, followed by curing and carbonization. The droplets of the oil phase are composed of phenolic resin (PFR, a good solvent (ethyl acetate and porogen (Poly(methyl methacrylate, PMMA. The microstructure was characterized in detail by scanning electron microscopy (SEM, transmission electron microscopy (TEM, nitrogen adsorption, and thermo gravimetric analysis (TGA. The obtained carbon particles have a capsular structure with a microporous carbon shell and a mesoporous carbon core. The BET surface area and porous volume are calculated to be 499 m2g-1 and 0.56 cm3g-1, respectively. The effects of the amount of porogen (PMMA, co-solvent (acetone and surfactant on the resultant structure were studied in detail.

  6. Preparation of graphitic carbon nitride by electrodeposition

    Institute of Scientific and Technical Information of China (English)

    LI Chao; CAO Chuanbao; ZHU Hesun

    2003-01-01

    The CNx thin film was deposited on Si(100) substrate from a saturated acetone solution of cyanuric trichloride and melamine (cyanuric trichloride/melamine=1︰1.5) at room temperature. X-ray diffraction (XRD) results showed that the diffraction peaks in the pattern coincided well with those of graphite-like carbon nitride calculated in the literature. The lattice constants (a=4.79 A, c=6.90 A) for g-C3N4 matched with those of ab initio calculations (a=4.74 A, c=6.72 A) quite well. X-ray photoelectron spectroscopy (XPS) measurements indicated that the elements in the deposited films were mostly of C and N (N/C=0.75), and N (400.00 eV) bonded with C (287.72 eV) in the form of six-member C3N3 ring. The peaks at 800 cm-1, 1310 cm-1 and 1610 cm-1 in the Fourier transform infrared (FTIR) spectrum indicated that triazine ring existed in the product. These results demonstrated that crystalline g-C3N4 was obtained in the CNx film.

  7. Carbon molecular sieve membranes prepared from porous fiber precursor

    NARCIS (Netherlands)

    Barsema, J.N.; van der Vegt, N.F.A.; Koops, G.H.; Wessling, Matthias

    2002-01-01

    Carbon molecular sieve (CMS) membranes are usually prepared from dense polymeric precursors that already show intrinsic gas separation properties. The rationale behind this approach is that the occurrence of any kind of initial porosity will deteriorate the final CMS performance. We will show that

  8. Carbon molecular sieve membranes prepared from porous fiber precursor

    NARCIS (Netherlands)

    Barsema, Jonathan N.; Vegt, van der N.F.A.; Koops, G.H.; Wessling, M.

    2002-01-01

    Carbon molecular sieve (CMS) membranes are usually prepared from dense polymeric precursors that already show intrinsic gas separation properties. The rationale behind this approach is that the occurrence of any kind of initial porosity will deteriorate the final CMS performance. We will show that i

  9. PREPARATION OF ACTIVATED CARBON FROM PALM OIL SHELL BY CHEMICAL ACTIVATION WITH Na2CO3 AND ZnCl2 AS IMPRENATED AGENTS FOR H2S ADSORPTION

    Directory of Open Access Journals (Sweden)

    Kanokorn Hussaro

    2014-01-01

    Full Text Available Hydrogen Sulfide (H2S, rotten-egg is one of the major environmental pollutants having its sources in natural and anthropogenic activities. It’s had smell gas produced by anaerobic digestion in acid condition from organic and inorganic compounds containing sulphur, presents dual problems of its toxicity and foul ordour. One of methods of its removal is adsorption. Activated carbon is a widely used adsorbent in the treatment of air pollution. Adsorption type and capacity are primarily based on the physical properties of pores, namely the surface area. Convetionnally, activated carbon is produced from biomass residues, wood coal and agricultural residuces. Today, one promising approach for the production of cheap and efficient activated carbon is used of waste from palm oil mill industries, which is palm oil shell. Palm oil shell is available in large quantities of approximately 0.53 million tonnes annually in Thailand. Palm oil shell is a by-products of the palm oil industry and was used as a raw material in this study due to its high carbon content, high density and low ash content. Normally, H2S in biogas, which is found the range between as low as about 50-10,000 ppm depending on the feed material composition to prodction, can cause corrosion to engine and metal substance via of SO2 from combustion. H2S must be removed from biogas product prior to further utilization. Therefore, in these research the usage of palm oil shell is especially important due to its high value added for produced activated carbon adsorbent for H2S adsorption in biogas product. In this study, fixed bed reactor (stainless steel with 54.1 mm internal diameter and 320 mm length was studied to observe the effect of char product: Chemical agent ratio (Na2CO3 and ZnCl2, 1:1 to 1:3, which there are activated at 700°C activation temperature for 2 h on the chemical and physical properties

  10. Studies relevant to the catalytic activation of carbon monoxide

    Energy Technology Data Exchange (ETDEWEB)

    Ford, P.C.

    1992-06-04

    Research activity during the 1991--1992 funding period has been concerned with the following topics relevant to carbon monoxide activation. (1) Exploratory studies of water gas shift catalysts heterogenized on polystyrene based polymers. (2) Mechanistic investigation of the nucleophilic activation of CO in metal carbonyl clusters. (3) Application of fast reaction techniques to prepare and to investigate reactive organometallic intermediates relevant to the activation of hydrocarbons toward carbonylation and to the formation of carbon-carbon bonds via the migratory insertion of CO into metal alkyl bonds.

  11. 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.

  12. 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.

  13. Preparation of porous carbon nanofibers derived from PBI/PLLA for supercapacitor electrodes

    Science.gov (United States)

    Jung, Kyung-Hye; Ferraris, John P.

    2016-10-01

    Porous carbon nanofibers were prepared by electrospinning blend solutions of polybenzimidazole/poly-L-lactic acid (PBI/PLLA) and carbonization. During thermal treatment, PLLA was decomposed, resulting in the creation of pores in the carbon nanofibers. From SEM images, it is shown that carbon nanofibers had diameters in the range of 100-200 nm. The conversion of PBI to carbon was confirmed by Raman spectroscopy, and the surface area and pore volume of carbon nanofibers were determined using nitrogen adsorption/desorption analyses. To investigate electrochemical performances, coin-type cells were assembled using free-standing carbon nanofiber electrodes and ionic liquid electrolyte. cyclic voltammetry studies show that the PBI/PLLA-derived porous carbon nanofiber electrodes have higher capacitance due to lower electrochemical impedance compared to carbon nanofiber electrode from PBI only. These porous carbon nanofibers were activated using ammonia for further porosity improvement and annealed to remove the surface functional groups to better match the polarity of electrode and electrolyte. Ragone plots, correlating energy density with power density calculated from galvanostatic charge-discharge curves, reveal that activation/annealing further improves energy and power densities.

  14. Preparation of porous carbon nanofibers derived from PBI/PLLA for supercapacitor electrodes.

    Science.gov (United States)

    Jung, Kyung-Hye; Ferraris, John P

    2016-10-21

    Porous carbon nanofibers were prepared by electrospinning blend solutions of polybenzimidazole/poly-L-lactic acid (PBI/PLLA) and carbonization. During thermal treatment, PLLA was decomposed, resulting in the creation of pores in the carbon nanofibers. From SEM images, it is shown that carbon nanofibers had diameters in the range of 100-200 nm. The conversion of PBI to carbon was confirmed by Raman spectroscopy, and the surface area and pore volume of carbon nanofibers were determined using nitrogen adsorption/desorption analyses. To investigate electrochemical performances, coin-type cells were assembled using free-standing carbon nanofiber electrodes and ionic liquid electrolyte. cyclic voltammetry studies show that the PBI/PLLA-derived porous carbon nanofiber electrodes have higher capacitance due to lower electrochemical impedance compared to carbon nanofiber electrode from PBI only. These porous carbon nanofibers were activated using ammonia for further porosity improvement and annealed to remove the surface functional groups to better match the polarity of electrode and electrolyte. Ragone plots, correlating energy density with power density calculated from galvanostatic charge-discharge curves, reveal that activation/annealing further improves energy and power densities.

  15. Preparation and characterization of carbon pillared clay material

    Institute of Scientific and Technical Information of China (English)

    2009-01-01

    Carbon pillared clay material was prepared from montmorillonite modified by C19H42BrN and C10H16ClN. SEM, FT-IR, XRD, N2 adsorption-desorption, thermal-gravimetric analysis and differential scanning calorimetry were employed to characterize the pore structure and test the effect of surfactant. The results show that organic modifier combines with montmorillonite particles by covalent bond and ion embedded. The microstructure of carbon pillared material looks like needle slice. The most probable pore size distribution is about 1.7 nm. The clay material slice mainly consists of two-dimensional aperture supported by a carbonization pillar. The high-temperature stability of carbon pillared clay is im- proved.

  16. Preparation and characterization of carbon pillared clay material

    Institute of Scientific and Technical Information of China (English)

    ZHANG ZengZhi; YANG ChunWei; NIU JunJie

    2009-01-01

    Carbon pillared clay material was prepared from montmorillonite modified by C19H42BrN and C10H16CIN.SEM, FT-IR, XRD, N2 adsorption-desorption, thermal-gravimetric analysis and differential scanning calorimetry were employed to characterize the pore structure and test the effect of surfactant. The re-sults show that organic modifier combines with montmorillonite particles by covalent bond and ion embedded. The microstructure of carbon pillared material looks like needle slice. The most probable pore size distribution is about 1.7 nm, The clay material slice mainly consists of two-dimensional ap-erture supported by a carbonization pillar. The high-temperature stability of carbon pillared clay is im-proved.

  17. Metal Nanoparticles Preparation In Supercritical Carbon Dioxide Solutions

    Energy Technology Data Exchange (ETDEWEB)

    Harry W. Rollins

    2004-04-01

    The novel optical, electronic, and/or magnetic properties of metal and semiconductor nanoparticles have resulted in extensive research on new methods for their preparation. An ideal preparation method would allow the particle size, size distribution, crystallinity, and particle shape to be easily controlled, and would be applicable to a wide variety of material systems. Numerous preparation methods have been reported, each with its inherent advantages and disadvantages; however, an ideal method has yet to emerge. The most widely applied methods for nanoparticle preparation include the sonochemical reduction of organometallic reagents,(1&2) the solvothermal method of Alivisatos,(3) reactions in microemulsions,(4-6) the polyol method (reduction by alcohols),(7-9) and the use of polymer and solgel materials as hosts.(10-13) In addition to these methods, there are a variety of methods that take advantage of the unique properties of a supercritical fluid.(14&15) Through simple variations of temperature and pressure, the properties of a supercritical fluid can be continuously tuned from gas-like to liquid-like without undergoing a phase change. Nanoparticle preparation methods that utilize supercritical fluids are briefly reviewed below using the following categories: Rapid Expansion of Supercritical Solutions (RESS), Reactive Supercritical Fluid Processing, and Supercritical Fluid Microemulsions. Because of its easily accessible critical temperature and pressure and environmentally benign nature, carbon dioxide is the most widely used supercritical solvent. Supercritical CO2 is unfortunately a poor solvent for many polar or ionic species, which has impeded its use in the preparation of metal and semiconductor nanoparticles. We have developed a reactive supercritical fluid processing method using supercritical carbon dioxide for the preparation of metal and metal sulfide particles and used it to prepare narrowly distributed nanoparticles of silver (Ag) and silver sulfide

  18. Removal of Heavy Metal Ions with Acid Activated Carbons Derived from Oil Palm and Coconut Shells

    Directory of Open Access Journals (Sweden)

    Mokhlesur M. Rahman

    2014-05-01

    Full Text Available In this work, batch adsorption experiments were carried out to investigate the suitability of prepared acid activated carbons in removing heavy metal ions such as nickel(II, lead(II and chromium(VI. Acid activated carbons were obtained from oil palm and coconut shells using phosphoric acid under similar activation process while the differences lie either in impregnation condition or in both pretreatment and impregnation conditions. Prepared activated carbons were modified by dispersing hydrated iron oxide. The adsorption equilibrium data for nickel(II and lead(II were obtained from adsorption by the prepared and commercial activated carbons. Langmuir and Freundlich models fit the data well. Prepared activated carbons showed higher adsorption capacity for nickel(II and lead(II. The removal of chromium(VI was studied by the prepared acid activated, modified and commercial activated carbons at different pH. The isotherms studies reveal that the prepared activated carbon performs better in low concentration region while the commercial ones in the high concentration region. Thus, a complete adsorption is expected in low concentration by the prepared activated carbon. The kinetics data for Ni(II, Pb(II and Cr(VI by the best selected activated carbon fitted very well to the pseudo-second-order kinetic model.

  19. 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.

  20. Cystamine preparations exhibit anticoagulant activity.

    Science.gov (United States)

    Aleman, Maria M; Holle, Lori A; Stember, Katherine G; Devette, Christa I; Monroe, Dougald M; Wolberg, Alisa S

    2015-01-01

    Transglutaminases are a superfamily of isoenzymes found in cells and plasma. These enzymes catalyze the formation of ε-N-(γ-glutamyl)-lysyl crosslinks between proteins. Cystamine blocks transglutaminase activity and is used in vitro in human samples and in vivo in mice and rats in studies of coagulation, immune dysfunction, and inflammatory disease. These studies have suggested cystamine blocks fibrin crosslinking and has anti-inflammatory effects, implicating transglutaminase activity in the pathogenesis of several diseases. We measured the effects of cystamine on fibrin crosslinking, tissue factor-triggered plasma clot formation and thrombin generation, and coagulation factor enzymatic activity. At concentrations that blocked fibrin crosslinking, cystamine also inhibited plasma clot formation and reduced thrombin generation. Cystamine inhibited the amidolytic activity of coagulation factor XI and thrombin towards chromogenic substrates. These findings demonstrate that cystamine exhibits anticoagulant activity during coagulation. Given the close relationship between coagulation and inflammation, these findings suggest prior studies that used cystamine to implicate transglutaminase activity in disease pathogenesis warrant re-examination.

  1. Cystamine preparations exhibit anticoagulant activity.

    Directory of Open Access Journals (Sweden)

    Maria M Aleman

    Full Text Available Transglutaminases are a superfamily of isoenzymes found in cells and plasma. These enzymes catalyze the formation of ε-N-(γ-glutamyl-lysyl crosslinks between proteins. Cystamine blocks transglutaminase activity and is used in vitro in human samples and in vivo in mice and rats in studies of coagulation, immune dysfunction, and inflammatory disease. These studies have suggested cystamine blocks fibrin crosslinking and has anti-inflammatory effects, implicating transglutaminase activity in the pathogenesis of several diseases. We measured the effects of cystamine on fibrin crosslinking, tissue factor-triggered plasma clot formation and thrombin generation, and coagulation factor enzymatic activity. At concentrations that blocked fibrin crosslinking, cystamine also inhibited plasma clot formation and reduced thrombin generation. Cystamine inhibited the amidolytic activity of coagulation factor XI and thrombin towards chromogenic substrates. These findings demonstrate that cystamine exhibits anticoagulant activity during coagulation. Given the close relationship between coagulation and inflammation, these findings suggest prior studies that used cystamine to implicate transglutaminase activity in disease pathogenesis warrant re-examination.

  2. 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.

  3. 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...

  4. 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.

  5. 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)

  6. 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.

  7. The application of prepared porous carbon materials: Effect of different components on the heavy metal adsorption.

    Science.gov (United States)

    Song, Min; Wei, Yuexing; Yu, Lei; Tang, Xinhong

    2016-06-01

    In this study, five typical municipal solid waste (MSW) components (tyres, cardboard, polyvinyl chloride (PVC), acrylic textile, toilet paper) were used as raw materials to prepare four kinds of MSW-based carbon materials (paperboard-based carbon materials (AC1); the tyres and paperboard-based carbon materials (AC2); the tyres, paperboard and PVC-based carbon materials (AC3); the tyres, paperboard, toilet paper, PVC and acrylic textile-based carbon materials (AC4)) by the KOH activation method. The characteristic results illustrate that the prepared carbon adsorbents exhibited a large pore volume, high surface area and sufficient oxygen functional groups. Furthermore, the application of AC1, AC2, AC3, AC4 on different heavy metal (Cu(2+), Zn(2+), Pb(2+), Cr(3+)) removals was explored to investigate their adsorption properties. The effects of reaction time, pH, temperature and adsorbent dosage on the adsorption capability of heavy metals were investigated. Comparisons of heavy metal adsorption on carbon of different components were carried out. Among the four samples, AC1 exhibits the highest adsorption capacity for Cu(2+); the highest adsorption capacities of Pb(2+) and Zn(2+) are obtained for AC2; that of Cr(3+) are obtained for AC4. In addition, the carbon materials exhibit better adsorption capability of Cu(2+) and Pb(2+) than the other two kind of metal ions (Zn(2+) and Cr(3+)).

  8. Carbon Dioxide (CO2) Adsorption by Activated Carbon Functionalized with Deep Eutectic Solvent (DES)

    Science.gov (United States)

    Zulkurnai, N. Z.; Ali, U. F. Md.; Ibrahim, N.; Manan, N. S. Abdul

    2017-06-01

    In recent years, carbon dioxide (CO2) emission has become a major concern as the amount of the emitted gas significantly increases annually. Consequently, this phenomenon contributes to global warming. Several CO2 capture methods, including chemical adsorption by activated carbon, have been proposed. In this study, activated carbon was prepared from sea mango (Cerbera odollam), which was functionalized with deep eutectic solvent (DES) composed of choline chloride and glycerol to increase the efficiency of CO2 capture. The samples underwent pre-carbonization and carbonization processes at 200 °C and 500 °C, respectively, with nitrogen gas and flowing several gases, namely, CO2 and steam, and then followed by impregnation with 50 phosphoric acid (H3PO4) at 1:2 precursor-to-activant ratio. The prepared activated carbon was impregnated with DES at 1:2 precursor-to-activant ratio. The optimum CO2 adsorption capacity of the activated carbon was obtained by using CO2 gas treatment method (9.851 mgCO2/gsol), followed by the absence of gases (9.685 mgCO2/gsol), steam (9.636 mgCO2/gsol), and N2 (9.536 mgCO2/gsol).

  9. 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 ...

  10. Preparation of Ceramic-Bonded Carbon Block for Blast Furnace

    Science.gov (United States)

    Li, Yiwei; Li, Yawei; Sang, Shaobai; Chen, Xilai; Zhao, Lei; Li, Yuanbing; Li, Shujing

    2014-01-01

    Traditional carbon blocks for blast furnaces are mainly produced with electrically calcined anthracite owing to its good hot metal corrosion resistance. However, this kind of material shows low thermal conductivity and does not meet the demands for cooling of the hearth and the bottom of blast furnaces. In this article, a new kind of a high-performance carbon block has been prepared via ceramic-bonded carbon (CBC) technology in a coke bed at 1673 K (1400 °C) using artificial graphite aggregate, alumina, metallic aluminum, and silicon powders as starting materials. The results showed that artificial graphite aggregates were strongly bonded by the three-dimensional network of ceramic phases in carbon blocks. In this case, the good resistance of the CBC blocks against erosion/corrosion by the hot metal is provided by the ceramic matrix and the high thermal conductivity by the graphite aggregates. The microstructure of this carbon block resembles that of CBC composites with a mean pore size of less than 0.1 μm, and up to 90 pct of the porosity shows a pore size <1 μm. Its thermal conductivity is higher than 30 W · m-1 · K-1 [293 K (20 °C)]. Meanwhile, its hot metal corrosion resistance is better than that of traditional carbon blocks.

  11. 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.

  12. 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.

  13. Preparation and Investigation of Diamond-like Carbon Stripper Foils

    Institute of Scientific and Technical Information of China (English)

    FAN; Qi-wen; DU; Ying-hui; ZHANG; Rong; XU; Guo-ji

    2013-01-01

    1 Preparation of DLC stripper foils For DLC stripper foils of about 5μg/cm2 thickness,the following methods were used.The DLC foils of about 4μg/cm2 thicknesses were produced by FCVA onto glass slides coated with betaine-saccharose as releasing agent,which was previously covered with the evaporated carbon layers of about 1μg/cm2

  14. Preparation and Thermal Characterization of Diamond-Like Carbon Films

    Institute of Scientific and Technical Information of China (English)

    BAI Su-Yuan; TANG Zhen-An; HUANG Zheng-Xing; Yu Jun; WANG Jing; LIU Gui-Chang

    2009-01-01

    Diamond-like carbon (DLC) films are prepared on silicon substrates by microwave electron cyclotron resonance plasma enhanced chemical vapor deposition. Raman spectroscopy indicates that the films have an amorphous structure and typical characteristics. The topographies of the films are presented by AFM images. Effective thermal conductivities of the films are measured using a nanosecond pulsed photothermal reflectance method. The results show that thermal conductivity is dominated by the microstructure of the films.

  15. Preparation of very long and open aligned carbon nanotubes

    Institute of Scientific and Technical Information of China (English)

    潘正伟; 常保和; 孙连峰; 钱露茜; 刘祖琴; 唐东升; 王刚; 解思深

    2000-01-01

    Very long and open aligned carbon nanotubes that reach about 2 mm long, an order of magnitude longer than previously reached, have been prepared by chemical vapor deposition over silica dioxide substrates on the surface, where iron/silica nano-composite particles are evenly positioned. The nanotubes are naturally opened at the bottom ends. The growth mechanism of the very long and open-ended nanotubes is also discussed.

  16. Preparation and Characterization of Visible-Light Response Activated Carbon with Antibacterial Behavior%可见光响应杀菌功能活性炭的制备及表征

    Institute of Scientific and Technical Information of China (English)

    张慧书; 王自强; 王锐; 刘守新

    2011-01-01

    以TiCl4为钛源,采用酸催化水解法在椰壳炭表面合成TiO2前驱体,在NH3/N2气氛中程序升温处理制得可见光响应杀菌功能活性炭(TiN/GAC).以大肠杆菌(E.coli)为实验菌种,考察了功能活性炭在可见光下的杀菌活性.采用X射线衍射(XRD)、扫描电镜(SEM)、傅立叶变换红外光谱(FTIR)及低温液氮物理吸附对杀菌功能活性炭进行晶相结构、表面形貌、光谱特征和孔结构进行表征.结果表明,负载活性炭对TiO2的晶相结构没有影响,负载TiO2的晶粒尺寸为9.8 nm.载体的非晶相层和强吸附力能够抑制TiO2晶粒增长,二者以Ti-O-C键牢固结合,使TiO2在活性炭表面形成致密的膜层.经500℃煅烧5h的样品对E.coli的杀菌率最高,4 h后杀菌率可达67%,效果优于相同条件下自然光杀菌率(39%).%A visible-light response activated carbon with antibacterial activity was prepared by calcinations of the mixture of TiO2 precursor obtained by acid catalyzed hydrolysis method and commercial granular activated carbon( CAC ) in NH3/N2 atmosphere. The antibacterial activity of the prepared activated carbon towards E. coil was investigated under the visible-light irradiation. X-ray diffraction( XRD), Scanning electron spectroscopy( SEM ) , Fourier transform infrared spectroscopy(FTIR) and N2 adsorption analyser were used to characterize the crystal phase structure, surface morphology, spectral characteristics and pore properties. The results show there is no influence for crystal phase structure of TiO2 supported AC. The crystal size of TiO2 is 9. 8 nm. Non-crystal phase layer and strong adsorption force of carrier can inhibit the grain growth of TiO2, and AC combines with TiO2 in Ti—O—C so that TiO2formestight film on AC. The sample calcinated at 500 ℃ for 5 h exhibites the highest bactericidal performance, and the bactericidal rate reached up to 67% after 4 h irradiation, which was better than that of nature light(39% ) in the same

  17. 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.

  18. Design of activated carbon/activated carbon asymmetric capacitors

    Science.gov (United States)

    Piñeiro-Prado, Isabel; Salinas-Torres, David; Ruiz Rosas, Ramiro; Morallon, Emilia; Cazorla-Amoros, Diego

    2016-03-01

    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.

  19. Adsorption of Acid Red 18 (AR18) by Activated Carbon from Poplar Wood- A Kinetic and Equilibrium Study

    OpenAIRE

    Reza Shokoohi; Vahid Vatanpoor; Mansuor Zarrabi; Akram Vatani

    2010-01-01

    Adsorption process by activated carbon is widely used for removal of dyes. Because of economical limits, activated carbon derived from low cost materials seem to be economical. The aim of this work is preparation of activated carbon from poplar wood and investigation of its ability to removal of (AR18) dye. In this work, we prepared the activated carbon by chemical activation method in electric furnace. In addition we have investigated effect of various parameters such as pH, contact time, dy...

  20. 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.

  1. 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.

  2. Facile preparation of nitrogen-doped hierarchical porous carbon with high performance in supercapacitors

    Energy Technology Data Exchange (ETDEWEB)

    Yan, Kun [State Key Laboratory of Advanced Processing and Recycling of Non-ferrous Metals, Lanzhou University of Technology, Lanzhou 730050 (China); Kong, Ling-Bin, E-mail: konglb@lut.cn [State Key Laboratory of Advanced Processing and Recycling of Non-ferrous Metals, Lanzhou University of Technology, Lanzhou 730050 (China); School of Materials Science and Engineering, Lanzhou University of Technology, Lanzhou 730050 (China); Shen, Kui-Wen; Dai, Yan-Hua; Shi, Ming; Hu, Bing [State Key Laboratory of Advanced Processing and Recycling of Non-ferrous Metals, Lanzhou University of Technology, Lanzhou 730050 (China); Luo, Yong-Chun; Kang, Long [School of Materials Science and Engineering, Lanzhou University of Technology, Lanzhou 730050 (China)

    2016-02-28

    Graphical abstract: Preparing and activating process of nitrogen-doped hierarchical porous carbon (NHPC). - Highlights: • The well-defined PAN-b-PMMA copolymer was synthesized by atom transfer radical polymerization with narrow molecular weight distribution. • Nitrogen-doped hierarchical porous structure (NHPC) was prepared through a simple carbonization procedure of PAN-b-PMMA precursor. • NHPC possessed hierarchical porous structure with high BET surface area of 257 m{sup 2} g{sup −1} and DFT mesopore size of 14.61 nm. • Effects of activation conditions on supercapacitive behavior were systematically studied. - Abstract: The nitrogen-doped hierarchical porous carbon (NHPC) material was successfully prepared through a simple carbonization procedure of well-defined diblock copolymer precursor containing nitrogen-enriched carbon source, i.e., polyacrylonitrile (PAN), and asacrificial block, i.e., polymethylmethacrylate (PMMA). PAN-b-PMMA diblock copolymer was synthesized by atom transfer radical polymeriation (ATRP) with narrow molecular weight distribution. The as-obtained NHPC possessed nitrogen-doped hierarchical porous structure with high BET surface area of 257 m{sup 2} g{sup −1} and Nonlocal density functional theory (NLDFT) mesopore size of 14.61 nm. Surface activated nitrogen-doped hierarchical porous carbon (A-NHPC) materials were obtained by subsequent surface activation with HNO{sub 3} solution. The effects of activation conditions on supercapacitive behavior were systematically studied, a maximum specific capacitance of 314 F g{sup −1} at a current density of 0.5 A g{sup −1} was achieved in 2 M KOH aqueous electrolyte. Simultaneously, it exhibited excellent rate capability of 67.8% capacitance retention as the current density increased from 0.5 to 20 A g{sup −1} and superior cycling performance of 90% capacitance retention after 10,000 cycles at the current density of 2 A g{sup −1}.

  3. Activated Carbon Fiber Monoliths as Supercapacitor Electrodes

    Directory of Open Access Journals (Sweden)

    Gelines Moreno-Fernandez

    2017-01-01

    Full Text Available Activated carbon fibers (ACF are interesting candidates for electrodes in electrochemical energy storage devices; however, one major drawback for practical application is their low density. In the present work, monoliths were synthesized from two different ACFs, reaching 3 times higher densities than the original ACFs’ apparent densities. The porosity of the monoliths was only slightly decreased with respect to the pristine ACFs, the employed PVDC binder developing additional porosity upon carbonization. The ACF monoliths are essentially microporous and reach BET surface areas of up to 1838 m2 g−1. SEM analysis reveals that the ACFs are well embedded into the monolith structure and that their length was significantly reduced due to the monolith preparation process. The carbonized monoliths were studied as supercapacitor electrodes in two- and three-electrode cells having 2 M H2SO4 as electrolyte. Maximum capacitances of around 200 F g−1 were reached. The results confirm that the capacitance of the bisulfate anions essentially originates from the double layer, while hydronium cations contribute with a mixture of both, double layer capacitance and pseudocapacitance.

  4. Preparation and Characterization of Nano-Structured SiO2 Thin Films on Carbon Steel

    Institute of Scientific and Technical Information of China (English)

    Rong Chun XIONG; Dong Zhou YAN; Gang WEI

    2003-01-01

    Nano-structured SiO2 thin films were prepared on the surface of carbon steel for the first time by LPD. The compositions of the films were analyzed by XPS, and the surface morphology of the thin films were observed by AFM. The thin films were constituted by compact particles of SiO2, and there was no Fe in the films. In the process of film forming, the SiO2 colloid particles were deposited or absorbed directly onto the surface of carbon steel substrates that were activated by acid solution containing inhibitor, and corrosion of the substrates was avoided. The nano-structured SiO2 thin films that were prepared had excellent protective efficiency to the carbon steel.

  5. H3PO4法制备核桃壳活性炭及其处理啤酒废水的研究%Preparation of Activated Carbons with Phosphoric Acid Method from Walnut Hull and its Application in Brewery Wastewater Treatment

    Institute of Scientific and Technical Information of China (English)

    董瑞; 肖凯军; 任源

    2011-01-01

    The preparation processing of activated carbons from walnut hull with phosphoric acid method was studied and the performance of prepared activated carbons to treat brewery wastewater was investigated. These results showed that the adsorptive values of prepared carbon to iodine and to methylene blue were 876.8 mg/L and 170.3 mg/L, respectively, under the following optimum conditions for activated carbon preparation: soaking regent of 60 % phosphoric acid solution, the ratio of phosphoric acid solution to activated carbon 1:20, soaking temperature 60 V, carbonizing time 80 min at 300℃ and activating time 80 min at 600℃. The CODCr and BOD removing rates of brewery wastewater at pH 7.0 were 83.9% and 66.5%, respectively, when the prepared active carbon with 170~200 meshes was used to adsorb at 60℃ for 80 min as the rate of active carbon to wastewater was 1:20.%本文研究了H3PO4法制备核桃壳活性炭的工艺条件,并探讨了其处理啤酒废水的影响因素.结果表明:浸渍比1:2.5,浸渍温度60℃,H3PO4浓度60%,300℃炭化80 min,600℃活化80min时,制备的活性炭对碘和亚甲基蓝的吸附值分别达到876.8 mg/L和170.3mg/L;在pH7.0的条件下,采用吸附粒径为170~200目的活性炭,以1:20的料液比,在40℃下处理啤酒废水80min,废水的CODCr去除率达到83.9%,BOD去除率达到66.5%.

  6. Preparation and Characterization of Activated Carbon-Silver Composite with Antibacterial Behavior via Vacuum Impregnation Method%醋酸银真空浸渍制备杀菌功能载银活性炭及其表征

    Institute of Scientific and Technical Information of China (English)

    王自强; 刘守新

    2011-01-01

    通过醋酸银真空浸渍法制备了银缓释杀菌功能载银活性炭(Ag/AC),研究了其对大肠杆菌(E.coil)的杀灭性能和抗银流失性能.以气体吸附仪测定活性炭的比表面积和孔结构,以扫描电子显微镜(SEM)观察Ag/AC表面形貌,以X射线衍射(XRD)考察Ag/AC晶体结构.结果表明,单质银均匀负载在活性炭表面.随着CH3COOAg浸溃浓度的增加,活性炭的载银量和银颗粒的粒径也随着增加,而比表面积、总孔容和平均孔径随之减少.当载银量为0.97%(质量分数)时,该法制备的Ag/AC在120 min内杀灭107CFU/mL浓度的E.coil,展示出与浸溃法制备的Ag/AC相近的杀菌活性;但在振荡30 d后,其银流失百分量仅为37.6%.抗银流失性能远高于浸渍法制备的Ag/AC.在保持较高杀菌活性前提下,可以实现银的缓释.%Activated carbon-silver composite(Ag/AC) for antibacterial performance by controlling silver release was prepared by silver acetate vacuum impregnation method. The antibacterial activity towards E. coil and resistance of water erosion was investigated through distilled water. Surface area and porosity analyzer, Scanning electron spectroscopy (SEM)and X-ray diffraction (XRD)were used to characterize the surface morphology and pore properties. The results show that Ago was deposited on AC symmetrically. The content of silver supported and particle size were increased by the increasing of the concentration of CH3 COOAg, while specific surface area, total pore volume and average pore size were decreased. Ag/AC prepared with silver content of 0. 97% which killed 107 CFU/mL concentration of E. coil in 120 min exhibited the similar antibacterial activity for E. coil with that prepared by traditional impregnation method. However, the silver loss of the Ag/AC prepared with silver content of 0. 97% was 37.6% , showing much higher resistance to water erosion. High antibacterial activity and control silver release can be simultaneously realized

  7. 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.

  8. Preparation of calcium carbonate particles coated with titanium dioxide

    Institute of Scientific and Technical Information of China (English)

    Hai Lin; Ying-bo Dong; Le-yong Jiang

    2009-01-01

    The preparation of a new mineral composite material, calcium carbonate particles coated with titanium dioxide, was stud-ied. The mechanism of the preparation process was proposed. The new mineral composite material was made by the mechanochemi-eal method under the optimum condition that the mass ratio of calcium carbonate particles to titanium dioxide was 6.5:3.5. The mass ratios of two different types of titanium dioxide (anatase to rutile) and grinding media to grinded materials were 8:2 and 4:1 respec-tively, and the modified density was 60%. Under this condition, the new material was capable of forming after 120-min modification.The hiding power and oil absorption of this new material were 29.12 g/m~2 and 23.30%, respectively. The results show that the modi-fication is based on surface hydroxylation. After coating with titanium dioxide, the hiding power of calcium carbonate can be im-proved greatly. The new mineral composite materials can be used as the substitute for titanium dioxide.

  9. Cryogenic Adsorption of Nitrogen and Carbon Dioxide in Activated Carbon

    Science.gov (United States)

    Shen, Fuzhi; Liu, Huiming; Xu, Dong; Zhang, Hengcheng; Lu, Junfeng; Li, Laifeng

    2017-09-01

    Activated carbon have been used for a long time at low temperature for cryogenic applications. The knowledge of adsorption characteristics of activated carbon at cryogenic temperature is essential for some specific applications. However, such experimental data are very scare in the literature. In order to measure the adsorption characteristics of activated carbon under variable cryogenic temperatures, an adsorption measurement device was presented. The experiment system is based on the commercially available PCT-pro adsorption analyzer coupled to a two-stage Gifford McMahon refrigerator, which allows the sample to be cooled to 4.2K. Cryogenic environment can be maintained steadily without the cryogenic liquid through the cryocooler and temperature can be controlled precisely between 5K and 300K by the temperature controller. Adsorption measurements were performed in activated carbon for carbon dioxide and nitrogen and the adsorption isotherm were obtained.

  10. Use of Activated Carbon Derived from Maize Cob and Mahogany ...

    African Journals Online (AJOL)

    MBI

    2015-12-28

    Dec 28, 2015 ... Shell for the Removal of Colour from Textile Effluent. Gumel, S. M. ... In the present study natural adsorbents Maize Cob (MC) and Mahogany Shells (MS) were carbonized and activated ... remove even minute amount of dyes in wastewaters. (Yakubu et .... were prepared by putting 10, 20, 30, 40 and 50 ml.

  11. Morphosynthesis of cubic silver cages on monolithic activated carbon.

    Science.gov (United States)

    Wang, Fei; Zhao, Hong; Lai, Yijian; Liu, Siyu; Zhao, Binyuan; Ning, Yuesheng; Hu, Xiaobin

    2013-11-14

    Cubic silver cages were prepared on monolithic activated carbon (MAC) pre-absorbed with Cl(-), SO4(2-), or PO4(3-) anions. Silver insoluble salts served as templates for the morphosynthesis of silver cages. The silver ions were reduced by reductive functional groups on MAC micropores through a galvanic cell reaction mechanism.

  12. Preparation and cellular response of porous A-type carbonated hydroxyapatite nanoceramics

    Energy Technology Data Exchange (ETDEWEB)

    Li Bo, E-mail: Leewave@126.com [Institute of Biomaterials and Living Cell Imaging Technology, School of Metallurgy and Materials Engineering, Chongqing University of Science and Technology, Chongqing 401331 (China) and National Engineering Research Center for Biomaterials, Sichuan University, Chengdu 610064 (China); Liao Xiaoling [Institute of Biomaterials and Living Cell Imaging Technology, School of Metallurgy and Materials Engineering, Chongqing University of Science and Technology, Chongqing 401331 (China); Zheng Li [National Engineering Research Center for Biomaterials, Sichuan University, Chengdu 610064 (China); He Huawei [Department of Prosthodontics, Beijing Stomatological Hospital, Capital Medical University, Beijing, 100050 (China); Wang Hong [National Engineering Research Center for Biomaterials, Sichuan University, Chengdu 610064 (China); Fan Hongsong, E-mail: hsfan68@hotmail.com [National Engineering Research Center for Biomaterials, Sichuan University, Chengdu 610064 (China); Zhang Xingdong [National Engineering Research Center for Biomaterials, Sichuan University, Chengdu 610064 (China)

    2012-05-01

    Microwave sintering using the activated carbon as embedding material was applied in preparation of porous A-type carbonated hydroxyapatite ceramics with nano(nCHA) and submicron (mCHA) structure. By examining the linear shrinkages and the compressive strengths of samples at different temperatures, a suitable microwave sintering temperature was achieved. The microwave sintering method was successfully used to prepare A-type CHA with nano or submicron structure, and the mechanism of the formation of A-type carbonate groups was discussed also. Compared with the samples prepared by the conventional sintering method (mHA), the nCHA bioceramics synthesized by the microwave sintering approach had smaller grain size and more uniform microstructure, and showed a compressive strength similar to the conventional samples. In vitro dissolution test proved that nCHA exhibits better degradation property in comparison to pure HA. Rat osteoblasts were cultured with nCHA, mCHA and mHA to evaluate their biocompatibility, and nCHA showed significant enhancement of cells in attachment, proliferation and differentiation. In conclusion, carbonate groups can be easily introduced to HA crystal structure using the activated carbon as embedding material, and microwave sintering is an effective and simple method in preparing A-type CHA with a nanostructure. Results from this in vitro biological study suggest that porous A-type carbonated hydroxyapatite nanoceramics may be a much better candidate for clinical use in terms of bioactivity. - Highlights: Black-Right-Pointing-Pointer We prepared porous A-type carbonated hydroxyapatite nanoceramics with microwave sintering. Black-Right-Pointing-Pointer We examined physico-chemical characterization and osteoblast response. Black-Right-Pointing-Pointer The nanoceramics have a comparable compressive strength to samples with conventional sintering method. Black-Right-Pointing-Pointer The nanoceramics enhance degradation property, osteoblast

  13. 碳掺杂的二氧化钛纳米管的制备及其可见光催化性能%Preparation and Visible Light Photocatalytic Activity of Carbon Doped Titanium Dioxide Nanotubes

    Institute of Scientific and Technical Information of China (English)

    李向清; 康诗钊; 唐韵秋; 李国栋; 穆劲

    2013-01-01

    Urea was used as a precursor of carbon to prepare carbon doped TiO2 nanotubes.The products obtained were characterized with Brunauer-Emmett -Teller surface area measurement (BET),X-ray diffraction (XRD) ,transmission electron microscopy (TEM) ,energy dispersive X-ray fluoresence spectroscopy ( EDX) ,X-ray photoelectron spectroscopy (XPS) ,solid diffuse reflection UV-Vis spectroscopy (DRS) and fluorescence spectroscopy.The results showed that the visible light photocatalytic activity of the TiO2 nanotubes was improved obviously after doping C.In addition,the influences of doping amount of C,calcination temperature,dosage of catalyst and pH on the photocatalytic degradation activity of the TiO2 nanotubes were investigated.The degradation efficiency of rodamine B could reach 91% under 3 h visible light irradiation when the amount of doping C was 5.3% ,calcination temperature was 400℃ ,dosage of catalyst was 1.5 g/L,pH of solution was 5.%以尿素作为碳元素前驱体对TiO2纳米管进行掺杂,采用比表面积测定、X射线衍射、透射电子显微镜、能量色散X射线荧光光谱、X射线光电子能谱、固体漫反射紫外-可见吸收光谱和荧光光谱对产物进行了表征.结果表明,以尿素作为前驱体可制备C掺杂的TiO2纳米管,C掺杂后,TiO2纳米管的可见光催化活性明显提高.此外,研究了C掺杂量、煅烧温度、催化剂用量和pH值对TiO2纳米管光催化降解活性的影响,发现当C的掺杂量为5.3%、催化剂用量为1.5 g/L、溶液的pH值为5时,在其催化作用下,可见光光照3h后罗丹明B的降解率可达到91%.

  14. Preparation and properties of gluten/calcium carbonate composites

    Institute of Scientific and Technical Information of China (English)

    Min Zuo; Zheng Zheng Lai; Yi Hu Song; Qiang Zheng

    2008-01-01

    Environment friendly thermosetting composites were prepared by blending wheat gluten (WG) as matrix, calcium carbonate (CaCO3) as filler and glycerol as plasticizer followed by compression molding the mixture at 120 ℃ to crosslink the WG matrix. Morphology observation showed that the CaCO3 particles were finely dispersed in matrix. Incorporation of CaCO3 up to 10 wt% into the composites caused Young's modulus and tensile strength to increase markedly. On the other hand, the moisture absorption and elongation at break decreased slightly.

  15. Direct Preparation of Carbon Nanotube Intramolecular Junctions on Structured Substrates

    Science.gov (United States)

    An, Jianing; Zhan, Zhaoyao; Sun, Gengzhi; Mohan, Hari Krishna Salila Vijayalal; Zhou, Jinyuan; Kim, Young-Jin; Zheng, Lianxi

    2016-12-01

    Leveraging the unique properties of single-walled carbon nanotube (SWNT) intramolecular junctions (IMJs) in innovative nanodevices and next-generation nanoelectronics requires controllable, repeatable, and large-scale preparation, together with rapid identification and comprehensive characterization of such structures. Here we demonstrate SWNT IMJs through directly growing ultralong SWNTs on trenched substrates. It is found that the trench configurations introduce axial strain in partially suspended nanotubes, and promote bending deformation in the vicinity of the trench edges. As a result, the lattice and electronic structure of the nanotubes can be locally modified, to form IMJs in the deformation regions. The trench patterns also enable pre-defining the formation locations of SWNT IMJs, facilitating the rapid identification. Elaborate Raman characterization has verified the formation of SWNT IMJs and identified their types. Rectifying behavior has been observed by electrical measurements on the as-prepared semiconducting-semiconducting (S-S) junction.

  16. Ni supported on activated carbon as catalyst for flue gas desulfurization

    Institute of Scientific and Technical Information of China (English)

    2010-01-01

    A series of Ni supported on activated carbon are prepared by excessive impregnation and the desulfurization activity is investigated. It has been shown that the activated carbon-supported Ni is an efficient solid catalyst for flue gas desulfurization. The activated carbon treated by HNO3 exhibits high desulfurization activity, and different amounts of loaded-Ni on activated carbon significantly influence the desulfurization activity. The catalysts are studied by X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS). The results of XRD and XPS indicate that the activated carbon treated by HNO3 can increase oxygen-containing functional groups. Ni on activated carbon after calcination at 800 °C shows major Ni phase and minor NiO phase, and with increasing Ni content on activated carbon, Ni phase increases and affects the desulfurization activity of the catalyst, which proves that Ni is the main active phase.

  17. 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.

  18. Multi-physical field coupling simulation of TCVI process for preparing carbon/carbon composites

    Institute of Scientific and Technical Information of China (English)

    2009-01-01

    To prepare Carbon/Carbon (C/C) composites with advanced performance, the thermal gradient chemical vapor infiltration (TCVI) process has been optimized by simulation. A 2D axisymmetric unstable model was built, which included convection, conduction, diffusion, densification reactions in the pores and the evolution of the porous medium. The multi-physical field coupling model was solved by finite element method (FEM) and iterative calculation. The time evolution of the fluid, temperature and preform density field were obtained by the calculation. It is indicated that convection strongly affects the temperature field. For the preform of carbon/carbon composites infiltrated for 100 h by TCVI, the radial average densities from simulation agrees well with those from experiment. The model is validated to be reliable and the simulation has capability of forecasting the process.

  19. Multi-physical field coupling simulation of TCVI process for preparing carbon/carbon composites

    Institute of Scientific and Technical Information of China (English)

    JIAO YanQiong; LI HeJun; LI KeZhi

    2009-01-01

    To prepare Carbon/Carbon (C/C) composites with advanced performance, the thermal gradient chemi-cal vapor infiltration (TCVI) process has been optimized by simulation.A 2D axisymmetric unstable model was built, which included convection, conduction, diffusion, densification reactions in the pores and the evolution of the porous medium.The multi-physical field coupling model was solved by finite element method (FEM) and iterative calculation.The time evolution of the fluid, temperature and pre-form density field were obtained by the calculation.It is indicated that convection strongly affects the temperature field.For the preform of carbon/carbon composites infiltrated for 100 h by TCVI, the radial average densities from simulation agrees well with those from experiment.The model is validated to be reliable and the simulation has capability of forecasting the process.

  20. Intercalated carbon nanotubes as a template for the preparation of supported heteroatomic nanoparticles.

    Science.gov (United States)

    Schouler, Marie-Claude; Chamssedine, Fadel; Claves, Daniel

    2011-03-01

    Chemistry in confined conditions is explored at the level of the interlayer space of multiwall carbon nanotubes. Starting from preliminary intercalated tubes, a ligand exchange reaction has been successfully conducted within the former Van der Waals gap, resulting in a final dispersion of heteroatomic particles, around 2 nm large and nearly homogeneous in size, on the outer surface of the tubes. Intercalated tubular carbon architectures thus prove to be interesting templates for a bottom-up preparation of chemically complex supported nanoparticles, with potential activities for versatile applications.

  1. Homogeneous Carbon Nanotube/Carbon Composites Prepared by Catalyzed Carbonization Approach at Low Temperature

    Directory of Open Access Journals (Sweden)

    Hongjiang Li

    2011-01-01

    Full Text Available We synthesize carbon nanotube (CNT/carbon composite using catalyzed carbonization of CNT/Epoxy Resin composite at a fairly low temperature of about 400∘C. The microstructure of the composite is characterized by scanning electron microscope (SEM, transmission electron microscope (TEM, and X-ray diffraction (XRD. The results indicate that CNTs and pyrolytic carbon blend well with each other. Pyrolytic carbon mainly stays in an amorphous state, with some of it forming crystalline structures. The catalyst has the effect of eliminating the interstices in the composites. Remarkable increases in thermal and electrical conductivity are also reported.

  2. Preparation of Hemp Stalk Activated Carbons for Decolorizing and Deodorizing of Bamboo Vinegar%汉麻杆活性炭的制备及对竹醋液脱色脱臭的研究

    Institute of Scientific and Technical Information of China (English)

    张婷; 高雅琳; 林小云; 周文富

    2012-01-01

    为了研究自制的汉麻活性炭对竹醋原液的脱色脱臭的最佳工艺,以单因素试验考察活性炭的用量、吸附时间、温度对竹醋原液(100℃蒸馏液)脱色脱臭的影响.结果表明:最佳工艺条件为单位体积竹醋原液汉麻活性炭用量24mg/mL,单位体积竹醋蒸馏液汉麻活性炭用量10mg/mL,吸附20min,吸附温度60℃,pH值为3.0,磷酸汉麻活性炭脱色率达85%以上;氯化锌脱色率达60%以上,磷酸汉麻活性炭吸附量高达385.3~427.3mg/g.结论:磷酸汉麻活性炭脱色率比其他活性炭脱色、脱臭率高,可应用于竹醋液的脱色脱臭.%The optimum process of decolorization and deodorization was studied, by using self-made hemp activated carbons and bamboo vinegar. The influence of adsorption dosage, time, and temperature on the decolorization and deodorization of bamboo vinegar liquid and its distillate(100℃) were explored by single factor. The results show that the optimum process conditions are. The hemp activated carbon is processed by phosphoric acid for bamboo vinegar liquid, dosage of activated carbons 24 mg/ml bamboo vinegar, dosage of activated carbons 10 mg/ml bamboo vinegar liquid and its distillate, adsorption time is 20 min, adsorption temperature is 60 ~C, pH=3.0, in this condition, the color removal rate of phosphoric acid processing hemp activated carbon is up to 85~; The color removal rate of zinc chloride processing hemp activated carbon is up to 60~/~o. The maximum adsorption of phosphoric acid processing hemp activated carbon is up to 358. 3~427.3 mg/g. The conclusion is drawn: The color removal rate and deodorizing rate of phosphoric acid processing activated carbon are higher than other activated carbons for the decolorization and deodorization of bamboo vinegar liquid.

  3. 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.

  4. Adsorptive removal of sulfate from acid mine drainage by polypyrrole modified activated carbons: Effects of polypyrrole deposition protocols and activated carbon source.

    Science.gov (United States)

    Hong, Siqi; Cannon, Fred S; Hou, Pin; Byrne, Tim; Nieto-Delgado, Cesar

    2017-10-01

    Polypyrrole modified activated carbon was used to remove sulfate from acid mine drainage water. The polypyrrole modified activated carbon created positively charged functionality that offered elevated sorption capacity for sulfate. The effects of the activated carbon type, approach of polymerization, preparation temperature, solvent, and concentration of oxidant solution over the sulfate adsorption capacity were studied at an array of initial sulfate concentrations. A hardwood based activated carbon was the more favorable activated carbon template, and this offered better sulfate removal than when using bituminous based activated carbon or oak wood activated carbon as the template. The hardwood-based activated carbon modified with polypyrrole removed 44.7 mg/g sulfate, and this was five times higher than for the pristine hardwood-based activated carbon. Various protocols for depositing the polypyrrole onto the activated carbon were investigated. When ferric chloride was used as an oxidant, the deposition protocol that achieved the most N(+) atomic percent (3.35%) while also maintaining the least oxygen atomic percent (6.22%) offered the most favorable sulfate removal. For the rapid small scale column tests, when processing the AMD water, hardwood-based activated carbon modified with poly pyrrole exhibited 33 bed volume compared to the 5 bed volume of pristine activated carbons. Copyright © 2017 Elsevier Ltd. All rights reserved.

  5. Inorganic Impurity on Preparation of Calcium Carbonate and Its Active Influence Oriented from Desulfurization Gypsum%脱硫石膏中无机杂质对制备碳酸钙及其活性的影响

    Institute of Scientific and Technical Information of China (English)

    史晨杰; 谭文轶; 闫怀晴; 郭霏霏; 徐幸福

    2012-01-01

    为了达到烟气脱硫石膏减量化处理,建立其资源化利用方法,在考虑到烟气脱硫石膏来源复杂性的基础上,分别考察了金属离子(如Mg2+,Fe3+)和非金属离子(如F-)对利用碳酸铵转化烟气脱硫石膏,制备碳酸钙粉末的影响.结果表明,F-,Mg2+,Fe3+等离子对脱硫石膏转化率有不同程度影响,但转化率均能达到70%以上,转化固体产物为较纯碳酸钙粉末.其中随着阳离子Mg2+,Fe3+含量增加,转化率下降;F-的水解作用以及络合物的生成将对转化率造成复杂影响,0.5wt%为最优的含量.转化产物经其吸收活性测试,其活度比天然石灰石略低,到达脱硫剂基本要求,但需注意杂质离子的积累效应.碳酸铵转化烟气脱硫石膏方法可制备微细碳酸钙粉末,是一种循环利用烟气脱硫石膏的有效途径.%To reduce gypsum produced from wet flue gas desulfurization (WFGD)process and to establish a resource approach to utilize desulfurization gypsum, the effect of metal ion such as Mg2+, Fe3+ and nonmetallic ion such as F" on productivity of calcium carbonate prepared from desulfurization gypsum was investigated, taking into consideration of complex composition of desulfurization gypsum. Results showed that the ions such as F", Mg2+, Fe3+ affect conversion of desulfurization gypsum to different extents, with conversion rate more than 70% and pure calcium carbonate as obtained solid powder. As cationic Mg2+, Fe3+ content increased, the conversion rate decreased. Both hydrolysis of F- and formation of the complicates conversion affected the conversion, with F- 0.5 wt% as the optimal content for conversion. It is verified that the solid product obtained has the potential activity to be recycled as desulfurization absorbent though impurities should be paid attentions. Conversion of desulfurization gypsum to calcium carbonate powder by ammonia carbonate is an effective method to recycle desulfurization gypsum.

  6. Preparation and characterization of activated carbon fiber material modified by CuO%活性炭纤维负载CuO改性及其性能表征

    Institute of Scientific and Technical Information of China (English)

    李海红; 薛慧; 杨清

    2016-01-01

    CuO/ACF electrode materials were prepared using activated carbon fiber (ACF) felt with HCl pretreatment as raw materials, which were loaded with copper oxide (CuO) by impregnation-burning method with Cu(NO3)2solution as the precursor. Physical and chemical properties of the ACF before and after loaded CuO samples were characterized by scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), specific surface area and pore size analysis, and fourier transform infrared spectroscopy (FTIR); the changes of electrochemical performance of the samples were analyzed by using electrochemical workstation. The results show that CuO/ACF electrode materials are successfully prepared. Specific surface area and total pore volume of CuO/ACF decrease by 31.94% and 33.95%, respectively. The surface oxygen groups increase, with obvious Cu—O bonds after loading with the metal oxides. The mass fraction of Cu in CuO/ACF is 13.7%; and the specific capacitance has an increase of 17.95% in comparison with original ACF after loading with CuO. CuO/ACF materials can be used as an electrode material for the removal of the inorganic ions in wastewater.%以Cu(NO3)2溶液作为前躯体,采用浸渍–煅烧法对盐酸预处理后的活性炭纤维(activated carbon fiber,ACF)毡进行负载氧化铜化学改性,制备CuO/ACF电极材料。通过扫描电镜(SEM)、X射线光电子能谱仪(XPS)、比表面积及孔径分析仪以及傅立叶变换红外光谱仪(FTIR)对ACF及其负载CuO后的形貌与结构、元素组成、比表面积、孔径等进行观察与分析,并利用电化学工作站测试其电化学性能。结果表明:经过负载 CuO 化学改性的CuO/ACF 电极材料,比表面积及孔容较改性前分别下降31.94%和33.95%,表面含氧基团增多,出现明显的 Cu—O键,CuO/ACF电极材料中Cu元素的质量分数为13.7%;负载CuO后比电容升高17.95%,电吸附性能提高。CuO/ACF材料可作为电极材料用于去

  7. Preparation of Two Kinds of Ultra-fine Activated Carbon Fibers and Adsorption of Formaldehyde on Them%两种超细活性碳纤维的制备及其甲醛吸附性能

    Institute of Scientific and Technical Information of China (English)

    余阳; 周美华; 吴小倩

    2011-01-01

    Two kinds of ultra-fine activated carbon fibers (UFACF-1 and UFACF-2) were prepared from ultra-fine preoxidized fiber mat via electric heating and microwave heating method, at the same relative humidity, the gaseous formaldehyde adsorption performance on the prepared ultra-fine activated carbon fibers was studied. The morphology and structural evolvement of ultra-fine preoxidized fiber during thermal treatment were characterized by field emission-scanning electron microscopy, FTIR spectroscopy and surface area and pore size analyses. UFACF-1 and UFACF-2 had differences in fiber morphology, structure and the formaldehyde adsorption performance, the surface area and the total pore volume of UFACF-1 were 805.25m2 · g-1 and 0. 366cm3 · g-1, and UFACF-2 were 733.32m2 · g-1 and 0. 386cm3 · g-1, respectively. UFACF-1 showed higher formaldehyde adsorption capacity than UFACF-2; UFACF-1 contained carbonyl and hydroxyl functional groups, which could have potential applications in removal of indoor formaldehyde.%以超细预氧化纤维毡为原料,采用电加热和微波加热方法制备两种超细活性碳纤维吸附剂(UFACF-1、UFACF-2),在相同湿度条件下,对两种超细活性碳纤维的甲醛吸附性能进行测定;采用场发射扫描电镜、傅里叶变换红外-拉曼光谱仪、全自动比表面和孔径分布分析仪对两种超细活性碳纤维吸附剂的纤维形态、结构、比表面积、孔容和孔径分布进行表征;两种超细活性碳纤维在纤维形态、结构和甲醛吸附性能上均有差别,其中,UFACF-1比表面积为805.25mz·g-1,总孔容为0.366cm3·g-1,UFACF-2比表面积为733.32m2·g-1,总孔容为0.386cm3·g-1,UFACF-1甲醛吸附性能优于UFACF-2;UFACF-1含有大量极微孔和含氧官能团,对于室内甲醛处理,是一种有应用潜力的新型吸附材料.

  8. Preparation of carbon alloy catalysts for polymer electrolyte fuel cells from nitrogen-containing rigid-rod polymers

    Energy Technology Data Exchange (ETDEWEB)

    Chokai, Masayuki [Department of Organic and Polymeric Materials, Tokyo Institute of Technology, Ookayama, Meguro-ku, Tokyo 152-8552 (Japan); Integrative Technology Research Institute, Teijin Ltd., 4-3-2, Asahigaoka, Hino, Tokyo 191-8512 (Japan); Taniguchi, Masataka; Shinoda, Tsuyoshi; Nabae, Yuta; Kuroki, Shigeki; Hayakawa, Teruaki; Kakimoto, Masa-aki [Department of Organic and Polymeric Materials, Tokyo Institute of Technology, Ookayama, Meguro-ku, Tokyo 152-8552 (Japan); Moriya, Shogo; Matsubayashi, Katsuyuki [Department of Organic and Polymeric Materials, Tokyo Institute of Technology, Ookayama, Meguro-ku, Tokyo 152-8552 (Japan); Business Development Division, Nisshinbo Holdings, Inc., 1-2-3, Onodai, Midori-ku, Chiba 267-0056 (Japan); Ozaki, Jun-ichi [Department of Organic and Polymeric Materials, Tokyo Institute of Technology, Ookayama, Meguro-ku, Tokyo 152-8552 (Japan); Department of Nanomaterial Systems, Graduate School of Engineering, Gunma University, 1-5-1, Tenjin-cho, Kiryu, Gunma 376-8515 (Japan); Miyata, Seizo [Department of Organic and Polymeric Materials, Tokyo Institute of Technology, Ookayama, Meguro-ku, Tokyo 152-8552 (Japan); New Energy and Industrial Technology Development Organization, 1310 Omiya-cho, Saiwai-ku, Kawasaki, Kanagawa 212-8554 (Japan)

    2010-09-15

    Carbon alloy catalysts (CAC), non-precious metal catalysts for the oxygen reduction reaction (ORR), were prepared from various kinds of nitrogen-containing rigid-rod aromatic polymers, polyimides, polyamides and azoles, by carbonization at 900 C under nitrogen flow. The catalytic activity for ORR was evaluated by the onset potential, which was taken at a current density of -2 {mu}A cm{sup -2}. Carbonized polymers having high nitrogen content showed higher onset potential. In particular, CACs derived from azole (Az5) had an onset potential of 0.8 V, despite being was prepared without any metals. (author)

  9. 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)

  10. Potassium vapor assisted preparation of highly graphitized hierarchical porous carbon for high rate performance supercapacitors

    Science.gov (United States)

    Liu, Zheng; Zeng, Ying; Tang, Qunli; Hu, Aiping; Xiao, Kuikui; Zhang, Shiying; Deng, Weina; Fan, Binbin; Zhu, Yanfei; Chen, Xiaohua

    2017-09-01

    Ultrahigh graphitized carbon microspheres with rich hierarchical pores (AGHPCM-1) have been successfully synthesized through the one-step activation-carbonization strategy (OACS) with porous sulfonated poly-divinylbenzene as the carbon precursor, iron as the hard template and catalyst, and potassium hydroxide (KOH) as activation agent. Through the XRD, TEM, Raman and BET analysis, AGHPCM-1 shows very high graphitization degree and rich micro-, meso- and macro-pores. More importantly, the mechanism for KOH to improve the graphitization degree of carbon materials in OACS has been illustrated by the thermodynamical theory. The tremendous heat releasing from the reaction between the catalyst precursor of Fe2O3 and potassium vapor plays a key role in the formation of graphitized carbon. It may provide a general direction to prepare highly graphitized porous carbon at a moderate temperature. Integrating the advantages of high graphitization degree and rich hierarchical porous structure, the AGHPCM-1 exhibits an excellent rate performance with a response to up to the high current density of 150 A g-1 and high scan rate of 2000 mV s-1. No obvious capacitance decay can be observed after 10000 charge/discharge cycles even at the high current density of 20 A g-1.

  11. Preparation of carbon-nitride bulk samples in the presence of seed carbon-nitride films

    Energy Technology Data Exchange (ETDEWEB)

    Kim, J. I. [Korea University of Technology and Education, Chonan (Korea, Republic of); Zorov, N. B. [Moscow State University, Moscow (Russian Federation)

    2004-05-15

    A procedure was developed for preparing bulk carbon-nitride crystals from polymeric alpha-C{sub 3}N{sub 4.2} at high pressure and high temperature in the presence of seeds of crystalline carbon-nitride films prepared by using a high-voltage discharge plasma combined with pulsed laser ablation of a graphite target. The samples were evaluated by using X-ray photoelectron spectroscopy (XPS), infrared (IR) spectroscopy, Auger electron spectroscopy (AES), secondary-ion mass spectrometry (SIMS), scanning electron microscopy (SEM) and X-ray diffraction (XRD). Notably, XPS studies of the film composition before and after thermobaric treatments demonstrated that the nitrogen composition in the alpha-C{sub 3}N{sub 4.2} material, which initially contained more than 58 % nitrogen, decreased during the annealing process and reached a common, stable composition of approx 45 %. The thermobaric experiments were performed at 10 - 77 kbar and 350 - 1200 .deg. C.

  12. Preparation of PAN/phenolic-based carbon/carbon composites with flexible towpreg carbon fiber

    Energy Technology Data Exchange (ETDEWEB)

    Li Wei [College of Materials Science and Engineering, Hunan University, Changsha 410082 (China)], E-mail: liwei5168@hnu.cn; Chen Zhenhua; Li Jin; Chen Xianhong; Xuan Hao; Wang Xiaoyi [College of Materials Science and Engineering, Hunan University, Changsha 410082 (China)

    2008-06-25

    Carbon/carbon composites made with flexible towpreg carbon fiber as reinforcement and phenolic resins as matrix precursor were impregnated with pitch during re-carbonization process. The structural characteristics of the composites were investigated by X-ray diffraction (XRD), scanning electron microscopy (SEM), three-point bending tests, Archimedes' method and water adsorption. Results showed that the density of the carbon/carbon composites increases from 1.45 to 1.54 g/cm{sup 3} with the cycles of pitch impregnated and re-carbonization. Open porosity measurement indicated that the increase of porosity resulted from the decomposition of phenolic resin matrix, and the open porosity of the composite gradually decreased after the impregnation and re-carbonization process. These composites also exhibited an improvement in flexural strength with increasing number of densification cycles. From SEM morphological observation, it was concluded that few cracks appeared in the surfaces and a few smaller pores with a diameter <1 {mu}m could be observed.

  13. 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.

  14. 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.

  15. Chemical Properties of Carbon Nanotubes Prepared Using Camphoric Carbon by Thermal-CVD

    Science.gov (United States)

    Azira, A. A.; Rusop, M.

    2010-03-01

    Chemical properties and surface study on the influence of starting carbon materials by using thermal chemical vapor deposition (Thermal-CVD) to produced carbon nanotubes (CNTs) is investigated. The CNTs derived from camphor were synthesized as the precursor material due to low sublimation temperature. The major parameters are also evaluated in order to obtain high-yield and high-quality CNTs. The prepared CNTs are examined using field emission scanning electron microscopy (FESEM) to determine the microstructure of nanocarbons. The FESEM investigation of the CNTs formed on the support catalysts provides evidence that camphor is suitable as a precursor material for nanotubes formation. The chemical properties of the CNTs were conducted using FTIR spectroscopy and PXRD analysis. The high-temperature graphitization process induced by the Thermal-CVD enables the hydrocarbons to act as carbon sources and changes the aromatic species into the layered graphite structure of CNTs.

  16. 聚丙烯酸/活性炭复合凝胶的制备及溶胀行为%Preparation and Swelling Mechanism of Polyacrylic Acid/Activate Carbon Composite Hydrogel

    Institute of Scientific and Technical Information of China (English)

    金淑萍; 岳国仁; 禹兴海; 张锋; 冯雷; 宋海

    2011-01-01

    采用自由基溶液聚合的方法,以过硫酸铵(APS)为引发剂,N,N′-亚甲基双丙烯酰胺(NNMBA)为交联剂,制备了聚丙烯酸(PAA)复合活性炭凝胶(PAA/AC)。考察了凝胶在生理盐水和不同pH值缓冲溶液中的平衡溶胀比及溶胀动力学,结果表明,活性炭能有效提高PAA凝胶的平衡溶胀比。蒸馏水中PAA/AC凝胶的平衡溶胀比可达到303(g/g),约为PAA凝胶平衡溶胀比的2.3倍;生理盐水(0.9%g/mL NaCl水溶液)中PAA/AC凝胶的平衡溶胀比可达到60(g/g),约为PAA凝胶平衡溶胀比的2.4倍;在实验设计的pH范围内PAA/AC凝胶的平衡溶胀比比PAA凝胶更高,具有更好的pH值敏感特性。%Polyacrylic acid hydrogels complex with activate carbon(PAA/AC) were prepared by free radical solution polymerization of acrylic acid(AA) using ammonium persulfate(APS) as an initiator and N,N′-methylene-bis acrylamide(NNMBA) as a crosslinker in the presence of activate carbon.The swelling behaviors of the hydrogels were studied in distilled water,normal saline solution and buffer solutions with different pH values.The results show that the PAA/AC hydrogel has a higher equilibrium degree of swelling(SWeq) than PAA hydrogel: the SWeq of PAA/AC is about 303(g/g) and 2.3 times more than that of PAA hydrogel in distilled water;it is about 60(g/g) and 2.4 times more than that of PAA hydrogel in normal saline solution;as well as an excellent pH-sensitivity over the range of pH investigated.

  17. 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.

  18. 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

  19. Porous Materials from Thermally Activated Kaolinite: Preparation, Characterization and Application

    Directory of Open Access Journals (Sweden)

    Jun Luo

    2017-06-01

    Full Text Available In the present study, porous alumina/silica materials were prepared by selective leaching of silicon/aluminum constituents from thermal-activated kaolinite in inorganic acid or alkali liquor. The correlations between the characteristics of the prepared porous materials and the dissolution properties of activated kaolinite were also investigated. The results show that the specific surface area (SSA of porous alumina/silica increases with silica/alumina dissolution, but without marked change of the BJH pore size. Furthermore, change in pore volume is more dependent on activation temperature. The porous alumina and silica obtained from alkali leaching of kaolinite activated at 1150 °C for 15 min and acid leaching of kaolinite activated at 850 °C for 15 min are mesoporous, with SSAs, BJH pore sizes and pore volumes of 55.8 m2/g and 280.3 m2/g, 6.06 nm and 3.06 nm, 0.1455 mL/g and 0.1945 mL/g, respectively. According to the adsorption tests, porous alumina has superior adsorption capacities for Cu2+, Pb2+ and Cd2+ compared with porous silica and activated carbon. The maximum capacities of porous alumina for Cu2+, Pb2+ and Cd2+ are 134 mg/g, 183 mg/g and 195 mg/g, respectively, at 30 °C.

  20. Preparation and Properties of Carbon Fiber Chiral Materials

    Institute of Scientific and Technical Information of China (English)

    ZHANG Ping; HUANG Zhixin; WANG Guoqing

    2008-01-01

    The chiral materials were prepared by using the carbon fiber helices as chiral inclusions,and the composite of Fe3O4 and polyaniline as matrix.The electromagnetic properties,including the rotation angles,the axial ratios and the complex chirality parameters,were measured by using a circular waveguide method in the 8.5-11.0 GHz frequency range.The dependence of these electromagnetic properties on the frequency and the concentration of the Fe3O4 in the composite matrix were analyzed.The results show that an appropriate concentration of Fe3O4 in the matrix is useful in improving the electromagnetic properties of the chiral material.

  1. Polymer/Carbon-Based Hybrid Aerogels: Preparation, Properties and Applications

    Directory of Open Access Journals (Sweden)

    Lizeng Zuo

    2015-10-01

    Full Text Available Aerogels are synthetic porous materials derived from sol-gel materials in which the liquid component has been replaced with gas to leave intact solid nanostructures without pore collapse. Recently, aerogels based on natural or synthetic polymers, called polymer or organic aerogels, have been widely explored due to their porous structures and unique properties, such as high specific surface area, low density, low thermal conductivity and dielectric constant. This paper gives a comprehensive review about the most recent progresses in preparation, structures and properties of polymer and their derived carbon-based aerogels, as well as their potential applications in various fields including energy storage, adsorption, thermal insulation and flame retardancy. To facilitate further research and development, the technical challenges are discussed, and several future research directions are also suggested in this review.

  2. Preparation and mechanism of calcium phosphate coatings on chemical modified carbon fibers by biomineralization

    Institute of Scientific and Technical Information of China (English)

    HUANG Su-ping; ZHOU Ke-chao; LI Zhi-you

    2008-01-01

    In order to prepare HA coatings on the carbon fibers, chemical modification and biomineralization processes were applied. The phase components, morphologies, and possible growth mechanism of calcium phosphate were studied by infrared spectroscopy(IR), X-ray diffractometry(XRD) and scanning electron microscopy(SEM). The results show that calcium phosphate coating on carbon fibers can be obtained by biomineralization. But the phase components and morphologies of calcium phosphate coatings are different due to different modification methods. Plate-like CaHPO4-2H2O (DCPD) crystals grow from one site of the active centre by HNO3 treatment. While on the para-aminobenzoic acid treated fibers, the coating is composed of nano-structural HA crystal homogeneously. This is because the -COOH functional groups of para-aminobenzoic acid graft on fibers, with negative charge and arranged structure, accelerating the HA crystal nucleation and crystallization on the carbon fibers.

  3. Ammonia Activation of Carbonized Polysaccharides and their Application for the Carbon Capture

    Energy Technology Data Exchange (ETDEWEB)

    Han, Tae Youl; Park, Seo Kyoung; Lee, Je Seung [Kyung Hee University, Seoul (Korea, Republic of)

    2016-05-15

    Porous carbons derived from polysaccharides (cellulose, chitosan, and alginic acid) have been prepared by heat treatment under N{sub 2} atmosphere and activated at high temperature under ammonia gas atmosphere. The CO{sub 2} adsorption capacities of prepared porous carbon materials and their dependence on the surface area and pore volume were investigated. The surface area of pristine carbon from cellulose, chitosan, and alginic acid at 800 .deg. C was measured as 406.5, 206.8, and 258.2 m{sup 2}/g with the pore volume of 0.27, 0.14, and 0.15 cm{sup 3}/g, respectively. The surface area and pore volume of carbons derived from cellulose, chitosan, and alginic acid further increased up to 976.6, 883.4, and 1031.9 m{sup 2}/g and 0.54, 0.45, and 0.65 cm{sup 3}/g, respectively, after the activation at high temperature under ammonia gas environment. The CO{sub 2} adsorption capacities of pristine carbons were measured as high as 1.85 mmol/g and further increased up to 2.44 mmol/g by ammonia activation.

  4. Preparation of carbon brushes with thermosetting resin binder

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    Carbon brushes with a resin binder were prepared according to an industrial process and the effects of the molding pressure, grains size and cure temperature on the properties of brush samples were discussed. The results show that the bulk density,bending strength and Rockwell hardness increase, while resistivity decreases with increasing molding pressure. Cure temperature has much more influence on the properties of brushes than molding pressure and grains size. Isothermal differential scanning calorimetry(DSC) was used to estimate the degree of cure of resin binder and a novel method of using the true density to measure the degree of cure of resin binder was presented and discussed briefly. Based on optimal process parameters carbon brushes were manufactured, durability tests for brushes were carried out on an alternate current motor and scanning electron microscope(SEM)was adopted to observe the morphology of worn surface of brushes. The results show that a luster oxide film can be formed on the surface of brushes and their service life reaches 380 h.

  5. Electric-Arc Plasma Installation for Preparing Nanodispersed Carbon Structures

    Institute of Scientific and Technical Information of China (English)

    P. STEFANOV; D. GARLANOV; G. VISSOKOV

    2008-01-01

    An electric-arc plasma installation operated in the hidden anode arrangement is constructed and used for the preparation of carbon nanostructures. A contracted plasma arc gen-erated by a plasma torch using an inert gas is used as heat source. The average mass temperature of arc is higher than 104 K, while its power density, which is directly transferred onto the electrode (anode), is ~ 2 kW/mm2. The anode contact area formed on the electrode moves against the arc by way of shifting the electrode and is hidden completely in the interior of plasma gas stream moving towards it. As a result of both the direct plasma attack and the opposite movement of streams in the hidden anode contact area, a temperature higher than 6000 K is reached. Thus, intensive vaporization takes place, which forms a saturated plasma-gas-aerosol phase of the initial material of electrode (anode). This gas phase is mixed in and carried by the plasma stream. Over that mixed plasma stream, a controlled process of quenching (fixation) is carried out by twisted turbulent fluid streams. After the fixation, the resultant carbon nano-structures are caught by a filter and collected in a bunker.

  6. Preparation and Visible Light Photocatalytic Activity of Titanium Dioxide Coated Multiwalled Carbon Nanotubes%二氧化钛涂覆多壁碳纳米管的制备及可见光催化活性

    Institute of Scientific and Technical Information of China (English)

    丛野; 秦云; 李轩科; 董志军; 袁观明; 崔正威

    2011-01-01

    以多壁碳纳米管(MWCNTs)为反应性模板,金属钛粉为钛源,采用熔盐法制备碳化钛涂覆的MWCNTs中间体,然后通过控制氧化制备二氧化钛涂覆的MWCNTs复合光催化剂.考察了熔盐反应温度、MWCNTs和钛粉的摩尔比及氧化温度等对产物的结构和形貌的影响.采用X射线衍射(XRD)、场发射扫描电子显微镜(FE-SEM)、透射电子显微镜(TEM)和X射线光电子能谱(XPS)等技术对其进行了系统的表征;以亚甲基蓝(MB)溶液的脱色降解为模型反应,考察了催化剂的可见光(λ>420 nm)催化活性.结果表明:所制备的催化剂基本保持了原始MWCNTs的纤维状形貌,二氧化钛涂层在MWCNTs表面分布均匀.并与MWCNTs之间结合紧密,形成了Ti-O-C键.MWCNTs增强了污染物亚甲基蓝在催化剂表面的吸附,Ti-O-C键的形成使得在二氧化钛价带附近形成了杂质能级,提高了对可见光的吸收和利用.因此所制备的TiO2/MWCNTs复合光催化剂表现出较高的可见光催化活性.%Titanium dioxide coated multiwalled carbon nanotubes (MWCNTs) composite photocatalysts were prepared by the controllable oxidation of titanium carbide coated MWCNTs obtained by the molten salt method using MWCNTs as a reaction template and metal titanium powder as a titanium source. The effects of the molten salt reaction temperature, the molar ratio of MWCNTs to titanium powder, and the oxidation temperature on the structure and morphology of the products were investigated. The samples were characterized by X-ray diffraction (XRD), field-emission scanning electron microscopy (FE-SEM),transmission electron microscopy (TEM), and X-ray photoelectron spectroscopy (XPS). The photodegradation of a methylene blue (MB) solution was used to evaluate the photocatalytic activity of the catalyst under visible light irradiation (λ>420 nm). The results suggest that the TiO2 coated MWCNTs keep the similar fibred morphology with the pristine MWCNTs. Uniform and fine

  7. Preparation and Photocatalytic Properties of SnO2 Coated on Nitrogen-Doped Carbon Nanotubes

    Directory of Open Access Journals (Sweden)

    Lingling Wang

    2012-01-01

    Full Text Available SnO2 nanoparticles coated on nitrogen-doped carbon nanotubes were prepared successfully via a simple wet-chemical route. The as-obtained SnO2/CNx composites were characterized using X-ray powder diffraction, scanning electron microscopy, and transmission electron microscopy. The photocatalytic activity of as-prepared SnO2/CNx for degradation Rhodamine B under UV light irradiation was investigated. The results show that SnO2/CNx nanocomposites have a higher photocatalytic activity than pure SnO2 and SnO2/CNTs nanocomposites. This enhanced photoresponse indicates that the photoinduced electrons in the SnO2 prefer separately transferring to the CNx, which has a high degree of defects. As a consequence, the radiative recombination of the electron-hole pairs is hampered and the photocatalytic activity is significantly enhanced for the SnO2/CNx photocatalysts.

  8. Attempts to prepare an all-carbon indigoid system

    Directory of Open Access Journals (Sweden)

    Şeref Yildizhan

    2015-03-01

    Full Text Available First attempts are described to prepare a precursor for an all-carbon analog of indigo, the tetracyclic triene 4. Starting from indan-2-one (9 the α-methylene ketone 13 was prepared. Upon subjecting this compound to a McMurry coupling reaction, it dimerized to the bis-indene derivative 17, rather than providing the tetramethyl derivative of 4, the hydrocarbon 14. In a second approach, indan-1-one (18 was dimerized to the conjugated enedione 21 through the bis-1-indene dimer 19. All attempts to methylenate 21 failed, however. When 19 was treated with the Tebbe reagent, the dimer 23 was produced, presumably through a Cope reaction of the intermediately generated isomer 22. The bis-indene derivative 23 can be alkylated with 1,2-dibromoethane to produce a 1:1 mixture of the spiro compounds 24 and 25. Although 9 could be reductively dimerized to 30, the conversion of this olefin to 14 failed.

  9. Preparation and characterization of dopamine-decorated hydrophilic carbon black

    Energy Technology Data Exchange (ETDEWEB)

    Zhu Lijun; Lu Yonglai [State Key Laboratory of Organic-Inorganic Composites, Beijing University of Chemical Technology, Beijing 100029 (China); Key Laboratory of Beijing City on Preparation and Processing of Novel Polymer Materials, Beijing 100029 (China); Wang Yiqing [State Key Laboratory of Organic-Inorganic Composites, Beijing University of Chemical Technology, Beijing 100029 (China); Key Laboratory of Carbon Fiber and Functional Polymers, Ministry of Education, Beijing 100029 (China); Zhang Liqun [State Key Laboratory of Organic-Inorganic Composites, Beijing University of Chemical Technology, Beijing 100029 (China); Key Laboratory of Beijing City on Preparation and Processing of Novel Polymer Materials, Beijing 100029 (China); Wang Wencai, E-mail: wangw@mail.buct.edu.cn [State Key Laboratory of Organic-Inorganic Composites, Beijing University of Chemical Technology, Beijing 100029 (China); Key Laboratory of Carbon Fiber and Functional Polymers, Ministry of Education, Beijing 100029 (China)

    2012-05-01

    Inspired by the bio-adhesive proteins secreted by mussels for attachment to almost all wet substrates, a facile method involving oxidative polymerization of dopamine was proposed to prepare highly hydrophilic carbon black (CB) particles. A self-assembled polydopamine (PDA) ad-layer was formed via the oxidative polymerization of dopamine on the surface of CB simply by dipping the CB into an alkaline dopamine solution and mildly stirring at room temperature. The process is simple, controllable, and environment-friendly. The surface composition and structure of the CB were characterized by X-ray photoelectron spectroscopy (XPS) and Fourier transform infrared spectroscopy (FTIR). The surface morphology of the CB was observed by scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The results showed that the PDA ad-layer was successfully deposited on the CB surfaces. The PDA-functionalized CB (CB-PDA) gave a stable colloidal dispersion in water. Contact angle measurement results indicated that the hydrophilicity of CB was significantly improved after dopamine modification. TGA results confirmed that the modified CB maintained good heat resistance. The method provided a facile route to prepare hydrophilic CB having terminal hydroxyl groups.

  10. Preparation and characterization of platinum/carbon and ruthenium/platinum/carbon nanocatalyst using the novel rotating disk-slurry electrode (RoDSE) technique

    Science.gov (United States)

    Santiago de Jesus, Diana

    An effort to develop electrochemically smaller and well-dispersed catalytic material on a high surface area carbon material is required for fuel cell applications. In terms of pure metal catalysts, platinum has shown to be the most common catalyst used in fuel cells, but suffers from poisoning when carbon monoxide is strongly adsorbed on its surface when used for direct methanol fuel cell applications. The addition of a metal with the ability to form oxides, such as ruthenium, helps to oxidize the carbon monoxide, freeing the platinum surface for new methanol oxidation. The deposition of catalysts of PtRu onto a carbon support helps to increase the active surface area of the catalyst. Vulcan X is the most commonly used of the amorphous carbon materials for fuel cell applications. Also, a high-surface-area carbon material of interest is carbon nano-onions (CNOs), also known as multilayer fullerenes. The most convenient synthetic method for CNOs is annealing nanodiamond particles, thus retaining the size of the precursors and providing the possibility to prepare very small nanocatalysts using electrochemical techniques. A rotating disk-slurry electrode (RoDSE) technique was developed as a unique method to electrochemically prepare bulk Pt/Carbon and PtRu/Carbon nanocatalysts avoiding a constant contact of the carbon support to an electrode surface during the electrodeposition process. The nanocatalysts were prepared by using a slurry that was saturated with functionalized Vulcan XC-72R and the metal precursor in sulfuric acid. The electrochemically prepared Pt/C and PtRu/C catalysts were characterized by using TEM, STEM, XRD, XRF, TGA, XPS and electrochemical techniques. A computational analysis also was done.

  11. 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...

  12. Preparation and characterization of hierarchical porous carbons derived from solid leather waste for supercapacitor applications.

    Science.gov (United States)

    Konikkara, Niketha; Kennedy, L John; Vijaya, J Judith

    2016-11-15

    Utilization of crust leather waste (CLW) as precursors for the preparation of hierarchical porous carbons (HPC) were investigated. HPCs were prepared from CLW by pre-carbonization followed by chemical activation using KOH at relatively high temperatures. Textural properties of HPC's showed an extent of micro-and mesoporosity with maximum BET surface area of 716m(2)/g. Inducements of graphitic planes in leather waste derived carbons were observed from X-ray diffraction and HR-TEM analysis. Microstructure, thermal behavior and surface functional groups were identified using FT-Raman, thermo gravimetric analysis and FT-IR techniques. HPCs were evaluated for electrochemical properties by cyclic voltammetry (CV), galvanostatic charge/discharge (GCD) and electrochemical impedance spectroscopy (EIS) by three electrode system. CLC9 sample showed a maximum capacitance of 1960F/g in 1M KCl electrolyte. Results achieved from rectangular curves of CV, GCD symmetric curves and Nyquist plots show that the leather waste carbon is suitable to fabricate supercapacitors as it possess high specific capacitance and electrochemical cycle stability. The present study proposes an effective method for solid waste management in leather industry by the way of converting toxic leather waste to new graphitic porous carbonaceous materials as a potential candidate for energy storage devices.

  13. Adsorption of Hydantoins on Activated Carbon,

    Science.gov (United States)

    1985-05-01

    covery, Garten and Weiss (1965) proposed the existence of chromene (benzpyran) groups on the surface of H-carbons. The acid reaction with the chromene ...presence of the chromene groups on the surface of H-carbons is responsible for the acid-adsorbing characteristics. Activation temperatures and

  14. 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.

  15. Preparation of asymmetrically distributed bimetal ceria (CeO₂) and copper (Cu) nanoparticles in nitrogen-doped activated carbon micro/nanofibers for the removal of nitric oxide (NO) by reduction.

    Science.gov (United States)

    Bhaduri, Bhaskar; Verma, Nishith

    2014-12-15

    A novel multi-scale web of carbon micro/nanofibers (ACF/CNF) was prepared by the catalytic chemical vapor deposition (CCVD), in which CeO2 and Cu nanoparticles (NPs) were in-situ incorporated during a synthesis step. The CVD temperature was adjusted such that the prepared material had asymmetric distribution of the bimetals, with the Cu NPs located at the tips of the CNFs and the CeO2 particles adhered to the surface of the ACF substrate. The prepared bimetals-dispersed web of ACF/CNF was treated with pyridine and the surface functionalized material was applied for the removal of NO by reduction. The complete reduction of NO was achieved at 500°C and for 400ppm NO concentration. Whereas the Cu NPs acted as the catalyst for the reduction, CeO2 facilitated the incorporation of nitrogen from the pyridine source into the ACF/CNF surface. The produced nitrogen containing surface functional groups enhanced the reactivity of the material toward the NO. The bimetals CeO2 and Cu nanoparticles (NPs)-dispersed ACF/CNF produced in this study is a potential candidate for effectively removing NO by reduction, without requiring urea or ammonia used in conventional abatement methods. Copyright © 2014 Elsevier Inc. All rights reserved.

  16. Synthesis of a Carbon-activated Microfiber from Spider Webs Silk

    Science.gov (United States)

    Taer, E.; Mustika, W. S.; Taslim, R.

    2017-03-01

    Carbon fiber of spider web silk has been produced through the simple carbonization process. Cobwebs are a source of strong natural fiber, flexible and micrometer in size. Preparation of micro carbon fiber from spider webs that consist of carbonization and activation processes. Carbonization was performed in N2 gas environment by multi step heating profile up to temperature of 400 °C, while the activation process was done by using chemical activation with KOH activating agent assistance. Measurement of physical properties was conducted on the surface morphology, element content and the degree of crystallinity. The measurement results found that micro carbon fiber from spider webs has a diameter in the range of 0.5 -25 micrometers. It is found that the carbon-activated microfiber takes the amorphous form with the carbon content of 84 %.

  17. METHOD OF INFRARED SPECTRA REGISTRATION OF ACTIVATED CARBONS IN POTASSIUM BROMIDE PELLETS

    Directory of Open Access Journals (Sweden)

    Diana Shepel

    2015-06-01

    Full Text Available This communication is devoted to the elaboration of a new optimal technique of infrared spectra registration of activated carbons in potassium bromide pellets. Authors investigated the dependence of the intensity of the least overlapping infrared bands of activated carbons on the conditions of preparation, recording of the spectrum, and the degree of homogenization with KBr.

  18. 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.

  19. 磺化石墨烯/活性炭复合电极的制备及其不对称电容器脱盐%Preparation of Sulfonated Graphene/Activated Carbon Composite Electrode for Asymmetric Capacitive Deionization

    Institute of Scientific and Technical Information of China (English)

    卢淼; 刘建允; 王世平; 程健

    2014-01-01

    在还原剂 NaBH4存在下,采用对氨基苯磺酸重氮盐与氧化石墨(GO)表面共价键合制备磺化石墨烯(GP-SO3 H).傅里叶变换红外光谱(FTIR)证明磺酸基团在石墨烯表面接枝.采用扫描电子显微镜(SEM)研究了磺化石墨烯的表面形貌.以磺化石墨烯为添加剂,制备了磺化石墨烯/活性炭(GP-SO3 H/ AC)复合电极.循环伏安及阻抗分析结果表明,该复合电极的电容特性及导电性有明显改善.以活性炭电极为对电极组装了不对称电容器(GP-SO3 H/ AC| AC),研究了该不对称电容器的电化学脱盐性能.与对称电容器(AC | AC)相比,不对称电容器中由于电极内磺酸基团对反离子的屏蔽作用,电容器的电流效率达到89.4%以上,脱盐量提高2.4倍,单个循环脱盐量达到10.87 mg/ g.%Sulfonated graphene( GP-SO3 H) was prepared by grafting reaction of sulfonated diazoniun salt. The sulfonated graphene was characterized by Fourier transform infrared spectrometry( FTIR) and scanning electron microscopy(SEM), respectively. The experimental results indicate that the sulfonic groups have been grafted onto graphene oxide. The sulfonated graphene / activated carbon composite electrode(GP-SO3 H/ AC) was prepared by mixing 10% ( mass fraction) GP-SO3 H as dopant. Compared with AC electrode, this composite electrode exhibits an ideal double layer capacitive behavior and high conductivity, confirmed by cyclic voltammetry and electrochemical impedance spectroscopy. The hybrid capacitor was assembled by the resultant GP-SO3 H/ AC as negative electrode and AC as counter electrode for capacitor deionization(CDI). Under the constant current charging-discharging condition, the salt removal amount of 10. 87 mg / g in single cycle was obtained, about 2. 4 times that of the normal AC capacitor. And the current efficiency was improved dramatically owing to the facile adsorption of sulfonic groups to cations, and the shielding effect of sulfonic groups

  20. 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