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过刊目录

    2012, Vol. 21, No. 3 Online: 2012-05-27
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    Special Column
    Carbon as a hard template for nano material catalysts (Special Column-Review)
    Kake Zhu, Junming Sun*, He Zhang, Jun Liu, Yong Wang*
    2012, 21(3): 215-232.  DOI: 10.1016/S1003-9953(11)60357-5
    摘要 ( 13382 )  
    As one of the naturally abundant elements, carbon can present in different molecular structures (allotropes) and thus lead to various physical/chemical properties of carbon-based materials which have found wide applications in a variety of fields including electrochemistry, optical, adsorption and catalysis, etc. On the other hand, its different allotropes also endow carbon-based materials with various morphostructures, which have been recently explored to prepare oxides and zeolites/zeotypes with tailored structures. In this review, we mainly summarize the recent advances in using carbon materials as hard templates to synthesize structural materials. Specifically, we focus on the development in the synthetic strategies, such as endotemplating, exotemplating approaches and using carbon materials as chemical reagents for the synthesis of metal carbides or nitrides, with an emphasis laid on the control of morphostructure. Meanwhile, the applications of the obtained materials will be highlighted, especially, in the field of heterogeneous catalysis where enhanced performances have been achieved with the materials derived from carbon-templated methods.
    Carbon nanotubes for supercapacitors: Consideration of cost and chemical vapor deposition techniques (Special Column-Review)
    Chao Zheng, Weizhong Qian*, Chaojie Cui, Guanghui Xu, Mengqiang Zhao, Guili Tian
    2012, 21(3): 233-240.  DOI: 10.1016/S1003-9953(11)60358-7
    摘要 ( 13413 )  
    In this topic, we first discussed the requirement and performance of supercapacitors using carbon nanotubes (CNTs) as the electrode, including specific surface area, purity and cost. Then we reviewed the preparation technique of single walled CNTs (SWNTs) in relatively large scale by chemical vapor deposition method. Its catalysis on the decomposition of methane and other carbon source, the reactor type and the process control strategies were discussed. Special focus was concentrated on how to increase the yield, selectivity, and purity of SWNTs and how to inhibit the formation of impurities, including amorphous carbon, multiwalled CNTs and the carbon encapsulated metal particles, since these impurities seriously influenced the performance of SWNTs in supercapacitors. Wish it be helpful to further decrease its product cost and for the commercial use in supercapacitors. .
    Selectivity modulation in the consecutive hydrogenation of benzaldehyde via functionalization of carbon nanotubes (Special Column)
    Yonghua Zhou, Jing Liu, Xingyun Li, Xiulian Pan*, Xinhe Bao*
    2012, 21(3): 241-245.  DOI: 10.1016/S1003-9953(11)60359-9
    摘要 ( 8195 )  
     Hydrogenation of benzaldehyde is a typical consecutive reaction, since the intermediate benzyl alcohol is apt to be further hydrogenated. Here we demonstrate that the selectivity of benzyl alcohol can be tuned via functionalization of carbon nanotubes (CNTs), which are used as the support of Pd. With the original CNTs, the selectivity of benzyl alcohol is 88% at a 100% conversion of benzaldehyde. With introduction of oxygen-containing groups onto CNTs, it drops to 27%. In contrast, doping CNTs with N atoms, the selectivity reaches 96% under the same reaction conditions. The kinetic study shows that hydrogenation of benzyl alcohol is significantly suppressed, which can be attributed to weakened adsorption of benzyl alcohol. This is most likely related to the modified electronic structure of Pd species via interaction with functionalized CNTs, as shown by XPS characterization.
    Carbonaceous residues from biomass gasification as catalysts for biodiesel production  (Special Column
    Rafael Luque*, Antonio Pineda, Juan C. Colmenares, Juan M. Campelo, Antonio A. R
    2012, 21(3): 246-250.  DOI: 10.1016/S1003-9953(11)60360-5
    摘要 ( 9174 )  
    Tars and alkali ashes from biomass gasification processes currently constitute one of the major problems in biomass valorisation, generating clogging of filters and issues related with the purity of syngas production. To date, these waste residues find no useful applications and they are generally disposed upon generation in the gasification process. A detailed analysis of these residues pointed out the presence of high quantities of Ca (>30 wt%). TG experiments indicated that a treatment under air at moderate temperatures (400-800 ℃) decomposed the majority of carbon species, while XRD indicated the presence of a crystalline CaO phase. CaO enriched valorized materials turned out to be good heterogeneous catalysts for biodiesel production from vegetable oils, providing moderate to good activities (50%-70% after 12 h) to fatty acid methyl esters in the transesterification of sunflower oil with methanol.
    Fabrication of functional hollow carbon spheres with large hollow interior as active colloidal catalysts  (Special Column)
    Qiang Sun, Guanghui Wang, Wencui Li, Xiangqian Zhang, Anhui Lu*
    2012, 21(3): 251-256.  DOI: 10.1016/S1003-9953(11)60361-7
    摘要 ( 8829 )  
    In this study, we have established a facile method to synthesize functional hollow carbon spheres with large hollow interior, which can act as active colloidal catalysts. The method includes the following steps: first, hollow polymer spheres with large hollow interior were prepared using sodium oleate as the hollow core generator, and 2, 4-dihydroxybenzoic acid and hexamethylene tetramine (HMT) as the polymer precursors under hydrothermal conditions; Fe3+ or Ag+ cations were then introduced into the as-prepared hollow polymer spheres through the carboxyl groups; finally, the hollow polymer spheres can be pseudomorphically converted to hollow carbon spheres during pyrolysis process, meanwhile iron or silver nanoparticles can also be formed in the carbon shell simultaneously. The structures of the obtained functional hollow carbon spheres were characterized by TEM, XRD, and TG. As an example, Ag-doped hollow carbon spheres were used as colloid catalysts which showed high catalytic activity in 4-nitrophenol reduction reaction.
    Preparation of phosphorus-doped carbon nanospheres and their electrocatalytic performance for O2 reduction  (Special Column)
    Ziwu Liu, Feng Peng*, Hongjuan Wang, Hao Yu, Wenxu Zheng, Xianyong Wei
    2012, 21(3): 257-264.  DOI: 10.1016/S1003-9953(11)60362-9
    摘要 ( 8467 )  
     Phosphorus-doped carbon nanospheres without any metal residues were synthesized and characterized. The results revealed that the doping phosphorus atoms could significantly improve the electrocatalytic activity of graphitic carbon for the oxygen-reduction reaction (ORR) both in acidic and alkaline media, and the materials exhibited high electrocatalytic activity, long-term stability, and excellent tolerance to crossover effects especially in alkaline media. Quantum mechanics calculations with the density functional theory demonstrated that the changes in charge density and energetic characteristics of frontier orbitals for the P-doped graphene sheet could facilitate the ORR.
    Cobalt phthalocyanine-graphene complex for electro-catalytic oxidation of dopamine  (Special Column)
    Jinghe Yang, Di Mu, Yongjun Gao, Juan Tan, Anhui Lu, Ding Ma*
    2012, 21(3): 265-269.  DOI: 10.1016/S1003-9953(11)60363-0
    摘要 ( 8066 )  
    Cobalt phthalocyanine-graphene (CoPc-Gr) complex are fabricated through π-π interaction of each components, with CoPc adsorbed/inserted on/in the graphene sheets. The obtained complex could be used in the electro-chemical detection of various medicines. CoPc-Gr modified glassy electrode shows excellent response to the electro-oxidation of dopamine (DA) and ascorbic acid (AA), much better than those of CoPc, graphene oxide (GrO) or graphene (Gr) modified electrode. Significantly, the detection of dopamine is a diffusion-controlled process, highly selective, and has a low detection limit and broad linear range.  
    Low temperature microwave-assisted vs conventional pyrolysis of various biomass feedstocks  (Special Column)
    Peter Shuttleworth, Vitaliy Budarin, Mark Gronnow, James H. Clark*, Rafael Luque
    2012, 21(3): 270-274.  DOI: 10.1016/S1003-9953(11)60364-2
    摘要 ( 7987 )  
    A comparison between conventional pyrolysis and a novel developed low-temperature microwave-assisted pyrolysis methodology has been performed for the valorisation of a range of biomass feedstocks including waste residues. Microwave pyrolysis was found to efficiently deliver comparable evolution of bio-gases in the system as compared with conventional pyrolysis at significantly reduced temperatures (120-180 ℃ vs 250-400 ℃). The gas obtained from microwave-assisted pyrolysis was found to contain CO2, CH4 and CO as major components as well as other related chemicals (e.g. acids, aldehydes, alkanes) which were obtained in different proportions depending on the selected feedstock.
    Easy synthesis of iron doped ordered mesoporous carbon with tunable pore sizes  (Special Column)
    Haodong Tang, Guojun Lan, Jian Zhong, Huazhang Liu, Ying Li*
    2012, 21(3): 275-281.  DOI: 10.1016/S1003-9953(11)60365-4
    摘要 ( 10495 )  
    Precise control of the pore sizes for porous carbon materials is of importance to study the confinement effect of metal particles because the pore size in nanosize range will decide the physical and chemical properties of the metal nanoparticles. In this paper, we report a new approach for the synthesis of iron doped ordered mesoporous carbon materials with adjustable pore size by using Fe-SBA-15 as hard template and boric acid as the pore expanding reagent. The pore size can be precisely adjusted by a step of 0.4 nm in the range of 3-6 nm. The carbonization temperature can be lowered to 773 K due to the catalytic role of the doped iron. The present approach is suitable for facile synthesis of metal imbedded porous carbon materials with tunable pore sizes.
    Review
    Conventional processes and membrane technology for carbon dioxide removal from natural gas: A review
    Zee Ying Yeo, Thiam Leng Chew, PengWei Zhu, Abdul Rahman Mohamed, SiangPiao Chai
    2012, 21(3): 282-298.  DOI: 10.1016/S1003-9953(11)60366-6
    摘要 ( 10201 )  
    Membrane technology is becoming more important for CO2 separation from natural gas in the new era due to its process simplicity, relative ease of operation and control, compact, and easy to scale up as compared with conventional processes. Conventional processes such as absorption and adsorption for CO2 separation from natural gas are generally more energy demanding and costly for both operation and maintenance. Polymeric membranes are the current commercial membranes used for CO2 separation from natural gas. However, polymeric membranes possess drawbacks such as low permeability and selectivity, plasticization at high temperatures, as well as insufficient thermal and chemical stability. The shortcomings of commercial polymeric membranes have motivated researchers to opt for other alternatives, especially inorganic membranes due to their higher thermal stability, good chemical resistance to solvents, high mechanical strength and long lifetime. Surface modifications can be utilized in inorganic membranes to further enhance the selectivity, permeability or catalytic activities of the membrane. This paper is to provide a comprehensive review on gas separation, comparing membrane technology with other conventional methods of recovering CO2 from natural gas, challenges of current commercial polymeric membranes and inorganic membranes for CO2 removal and membrane surface modification for improved selectivity.
    Communication
    Accelerated nucleation of tetrahydrofuran (THF) hydrate in presence of ZIF-61 (Communication)
    Yanhong Wang, Xuemei Lang, Shuanshi Fan*
    2012, 21(3): 299-301.  DOI: 10.1016/S1003-9953(11)60367-8
    摘要 ( 8551 )  
    Clathrate hydrate can be used in energy gas storage and transportation, CO2 capture and cool storage etc. However, these technologies are difficult to be used due to the low formation rate and long induction time of hydrate formation. In this paper, ZIF-61 (zeolite imidazolate framework, ZIF) was first used in hydrate formation to stimulate hydrate nucleation. As an additive of clathrate hydrate, ZIF-61 promoted obviously the acceleration of tetrahydrofuran (THF) hydrate nucleation. It shortened the induction time of THF hydrate formation from 2-5 h to 0.3-1 h mainly due to the template function of ZIF-61 by which the nucleation of THF hydrate has been promoted.
    article
    Band gap narrowing of TiO2 by compensated codoping for enhanced photocatalytic activity
    Jindou Huang, Shuhao Wen, Jianyong Liu*, Guozhong He
    2012, 21(3): 302-307.  DOI: 10.1016/S1003-9953(11)60368-X
    摘要 ( 8894 )  
    In this study, we have performed first-principles screened exchanged hybrid density function theory with the HSE06 function calculations of the C-Mo, C-W, N-Nb and N-Ta codoped anatase TiO2 systems to investigate the effect of codoping on the electronic structure of TiO2. The calculated results demonstrate that (W(s)+C(s)) codoped TiO2 narrows the band gap significantly, and have little influence on the position of conduction band edges, therefore, enhances the efficiency of the photocatalytic hydrogen generation from water and the photodegradation of organic pollutants. Moreover, the proper oxygen pressure and temperature are two key factors during synthesis which should be carefully under control so that the desired (W(s)+C(s)) codoped TiO2 can be obtained.
    Rule of 100: An inherent limitation or performance measure in oxidative coupling of methane?
    Saeed Sahebdelfar, Maryam Takht Ravanchi*, Mahtab Gharibi, Marzieh Hamidzadeh
    2012, 21(3): 308-313.  DOI: 10.1016/S1003-9953(11)60369-1
    摘要 ( 8666 )  
    The oxidative coupling of methane over La2O3/CaO type-catalyst in a fixed-bed reactor is studied under a wide range of operating conditions (973<T<1103 K, 55<ptotal<220 kPa, and 3.7<mcat/VSTP<50 kg·s/m3). A ten-step kinetic model incorporating all main products was used to predict the behavior of the system. Methane conversions and C2 selectivities were calculated by varying methane to oxygen ratios in the feed under different operating conditions which were also compared with the rule of 100. The results show that deviation from this rule depends on the operating conditions. Within the range studied, an increase in pressure, temperature and contact time results in smaller deviation from the rule. This rule is best approximated when the catalyst operates near its optimal performance. For negative deviations, common to the most catalysts, it is found that the optimal performance should occur at methane conversion levels lower than 50%. A plot of selectivity versus conversion for high-yield reported performance data of a large variety of catalysts shows that data points concentrated roughly in 20%-50% methane conversion region, confirming the generality and prediction of modeling.
    Partial amination of cationic exchange resins and its application in the hydration of butene
    Deren Fang*, Wanzhong Ren, Hongying Lü, Hongtao Yang
    2012, 21(3): 314-318.  DOI: 10.1016/S1003-9953(11)60370-8
    摘要 ( 7987 )  
    In this work, the amination of sulfonated polystyrene resin with alkyl secondary amine is investigated. The catalytic activities of the modified resins are determined through the hydration of 1-butene. The optimum chain length and the best range of amination rate are determined. It is found that the single-pass conversion of 1-butene was raised 2% on average, and the relative activity was increased over 30% after modification. A hypothesis about the enhancement of catalytic activities by the inclusion of alkyl chain to wrap up the butene molecule is proposed.
    Efficient CO2 capture on low-cost silica gel modified by polyethyleneimine
    Ke Wang, Hongyan Shang, Lin Li, Xinlong Yan, Zifeng Yan, Chenguang Liu, Qingfang
    2012, 21(3): 319-323.  DOI: 10.1016/S1003-9953(11)60371-X
    摘要 ( 8190 )  
    In this work, a series of polyethyleneimine (PEI) functionalized commercial silica gel were prepared by wet impregnation method and used as CO2 sorbent. The as-prepared sorbents were characterized by N2 adsorption, FT-IR and SEM techniques. CO2 capture was tested in a fixed bed reactor using a simulated flue gas containing 15.1% CO2 in a temperature range of 25-100 ℃. The effects of sorption temperature and amine content on CO2 uptake of the adsorbents were investigated. The silica gel with a 30 wt% PEI loading manifested the largest CO2 uptake of 93.4 mgCO2/gadsorbent (equal to 311.3 mgCO2/gPEI) among the tested sorbents under the conditions of 15.1% (v/v) CO2 in N2 at 75 ℃ and atmospheric pressure. Moreover, it was rather low-cost. In addition, the PEI-impregnated silica gel exhibited stable adsorption-desorption behavior during 5 consecutive test cycles. These results suggest that the PEI-impregnated silica gel is a promising and cost-effective sorbent for CO2 capture from flue gas and other stationary sources with low CO2 concentration.
    Effect of cerium addition on catalytic performance of PtSnNa/ZSM-5 catalyst for propane dehydrogenation
    Mengwei Xue, Yuming Zhou*, Yiwei Zhang, Xuan Liu, Yongzheng Duan, Xiaoli Sheng
    2012, 21(3): 324-331.  DOI: 10.1016/S1003-9953(11)60372-1
    摘要 ( 9212 )  
    The effect of cerium addition on the catalytic performance of propane dehydrogenation over PtSnNa/ZSM-5 catalyst has been investigated by reaction tests and some physicochemical characterization such as XRD, BET, TEM, XPS, NH3-TPD, H2 chemisorption, TPR and TPO techniques. It has been found that with suitable amount of cerium addition, the platinum dispersion increased, while the carbon deposition tended to be eliminated easily. In these cases, the presence of cerium could not only realize the better distribution of metallic particles on the support, but also strengthen the interactions between Sn species and the support. Additionally, XPS spectra confirmed that more amounts of tin could exist in oxidized form, which was advantageous to the reaction. In our experiments, PtSnNaCe (1.1 wt%)/ZSM-5 catalyst exhibited the best catalytic performance. After running the reaction for 750 h, propane conversion was maintained higher than 30% with the corresponding selectivity to propylene of about 97%.
    Selective catalytic reduction of NO by C2H2 over Ce-Al2O3 catalyst with rate-determining step of NO oxidation
    Suhua Yan, Xinping Wang*, Wenchen Wang, Zequn Liu, Jiahao Niu
    2012, 21(3): 332-338.  DOI: 10.1016/S1003-9953(11)60373-3
    摘要 ( 10356 )  
    Ce-Al2O3 catalysts prepared by co-precipitation are investigated both in NO oxidation by O2 and in selective catalytic reduction of NO by C2H2 (C2H2-SCR). It is found that C2H2-SCR is initiated and controlled by NO oxidation to NO2 over Al2O3. Ce loading on Al2O3 is almost inactive for NO oxidation below 350 ℃, since NO2 strongly adsorbs on cerium oxide, leading to the active sites being blocked, which was characterized by temperature-programmed desorption of NO and NO2 and Fourier transform infrared spectroscopy after NO+O2 coadsorption over the samples. However, in the case of C2H2-SCR, Ce loading on Al2O3 significantly improves the reaction by accelerating the NO oxidation step in the temperature range of 250-450 ℃, since the nitrate species produced by NO2 adsorption is an active intermediate required by C2H2-SCR.
    Enhancement of CO2 adsorption on nanoporous chromium terephthalate (MIL-101) by amine modification
    Mansoor Anbia*, Vahid Hoseini
    2012, 21(3): 339-343.  DOI: 10.1016/S1003-9953(11)60374-5
    摘要 ( 8714 )  
    Carbon dioxide (CO2) adsorption on a standard metal-organic framework MIL-101 and a pentaethylenehexamine modified MIL-101 (PEHA-MIL-101) are investigated and compared in this study. The adsorbent samples were characterized by XRD, FT-IR and nitrogen adsorption-desorption isotherms analysis. CO2 adsorption capacity was measured by a volumetric method. MIL-101 and PEHA-MIL-101 exhibited CO2 adsorption capacities of 0.85 and 1.3 mmol\rmCO2/g\rmadsorbent at 10 bar and 298 K, respectively. It is observed that CO2 adsorption capacity was fairly improved about 50% after amine modification.
    Optimization of hydrothermal synthesis of H-ZSM-5 zeolite for dehydration of methanol to dimethyl ether using full factorial design
    Samaneh Hosseini, Majid Taghizadeh*, Ali Eliassi
    2012, 21(3): 344-351.  DOI: 10.1016/S1003-9953(11)60375-7
    摘要 ( 10693 )  
    H-ZSM-5 zeolite was synthesized by hydrothermal method. The effects of different synthesis parameters, such as hydrothermal crystallization temperature (170--190 ℃) and Si/Al molar ratio (100--150), on the catalytic performance of the dehydration of methanol to dimethyl ether (DME) over the synthesized H-ZSM-5 zeolite were studied. The catalysts were characterized by N2 adsorption-desorption, XRD, NH3-TPD, TGA/DTA, and SEM techniques. The full factorial design of experiments was applied to the synthesis of H-ZSM-5 zeolite and the effects of synthesis conditions and their interaction on the yield of DME as the response variable were determined. Analysis of variance showed that two variables and their interaction significantly affected the response. According to the experimental results, the optimized catalyst prepared at 170 ℃ with the Si/Al molar ratio of 100 showed the best catalytic performance among the tested H-ZSM-5 zeolite.
    Preparation of mesoporous alumina with large pore size and their supported rhenium oxide catalysts in metathesis of 1-butene and 2-butene to propene
    Lei Sang, Sheng-Li Chen*, Guimei Yuan, Zheng Zhou, Rui Li, Aicheng Chen, Min Zhe
    2012, 21(3): 352-359.  DOI: 10.1016/S1003-9953(11)60376-9
    摘要 ( 8975 )  
    Mesoporous γ-aluminas with large pore size (up to 19 nm, denoted as MA19) are prepared from dispersed pseudo-boehmite using pluronic P123 as template. It is found that these mesoporous alumina supported rhenium oxide catalysts were more active and have far longer working life-span in gas-phase metathesis of 1-butene and 2-butene to propene than rhenium oxide on conventional alumina with small pore size (5 nm). At 60 ℃ and atmospheric pressure with WHSV = 1 h-1, the similar stable conversions of butene (ca. 55%) for all the 13 wt% Re2O7/alumina catalysts were obtained near the chemical equilibrium, and the stable working life-spans of Re2O7/MA19 were far longer than that of Re2O7/Al2O3, being about 70 h and 20 h, respectively.
    Enhanced catalytic performance for direct synthesis of dimethyl ether from syngas over a La2O3 modified Cu-ZrO2/γ-Al2O3 hybrid catalyst
    Zhuo Li, Jianqing Li, Cheng Yang*, Jinhu Wu*
    2012, 21(3): 360-365.  DOI: 10.1016/S1003-9953(11)60377-0
    摘要 ( 8502 )  
    A series of hybrid catalysts were made by physically mixing Cu-ZrO2 and γ-Al2O3, for former it was modified with different loadings of La2O3 prepared by co-precipitation method. The catalysts were characterized by BET, XRD, N2O-adsorption, EXAFS, H2-TPR, NH3-TPD techniques and evaluated in the synthesis of dimethyl ether from syngas. The results show that La2O3 promoted catalysts displayed a significantly better catalytic performance compared with Cu-ZrO2/γ-Al2O3 catalyst in CO conversion and DME selectivity, and the optimum catalytic activity was obtained when the content of La2O3 was 12 wt%. The characterizations reveal that high copper dispersion, facile reducibility of copper particles and appropriate amount of acidic sites are responsible for the superior catalytic performance.