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五种典型浸矿微生物的耐氟性状对比研究 被引量:6
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作者 李乾 丁德馨 +7 位作者 王清良 史文革 胡鄂明 李会娟 马丽媛 肖云花 曹杨 刘学端 《南华大学学报(自然科学版)》 2013年第2期16-22,共7页
在微生物冶金体系中,浸矿环境的压力很可能超出了浸矿菌种的耐受能力,提高浸矿菌种的耐受性是一个极具挑战性的难题.氟化物对微生物的生长具有很强的抑制或杀死作用.在本文所研究的五种浸矿细菌中,A.ferrooxidans的氟耐受性是最好的,其... 在微生物冶金体系中,浸矿环境的压力很可能超出了浸矿菌种的耐受能力,提高浸矿菌种的耐受性是一个极具挑战性的难题.氟化物对微生物的生长具有很强的抑制或杀死作用.在本文所研究的五种浸矿细菌中,A.ferrooxidans的氟耐受性是最好的,其次是A.thiooxidans,再次是L.ferriphilum与A.caldus,最差的是S.thermosulfi-dooxidans.由此看出,中度嗜热浸矿菌比常温浸矿菌更容易被氟离子抑制. 展开更多
关键词 浸矿微生物 氟耐受性 硫氧化活性
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Catalytic Oxidative Desulfurization of Gasoline Using Vanadium(V)-substituted Polyoxometalate/H_2O_2/Ionic Liquid Emulsion System 被引量:2
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作者 Ge Jianhua Zhou Yuming +1 位作者 Yang Yong Xue Mengwei 《China Petroleum Processing & Petrochemical Technology》 SCIE CAS 2012年第1期25-31,共7页
Aiming at deep desulfurization of gasoline,three amphiphilic catalysts [C18H37N(CH3)3]3+x [PMo12-xVxO40](x=1,2,or 3) were prepared and characterized.The amphiphilic vanadium(V)-substituted polyoxometalates were dissol... Aiming at deep desulfurization of gasoline,three amphiphilic catalysts [C18H37N(CH3)3]3+x [PMo12-xVxO40](x=1,2,or 3) were prepared and characterized.The amphiphilic vanadium(V)-substituted polyoxometalates were dissolved in water-immiscible ionic liquid([Bmim]PF6),forming a H2O2-in-[Bmim]PF6 emulsion desulfurization system with 30 m% H2O2 serving as the oxidant.The catalytic oxidation of sulfur-containing model oil has been studied in detail under various reaction conditions using this system.The ionic liquid emulsion system showed high catalytic oxidative activity in the treatment of commodity gasoline.Furthermore,the mechanism of catalytic oxidative desulfurization was also elaborated. 展开更多
关键词 DESULFURIZATION vanadium (V)-substituted polyoxometalates ionic liquid emulsion catalytic oxidation
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Effect of the surface properties of an activated coke on its desulphurization performance 被引量:10
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作者 ZHANG Xiang-lan ZHANG Yan DING Fang-sheng HUANG Qi-jiang LI Yuan 《Mining Science and Technology》 EI CAS 2009年第6期769-774,共6页
Commercial coke was modified by H2O2 and/or NH3.H2O to obtain an activated coke containing additional oxygen functional groups and/or nitrogen functional groups. The aim of the modification was to enhance the SO2 adso... Commercial coke was modified by H2O2 and/or NH3.H2O to obtain an activated coke containing additional oxygen functional groups and/or nitrogen functional groups. The aim of the modification was to enhance the SO2 adsorption capacity of the activated coke. Several techniques, including total nitrogen content measurements, SO2 adsorption, XPS and FTIR analysis, were used to characterize the coke samples. The XPS and FTIR spectra suggest the existence of -CONH2 groups in the H2O2 plus ammonia modified coke. The SO2 adsorption capacity of an activated coke increases slightly with an increase in H2O2 concentration during the modification process. The desulphurization performance of a modified coke is considerably enhanced by increasing the treatment temperature during ammonia modification. The amount of nitrogen in a coke modified by H2O2 plus NH3.H2O is the highest, and the SO2 adsorption capacity of the coke is also the highest (89.9 mg/gC). The NH3.H2O (only) modified sample has lower nitrogen content and lower desulphurization capacity (79.9 mg/gC). H2O modification gives the lowest SO2 adsorption capacity (28.9 mg/gC). The H2O2 pre-treatment is beneficial for the introduction of nitrogen onto the surface of a sample during the following ammonia treatment process. 展开更多
关键词 activated coke surface property desulphurization property
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Oxidative Desulfurization over Molybdenum-containing MCM-41 被引量:1
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作者 Xu Li Zhang Wenhao +4 位作者 Fan Heli Xie Chaogang Wang Danhong Peng Zhien Wang Xieqing 《China Petroleum Processing & Petrochemical Technology》 SCIE CAS 2009年第3期39-47,共9页
Two series of molybdenum-containing MCM-41 catalysts were prepared for oxidative desulfurization ofdibenzothiophene (DBT) using t-butylhydroperoxide (TBHP) as the oxidant. The electronic properties, pore dimension... Two series of molybdenum-containing MCM-41 catalysts were prepared for oxidative desulfurization ofdibenzothiophene (DBT) using t-butylhydroperoxide (TBHP) as the oxidant. The electronic properties, pore dimension and hydrophilic properties of the catalysts were studied by XRD, BET, and 1R spectrometry. The Mo-Al2O3 catalyst and TiMCM-3% were also studied for comparison. The two series of MCM-41 zeolite with MoO3 in the framework or impregnated on the surface exhibited considerable activities at low MoO3 content and both were faxbetter than the Mo-Al2O3 catalyst, but had lower activities as compared to the TiMCM-3% catalyst. The catalysts with the highest activity were evaluated in a fixed-bed reactor. The concentration of DBT in model diesel upon oxidative desulfurization was successfully reduced from 5000 ppm to less than 150 ppm, but the catalysts were deactivated very fast. The probable reason was the high affinity of DBTO2 to the MCM-41 skeleton, especially to MoO3. The catalysts could restore most of its original activity by treating with alcohol. 展开更多
关键词 oxidative desulfurization MCM-41 MOO3
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