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Towards carbon neutrality of calcium carbide-based acetylene production with sustainable biomass resources 被引量:2
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作者 Peng Jiang Guanhan Zhao +4 位作者 Hao Zhang Tuo Ji Liwen Mu Xiaohua Lu Jiahua Zhu 《Green Energy & Environment》 SCIE EI CAS CSCD 2024年第6期1068-1078,共11页
Acetylene is produced from the reaction between calcium carbide(CaC_(2))and water,while the production of CaC_(2) generates significant amount of carbon dioxide not only because it is an energy-intensive process but a... Acetylene is produced from the reaction between calcium carbide(CaC_(2))and water,while the production of CaC_(2) generates significant amount of carbon dioxide not only because it is an energy-intensive process but also the raw material for CaC_(2) synthesis is from coal.Here,a comprehensive biomass-to-acetylene process was constructed that integrated several units including biomass pyrolysis,oxygen-thermal CaC_(2) fabrication and calcium looping.For comparison,a coal-to-acetylene process was also established by using coal as feedstock.The carbon efficiency,energy efficiency and environmental impacts of the bio-based calcium carbide acetylene(BCCA)and coal-based calcium carbide acetylene(CCCA)processes were systematically analyzed.Moreover,the environmental impacts were further evaluated by applying thermal integration at system level and energy substitution in CaC_(2) furnace.Even though the BCCA process showed lower carbon efficiency and energy efficiency than that of the CCCA process,life cycle assessment demonstrated the BCCA(1.873 kgCO_(2eq) kg-prod^(-1))a lower carbon footprint process which is 0.366 kgCO_(2eq) kg-prod^(-1) lower compared to the CCCA process.With sustainable energy(biomass power)substitution in CaC_(2) furnace,an even lower GWP value of 1.377 kgCO_(2eq) kg-prod^(-1) can be achieved in BCCA process.This work performed a systematic analysis on integrating biomass into industrial acetylene production,and revealed the positive role of biomass as raw material(carbon)and energy supplier. 展开更多
关键词 Biomass pyrolysis CO_(2)mitigation Calcium carbide acetylene Calcium loop
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Effect of Calcination Temperature on La-Modified Al2O3 Catalysts for Vapor Phase Hydrofluorination of Acetylene to Vinyl Fluoride 被引量:4
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作者 毕庆员 鲁继青 +2 位作者 邢丽琼 郭明 罗孟飞 《Chinese Journal of Chemical Physics》 SCIE CAS CSCD 2010年第1期89-94,I0002,共7页
A La-modified Al2O3 catalyst was prepared with deposition-precipitation method. The effect of calcination temperature on the reactivity for vapor phase hydrofluorination of acetylene to vinyl fluoride. The catalysts c... A La-modified Al2O3 catalyst was prepared with deposition-precipitation method. The effect of calcination temperature on the reactivity for vapor phase hydrofluorination of acetylene to vinyl fluoride. The catalysts calcined at different temperatures were characterized using NH3-TPD, pyridine-FTIR, X-ray diffraction, and Raman techniques. It was found that the calcination process could not only change the structure of these catalysts but also modify the amount of surface acidity on the catalysts. The catalyst calcined at 400 ℃ exhibited the highest conversion of acetylene (94.6%) and highest selectivity to vinyl fluoride (83.4%) and lower coke deposition selectivity (0.72%). The highest activity was related to the largest amount of surface acidity on the catalyst, and the coke deposition was also related to the total amount of surface acidic sites. 展开更多
关键词 La2O3-Al2O3 catalyst Hydrofluorination reaction Vinyl fluoride acetylene Calcination temperature
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水热法制备Ni/CeO_(2)-Al_(2)O_(3)及催化乙炔选择性加氢
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作者 王颖侠 潘柳依 +3 位作者 苏涛 李冬 牛梦龙 李稳宏 《精细化工》 EI CAS CSCD 北大核心 2024年第11期2472-2478,共7页
首先,采用水热法制备了不同CeO_(2)质量分数(x%)的xCeO_(2)-Al_(2)O_(3)载体;然后,采用初湿浸渍法制备了Ni质量分数为2%的Ni/xCeO_(2)-Al_(2)O_(3),以乙炔选择性加氢制乙烯反应为探针反应,结合XRD、SEM、H_(2)-TPR、BET、XPS、NH_(3)-TP... 首先,采用水热法制备了不同CeO_(2)质量分数(x%)的xCeO_(2)-Al_(2)O_(3)载体;然后,采用初湿浸渍法制备了Ni质量分数为2%的Ni/xCeO_(2)-Al_(2)O_(3),以乙炔选择性加氢制乙烯反应为探针反应,结合XRD、SEM、H_(2)-TPR、BET、XPS、NH_(3)-TPD、TG评价了Ni/xCeO_(2)-Al_(2)O_(3)催化性能。结果表明,Ni/5CeO_(2)-Al_(2)O_(3)表现出最佳的催化性能,在280℃下,乙炔转化率为99.7%,乙烯选择性为94.9%。Ni/5CeO_(2)-Al_(2)O_(3)具有最大的比表面积(164.2 m^(2)/g)和孔径(7.2 nm),适当的氧空位含量〔9.2%,即Ce^(3+)峰面积/(Ce^(3+)峰面积+Ce^(4+)峰面积),下同〕。CeO_(2)的添加减弱了Ni/Al的强相互作用,减少了惰性NiAl2O4尖晶石相的生成,有效提升了催化剂的活性、选择性和稳定性。在30 h的反应时间内,乙炔转化率降至90.0%,原因在于反应过程中造成的炭沉积降低了Ni/5CeO_(2)-Al_(2)O_(3)的比表面积(151.5 m^(2)/g)和孔径(6.6 nm)。 展开更多
关键词 催化剂 复合载体 乙炔加氢 乙烯选择性 NiAl_(2)O_(4)尖晶石相 催化技术
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Catalytic Performance and Characterization of Anatase TiO_(2) Supported Pd Catalysts for the Selective Hydrogenation of Acetylene 被引量:4
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作者 GAO Xiao-Ping GUO Zhang-Long +2 位作者 ZHOU Ya-Nan JING Fang-Li CHU Wei 《物理化学学报》 SCIE CAS CSCD 北大核心 2017年第3期602-610,共9页
Anatase TiO_(2)nanospindles containing 89%exposed{101}facets(TIO_(2)-101)and nanosheets with 77%exposed{001}facets(TiO_(2)-001)were hydrothermally synthesized and used as supports for Pd catalysts.The effects of the T... Anatase TiO_(2)nanospindles containing 89%exposed{101}facets(TIO_(2)-101)and nanosheets with 77%exposed{001}facets(TiO_(2)-001)were hydrothermally synthesized and used as supports for Pd catalysts.The effects of the TiO_(2)materials on the catalytic performance of Pd/TiO_(2)-101 and Pd/TiO_(2)-001 catalysts were investigated in the selective hydrogenation of acetylene to polymer-grade ethylene.The PdfTiO_(2)-101 catalyst exhibited enhanced performance in terms of acetylene conversion and ethylene yield.To understand these effects,the catalysts were characterized by H_(2)temperature-programmed desorption(H_(2)-TPD),H_(2)temperature-programmed reduction(H=-TPR),transmission electron microscopy(TEM),pulse CO chemisorption,X-ray photoelectron spectroscopy(XPS),and thermogravimetric analysis(TGA).The TEM and CO chemisorption results confirmed that Pd nanoparticles(NPs)on the TiO_(2)-101 support had a smaller average particle size(1.53 nm)and a higher dispersion(15.95%)than those on the TiO_(2)-001 support(average particle size of 4.36 nm and dispersion of 9.06%).The smaller particle size and higher dispersion of Pd on the Pd/TiO_(2)-101 catalyst provided more reaction active sites,which contributed to the improved catalytic activity of this supported catalyst. 展开更多
关键词 Pd/TiO_(2)catalyst acetylene selective hydrogenation Anatase TiO_(2) {101}plane Structure characterization
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Synthesis and Infrared Spectra Computation of Sterically Congested 2,2-Disubstituted Indane-1,3-dione Derivatives 被引量:2
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作者 Seyed Mohammad Shoaei Ali Reza Kazemizadeh Ali Ramazani 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 2011年第4期568-574,共7页
Sterically congested 2,2-disubstituted indane-1,3-dione derivatives have been syn-thesized and characterized by 1H NMR,13C NMR,FT-IR and elemental analysis.The B3LYP/HF calculations for computation of IR spectra have ... Sterically congested 2,2-disubstituted indane-1,3-dione derivatives have been syn-thesized and characterized by 1H NMR,13C NMR,FT-IR and elemental analysis.The B3LYP/HF calculations for computation of IR spectra have been carried out for the title compounds at the 6-31G and 6-311++G basis set levels.Predicted vibrational frequencies have been assigned and compared with the experimental FT-IR spectra and they are supported each other. 展开更多
关键词 vibrational frequency DFT HF FT-IR spectra 2 2-disubstituted indane-1 3-dione ISOCYANIDE
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One-pot Synthesis of 2,5-Disubstituted Oxazoles Using Poly[styrene(iodosodiacetate)] 被引量:1
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作者 JiangMinCHEN LuLingWU XianHUANG 《Chinese Chemical Letters》 SCIE CAS CSCD 2004年第2期143-144,共2页
Disubstituted oxazoles were prepared conveniently by treatment of aromatic -methyl ketones and nitriles with poly[styrene(iodosodiacetate)] in one-pot process.
关键词 Poly[styrene(iodosodiacetate)] one-pot synthesis 2 5-disubstituted oxazoles.
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Synthesis and <i>in Vitro</i>Biological Activities of 4,5-Disubstituted 1,2,4-Triazole-3-Thiols 被引量:1
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作者 Humaira Nadeem Muhammad Mohsin +3 位作者 Hasan Afzaal Sadaf Riaz Ammar Zahid Syed Aun Muhammad 《Advances in Microbiology》 2013年第4期366-375,共10页
Purpose: The triazole nucleus is an important part of the therapeutically interesting drug candidate as antimicrobial, analgesic, anticancer, anticonvulsant and anti-inflammatory agents. Methods: Therefore, in this st... Purpose: The triazole nucleus is an important part of the therapeutically interesting drug candidate as antimicrobial, analgesic, anticancer, anticonvulsant and anti-inflammatory agents. Methods: Therefore, in this study, twelve 4,5-disubstituted-1,2,4-triazole-3-thiols were synthesized by the reaction of substituted isothiocyanates and hydrazides using the common method of base catalysed intramolecular dehydrative cyclization of substituted thiosemicarbazides 3(a-f) and 4(a-f). The structures of these compounds were characterized by means of FT-IR, 1H-NMR, and elemental analysis data. All these compounds were screened for antibacterial, antioxidant, antitumor and cytotoxic activities. Results: Among these compounds: 5c, 5f and 6f were found active against gram positive cocci, the compounds 5a, 5b, 5d, 6a and 6f showed 85% free radical scavenging effect at 3 ppm when tested for antioxidant activity, 75% tumors inhibition was recorded using 5c, 5d and 6a and brine shrimps lethality assay declared 5a, 5b and 6d was 129.62 μg/ml, 161.577 μg/ml and 81.56 μg/ml respectively. Conclusion: Compounds carrying significant bioactivity can be further studied using animal models to establish their safety profile prior to initiating clinical trials. 展开更多
关键词 4 5-disubstituted 1 2 4-Triazole-3-Thiols Antibacterial Antitumor Antioxidant Cytotoxic
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PLASMA POLYMERIZATION OF ACETYLENE/CO_2/H_2
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作者 郑继 方月娥 +1 位作者 史天义 井上祥平 《Chinese Journal of Polymer Science》 SCIE CAS CSCD 1989年第3期202-206,共5页
A study has been made on the plasma polymerization of acetylene/CO_2/H_2 in a capacitively coupled RF plasma. The monomer mixture yielded a crosslinked film with light brown color. A kinetic study is reported for the ... A study has been made on the plasma polymerization of acetylene/CO_2/H_2 in a capacitively coupled RF plasma. The monomer mixture yielded a crosslinked film with light brown color. A kinetic study is reported for the plasma polymer ization of acetylene/CO_2/H_2. The effects of discharge power level and reactor geometry on the rate of polymer formation are reported. The structure of the plasma polymer is investigated by IR study. 展开更多
关键词 Plasma polymerization acetylene/CO_2/H_2 KINETICS IR
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Solid-Phase Stereoselective Synthesis of (E)-1, 2-Disubstituted Ethenes from Polymer-Sopported a-Selenoaldehydes
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作者 ShouRiSHENG LuLingWU XianHUANG 《Chinese Chemical Letters》 SCIE CAS CSCD 2003年第10期991-992,共2页
Reaction of polymer-supported a-selenoaldehydes with Grignard reagents afforded polymer-bound B-hydroxyalkyl selenides, which treated with thionyl chloride and triethylamine leading to (E)-1, 2-disubstituted ethenes i... Reaction of polymer-supported a-selenoaldehydes with Grignard reagents afforded polymer-bound B-hydroxyalkyl selenides, which treated with thionyl chloride and triethylamine leading to (E)-1, 2-disubstituted ethenes in good yield. 展开更多
关键词 Solid phase organic synthesis a-selenoaldehyde (E)-1 2-disubstituted ethene.
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SYNTHESIS OF 4,6-DISUBSTITUTED 5-THIOXO-1,2,4-TRIAZIN-3-ONE FROM BENZOTHIOFORMANILIDE
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作者 Zhong E LU Tian Lin XU Xiao Dong SHI Department of Chemistry,Suzhou University,Suzhou,215006 《Chinese Chemical Letters》 SCIE CAS CSCD 1991年第7期525-526,共2页
A method of synthesis of 4,6-disubstituted 5-thioxo-1,2,4-triazin- 3-ones from benzothioformanilides and semicarbazide is described.And six new compounds were synthesized by this method.
关键词 SYNTHESIS OF 4 6-disubstituted 5-THIOXO-1 2 4-TRIAZIN-3-ONE FROM BENZOTHIOFORMANILIDE
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Synthesis and Antibacterial Activities of 1,4-Disubstituted Phenyl-5-(halo-2-hydroxyphenyl)imino-1,2,3-triazole
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作者 ZHAO Xu LU Jun-rui +6 位作者 XIN Chun-wei LU Bo-wei BAO Xiu-rong LI Jian-fa LIU Ya YANG Xu-yun YUAN Yi 《Chemical Research in Chinese Universities》 SCIE CAS CSCD 2012年第3期424-429,共6页
According to the superposition principle of reinforcement of biological activities, 24 novel 1,4- disubstituted phenyl-5-(halo-2-hydroxyphenyl)imino-l,2,3-triazoles was synthesized and characterized by 1H NMR, ^13C ... According to the superposition principle of reinforcement of biological activities, 24 novel 1,4- disubstituted phenyl-5-(halo-2-hydroxyphenyl)imino-l,2,3-triazoles was synthesized and characterized by 1H NMR, ^13C NMR, elemental analysis and IR. All the target compounds were screened for their antibacterial potential in vitro against Monilia albican, Escherichia coli and Staphylococcus aureus. It was shown that all the compounds possessed efficient antibacterial activities at a concentration of 0.1 mg/mL, even at a concentration of 0.01 mg/mL, some of the compounds still exhibited antibacterial activities against Escherichia coli and Monilia albican. At last, the struc- ture-activity relationship was discussed based on the antibacterial results. 展开更多
关键词 1 4-disubstituted phenyl-5-(halo-2-hydroxyphenyl)imino-l 2 3-triazole Antibacterial activity Structure-activity relationship
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Bifunctional two-carbon reagent made from acetylene via 1,2-difunctionalization and its applications
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作者 Bo Yang Kangkui Li +1 位作者 Yongdong Wang Shifa Zhu 《Science China Chemistry》 SCIE EI CAS CSCD 2024年第3期936-944,共9页
There are very limited approaches to directly gluing two molecules for the production of internal alkenes using the vastly abundant acetylene via 1,2-difunctionalization. Conversion of gaseous acetylene to internal al... There are very limited approaches to directly gluing two molecules for the production of internal alkenes using the vastly abundant acetylene via 1,2-difunctionalization. Conversion of gaseous acetylene to internal alkenes via 1,2-difunctionalization in a desired manner is not as easy as it might be expected due to the potential competition reactions between acetylene and alkene produced and the difficulty in handling this harmful reagent and controlling the regio-and stereoselectivity. In this work, we designed an efficient catalytic system for the incorporation of acetylene gas into tremendous(E)-β-bromo vinylsulfones, which are bench-stable, easy to operate, and can function as bifunctional acetylene and show a rich reactivity profile in Sonogashira coupling, Heck coupling, substituted reaction, and various desulfonylation transformations, providing numerous internal alkenes. 展开更多
关键词 acetylene 1 2-difunctionalization PHOTOCATALYSIS vinylsulfone
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The ligand coordination approach for improving the stability of low-mercury catalyst in the hydrochlorination of acetylene 被引量:1
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作者 Xiaolong Xu Haihua He +3 位作者 Jia Zhao Bailin Wang Shanchuan Gu Xiaonian Li 《Chinese Journal of Chemical Engineering》 SCIE EI CAS CSCD 2017年第9期1217-1221,共5页
Mercuric chloride supported on activated carbon(HgCl_2/AC) is used as an industrial catalyst for the hydrochlorination of acetylene. Loss of HgCl_2 by sublimating from the surface of activated carbon causes the irreve... Mercuric chloride supported on activated carbon(HgCl_2/AC) is used as an industrial catalyst for the hydrochlorination of acetylene. Loss of HgCl_2 by sublimating from the surface of activated carbon causes the irreversible deactivation of mercury catalyst and environmental pollution. In this work, a ligand coordination approach based on the Principle of Hard and Soft Acids and Bases(HSAB) was employed to design more stable lowmercury catalyst. The low-mercury catalysts(4% HgCl_2 loading) were prepared by using HgCl_2 and potassium halides(KX, X = Cl, I) as precursors. The HgCl_2-4KI/AC catalyst showed best catalytic stability than HgCl_2/AC and HgCl_2-4KCl/AC in the hydrochloriantion of acetylene. HgCl_2 could form more stable complex with KI,K_2HgI_4 as the main active component of the HgCl_2-4KI/AC catalyst. The characterizations of XRD and EDX analysis illustrated that the active component of HgCl_2-4KI/AC was highly dispersed on the surface of activated carbon.The sublimation rates of HgCl_2 from the catalysts verified that the active component with larger stability constant had better thermal stability. Using Hg(Ⅱ) complexes with high stability constant as the active component may be the research direction of developing highly stable low-mercury catalyst for the hydrochlorination of acetylene. 展开更多
关键词 Low-mercury catalyst SUBLIMATION K2HgI4 Ligand coordination acetylene hydrochlorination
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Robot系统测定旱地N_(2)排放的方法优化及其与其他方法的对比研究 被引量:1
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作者 李承霖 魏志军 +2 位作者 吴敏 单军 颜晓元 《土壤学报》 CAS CSCD 北大核心 2023年第3期694-704,共11页
反硝化是生态系统氮循环的最后一环同时也是活性氮转化为惰性氮(N2)的最主要过程。由于空气中背景N2浓度高达78%,在如此高的背景浓度N2环境中直接和准确测定反硝化过程产生的微量N2,一直是个巨大的挑战。Robot系统(Robotized incubation... 反硝化是生态系统氮循环的最后一环同时也是活性氮转化为惰性氮(N2)的最主要过程。由于空气中背景N2浓度高达78%,在如此高的背景浓度N2环境中直接和准确测定反硝化过程产生的微量N2,一直是个巨大的挑战。Robot系统(Robotized incubation and analyzing system)是基于无N2背景(氦环境)的用以研究纯菌或土壤体系N2排放速率的方法,该系统平台搭建简单且测定效率高,目前应用比较广泛。但该系统在运行过程中需要频繁利用微量注射器进行取样和测定,极易造成外界N2的渗漏。为解决这一问题,通过使用预先置于氦环境的橡胶隔垫、采用充氦后的蒸馏水配制溶液及实施破坏性取样的处理,对Robot系统测定旱地N2排放速率的方法进行优化,同时与乙炔抑制法和RoFlow系统(Robotized continuous flow incubation system)的测定结果进行对比。研究结果表明,通过方法优化,可以大幅降低Robot系统的N2渗漏率,方法优化后系统的渗漏率在0~0.78μL·L^(–1)·h^(–1)之间。优化后的Robot系统对碳源和氮源添加后N2排放速率差异的响应较好,并且对旱地土壤N2排放速率的测定误差最小(0.003~0.045 mg·kg^(–1)·d^(–1)),显著优于乙炔抑制法(0.34~3.29 mg·kg^(–1)·d^(–1))和RoFlow系统(0.41~1.02 mg·kg^(–1)·d^(–1))。综上,优化后的Robot系统在测定旱地N2排放速率时具有N2渗漏率低,对外源底物添加响应好及测定结果精确度高的特点,未来在研究旱地土壤背景N2排放及相关机理方面有较好的应用前景。 展开更多
关键词 N_(2)排放 乙炔抑制法 Robot系统(Robotized incubation and analyzing system) RoFlow系统(Robotized continuous flow incubation system)
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Al_(2)O_(3)负载Cu基催化剂的制备及其催化乙炔选择性加氢性能
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作者 汝绪阳 曾傲楠 +4 位作者 王瑶 刘颖雅 孙志超 遇治权 王安杰 《化学反应工程与工艺》 CAS 2023年第1期11-19,共9页
采用等体积浸渍法合成了Cu(OH)_(2)/Al_(2)O_(3)前体,经乙炔处理、氢气还原制备了Al_(2)O_(3)负载的Cu基催化剂。采用X射线衍射(XRD)、透射电镜(TEM)和N2物理吸附对催化剂前体以及催化剂进行了表征,并在固定床反应器中系统考察了氢氧化... 采用等体积浸渍法合成了Cu(OH)_(2)/Al_(2)O_(3)前体,经乙炔处理、氢气还原制备了Al_(2)O_(3)负载的Cu基催化剂。采用X射线衍射(XRD)、透射电镜(TEM)和N2物理吸附对催化剂前体以及催化剂进行了表征,并在固定床反应器中系统考察了氢氧化铜负载量、乙炔处理温度、乙炔处理时间以及氢气还原温度对所制备催化剂催化乙炔选择性加氢性能的影响。研究结果表明:当Cu(OH)_(2)负载量为30%(质量分数),乙炔处理温度为140℃,乙炔处理时间为2 h,氢气还原温度为150℃时,催化剂具有较高的低温乙炔选择性加氢活性。当反应温度为115℃时,乙炔转化率为98.50%,乙烯的选择性为66.15%,乙烷的选择性为15.75%,C_(4)的选择性为18.10%。 展开更多
关键词 氢氧化铜 乙炔 Al_(2)O_(3) 载体 选择性加氢
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Fe_(2)O_(3)/C锂离子电池负极材料的制备及电化学性能研究 被引量:2
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作者 刘科 钟志成 《功能材料》 CAS CSCD 北大核心 2023年第10期10175-10179,10230,共6页
以纳米Fe_(2)O_(3)和乙炔炭黑为原料,通过加入不同质量分数(25%,35%,45%,55%)的乙炔炭黑制备出了Fe_(2)O_(3)/C负极材料,研究了乙炔炭黑占比对Fe_(2)O_(3)/C负极材料的晶体结构、微观形貌及电化学性能的影响。结果表明,Fe_(2)O_(3)/C负... 以纳米Fe_(2)O_(3)和乙炔炭黑为原料,通过加入不同质量分数(25%,35%,45%,55%)的乙炔炭黑制备出了Fe_(2)O_(3)/C负极材料,研究了乙炔炭黑占比对Fe_(2)O_(3)/C负极材料的晶体结构、微观形貌及电化学性能的影响。结果表明,Fe_(2)O_(3)/C负极材料具有较高的结晶度,属于六方晶系结构,呈现出微球状颗粒,掺入适量的乙炔炭黑后改善了Fe_(2)O_(3)颗粒分布的均匀性,Fe_(2)O_(3)纳米颗粒被乙炔炭黑连接起来,形成了致密均匀的网格结构。以Fe_(2)O_(3)/C为负极材料制备了CR2025型纽扣电池,随着乙炔炭黑掺杂量的增大,Fe_(2)O_(3)/C负极材料的首次放电容量表现出先增大后降低的趋势,当乙炔炭黑的掺杂量为45%(质量分数)时,Fe_(2)O_(3)/C负极材料的首次放电容量达到最大值483.6 mAh/g。随着循环次数的增加,电池放电比容量衰减逐渐增大,放电过程中电压在0.15 V附近出现了较宽的放电平台,在达到30次充放电循环时,当乙炔炭黑的掺杂量为45%(质量分数)时,Fe_(2)O_(3)/C负极材料的放电比容量降低至115.6 mAh/g,保持率最高为23.91%,经过0.5,1.0,2.0和3.0 C的电流密度放电后,再将电流密度给定到0.5 C时,电池的放电容量变化较小,具有优异的倍率性能。 展开更多
关键词 Fe_(2)O_(3)/C 锂离子电池 负极材料 乙炔炭黑 电化学性能
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乙炔抑制法对农田土壤反硝化潜势不确定性的量化
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作者 曹文超 王娅静 +6 位作者 李艳青 潘好芹 赵飞 肖万里 王翠翠 王敬国 宋贺 《中国环境科学》 EI CAS CSCD 北大核心 2024年第10期5733-5742,共10页
通过利用Robot培养系统进行厌氧泥浆培养试验,旨在明确乙炔抑制法在定量设施菜田与粮田土壤实际的反硝化潜势时是否均存在低估现象.以寿光地区设施菜田土壤与相邻粮田土壤为研究对象,分别设置了添加10%乙炔和未添加10%乙炔处理.结果表明... 通过利用Robot培养系统进行厌氧泥浆培养试验,旨在明确乙炔抑制法在定量设施菜田与粮田土壤实际的反硝化潜势时是否均存在低估现象.以寿光地区设施菜田土壤与相邻粮田土壤为研究对象,分别设置了添加10%乙炔和未添加10%乙炔处理.结果表明,厌氧泥浆培养3h后,设施菜田与粮田土壤在10%乙炔处理中的N_(2)O累积浓度均显著高于未添加乙炔处理,而N_(2)累积浓度呈现相反趋势;在10%乙炔下,设施菜田和粮田土壤在厌氧培养63h内分别有7.92%和34.2%的N_(2)O被还原为N_(2);添加10%乙炔设施菜田与粮田土壤实际的反硝化潜势均显著增加,但并未显著影响土壤的呼吸作用;由乙炔抑制法对土壤实际的反硝化潜势计算的偏差(AIT-bias)来看,乙炔抑制法高估设施菜田土壤实际的反硝化潜势比例为22.0%,而对粮田土壤低估了11.4%.综合来看,在设施菜田与粮田土壤中,乙炔抑制法均未完全抑制N_(2)O还原为N_(2);乙炔抑制法对土壤实际反硝化潜势的不确定性受种植系统的深刻影响,这可能与不同种植系统下土壤养分、土壤类型等因素存在差异有关,需要进一步评估该方法在不同土壤条件下的准确性. 展开更多
关键词 乙炔抑制法 反硝化潜势 氮气(N_(2)) 氧化亚氮(N_(2)O) N_(2)/(N_(2)O+N_(2)) 自动采样与分析系统
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2-硅萘与乙炔和苯乙炔杂Diels-Alder反应的理论研究 被引量:5
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作者 曾小兰 王岩 +2 位作者 翟秋阁 朱建君 裴强 《信阳师范学院学报(自然科学版)》 CAS 2010年第1期63-67,共5页
采用密度泛函理论(DFT)方法在B3LYP/6-311G(d,p)水平上研究了2-硅萘与乙炔和苯乙炔的杂Diels-Alder反应的微观机理和势能剖面,考察了反应的取代基效应和溶剂效应,并与硅苯参与的类似反应进行了比较.计算结果表明,所研究反应均以协同非... 采用密度泛函理论(DFT)方法在B3LYP/6-311G(d,p)水平上研究了2-硅萘与乙炔和苯乙炔的杂Diels-Alder反应的微观机理和势能剖面,考察了反应的取代基效应和溶剂效应,并与硅苯参与的类似反应进行了比较.计算结果表明,所研究反应均以协同非同步的方式进行.乙炔分子中碳原子上的苯基取代基对反应活化能垒的影响与产物中苯基所处的位置有关.2-硅萘分子中硅原子上的C(CH3)3或NH2取代基对反应势能剖面的影响一般都比较小,而其上的CCl3取代基对反应势能剖面的影响则比较复杂.苯溶剂对所研究反应的势能剖面影响不大.2-硅萘参与的杂Diels-Alder反应在热力学和动力学上均不如涉及硅苯的相应反应容易进行. 展开更多
关键词 2-硅萘 乙炔 苯乙炔 杂Diels-Alder反应 密度泛函理论
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2-甲基吡啶的合成工艺 被引量:3
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作者 邹华生 潘学敏 林岗 《华南理工大学学报(自然科学版)》 EI CAS CSCD 北大核心 2008年第11期34-37,44,共5页
探讨了以乙炔和乙腈为原料制备高纯度2-甲基吡啶的合成工艺,通过实验确定了适宜的反应条件.结果表明,乙炔压力为1.1MPa、乙炔耗用量为7.332 g、反应温度为180℃、有机钴类催化剂用量为200mg、反应时间为12 h时,2-甲基吡啶收率可达50.88%... 探讨了以乙炔和乙腈为原料制备高纯度2-甲基吡啶的合成工艺,通过实验确定了适宜的反应条件.结果表明,乙炔压力为1.1MPa、乙炔耗用量为7.332 g、反应温度为180℃、有机钴类催化剂用量为200mg、反应时间为12 h时,2-甲基吡啶收率可达50.88%.反应生成的混合溶液经过滤、间歇精馏制得含量大于98%的2-甲基吡啶产品.该工艺操作简单,收率较高,具有潜在的工业应用价值. 展开更多
关键词 乙炔 乙腈 2-甲基吡啶 催化 合成
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[Co(NH_3)_6]^(2+)催化乙炔氧化缩聚合成β型线型碳 被引量:1
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作者 张振 王茹 《化学研究与应用》 CAS CSCD 北大核心 2011年第6期767-770,共4页
在T=35℃的条件下,以盐酸为酸化剂、[Co(NH3)6]2+为催化剂,催化乙炔氧化缩聚合成了β型线型碳。通过红外光谱、拉曼光谱和X-衍射对产物进行了结构表征。pH=6,六水氯化钴(Ⅱ)用量为0.4g时,β型线型碳的产率为61.18%,其中Co(II)的含量为1.... 在T=35℃的条件下,以盐酸为酸化剂、[Co(NH3)6]2+为催化剂,催化乙炔氧化缩聚合成了β型线型碳。通过红外光谱、拉曼光谱和X-衍射对产物进行了结构表征。pH=6,六水氯化钴(Ⅱ)用量为0.4g时,β型线型碳的产率为61.18%,其中Co(II)的含量为1.72%。TG和DTA分析结果表明:在227.4℃时,β型线型碳向α型线型碳转化,而在370℃~420℃时,β型线型碳实现了向金刚石的转化。 展开更多
关键词 β型线型碳 [Co(NH3)6]2+ 催化 乙炔 缩聚
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