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微波碳热还原法制备Li_3V_2(PO_4)_3及其性能研究 被引量:13
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作者 应皆荣 姜长印 +3 位作者 唐昌平 高剑 李维 万春荣 《稀有金属材料与工程》 SCIE EI CAS CSCD 北大核心 2006年第11期1792-1796,共5页
将一定配比的LiOH·H2O,V2O5,H3PO4和蔗糖(C12H22O11)通过球磨均匀混合,烘干后埋入石墨粉中,在功率为800W的家用微波炉中高火加热15min,通过碳热还原合成Li3V2(PO4)3。用X射线衍射和扫描电镜对材料的结构和形貌进行了表征。充放电... 将一定配比的LiOH·H2O,V2O5,H3PO4和蔗糖(C12H22O11)通过球磨均匀混合,烘干后埋入石墨粉中,在功率为800W的家用微波炉中高火加热15min,通过碳热还原合成Li3V2(PO4)3。用X射线衍射和扫描电镜对材料的结构和形貌进行了表征。充放电测试表明,在电压范围为3V^4.3V和3V^4.8V时,Li3V2(PO4)3正极材料具有较高的比容量、优良的循环性能和倍率特性。在电压范围为1.5V^4.8V时,Li3V2(PO4)3正极材料具有很高的比容量,但循环性能较差。该材料有望用于锂离子电池部分取代昂贵的LiCoO2,也可望应用于动力型和储能型锂离子电池。 展开更多
关键词 锂离子电池 正极材料 LI3V2(PO4)3 微波碳热还原
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微波碳热还原法合成锂离子电池正极材料Li_2FeSiO_4/C 被引量:8
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作者 曹雁冰 胡国荣 +2 位作者 彭忠东 杜柯 刘艳 《功能材料》 EI CAS CSCD 北大核心 2010年第6期990-993,共4页
以Li2CO3、FeOOH、纳米Si O2为原料,聚乙烯醇和超导碳为碳源,采用微波碳热合成法合成了Li2FeSi O4/C材料。通过XRD、SEM和恒流充放电测试,对样品结构、形貌和电化学性能进行了表征和分析。结果表明,微波合成法可以快速制备具有正交结构... 以Li2CO3、FeOOH、纳米Si O2为原料,聚乙烯醇和超导碳为碳源,采用微波碳热合成法合成了Li2FeSi O4/C材料。通过XRD、SEM和恒流充放电测试,对样品结构、形貌和电化学性能进行了表征和分析。结果表明,微波合成法可以快速制备具有正交结构的Li2FeSi O4材料;在处理温度650℃、时间12min的条件下获得了高纯度、晶粒细小均匀的产物,并具有良好的电化学性能。以C/20倍率进行充放电测试,首次放电容量为127.5mAh/g,20次循环后容量仍有124mAh/g。 展开更多
关键词 锂离子电池 正极材料 LI2FESIO4 微波碳热还原
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微波碳热还原法制备氮化铝粉末的工艺研究 被引量:10
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作者 肖劲 周峰 陈燕彬 《无机材料学报》 SCIE EI CAS CSCD 北大核心 2009年第4期755-758,共4页
采用微波碳热还原法制备了氮化铝粉末,研究了铝源、碳源和添加剂对制备氮化铝粉末的影响.通过对所合成的产物进行XRD检测分析表明,氢氧化铝和乙炔黑是最合适的铝源和碳源、单质添加剂的氮化催化效果最明显.以氢氧化铝和乙炔黑为原料,加... 采用微波碳热还原法制备了氮化铝粉末,研究了铝源、碳源和添加剂对制备氮化铝粉末的影响.通过对所合成的产物进行XRD检测分析表明,氢氧化铝和乙炔黑是最合适的铝源和碳源、单质添加剂的氮化催化效果最明显.以氢氧化铝和乙炔黑为原料,加入单质添加剂,在氮气气氛下反应温度为1300℃、反应时间为1h时能获得完全氮化的氮化铝粉末,可见微波碳热还原工艺能够大大降低碳热还原法制备氮化铝粉末的反应温度,并缩短反应时间. 展开更多
关键词 微波碳热还原 添加剂 氮化铝粉末
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溶胶-凝胶和微波碳热还原氮化法合成β-sialon超细粉 被引量:7
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作者 付芳 贾晓林 张海军 《硅酸盐学报》 EI CAS CSCD 北大核心 2007年第3期317-321,共5页
以正硅酸乙酯(tetraethoxysilane,TEOS),硝酸铝,蔗糖等为原料,通过溶胶-凝胶和微波碳热还原氮化法合成了β-sialon超细粉。研究了铝碳摩尔比、温度、埋粉条件、晶种、添加剂等工艺条件对合成β-sialon超细粉的影响。结果表明:铝碳摩尔... 以正硅酸乙酯(tetraethoxysilane,TEOS),硝酸铝,蔗糖等为原料,通过溶胶-凝胶和微波碳热还原氮化法合成了β-sialon超细粉。研究了铝碳摩尔比、温度、埋粉条件、晶种、添加剂等工艺条件对合成β-sialon超细粉的影响。结果表明:铝碳摩尔比显著影响β-sialon超细粉的合成,过量碳有利于形成β-sialon超细粉。1573~1623K为最佳合成温度。埋粉不利于β-sialon超细粉的合成。晶种对β-sialon超细粉的合成没有显著影响,添加剂Fe2O3对反应有明显促进作用。用场发射扫描式电子显微镜观察产物的显微形貌,结果表明:合成β-sialon超细粉的粒度大约为100nm。 展开更多
关键词 Β-SIALON 微波碳热还原氮化 溶胶-凝胶 超细粉
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鲕状赤铁矿微波碳热还原-磁选提铁脱磷实验研究 被引量:9
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作者 何文浩 陈雯 +2 位作者 王鑫 雷鹰 李雨 《矿冶工程》 CAS CSCD 北大核心 2019年第5期92-94,99,共4页
采用微波碳热还原 磁选工艺对鲕状赤铁矿提铁脱磷进行了研究,考察了还原温度、碱度、添加剂用量和原矿粒度等因素对提铁脱磷效果的影响。结果表明,最佳还原条件为:还原温度1150℃、碱度0.8、配碳量1.0、钠盐添加剂用量15%、原矿粒度0.15... 采用微波碳热还原 磁选工艺对鲕状赤铁矿提铁脱磷进行了研究,考察了还原温度、碱度、添加剂用量和原矿粒度等因素对提铁脱磷效果的影响。结果表明,最佳还原条件为:还原温度1150℃、碱度0.8、配碳量1.0、钠盐添加剂用量15%、原矿粒度0.15 mm;将还原所得球团磨至-0.15 mm,在65 mT磁场强度下磁选,可得到全铁含量87.98%、铁回收率95.48%、脱磷率69.42%的指标。 展开更多
关键词 鲕状赤铁矿 微波碳热还原 磁选 铁品位 脱磷率
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锆英石微波碳热还原合成ZrC-SiC复合粉体 被引量:3
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作者 刘江昊 杜爽 +4 位作者 邓先功 李发亮 段红娟 张海军 张少伟 《稀有金属材料与工程》 SCIE EI CAS CSCD 北大核心 2015年第S1期217-221,共5页
以锆英石和活性炭为原料,采用微波碳热还原法制备了Zr C-Si C复合粉体,对其合成过程进行了热力学分析,并研究了反应温度、添加剂的用量和埋粉等工艺条件对合成的Zr C-Si C复合粉体的物相组成和显微结构的影响。结果表明,提高反应温度和... 以锆英石和活性炭为原料,采用微波碳热还原法制备了Zr C-Si C复合粉体,对其合成过程进行了热力学分析,并研究了反应温度、添加剂的用量和埋粉等工艺条件对合成的Zr C-Si C复合粉体的物相组成和显微结构的影响。结果表明,提高反应温度和在反应物中添加B2O3有助于促进Zr C-Si C复合粉体的合成,而将反应物埋入Si C粉对该复合粉体的合成则有抑制作用。与常规加热相比,微波加热法可以有效地降低碳热还原反应的起始温度,并且减少制备过程的时间和能耗。 展开更多
关键词 锆英石 微波碳热还原 化锆 化硅 复合粉体
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微波助溶胶-凝胶碳热还原合成SiC超细粉 被引量:5
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作者 付芳 贾晓林 张海军 《稀有金属材料与工程》 SCIE EI CAS CSCD 北大核心 2008年第A01期153-155,共3页
以正硅酸乙酯(TEOS)、蔗糖、无水乙醇等为原料,通过溶胶-凝胶、微波碳热还原的方法合成SiC超细粉。研究了合成SiC超细粉的工艺条件。使用FE-SEM和XRD对合成的超细粉进行了表征。结果表明:硅碳摩尔比对SiC的合成有一定影响。1573 K可以... 以正硅酸乙酯(TEOS)、蔗糖、无水乙醇等为原料,通过溶胶-凝胶、微波碳热还原的方法合成SiC超细粉。研究了合成SiC超细粉的工艺条件。使用FE-SEM和XRD对合成的超细粉进行了表征。结果表明:硅碳摩尔比对SiC的合成有一定影响。1573 K可以合成高纯SiC超细粉。适当延长合成时间有利于SiC超细粉的合成。FE-SEM和比表面积的结果表明,合成SiC超细粉的粒度在100 nm以下。 展开更多
关键词 化硅 超细粉 微波碳热还原
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钛铁矿的还原技术研究现状 被引量:7
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作者 唐昭辉 彭金辉 +3 位作者 张世敏 郭胜惠 张利波 李静 《钛工业进展》 CAS 2010年第2期9-12,共4页
在简要分析当前钛铁矿还原富集技术中存在的问题的基础上,阐述了钛铁矿的非碳热还原及常规碳热还原技术的国内外研究现状。结合微波加热的特点,重点阐述了钛铁矿的微波碳热还原的国内外研究现状。指出,微波加热应用于钛铁矿的碳热还原,... 在简要分析当前钛铁矿还原富集技术中存在的问题的基础上,阐述了钛铁矿的非碳热还原及常规碳热还原技术的国内外研究现状。结合微波加热的特点,重点阐述了钛铁矿的微波碳热还原的国内外研究现状。指出,微波加热应用于钛铁矿的碳热还原,能明显提高炭的还原能力,提高还原速率,缩短反应时间,大幅度降低能耗,显示出良好的经济价值和潜在的工业化前景,同时也指出了钛铁矿微波碳热还原技术中需要解决的问题。 展开更多
关键词 钛铁矿 还原 微波碳热还原
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Thermodynamics and kinetics of carbothermal reduction of zinc ferrite by microwave heating 被引量:2
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作者 王欣 杨大锦 +2 位作者 巨少华 彭金辉 段昕辉 《Transactions of Nonferrous Metals Society of China》 SCIE EI CAS CSCD 2013年第12期3808-3815,共8页
The kinetics of carbon reduction of ZnFe2O4 in the temperature range of 550-950 °C was investigated in a microwave tank-type reactor. The mechanism of formation of ZnO and Fe3O4/FeO by the decomposition of ZnFe2O... The kinetics of carbon reduction of ZnFe2O4 in the temperature range of 550-950 °C was investigated in a microwave tank-type reactor. The mechanism of formation of ZnO and Fe3O4/FeO by the decomposition of ZnFe2O4 was detailed using the equilibrium calculations and thermodynamics analysis by HSC chemistry software 6.0. In addition, the effects of decomposition temperature, the C/ZnFe2O4 ratio, the particle size and the microwave power were assessed on the kinetics of decomposition. Zn recovery as high as 97.93%could be achieved at a decomposition temperature of 750 °C with C/ZnFe2O4 ratio of 1:3, particle size of 61-74 μm and microwave power of 1200 W. The kinetics of decomposition was tested with different kinetic models and carbon gasification control mechanism was identified to be the appropriate mechanism. The activation energy for the carbon gasification reaction was estimated to be 38.21 kJ/mol. 展开更多
关键词 zinc ferrite activation energy MICROWAVE carbothermal reduction
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Synthesis of (Ca, Mg)-α′-Sialon-AlN-BN powders from boron-rich blast furnace slag by microwave carbothermal reduction-nitridation 被引量:4
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作者 姜涛 薛向欣 《Transactions of Nonferrous Metals Society of China》 SCIE EI CAS CSCD 2012年第12期2984-2990,共7页
(Ca, Mg)-α′-Sialon-AlN-BN powders were synthesized by the carbothermal reduction and nitridation (CRN) method using boron-rich slag, one of the intermediate products from pyrometallurgy separation of pageit, as the ... (Ca, Mg)-α′-Sialon-AlN-BN powders were synthesized by the carbothermal reduction and nitridation (CRN) method using boron-rich slag, one of the intermediate products from pyrometallurgy separation of pageit, as the staring material. The influences of synthesis temperature and holding time on the phase composition and microstructure during the microwave CRN were studied by XRD, SEM and EDS. The comparison between two heating techniques, conventional and microwave heating, on the synthesized powder was presented as well. The experimental results revealed that the phase compositions and microstructures of the synthesized products were greatly affected by the synthesis temperature and holding time. With an increase in the synthesis temperature or holding time, the relative amount of α′-Sialon increased and α′-Sialon became the main crystalline phase at 1400 °C for 6 h. The synthesized products also contained AlN, BN and a small amount of β-SiC. Elongated α′-Sialon grains, short rod AlN grains, aggregate nanoscale BN grains were observed in the synthesized powders. The reaction temperature of microwave heating method was reduced by 80 °C, the reaction time was shortened by 2 h, and more elongated α′-Sialon grains with large aspect ratio were observed. 展开更多
关键词 boron-rich blast furnace slag carbothermal reduction-nitridation MICROWAVE (Ca Mg)-α′-Sialon-AlN-BN POWDERS
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Direct carbothermic reduction of ilmenite concentrates by adding high dosage of Na_(2)CO_(3) in microwave field 被引量:6
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作者 Zhi-gang YU Jing-wu XIAO +1 位作者 Hai-yan LENG Kuo-chih CHOU 《Transactions of Nonferrous Metals Society of China》 SCIE EI CAS CSCD 2021年第6期1818-1827,共10页
A clean and efficient route for the utilization of ilmenite concentrates was proposed by direct carbothermic reduction in microwave field.High dosage of Na_(2)CO_(3),which can be recycled,was added to accelerate the r... A clean and efficient route for the utilization of ilmenite concentrates was proposed by direct carbothermic reduction in microwave field.High dosage of Na_(2)CO_(3),which can be recycled,was added to accelerate the reduction reaction of ilmenite concentrates.After microwave heating in the temperature range of 1073−1123 K for 20 min,the main products were Na_(2)TiO_(3) and metallic Fe with the metallization ratios being as high as 92.67%−93.21%.The reduction products were processed by water leaching,ball-milling in CO2 atmosphere and magnetic separation in turn.The final products after magnetic separation were Fe-rich materials and Ti-rich materials(90.04 wt.%TiO2),which can be used to produce iron and TiCl4 or TiO2.The optimized heating temperature was 1123 K in terms of metallization ratios,magnetic separation and caking property of the reduction products.Besides,the reduction mechanism of ilmenite concentrates with the addition of Na_(2)CO_(3) in microwave field was also proposed. 展开更多
关键词 ilmenite concentrates MICROWAVE Na_(2)CO_(3) carbothermic reduction
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Direct reduction of carburized pre-reduced pellets by microwave heating 被引量:2
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作者 胡兵 黄柱成 +1 位作者 易凌云 姜涛 《Journal of Central South University》 SCIE EI CAS 2014年第1期351-357,共7页
A new iron-making process using carburized pre-reduced iron ore pellets and microwave heating is investigated. The pre-reduced pellets, with a porous structure, and fine particles are carburized homogeneously at 400-6... A new iron-making process using carburized pre-reduced iron ore pellets and microwave heating is investigated. The pre-reduced pellets, with a porous structure, and fine particles are carburized homogeneously at 400-650 ℃ in a CO atmosphere. The carburized carbon not only acts reaction as a reduction agent, but also absorbs microwave in the reduction process. Hence, the carburized pre-reduced pellets can be rapidly reduced by microwave heating. There are three procedures involved in the process, namely, gas-based pre-reduction, low-temperatttre carburization and deep reduction by microwave heating. Carburized pre-reduced iron ore pellets show a rapid temperature rise that is twice as fast as the results for pre-reduced pellets in the laboratory. This not only improves the efficiency of the microwave heating, but also accelerates the reduction of iron oxides. The temperature of the pre-reduced pellets rises to 1050 ℃ in 45 min when the carburization rate is 2.02%, and the metallization rate and compressive strength reach 94.24% and 1725 N/pellet, respectively. 展开更多
关键词 oxidized pellets PRE-REDUCTION CARBURIZING microwave heating direct reduction
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