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生物油加氢精制工艺研究进展
引用本文:李雁斌,徐莹,马隆龙,陈冠益,王铁军,张琦.生物油加氢精制工艺研究进展[J].农业工程学报,2014,30(9):183-191.
作者姓名:李雁斌  徐莹  马隆龙  陈冠益  王铁军  张琦
作者单位:1. 中国科学院广州能源研究所,广州 5106402. 天津大学环境学院生物质能研究中心/内燃机燃烧学国家重点实验室,天津 300072;1. 中国科学院广州能源研究所,广州 5106403. 中国科学院广州能源研究所可再生能源重点实验室,广州 510640;1. 中国科学院广州能源研究所,广州 5106402. 天津大学环境学院生物质能研究中心/内燃机燃烧学国家重点实验室,天津 3000723. 中国科学院广州能源研究所可再生能源重点实验室,广州 510640;2. 天津大学环境学院生物质能研究中心/内燃机燃烧学国家重点实验室,天津 300072;1. 中国科学院广州能源研究所,广州 5106403. 中国科学院广州能源研究所可再生能源重点实验室,广州 510640;1. 中国科学院广州能源研究所,广州 5106403. 中国科学院广州能源研究所可再生能源重点实验室,广州 510640
基金项目:国家自然科学基金资助项目(51036006&51106108),所长基金(y307r91001)。
摘    要:该文针对近年来生物油加氢精制方面的研究进行了探讨,介绍了加氢精制原理,总结了国内外生物油加氢精制工艺研究取得的进展,包括催化剂性能,反应机理和工艺路线的创新与研究。详细说明了分段加氢、加氢酯化、原位加氢等工艺流程的创新和缺点;传统加氢催化剂:如NiMo、CoMo催化剂,以及Ru、Pt、Pd、Rh等贵金属催化剂,在加氢工艺中的特点,前者价格便宜但效果较差,失活现象更严重;后者具有更强的反应活性,但价格昂贵且须在反应后回收。同时,该文对模型化合物、生物油部分相以及生物油真实体系的加氢试验分别进行了详述。最后,针对目前研究中遇到的无法长时间连续运行,成本过高工艺复杂以及缺乏合适催化剂等问题,预测了该技术未来加强催化剂抗结焦能力和低温活性,简化工艺流程并降低成本的研究方向。

关 键 词:生物质  燃料  催化剂  生物油  加氢  原位加氢  加氢酯化  分段加氢
收稿时间:2013/11/15 0:00:00
修稿时间:1/3/2014 12:00:00 AM

Development in hydrotreating process of bio-oil
Li Yanbin,Xu Ying,Ma Longlong,Chen Guanyi,Wang Tiejun and Zhang Qi.Development in hydrotreating process of bio-oil[J].Transactions of the Chinese Society of Agricultural Engineering,2014,30(9):183-191.
Authors:Li Yanbin  Xu Ying  Ma Longlong  Chen Guanyi  Wang Tiejun and Zhang Qi
Institution:1. Guangzhou Institute of Energy Conversion, Chinese Academy of Sciences, Guangzhou 510640, China2. Faculty of Environmental Science and Engineering/State Key Lab of international Combustion Engine, Tianjin University, Tianjin 300072, China;1. Guangzhou Institute of Energy Conversion, Chinese Academy of Sciences, Guangzhou 510640, China3. Key Laboratory of Renewable Energy, Guangzhou Institute of Energy Conversion, Chinese Academy of Sciences, Guangzhou 510640, China;1. Guangzhou Institute of Energy Conversion, Chinese Academy of Sciences, Guangzhou 510640, China2. Faculty of Environmental Science and Engineering/State Key Lab of international Combustion Engine, Tianjin University, Tianjin 300072, China3. Key Laboratory of Renewable Energy, Guangzhou Institute of Energy Conversion, Chinese Academy of Sciences, Guangzhou 510640, China;2. Faculty of Environmental Science and Engineering/State Key Lab of international Combustion Engine, Tianjin University, Tianjin 300072, China;1. Guangzhou Institute of Energy Conversion, Chinese Academy of Sciences, Guangzhou 510640, China3. Key Laboratory of Renewable Energy, Guangzhou Institute of Energy Conversion, Chinese Academy of Sciences, Guangzhou 510640, China;1. Guangzhou Institute of Energy Conversion, Chinese Academy of Sciences, Guangzhou 510640, China3. Key Laboratory of Renewable Energy, Guangzhou Institute of Energy Conversion, Chinese Academy of Sciences, Guangzhou 510640, China
Abstract:Abstract: This paper reviews catalytic the hydrotreatment upgrading technology of biomass-derived oil. It provides an overview of the reaction mechanism and the condition of the operation, then summarizes the process of bio-oil hydrogenation at home and abroad. Detailed comparison of various technological processes such as multi-stage hydrogenation, hydrogenation-esterification, in-situ hydrogenation, etc. are made. Multi-stage hydrogenation, which separates the hydroprocessing into two stages (mild hydrotreating and deep hydrotreating), can improve the selectivity of products, moreover avoiding an economic penalty by using less hydrogen. Hydrogenation-esterification combines hydrogenation and esterfication to establish a new upgrading method. Through the method, unstable compounds of biomass-derived oil can be converted more effectively. In-situ hydrogenation, which leads to reducing the cost and enhancing the safety, uses other reagents as resources of hydrogen, simultaneously generating hydrogen and hydrotreating in one reaction system to replace transporting hydrogen from outside. The reasonable optimization of the process routes benefits improving product quality. Research in this area is expected to become a main research direction for bio-oil hydrotreatment.Experimental data were collected about various model compounds including cresol, phenol, guaiacol, acetone, aldehyde, etc. and bio-oil from the literature in the field of this study. Also, a test is reviewed about a range of catalysts including the conventional and novel types of supported noble metal and transition metal catalytic materials and their performance in bio-oil hydroprocessing. Conventional catalysts, such as NiMo and CoMo, have economic advantages; the reaction using noble metal catalysts have better reactivity; amorphous catalysts have both advantages of these two types of catalysts, but amorphous catalysts have terrible thermal stability, and can only be used below 473 K; then, zeolite catalysts and mesoporous catalysts exhibit magnificent effects on reducing oxygen content and moisture content in bio-oil, but still can't avoid coking in the reaction. Unfortunately, researchers have not found any catalyst's hydrothermal stability good enough to improve the effect of reaction continuously (more than seven days), Deactivation and coking of catalysts are still main problems. Obviously, further study is required to prepare these catalysts which have better durability.Finally, this article gives information about the problems which researchers may meet, including equipment plugging, catalyst deactivation, and high operation costs etc., and predicts that the future research directions of this technology is to optimize the hydrogenation process, and to develop new types of composite catalysts which exhibit excellent activity at low temperature and anti-coking performance. The technology development is still on the way but can play a significant role in supplying increasingly expensive petroleum.
Keywords:biomass  fuels  catalysts  bio-oil  hydroprocessing  in-situ hydrogenation  hydrogenation- esterification  multi-stage hydrogenation
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