中文   |   English   |   Email Alert

催化甘油脱水氧化连串反应制丙烯酸

花东龙1, 庄晓煜1, 童东绅1, 俞卫华1, 周春晖1,2*

化学进展 ›› 2016, Vol. 28 ›› Issue (2/3) :375-390

PDF (4481KB)
化学进展 ›› 2016, Vol. 28 ›› Issue (2/3) :375-390 DOI: 10.7536/PC150604
综述与评论
扫码查看或转发全文

催化甘油脱水氧化连串反应制丙烯酸

    花东龙1, 庄晓煜1, 童东绅1, 俞卫华1, 周春晖1,2*
作者信息 +

Catalytic Oxidehydration of Glycerol to Acrylic Acid

  • Hua Donglong1, Zhuang Xiaoyu1, Tong Dongshen1, Yu Weihua1, Zhou Chunhui1,2*
Author information +
文章历史 +

摘要

本文综述了近年来单反应器中甘油脱水氧化连串反应制备丙烯酸的研究进展。文中简介了甘油来源及丙烯酸的需求背景;概括了当前对单反应器中的催化体系、反应温度、接触时间、氧气分压及甘油浓度等的研究状况;重点讨论了单、双床层气固相体系中复合氧化物型催化剂和分子筛负载型催化剂的催化性能及其影响因素,涉及的催化剂有V-P、Fe-P、W-V、Mo-V、CsPW-Nb、VMo-SiC等复合氧化物和V2O5/BEA、V2O5/MFI分子筛负载型催化剂等;总结了当前研究对气固相催化反应机理和可能发生的副反应的认识;评述了催化剂的失活现象与再生问题;此外,还讨论了液固相体系中Cu/SiO2-MnO2 和POM/Al2O3催化剂的催化特点及反应机理。最后分析了单反应器中甘油脱水氧化连续反应制丙烯酸反应过程尚存的难题,从反应体系的选取、催化剂性能的改进以及催化剂积炭消除等方面展望了可能的解决途径和方向。

Abstract

This article deals with the recent research and development on catalytic oxidehydration of glycerol into acrylic acid in a single reactor. The biorenewable glycerol as a platform chemical for the production of acrylic acid is introduced. The reaction parameters such as temperature, contact time, partial pressure of oxygen and glycerol concentration in the gas-solid systems and the liquid-solid systems are examined. The catalytic performances of oxide composites and molecular sieve-supported catalysts in a single-bed system and a double-bed gas-solid system are discussed. The catalysts include V-P, Fe-P, W-V, Mo-V, CsPW-Nb, VMo-SiC oxide composites, V2O5/BEA and V2O5/MFI. The postulated reaction mechanisms and probable side reactions in the gas-solid system are presented, followed by the discussion on the issues of catalyst deactivation and regeneration. Then the catalytic characteristics of Cu/SiO2-MnO2 and POM/Al2O3 catalysts and the reaction mechanism in the liquid-solid system are remarked. The problems and the prospects in the selection of catalytic system, the improvement of catalysts and the elimination of coking of catalysts are commented.

Contents
1 Introduction
2 Gas-solid catalytic reactions
2.1 Gas-solid catalytic reactions in a single-bed reactor
2.2 Gas-solid catalytic reactions in a double-bed reactor
2.3 Mechanism of gas-solid catalytic reactions
2.4 Deactivation and regeneration of catalysts
3 Liquid-solid catalytic reactions
3.1 Reaction conditions of liquid-solid catalytic reactions
3.2 Catalysts of liquid-solid catalytic reactions
3.3 Mechanism of liquid-solid catalytic reactions
4 Conclusion

Graphical abstract

关键词

甘油 / 催化剂 / 脱水反应 / 氧化反应 / 丙烯酸 / 反应机理

Key words

glycerol / catalysts / dehydration / oxidation / acrylic acid / reaction mechanism

引用本文

引用格式 ▾
花东龙, 庄晓煜, 童东绅, 俞卫华, 周春晖. 催化甘油脱水氧化连串反应制丙烯酸[J]. 化学进展, 2016, 28(2/3): 375-390 DOI:10.7536/PC150604
Hua Donglong, Zhuang Xiaoyu, Tong Dongshen, Yu Weihua, Zhou Chunhui. Catalytic Oxidehydration of Glycerol to Acrylic Acid[J]. Progress in Chemistry, 2016, 28(2/3): 375-390 DOI:10.7536/PC150604

登录浏览全文

4963

注册一个新账户 忘记密码

参考文献

[1] Talebian-Kiakalaieh A, Amin N A S, Hezaveh H. Renew. Sust. Energ. Rev., 2014, 40:28.
[2] Katryniok B, Paul S, Capron M, Dumeignil F. ChemSusChem., 2009, 2(8):719.
[3] Sereshki B R, Balan S J, Patience G S, Dubois J L. Ind. Eng. Chem. Res., 2009, 49(3):1050.
[4] McKendry P. Bioresource Technol., 2002, 83(1):55.
[5] Demirbas A. Appl. Energ., 2009, 86:S108.
[6] Zhou C H, Xia X, Lin C X, Tong D S, Beltramini J. Chem. Soc. Rev., 2011, 40(11):5588.
[7] 冯建(Feng J),袁茂林(Yuan M L), 陈华(Chen H),李贤均(Li X J). 化学进展(Progress in Chemistry), 2007, 19(5):651.
[8] 李明燕(Li M Y),周春晖(Zhou C H), Beltramini J N,俞卫华(Yu W H),范永仙(Fan Y C). 化学进展(Progress in Chemistry), 2008, 20(10):1474.
[9] Ilyushin V V, Motiyenko R A, Lovas F J, Plusquellic D F. J. Mol. Spectrosc., 2008, 251(1):129.
[10] Israel A U, Obot I B, Asuquo J E. J. Chem., 2008, 5(4):940.
[11] Díaz G C, Tapanes N C O, Câmara L D T, Aranda D A G. Renew. Energ., 2014, 64:113.
[12] Saleh J, Tremblay A Y, Dubé M A. Fuel, 2010, 89(9):2260.
[13] Beerthuis R, Rothenberg G, Shiju N R. Green Chem., 2015, 17(3):1341.
[14] Arroyo-López F N, Pérez-Torrado R, Querol A, Barrio E. Food Microbial., 2010, 27(5):628.
[15] Modig T, Granath K, Adler L, Liden G. Appl. Microbial. Biotechnol., 2007, 75(2):289.
[16] Seo H B, Yeon J H, Jeong M H, Kang D H, Lee H Y, Jung K H. Biotechnol. Bioproc. E., 2009, 14(5):599.
[17] Wang Z, Zhu G J, Fang H, Prior B A. Biotechnol. Adv., 2001, 19(3):201.
[18] Zhao H, Zhou C H, Wu L M, Lou J Y, Li N, Yang H M, Tong D S, Yu W H. Appl. Clay Sci., 2013, 74:154.
[19] Johnson D T, Taconi K A. Environ. Prog., 2007, 26(4):338.
[20] Tan K T, Lee K T, Mohamed A R. Bioresource Technol., 2010, 101(3):965.
[21] OECD-FAO. OECD-FAO Agricultural Outlook 2014~2023. OECD Publishing. 2014, 111.
[22] Yaakob Z,Mohammad M,Alherbawi M, Alherbawi M, Alam Z, Sopian K.Renew. Sust. Energ. Rev., 2013, 18:184.
[23] Jerzykiewicz M, Cwielag I, Jerzykiewicz W. J. Chem. Technol. Biot., 2009, 84(8):1196.
[24] Sharninghausen L S, Campos J, Manas M G, Crabtree R H. Nat. Commun., 2014, 5:5084.
[25] Possato L G, Cassinelli W H, Garetto T, Pulcinelli S H, Santilli C V, Martins L. Appl. Catal. A:Gen., 2015, 492:243.
[26] Zhou C H, Zhao H, Tong D S, Wu L M, Yu W H. Catal. Rev., 2013, 55(4):369.
[27] Katryniok B, Paul S, Dumeignil F. ACS Catal., 2013, 3(8):1819.
[28] Raksaphort S, Pengpanich S, Hunsom M. React. Kinet. Catal. Lett., 2014, 55(4):434.
[29] Viswanadham B, Pavankumar V, Chary K V R. Catal. Lett., 2014, 144(4):744.
[30] Zhou C H, Beltramini J N, Fan Y X, Lu G Q. Chem. Soc. Rev., 2008, 37(3):527.
[31] Pagliaro M, Ciriminna R, Kimura H, Rossi M, Pina C D. Angew. Chem. Int. Ed., 2007, 46(24):4434.
[32] Wang Z C, Wang L Z, Jiang Y J, Hunger M, Huang J. ACS Catal., 2014, 4(4):1144.
[33] Rajan N P, Rao G S, Putrakumar B, Chary K V R. RSC Adv., 2014, 4(96):53419.
[34] Cui Y, Galvita V, Rihko-Struckmann L, Lorenz H, Sundmacher K. Appl. Catal. B:Environ., 2009, 90(1):29.
[35] Ciriminna R, Palmisano G, Della Pina C, Rossi M, Pagliaro M. Tetrahedron Lett., 2006, 47(39):6993.
[36] Zhang Y, Gao F, Zhang S P, Su Z G, Ma G H,Wang P. Bioresource Technol., 2011, 102(2):1837.
[37] Feng X Z, Sun B, Yao Y, Su Q, Ji W J, Au C T. J. Catal., 2014, 314:132.
[38] Abdel-Halim E S, Al-Hoqbani A A. Bioresources, 2015, 10(2):3112.
[39] Schwenk E, Gehrke M, Aichner F. US 1916743, 1933.
[40] Vitry D, Morikawa Y, Dubois J L, Ueda W. Appl. Catal. A:Gen., 2003, 251(2):411.
[41] Han S, Frick C D, Kraptchetov D A, Martenak D J, Quiros N I, Donnelly T J. US20140243554 A1, 2012.
[42] Soares R R, Simonetti D A, Dumesic J A. Angew. Chem. Int. Ed., 2006, 118(24):4086.
[43] Pagliaro M, Ciriminna R, Kimura H, Rossi M, Della Pina C. Angew. Chem. Int. Ed., 2007, 119(24):4516.
[44] Kampe P, Giebeler L, Samuelis D, Kunert J, Drochner A, Haaß F, Adams A H, Ott J, Endres S, Schimanke G, Buhrmester T, Martin M, Fuess H, Vogel H. Phys. Chem. Chem. Phys., 2007, 9(27):3577.
[45] Manosak R, Limpattayanate S, Hunsom M. Fuel Process. Technol., 2011, 92(1):92.
[46] López J Á S, Santos M Á M, Pérez A F C, Martin A M. Bioresource Technol., 2009, 100(23):5609.
[47] Devi P, Bethala L A, Gangadhar K N, Sai Prasad P S, Jagannadh B, Prasad R B. ChemSusChem., 2009, 2(7):617.
[48] Ayoub M, Abdullah A Z. Renew. Sust. Energ. Rev., 2012, 16(5):2671.
[49] Zhou C H, Beltramini J N, Lin C X, Xu Z P, Lu G Q, Tanksale A. Catal. Sci. Technol., 2011, 1(1):111.
[50] Wang F, Xu J, Dubois J L, Ueda W. ChemSusChem., 2010, 3(12):1383.
[51] Chieregato A, Basile F, Concepción P, Guidetti S, Liosi G, Soriano M D, Nieto J M L. Catal. Today, 2012, 197(1):58.
[52] Arntz D, Höpp M, Jacobi S, Sauer J, Ohara T, Sato T, Wei B O. Acrolein and Methacrolein. NJ:Wiley-VCH. 2012.
[53] Sithambaram S, Kumar R, Son Y C, Suib S L. J. Catal., 2008, 253(2):269.
[54] Bohmer N, Roussiere T, Kuba M, A Schunk S. Comb. Chem. High T. Scr., 2012, 15(2):123.
[55] Nimlos M R, Blanksby S J, Qian X, Himmel M E, Johnson D K. J. Phys. Chem. A, 2006, 110(18):6145.
[56] Fritz-Langhals E. Org. Process Res. Dev., 2005, 9(5):577.
[57] Soriano M D, Concepción P, Nieto J M L, Cavani F, Guidetti S, Trevisanut C. Green Chem., 2011, 13(10):2954.
[58] Yun Y S, Lee K R, Park H, Kim T Y,Yun D, Han J W,Yi J. ACS Catal., 2014, 5(1):82.
[59] Shen L Q, Yin H G, Wang A L, Lu X F, Zhang C H. Chem. Eng. J., 2014, 244:168.
[60] Chieregato A, Soriano M D, Basile F, Liosi G, Zamora S, Concepción P, Nieto J M L. Appl. Catal. B:Environ., 2014, 150:37.
[61] Possato L G, Cassinelli W H, Garetto T, Pulcinelli S H, Santilli C V, Martins L. Appl. Catal. A:Gen., 2015, 492:243.
[62] Khenkin A M, Neumann R. Angew. Chem. Int. Ed., 2000, 39(22):4088.
[63] Khenkin A M, Weiner L, Wang Y, Neumann R. J. Am. Chem. Soc., 2001, 123(35):8531.
[64] Vannice M A. Catal. Today, 2007, 123(1):18.
[65] Efremenko I, Neumann R. J. Am. Chem. Soc., 2012, 134(51):20669.
[66] Ennaciri S A, Malka K, Louis C, Barboux P, R'Kha C, Livage J. Catal. Lett., 1999, 62(1):79.
[67] Wang F, Dubois J L, Ueda W. J. Catal., 2009, 268(2):260.
[68] Kamiya Y, Nishiyama H, Yashiro M, Satsuma A, Hattori T. J. Jpn. Petrol. Inst., 2003, 46(1):62.
[69] Coulston G W, Thompson E A, Herron N. J. Catal., 1996, 163(1):122.
[70] Liu R, Wang T, Cai D, Jin Y. Ind. Eng. Chem. Res., 2014, 53(21):8667.
[71] Muneyama E, Kunishige A, Ohdan K, Ai M. J. Mol. Catal., 1994, 89(3):371.
[72] Ai M. J. Mol. Catal. A-Chem., 1996, 114(1):3.
[73] Ai M, Ohdan K. Appl. Catal. A:Gen, 1999, 180(1):47.
[74] Deleplanque J, Dubois J L, Devaux J F, Ueda W. Catal. Today, 2010, 157(1):351.
[75] Muneyama E, Kunishige A, Ohdan K, Ai, M. J. Mol. Catal., 1994, 89(3):371.
[76] Millet J, Bouchard A, Édelin C. Acta biotheor., 1998, 46(1):1.
[77] Song H, Sun Y, Jia X. Mater. Charact., 2015, 107:182.
[78] 王峰(Wang F), 徐杰(Xu J). CN102249890A, 2011.
[79] Vitry D, Morikawa Y, Dubois J L, Ueda W. Appl. Catal. A:Gen, 2003, 251(2):411.
[80] Ueda W, Vitry D, Katou T. Catal. Today, 2005, 99(1):43.
[81] Sadakane M, Yamagata K, Kodato K, Endo K, Toriumi K, Ozawa Y, Ueda W. Angew. Chem. Int. Ed., 2009, 121(21):3840.
[82] Chieregato A, Soriano M D, García-González E, Puglia G, Basile F, Concepción P, Bandinelli C, López Nieto J M, Cavani F. ChemSusChem, 2014, 8(2):398.
[83] Liu L C, Wang B, Du Y H, Zhong Z Y, Borgna A. Appl. Catal. B, Environ., 2015, 174:1.
[84] Atia H, Armbruster U, Martin A. Appl. Catal. A, Gen., 2011, 393(1):331.
[85] Paniagua M, Saravanamurugan S, Melian-Rodriguez M, Melero J A, Riisager A. ChemSusChem, 2015, 8(6):1088.
[86] Vjunov A, Hu M Y, Feng J, Camaioni D M, Mei D, Hu J Z, Lercher J A. Angew. Chem. Int. Ed., 2014, 53(2):479.
[87] Mahdavi V, Soleimani S. Mater. Res. Bull., 2014, 51:153.
[88] Sutradhar M, Martins L M, da Silva M F C G, Pombeiro A J. Coordin. Chem. Rev., 2015.
[89] Price S P, Tong X, Ridge C, Neilson H L, Buffon J W, Robins J, Buratto S K.J. Phys. Chem. A, 2014, 118(37):8309.
[90] Pestana C F M, Guerra A C O, Ferreira G B, Turcia C C, Mota C J A. J. Brazil. Chem. Soc., 2013, 24(1):100.
[91] Witsuthammakul A, Sooknoi T. Appl. Catal. A, Gen., 2012, 413:109.
[92] Ovsitser O, Uchida Y, Mestl G, Weinberg G, Blume A, Jäger J, Dieterle M, Hibst H, Schlögl R. J.Mol. Cataly. A:Chem., 2002, 185(1):291.
[93] Adams A H, Haaß F, Buhrmester T, Kunert J, Ott, Vogel H, Fuess H. J. Mol. Catal. A:Chem., 2004, 216(1):67.
[94] Katou T, Vitry D, Ueda W. Catal. Today, 2004, 91:237.
[95] Guliants V V, Bhandari R, Swaminathan B, Vasudevan V K, Brongersma H H, Knoester A, Han S. J. Phys. Chem. B, 2005, 109(50):24046.
[96] Katou T, Vitry D, Ueda W. Chem. Lett., 2003, 32(11):1028.
[97] Kuznetsova T G, Andrushkevich T V, Gorshkova T P. React. Kinet. Catal. L., 1986, 30(1):149.
[98] Okuhara T, Watanabe H, Nishimura T, Inumaru K, Misono M. Chem. Mater., 2000, 12(8):2230.
[99] Kamiya Y, Okuhara T, Misono M, Miyaji A, Tsuji K, Nakajo T. Catal. Surv. Asia, 2008, 12(2):101.
[100] Chai S H, Wang H P, Liang Y, Xu B Q. J.Catal., 2007, 250(2):342.
[101] Tsukuda E, Sato S, Takahashi R, Sodesawa T. Catal. Commun., 2007, 8(9):1349.
[102] Keulks G W, Krenzke L D, Notermann T M. Adv. Catal., 1979, 27:183.
[103] Corma A, Huber G W, Sauvanaud L, O'Connor P. J. Catal., 2008, 257(1):163.
[104] Suprun W, Lutecki M, Haber T, Papp H. J. Mol. Catal. A:Chem., 2009, 309(1):71.
[105] Alhanash A, Kozhevnikova E F, Kozhevnikov I V. Appl. Catal. A:Gen., 2010, 378(1):11.
[106] Chai S H, Wang H P, Liang Y, Xu B Q. Green Chem., 2007, 9(10):1130.
[107] Martinuzzi I, Azizi Y, Devaux J F, Tretjak S, Zahraa O, Leclerc J P. Chem. Eng. Sci., 2014, 116:118.
[108] Erfle S, Armbruster U, Bentrup U, Martin A, Brückner A. Appl. Catal. A:Gen., 2011, 391(1-2):102.
[109] Katryniok B, Paul S, Bellière-Baca V, Rey P, Dumeignil F. Green Chem., 2010, 12(12):2079.
[110] Park H, Yun Y S, Kim T Y, Lee K R, Baek J, Yi J. Appl. Catal. B:Environ., 2015, 176:1.
[111] Dubois J L, Duquenne C, Hoelderich W. WO 2006087083, 2006.
[112] O'Connor P, Corma C, Huber G, Savanaud L. WO 2008052993, 2008.
[113] Painter R M, Pearson D M, Waymouth R M. Angew. Chem. Int. Ed., 2010, 49(49):9456.
[114] Sarkar B, Pendem C, Konathala L N S, Tiwari R, Sasaki T, Bal R. Chem. Commun., 2014, 50(68):9707.
[115] Thanasilp S, Schwank J W, Meeyoo V, Pengpanich S, Hunsom M. J. Mol. Catal. A:Chem., 2013, 380:49.
[116] Hoffman R V, Bishop R D, Fitch P M, Hardenstein R. J. Org. Chem., 1980, 45(5):917.
[117] Ragupathi C, Vijaya J J, Kumar R T L, Kennedy J. J.Mol. Struct., 2015, 1079:182.
[118] Tenten A, Weidlich P. US 5446004. 1995.
[119] Tran B L, Driess M, Hartwig J F. J. Am. Chem. Soc., 2014, 136(49):17292.
[120] Seubsai A, Kahn M, Zohour B, Noon D, Charoenpanich M, Senkan S. Ind. Eng. Chem. Res., 2015, 54(10):2638.
[121] Pope M T, Müller A. Angew. Chem. Int. Ed., 1991, 30(1):34.
[122] Nishiyama Y, Nakagawa Y, Mizuno N. Angew. Chem. Int. Ed., 2001, 40(19):3639.
[123] Long D L, Burkholder E, Cronin L. Chem. Soc. Rev., 2007, 36(1):105.
[124] Li Y, Wu X, Wu Q, Ding H, Yan W. Dalton T., 2014, 43(36):13591.
[125] Atia H, Armbruster U, Martin A. J. Catal., 2008, 258(1):71.
[126] Shen L, Yin H, Wang A, Feng Y G, Shen Y T, Wu Z N, Jiang T S. Chem. Eng. J., 2012, 180:277.
[127] Thanasilp S, Schwank J W, Meeyoo V, Pengpanich S, Hunsom M. Chem. Eng. J., 2015, 275:113.
[128] Ott L, Bicker M, Vogel H. Green Chem., 2006, 8(2):214.
PDF (4481KB)

6249

访问

0

被引

详细

导航
相关文章

/

〈 〉