Metal-free bifunctional silica for conversion of waste glycerol from biodiesel: Sustainable production of formic acid

被引:25
作者
Chagas, Poliane [1 ]
Thibau, Mariana A. [1 ]
Breder, Samuel [1 ]
Souza, Patterson P. [2 ]
Caldeira, Gabriela S. [2 ]
Portilho, Marcio F. [3 ]
Castro, Cinthia S. [1 ]
Oliveira, Luiz C. A. [1 ]
机构
[1] Univ Fed Minas Gerais, Dept Chem, BR-31270901 Belo Horizonte, MG, Brazil
[2] Fed Ctr Technol Educ Minas Gerais, BR-30421169 Belo Horizonte, MG, Brazil
[3] CENPES Petrobras, Cidade Univ,Q7, BR-21949900 Rio De Janeiro, RJ, Brazil
关键词
Residual glycerol; Oxidative clivage; Formic acid; Synthetic silica; CATALYTIC DEHYDRATION; SELECTIVE OXIDATION; HYDROGEN-PEROXIDE; MCM-41; SITES; DECOMPOSITION; ACROLEIN; ACETOL; LEWIS; WATER;
D O I
10.1016/j.cej.2019.03.068
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
This work describes for the first time the conversion of the waste glycerol from biodiesel production using a metal-free bifunctional silica with high porosity as catalyst. The mesoporous silica (synthetic SiO2) with high specific surface area of 1489 m(2)g(-1) was used in the conversion of the residual glycerol (supplied by Petrobras, without any purification) using continuous flow (PBR) reactor. Surprisingly, this metal-free silica showed high selectivity for the oxidative cleavage product (formic acid), reaching 83% in continuous flow. This indicates that there is no need for the use of supported metals as in the most of the works in the literature, which can reduce the cost of the catalyst. The surface defects in the synthetic SiO2 generated a high amount of Lewis acid sites (identified by pyridine adsorption experiments). Thus, the acid sites reacted in situ with the H2O2 (used as oxidizing agent during reaction for glycerol conversion), generating very active oxygen species on the catalyst surface. Therefore, the data presented in this work suggest that the prepared SiO2 is a bifunctional catalyst that presents Lewis acid sites besides reactive oxygen species.
引用
收藏
页码:1102 / 1108
页数:7
相关论文
共 39 条
[1]   Oxidation of 3,4-dihydroxybenzoic acid by means of hydrogen peroxide in aqueous goethite slurry [J].
Andreozzi, R ;
Caprio, V ;
Marotta, R .
WATER RESEARCH, 2002, 36 (11) :2761-2768
[2]   The potential of glycerol as a value-added commodity [J].
Anitha, M. ;
Kamarudin, S. K. ;
Kofli, N. T. .
CHEMICAL ENGINEERING JOURNAL, 2016, 295 :119-130
[3]   GLYCEROL: A BRIEF HISTORY AND THEIR APPLICATION IN STEREOSELECTIVE SYNTHESES [J].
Beatriz, Adilson ;
Araujo, Yara J. K. ;
de Lima, Denis Pires .
QUIMICA NOVA, 2011, 34 (02) :306-319
[4]   Towards Sustainable Production of Formic Acid [J].
Bulushev, Dmitri A. ;
Ross, Julian R. H. .
CHEMSUSCHEM, 2018, 11 (05) :821-836
[5]   Ga-MCM-41 nanoparticles: Synthesis and application of versatile heterogeneous catalysts [J].
Collard, Xavier ;
Li, Li ;
Lueangchaichaweng, Warunee ;
Bertrand, Arnaud ;
Aprile, Carmela ;
Pescarmona, Paolo P. .
CATALYSIS TODAY, 2014, 235 :184-192
[6]   The influence of impurities on the acid-catalyzed reaction of glycerol with acetone [J].
da Silva, Carolina X. A. ;
Mota, Claudio J. A. .
BIOMASS & BIOENERGY, 2011, 35 (08) :3547-3551
[7]   Oxidation of hydroxyacetone (acetol) with hydrogen peroxide in acetonitrile solution catalyzed by iron(III) chloride [J].
de Araujo, Marcos L. ;
Mandelli, Dalmo ;
Kozlov, Yuriy N. ;
Carvalho, Wagner A. ;
Shul'pin, Georgiy B. .
JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL, 2016, 422 :103-114
[8]   Catalytic amination of glycerol with dimethylamine over different type ofheteropolyacid/Zr-MCM-41 catalysts [J].
Ding, Jianfei ;
Cui, Mingyu ;
Ma, Tianlin ;
Shao, Rong ;
Xu, Wei ;
Wang, Pengfei .
MOLECULAR CATALYSIS, 2018, 457 :51-58
[9]   Formic acid as the in-situ hydrogen source for catalytic reduction of nitrate in water by PdAg alloy nanoparticles supported on amine-functionalized SiO2 [J].
Ding, Yajun ;
Sun, Wuzhu ;
Yang, Weiyi ;
Li, Qi .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2017, 203 :372-380
[10]   Efficient production of 1,3-butadiene in the catalytic dehydration of 2,3-butanediol [J].
Duan, Hailing ;
Yamada, Yasuhiro ;
Sato, Satoshi .
APPLIED CATALYSIS A-GENERAL, 2015, 491 :163-169