Production of formic acid from biomass-based compounds using a filter press type electrolyzer

被引:16
作者
Muiuane, V. P. [1 ]
Ferreira, M. [1 ]
Bignet, P. [1 ]
Bettencourt, A. P. [1 ]
Parpot, P. [1 ]
机构
[1] Univ Minho, Dept Quim, Campus Gualtar, P-4710057 Braga, Portugal
关键词
Biomass valorization; Nickel oxyhydroxide; Lead oxide; DSA; Formic acid; FM01-LC;
D O I
10.1016/j.jece.2013.09.014
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
There has been a growing interest for the sustainable production of formic acid ( FA) in recent years considering its potential use as a hydrogen storage compound. In this context, the electrochemical transformation of carbohydrate-based biomass into formic acid in aqueous media was investigated using a filter-press type electrochemical cell. Therefore the oxidation of mono and disaccharides was carried out at NiOOH, RuO2/Ti ( DSA) and PbO2 anodes, in FM01-LC ( ICI) electrolyzer. The effect of carbon number of biomass compound, anode material and pH on product distribution was determined. Between the readily available carbohydrates studied in this work at NiOOH anode, in alkaline medium, D-xylose provides the highest selectivity towards formate anion, i.e. 42%. The transformation of D-glucose into formic acid, with 38% selectivity, was achieved at RuO2/Ti ( DSA) in 0.5 M NaOH medium, applying a current density of 80 A m (2). The production of formate anion is mostly accompanied by the formation of oxalate anion and carbonates which constitute the by-products of the reaction. Considering that after acidification of carbonates the resulting CO2 can be easily removed and trapped by the growing plants which provide new biomass-based material, the transformation of oxalate anion ( OA) into CO32 is of major importance. For this reason the oxidation of OA at DSA in 0.1 MNaOH medium was also studied. In these conditions 60% of the initial oxalate anion was transformed to CO32 at 2.5 V vs. SCE. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1237 / 1244
页数:8
相关论文
共 20 条
[1]   Selective electrocatalytic oxidation of 2,5-dihydroxymethylfuran in aqueous medium:: a chromatographic analysis of the reaction products [J].
Al Baradii, A ;
Kokoh, KB ;
Huser, H ;
Lamy, C ;
Léger, JM .
ELECTROCHIMICA ACTA, 1999, 44 (16) :2779-2787
[2]  
Alves PDP, 2004, J BRAZIL CHEM SOC, V15, P626
[3]   Main routes for the thermo-conversion of biomass into fuels and chemicals. Part 1: Pyrolysis systems [J].
Balat, Mustafa ;
Balat, Mehmet ;
Kirtay, Elif ;
Balat, Havva .
ENERGY CONVERSION AND MANAGEMENT, 2009, 50 (12) :3147-3157
[4]   Structure-Activity Correlations in a Nickel-Borate Oxygen Evolution Catalyst [J].
Bediako, D. Kwabena ;
Lassalle-Kaiser, Benedikt ;
Surendranath, Yogesh ;
Yano, Junko ;
Yachandra, Vittal K. ;
Nocera, Daniel G. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2012, 134 (15) :6801-6809
[5]   Catalysis for conversion of biomass to fuels via pyrolysis and gasification: A review [J].
Bulushev, Dmitri A. ;
Ross, Julian R. H. .
CATALYSIS TODAY, 2011, 171 (01) :1-13
[6]  
Castanho M., 2006, APPL CATAL B-ENVIRON, V62, P193
[7]   EXPERIMENTAL EVALUATION OF ADSORPTION BEHAVIOR OF INTERMEDIATES IN ANODIC OXYGEN EVOLUTION AT OXIDIZED NICKEL SURFACES [J].
CONWAY, BE ;
LIU, TC .
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS I, 1987, 83 :1063-1079
[8]   Electrochemical treatment of tannery wastewater using DSA® electrodes [J].
Costa, Carla Regina ;
Botta, Clarice M. R. ;
Espindola, Evaldo L. G. ;
Olivi, Paulo .
JOURNAL OF HAZARDOUS MATERIALS, 2008, 153 (1-2) :616-627
[9]   OXIDATION OF ORGANIC COMPOUNDS AT A NICKEL ANODE IN ALKALINE SOLUTION [J].
FLEISCHMANN, M ;
KORINEK, K ;
PLETCHER, D .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1971, 31 (01) :39-+
[10]   Electrochemical approaches to environmental problems in the process industry [J].
Jüttner, K ;
Galla, U ;
Schmieder, H .
ELECTROCHIMICA ACTA, 2000, 45 (15-16) :2575-2594