Adsorption of dyes by ACs prepared from waste tyre reinforcing fibre. Effect of texture, surface chemistry and pH

被引:40
作者
Acevedo, Beatriz [1 ]
Rocha, Raquel P. [2 ]
Pereira, Manuel F. R. [2 ]
Figueiredo, Jose L. [2 ]
Barriocanal, Carmen [1 ]
机构
[1] CSIC, Inst Nacl Carbon, INCAR, E-33080 Oviedo, Spain
[2] Univ Porto, Fac Engn, Dept Engn Quim, LCM,Lab Associado LSRE LCM, P-4200465 Oporto, Portugal
关键词
Reinforcing fibre; Coal; Activated carbons; Surface chemistry; pH; ACTIVATED CARBONS; AQUEOUS-SOLUTIONS; CATIONIC DYES; TEXTILE DYES; REMOVAL; DECOLORIZATION; OXIDES; TPD;
D O I
10.1016/j.jcis.2015.07.068
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
This paper compares the importance of the texture and surface chemistry of waste tyre activated carbons in the adsorption of commercial dyes. The adsorption of two commercial dyes, Basic Astrazon Yellow 7GLL and Reactive Rifafix Red 3BN on activated carbons made up of reinforcing fibres from tyre waste and low-rank bituminous coal was studied. The surface chemistry of activated carbons was modified by means of HCl HNO3 treatment in order to increase the number of functional groups. Moreover, the influence of the pH on the process was also studied, this factor being of great importance due to the amphoteric characteristics of activated carbons. The activated carbons made with reinforcing fibre and coal had the highest S-BET, but the reinforcing fibre activated carbon samples had the highest mesopore volume. The texture of the activated carbons was not modified upon acid oxidation treatment, unlike their surface chemistry which underwent considerable modification. The activated carbons made with a mixture of reinforcing fibre and coal experienced the largest degree of oxidation, and so had more acid surface groups. The adsorption of reactive dye was governed by the mesoporous volume, whilst surface chemistry played only a secondary role. However, the surface chemistry of the activated carbons and dispersive interactions played a key role in the adsorption of the basic dye. The adsorption of the reactive dye was more favored in a solution of pH 2, whereas the basic dye was adsorbed more easily in a solution of pH 12. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:189 / 198
页数:10
相关论文
共 44 条
  • [1] Identification of polymers in waste tyre reinforcing fibre by thermal analysis and pyrolysis
    Acevedo, B.
    Fernandez, A. M.
    Barriocanal, C.
    [J]. JOURNAL OF ANALYTICAL AND APPLIED PYROLYSIS, 2015, 111 : 224 - 232
  • [2] Pyrolysis of blends of coal and tyre wastes in a fixed bed reactor and a rotary oven
    Acevedo, B.
    Barriocanal, C.
    Alvarez, R.
    [J]. FUEL, 2013, 113 : 817 - 825
  • [3] Acevedo B., 2015, FUEL PROC TECHNOL
  • [4] Effect of carbon surface chemistry on the removal of reactive dyes from textile effluent
    Al-Degs, Y
    Khraisheh, MAM
    Allen, SJ
    Ahmad, MN
    [J]. WATER RESEARCH, 2000, 34 (03) : 927 - 935
  • [5] SOME ASPECTS OF THE SURFACE-CHEMISTRY OF CARBON-BLACKS AND OTHER CARBONS
    BOEHM, HP
    [J]. CARBON, 1994, 32 (05) : 759 - 769
  • [6] Surface oxides on carbon and their analysis: a critical assessment
    Boehm, HP
    [J]. CARBON, 2002, 40 (02) : 145 - 149
  • [7] Application of cupuassu shell as biosorbent for the removal of textile dyes from aqueous solution
    Cardoso, Natali F.
    Lima, Eder C.
    Pinto, Isis S.
    Amavisca, Camila V.
    Royer, Betina
    Pinto, Rodrigo B.
    Alencar, Wagner S.
    Pereira, Simone F. P.
    [J]. JOURNAL OF ENVIRONMENTAL MANAGEMENT, 2011, 92 (04) : 1237 - 1247
  • [8] Membrane separation for wastewater reuse in the textile industry
    Ciardelli, G
    Corsi, L
    Marcucci, M
    [J]. RESOURCES CONSERVATION AND RECYCLING, 2001, 31 (02) : 189 - 197
  • [9] Synthesis of lignin-base cationic flocculant and its application in removing anionic azo-dyes from simulated wastewater
    Fang, Run
    Cheng, Xiansu
    Xu, Xiaorong
    [J]. BIORESOURCE TECHNOLOGY, 2010, 101 (19) : 7323 - 7329
  • [10] Adsorption of anionic and cationic dyes on activated carbons with different surface chemistries
    Faria, PCC
    Orfao, JJM
    Pereira, MFR
    [J]. WATER RESEARCH, 2004, 38 (08) : 2043 - 2052