A kinetic study of the depolymerisation of poly(ethylene terephthalate) by phase transfer catalysed alkaline hydrolysis

被引:44
作者
Lopez-Fonseca, R. [1 ]
Gonzalez-Marcos, M. P. [1 ]
Gonzalez-Velasco, J. R. [1 ]
Gutierrez-Ortiz, J. I. [1 ]
机构
[1] Univ Pais Vasco EHU, Fac Sci & Technol, Dept Chem Engn, Chem Technol Environm Sustainabil Grp, E-48080 Bilbao, Spain
关键词
chemical recycling; PET; alkaline hydrolysis; kinetics; phase transfer catalysts; quaternary phosphonium salts; WASTE POLY(ETHYLENE-TEREPHTHALATE); POLYETHYLENE TEREPHTHALATE; PET; ACID; RECOVERY;
D O I
10.1002/jctb.2011
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
BACKGROUND: Chemical or tertiary recycling of waste polymers including PET, poly(ethylene terephthalate), leads to the formation of raw starting monomers by different depolymerisation routes. This work was focused on the identification of the catalytic behaviour, if any, of a series of quaternary phosphonium and ammonium salts as phase transfer catalysts for the alkaline hydrolysis of PET, and on the determination of the kinetics of the phase transfer catalysed process. RESULTS: Among the salts examined tributylhexadecylphosphonium bromide was found to be the most effective catalyst. The proposed kinetic model accounted for the uncatalysed and catalysed reactions and predicted a linear correlation for the reaction rate with the concentration of the quaternary salt. The notable increase in the phase transfer catalysed reaction rate was related mainly to the greater value of the pre-exponential factor while the value of the activation energy was hardly modified by the presence of the quaternary phosphonium salt, thereby suggesting a similar mechanism for the alkaline hydrolysis with or without phase transfer catalyst. CONCLUSIONS: The use of selected phosphonium quaternary salts exhibited a remarkably positive effect on the experimental conditions under which the depolymerisation of poly(ethylene terephthalate) by alkaline hydrolysis can be carried out, especially in terms of low operating temperature. Kinetic correlations provided a reliable mathematical reaction model for this recycling process, which is in agreement with the principles of sustainable development. (C) 2008 Society of Chemical Industry
引用
收藏
页码:92 / 99
页数:8
相关论文
共 31 条
  • [1] Recycling of PET
    Awaja, F
    Pavel, D
    [J]. EUROPEAN POLYMER JOURNAL, 2005, 41 (07) : 1453 - 1477
  • [2] CATALYZED-HYDROLYSIS OF POLYETHYLENE TEREPHTHALATE MELTS
    CAMPANELLI, JR
    COOPER, G
    KAMAL, MR
    [J]. JOURNAL OF APPLIED POLYMER SCIENCE, 1994, 53 (08) : 985 - 991
  • [3] Chemical recycling of poly(ethylene terephthalate) (PET) by hydrolysis and glycolysis
    Carta, D
    Cao, G
    D'Angeli, C
    [J]. ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH, 2003, 10 (06) : 390 - 394
  • [4] Das J, 2007, INDIAN J CHEM TECHN, V14, P173
  • [5] Depolymerization mechanism of poly(ethylene terephthalate) in supercritical methanol
    Genta, M
    Iwaya, T
    Sasaki, M
    Goto, M
    Hirose, T
    [J]. INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 2005, 44 (11) : 3894 - 3900
  • [6] Depolymerisation of poly(ethylene terephthalate) fibre wastes using ethylene glycol
    Ghaemy, M
    Mossaddegh, K
    [J]. POLYMER DEGRADATION AND STABILITY, 2005, 90 (03) : 570 - 576
  • [7] Goje AS, 2004, POLYM-PLAST TECHNOL, V43, P1093, DOI 10.1081/PPT-120038616
  • [8] Glycolytic aminolysis of poly(ethylene terephthalate) waste for recovery of value-added comonomer at atmospheric pressure
    Goje, AS
    Thakur, SA
    Patil, TM
    Mishra, S
    [J]. JOURNAL OF APPLIED POLYMER SCIENCE, 2003, 90 (12) : 3437 - 3444
  • [9] Degradation kinetics of polyethylene terephthalate in supercritical methanol
    Goto, M
    Koyamoto, H
    Kodama, A
    Hirose, T
    [J]. AICHE JOURNAL, 2002, 48 (01) : 136 - 144
  • [10] BEHAVIOR OF HIGHLY DISPERSED PLATINUM CATALYSTS IN LIQUID-PHASE HYDROGENATIONS
    GUTIERREZORTIZ, MA
    GONZALEZMARCOS, JA
    GONZALEZMARCOS, MP
    GONZALEZVELASCO, JR
    [J]. INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 1993, 32 (06) : 1035 - 1040