Chemical recycling of polycarbonate in dilute aqueous ammonia solution under hydrothermal conditions

被引:47
作者
Hatakeyama, Kouhei [1 ]
Kojima, Tomoharu [1 ]
Funazukuri, Toshitaka [1 ]
机构
[1] Chuo Univ, Dept Appl Chem, Bunkyo Ku, Tokyo 1128551, Japan
基金
日本学术振兴会;
关键词
Ammonia; Bisphenol A; Chemical recycling; Hydrothermal; Polycarbonate; Rate; POLY(ETHYLENE-TEREPHTHALATE); DEPOLYMERIZATION; RECOVERY; ACID;
D O I
10.1007/s10163-013-0151-8
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Polycarbonate (PC) pellets were subjected to dilute aqueous ammonia solution under hydrothermal conditions in a semi-batch reactor at temperatures ranging from 433 to 463 K and at a pressure of 10 MPa. The PC pellets were almost completely converted to bisphenol A (BPA). During an initial certain period, referred to as an induction time, neither BPA nor total organic carbon in solution were detected, and the BPA yield increased with time. The monomer yield was well represented by a surface reaction model, two-thirds-order reaction with respect to the mass of unreacted PC. The overall rate constant of the reaction in 0.6 mol/kg aqueous ammonia solution at 433 K was about 15 times greater than that in 0.6 mol/kg NaOH solution. The rate constant at 433 K was proportional to the ammonia or NaOH concentration. There was a correlation between the induction time and temperature, as well as the ammonia or NaOH concentration. By carrying out the reaction in aqueous mixtures of (NH4)(2)SO4 and NaOH at various concentrations of NaOH, ammonia was confirmed not to function as an alkaline reagent, but as a nucleophile reagent.
引用
收藏
页码:124 / 130
页数:7
相关论文
共 14 条
[1]  
[Anonymous], 2011, YB CHEM IND STAT 201
[2]   Reaction kinetics of hydrothermal depolymerization of poly(ethylene naphthalate), poly(ethylene terephthalate), and polycarbonate with aqueous ammonia solution [J].
Arai, Risa ;
Zenda, Kentaro ;
Hatakeyama, Kohei ;
Yui, Kazuko ;
Funazukuri, Toshitaka .
CHEMICAL ENGINEERING SCIENCE, 2010, 65 (01) :36-41
[3]   Chemical recycling of plastics using sub- and supercritical fluids [J].
Goto, Motonobu .
JOURNAL OF SUPERCRITICAL FLUIDS, 2009, 47 (03) :500-507
[4]   Chemical conversion of poly(carbonate) to 1,3-dimethyl-2-imidazolidinone (DMI) and bisphenol A: a practical approach to the chemical recycling of plastic wastes [J].
Hata, S ;
Goto, H ;
Yamada, E ;
Oku, A .
POLYMER, 2002, 43 (07) :2109-2116
[5]   Viable utilization of polycarbonate as a phosgene equivalent illustrated by reactions with alkanedithiols, mercaptoethanol, aminoethanethiol, and aminoethanol: A solution for the issue of carbon resource conservation [J].
Hata, S ;
Goto, H ;
Tanaka, S ;
Oku, A .
JOURNAL OF APPLIED POLYMER SCIENCE, 2003, 90 (11) :2959-2968
[6]  
JSME, 1999, STREAM TABL BAS IAPW
[7]   Ammonolysis of polycarbonates with (supercritical) ammonia: An alternative for chemical recycling [J].
Mormann, W ;
Spitzer, D .
ADVANCES IN POLYCARBONATES, 2005, 898 :244-261
[8]  
Mormann W., 2004, Supercritical Fluids as Solvents and Reaction Media ed, P593, DOI [DOI 10.1016/B978044451574-2/50025-0, 10.1016/B978-044451574-2/50025-0, DOI 10.1016/B978-044451574-2/50025-0]
[9]   Chemical recycling of polycarbonate in a semi-continuous lab-plant.: A green route with methanol and methanol-water mixtures [J].
Piñero, R ;
García, J ;
Cocero, MJ .
GREEN CHEMISTRY, 2005, 7 (05) :380-387
[10]   Nonstationary model of the semicontinuous depolymerization of polycarbonate [J].
Pinero-Hernanz, Raul ;
Garcia-Serna, Juan ;
Jose Cocero, Maria .
AICHE JOURNAL, 2006, 52 (12) :4186-4199