Advanced degradation of brominated epoxy resin and simultaneous transformation of glass fiber from waste printed circuit boards by improved supercritical water oxidation processes

被引:39
作者
Liu, Kang
Zhang, Zhiyuan
Zhang, Fu-Shen [1 ]
机构
[1] Chinese Acad Sci, Res Ctr Ecoenvironm Sci, Dept Solid Waste Treatment & Recycling, 18 Shuangqing Rd, Beijing 100085, Peoples R China
基金
中国国家自然科学基金;
关键词
Waste PCBs; Advanced degradation; Supercritical water; Mechanism; Anorthite; METAL RECOVERY; DECOMPOSITION; MECHANISM; PHENOL; ACID; RETARDANT; AU; CU;
D O I
10.1016/j.wasman.2016.05.022
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 investigated various supercritical water oxidation (SCWO) systems, i.e. SCWO1 (only water), SCWO2 (water +H2O2) and SCWO3 (water + H2O2/NaOH), for waste printed circuit boards (PCBs) detoxification and recycling. Response surface methodology (RSM) was applied to optimize the operating conditions of the optimal SCWO3 systems. The optimal reaction conditions for debromination were found to be the NaOH of 0.21 g, the H2O2 volume of 9.04 mL, the time of 39.7 min, maximum debromination efficiency of 95.14%. Variance analysis indicated that the factors influencing debromination efficiency was in the sequence of NaOH > H2O2 > time. Mechanism studies indicated that the dissociated ions from NaOH in supercritical water promoted the debromination of brominated epoxy resins (BERs) through an elimination reaction and nucleophilic substitution. HO2, produced by H2O2 could induce the oxidation of phenol ring to open (intermediates of BERs), which were thoroughly degraded to form hydrocarbons, CO2, H2O and NaBr. In addition, the alkali-silica reaction between OH- and SiO2 induced the phase transformation of glass fibers, which were simultaneously converted into anorthite and albite. Waste PCBs in H2O2/NaOH improved SCWO system were fully degraded into useful products and simultaneously transformed into functional materials. These findings are helpful for efficient recycling of waste PCBs. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:423 / 430
页数:8
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