Dechlorination of polychlorobiphenyls using NaBH4 and NaBH4/LiCl at 120-310°C in glyme solvents

被引:17
|
作者
Pittman, CU [1 ]
Yang, CM [1 ]
机构
[1] Mississippi State Univ, Dept Chem, Ind Chem Res Ctr, Mississippi State, MS 39762 USA
关键词
dechlorination; polychlorobiphenyls; sodium borohydride; glyme solvents; high temperature reductions;
D O I
10.1016/S0304-3894(01)00175-3
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
High temperature PCB dechlorination (Aroclor 1016) occurred using NaBH4 alone in tetraglyme at 290-310 degreesC within 2 h in a sealed tube. Aroclor 1016 dechlorination was also quantitatively achieved using NaBH4/LiCl/glyme solvents (di-, tri-, or tetraglyme) at 125-135 degreesC. The best results were obtained by prestirring NaBH4, LiCl and the glyme solvent at room temperature before heating at 125-135 degreesC. At equivalent conditions, PCB dechlorination rates were found to depend on solvent in the order: tetraglyme, triglyme > diglyme. At 130 degreesC, Aroclor 1016 can be dechlorinated in NaBH4/LiCl/tetraglyme in 4 h. 2-Chlorobiphenyl and 2,2'-dichlorobiphenyl were the least reactive congeners in dechlorinations with NaBH4/LiCl in diglyme. Competitive dechlorinations with NaBH4/LiCl in diglyme showed 3-chloro- and 4-chlorobiphenyl reacted faster than 2-chlorobiphenyl at 130 degreesC. The reactions were clean with no solvent decomposition in the range of 120- 162 degreesC. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:299 / 311
页数:13
相关论文
共 50 条
  • [41] DECOMPOSITION OF NABH4 IN AN ELECTROLESS NICKEL BATH
    LO, YL
    HWANG, BJ
    INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 1994, 33 (01) : 56 - 61
  • [42] REACTIONS OF THE SYNTHESIS TETRAHYDROBORATES OF ZIRCONIUM AND HAFNIUM USING NABH4
    VOLKOV, VV
    MYAKISHEV, KG
    IZVESTIYA SIBIRSKOGO OTDELENIYA AKADEMII NAUK SSSR SERIYA KHIMICHESKIKH NAUK, 1986, (04): : 68 - 72
  • [43] An efficient and chemoselective deoxygenation of hetero cyclic N-Oxides using LiCl/NaBH4
    Ram, SR
    Chary, KP
    Iyengar, DS
    SYNTHETIC COMMUNICATIONS, 2000, 30 (19) : 3511 - 3515
  • [44] EPIMERIZATION IN NABH4 REDUCTION OF ASYMMETRIC KETONES
    HACH, V
    FRYBERG, EC
    MCDONALD, E
    TETRAHEDRON LETTERS, 1971, (28) : 2629 - &
  • [45] Understanding the Kinetics and Reduction of Methylene Blue Using NaBH4
    Patel, P.
    Maliekal, P. J.
    Lingayat, S.
    Badani, P. M.
    RUSSIAN JOURNAL OF PHYSICAL CHEMISTRY B, 2022, 16 (05) : 869 - 876
  • [46] Continuous Reductions and Reductive Aminations Using Solid NaBH4
    Gilmore, Kerry
    Vukelic, Stella
    McQuade, D. Tyler
    Koksch, Beate
    Seeberger, Peter H.
    ORGANIC PROCESS RESEARCH & DEVELOPMENT, 2014, 18 (12) : 1771 - 1776
  • [47] Understanding the Kinetics and Reduction of Methylene Blue Using NaBH4
    P. Patel
    P. J. Maliekal
    S. Lingayat
    P. M. Badani
    Russian Journal of Physical Chemistry B, 2022, 16 : 869 - 876
  • [48] Regeneration of spent-NaBH4 back to NaBH4 by using high-energy ball milling
    Hsueh, Chan-Li
    Liu, Cheng-Hong
    Chen, Bing-Hung
    Chen, Chuh-Yung
    Kuo, Yi-Chia
    Hwang, Kuo-Jen
    Ku, Jie-Ren
    INTERNATIONAL JOURNAL OF HYDROGEN ENERGY, 2009, 34 (04) : 1717 - 1725
  • [49] High pressure polymorphism of LiBH4 and of NaBH4
    Marizy, Adrien
    Geneste, Gregory
    Garbarino, Gaston
    Loubeyre, Paul
    RSC ADVANCES, 2021, 11 (41) : 25274 - 25283
  • [50] 用SBH(NaBH4)回收贵金属
    伊贺久矩
    于君杰
    黄金, 1986, (03) : 33 - 35