Characterization and recovery of mercury from spent fluorescent lamps

被引:89
作者
Jang, M [1 ]
Hong, SM [1 ]
Park, JK [1 ]
机构
[1] Univ Wisconsin, Dept Civil & Environm Engn, Madison, WI 53706 USA
关键词
D O I
10.1016/j.wasman.2004.09.008
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Fluorescent lamps rely on mercury as the source of ultraviolet radiation for the production of visible light. Partitioning of mercury among vapor phase, loose phosphor powders produced during breaking and washing steps, glass matrices, phosphor powders attached on the glass and aluminum end caps was examined from simulated laboratory lamp recycling tests for different types of spent and new fluorescent lamps. Mercury concentrations in lamp glasses taken from commercial lamp recyclers were also analyzed for comparison with the simulated results of spent and new lamps of different types. The mercury content of the glass from spent lamps was highly variable depending on the lamp type and manufacturer; the median values of the mercury concentration in glasses for spent 26- (T8) and 38-mm (T12) diameter fluorescent lamps were approximately 30 and 45 mug/g, respectively. The average mercury concentration of samples taken from recycler A was 29.6 mug/g, which was about 64% of median value measured from the spent T 12 lamps. Over 94% of total mercury in lamps remained either as a component of phosphor powders attached inside the lamp or in glass matrices. New T12 lamps had a higher partitioning percentage of elemental mercury in the vapor phase (0.17%) than spent T12 lamps (0.04%), while spent lamps had higher partitioning percentages of mercury resided on end-caps and phosphor powders detached from the breaking and washing steps. The TCLP values of simulated all lamp-glasses and samples obtained from recyclers were higher than the limit of LDR standard (0.025 mg/L). After investigating acid treatment and high temperature treatment as mercury reclamation techniques, it was found that heating provided the most effective mercury capture. Although the initial mercury concentrations of individual sample were different, the mercury concentrations after I h exposure at 100 degreesC were below 4 mug/g for all samples (i.e., <1% remaining). Therefore, it is recommended that heating be used for recovering mercury from spent fluorescent lamps. (C) 2004 Elsevier Ltd. All rights reserved.
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页码:5 / 14
页数:10
相关论文
共 18 条
[1]   Release of mercury from broken fluorescent bulbs [J].
Aucott, M ;
McLinden, M ;
Winka, M .
JOURNAL OF THE AIR & WASTE MANAGEMENT ASSOCIATION, 2003, 53 (02) :143-151
[2]  
BATTYE W, 1994, EVALUATION MERCURY E
[3]  
DOMINSKI P, 1985, AUTOMATED COLD VAPOR
[4]   MERCURY-GLASS INTERACTIONS IN FLUORESCENT LAMPS [J].
DOUGHTY, DA ;
WILSON, RH ;
THALER, EG .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1995, 142 (10) :3542-3550
[5]  
*EPA, 1998, MERC EM DISP FLUOR L
[6]  
*EPA, 1992, AN RES MERC FLUOR LA
[7]  
*EPA, 1999, FED REGISTER, V64, P36466
[8]   Reduction of mercury loss in fluorescent lamps coated with thin metal-oxide films [J].
Hildenbrand, VD ;
Denissen, CJM ;
van der Pol, AJHP ;
Hendriks, AHC ;
van der Marel, C ;
Snijders, JHM ;
Tamminga, Y ;
Brongersma, HH ;
Viitanen, MM .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2003, 150 (07) :H147-H155
[9]   Interactions of thin oxide films with a low-pressure mercury discharge [J].
Hildenbrand, VD ;
Denissen, CJM ;
Geerdinck, LM ;
van der Marel, C ;
Snijders, JHM ;
Tamminga, Y .
THIN SOLID FILMS, 2000, 371 (1-2) :295-302
[10]  
ISKANDER MS, 1994, INT J ENVIRON POLLUT, V4, P229