Photochemical destruction of cyanide in landfill leachate

被引:26
作者
Kim, BR
Podsiadlik, DH
Kalis, EM
Hartlund, JL
Gaines, WA
机构
[1] Ford Motor Co, Res Lab, Dearborn, MI 48121 USA
[2] Ford Motor Co, Sandusky Plant, Sandusky, OH 44070 USA
[3] Ford Motor Co, Envir Qual Ofc, Fac Envir Control Engr, Dearborn, MI 48126 USA
来源
JOURNAL OF ENVIRONMENTAL ENGINEERING-ASCE | 1998年 / 124卷 / 11期
关键词
D O I
10.1061/(ASCE)0733-9372(1998)124:11(1108)
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The Alien Park Clay Mine Landfill, owned by Ford, produces a leachate that occasionally contains cyanide at levels marginally below the discharge limit. The form of the cyanide in the leachate was found to be iron-cyanide complexes that resist oxidation by a conventional treatment method, alkaline oxidation. Furthermore, the leachate also was found to contain a relatively large amount of organics (>1,000 mg/L of chemical oxygen demand), which would exert additional demand for oxidizing agents (e.g., chlorine). A study was performed to determine what treatment technology could be employed in the event treatment becomes necessary because of potential changes in the leachate characteristics and/or discharge limits. In this study, among several chemical oxidation methods, ultraviolet (UV) irradiation with or without ozone was investigated as a treatment option. The following are the primary findings: (1) UV irradiation alone was effective for removing the iron-cyanide complex in both the leachate and the clean water; (2) the demand for UV or ozone by chemical oxygen demand was relatively low for this leachate; (3) ozone alone was not effective for removing the iron-cyanide complex; and (4) UV irradiation alone and UV irradiation with ozone resulted in the same removal for total cyanide in clean-water experiments, but the UV irradiation alone left some free cyanide whereas the UV irradiation with ozone did not.
引用
收藏
页码:1108 / 1113
页数:6
相关论文
共 21 条
[1]  
[Anonymous], 1992, STAND METH EX WAT WA
[2]  
BERNARDIN FE, 1973, J WATER POLLUT CON F, V45, P221
[3]   KINETICS AND MECHANISM OF OZONATION OF FREE CYANIDE SPECIES IN WATER [J].
GUROL, MD ;
BREMEN, WM .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1985, 19 (09) :804-809
[4]  
GUROL MD, 1989, P 21 MID ATL IND WAS, P282
[5]  
*HACH CO, 1992, WAT AN HDB
[6]   ROLE OF HYDROXYL RADICAL REACTIONS IN OZONATION PROCESSES IN AQUEOUS-SOLUTIONS [J].
HOIGNE, J ;
BADER, H .
WATER RESEARCH, 1976, 10 (05) :377-386
[7]   CHEMICAL-STABILITY AND DECOMPOSITION RATE OF IRON CYANIDE COMPLEXES IN SOIL SOLUTIONS [J].
MEEUSSEN, JCL ;
KEIZER, MG ;
DEHAAN, FAM .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1992, 26 (03) :511-516
[8]   SPECTROPHOTOMETRIC DETERMINATION OF TOTAL CYANIDE, IRON-CYANIDE COMPLEXES, FREE CYANIDE AND THIOCYANATE IN WATER BY A CONTINUOUS-FLOW SYSTEM [J].
MEEUSSEN, JCL ;
TEMMINGHOFF, EJM ;
KEIZER, MG ;
NOVOZAMSKY, I .
ANALYST, 1989, 114 (08) :959-963
[9]   PHOTOCHEMISTRY OF CO-ORDINATION COMPOUNDS .15. CYANIDE COMPLEXES [J].
MOGGI, L ;
BOLLETTA, F ;
BALZANI, V ;
SCANDOLA, F .
JOURNAL OF INORGANIC & NUCLEAR CHEMISTRY, 1966, 28 (11) :2589-&
[10]  
NUTT SG, 1984, P 38 PURD IND WAST C, P357