中国有色金属学报
中國有色金屬學報
중국유색금속학보
THE CHINESE JOURNAL OF NONFERROUS METALS
2015年
6期
1694-1704
,共11页
李天国%占强%徐晓军%凤世林%李昊%刘树丽%武英魁
李天國%佔彊%徐曉軍%鳳世林%李昊%劉樹麗%武英魁
리천국%점강%서효군%봉세림%리호%류수려%무영괴
浮选废水%铅%苯胺黑药%脉冲电催化%内电解%流化床
浮選廢水%鉛%苯胺黑藥%脈遲電催化%內電解%流化床
부선폐수%연%분알흑약%맥충전최화%내전해%류화상
flotation wastewater%lead%dianilino dithiophosphoric acid%pulsed electro-catalysis%internal micro-electrolysis%fluidized bed
采用脉冲电催化内电解流化床技术同时去除浮选废水中的Pb2+和苯胺黑药,运用序批试验和SEM、XPS等分析研究影响污染物去除的工艺条件、脉冲电催化效应、Pb2+和苯胺黑药的去除或降解机制。结果表明:当pH为4、电流密度为20 mA/cm2、脉冲周期为2 s、停留时间为90 min时,Pb2+和苯胺黑药的去除率分别为99.80%和78.83%,BOD5/CODCr值由0.15上升至0.41。该技术能较好地同时去除浮选废水中的Pb2+和苯胺黑药,显著提高废水的可生化性。Pb2+和苯胺黑药的去除得益于脉冲电催化内电解体系下的氧化还原反应、电沉积和高聚合度铁氢氧化物的絮凝沉淀作用等;苯胺黑药在新生态 Fe2+、[H]、H2O2、?OH 等活性物质的作用下先后脱除二硫代磷酸基、脱氨基、苯环开环断裂而被降解为有机小分子和无机物。
採用脈遲電催化內電解流化床技術同時去除浮選廢水中的Pb2+和苯胺黑藥,運用序批試驗和SEM、XPS等分析研究影響汙染物去除的工藝條件、脈遲電催化效應、Pb2+和苯胺黑藥的去除或降解機製。結果錶明:噹pH為4、電流密度為20 mA/cm2、脈遲週期為2 s、停留時間為90 min時,Pb2+和苯胺黑藥的去除率分彆為99.80%和78.83%,BOD5/CODCr值由0.15上升至0.41。該技術能較好地同時去除浮選廢水中的Pb2+和苯胺黑藥,顯著提高廢水的可生化性。Pb2+和苯胺黑藥的去除得益于脈遲電催化內電解體繫下的氧化還原反應、電沉積和高聚閤度鐵氫氧化物的絮凝沉澱作用等;苯胺黑藥在新生態 Fe2+、[H]、H2O2、?OH 等活性物質的作用下先後脫除二硫代燐痠基、脫氨基、苯環開環斷裂而被降解為有機小分子和無機物。
채용맥충전최화내전해류화상기술동시거제부선폐수중적Pb2+화분알흑약,운용서비시험화SEM、XPS등분석연구영향오염물거제적공예조건、맥충전최화효응、Pb2+화분알흑약적거제혹강해궤제。결과표명:당pH위4、전류밀도위20 mA/cm2、맥충주기위2 s、정류시간위90 min시,Pb2+화분알흑약적거제솔분별위99.80%화78.83%,BOD5/CODCr치유0.15상승지0.41。해기술능교호지동시거제부선폐수중적Pb2+화분알흑약,현저제고폐수적가생화성。Pb2+화분알흑약적거제득익우맥충전최화내전해체계하적양화환원반응、전침적화고취합도철경양화물적서응침정작용등;분알흑약재신생태 Fe2+、[H]、H2O2、?OH 등활성물질적작용하선후탈제이류대린산기、탈안기、분배개배단렬이피강해위유궤소분자화무궤물。
Pulsed electro-catalytic internal micro-electrolysis fluidized bed (PEIMEF) was used for simultaneous removal of Pb2+ and dianilino dithiophosphoric acid (DDA) from flotation wastewater. Sequencing batch tests and SEM, XPS were conducted to investigate the process conditions, the effect of pulsed electro-catalytic and removal mechanism. The results show that the removal efficiency of Pb2+ and DDA are 99.80% and 78.83%, respectively, and BOD5/CODCr increases to 0.41 from 0.15 at pH of 4, current density of 20 mA/cm2, pulse time of 2 s and hydraulic retention time of 90 min. PEIMEF can removes Pb2+and DDA well, and improve the biodegradability significantly. The removal of Pb2+and DDA is due to the redox reaction, electro-deposition and flocculation precipitation of iron hydroxide of high degree of polymerization under the function of PEIMEF. The degradation of DDA to small organic molecule and inorganic substance may be attributed to the repture of dithiophosphate groups, deamination and ring opening of benzene ring successively by the catalytic redox of the generated active substances of Fe2+, [H], H2O2,?OH.