北京化工大学学报(自然科学版)
北京化工大學學報(自然科學版)
북경화공대학학보(자연과학판)
JOURNAL OF BEIJING UNIVERSITY OF CHEMICAL TECHNOLOGY(NATURAL SCIENCE EDITION)
2010年
3期
35-40
,共6页
刘佳%陈咏梅%李天玉%宋冠军%万平玉
劉佳%陳詠梅%李天玉%宋冠軍%萬平玉
류가%진영매%리천옥%송관군%만평옥
海绵铁%镍盐溶液活化%三氯乙酸%降解
海綿鐵%鎳鹽溶液活化%三氯乙痠%降解
해면철%얼염용액활화%삼록을산%강해
sponge iron%activated by nickel salt%TCAA%degradation
海绵铁经酸浸活化处理或外加镍盐溶液活化处理,可以显著提高其降解水中三氯乙酸(TCAA)的反应速率.实验结果表明,海绵铁降解TCAA反应属于一级反应,酸浸活化和镍盐活化处理都没有改变海绵铁降解三氯乙酸的反应级数,对反应活化能的影响也不大,但都可以显著提高其表观反应速率常数Kobs,经酸浸处理和经镍盐活化处理后海绵铁降解TCAA表观反应速率常数分别提高了3倍和8倍.此外,减小海绵铁粒径,提高单位水体海绵铁用量(mFe/VTCAA)也有利于提高海绵铁对三氯乙酸的降解速率.对于20℃,海绵铁用量为mFe/VTCAA=50g/L时,经镍盐活化处理的海绵铁降解TCAA表观反应速率常数Kobs可达到0.855h-1.
海綿鐵經痠浸活化處理或外加鎳鹽溶液活化處理,可以顯著提高其降解水中三氯乙痠(TCAA)的反應速率.實驗結果錶明,海綿鐵降解TCAA反應屬于一級反應,痠浸活化和鎳鹽活化處理都沒有改變海綿鐵降解三氯乙痠的反應級數,對反應活化能的影響也不大,但都可以顯著提高其錶觀反應速率常數Kobs,經痠浸處理和經鎳鹽活化處理後海綿鐵降解TCAA錶觀反應速率常數分彆提高瞭3倍和8倍.此外,減小海綿鐵粒徑,提高單位水體海綿鐵用量(mFe/VTCAA)也有利于提高海綿鐵對三氯乙痠的降解速率.對于20℃,海綿鐵用量為mFe/VTCAA=50g/L時,經鎳鹽活化處理的海綿鐵降解TCAA錶觀反應速率常數Kobs可達到0.855h-1.
해면철경산침활화처리혹외가얼염용액활화처리,가이현저제고기강해수중삼록을산(TCAA)적반응속솔.실험결과표명,해면철강해TCAA반응속우일급반응,산침활화화얼염활화처리도몰유개변해면철강해삼록을산적반응급수,대반응활화능적영향야불대,단도가이현저제고기표관반응속솔상수Kobs,경산침처리화경얼염활화처리후해면철강해TCAA표관반응속솔상수분별제고료3배화8배.차외,감소해면철립경,제고단위수체해면철용량(mFe/VTCAA)야유리우제고해면철대삼록을산적강해속솔.대우20℃,해면철용량위mFe/VTCAA=50g/L시,경얼염활화처리적해면철강해TCAA표관반응속솔상수Kobs가체도0.855h-1.
When sponge iron was activated by immersion in acid or nickel salt solutions,its activity for the degradation of trichloroacetic acid(TCAA)in water was significantly increased.The experimental results showed that the degradation of TCAA by sponge iron is a first order reaction,and being activated by immersion in acid or nickel salts neither changed the order of the degradation reaction nor greatly affected the activation energy,but did significandy increase the apparent rate constant of the reaction,Kobs,by factors of three and eight,respectively.Moreover,a decrease in the radius of the sponge iron and an increase in the amount of sponge iron acting on a fixed volnine of TCAA(mFe/VTCAA)both resulted in an increase in the degradation rate.The apparent rate constant of the degradation of TCAA by sponge iron activated by nickel salts reached 0.855 h-1 when the reaction was carried out at 20 ℃ with mFe/VTCAA equal to 50g/L.