化工学报
化工學報
화공학보
JOURNAL OF CHEMICAL INDUSY AND ENGINEERING (CHINA)
2015年
2期
306-313
,共8页
唐海%沙俊鹏%欧阳龙%仲达%刘桂中
唐海%沙俊鵬%歐暘龍%仲達%劉桂中
당해%사준붕%구양룡%중체%류계중
硫酸根自由基%剩余污泥%强化脱水%氧化破解%响应面优化
硫痠根自由基%剩餘汙泥%彊化脫水%氧化破解%響應麵優化
류산근자유기%잉여오니%강화탈수%양화파해%향응면우화
sulfate radical%excess sludge%dewatering enhancement%oxidation disintegration%response surface method
采用 Fe(Ⅱ)活化过硫酸盐,产生强氧化性硫酸根自由基(SO?4·),以污泥释放的溶解性COD(SCOD)、相对疏水性(RH)和污泥比阻(SRF)为表征,考察了SO?4·氧化破解剩余污泥强化脱水的影响因素,并解析了机理。结果表明:当初始pH为4.5,n(S2O82?)=2.2 mmol·(g VSS)?1,n(Fe2+)=1.32 mmol·(g VSS)?1,常温下反应3 h后,SCOD由66.5 mg·L?1增加到472.3 mg·L?1,RH由26.9%升高到41.1%,SRF由24.9×108 S2·g?1降低至4.5×108 S2·g?1;在此基础上利用响应面法,根据Box-Benhnken中心组合试验设计,以SRF为响应指标,优化条件为pH 4.27, n(S2O82?)=2.6 mmol·(g VSS)?1,n(Fe2+)=1.59 mmol·(g VSS)?1时,SRF为3.8×108 S2·g?1,泥饼含水率为72.7%。镜检发现,破解后污泥变为颗粒碎片状;傅里叶红外光谱显示污泥表面官能团对应的特征吸收峰强度有一定程度的减弱;热重分析表明无明显物理吸附水失重区。证实了在 SO?4·作用下,污泥菌胶团结构破坏,溶胞释放了有机物,使表观疏水性更强,与水结合力明显减弱,脱水性得到了较大提高,有利于污泥减量化应用。
採用 Fe(Ⅱ)活化過硫痠鹽,產生彊氧化性硫痠根自由基(SO?4·),以汙泥釋放的溶解性COD(SCOD)、相對疏水性(RH)和汙泥比阻(SRF)為錶徵,攷察瞭SO?4·氧化破解剩餘汙泥彊化脫水的影響因素,併解析瞭機理。結果錶明:噹初始pH為4.5,n(S2O82?)=2.2 mmol·(g VSS)?1,n(Fe2+)=1.32 mmol·(g VSS)?1,常溫下反應3 h後,SCOD由66.5 mg·L?1增加到472.3 mg·L?1,RH由26.9%升高到41.1%,SRF由24.9×108 S2·g?1降低至4.5×108 S2·g?1;在此基礎上利用響應麵法,根據Box-Benhnken中心組閤試驗設計,以SRF為響應指標,優化條件為pH 4.27, n(S2O82?)=2.6 mmol·(g VSS)?1,n(Fe2+)=1.59 mmol·(g VSS)?1時,SRF為3.8×108 S2·g?1,泥餅含水率為72.7%。鏡檢髮現,破解後汙泥變為顆粒碎片狀;傅裏葉紅外光譜顯示汙泥錶麵官能糰對應的特徵吸收峰彊度有一定程度的減弱;熱重分析錶明無明顯物理吸附水失重區。證實瞭在 SO?4·作用下,汙泥菌膠糰結構破壞,溶胞釋放瞭有機物,使錶觀疏水性更彊,與水結閤力明顯減弱,脫水性得到瞭較大提高,有利于汙泥減量化應用。
채용 Fe(Ⅱ)활화과류산염,산생강양화성류산근자유기(SO?4·),이오니석방적용해성COD(SCOD)、상대소수성(RH)화오니비조(SRF)위표정,고찰료SO?4·양화파해잉여오니강화탈수적영향인소,병해석료궤리。결과표명:당초시pH위4.5,n(S2O82?)=2.2 mmol·(g VSS)?1,n(Fe2+)=1.32 mmol·(g VSS)?1,상온하반응3 h후,SCOD유66.5 mg·L?1증가도472.3 mg·L?1,RH유26.9%승고도41.1%,SRF유24.9×108 S2·g?1강저지4.5×108 S2·g?1;재차기출상이용향응면법,근거Box-Benhnken중심조합시험설계,이SRF위향응지표,우화조건위pH 4.27, n(S2O82?)=2.6 mmol·(g VSS)?1,n(Fe2+)=1.59 mmol·(g VSS)?1시,SRF위3.8×108 S2·g?1,니병함수솔위72.7%。경검발현,파해후오니변위과립쇄편상;부리협홍외광보현시오니표면관능단대응적특정흡수봉강도유일정정도적감약;열중분석표명무명현물리흡부수실중구。증실료재 SO?4·작용하,오니균효단결구파배,용포석방료유궤물,사표관소수성경강,여수결합력명현감약,탈수성득도료교대제고,유리우오니감양화응용。
Released soluble COD (SCOD), relative hydrophobicity (RH), and specific resistance of sludge (SRF) were used to characterize sludge disintegration degree, surface hydrophobicity and dewatering performance. The enhanced dewatering influence factors and mechanism of oxidation disintegration of excess sludge were investigated by oxidative sulfate radical (SO?4·) generated from persulfate activated by Fe(Ⅱ). SCOD increased from 66.5 mg·L?1 to 472.3 mg·L?1, RH increased from 26.9%to 41.1%, SRF decreased from 24.9×108 S2·g?1 to 4.5×108 S2·g?1 after disintegration reaction when pH was 4.5, n(S2O82?) was 2.2 mmol·(g VSS)?1, n(Fe2+)=1.32 mmol · (g VSS)?1 and reaction time was 3 h at room temperature. According to the center combination experimental design of Box-Benhnken based on the response surface method, the optimal results were pH=4.27, n(S2O82?)=2.6 mmol·(g VSS)?1, n(Fe2+)=1.59 mmol·(g VSS)?1, SRF=3.8×108 S2·g?1 and sludge cake moisture content rate = 72.7% when SRF was taken as response. Microscopic observation revealed that floc sludge was disintegrated into smaller particles and debris. FT-IR showed the surface functional group corresponding to the absorption peak intensity of sludge decreased to some extent, and thermogravimetric analysis indicated that physical adsorption combined water loss region disappeared. The above results suggested that under the influence of SO?4·, stable sludge zoogloea structure was destroyed, cell lysis and organic matter was released into the liquid phase, sludge surface was more hydrophobic, water binding capacity decreased and sludge dewatering performance was improved considerably, thus facilitating sludge reduction application.