Phenol removal through combined biological and enzymatic treatments

被引:63
作者
Bevilaqua, JV
Cammarota, MC
Freire, DMG
Sant-Anna, GL
机构
[1] Univ Fed Rio de Janeiro, Inst Chem, Ctr Tecnol, BR-21945900 Rio De Janeiro, Brazil
[2] Univ Fed Rio de Janeiro, Sch Chem, Rio De Janeiro, Brazil
[3] Univ Fed Rio de Janeiro, COPPE, Chem Engn Program, BR-21945 Rio De Janeiro, Brazil
关键词
tyrosinase; phenol removal; biological treatment;
D O I
10.1590/S0104-66322002000200010
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
This work studies the use of biological and combined biological/enzymatic treatments in phenol degradation. The systems studied were conventional batch aerobic biological followed or preceded by enzymatic treatment. Tyrosinase extracted from the mushroom Agaricus bispora was employed. Biological treatment efficiently degraded effluents containing up to 420 mg.L-1 of phenol, removing 97% of the COD and 99% of the phenol in 48-hour batches. Alterations in phenol concentration intake reduced treatment efficiency significantly. Enzymatic polishing of biotreated effluent removed up to 75% of the remaining phenol in a four-hour reaction with 46 U.mL(-1) of tyrosinase and 50 mg.L-1 of chitosan (used as coagulant).. Enzymatic pretreatment with 20 U.mL-1 of tyrosinase reduced the phenol concentration by 25% after 2 hours of reaction, although initial COD increased up to 58%. The subsequent biological treatment of that enzymatic pretreated effluent reduced COD to 151 mgO(2).L-1 and phenol concentration to 1 mg.L-1 in 24-hours batches.
引用
收藏
页码:151 / 158
页数:8
相关论文
共 12 条
[1]  
*APHA, 1992, STAND METH EX WAT WA
[2]   DEPHENOLIZATION OF INDUSTRIAL WASTEWATERS CATALYZED BY POLYPHENOL OXIDASE [J].
ATLOW, SC ;
BONADONNAAPARO, L ;
KLIBANOV, AM .
BIOTECHNOLOGY AND BIOENGINEERING, 1984, 26 (06) :599-603
[3]  
BEVILAQUA JV, 2000, THESIS UFRJ RIO DE J
[4]  
DUCKWORTH HW, 1970, J BIOL CHEM, V245, P1613
[5]  
FLURKEY WH, 1991, J FOOD SCI, P5693
[6]  
GANGIDOUST H, 1996, WAT SCI TECH, V34, P151
[7]  
Karam J, 1997, J CHEM TECHNOL BIOT, V69, P141, DOI 10.1002/(SICI)1097-4660(199706)69:2&lt
[8]  
141::AID-JCTB694&gt
[9]  
3.0.CO
[10]  
2-U