2010•Environmental Science & TechnologyRequires access

Immobilization and Degradation Perpormance of Efficient Phenol-degrading Bacteria Bacillus sp.JY01

Yuan Li

Open publisher page 0 citations

Abstract

One strain of phenol-degrading Bacillus sp.JY01 was immobilized in sodium alginate.Optimal preparation condition of the strain immobilization was ascertained by the cross-test experiments.The phenol-degrading performance of the immobilized cells and free cells were studied and compared.Results indicated that sodium alginate 's mass fraction was 3% and the volume ratio for bacterial:sodium alginate aqueous solution was 4:30,CaCl2 content was 3%,calsifying time was 8h and the best temperature of degrading phenol was 32℃ ,the optimal pH value range was 7.0 ~7.5.Under this condition,immobilized microorganism can degradate phenol solution with concentration of 1300mg/L efficiently.After immobilized cells were recycled 8 times phenol degradation rate still reached 96.8% .Results showed that the degradation performance of immobilized cells was apparently superior to that of free cells.This experiment offered a comparatively reliable parameter for the phenolic effluent biological treatment by this bacterial.

About this research paper

What this paper is about

One strain of phenol-degrading Bacillus sp.JY01 was immobilized in sodium alginate.Optimal preparation condition of the strain immobilization was ascertained by the cross-test experiments.The phenol-degrading performance of the immobilized cells and free cells were studied and compared.Results indicated that sodium alginate 's mass fraction was 3% and the volume ratio for bacterial:sodium alginate aqueous solution was 4:30,CaCl2 content was 3%,calsifying time was 8h and the best temperature of degrading phenol was 32℃ ,the optimal pH value range was 7.0 ~7.5.Under this condition,immobilized microorganism can degradate phenol solution with concentration of 1300mg/L efficiently.After immobilized cells were recycled 8 times phenol degradation rate still reached 96.8% .Results showed that the degradation performance of immobilized cells was apparently superior to that of free cells.This experiment offered a comparatively reliable parameter for the phenolic effluent biological treatment by this bacterial.

Why it matters

A significance statement is not available in the OpenAlex record.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

One strain of phenol-degrading Bacillus sp.JY01 was immobilized in sodium alginate.Optimal preparation condition of the strain immobilization was ascertained by the cross-test experiments.The phenol-degrading performance of the immobilized cells and free cells were studied and compared.Results indicated that sodium alginate 's mass fraction was 3% and the volume ratio for bacterial:sodium alginate aqueous solution was 4:30,CaCl2 content was 3%,calsifying time was 8h and the best temperature of degrading phenol was 32℃ ,the optimal pH value range was 7.0 ~7.5.Under this condition,immobilized microorganism can degradate phenol solution with concentration of 1300mg/L efficiently.After immobilized cells were recycled 8 times phenol degradation rate still reached 96.8% .Results showed that the degradation performance of immobilized cells was apparently superior to that of free cells.This experiment offered a comparatively reliable parameter for the phenolic effluent biological treatment by this bacterial.

Key concepts: Phenol, Effluent, Chemistry, Degradation (telecommunications), Sodium alginate, Bacteria, Biodegradation, Sodium

Related papers

Back to paper searchBrowse research topicsOriginal source
Immobilization and Degradation Perpormance of Efficient Phenol-degrading Bacteria Bacillus sp.JY01 — Research Paper | ScholarLens