<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Hsu JS</submitter><funding>Ministry of science and technology, Taiwan</funding><pagination>402</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8877889</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>10(2)</volume><pubmed_abstract>A novel chitosan immobilization technique that entraps photocatalyst and microbes was developed and applied to decompose decabromodiphenyl ether (BDE-209) in a clay slurry microcosm. The optimized conditions for immobilization were obtained by mixing 1.2% (w/v) chitosan dissolved in 1% (v/v) acetic acid with nano-TiO2 particles and the BDE-209-degrading bacterial mixed culture. This aqueous mixture was injected into 1% (w/v) water solution containing sodium tripolyphosphate to form spherical immobilized beads. The surface of the immobilized beads was reinforced by 0.25% (v/v) glutaraldehyde cross-linking. These beads had enough mechanical strength during BDE-209 degradation to maintain their shape in the system at a stirring rate of 200-rpm, while undergoing continuous 365 nm UVA irradiati</pubmed_abstract><journal>Microorganisms</journal><pubmed_title>Degradation of Decabromodiphenyl Ether in an Aerobic Clay Slurry Microcosm Using a Novel Immobilization Technique.</pubmed_title><pmcid>PMC8877889</pmcid><funding_grant_id>MOST108-2918-I-031-001, MOST110-2221-E-031-002</funding_grant_id><pubmed_authors>Yu TY</pubmed_authors><pubmed_authors>Jane WN</pubmed_authors><pubmed_authors>Hsu JS</pubmed_authors><pubmed_authors>Chang YT</pubmed_authors><pubmed_authors>Wei DJ</pubmed_authors></additional><is_claimable>false</is_claimable><name>Degradation of Decabromodiphenyl Ether in an Aerobic Clay Slurry Microcosm Using a Novel Immobilization Technique.</name><description>A novel chitosan immobilization technique that entraps photocatalyst and microbes was developed and applied to decompose decabromodiphenyl ether (BDE-209) in a clay slurry microcosm. The optimized conditions for immobilization were obtained by mixing 1.2% (w/v) chitosan dissolved in 1% (v/v) acetic acid with nano-TiO2 particles and the BDE-209-degrading bacterial mixed culture. This aqueous mixture was injected into 1% (w/v) water solution containing sodium tripolyphosphate to form spherical immobilized beads. The surface of the immobilized beads was reinforced by 0.25% (v/v) glutaraldehyde cross-linking. These beads had enough mechanical strength during BDE-209 degradation to maintain their shape in the system at a stirring rate of 200-rpm, while undergoing continuous 365 nm UVA irradiati</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Feb</publication><modification>2025-04-04T14:59:05.803Z</modification><creation>2025-02-19T03:58:57.819Z</creation></dates><accession>S-EPMC8877889</accession><cross_references><pubmed>35208857</pubmed><doi>10.3390/microorganisms10020402</doi></cross_references></HashMap>