Cell immobilization technique for biotrickle filtering of isopropyl alcohol waste vapor generated by high-technology industries

Shen Long Tsai, Chi Wen Lin*, Chih Hung Wu, Baoping Xin

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

9 Citations (Scopus)

Abstract

BACKGROUND: A bench-scale biotrickling filter coupled with Pseudomonas citronellolis YAIP521-immobilized polyvinyl alcohol (PVA)/alginate beads was developed for kinetic analysis of microbial removal of isopropyl alcohol (IPA), an organic solvent widely used for fabricating wafers and printed circuit boards. RESULTS: Response surface methodology (RSM) showed that the optimal ratio of PVA to alginate was 7.5 g to 0.8 g. More than 95% of IPA removal could be achieved at an inlet concentration of 220 ± 34 ppm (w/w) under short residency time. System stability decreased under high IPA concentration and intermittent shock-loading conditions but increased when using cell-immobilized beads because the buffer effect limited the adverse impacts of high IPA concentrations on microorganisms, and the system gradually stabilized with IPA removal efficiency as high as 95%. Nevertheless, qPCR indicated that intermittent shock-loading decreased the biomass in the beads. CONCLUSION: The experimental results showed that the biotrickling filter system developed effectively diminishes the inhibitory effects of elevated IPA concentration on microbial growth, thereby solving the problem of high IPA loading often encountered in the electronic high-tech industries. The design of the system along with the population dynamics and reaction kinetics provide superior information to ensure the success of the biotrickling filter system.

Original languageEnglish
Pages (from-to)364-371
Number of pages8
JournalJournal of Chemical Technology and Biotechnology
Volume88
Issue number3
DOIs
Publication statusPublished - Mar 2013

Keywords

  • Biotrickling filter
  • Cell-immobilized beads
  • Isopropyl alcohol (IPA)
  • Kinetics
  • Real-time PCR

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