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dc.contributor.authorChen, Xiao
dc.contributor.authorStewart, Philip S.
dc.date.accessioned2018-01-31T20:53:43Z
dc.date.available2018-01-31T20:53:43Z
dc.date.issued1996-01
dc.identifier.citationChen, X. and P.S. Stewart, “Chlorine Penetration into Artificial Biofilm is Limited by a ReactionDiffusion Interaction,” Environmental Science & Technology, 30(6):2078-2083 (1996).en_US
dc.identifier.issn0013-936X
dc.identifier.urihttps://scholarworks.montana.edu/xmlui/handle/1/14264
dc.description.abstractThe retarded penetration of chlorine into artificial biofilms of Pseudomonas aeruginosa entrapped in agarose gel slabs was investigated experimentally and shown to be consistent with an unsteady reaction−diffusion model. A chlorine microelectrode was used to measure transient chlorine concentration profiles in artificial biofilms in a flow cell. While chlorine penetrated relatively quickly into pure agarose films (∼15 min), its penetration into biofilms was greatly retarded when cells were present. The degree of retardation was proportional to the initial cell density in the biofilm. After 3 h of treatment with a flowing chlorine solution, the chlorine concentration at the substratum under a 526 μm thick biofilm containing 14 400 mg L-1 cell mass had only risen to 10% of the bulk solution value. A mathematical model of the transient reaction−diffusion interaction correctly captured the qualitative behavior of experimentally measured chlorine concentration profiles. Parameter values for the simulations were obtained from the literature and from independent investigations of biomass−chlorine reactions using well-mixed suspensions. Kinetic and stoichiometric coefficients for the reactions of agarose and cell mass with chlorine were obtained by fitting a simple first-order (in both reactants) kinetic model to chlorine versus time data. The reaction rate coefficient for chlorine−cell reaction (1.1 × 10-3 L mg-1 s-1) exceeded that of chlorine−agarose reaction (3.7 × 10-6 L mg-1 s-1) by 2 orders of magnitude. The yield coefficient relating the amount of cell mass consumed to the amount of chlorine consumed ranged from 0.6 to 4.3 mg mg-1, depending on the duration of the experiment. This study shows that the reaction rate of chlorine with cellular biomass is fast enough that diffusion of this disinfectant into the biofilm readily becomes rate limiting. This reaction−diffusion interaction affords an excellent explanation for the poor efficacy of chlorine when used against biofilm microorganisms.en_US
dc.titleChlorine penetration into artificial biofilm is limited by a reaction-diffusion interactionen_US
dc.typeArticleen_US
mus.citation.extentfirstpage2078en_US
mus.citation.extentlastpage2083en_US
mus.citation.issue6en_US
mus.citation.journaltitleEnvironmental Science & Technologyen_US
mus.citation.volume30en_US
mus.identifier.categoryEngineering & Computer Scienceen_US
mus.identifier.doi10.1021/es9509184en_US
mus.relation.collegeCollege of Engineeringen_US
mus.relation.departmentCenter for Biofilm Engineering.en_US
mus.relation.departmentChemical & Biological Engineering.en_US
mus.relation.departmentChemical Engineering.en_US
mus.relation.universityMontana State University - Bozemanen_US
mus.relation.researchgroupCenter for Biofilm Engineering.en_US
mus.data.thumbpage3en_US
mus.contributor.orcidStewart, Philip S.|0000-0001-7773-8570en_US


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