Ahn I S, Lion L W, Shuler M L
School of Chemical Engineering, Cornell University, Ithaca, New York.
Biotechnol Bioeng. 1996 Jul 5;51(1):1-14. doi: 10.1002/(SICI)1097-0290(19960705)51:1<1::AID-BIT1>3.0.CO;2-I.
A mathematical model to describe polynuclear aromatic hydrocarbon (PAH) desorption, transport, and biodegradation in saturated soil was constructed by describing kinetics at a microscopic level and incorporating this description into macroscale transport equations. This approach is novel in that the macroscale predictions are made independently from a knowledge of microscale kinetics and macroscopic fluid dynamics and no adjustable parameters are used to fit the macroscopic response. It was assumed that soil organic matter, the principal site of PAH sorption, was composed of a continuum of compartments with a gamma distribution of desorption rate coefficients. The mass transport of substrates and microorganisms in a mesopore was described by diffusion and that in a macropore by one-dimensional advection and dispersion. Naphthalene was considered as a test PAH compound for initial model simulations. Three mechanisms of naphthalene biodegradation were considered: growth-associated degradation as a carbon and energy source for microbial growth; degradation for maintenance energy; and growth-independent degradation. The Haldane modification of the Monod equation was used to describe microbial growth rates and to account for possible growth inhibition by naphthalene. Multisubstrate interactions were considered and described with a noninteractive model for specific growth rates. The sensitivity of selected model parameters was analyzed under conditions when naphthalene was the sole growth-rate-limiting substrate. The time necessary to achieve a specific degree of naphthalene biodegradation was found to be proportional to the initial concentration of naphthalene in soil organic matter. The biodegradation rate of naphthalene increased when the sorption equilibrium constant of naphthalene was reduced. The presence of an alternative carbon source inhibited naphthalene biodegradation in spite of the calculated increase in biomass. (c) 1996 John Wiley & Sons, Inc.
通过在微观层面描述动力学并将其纳入宏观传输方程,构建了一个描述多环芳烃(PAH)在饱和土壤中解吸、传输和生物降解的数学模型。这种方法的新颖之处在于,宏观预测是独立于微观动力学知识和宏观流体动力学做出的,并且不使用可调参数来拟合宏观响应。假设土壤有机质作为PAH吸附的主要位点,由具有解吸速率系数伽马分布的连续隔室组成。中孔隙中底物和微生物的质量传输通过扩散描述,大孔隙中的质量传输通过一维平流和弥散描述。萘被视为初始模型模拟的测试PAH化合物。考虑了萘生物降解的三种机制:作为微生物生长的碳和能源的生长相关降解;维持能量的降解;以及生长非依赖降解。使用莫诺德方程的霍尔丹修正来描述微生物生长速率,并考虑萘可能的生长抑制作用。考虑了多底物相互作用并用特定生长速率的非相互作用模型进行描述。在萘是唯一生长速率限制底物的条件下,分析了选定模型参数的敏感性。发现实现特定程度萘生物降解所需的时间与土壤有机质中萘的初始浓度成正比。当萘的吸附平衡常数降低时,萘的生物降解速率增加。尽管计算得出生物量增加,但替代碳源的存在抑制了萘的生物降解。(c)1996约翰威立国际出版公司