首页> 外文会议>IWA(International Water Association) International Conference on Biofilm Systems; 20030914-18; Cape Town(ZA) >Results from the multi-species Benchmark Problem 3 (BM3) using two-dimensional models
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Results from the multi-species Benchmark Problem 3 (BM3) using two-dimensional models

机译:使用二维模型的多物种基准问题3(BM3)的结果

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In addition to the one-dimensional solutions of a multi-species benchmark problem (BM3) presented earlier (Rittmann et al., 2004), we offer solutions using two-dimensional (2-D) models. Both 2-D models (called here DN and CP) used numerical solutions to BM3 based on a similar mathematical framework of the one-dimensional AQUASIM-built models submitted by Wanner (model W) and Morgenroth (model M1), described in detail elsewhere (Rittmann et al., 2004). The CP model used differential equations to simulate substrate gradients and biomass growth and a particle-based approach to describe biomass division and biofilm growth. The DN model simulated substrate and biomass using a cellular automaton approach. For several conditions stipulated in BM3, the multidimensional models provided very similar results to the 1-D models in terms of bulk substrate concentrations and fluxes into the biofilm. The similarity can be attributed to the definition of BM3, which restricted the problem to a flat biofilm in contact with a completely mixed liquid phase, and therefore, without any salient characteristics to be captured in a multidimensional domain. On the other hand, the models predicted significantly different accumulations of the different types of biomass, likely reflecting differences in the way biomass spread within the biofilm is simulated.
机译:除了较早提出的多物种基准问题(BM3)的一维解决方案(Rittmann et al。,2004)外,我们还提供使用二维(2-D)模型的解决方案。两种2-D模型(在此称为DN和CP)都使用了BM3的数值解决方案,该模型基于Wanner(模型W)和Morgenroth(模型M1)提交的一维AQUASIM建造模型的类似数学框架,在其他地方进行了详细介绍(Rittmann等,2004)。 CP模型使用微分方程来模拟基质梯度和生物量的增长,并使用基于粒子的方法来描述生物量的划分和生物膜的增长。 DN模型使用细胞自动机方法模拟了底物和生物量。对于BM3中规定的几种条件,多维模型在整体底物浓度和进入生物膜的通量方面提供了与1-D模型非常相似的结果。相似性可以归因于BM3的定义,该定义将问题限制在与完全混合的液相接触的平坦生物膜上,因此没有在多维域中捕获的任何显着特征。另一方面,模型预测了不同类型生物质的显着不同积累,这很可能反映了生物质在生物膜内扩散方式的模拟差异。

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