厌氧移动床生物膜反应器的性能模拟。

IF 3.5 2区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Yuhang Cai, Joshua P. Boltz, Bruce E. Rittmann
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引用次数: 0

摘要

结合代表微生物和水解酶、一维生物膜和生物反应器转化过程的子模型,模拟厌氧移动床生物膜反应器(AnMBBR)中的有机物发酵和甲烷(CH4)产生。综合模型正确地代表了所有实验观察结果,并确定了当总化学需氧量(TCOD)的体积加载率(VLR)从3.9 kg CODT/m3- 3增加到19.5 kg CODT/m3- 3时,AnMBBR性能如何以及为什么会发生变化的机制。随着TCOD的VLR的增加,TCOD的分式去除率和CH4的产生量下降,部分原因是生物膜厚度的增加,填充了塑料载体内部的保护通道,导致生物膜表面积的减少和传质边界层的增加。此外,TCOD每次VLR ~25天的持续时间太短,无法使生物膜在生物膜厚度方面建立新的准稳定状态。了解生物膜特性和工艺性能如何响应TCOD VLR的增加,可以应用于工程实践,以改进AnMBBR工艺的设计和运行。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Modeling the Performance of an Anaerobic Moving Bed Biofilm Reactor

Modeling the Performance of an Anaerobic Moving Bed Biofilm Reactor

Sub-models representing transformation processes by microorganisms and hydrolases, a one-dimensional (1-D) biofilm, and a bioreactor were integrated to simulate organic-matter fermentation and methane (CH4) production in an anaerobic moving bed biofilm reactor (AnMBBR). The integrated models correctly represented all experimental observations and identified mechanisms underlying how and why AnMBBR performance changed when the volumetric loading rate (VLR) of total chemical oxygen demand (TCOD) increased from 3.9 to 19.5 kg CODT/m3-d. The fractional removal of TCOD and CH4 production decreased as the VLR of TCOD increased, in part, due to an increasing biofilm thickness that filled the protected channels in the interior of the plastic carriers and led to a decrease in biofilm surface area and an increase in the mass-transfer boundary layer. Also, the ~25-day duration for each VLR of TCOD was too brief to allow the biofilm to establish a new quasi-steady state with respect to biofilm thickness. The mechanistic understanding of how biofilm characteristics and process performance respond to increased VLR of TCOD can be applied in engineering practice to improve AnMBBR process design and operation.

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来源期刊
Biotechnology and Bioengineering
Biotechnology and Bioengineering 工程技术-生物工程与应用微生物
CiteScore
7.90
自引率
5.30%
发文量
280
审稿时长
2.1 months
期刊介绍: Biotechnology & Bioengineering publishes Perspectives, Articles, Reviews, Mini-Reviews, and Communications to the Editor that embrace all aspects of biotechnology. These include: -Enzyme systems and their applications, including enzyme reactors, purification, and applied aspects of protein engineering -Animal-cell biotechnology, including media development -Applied aspects of cellular physiology, metabolism, and energetics -Biocatalysis and applied enzymology, including enzyme reactors, protein engineering, and nanobiotechnology -Biothermodynamics -Biofuels, including biomass and renewable resource engineering -Biomaterials, including delivery systems and materials for tissue engineering -Bioprocess engineering, including kinetics and modeling of biological systems, transport phenomena in bioreactors, bioreactor design, monitoring, and control -Biosensors and instrumentation -Computational and systems biology, including bioinformatics and genomic/proteomic studies -Environmental biotechnology, including biofilms, algal systems, and bioremediation -Metabolic and cellular engineering -Plant-cell biotechnology -Spectroscopic and other analytical techniques for biotechnological applications -Synthetic biology -Tissue engineering, stem-cell bioengineering, regenerative medicine, gene therapy and delivery systems The editors will consider papers for publication based on novelty, their immediate or future impact on biotechnological processes, and their contribution to the advancement of biochemical engineering science. Submission of papers dealing with routine aspects of bioprocessing, description of established equipment, and routine applications of established methodologies (e.g., control strategies, modeling, experimental methods) is discouraged. Theoretical papers will be judged based on the novelty of the approach and their potential impact, or on their novel capability to predict and elucidate experimental observations.
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