粒子群优化与遗传算法在蛋白质生产多产品批量装置设计中的比较

Y. Hamzaoui, J. Arellano
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引用次数: 1

摘要

制药研究人员和生物技术公司致力于开发药物,如:治疗蛋白质,人胰岛素,肝炎疫苗,食品级蛋白质,凝乳酶洗涤酶,以及低温蛋白酶。这可以让患者活得更长、更健康、更有成效。然而,近年来,人们对化学、食品和制药工业中批处理设计的系统方法的发展越来越感兴趣。基本上,批处理装置由以不连续方式运行的物品组成,其中每个批处理然后访问固定数量的设备物品,这是给定合成顺序(即生产配方)的要求。在批量工艺设计的文献中,许多工作都是基于将批量大小与设备尺寸线性相关的表达式。1-10每个阶段所需的并联设备单元的体积和尺寸的数量有待确定。然而,间歇式工厂的设计需要考虑设备的使用方式。然而,你看它的多产品批次化学工艺的优化设计涉及到每个产品的生产要求和所有产品的总生产时间已被考虑。确定各阶段并联设备单元的数量和大小以及中间存储的位置和大小,以使投资成本最小化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comparison of particle swarm optimization and genetic algorithm for multiproduct batch plant design of protein production
Pharmaceutical researchers and biotechnology companies are devoted to developing medicines, such as: therapeutic proteins, human insulin, vaccines for hepatitis, food grade protein, chymosin detergent enzyme, and cryophilic protease. This allows patients to live longer, heathier, and more productive. However, in recent years, there has been an increased interest development of systematic method for the design of batch process in chemicals, food products, and pharmaceutical industries. Basically, batch plants are composed of items operating in a discontinuous way, where each batch then visits a fixed number of equipment items, as required by a given synthesis sequence so called production recipe. Many works in the literature on batch process design are based on expressions that relate the batch sizes linearly with the equipment sizes.1–10 The number required of volume and size of parallel equipment units in each stage is to be determined. Nevertheless, the design of batch plants requires involving how equipment may be utilized. However you look at it the optimal design of a multiproduct batch chemical process involves the production requirement of each product and the total production time available for all products has been considered. The number and size of parallel equipment units in each stage as well as the location and size of intermediate storage are to be determined in order to minimize the investment cost.
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