Crystallization is one of the oldest methods known for recovering pure solids from a solution. The Chinese, for example, were using crystallization to recover common salt from water some 5000 years ago. The perfection and beauty of the crystal which fascinated the early tribes now leads to a product of high purity and attractive appearance

The drying operation is often the final step of a manufacturing process. Indirect drying will be discussed in this section; it is the process of removing liquid by conductive heat transfer. Sometimes drymg is apart ofthe manufacturing process itself, as in the case of seasoning oftimber or in paper making, but generally, the reasons for carrying out a drying operation are:

The purpose ofthis chapter is to review various forms of solids dryers and auxiliary components. It is intended to be a practical guide to dryer selection (as opposed to the theory of drying, which is addressed in various technical manuals referenced in the bibliography). From a microscopic

一、什么是生物技术制药 二、为什么我们要学习生物技术制药？ 三、生物技术制药的主要研究内容 基因工程制药 细胞发酵工程制药 酶工程制药 抗体工程制药 四、生物技术制药的特征 高技术 高投入 长周期 高风险 高收益 五、生物技术发展简史 六、医药生物技术新进展 七、我国的医药生物技术 八、医药生物技术发展展望

Capital cost projects begin when a need is defined that cannot be satisfied in existing facilities. Thus begins the life cycle of a capital project (Fig. 1). Once started, the project will progress through all of the following phases or be canceled. It all starts with the recognition of a need that will require capital plant. In the conceptual phase of the project, multiple approaches will be evaluated and one or more plans will be evaluated for meeting these needs

Copyright 8 1997 by Noyes Publications No part of this book may be reproduced or utilized in any form or by any means, electronic or mechanical, including photocopying, recording or by any information storage and retrieval system, without permission in writing from the Publisher. Library of Congress Catalog Card Number: 96-29055 Printed in the United States

The second edition ofthe Fermentation andBiochemica1 Engineer￾ing Handbook, like the previous edition, is intended to assist the develop￾ment, design and production engineer who is engaged in the fermentation industry. Particular emphasis is give to those unit operations most frequently encountered in the commercial production ofchemicals and pharmaceuticals via fermentation

Common, everyday water is a major consideration in a pharmaceu￾tical plant. The final product or any of its intermediate materials can only be as contaminant-free as the water available at that stage. Water may be an ingredient or used principally to wash and rinse product contact components and equipment. Water is also used to humidiethe air, to generate clean steam for sterilization, to cool or heat, as a solvent, for drinking and sanitary uses, etc. To better control this critical media

Cross-flow filtration (CFF) also known as tangential flow filtration is not of recent origin. It began with the development of reverse osmosis (RO) more than three decades ago. Industrial RO processes include desalting of sea water and brackish water, and recovery and purification of some fermentation products. The cross-flow membrane filtration technique was next applied to the concentration and fractionation ofmacromolecules commonly recognized

2.1 The Microbiological Laboratories Isolation of organisms for new products normally does not occur in laboratories associated with production cultures, however, production (mi￾crobiological) laboratories frequently do mutation and isolation work to produce strains with higher yields, to suppress a by-product, to reduce the formation of a surfactant, to change the physical properties of the broth to facilitate the product recovery