دسترسی نامحدود
برای کاربرانی که ثبت نام کرده اند
برای ارتباط با ما می توانید از طریق شماره موبایل زیر از طریق تماس و پیامک با ما در ارتباط باشید
در صورت عدم پاسخ گویی از طریق پیامک با پشتیبان در ارتباط باشید
برای کاربرانی که ثبت نام کرده اند
درصورت عدم همخوانی توضیحات با کتاب
از ساعت 7 صبح تا 10 شب
دسته بندی: فن آوری ویرایش: نویسندگان: William Whyte سری: ISBN (شابک) : 9780471868422, 0471868426 ناشر: Wiley سال نشر: 2001 تعداد صفحات: 312 زبان: English فرمت فایل : PDF (درصورت درخواست کاربر به PDF، EPUB یا AZW3 تبدیل می شود) حجم فایل: 27 مگابایت
در صورت تبدیل فایل کتاب Cleanroom Technology: Fundamentals of Design, Testing and Operation به فرمت های PDF، EPUB، AZW3، MOBI و یا DJVU می توانید به پشتیبان اطلاع دهید تا فایل مورد نظر را تبدیل نمایند.
توجه داشته باشید کتاب فناوری Cleanroom: اصول طراحی ، آزمایش و بهره برداری نسخه زبان اصلی می باشد و کتاب ترجمه شده به فارسی نمی باشد. وبسایت اینترنشنال لایبرری ارائه دهنده کتاب های زبان اصلی می باشد و هیچ گونه کتاب ترجمه شده یا نوشته شده به فارسی را ارائه نمی دهد.
اتاق تمیز یک محیط کنترل شده با آلودگی است و در تولید صنعتی بسیاری از محصولات الکترونیکی، نیمه هادی، نوری، دارویی و پزشکی ضروری است. استفاده از اتاق های تمیز برای تولید طیف وسیعی از محصولات مانند ریزپردازنده ها، پخش کننده های سی دی، لیزرها، داروها و دستگاه های پزشکی همچنان در حال رشد است و بسیاری از شرکت ها برای اولین بار از اتاق های تمیز استفاده می کنند. در عین حال، محصولات فناوری جدید که فقط در اتاق های تمیز تولید می شوند در حال توسعه هستند. این مروری جامع از اصول، طراحی، آزمایش و عملکرد سیستمهای اتاق تمیز، مقدمهای با این فناوری پیشرفته و متخصصان را با ارجاع در دسترس به استانداردهای فعلی به تازهکاران ارائه میدهد. خوانندگان از تجربه 35 ساله نویسنده در تحقیق و توسعه فناوری اتاق تمیز، مشاوره و تدریس بهره خواهند برد. این متن مکمل ساختار و محتوای دوره های اتاق تمیز خود و بسیاری از دوره های داخلی در صنایع الکترونیک و داروسازی است. · مکمل طراحی بسیار موفق Cleanroom، ویرایش دوم و آزمایش و اجرای Cleanroom آتی توسط همان نویسنده · اصول و آخرین استانداردها برای طراحی، اعتبار سنجی، آزمایش و اجرای سیستم های اتاق تمیز را ارائه می دهد که در سطح مقدماتی و متناسب با آن طراحی شده است. الزامات آموزشی دانشمندان و مهندسان تازه وارد در فناوری اتاق تمیز
را برآورده کنید
A cleanroom is a contamination-controlled environment and is essential in the industrial manufacture of many electronic, semiconductor, optical, pharmaceutical and medical products. The use of cleanrooms for the manufacture of a large range of products such as microprocessors, CD players, lasers, pharmaceuticals and medical devices continues to grow and many companies are using cleanrooms for the first time. At the same time, new technology products that can only be produced in cleanrooms are being developed. This comprehensive overview of the fundamentals, design, testing and operation of cleanroom systems provides novices with a introduction to this state-of-the-art technology and professionals with an accessible reference to the current standards. Readers will benifit from the author's 35 years of experience in cleanroom technology R&D, consultancy and teaching. The text is complementary to the structure and content of Whyte's own and many in-house cleanroom courses in the electronics and pharmaceutical industries. В· Complementary to the highly successful Cleanroom Design, Second Edition and the forthcoming Cleanroom Testing and Running by the same author В· Presents the fundamentals and latest standards for the design, validation, testing and running of cleanroom systems Pitched at introductory level and tailored to fulfil the training requirements of scientists and engineers new to cleanroom technology
Content: About the Author. Preface. Acknowledgements. 1 Introduction. 1.1 What is a Cleanroom? 1.2 The Need for Cleanrooms. 1.3 Types of Cleanrooms. 1.4 What is Cleanroom Technology? 2 The History of Cleanrooms. 2.1 The Earliest Years. 2.2 Ventilated Operating Rooms. 2.3 Early Industrial Cleanrooms. 2.4 Unidirectional Airflow Cleanrooms. 3 Cleanroom Classification Standards. 3.1 The History of Standards. 3.2 The Basis of Cleanroom Standards. 3.3 Federal Standard 209. 3.4 ISO Standard 14644-1:1999. 3.5 Pharmaceutical Cleanroom Classification. 3.6 Classification of Cleanrooms with Airborne Chemical Contamination. 3.7 Classification of Cleanrooms with Surface Contamination. 4 Information Sources. 4.1 The International Confederation of Contamination Control Societies (ICCCS). 4.2 The ICEB. 4.3 International Cleanroom Standards. 4.4 Cleanroom Books. 4.5 Recommended Practices and Guides of the Institute of Environmental Sciences and Technology (IEST). 4.6 Cleanroom Journals and Magazines. 4.7 Sources of Pharmaceutical Cleanroom Documents. 4.8 Training Videos/DVDs. 5 Non-unidirectional Airflow and Ancillary Cleanrooms. 5.1 Non-unidirectional Airflow Cleanrooms. 5.2 Ancillary Cleanrooms. 6 Unidirectional Airflow Cleanrooms. 6.1 Types of Unidirectional Cleanrooms. 6.2 Vertical Unidirectional Airflow Cleanrooms. 6.3 Horizontal Unidirectional Airflow Rooms. 6.4 The Application of Unidirectional Airflow. 7 Separative Clean Air Devices and Containment Zones. 7.1 Unidirectional Airflow Devices. 7.2 Mini-environments, Isolators and RABS. 7.3 Containment Zones. 8 Construction and Clean-build. 8.1 Constructional Materials and Methods. 8.2 Outgassing and Electrostatic Properties. 8.3 Clean-build. 9 High Efficiency Air Filtration. 9.1 Air Filters Used in Cleanrooms. 9.2 The Construction of High Efficiency Filters. 9.3 Particle Removal Mechanisms. 9.4 Testing of High Efficiency Filters. 9.5 Scan Testing of High Efficiency Filters. 9.6 Filter Housings for High Efficiency Filters. 9.7 Removal of Airborne Chemical Contamination. 10 Cleanroom Testing and Monitoring. 10.1 Principles of Cleanroom Testing. 10.2 Cleanroom Tests. 10.3 Testing in Relation to Room Type and Occupation State. 10.4 Re-testing to Demonstrate Compliance. 10.5 Monitoring of Cleanrooms. 11 Measurement of Air Quantities and Pressure Differences. 11.1 Air Quantities. 11.2 Differential Pressure Tests. 12 Air Movement Control: Containment, Visualization and Recovery. 12.1 Cleanroom Containment Leak Testing. 12.2 Air Movement Control within a Cleanroom. 12.3 Recovery Test Methods. 12.4 Recovery Rate Requirement in the EU GGMP. 13 Filter Installation Leak Testing. 13.1 The Use of Aerosol Test Challenges. 13.2 Artificial Aerosol Test Challenges. 13.3 Apparatus for Measuring Aerosol Penetration. 13.4 Methods of Testing Filters and Filter Housings. 13.5 Repair of Leaks. 14 Airborne Particle Counts. 14.1 Airborne Particle Counters. 14.2 Continuous Monitoring Apparatus for Airborne Particles. 14.3 Particle Counting in Different Occupancy States. 14.4 Measurement of Particle Concentrations. 14.5 Worked Example of ISO 14644-1 Test Method. 15 Microbial Sampling. 15.1 Microbial Sampling of the Air. 15.2 Microbial Deposition onto Surfaces. 15.3 Microbial Surface Sampling. 15.4 Personnel Sampling. 16 Operating a Cleanroom: Managing the Risk from Contamination. 16.1 Step 1: Identification of Sources and Routes of Contamination. 16.2 Step 2: Risk Assessment and the Control of Sources of Contamination. 16.3 Step 3: Establish an Effective Monitoring Programme. 16.4 Step 4: Verification and Reappraisal of the System. 16.5 Step 5: Documentation. 16.6 Step 6: Staff Training. 17 Cleanroom Disciplines. 17.1 People Allowed into Cleanrooms. 17.2 Personal Items Not Allowed into the Cleanroom. 17.3 Disciplines within the Cleanroom. 17.4 Maintenance and Service Personnel. 18 Entry and Exit of Personnel. 18.1 Prior to Arriving at the Cleanroom. 18.2 Changing into Cleanroom Garments. 18.3 Exit Changing Procedures. 19 Materials, Equipment and Machinery. 19.1 Choice of Materials for use in a Cleanroom. 19.2 Items Supplied from Outside Manufacturing Sources. 19.3 Wrapping and Transportation of Materials. 19.4 Transfer of Items and Small Pieces of Equipment through a Material Transfer Airlock. 19.5 Entry of Heavy Machinery and Bulky Items. 19.6 Transfer of Materials through Hatches and Sterilisers. 20 Cleanroom Clothing. 20.1 Sources and Routes of Inert Airborne Particle Dispersion. 20.2 Routes and Sources of Microbial Dispersion. 20.3 Types of Cleanroom Clothing. 20.4 Processing of Cleanroom Garments and Change Frequency. 20.5 The Effect of Laundering and Wear. 20.6 Testing of Cleanroom Clothing. 20.7 Static Dissipative Properties of Clothing. 21 Cleanroom Masks and Gloves. 21.1 Cleanroom Masks. 21.2 Cleanroom Gloves. 22 Cleaning a Cleanroom. 22.1 Why a Cleanroom must be Cleaned. 22.2 Cleaning Methods and the Physics of Cleaning Surfaces. 22.3 Implements Used to Clean Cleanrooms. 22.4 Liquids Used in Cleaning Cleanrooms. 22.5 How Should a Cleanroom be Cleaned? 22.6 Cleaning Programme. 22.7 Test Methods. Index.