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Wednesday, August 28, 2013
Sunday, July 4, 2010
A Guide to Safe Material and Chemical Handling (Wiley-Scrivener)
- Wiley-Scrivener
- Number Of Pages: 480
- Publication Date: 2010-03-15
- ISBN-10 / ASIN: 0470625821
- ISBN-13 / EAN: 9780470625828
There have been many volumes written that claim to be the most "comprehensive" compendium or on chemical data. These wieldy volumes are often too big and extraneous to be useful to the practicing engineer. This new volume aims to be the most useful "go to" volume for the working engineer, scientist, or chemist who needs quick answers to daily questions about materials or and doesn't want to go on long searches through voluminous tomes or lengthy internet searches. Covering only the most commonly used chemicals in the most important processes in industry,A Guide to Safe Material and Chemical Handling includes industrial chemicals, such as gases, fuels, and , which are not incorporated in most "comprehensive" on materials and chemical properties. Safety plans and procedures that can be implemented by any engineer or plant manager by following the easy, step-by-step instructions in the book are also provided.
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http://ifile.it/ws80lyq/0470625821.pdf
Sunday, May 30, 2010
Chemstations CHEMCAD 6.1.4.3059

Tuesday, May 25, 2010
Safety Assessment for Chemical Processes by Jorg Steinbach

Saturday, February 13, 2010
Compatibility of Pharmaceutical Solutions and Contact Materials: Safety Assessments of Extractables and Leachables for Pharmaceutical Products
- Publisher: Wiley-Interscience
- Number Of Pages: 379
- Publication Date: 2009-06-02
- ISBN-10 / ASIN: 0470281766
- ISBN-13 / EAN: 9780470281765
Dennis Jenke
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Sunday, November 29, 2009
Pharmaceutical Suspensions: From Formulation Development to Manufacturing
- Publisher: Springer
- Number Of Pages: 323
- Publication Date: 2009-10-16
- ISBN-10 / ASIN: 1441910867
- ISBN-13 / EAN: 9781441910868
The suspension dosage form has long been used for poorly soluble active ingredients for various therapeutic indications. Development of stable dispersions over the shelf life of the drug product continues to be a challenge on many fronts.
A good understanding of fundamentals of disperse systems is essential in the development of a suitable pharmaceutical suspension. The development of suspension dosage form follows a very complicated path. The selection of the proper excipients (surfactants, viscosity imparting agents etc.) is important. The particle size distribution in the finished drug product dosage form is a critical parameter that significantly impacts the bioavailability and pharmacokinetics of the product. Appropriate analytical methodologies and instruments (chromatographs, viscometers, particle size analyzers, etc.) must be utilized to properly characterize the suspension formulation. The development process continues with a successful scale-up of the manufacturing process. Regulatory agencies around the world require clinical trials to establish the safety and efficacy of the drug product. All of this development work should culminate into a regulatory filing in accordance with regulatory guidelines. Pharmaceutical Suspensions, in its organization, follows the development approach used widely in the pharmaceutical industry. The primary focus of this book is on the classical disperse system – poorly soluble active pharmaceutical active dispersed in a suitable vehicle.
After discussing various disperse systems, the theory of disperse systems and commonly used excipients, the remaining chapters in this textbook systematically detail the development of pharmaceutical suspensions, from pre-formulation stage to clinical development, regulatory submission and commercial manufacturing. Additionally, the emerging area of nano-suspensions as applied to pharmaceutical filed is also discussed. Each of the chapters in Pharmaceutical Suspensions was written independently by scientists skilled in their specific areas. Contributing authors represent a cross-sections of scholars from Academic Institutions, Pharmaceutical Industries and Regulatory Agency.
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Monday, November 9, 2009
Wiley Guide to Chemical Incompatibilities, 3rd Edition
- Publisher: Wiley
- Number Of Pages: 1110
- Publication Date: 2009-08-17
- ISBN-10 / ASIN: 0470387637
- ISBN-13 / EAN: 9780470387634
The authoritative resource on dangerous chemical interactions now enlarged, revised, and even more useful.
The term "incompatibilities" describes a wide range of chemical reactions that produce undesirable results in noncontrolled situations: the generation of toxic gases, fire, explosions, corrosive activity, polymerization, ruptured containers, creation of more dangerous compounds, and the like. A portable and easy-to-use reference on reactive substances commonly found in commerce, the Wiley Guide to Chemical Incompatibilities, Third Edition compiles hard-to-find data on over 11,000 chemical compounds, providing chemists, technicians, and engineers a thorough, lightning-quick resource to use during experimental preparation and in the event of an emergency.
More than a revision of the previous edition, this Third Edition has been rewritten and expanded to broaden coverage and improve its usefulness. It contains nearly 9,000 chemical incompatibility profiles and nearly 250 new entries, covering flammability, violent and explosive binary reactions, incompatibilities, and reactions that may result from physical change. Alphabetical organization provides concise incompatibility profiles for thousands of commonly used commercial chemicals, allowing readers to look up a given substance and instantly learn whether it is incompatible with common materials, other chemical substances, structural materials, or personal protective equipment.
New for the Third Edition:
- Chemicals that have the potential to cause disasters
- Chemical formulas and autoignition temperatures
- More flash points, as well as molecular formulas, lower and upper explosive limits, autoignition temperatures, and NFPA®-type (Red) numerical fire codes
- Safety reminders
- All entries keyed by CAS numbers to eliminate possible confusion among synonyms
- Spanish-, French-, and German-language entries for international use
- Revised glossary helps users who may not be chemists with general chemical terms
Pharmaceutical Suspensions: From Formulation Development to Manufacturing
- Publisher: Springer
- Number Of Pages: 323
- Publication Date: 2009-10-16
- ISBN-10 / ASIN: 1441910867
- ISBN-13 / EAN: 9781441910868
The suspension dosage form has long been used for poorly soluble active ingredients for various therapeutic indications. Development of stable dispersions over the shelf life of the drug product continues to be a challenge on many fronts.
A good understanding of fundamentals of disperse systems is essential in the development of a suitable pharmaceutical suspension. The development of suspension dosage form follows a very complicated path. The selection of the proper excipients (surfactants, viscosity imparting agents etc.) is important. The particle size distribution in the finished drug product dosage form is a critical parameter that significantly impacts the bioavailability and pharmacokinetics of the product. Appropriate analytical methodologies and instruments (chromatographs, viscometers, particle size analyzers, etc.) must be utilized to properly characterize the suspension formulation. The development process continues with a successful scale-up of the manufacturing process. Regulatory agencies around the world require clinical trials to establish the safety and efficacy of the drug product. All of this development work should culminate into a regulatory filing in accordance with regulatory guidelines. Pharmaceutical Suspensions, in its organization, follows the development approach used widely in the pharmaceutical industry. The primary focus of this book is on the classical disperse system – poorly soluble active pharmaceutical active dispersed in a suitable vehicle.
After discussing various disperse systems, the theory of disperse systems and commonly used excipients, the remaining chapters in this textbook systematically detail the development of pharmaceutical suspensions, from pre-formulation stage to clinical development, regulatory submission and commercial manufacturing. Additionally, the emerging area of nano-suspensions as applied to pharmaceutical filed is also discussed. Each of the chapters in Pharmaceutical Suspensions was written independently by scientists skilled in their specific areas. Contributing authors represent a cross-sections of scholars from Academic Institutions, Pharmaceutical Industries and Regulatory Agency.
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Wednesday, November 4, 2009
2006 International Fire Code: Softcover Version by International Code Council

http://ebooks4science.blogspot.com/
Enclosure Fire Dynamics (Environmental and Energy Engineering Series) by Bjorn Karlsson and James Quintiere

http://ebooks4science.blogspot.com/
Physical Properties of Hydrocarbons: Volume 1 + Volume 2, Second Edition by Robert W. Gallant
Tuesday, October 6, 2009
Industrial Fire Safety Guidebook
- Publisher: William Andrew
- Number Of Pages: 539
- Publication Date: 1999-01-14
- ISBN-10 / ASIN: 0815514204
- ISBN-13 / EAN: 9780815514206
This reference has been written for emergency response personnel, plant safety specialists, and emergency response coordinators. It has been prepared at a practical level to assist both in training safety personnel and to provide technical information that can assist in responding to a hazard material incident that could lead to a fire hazard situation. Considerable information and technical data are given on petroleum based products since these are among the most widely consumed products, however, the reader will find ample information on other chemicals. Fire situations pose one of the most serious problems in an industrial setting, with the potential loss of lives and property, as well as damage to the environment. Proper response by trained personnel, as well as careful preplanning can minimize the risk and damage caused by fire.
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Handbook of Pharmaceutical Excipients (Rowe, Handbook of Pharmaceutical Excipients)
- Publisher: Pharmaceutical Press
- Number Of Pages: 917
- Publication Date: 2009-07-31
- ISBN-10 / ASIN: 0853697922
- ISBN-13 / EAN: 9780853697923
"The Handbook of Pharmaceutical Excipients" is internationally recognised as the authoritative source of information on pharmaceutical excipients. "The Handbook of Pharmaceutical Excipients" is a comprehensive guide to the uses, properties and safety of pharmaceutical excipients and is an essential reference for those involved in the development, production, control or regulation of pharmaceutical preparations. The handbook collects together essential data on the physical properties of excipients as well as providing information on their safe use and potential toxicity. All monographs are also thoroughly cross-referenced and indexed to allow their identification by chemical, non-proprietary or trade names.
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http://rapidshare.com/files/288283687/0853697922_Pharmaceutical_excipients.rar
Tuesday, September 22, 2009
Dust Explosions in the Process Industries, Third Edition
Monday, September 7, 2009
Building Facade Maintenance, Repair, and Inspection
Friday, August 7, 2009
Rapid Microbiological Methods in the Pharmaceutical Industry
Download:-http://rapidshare.com/files/144839279/trapmicro_meth_pharma_ind.zip
Sunday, August 2, 2009
Quality Systems and Controls for Pharmaceuticals
Saturday, August 1, 2009
Guidelines for Engineering Design for Process Safety
Wiley-AIChE | 1993-09-01 | ISBN: 0816905657 | 608 pages | PDF | 27.9 MB
Inherently safer plants begin with the initial design. Here is where integrity and reliability can be built in at the lowest cost, and with maximum effectiveness. This book focuses on process safety issues in the design of chemical, petrochemical, and hydrocarbon processing facilities. It discusses how to select designs that can prevent or mitigate the release of flammable or toxic materials, which could lead to a fire, explosion, or environmental damage. All engineers on the design team, the process hazard analysis team, and those who make basic decisions on plant design, will benefit from its comprehensive coverage, its organization, and the extensive references to literature, codes, and standards that accompany each chapter DOWNLOAD LINK: rapidshare |