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Chemical Hazards in the Workplace. Measurement and Control PDF

597 Pages·1981·10.056 MB·English
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1 0 0 w 9.f 4 1 0 1- 8 9 1 Chemical Hazards k- b 1/ 2 0 1 0. in the Workplace 1 oi: d 1 | 8 9 1 2, pril A e: at D n o ati c bli u P 1 0 0 w 9.f 4 1 0 1- 8 9 1 k- b 1/ 2 0 1 0. 1 oi: d 1 | 8 9 1 2, pril A e: at D n o ati c bli u P Chemical Hazards in the Workplace Measurement and Control Gangadhar Choudhary, EDITOR National Institute for Occupational Safety and Health 1 0 0 w 9.f 4 1 0 1- 98 Based on a symposium 1 k- b 21/ sponsored by the Division of 0 1 0. 1 oi: Chemical Health and Safety at the d 1 | 8 19 Second Chemical Congress of the 2, April North American Continent e: at D n (180th ACS National Meeting), o ati c bli Las Vegas, Nevada, u P August 25-28, 1980. ACS SYMPOSIUM SERIES 149 AMERICAN CHEMICAL SOCIETY WASHINGTON, D. C. 1981 Library of Congress CIP Data Chemical hazards in the workplace. (ACS symposium series; 149) "Based on a symposium sponsored by the Division of Chemical Health and Safety at the Second Chemical Congress of the North American Continent (180th 1 0 ACS National Meeting), Las Vegas, Nevada, August 0 w 25-28, 1980." 9.f 4 Includes bibliographies and index. 1 0 1- 1. Industrial toxicology—Congresses. 2. Industrial 8 hygiene—Congresses. 3. Environmental monitoring— 9 1 Congresses. 4. Work environment—Congresses. bk- I. Choudhary, Gangadhar, 1935- . II. American 1/ Chemical Society. Division of Chemical Health and 2 0 Safety. III. Chemical Congress of the North American 1 0. Continent (2nd: 1980: Las Vegas, Nev.) IV. Series. 1 oi: RA1229.C46 615.9Ό2 81-130 d ISBN 0-8412-0608-2 ACSMC8 149 1-628 1981 1 | AACR2 8 9 1 2, pril A e: Copyright © 1981 at D American Chemical Society n o ati All Rights Reserved. The appearance of the code at the bottom of the first page of each c article in this volume indicates the copyright owner's consent that reprographic copies of bli the article may be made for personal or internal use or for the personal or internal use of u P specific clients. This consent is given on the condition, however, that the copier pay the stated per copy fee through the Copyright Clearance Center, Inc. for copying beyond that permitted by Sections 107 or 108 of the U.S. Copyright Law. This consent does not extend to copying or transmission by any means—graphic or electronic—for any other purpose, such as for general distribution, for advertising or promotional purposes, for creating new collective work, for resale, or for information storage and retrieval systems. The citation of trade names and/or names of manufacturers in this publication is not to be construed as an endorsement or as approval by ACS of the commercial products or services referenced herein; nor should the mere reference herein to any drawing, specification, chemical process, or other data be regarded as a license or as a conveyance of any right or permission, to the holder, reader, or any other person or corporation, to manufacture, repro­ duce, use, or sell any patented invention or copyrighted work that may in any way be related thereto. PRINTED IN THE UNITED STATES OF AMERICA ACS Symposium Series M. Joan Comstock, Series Editor 1 0 0 Advisory Board w 9.f 4 01 David L. Allara James P. Lodge 1- 8 9 1 Kenneth B. Bischoff Marvin Margoshes k- b 1/ 02 Donald D. Dollberg Leon Petrakis 1 0. 1 oi: Robert E. Feeney Theodore Provder d 1 | 8 Jack Halpern F. Sherwood Rowland 9 1 2, pril Brian M. Harney Dennis Schuetzle A ate: W. Jeffrey Howe Davis L. Temple, Jr. D n atio James D. Idol, Jr. Gunter Zweig c bli u P FOREWORD The ACS SYMPOSIUM SERIES was founded in 1974 to provide a medium for publishing symposia quickly in book form. The format of the Series parallels that of the continuing ADVANCES IN CHEMISTRY SERIES except that in order to save time the papers are not typeset but are reproduced as they are sub mitted by the authors in camera-ready form. Papers are re viewed under the supervision of the Editors with the assistance 1 0 0 of the Series Advisory Board and are selected to maintain the w 9.f integrity of the symposia; however, verbatim reproductions of 4 01 previously published papers are not accepted. Both reviews 1- 8 and reports of research are acceptable since symposia may 9 1 k- embrace both types of presentation. b 1/ 2 0 1 0. 1 oi: d 1 | 8 9 1 2, pril A e: at D n o ati c bli u P PREFACE The workplace environment is a significant part of the total ecological system. Since it can be measured, some control over it can be achieved, and improvements in the control technologies in the workplace can be made. Because of the rapidly growing production of complex chemical substances and the use of these in modern living during the past three decades, the existence of chemical hazards in workplaces in relation to worker health and safety has become the subject of great concern. Although the industrial hygiene considerations and the federal govern ment involvement in worker health and safety in the United States began 1 0 0 a long time ago, concerted effort and increased attention toward this work- pr 9. related problem—either by government or by industry—did not become 4 01 possible until about ten years ago when two sister agencies of the govern 1- 8 ment were created, namely, the Occupational Safety and Health Adminis 9 1 k- tration (OSHA), which is part of the Department of Labor, and the b 1/ National Institute for Occupational Safety and Health (NIOSH), which is 2 0 1 part of the Department of Health and Human Services. The functions of 0. oi: 1 these agencies are to clean up the workplace environment and to protect d workers' health through worker and industry participation, recognition of 1 | 8 potential hazards, and conduction of on-site evaluations. The fulfillment of 9 1 2, these responsibilities requires the development of new measurement and pril control methods as well as improving the existing technology. A e: To achieve meaningful health hazard evaluations and control tech Dat nologies for the workplace environment, knowledge of correct measurement on and monitoring techniques is necessary. The increased number and com cati plexity of chemical species in workplaces has 'made the occupational ubli environment intricate in nature. Careful measurements are required for P any meaningful controls. Therefore, analytical chemists and industrial hygienists working in the occupational health field face a great challenge in measuring and evaluating the workplace environment. New problems are encountered and solutions are sought on a continuing basis. For instance, the work atmosphere could contain various gases and vapors, aerosols, particulates, vapor-particulate mixtures at various temperatures, humidities, and concentrations to which workers may be exposed. Sam pling and analytical methods for the substances must be available before any measurement and control efforts are made to meet their health and xi safety threatening challenges. In addition, quality control and compliance statistics must be maintained for any meaningful efforts in this regard. The symposium upon which this book is based was designed to present a current perspective on the measurement and control of chemical hazards in the workplace and to encourage an exchange of ideas among specialists in related areas. This symposium presented both the state-of-the-art and future directions of monitoring and measurement procedures for the occu pational environment. Specific topics included: new analytical techniques and methods development; occupational environmental monitoring and control technology (including medical monitoring and analysis); and quality assurance and requirements of compliance statistics. The authors represent an excellent cross section of the current knowl edge in the field of the measurement and control of the occupational environment. The chapters are organized into sections (based on the logical categorization developed for the symposium) on methodology, 1 monitoring and control, special toxicants, quality assurance, and new 0 pr0 technologies. I hope that this book will be a source of useful information 49. to those working in the field, and also a valuable contribution to the 1 1-0 literature. 8 9 I wish to acknowledge, with sincere appreciation, the contributions 1 k- of the authors and reviewers; without their time-consuming efforts this b 21/ work would not have been possible. I would also like to thank the ACS 0 1 0. Division of Chemical Health and Safety for inviting me to organize the 1 oi: symposium, and the National Institute for Occupational Safety and Health d 1 | for supporting my participation in this activity. 8 9 1 2, GANGADHAR CHOUDHARY pril National Institute for A e: Occupational Safety and Health at n D Cincinnati, Ohio o ati October 2, 1980 c bli u P xii 1 Sampling and Analytical Methodology for Workplace Chemical Hazards State of the Art and Future Trends C. CLARINE ANDERSON, ELLEN C. GUNDERSON, and DALE M. COULSON SRI International, Menlo Park, CA 94025 Industrial hygiene sampling and analysis is a rapidly expand ing activity in government and industry. Exposures of individuals 1 to toxic substances in workplace environments requires accurate 0 h0 sampling and measurement of gases, liquids and solids. Acceptable c 9. methods are now available for at least 400 substances as a result 4 1 of the NIOSH Standards Completion Program. Miniature impingers and 0 1- bubblers have been long used for workplace sampling. They are in 8 19 convenient to use. Solid sorbent tubes are easier to use and are bk- finding wide applicability. 21/ The conversion to solid sorption media from liquid absorption 0 1 solutions for collection of gases and vapors is a continuing pro 0. 1 cess. The solid sorbent sampling tube is a small device, easily oi: manipulated, and not prone to lose its contents when being used d 1 | under awkward sampling conditions or during shipping. These physi 8 9 cal factors can improve the accuracy of the final result. 1 2, Filter collection media have become available in a wide vari pril ety of materials including glass fibers and many synthetic plastic A films. This allows for selection of a filter that is compatible ate: with the analytical method in addition to not altering the physical D and chemical characteristics of the particles collected. The field n o of aerosol technology has grown significantly and with the increased cati knowledge of particle characterization methodology the effects of ubli specific ranges of particulate matter can be analyzed. P Analytical techniques have gone through considerable changes in the past 20 years. With the development of more sensitive and selective analytical instrumentation the analyst has been able to detect and identify minute quantities of materials never before seen. This has brought about a keen awareness of the widespread distribution of toxic hazards and also the need to study the long term effects of low level exposures. The development of new method ology is a dynamic process. However, new methods should always be thoroughly tested to demonstrate the precision and accuracy of the results obtained. SRI International and Arthur D. Little, Inc. carried out an extensive development and validation study between 1974 and 1979 0097-6156/81/0149-0003$05.00/0 © 1981 American Chemical Society 4 CHEMICAL HAZARDS IN THE WORKPLACE for NIOSH in which approximately 400 methods were studied. (.1,2) The study was carried out in two phases. In the first phase the major emphasis was on laboratory validation of existing methods. In the second phase more emphasis was placed on methods development and the substances that were studied were selected from those for which validation methods were not available from the first phase. The results of these studies were presented as individual reports for each substance. They are a sampling and analytical method (SAM), a sampling data sheet (SDS), and a backup data report (BUD). The reports on methods have been published by NIOSH and are avail able through the U.S. Government Printing Office, Washington, D.C Protocol for Methods Validation A detailed protocol for laboratory validation of sampling and analytical methods for toxic substances in workplace environments 1 0 is given in Figure 1. The literature was searched and a method of 0 ch sampling and analysis was selected. The next step was to evaluate 49. and, if necessary, develop an analytical method that was compatible 1 0 with the sampling medium. If a satisfactory analytical method be 1- 8 came available only then did we undertake generation of a test atmo 9 k-1 sphere. Then samples were collected with the appropriate collection 1/b medium. Both capacity and collection efficiency were evaluated. 02 For each method 18 samples were collected and analyzed—6 sam 1 0. ples at each of the 1/2, 1, and 2 times the OSHA Standard level. 1 oi: If the results to this point indicated a successful method, then d storage stability was evaluated. If all requirements of the proto 1 | col were met, the method was considered laboratory-validated and 8 9 1 appropriate reports were prepared. At various stages of the proto pril 2, ceoalc,h wmee tehvoad.l uatIefd a tt haen yp rtoibmaeb iilti tbye coafm es uacpcpeasrse nwti tthhiant tthhee bmuedtgheotd f or A e: study could not be successfully completed within budget, laboratory at work was discontinued and a failure report was prepared. D n The basic criterion for successful validation was that a o ati method should come within 25% of the "true value" at the 95% confi blic dence level. To meet this criterion, the protocol for experimental u testing and method validation was established with a firm statisti P cal basis. A statistical protocol provided methods of data analysis that allowed the accuracy criterion to be evaluated with statisti cal parameters estimated from the laboratory test data. It also gave a means to evaluate precision and bias, independently and in combination, to determine the accuracy of sampling and analytical methods. The substances studied in the second phase of the study are summarized in Table I. Selection of Methods of Sampling and Analysis A literature search was usually the first step that resulted in the selection of an analytical method consistent with one of the common sampling methods. The objective of these methods is to

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