ImageVerifierCode 换一换
格式:PDF , 页数:8 ,大小:358.12KB ,
资源ID:543209      下载积分:10000 积分
快捷下载
登录下载
邮箱/手机:
温馨提示:
如需开发票,请勿充值!快捷下载时,用户名和密码都是您填写的邮箱或者手机号,方便查询和重复下载(系统自动生成)。
如填写123,账号就是123,密码也是123。
特别说明:
请自助下载,系统不会自动发送文件的哦; 如果您已付费,想二次下载,请登录后访问:我的下载记录
支付方式: 支付宝扫码支付 微信扫码支付   
注意:如需开发票,请勿充值!
验证码:   换一换

加入VIP,免费下载
 

温馨提示:由于个人手机设置不同,如果发现不能下载,请复制以下地址【http://www.mydoc123.com/d-543209.html】到电脑端继续下载(重复下载不扣费)。

已注册用户请登录:
账号:
密码:
验证码:   换一换
  忘记密码?
三方登录: 微信登录  

下载须知

1: 本站所有资源如无特殊说明,都需要本地电脑安装OFFICE2007和PDF阅读器。
2: 试题试卷类文档,如果标题没有明确说明有答案则都视为没有答案,请知晓。
3: 文件的所有权益归上传用户所有。
4. 未经权益所有人同意不得将文件中的内容挪作商业或盈利用途。
5. 本站仅提供交流平台,并不能对任何下载内容负责。
6. 下载文件中如有侵权或不适当内容,请与我们联系,我们立即纠正。
7. 本站不保证下载资源的准确性、安全性和完整性, 同时也不承担用户因使用这些下载资源对自己和他人造成任何形式的伤害或损失。

版权提示 | 免责声明

本文(BS 2690-117-1983 Methods of testing water used in industry - Long-chain fatty amines spectrophotometric method《工业用水试验方法 第117部分 长链脂肪胺 分光光度法》.pdf)为本站会员(ideacase155)主动上传,麦多课文库仅提供信息存储空间,仅对用户上传内容的表现方式做保护处理,对上载内容本身不做任何修改或编辑。 若此文所含内容侵犯了您的版权或隐私,请立即通知麦多课文库(发送邮件至master@mydoc123.com或直接QQ联系客服),我们立即给予删除!

BS 2690-117-1983 Methods of testing water used in industry - Long-chain fatty amines spectrophotometric method《工业用水试验方法 第117部分 长链脂肪胺 分光光度法》.pdf

1、BRITISH STANDARD BS 2690-117: 1983 Methods of testing Water used in industry Part 117: Long-chain fatty amines: spectrophotometric method IMPORTANT NOTE. It is essential that this Part be read in conjunction with the information in Part 100 of this standard, “Foreword, scope and general requirements

2、 which is published separately. UDC 628.1:663.63.01:543.3:543.42.062:547.233BS2690-117:1983 This British Standard, having been prepared under the directionof the Environment andPollution Standards Committee, was published underthe authority of the BoardofBSI and comes intoeffecton 31 May 1983 BSI

3、07-1999 The following BSI references relate to the work on this standard: Committee reference EPC/37 Special announcement in BSINews March 1983 ISBN 0 580 11973 4 A British Standard does not purport to include all the necessary provisions of a contract. Users of British Standards are responsible for

4、 their correct application. Compliance with a British Standard does not of itself confer immunity from legal obligations. Summary of pages This document comprises a front cover, an inside front cover, pages i and ii, pages1 and 2, an inside back cover and a back cover. This standard has been updated

5、 (see copyright date) and may have had amendments incorporated. This will be indicated in the amendment table on the inside front cover. Amendments issued since publication Amd. No. Date of issue CommentsBS 2690-117:1983 BSI 07-1999 i Contents Page 0 Introduction 1 1 Scope 1 2 Range 1 3 Principle 1

6、4 Interferences 1 5 Reagents 1 6 Treatment of apparatus 1 7 Sampling 1 8 Preparation of calibration graph 2 9 Procedure 2 10 Calculation 2 Publications referred to Inside back coverii blankBS2690-117:1983 BSI 07-1999 1 0 Introduction BS 2690-115, BS 2690-116 and BS 2690-117 together supersede BS 269

7、0-8:1969. This Part is a revision of clause 4. 1 Scope The method described is for the determination of long-chain fatty amines in industrial waters by a spectrophotometric method. 2 Range From 5 4g to 200 4g of long-chain fatty amine, expressed as octadecylamine, in a test portion not exceeding 100

8、 mL. 3 Principle The primary, secondary and tertiary forms of long-chain fatty amines react with methyl orange atpH 3 to 4 to form yellow complexes which are extracted into dichloromethane and determined colorimetrically. The calibration graph is prepared with the fatty amine that is added to the st

9、eam plant under investigation. As octadecylamine is the most commonly added fatty amine, it is used in the following method. 4 Interferences Cyclohexylamine, morpholine and ammonia do not interfere. Detergents interfere seriously and shall not be used for cleaning any glassware used in the test. 5 R

10、eagents 5.1 Buffer solution. Dissolve 125 g of potassium chloride and 70 g of sodium acetate trihydrate in500 mL of water. Add 300 mL of glacial acetic acid and dilute to 1 L with water. The pH value is 3.4. 5.2 Dichloromethane WARNING. Dichloromethane is harmful by inhalation. Avoid breathing its v

11、apour and contact with skin and eyes. 5.3 Propan-2-ol 5.4 Methyl orange solution. Dissolve 100 mg of methyl orange in 200 mL of water and add 50 mL of industrial methylated spirits (see 3.8 of BS 2690-100:1978). 5.5 Octadecylamine standard solutions 5.5.1 Octadecylamine stock solution. Weigh 0.500 g

12、 of octadecylamine into a 250 mL beaker, add 50 mL of glacial acetic acid and stir to dissolve. Transfer the solution to a 500 mL one-mark volumetric flask and dilute to the mark with water. Mix well. 5.5.2 Octadecylamine working solution. Dilute10.0mL of the octadecylamine stock solution(5.5.1) wit

13、h water to the mark in a1000mL one-mark volumetric flask(1mLN 104g of octadecylamine). Prepare this solution fresh before each calibration. 6 Treatment of apparatus Long-chain fatty amines tend to be absorbed on to glass surfaces and therefore all glassware apart from the optical cells shall be sili

14、cone-coated. This can be done by first cleaning the glassware with chromic acid and then rinsing the clean and dry surface of the glassware with a proprietary silicone emulsion, in accordance with the manufacturers instructions. The coating will usually last for about6 months and the glassware shall

15、 be re-treated when a normal water meniscus appears. 7 Sampling If the temperature of the water being sampled is above 30 C, the sampling line shall contain a small, permanently fixed, stainless steel cooling coil capable of reducing the temperature of the sample to about 25 C to 30 C. The sampling

16、line shall be kept as short as possible and the sample allowed to run to waste for at least 30 min before collection. Run the sample into a stoppered 250 mL silicone-coated glass bottle and analyse immediately.BS2690-117:1983 2 BSI 07-1999 8 Preparation of calibration graph Add 0, 1.0, 2.0, 5.0, 10.

17、0, 15.0 and 20.0 mL of the octadecylamine working solution (5.5.2) to a series of 150 mL separating funnels. This will correspond to 0, 10, 20, 50, 100, 150 and 200 4g of octadecylamine in a separating funnel. Treat the contents of each funnel as follows. Dilute to 100 mL with water, add 4.0 mL of t

18、he buffer solution (5.1), 2.0 mL of the methyl orange solution (5.4) and 20.0 mL of the dichloromethane(5.2), stopper and shake for 5 min. Invert the funnel and dry the stem with a spill of filter paper extending to the open tap. Close the stopcock and allow the funnel to stand upright for3min. Run

19、the dichloromethane layer into a dry50 mL separating funnel. Add 0.5 mL of the propan-2-ol (5.3) to the separated dichloromethane layer to remove any turbidity and swirl gently. Run off the dichloromethane into a 10 mm cell. Immediately measure the absorbance of the dichloromethane solution at a kno

20、wn temperature between 20 C and 25 C in a spectrophotometer at the wavelength corresponding to maximum absorption (approximately 430 nm, but the exact wavelength shall be checked for each spectrophotometer), using 10 mm cells. Use dichloromethane in the compensating cell. Deduct the reading for the

21、blank from those for the standard solutions and plot a calibration graph of absorbance against the number of micrograms of octadecylamine. The absorbance given by 200 4g of octadecylamine in the total volume of test solution is approximately1.2. 9 Procedure Measure a suitable volume of the sample (c

22、ontaining less than 200 4g of octadecylamine) into a 150 mL separating funnel and, if necessary, dilute to 100 mL with water. Add 100 mL of water to a second separating funnel to act as a blank. Treat the contents of each funnel as follows. To each funnel add 4.0 mL of the buffer solution(5.1), 2.0

23、mL of the methyl orange solution(5.4) and 20.0 mL of the dichloromethane(5.2), stopper and shake for 5 min. Invert the funnel and dry the stem with a spill of filter paper extending to the open tap. Close the tap and allow the funnel to stand upright for 3 min. Run the dichloromethane layer into a d

24、ry 50 mL separating funnel. Add 0.5 mL of the propan-2-ol (5.3) to the separated dichloromethane layer to remove any turbidity and swirl gently. Run off the dichloromethane into a 10 mm cell. Immediately measure the absorbance of the dichloromethane solution at the wavelength used for the calibratio

25、n graph and at a temperature within 1 C of that at which the calibration graph was prepared in the spectrophotometer. Use dichloromethane in the compensating cell. 10 Calculation Deduct the reading obtained for the blank from that for the sample and read off the octadecylamine content in micrograms

26、from the calibration graph. The concentration, in milligrams per litre, of octadecylamine is given by where m is the mass of octadecylamine from the calibration graph (in 4g); V is the volume of sample (in mL). m V -BS 2690-117:1983 BSI 07-1999 Publications referred to BS 2690, Methods of testing wa

27、ter used in industry. BS 2690-115, Cyclohexylamine: spectrophotometric method 1) . BS 2690-116, Morpholine: spectrophotometric method 1) . 1) Referred to in the introduction only.BS 2690-117: 1983 BSI 389 Chiswick High Road London W4 4AL BSIBritishStandardsInstitution BSI is the independent national

28、 body responsible for preparing BritishStandards. It presents the UK view on standards in Europe and at the international level. It is incorporated by Royal Charter. Revisions BritishStandards are updated by amendment or revision. Users of BritishStandards should make sure that they possess the late

29、st amendments or editions. It is the constant aim of BSI to improve the quality of our products and services. We would be grateful if anyone finding an inaccuracy or ambiguity while using this BritishStandard would inform the Secretary of the technical committee responsible, the identity of which ca

30、n be found on the inside front cover. Tel:02089969000. Fax:02089967400. BSI offers members an individual updating service called PLUS which ensures that subscribers automatically receive the latest editions of standards. Buying standards Orders for all BSI, international and foreign standards public

31、ations should be addressed to Customer Services. Tel:02089969001. Fax:02089967001. In response to orders for international standards, it is BSI policy to supply the BSI implementation of those that have been published as BritishStandards, unless otherwise requested. Information on standards BSI prov

32、ides a wide range of information on national, European and international standards through its Library and its Technical Help to Exporters Service. Various BSI electronic information services are also available which give details on all its products and services. Contact the Information Centre. Tel:

33、02089967111. Fax:02089967048. Subscribing members of BSI are kept up to date with standards developments and receive substantial discounts on the purchase price of standards. For details of these and other benefits contact Membership Administration. Tel:02089967002. Fax:02089967001. Copyright Copyri

34、ght subsists in all BSI publications. BSI also holds the copyright, in the UK, of the publications of the internationalstandardization bodies. Except as permitted under the Copyright, Designs and Patents Act 1988 no extract may be reproduced, stored in a retrieval system or transmitted in any form o

35、r by any means electronic, photocopying, recording or otherwise without prior written permission from BSI. This does not preclude the free use, in the course of implementing the standard, of necessary details such as symbols, and size, type or grade designations. If these details are to be used for any other purpose than implementation then the prior written permission of BSI must be obtained. If permission is granted, the terms may include royalty payments or a licensing agreement. Details and advice can be obtained from the Copyright Manager. Tel:02089967070.

copyright@ 2008-2019 麦多课文库(www.mydoc123.com)网站版权所有
备案/许可证编号:苏ICP备17064731号-1