ImageVerifierCode 换一换
格式:PDF , 页数:14 ,大小:288.92KB ,
资源ID:227520      下载积分:5000 积分
快捷下载
登录下载
邮箱/手机:
温馨提示:
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   
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-227520.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(SN T 1950-2007 进出口茶叶中多种有机磷农药残留量的检测方法 气相色谱法.pdf)为本站会员(sofeeling205)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!

SN T 1950-2007 进出口茶叶中多种有机磷农药残留量的检测方法 气相色谱法.pdf

1、5日串中华人民共和国出入境检验检疫行业标准SN/T 1950-2007 进出口茶叶中多种有机磷农药残留量的检测方法气相色谱法Determination of organphosphorus pesticides multiresidues in tea for import and export-Gas chromatography 2007-08-06发布2008-曰-01实施在重重坏培v垂直司z槌HZ酣幽阳,可当7中y华人民共和国发布罔家质量监督检验检夜总局前言本标准的附录A为资料性附录。本标准出国家认证认可监督管理委员会提出并归口。本标准起草单位:巾华人民共和国湖南出入境检验检疫局。本标

2、x1主要起草人z张莹、颜鸿飞、孙非、黄志强、王美玲、李拥军。本标准系首次发布的出入境检检疫行业标准。SN/T 1950一20071 范围进出口茶叶中多种有机磷农药残留量的检测方法气相色谱法SN/T 1950-2007 本标准规定了茶叶中敌敌畏、甲胶磷、乙眈甲胶磷、甲拌磷、氧乐果、乙拌陈、异稻瘟净、乐泉、皮蝇磷、毒死蝇、杀奴硫磷、对硫磷、7240C(lmin), c) 进样口温度,250C;dl 检测器温度,250C,e) 我气:氮气,纯度大于等于99.99%. m: Gt 5.0 m1 fl 氢气,75mL/min , g) 空气,100mL/min; h) F6吹气,20mL/min; 。进

3、样方式无分流进样,1.0 进样量,2L。色谱测定抑14.0min、杀螺硫磷14.8min、对硫磷15.5min.水胶硫磷16.1 min、杀扑磷17.3min、乙硫磷19.6 min.三瞠磷21.3 min.芬硫磷22.3 min、末硫磷23.1 m川、亚胶硫磷23.5 min.伏杀硫磷24.6 min、毗陪磷25.5min , 标准品的色谱分离因参见附录A中阁A.l,6.4 空白试验除不加试样外,按上述测定步骤进行。7 结果计算和表述用色i汗数据处理机或投式(1)计算试样中有机磷残留量.f-1):结果需扣除空白值。2 ( 1 ) SNjT 1950-2007 式中zX 样品中有机磷含量,单位

4、为毫克每千克(mg/kg), A一样液中有机磷的峰回积1As一-一标准工作溶液中有机磷的峰面积;c 标准工作溶液中有机磷的浓度,单位为做克每毫升(lg/mL), V一一样l!i最终定容你积,单位为毫升(mL),m 称取的试样质量,单位为克(g)。B 方法的测定低限、回收率本方法的测定低限和1回收率数据见表10测定低限和回收率数据农药名称添加范罔/C可Ikg)回收率范t可fYc测定低限/Cmg/kg)敌敌畏O. 02 .a 也7声84.01050.02 甲胶磷O. 020. 2 ./ 79.5122,7/ 0.02 乙I!:t甲胶磷0.020.2 /卢l79).118 0.02 甲拌磷20扩/J

5、J dST庐094.00.02 氧乐果O. 02 , I , ., .:;0. 1 0.02 乙拌磷0.02 69.8101 0.02 异稻瘟净O. 01 幅L.82. Q土气J.8卢, 0.01 乐果O. 020. 2 / 何h0.02 皮蝇磷O. 020. /凡川17_,0.02 毒死蝉0.02-1- 2 f 7L9lCI 0日2JA鲤硫磷0.02 10.2 7旷主斗1.l0.02 对硫磷0.02 :_C.2 f 0.02 水胶硫磷0.01 卡0.1jsu12 0.01 杀扑磷0.02 -e.2、.f 77. 7rfS 0.02 乙硫磷0.0匈2/842 119 / 0.02 三Il磷。f

6、 78.4 俨1D2J/0.02 芬硫磷O. 01O. 1 ._.,且78. 525 0.01 苯硫磷O. 01 O. 1 74. 898. 6 0.01 亚胶硫磷0.02-0.2 77.2-115 0.02 伏杀硫磷O. 020. 2 85.0-119 。.02口吐畸磷0.01-0.1 83. 5119 0.02 3 SN/T 1950-2007 4 900 。800 700 600 500 400 300 200 100 。l 敌敌畏$2 甲胶磷53 乙酌甲胶磷34 甲拌磷g5 氧乐果$6 乙拌磷g7 异韬瘟净$8 乐果g9 皮蝇磷s10-毒死牌g11-杀蟆硫磷$12 对硫磷,13 水胶硫

7、磷$14一杀扑磷g15一一乙硫磷,16 三略磷;17一芬硫磷$18 苯硫磷z19 亚胶硫陇320一伏杀硫磷$21 毗晴磷.附录A资料性附录)21种有机磷农药的标准气相色i昔图2 5 10 15 20 25 mm 图A.1 21种有机磷农药标准品的气中目色i普图-SN/T 1950-2007 Foreword Annex A 01 this standard is an inlormative annex. This standard was proposed by and is under the charge 01 the Certilication and Accreditation Ad

8、min istration 01 the Peoples Republic 01 China This standard was dralted by Hunan Entry-Exit Inspection and Quarantine Bureau 01 the Peoples Re public 01 China The main drafters 01 this standard are Zhang Ying Yan Honglei Huang Zhiqiang Wang Meiling Li Yongjun This standard is a prolessional standar

9、d lor entry-ex!t inspection and quarantine promulgated lor the lirst time Note; This English vers旧atranslation from the Chnese text is soleJy for guidance. P J a SN/T 195-2007 Determination of organophosphorus pesticide multi-residues in tea for import and export-Gas chromatograph 1 Scope This stand

10、ard specifies the method for the determination of dichlorvos. methodophos acephate phorate omethoate disulfoton IBP dimelhoate fenchlorphos chlorpyrifos fe41itrothion parathion isocar bophosl methidathion ethion triazoph吟fensthionoateEPN phosm叫pho$lonepyrazophos residues by gas chromatography in tea

11、 for impo凹nnrt.-c.;-3 Reagents and materials 。rdeionized water 3. 1 Ethyl acetat: Redistilled. 3.2 Hexane: Redistilled. 3.3 Acetone:Redistilled. 3.4 Anhydrous sodium sulfate: Ignite at 650t for 4 h. 3.5 Organophosphorus pesticide standard: Purity二,98%.3. 6 Organophosphorus pesticide standard solutio

12、n: Accurately weigh proper amount of organophos phorus pesticide standard. to prepare a solution of 100 19 mL in acetone as the standard stock solu tion Accordin9 to the requirement prepare a standard working solution of appropriate concentration 6 SN/T 1950-2007 in ethyl acetate. 3.7 Envl-Carb colu

13、mn 3 mLsupelco or equivalent). 4 Apparatus and equipment 4. 1 Gas chromatograph equipped with a flame ph口tometricdetector FPD with a specific filter for phosphorus at 526 nm 4.2 Vortex mixer. 4.3 4.4 4.5 4.6 Test-tube, 10 mL. 4.7 Glass capillary-tip pipettes. The test samples of tea should be stored

14、 below OC -4(; In the course of sampling and sample prep arat旧n.precaution must be taken to avoid contamir旧tionor any factors which may cause the change 。fresidue content 6 Test Procedure 6. 1 Extraction Weigh O. 5 9 of the test sample accurate to O. 001 9 in 10 mL centrifuge tube. Marinate the test

15、 sam-7 SN/T 1950-2007 ple in 1 mL of water for 10 min Add enough anhydrous sodium sulfate. and vortex for 2 min. Extract with 2 x 2 ml ethyl acetate by vortex for 2 min. and centrifuge for 3 min. Add 2 mL ethyl acetate hexane (1 + 1) to the pellet vortex and repeat steps above combining supernatants

16、 6.2 Cleanup Add anhydrous sodium sulfate on the Envl-Carb SPE column to the height of 1 cm Condition the col umn with 4 mL ethyl acetate. Load the extract solution (6.1) on the column Elute with 4 mL ethyl acetate and 2 mL ethyl acetate-hexane (1 + 1 ). Evaporate the eluate to O. 50 mL under nitrog

17、en stream at 40t The solution is ready for GC analysis 6.3 Determination 6.3. 1 GC operating conditions a) Column: EQUITY-1701.fused silica臼pillarycolumn 3D m x O. 53 mm(i d x 1. 0 I,m. or equiva lent, 10t/min ._- ,. 5t/min b) Column temperature: 100t (1 min)一一160t(1 min)-=一一一:2400C(8 min) , c) Inje

18、ction port temperature: 250t , d) Detector temperature: 250t , e) Carrier gas: Nitrogen. purity二,99.99%.5.0 mL/min, f) Hydrogen: 75 mL/min, gl Oxygen 100 mL/min, hl Make-up gas:20 mL/min, il Injection mode: Splitless, j) Injection volume:2L 6.3.2 GC determination According to the approximate concent

19、ration of organophosphorus pesticide in the test sample solu. tion select the standard working solution with similar peak area to that of sample solution The re sponses of multiple organophosphorus pesticides in the standard working solution and sample solu tion should be within the linear range of

20、the instrumental detection The standard working solution B SN/T 1950-2007 should be injected randomly in between the injections of sample solution of equal volume Under the above GC opening conditions, chromatogram of organophosphorus pesticide standards are shown in Figre A. 1 in Annex A 6.3.3 Blan

21、k test The operation of the blank test is the same as that described in the method of determination but with omission of sample addition. 7 Calculation and expression of result The calculation of organophosphorus pesticide content in the sample is carried out by GC data pro cessor or according to th

22、e formula (1) , The blank value should be subtracted from the result of calcu lation A.c.V x=一一一一一(1 ) As.m where X-the residue content of multiple organophosphorus in the test sample , mg/kg , A -the peak area of multiple organophosphorus in the sample solution, As-the peak area of multiple organop

23、hosphorus in the standard working solution, c-the concentration of multiple organophosphorus in the standard working solution,g/mL, V-the final volume of sa门、口lesolution mL, m-the corresponding mass of test sample in the final sample solution,g. 8 limit of determination and recovery The limit of det

24、ermination of this method and its corresponding recoveries of fortifying concentra tions show on table 1 Table l-Li mit of determination and recovery Pesticides Spiked level/(mg/kg) Recove叩1%lOD!(mg!kg) dichlorvos 0.02-0.2 84.0-105 0.02 methodophos 0.02-0.2 79.5-122 0.02 acephate 0.02-0.2 79.0-118 0

25、.02 phora飞e0.02-0.2 70.0-94.0 0.02 omethoate 0.02-0.2 73.5-96.1 。口2disulfoton 0.02-0.2 69.8-101 0.02 IBP 0.01-口182.0-128 0.01 dimethoate 0.02-0.2 88.9-113 0.02 fenchlorphos 0.02-0.2 76.4-117 0.02 9 8:1/1 1950-2007 Table 1 (continue) Pesticides Spiked level!(mg/kg) Recoverv/% LOD/(mg!kgJ chlorpyrfos

26、0.02-0.2 71.9-104 0.02 fenitrothion 0.02-0.2 76.6-111 0.02 parathion 。口2-0.279.7-110 0.02 socarbophosl 0.01-0.1 86.3-125 0.01 methidathion 0.02-0.2 77.7-115 0.02 ethion 0.02-0.2 84.2-119 0.02 triazophos 0.02-0.2 78.4-109 。.02fensthionoate 0.01 ,-,-EPN 74日-9丘6。.01phosmet 0.02-0.2,阜n2-115 O. 02 phosa!

27、one 口M泣气一85.0-1;町0.02 pyrazophos 。01-0.83.r:.119 0.02 / 10 1飞i800 700 600 500 400 300 200 100 。l-Dichlorvos; 2-methodophos; 3 - Acephate; 4-Phorate; 5-0methoate; 6-Disulfoton; 7-IBP; B口imethoate;9-Fenchlorphos; 10-Chlorpyrifos; 11一-Fenitrothion; 12-Parathion; 13一Isocarbophosl;14 -Methidathion; 15-Et

28、hion; 16一Triazophos;7-Fensthionoate; 18-EPN; 19-Phosmet; 20-Phosalone; 21-Pyrazophos 手5 Annex A (1 nformative) Chromatogram of the standards 10 15 20 SN/T 1950-2007 25 mm Figure A. 1-Chromatogram of mixed solution of organophosphorus pesticide standards 中华人民共和国出入境检验检疫行业标准进出口茶叶中多种有机磷农药残留量的检测方法气相色谱法SNjT 1950-2007 3峰中国标准出版社出版北京复兴门外三里河北街16号邮政编码100045阿址电话,6852394668517548 中国标准出版社秦皇岛印刷厂印刷峰开本880X12301/16 印张1字数24干字2007年11月第一版2007年11月第一次印刷印数1-2000晤书号:155066.2-18232 定价10.00元

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