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机构地区:[1]中国科学院地质与地球物理研究所,中国科学院工程地质力学重点实验室,北京100029 [2]生物地质与环境地质国家重点实验,中国地质大学(武汉),武汉430074
出 处:《分析化学》2013年第12期1915-1918,共4页Chinese Journal of Analytical Chemistry
基 金:国家重点基础研究发展计划(No.2010CB428801);国家自然科学基金(No.21207120)资助
摘 要:采用O2作为反应气,将75As+氧化成75As16O+后在m/z 91处测定,有效消除了m/z 75处40Ar35Cl+,40Ca35Cl+,39K36Ar+形成的质谱干扰,建立了电感耦合等离子体质谱法(ICP-MS)直接测定高盐氯化钙型地下水中痕量总砷的方法。优化了反应池(DRC)的参数,在O2流速为0.1 mL/min,反应池抑制参数R pq=0.55时,背景等效浓度(BEC)最小。样品中加入3%甲醇可以提高75As16O+的信号强度3.6倍。方法采用海水标准物质NASS-4和CASS-5进行了验证,结果令人满意。方法的检出限为0.01μg/L,1.0μg/L As的7次平行测定的相对标准偏差为1.8%。A new procedure for the direct determination of total arsenic in high salinity and CaCl2 type groundwater has been developed. In order to remove the polyatomic interferences 40Ar35Cl+,40Ca35Cl+,39K36Ar+ arising from the direct analysis of high salinity and CaC12 type groundwater, 75As+, the mass for general detection, was effectively changed to 75As160+ which could be detected at m/z 91 by reaction with oxygen in a Dynamic Reaction Cell (DRC). The DRC parameters were optimized, the background equivalent concentration (BEC) was minimum when 02 gas flow rate was 0. 1 mL/min and the rejection parameter q (RPq) of DRC was 0.55. The signal intensity of 75As160+ was improved 4-fold by addition of 3% methanol into sample solution. The accuracy was verified by the analysis of certified reference materials of sea-water (CASS-5, NASS-4). Detection limits of 0. 011μg/L and the relative standard deviation of 1.8% were obtained.
关 键 词:电感耦合等离子体质谱 总砷 氯化钙 高盐地下水
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