摘要
在pH1.8～3.0的Britton-Robinson(BR)缓冲溶液中,钴(Ⅱ)与2-(5-溴-2-吡啶偶氮)-5-二乙氨基酚(5-Br-PADAP)(HL)反应形成紫红色螯合阳离子,此时仅能引起吸收光谱的变化,不能导致共振瑞利散射(RRS)的增强.当钴(Ⅱ)-5-Br-PADAP螯合阳离子与阴离子表面活性剂十二烷基苯磺酸钠(SDBS)、十二烷基磺酸钠(SLS)和十二烷基硫酸钠(SDS)作用时,仅能与SDBS进一步反应形成三元离子缔合物并引起RRS的显著增强,而不与SDS和SLS产生类似反应.离子缔合物的RRS峰分别位于306,370和650nm处,在一定范围内RRS增强(ΔⅠ)与SDBS浓度成正比,当用650nm处测量时,其检出限为0.043μg·mL-1,线性范围为0.14～6.0μg·mL-1.文中研究了反应产物的RRS光谱特征,适宜的反应条件及分析化学性质,据此发展了一种在一定量SDS和SLS等阴离子表面活性剂存在下选择性测定SDBS的新方法,方法灵敏、简便、快速,用于天然水和污水中SDBS的测定,获得满意结果.文中还对反应机理进行了讨论.
In pH 1.8~3.0 BR buffer medium, Co（Ⅱ） was reacted with 2-（5-bromo-2-pyridylaro）-5-di- ethylaminophenol （5-Br-PADAP）（HL） to form a cationic chelate Co[（HL）2]2＋. In this case, only the characteristics of the absorption spectra were changed, but the intensities of the resonance Rayleigh scattering （RRS） did not increase. When the cationic chelate was further reacted with some anionic surfactants such as sodium dodecylbenzenesulfonate （SDBS）, sodium dodecyl sulfate （SDS） and sodium laurylsulfonate （SLS）, only SDBS formed a ternary ion-association complex resulting in the great enhancement of the RRS. The RRS peaks for the ion-association complex are located at 306, 370 and 650 nm, respectively. There was a linear relationship between the RRS intensity （△I） and the SDBS concentration in a certain range. The detection limit was 0.043 μg·mL^-1 and the linear range was 0.14~6.0 μg·mL^-1 at 650 nm. In this work, the characteristics of the RRS spectra, the optimum conditions of the reaction and the properties of analytical chemistry were investigated. A new method for the selective determination of SDBS in the presence of some other anionic surfactants such as SDS and SLS has been developed, which is sensitive, simple and fast. It can be applied to the determination of SDBS in natural water and waste water sampies with satisfactory results. In addition, the reaction mechanism was also discussed.
出处
《化学学报》
SCIE
CAS
CSCD
北大核心
2008年第21期2371-2378,共8页
Acta Chimica Sinica
基金
国家自然科学基金(No.20475045)
重庆市自然科学基金(Nos.CSTC2006BB7267,CSTC2006BA7026)
重庆市环科院环保基金(Nos.200603,200705)
发光与实时分析重庆市重点实验室(西南大学)(No.CSTC2006CA8006)资助项目
