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出 处:《冶金分析》2007年第7期70-72,共3页Metallurgical Analysis
基 金:广西大学科研基金资助项目(X051108)
摘 要:本文研究了萃取一分光光度法测定钢中硼。考察了萃取剂的种类、体积及萃取体系的酸度等因素对萃取率的影响。在PH3.7的甲酸一甲酸钠缓冲溶液中,硼、苯羟乙酸和[Fe(phen)3]^2+络合生成具有较大疏水性的化合物,1,2-二氯乙烷萃取后采用分光光度法测定有机相中的铁,间接测定硼含量。结果表明,络合体系的最大吸收波长为513nm,硼量在0.11~3.2μg/mL范围内呈良好线性关系,方法的检出限为0.032ug/mL。方法用于钢中硼的测定,相对标准偏差为0.8%~2.0%,结果同认定值相吻合。Indirect determination of boron in steel was investigated UV-spectrophotometrically. The effect of solvents, volumes and acidity in the extraction system on extractability of boron was experimentally explored. In a medium of formic acid--sodium formate buffer solution of pH 3. 7, borax , mandelic acid and [Fe(phen) 3 ]^2+ form a hydrophobic association complex which can be extracted with 1,2-dichloroethane. The indirect determination of boron in steel samples is achieved by determining iron in organic phase UV-spectrophotometrically. The results show that the maximum absorption wavelength of the complex is at 513 nm, and the detection limit is 0. 032 μg/mL. The calibration curve is linear over the range 0. 11-3. 2μg/mL for boron. The method has been applied in the determination of boron in steel,giving the relative standard deviation of 0. 8 %--2. 0%. The results are consistent with the certified values.
分 类 号:TG115.3[金属学及工艺—物理冶金]
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