冶金分析
冶金分析
야금분석
METALLURGICAL ANALYSIS
2015年
6期
57-60
,共4页
催化动力学光度法%高碘酸钾%亚甲基蓝%钼酸铵%钼
催化動力學光度法%高碘痠鉀%亞甲基藍%鉬痠銨%鉬
최화동역학광도법%고전산갑%아갑기람%목산안%목
catalytic kinetic spectrophotometry%potassium periodate%methylene blue%ammonium molybdate%mo-lybdenum
实验研究发现,在硫酸存在的情况下,高碘酸钾可以氧化亚甲基蓝褪色,钼Ⅵ对该褪色反应有催化作用,据此,建立了催化动力学光度法测定钼尾矿中钼的新方法。实验表明:当显色体系中亚甲基蓝浓度为0.012 g/L、硫酸浓度为0.001 mol/L、高碘酸钾浓度为0.0004 mol/L时,于60℃加热13 min,钼Ⅵ在0.02~0.6 mg/L范围内与吸光度变化值呈良好的线性关系,方法检出限为0.05 mg/L。在最佳实验条件下,催化体系的表观活化能 E a=47.31 kJ/moL,反应速率常数k=3.5×10-4/s。方法应用于3个不同地区钼尾矿中钼的测定,测定结果与原子吸收光谱法(AAS)吻合,相对标准偏差(RSD,n=11)为2.1%~2.9%,回收率为97%~102%。
實驗研究髮現,在硫痠存在的情況下,高碘痠鉀可以氧化亞甲基藍褪色,鉬Ⅵ對該褪色反應有催化作用,據此,建立瞭催化動力學光度法測定鉬尾礦中鉬的新方法。實驗錶明:噹顯色體繫中亞甲基藍濃度為0.012 g/L、硫痠濃度為0.001 mol/L、高碘痠鉀濃度為0.0004 mol/L時,于60℃加熱13 min,鉬Ⅵ在0.02~0.6 mg/L範圍內與吸光度變化值呈良好的線性關繫,方法檢齣限為0.05 mg/L。在最佳實驗條件下,催化體繫的錶觀活化能 E a=47.31 kJ/moL,反應速率常數k=3.5×10-4/s。方法應用于3箇不同地區鉬尾礦中鉬的測定,測定結果與原子吸收光譜法(AAS)吻閤,相對標準偏差(RSD,n=11)為2.1%~2.9%,迴收率為97%~102%。
실험연구발현,재류산존재적정황하,고전산갑가이양화아갑기람퇴색,목Ⅵ대해퇴색반응유최화작용,거차,건립료최화동역학광도법측정목미광중목적신방법。실험표명:당현색체계중아갑기람농도위0.012 g/L、류산농도위0.001 mol/L、고전산갑농도위0.0004 mol/L시,우60℃가열13 min,목Ⅵ재0.02~0.6 mg/L범위내여흡광도변화치정량호적선성관계,방법검출한위0.05 mg/L。재최가실험조건하,최화체계적표관활화능 E a=47.31 kJ/moL,반응속솔상수k=3.5×10-4/s。방법응용우3개불동지구목미광중목적측정,측정결과여원자흡수광보법(AAS)문합,상대표준편차(RSD,n=11)위2.1%~2.9%,회수솔위97%~102%。
It was found through experiments that potassium periodate could oxidize methylene blue for fading in presence of sulfuric acid. Based on molybdenumⅥhad catalytic effect on this fading reaction, a new determination method of molybdenum was established in molybdenum tailing by catalytic kinetic spectrophotometry. The results showed that when the concentration of methylene blue, sulfuric acid and potassium periodate in coloring system was 0. 012 g/L, 0. 001 mol/L and 0. 000 4 mol/L, respectively, the concentration of molybdenumⅥin range of 0. 02-0. 6 mg/L exhibited good linearity to the absorbance change after the coloring system was heated at 60 ℃ for 13 min. The detection limit of method was 0. 05 mg/L. Under the optimized experimental conditions, the apparent ac-tivation energy of catalytic system was Ea=47. 31 kJ/mol, and the reaction rate constant was k=3. 5×10-4/s. The proposed method was applied to the determination of molybdenum in molybdenum tailings from three different areas. The results were consistent with those obtained by atomic absorption spectrometry( AAS) . The relative standard de-viation (RSD, n=11) was 2. 1%-2. 9%, and the recoveries were between 97% and 102%.