岩矿测试
巖礦測試
암광측시
ROCK AND MINERAL ANALYSIS
2014年
6期
828-833
,共6页
刘江斌%余宇%段九存%赵伟华%李瑞仙%黄兴华%和振云%党亮
劉江斌%餘宇%段九存%趙偉華%李瑞仙%黃興華%和振雲%黨亮
류강빈%여우%단구존%조위화%리서선%황흥화%화진운%당량
锑矿石%锑%微量元素%伴生元素%四硼酸锂-偏硼酸锂-氟化锂混合熔剂%X射线荧光光谱法
銻礦石%銻%微量元素%伴生元素%四硼痠鋰-偏硼痠鋰-氟化鋰混閤鎔劑%X射線熒光光譜法
제광석%제%미량원소%반생원소%사붕산리-편붕산리-불화리혼합용제%X사선형광광보법
antimony ore%antimony%trace elements%associated elements%lithium teraborate-lithium metaborate-lithium mixed flux%X-ray Fluorescence Spectrometry
锑矿石分析通常分别采用酸分解系统和碱熔系统,萃取分离后应用容量法、原子吸收光谱法、原子荧光光谱法等分析手段进行单项测定,样品处理繁琐、操作复杂,分析过程常因熔矿不完全而导致结果偏低或失真,难以满足地质测试的需要。本文建立了玻璃熔融制样,波长色散X射线荧光光谱测定锑矿石中的锑及14种次量元素与伴生元素(Cu、Pb、Zn、As、Co、Ni、W、Ba、S、SiO2、Al2 O3、TFe、CaO、MgO)的快速分析方法。用国家标准物质和人工合成标准参考物质拟合校准曲线,对熔融条件进行了研究。确定样品与四硼酸锂-偏硼酸锂-氟化锂复合熔剂的熔融稀释比例为1∶20,以硝酸铵为氧化剂,碳酸锂为保护剂,700℃预氧化,在1050℃温度下熔融完全,有效地防止了As、S的挥发损失,解决了化学法测试样品处理复杂、不能同时测定多元素、测试元素偏少的问题。一些元素的检出限为Sb 0.14%,Cu 0.0027%,Pb 0.0025%,Zn 0.0046%,As 0.0028%,S 0.021%;方法精密度(RSD,n=12)小于5%;选用合成标准物质和实际生产锑矿石试样进行验证,测定结果与参考值或化学值一致性良好。本法大部分元素检出限都要稍高于粉末压片法,但操作简单,测试范围更宽,适用于实验室对不同锑矿矿种批量样品中多元素快速、准确检测的需要。
銻礦石分析通常分彆採用痠分解繫統和堿鎔繫統,萃取分離後應用容量法、原子吸收光譜法、原子熒光光譜法等分析手段進行單項測定,樣品處理繁瑣、操作複雜,分析過程常因鎔礦不完全而導緻結果偏低或失真,難以滿足地質測試的需要。本文建立瞭玻璃鎔融製樣,波長色散X射線熒光光譜測定銻礦石中的銻及14種次量元素與伴生元素(Cu、Pb、Zn、As、Co、Ni、W、Ba、S、SiO2、Al2 O3、TFe、CaO、MgO)的快速分析方法。用國傢標準物質和人工閤成標準參攷物質擬閤校準麯線,對鎔融條件進行瞭研究。確定樣品與四硼痠鋰-偏硼痠鋰-氟化鋰複閤鎔劑的鎔融稀釋比例為1∶20,以硝痠銨為氧化劑,碳痠鋰為保護劑,700℃預氧化,在1050℃溫度下鎔融完全,有效地防止瞭As、S的揮髮損失,解決瞭化學法測試樣品處理複雜、不能同時測定多元素、測試元素偏少的問題。一些元素的檢齣限為Sb 0.14%,Cu 0.0027%,Pb 0.0025%,Zn 0.0046%,As 0.0028%,S 0.021%;方法精密度(RSD,n=12)小于5%;選用閤成標準物質和實際生產銻礦石試樣進行驗證,測定結果與參攷值或化學值一緻性良好。本法大部分元素檢齣限都要稍高于粉末壓片法,但操作簡單,測試範圍更寬,適用于實驗室對不同銻礦礦種批量樣品中多元素快速、準確檢測的需要。
제광석분석통상분별채용산분해계통화감용계통,췌취분리후응용용량법、원자흡수광보법、원자형광광보법등분석수단진행단항측정,양품처리번쇄、조작복잡,분석과정상인용광불완전이도치결과편저혹실진,난이만족지질측시적수요。본문건립료파리용융제양,파장색산X사선형광광보측정제광석중적제급14충차량원소여반생원소(Cu、Pb、Zn、As、Co、Ni、W、Ba、S、SiO2、Al2 O3、TFe、CaO、MgO)적쾌속분석방법。용국가표준물질화인공합성표준삼고물질의합교준곡선,대용융조건진행료연구。학정양품여사붕산리-편붕산리-불화리복합용제적용융희석비례위1∶20,이초산안위양화제,탄산리위보호제,700℃예양화,재1050℃온도하용융완전,유효지방지료As、S적휘발손실,해결료화학법측시양품처리복잡、불능동시측정다원소、측시원소편소적문제。일사원소적검출한위Sb 0.14%,Cu 0.0027%,Pb 0.0025%,Zn 0.0046%,As 0.0028%,S 0.021%;방법정밀도(RSD,n=12)소우5%;선용합성표준물질화실제생산제광석시양진행험증,측정결과여삼고치혹화학치일치성량호。본법대부분원소검출한도요초고우분말압편법,단조작간단,측시범위경관,괄용우실험실대불동제광광충비량양품중다원소쾌속、준학검측적수요。
The analysis of antimony ores usually uses acid decomposition and an alkali fusion system,each component is seperated with solvent extraction and then determined by various analytical methods such as volumetric method,Atomic Absorption Spectrometry and Atomic Fluorescence Spectrometry.These methods not only have complicated operations with long time consuming,but also obtain low value or become distorted due to incomplete digestion or serious interferences,which subsequently make it difficult to meet the needs of geological analysis.The glass fusion preparation technique and establishing the rapid analysis method by using wavelength dispersion X-ray Fluorescence Spectrometry (XRF)are discussed and presented in this paper to determine antimony and 1 4 kinds of trace and associated elements (Cu,Pb,Zn,As,Co,Ni,W,Ba,S,SiO2,Al2O3,TFe,CaO and MgO)in antimony ores.The calibration cure was calibrated by using the national standard material and synthetic standard reference material,in order to study melting conditions.The sample and lithium teraborate-lithium metaborate-lithium fluoride were melted with dilution ratio of 1 ∶20 with ammonium nitrate as oxidant and lithium carbonate as protective agent.The sample was preoxidated at 700℃,and was completely melted at 1 050℃,which effectively prevented the volatilization of As and S to solve the problems of complex procedure,the inability to simultaneous determine elements and insufficient test elements by chemical method.The detection limits of method are lower than previous methods (Sb:0.1 4%,Cu:0.0027%,Pb:0.0025%,Zn:0.0046%,As:0.0028% and S:0. 021%)and the precision (RSD,n=1 2)is lower than 5%.Verified by synthetic standard material and the actual production of an antimony ore sample,the results show good consistency with the reference values obtained by the chemical method.Although the detection limits are higher than those for the powder pellet method,the operation of this method was simple,rapid and accurate,making it applicable to laboratory analysis requirements of varied and batch antimony ores samples.