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1.
刘先国  王锝 《岩矿测试》2000,19(4):292-294
拟定了电感耦合等离子体原子发射光谱法测定高纯氧化钇中14个稀土杂质的方法,选择了仪器的最佳工作条件,考察了基体效应的影响,在选定条件下,14个稀土元素的检出限为(0.06~1.10)μg/g,相对标准偏差(n≥10)为0.98%~9.3%,加标回收率为93%~114%。方法不经预分离富集处理,在大量基体中成功地测定了含量在μg/g级的稀土杂质元素。  相似文献   

2.
辛仁轩  董仁杰 《岩矿测试》1996,15(3):203-206
用5709萃取树脂还原色层法分离富集高纯氧化铕中微量稀土杂质,随后用顺序扫描等离子体光电光谱法测定。色层分离的条件:上柱稀土基体的质量浓度为20g/L,pH2-3,流速为2.5mL/min,洗脱液为6mol/L的HCl溶液。共测定铈,镨,钕钐,钆和镝6种稀土杂质。  相似文献   

3.
用5709萃淋树脂还原色层法分离富集高纯氧化铕中微量稀土杂质,随后用顺序扫描等离子体光电光谱法测定。色层分离的条件:上柱稀土基体的质量浓度为20g/L,pH2~3,流速为25mL/min,洗脱液为6mol/L的HCl溶液。共测定铈、镨、钕、钐、钆和镝6种稀土杂质。回收率为89%~105%,相对标准偏差≤4%。方法可用于荧光级氧化铕中杂质稀土的测定  相似文献   

4.
李冰 《岩矿测试》1994,13(1):20-24
研究了用感耦等离子体发射光谱(ICP-AES)测定纯氧化镧中Ce,Pr,Nd,Sm,Y,Fe,Al,Ca,Mg和Si10个杂质元素的方法。考察了基体镧的光谱干扰,共存元素间光谱干扰及校正方法,方法检出限为0.0005-0.039μg/ml;标准加入量1μg/ml时,回收率为95%-106%;10μg/ml的标准溶液,测定10次,RSD为0.24%-1.01%。方法简单,快速,不震分离富集,适用于氧  相似文献   

5.
直流等离子体原子发射光谱在纯钕中稀土杂质分析的应用   总被引:2,自引:0,他引:2  
陈俊芬 《岩矿测试》1998,17(4):254-258
应用直流等离子体中阶梯光栅直读光谱仪进行纯钕中14个稀土杂质元素的分析,选定了干扰小、检出限低的最佳分析线,对干扰的来源和性质作了研究,从而拟定了纯钕中稀土杂质元素的分析方法。该方法的检出限在3~81μg/L,RSD(n=11)在1%~3.6%,加标回收率为92%~108%。方法已用于纯金属钕和氧化钕中杂质稀土的分析。  相似文献   

6.
萃取—原子吸收法测定高纯氧化钐中的镍   总被引:3,自引:0,他引:3  
霍广进  王嘉 《岩矿测试》1997,16(4):316-318
在pH3的弱酸性介质中,用二乙基二硫代氨基甲酸钠_甲基异丁基酮萃取分离氧化钐以消除基体干扰,用4mol/LHNO3溶液反萃取后火焰原子吸收测定被富集的杂质镍。萃取时水相与有机相体积比为5∶1,反萃时体积比为1∶1,萃取时间5min,测定高纯氧化钐中杂质镍的回收率达98%。分离后的共存非稀土元素对测定镍无干扰。方法检出限为40μg/LNi,对w(Ni)=03×10-6的氧化钐测定6次,RSD=71%,试样加标回收率在93%~104%。  相似文献   

7.
周丽沂  张勤 《岩矿测试》1995,14(1):45-48
在0.2mol/L HCl-1.0mol/LNaCl-0.15mol/L抗坏血酸介质中,用电流氧化微分溶出计时电位法直接测定地质物料中微量Cu。富集电位-0.55V,时间20~40s;电极转速2500r/min;溶出电流0.2~1μA;记录电位范围-0.2~-1.20V;清洗电位-0.10V,时间10s。方法检出限0.2μg/g,线性范围2~400ng/ml,精密度(RSD,n=11,4.1μg/  相似文献   

8.
青藏高原五道梁冻土活动层表面二氧化碳和甲烷的排放   总被引:9,自引:3,他引:9  
林清  金会军  程国栋  李宁 《冰川冻土》1996,18(4):325-330
通过静态箱取样方法,首次获得青藏高原冻土活动层排放气体。分析测定结果表明,CH4含量为0.63~1.54μg/g,平均为1.19μg/g,大多数样品CH4含量低于当地大气CH4含量(1.32μg/g);CO2含量为0.15%~0.27%,平均为0.21%,明显高于大气CO2的浓度(0.069%)。CH4、CO2含量具有一定的日变化特征。CH4排放率为-0.032~0.048mgm-2h-1,平均为0.001mgm-2h-1;CO2排放率为-56.503~61.425mgm-2h-1,平均为0.095mgm-2h1。从所获得的冻土排放气体中CH4和CO2的浓度来看,这种干燥寒冷的高原冻土活动层表面CH4排放较少,CO2的排放较高  相似文献   

9.
发展了一种可在野外快速测定0.010—50μg/g银量的新方法。此法由两个各自独立而又配套的部分组成。一是直接测定0.25—50μg/g银量的Ag-TMK-SDS三元络合物光导比色测定法;二是测定0.010—0.25μg/g银量的巯基棉分离富集微珠析出比色法。可在同一份试液中依次完成。前者检出限为0.006μg/ml(K=3);测定铜、铅和锌矿石标样GSO-Cu-1(含银3.87μg/g)、GSO-Ph-1(含银14.7μg/g)和GSO-Zn-1(含银13.5μg/g)中的银,RDS(n=11)分别为1.6%、3.7%和3.4%;后法可检出5ng/g银;测定地球化学标样GSD-3(含银0.59μg/g)中的银,RSD(n=11)为6.t%。方法较为简便、快速、准确和灵敏。用光导比色计测定,结果准确度、精度均有较大改善,且与室内原子吸收法相当。故所定方法具有广阔的应用前景。  相似文献   

10.
对P507萃淋树脂分离稀土元素的条件进行了实验,拟定了以P507萃淋树脂为固定相,HCl为流动相分离4N级荧光材料Eu_2O_3中14种稀土杂质元素的流程,使被测杂质与基体Eu_2O_3达到了较好的分离;再用阳离子交换树脂分离被测液中非稀土杂质元素。选择了端视ICP-AES测量稀土杂质元素的最佳条件。称样量50mg时各杂质组分的测定下限(ug/g)为:CeO_2、Pr_6O_(11)、Nd_2O_3、Sm_2O_3、Tb_4O_7、Ho_2O_3、Er_2O_3,Tm_2O_3、Lu_2O_30.4,La_2O_3、Gd_2O_3、0.2,Dy_2O_3、Y_2O_30.04,Yb_2O_30.02。6次取样分析,各杂质组分加入量为10ug/g(CeO_2为2ug/g),加入回收率在84%~112%;RSD<13%。方法可用于纯度在99.99%~99.9995%Eu_2O_3中14种稀土杂质元素的测定。  相似文献   

11.
Lithostratigraphy, physicochemical stratigraphy, biostratigraphy, and geochronology of the 77–70 Ma old series bracketing the Campanian–Maastrichtian boundary have been investigated by 70 experts. For the first time, direct relationships between macro- and microfossils have been established, as well as direct and indirect relationships between chemo-physical and biostratigraphical tools. A combination of criteria for selecting the boundary level, duration estimates, uncertainties on durations and on the location of biohorizons have been considered; new chronostratigraphic units are proposed. The geological site at Tercis is accepted by the Commission on Stratigraphy as the international reference for the stratigraphy of the studied interval. To cite this article: G.S. Odin, C. R. Geoscience 334 (2002) 409–414.  相似文献   

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14.
正1 Introduction Geological studies established on several sections in Lanping-Simao basin have shown that the salt-bearing strata of Mengyejing formation(Yunlong Fm.in Lanping basin)are constituted by an alternation of salt layers and interbedded facies.The latter consists mainly of mudstones,and mudstone-rich conglomerate.The mineralogy and geochemistry of salt-bearing beds and  相似文献   

15.
正On 22nd April 2014,with the approach of the 45th World Earth Day,China’s Ministry of Land and resources issued the status of China’s mineral resources in 2013.The first task of the prospecting breakthrough strategy action implemented in the last five years has been completed,and China’s security capacity for mineral resources has been significantly improved.In the  相似文献   

16.
正There are more than 700 salt lakes with area of more than 1km2 on the Qinghai-Tibet Plateau of China.In recent years,an oilfield brine was also found in the Nanyishan Section of Qaidam Basin in the Qinghai-Tibet  相似文献   

17.
正1 Introduction Physical and numerical models are constructed to investigate the evolution and mechanism of salt migration driven by tectonic processes.In recent years,we have designed and ran series of models to simulate salt  相似文献   

18.
正The study of Cretaceous-Palaeogene salt-bearing strata of the Khorat Basin Laos and the Lanping-Simao Basin in Yunnan,China has an great significance not only in explaining the basin evolution and the genesis of potash  相似文献   

19.
正Potash is one of the long-term scare deposits in China,and potash prospecting has long been listed as a key brainstorm project for our nation and geological prospecting units.There have been considerable studies in search for potash deposits in the Kuqa depression of the Tarim basin(Jackson et al.,1991;Gemmer et al.,2004;Vendeville,2005;Vendeville and Jackson,1992a,1992b),  相似文献   

20.
正1 Introduction Qaidam Basin in Qinghai,including 43 salt lakes with multiple dominant mineral such as potassium,magnesium,lithium etc.,is the most intensive distribution of Saline  相似文献   

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