988 resultados para ICP


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本文采用国产WP-2L型平面光栅摄谱仪配置国产GP3.5D型ICP光源进行了彩色电视荧光级氧化钇中14个稀土杂质元素分析方法的研究。样品溶液以不去溶方式引入ICP。当样品溶液中Y2O3的浓度为20mg/ml时,测定下限分别为铕、镱和0.00020%,镧、铈、钛、钆、镝、钬、铒和铥0.00050%,镨、钐和铽0.0010%。相对标准偏差为3.2~9.8%。

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本文提出了用ICP-AES法直接对海洋沉积物标准样品中多元素同时分析。ICP-AES法具有灵敏度高,测量精度好,线性范围宽等优点[I-4]。在此文中对样品前处理做了方法的研究。选用了多元素同时测定,空白值低、省时的溶解方法。相对标准偏差为0.03-6.9%,同时对GSD-9标准样进行了分析,结果与标准样值相符。

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本文研究了用ICP-AES法,不必化学分离,一次同时测定混合稀土铜合金名14种稀土和非稀土元素,获得满意结果。

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本文将自模型曲线分辨方法(SMCR)应用于ICP-AES谱线重叠光谱干扰的校正,并就测量误差对重叠光谱解析结果的影响作了详细的研究和讨论。两谱线的重叠程度越大,随机误差对光谱干扰校正的影响越大。对测量数据作平滑处理。可以减小数据随机误差对结果的影响,但平滑次数增加,将导致光谱图变形,使干扰校正结果产生较大的误差。数据的平滑不能减小光谱偏离加和性的误差。本工作对两条光谱重叠的情况作了讨论,并取得了较好的结果,表明SMCR法是校正ICP-AES中重叠谱线干扰的一种简便、快速的方法。

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本文研究了乙醇对ICP激发温度、气体温度、电子数密度以及易电离元素基体效应的影响,讨论了“有机ICP”的局部热平衡特性及扩张效应。

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本文对ICP-AES分析中2种线性回归方法的校准曲线作了比较和讨论。对大多数元素而言,用加权法得到的校准曲线的斜率比不加权校准曲线的斜率略大,减小3校准曲线在低浓度部分的弯曲,曲线明显优于不加权校准曲线。将2种方法得到的校准曲线进行比较时,应将剩余标准偏差(或剩余变差平方和)及曲线截距等加以综合考虑。用含零标的标准系列制作校准曲线可使曲线的截距更接近原点,有利于提高在低浓度部分校准分析的准确性。

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本文研究了以流动注射进样的ICP-AES分析方法和NaCl的基体效应。0.25-2.5%NaCl对11个元素的影响结果表明,FI进样可克服常规连续雾化的信号漂移,从而改善了测量精度。不同功率下的NaCl基体的影响不同。结果表明,NaCl的基体效应主要存在于气溶胶微粒在ICP中的蒸发—原子化—激发过程。

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从放电稳定性、激发特性、辐射特性及分析特性几方面,讨论了“有机 ICP”的若干基本问题及其研究进展。

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本文提出了用ICP-AES直接同时测定高纯金属钕中镧、铈、镨、钐和钇的新方法。描述了在钕样品溶液中加入乙醇后对测定灵敏度的影响,乙醉量的影响以及ICP的几个主要工作参数的选择等。当样品溶液中稀土元素的总浓度为5毫克/毫升,乙醇浓度为70%(V/V)时,测定下限分别为镧0.0020%,铈0.0030%,镨0.010%,钐0.0050%和钇0.0010%其相对标准偏差为2.9-5.7%。

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A method of analysis of high purity yttrium oxide with ICP-AES was described with emphasis on the study of Y_2O_3 matrix effects. The results showed that the line intensities of ana]ytes decreased with the increase of Y_2O_3 concentration in solution because of following factors. (1) The presence of matrix resulted in the decrease of the amount of analytes reaching ICP. (2) Matrix Y_2O_3 entering the plasma decreased the excitation temperature of the plasma and depressed the ionization of analytes in the pl...

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本工作利用一种改进型旋流雾室雾化氢化物发生装置,建立同时测定铅、砷、锑、铋、锗、锡及非氢化物元素的ICP-AES法。溶液中的Pb(Ⅱ)首先以H_2O_2-(NH_4)_2S_2O_8溶液氧化为Pb(Ⅳ),然后再与NaBH_4溶液反应产生氢化物,与由气动雾化产生的样品气溶胶一起被导入等离子体中。Pb,As,Sb,Bi,Sn,Ge的检出限分别为1.4,7.6,2.8,1.3,2.4和15μg/L,较通常的气动雾化法低20-60倍,硒、碲在氧化剂存在下不能产生氢化物。研究了共存元素的干扰及消除方法。实际样品(沉积物)分析结果与推荐值吻合。

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本文研究了ICP-AES法测定高纯氧化铥中十四种其它稀土杂质的方法。研究了有机溶剂的影响,加热去溶效果等。确定了折衷工作条件。本方法可以测定99.99%高纯氧化铥中十四种稀土杂质,回收率为82.5-110%相对标准偏差为1.9-9.3%。

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本文介绍了空心阴极激发的ICP原子荧光光谱的原理、仪器、光谱特性及元素的检出限,评述了该技术的应用情况以及近年来的某些改进,讨论了进一步改善某些元素检测限的可能途径。

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本文结合溶剂萃取研究了非水介质中氢化物发生-ICP-AES的分析条件、干扰等因素的影响。利用KI~+H_2SO_4/MIBK萃取体系将As,Sb,Bi萃取到MIBK中而与基体元素分离,然后将该有机相与甲酸按等体积混合后,即可直接进行氢化物发生-ICP-AES分析。还对影响萃取和氢化物发生的一些因素及共存元素的干扰进行了讨论。该方法应用于Ni-Fe基合金中As和Sb的分析,取得了较满意的结果。

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An off-line chelation system combined with ICP-MS technique was developed for the quantitative determination of trace elements in seawater, namely V, Co, Ni, Cu, Zn, Mo, Cd, Pb, U and rare earth elements(REEs). The system was built based on an ion chromatography equipped with MetPac((R)) CC-I chelation columns which had a strong selective chelation to these target elements within a pH range 5.2-5.6. Acidified seawater samples and NH4Ac(2 mol/L) were blended to meet suitable pH before being injected into the chelation column, thus target elements were retained while alkali and alkaline metals were excluded. Then chelated elements were eluted by HNO3 (1 mol/L) and samples were collected for ICP-MS analysis. Varying the ratio of input( gen. 200 mL) to output( gen. 5 mL), the target elements which were concentrated as 40 times as their concentrations were far beyond instrumental quantification limits. At last, a certificated seawater CASS-4 was introduced and our detected values were in good agreement with those certified values.