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Determination of alloy and impurity elements in the WC-Co based cemented carbide by microwave digestion-inductively coupled plasma atomic emission spectrometry

机译:微波消解-电感耦合等离子体原子发射光谱法测定WC-Co基硬质合金中的合金和杂质元素

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Using high-pressure sealed microwave heating method,the WC-Co based cemented carbide samples were digested completely by nitric acid and phosphoric acid (VHNO3∶VH3PO4=5∶1).Then the digestion solution was diluted with water to a constant volume,and directly using inductively coupled plasma atomic emission spectrometry (ICP-OES) determination of the content of 0.005 to 10% Co and 0.005 ~ 1% of Fe,Nb,Ta,V,Cr,Mo and Ni.This paper examine the best digestion conditions,including reagent composition,ratio,and microwave control parameters,etc.,then establish a set of microwave digestion and by complex reactions with inorganic reagents to stabilize the high tungsten matrix digestion method,in order to quickly and completely digest the tungsten-cobalt-based samples and avoid the generation of tungsten acid precipitation resulting in the loss of some of the analyte and impact of organic complex agents on the spectral determination.The results showed that:the control parameters of using 5 min to heat the sample to 130 °C and keep for 5 min,then heated to 190 °C in 5 min and keep for 15 min is better to maintain the digestion.By optimizing elemental analysis line,ICP measurement parameters and matrix matching and synchronization of background correction method,the high tungsten matrix effects and spectral interference are eliminated; ensure the detection performance of the method.Background equivalent concentration of 5μg/L (Nb) ~ 18μg/L (Fe),elements of the detection limit of 4μg/L (Nb) ~ 13μg/L (Fe),which used for the determination of impurities in the alloy or elements with the results is RSD <3%,recovery 97.0% ~ 103.5% corresponding with the national standard examination method.
机译:采用高压密封微波加热法,将硝酸钴和磷酸(VHNO3∶VH3PO4 = 5∶1)对WC-Co基硬质合金样品进行完全消解,然后将消解液用水稀释至恒定体积,然后直接使用电感耦合等离子体原子发射光谱法(ICP-OES)测定Fe,Nb,Ta,V,Cr,Mo和Ni的0.005至10%Co和0.005〜1%的含量。 ,包括试剂组成,比例和微波控制参数等,然后建立一套微波消解方法,并通过与无机试剂的复杂反应来稳定高钨基消解方法,以便快速,完全地消解钨钴钴。避免了钨酸沉淀的产生,从而导致一些分析物的损失以及有机络合剂对光谱测定的影响。结果表明:控制参数使用5 min至h将样品在130°C下保温5分钟,然后在5分钟内加热到190°C保温15分钟,以更好地保持消化。通过优化元素分析线,ICP测量参数和基质匹配以及背景同步校正方法,消除了高钨基体效应和光谱干扰;保证了该方法的检测性能。背景当量浓度为5μg/ L(Nb)〜18μg/ L(Fe),元素检测限为4μg/ L(Nb)〜13μg/ L(Fe),用于合金或元素中杂质的测定,RSD <3%,回收率97.0%〜103.5%,符合国家标准检验方法。

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