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悬浮液进样

悬浮液进样的相关文献在1992年到2022年内共计126篇,主要集中在化学、轻工业、手工业、中国医学 等领域,其中期刊论文122篇、会议论文4篇、专利文献440945篇;相关期刊62种,包括湖南文理学院学报(自然科学版)、药物分析杂志、理化检验-化学分册等; 相关会议4种,包括第十七届全国光谱仪器与分析学术研讨会、第三届科学仪器前沿技术及应用学术研讨会、中国化学会第七届分析化学年会暨原子光谱学术会议等;悬浮液进样的相关文献由246位作者贡献,包括刘立行、梁保安、汪正等。

悬浮液进样—发文量

期刊论文>

论文:122 占比:0.03%

会议论文>

论文:4 占比:0.00%

专利文献>

论文:440945 占比:99.97%

总计:441071篇

悬浮液进样—发文趋势图

悬浮液进样

-研究学者

  • 刘立行
  • 梁保安
  • 汪正
  • 徐强
  • 林建原
  • 雷金禄
  • 付华峰
  • 刘汉东
  • 张启凯
  • 王明勇
  • 期刊论文
  • 会议论文
  • 专利文献

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    • 程光磊; 王学江
    • 摘要: 探讨了固体悬浮液进样石墨炉原子吸收光谱法(GFAAS)测定土壤中微量银的方法,对悬浮液种类及浓度的选择、稳定性考察、灰化温度、原子化温度、等分析条件进行了讨论和优化。采用0.1%琼脂溶液为悬浮剂制成土壤悬浮液,并通过自动进样器将其注入石墨炉中,磷酸二氢铵溶液作基体改进剂,石墨炉原子吸收光谱法(GFAAS)测土壤中银,避免了传统样品前处理时繁琐的消解过程和可能的样品污染与损失。条件经优化后,本法测定银的检出限为0.43pg,银的质量浓度在0~6μg·L^(-1)以内呈线性关系,相关系数0.9988,测定土壤标准样品(型号ESS-5、GSS-6、ESS-15)结果与标准值一致。
    • 孙杨杨; 陈玉娥; 钟慧怡; 黄海波
    • 摘要: 取经烘干粉碎并通过0.074 mm网筛的巴戟天样品0.0500 g,加入琼脂溶液10.0 mL(其中含磷酸二氢铵0.1 g,作为基体改进剂),超声振荡5 min,制成样品的悬浮液,直接进样,采用石墨炉原子吸收光谱法测定其中铅和镉的含量.设置铅和镉的灰化温度分别为850°C和800°C.结果表明:铅和镉的质量浓度在一定范围内与其吸光度呈线性关系,铅和镉的检出限(3s×V/b)分别为2.17×10-9 mg和3.4×10-10 mg.按照标准加入法进行加标回收试验,铅和镉的回收率分别在98.8%~103%和98.3%~104%之间.精密度试验表明铅和镉的测定值的相对标准偏差(n=7)分别为2.7%和1.2%.
    • 邹慧君; 汪正; 李青; 黄楚楚
    • 摘要: 针对高纯氮化硅粉体中的9种微量杂质元素(Al、Ca、Co、Fe、K、Mg、Mn、Na、Ni),建立了悬浮液进样-液体阴极辉光放电原子发射光谱定量分析方法.考察了制备稳定悬浮液对样品颗粒度的要求,并通过六通阀将悬浮液引入液体阴极辉光放电原子发射光谱装置检测.本方法采用水溶液标准进行定量分析,无需对悬浮液的pH值进行精确调节,能够保持液体阴极辉光等离子体的稳定性.研究了仪器装置的操作电压、载液流速、光电倍增管积分时间等因素对检出限的影响.优化后得到的最佳实验条件为操作电压1080 V,载液流速1.2 mL/min,光电倍增管积分时间800 ms.利用六通阀进样系统对原有的液体阴极辉光放电原子发射光谱装置进行改进,从而实现悬浮液直接进样检测.用此装置对氮化硅实际样品进行检测,得到各种元素的检出限在0.2~53 mg/kg之间,RSD在1.1%~5.0%之间.通过对氮化硅标准参考物质ERM-ED101进行分析,其测定结果与高温高压消解-电感耦合等离子体发射光谱法一致,并与标准参考值吻合,表明此方法可用于氮化硅粉体的悬浮液直接进样检测,结果准确可靠,灵敏度高,具备应用价值.%Trace impurities of Al, Ca, Co, Fe, K, Mg, Mn, Na, Ni in silicon nitride powder were determined by slurry introduction into a solution-cathode glow discharge-atomic emission spectrometer (SCGD-AES).The effect of particle size on the stability of suspension was investigated.A 6-port valve was selected to link sampling system and SCGD-AES, by which the suspension could be introduced into the SCGD-AES to get instantaneous spectrum signal.The calibration curves for quantitative analysis could be established using aqueous standards and the pH of suspension was not required to be adjusted accurately.The applied voltage, solution flow rate, and integral time of PMT were set to 1080 V, 1.2 mL/min and 800 ms, respectively.In this work, slurry sampling was combined with SCGD-AES by a 6 port 2-pos valve.Powder Si3N4 was tested by this way and the limits of detection for all nine elements were 0.2-53.0 mg/kg.The RSDs were 1.1%-5.0%.The detection result of trace impurities in standard reference material ERM-ED101 agreed with that obtained from inductively coupled plasma atomic emission spectrometry.This method was proved to be accurate, reliable and valuable.
    • 黄楚楚; 李青; 张国霞; 汪正
    • 摘要: 以石英超细纤维滤膜采集上海市长宁区的大气颗粒物(PM2.5)样品,采用球磨机将滤膜研磨成细微颗粒,并以0.7% Triton X-100作为分散剂,制备了稳定均一悬浮液,建立了一种简便、绿色、快速的悬浮液进样-石墨炉原子吸收法测定PM2.5中铅和镉的方法.铅在0.1~75 μg/L范围内,镉在0.2~3 μg/L范围内,校正曲线的线性相关性大于0.998;铅和镉的检出限分别为0.36和0.06 μg/L,相对标准偏差小于5%.采用HF-HN03体系酸消解样品,并与电感耦合等离子体质谱法和石墨炉原子吸收光谱法测试结果对比,验证了方法的准确性.采用本方法对2014年11月~ 2015年5月期间上海市区大气中PM2.5及铅和镉的污染特性进行分析,结果表明,铅和镉的质量浓度随时间变化趋势与PM2.5的质量浓度随时间的变化趋势呈现良好的一致性.
    • 龙安应; 刘全亨; 吴胜金; 王士魁; 李悦
    • 摘要: The composition of coal is complicated .The content of cadmium in coal is low ,and it is easily volatile .According to these characteristics ,the coal was firstly pretreated by oxygen plasma low tempera‐ture ashing .Then ,the palladium nitrate was added as matrix modifier to make cadmium form non‐dissoci‐ative substance in ashing process .The determination method of cadmium in coal by graphite furnace atomic absorption spectrometry(GFAAS) with slurry sampling was established .The influence of sample matrix was mainly studied .The samples before and after low temperature ashing were compared and analyzed . The results indicated that the analytical sensitivity and precision could be significantly improved by low temperature ashing treatment .T he ashing temperature and atomization temperature of slurry sample and the dosage of matrix modifier were optimized .The ashing temperature and atomization temperature was 650 °C and 2 200 °C ,respectively .T he optimal mass concentration of matrix modifier (i .e .,palladium ni‐trate) was 1.0 g/L .Under the optimized conditions ,the standard slurry sample showed good linear in range of 0.1‐2.0 μg/L for cadmium .The linear correlation coefficient was 0.999 5 .The detection limit was 0.012 mg/kg .The actual sample and certified reference material of coal were analyzed according to the experimental method .The relative standard deviation (RSD ,n=5) was between 2.9% and 5.9% .The found results were consistent with those obtained by airtight digestion method or the certified values .%针对煤质复杂,而煤中的镉元素具有低含量且易挥发的特点,提出了采用氧等离子体低温灰化技术对煤进行预处理,再加入硝酸钯作为基体改进剂使镉在灰化过程中生成难离解物质,建立了悬浮液进样石墨炉原子吸收光谱法(GFAAS)测定煤中镉的方法。研究过程中主要探讨了样品基质的影响,通过对比分析低温灰化前后的样品,发现低温灰化处理明显提高了分析的灵敏度和精密度;优化了悬浮液样品的灰化温度和原子化温度及基体改进剂的用量,确定灰化温度和原子化温度分别为650°C和2200°C,基体改进剂硝酸钯的最佳质量浓度为1.0 g/L。实验表明,在优化条件下,标准悬浮液样品中镉在0.1~2.0μg/L范围内呈现较好的线性关系,线性相关系数为0.9995。方法检出限为0.012 mg/kg。对煤实际样品和标准物质进行分析,相对标准偏差(RSD ,n=5)为2.9%~5.9%,测定结果与密闭消解法处理样品后的测定值或认定值吻合。
    • 陈雪; 郝伟; 何咏; 李烨
    • 摘要: In this paper a graphite furnace atomic absorption spectrometry method was proposed as a quick way to analyze Pb content in teas with slurry injection.The tea samples were digested rapidly with HNO3 and the constant volume of triton X-100 was applied to form slurry injection to determine lead.The result showed that the detection limit is 3.55 ×10 -2 mg/kg;the recoveries of the lead in the tea samples from four different producing areas are 86%—118%and RSD is less than 4%.This is a simple,rapid and accurate method with high efficiency to analyze lead in tea samples.%建立一种快速测定茶叶样品中铅的石墨炉原子吸收的方法.茶叶样品经浓硝酸快速消解,采用曲拉通X-100定容制成悬浮液直接进样测定铅含量.结果表明,茶叶样品中铅的检出限为3.55×10-2 mg/kg;4个不同产地茶叶样品中铅的加标回收率在86%~118%之间;相对标准偏差在4%以内;该方法简便、快速、准确,明显提高工作效率,可实现茶叶样品中铅的快速分析.
    • 周陶鸿; 林津; 彭青枝; 朱影; 刘杰
    • 摘要: Objective To establish a method for the direct determination of chromium in milk powder dissolved by water and triton using Graphite Furnace Atomic Absorption Spectrometry(GF-AAS).Methods Using NH4H2PO4as matrix modifier could reduce the temperature of atomization and solve the trailing phenomenon. The loss in ashing step could be lower using optimized step of drying and ashing procedure in graphite furnace temperature program.Results During the range line of 0~30μg/L, the correlation coefficient was 0.9995. At the same time, the detection limit was 4μg/kg. The results showed that using the method ofdetermination of chromium in milk powder standards, the value of recovery was 98.9% with RSD (n=6) 3.0%. Ten batches of milk powder were determined by using this method, all the results were less than 0.1mg/kg. There was no significant difference between the national standard and this method.Conclusion This method was simple, high sensitive and environmental, and it was applicable to determine the trace chromium of milk powder and liquid milk accurately.%目的:建立了乳粉加水和曲拉通溶解,利用石墨炉原子吸收光谱法直接测定铬的检测方法。方法采用 NH4H2PO4作基体改进剂,降低原子化温度,解决拖尾现象;在石墨炉升温过程中采用分步干燥和分步灰化优化升温程序,降低灰化损失。结果铬浓度在0~30μg/L 范围内具有良好的线性关系,相关系数为0.9995;方法检出限为4μg/kg;利用该法测定乳粉考核样品中铬的含量,回收率为98.9%,相对标准偏差(n=6)为3.0%;利用本法对10批奶粉进行测定,结果均低于0.1mg/kg,与国标方法无显著差异。结论该法简便快速、灵敏度高、污染少,适用于乳粉以及液体乳中痕量铬的快速准确测定。
    • 陈张好; 宋向岗
    • 摘要: 汞、砷、铅等有害金属元素是化妆品质量控制的重要指标。对近年来国内外化妆品中金属元素分析方法的研究现状进行了综述,主要比较了各分析方法的特点及优缺点,并对化妆品中金属元素分析方法的发展趋势进行了展望。%The content of harmful metal,such as Hg,As and Pb,is an important quality control index in cosmetic.Advances of analytical methods for metal elements in cosmetics in recent years were reviewed.Different analytical methods were described and compared,and the main problems and key points of future development with personal perspectives were discussed.
    • 杨兴华; 马仁乐
    • 摘要: 建立了一种应用琼脂悬浮液直接进样—石墨炉原子吸收法测定大米中痕量铅的新方法.研究了大米悬浮液的均匀性和稳定性,并优化了石墨炉升温程序:干燥分两段进行,150°C用时20秒,250°C用时10秒;灰化温度750°C,用时23秒;原子化温度2550°C,用时2秒.结果显示,标准工作曲线 A =0.004634CPb +0.00435,相关系数 r=1.00,线性良好.方法检出限:0.22 ng∕mL.精密度 RSD 为3.61%.5次重复性试验 RSD 小于5%.回收率96.0%~99.0%之间.该方法简便、准确,灵敏度高,完全适用于大米及类似样品中铅的测定.%Established a direct injections of agar suspension — the research of determination of Lead in Rice by graphite furnace atomic absorption spectrometry .Study the homogeneity and stability of rice suspension .and optimize the graphite furnace temperature program : drying in two stages :150 °C with 20 seconds ,250 °C with 10 seconds ;Ashing temperature of 750 °C with 23 seconds ; atomic temperature of 2 550 °C with 2 seconds .The results showed that standard curves A = 0.004634CPb + 0.00435 , the correlation coefficient r = 1.00 ,good linearity .The detection limit : 0.22 ng∕mL .RSD of 3.61% .5 repeatability RSD%less than 5% .Recoveries between 96.0% to 99.0% .The method is simple ,accurate and sensitive ,fully determination of lead in rice and similar samples .
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