Determination of Cadmium and Lead in Sugarcane by Graphite Furnace Atomic Absorption Spectrometer with Zeeman Correction

[Objective] The aim was to develop a rapid,simple method for determination of cadmium and lead in sugarcane samples by graphite furnace atomic absorption spectrometry.[Method] The method for determination of Cd and Pb in sugarcane by combined graphite furnace atomic absorption spectrometry and microwave digestion was used.[Result] The concentration curve was linear within the range of 0-0.80 μg/L the detection limits of Cd and Pb was 0.015 and 0.030 μg/L,respectively.The precision for elevenfold determination of Cd and of Pb at the 0.40 μg/L level were 1.8% and 2.3%（RSD）,respectively.Recoveries of 96.7%-98.2% for Cd and 104.6%-106.7% for Pb were obtained for two sugarcane samples and one certified reference material.[Conclusion] The proposed method has the advantages of simple operation,high sensitivity,and high efficiency;it was successfully used for determination of Cd and Pb in sugarcane samples.

Determination of Trace Amounts of Nickel (Ⅱ) by Graphite Furnace Atomic Absorption Spectrometry Coupled with Cloud Point Extraction

A new method based on the cloud point extraction（CPE） for separation and preconcentration of nickel（Ⅱ） and its subsequent determination by graphite furnace atomic absorption spectrometry（GFAAS） was proposed, 8-hydroxyquinoline and Triton X-100 were used as the ligand and surfactant respectively. Nickel（Ⅱ） can form a hy-drophobic complex with 8-hydroxyquinoline, the complex can be extracted into the small volume surfactant rich phase at the cloud point temperature（CPT） for GFAAS determination. The factors affecting the cloud point extraction, such as pH, ligand concentration, surfactant concentration, and the incubation time were optimized. Under the optimal conditions, a detection limit of 12 ng/L and a relative standard deviation（RSD） of 2.9% were obtained for Ni（Ⅱ） determination. The enrichment factor was found to be 25. The proposed method was successfully applied to the determination of nickel（Ⅱ） in certified reference material and different types of water samples and the recovery was in a range of 95%―103%.

A Study of the Background Absorption of Chitosan in the Graphite Furnace Atomic Absorption Spectrometry

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Preconcentration of Vanadium(Ⅴ) on Crosslinked Chitosan and Determination by Graphite Furnace Atomic Absorption Spectrometry

A new method is proposed for the preconcentration of vanadium(Ⅴ) with crosslinked chitosan (CCTS) and determination by graphite furnace atomic absorption spectrometry (GFAAS). The adsorption rate of vanadium(Ⅴ) by CCTS was 97% at pH 4.0, and vanadium(Ⅴ) was eluted from crosslinked chitosan with 2 mL 2.0 mol·L -1 chlorhydric acid and determined by GFAAS. The detection limit (3σ,n=7) for vanadium(Ⅴ) was 4.8×1 0 -12g and the relative standard deviation (R.S.D) at concentration level of 2.6 μg·L -1 is less than 3.6%. The method shows a good selectivity and high sensitivity, and it was applied to determination of vanadium(Ⅴ) in oyster and water samples. The analytic recoveries are (97±5)%.

Determination of Trace Iron in High Purity Sodium Fluoride by Graphite Furnace Atomic Absorption Spectrometry

A method is described for the direct determination of iron in high purity sodium fluoride using graphite furnace atomic absorption spectrometry. Interferences caused by the matrix are investigated. It is shown that the ashing temperature can be increased to 1 400°C and matrix interferences eliminated, the sensitivity of iron increased in 1. 27 fold by the addition of nickel nitrate. The method is applied to the determination of iron in sodium fluoride and satisfactory results are obtained.

Determination of Trace Amounts of Lead by Modified Graphite Furnace Atomic Absorption Spectrometry after Liquid Phase Microextraction with Pyrimidine-2-thiol

The liquid phase microextraction (LPME) was combined with the modified Graphite furnace atomic absorption spectrometry (GF-AAS) for determination of lead in the water and solid samples. In a preconcentration step, lead was extracted from a 2 ml of its aqueous sample in the pH = 5 as lead-Pyrimidine-2-thiol cationic complex into a 4 μl drop of 1,2 dichloroethane and ammonium tetraphenylborate as counter ion immersed in the solution. In the drop, the lead-Pyrimidine-2-thiol ammonium tetraphenylborate ion associated complex was formed. After extraction, the microdrop was retracted and directly transferred into a graphite tube modified by [W.Pd.Mg] (c). Some effective parameters on extraction and complex formation, such as type and volume of organic solvent, pH, concentration of chelating agent and counter ion, extraction time, stirring rate and effect of salt were optimized. Under the optimum conditions, the enrichment factor and recovery were 525% and 94%, respectively. The calibration graph was linear in the range of 0.01 - 12 μg?L–1 with correlation coefficient of 0.9975 under the optimum conditions of the recommended procedure. The detection limit based on the 3Sb criterion was 0.0072 μg?L–1 and relative standard deviation (RSD) for ten replicate measurement of 0.1 μg?L–1 and 0.4 μg?L–1 lead was 4.5% and 3.8% respectively. The characteristic concentration was 0.0065 μg?L–1 equivalent to a characteristic mass of 26 fg. The results for determination of lead in reference materials, spiked tap water and seawater demonstrated the accuracy, recovery and applicability of the presented method.

A Study of the Background Absorption of Slurry Algae in the Graphite Furnace Atomic Absorption Spectrometry

In general, biological organisms have the ability to absorb a specific element selectively. Holcombe and his co-workers reported that copper, nickel and cobalt could be separated from riverine and sea-water samples and cadmium from river water samples by unicellular green algae and were determined by slurry GFAAS. Dar-

Determination of Pb Content in Soil Samples by Graphite Furnace Atomic Absorption Spectrometry

[ Objective] A method was established to determine trace Pb in soil by graphite furnace atomic absorption spectrometry. [ Method] The pre-treatment of soil sample was conducted by nitric acid -perchloric acid -hydrochloric acid system. Palladium nitrate was added to eliminate ma- trix interference. Digestion acid, ashing and atomization temperature of the sample were selected. The operating parameters of instrument and tem- perature-rise program of graphite furnace were optimized. National standard matter was used to verify accuracy of the method. [Result] The detec- tion limit for Pb was 0.27 μg/g by graphite furnace atomic absorption spectrometry, and the recovery rate was 91.0% -96.1%. [ Conclusion The method had rapid analysis velocity, high sensitivity, less interference and easy operation. When applied to determination of trace Pb in the soil, the method obtained satisfactory results.

Investigation of Distribution for Trace Lead and Cadmium in Chinese Herbal Medicines and Their Decoctions by Graphite Furnace Atomic Absorption Spectrometry

Lead and cadmium in herbal medicines are highly toxic to living organisms even in low concentrations. An effective method is developed for analysis of trace lead and cadmium in Chinese herbal medicines and their decoctions by graphite furnace atomic absorption spectrometry (GFAAS). The effects of analytical conditions on absorbance were investigated and optimized. A water-dissolving capability for Pb and Cd was investigated, and the contents of different species in five Chinese herbal medicines and their decoctions were analyzed. The content ratios (kow) of n-octanol-soluble Pb or Cd to water-soluble Pb or Cd were evaluated, and the distribution of Pb and Cd in water decoction at stomach and intestine acidities was developed, in the first time. The contents of water-soluble Pb and Cd, n-octanol-soluble Pb and Cd, and their content ratios were related with the kind of medicine and the acidity of the decoction. The proposed method has the advantages of simple operation, high sensitivity and high speed, with 3 σ detection limits of 4.2 pg for Pb and 0.1 pg for Cd.

Measuring Conditions for the Determination of Lead in Iron-Matrix Samples Using Graphite Atomizers with/without a Platform in Graphite Furnace Atomic Absorption Spectrometry

In graphite furnace atomic absorption spectrometry (GF-AAS), the atomization process of lead occurring in graphite atomizers with/without a platform plate was investigated when palladium was added to an iron-matrix sample solution containing trace amounts of lead. Absorption profiles of a lead line were meas- ured at various compositions of iron and palladium. Variations in the gas temperature were also estimated with the progress of atomization, by using a two-line method under the assumption of a Boltzmann distribu- tion. Each addition of iron and palladium increased the lead absorbance in both the atomizers, indicating that iron or palladium became an effective matrix modifier for the determination of lead. Especially, palladium played a significant role for controlling chemical species of lead at the charring stage in the platform-type atomizer, to change several chemical species to a single species and eventually to yield a dominant peak of the lead absorbance at the atomizing stage. Furthermore, the addition of palladium delayed the peak after the gas atmosphere in the atomizer was heated to a higher temperature. These phenomena would be because the temperature of the platform at the charring stage was elevated more slowly compared to that of the furnace wall, and also because a thermally-stable compound, such as a palladium-lead solid solution, was produced by their metallurgical reaction during heating of the charring stage. A platform-type atomizer with palladium as the matrix modifier is recommended for the determination of lead in GF-AAS. The optimum condition for this was obtained in a coexistence of 1.0 × 10–2 g/dm3 palladium, when the charring at 973 K and then the atomizing at 3073 K were conducted.

Determination of Heavy Metals at Sub-ppb Levels in Water by Graphite Furnace Atomic Absorption Spectrometry Using a Direct Introduction Technique after Preconcentration with an Iminodiacetate Extraction Disk

A direct analysis method combining an iminodiacetate extraction disk (IED) with graphite furnace atomic absorption spectrometry was developed for the determination of Co, Ni, Cu, Cd, Sn, Pb, and Bi at sub-ppb levels in water. A 100 mL water sample was adjusted to pH 5.6 with nitric acid and a 1 mol?L–1 ammonium acetate solution, and then passed through an IED (diameter, 47 mm;effective filtering diameter, 35 mm) at a flow rate of 80 - 100 mL?min–1 to preconcentrate seven analytes. The IED was dried at 100?C for 20 min in an electric oven, and 110 - 145 small disks, each 2 mm in diameter, were punched out from the IED. A small disk was introduced into the graphite furnace and atomized according to a heating program. For Cd, Sn, Pb, and Bi measurements, Pd was used as a chemical modifier to enhance the absorbances. Calibration was performed using aqueous standard solutions. The detection limits, corresponding to three times the standard deviation (n = 5) of the blank values, were 0.092 μg·L–1 for Co, 0.12 μg·L–1 for Ni, 0.40 μg·L–1 for Cu, 0.077 μg·L–1 for Cd, 0.92 μg·L–1 for Sn, 0.61 μg·L–1 for Pb, and 0.80 μg·L–1 for Bi with an enrichment factor of 140 using a 100-mL water sample. A spike test for the seven analytes in tap water, rainwater, river water, and mineral drinking water showed quantitative recoveries (93% - 108%).

悬滴微萃取-高分辨连续光源石墨炉原子吸收光谱法测定高纯石墨中的超痕量金

准确测定高纯石墨中的超痕量金,难点是如何在最大程度地减少样品前处理过程中器皿、试剂、材料、环境及设备所引入的二次污染的前提下,实现对样品溶液中超痕量金(0.1~1ng/mL)的有效分离和高倍富集。本文建立了铂皿中灰化、酸解、磷酸三丁酯悬滴微萃取的方法用于高纯石墨中超痕量金分析。首先于铂皿中高温灼烧除去样品中的固定碳,然后采用氢氟酸-王水-高氯酸将灰分消解完全制备成样品溶液,再以微升级磷酸三丁酯悬滴作为萃取剂,分离富集样品溶液中的金,最后采用高分辨连续光源石墨炉原子吸收光谱法(GFAAS)对悬滴中的金进行测定。实验结果表明,使用2.5μL磷酸三丁酯悬滴(氯仿体积为20%)作为萃取剂,在10%盐酸介质的样品溶液中萃取金2min,对金的富集倍数可达283倍。在实验条件下,金的质量浓度在0.1~2.0ng/mL范围内与其吸光度呈良好的线性关系,相关系数r为0.999,检出限为0.11ng/g,样品溶液中一定量的共存元素(如钠、镁、铝)对金的测定无干扰。按照实验方法测定5个高纯石墨实际样品中的金含量,测定结果的相对标准偏差(RSD,n=6)为1.5%~4.9%,加标回收率为94.9%~105.3%。

石墨炉原子吸收光谱法测量干香菇镉含量的不确定度来源评定

依据国家计量技术规范《测量不确定评定与表示》(JJF 1059.1—2012),针对干香菇镉含量的原子吸收光谱法(石墨炉法)检测过程,分析测量不确定度的来源,不确定度主要来源于测量重复性、标准物质、样品制备、线性拟合标准曲线、石墨炉原子吸收光谱仪等5个方面,通过建立相应的数学模型,计算评定上述5个方面来源的相对标准不确定度分别为0.00743、0.00268、0.02275、0.00866和0.00005,合成标准不确定度为0.0151 mg∕kg,最终得出测量结果的扩展不确定度为0.03 mg∕kg。结果表明,在该试验中标准曲线线性拟合计算质量浓度是不确定度引入的最主要因素。

Cd在污泥厌氧消化中的检测及其对产沼气的抑制研究

为了研究重金属Cd对污泥厌氧消化产甲烷的影响,在序批式反应器中,通过控制进料中Cd的浓度,分析了Cd在污泥处理系统内的检出与去除规律,以及Cd对污泥厌氧消化产甲烷的影响。研究结果表明,石墨炉原子吸收光谱法能有效检测污泥中Cd的浓度,且Cd的初始浓度会影响Cd的去除效率;浓度>1.0 mg·L-1的Cd抑制了污泥厌氧消化产甲烷,最低甲烷产量为77.9 mL·g-1;Cd降低了污泥厌氧消化内有机质的水解,5.0 mg·L-1的Cd暴露组中溶解性COD和挥发性脂肪酸(VFA)的最大值分别为1455 mg·L-1和794 mg·L-1,低于对照组。高浓度Cd会降低污泥减量率,至24.5%,增加了污泥后续处理的难度。

纺织品及附件铅释放量的测定

文章建立以人工睡液为萃取介质,测定纺织品及纺织品附件中铅释放量的试验方法,优化样品前处理条件和测试仪器参数。试验结果表明:采用电感耦合等离子体发射光谱法测定的定量限为0.02μg/(cm^(2)·h),在低、中、高3个加标浓度下的回收率在93.26%~107.65%,相对标准偏差为1.03%~5.99%(n=7);采用石墨炉原子吸收光谱法测定的定量限为0.01μg/(cm^(2)·h),在低、中、高3个加标浓度下的回收率在82.65%~110.32%,相对标准偏差为1.08%~4.61%(n=7)。该方法前处理步骤简单,检测流程短,结果准确度高,适用于可放入婴幼儿和儿童口中的纺织品及其附件的检测。

火焰原子吸收法测定青阳地区农田土壤中的锌

建立了全自动石墨消解-火焰原子吸收法,对安徽省耕地质量调查中青阳地区农田土壤的锌进行了样品消解和分析检测,土壤消解体系采用1.5 m L HNO3-4.5 mL HCl-3 mL HF-1 m L HClO4进行,通过设定的消解程序完成对土壤样品消解后在火焰原子吸收分光光度计上对Zn的测定,通过对土壤标准物质GBW 07385、GBW 07387、GBW 07388的测定,结果表明,其测定结果平均值与认定值相吻合,精密度符合要求。将优化后的测量方法用于青阳地区农田土壤实际样品测定,其结果与平行实验室间测定平均值的对比结果线性相关性极显著,证明了该方案的有效性。

双水相萃取-连续光源石墨炉原子吸收光谱法测定水样中的痕量锑

提出了以吡咯烷基二硫代氨基甲酸铵(APDC)为螯合剂,乙腈为萃取剂,氯化钠为无机盐的双水相萃取-连续光源石墨炉原子吸收光谱法测定水样中痕量锑的方法。优化的双水相萃取Sb^(3+)的条件如下:螯合反应体系酸度为pH 4,0.5 mL的2 g·L^(-1)APDC储备溶液,1.6 mL的乙腈,1.2 g的氯化钠,反应时间为20 min。在此试验条件下,Sb^(3+)的质量浓度在1.00~20.00μg·L^(-1)内与对应的吸光度呈线性关系,检出限(3 s/k)为0.048μg·L^(-1)。分别对5.00,10.00μg·L^(-1)的Sb^(3+)标准溶液测定10次,测定值的相对标准偏差为4.6%和3.3%。按照标准加入法对实际样品进行回收试验,回收率为95.8%~102%。将此方法用于检测自来水、河水、湖水中的痕量锑,显示这些环境样品中含有部分痕量锑。

永泰县话梅中铅含量的检测分析

为调查研究永泰县话梅中铅含量情况,采购永泰县当地产话梅200份,采用石墨炉原子吸收光谱法对其铅含量进行检测分析。结果表明,永泰县话梅中铅的含量为0~1.10 mg·kg^(-1),平均含量为0.31 mg·kg^(-1),仅有1份话梅样品中铅含量超过0.8 mg·kg^(-1)的国家限量标准。200份话梅样本中铅检出率为85%,铅含量为0.41~0.80 mg·kg^(-1)的占17%,0.4 mg·kg^(-1)以下的占82.5%,整体合格率为99.5%,说明目前永泰县话梅质量安全较高,生产卫生较好。

Tamm溶液提取-石墨炉原子吸收光谱法测定土壤中有效钼

提出了Tamm溶液提取-石墨炉原子吸收光谱法对土壤样品中有效钼的测定方法。有效钼标准曲线的相关系数为0.9995,方法检出限为0.005 mg/kg,定量限为0.018 mg/kg;采用有证标准物质对方法适用性进行了考察,本方法测定值与认定值基本一致,且相对误差(RE)不大于4.17%,相对标准偏差(RSD)不大于7.87%,本方法检出限低、精密度和正确度较好,满足土壤样品测试工作的要求,简化了工作流程,提高了工作效率,适用于批量土壤样品中有效钼的测定。

基围虾中铅镉元素快速检测法的可行性分析

目的分析基围虾中铅元素、镉元素快速检测法的可行性。方法以基围虾作为研究对象,依据国标要求,筛选出5个符合规格的快速检测产品。通过5个快速检测产品对阴性样、1.0倍以及1.8倍限量值的阳性样中的重金属铅和镉进行快速测定,并通过石墨炉原子吸收光谱法对铅镉的快速检测结果进行验证。结果快检1和快检2在铅镉元素含量分别大于0.413 mg/kg及0.488 mg/kg时,检测结果显示为阳性;快检3和快检5在铅镉元素含量分别大于0.607mg/kg及0.604mg/kg时,检测结果显示为阳性,这说明海产品铅镉元素的快速检测产品对基围虾中铅镉元素快速测定具有一定的可行性,检测结果存在一定的差异,主要的原因可能为不同牌子的产品,在技术上存在一定的差异,导致产品的灵敏度存在差异。结论快速检测法测定基围虾中铅、镉元素具有可行性,这为海产品重金属元素测定提供了参考依据。