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1.
采用微波消解电感耦合等离子体质谱法同时测定大气颗粒物中13种元素,选择硝酸体系消解20 min,硝酸加入体积为8 mL。Cu、Ni、Cr、Pb、Al、Mg、Mn、Ca在0μg/L~100μg/L,Ag、Ba、Co、Cd、Sn在0μg/L~5.00μg/L范围内线性良好,除Al、Mg、Ca检出限较高外,其他10种元素的检出限为0.07 ng/m3~1.82 ng/m3(按采样体积0.688 m3、定容体积50 mL计),滤膜样品平行测定3次的RSD≤1.2%,加标回收率在92%~108%之间。  相似文献   

2.
采用全自动固相萃取处理废水,气相色谱-质谱联用法测定废水中的15种硝基苯类化合物,通过优化试验条件,使方法在0.100mg/L~10.0mg/L范围内线性良好。方法检出限为0.012μg/L~0.038μg/L,标准溶液11次测定结果的RSD为1.0%~7.5%。对实际水样做2个质量浓度水平的加标回收试验,平均加标回收率为78.0%~107%。  相似文献   

3.
采用微波消解处理鱼肉样品,用电感耦合等离子体质谱法测定样品中砷和汞。通过试验优化微波消解参数、酸体系及赶酸温度,用在线加入内标方法消除基体干扰及仪器漂移对测定的影响。方法在0μg/L~40. 0μg/L范围内线性良好,砷和汞的方法检出限分别为0. 002 mg/kg和0. 001 mg/kg,实际样品6次测定结果的RSD为5. 4%~15. 6%,加标回收率为90. 0%~110%。将该方法用于测定芹菜和扇贝标准物质,测定值在标准值不确定度范围内。  相似文献   

4.
采用顶空进样-气相色谱/质谱联用法(HS-GC/MS)测定水和废水中苯、甲苯、乙苯、对二甲苯、间二甲苯、邻二甲苯、异丙苯、苯乙烯等8种苯系物,优化了分析条件,讨论了色谱柱极性、加热温度、平衡时间和进样次数对测定结果的影响。8种苯系物在1.00μg/L~1 000μg/L范围内线性良好,方法检出限为0.22μg/L~0.38μg/L,实际样品平行测定的相对标准偏差5.0%,加标回收率在86.0%~115%之间。  相似文献   

5.
采用微波消解-电感耦合等离子体质谱法测定水系沉积物中12种元素,通过优化试验相关条件消除质谱干扰和非质谱干扰对测定的影响,使方法在0μg/L~200μg/L范围内线性良好,当取样质量为0.25 g,定容体积为50 m L时,各元素的方法检出限为0.002 mg/kg~0.05 mg/kg。用该方法测定沉积物标准物质,6次测定结果均在标准值范围内,RSD为1.3%~6.1%,实际样品的加标回收率为83.0%~97.0%。  相似文献   

6.
水样经硝酸和过氧化氢消解,Tl~+被氧化为Tl~(3+),在王水和Fe~(3+)介质中,TlCl~-_4被聚氨酯泡塑吸附富集,沸水脱附后用石墨炉原子吸收光谱法测定。用硝酸钯-抗坏血酸基体改进剂提高测定灵敏度,方法在0μg/L~25.0μg/L范围内线性良好,方法检出限为0.01μg/L。实际样品加标后6次测定结果的RSD为3.0%~11.0%,平均加标回收率为95.0%~99.8%。有证标准物质的测定结果在标准值范围内,相对误差为-4.8%。  相似文献   

7.
采用全自动石墨消解仪代替水浴锅加热王水消解法处理土壤样品,用原子荧光法测定消解液中的砷和汞。该方法在0μg/L~20.0μg/L范围内线性良好,测定有证标准土壤样品的结果均在标准值允许范围内,砷、汞测定结果的RSD分别为2.5%~4.8%、2.9%~5.4%,比王水消解法的测定结果更靠近标准值,实际土壤样品的加标回收率分别为94.6%~104%、92.6%~105%。  相似文献   

8.
电感耦合等离子体原子发射光谱法测定废水中的铊   总被引:1,自引:0,他引:1  
采用电感耦合等离子体原子发射光谱仪(ICP-AES)测定废水中铊,并对测定波长、介质及其酸度、共存元素干扰等因素进行分析和条件优化,使该方法在0 mg/L~5.00 mg/L范围内线性良好,相关系数为0.999 9。方法检出限为22μg/L,该方法对铊标准样品测定的结果在保证值范围内,4份废水样7次测定结果的RSD为0.2%~0.8%,实际废水样品的加标回收率为98.0%~100%。  相似文献   

9.
氢化物发生-原子荧光光谱法测定土壤中镉   总被引:1,自引:0,他引:1       下载免费PDF全文
采用氢化物发生-原子荧光光谱法测定土壤中的镉,优化了试验条件,讨论了共存元素的干扰及消除办法。方法在0μg/L~120μg/L范围内线性良好,检出限为0.003 mg/kg(按取样0.600 g定容至45 mL计),土壤标准样品测定的RSD≤3.7%,加标回收率为94.8%,与石墨炉原子吸收分光光度法的测定结果相吻合。  相似文献   

10.
采用微波消解-石墨炉原子吸收分光光度法测定北方某市环境空气PM10及PM2.5样品中的镉,并比较了硝酸-盐酸体系与硝酸-过氧化氢体系的消解效果。结果表明,硝酸-盐酸体系与硝酸-过氧化氢体系的方法检出限分别为0.006、0.008μg/L,相对偏差分别为5.4%、7.9%,加标回收率为85%~110%,其检出限、精密度与加标回收率均满足要求。2种消解体系均能较好地提取颗粒物中的镉,测定结果无显著差异(P0.05),但硝酸-过氧化氢体系更适合作为多种分析仪器测试通用的前处理体系。  相似文献   

11.
Forty-two soil and apple samples from central Greece were collected and analyzed with regards to the content in major (Ca, Fe, K, Mg, Na, P, and S) and trace elements (As, B, Ba, Cd, Co, Cr, Cu, Hg, Mn, Mo, Ni, Pb, Sb, Sc, Se, Sr, Ti, and Zn). Soil samples were analyzed by inductively coupled plasma atomic emission spectrometry, while for the apples inductively coupled plasma mass spectrometry was implemented. Several elements such as As, B, Cd, Cr, Cu, Fe, Mn, Ni, Pb, Se, Ti, and Zn, represent high concentrations in apples from the study area. These relatively high concentrations may be a consequence of the local geology, along with the excessive application of agricultural products such as fertilizers and agrochemicals.  相似文献   

12.
干旱区中小城市降雪中金属元素沉降通量研究   总被引:1,自引:0,他引:1  
文章以干旱区中小城市昌吉市为研究区,选择2011年12月至2012年2月期间较为典型的6场次降雪进行采样,利用ICP-MS测定降雪中20种金属元素,并探讨金属元素的沉降通量、富集特征及其来源。研究表明,降雪中Al的年沉降通量最大,为10.32 mg/m2;Fe、Ba、Zn、V、Cu的年沉降通量次之,集中在1.40~6.11 mg/m2;As、Ni、Mn、Cr、Mo、Sb年沉降通量较小,集中在0.08~0.39 mg/m2;Be、Co、Cd、Pb、Hg、Tl、Th、U的年沉降通量最小,集中在0.001~0.053 mg/m2。Al、Fe、Mn、Be、Th富集系数在0.32~3.05之间,这些金属元素主要来自自然来源;Cd与Hg富集系数分别为923.23、2511.47,达到严重富集的程度;其余金属元素富集系数在10~500之间,属中度富集。昌吉州境内煤炭资源丰富,近年煤炭开采量较大,城区供暖面积不断加大,供暖不断加强;市区车流量急剧增加,运输排放加剧;近郊及周边地区各类工业的分布等是各类金属元素在雪中富集的主要原因。冰雪节后冰灯拆除,降雪可有效捕集大气中的汞,冬季气温不利于Hg挥发等对Hg的严重富集也有重要影响。  相似文献   

13.
The aim of this paper is to evaluate total and bioavailable concentration of heavy metals in agricultural soils in order to estimate their distribution, to identify the possible correlations among toxic elements and the pollution sources, to distinguish the samples in relation to sampling site or to sampling depth, and to evaluate the available fraction providing information about the risky for plants. In particular, we reinvestigated total concentrations of As, Be, Cd, Cr, Cu, Fe, Hg, Mn, Ni, Pb, Sb, V, and Zn and available concentrations of As, Be, Cd, Cr, Cu, Hg, Ni, Pb, Sb, and Zn in soil from Apulia (Southern Italy). Analytical results showed that total concentrations, for all soils, are in the range permitted by regulations in force in Italy, but some soils evidence slight enrichment of Cd, Cr, Cu, Pb, and Zn. All the heavy metals in the available fraction were below the detection limits of the analytical techniques used except Cu, Ni, Pb, and Zn.  相似文献   

14.
Kidney and muscle samples were collected from 197 bovine and 33 porcine carcasses and liver and muscle from 115 poultry carcasses across the province. These tissues were analyzed for the following 13 elements, Ag, As, Cd, Co, Cr, Cu, Hg, Mo, Ni, Pb, Sb, Se, and Zn. The intent of the study was to determine normal background levels. Tissue concentration of these elements fell into five orders of magnitude ranging from < 10 g kg–1 for Ag to over 10 mg kg–1 for Zn. Similar concentrations were observed in the three specie tissues being compared except for higher concentrations of Cd and Sb in bovine kidneys. In avian tissues Mo contents were higher in liver than muscle. When samples from all three species were grouped by age, no distinct trends were observed to indicate an increase in metal contents with age, with the exception of Cd in bovine kidneys.  相似文献   

15.
2021年1-3月,采集湖南省某典型金属冶炼城市不同功能区的降尘样品,分析测定了17种重金属元素含量,其中15种重金属元素含量超出了湖南背景值,分别为Ag、Fe、Cd、Ti、Sb、Tl、Pb、As、Zn、Cu、Mo、Ni、Cr、Ba、Mn。采用地累积指数法、潜在生态危害指数法和健康风险评价模型对大气降尘中重金属可能造成的生态风险和健康风险进行评价。结果表明:受长期的有色金属冶炼影响,Ag、Cd、Fe、Sb、Ti、Tl 6种重金属达到了极重度污染,Pb、As、Zn、Cu、Mo在中度污染程度以上。工业区的综合生态危害指数远高于工业居民混合区、工业农业混合区、居民区和交通区,达到了极强生态危害级别。健康风险评价结果显示:大气降尘中As和Pb存在非致癌风险,As、Cd和Ni存在致癌风险,且经口摄入是最主要的暴露途径。与青少年和儿童相比,大气降尘中重金属对成人造成的风险较高,且成年女性面临的风险高于成年男性。  相似文献   

16.
Concentrations of 12 metals (Fe, Mn, Cr, Mo, Ni, Pb, Se, Sr, U, V, Zn, and Zr) in surface sediments of Karachi Coast, Pakistan were determined to evaluate their distribution and pollution assessment. The measured metals in the sediments were found to be in the range of Fe, 0.84–6.96 %; Mn, 300–1,300 μg/g; Cr, 12.0–319.84 μg/g; Mo, 0.49–2.03 μg/g; Ni, 1.53–58.86 μg/g; Pb, 9.0–49.46 μg/g; Se, 0.25–.86 μg/g; Sr, 192–1185 μg/g; U, 0.19–1.66 μg/g; V, 15.80–118.20 μg/g; Zn, 15.60–666.28 μg/g; and Zr, 44.02–175.26 μg/g. The mean contents of the metal studied were: Fe, 3.07 %, Mn, 0.05 %; Cr, 96.75 μg/g; Mo, 1.34 μg/g; Ni, 31.39 μg/g; Pb, 23.24 μg/g; Se, 0.61 μg/g; Sr, 374.83 μg/g; U, 0.64 μg/g; V, 61.75 μg/g; Zn, 204.75 μg/g; and Zr:76.27 μg/g, and arrangement of the metals from higher to lower mean content in this area is: Fe?>?Zn?>?Mn?>?Sr?>?Zn?>?Cr?>?Zr?>?V?>?Ni?>?Pb?>?Mo?>?U?>?Se. There is no significant correlation among most of these metals, indicating different anthropogenic and natural sources. To assess ecotoxic potential of marine sediments, Numerical Sediment Quality Guidelines were also applied. The concentration of Pb in all the sediments except one was lower than the threshold effect concentration (TECs) showing that there are no harmful effects to marine life from Pb. On the other hand, the concentrations of Cr, Ni, and Zn exceeded TEC in three stations, indicating their potential risk. The degree of pollution in sediments for metals was assessed by calculating enrichment factor (EF) and pollution load index (PLI). The results indicated that sediments of Layari River Mouth Area, Fish Harbour, and KPT Boat Building Area are highly enriched with Cr and Zn (EF?>?5). Sediments of Layari River Outfall Zone were moderately enriched with Ni and Pb (EF?>?2). The pollution load index was found in the range of 0.98 to 1.34. Lower values of PLI (≤1) at most of sampling locations imply no appreciable input from anthropogenic sources. However, relatively higher PLI values (>1) at Layari River Mouth Area, Fish Harbour, and KPT Boat Building Area are attributed to increased human activity in the area.  相似文献   

17.
In this study, the concentrations of 13 elements (Al, Fe, Mn, Cr, Ni, Zn, Co, As, Pb, Cu, Mo, Hg, and Cd) were determined in the sediments of three different sites in the Kapulukaya Dam Lake between May 2007 and November 2008. They ranged from 1.47 to 4.64 for Al, 0.92 to 3.48 for Fe (in percent), 326.60 to 1053.00 for Mn, 98.00 to 1,116.00 for Cr, 24.70 to 127.10 for Ni, 14.80 to 124.20 for Zn, 11.0 to 43.20 for Co, 5.00 to 29.30 for Cu, 9.10 to 69.70 for As, 8.60 to 34.00 for Pb, 2.50 to 5.20 for Mo, 1.00 to 1.60 for Hg, and 0.50 to1.80 for Cd in microgram per gram dry weight sediment. The contamination degree of the sediment was assessed on the basis of enrichment factor and corresponding sediment quality guideline. The calculated enrichment factors (EF, measured metal vs. background concentrations) indicated that the effect of man-made activities on the occurrence of concentrations could be accounted for the majority of heavy metals namely Mn, As, Ni, Cu, Zn, Cr, Co, Mo, and Cd, whereas such affect was not detected for Hg and Pb. The maximum values of the EF were represented by As, minimum values by Hg at all sites. Mean EF values were 36.60 and 0.70 for As and Hg, respectively. This study has clearly assessed a certain level of heavy metal pollution in the region, based particularly on the findings from sediment.  相似文献   

18.
Metallic elements (As, Be, Ca, Cd, Co, Cr, Fe, K, Mn, Ni, Pb, Sb, Se, and Zn) in PM10 aerosols were determined at urban and industrial sites, which are affected by traffic and residential sources, metallurgical activity, and petrochemical and steel works. The effect of the long-range transported Asian Dust on the metal content of aerosols was also examined. At the urban sampling site, concentrations of As, Cd, Pb, Se, and Zn were assigned to road traffic and combustion sources, Ca and Fe to soil dust sources from long-range transported Asian Dusts, and Cr and Ni to metallurgical sources transported from the nearby industrial complex, based on Principal Component Analysis (PCA). Enhanced Cr and Ni concentrations at the metallurgical industrial site suggest that local emissions from metal-assembly facilities and manufacture of alloys contributed to elevated levels of those metals. We also observed that petrochemical activities contributed to increased levels of Sb and Zn. When Asian Dust events occurred, Ca, Fe, K, and Zn concentrations dramatically increased compared to values without the Asian Dust. Two different types of Asian Dust events were observed. For the Asian Dust event 1 (4/1/2007), the Fe and K concentrations were much higher by a factor of 2–3 than those for the Asian Dust event 2 (3/2/2008), while As, Mn, and Zn concentrations were significantly higher on the Asian Dust event 2. Backward trajectory analysis showed that for the Asian Dust event 2, the air mass had passed over the heavily industrialized zones in China during long-range transport to the current sampling site, suggesting that the As, Mn, and Zn may have originated from industrial sources.  相似文献   

19.
Heavy Metal Pollution of Surface Soil in the Thrace Region, Turkey   总被引:1,自引:0,他引:1  
Abstact Samples of surface soil were collected at 73 sites in the Thrace region, northwest part of Turkey. Two complementary analytical techniques, epithermal neutron activation analysis (ENAA) and atomic absorption spectrometry (AAS) with flame and graphite furnace atomization were used to determine 35 elements in the soil samples. Concentrations of As, Cd, Co, Cu, Mn, Ni, Pb and Zn were determined using AAS and GF AAS, and ENAA was used for the remaining 27 elements. Results for As, Ba, Br, Ca, Cd, Ce, Co, Cr, Cs, Cu Eu, Fe, Hf, I, In, K, La, Mn, Mo, Na, Nd, Ni, Pb, Rb, Sb, Sc, Sm, Sr, Ta, Tb, Th, Ti, U, V and Zn are reported for the first time for soils from this region. The results show that concentrations of most elements were little affected by the industrial and other anthropogenic activities performed in region. Except for distinctly higher levels of Pb, Cu, Cd and Zn in Istanbul district than the median values for the Thrace region, the observed distributions seem to be mainly associated with lithogenic variations. Spatial distributions of As, Cd, Cr, Cu, Ni, Pb and Zn were plotted in relation to the concentration values in soil using Geographic Information System (GIS) technology  相似文献   

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