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三价铬的溶解度及其对使用美国环境保护局(EPA)方法6800测定环境颗粒物中六价铬含量的影响。

Trivalent chromium solubility and its influence on quantification of hexavalent chromium in ambient particulate matter using EPA method 6800.

作者信息

Huang Lihui, Yu Chang Ho, Hopke Philip K, Shin Jin Young, Fan Zhihua

机构信息

Department of Building Science, Tsinghua University, Beijing, China.

出版信息

J Air Waste Manag Assoc. 2014 Dec;64(12):1439-45. doi: 10.1080/10962247.2014.951745.

Abstract

Measurement of carcinogenic Cr(VI) in ambient PM is challenging due to potential errors associated with conversion between Cr (VI) (a carcinogen) and Cr(III) (an essential nutrient). Cr(III) conversion is a particular concern due to its > 80% atomic abundance in total Cr. US. Environmental Protection Agency (EPA) method 6800 that uses water-soluble isotope spikes can be used to correct the interconversion. However, whether the enriched Cr(III) isotope spikes can adequately mimic the Cr(III) species originally in ambient PM is unknown. This study examined the water solubility of Cr(III) in ambient PM and discussed its influence on Cr(VI) measurement. Ambient PM10 samples were collected on Teflon filters at four sites in New Jersey that may have different Cr emission sources. The samples were ultrasonically extracted with 5 mL DI-H2O (pH 5.7) at room temperature for 40 min, and then analyzed by ion chromatography-inductively coupled plasma mass spectrometry (IC-ICPMS). Cr(III) was below detection limit (0.06 ng/m3) for all samples, suggesting water-soluble Cr(III) species, such as CrCl3, Cr(NO3)3, and amorphous Cr(OH)3, in the ambient PM were negligible. Therefore, the enriched 50Cr(III) isotope spike (in the form of Cr(NO3)3) could not mimic the original ambient Cr(III). Only the conversion of 53Cr(VI) (in the form of K2CrO4) was taken into account when correcting the interconversion. We then used NaHCO3-pretreated MCE filters (prespiked with enriched isotope species) to measure Cr(VI) in the ambient PM10. The samples were ultrasonically extracted at 60 C pH 9 solutions for 40 min followed by IC-ICPMS analysis. Due to the correction of Cr(VI) reduction, the Cr(VI) concentrations determined by EPA method 6800, 0.26 ± 0.16 (summer) and 0.16 ± 0.11(winter) ng/m3 (n = 64), were significantly greater than those by the external standard curve, 0.21 ± 0.17 (summer) and 0.10 ± 0.07 (winter) ng/m3 (n = 56) (p < 0.01, Student's t-test). Our study revealed that appropriate application of EPA method 6800 is important because it only applies to soluble fraction of Cr species in ambient PM. Implications: Accurate measurement of carcinogenic Cr(VI) in ambient PM is challenging due to conversion between Cr(VI) (a human carcinogen) and Cr(III) (a human essential nutrient). The conversion of CR(III) is of particular concern due to its dominant presence in total Cr (>80%). This study examined the water solubility of Cr(III) in ambient PM that was collected at four locations in New Jersey. Then we discussed the influence of Cr(III) solubility on the application of EPA method 6800, which utilizes enriched isotope spikes to correct the interconversion. Our results suggested that appropriate application of EPA method 6800 is important because it only applies to soluble fraction of Cr species.

摘要

由于与致癌物六价铬(Cr(VI))和必需营养素三价铬(Cr(III))之间的转化相关的潜在误差,测量环境颗粒物(PM)中的致癌性Cr(VI)具有挑战性。由于Cr(III)在总铬中的原子丰度超过80%,其转化是一个特别值得关注的问题。美国环境保护局(EPA)的方法6800使用水溶性同位素示踪剂可用于校正这种相互转化。然而,富集的Cr(III)同位素示踪剂是否能充分模拟环境PM中原本的Cr(III)物种尚不清楚。本研究考察了环境PM中Cr(III)的水溶性,并讨论了其对Cr(VI)测量的影响。在新泽西州四个可能具有不同Cr排放源的地点,用特氟龙滤膜采集环境PM10样本。在室温下用5 mL去离子水(pH 5.7)对样本进行40分钟的超声提取,然后通过离子色谱 - 电感耦合等离子体质谱法(IC - ICPMS)进行分析。所有样本中的Cr(III)均低于检测限(0.06 ng/m³),这表明环境PM中水溶性的Cr(III)物种,如氯化铬(CrCl₃)、硝酸铬(Cr(NO₃)₃)和无定形氢氧化铬(Cr(OH)₃)含量可忽略不计。因此,富集的⁵⁰Cr(III)同位素示踪剂(以Cr(NO₃)₃的形式)无法模拟原始环境中的Cr(III)。在校正相互转化时,仅考虑了⁵³Cr(VI)(以K₂CrO₄的形式)的转化。然后我们使用经碳酸氢钠预处理且预先添加了富集同位素物种的混合纤维素酯(MCE)滤膜来测量环境PM10中的Cr(VI)。样本在60℃、pH 9的溶液中超声提取40分钟,随后进行IC - ICPMS分析。由于对Cr(VI)还原的校正,EPA方法6800测定的Cr(VI)浓度为0.26±0.16(夏季)和0.16±0.11(冬季)ng/m³(n = 64),显著高于外标曲线法测定的浓度,分别为0.21±0.17(夏季)和0.10±0.07(冬季)ng/m³(n = 56)(p < 0.01,学生t检验)。我们的研究表明,正确应用EPA方法6800很重要,因为它仅适用于环境PM中Cr物种的可溶部分。研究启示:由于人类致癌物Cr(VI)与人类必需营养素Cr(III)之间的转化,准确测量环境PM中的致癌性Cr(VI)具有挑战性。由于Cr(III)在总铬中占主导地位(>80%),其转化尤其值得关注。本研究考察了在新泽西州四个地点采集的环境PM中Cr(III)的水溶性。然后我们讨论了Cr(III)溶解度对EPA方法6800应用的影响,该方法利用富集同位素示踪剂校正相互转化。我们的结果表明,正确应用EPA方法6800很重要,因为它仅适用于Cr物种的可溶部分。

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