[气相色谱-质谱法测定土壤中的 14 种苯胺和联苯胺化合物]。

IF 1.2 4区 化学 Q4 CHEMISTRY, ANALYTICAL
Lijuan Wu, Lili Yang, Enyu Hu, Meifei Wang, Chao Yang, Mingming Yin
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引用次数: 0

摘要

土壤样品基质复杂,苯胺化合物的提取效率低,这限制了许多检测土壤中苯胺和联苯胺化合物的方法。本研究开发了一种基于气相色谱-质谱法的快速、灵敏的方法,用于同时测定土壤中的 14 种苯胺和联苯胺化合物。比较了加速溶剂萃取和振荡分散萃取的萃取效率,发现加速溶剂萃取的回收率较低。因此,采用了三相振荡分散萃取法。由于苯胺和联苯胺化合物是弱碱性物质,因此在萃取过程中向试验体系中加入一定量的碱性水溶液以提高萃取效率。当萃取水相的 pH 值大于 12 时,回收率相对较高。接着,加入乙酸乙酯-二氯甲烷(1∶4,v/v)混合溶剂,振荡 20 分钟萃取目标化合物。通过离心丢弃固相,然后将水相和有机相转移到液体分离漏斗中进一步分离。最后保留有机相。这种预处理过程可防止酸性化合物或其他杂质的共萃取,从而提高该方法的纯化能力。固相萃取(SPE)通常被推荐用于土壤萃取和净化。初步测试表明,与其他固相萃取柱相比,Florisil 固相萃取柱能更好地保留目标物质,并表现出更高的洗脱效率。纯化后,使用氮气鼓风机将有机相浓缩至 1 mL。使用毛细管色谱柱(DB-35MS,30 m×0.25 mm×0.25 μm)对分析物进行气相色谱-质谱分析。对温度程序进行了优化,以分离基线上的目标化合物。具体来说,烘箱初始温度设定为 60 ℃,保持 2 分钟,然后以 5 ℃/分钟的速度升至 130 ℃,再以 30 ℃/分钟的速度升至 300 ℃,保持 4 分钟。进样器和离子源的温度分别为 250 ℃ 和 300 ℃。以苯胺-d5 和苊-d10 为内标进行定量。考察了抗氧化剂添加、萃取溶剂类型、盐析等因素对萃取效率的影响。结果表明,以实际土壤为样品基质,在优化的实验条件下,该方法的性能良好。验证了该方法的准确性和精密度。14种苯胺和联苯胺化合物在0.5-100 mg/L范围内线性关系良好。方法检出限(MDL)为0.02-0.07 mg/kg,定量限(LOQ)为0.08-0.28 mg/kg。目标化合物的添加量为 1 和 10 mg/kg。14种目标化合物在实际土壤中的加标回收率为62.9%~101%,6次精密度试验的相对标准偏差为3.8%~10.3%。该方法有效地抑制了苯胺和联苯胺化合物在萃取过程中的氧化作用,目标化合物在三相作用下的回收率高且稳定性好。此外,该方法操作步骤简单,易于实现。将所提出的方法应用于从江苏省某工业企业采集的疑似苯胺污染土壤,结果检测出两种苯胺化合物。该方法所需样品量少,保存步骤简单有效。此外,该方法还可应用于各类实际土壤。该方法符合现行土壤污染风险管控标准对土壤中苯胺和联苯胺化合物的要求。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Determination of 14 aniline and benzidine compounds in soil by gas chromatography-mass spectrometry].

The complex matrix of soil samples and low extraction efficiency of aniline compounds limit many methods developed for detecting aniline and benzidine compounds in soil. In this study, a rapid and sensitive method based on gas chromatography-mass spectrometry was developed for the simultaneous determination of 14 aniline and benzidine compounds in soil. The collected soil samples were sealed with 5% sodium sulfite solution and refrigerated to inhibit the oxidation of the target compounds for up to 7 d. The extraction efficiencies of accelerated solvent extraction and oscillating dispersion extraction were compared, and the recovery of accelerated solvent extraction was found to be unsuitable. Hence, three-phase oscillating dispersion extraction was adopted. A certain amount of alkaline aqueous solution was added to the test system during extraction to improve the extraction efficiency because aniline and benzidine compounds are weakly alkaline substances. When the pH of the extracted water phase was greater than 12, relatively good recoveries were obtained. Next, a mixed solvent of ethyl acetate-methylene chloride (1∶4, v/v) was added to extract the target compounds via oscillation for 20 min. The solid phase was discarded via centrifugation, and the aqueous and organic phases were transferred to a liquid separation funnel for further separation. Finally, the organic phase was retained. This pretreatment process prevents the co-extraction of acidic compounds or other impurities, thereby enhancing the purification ability of the method. Solid phase extraction (SPE) is generally recommended for soil extraction and purification. A preliminary test showed that compared with other columns, the Florisil SPE column could better retain the target substances and exhibited higher elution efficiency. After purification, the organic phase was concentrated to 1 mL using a nitrogen blower. The analytes were analyzed by gas chromatography-mass spectrometry using a capillary column (DB-35MS, 30 m×0.25 mm×0.25 μm). The temperature program was optimized to separate the target compounds at the baseline. Specifically, the initial oven temperature was set to 60 ℃, held for 2 min, increased to 130 ℃ at a rate of 5 ℃/min, increased to 300 ℃ at a rate of 30 ℃/min, and held for 4 min. The injector and ion source temperatures were 250 and 300 ℃, respectively. Aniline-d5 and acenaphthene-d10 were used as the internal standards for quantification. The effects of antioxidant addition, extraction solvent type, salting out, and other factors on extraction efficiency were investigated. The results showed that the method performed well under the optimized experimental conditions when actual soils were used as real sample matrices. The accuracy and precision of the proposed method were verified. A total of 14 aniline and benzidine compounds demonstrated good linearities in the range of 0.5-100 mg/L. The method detection limits (MDLs) ranged from 0.02 to 0.07 mg/kg, and the limits of quantification (LOQs) ranged from 0.08 to 0.28 mg/kg. The target compounds were spiked at contents of 1 and 10 mg/kg. The spiked recoveries of the 14 targets in actual soils were 62.9%-101%, and the relative standard deviations (RSDs) of six precision tests were 3.8%-10.3%. The proposed method effectively inhibited the oxidation of aniline and benzidine compounds during extraction, and the target compounds exhibited high recoveries and good stabilities in the presence of three phases. Moreover, the operating procedure was simple and easy to implement. The proposed method was applied to the soil collected from an industrial enterprise in Jiangsu province that was suspected to be contaminated with aniline, and two aniline compounds were detected. The developed method requires a small sample size, and the preservation step is simple and effective. In addition, it can be applied to various types of actual soils. The method meets the requirements of current soil pollution risk control standards for aniline and benzidine compounds in soils.

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色谱
色谱 CHEMISTRY, ANALYTICAL-
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1.30
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42.90%
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