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Elemental Analysis of Atmospheric Fine Particles at Trace and Ultra-Trace Levels using Microwave Acid Digestion and Inductively Coupled Plasma - mass Spectrometry

机译:使用微波酸消化和电感耦合等离子体质谱法在痕量和超痕量水平下大气细粒的元素分析

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The toxicity of trace metals that only constitute a small fraction of total particulate mass (PM) and their use as markers in source - receptor modeling studies have resulted in a need to accurately determine the elemental composition of airborne PM. Data on metals composition of PM are also useful in determining the anthropogenic and non-anthropogenic sources of PM to develop effective air quality management strategies. High temperature - high pressure microwave assisted acid digestion followed by inductively coupled plasma - mass spectrometry (ICP-MS) is capable of accurately quantitating a wide variety of elements in airborne PM. To date, the vast majority of studies have focused on determining only the main groups and main transition series elements. These studies have not quantified rare earth elements (REEs) that can be unique tracers to track PM emissions from petroleum refining operations. The loss of REE enriched zeolite catalysts from refineries' fluidized bed catalytic cracking (FCC) is the major source of REEs in atmospheric fine particles (PM{sub}2.5). Therefore, it is crucial to analyze REEs in ambient PM{sub}2.5 and FCC catalysts. A major challenge in quantifying FCC emissions is that they are present in trace to ultra-trace levels in ambient PM{sub}2.5 and the lack of an analytical method (using ICP-MS) due to absence of certified reference material for FCC catalysts. The principal goal of this presentation will be to document some of our recent research on developing innovative microwave digestion methods and on the impacts of petroleum refining operations on REEs in Houston area fine particles. Specific objectives are to: (1) develop a PM dissolution method using microwave assisted acid digestion followed by ICP-MS analysis to accurately quantify wide range of elements in the atmospheric PM at trace levels (2) evaluate feasibility of generating HF in-situ in closed Teflon lined vessels during digestion to avoid direct handling of hazardous HF, and (3) optimize the digestion method for accurate and precise quantification of REEs in FCC catalysts, which can also be used to determine REE concentrations in ambient PM{sub}2.5.
机译:痕量金属的毒性仅构成少量颗粒物质(PM)及其作为源 - 受体建模研究中的标志物的用途,导致需要准确地确定空气中PM的元素组成。 PM金属组合物的数据也可用于确定PM的人为和非人为植物来源,以开发有效的空气质量管理策略。高温高压微波辅助酸消解,然后进行电感耦合等离子体 - 质谱(ICP-MS)能够精确定量空气中PM中的各种元素。迄今为止,绝大多数研究都集中在仅确定主要组和主要过渡序列元素。这些研究没有量化稀土元素(REES),可以是独特的示踪剂,以跟踪来自石油精炼操作的PM排放。 REE富含炼油厂流化床催化裂化(FCC)的富含沸石催化剂的损失是大气细粒(PM {SUB} 2.5)中的主要来源。因此,在环境PM {Sub} 2.5和FCC催化剂中分析REES至关重要。定量FCC排放的主要挑战是它们在痕量至外部痕量水平中存在于环境PM {Sub} 2.5中,并且由于缺乏FCC催化剂的认证参考材料而缺乏分析方法(使用ICP-MS)。本演示文稿的主要目标将是我们最近的一些关于开发创新微波消解方法的研究以及石油精炼业务对休斯顿地区细颗粒的芦苇的影响。具体目标是:(1)使用微波辅助酸消解开发PM溶解方法,然后进行ICP-MS分析,以精确地量化在痕量水平(2)中的大气PM中的各种元素(2)评估原位产生HF的可行性消化过程中封闭的铁氟龙衬里血管,以避免直接处理危险的HF,(3)优化FCC催化剂中REES的准确和精确定量的消化方法,其也可用于确定环境温度下PM {SUB} 2.5中的REE浓度。

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