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3차 정제수를 활용한 이온크로마토그래피의 대기 중 유기 지방산류 분석법에 대한 검토 KCI 등재

A study on an analytical method for volatile fatty acids (VFAs) in the atmosphere by using ion chromatography and ultrapure water

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실내환경 및 냄새 학회지 (Journal of Odor and Indoor Environment)
한국냄새환경학회 (Korean Society Of Odor Research And Engineering)
초록

Since 2010, the Odor Prevention Act has identified and regulated four types of fatty acids as substances that cause odors. Four types of fatty acids are contributors to odor pollution and are sensitive to changes in temperature and humidity. However, the current analysis method has several limitations, including dependency on the timing of sampling before and after the procedure, as well as dependency on the specific analysis method employed. The aim of this study is to assess the efficacy of the ion chromatography analysis method by utilizing ultrapure distilled water as a means to improve the current approach. Initially, the analysis system underwent a quality assessment. The results indicated a linearity (R2) of 0.99, a limit of 10 nmol/mol or lower, supporting the conclusion that it is suitable. Furthermore, the investigation focused on the substance’s tendency to change over time in ultrapure water and under alkali absorption (0.01N NaOH). At a concentration of 0.95 ng (low-concentration standard sample), the confirmed peak area values ranged from 0.0004 μg/min to 0.0010 μg/min, resulting in an injection variation of approximately ± 0.001. At 23.7 ng (high-concentration standard sample), the peak area value fluctuated between 0.008 μg/min and 0.013 μg/ min, with an average of ± 0.002. Therefore, storing the material at temperatures below 4°C for up to 3 days (72 hours) after manufacturing seemed to facilitate the optimal conditions for maintaining its stability without significant changes taking place. Finally, blank samples from the laboratory, equipment, and site were analyzed. Out of the four substances analyzed, only n-butyl acid was detected in all three background samples. It was confirmed that it represented 4% of the peak area in the 4.94 ng standard sample.

목차
1. 서 론
2. 연구 방법
    2.1 표준용액의 조제 및 이온크로마토그래피의 분석 조건
    2.2 시간 경과에 따른 흡수액 내 분석 대상 물질의변화 경향
    2.3 바탕시료의 확인
3. 분석결과
    3.1 이온크로마토그래피의 직전성, 재현성 및 방법검출한계
    3.2 시간 경과에 따른 흡수액 내 분석 대상물질의변화 경향
    3.3 바탕시료 확인
4. 고 찰
5. 결 론
감사의 글
References
저자
  • 강희주(한국공학대학교 생명화학공학과) | Hee Ju Kang (Department of Chemical Engineering & Biotechnology, Tech University of Korea)
  • 박승준(한국공학대학교 생명화학공학과) | Seung Joon Park (Department of Chemical Engineering & Biotechnology, Tech University of Korea) Corresponding author