• 제목/요약/키워드: pyrolysis-GC/MS

검색결과 109건 처리시간 0.021초

인화성액체를 촉진제로 사용한 방화화재의 감식기법에 관한 연구 (Arson Fire Analysis Involving the Use of Flammable Liquilds as Accelerants)

  • 최민기;한동훈;최돈묵
    • 한국화재소방학회논문지
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    • 제28권4호
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    • pp.64-72
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    • 2014
  • 본 연구에서는 연소잔류물에 남아있는 미세한 인화성액체의 성분을 검출하기 위해 가스검지관, Gas Chromatograph/Mass Spectrometer (GC/MS), 열분해분석장비를 활용하였다. 일반적으로 연소했을 경우와 인화성액체를 첨가하여 연소된 경우의 성분분석결과를 비교하였다. 결과적으로 인화성액체를 첨가하지 않고 연소 후 생성된 화재잔해물에서도 가스검지관이 반응하는 것을 확인할 수 있었다. 일반적인 연소와 열분해를 통해 생성된 화학성분의 차이가 있었으며, 이는 연소 환경의 차이로 인한 것으로 판단된다. 대표적인 석유화학제품인 우드데코타일(PVC) 시료는 인화성액체를 첨가하지 않고 일반적으로 연소시켰을 경우에도 감정인의 정확한 판단을 방해할 수 있는 방해물질인 Toluene, Ethylbenzene, Undecane, Dodecane 등이 검출되는 것을 확인하였다.

ZnO를 첨가한 PVC와 PS 혼합물의 열분해 특성에 관한 연구 (A Study on the Co-pyrolysis Characteristics of PVC and PS Mixtures with ZnO)

  • 오세천;정명욱;김희택;이해평
    • 공업화학
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    • 제16권4호
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    • pp.513-518
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    • 2005
  • 혼합비율 및 반응온도의 변화에 따른 ZnO가 첨가된 PVC와 PS의 혼합 열분해 특성에 관한 연구를 TG와 GC-MS를 이용하여 수행하였다. 본 연구로부터 혼합물에 있어서 PS의 양이 증가할수록 액상 생성물은 증가하였으며 기상 생성물은 감소함을 알 수 있었다. 또한 ZnO의 첨가량이 증가할수록 기상 생성물과 염화수소의 발생량은 감소하였으며 염화수소의 발생 억제 및 액상 생성물의 최대수율을 얻기 위한 최적의 반응온도는 $500^{\circ}C$임을 알 수 있었다.

Formation of Polybrominated Dibenzo-p-dioxins/Furans (PBDDs/Fs) by the Pyrolysis of 2,4-Dibromophenol, 2,6-Dibromophenol, and 2,4,6-Tribromophenol

  • Na, Yun-Cheol;Hong, Jong-Ki;Kim, Kang-Jin
    • Bulletin of the Korean Chemical Society
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    • 제28권4호
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    • pp.547-552
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    • 2007
  • This study examined the thermal reactions of 2,4-dibromophenol (diBP), 2,6-diBP and 2,4,6-triBP. The products obtained under pyrolytic conditions were analyzed by gas chromatography/mass spectrometry (GC/MS). 2,7-dibromodibenzo-p-dioxin (diBDD) was the major compound produced from the thermal reaction of 2,4-diBP. In addition, monoBDD and triBDDs were obtained through a process of debromination and bromination, respectively. The pyrolysis of 2,6-diBP and 2,4,6-triBP produced two major brominated dioxin isomers through direct condensation and a Smiles rearrangement. The two ortho-Brs in 2,6-diBP and 2,4,6-triBP mainly led to the production of dioxins, whereas in addition to 2,7-diBDD, 2,4-diBP produced two furans as minor products, 2,8-dibromodibenzofuran (diBDF) and 2,4,8-triBDF, through the intermediate dihydroxybiphenyl (DOHB). The maximum yield of the major dioxins was obtained at 400 oC, and decomposition by debromination at 500 oC resulted in less substituted bromodioxins.

Transformation of dissolved organic matter in a constructed wetland: A molecular-level composition analysis using pyrolysis-gas chromatography mass spectrometry

  • Park, Jongkwan;Choi, Mijin;Cho, Jaeweon;Chon, Kyongmi
    • Environmental Engineering Research
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    • 제23권4호
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    • pp.390-396
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    • 2018
  • This study investigated the transformation of dissolved organic matter (DOM) in a free-water surface flow constructed wetland. Pyrolysis gas chromatography-mass spectrometry (Py-GC/MS) coupled with preparative high-performance liquid chromatography (prep-HPLC) was used to analyze the compositions of biopolymers (polysaccharides, amino sugars, proteins, polyhydroxy aromatics, lipids and lignin) in DOM according to the molecular size at three sampling points of the water flow: inflow, midflow, and outflow. The prep-HPLC results verified the decomposition of DOM through the decrease in the number of peaks from three to one in the chromatograms of the sampling points. The Py-GC/MS results for the degradable peaks indicated that biopolymers relating to polysaccharides and proteins gradually biodegraded with the water flow. On the other hand, the recalcitrant organic fraction (the remaining peak) in the outflow showed a relatively high concentration of aromatic compounds. Therefore, the ecological processes in the constructed wetland caused DOM to become more aromatic and homogeneous. This indicated that the constructed wetland can be an effective buffer area for releasing biochemically stable DOM, which has less influence on biological water quality indicators, e.g., biochemical oxygen demand, into an aquatic ecosystem.

적외선분광분석과 Py-GC/MS를 이용한 옻칠 및 캐슈칠도막 분석 (Analysis of Lacquer and CNSL Using Infrared Spectrometer and Pyrolysis-GC/MS)

  • 최재완;김수철
    • Journal of the Korean Wood Science and Technology
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    • 제46권1호
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    • pp.1-9
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    • 2018
  • 칠기문화재 보존에 옻칠이 사용되지만 근대화로 인해 캐슈칠과 같은 합성도료가 같이 사용되는 추세이다. 보존윤리에서는 문화재 보존 시 동일 재료가 사용되어야 한다고 명시되어있다. 따라서 칠기문화재 보존에는 옻칠과 같은 천연 도료가 사용되어야 한다. 하지만 옻칠과 캐슈칠의 성분이 유사하여 전문가들도 쉽게 구분하지 못하는 실정이다. 본 연구에서는 IR과 Py-GC/MS를 이용하여 이를 분석하고 식별 키워드를 찾고자 하였다. IR 분석 결과 옻칠은 $720cm^{-1}$ 대에서 피크가 확인되었으며 캐슈칠은 $750cm^{-1}$, $720cm^{-1}$, $700cm^{-1}$ 대에서 피크가 확인되었다. Py-GC/MS 결과 두 종류의 시료에서 Benzene과 Phenol계 화합물과 알킬사슬고리에 기인하는 성분이 검출되었다. 하지만, 캐슈칠에서는 Hexanoic acid라는 성분이 검출되었고 옻칠에서는 검출되지 않았다. 이러한 분석방법을 토대로 진정성 있는 칠기문화재 보존처리 및 복원에 활용될 수 있을 것이라 판단된다.

Analysis of Minor Additives and Polymer in Used-stripper Using Pyrolysis-Gas Chromatography/Mass Spectrometry and Electrospray Mass Spectrometry

  • Koo, Jeong-Boon;Park, Chang-Hyun;Han, Cheol;Na, Yun-Cheol
    • Bulletin of the Korean Chemical Society
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    • 제30권2호
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    • pp.368-372
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    • 2009
  • The trace polymer and additives in used stripper solutions were analyzed by a combination of Py-GC/MS and ESI-MS. In the comparison of the pyrolysates produced by the pyrolysis of the pure stripper and photoresist at $500{^{\circ}C}$, the presence of novolac polymer in the used stripper was confirmed by the presence of the characteristic peaks of its pyrolysates, such as those of the methylphenol, di-methylphenol and methylenebis(methylphenol) isomers. The intact trace polymer was measured by ESI-MS, which showed the distribution of oligomers at intervals of 120 Da, indicating di-methylphenol to be the repeat unit. Additional MS/MS measurements demonstrated that the end group is methylphenol and the repeat groups are di-methylphenol. Some modified oligomers caused by the methylation or di-methylation of the repeat unit were also identified. Although the polymer is only present at a trace level in the used stripper, these combined analytical methods provided the means to qualify the stripper solution through the identification and structural determination of the polymer.

Identification of Coffee Fragrances Using Needle Trap Device-Gas Chromatograph/Mass Spectrometry (NTD-GC/MS)

  • Eom, In-Yong;Jung, Min-Ji
    • Bulletin of the Korean Chemical Society
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    • 제34권6호
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    • pp.1703-1707
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    • 2013
  • A fast and simple sampling and sample preparation device, (NTD) has been developed and applied to sample and analyze volatile components from ground coffee beans. Coffee fragrances and other volatile organic compounds (VOCs) were sampled by the NTD and then analyzed by gas chromatograph-mass spectrometry (GC/MS). Divinylbenzene (DVB) particles (80/100 mesh size) were the sorbent bed of the NTD. More than 150 volatile components were first identified based on the database of the mass library and then finally 30 fragrances including caffeine were further confirmed by comparing experimental retention indices (i.e. Kovat index) with literature retention indices. Total sampling time was 10 minutes and no extra solvent extraction and/or reconstitution step need. Straight n-alkanes (C6-C20) were used as retention index probes for the calculation of experimental retention indices. In addition, this report suggests that an empty needle can be an alternative platform for analyzing polymers by pyrolysis-GC/MS.

유동층(流動層) 급속열분해(急速熱分解)에 의한 폐(廢) Polypropylene fraction으로부터 BTEX-aromatics의 회수(回收) (Recovery of BTEX-aromatics from Post-consumer Polypropylene Fraction by Pyrolysis Using a Fluidized Bed)

  • 조민환;정수화;김주식
    • 자원리싸이클링
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    • 제17권6호
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    • pp.50-56
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    • 2008
  • Post-consumed플라스틱 중 폐 polypropylene fraction으로 분리된 재료를 이용하여 열분해 실험을 수행하였다. 본 연구의 목적은 열분해 생성오일 중 용제로 사용이 가능한 BTEX-aromatics 수율이 반웅온도에 따라 어떤 영향을 받는지 고찰하는 것이었다. 이를 위하여 열전달이 우수한 유동층 반응기를 이용하여 $650^{\circ}C$에서 $700^{\circ}C$ 사이의 반응온도에서 열분해 실험을 진행하였다. 본 실험에서는 오일생성 극대화를 위해 열분해 반응 중 생성되는 가스를 유동화 가스로 사용하였으며, 유동화 가스의 유량과 시료 투입율은 실험 중에 일정하게 유지하였다. 실험결과 gas, oil 및 char가 반응 생성물로 얻어졌다. 생성 가스는 GCs(TCD, FID)를 사용하여 정량 분석하였고 정성적 분석을 위해서는 GC-MS 시스템을 이용하였다 정확한 분석을 위해서 생성오일은 진공 증류하여 distillation residue를 분리하였으며, 증류한 oil은 GC-MS 통해 정성 및 정량적 분석을 수행하였다. 반응온도가 높아질수록 distillation oil중의 BTEX-aromatics의 함량은 증가하였으며 $695^{\circ}C$에서 약 30% 정도의 함량을 나타내었다. 생성 가스는 대부분 $CH_4$, $C_2H_4$, $C_2H_6$, $C_3H_6$, $C_4H_{10}$로 구성되어 있었으며, 고위 발열량은 약 45 MJ/kg로서 열분해 공정 에너지원이나 기타 연료용 에너지원으로 사용가능할 것으로 평가되었다.

Thermal Degradation Kinetics of Antimicrobial Agent, Poly(hexamethylene guanidine) Phosphate

  • Lee, Sang-Mook;Jin, Byung-Suk;Lee, Jae-Wook
    • Macromolecular Research
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    • 제14권5호
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    • pp.491-498
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    • 2006
  • The thermal degradation of poly(hexamethylene guanidine) phosphate (PHMG) was studied by dynamic thermogravimetric analysis (TGA) and pyrolysis-GC/MS (p-GC). Thermal degradation of PHMG occurs in three different processes, such as dephosphorylation, sublimation/vaporization of amine compounds and decomposition/ recombination of hydrocarbon residues. The kinetic parameters of each stage were calculated from the Kissinger, Friedman and Flynn-Wall-Ozawa methods. The Chang method was also used for comparison study. To investigate the degradation mechanisms of the three different stages, the Coats-Redfern and the Phadnis-Deshpande methods were employed. The probable degradation mechanism for the first stage was a nucleation and growth mechanism, $A_n$ type. However, a power law and a diffusion mechanism, $D_n$ type, were operated for the second degradation stage, whereas a nucleation and growth mechanism, $A_n$ type, were operated again for the third degradation stage of PHMG. The theoretical weight loss against temperature curves, calculated by the estimated kinetic parameters, well fit the experimental data, thereby confirming the validity of the analysis method used in this work. The life-time predicted from the kinetic equation is a valuable guide for the thermal processing of PHMG.

Influence of Maleic Anhydride Grafted onto Polyethylene on Pyrolysis Behaviors

  • Chung, Yu Yeon;Choi, Sung-Seen
    • Elastomers and Composites
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    • 제51권3호
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    • pp.233-239
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    • 2016
  • Polyethylene (PE) and maleic anhydride-grafted PE (PE-g-MAH) were pyrolyzed, and their pyrolysis products were analyzed using gas chromatography/mass spectrometry (GC/MS) to investigate the influence of MAH grafted onto PE on pyrolysis behaviors. Major pyrolysis products of PE and PE-g-MAH were n-alkanes, 1-alkenes, ${\alpha},{\omega}$-alkadienes, and aromatic compounds. 1-Alkenes were more formed than n-alkanes, ${\alpha},{\omega}$-alkadienes, and aromatic compounds. Butadiene was more produced from PE than PE-g-MAH, whereas toluene and ethyl benzene were more generated from PE-g-MAH than PE. Difference in the pyrolysis behaviors between PE and PE-g-MAH were explained by initial decomposition of MAH moiety.