• 제목/요약/키워드: exothermic peak

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니트로페닐하이드라진의 열분해 특성에 관한 연구 (A Study on the Thermal Decomposition Characteristics of Nitrophenylhydrazine)

  • 김관응;이근원
    • 한국안전학회지
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    • 제16권2호
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    • pp.75-79
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    • 2001
  • For handling and storage of reactive chemicals, the hazard evaluations have been extremely important. In the chemical industry, the most concerns are focused on the thermal harzards such as runaway reactions and thermal decompositions, which are mostly governed by thermodynamics and reaction kinetics or these reactive chemical in the system. This study no investigated the thermal decomposition characteristics of nitrophenylhydrazine isomers by using differential scanning calorimeter(DSC) and accelerating rate calorimeter(ARC). Experimental results showed that exothermic onset-temperatures in nitrophenylhydrazine(NPH) isomers were about 160-$210^{\circ}C$ by DSC and 100-$150^{\circ}C$ by ARC. The decomposition temperature acquired by ARC was about 50-$60^{\circ}C$ lower than that by DSC. Reaction heats were about 40-100cal/g by DSC and 330-750ca1/g by ARC. While ortho isomer of NPH show two distinct exothermic peaks, para isomer shows a single peak in DSC curves. The first exothermic peak for 2-NPH is mainly due to intramolecular dehydration forming 1-hydroxybenzotriazole(HOBT) and the second exothermic peak is mainly due to the decomposition of HOBT formed in the first step of decomposition. The exothermin peak in the DSC curve for 4-NPH is mainly due to dissociation of hydrazino and nitro groups.

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열적 피로에 의한 전원코드의 발화 특성과 전기화재 분석에 관한 연구 (A Study on the Electrical-Fire Analysis and Firing Characteristics of Power Cord by Thermal Stress)

  • 최충석;송길목;김향곤;김동욱;김동우
    • 한국화재소방학회:학술대회논문집
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    • 한국화재소방학회 2003년도 춘계학술논문발표회논문집
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    • pp.164-170
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    • 2003
  • In this paper, we studied on the firing characteristics and electrical fire analysis of power cord deteriorated by thermal stress. The cross section of PVC insulating cord deteriorated by indirect flame decreased through heat convection. PVC insulating cord deteriorated by direct flame was bumpy shape. The exothermic peak of normal cord was shown at ($526.7^{\circ}C$), but the peaks or on(heat treatment temperature) ($150^{\circ}C$) cord was shown at ($299.6^{\circ}C$) and [$502.2^{\circ}C$]. The exothermic peaks according to high temperature were similar to those of amorphous carbon. In the FT-IR analysis, the absorption peak of normal cord indicated double bond of oxygen and carbon in benzene ring at 1720.0$cm^{1}$. As the HTT was high, the height of characteristic peak decreased and the peak of carbonyl group was shown at about 1625.7$cm^{-1}$. The characteristic peak of single bond(O-H) was shown at about 3479.2$cm^{-1}$. In case of the internal part of wire covering deteriorated by over current, the characteristic peak were shown at about 3417.3$cm^{-1}$ and 1600.2$cm^{-1}$. The above results show that we can distinguish the differences according to the fire pattern through the internalㆍexternal analysis of wire covering deteriorated by heat.

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트래킹에 의해 열화된 페놀수지의 탄화 특성 (Carbonization Characteristics of Phenolic Resin Deteriorated by Tracking)

  • 송길목;최충석;노영수;곽희로
    • 대한전기학회논문지:전기물성ㆍ응용부문C
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    • 제53권1호
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    • pp.1-7
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    • 2004
  • This paper describes the carbonization characteristics of a phenolic resin deteriorated by tracking under the environment of a fire. In the experiment, a liquids droplet of 1[%] NaCl was dripped on the phenolic resin to cause a tracking with 110[V], 220[V] voltages applied. It can be addressed from the experimental results that when an insulator is carbonized by an external fire, its structure is amorphous. If an insulator is carbonized by electrical cause, on the other hand, its structure would be crystalline. In order to observe the surface change of the phenolic resin, the tracking process was analyzed by using SEM. In the case that the materials are carbonized under heat or fire, the exothermic peak appears around 500[$^{\circ}C$]. This is one of the important factors to determine the cause of fires. As a result of DTA, the exothermic peaks of an untreated sample showed at 333.4[$^{\circ}C$], 495.7[$^{\circ}C$] but those of a sample deteriorated by tracking appeared at 430.6[$^{\circ}C$], 457.6[$^{\circ}C$] in a voltage of 110[V], and at 456.2[$^{\circ}C$], 619.7[$^{\circ}C$] in a voltage of 220[V]. It is possible, therefore, to distinguish a virgin sample from carbonized samples(graphite) by the exothermic peak.

진공증착법을 이용한 PVDF 유기박막의 제조와 전기전도현상 (The Fabrication of PVDF Organic Thin Films by Physical Vapor Deposition Method and Their Electrical Conductivity Phenomena)

  • 임응춘;이덕출
    • E2M - 전기 전자와 첨단 소재
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    • 제10권3호
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    • pp.217-225
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    • 1997
  • In this study, the PVDF organic thin film was fabricated by the physical vapor deposition method to be dry-process. The distance of heat source and substrate was 5[cm] and the temperature of substrate was 30[.deg. C], when the pressure had reached 2.0 x 10$^{-5}$ [Torr], the temperature of heat source was reached to 285[.deg. C] to heat at 6-8[.deg. C/min] rate, the shutter was opened and deposition was started. TG-DTA(Thermogravimetric-Differential Thermal Analysis) spectrum of PVDF pellets showed that endothermic peak arose at 170[.deg. C] and exothermic peak at 524[.deg. C], but that of thin PVDF film showed that endothermic peak arose at 145[.deg. C] and exothermic peak at 443[.deg C]. The current density was increased linearly with increasing voltage but increased nonlinearly with higher electric field than 250[kV/cm] and activation energy was about 0.667[eV] at the temperature of 30-90[.deg. C].

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Thermite Reaction Between CuO Nanowires and Al for the Crystallization of a-Si

  • Kim, Do-Kyung;Bae, Jung-Hyeon;Kim, Hyun-Jae;Kang, Myung-Koo
    • Transactions on Electrical and Electronic Materials
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    • 제11권5호
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    • pp.234-237
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    • 2010
  • Nanoenergetic materials were synthesized and the thermite reaction between the CuO nanowires and the deposited nano-Al by Joule heating was studied. CuO nanowires were grown by thermal annealing on a glass substrate. To produce nanoenergetic materials, nano-Al was deposited on the top surface of CuO nanowires. The temperature of the first exothermic reaction peak occurred at approximately $600^{\circ}C$. The released heat energy calculated from the first exothermic reaction peak in differential scanning calorimetry, was approximately 1,178 J/g. The combustion of the nanoenergetic materials resulted in a bright flash of light with an adiabatic frame temperature potentially greater than $2,000^{\circ}C$. This thermite reaction might be utilized to achieve a highly reliable selective area crystallization of amorphous silicon films.

Nb-25 at%Al 혼합분말의 기계적 합금화 거동 (Alloying Behavior of Nb-25 at%Al Powder Mixtures by Mechanical Alloying)

  • 이상호
    • 한국분말재료학회지
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    • 제3권1호
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    • pp.42-48
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    • 1996
  • To investigate the phase transformation behaviors of mechanically alloyed Nb-25 at%Al powders, the mixed Nb-25 at%Al powders were mechanically alloyed in SPEX 8000 Mixer/Mill. Mechanical alloying(MA) time was varied between 0.5 hour and 72 hours. The phase formation behaviors of these mechanically alloyed powders were examined using X-ray diffraction(XRD), scanning electron microscopy(SEM), transmission electron microscopy(TEM), and differential thermal analysis(DTA). Appreciable amorphization started from 6 hours of MA. The powders mechanically alloyed for 10 hours were in almost amorphous phase. DTA results showed that the powders mechanically alloyed for 12 hours had a strong exothermic peak about$600^{\circ}C$, whereas the powders mechanically alloyed for 6 hours had two exothermic peaks. The first peak was found to be due to the stress relief effect and the second one due to the formation of$Nb_{3}Al,Nb_{2}Al and Nb_{2}C$phases by crystallization.

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STS304의 레이저 절단에서 보조가스 압력이 미치는 영향 (Effect of Assistant Gas Pressure on Laser Cutting of STS304)

  • 이호준;조용무;유웅재;김재도
    • 한국정밀공학회지
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    • 제12권3호
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    • pp.15-22
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    • 1995
  • This paper presents the effects of assistant gas pressure on laser cutting. To investigate the effects of assistant gas pressure, pressure measuring system was constructed with good handling and precision at low price. The measured results discussed compare with that of laser cutting of STS304. The assistant gas pressure varied with the variation of distance between nozzle and workpiece. The peak pressure existed at some distance and could be known by using the deviced pressure measuring system. The higher assistant gas pressure helps to remove the dross and the exothermic energy out of the material. The quantity of dross beneath the workpiece decreases and the kerf width narrows at measured peak pressure.

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누전차단기 외함 전원측 단자사이의 트래킹에 의한 탄화특성 분석 (The Analysis of the Carbonization Properties between RCD Source Terminals Deteriorated by Tracking)

  • 최충석;송길목;김동우
    • 한국화재소방학회논문지
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    • 제17권4호
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    • pp.13-19
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    • 2003
  • 본 논문은 누전차단기 외함 전원측 단자사이에서 발생하는 전기화재 원인에 대한 분석을 연구하였다. 누전차단기는 보호범위의 전기시설물에서 누전 또는 과부하에 의한 차단을 목적으로 한다 누전차단기의 전원측 단자는 트래킹에 의해 화재로 쉽게 이어질 수 있다. 따라서, 누전차단기의 재현실험을 통해 트래킹시료($E_1$)와 화재현장에서 트래킹된 것($S_1$)을 비교분석하여 전기화재의 원인을 밝히는데 중요한 자료가 되도록 하였다. 실험은 IEC Publ. 112법을 응용하여 실시하였고 누전차단기에서 미소방전과 건조대가 발생한 후 소손되는 것을 확인하였다. $_1$에서 전원측 단자간의 절연저항은 약 25.7Ω이고 $S_1$의 절연저항은 약 58.6Ω이었다. $E_1$의 발열피크는 $491.0^{\circ}C$$603.2^{\circ}C$였다. $603.2^{\circ}C$에서의 발열피크는 트래킹에 의한 것이다. $S_1$의 발열피크는 $593.1^{\circ}C$에서 나타났다. 트래킹에 의해 변화된 시료는 IR 흡수스펙트럼에서 $1590 cm^{-1}$ 에서 흡광피크가 나타나지 않았다.

수용성 페놀-포름알데히드 수지의 열안정성 및 경화거동 (Thermal Stability and Cure Behavior of Waterborne Phenol-Formaldehyde Resin)

  • 윤성봉;김진우;조동환
    • 접착 및 계면
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    • 제7권1호
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    • pp.16-22
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    • 2006
  • 본 연구에서는 페놀수지 SMC 제조에 사용되는 수용성 레졸형 페놀-포름알데히드 수지의 열안정성과 경화 발열반응 피크의 변화에 미치는 경화온도 및 경화시간의 영향을 열중량분석기와 시차주사열량계를 사용하여 조사하였다. 수용성 페놀-포름알데히드 수지의 중량감소는 주로 $200^{\circ}C,\;400^{\circ}C$ 그리고 $500^{\circ}C$ 부근에서 세 단계로 발생하였다. 경화된 수지의 $750^{\circ}C$에서 탄화수율은 약 62%~65%이었다. 수용성 페놀수지의 열안정성은 경화온도와 경화시간이 증가할수록 증가하였다. 경화시 발열반응은 약 $120^{\circ}C{\sim}190^{\circ}C$ 사이에서 진행되며, 발열피크의 최대점은 약 $165^{\circ}C{\sim}170^{\circ}C$ 사이에서 관찰되었다. 발열반응 곡선의 형태와 발열피크의 최대점은 주어진 경화온도와 경화시간에 의존하였다. 경화되지 않은 수지에 포함되어 있는 $H_2O$ 및 휘발성분을 제거하기 위하여 경화 또는 성형 전에 적어도 $100^{\circ}C$ 이상에서 약 60분 이상의 열처리가 요구되었다. $130^{\circ}C$에서 120분 동안의 경화는 수용성 페놀-포름알데히드 수지의 발열피크를 사라지게 하며, $180^{\circ}C$에서 60분 동안이 후경화는 수지의 열안정성을 더욱 향상시켜 주었다.

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딕카이트의 열적 특성 연구 (Thermal Behavior of Dickite)

  • 조현구
    • 한국광물학회지
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    • 제12권1호
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    • pp.11-22
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    • 1999
  • Thermal behavior of dickite was studied by thermal analysis, X-ray diffraction analysis, electron microprobe analysis, and scanning electron microscopy, Dickite has an endothermic peak at about$ 650^{\circ}C$ and an exothermic one at $960^{\circ}C$ in the differential thermal analysis. The endothermic reaction is assigned to the decomposition of dickite to meta-dickite. Hydroxyl radicals are removed from dickite structure by the reaction, resulting in the weight loss about 10.5~14.5% and appearance of a 14$\AA$ phase different from other kaolin minerals. The reaction slowly proceed in the range of $200^{\circ}C$. As the completion of decomposition, aciclular mullite forms at the expense of meta-dickite plates with random crystallographic relationship. Mullites have diverse silica versus alumina ratio. The exothermic reaction without weight loss seems to be due to the formation of spinel and amorphous silica. The spinel phase shows cryptocrystalline globular morphology accompanying a little amount of silica. From spinel phase shows cryptocrystalling globular morphology accompanying a little amount of silica. From this work, it is suggested that mullite is formed from meta-dickite much lower temperature than the reported one in the previous works.

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