• Title/Summary/Keyword: Sarin(GB)

Search Result 7, Processing Time 0.024 seconds

Hydrolysis of Sarin(GB) in Aqueous NaOH Solution (가성소다 수용액에서 사린(GB)의 가수분해)

  • Lee, Yong-Han;Lee, Jong-Chol;Hong, Deasik
    • Korean Chemical Engineering Research
    • /
    • v.45 no.2
    • /
    • pp.172-177
    • /
    • 2007
  • The hydrolysis reaction of sarin(GB), one of the nerve agents was studied in aqueous sodium hydroxide(NaOH) solutions to find the experimental conditions which can convert GB into the less toxic compounds. 10 wt% of GB was added into the aqueous NaOH(2.05 eq) in a small-scale jacket-attached reactor connected to a circulator. The reaction rate constants were measured at three temperatures(50, 70 and $90^{\circ}C$) and the reaction times required to degrade the material to > 99% were calculated at different temperatures. In this study, 10 wt% of GB was degraded to 99.99% in 1.2hr at $90^{\circ}C$ by the aqueous NaOH solution. The major hydrolysate of GB was isopropyl methylphosphonate.

A Study on the Hydrolysis of Sarin and Soman by Merrifield-Type Diaminatedpolystyrene-Cu (II) Heterogeneous Polymers (Merrifield-Type Diaminatedpolystyrene-Cu (II) 불균일 촉매에 의한 Sarin과 Soman 분해반응 연구)

  • 정우영;계영식
    • Journal of the Korea Institute of Military Science and Technology
    • /
    • v.3 no.1
    • /
    • pp.164-175
    • /
    • 2000
  • Three compounds of Cu(II)-loaded N,N,N'-trimethylethylenediaminated Merrifield-type polymers were synthesized with yields higher than 80%, and the hydrolysis reaction rates of O-isopropylmethyl-phosphonofluoridate(GB) and O-pinacolylmethylphosphonofluoridate (GD) catalyzed by them have been surveyed. GB and GD hydrolysis by Cu(II)-loaded polymers occurs via intermediate complex mechanism where rapid equilibrium to form intermediate complex between substrate and Cu(II)-loaded polymers($K_f$) is followed by rate determining hydrolysis step($k_1$). The measured activation parameters for $k_1$ are ${\Delta}H^{\ddag}$ : $17.75{\pm}0.98kJ/mol$ ${\Delta}S^{\ddag}$ / : $-218.42{\pm}3.35J/mol$ K, $E^{\circ}_a$ : $20.22{\pm}0.98kJ/mo1$ for GB and ${\Delta}H^{\ddag}$ / : $11.16{\pm}1.15kJ/mol,$${\Delta}S^{\ddag}$ /: $-258.57{\pm}3.93J/mol$ K, $E^{\circ}_a$ : $13.64{\pm}1.15 kJ/mol$ for GD. Standard enthalpy/entropy changes corresponding to the intermediate complex formation constant $K_f$ are ${\Delta}H^{\circ}$ : $37.05{\pm}2.19 kJ/mo1,$$ {\Delta}S^{\circ}$ : $163.12{\pm}7.49 J/mol$ K and ${\Delta}H^{\circ}$ : 418.59{\pm}2.04 kJ/mol,$ ${\Delta}S^{\circ}$ : 4111.92{\pm}6.98 J/mol$ K for GB and GD, respectively, The electron push-pull mechanism by Cu(II)-loaded polymers lowers the P-F bond breaking energy(~400 kJ/mol) to less than 1/20 compared to the case in which no Cu(II)-loaded resin presents. Analysis of $K_f$ and 4k_1$ over pH=6.5~8.0 range suggest that the GB and GD hydrolysis occurs intramolecularily with $pK_a$ =7.29 for ligated $H_2O$ and $t_{1/2}$=36.9 sec, $pK_a$ = 7.06 and $t_{1/2}$=177.7 sec for GB and GD, respectively.

  • PDF

Hazards of Chemical Agents and Its mechanism of Action (화학무기의 유해성과 작용 메카니즘)

  • Chung, Yeong-Jin
    • Proceedings of the Korea Institute of Fire Science and Engineering Conference
    • /
    • 2013.11a
    • /
    • pp.115-116
    • /
    • 2013
  • 본 연구에서는 유기인 유도체 중 생리활성이 커서 독성이 있는 화합물의 구조를 분석하였다. 5-[(b-monoaza-15-crown-5)ethyloxy]-2iodosbenzoic acid의 IBA 촉매를 합성하여 그 반응성을 p-nitrophenyldiphenylphosphate (PNPDPP)와 Isopropyl methylphosphonofluoridate (Sarin GB), Pinacolyl methylphosphonofluoridate (Soman, GD)를 기질로 하여 연구하였다. PNPDPP 가수분해 반응에서는 긴 알킬작용기로 친유성을 증가시킨 촉매가 더 상전이 촉매로 작용함이 확인되었다.(t1/2 = 5 sec, pH = 8.07)

  • PDF

Chemical Agent Disposal Technology by a 2-step Process(II) (Agent Hydrolysis followed by Supercritical Water Oxidation) (화학작용제의 2단계 폐기기술(II) (작용제 가수분해 후 초임계수 산화처리))

  • Lee, Jong-Chol;Bambang, Veriansyah;Song, Eun-Suk;Kim, Jae-Duck
    • Journal of the Korea Institute of Military Science and Technology
    • /
    • v.10 no.1
    • /
    • pp.123-129
    • /
    • 2007
  • A 2-step process for the safe destruction of chemical wafare agents(agent hydrolysis followed by supercritical water oxidation) was studied to obtain kinetic data for the pilot plant design. This process is simple to operate by using commercial equipments and could be applied as an alternative technology to incineration. Sarin(GB) and sulfur mustard(HD) were hydrolysed in sodium hydroxide and water respectively and their hydrolysates and OPA, which is binary agent for GB were oxidized in a continuous flow supercritical water oxidation system. Destruction efficiencies of the materials were above 99.99% in supercritical water.

A Study on the Chemical Warfare Agents Dispersion Modelling in a Naturally Ventilated Indoor System (자연환기상태 실내공간에서의 화학작용제 확산 모델링 연구)

  • Kye, Young-Sik;Chung, Woo-Young;Kim, Yong-Joon
    • Journal of the Korea Institute of Military Science and Technology
    • /
    • v.11 no.4
    • /
    • pp.133-140
    • /
    • 2008
  • The purpose of this study is to provide response methods to minimize the damage from chemical terrorism in a naturally ventilated indoor system using several types of dispersion simulations. Three chemical warfare agents such as sarin(GB), phosgene and chlorine gas which have high potential to be used in terror or to be involved with accidents were selected in this simulation. Fire dynamic simulation based on Large Eddy Simulation which is effective because of less computational effort and detailed expression of the dispersion flow was adopted to describe the dispersion behavior of these agents. When the vent speed is 0.005m/s, the heights of 0.1 agent mass fraction are 0.9m for sarin, 1.0m for phosgene and 1.1m for chlorine gas, and the maximum mass fraction are 0.27 for all three agents. However, when the vent speed is increased to 0.05m/s, the heights of 0.1 agent mass fraction become 1.6m for all three agents and maximum mass fraction inside the room increase to 0.70 for sarin, 0.58 for phosgene and 0.53 for chlorine gas. It is shown that molecular weight of the agents has an important role for dispersion, and it is important to install ventilation system with height less than 1.6m to minimize the damage from chemical toxicity.

Chemical Agent Disposal Technology by a 2-step Process(I) (Agent Hydrolysis followed by Incineration) (화학작용제의 2단계 폐기기술(I) (작용제 가수분해 후 액중배기식 소각처리))

  • Lee, Jong-Chol;Lee, Yong-Han;Oh, Sok-Chong;Hong, Dea-Sik
    • Journal of the Korea Institute of Military Science and Technology
    • /
    • v.10 no.1
    • /
    • pp.116-122
    • /
    • 2007
  • A 2-step process for the safe disposal of chemical warfare agents(agent hydrolysis followed by incineration In the submerged-quench incinerator) was studied to obtain basic data for the design of pilot plant in the future. Sample materials used for the hydrolysis reaction were sarin(GB), sulfur mustard (HD), and methylphosphonic difluoride(DF). The hydrolysates of these materials were thermally destroyed in a submerged-quench incineration system. Experimental conditions for achieving destruction efficiency of 99.99% in both steps were established and phosphoric acid was recovered from the waste water when destroying DF hydrolysate in the incinerator. Treated water could be reused as process water for the agent hydrolysis.

Liquid-phase Microextraction Pretreatment Techniques for Analysis of Chemical Warfare Agents and Their Degradation Byproducts in Environmental Aqueous Samples (환경샘플 내 화학작용제 및 분해물질 분석을 위한 Liquid Phase Microextraction (LPME) 전처리 기법)

  • Kim, Dongwook;Chung, Wooyoung;Kye, Youngsik
    • Applied Chemistry for Engineering
    • /
    • v.26 no.1
    • /
    • pp.17-22
    • /
    • 2015
  • International interests in chemical warfare agents (CWAs) have been increased recently because of the use of sarin (GB) in Syrian civil war which caused around 1,300 casualties in 2013. After exposing to natural environments, CWAs undergo hydrolysis or photodegrade to non-toxic degradation byproducts. Generally, CWAs and their degradation byproducts are present at very low concentration (e.g. several ppb), thus pretreatment processes including separation, extraction and concentration are required prior to any analyses. Liquid-liquid extraction and solid-phase extraction (SPE) are common techniques to pretreat environmental samples. Recently, a novel pretreatment method, liquid phase miecoextraction (LPME), has been applied to CWAs analysis, which could reduce amounts of solvent used but promote analytical efficiencies. Fundamental backgrounds of LPME and its application to CWAs analysis were reviewed.