From the Decomposition of Chemical Warfare Agents to the Decontamination of Cytostatics

被引:7
|
作者
Stengl, Vaclav [1 ,2 ]
St'astny, Martin [1 ,3 ]
Janos, Pavel [3 ]
Mazanec, Karel [4 ]
Perez-Diaz, Jose Luis [5 ]
Stenglova-Netikova, Irena R. [2 ]
机构
[1] Inst Inorgan Chem ASCR Vvi, Dept Mat Chem, Husinec Rez 25068, Czech Republic
[2] Charles Univ Prague, Fac Med 1, Dept Oncol, Katerinska 32, Prague 12800 2, Czech Republic
[3] JE Purkyne Univ Usti Nad Labem, Fac Environm, Kralova Vysina 7, Usti Nad Labem 40096, Czech Republic
[4] Mil Res Inst, Veslarska 230, Brno 63700, Czech Republic
[5] EPS Univ Alcala, Madrid 28805, Spain
关键词
NANOSTRUCTURED METAL-OXIDES; MESOPOROUS MANGANESE OXIDE; SULFUR MUSTARD; STOICHIOMETRIC DEGRADATION; PARATHION METHYL; DOPED TITANIA; MIXED OXIDES; VX; DESTRUCTION; TIO2;
D O I
10.1021/acs.iecr.7b04253
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
The ability of pilot samples of destructive metal oxide sorbents to decompose a sulfur mustard-type chemical warfare agent into nontoxic products in a nonaqueous solvent was compared with that of the commercial product FAST-ACT. Additionally, samples of the destructive metal oxide sorbents were used to decompose nitrogen mustards, which are used as chemotherapeutic agents, in water, and the results, were compared with those of FAST-ACT. All the prepared pilot samples exhibited stoichiometric activities, i.e., the degradation rate expressed by the rate constant, k [s(-1), min(-1), and the decomposition efficiencies, which are expressed by the degree of conversion d [%], higher than those of the comparative commercial product FAST-ACT. Scaling up the sulfur mustard decomposition from the laboratory conditions (reaction volume, 4 L) to quarter operating (pilot) reaction conditions (reaction volume, 100 L) had a positive effect on the reaction and final product.
引用
收藏
页码:2114 / 2122
页数:9
相关论文
共 50 条
  • [1] DECONTAMINATION OF CHEMICAL WARFARE AGENTS
    YANG, YC
    BAKER, JA
    WARD, JR
    CHEMICAL REVIEWS, 1992, 92 (08) : 1729 - 1743
  • [2] Study of Decomposition of Chemical Warfare Agents using Solid Decontamination Substances
    Capoun, Tomas
    Krykorkova, Jana
    TOXICS, 2019, 7 (04)
  • [3] Decontamination of Chemical Warfare Agents by Photocatalysis
    Hirakawa, Tsutomu
    Mera, Nobuaki
    Sano, Taizo
    Negishi, Nobuaki
    Takeuchi, Koji
    YAKUGAKU ZASSHI-JOURNAL OF THE PHARMACEUTICAL SOCIETY OF JAPAN, 2009, 129 (01): : 71 - 92
  • [4] Decontamination of Chemical and Biological Warfare Agents
    Seto, Yasuo
    YAKUGAKU ZASSHI-JOURNAL OF THE PHARMACEUTICAL SOCIETY OF JAPAN, 2009, 129 (01): : 53 - 69
  • [5] Recent Advances in Decontamination of Chemical Warfare Agents
    Khan, Abdul Wadood
    Kotta, Sabna
    Ansari, Shahid Husain
    Ali, Javed
    Sharma, Rakesh Kumar
    DEFENCE SCIENCE JOURNAL, 2013, 63 (05) : 487 - 496
  • [6] DECONTAMINATION OF WATER CONTAINING CHEMICAL WARFARE AGENTS
    LINDSTEN, DC
    JOURNAL AMERICAN WATER WORKS ASSOCIATION, 1978, 70 (02): : 90 - 92
  • [7] RECOVERY OF DNA FROM EXHIBITS CONTAMINATED WITH CHEMICAL WARFARE AGENTS: A PRELIMINARY STUDY OF THE EFFECT OF DECONTAMINATION AGENTS AND CHEMICAL WARFARE AGENTS ON DNA
    Wilkinson, Della
    Sweet, David
    Fairley, Diane
    CANADIAN SOCIETY OF FORENSIC SCIENCE JOURNAL, 2007, 40 (01) : 15 - 22
  • [8] Rapid nucleophilic/oxidative decontamination of chemical warfare agents
    Wagner, GW
    Yang, YC
    INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 2002, 41 (08) : 1925 - 1928
  • [9] Decontamination of Chemical Warfare Agents with Nanosize Metal Oxides
    Wagner, George W.
    NANOSCALE MATERIALS IN CHEMISTRY : ENVIRONMENTAL APPLICATIONS, 2010, 1045 : 125 - 136
  • [10] Personal decontamination and detoxification of chemical warfare agents (CWA)
    Gordon, RK
    Owens, RR
    Baker, K
    Askins, LY
    Doctor, BP
    Clarkson, ED
    Mitcheltree, LW
    Schutz, S
    Kelleher, C
    Washington, N
    Railer, R
    FASEB JOURNAL, 2005, 19 (04): : A489 - A489