ライフサイエンスコーパス: chemical warfare agent

1 and used in the catalytic decontamination of chemical warfare agents.

2 phorous chemicals including insecticides and chemical warfare agents.

3 rable characteristics for the destruction of chemical warfare agents.

4 xification of organophosphate pesticides and chemical warfare agents.

5 by selected organophosphorus pesticides and chemical warfare agents.

6 counterterrorism responses to biological and chemical warfare agents.

7 oxification of agricultural insecticides and chemical warfare agents.

8 on of organophosphate-based insecticides and chemical warfare agents.

9 off from sites that produce the compounds as chemical warfare agents.

10 In addition, these toxins are suspected chemical warfare agents.

11 xification of toxic industrial chemicals and chemical warfare agents.

12 The VX nerve agent is one of the deadliest chemical warfare agents.

13 drome" among veterans potentially exposed to chemical warfare agents; 2) compare the findings of fact

14 Organophosphorus (OP) insecticides and chemical warfare agents act primarily by inhibiting acet

15 a vesicant, similar to Lewisite, a potential chemical warfare agent and an environmental contaminant.

16 hydrocarbons and the high-speed analysis of chemical warfare agent and explosive markers.

17 The investigated compounds include an intact chemical warfare agent and structurally related molecule

18 luoridates, which are common constituents of chemical warfare agents and agricultural pesticides.

19 ompounds, a class of chemicals that includes chemical warfare agents and flame retardants.

20 screening, identification, and validation of chemical warfare agents and other small-molecule analyte

21 nger countermeasure against organophosphorus chemical warfare agents and pesticides is warranted.

22 A series of ~20 drugs, V-type chemical warfare agents and pesticides, simulating toxic

23 A wide range of chemical warfare agents and their simulants are catalyti

24 espread use for the screening of explosives, chemical warfare agents, and illicit drugs.

25 Most of the organophosphate chemical warfare agents are a mixture of two stereoisome

26 for the in-the-field detection of traces of chemical warfare agents as well as to differentiate betw

27 veterans who had witnessed the demolition of chemical warfare agents at the Khamisiyah site in Iraq h

28 f organophosphates, including pesticides and chemical warfare agents, at rates approaching the diffus

29 os that mimic real-world events, including a chemical warfare agent attack, the contamination of a ho

30 Chemical warfare agents containing phosphonate ester bon

31 ection limits is observed in the analysis of chemical warfare agent (CWA) degradation products in env

32 ped to determine oxidation products of three chemical warfare agent (CWA) related phenylarsenic compo

33 ht mass spectrometer (IM(tof)MS) to detect a chemical warfare agent (CWA) simulant from aerosol sampl

34 ed identification of single particles of the chemical warfare agent (CWA) simulants at each laser flu

35 ight mass spectrometer (IM(tof)MS) to detect chemical warfare agent (CWA) simulants from both aqueous

36 Aerosolized chemical warfare agent (CWA) simulants trimethyl phospha

37 Detection of chemical warfare agent (CWA) simulants, illicit drugs, a

38 Ion mobility spectra of chemical warfare agent (CWA) stimulant dimethyl methylph

39 f catalytic oxidative decontamination of the chemical warfare agent (CWA) sulfur mustard (HD, bis(2-c

40 vice when using fixed sampling times for the chemical warfare agent (CWA) surrogate compound, diisopr

41 ironment, are examined as decontaminants for chemical warfare agents (CWA).

42 Organophosphorus chemicals, including chemical warfare agents (CWAs) and insecticides, are acu

43 or degradation of toxic chemicals, including chemical warfare agents (CWAs) and toxic industrial chem

44 of highly toxic substances in air, including chemical warfare agents (CWAs) and toxic industrial chem

45 After an incident with suspected use of chemical warfare agents (CWAs) has occurred, fast and re

46 phenylarsenic chemicals that originated from chemical warfare agents (CWAs) have been detected and id

47 The recent alleged use of A-series chemical warfare agents (CWAs) highlights the urgent nee

48 The threat associated with chemical warfare agents (CWAs) motivates the development

49 ions (3-30%) efficiently decomposes adsorbed chemical warfare agents (CWAs) on microporous activated

50 rus nerve agents, a class of extremely toxic chemical warfare agents (CWAs), have remained a threat t

51 avenues for the mitigation of the effects of chemical warfare agents (CWAs), including sensing, catal

52 al forensics, it has not yet been applied on chemical warfare agents (CWAs).

53 ion of a CE-based method for the analysis of chemical warfare agent degradation products in agent neu

54 hods have been developed for the analysis of chemical warfare agent degradation products in reaction

55 the detection of narcotics, explosives, and chemical warfare agents, drift tube ion mobility spectro

56 ng of pharmaceutical compounds, detection of chemical warfare agents, environmental hygiene technolog

57 SARS-CoV-2 outbreak and the alarming use of chemical warfare agents highlight the necessity to produ

58 ger group of veterans potentially exposed to chemical warfare agents; however, veterans who had witne

59 Recently, a new class of reactivators of chemical warfare agent inhibited acetylcholinesterase (A

60 Lewisite is a potent arsenic-based chemical warfare agent known to induce painful cutaneous

61 by several organophosphorus (OP) pesticides, chemical warfare agents, lubricants, and plasticizers, l

62 derstanding the hydrolysis of the very toxic chemical warfare agent mustard (bis(2-chloroethyl)sulfid

63 ased adsorbent design for protection against chemical warfare agents (organophosphorus nerve agents,

64 environmental remediation, detoxification of chemical warfare agents, photocatalytic energy conversio

65 widely utilized insecticide paraoxon and the chemical warfare agent sarin.

66 rca 20-fold increase in activity against the chemical warfare agent simulant dimethyl-4-nitrophenyl p

67 tection for the trace analysis in air of the chemical warfare agent simulant methyl salicylate (1.24

68 mechanism of adsorption and decomposition of chemical warfare agent simulants on Zr-based MOFs open n

69 Using a set of chemical warfare agent simulants with nominally the same

70 diacetylmorphine), organic salts, peptides, chemical warfare agent simulants, and other small organi

71 ructurally related precursor ions, including chemical warfare agent simulants, fentanyls and other op

72 Data are given for chemical warfare agent simulants, methyl salicylate, and

73 specificity for NPPMP, the analogue for the chemical warfare agent soman.

74 on the capture and catalytic degradation of chemical warfare agents such as sarin and sulfur mustard

75 Incorporation of the chemical warfare agent sulfur mustard (SM) produces a co

76 important precursors of the extremely toxic chemical warfare agent sulfur mustard and classified, re

77 n-hexane, used as a structural mimic for the chemical warfare agent sulfur mustard gas.

78 numerous positive and negative ions with VX chemical warfare agent surrogates representing the amine

79 Among the chemical warfare agents, the extremely toxic nerve agent

80 rganophosphates have been adapted for use as chemical warfare agents; the most well-known are GA, GB,

81 ents to organophosphorus (OP) pesticides and chemical warfare agents; therefore, they warrant explora

82 low-cost technique for the identification of chemical warfare agents, toxic chemicals, or explosives

83 tremely toxic and environmentally persistent chemical warfare agent VX (O-ethyl S-2-(diisopropylamino

84 or demeton S (P-S bond), an analogue for the chemical warfare agent VX.

85 Chemical warfare agents were demolished by US soldiers a

86 omise for monitoring degradation products of chemical warfare agents, with advantages of speed/warnin