ライフサイエンスコーパス: trinitrotoluene

1 4,6-trinitrophenylmethylnitramine), and TNT (trinitrotoluene).

2 tranitro-1,3,5,7-Tetrazocine)) or TNT (2,4,6-trinitrotoluene).

3 l enterotoxin B) and a small molecule (2,4,6-trinitrotoluene).

4 ed in a plant species to sense environmental trinitrotoluene.

5 Aromatic explosives such as 2,4,6-trinitrotoluene (2,4,6-TNT) are more effective quenchers

6 ses each of the munitions constituents 2,4,6-trinitrotoluene, 2,4-dinitrotoluene, 2,6-dinitrotoluene,

7 an MICP material for the detection of 2,4,6-trinitrotoluene and related nitroaromatic compounds.

8 cation of enzymes capable of degrading 2,4,6-trinitrotoluene and this still remains elusive, although

9 dynamic voltammograms of nitrobenzene, 2,4,6-trinitrotoluene, and hexahydro-1,3,5-trinitro-1,3,5-tria

10 -nitrotoluene, 2,4-dinitrotoluene, and 2,4,6-trinitrotoluene, as well as the peroxide-based explosive

11 of 1 mM glycerol trinitrate (GTN) or 0.05 mM trinitrotoluene, at concentrations that inhibited germin

12 dual nitroaromatic explosives (such as 2,4,6-trinitrotoluene) can be easily detected in amounts as lo

13 haracterizing, plant genes involved in 2,4,6-trinitrotoluene detoxification and the biochemical pathw

14 Results for trinitrotoluene, dinitrotoluenes, and nitrotoluenes are

15 sed to construct soluble receptors that bind trinitrotoluene, l-lactate or serotonin with high select

16 gene expression in response to extracellular trinitrotoluene or l-lactate.

17 efinition of the polymorphic nature of 2,4,6-trinitrotoluene precipitated from solution.

18 n and tissue residue of two chemicals, 2,4,6-trinitrotoluene (TNT) and 1,3,5-trinitro-1,3,5-triazacyc

19 The trinitroaromatic explosives, 2,4,6-trinitrotoluene (TNT) and 1,3,5-trinitrobenzene (TNB), a

20 this study, the alkaline hydrolysis of 2,4,6-trinitrotoluene (TNT) and 2,4-dinitroanisole (DNAN) was

21 Trace vapours of the explosives 2,4,6-trinitrotoluene (TNT) and 2,4-dinitrotoluene (DNT) intro

22 security concerns, including the explosives trinitrotoluene (TNT) and ammonium nitrate.

23 Utilizing phage display techniques against trinitrotoluene (TNT) and dinitrotoluene (DNT) targets,

24 The principle is exemplified via trinitrotoluene (TNT) and dinitrotoluene (DNT) with inhe

25 miluminescence enzyme immunoassays for 2,4,6-trinitrotoluene (TNT) and pentaerythritol tetranitrate (

26 ne coated with antibodies specific for 2,4,6-trinitrotoluene (TNT) and the other specific for hexahyd

27 s) and characterized biodegradation of 2,4,6-trinitrotoluene (TNT) and two dinitrotoluene isomers (2,

28 hase marker compounds of the explosive 2,4,6-trinitrotoluene (TNT) at sub-parts-per-billion (<ppb) co

29 nd characterization of an amperometric 2,4,6-trinitrotoluene (TNT) biosensor based on the surface imm

30 e report high-sensitivity detection of 2,4,6-trinitrotoluene (TNT) by using laser photoacoustic spect

31 ree detection of explosive molecules such as trinitrotoluene (TNT) down to 10(-10)M in concentration

32 is roots and assess their responses to 2,4,6-trinitrotoluene (TNT) exposure.

33 for rapid preconcentration and extraction of trinitrotoluene (TNT) for electrochemical analysis and d

34 ,3,5-trinitro-1,3,5-triazine (RDX) and 2,4,6-trinitrotoluene (TNT) from poly(tetrafluoroethylene) (PT

35 erned array of antibodies specific for 2,4,6-trinitrotoluene (TNT) immobilized onto the surface of a

36 e spectroscopy (EIS) is used to detect 2,4,6-trinitrotoluene (TNT) in a novel sandwiched structure wh

37 he specific detection of the explosive 2,4,6-trinitrotoluene (TNT) in aqueous environments.

38 or detection of the explosive compound 2,4,6-trinitrotoluene (TNT) in aqueous solution was developed

39 ct and quantify the explosive compound 2,4,6-trinitrotoluene (TNT) in aqueous solutions is demonstrat

40 t of 2 x 10(-12) mol (i.e., 2 pmol) of 2,4,6-trinitrotoluene (TNT) in connection with 47 nL of inject

41 asing use of DNAN as a replacement for 2,4,6-trinitrotoluene (TNT) in insensitive explosive formulati

42 re, our results indicated that it can detect trinitrotoluene (TNT) in liquid at a concentration as lo

43 or for the detection of the explosive, 2,4,6-trinitrotoluene (TNT) in seawater using a reversed-displ

44 X), pentaerythritol tetranitrate (PETN), and trinitrotoluene (TNT) in their crystalline forms and alu

45 The explosive 2,4,6-trinitrotoluene (TNT) is a highly toxic and persistent e

46 The explosive 2,4,6-trinitrotoluene (TNT) is a major worldwide military poll

47 The explosive 2,4,6-trinitrotoluene (TNT) is a significant, global environme

48 Trinitrotoluene (TNT) is a widely used explosive in land

49 e, selective and portable detection of 2,4,6-trinitrotoluene (TNT) is in high demand for public safet

50 2,4,6-Trinitrotoluene (TNT) is one of the most recalcitrant an

51 The toxic pollutant 2,4,6-trinitrotoluene (TNT) is recalcitrant to degradation in

52 ndence in the detection sensitivity of 2,4,6 trinitrotoluene (TNT) on the reduced electric field (E/N

53 Higher trinitrotoluene (TNT) quantity and closer explosion caus

54 explosive detection is reported using 2,4,6-trinitrotoluene (TNT) specific aptamer and antibodies ta

55 the selective detection of trace amounts of trinitrotoluene (TNT) still remains a big challenge for

56 e) and 1,3,5-trimethylbenzene (TMB) (a 2,4,6-trinitrotoluene (TNT) surrogate) in a mixture of N(2) an

57 The electrochemical reduction of 2,4,6-trinitrotoluene (TNT) was investigated using films of va

58 tra from 1000 single particles each of 2,4,6-trinitrotoluene (TNT), 1,3,5-trinitro-1,3,5-triazinane (

59 including 2,4,6-trinitrophenol (TNP), 2,4,6-trinitrotoluene (TNT), 1,3,5-trinitrobenzene (TNB), and

60 It was used to identify the explosives 2,4,6-trinitrotoluene (TNT), 2,4,6-trinitrophenyl-N-methylnitr

61 on of nitroaromatic compounds, such as 2,4,6-trinitrotoluene (TNT), 2,4-dinitrotoluene (2,4-DNT), 2,6

62 using newly measured kinetic data for 2,4,6-trinitrotoluene (TNT), 2,4-dinitrotoluene (2,4-DNT), and

63 ysis of three nitroaromatic compounds: 2,4,6-trinitrotoluene (TNT), 2,4-dinitrotoluene (DNT), and 2,4

64 l detection of nitroaromatic compounds 2,4,6-trinitrotoluene (TNT), 2,4-dinitrotoluene (DNT), and fen

65 rinitroper-hydro-1,3,5-triazine (RDX), 2,4,6-trinitrotoluene (TNT), 2-amino-4,6-dinitrotoluene (ADNT)

66 (AOC), 2 mm metolachlor (MOC), 0.6 mm 2,4,6-trinitrotoluene (TNT), and 0.3 mm hexahydro-1,3,5-trinit

67 .4-dichlorophenoxyacetic acid (2,4-D), 2,4,6-trinitrotoluene (TNT), and 1,3,5-trinitroperhydro-1,3,5-

68 esulting in the detection of 0.6 ng of 2,4,6-trinitrotoluene (TNT), and low explosives (several smoke

69 enzene (NB), 2,4-dinitrotoluene (DNT), 2,4,6-trinitrotoluene (TNT), and picric acid (PA), has been ex

70 ecause RDX is 10(3) less volatile than 1,3,5-trinitrotoluene (TNT), corresponding to a parts-per-tril

71 micals [pentaerythritol tetranitrate (PETN), trinitrotoluene (TNT), cyclo-1,3,5-trimethylenetrinitram

72 The generation of trace 2,4,6-trinitrotoluene (TNT), cyclotrimethylenetrinitramine (RD

73 ntrations of 1 ppm of trinitrobenzene (TNB), trinitrotoluene (TNT), dinitrobenzene (DNB), tetryl, and

74 ) at 100-fold ratios nor nitro-explosives of trinitrotoluene (TNT), hexahydro-1,3,5-trinitro-1,3,5-tr

75 on of a model nitroaromatic explosive, 2,4,6-trinitrotoluene (TNT), is presented as a prime example.

76 ,4-DNT), 2,6-dinitrotoluene (2,6-DNT), 2,4,6-trinitrotoluene (TNT), nitroglycerin (NG), 1,3,5-trinitr

77 -tetranitro-1,3,5,7-tetrazocine (HMX), 2,4,6-trinitrotoluene (TNT), Pentaerythritol tetranitrate (PET

78 different analytes, including the explosives trinitrotoluene (TNT), tetryl, and RDX, various explosiv

79 ermore, sensors composed of phage displaying trinitrotoluene (TNT)-binding peptide motifs identified

80 NACs), displaying superior detection toward trinitrotoluene (TNT).

81 ate (PETN) and significantly exceeds that of trinitrotoluene (TNT).

82 c response of Daphnia magna to the energetic trinitrotoluene (TNT).

83 tiate NAD(P)H-dependent denitration of 2,4,6-trinitrotoluene (TNT).

84 One such compound is the explosive 2,4,6-trinitrotoluene (TNT).

85 hexen-1-one but did not readily reduce 2,4,6-trinitrotoluene (TNT).

86 active catalysts for the reduction of 2,4,6-trinitrotoluene to 2,4,6-triaminotoluene and subsequent

87 a series of dinitrotoluenes, dinitrobenzene, trinitrotoluene, trinitrobenzene, two aminodinitrotoluen

88 or 60 repetitive measurements of 5 ppm 2,4,6-trinitrotoluene (vs RSD of 10.8% at the thick-film carbo