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2.5- Dimercapto 1,3,4-thiadiazole

Figure 17-12. Biocides for hydraulic fracturing fluids 2-mercaptobenzoim-idazole, 2-mercaptobenzothiazole, 2-mercaptobenzoxazole, 2-mercapto-thiazoline, 2,5-dimercapto-1,3,4-thiadiazole, and 2-imidazolidinethion. Figure 17-12. Biocides for hydraulic fracturing fluids 2-mercaptobenzoim-idazole, 2-mercaptobenzothiazole, 2-mercaptobenzoxazole, 2-mercapto-thiazoline, 2,5-dimercapto-1,3,4-thiadiazole, and 2-imidazolidinethion.
Figure 2. Nitrogen adsorption isotherms at 77K for the OMM samples with multifunctional mercury-specific ligands 1-benzoyl-3-propylthiourea (OMM-1 and OMM-2), 2,5-dimercapto-1,3,4-thiadiazole (OMM-3) and the corresponding differential pore size distributions. OMM-a, OMM-b and OMM-c refer to the calcined MCM-41, MCM-48 and SBA-15 samples, respectively. For clarity the isotherms are offset vertically by 1000 ccSTP/g for OMM-a and OMM-1 samples and by 500 ccSTP/g for OMM-b and OMM-2 samples. The PSD plots are offset vertically by 2 ccg 1nm 1 for OMM-a and OMM-1 and by lccg-1 nm"1 for OMM-b and OMM-2 samples. Figure 2. Nitrogen adsorption isotherms at 77K for the OMM samples with multifunctional mercury-specific ligands 1-benzoyl-3-propylthiourea (OMM-1 and OMM-2), 2,5-dimercapto-1,3,4-thiadiazole (OMM-3) and the corresponding differential pore size distributions. OMM-a, OMM-b and OMM-c refer to the calcined MCM-41, MCM-48 and SBA-15 samples, respectively. For clarity the isotherms are offset vertically by 1000 ccSTP/g for OMM-a and OMM-1 samples and by 500 ccSTP/g for OMM-b and OMM-2 samples. The PSD plots are offset vertically by 2 ccg 1nm 1 for OMM-a and OMM-1 and by lccg-1 nm"1 for OMM-b and OMM-2 samples.
Badische Anilin- und Soda-Fabrik A. G. 2,5-dimercapto-1,3.4-thiadiazole. [Pg.182]

Poly(oxyethylene) combinations with various other comonomers [46], are of interest as solid polymer electrolytes after complex formation with Li(I) (complexation with Na(I), K(I), Mg(II), Ba(II), etc. has also been studied) [1,5,46-48]. The synthesis is carried out by direct interaction of the ligand and metal ions in solution or, if cross-linked poly(oxyethylene) is employed, by immersing the polymer ligand into a solution of the metal salt. Poly(oxypropylene), modified polysiloxanes, cross-linked phosphate esters and ethers [46,49,50], and structurally different ligands such as 2,5-dimercapto-1,3,4-thiadiazol-polyaniline [51] have also been used as polymer ligands, The developments in this field are reviewed in [46], In this review the segmental motion of Li(I) in a poly(oxyethylene) is described as shown in Fig. 5-4. [Pg.184]

Bismuth (III) iodide. See Bismuth iodide Bismuthiol I. See 2,5-Dimercapto-1,3,4-thiadiazole Bismuth nitrate... [Pg.522]

Dimer acid 2,5-Dimercapto-1,3,4-thiadiazole Dimethyl ami noethyl methacrylate Dimethyl lauramine 2,6-Dimethylmorpholine Dimethyl myristamine Dimethyl oleic-linolenic amine Dimethyl tallowamine 2,4-Dinitroaniline Dioctyl amine Dipropylamine Disodium cocoyl glutamate Disodium tetrapropenyl succinate Ditallowamine Erucic acid Ethanolamine Ethanolaminebis (methylenephosphonic acid) Ethylene/acrylic acid copolymer 2-Ethylhexyl oleate Ferric nitrate... [Pg.5014]

S. J. Visco et al. proposed a new rechargeable battery system at room temperature by using reversible polymerization reaction of organic sulfur compound in place of inorganic sulfur. As for 2,5-dimercapto 1,3,4-thiadiazole (DMcT) chemical... [Pg.421]

BD = a-benzildioxime BO = a-benzoinooxime BP = 2,2 -bipyridine CA = chloranilic acid DHN=2,3-dihydroxynaphthalene DMG =dimethylglyoxime DMTD = 2,5-dimercapto-1,3,4-thiadiazole DTPA = diethylenetriaminepentaacetic acid FD=a-futildioxime HNB = A/-hydroxy-A/-nitroso benzeneamine MA = mandelic acid NO = nioxime NN = 1-Nitroso-2-naphthol PAN = 1-(2 -Pyridylazo)-2-naphthol PC = pyrocatechol TTHA=triethylenetetraminehexaacetic acid. [Pg.4963]

Dias Filho NL, do Carmo DR (2005) Stripping voltammetry of mercury(II) with a chemically modified carbon paste electrode containing silica gel functionalized with 2,5-dimercapto-1,3,4-thiadiazole. Electroanalysis 17 1540-1546... [Pg.486]

DMTD 2,5-Dimercapto- 1,3,4-thiadiazole (WTR) DSTDP Distearyl 3,3 -dithiopropionate... [Pg.2251]

This article describes the performance of a new curative for polychloroprene, a derivative of 2,5-dimercapto-1,3,4-thiadiazole (DMTD). This curative provides long Mooney scorch times, rapid cure rate resulting in short cure times and an exceptionally flat cure plateau. Other performance characteristics are presented, including the effect of other additives in a typical polychloroprene formulation. 5 refs. [Pg.108]


See other pages where 2.5- Dimercapto 1,3,4-thiadiazole is mentioned: [Pg.292]    [Pg.253]    [Pg.574]    [Pg.617]    [Pg.111]    [Pg.209]    [Pg.310]    [Pg.565]    [Pg.617]    [Pg.4071]    [Pg.213]    [Pg.1373]    [Pg.4405]    [Pg.4405]    [Pg.4661]    [Pg.6163]    [Pg.1145]    [Pg.203]    [Pg.425]    [Pg.442]    [Pg.1008]   
See also in sourсe #XX -- [ Pg.253 ]




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1,2,3-thiadiazole

1,2,5-Thiadiazoles

1,3,4-Thiadiazol

2.4- Dimercapto

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