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Di- hydrogen

The main use of these clays is to control, or adjust, viscosity in nonaqueous systems. Organoclays can be dispersed in nonaqueous fluids to modify the viscosity of the fluid so that the fluid exhibits non-Newtonian thixotropic behavior. Important segments of this area are drilling fluids, greases (79,80), lubricants, and oil-based paints. The most used commercial products in this area are dimethyl di (hydrogen a ted tallow) alkylammonium chloride [61789-80-8] dimethyl (hydrogen a ted tallow)aLkylbenzylammonium chloride [61789-72-8] and methyldi(hydrogenated tallow)aLkylbenzylammonium chloride [68391-01-5]. [Pg.383]

At the end of last century, a near frictionless carbon (NFC) coating was reported, which is practically hydrogen contained DLC film grown on steel and sapphire substrates using a plasma enhanced chemical vapor deposition (PECVD) system [50]. By using a ball on a disk tribo-meter, a super low friction coefficient of 0.001-0.003 between the films coated on both the ball and the disk was achieved [50]. A mechanistic model was proposed that carbon atoms on the surface are partially di-hydrogenated, resulting in the chemical inertness of the surface. Consequently, adhesive interaction becomes weak and super low friction is achieved [22],... [Pg.151]

DI-SODIUM HYDROGEN PHOSPHATE POTASSIUM DI-HYDROGEN PHOSPHATE 6.7 6.5 to 7.5... [Pg.188]

Small ey(Ib) that cobalt and niobium clusters react in a very selective fashion with deuterium was rapidly followed by similar studies on a variety of other metal systems. Three groups simultaneously reported similar dramatic behavior for iron c usters( 2b, 3b). Di hydrogen or di deuteri urn addition reactions have been reported for vanadium( 3e), i ron(lc,2a-d,3b), cobalt(lb),... [Pg.52]

Nitrogen. The Rice group reported that the reactions of di nitrogen wi th ni obi urn and cobalt c usters( lc) exhibit reactivity patterns very similar to di hydrogen. Iron has not yet been observed to react in the gas phase with di nitrogen. The Rice group did report some... [Pg.56]

Figure 9. Plots of the rate constants (X) of iron, vanadium and niobium clusters reacting with di hydrogen/di denteri urn, and their respective bare cluster ionization potentials (solid lines) scaled as described in the text. Figure 9. Plots of the rate constants (X) of iron, vanadium and niobium clusters reacting with di hydrogen/di denteri urn, and their respective bare cluster ionization potentials (solid lines) scaled as described in the text.
Figure 11.5 Covalent bonding, (a) shows two isolated hydrogen atoms coming together to form a covalently bonded (di)hydrogen molecule, (b) shows a simple model of the bonding in a dihydrogen molecule, with the single Is orbital electron from each atom being shared by the molecule, to give each atom a closed shell. Figure 11.5 Covalent bonding, (a) shows two isolated hydrogen atoms coming together to form a covalently bonded (di)hydrogen molecule, (b) shows a simple model of the bonding in a dihydrogen molecule, with the single Is orbital electron from each atom being shared by the molecule, to give each atom a closed shell.
E. Matthijs, P. Gerike, H. Klotz, J.G.A. Kooijman, H.G. Karber and J. Waters, Removal and Mass Balance of the Cationic Fabric Softener Di(Hydrogenated)Tallow Dimethyl Ammonium Chloride in Activated Sludge Sewage Treatment Plants European Association of Surfactant Manufacturers (AIS/CESIO), Brussels, Belgium, 1992. [Pg.77]

Fig. 2.12.6. Identification of esterquat compounds FIA-APCI-MS-MS(+) (CID) product ion mass spectrum of selected [M — RCO]+ base peak ion of cationic surfactant blend of di-hydrogenated tallowethyl hydroxyethyl ammonium methane sulfate type (mlz 692 general formula (R(C0)0CH2CH2)2-N (CH3)-CH2CH2(0H)CH30S03) fragmentation behaviour under CID... Fig. 2.12.6. Identification of esterquat compounds FIA-APCI-MS-MS(+) (CID) product ion mass spectrum of selected [M — RCO]+ base peak ion of cationic surfactant blend of di-hydrogenated tallowethyl hydroxyethyl ammonium methane sulfate type (mlz 692 general formula (R(C0)0CH2CH2)2-N (CH3)-CH2CH2(0H)CH30S03) fragmentation behaviour under CID...
The acidity probes discussed above are the most commonly used. However, the use of many different probes has been reported in the literature. This list includes nitriles, alkanes, amines, water, di-hydrogen, deuterium, isotopically labeled molecules, benzene, etc. Probe molecules can also be used to measure basicity on zeohtes. In this case, weakly acidic molecules such as CO2, pyrrole, acetic acid and halogenated light paraffins have been used. Space does not permit discussion of these in any detail, but information about these probes and their applications can be found in the following references [87, 127-130]. [Pg.135]

The dominating use of ester quats is as fabric softener and the transition from the traditional di(hydrogenated tallow)dimethylammonium chloride, which had been the work-horse softener for more than three decades, to ester quats was made in Europe in the early 1990s as a response to pressure from environmental authorities in the European Union [23]. The transition has been less rapid in the United States, but ester quats have gradually replaced the traditional quats in most of the major softener products there as well. The same trend is ongoing in the rest of the world. [Pg.69]

A variety of other anionic initiators promote the polymerization of thio-carbonyl fluoride. Among them are aluminum isopropoxide, di(hydrogenated tal-low)dimethylammonium methoxide and chloride, N-nitrosodimethylamine, diisopropylamine, and triethylamine (59). Combinations of either [(C6H 5)3 P] 3RhCl or... [Pg.93]

To be reconstituted with Sodium di-hydrogen phosphate ILP (Isolated limb... [Pg.447]

The difficulties encountered in firmly establishing the structure of the first di-hydrogen complex still have not been entirely overcome. The H—D coupling constant experiment described above offers a method of distinguishing between the classical and nonclassical forms, but it is not applicable if the system is rapidly fluxional. [Pg.860]

Cadmium Arsenates.—The hydrated normal cadmium orthoarsenate, 2Cd3(As04)2.3H20, falls as a white voluminous precipitate on adding alkali to a solution of cadmium mono- or di-hydrogen arsenate in hydrochloric acid,4 or on addition of sodium orthoarsenate to a solution of cadmium sulphate.5 On drying at 100° C. the anhydrous salt remains. [Pg.196]


See other pages where Di- hydrogen is mentioned: [Pg.315]    [Pg.374]    [Pg.376]    [Pg.377]    [Pg.379]    [Pg.382]    [Pg.382]    [Pg.382]    [Pg.383]    [Pg.364]    [Pg.20]    [Pg.63]    [Pg.60]    [Pg.249]    [Pg.229]    [Pg.257]    [Pg.392]    [Pg.394]    [Pg.325]    [Pg.513]    [Pg.81]    [Pg.82]    [Pg.89]    [Pg.89]    [Pg.90]    [Pg.92]    [Pg.94]    [Pg.96]    [Pg.379]    [Pg.174]    [Pg.191]    [Pg.282]   
See also in sourсe #XX -- [ Pg.325 ]




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D-Mannofuranose, 2,3:5,6-di-O-isopropylidenetransfer hydrogenation

Di(hydrogenated

Di- hydrogen phosphate as reagent

Di-2-ethylhexyl hydrogen phosphate

Di-hydrogen bonds

Di-isopropyl hydrogen phosphite

Di-p-nitrophenyl hydrogen phosphate

Diphenylphosphorodiamidic chloride di-isopropyl hydrogen phosphite

Sodium di- hydrogen phosphate

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