Nitrogen hydrate

Seo, Y.-T. Kang, S.-P. Lee, H. (2001). Experimental determination and thermodynamic modeling of methane and nitrogen hydrates in the presence of THF, propylene oxide, 1,4-dioxane and acetone. Fluid Phase Equilibria, 189, 99-110. 

Yoon, J.-H. Kawamura, T. Ohtake, M. Takeya, S. Komai, T. Yamamoto, Y. Emi, H. Kohara, M. Tanaka, S. Takano, O. Uchida, K. (2006). Highly selective encaging of carbon dioxide molecules in the mixed carbon dioxide and nitrogen hydrate at low temperatures. J. Phys. Chem. B, 110 (35), 17595-17599. 

Tohidi et al. (2001) also suggested that the stability of simple methane and nitrogen hydrates could be increased by using sH large guest formers. They suggested that the C6 Cio fraction of real petroleum fluids are potential sH hydrate formers, though no evidence exists so far that real reservoir fluids are more likely to form structure H. 

Figure 6.55 Inhibition of methane + nitrogen hydrates with sodium chloride and magnesium chloride.

Figure 4 Comparisons of phase transformation pressures between the X-ray diffraction (XRD) and neutron diffraction (ND) studies and the present results by microscopic observations and in-situ Raman scattering measurements for krypton hydrate, nitrogen hydrate, and methane hydrate.

For this second reaction Kjgs = 181 x 10" and hence pK, for ammonia solution is 4.75. The entity NHj. H2O is often referred to as ammonium hydroxide, NH4OH, a formula which would imply that either nitrogen has a covalency of five, an impossible arrangement, or that NH4OH existed as the ions NH4 and OH". It is possible to crystallise two hydrates from concentrated ammonia solution but neither of these hydrates is ionic. Hence use of the term ammonium hydroxide is to be discouraged in favour of ammonia solution . 

Anhydrous sodium sulphide. The hydrated salt, NajS.QH O, is heated in a Pyrex distilling flask or retort in a stream of hydrogen or of nitrogen until water ceases to be evolved. The solid cake of anhydrous sodium sulphide is removed from the vessel with the aid of a copper wire hook or by other suitable means. No attempt should be made to fuse the sodium sulphide since at high temperatiues sodium sulphide is readily oxidised to sodium sulphate. 

This genera] scheme could be used to explain hydrogen exchange in the 5-position, providing a new alternative for the reaction (466). This leads us also to ask whether some reactions described as typically electrophilic cannot also be rationalized by a preliminary hydration of the C2=N bond. The nitration reaction of 2-dialkylaminothiazoles could occur, for example, on the enamine-like intermediate (229) (Scheme 141). This scheme would explain why alkyl groups on the exocyclic nitrogen may drastically change the reaction pathway (see Section rV.l.A). Kinetic studies and careful analysis of by-products would enable a check of this hypothesis. 

The evidence obtained in compaction experiments is of particular interest in the present context. Figure 3.22 shows the results obtained by Avery and Ramsay for the isotherms of nitrogen on compacts of silica powder. The hysteresis loop moved progressively to the left as the compacting pressure increased, but the lower closure point did not fall below a relative pressure of 0-40. Similar results were obtained in the compaction of zirconia powder both by Avery and Ramsay (cf. Fig. 4.5), and by Gregg and Langford, where the lower closure point moved down to 0-42-0-45p° but not below. With a mesoporous magnesia (prepared by thermal decomposition of the hydrated carbonate) the position of the closure point... 

Thorium compounds of anionic nitrogen-donating species such as [Th(NR2)4], where R = alkyl or sdyl, are weU-known. The nuclearity is highly dependent on the steric requirements of R. Amides are extremely reactive, readily undergoing protonation to form amines or insertion reactions with CO2, COS, CS2, and CSe2 to form carbamates. Tetravalent thorium thiocyanates have been isolated as hydrated species, eg, Th(NCS)4(H20)4 [17837-16-0] or as complex salts, eg, M4 Th(NCS)g] vvH20, where M = NH, Rb, or Cs. 

Tin does not react directly with nitrogen, hydrogen, carbon dioxide, or gaseous ammonia. Sulfur dioxide, when moist, attacks tin. Chlorine, bromine, and iodine readily react with tin with fluorine, the action is slow at room temperature. The halogen acids attack tin, particularly when hot and concentrated. Hot sulfuric acid dissolves tin, especially in the presence of oxidizers. Although cold nitric acid attacks tin only slowly, hot concentrated nitric acid converts it to an insoluble hydrated stannic oxide. Sulfurous, chlorosulfuric, and pyrosulfiiric acids react rapidly with tin. Phosphoric acid dissolves tin less readily than the other mineral acids. Organic acids such as lactic, citric, tartaric, and oxaUc attack tin slowly in the presence of air or oxidizing substances. 

---