Defective hydration

Coal mine gas (called Coal bed Gas) is a kind of associated gas from the coal seam in coal mine exploitation process in different forms, which is one of the main reasons of the coal mine accident. As the first fatal factor in coal mine, the gas accident not only causes a large number of casualties and huge economic losses, and imperils the safety of coal mine production seriously once it occurs. Gas concerns the major issues of environmental pollution, the greenhouse effect and the future of new energy. It can be used after recovered rapidly if the coal mine gas develops, storages and transports high-efficiently in moderate environment. Meanwhile it will be reduced that the cost, the hidden safety trouble and the gas emission pollution to the environment. Thus it is badly in need of a new type of gas utilization technology to make up for the current technical defects. Hydrate method is an optional way. 

As both species—the ion and the vacancy—are defective, they both carry effective charge and thus contribute to conductivity this allows further interaction with other defects and elucidation of the behavior of minority defects. Hydration can be written ... 

L. Paz, J. M. Di Meglio, M. Dvolaitzky, R. Ober, C. Taupin. Highly curved defects in lyotropic (nonionic) lamellar phases. Origin and role in hydration processes. J Phys Chem 55 3415-3418, 1984. 

Nonstoichiometry of the oxides can be due to a number of reasons, such as hydration,159 incomplete oxidation,158 and the generation of defects at interfaces.157 An important factor affecting the chemical composition of the oxides is the incorporation of electrolyte species into the growing alumina. There have even been suggestions to use this for impurity doping of oxides and modifying their properties.161 Various kinds of anion distributions and mechanisms of anion incorporation and their influence on oxide properties have been reported. The problems attracting attention are ... 

Models of lipid bilayers have been employed widely to investigate diffusion properties across membranes through assisted and non-assisted mechanisms. Simple monovalent ions, e.g., Na+, K+, and Cl, have been shown to play a crucial role in intercellular communication. In order to enter the cell, the ion must preliminarily permeate the membrane that acts as an impervious wall towards the cytoplasm. Passive transport of Na+ and Cl ions across membranes has been investigated using a model lipid bilayer that undergoes severe deformations upon translocation of the ions across the aqueous interface [126]. This process is accompanied by thinning defects in the membrane and the formation of water fingers that ensure appropriate hydration of the ion as it permeates the hydrophobic environment. 

Fig. 2 Mechanically oriented bilayer samples as a membrane model for ssNMR. (a) Illustration of the hydrated lipid bilayers with MAPs embedded, the glass supports, and the insulating wrapping, (b) A real sample consists of 15 stacked glass slides, (c) Schematic solid-state 19F-NMR lineshapes from an oriented CF3-labelled peptide (red), and the corresponding powder lineshape from a non-oriented sample (grey), (d) Illustration of typical orientational defects in real samples - the sources of powder contribution in the spectra...

Defect clusters are similarly prominent in hydrated phases. For example, anatase nanocrystals prepared by sol-gel methods contain high numbers of vacancies on titanium sites, counterbalanced by four protons surrounding the vacancy, making a (Vxi 4H ) cluster. In effect the protons are associated with oxygen ions to form OH- ions, and a vacancy-hydroxyl cluster is an equally valid description. Similar clusters are known in other hydrated systems, the best characterized being Mn4+ vacancies plus 4H in y-Mn02, known as Reutschi defects. 

From the frequency measurements of the LB-film-deposited QCM plate in water, the behavior of phospholipid LB films can be classified into three types (i) phospholipids having relatively hydrophilic head groups such as DPPC and DPPG are hydrated and then easily flaked from the substrate in the fluid liquid crystalline state above Tc (ii) DPPE and DPPS having the less hydrophilic head groups are hydrated only near their Tc (iii) cholesterol LB films show relatively large hydration behavior even at low temperatures due to the water penetration into the structure defects in the membrane. 

In terms of reinforcement, hydrocalumite/polymer nanocomposites may also be considered as promising in the field of cement-related materials. The so-called macro-defect-free (MDF) cements are based on the filHng by polymer of the macroscopic voids responsible for the breakdown of cement. The hydrocalumite phase is formed during the hydration of cement and is known to readily incorporate polymers between its layers [71-75]. 

The situation for hydrated Nafion in the acid form, or as containing aqueous acids or strong bases, is more complex because protons and defect protons (i.e., OH ions), migrate according to a somewhat different mechanism. Proton transfer in either case occurs throughout and between clusters of hydrogen bonded water molecules to a degree that depends on the relative water content. 

Mauritz and Gray analyzed the IR continuous absorption of hydrated Na OH - and K OH -imbibed Nafion sulfonate membranes for the purpose of correlating this phenomenon to the current efficiency (cation transference number) of chlor-alkali electrochemical cells.In this case, the similar issue of OH ( defect proton ) conductivity is important. A distinct continuous absorption appeared in the spec-... 

Figure 27. Defective structure of solid trifluoromethane-sulfonic acid hydrate (CF3S0sH H20)4 found using ab initio molecular dynamics (AIMD see Section 2.2.3 for a description of the technique), showing two hydronium ions hydro-gen-bonded to sulfonate groups (as found in the perfect structure) but, more importantly, two shared protons (one between two sulfonate groups and the other as part of a Zundel ion see text). Note that the energy of the defective structure is only --30 kj/mol higher than that of the perfect structure.

Specific examples of RWA are further described. Raney copper precursor with a small amount of Pd was prepared by this process. Rapid solidification was effective in keeping most of the added Pd dissolved in the precursor. The specific surface area of the leached specimen increased by about 3 times in comparison with that of ordinary Raney copper catalyst. The conversion from acrylonitrile to acrylamide by the hydration reaction was about 60%, or more than 20% higher than that from ordinary Raney copper catalyst. In case of Ti or V addition, the conversion increased to 70-80%. Rapid solidification was quite effective in decreasing the defect rate of Raney catalysts from some precursors. The potential for design of new catalysts may be widely extended by rapid solidification. 

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