Hydrates, water content

Drugs that associate with water to produce crystalline forms are called hydrates. Water content of the hydrate forms of sodium cefazolin as a function of relative humidity is seen in Fig. 1. As shown in Fig. 1, the sesquihydrate is the most stable structure when exposed to extreme humidity conditions [6], This figure also shows the importance of choosing the proper combination of hydrate and humidity conditions when designing a manufacturing process or facility. 

Hydration (water content) of the stratum comeurn affects penetrability. 

The course of the reaction between A -methylmorpholine-A -oxide 290 (NMMO) and cyanuric chloride is strictly dependent on the hydrate water content of the amine oxide (Scheme 55). The reaction can be conducted in such a way that a clean deoxygenative demethylation is achieved <2002T9809>. 

Table 38.2 gives the conductivity of crystalline materials, all containing some water molecules, and used in ECDs. Phosphotungstic acid (PWA) has been used either as an electrochromic electrolyte able to undergo a colour change during oxidation or as an electrolyte or associated with WOj . Zirconium phosphate showed a good conductivity but a fast dissolution of WO3 was observed similar to that found with WO3 in pure water . However, both compounds are susceptible to variations of the hydrated water content and react with WO3 films. Compared to the above... 

Two different complexes between trilaurylammoniumchloride and ferric chloride have been observed in the organic phase after extraction from 1 M HCl. A complex containing 2 molecules of amine salt per molecule of ferric chloride (2 1 complex) exists when the equilibrium concentration of iron in the aqueous phase is small, A 1 1 complex, however, is extracted either from 1 M HCl containing up to 3 M/1 FeCl, or from 10 M HCl which in the last case is accompanied by a decrease in excess acid content in the organic phase. The formation of these different complexes and the decrease of hydration water content, as followed by chemical analysis of the equilibrium solutions, are confirmed by infrared spectra of the organic phases. In both cases, formation of 2 1 or 1 1 complexes, visible spectra indicate the existence of tetrachloroferrate ion in the organic phase,... 

Table 3. Structurally critical hydrate water contents (CHI — cellulose hydrate I)...

Membrane Type pKa Hydration Water Content Current Efficiency (%) Conductivity Chemical Stability pH in Anode... 

In a substance such as a salt hydrate (for example BaCl2.2H20) water can be determined by heating until it is all driven off. Provided that only water is evolved on heating, the difference in weight gives the water content. If water is mixed with other decomposition... 

The hydration shell is formed with the increasing of the water content of the sample and the NA transforms from the unordered to A- and then to B form, in the case of DNA and DNA-like polynucleotides and salt concentrations similar to in vivo conditions. The reverse process, dehydration of NA, results in the reverse conformational transitions but they take place at the values of relative humidity (r.h.) less than the forward direction [12]. Thus, there is a conformational hysteresis over the hydration-dehydration loop. The adsorption isotherms of the NAs, i.e. the plots of the number of the adsorbed water molecules versus the r.h. of the sample at constant temperature, also demonstrate the hysteresis phenomena [13]. The hysteresis is i( producible and its value does not decrease for at least a week. 

Taking into account the hydration shell of the NA and the possibility of the water content changing we are forced to consider the water -I- nucleic acid as an open system. In the present study a phenomenological model taking into account the interdependence of hydration and the NA conformation transition processes is offered. In accordance with the algorithm described above we consider two types of the basic processes in the system and thus two time intervals the water adsorption and the conformational transitions of the NA, times of the conformational transitions being much more greater... 

Several aqueous systems should be considered in a similar manner. For example, in the selective removal of divalent cations from a saturated salt solution, the hydrated resin gives up a portion of its normal water content as it contacts the salt stream. In so doing, the particles shrink, and the inner pathways for ion migration become smaller. 

X 10 J/T (5.71 //g) at room temperature. It is air stable at 25°C, but is slowly converted to Fe202 and bromine at 310°C. The light yellow to brown hydroscopic sohd is soluble ia water, alcohol, ether, and acetonitrile. Iron(II) bromide forms adducts with a wide range of donor molecules. Pale green nona-, hexa-, tetra-, and dihydrate species can be crystallized from aqueous solutions at different temperatures. A hydrate of variable water content,... 

Some commercially available molecular-sieve products and related materials are shown in Table 6, classified according to the basic 2eohte stmcture types. In most cases, the water content of the commercial product is below 1.5—2.5 wt % certain products, however, are sold as fully hydrated crystalline powders. 

Microscopic sheets of amorphous silica have been prepared in the laboratory by either (/) hydrolysis of gaseous SiCl or SiF to form monosilicic acid [10193-36-9] (orthosihcic acid), Si(OH)4, with simultaneous polymerisation in water of the monosilicic acid that is formed (7) (2) freesing of colloidal silica or polysilicic acid (8—10) (J) hydrolysis of HSiCl in ether, followed by solvent evaporation (11) or (4) coagulation of silica in the presence of cationic surfactants (12). Amorphous silica fibers are prepared by drying thin films of sols or oxidising silicon monoxide (13). Hydrated amorphous silica differs in solubility from anhydrous or surface-hydrated amorphous sdica forms (1) in that the former is generally stable up to 60°C, and water is not lost by evaporation at room temperature. Hydrated sdica gel can be prepared by reaction of hydrated sodium siUcate crystals and anhydrous acid, followed by polymerisation of the monosilicic acid that is formed into a dense state (14). This process can result in a water content of approximately one molecule of H2O for each sdanol group present. 

Hydrated Stannic Oxide. Hydrated stannic oxide of variable water content is obtained by the hydrolysis of stannates. Acidification of a sodium stannate solution precipitates the hydrate as a flocculent white mass. The colloidal solution, which is obtained by washing the mass free of water-soluble ions and peptization with potassium hydroxide, is stable below 50°C and forms the basis for the patented Tin Sol process for replenishing tin in staimate tin-plating baths. A similar type of solution (Staimasol A and B) is prepared by the direct electrolysis of concentrated potassium staimate solutions (26). 

Calcium Hypochlorite. High assay calcium hypochlorite [7778-54-3] was first commercialized in the United States in 1928 by Mathieson Alkali Works, Inc. (now Olin Corp.) under the trade name HTH. It is now produced by two additional manufacturers in North America (Table 5). Historically, it usually contained about 1% water and 70—74% av CI2, so-called anhydrous product, but in 1970, a hydrated product was introduced (234). It is similar in composition to anhydrous Ca(OCl)2 except for its higher water content of about 6—12% and a slightly lower available chlorine content. This product has improved resistance to accidental initiation of self-sustained decomposition by a Ht match, a Ht cigarette, or a small amount of organic contamination. U.S. production in the 1990s consists primarily of partially hydrated Ca(OCl)2, which is sold as a 65% av CI2 product mainly for swimming pool use. Calcium hypochlorite is also sold as a 50% av CI2 product as a sanitizer used by dairy and food industries and in the home, and as a 32% product for mildew control. 

Emulsion components enter the stratum corneum and other epidermal layers at different rates. Most of the water evaporates, and a residue of emulsifiers, Hpids, and other nonvolatile constituents remains on the skin. Some of these materials and other product ingredients may permeate the skin others remain on the surface. If the blend of nonvolatiles materially reduces the evaporative loss of water from the skin, known as the transepidermal water loss (TEWL), the film is identified as occlusive. AppHcation of a layer of petrolatum to normal skin can reduce the TEWL, which is normally about 4—8 g/(m h), by as much as 50 to 75% for several hours. The evaporated water is to a large extent trapped under the occlusive layer hydrating or moisturizing the dead cells of the stratum corneum. The flexibiHty of isolated stratum corneum is dependent on the presence of water dry stratum corneum is britde and difficult to stretch or bend. Thus, any increase in the water content of skin is beHeved to improve the skin quaHty. 

Aluminium fluoride (anhydrous) [7784-18-4] M 84.0, m 250°. Technical material may contain up to 15% alumina, with minor impurities such as aluminium sulfate, cryolite, silica and iron oxide. Reagent grade AIF3 (hydrated) contains only traces of impurities but its water content is very variable (may be up to 40%). It can be dried by calcining at 600-800° in a stream of dry air (some hydrolysis occurs), followed by vacuum distn at low pressure in a graphite system, heated to approximately 925° (condenser at 900°) [Henry and Dreisbach J Am Chem Soc 81 5274 1959]. 

Sodium borate (decahydrate, hydrated borax) [1303-96-4] M 381.2, m 75 (loses 5H2O at 60 ), d 1.73. Crystd from water (3.3mL/g) keeping below 55° to avoid formation of the pentahydrate. Filtered at the pump, washed with water and equilibrated for several days in a desiccator containing an aqueous solution saturated with respect to sucrose and NaCl. Borax can be prepared more quickly (but its water content is somewhat variable) by washing the recrystd material at the pump with water, followed by 95% EtOH, then Et20, and air dried at room temperature for 12-18h on a clock glass. 

In the feed preparation section, those materials are removed from the reactor feed which would either poison the catalyst or which would give rise to compounds detrimental to product quality. Hydrogen sulfide is removed in the DBA tower, and mercaptans are taken out in the caustic wash. The water wash removes traces of caustic and DBA, both of which are serious catalyst poisons. Also, the water wash is used to control the water content of the reactor feed (which has to be kept at a predetermined level to keep the polymerization catalyst properly hydrated) and remove NH3, which would poison the catalyst. Diolefins and oxygen should also be kept out of poly feed for good operation. 

Extensive drying or dewatering of the waste is not required because cement mixtures require water in the hydration process, and thus the amount of cement added can be adjusted to accommodate a wide range of waste water contents. 

FIG. 13 Average number of hydrogen bonds (for definition see text) as a function of p in five simulations at different levels of hydration in a Vycor pore. Full hues show the number of water-water bonds, long-dashed hnes show the number of bonds between water molecules and Vycor, and short-dashed lines denote the sum of the two. From top to bottom, the frames correspond to a water content of about 96, 74, 55, 37, and 19% of the maximum possible (corresponding to 2600, 2000,1500, 1000, and 500 water molecules in a cylindrical cavity of about 4nm diameter and 7.13 nm length). (From Ref. 24.)... 

Protein crystals contain between 25 and 65 vol% water, which is essential for the crystallisation of these biopolymers. A typical value for the water content of protein crystals is 45% according to Matthews et al. l49,150). For this reason it is possible to study the arrangement of water molecules in the hydration-shell by protein-water and water-water interactions near the protein surface, if one can solve the structure of the crystal by X-ray or neutron diffraction to a sufficiently high resolution151 -153). 

HNO3 in the spent acid. The vertical line corresponds to the mole ratio of H20/H2S04 to form the mo no hydrate H2SO4.H2O. Note that the max HNO3 solubility for each curve occurs dose to this vertical line. It is clear that both water content and HN03 content of the spent acid should be kept low in order to minimize HN03 solubility in the NG... 

The amount of water boimd to the proteins and polysaccharides depends primarily on the ratio of water to the biopolymer in the investigated system The two extreme cases are the dry biopolymer (water content tend to zero) and highly diluted aqueous solutions of the biopolymers. The dry biopolymer undergoes hydration if is exposed to the water vapor of increased vapor pressure. The extent of hydration can be determined y measuring the... 

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