Low water

Alkynes resemble alkanes and aUcenes m their physical properties They share with these other hydrocarbons the properties of low density and low water solubility They are slightly more polar and generally have slightly higher boiling points than the corre spondmg alkanes and alkenes... 

Key properties of cellulose nitrate are good dimensional stability, low water absorption, and toughness. Its disadvantages are its flammability and lack of stability to heat and sunlight. 

This thermoplastic shows good tensile strength, toughness, low water absorption, and good frictional properties, plus good chemical resistance and electrical properties. 

Dew retting iuvolves the action of dew, sun, and fungi on the plants spread thinly on the ground. Dew retting takes 4—6 weeks, but the action is not uniform and it tends to yield a dark-colored fiber. However, it is far less labor iatensive and less expensive than water retting. It is commonly used iu regions of low water supply and accounts for 85% of the Western European crop, especially iu France, and also iu the former Soviet Union. 

Hard baked goods such as cookies and crackers have a relatively low water and high fat content. Water can be absorbed, and the product loses its desirable texture and becomes subject to Hpid rancidity. Packagiag for cookies and crackers includes polyolefin-coextmsion film pouches within paperboard carton sheUs, and polystyrene trays overwrapped with polyethylene or oriented polypropylene film. Soft cookies are packaged in high water-vapor-barrier laminations containing aluminum foil. 

Hard sugar candies have very low moisture content. They are sealed in low water vapor-transmission packaging such as aluminum foil or oriented polypropylene film. 

Fish proteia coaceatrates vary widely ia fuactioaal characteristics, ranging from those having high proteia coateat and low water solubiUty, to those having lower proteia coateats but improved water solubiUty. Attempts have beea made to improve fuactioaal properties of fish proteia by enzyme hydrolysis (141), or by modificatioa of the myofibrillar proteia by succiaylatioa (142). 

Formaldehyde—Alcohol Solutions. These solutions are blends of concentrated aqueous formaldehyde, the alcohol, and the hemiacetal. Methanol decreases the average molecular weight of formaldehyde oligomers by formation of lower molecular weight hemiacetals. These solutions are used to produce urea and melamine resins the alcohol can act as the resin solvent and as a reactant. The low water content can improve reactivity and reduce waste disposal and losses. Typical specifications for commercially available products are shown in Table 7 (117). 

Paraformaldehyde is used by resin manufacturers seeking low water content or more favorable control of reaction rates. It is often used in making phenol—, urea—, resorcinol—, and melamine—formaldehyde resins. 

Unsaturated resias based on 1,4-cyclohexanedimethanol are useful ia gel coats and ia laminating and molding resias where advantage is taken of the properties of very low water absorption and resistance to boiling water (6). Thermal stabiHty is imparted to molding resias, both thermoplastic (71,72) and thermoset (73—76), enabling retention of physical and electrical properties at elevated temperatures (77). Additionally, resistance to chemical and environmental exposure is characteristic of products made from these resias (78). 

Fluridone is a weak base with low water solubiUty. Sorption of fluridone increases with decreasing pH (436). Leaching of fluridone was not significant in field study, and the persistence has been determined to be less than 365 days. The degradation of fluridone appears to be microbial in nature, and accelerated breakdown of the herbicide occurs upon repeated appHcations (437). Fluorochloridone is shown to degrade by hydrolysis at pH 7 and 9, but not at lower pH. The half-Hves for this reaction are 190 and 140 days for pH 7 and 9, respectively. Breakdown by photolysis occurs rapidly with a half-hfe of 4.3 days at pH 7 (438). An HA is available for acifluorfen. 

The immersion of glass electrodes in strongly dehydrating media should be avoided. If the electrode is used in solvents of low water activity, frequent conditioning in water is advisable, as dehydration of the gel layer of the surface causes a progressive alteration in the electrode potential with a consequent drift of the measured pH. Slow dissolution of the pH-sensitive membrane is unavoidable, and it eventually leads to mechanical failure. Standardization of the electrode with two buffer solutions is the best means of early detection of incipient electrode failure. 

The TPX experimental product of Mitsubishi Petrochemical Ind. (221) is an amorphous, transparent polyolefin with very low water absorption (0.01%) and a glass-transition temperature comparable to that of BPA-PC (ca 150°C). Birefringence (<20 nm/mm), flexural modulus, and elongation at break are on the same level as PMMA (221). The vacuum time, the time in minutes to reach a pressure of 0.13 mPa (10 torr), is similarly short like that of cychc polyolefins. Typical values of TPX are fisted in Table 11. A commercial application of TPX is not known as of this writing. 

Vinyl-coated fabrics exhibit high density, extremely low water vapor and air permeabiUty, cold touch, poor flex endurance, and plasticizer migration. However, they have good scratch resistance and colorabiUty and are inexpensive. 

The high solubility of the salt and resultant low water vapor pressure (58) of its aqueous solutions ate usehil ia absorption air conditioning (qv) systems. Lithium bromide absorption air conditioning technology efficiencies can surpass that of reciprocal technology usiag fluorochlorocarbon refrigerants. 

Lithium hydroxide can be used for preparation of numerous lithium salts. The dominant use is the preparation of lithium stearate [4485-12-5], which is added to lubricating greases in amounts up to about 10% by weight. This salt has very low water solubiHty and extends the acceptable viscosity for the grease to both low and high temperatures (see Lubrication and lubricants). Lithium hydroxide is also used in production of dyes (62) and has been proposed as a source of lithium ion for inhibition of alkaH-aggregate expansive reactivity in concrete (63). 

A variety of methods have been devised to stabilize shales. The most successful method uses an oil or synthetic mud that avoids direct contact between the shale and the emulsified water. However, preventing direct contact does not prevent water uptake by the shale, because the organic phase forms a semipermeable membrane on the surface of the wellbore between the emulsified water in the mud and the water in the shale. Depending on the activity of the water, it can be drawn into the shale (activity lower in the shale) or into the mud (activity higher in the shale) (95—97). This osmotic effect is favorable when water is drawn out of the shale thus the aqueous phase of the oil or synthetic mud is maintained at a low water activity by a dding a salt, either sodium chloride or more commonly, calcium chloride. The salt concentration is carried somewhat above the concentration required to balance the water activity in the shale to ensure water movement into the mud. 

Another process employs a pH maintained at 4—7 and a catalyst that combines a divalent metal cation and an acid. Water is removed continuously by azeotropic distillation and xylene is recycled. The low water content increases the reaction rate. The dibenzyl ether groups are decomposed by the acid the yield of 2,2 -methylene can be as high as 97% (34). 

Aquatic Toxicity. The standard tests to measure the effect of substances on the aquatic environment are designed to deal with those that are reasonably soluble ia water. Unfortunately this is a disadvantage for the primary phthalates because they have a very low water solubiUty (ca 50 p.g/L) and this can lead to erroneous test results. The most common problem is seen ia toxicity tests on daphnia where the poorly water-soluble substance forms a thin film on the water surface within which the daphnia become entrapped and die. These deaths are clearly not due to the toxicity of the substance but due to unsuitable test design. 

Several nonequilihrium forms of aluminum oxides have been observed (11,12) in hydrothermal experiments at low water vapor pressures in the temperature region of 300—500°C. The KI—AI2O2 form, also known as tondite [12043-15-1] AI2O2 I/5H2O, is characterized by a distinct x-ray diffraction pattern. 

Liquid cycloahphatic amines and diamines have exacting purity and color standards. Almost all are sold to specification, not performance standards. Use as isocyanate precursors requites low water content criteria for these hygroscopic fluids, hence nitrogen blanketing is often specified for product sampling as well as storage and transport. 

Table 8 summarizes domestic consumption by use for amyl alcohols. About 55% of the total 1-pentanol and 2-methyl-1-butanol production is used for zinc diamyldithiophosphate lubrication oil additives (150) as important corrosion inhibitors and antiwear additives. Amyl xanthate salts are useful as frothers in the flotation of metal ores because of their low water solubiUty and miscibility with phenoHcs and natural oils. Potassium amyl xanthate, a collector in flotation of copper, lead, and zinc ores, is no longer produced in the United States, but imports from Germany and Yugoslavia were 910 —1100 t in 1989 (150). 

Equation 7 shows that as AP — oo, P — 1. The principal advantage of the solution—diffusion (SD) model is that only two parameters are needed to characterize the membrane system. As a result, this model has been widely appHed to both inorganic salt and organic solute systems. However, it has been indicated (26) that the SD model is limited to membranes having low water content. Also, for many RO membranes and solutes, particularly organics, the SD model does not adequately describe water or solute flux (27). Possible causes for these deviations include imperfections in the membrane barrier layer, pore flow (convection effects), and solute—solvent—membrane interactions. 

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