Room temperature wet

T. Ohmi, Total room temperature wet cleaning for Si substrate surface, J. Electrochem. Soc. 143, 2957, 1996. 

RMSD root mean square difference RTW room temperature wet... 

Besides our prediction of the phenomenon of water droplets on water monolayers, there are more observations on real surfaces to support the existence of this phenomenon at room temperature. Recently, several simulation or experimental works have observed the phenomenon of water droplets on water monolayers on some real soUd surfaces. All of these results provide solid evidence that this room temperature wetting phenomenon generally exists in the nature. 

The method for total room temperature wet cleaning of silicon surface comprises the use of HF, H2O2 and ozonized water and is with 5% more economical than that the standard procedure of wet cleaning [161],... 

Six protective groups for alcohols, which may be removed successively and selectively, have been listed by E.J. Corey (1972B). A hypothetical hexahydroxy compound with hydroxy groups 1 to 6 protected as (1) acetate, (2) 2,2,2-trichloroethyl carbonate, (3) benzyl ether, (4) dimethyl-t-butylsilyl ether, (5) 2-tetrahydropyranyl ether, and (6) methyl ether may be unmasked in that order by the reagents (1) KjCO, or NH, in CHjOH, (2) Zn in CHjOH or AcOH, (3) over Pd, (4) F", (5) wet acetic acid, and (6) BBrj. The groups may also be exposed to the same reagents in the order A 5, 2, 1, 3, 6. The (4-methoxyphenyl)methyl group (=MPM = p-methoxybenzyl, PMB) can be oxidized to a benzaldehyde derivative and thereby be removed at room temperature under neutral conditions (Y- Oikawa, 1982 R. Johansson, 1984 T. Fukuyama, 1985). 

Three forms of set may be conferred to wool fibers. (/) Cohesive set is imparted when the fibers are dried under strain or set in steam and is lost when the fibers are relaxed in water at room temperature. (2) Temporary set is imparted at higher temperatures and is lost when the fibers are wet out in hot (70°C) water. (2) Permanent set is imparted in boiling water and in high pressure steam, and is stable to release in hot water. 

Minimum Wetting Rate The minimum liquid rate required for complete wetting of a vertical surface is about 0.03 to 0.3 kg/m s for water at room temperature. The minimum rate depends on the geom-etiy and nature of the vertical surface, liquid surface tension, and mass transfer between surrounding gas and the liquid. See Ponter, et al. Int. J. Heat Mass Tran.fer 10, 349-359 [1967] Trans. Inst. Chem. Eng. [London], 45, 345—352 [1967]), Stainthorp and Allen Trans. Inst. Chem. Eng. [London], 43, 85-91 [1967]) and Watanabe, et al. ]. Chem. Eng. [Japan], 8[1], 75 [1975]). 

Aluminum is not embrittled by low temperatures and is not subject to external corrosion when exposed to normal atmospheres. At 200°C (400°F) its strength is less than half that at room temperature. It is attacked by alkahes, by traces of copper, nickel, mercuiy, and other heaw-metal ions, and by prolonged contact with wet insiilation. It suffers from galvanic corrosion when coupled to copper, nickel, or lead-... 

C. Thymoquinone.—The wet aminothymol thus prepared is immediately dissolved in no cc. of concentrated sulfuric acid diluted to 4 1. and contained in a 12-I. flask. To this solution is added 150 g. of sodium nitrite (2.18 moles), in 5-10-g. portions, with shaking after each addition. The resulting mixture is heated to 60° on a steam bath, with occasional shaking, for half an hour (Note 5), and is then distilled in a current of steam, by means of the apparatus described in Org. Syn. 2, 80 (Note 6). All the thymoquinone passes over with the first 3 1. of distillate it solidifies on cooling, and is filtered with suction (Note 7), washed, and dried at room temperature. The yield is 80-87 g. (73-80 per cent of the theoretical amount) of bright yellow crystals, melting at 43-45° (Note 8). 

Cetyltrimethylammonium bromide (cetrimonium bromide, CTAB) [57-09-0] M 364.5, m 227-235"(dec). Crystd from EtOH, EtOH/ benzene or from wet acetone after extracting twice with pet ether. Shaken with anhydrous diethyl ether, filtered and dissolved in a little hot MeOH. After cooling in the refrigerator, the ppte was filtered at room temperature and redissolved in MeOH. Anhydrous ether was added and, after warming to obtain a clear soln, it was cooled and crystalline material was filtered. [Dearden and Wooley J Phys Chem 91 2404 7957 Hakemi et al. J Am Chem Soc 91 120 1987.]... 

Ammonium peroxydisulfate [7727-54-0] M 228.2, m dec when heated wet liberating oxygen, d 1.98. Recrystd at room temperature from EtOH/water. 

Polyester diols are often combined with polyether diols to provide green strength through crystallization or elevated r . Most prevalent and least expensive is hexamethylene diol adipate (HDA) with a Tm of about 60°C. A variety of polyesters are available with various levels of crystallinity — from wax-like to amorphous — and crystallization rate, and with values ranging well below 0°C to above room temperature. Polybutadiene diols are the most expensive and most hydrophobic. They provide low surface tension and thus good wet out of non-polar surfaces. 

Plasticizers soften the film and increase the adhesion and the setting speed. The most common are phthalates, adipates and benzoates. The amount added can be in a broad range of 10-50%. They affect the swelling and softening of the PVAc emulsion particles, ensure film formation at room temperature, and the tack of the still wet adhesive. They also provide improved moisture resistance of the bond. Disadvantages are the lower resistance of the bond line against heat, possible migration of the plasticizers and enhanced cold flow. 

Two other methods worth discussing are wet air oxidation and regeneration by steam. Wet oxidation may be defined as a process in which a substance in aqueous solution or suspension is oxidized by oxygen transferred from a gas phase in intimate contact with the liquid phase. The substance may be organic or inorganic in nature. In this broad definition, both the well known oxidation of ferrous salts to ferric salts by exposure of a solution to air at room temperature and the adsorption of oxygen by alkaline pyrogallol in the classical Orsat gas analysis would be considered wet oxidations. 

Figure 13 Influence of coupling agents and fiber content on the characteristic values of kenafreinforced recycled PE at room temperature (dry state) and after exposure in boiling water (wet-state) [57].

Halogens Although tantalum is severely attacked by flourine at room temperature it does not react with liquid chlorine, bromine and iodine up to 150°C and the metal suffers no appreciable attack in wet or dry bromine, chlorine and iodine below 250°C. It is virtually uncorroded by hydrogen bromide and hydrogen chloride below 370°C, attack starting at about 375 and 410°C respectively. 

The terms hot corrosion or dry corrosion are normally taken to apply to the reactions taking place between metals and gases at temperatures above 100 C i.e. temperatures at which the presence of liquid water is unusual. The obvious cases of wet corrosion at temperatures above 100 C, i.e. in pressurised boilers or autoclaves, are not considered here. In practice, of course, common metals and alloys used at temperatures above normal do not suffer appreciable attack in the atmosphere until the temperature is considerably above 100 C. Thus iron and low-alloy steels form only the thinnest of interference oxide films at about 200 C, copper shows the first evidence of tarnishing at about 180 C, and while aluminium forms a thin oxide film at room temperature, the rate of growth is extremely slow even near the melting point. 

The 14e compound MTO readily forms coordination complexes of the type MTO-L and MTO-L2 with anionic and uncharged Lewis bases [96], These yellow adducts are typically five- or six-coordinate complexes, and the Re-L system is highly labile. Apart from their fast hydrolysis in wet solvents, MTO-L adducts are much less thermally stable then MTO itself. The pyridine adduct of MTO, for instance, decomposes even at room temperature. In solution, methyltrioxorhenium displays high stability in acidic aqueous media, although its decomposition is strongly accelerated at increased hydroxide concentrations [97, 98], Thus, under basic aqueous conditions MTO decomposes as shown in Equation (4). 

The sodium salt still wet with ether is dissolved in 1300 cc. of distilled water at room temperature, the solution cooled to o°, and the nitrile precipitated by adding slowly, with vigorous shaking, 90 cc. of glacial acetic acid, while the temperature is kept below io°. The precipitate is separated by suction filtration... 

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