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Room temperature, standard

Errors in density result from errors in temperature measurement or control calibration of instruments transfer, handling and weighing of samples and impurities in the samples. At temperatures well below the critical temperature and near room temperature, standard techniques easily achieve accuracies of +0.05%. For the compounds in this compilation, that level corresponds to about +0.4 kg m"3. Under these conditions, errors in temperature are not very significant. This level of accuracy only requires... [Pg.10]

Equilibrium room temperature (standard state) phase. [Pg.752]

Handlina Safety Availability - Store at room temperature. - Standard sample was supplied. [Pg.254]

For a free energy of fonnation, the preferred standard state of the element should be the thennodynamically stable (lowest chemical potential) fonn of it e.g. at room temperature, graphite for carbon, the orthorhombic crystal for sulfiir. [Pg.367]

The reaction product is cooled to room temperature, is washed with 10 ml of H2O to the purpose of removing lithium iodide and is then dehydrated over NaiS04. 3.57 g is obtained of dimethoxy-phenylacetone (III), as determined by gas-chromatographic analysis with an inner standard of 4,4 -dimethoxybeniophenone. The yield of ketone (III) relative to the olefin ( ) used as the starting material is of 87.1%. [Pg.190]

The reaction of an aryl diazonium salt with potassium iodide is the standard method for the preparation of aryl iodides The diazonium salt is prepared from a primary aro matic amine m the usual way a solution of potassium iodide is then added and the reac tion mixture is brought to room temperature or heated to accelerate the reaction... [Pg.947]

After heating to 50 °C in a water bath, the sample was cooled to below room temperature and filtered. The residue was washed with two 5-mL portions of CCI4, and the combined filtrates were collected in a 25-mL volumetric flask. After adding 2.00 mL of the internal standard solution, the contents of the flask were diluted to volume with CCI4. Analysis of an approximately 2- tL sample gave LfD signals of f3.5 for the terpene hydrate and 24.9 for the camphor. Report the %w/w camphor in the analgesic ointment. [Pg.616]

The widely used Parylene C owes its popularity ptincipaHy to the room temperature volatiUty of its monomer. The Parylene C monomer, chloro-A-xylylene, has become the de facto performance standard. By comparison, the Parylene N monomer, A"xylylene itself, is too volatile and would perform better ia a sub-ambient temperature deposition system. The Parylene D monomer, dichloro-A-xyljlene [85586-88-5] is too heavy, and causes distribution problems ia larger deposition systems. [Pg.429]

Cyanoacrylate adhesives (Super-Glues) are materials which rapidly polymerize at room temperature. The standard monomer for a cyanoacrylate adhesive is ethyl 2-cyanoacrylate [7085-85-0], which readily undergoes anionic polymerization. Very rapid cure of these materials has made them widely used in the electronics industry for speaker magnet mounting, as weU as for wire tacking and other apphcations requiring rapid assembly. Anionic polymerization of a cyanoacrylate adhesive is normally initiated by water. Therefore, atmospheric humidity or the surface moisture content must be at a certain level for polymerization to take place. These adhesives are not cross-linked as are the surface-activated acryhcs. Rather, the cyanoacrylate material is a thermoplastic, and thus, the adhesives typically have poor temperature resistance. [Pg.233]

THPC—Amide Process. The THPC—amide process is the first practical process based on THPC. It consists of a combination of THPC, TMM, and urea. In this process, there is the potential of polymer formation by THPC, melamine, and urea. There may also be some limited cross-linking between cellulose and the TMM system. The formulation also includes triethanolamine [102-71-6J, an acid scavenger, which slows polymerization at room temperature. Urea and triethanolamine react with the hydrochloric acid produced in the polymerization reaction, thus preventing acid damage to the fabric. This finish with suitable add-on passes the standard vertical flame test after repeated laundering (80). [Pg.489]

Storage. For receiving glycerol from standard 30.3-m (8000-gal) tank cars (36.3-t), a storage tank of 38—45-m ((10-12) x 10 — gal) capacity should be employed. Preferably it should be of stainless steel (304 or 316), of stainless- or nickel-clad steel, or of aluminum. Certain resin linings such as Lithcote have also been used. Glycerol does not seriously corrode steel tanks at room temperature but gradually absorbed moisture may have an effect. Therefore, tanks should be sealed with an air-breather trap. [Pg.349]

Krypton difluoride cannot be synthesized by the standard high pressure-high temperature means used to prepare xenon fluorides because of the low thermal stabitity of KrF. There are three low temperature methods which have proven practical for the preparation of gram and greater amounts of KrF (141—143). Radon fluoride is most conveniently prepared by reaction of radon gas with a tiquid halogen fluoride (CIE, CIE, CIE, BrE, or lE ) at room temperature (144,145). [Pg.25]

Oxygen scavengers other than hydrazine are also used, especially catalyzed sodium sulfite, which reacts rapidly with oxygen even at room temperatures to form sodium sulfate. Catalyzed hydrazine formulations are now commercially available that react with oxygen at ambient temperatures at rates comparable to catalyzed sulfite (189). At elevated temperatures, the reaction rates are all similar. Table 14 Hsts the standard hydrazine solution products offered by Olin Corp. for sale to the water-treatment market. Other concentrations are available and other companies offer similar products. [Pg.290]

The higher concentration (0,5, 1,0 M) HMTA solutions are recommended to use as initial standards for determination of acids concentrations. It is recommended to keep them at room temperature because they are more stable under these conditions. [Pg.38]

The method was validated in accordance to the guidelines of the international conference on harmonization (ICH). Data with respect to accuracy, within- and between run precision, recovery, detection and quantitation limits were reported and found to be within the accepted international criteria. Neither endogeneous substances nor the commonly used dmgs were found to interfere with the retention times of the analytes. Standard solutions of the dmg and quality control preparations at high and low level concentrations were demonstrated to be stable at room temperature and/or -20°C for long and short periods of time. [Pg.395]


See other pages where Room temperature, standard is mentioned: [Pg.520]    [Pg.258]    [Pg.401]    [Pg.258]    [Pg.258]    [Pg.130]    [Pg.520]    [Pg.258]    [Pg.401]    [Pg.258]    [Pg.258]    [Pg.130]    [Pg.856]    [Pg.1474]    [Pg.2806]    [Pg.197]    [Pg.534]    [Pg.297]    [Pg.365]    [Pg.399]    [Pg.312]    [Pg.73]    [Pg.154]    [Pg.365]    [Pg.53]    [Pg.160]    [Pg.300]   
See also in sourсe #XX -- [ Pg.20 ]




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