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Vapor organic solvent

A crystalline or semicrystalline state in polymers can be induced by thermal changes from a melt or from a glass, by strain, by organic vapors, or by Hquid solvents (40). Polymer crystallization can also be induced by compressed (or supercritical) gases, such as CO2 (41). The plasticization of a polymer by CO2 can increase the polymer segmental motions so that crystallization is kinetically possible. Because the amount of gas (or fluid) sorbed into the polymer is a dkect function of the pressure, the rate and extent of crystallization may be controUed by controlling the supercritical fluid pressure. As a result of this abiHty to induce crystallization, a history effect may be introduced into polymers. This can be an important consideration for polymer processing and gas permeation membranes. [Pg.223]

Ethylene oxide is a colorless gas that condenses at low temperatures into a mobile Hquid. It is miscible in all proportions with water, alcohol, ether, and most organic solvents. Its vapors are flammable and explosive. The physical properties of ethylene oxide are summarized in Tables 1—7. [Pg.450]

Vapor Permeation Vapor permeation is similar to vapor perva-poration except that the feed stream for permeation is a gas. The futnre commercial viability of this process is based npon energy and capital costs savings derived from the feed already being in the vapor-phase, as in fractional distillation, so no additional heat inpnt wonld be req iired. Its foreseen application areas wonld be the organics recov-eiy from solvent-laden vapors and pollntion treatment. One commercial nnit was installed in Germany in 1989 (Ref. 26). [Pg.2195]

Catalytic afterburners are currently used primarily in industry for the control of solvents and organic vapor emissions from industrial ovens. They are used as emission control devices for gasoline-powered automobiles (see Chapter 31). [Pg.483]

Catalysts that in themselves are completely safe may catalyze combustion of hydro n or of organic vapors or solvents. Compounds that are de-hydro nated readily, such as lower alcohols and cyclohexene, are particularly apt to ignite. Other solvents are ignited with much more difficulty and very rarely, but this should not be relied on, and in all cases due precaution should be taken. [Pg.12]

Other workers do the opposite and add catalyst to the solvent (which again may be cooled) after first sweeping the flask with inert gas to remove air. It appears that if catalyst and solvent are mixed without removal of air (which is certainly not advised) fires are more likely to occur when catalyst is added to the solvent. Catalyst particles falling through organic vapor cannot be eflectively cooled and may enter the liquid glowing. On the other hand, when solvent is added rapidly to the catalyst, any tendency of the catalyst to heat is limited by quenching with a massive amount of liquid. [Pg.13]

Caution Potassium is highly reactive. Although it may be handled safely in air if it is covered with a hydrocarbon solvent such as heptane or mineral oil, it will spark and ignite flammable organic vapors on contact with water. The magnesium formed in this reaction is highly reactive and pyrophoric (Note 1). Accordingly, Parts C and D of this procedure should be carried out behind a safety shield. [Pg.179]

The use of absorption as the primary control technique for organic vapors is subject to several limiting factors. One factor is the availability of a suitable solvent. The VOC must be soluble in the absorbing liquid and even then, for any given absorbent liquid, only VOCs that are soluble can be removed. [Pg.227]

Ligocki MP, Pankow JF. 1985. Assessment of adsorption/solvent extraction with polyurethane foam and adsorption/thermal desorption with Tenax-GC for the collection and analysis of ambient organic vapors. Anal Chem 57 1138-1144. [Pg.155]

Henry s Law is obeyed with organic pollutants of low solubility provided the pressures are not high or temperatures too low - conditions under which one might expect deviations from ideal behavior. Experimental values for Henry s Law constant may be obtained by equilibrating a pollutant between the solvent and vapor phase and measuring its concentration in those two phases. Providing the solubility is low (PA< 0.1) Henry s Law constant can be calculated from the equilibrium vapor pressure (PA) and solubility (S) ... [Pg.250]

Many of the charcoal tube methods are based on NIOSH Method P CAM 127 (4) for organic solvents. In this method, a known volume of air is drawn through a charcoal tube to trap organic vapors, the charcoal is transferred to a vial, and the sample is desorbed with carbon disulfide. The sample is analyzed by gas chromatography (GC) with flame ionization detection (FID). Most methods use CS2 as the desorption solvent because it yields good recoveries from charcoal and produces a very low flame response. [Pg.184]

As with any laboratory method, there are precautions and limitations of lyophilization that must be understood. Only aqueous solutions should be lyophilized. Organic solvents lower the melting point of aqueous solutions and increase the chances that the sample will melt and become denatured during freeze-drying. There is also the possibility that organic vapors will pass through the cold trap into the vacuum pump, where they may cause damage. [Pg.53]

Organic vapors are generated in the work place wherever organic solvents are used. The quantity of... [Pg.189]

A flammable chemical substance is a solid, liquid, vapor, or gas that ignites easily and burns rapidly in air. Many of the flammable chemicals used in laboratories are flammable liquids and organic solvents. The vapors of these chemical substances form ignitable mixtures with air. Based on the flash points of these chemicals, classifications are made. The flash point of a chemical substance is defined as the lowest temperature at which a fuel-air mixture present above the surface of a liquid will ignite, if an ignition source is present. The common flammable chemical substances include, but are not restricted to, acetone, benzene, cyclohexane, ethanol, ethyl acetate, ethyl ether, gasoline, hexane, isopropyl alcohol, methanol, propanol, tetrahydro-furan and toluene, and xylene. [Pg.253]

Most of the 300+ organic vapors that may be found in indoor pollution are derived from paints, paint strippers and other solvents, wood preservatives, aerosol sprays, cleansers and disinfectants, moth repellents, air fresheners, in addition to fuels and automotive products, and dry-cleaners. Many of these compounds are halogenated hydrocarbons, PAH, ketones and aldehydes, which exhibit different degrees of toxicity. [Pg.180]


See other pages where Vapor organic solvent is mentioned: [Pg.387]    [Pg.388]    [Pg.75]    [Pg.392]    [Pg.448]    [Pg.451]    [Pg.922]    [Pg.385]    [Pg.388]    [Pg.31]    [Pg.742]    [Pg.560]    [Pg.565]    [Pg.223]    [Pg.402]    [Pg.135]    [Pg.450]    [Pg.67]    [Pg.519]    [Pg.44]    [Pg.575]    [Pg.75]    [Pg.247]    [Pg.146]    [Pg.372]    [Pg.190]    [Pg.215]    [Pg.239]    [Pg.34]    [Pg.35]   
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