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Acetates aromatics

PMMA is not affected by most inorganic solutions, mineral oils, animal oils, low concentrations of alcohols paraffins, olefins, amines, alkyl monohahdes and ahphatic hydrocarbons and higher esters, ie, >10 carbon atoms. However, PMMA is attacked by lower esters, eg, ethyl acetate, isopropyl acetate aromatic hydrocarbons, eg, benzene, toluene, xylene phenols, eg, cresol, carboHc acid aryl hahdes, eg, chlorobenzene, bromobenzene ahphatic acids, eg, butyric acid, acetic acid alkyl polyhaHdes, eg, ethylene dichloride, methylene chloride high concentrations of alcohols, eg, methanol, ethanol 2-propanol and high concentrations of alkahes and oxidizing agents. [Pg.262]

Petrochemicals and fossil fuels entail chemicals produced from hydrocarbon feedstocks, such as crude oil products and natural gas. They include such chemicals as hydrocarbons and industrial chemicals (e.g., alcohols, acrylates, acetates), aromatics (e.g., benzene, toluene, xylenes), and olefins (e.g., ethylene, propylene, butadiene, methanol). [Pg.50]

Polyvinyl acetate Aromatic hydrocarbons, ketones, chlorinated hydrocarbons, alcohols Petrol... [Pg.101]

Mechanistically, the Beirut reaction is a heterocycle expansion-process where the nucleophile attack conducts, after atomic rearrangements, to a new diazine system. In general, a further elimination—i.e., of H2O, amines, acetate—aromatizes the new heterocycle. [Pg.184]

A solution or suspension of the acid (1 mmol) in carbon tetrachloride (75 ml) containing DIB (0.55 mmol) and iodine (0.5 mmol) was irradiated with two 100 W tungsten-filament lamps for 45 min at reflux temperature. Another portion of DIB (0.55 mmol) was then added and irradiation was continued for 45 min at reflux. The reaction mixture was washed with dilute sodium thiosulphate and water, concentrated and chromatographed (silica gel column, 9 1 hexanes-ethyl acetate) to afford the alkyl iodide. Several steroidal acids with the carboxyl group attached at a 1° or 2° carbon atom gave the corresponding iodides in good yields. Acids with a 3° a-C instead of the iodide afforded alkenes similarly, alkenes were formed with a fivefold excess of DIB in the presence of cupric acetate. Aromatic acids also underwent iododecarboxylation, in moderate yields very effective was the otherwise difficult transformation of 1,8-naphthalenedicarboxylic acid to 1,8-diiodonaphthalene (80%) [68]. Cubyl and homocubyl iodides were also prepared in excellent yield [69]. [Pg.73]

This product is best obtained by heating dehydroquininc with about five times its weight of arsenic trichloride in an oil-bath at 130" to 135" for three hours, in the absence of a solvent. It may also be prepared by digesting the previous compound with aqueous ammonium carbonate. It darkens at 199° to 200° C., sinters at about 204° C., and melts at 207 to 209° C. it is easily soluble in alcohols and pyridine, very sparingly soluble in chloroform and acetone, and insoluble in ether, ethyl acetate, aromatic hydrocarbons, and carbon disulphide. Its salts arc not crystalline. The fact that it forms a benzoyl derivative shows the presence of a free hydroxyl group, and consequently the attachment of the arsenic to the vinyl group. [Pg.480]

A variety of reverse osmosis membrane systems based on cellulose acetate, aromatic polyamides, and other polymers have been tested for their potential applications. Reverse osmosis membrane equipment is available for large-scale operation since the process is widely used for the production of potable water from sea or brackish waters and upstream of ion exchange in the preparation of ultrapure water for steam-generating boilers. In these applications, the feed concentrations may vary from 500 to 40,000 mg/L of dissolved solids. The RO technique can be used at pH values between 3 and 12 and up to 45°C. [Pg.831]

The essential step of this method is the electrocyclization of the azahexatriene system in 5-[(arylmethylene)amino]-6-[(./V,./V-dimethylamino)vinyl]-l, 3-dimethyluracils 5, which rearrange in situ following their formation from 5-(arylidene imino)-1,3,6-trimcthyluracils 4 and dimethylformamide dimethyl acetal. Aromatization then occurs by elimination of dimethyl-amine. The intermediate 6-[(W,Af-dimethylamino)vinyl] compounds 5 may be isolated in low yield.440 441... [Pg.170]

Reverse osmosis was not commercially practical until techniques for increasing productivity were developed. The principal discovery (32) involved a casting procedure that results in asymmetric membranes having a thin dense layer of polymer, approximately 0.2)a thick, supported on a porous sublayer as Illustrated in Figure 8. These membranes are called Loeb membranes (33). Current commercial membranes of this type are made of cellulose acetate, aromatic polyamides, and certain composites that achieve water fluxes of the order of 1.0 m /m day with NaCl rejections of 99% or more (27). As seen in Equation 25, rejection increases with applied pressure. [Pg.270]

Several families of polymers may be used for this application, including cellulose acetates, aromatic polyamides and polysulfones, but progress remains to be made regarding the nature of membranes and their implementation to control the morphologies of the interface. [Pg.390]

Poly(vinyl acetate) Aromatic hydrocarbons. chlorinated hydrocarbons, ketones, methanol Aliphatic hydrocarbons... [Pg.376]

Many polymeric materials are used for membrane fabrication. The most widely used polymers are cellulose acetate and its derivatives, aromatic polyamide, polyamide hydrazide, polysulfone, polyphenylene, polypropylene, etc. Among these cellulose acetate, aromatic polyamide, and polysulfone are more commonly used. In addition, some membranes are made from glasses, ceramics, and metal oxides. [Pg.690]

It was mentioned earlier that composite membranes have superior properties as compared with asymmetric memberanes. There is better control on memberane active and support layers concerning chemical stability, wider pH range, selectivity, solubility, and permeability. The active layer can be made as thin as possible for higher permeability (low-pressure operation). They can be designed with good control on properties for any particular application. Finally, the pH range of application is normally much wider than for asymmetric memberanes as was shown in Table 1. Active surface layer of composite membranes is made from cellulose acetate, aromatic polyamide, polyvinyl alcohol, etc., whereas the support layer is typically made from cellulose acetate, polysulfone, polyester, etc. [Pg.694]

Aromatic polyisocyanurate in butyl acetate Aromatic polyisocyanurate in DOP Contains no solvents... [Pg.121]

Properties Colorless clear appearance sol. in alcohols, esters, ketones, glycol ethers, glycol ether acetates, aromatic and chlorinated hydrocarbons, dearomatized hydrocarbons and isoparaffins dens. 1.04 g/cm (20 C) vise. 20-50 Pa s (23 C) acid no. < 1 flash pt. 109 C surf. tens. 28 0.4mN/m >98.5%NV Acronal NX 4786 [BASF]... [Pg.16]

Chem. Descrip. Methyl methacrylate/modified PVC-based polymer Uses Heat-sealing raw material for pkg. of foods and pharmaceuticals adhesive/bonding agent for finishing PVC leatherette and film binder in printing inks and spray paints for PVC, ABS, PS coatings and films Properties Bead in powd. form sol. in ethyl acetate, MEK, acetone, cyclohexanone, butyl acetate, butyl glycol acetate, aromatics, tetrahydro-furan, chlorinated hydrocarbons insol. in naphtha and alcohols dens. 1.36 g/cm reduced vise. 45-55 em /g (20 C)... [Pg.701]

Chem. Descrip. Modified thermoplastic acrylic in PM acetate/Aromatic 100 solv. blend... [Pg.861]

Chem. Descrip. Polyisocyanate prepolymer Uses Crosslinking agent for two-component polyurethane paints Properties SI. yel. liq. sp.gr. 1.06 g/cm (15 C) 70% solids in n-butyl acetate/Aromatic 100 (1 2) 11.9% NCO Vestanat T1890 M [Degussa AG/Marl]... [Pg.910]

This water-white, primary aliphatic amine is available commercially in an anhydrous form. It is soluble In water, methyl and ethyl alcohols, ethyl ether, ethyl acetate, aromatic and aliphatic hydrocarbons, acetone, mineral oil, fixed oils, oleic and stearic acids. It is soluble In hat paraffin and carnouba waxes, which solidify on cooling. It is potentially useful os on intermediate In such manufactured products as dyestuffs, surface-active agents, textile specialties, pharmaceuticals, bactericides, insecticides, and cleaning compounds. It is also used os o dehoiring ogent in the leather industry. [Pg.692]

Di-n-butylethanolamine (Di-n-Butylaminocthanol, (C H )jNCH CH -OH). This alkylolamine is a water-white liquid with a faintly amine odor. It is insoluble in water but soluble in ethyl alcohol, methyl alcohol, ethyl ether, ethyl acetate, aromatic hydrocarbons, fixed oils, mineral oil, oleic and hot steai-ic acids, and hot paraffin and carnauba waxes, the latter two solidifying when cooled. It is slightly soluble in paraffinic hydrocarbons. [Pg.766]

Properties Grayish-green to greenish-yel. powd., gran., or flakes si. odor tasteless sol. in benzene, ether, hot acetic acid, 21% in acetone, 15% in ethyl amyl ketone, 11% in ethyl acetate, aromatic soivs. si. sol. in alcohol, min. oils pract. insol. in water, chloroform, petrol, ether m.w. 199.26 m.p. 185 C subl. 130 C (1 mm Hg) b.p. 371 C... [Pg.3298]

Definition Synthetic acetal aromatic Empirical C16H26O2... [Pg.3303]

Cellulose Acetate Aromatic Polyamide Polybenzimidazole Polybenzimidzolone Aromatic Polyhydrazide Polyamidimide... [Pg.665]

Scheme 9.14 (a) Acetonitrile, rt, 3-5 h, (b) Acetic acid, ammonium acetate, aromatic/hetero-aro-matic aldehydes, 90 °C, 4-6 h... [Pg.265]

Joshi et al. [67] developed an efficient and simple one-pot synthesis of some new symmetrical, unsymmetrical, and iV-substituted Hantzsch 1,4-DHPs 48 and 49 using molecular iodine as catalyst by the reaction of aldehydes, 1,3-dicarbonyl compound, and ammonium acetate/aromatic amine in EtOH. This new method has the advantage of good to excellent product yields and shorter reaction times at ambient temperature (Scheme 10.32). [Pg.299]

Acetic Anhydride Acetone Acetyl Bromide Acetyl Chloride Ammonium Hydroxide Amyl Acetate Aromatic Hydrocarbons Butyl Acetate Carbon Bisulfide... [Pg.67]

Polyvinyl acetate Aromatic and chlorinated hydrocarbons, methanol, ketones Gasoline... [Pg.139]

Many polymers have been screened for use as reverse osmosis membranes, but only a few have proved to be suitable. Examples of current interest include cellulose acetate, aromatic polyamides and certain thin-film composite membranes of polyamides. [Pg.666]


See other pages where Acetates aromatics is mentioned: [Pg.73]    [Pg.120]    [Pg.989]    [Pg.3]    [Pg.97]    [Pg.73]    [Pg.392]    [Pg.13]    [Pg.2000]    [Pg.403]    [Pg.1205]    [Pg.1269]    [Pg.2684]    [Pg.23]    [Pg.259]    [Pg.249]    [Pg.760]    [Pg.4627]    [Pg.73]    [Pg.111]    [Pg.332]   
See also in sourсe #XX -- [ Pg.2 , Pg.3 , Pg.4 , Pg.5 , Pg.7 ]

See also in sourсe #XX -- [ Pg.2 , Pg.3 , Pg.4 , Pg.5 , Pg.7 , Pg.11 ]




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Acetates aromatic

Acetates aromatic

Acetates aromatic amines

Acetic acid aromatic

Acetic anhydride aromatic ethers acylation

Acetic anhydride aromatics acetylation

Aromatic acetals

Aromatic compounds reaction with acetals

Aromatic cyanohydrin acetates

Aromatic with acetic anhydride

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