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Phtalic anhydride

Fig. 3.116. Preparation of D C Yellow No. 10 by condensing quinaldine, 1 with phtalic anhydride, 2 and sulphonating the condensation product, 3. Reprinted with permission from A. Weiszet al. [172]. Fig. 3.116. Preparation of D C Yellow No. 10 by condensing quinaldine, 1 with phtalic anhydride, 2 and sulphonating the condensation product, 3. Reprinted with permission from A. Weiszet al. [172].
Figure 4. FT-IR spectra of the adsorbed species arising from contact of the catalyst with o-xylene/oxygen at r.t. (a), 373 K (b), 423 K (c), 473 K (d), and 523 K (e). (f) phtalic anhydride adsorbed at r.t., producing also phtalate ions. Figure 4. FT-IR spectra of the adsorbed species arising from contact of the catalyst with o-xylene/oxygen at r.t. (a), 373 K (b), 423 K (c), 473 K (d), and 523 K (e). (f) phtalic anhydride adsorbed at r.t., producing also phtalate ions.
Friedel-Crafts acylation is used, for example, in the synthesis of anthraquinone from benzene and phtalic anhydride. [Pg.113]

Photosensitized crosslinking of polymers has been the subject of numerous publications [l - 30], concerned mainly with poly(ethylene), poly(vinyl alcohol), various vinyl copolymers, copolymers of maleic anhydride and/or phtalic anhydride with styrene and some polymers derivated from cinnamic acid. The following compounds were used as sensitizers benzophenone, 4-chloro- and 4,4-dimethylbenzophenone [l, 3-6, 8, 9l, oC -and -derivatives of anthraquinone [3, 23] acetophenone, hydroquinone, triphenylmethane and pyridine li.] chlorobenzene and no less than trichlorinated n-paraffins [6], a complex of zink chloride with o-dia-nizidine fill potassium bichromate [l2j, anthracene fl3, 14] 2,5-methoxy-4-amino-trans-stilbene [l5], benzyl ideneacetophenone fl6-l8] -thiophenylacetophenone,... [Pg.58]

Polyester of Maleic/Phtalic Anhydrides and Ethylene Glycol in Styrene V... [Pg.66]

V. A. Nikolov, D. G. Klissurski, and K. I. Hadjiivanov, "Deactivation of a V205-Ti02 Catalysts for the Oxidation of o-Xylene to Phtalic Anhydride", in Catalyst Deactivation 1987, eds. Delmon Froment, Elsevier, Amsterdam, 1987, pp. 173-82. [Pg.176]

Desublimation. Sometimes a solid phase can be obtained directly by desublimation, as for example the separation of phtalic anhydride by the oxidation of ortho-xylene. [Pg.265]

Another solution is the use of a flash as pre-separator of lights from heavies, while the purification of the bulk component takes place in a second side-stream column. This device offers the simultaneous removal of lights and heavies. A practical example is the purification of phtalic anhydride (Dimian, 1997). [Pg.273]

Ellington, J. B., K. M. Park, and J. F. Brennecke. 1994. Effect of local composition enhancements on the esterification of phtalic-anhydride with methanol in supercritical carbon-dioxide. Industrial and Engineering Chemistry Research. 33,965. [Pg.333]

Besidesfluoroepoxides, fluoroanhydrides (76,79) have been synthesized. The structure of the substituted phtalic anhydride is as follows ... [Pg.26]

Cyclic anhydrides have been studied as chemical reagents for wood modification phtalic anhydride, maleic anhydride, glutaric anhydride, succinic anhydride and alkenyl succinic anhydrides (ASA) [42]. Scots pine-treated samples with petrochemical octenyl succinic anhydrides (ASAs) dissolved in pyridine that after treatment did not present enough resistance against fungi decay but increased dimensional stability. [Pg.321]

Figure 17. Magnetic force as a function of the castor oil amount and phtalic anhydride amount. Figure 17. Magnetic force as a function of the castor oil amount and phtalic anhydride amount.
Figiire 20. Oil removal capability as a function of the petroleum and phtalic anhydride amounts. [Pg.261]

Toluene Sulfonic Acid 94 122-257 50-125 E - - plus phthalic acid, alcohols, water, weak H S0<, activated carbon. CO m esterification of phtalic anhydride. Alloy C 0.1 mpy... [Pg.718]

Analysis of TG-MS data yields additional information about emission of volatiles. Analysis of the volatile deeomposition products by FT-MS spectroscopy revealed that during eontrolled heating emission of phtalic anhydride takes place at ca. 330°C, than, at ca. 380 C styrene and a complex mixture of other aromatic compounds are evolved. [Pg.230]


See other pages where Phtalic anhydride is mentioned: [Pg.217]    [Pg.217]    [Pg.80]    [Pg.638]    [Pg.101]    [Pg.52]    [Pg.60]    [Pg.151]    [Pg.318]    [Pg.101]    [Pg.607]    [Pg.27]    [Pg.604]    [Pg.166]    [Pg.210]    [Pg.223]    [Pg.218]    [Pg.259]    [Pg.198]    [Pg.246]   
See also in sourсe #XX -- [ Pg.642 ]

See also in sourсe #XX -- [ Pg.12 , Pg.31 , Pg.40 , Pg.57 ]




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