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Arco

Characteristics of an extremely" reformulated gasoline and its impact on the environment Source Arco. [Pg.264]

Chartler A, D Arco P, DovesI R and Saunders V R 1999 Ab initio Flartree-Fock Investigation of the structural, electronic, and magnetic properties of MOjO Pbys. Rev. B 60 14 042-8, and references therein... [Pg.2233]

ArCOCl + CsHjN + ArCOOH -----> ArCO—0—COAr + CgHgN.HCl... [Pg.794]

ARCO s Xylenes Plus, and Mobil s MTDP and STOP. [Pg.415]

Currendy, about 40% of the PX produced woddwide uses crystallization technology. A number of crystallization processes have been commercialized over the years. The more common ones are those developed by Chevron, Kmpp, Amoco, ARCO (LyondeU), and Phillips. Some of the features of these processes are discussed herein. [Pg.417]

ARCO has developed a coproduct process which produces KA along with propylene oxide [75-56-9] (95—97). Cyclohexane is oxidized as in the high peroxide process to maximize the quantity of CHHP. The reactor effluent then is concentrated to about 20% CHHP by distilling off unreacted cyclohexane and cosolvent tert-huty alcohol [75-65-0]. This concentrate then is contacted with propylene [115-07-1] in another reactor in which the propylene is epoxidized with CHHP to form propylene oxide and KA. A molybdenum catalyst is employed. The product ratio is about 2.5 kg of KA pet kilogram of propylene oxide. [Pg.242]

It has been known since the early 1950s that butadiene reacts with CO to form aldehydes and ketones that could be treated further to give adipic acid (131). Processes for producing adipic acid from butadiene and carbon monoxide [630-08-0] have been explored since around 1970 by a number of companies, especially ARCO, Asahi, BASF, British Petroleum, Du Pont, Monsanto, and Shell. BASF has developed a process sufficiendy advanced to consider commercialization (132). There are two main variations, one a carboalkoxylation and the other a hydrocarboxylation. These differ in whether an alcohol, such as methanol [67-56-1is used to produce intermediate pentenoates (133), or water is used for the production of intermediate pentenoic acids (134). The former is a two-step process which uses high pressure, >31 MPa (306 atm), and moderate temperatures (100—150°C) (132—135). Butadiene,... [Pg.244]

CO, and methanol react in the first step in the presence of cobalt carbonyl catalyst and pyridine [110-86-1] to produce methyl pentenoates. A similar second step, but at lower pressure and higher temperature with rhodium catalyst, produces dimethyl adipate [627-93-0]. This is then hydrolyzed to give adipic acid and methanol (135), which is recovered for recycle. Many variations to this basic process exist. Examples are ARCO s palladium/copper-catalyzed oxycarbonylation process (136—138), and Monsanto s palladium and quinone [106-51-4] process, which uses oxygen to reoxidize the by-product... [Pg.244]

K. Boekhaus and co-workers, "Reformulated GasoHne for Clean Air An ARCO Assessment," 2nd Biennial U.C. Davis Conf. on yiltemative Fuels (July 12, 1990). [Pg.436]

Fig. 10. Simplified flow diagram depicting the ARCO gas-to-gasoline process for a conceptual gasoline production plant (72). Fig. 10. Simplified flow diagram depicting the ARCO gas-to-gasoline process for a conceptual gasoline production plant (72).
J. A. Sofranko, "Gas to Gasohne The ARCO GTG Process," paper presented at Bicentenay Catalysis Meeting, Sydney, AustraUa, Sept. 1988. [Pg.98]

ARCO Chemical Co., Testimony to the Colorado Air Quality Control Commission on Proposed Regulation Mo. 13 (Oyygenate Mandate Program), Denver, Colo., June 4,1987. [Pg.98]

Attempts have been made to develop methods for the production of aromatic isocyanates without the use of phosgene. None of these processes is currently in commercial use. Processes based on the reaction of carbon monoxide with aromatic nitro compounds have been examined extensively (23,27,76). The reductive carbonylation of 2,4-dinitrotoluene [121 -14-2] to toluene 2,4-diaLkylcarbamates is reported to occur in high yield at reaction temperatures of 140—180°C under 6900 kPa (1000 psi) of carbon monoxide. The resultant carbamate product distribution is noted to be a strong function of the alcohol used. Mitsui-Toatsu and Arco have disclosed a two-step reductive carbonylation process based on a cost effective selenium catalyst (22,23). [Pg.454]

Sales demand for acetophenone is largely satisfied through distikative by-product recovery from residues produced in the Hock process for phenol (qv) manufacture. Acetophenone is produced in the Hock process by decomposition of cumene hydroperoxide. A more selective synthesis of acetophenone, by cleavage of cumene hydroperoxide over a cupric catalyst, has been patented (341). Acetophenone can also be produced by oxidizing the methylphenylcarbinol intermediate which is formed in styrene (qv) production processes using ethylbenzene oxidation, such as the ARCO and Halcon process and older technologies (342,343). [Pg.501]

ARCO to Exit MEK Busiuess Citing Eeedstock, Plant Age," Chem. Mark. Rep. (fan. 7,1991). [Pg.502]

The addition of an oxygen atom to an olefin to generate an epoxide is often catalyzed by soluble molybdenum complexes. The use of alkyl hydroperoxides such as tert-huty hydroperoxide leads to the efficient production of propylene oxide (qv) from propylene in the so-called Oxirane (Halcon or ARCO) process (79). [Pg.477]

Functional Olefin Hydroformylation. There has been widespread academic (18,19) and industrial (20) interest in functional olefin hydroformylation as a route to polyfiinctional molecules, eg, diols. There are two commercially practiced oxo processes employing functionalized olefin feedstocks. Akyl alcohol hydroformylation is carried out by Arco under Hcense from Kuraray (20,21). 1,4-Butanediol [110-63 ] is produced by successive hydroformylation of aHyl alcohol [107-18-6] aqueous extraction of the intermediate 2-hydroxytetrahydrofuran, and subsequent hydrogenation. [Pg.470]

Chevron Chemical Co. began commercial production of isophthahc acid in 1956. The sulfur-based oxidation of / -xylene in aqueous ammonia at about 320°C and 7,000—14,000 kPa produced the amide. This amide was then hydrolyzed with sulfuric acid to produce isophthahc acid at about 98% purity. Arco Chemical Co. began production in 1970 using air oxidation in acetic acid catalyzed by a cobalt salt and promoted by acetaldehyde at 100—150°C and 1400—2800 kPa (14—28 atm). The cmde isophthahc acid was dissolved and recrystallized to yield a product exceeding 99% purity. The Arco technology was not competitive and the plant was shut down in 1974. [Pg.493]


See other pages where Arco is mentioned: [Pg.264]    [Pg.794]    [Pg.21]    [Pg.126]    [Pg.202]    [Pg.202]    [Pg.69]    [Pg.69]    [Pg.416]    [Pg.423]    [Pg.423]    [Pg.94]    [Pg.109]    [Pg.424]    [Pg.424]    [Pg.424]    [Pg.120]    [Pg.372]    [Pg.444]    [Pg.86]    [Pg.88]    [Pg.170]    [Pg.365]    [Pg.370]    [Pg.477]    [Pg.483]    [Pg.460]    [Pg.460]    [Pg.460]    [Pg.134]    [Pg.316]    [Pg.294]   
See also in sourсe #XX -- [ Pg.13 , Pg.23 , Pg.111 , Pg.145 , Pg.153 , Pg.154 , Pg.159 , Pg.171 , Pg.172 ]




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