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Methanol material factor

Polybutene resins. These liquid resins are obtained by cationic polymerization of petroleum C4 streams in the presence of AICI3 at relatively low temperature. Temperature and AICI3 concentration are important factors as they influence the molecular weight and viscosity of the final resin. After reaction, the mixture is deactivated with water, methanol, ammonia or aqueous sodium hydroxide. The organic layer is separated and distilled to remove solvent and unconverted material. [Pg.610]

Cheaper raw materials are another way to reduce production costs. This includes, e.g., the minimization of the melamine content in a MUF-resin. An impeding factor can be the (often temporary) shortage of raw materials for the adhesives, as it was the case with sudden price increases for methanol (from which formaldehyde is obtained industrially) and melamine within the last decade. [Pg.1043]

Mesoporous carbon materials were prepared using ordered silica templates. The Pt catalysts supported on mesoporous carbons were prepared by an impregnation method for use in the methanol electro-oxidation. The Pt/MC catalysts retained highly dispersed Pt particles on the supports. In the methanol electro-oxidation, the Pt/MC catalysts exhibited better catalytic performance than the Pt/Vulcan catalyst. The enhanced catalytic performance of Pt/MC catalysts resulted from large active metal surface areas. The catalytic performance was in the following order Pt/CMK-1 > Pt/CMK-3 > Pt/Vulcan. It was also revealed that CMK-1 with 3-dimensional pore structure was more favorable for metal dispersion than CMK-3 with 2-dimensional pore arrangement. It is eoncluded that the metal dispersion was a critical factor determining the catalytic performance in the methanol electro-oxidation. [Pg.612]

Common standard compounds for reversed phase columns are toluene and naphthalene, which have retention factors, k, of about 3. The eluent modifier is methanol or acetonitrile at a concentration of 50-80%, depending on the hydrophobicity of the stationary phase material. For other stationary phase materials, corresponding analytes, with k = 3-5, can be used. [Pg.39]

Although a reductase was not actually applied, separation of 26 from (S)/(R)-20 was accomplished by use of reversed-phase silica as the column material and methanol/ water as the eluant. In view of the observed dependence of the g factor on concentration, aggregation in this protic medium was excluded. In the HPLC setup, the mixture was fully separated within less than 1.5 min. By use of the JASCO-CD-1595 instrument in conjunction with a robotic autosampler, it was possible to perform about 700—900 rather exact ee determinations per day (111). [Pg.30]

Goewie et al. (19) developed an organometallic-silica bonded phase for the selective retention of phenylurea herbicides and anilines from water. Seven-micrometer diameter silica was derivatized with 2-amino-1-cyclopentene-l-dithiocarboxylic acid (ACDA), resulting in Structure I. Capacity factors of phenylurea herbicides and corresponding anilines were measured on the ACDA-silica and ACDA-metal-loaded silica. The platinum-loaded material was found to selectively retain the anilines. Anilines could be eluted with acetonitrile, but not with methanol or tetrahydrofuran, because of the strength with which acetonitrile forms complexes with platinum and thus displaces the anilines. Application of the ACDA-Pt precolumn in series with an ODS-silica precolumn for... [Pg.113]

The fact that silanol persistence can be favored by equilibrium conditions rather than control of condensation kinetics by steric or electronic factors is usually not considered. The phase separation which results from highly condensed systems continuously removes material from deposition solutions, depleting soluble silane species. While condensed silanols or siloxanes are typically not regarded as participating in a reversible reaction with water or alcohol, they do indeed participate in an equilibrium reaction. Iler [16] has shown that even hydrated amorphous silicon dioxide has an equilibrium solubility in methanol, which implies the formation of soluble low molecular... [Pg.95]

The process shown in Figure 9.21 was first developed by Separex, using cellulose acetate membranes. The separation factor for methanol from MTBE is high (>1000) because the membrane material, cellulose acetate, is relatively glassy and hydrophilic. Thus, both the mobility selectivity term and the sorption term in Equation (9.5) significantly favor permeation of the smaller molecule, methanol, because methanol is more polar than MTBE or isobutene, the other feed components. These membranes are reported to work well for feed methanol concentrations up to 6%. Above this concentration, the membrane is plasticized, and selectivity is lost. More recently, Sulzer (GFT) has also studied this separation using their plasma-polymerized membrane [56],... [Pg.388]

For adhesive bonding of PES to itself or to other materials, epoxy adhesives are generally used. Cyanoacrylates provide good bond strength if environmental resistance is not a factor. Parts made from PES can be cleaned using ethanol, methanol, isopropanol, or low-boiling petroleum ether. Solvents that should not be used are acetone, MEK, perchloroeth-ylene, tetrahydrofuran, toluene, and methylene chloride. [Pg.377]


See other pages where Methanol material factor is mentioned: [Pg.34]    [Pg.180]    [Pg.333]    [Pg.195]    [Pg.461]    [Pg.118]    [Pg.454]    [Pg.519]    [Pg.66]    [Pg.428]    [Pg.99]    [Pg.177]    [Pg.12]    [Pg.36]    [Pg.124]    [Pg.427]    [Pg.35]    [Pg.196]    [Pg.60]    [Pg.29]    [Pg.402]    [Pg.139]    [Pg.87]    [Pg.32]    [Pg.195]    [Pg.453]    [Pg.795]    [Pg.170]    [Pg.227]    [Pg.497]    [Pg.108]    [Pg.309]    [Pg.142]    [Pg.461]    [Pg.107]    [Pg.434]    [Pg.174]    [Pg.283]    [Pg.18]    [Pg.165]    [Pg.266]   
See also in sourсe #XX -- [ Pg.440 ]




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