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Formaldehyde methanol

In methanol—formaldehyde—water solutions, increasing the concentration of either methanol or formaldehyde reduces the volatility of the other. Vapor-hquid-equihbrium data (8,27) for several methanolic formaldehyde solutions ate given in Table 2. The flash point varies with composition, decreasing from 83 to 60°C as the formaldehyde and methanol concentrations increase (17,18). [Pg.491]

Most formaldehyde producers recommend a minimum storage temperature for both stabilized and unstabilized solutions. Figure 3 is a plot of data (17,18,122,126) for uiiinhibited (<2.0 wt% methanol) formaldehyde. The minimum temperature to prevent paraformaldehyde formation in unstabilized 37% formaldehyde solutions stored for one to about three months is as follows 35°C with less than 1% methanol 21°C with 7% methanol 7°C with 10% methanol and 6°C with 12% methanol (127). [Pg.496]

Fiaal purification of propylene oxide is accompHshed by a series of conventional and extractive distillations. Impurities ia the cmde product iaclude water, methyl formate, acetone, methanol, formaldehyde, acetaldehyde, propionaldehyde, and some heavier hydrocarbons. Conventional distillation ia one or two columns separates some of the lower boiling components overhead, while taking some of the higher boilers out the bottom of the column. The reduced level of impurities are then extractively distilled ia one or more columns to provide a purified propylene oxide product. The solvent used for extractive distillation is distilled ia a conventional column to remove the impurities and then recycled (155,156). A variety of extractive solvents have been demonstrated to be effective ia purifyiag propylene oxide, as shown ia Table 4. [Pg.139]

On the base of alcohol oxidase and flavocytochrome b, the enzymatic kits for selective assay of ethanol, methanol, formaldehyde and L-lactate were developed. [Pg.347]

Chemical compounds manufactured at petrochemical plants include methanol, formaldehyde, and halogenated hydrocarbons. Formaldehyde is used in the manufacture of plastic resins, including phenolic, urea, and melamine resins. Halogenated hydrocarbons are used in the manufacture of silicone, solvents, refrigerants, and degreasing agents. [Pg.54]

Reaction of (+)-sedridine (118) and a 37% aqueous solution of CH2O in MeOH at room temperature gave 3-methylperhydropyrido[l,2-c][l,3]oxa-zine (81) (97TA109). Similarly, reaction of andrachcinidine alkaloid, cis-2,6-H-2-(2-oxopropyl)-6-(2-hydroxypentyl)piperidine with 1.5% methanolic formaldehyde solution afforded cw-3,4n,9-H-9-(2-oxopropyl)-3-propylper-hydropyrido[l, 2-c][ 1,3]oxazine (00MI71). [Pg.244]

To balance the methanol-formaldehyde halfreaction we write, as a start,... [Pg.333]

Interest in fuel cells has stimulated many investigations into the detailed mechanisms of the electrocatalytic oxidation of small organic molecules such as methanol, formaldehyde, formic acid, etc. The major problem using platinum group metals is the rapid build up of a strongly adsorbed species which efficiently poisons the electrodes. [Pg.556]

Methanol, Formaldehyde, and Formic Acid Adsorption/Oxidation on a Carbon-Supported Pt Nanoparticle Fuel Cell Catalyst A Comparative Quantitative OEMS Study... [Pg.411]

The adsorption and oxidation of the Ci molecules methanol, formaldehyde, and formic acid over a carbon-supported Pt/C fuel cell catalyst under continuous electrolyte flow have been investigated in a quantitative, comparative online DBMS study. [Pg.451]

Perez JM, Munoz E, Moralldn E, Cases F, Vazquez JL, Aldaz A. 1994. Formation of CO during adsorption on platinum electrodes of methanol, formaldehyde, ethanol and acetaldehyde in carbonate medium. J Electroanal Chem 368 285-291. [Pg.461]

This chapter compares the reaction of gas-phase methylation of phenol with methanol in basic and in acid catalysis, with the aim of investigating how the transformations occurring on methanol affect the catalytic performance and the reaction mechanism. It is proposed that with the basic catalyst, Mg/Fe/0, the tme alkylating agent is formaldehyde, obtained by dehydrogenation of methanol. Formaldehyde reacts with phenol to yield salicyl alcohol, which rapidly dehydrogenates to salicyladehyde. The latter was isolated in tests made by feeding directly a formalin/phenol aqueous solution. Salicylaldehyde then transforms to o-cresol, the main product of the basic-catalyzed methylation of phenol, likely by means of an intramolecular H-transfer with formaldehyde. With an acid catalyst, H-mordenite, the main products were anisole and cresols moreover, methanol was transformed to alkylaromatics. [Pg.399]

The results obtained indicate that in the reaction between phenol and methanol, formaldehyde is the trae methylating agent when basic catalysts are used. This indicates that the type of transformation occurring with methanol is the factor that mainly differentiates performances in phenol methylation when catalyzed by either basic or acid catalysts. The catalyst plays its role in the generation of the methylating species the nature of the latter then determines the type of phenolic products obtained. [Pg.404]

Clearly some molecular processing occurs in the coma to produce larger molecules such as methanol, formaldehyde and more complex still, but the detection and identification of bigger molecules are limited by the sensitivity and resolution of the instruments. The inventory, however, is probably a guide to an untold story... [Pg.184]

Walker A process for partially oxidizing natural gas or LPG, forming a mixture of methanol, formaldehyde, and acetaldehyde. Air is the oxidant and aluminum phosphate the catalyst. Invented by J. C. Walker in the 1920s and operated by the Cities Service Corporation, OK, in the 1950s. [Pg.287]

Methanol conversion, in formaldehyde manufacture, 12 115 Methanol converters, 16 308 Methanol-formaldehyde-water solutions, 12 109... [Pg.574]

Fuel cells using directly liquid fuels are advantageous in this aspect. Methanol, formaldehyde (water solution), formic acid (water solution) and hydrazine are among fuels relatively easy to oxidize electrochemically. Alcohol and hydrocarbon with larger molecular weight are much harder to oxidize completely to C02- Other qualifications to be considered are price, availability, safety, energy density and ease of handling. [Pg.27]

The toxic emissions with CNG, without exception, are lower than for any other hydrocarbon fuel. This is a direct result of the fact that CNG is a single hydrocarbon, 90% methane, whereas all of the other fuels are a mix of hydrocarbons. LPG is a relatively simple mix of propane, butane, and pentane compared to CNG and the complex mix that makes up the gasoline and diesel typically pnrchased at the service station. Gasoline and diesel emit compounds into the air methanol, formaldehyde, aldehydes, acrolein, benzene, toluene, xylene, etc., some of which ate not yet part of any established emission standard but certainly are not beneficial to people s health (Demiibas, 2002). [Pg.93]

We can push this to completion. In formaldehyde, H2C=0, only two bonding electrons are assigned to the carbon atom so it has been oxidized again. In formic acid, HCOOH, only one electron is assigned to the carbon atom and in carbon dioxide, CO2, none are. So the states of increasing oxidation are methane, methanol, formaldehyde, formic acid, and carbon dioxide. [Pg.73]

Ammonia Derivatives Methyl t-butyl ether -Butyraldehyde Dimethyl terephthalate Methanol Formaldehyde Acetic acid... [Pg.205]

Lee, E. S., Chen, H., Hardman, C., Simm, A., and Charlton, C. (2008). Excessive S-adenosyl-1-methionine-dependent methylation increases levels of methanol, formaldehyde and formic add in rat brain striatal homogenates Possible role in S-adenosyl-l-methionone-induced Parkinsons s disease-like disorders. Life Sci. 83, 821-827. [Pg.144]

We have discussed these reactions previously in connection with equilibrium limitations on reactions, and we will discuss them again in Chapter 7, because both use catalysts. These reactions are very important in petrochemicals, because they are used to prepare industrial H2 and CO as well as methanol, formaldehyde, and acetic acid. As noted previously, these processes can be written as... [Pg.236]

Instead of methanol, formaldehyde can be used as an intermediate derived from syngas. As is exemplified in Table III, various chemicals can be derived directly from formaldehyde. [Pg.13]

Total sulfate may be determined in a 50 50 water-methanolic formaldehyde solution by titration with standardized 0.1//lead perchlorate. Endpoint detection is effected using a combination lead ion-selective electrode, and the level of sulfate is typically 13.8 wt % [14]. [Pg.349]

Methanol Formaldehyde Ethylene Propylene oxide Phenol 1,4-Butanediol Tetrahydrofuran Ethylene glycol Adipic acid Isocyanates Styrene Methyl methacrylate Methyl formate Two-step, via CH4 steam reforming Three-step, via methanol Cracking of naphtha Co-product with t-butyl alcohol or styrene Co-product with acetone Reppe acetylene chemistry Multi-step Hydration of ethylene oxide Multi-step Phosgene chemistry Co-product with propylene oxide Two-step, via methacrolein Three-step, via methanol... [Pg.6]


See other pages where Formaldehyde methanol is mentioned: [Pg.18]    [Pg.287]    [Pg.43]    [Pg.1265]    [Pg.442]    [Pg.603]    [Pg.696]    [Pg.63]    [Pg.273]    [Pg.311]    [Pg.185]    [Pg.413]    [Pg.416]    [Pg.420]    [Pg.375]    [Pg.770]    [Pg.138]    [Pg.106]    [Pg.247]    [Pg.229]    [Pg.84]    [Pg.7]   


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