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Solutions, formaldehyde State

Formaldehyde is a gas, b.p. — 21°, and cannot obviously be stored as such moreover, it polymerises readily in the liquid and the gaseous state. The commercial preparation, formalin, is an aqueous solution containing 35-40 per cent, of formaldehyde and some methyl alcohol. The preparation of a solution of formaldehyde may be demonstrated by the following experiment. [Pg.325]

Urea.—Forma.IdehydeResins. Cellular urea—formaldehyde resins can be prepared in the following manner an aqueous solution containing surfactant and catalyst is made into a low density, fine-celled foam by dispersing air into it mechanically. A second aqueous solution consisting of partially cured urea—formaldehyde resin is then mixed into the foam by mechanical agitation. The catalyst in the initial foam causes the dispersed resin to cure in the cellular state. The resultant hardened foam is dried at elevated temperatures. Densities as low as 8 kg/m can be obtained by this method (117). [Pg.408]

It is stated that in time the acidity (up to 2,5 units) of 0,1-1,0 M HMTA aqueous solutions changes maximally at 1°C, in comparatively to other temperatures (11, 16, 21°C). When the temperature arises the change of HMTA aqueous solutions pH values decreases in time. Formaldehyde and ammonium ions (end products of HMTA hydrolysis) have been fixed only in more diluted solutions (0,10 and 0,25M). The concentration of NH in them in some times is higher than H2C=0 concentration that is caused by oxidation of the last one to a formic acid, being accompanied by the change of the system platinum electrode potential. It is stated that concentration NH in solutions does not exceed 5% from HMTA general content. The conclusion the mechanism of HMTA destruction in H,0 to depend essentially on its concentration and temperature has been made. [Pg.38]

Formaldehyde is a gas with a boiling point of -21 °C. It is usually supplied as a stabilised aqueous solution ( 40% formaldehyde) known as formalin. When formalin is used as the source of the aldehyde, impurities present generally include water, methanol, formic acid, methylal, methyl formate and carbon dioxide. The first three of these impurities interfere with polymerisation reactions and need to be removed as much as possible. In commercial polymerisation the low polymers trioxane and paraformaldehyde are convenient sources of formaldehyde since they can be obtained in a greater state of purity. [Pg.532]

Formaldehyde has been rated as a possible carcinogen by the United States Occupational Safety and Health Act (OSHA) rules and should be handled with due caution. It is also a strong lacrymator and choking respiratory irritant. It irritates the skin, eyes, and mucous membranes [76]. Since it is used for tanning leather, it is obvious that fonnaldehyde has a high potential for reactions with proteins. Formaldehyde gas is flammable and most formalin solutions contain significant amounts of methanol, which is also volatile, toxic, and flammable. [Pg.875]

Taurolidine (bis-[l,l-dioxoperhydro-l,2,4-thiadiazinyl-4] methane) is a condensate of two molecules of the amino acid taurine and three molecules of formaldehyde. It is more stable than noxythiolin in solution and has similar uses. The activity oftaurolidine is stated to be greater than that of formaldehyde. [Pg.216]

Sometimes, extra chemicals are added to the main chemical as stabilizers. For example, formaldehyde is too reactive in its pure state to exist as formaldehyde for any length of time. It will dimerize or polymerize on standing. Formaldehyde is normally sold as a 40 vol% solution in water, with a methanol stabilizer (12 vol%) to slow down the polymerization. [Pg.127]

The technological circuit of ZnCFO synthesis is developed in the Ukrainian State Chemical-Technological University. ZnCFO is the product of reaction of carbamide and formaldehyde polycondensation in zinc salts solution at recycling of metalcontaining wastes of chemical manufactures. The material base of ZnCFO manufacture are fulfilled catalysts, solutions from zincing and others zinccontaining wastes of various origin. [Pg.190]

Properties and handling. Formaldehyde is a colorless, toxic gas at room temperature, with a pungent, irritating odor. It is flammable and explosive in presence of air. Both gaseous and liquid forms of formaldehyde polymerize at room temperature, and because of this, it can only be maintained in the pure state for a very short period. Because of these unhandy conditions, there are two ways formaldehyde gets into commerce, as a water solution called formalin and as a solid called paraformaldehyde or trioxane. [Pg.231]

Both liquid and gaseous formaldehyde polymerize readily at low temperatures and can be kept in the pure monomeric state only for a limited time. Because of these facts, formaldehyde is sold and transferred either in solution or in polymerized form, such as paraformaldehyde and trioxane, described here under Formaldehyde polymers Commercial, 37% solution of formaldehyde (So-called Methanol-free)... [Pg.546]

Oxidation of Methane. A variety of new catalyst systems have been disclosed, and new reagents were developed with the aim to perform selective transformation of methane to methanol, methyl esters, and formaldehyde. Much work was carried out in strongly acidic solutions, which enhances the electrofilicity of the metal ion catalyst, and the ester formed is prevented from further oxidation. An important advance in the selective oxidation of methane to methanol is Periana s 70% one-pass yield with high selectivity in sulfuric acid solution under moderate conditions.1073 The most effective catalyst is a Pt-bipyrimidine complex. Pt(II) was shown to be the most active oxidation state generating a Pt-methyl intermediate that is oxidized to yield the product methyl ester. A density functional study... [Pg.519]


See other pages where Solutions, formaldehyde State is mentioned: [Pg.440]    [Pg.18]    [Pg.352]    [Pg.1169]    [Pg.531]    [Pg.86]    [Pg.148]    [Pg.371]    [Pg.182]    [Pg.1038]    [Pg.201]    [Pg.215]    [Pg.215]    [Pg.424]    [Pg.427]    [Pg.257]    [Pg.271]    [Pg.278]    [Pg.326]    [Pg.264]    [Pg.247]    [Pg.249]    [Pg.1438]    [Pg.146]    [Pg.782]    [Pg.176]    [Pg.125]    [Pg.97]    [Pg.167]    [Pg.91]    [Pg.531]    [Pg.236]    [Pg.179]    [Pg.117]    [Pg.26]    [Pg.278]    [Pg.311]   
See also in sourсe #XX -- [ Pg.29 ]




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