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Formaldehyde reactivity

Aniline—formaldehyde resins were once quite important because of their excellent electrical properties, but their markets have been taken over by newer thermoplastic materials. Nevertheless, some aniline resins are stiU. used as modifiers for other resins. Acrylamide (qv) occupies a unique position in the amino resins field since it not only contains a formaldehyde reactive site, but also a polymerizable double bond. Thus it forms a bridge between the formaldehyde condensation polymers and the versatile vinyl polymers and copolymers. [Pg.322]

Zavitsas et al. account for the effects of water in their calculations. Water promotes depolymerization of the paraformaldehyde as well as the hemiformals. Their modifications correct for the apparent reduction in methylolation rate as the extent of reaction proceeds, in that the hemiformals remove formaldehyde reactivity from the reaction mixture. Their rate constants look large because they are written for phenate concentrations rather than phenol and because of the formaldehyde equilibrium adjustments. They note that unsalted phenol is a by-... [Pg.901]

Low temperature steam and formaldehyde Reactive chemical Indicator paper impregnated with a formaldehyde-, steam- and temperature-sensitive reactive chemical which changes colour during the sterilization process Gas concentration, temperature, time (selected cycles)... [Pg.444]

Only a few studies have tackled the problem of deriving a detailed kinetic model of the phenol-formaldehyde reactive system, mainly because of its complexity. In recent years, a generalized procedure has been reported in [11,14] that allows one to build a detailed model for the synthesis of resol-type phenolic resins. This procedure is based on a group contribution method and virtually allows one to estimate the kinetic parameters of every possible reaction taking place in the system. [Pg.24]

In this section, the phenol-formaldehyde reactive system is considered as an example of identification of reduced kinetic models. The kinetic model containing 13 components and 89 reactions, developed in Sect. 2.4 to study the production of 1,3,5-methylolphenol, is too detailed and complex for control and monitoring purposes. Thus, in this section this model is referred to as detailed model, while four reduced kinetic models, based on lumped components and reactions, are developed. [Pg.56]

In this section, the proposed approach has been tested in a simulation case study, developed in the MATLAB/SIMULINK environment. In detail, the problem of temperature control of the phenol-formaldehyde reactive system, developed in Sect. 2.4, has been considered. [Pg.108]

Formaldehyde reactive polyphenolic compounds (Stiasny number). 2Extract modified with 2% phenol (ovendry weight). [Pg.232]

A major distinction for nucleophilic reactions with ambident anions is whether they proceed with kinetic or thermodynamic control.80 N-Substituted saccharins (10) should be thermodynamically more stable because of amide character than the isomeric pseudosaccharin (3) of imidate structure. In fact 3 may be rearranged thermally to 10 in an irreversible reaction.96 The threshold for thermodynamic control appears to be lowered for electrophiles with multiple bonds, e.g., formaldehyde, reactive derivatives of carboxylic acids, but also quaternary salts of N-heterocyclic compounds.80 It will be seen that in those cases substitution indeed occurs at the nitrogen, not necessarily through thermodynamic control. [Pg.244]

The easy-care treatment of cellulose fabrics uses padding with methylol-urea resins and curing them to cross-link inside the fibres. Consequently formaldehyde is the most important pollutant accompanying the easy-care finish. Alternatives were developed with resins without formaldehyde (reactive elas-tomere silicones, or dicarboxylic acids able to react with the OH groups of cellulose) but the results need still to be improved. Ammonia may also be used for improving the easy-care treatment in a mercerization-like process. This produces, on the other side, ammonia pollutants. [Pg.390]

Figure 3. Changes in the degree of polymerization as a function of the extent of reaction calculated from equation 2 (a) changes in the ratio of phenol to formaldehyde reactive sites (r) for constant (f) and (p) (f=3, p=l), (b) changes in the functionality or number of reactive sites on a individual phenolic molecule (f) for constant (r) and (p) (r=l, p=l), and (c) changes in the amount of monofunctional phenolics (p) for constant (f) and (r) (fr=l, r=l). Figure 3. Changes in the degree of polymerization as a function of the extent of reaction calculated from equation 2 (a) changes in the ratio of phenol to formaldehyde reactive sites (r) for constant (f) and (p) (f=3, p=l), (b) changes in the functionality or number of reactive sites on a individual phenolic molecule (f) for constant (r) and (p) (r=l, p=l), and (c) changes in the amount of monofunctional phenolics (p) for constant (f) and (r) (fr=l, r=l).
Methanol Majority of APIs soluble in methanol. UV transparent Reactive toward many functional groups, especially in acid/base. May contain trace formaldehyde reactive with amines... [Pg.69]


See other pages where Formaldehyde reactivity is mentioned: [Pg.136]    [Pg.274]    [Pg.275]    [Pg.297]    [Pg.299]    [Pg.337]    [Pg.139]    [Pg.144]    [Pg.85]    [Pg.113]    [Pg.114]    [Pg.163]    [Pg.136]    [Pg.274]    [Pg.275]    [Pg.297]    [Pg.299]    [Pg.337]    [Pg.180]    [Pg.4437]   
See also in sourсe #XX -- [ Pg.47 , Pg.48 ]

See also in sourсe #XX -- [ Pg.165 ]

See also in sourсe #XX -- [ Pg.47 ]

See also in sourсe #XX -- [ Pg.47 ]




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Reactivity with formaldehyde

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