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Polyurethanes diisocyanates used

A different diisocyanate used in polyurethane synthesis is methylene diisocyanate (MDI), which is prepared from aniline and formaldehyde. The diamine product is reacted with phosgene to get MDI. [Pg.343]

Most of the hexamethylenediamine produced is used for the manufacture of Type 66 nylon by polymerization with adipic acid. A minor use is for the preparation of hexamethylene diisocyanate used in light-stable polyurethane coatings. [Pg.136]

Figure 25.6 Examples of diisocyanates used in the manufacture of polyurethanes a TDI,b) MDi,c) NDI,and d) hexamethyiene diisocyanate... Figure 25.6 Examples of diisocyanates used in the manufacture of polyurethanes a TDI,b) MDi,c) NDI,and d) hexamethyiene diisocyanate...
The properties of the polyurethanes depend on the nature of the diisocyanate used in their preparation. [Pg.183]

Other commercially available aliphatic and aromatic diisocyanates used in the polyurethane industry are listed in Table 2.2. These diisocyanates represent 3 to 4% of the market use. The remainder is TDI and MDI. [Pg.19]

LAWSON G, BARTRAM s, FiTCHNER s and WOODLAND E (2000) MALDl-MS and colorimetric analysis of diisocyanate and polyol migrants from model polyurethane adhesives used in food packaging, Analyst, 125, 115-118. [Pg.369]

Polyurethanes are formed from the copolymerization of a diol with a diisocyanate. Polyurethanes are used in foamed insulation and a variety of other construction materials. What is the structure of the polyurethane formed by the following reaction ... [Pg.1068]

The polyurethane foam used for home insulation uses methanediphenyl-diisocyanate (MDl) as monomer. The MDl is prepared by acid-caralyzed reaction of aniline with formaldehyde, followed by treatment with phosgene, COCI2. Propose mechanisms for both steps. [Pg.1223]

Wood stains and varnishes used indoors contain aliphatic and aromatic hydrocarbons, isocyanates, ketones, and esters. Though these have limited use compared with paint, newly finished building interiors often contain toxic levels of these. Toluene diisocyanate, used as a catalyst in polyurethane wood finishes, is a powerful respiratory irritant and sensitizer. 13 ... [Pg.179]

Hafnium triflate has also been used for acylation and alkylation of aromatic compounds.64 It has also been used in aromatic nitration in a process (6.18) that eliminates the usual waste acid from such reactions.65 The products are intermediates in the synthesis of toluene diisocyanates used in making polyurethanes. The catalyst could be reused with... [Pg.143]

Polyurethanes are produced by the chemical action of di-isocyanate and polyol. The properties can be varied by the type of isocyanate used and the proportion of the two monomers. There are four main groups of classification for the thermoplastic groups of polyurethane, i.e. rigid foam, flexible foam, non-cellular and cellular polymers. Two main isocyanates used are toluene di-isocyanate (TDI) and diphenylmethane diisocyanate (MDI). Polyurethanes have limited application in the pharmaceutical or medical industries. Polyurethane is used as an adhesive for laminations (thermosetting material). Like thermosetting polyurethane, thermoplastic polyurethanes can be found as esters and ethers. [Pg.197]

Toluene diisocyanate used in flexible polyurethane foam is formed as a number of isomers. The most common TDI mixture is supplied as an 80 20 mix of the 2,4 isomer and the 2,6 isomer. Other ratios are commer-... [Pg.229]

Previous studies( ) have shown how the number fraction of ring structures formed during irreversible linear random polymerisations leading to polyurethanes may be measured. The work has been extended(7,8) to non-linear polyurethane formation using hexa-methylene diisocyanate(HDI) and POP triols. For non-linear polymerisations, it is found that the number of ring structures per molecule(Nr) is always significant, even in bulk reactions. [Pg.2]

An important class of waterborne coatings is the family of polyurethane dispersions (PUDs). lonizable groups (usually carboxyl) incorporated to the PU backbone allow the polymer to be dispersed in water after neutralization with amines. The properties can be varied substantially depending on the structure of the polyol and diisocyanate used to prepare them. Aliphatic and cycloaliphatic isocyanates are preferred because of their low reactivity with water and... [Pg.526]

Polyurethanes were used that were based on trimethylolpropane-toluylene diisocyanate (TMP-TDI) and tetrahydrofuran and propylene oxide copolymer (THF-PO) obt dned with various ratios of isocyanate... [Pg.278]

Among these, the most common diisocyanates used on a large scale are toluene diisocyanate (TDI) and MDI.TDI was the first commercially available isocyanate and is available as a mixture of 80% 2,4- and 20% 2,6-toluene diisocyanate isomers (Table 6.2), although they are also available as pure single isomers. Similarly, MDI has three isomers, namely 4,4 -, 2,4 -and 2,2 -diphenylmethane diisocyanate. However, only the 4,4 -isomer is used for commercial purposes although all the isomers are present in polymeric methylene diphenyl diisocyanate (PMDI) which is also used in the preparation of polyurethane. [Pg.155]

Polyurethanes are very versatile polymers. They are used as flexible and rigid foams, elastomers, and coatings. Polyurethanes are available as both thermosets and thermoplastics. In addition, their hardnesses span the range from rigid material to elastomer. Thermoplastic polyurethanes will be the focus of this section. The term polyurethane is used to cover materials formed from the reaction of isocyanates and polyols. The general reaction for a polyurethane produced through the reaction of a diisocyanate with a diol is shown in Fig. 2.35. [Pg.99]

The term polyurethane is used to cover materials formed from the reaction of isocyanates and polyols. The general reaction for a polyurethane produced through the reaction of a diisocyanate with a diol is shown in Fig. 1.38. [Pg.73]

Fig. 1.9a. Aromatic diisocyanates used in polyurethane elastomer synthesis, t... Fig. 1.9a. Aromatic diisocyanates used in polyurethane elastomer synthesis, t...
Fig. 3.15. Relation between tensile strength at different temperatures and the excess amount of diisocyanate used for crosslinking CHDI-based polyurethane (a) BDO chain-extended polyurethane, formulation CAPA 225 1, CHDI 2, 1,4 BDO 1 (b) BDO/CHDM chain-extended polyurethane, formulation CAPA 225 1, CHDI 3, 1,4 CHDM 1. Fig. 3.15. Relation between tensile strength at different temperatures and the excess amount of diisocyanate used for crosslinking CHDI-based polyurethane (a) BDO chain-extended polyurethane, formulation CAPA 225 1, CHDI 2, 1,4 BDO 1 (b) BDO/CHDM chain-extended polyurethane, formulation CAPA 225 1, CHDI 3, 1,4 CHDM 1.

See other pages where Polyurethanes diisocyanates used is mentioned: [Pg.341]    [Pg.32]    [Pg.221]    [Pg.237]    [Pg.378]    [Pg.84]    [Pg.471]    [Pg.597]    [Pg.683]    [Pg.310]    [Pg.310]    [Pg.178]    [Pg.12]    [Pg.39]    [Pg.602]    [Pg.47]    [Pg.393]    [Pg.566]    [Pg.156]    [Pg.175]    [Pg.439]    [Pg.316]    [Pg.269]    [Pg.275]    [Pg.48]    [Pg.13]    [Pg.57]   


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