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Ethers reactivity

Butyl glycidyl ether reactive diluent (HELOXY 61 Resolution 20... [Pg.374]

Thus a plot of [M2 ] /O against [Mj ] allows determination of the value of Ki from the intercept and r2 from the slope. The resulting kinetic parameters are summarized in Table 13. The comparison with the basicity values, here given in terms of pi b > ain shows that in a copolymerization of cyclic ethers, reactivity correlates well with basicity. [Pg.323]

Gorman, A. A., Gould, I. R., Hamblett, I., Time resolved Study of the Solvent and Temperature Dependence of Singlet Oxygen ( Ag) Reactivity toward Enol Ethers Reactivity Parameters Typical of Rapid Reversible Exciplex Formation, J. Am. Chem. Soc. 1982, 104, 7098 7104. [Pg.542]

Rapi-Cure. [ISP] Vinyl ethers reactive diluent... [Pg.308]

Heloxy . hone-Pouloic/Peif. Resim Coatings] Glyddyl ethers reactive diluoit for epoxy resins used in cast-ii%, laminating, toolii, potting, elec., adi ve, flotuing, and groutiiig qipli-cations. [Pg.168]

Liquid epoxy resin Butyl glycidyl ether (reactive diluent)... [Pg.52]

Poly bd R-20LM Poly bd R-45HTLO reaction medium, polymerizations PF-5030 PF-6040 PF-5050 PF-5052 PF-5060 PF-5070 PF-5080 reaction medium, purification PF-5030 PF-5040 PF-5050 PF-5052 PF-5060 PF-5070 PF-5080 reaction medium, separation processes PF-5030 PF-5040 PF-5050 PF-5052 PF-5060 PF-5070 PF-5080 reactive agent, photopolymerizable compositions Pentaerythrityl triallyl ether reactive building block automotive coatings Desmodur I... [Pg.1585]

Pentaerythrityl triallyl ether reactive diluent, epoxies electrical... [Pg.5594]

Butanediol diglycidyl ether reactive diluent, hot-melt prepregs... [Pg.5594]

Furan telechelic PIB macromonomers with well-defined M s and narrow MWD were synthesized by end quenching hving PIB with 2-tributylstannylfuran or 2,2-difurylpropane [137, 161]. Three-arm star, furan functional PlBs were obtained under identical conditions except 1,3,5-tricumyl chloride was used as initiator. The resulting telechelic PI Bs could be efficiently photocured by ultraviolet (U V) radiation in the presence of a cationic photoinitiator and a divinyl ether reactive diluent [162]. Owing to the lower reactivity of thiophene compared to furan the reaction of unsubstituted thiophene with hving PIB resulted in rapid and quantitative monoaddition and the quantitative formation of 2-polyisobutylenyl-thiophene [163]. [Pg.795]

Bisowarno B.H. and Tade M.O. (2000). Dynamic simulation of startup in ethyl tert-butyl ether reactive distillation with input multiplicity. Process Design and Control 39, 1950-1954. 2.9.1.2, 2.9.1.2, 2.9.2... [Pg.233]

Subsequently, a more direct verification of formation of persistent nanoscale domains was done by running the FRRPP of MAA/water in a quiescent fluid, and then doing a morphological analysis of the product polymer material from liquid samples that were frozen to preserve the polymer structure from the liquid before drying. The result is a picture from the atomic force micrograph (AFM) of nanoparticles from a polystyrene/ether reactive FRRPP system, shown in Fig. 2.1.2. [Pg.106]

Figure 2.4.3 shows conversion-time comparison for the polystyrene-styrene-ether reactive system between experimental data and computer simulation results at... [Pg.156]

Fig. 2.4.3 Conversion-time comparison for the polystyrene/styrene/ether reactive system between experimental data and computer simulation results at 80°C for the two initial monomer and initiator concentrations (Replotted from Dar, 1999 Dar and Caneba, 2002 with permission)... Fig. 2.4.3 Conversion-time comparison for the polystyrene/styrene/ether reactive system between experimental data and computer simulation results at 80°C for the two initial monomer and initiator concentrations (Replotted from Dar, 1999 Dar and Caneba, 2002 with permission)...
Fig. 2.4.7 Simulation result for the center temperature of laige particles from the reactive polystyrene/styrene/ether reactive system at 80° C... Fig. 2.4.7 Simulation result for the center temperature of laige particles from the reactive polystyrene/styrene/ether reactive system at 80° C...
Table 9. Some Common Commercial Glycidyl Ether Reactive Diluents... Table 9. Some Common Commercial Glycidyl Ether Reactive Diluents...
EL23 Bisphenol-A Alkyl glycidyl ether (Reactive) 1.15 1.1 -1.6... [Pg.125]


See other pages where Ethers reactivity is mentioned: [Pg.728]    [Pg.405]    [Pg.299]    [Pg.84]    [Pg.242]    [Pg.168]    [Pg.230]    [Pg.143]    [Pg.84]    [Pg.514]   
See also in sourсe #XX -- [ Pg.169 ]




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Crown ethers enolate reactivity, effect

Crown-ether complexes, stability and reactivity

Cyclic ethers, reactivity

Ethers Reactivity Chart

Ethers reactivity toward nucleophilic substitution

Ethers reactivity toward oxygen

Reactive distillation ether

Reactivity charts as ethers

Stability and reactivity of crown-ether

Stability and reactivity of crown-ether complexes

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