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Triethanolamine sucrose mixtures

The mixtures of sucrose - triethanolamine, usually of 1-1.5/1 (sucrose/triethanolamine) [9] are very stirrable mixtures, at the propoxylation temperature, and are frequently used in practice. Triethanolamine can be replaced by diethanolamine, monoethanolamine and even by ammonia [59]. The triol is formed in situ by the reaction of ammonia or primary or secondary ethanolamines with PO. The polyols based on sucrose - triethanolamine (Table 13.6) are frequently used to make rigid PU foams for thermoinsulation of freezers. The mixtures of sucrose - sorbitol lead easily to high functionality polyols, sorbitol having an excellent solvating capability for solid sucrose. [Pg.358]

This method of direct propoxylation of mixtures between sucrose and a second polyol is often used in practice, the most important polyols being based on sucrose - glycerol, sucrose - triethanolamine and sucrose - diethyleneglycol. [Pg.358]

One can easily imagine that if the glycerol is replaced by triethanolamine [9, 10] or by DEG [51], the resulting polyols are of course a mixture of propoxylated sucrose with propoxylated triethanolamine or propoxylated DEG (13.29). [Pg.362]

E3 UDP-sugar phosphorylase. E4 pyrophosphatase. (Below) Synthesis of 6 -deoxy-6 -fluorosucrose. El, sucrose synthetase E2, pyruvate kinase E3, UDP-glucose pyrophosphorylase E4, pyrophosphatase. All enzymes (150 U each) are co-immobilized in polyacrylamide gel. The reactions are carried out in triethanolamine buffer (50 mM) containing MgCl2 (10 mM) with pH being controlled at 7.5 by addition of IN NaOH. The 500-mL reaction mixture contains glucose-... [Pg.40]


See other pages where Triethanolamine sucrose mixtures is mentioned: [Pg.134]    [Pg.353]    [Pg.357]    [Pg.358]    [Pg.370]   
See also in sourсe #XX -- [ Pg.357 , Pg.359 , Pg.362 ]




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