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Dextrins reducibility changes

Thus, we see that Freudenberg passed through a change in views, from the notion that the Schardinger dextrins were chain molecules with a peculiar chain termination which rendered them non-reducing, to the current... [Pg.205]

Fig. 17.—Changes of Reducibility of Dextrins from Potato Starch Depending on Time of Roasting at 165° andpH 2.9. [Starchacidifiedwith(l)hydrochloricacid, (2) nitric acid, and (3) phosphoric acid. ]... Fig. 17.—Changes of Reducibility of Dextrins from Potato Starch Depending on Time of Roasting at 165° andpH 2.9. [Starchacidifiedwith(l)hydrochloricacid, (2) nitric acid, and (3) phosphoric acid. ]...
In the case of the White dextrins, pyrolysis induces an apparent hydrolytic reaction, because, with time, there is a steady increase in reducing power and cold-water solubility and a steady decrease in viscosity. These characteristic changes are shown in Fig. 1. Pastes made from such dextrins show gelation, or set-back, properties comparable to those of the original starch. [Pg.485]

The first investigation which used amylose as a model compound for dextrinization was that of Brimhall. She pyrolyzed amylose at 200°, and found that the changes observed in the reducing power, methylation end-group assay, /3-amylolysis limit, and solubility were all consistent with the concept that dextrinization causes the molecule to become branched. [Pg.493]


See other pages where Dextrins reducibility changes is mentioned: [Pg.425]    [Pg.431]    [Pg.104]    [Pg.262]    [Pg.849]    [Pg.212]    [Pg.91]    [Pg.249]    [Pg.766]    [Pg.207]    [Pg.35]    [Pg.195]    [Pg.203]    [Pg.226]    [Pg.229]    [Pg.232]    [Pg.8]    [Pg.286]    [Pg.293]    [Pg.315]    [Pg.494]    [Pg.128]    [Pg.351]    [Pg.78]    [Pg.73]    [Pg.314]    [Pg.681]    [Pg.782]    [Pg.11]    [Pg.267]    [Pg.421]   
See also in sourсe #XX -- [ Pg.47 , Pg.294 , Pg.296 ]




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