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Starch and Cellulose

One of the most important differences between cellulose and starch is that animals can digest starch Because the glycosidic linkages m starch are a an animal s a glycosidase enzymes can catalyze then hydrolysis to glucose When more glucose is... [Pg.1049]

Polysaccharides are macromolecules which make up a large part of the bulk of the vegetable kingdom. Cellulose and starch are, respectively, the first and second most abundant organic compounds in plants. The former is present in leaves and grasses the latter in fruits, stems, and roots. Because of their abundance in nature and because of contemporary interest in renewable resources, there is a great deal of interest in these compounds. Both cellulose and starch are hydrolyzed by acids to D-glucose, the repeat unit in both polymer chains. [Pg.16]

Many of these reactions are reversible, and for the stronger nucleophiles they usually proceed the fastest. Typical examples are the addition of ammonia, amines, phosphines, and bisulfite. Alkaline conditions permit the addition of mercaptans, sulfides, ketones, nitroalkanes, and alcohols to acrylamide. Good examples of alcohol reactions are those involving polymeric alcohols such as poly(vinyl alcohol), cellulose, and starch. The alkaline conditions employed with these reactions result in partial hydrolysis of the amide, yielding mixed carbamojdethyl and carboxyethyl products. [Pg.133]

The dipping solution can also be employed as spray reagent, in this event 60% [6], 80% [5] or 95% ethanol [9] have been recommended in the literature. The reagent can be employed on silica gel, Dowex 50X4 (Na ), cellulose and starch layers. The detection limit for 1,4-benzodiazapines is 100 ng per chromatogram zone [11]. [Pg.311]

This is a highly selective process and very good results on cellulose and starch grafting have been observed. Ceric ion initiated grafting is usually carried out at lower temperatures and, therefore, wastage of monomer in chain transfer reactions is minimal. [Pg.487]

Polysaccharides, which are condensation polymers containing from several hundred to several thousand monosaccharide units. Cellulose and starch are the most common polysaccharides. [Pg.617]

In 1833 Braconnot obtained nitric esters of cellulose and starch by acting with nitric acid on plant fibres and starch, at low temperature. [Pg.225]

Note. Examples of established usage of the -an ending are xylan for polymers of xylose, mannan for polymers of mannose, and galactan for polymers of galactose. Cellulose and starch are both glucans, as they are composed of glucose residues. [Pg.163]

Cellulose and starch are macromolecules with empirical formulas that resemble hydrated carbon, CX (H2 0)y, where x and y are integers. The monomers from which these macromolecules are consfructed are sugars such as glucose and fructose. These monomers and macromolecules are the carbohydrates. Structurally, carbohydrates are very different from simple combinations of carbon and water. Even the smallest carbohydrates contain carbon chains with hydrogen atoms, OH groups, and occasional ether linkages. [Pg.919]

Approximate conformity of the composition of cellulose and starch with the formula CeHioOs was deduced very early, but often the literal exactness of this formula was obscured by failure to obtain the polymer in the anhydrous condition. In the first decade of the present century the CeHioOs formula was shown to represent the composition of... [Pg.10]

Figure 1.32 The repeating units of cellulose and starch, two of the most common polysaccharides in nature. Figure 1.32 The repeating units of cellulose and starch, two of the most common polysaccharides in nature.
The sorption of water by excipients derived from cellulose and starch has been considered by numerous workers, with at least three thermodynamic states having been identified [82]. Water may be directly and tightly bound at a 1 1 stoichiometry per anhydroglucose unit, unrestricted water having properties almost equivalent to bulk water, or water having properties intermediate between these two extremes. The water sorption characteristics of potato starch and microcrystalline cellulose have been determined, and comparison of these is found in Fig. 11. While starch freely adsorbs water at essentially all relative humidity values, microcrystalline cellulose only does so at elevated humidity values. These trends have been interpreted in terms of the degree of available cellulosic hydroxy groups on the surfaces, and as a function of the amount of amorphous material present [83]. [Pg.30]

Xylan occurs in practically all land plants and is said to be present in some marine algae.6 In both wide botanical distribution and abundance in nature it closely follows cellulose and starch. It is most abundant in annual crops, particularly in agricultural residues such as corn cobs, corn stalks, grain hulls and stems. Here it occurs in amounts ranging from 15 to 30%. Hard woods contain 20 to 25% xylan while soft woods contain 7 to 12 %. Spring wood has more pentosan than summer wood. 7 Low strength vegetable fibers of commerce such as jute, sisal, Manila... [Pg.283]

Ce Ion Initiation. Initiation of grafting with Ce ions was introduced by Mino et al. 7. The process has been widely studied and even applied to industrial production of cellulose and starch graft copolymers. A mechanism is derived from model experiments with low molecular weight vicinal diols in acid aqueous solution. The first step (22) is OH OH... [Pg.259]

Chemical Conversions. Although D-glucose is the component sugar of cellulose and starch, only the latter is the raw material for its commercial... [Pg.33]

Some natural polysaccharides. For cellulose and starch, n and x reflect the different orientations of glucose, which distinguishes these two polymers. [Pg.585]

Two glucose polymers of plant origin are of special importance among the polysaccharides pi 4-linked polymer cellulose and starch, which is mostly al 4-linked. [Pg.42]

The best known homopolysaccharides are derived from o-glucose and known as glucans. Glucose has a number of reactive sites and a wide variety of polymers formed utilizing combinations of these reactive sites are found in nature. We have already visited the two most well-known members of this group—cellulose and starch containing amylose and amylopectin. Here we will visit some other important members. [Pg.275]

The important difference between a and 3 glycosidic bonds can be seen in the digestibility of the major plant polysaccharides cellulose and starch. [Pg.44]

Complex Carbohydrate polysaccharides such as cellulose and starch Compound a substance consisting of atoms of two or more different elements chemically bonded... [Pg.338]


See other pages where Starch and Cellulose is mentioned: [Pg.75]    [Pg.314]    [Pg.430]    [Pg.477]    [Pg.450]    [Pg.732]    [Pg.417]    [Pg.543]    [Pg.1000]    [Pg.425]    [Pg.191]    [Pg.142]    [Pg.22]    [Pg.5]    [Pg.408]    [Pg.110]    [Pg.34]    [Pg.322]    [Pg.259]    [Pg.261]    [Pg.263]    [Pg.623]    [Pg.27]    [Pg.94]    [Pg.38]    [Pg.261]    [Pg.273]    [Pg.297]    [Pg.267]   
See also in sourсe #XX -- [ Pg.129 ]




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Adsorption of Starch on Cellulose and Pigments

Biosynthesis of Starch, Glycogen, and Cellulose

Cellulose, Starch, and Chitin

Cellulose, Starch, and Chitin Reinforcement

Cellulose-Based Starch Composites Structure and Properties

Polysaccharides cellulose and starch

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