Cellulose other derivatives

Cellulose derivatives Sodium carboxymethyl cellulose Methylcellulose Hydroxyethylcellulose Hydroxypropylmethyl cellulose Other derivatives Modified starches Low-Methoxyl pectins Propylene glycoalginates... 

Cellulose (qv) is one of nature s most abundant stmctural materials, providing the primary framework of most plants. For industrial purposes cellulose is derived from two primary sources, cotton linters and wood pulp. Linters are derived from the machine by the same name used for removing the short fibers adhering to cotton seeds after ginning and consist essentially of pure cellulose (see Cotton). Wood (qv), on the other hand, contains 40—60% cellulose, which must be extracted by the chemical degradation of the wood stmcture. 

UV absorbers have been found to be quite effective for stabilization of polymers and are very much in demand. They function by the absorption and harmless dissipation of the sunlight or UV-rich artificial radiation, which would have otherwise initiated degradation of a polymer material. Meyer and Geurhart reported, for the first time in 1945 [10], the use of UV absorber in a polymer. They found that the outdoor life of cellulose acetate film was greatly prolonged by adding phenyl salicylate (salol) [10]. After that, resorcinol monobenzoate, a much more effective absorber, was introduced in 1951 [11] for stabilization of PP, but salol continued to be the only important commercial stabilizer for several years. The 2,4-dihydroxybenzophenone was marketed in 1953, followed shortly by 2-hydroxy-4-methoxybenzophenone and other derivatives. Of the more commonly known UV absorbers, the 2-hydroxybenzophenones, 2-hy-droxy-phenyl-triazines, derivatives of phenol salicylates, its metal chelates, and hindered amine light stabilizers (HALS) are widely used in the polymer industry. 

Bran, a grain milling waste product, and linseed (flaxseed) are both rich in cellulose. Other hydrophilic colloids derive from the seeds of Plantago species or karaya gum. Ingestion of hydrophilic gels for the prophylaxis of constipation usually entails a low risk of side effects. However, with low fluid intake in combination with a pathological bowel stenosis, mucilaginous viscous material could cause bowel occlusion (ileus). 

The particular array of chemical shifts found for the nuclei of a given polymer depends, of course, on such factors as bond orientation, substituent effects, the nature of nearby functional groups, solvation influences, etc. As a specific example, derivatives of the carbohydrate hydroxyl moieties may give rise to chemical shifts widely different from those of the unmodified compound, a fact that has been utilized, e.g., in studies (l ) on commercially-important ethers of cellulose. Hence, as illustrated in Fig, 2, the introduction of an 0-methyl function causes (lU,15) a large downfield displacement for the substituted carbon. This change allows for a convenient, direct, analysis of the distribution of ether groups in the polymer. Analogously, carboxymethyl, hydroxyethyl and other derivatives may be characterized as well... 

In addition to being necessary for all forms of life, biopolymers, especially enzymes (proteins), have found commercial applications in various analytical techniques (see Automated instrumentation, clinical chemistry Automated instrumentation, hemtatology Biopolymers, analytical techniques Biosensors Immunoassay) in synthetic processes (see Enzyme applications, industrial Enzyme applications in organic synthesis) and in prescribed therapies (see Enzyme applications, THERAPEUTICS IMMUNOTHERAPEUTIC AGENTS Vitamins). Other naturally occurring biopolymers having significant commercial importance are the cellulose (qv) derivatives, eg, cotton (qv) and wood (qv), which are complex polysaccharides. 

Introduction. Today nitrocellulose is one of most important derivatives of cellulose used in industry and commerce, and a major product of the chemical industry. Its wide and manifold applications are due mainly to its extraordinary physical properties. Thus a protective coating of nitrocellulose varnish, a nitrocellulose film or a tube of smokeless powder — all are characterized by relatively high elasticity and mechanical strength. These properties are a direct consequence of the microstructure of cellulose, which is composed of highly oriented long-chain molecules of polysaccharide. Not only nitrocellulose, but also other derivatives of cellulose, such as other esters and ethers, demonstrate similar characteristics. 

Chemical Cellulose White fibers, consisting mostly of alpha-cellulose, obtained from vegetable matter(such as wood or cotton linters) by treatment with sulfite dilute NaOH soln or other reagent. Material obtained by treatment of cotton linters with dilute NaOH is also known as chemical cotton (See also CELLULOSE AND DERIVATIVES) Ref Merriam-Webster s(196l), 360 384... 

An ingenious treatment of cellulose was discovered by Charles Cross and Edward Bevan in England in 1892. It involved first preparing a chemical derivative called cellulose xanthate in a process that is conceptually no different from converting cellulose into other derivatives such as cellulose acetate or cellulose nitrate. What made this different, however, is that xan-thates are reactive chemical intermediates that can be converted easily into still different compounds, or returned to the starting material, in this case cellulose. See Equation 3. 

The carboxymethyl cellulose (CMC) derivatives and carboxymethyl starch (CMS) are effective antiredeposition agents that are cellulose-containing fibers such as cotton and blends of cotton and synthetic fibers. However, CMC has virtually no effect on pure synthetic fibers. Other effective antiredeposition agents and soil repellents have been developed (Fig. 5.4) [20]. 

Paper. Paper is a matted, dried mass of cellulose fibers derived from wood, cotton linters or, more rarely, sugar cane bagasse or other plant stalks. Related products are cardboard and sound-proofing material. 

NITRIC ESTERS OF POLYSACCHARIDES OTHER THAN CELLULOSE. NITRO-DERIVATIVES OF LIGNIN AND ABIETIC ACID... 

Chapter XVI. Nitric Esters of Polysaccharides other than Cellulose Nitro-Derivatives of Lignin and Abietic Acid... 

Although cyclic and acyclic carbonates of monosaccharides have been known for some time, little interest had been taken in such derivatives of polysaccharides, probably because the conditions could not be controlled to give any degree of specificity. The formation of cyclic carbonate rings involves treatment of the polysaccharide with ethyl chloro-formate heterogeneous reactions occur, and acyclic carbonate (ethy-oxycarbonyl) groups are also formed. The reaction conditions suitable for maximum cyclic carbonate and minimum acyclic substitution have been investigated in detail for cellulose. Other chloroformates have... 

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