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Green cellulose

TABLE 13.1 Non-Green Cellulose Extraction from Various Feed Stocks... [Pg.391]

C rbocyclic Azo Dyes. These dyes are the backbone of most commercial dye ranges. Based totally on benzene and naphthalene derivatives, they provide yellow, red, blue, and green colors for all the major substrates such as polyester, cellulose, nylon, polyacrylonitrile, and leather. Typical stmctures (26—30) are shown in Figure 4. [Pg.277]

Avidin (from egg white) [1405-69-2] Mr -70,000. Purified by chromatography of an ammonium acetate soln on CM-cellulose [Green Biochem J 101 774 1966]. Also purified by affinity chromatography on 2-iminobiotin-6-aminohexyl-Sepharose 4B [Orr 7 Bio/C/iew 256 761 1981]. It is a biotin binding protein. [Pg.513]

FIGURE 7.27 The structure of cellulose, showing the hydrogen bonds (blue) between the sheets, which strengthen the structure. Intrachain hydrogen bonds are in red and interchain hydrogen bonds are in green. [Pg.232]

Fig. 4.1.17 Graphic illustration of Forster-type resonance energy transfer from aequorin to Aequorea GFP. In the vessel at left, a solution contains the molecules of aequorin and GFP randomly distributed in a low ionic strength buffer. The vessel at right contains a solution identical with the left, except that it contains some particles of DEAE cellulose. In the solution at right, the molecules of aequorin and GFP are coadsorbed on the surface of DEAE particles. Upon an addition of Ca2+, the solution at left emits blue light from aequorin (Xmax 465 nm), and the solution at right emits green light from GFP (Xmax 509 nm). Fig. 4.1.17 Graphic illustration of Forster-type resonance energy transfer from aequorin to Aequorea GFP. In the vessel at left, a solution contains the molecules of aequorin and GFP randomly distributed in a low ionic strength buffer. The vessel at right contains a solution identical with the left, except that it contains some particles of DEAE cellulose. In the solution at right, the molecules of aequorin and GFP are coadsorbed on the surface of DEAE particles. Upon an addition of Ca2+, the solution at left emits blue light from aequorin (Xmax 465 nm), and the solution at right emits green light from GFP (Xmax 509 nm).
Chromatography on thin layers of Avicel C (microcrystalline cellulose from American Viscose Division, F.M.C. Corp., Newark, Del.), in 1-butanol-water-acetic acid (4 5 1) with bromocresol green as indicator. Countercurrent distribution in same solvent by single withdrawal procedure with 299 transfers and 100 elements... [Pg.86]

Green chemistry, principles of Green chemistry, application to cellulose... [Pg.103]

The discussion is organized in the following order First the advantages of HRC scheme, relative to the industrial (i.e., heterogenous) process are briefly commented on second, the relevance of celMose activation and the physical state of its solution to optimization of esterification are discussed. Finally, the use of recently introduced solvent systems and synthetic schemes, designed in order to obtain new, potentially useful cellulose esters with controlled, reproducible properties is reviewed. A comment on the conformity of these methods with the concepts of green chemistry is also included. [Pg.107]

While this works progresses, a part of our attention should be focused on potential industrial applications. In this regard, the path is set, because important principles of green chemistry are inherent to cellulose derivatives, namely the raw material is renewable, and the products are biodegradable. With regard to these principles, consider the following ... [Pg.141]

The reagent can be used most advantageously on aluminium oxide, silica gel, kieselguhr. Si 50000, cellulose, diol and water-wettable RP 18 layers there is less contrast in color on strongly hydrophobic RP 18 phases. NH2 and polyamide layers are not suitable because the iodine is too strongly bound and the whole layer is colored green-yellow. [Pg.150]

Biopolymers have diverse roles to play in the advancement of green nanotechnology. Nanosized derivatives of polysaccharides like starch and cellulose can be synthesized in bulk and can be used for the development of bionanocomposites. They can be promising substitutes of environment pollutant carbon black for reinforcement of rubbers even at higher loadings (upto SOphr) via commercially viable process. The combined effect of size reduction and organic modification improves filler-matrix adhesion and in turn the performance of polysaccharides. The study opens up a new and green alternative for reinforcement of rubbers. [Pg.138]

Wood chips can also be utilized as such to produce bioethanol. The cellulose and hemicellulose material is hydrolyzed in the presence of acids (H2SO4, HCl, or HCOOH) or enzymes to yield glucose and other monosaccharides [16]. Lignin is separated by filtration as a solid residue and the monosaccharides are fermented to ethanol, which, in turn, is separated from water and catalyst by distillation. Ethanol can be used not only as energy source but also as a platform component to make various chemicals, such as ethene and polyethene. Today green acetaldehyde and acetic acid from wood-derived bioethanol is manufactured by SEKAB Ab, at the Ornskoldsvik Biorefinery of the Future industrial park. [Pg.166]

Green coffee beans, as expected, contain storage polysaccharides such as starch, and structural support compounds such as cellulose and lignin. Mono- and di-saccharides are represented, as well as the related compounds quinic acid and myo inositol. [Pg.139]

Pectins occur naturally in both soluble and insoluble forms. Soluble pectin occurs in plant juices and is particularly abundant in those juices which form jellies, such as black-currant and gooseberry. Insoluble pectins tend to occur in the green parts of plants, in fruit and in root crops.1 This insolubility is apparently due either to the presence of the pectin as its insoluble calcium or magnesium salt or because it is combined (esterified ) with cellulose or some other insoluble polysac-... [Pg.254]

A. Onda, T. Ochi, and K. Yanagisawa, Selective hydrolysis of cellulose into glucose over solid acid catalysts, Green Chem., 10 (2008) 1033-1037. [Pg.95]


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See also in sourсe #XX -- [ Pg.184 ]




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