Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Cellulose amide

The nucleophilic substitution reaction may take place when a durable synthetic polymer is mixed with agar or yeast, cellulose, amides and water. The hydroxyl groups present in the cellulose become attached to the hydroxyl groups of agar and yeast in a link resembling a glycosidic linkage. [Pg.46]

Ethyl cellulose Amide Single Tg FTIR n was a (x lyamide with PA-6, PA-6,6, and PA-10,10 units Zhang et aL (2012b)... [Pg.1985]

Cellulose-acetate-butyrate resin Poly(amide-imide)... [Pg.1010]

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]

THPC—Amide Process. The THPC—amide process is the first practical process based on THPC. It consists of a combination of THPC, TMM, and urea. In this process, there is the potential of polymer formation by THPC, melamine, and urea. There may also be some limited cross-linking between cellulose and the TMM system. The formulation also includes triethanolamine [102-71-6J, an acid scavenger, which slows polymerization at room temperature. Urea and triethanolamine react with the hydrochloric acid produced in the polymerization reaction, thus preventing acid damage to the fabric. This finish with suitable add-on passes the standard vertical flame test after repeated laundering (80). [Pg.489]

Ammonia—Gas-Cured Flame Retardants. The first flame-retardant process based on curing with ammonia gas, ie, THPC—amide—NH, consisted of padding cotton with a solution containing THPC, TMM, and urea. The fabric was dried and then cured with either gaseous ammonia or ammonium hydroxide (96). There was Httle or no reaction with cellulose. A very stable polymer was deposited in situ in the cellulose matrix. Because the fire-retardant finish did not actually react with the cellulose matrix, there was generally Httle loss in fabric strength. However, the finish was very effective and quite durable to laundering. [Pg.489]

Tables 1 and 2 Hst the important physical properties of formamide. Form amide is more highly hydrogen bonded than water at temperatures below 80°C but the degree of molecular association decreases rapidly with increa sing temperature. Because of its high dielectric constant, formamide is an excellent ionizing solvent for many inorganic salts and also for peptides, proteias (eg, keratin), polysaccharides (eg, cellulose [9004-34-6] starch [9005-25-8]) and resias. Tables 1 and 2 Hst the important physical properties of formamide. Form amide is more highly hydrogen bonded than water at temperatures below 80°C but the degree of molecular association decreases rapidly with increa sing temperature. Because of its high dielectric constant, formamide is an excellent ionizing solvent for many inorganic salts and also for peptides, proteias (eg, keratin), polysaccharides (eg, cellulose [9004-34-6] starch [9005-25-8]) and resias.
The Fourier Trairsform Infrared (FTIR) spectrum obtained from non-adapted tomato cell walls is very similar to that from the onion parenchyma cell wall (both contain cellulose, xyloglucan and pectin) although there is more protein in the tomato walls (amide stretches at 1550 and 1650 cm-i) (Fig 4). In DCB-adapted tomato cell walls, the spectrum more closely resembles that of either purified pectins or of a commercial polygalacturonic acid sample from Sigma with peaks in common at 1140, 1095, 1070, 1015 and 950 cm-t in the carbohydrate region of the spectrum as well as the free acid stretches at 1600 and 1414 cm-i and an ester peak at 1725 cm-k An ester band at 1740 cm-i is evident in both onion parenchyma and non-adapted tomato cell wall samples. It is possible that this shift in the ester peak simply reflects the different local molecular environment of this bond, but it is also possible that a different ester is made in the DCB-adapted cell walls, as phenolic esters absorb around 1720 cm-i whilst carboxylic esters absorb at 1740 cm-k The... [Pg.96]

Carboxymethylcellulose, polyethylene glycol Combination of a cellulose ether with clay Amide-modified carboxyl-containing polysaccharide Sodium aluminate and magnesium oxide Thermally stable hydroxyethylcellulose 30% ammonium or sodium thiosulfate and 20% hydroxyethylcellulose (HEC) Acrylic acid copolymer and oxyalkylene with hydrophobic group Copolymers acrylamide-acrylate and vinyl sulfonate-vinylamide Cationic polygalactomannans and anionic xanthan gum Copolymer from vinyl urethanes and acrylic acid or alkyl acrylates 2-Nitroalkyl ether-modified starch Polymer of glucuronic acid... [Pg.12]

Like evaporators, RO works on most plating baths and rinse tanks. Most RO systems consist of a housing that contains a membrane and feed pump. There are four basic membrane designs plate-and-frame, spiral-wound, tubular, and hollow-fiber. The most common types of membrane materials are cellulose acetate, polyether/amide, and polysulfones.29... [Pg.239]

Biosorption is a rather complex process affected by several factors that include different binding mechanisms (Figure 10.4). Most of the functional groups responsible for metal binding are found in cell walls and include carboxyl, hydroxyl, sulfate, sulfhydryl, phosphate, amino, amide, imine, and imidazol moieties.4 90 The cell wall of plant biomass has proteins, lipids, carbohydrate polymers (cellulose, xylane, mannan, etc.), and inorganic ions of Ca(II), Mg(II), and so on. The carboxylic and phosphate groups in the cell wall are the main acidic functional groups that affect directly the adsorption capacity of the biomass.101... [Pg.398]

This reactivity with diols provides a unique aspect to the linked amide/blocked aldehydes and offers a basis for explaining their good performance at low molar levels of Incorporation on cellulose (Table IV). [Pg.474]

Fig. 7 Maltotetraose hybrids with various carriers resulting in different chain architectures A poly(ethylene oxide) Ba and Bb poly(acrylic acid), amylose, cellulose, and other polysaccharides Ca cyclodextrin and multifunctional acids Cb amylopectin D crosslinked poly(acryl amide) [156] - Reproduced by permission of Wiley... Fig. 7 Maltotetraose hybrids with various carriers resulting in different chain architectures A poly(ethylene oxide) Ba and Bb poly(acrylic acid), amylose, cellulose, and other polysaccharides Ca cyclodextrin and multifunctional acids Cb amylopectin D crosslinked poly(acryl amide) [156] - Reproduced by permission of Wiley...

See other pages where Cellulose amide is mentioned: [Pg.1087]    [Pg.1087]    [Pg.143]    [Pg.295]    [Pg.295]    [Pg.351]    [Pg.487]    [Pg.23]    [Pg.539]    [Pg.301]    [Pg.173]    [Pg.112]    [Pg.116]    [Pg.117]    [Pg.129]    [Pg.140]    [Pg.931]    [Pg.182]    [Pg.341]    [Pg.908]    [Pg.126]    [Pg.488]    [Pg.196]    [Pg.167]    [Pg.98]    [Pg.117]    [Pg.204]    [Pg.231]    [Pg.153]    [Pg.85]    [Pg.225]    [Pg.171]    [Pg.493]    [Pg.66]    [Pg.351]    [Pg.22]   
See also in sourсe #XX -- [ Pg.139 ]




SEARCH



Amide derivatives, cellulose, reaction

Cellulose amide derivatives

Formaldehyde amide derivatives, cellulose

© 2024 chempedia.info