Cellulosic surfactants

A very recent study by Pichot and Charreyre [35] dealt with cellulosic surfactants with a methacrylic group at the end of an hydrocarbon chain (6 to... 

Carbon-carbon, free radical initiators 91-94 Cardo amines 210 Cellulosic surfactants 53 4-Chloroformyl(naphthalic anhydrides) 129-132... 

Uses Whitener for cotton and other cellulosics surfactant in anionic and nonionic laundry detergents, dry bleaches, fabric softeners, commercial laundry prods. vise, control agent Trade Names Containing Uvitex NFW Liq. 

Hazardous Decomp. Prods. Heated to decomp., emits toxic fumes of SOx and Na20 Uses Whitener for cotton and other cellulosics surfactant in anionic and nonionic laundry detergents, dry bleaches, fabric softeners, commercial laundry prods. vise, control agent Trade Name Synonyms Eutex CBS [Aceto http //www.aceito.com], Tinopal CBS-X [Ciba Spec. Chems./Plastic Addit. http //WWW. cibasc. com]... 

Uses Scouring agent tor synthetics and cellulosics surfactant for gannent scouring detergent with nonredeposItion props, for min. oils, motor oils, grease, butyl stearate stains Features Enzyme-stable... 

Drawing ink A suspension of carbon black in a colloidal solution of - shellac soap, stabilized with animal glue (- glue, animal, - methylcellu-lose, - hydroxyethyl cellulose or - carboxymethyl cellulose - surfactants are also used ... 

Barnes and co-workers have studied mixed-monolayer systems [278,281,283,284] and found some striking nonidealities. Mixed films of octadecanol and cholesterol, for example, show little evaporation resistance if only 10% cholesterol is present [278] apparently due to an uneven granular microstructure in films with cholesterol [284]. Another study of cellulose decanoate films showed no correlation between holes in the monolayer and permeation rate [285]. Polymerized surfactants make relatively poor water evaporation retarders when compared to octadecanol [286]. There are problems in obtaining reproducible values for r [287] due to impurities in the monolayer material or in the spreading solvent. 

Major industrial uses for chloroacetic acid are in the manufacture of cellulose ethers (mainly carboxymethylceUulose, CMC), herbicides, and thioglycolic acid. Other industrial uses include manufacture of glycine, amphoteric surfactants, and cyanoacetic acid. 

Both mechanical and chemical action promote ink detachment from cellulose fibers during pulping. Mechanical action includes interfiber abrasion and fiber flexing and bending. Chemical action includes fiber swelling and surfactant-promoted ink particle emulsification and solubilization. 

Flotation. Flotation (qv) is used alone or in combination with washing and cleaning to deink office paper and mixtures of old newsprint and old magazines (26). An effective flotation process must fulfill four functions. (/) The process must efficiently entrain air. Air bubble diameter is about 1000 p.m. Typically air bubbles occupy 25—60% of the flotation cell volume. Increa sing the airRquid ratio in the flotation cell is said to improve ink removal efficiency (27). (2) Ink must attach to air bubbles. This is primarily a function of surfactant chemistry. Air bubbles must have sufficient residence time in the cell for ink attachment to occur. (3) There must be minimal trapping of cellulose fibers in the froth layer. This depends on both cell design and surfactant chemistry. (4) The froth layer must be separated from the pulp slurry before too many air bubbles coUapse and return ink particles to the pulp slurry. 

Poly(vinyl acetate) emulsions can be made with a surfactant alone or with a protective coUoid alone, but the usual practice is to use a combination of the two. Normally, up to 3 wt % stabilizers may be included in the recipe, but when water sensitivity or tack of the wet film is desired, as in some adhesives, more may be included. The most commonly used surfactants are the anionic sulfates and sulfonates, but cationic emulsifiers and nonionics are also suitable. Indeed, some emulsion compounding formulas require the use of cationic or nonionic surfactants for stable formulations. The most commonly used protective coUoids are poly(vinyl alcohol) and hydroxyethyl cellulose, but there are many others, natural and synthetic, which are usable if not preferable for a given appHcation. 

Emulsion polymerizations of vinyl acetate in the presence of ethylene oxide- or propylene oxide-based surfactants and protective coUoids also are characterized by the formation of graft copolymers of vinyl acetate on these materials. This was also observed in mixed systems of hydroxyethyl cellulose and nonylphenol ethoxylates. The oxyethylene chain groups supply the specific site of transfer (111). The concentration of insoluble (grafted) polymer decreases with increase in surfactant ratio, and (max) is observed at an ethoxylation degree of 8 (112). 

Cellulose Diacetate. When preparing cellulose diacetate for dyeing, strong alkahes must be avoided in the scouring of acetate because the surface of the cellulose acetate would be saponified by such treatment. Many fabrics tend to crease and therefore requke open-width handling. Scouring is frequendy carried out on a jig or beam using 1.0 g/L of surfactant and 0.5—1.0 g/L tetrasodium pyrophosphate for 30 min at 70—80°C. 

Cellulose Triacetate. Cellulose acetate having 92% or more of the hydroxyl groups acetylated is referred to as triacetate. This fiber is characteristically more resistant to alkaU than the usual acetate and may be scoured, generally, in openwidth, with aqueous solutions of a synthetic surfactant and soda ash. 

Nonionic Surface-Active Agents. Approximately 14% of the ethyleae oxide consumed ia the United States is used in the manufacture of nonionic surfactants. These are derived by addition of ethylene oxide to fatty alcohols, alkylphenols (qv), tall oil, alkyl mercaptans, and various polyols such as poly(propylene glycol), sorbitol, mannitol, and cellulose. They are used in household detergent formulations, industrial surfactant appHcations, in emulsion polymeri2ation, textiles, paper manufacturing and recycling, and for many other appHcations (281). 

Albertsson (Paiiition of Cell Paiiicle.s and Macromolecules, 3d ed., Wiley, New York, 1986) has extensively used particle distribution to fractionate mixtures of biological products. In order to demonstrate the versatility of particle distribution, he has cited the example shown in Table 22-14. The feed mixture consisted of polystyrene particles, red blood cells, starch, and cellulose. Liquid-liquid particle distribution has also been studied by using mineral-matter particles (average diameter = 5.5 Im) extracted from a coal liquid as the solid in a xylene-water system [Prudich and Heniy, Am. Inst. Chem. Eng. J., 24(5), 788 (1978)]. By using surface-active agents in order to enhance the water wettability of the solid particles, recoveries of better than 95 percent of the particles to the water phase were obsei ved. All particles remained in the xylene when no surfactant was added. 

Modified cellulose-based thickeners are often used, along with the surfactant-based thickeners already mentioned. 

Cellulosic, polyester, and acrylic fibers lubricated with a surfactant-based oiling composition containing an organic phosphorus ester neutralized with an amine showed less pilling, good antistatic properties, and anticorrosiveness. The phosphorus ester salts were hexyl phosphate trimethylamine salt, dodecamethy-lene caproate phosphonate ethylamine salt, and polyethylene glycol dodecyl ether phosphate dimethylamine salt [262]. 

The heat exchanger fins from aluminum or its alloy are coated with aqueous solution containing a water-soluble cellulose resin or polyvinyl alcohol and a surfactant to form a hydrophilic film. Phosphoric acid ester was used as anionic surfactant (0.05-4.5%) in aqueous solution to form a hydrophilic film showing contact angle with water of 5-32° [288]. 

Paraformaldehyde/DMSO dissolves cellulose rapidly, with neghgible degradation, and forms the hydoxymethyl (methylol) derivative at Ce [ 140-142]. Therefore, cellulose derivatives at the secondary carbon atoms are easily obtained after (ready) hydrolysis of the methylol residue. Additionally, fresh formaldehyde may add to the methylol group, resulting in longer methylene oxide chains, that can be functionahzed at the terminal OH group, akin to non-ionic, ethylene oxide-based surfactants [143,144]. 

Suspension of water soluble solids in oil can be achieved by a variety of chemical additives. Chemical suspension additives that have been suggested include alkyl mercaptophosphonic acids(174), organophylic clay plus hydroxypropyl cellulose(175), polyols(176), aluminum stearate(177), organophylic clay plus surfactant(178-181), aluminum phosphate esters(182), and acrylate copolymers(183-184). 

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