Cellulose surface activation

Cellulose activated with ethylenediarnine [107-15-3] is used to prepare high molecular-weight cellulose butyrate (23). Cellulose so activated has a larger measured surface area (120 m /g) than cellulose activated with acetic acid (4.8 m /g). The diamine is removed with water, followed by solvent exchange with acetic acid and butyric acid before esterification. 

Properties. Hydroxypropylcellulose [9004-64-2] (HPC) is a thermoplastic, nonionic cellulose ether that is soluble in water and in many organic solvents. HPC combines organic solvent solubiUty, thermoplasticity, and surface activity with the aqueous thickening and stabilising properties characteristic of other water-soluble ceUulosic polymers described herein. Like the methylceUuloses, HPC exhibits a low critical solution temperature in water. 

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. 

Electric discharge (corona, cold plasma) is another method of physical treatment. Corona treatment is one of the most interesting techniques for surface oxidation activation. This process changes the surface energy of the cellulose fibers [28]. In the case of wood surface activation it increases the amount of aldehyde groups [291. 

Electrokinetic processes are widely used in different fields of science and technology. We had already mentioned the use of electrokinetic processes for research into the electric properties of surface layers of insulating materials. Such measurements are used, in particular, when studying the surface properties of polymeric materials, their behavior in different media, and their interactions with other materials (e.g., with adsorbing surface-active substances). The results of this research are used in textile, cellulose and paper, and other industries. 

Thickeners and binders such as acacia, agar, starch, sodium alig-nate, gelatin, methyl cellulose, bentonite, and silica are used to improve product stability and enhance the convenience of the administration of a liquid formulation. Surface-active agents, colors, flavors and preservatives may also be used in the final formulation (Garcia et ah. Bioseparation Process Science, Blackwell Science, Malden, Mass., 1999, p. 374). 

The classic studies of Saunders( 17) demonstrated that in the presence of excess surfactant methyl cellulose (MC) would desorb from monodispersed polystyrene latices. MC is one of the most surface active water-soluble polymers (W-SPs) and it will readily dominate the surface pressure 7T (7T = cre - cr t where cr is the surface tension of water and is the surface tension of the aqueous polymer solution) of the aqueous solution. For example, hydroxyethyl cellulose (HEC) lowers the surface tension of water much less than MC or HPMC, and when the combination of HEC and MC or HPMC in water is studied, there is no notable influence of HEC on the surface pressure (Figure 2). 

A new class of amphiphilic, surface-active graft copolymers, hydrophobically modified hydroxyethyl celluloses (HM-HEC s), are comprised of a cellulose backbone with short polyethylene oxide (PEO) and grafted alkyl side chains. They are excellent steric stabilizers of 0/W emulsions. 

The stabilizing of aqueous latexes succeeded by using emulsifiers (anionic, nonionic) and/or their mixture, steric stabilizators (polyvinyl alcohol (PVOH), hydroxyethyl cellulose, polyethylene glycol, new protective colloids etc.), and polymerizable surfaces active agents, in general. Vinyl acetate (VAc) emulsion homopolymers and copolymers (latexes) are widely used as binders in water-based interior and exterior architectural paints, coatings, and adhesives, since they have higher mechanical and water resistance properties than the homopolymers of both monomers [2, 4, 7]. 

PF had been proposed as the terminal complex (23) and associated pores were reported on the outer membrane EF (24). Due to their proximity to the site of cellulose ribbon extrusion from the cell surface, these structures were assumed to be responsible for cellulose synthesis. A model was advanced in which cellulose synthase was localized on the outer membrane, which invoked adhesion sites between the outer and plasma membranes as a mechanism to explain the transfer of uridine-diphosphoryl-glucose (UDPG) from the cytoplasm to the cellulose synthases (25,26). However, when the outer and plasma membranes of Acetobacter were isolated separately by density-gradient centrifugation, the cellulose synthase activity was localized only in the plasma membrane fraction (27). Therefore, the linear structures observed on the Acetobacter outer membrane, while they may be associated in some manner with cellulose biosynthesis, are probably not the cellulose synthase terminal complexes. Since no ultrastructural evidence for adhesion sites between the outer and plasma membranes has been presented, a thorough investigation of the mechanism of / (1-4) glucan chain translocation from the cytoplasmic membrane to the outer membrane in Acetobacter xylinvm is now in order. 

In an attempt to separate the domains from the cores, we used limited degradation with several proteases. CBH I (65 kda) and CBH II (58 kda) under native conditions could only be cleaved successfully with papain (15). The cores (56 and 45 kda) and terminal peptides (11 and 13 kda) were isolated by affinity chromatography (15,16) and the scission points were determined unequivocally. The effect on the activity of these enzymes was quite remarkable (Fig. 7). The cores remained perfectly active towards soluble substrates such as those described above. They exhibited, however, a considerably decreased activity towards native (microcrystalline) cellulose. These effects could be attributed to the loss of the terminal peptides, which were recognized as binding domains, whose role is to raise the relative concentration of the intact enzymes on the cellulose surface. This aspect is discussed further below. The tertiary structures of the intact CBH I and its core in solution were examined by small angle X-ray scattering (SAXS) analysis (17,18). The molecular parameters derived for the core (Rj = 2.09 mm, Dmax = 6.5 nm) and for the intact CBH I (R = 4.27 nm, Dmax = 18 nm) indicated very different shapes for both enzymes. Models constructed on the basis of these SAXS measurements showed a tadpole structure for the intact enzyme and an isotropic ellipsoid for the core (Fig. 8). The extended, flexible tail part of the tadpole should thus be identified with the C-terminal peptide of CBH I. 

Other paint stripper ingredients include surface-active agents (surfactants), emulsifiers, thickeners, sealants, and corrosion inhibitors. Thickeners such as methyl cellulose derivatives are used to thicken the stripper so that it can be brushed onto vertical surfaces. Sealants snch as crude or refined paraffin act to retard evaporation of the CH2CI2 so that the stripper remains effective over a long period of time. 

Adsorption This method is the simplest way to immobilize enzymes. Enzymes can be adsorbed physically on a surface-active adsorbent by contacting an aqueous solution of enzyme with an adsorbent. Commonly employed adsorbents are (Zaborsky, 1973) alumina, amon-exchange resins, calcium carbonate, carbon, cation-exchange resins, celluloses, clays, collagen, colloid-ion, conditioned metal, glass plates, diatomaceous earth, and hydroxyapatite. The advantages of adsorption techniques are as follows ... 

Methylcellulose occurs as a white, fibrous powder or granules. It is the methyl ether of cellulose. It is soluble in water and in a limited number of organic solvent systems. Aqueous solutions of Methylcellulose are surface active, form films upon drying, and undergo a reversible transformation from sol to gel upon heating and cooling, respectively. 

Typical suspension stabilizers for the production of EPS are water-soluble, surface-active macromolecules, such as poly (vinyl alcohol) (PVA), hydroxyethyl-cellulose (HEC) and polyvinylpyrrolidone (PVP), or natural products, such as gelatin [36-40], and insoluble inorganic powders, such as tricalcium phosphate (TCP), also called picketing stabilizer , mostly in combination with surfactants called extenders [33-35,44], or a combination of these [129]. The differences and specialties of these stabilizing mechanism are described briefly below ... 

Other Vinyl Derivatives. PVP is a nonionic surfactant used in 3% to 5% concentrations to increase viscosity of solutions. Although it exhibits surface-active properties similar to the cellulose ethers, PVP appears to have less abiUty to lower the interfacial tension at a water-oil interface. Nevertheless, in contrast to the cellulose ethers, PVP appears capable of forming hydrophilic coatings in the form of adsorbed layers. Because conjunctival mucin is believed to interact with the ocular surfece to form an adsorbing surface for aqueous tears, the formation by artificial means of a hydrophilic layer that would mimic conjimctival mucin (mucomimetic) appears to be clinically desirable. Both mucin- and aqueous-deficient dry eyes would benefit, because the wetting ability of the corneal surfece would be enhanced. 

Colloidal Properties of Surface-Active Cellulosic Pofymer... 

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