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Cellulose, surface-active polymers

Table 1.3 shows, for example, the surface tension of the solutions of some water-soluble polymers at 25°C (0.1% aqueous solutions of the polymers). Hydroxypropylcellulose (HPC) is a good example of a surface-active polymer. Water solutions greatly reduced surface and interfacial tensions. HPC functions as an assistant in both emulsifying and whipping. HPC combines organic solvent solubility, thermoplasticity and surface activity with the aqueous thickening and stabilizing properties of other water soluble cellulose pol miers. [Pg.15]

Finally, the area is enlarged a bit by looking at larger surface-active molecules that one could describe as surface-active polymers or polymeric surfactants. Here mature types of products like cellulose derivatives and lignosulfonates, as well as the newer inulin products, are treated. [Pg.338]

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. [Pg.279]

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). [Pg.116]

A new class of water soluble cellulosic polymers currently receiving attention Is characterized by structures with hydrophobic moieties. Such polymers exhibit definite surface activity at alr-llquld and liquid-liquid Interfaces. By virtue of their hydrophobic groups, they also exhibit Interesting association characteristics In solution. In this paper, results are presented on the solution and Interfaclal properties of a cationic cellulosic polymer with hydrophobic groups and Its Interactions with conventional surfactants are discussed. [Pg.297]

In this section, we discuss about the screen printed electrode (SPE) based AChE sensors for the selective determination of OP and CA pesticides. In the past decades, several attempts were made by the researchers to develop SPE based pesticide sensors, where the enzyme AChE was immobilized either directly onto the electrode or above other matrices incorporated SPE surfaces. Both approaches resulted in the good, rapid detection of OP and CA pesticides. Earlier, Hart et al. employed AChE/SPE to detect OP and CA pesticides [21], They measured the enzyme activity from the rate of hydrolysis of acetylthiocholine iodide. Three polymers such as hydroxyethyl cellulose, dimethylaminoethyl methacrylate, and polyethyleneimine were used as enzyme immobilization matrices. Initially, electrodes were exposed to drops of water or pesticide solution, dried and their activity was screened after 24 h. They found that, when the enzyme matrix was hydroxyethyl cellulose, electrode activity inhibited both by water as well as by pesticides. While with co-polymer matrix, a significant response towards pesticides alone was observed. Further, the long-term storage stability of electrodes was highest when the enzyme matrix consisted of the co-polymer. The electrodes retained their activity for nearly one year. In contrast, the electrodes made of hydroxyethyl cellulose or polyethyleneimine possess less stability. [Pg.287]

In many applications and formulations, WSPs with surface-active properties are desirable. These properties are imparted to a polymer by chemical modification of the hydrophilic WSP with appropriate hydrophobic substituents. Examples of commercially available surface-active WSPs based on cellulose include its methyl, hydroxypropyl, and methylhydroxypropyl derivatives. [Pg.344]

A few years ago, Landoll (2-4) reported that grafting a small amount of long-chain alkyl hydrophobes onto a nonionic water-soluble polymer leads to associative thickening behavior (i.e., enhanced viscosity, surface activity, and unusual rheological properties). This chapter deals with the general methods of preparation and solution properties of hydrophobically modified nonionic WSPs. Particularly described are the solution properties of hydrophobically modified (hydroxyethyl)cellulose (HMHEC) in aqueous and surfactant systems. [Pg.344]

In the modification with water-soluble polymers such as cellulose derivatives and polyvinyl alcohol, small amounts of the polymers are added as powders or aqueous solutions to cement mortar and concrete during mixing. Such a modification mainly improves their workability because of the surface activity of the water-soluble polymers, and prevents the dryout phenomena (explained in Ch. 4, Sec. 3.1, Water Retention). The prevention of the dry-out is interpreted in terms of an increase in the viscosity of the water phase in the modified cement mortar and concrete and a sealing effect due to the formation of very thin and water-impervious film in them. In general, the water-soluble polymers hardly contribute to an improvement in the strength of the modified systems. [Pg.19]

Modification of cement mortar and concrete by small amounts of water-soluble polymers such as cellulose derivatives and polyvinyl alcohol is used popularly for improving workability. In this case, the water-soluble polymers are mixed with the mortar and concrete as powders or aqueous solutions, and act as plasticizers because of their surface activity. [Pg.224]

As flocculants for a wide range of substrates (such as cellulose fibres) and in water treatment. Reverse latexes are destabilised and reversed by adding excess water or possibly another surface active agent. Microlatexes prepared in microemulsion polymerisation are self-reversing and therefore do not require addition of another surfactant to favour this transformation. Furthermore, the corresponding polymers, confined within such small particles, with such low polydispersity, should exhibit better characteristics in this respect. [Pg.203]

This is the final category considered when the polymer is itself markedly surface active, the situation becomes very different in many cases the polymer alone will be able to sustain a foam generated from its aqueous solution. An example (61) of this is the hydro-phobically substituted cationic cellulose polymer Quatrisoft LM 200. Many other examples can be found in the literature, including proteins themselves and their derivatives. On addition of a surfactant, mixed adsorbed films will form and the film and foaming characteristics will depend very much on the specifics of the components themselves, the nature of their interaction, and their relative concentration. (See Fig. 11.)... [Pg.212]

Properties. Methylcellulose [9004-67-5] (MC) and its alkylene oxide derivatives hydroxypropylmethylcellulose [9004-65-3] (HPMC), hydroxyethylmethyl-cellulose [9032-42-2] (HEMC), and hydroxybutylmethylcellulose [9041-56-9] (HBMC) are nonionic, surface-active, water-soluble polymers. Each type of derivative is available in a range of methyl and hydroxyalkyl substitutions. The extent and imiformity of the methyl substitution and the specific type of hydroxyalkyl substituent affect the solubility, surface activity, thermal gelation, and other properties of the poljuners in solution. [Pg.1141]


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Active polymers

Cellulose activation

Cellulose activity

Cellulose surface activation

Cellulosic polymers

Polymer activities

Polymer cellulose

Polymers activator

Polymers, activation

Surface-Active Polymers from Cellulose

Surface-active cellulosic polymer

Surface-active cellulosic polymer

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