Big Chemical Encyclopedia

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

Articles Figures Tables About

Preparation surfactants

The third generation are latices made with independentiy prepared surfactant to mimic the in situ prepared functional monomer surfactant. These emulsifiers are often A—B block polymers where A is compatible with the polymer and B with the aqueous phase. In this way surface adsorption of the surfactant is more likely. These emulsions are known to exhibit excellent properties. [Pg.25]

One of the longest known synthetically prepared surfactants are the fatty alcohol sulfates, which were prepared on technical scale before 1940. Along with their ethoxylated counterparts, the fatty alcohol ether sulfates, which appeared on the stage shortly after, their use in toiletries is very popular but they can also be found in products for textile industry and auxiliaries in emulsion polymerization. With the exception of soaps, the mentioned anionic surfactants all have a sulfur-containing functional group. Denying the differences between these, their skin irritancy potential is remarkably high. [Pg.502]

Fatty Acid Esters and Fatty Alcohols Fatty acid esters are obtained by transesterification of triglycerides (vegetable oils) or by esterification of fatty acid with alcohol or polyols. Fatty alcohols are obtained by hydrogenation of esters on metal catalysts. Fatty acid esters and fatty alcohols are useful platform molecules to prepare surfactants, emulsifier, lubricants and polymers. [Pg.62]

Since L-arabinose (15) and o-xylose (16) (Fig. 8) are easily extracted from wheat straw and bran [26, 27], the telomerization of 1 with these pentoses constitutes an attractive route to prepare surfactants without the use of expensive protection and deprotection steps. [Pg.101]

Mayonnaise. Mayonnaise is an oil-in-water emulsion prepared generally by using either whole egg or egg yolk. Instead of these, gelatin-Leu-OCi2 (15 min) (see Table IV) was tried as an emulsifying surfactant to prepare a mayonnaise-like food. Tween-60 as well as whole egg and egg yolk were used as controls. The final adopted ingredient composition was as follows 54 g soybean oil 0.9 g table salt 10 g surfactant dispersion. To prepare surfactant dispersions of two different concentra-... [Pg.215]

The author [4] prepared surfactant pairs as provided in Table 3 for the RAFT polymerization of styrene using dibenzyltrithiocarbonate as the chain transfer agent. [Pg.598]

Figure 1. Schematic pathway for preparing surfactant-templated mesoporous silicas, illustrating a formation mechanism based on preformed liquid crystal (LC) mesophase (route A) or a cooperative process (route B). Reprinted from [20], Copyright (2008) WILEY-VCH Verlag GmbH Co. Figure 1. Schematic pathway for preparing surfactant-templated mesoporous silicas, illustrating a formation mechanism based on preformed liquid crystal (LC) mesophase (route A) or a cooperative process (route B). Reprinted from [20], Copyright (2008) WILEY-VCH Verlag GmbH Co.
Aqueous stock solutions of selected anionic surfactants were prepared if alcohol was to be added, it was incorporated in the stock surfactant solution. These surfactants were desalted and deoiled. Aqueous NaCl solutions were also prepared. Surfactant (or surfactant/alcohol) and NaCl solutions were mixed in 10 ml screw-capped test tubes in the proportions necessary to give the desired final concentration of each constituent. After thorough mixing, the test tubes were set aside and observed periodically for clarity and/or precipitation. The results are summarized in Table I. [Pg.12]

In the present case, at time t = t, the adsorption layer has reached an intermediate coverage and consists of almost only molecules of type A. After a time t = tj, equilibrium has not yet been reached, but component B occupies already a remarkable part of the interfacial area. The final equilibrium state of the adsorbed layer is established at time t > tj, and the interfacial properties are mainly controlled by the contaminant B. The evolution of the adsorbed layer composition with time is on a logarithmic scale. The absolute time ranges are a function of the absolute concentration, the time differences and concentration ratios at the interface and the surface activities of the two components. In practical cases, surfactants are not only contaminated by one but often by several components of different surface activity. This complicates the analysis of purification procedures and the grade of purity of prepared surfactant solutions. [Pg.144]

To increase dispersion or surface area of salt-enzyme preparations in organic media, a method of preparing surfactant-assisted salt enzyme nanodispersions (SSENDs) was explored. The goal was to create a fine dispersion of the salt enzyme lyophilized particles with the use of a siufactant prior to lyophilization by creation of a fine emulsion, followed by removal of solvent and water by lyophilization. Microscopic observation of the emulsion indicated a submicron dispersion of the aqueous phase in the solvent. The results of the ertzyme assay using SSENDs catalyst is shown in Table 3. This experiment was conducted in hexane to determine if such a preparation can enhance activity of the enzyme because posdyophilization addition of the surfactant did not improve the rate of the reaction. The results show that a two- to threefold higher rate can be obtained by preparation of the salt-SC using the SSENDs preparation method. [Pg.342]

Lin et al. (2006) revealed that the cleavage of the prepared surfactants leads to the formation of a water-insoluble silanol moiety and two water-soluble products after plasma treatment at different pressures and powers and for different lengths of time. The hydrophobic silanol moiety readily undergoes polymerization through silanol condensation and deposits a hydrophilic film onto the fiber. This film, which consists of hydrocarbon chains attached to and oriented on the fiber surface through polar groups, imparts water repellency and softness to the fabrics (Shenai, 1976). [Pg.100]

SEM images show that silicone has filled and sealed the inter-monofilament pores and voids and indicates that the PEG silicone surfactants coating the fabrics were decomposed after plasma treadnent. The cleaved products coating the nylon fabric appear to be distributed very uniformly. This phenomenon is consistent with the results of the contact angle measuranents cleavage of the prepared surfactants leads to water-insoluble silanol moieties and two water-soluble products this process imparts excellent water repellency to the nylon fabric. Zhang et al. (2003) determined antibacterial properties qualitatively through measurements of areas from which S. aureus and K. pneumonia have been eradicated. The silicone coat at the eradicated area is not transparent. Biocidal treatments with both the silicone and PEG 2000 silicone surfactants improved the antibacterial properties of the nylon fabrics. The results we obtained before and alter plasma treatment were similar, especially for S. aureus. Thus, the sample treated with PEG 2000 silicone retained its antibacterial activity and water repellency after plasma treatment (Lin et al., 2006). [Pg.101]

Fig. 3 Schematic representation of aqueous vesicle method of preparing surfactant fihns containing proteins, showing an idealized view of static structure... Fig. 3 Schematic representation of aqueous vesicle method of preparing surfactant fihns containing proteins, showing an idealized view of static structure...
As displayed in Table 1, the highest incorporation of starch nanopartides within reverse micelles was found by using the AOT/isooctane microemulsion system. Based on these results, the AOT/isooctane system was used to prepare surfactant coated starch nanopartides. To isolate the AOT-coated starch nanopartides, the isooctane was removed under reduced pressure. Previous studies in our laboratory showed that toluene was a preferred organic medium in which to perform Novozyme 435 catalyzed transesterification reactions(29). Hence, the AOT-coated starch nanospheres were solubilized in toluene and evaluated for modification reactions. [Pg.252]

Pulsed laser deposition involves striking a target made of pre-prepared surfactant-templated inorganic material with an intense laser beam, causing the ejection of atoms, ions and fragments containing template that deposit onto a substrate. Continuous well-adhered films of nanometer scale particles of mesophase material tens of nanometers to... [Pg.588]

Furusawa K, Norde W, Lyklema J (1972) Method for preparing surfactant-free polystyrene latices of high surface charge. Kolloid-Z u Z Polymeie 250(9) 908... [Pg.239]

CAS 31566-31-1 (generic) EINECS/ELINCS 234-325-6 Uses O/w emulsifier for all types of skin care preparations surfactant for w/o emulsions... [Pg.908]

Non-metabolisable oils may also be included in different montanide preparations surfactants may also be added. [Pg.255]


See other pages where Preparation surfactants is mentioned: [Pg.376]    [Pg.608]    [Pg.274]    [Pg.125]    [Pg.68]    [Pg.943]    [Pg.510]    [Pg.265]    [Pg.71]    [Pg.82]    [Pg.31]    [Pg.689]    [Pg.214]    [Pg.616]    [Pg.193]    [Pg.120]    [Pg.173]    [Pg.190]    [Pg.129]    [Pg.164]    [Pg.159]   
See also in sourсe #XX -- [ Pg.106 ]




SEARCH



Advantages of bioprocessing to prepare bio-based non-ionic surfactants

Amino acid surfactants preparation

Preparation of Mesoporous Materials with Nonhydrocarbon Surfactants

Preparation of bio-based surfactants via enzymes in non-aqueous media

Preparation with fluorinated surfactants

Silicone surfactants preparation

Surfactants Removal Process and Bulk Samples Preparation

Surfactants material preparation

Surfactants parenteral preparations

© 2024 chempedia.info