Big Chemical Encyclopedia

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

Articles Figures Tables About

Nonionic surfactants ethers

Relationship between HLB values of nonionic surfactant ethers and esters and the nasal absorption of insulin (lOU/kg) in rata measured as a percentage reduction (D) in glucose levels from 0-4h. Surfactant applied at a concentration of 1 . 9 ethers, 0 esters. Data... [Pg.194]

Anionic surfactants are the most commonly used class of surfactant. Anionic surfactants include sulfates such as sodium alkylsulfate and the homologous ethoxylated versions and sulfonates, eg, sodium alkylglycerol ether sulfonate and sodium cocoyl isethionate. Nonionic surfactants are commonly used at low levels ( 1 2%) to reduce soap scum formation of the product, especially in hard water. These nonionic surfactants are usually ethoxylated fatty materials, such as H0CH2CH20(CH2CH20) R. These are commonly based on triglycerides or fatty alcohols. Amphoteric surfactants, such as cocamidopropyl betaine and cocoamphoacetate, are more recent surfactants in the bar soap area and are typically used at low levels (<2%) as secondary surfactants. These materials can have a dramatic impact on both the lathering and mildness of products (26). [Pg.158]

Liquid Third Phase. A third Hquid with coUoidal stmcture has been a known component in emulsions since the 1970s (22) for nonionic surfactants of the poly(ethylene glycol) alkylaryl ether type. It allows low energy emulsification (23) using the strong temperature dependence of the coUoidal association stmctures in the water—surfactant—hydrocarbon systems. [Pg.201]

Poloxamers are used primarily in aqueous solution and may be quantified in the aqueous phase by the use of compleximetric methods. However, a major limitation is that these techniques are essentially only capable of quantifying alkylene oxide groups and are by no means selective for poloxamers. The basis of these methods is the formation of a complex between a metal ion and the oxygen atoms that form the ether linkages. Reaction of this complex with an anion leads to the formation of a salt that, after precipitation or extraction, may be used for quantitation. A method reported to be rapid, simple, and consistently reproducible [18] involves a two-phase titration, which eliminates interferences from anionic surfactants. The poloxamer is complexed with potassium ions in an alkaline aqueous solution and extracted into dichloromethane as an ion pair with the titrant, tet-rakis (4-fluorophenyl) borate. The end point is defined by a color change resulting from the complexation of the indicator, Victoria Blue B, with excess titrant. The Wickbold [19] method, widely used to determine nonionic surfactants, has been applied to poloxamer type surfactants 120]. Essentially the method involves the formation in the presence of barium ions of a complex be-... [Pg.768]

Ethylene oxide is an important intermediate chemical not only for the production of nonionic surfactants like fatty alcohol ethoxylates, alkylphenol ethoxy lates, or propylene oxide/ethylene oxide block copolymers, but also for manufacturing of anionic surfactants like alcohol ether sulfates. [Pg.32]

Subacute and chronic toxicity of alcohol and alcohol ether sulfates has been extensively tested in several animals and sometimes humans. The duration of the tests was in some cases as long as 2 years. When administered below the toxic amount no specific damages were observed in any of the species tested [333]. No severe side effects were observed in the study by Swisher, carried out with volunteers who ingested considerable amounts of anionic and nonionic surfactants over long periods [348]. Similarly, the effects produced by the intake of daily doses of 1 g of alcohol sulfate per person over 8 weeks [349],... [Pg.288]

Van Paassen [57], Stroink [61], and Meijer [64] described the influence of fatty chain, ethoxylation degree, and pH on the surface tension. It can be concluded that the ether carboxylates behave at low pH as nonionic surfactants with a lower surface tension than at higher pH, where they behave more as anionic surfactants (Fig. 1). Furthermore a higher EO chain or a shorter fatty chain increases the surface tension. [Pg.323]

It has been found that the CMC values are higher and the micelle aggregation numbers smaller than those of the corresponding nonionic surfactants. The CMC increases with increasing EO chain, which is, according to the authors, opposite to the results for sodium alkyl ether sulfate. [Pg.325]

From the apparent ionization degree it was concluded that the EO chain probably behaves as part of the headgroup. As with Aalbers [49], a low surface charge of the sodium alkyl ether carboxylate micelles was mentioned. The micelle aggregation number N increases with the C chain much more than for the corresponding nonionic surfactants. In the case of C8 there was no influence of temperature. A small decrease was found with increasing EO, but much smaller than in the case of nonionics. [Pg.326]

Adsorption and retention studies of surfactants to sand in high-salinity reservoirs showed no differences between nonionics and ether carboxylates [185— 187] low retention and a positive behavior for good oil recovery has been found. [Pg.343]

The colloid probe technique was first applied to the investigation of surfactant adsorption by Rutland and Senden [83]. They investigated the effect of a nonionic surfactant petakis(oxyethylene) dodecyl ether at various concentrations for a silica-silica system. In the absence of surfactant they observed a repulsive interaction at small separation, which inhibited adhesive contact. For a concentration of 2 X 10 M they found a normalized adhesive force of 19 mN/m, which is small compared to similar measurements with SEA and is probably caused by sufactant adsorption s disrupting the hydration force. The adhesive force decreased with time, suggesting that the hydrophobic attraction was being screened by further surfactant adsorption. Thus the authors concluded that adsorption occurs through... [Pg.49]

In addition, water motion has been investigated in reverse micelles formed with the nonionic surfactants Triton X-100 and Brij-30 by Pant and Levinger [41]. As in the AOT reverse micelles, the water motion is substantially reduced in the nonionic reverse micelles as compared to bulk water dynamics with three solvation components observed. These three relaxation times are attributed to bulklike water, bound water, and strongly bound water motion. Interestingly, the overall solvation dynamics of water inside Triton X-100 reverse micelles is slower than the dynamics inside the Brij-30 or AOT reverse micelles, while the water motion inside the Brij-30 reverse micelles is relatively faster than AOT reverse micelles. This work also investigated the solvation dynamics of liquid tri(ethylene glycol) monoethyl ether (TGE) with different concentrations of water. Three relaxation time scales were also observed with subpicosecond, picosecond, and subnanosecond time constants. These time components were attributed to the damped solvent motion, seg-... [Pg.413]

Surfactants. The use of surfactants is greatly restricted in formulating ophthalmic solutions. The order of surfactant toxicity is anionic > cationic >> nonionic. Several nonionic surfactants are used in relatively low concentrations to aid in dispersing steroids in suspensions and to achieve or to improve solution clarity. Those principally used are the sorbitan ether esters of oleic acid (Polysorbate or Tween 20 and 80), polymers of oxyethylated octyl phenol (Tyloxapol), and polyoxyl 40 stearate. The lowest concentration possible is used to perform the desired function. Their effect on preservative efficacy and their possible binding by macromolecules must be taken into account, as well as their effect on ocular irritation. The use of surfactants as cosolvents for an ophthalmic solution of chloramphenicol has been described [271]. This com-... [Pg.458]

The great technical and economic Tmportance of this product group was reached despite its higher price only because of its special properties. Due to the ionic sulfate group and the adjacent ether groups, ether sulfates combine the classical elements of ionic and nonionic surfactants in one molecule. This provides a number of properties, one of which, the Krafft-Point, is of special importance for the technical application of these compounds. [Pg.4]

Therefore, the hypothesis of an increasing nonionic character of alkyl ether sulfates with increasing number of oxyethylene groups is not tenable. Some time ago (30), it was suggested that a certain hydrophobic nature can be attributed to the polyoxyethylene chain of alkyl ether sulfates. At first, this appears to be in contradiction to the decidedly hydrophilic character of the polyoxyethylene chain for nonionic surfactants. However, the possibility of EO group hydration impairment by the sulfate group cannot be excluded. [Pg.9]

Table III shows some data regarding the possible hydrophobic nature of ether sulfates. From several investigations, it is known that, for nonionic surfactants with identical hydrophobic groups, an increase in the hydrophilic part of the molecule causes a decrease in the aggregation number (28). This is caused by the... Table III shows some data regarding the possible hydrophobic nature of ether sulfates. From several investigations, it is known that, for nonionic surfactants with identical hydrophobic groups, an increase in the hydrophilic part of the molecule causes a decrease in the aggregation number (28). This is caused by the...
In Figure 1, the log of the cmc is shown as a function of the number of carbon atoms in the hydrocarbon chain, n, . It is clear that the nonionic surfactants (hexaethyleneglycol alkyl ethers) and the zwitterionic surfactants (N-alkyl betaines) exhibit linear relations with similar slopes of about -0.5... [Pg.75]

The difficulty with HLB as an index of physicochemical properties is that it is not a unique value, as the data of Zaslavsky et al. (1) on the haemolytic activity of three alkyl mercaptan polyoxyethylene derivatives clearly show in Table 1. Nevertheless data on promotion of the absorption of drugs by series of nonionic surfactants, when plotted as a function of HLB do show patterns of behaviour which can assist in pin-pointing the necessary lipophilicity required for optimal biological activity. It is evident however, that structural specificity plays a part in interactions of nonionic surfactants with biomembranes as shown in Table 1. It is reasonable to assume that membranes with different lipophilicities will"require" surfactants of different HLB to achieve penetration and fluidization one of the difficulties in discerning this optimal value of HLB resides in the problems of analysis of data in the literature. For example, Hirai et al. (8 ) examined the effect of a large series of alkyl polyoxyethylene ethers (C4,C0, Cj2 and C 2 series) on the absorption of insulin through the nasal mucosa of rats. Some results are shown in Table II. [Pg.192]

In some biological systems nonionic surfactants have an intrinsic biological activity the Ci2 alkyl ethers were too toxic to be used in the experiments of drug absorption with goldfish. The activity of the C12 ethers was quantified by measurement of the fish turnover time, T. When the reciprocal of the turnover time is plotted against alkyl chain length for the series Cx and Ejq and C12 compound is distinguished by its marked effect. (12). [Pg.195]

The melting point of the L mesomorphic phase of alkyl ether nonionic surfactants taken from the results of Mitchell et (1983) showing the influence of alkyl and hydrophilic (EO) chain lengths. [Pg.201]

When an aqueous solution containing chlorobenzene (190 pM) and a nonionic surfactant micelle (Brij 58, a polyoxyethylene cetyl ether) was illuminated by a photoreactor equipped with 253.7-nm monochromatic UV lamps, phenol, hydrogen, and chloride ions formed as major products. It was reported that aromatic aldehydes, organic acids, and carbon dioxide would form from the photoreaction of chlorobenzene in water under similar conditions. A duplicate experiment was conducted using an ionic micelle (triethylamine, 5 mM), which serves as a hydrogen source. Products identified were phenol and benzene (Chu and Jafvert, 1994). [Pg.281]


See other pages where Nonionic surfactants ethers is mentioned: [Pg.2578]    [Pg.534]    [Pg.322]    [Pg.333]    [Pg.339]    [Pg.473]    [Pg.564]    [Pg.600]    [Pg.130]    [Pg.428]    [Pg.128]    [Pg.556]    [Pg.557]    [Pg.42]    [Pg.29]    [Pg.354]    [Pg.351]    [Pg.97]    [Pg.128]    [Pg.51]    [Pg.21]    [Pg.189]    [Pg.190]    [Pg.342]   
See also in sourсe #XX -- [ Pg.31 , Pg.32 , Pg.33 , Pg.34 ]




SEARCH



Alkyl ether nonionic surfactants, polyoxyethylene

Nonionic ethers

Nonionic surfactants

Nonionizing

Surfactants Nonionics

© 2024 chempedia.info