Relaxation surfactant

It was determined, for example, that the surface tension of water relaxes to its equilibrium value with a relaxation time of 0.6 msec [104]. The oscillating jet method has been useful in studying the surface tension of surfactant solutions. Figure 11-21 illustrates the usual observation that at small times the jet appears to have the surface tension of pure water. The slowness in attaining the equilibrium value may partly be due to the times required for surfactant to diffuse to the surface and partly due to chemical rate processes at the interface. See Ref. 105 for similar studies with heptanoic acid and Ref. 106 for some anomalous effects. 

Figrue BE 16.20 shows spectra of DQ m a solution of TXlOO, a neutral surfactant, as a function of delay time. The spectra are qualitatively similar to those obtained in ethanol solution. At early delay times, the polarization is largely TM while RPM increases at later delay times. The early TM indicates that the reaction involves ZnTPPS triplets while the A/E RPM at later delay times is produced by triplet excited-state electron transfer. Calculation of relaxation times from spectral data indicates that in this case the ZnTPPS porphyrin molecules are in the micelle, although some may also be in the hydrophobic mantle of the micelle. Furtlier,... 

Figure 5.8. Paramagnetic ion-induced spin-lattice relaxation rates (rp) of the protons of 5.1c and 5.1 f in CTAB solution and of CTAB in the presence of 5.1c or 5.1 f, normalised to rpfor the surfactant -CH-j. The solutions contained 50 mM of CTAB, 8 mM of 5.1c or 5.1f and 0 or 0.4 mM of [Cu (EDTA) f ...

For example, for alkyl (8-16) glycoside (Plantacare 818 UP) non-ionic surfactant solution of molecular weight 390 g/mol, an increase in surfactant concentration up to 300 ppm (CMC concentration) leads to a significant decrease in surface tension. In the range 300 < C < 1,200 ppm the surface tension was almost independent of concentration. In all cases an increase in liquid temperature leads to a decrease in surface tension. This surface tension relaxation is a diffusion rate-dependent process, which typically depends on the type of surfactant, its diffusion/absorption kinetics, micellar dynamics, and bulk concentration levels. As the CMC is approached the absorption becomes independent of the bulk concentration, and the surfactant... 

The addition of salts modifies the composition of the layer of charges at the micellar interface of ionic surfactants, reducing the static dielectric constant of the system [129,130]. Moreover, addition of an electrolyte (NaCl or CaCli) to water-containing AOT-reversed micelles leads to a marked decrease in the maximal solubihty of water, in the viscosity, and in the electrical birefringence relaxation time [131],... 

Surfactant Cone. (M) In-plane rotational relaxation time (ns) Interfacial viscosity (Pas)... 

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-... 

Interpretation of NMR well logs is usually made with the assumption that the formation is water-wet such that water occupies the smaller pores and oil relaxes as the bulk fluid. Examination of crude oil, brine, rock systems show that a mixed-wet condition is more common than a water-wet condition, but the NMR interpretation may not be adversely affected [47]. Surfactants used in oil-based drilling fluids have a significant effect on wettability and the NMR response can be correlated with the Amott-Harvey wettability index [46]. These surfactants can have an effect on the estimation of the irreducible water saturation unless compensated by adjusting the T2 cut-off [48]. 

The difference between the static or equilibrium and dynamic surface tension is often observed in the compression/expansion hysteresis present in most monolayer Yl/A isotherms (Fig. 8). In such cases, the compression isotherm is not coincident with the expansion one. For an insoluble monolayer, hysteresis may result from very rapid compression, collapse of the film to a surfactant bulk phase during compression, or compression of the film through a first or second order monolayer phase transition. In addition, any combination of these effects may be responsible for the observed hysteresis. Perhaps understandably, there has been no firm quantitative model for time-dependent relaxation effects in monolayers. However, if the basic monolayer properties such as ESP, stability limit, and composition are known, a qualitative description of the dynamic surface tension, or hysteresis, may be obtained. 

A microemulsion droplet is a multicomponent system containing oil, surfactant, cosurfactant, and probably water therefore there may be considerable variation in size and shape depending upon the overall composition. The packing constraints which dictate size and shape of normal micelles (Section 1) should be relaxed in microemulsions because of the presence of cosurfactant and oil. However, it is possible to draw analogies between the behavior of micelles and microemulsion droplets, at least in the more aqueous media. 

With the more conductive liquids, the ion concentration becomes so great that ion concentration fluctuations on a statistical basis are likely to be small. However, charging can take place by three other mechanisms (1) mechanical disruption of any double layer of ions that may exist at the surface in times that are short compared with the relaxation time, with a predominance of the surface ions going to the portion of fluid coming from the surface (2) unequal ion mobility with the larger ions unable to return to the bulk of liquid as readily as the smaller and more mobile ones and (3) contaminating materials, such as dust or surfactants at the interfaces serving as ion carriers into one portion or the other of the ruptured liquid. 

Some of the exchanged resins were coated with cellulose acetate butyrate or cellulose acetate phthalate. The results showed relaxation rate enhancement in 25% water suspensions containing 2% carboxymethylcellulose (CMC) as a surfactant. The relaxivities, however, were rather low. It should be noted, however, that the measurements were made at high field, 300 MHz, where the relaxivity enhancements are always smaller. 

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