Wetting characterization measurements

Figure 5 Representative combing forces for wet hair. Measurements were taken following application of aminofunctional silicone fluids and again after eight shampooing cycles. Harr treated with trimethylsilylamodimethicone fluids characterized by low, medium, and high levels of amine modi-flcation are compared to an untreated control.

CHARACTERIZATION OF HIGH SURFACE AREA POLYESTER FILAMENTS BY MEANS OF WETTING FORCE MEASUREMENTS... 

One of the main uses of these wet cells is to investigate surface electrochemistry [94, 95]. In these experiments, a single-crystal surface is prepared by UFIV teclmiqiies and then transferred into an electrochemical cell. An electrochemical reaction is then run and characterized using cyclic voltaimnetry, with the sample itself being one of the electrodes. In order to be sure that the electrochemical measurements all involved the same crystal face, for some experiments a single-crystal cube was actually oriented and polished on all six sides Following surface modification by electrochemistry, the sample is returned to UFIV for... 

Methods of Measurement Methods of characterizing the rate process of wetting include four approaches as illustrated in Table 20-37. The first considers the ability of a drop to spread across the powder. This approach involves the measurement of a contact angle of a drop on a powder compact. The contact angle is a measure of the affinity of the fluid for the solid as given by the Young-Dupre equation, or... 

The second approach to characterize wetting considers the abihty of the fluid to penetrate a powder bed. It involves the measurement of the extent and rate of fluid rise by capillaiy suction into a column of powder, better known as the Washburn test. Considering the powder to consist of capillaries of radius R, the equilibrium height of rise... 

An excellent review of experimental techniques for measuring electrical resistivity in aqueous solutions is available [34], Separators used in nonaqueous systems can be characterized by wetting them with a surfactant and measuring the electrical resistivity in an aqueous solution. Then the resistivity in a nonaqueous membrane can be estimated from Eq. (2). 

Most suitable for the examination of the surface is x-ray photoelectron spectroscopy, whereas the wettability determination can be established by a detailed interpretation of core flooding experiments and wettability index measurements. The results of such studies show that the organic carbon content in the surface is well correlated with the wetting behavior of the material characterized by petrophysical measurements [1467,1468]. 

One problem with methods that produce polycrystalline or nanocrystalline material is that it is not feasible to characterize electrically dopants in such materials by the traditional four-point-probe contacts needed for Hall measurements. Other characterization methods such as optical absorption, photoluminescence (PL), Raman, X-ray and electron diffraction, X-ray rocking-curve widths to assess crystalline quality, secondary ion mass spectrometry (SIMS), scanning or transmission electron microscopy (SEM and TEM), cathodolumi-nescence (CL), and wet-chemical etching provide valuable information, but do not directly yield carrier concentrations. 

For this purpose, all three catalyst supports were initially synthesized by a chemical vapor deposition (CVD) process and thereafter, using a wet impregnation method, loaded with cobalt as the active component for FTS. The as-synthesized Co/nanocatalysts were then characterized by applying electron microscopic analysis as well as temperature-programmed desorption, chemi- and physisorption measurements, thermogravimetric analysis, and inductively coupled plasma... 

Four samples of faujasite were synthesized at Si/Al ratios of 2.61, 2.80, 2.97 and 3.03 using published methods from seeded slurries (8-9) and using proprietary methods. One additional sample of Si/Al ratio 2.58 was purchased from Union Carbide. The samples were characterized by X-ray powder diffraction, by surface area measurements, and by wet chemical analysis. The results of these measurements are contained in Table I. 

Some tests, like lather volume, involved objective laboratory measurements. For example, a technician might produce lather by a prescribed washing procedure intended to consistently reproduce the same motions, and this lather volume would be measured in a graduated cylinder to give an objective measure [12], Other tests, like wet bar feel, required the subjective measurement of trained assessors. For example, the wet feel of a bar would be subjectively characterized as draggy or slippery by an expert panel of evaluators [13]. 

Fairweather et al. [204] developed a microfluidic device and method to measure the capillary pressure as a function of fhe liquid water saturation for porous media wifh heferogeneous wetting properties during liquid and gas intrusions. In addition to being able to produce plots of capillary pressure as a function of liquid wafer safuration, their technique also allowed them to investigate both hydrophilic and hydrophobic pore volumes. This method is still in its early stages because the compression pressure and the temperatures were not controlled however, it can become a potential characterization technique that would permit further understanding of mass transport within the DL. 

The testing of battery separators and control of their pore characteristics are important requirements for proper functioning of batteries. Mercury porosim-etry has been historically used to characterize the separators in terms of percentage porosity, mean pore size and pore size distribution. In this method, the size and volume of pores in a material are measured by determining the quantity of mercury, which can be forced into the pores at increasing pressure. Mercury does not wet most materials, and a force must be applied to overcome the surface tension forces opposing entry into the pores. 

Even if MIP and BET are widely accepted regarding the characterization of HPLC stationary phases, they are only applicable to the samples in the dry state. In order to investigate the impact of polymerization time on the porous properties of wet monolithic columns, ISEC measurements of 200 jm I.D. poly(p-methylstyrene-co-l,2-bis(vinylphenyl)ethane) (MS/BVPE) capillary columns (prepared using a total polymerization time ranging from 45 min to 24 h) have been additionally evaluated (see Table 1.2 for a summary of determined e values). On a stepwise decrease in the time down to 45 min, the total porosity (St) is systematically increasing to about 30% in total (62.8% for 24 h and 97.2% for 45 min). This is caused by a simultaneous increase in the fraction of interparticulate porosity (e. ) as well as the fraction of pores (Cp). The ISEC measurements are in agreement with those of the MIP as well as BET analyses, as an increase in should be reflected in an increase in 8p and as the relative increase in the total porosity (caused by decreasing the polymerization time... 

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