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Polar liquid, test

Aniline and mixed aniline point (DIN 51 775 modified). It is similar to the cloud point test except that the solvent is aniline, a very polar liquid. The aniline point is defined as the temperature at which a mixture of equal parts of aniline and the resin show the beginning of phase separation (i.e. the onset of clouding). Phase separation for aromatic resins occurs between I5°C and below zero for resins with intermediate aromaticity, it lies between 30 and 50°C and for non-aromatic resins, it is 50 to 100°C. Sometimes the mixed aniline point is used. It is similar to the aniline point except that the solvent is a mixture of one part of aniline and one part of w-heptane. The problem of both procedures is that precipitation of resins can be produced before the cloud is generated. [Pg.617]

Following are some properties of AECP explosion /emp(PA method) 305—10°(5 sec) impact test with 2kg wt—detonated at 12" bygroscopicity(% gain in wt at RT and 77% RH) 23% after 6 days and 22.3% after 13 days thermal stability—relatively stable at 85° for long periods of time but decomp extensively at 125° within a week tensile strength—decreases with increase in perchlorate content solubility—insol in common solvents, sometimes dissolved at elevated temps with decompn, swelled in some polar liquids dissociated to some extent in HaO compatibility with NC—incompatible... [Pg.204]

Fowkes, F. M., F. L. Riddle Jr., W. E. Pastore, and A. E. Weber, Interfacial interactions between self-associated polar liquids and squalane used to test equations for solid-liquid interactions , Colloids and Surfaces, 43, 367-387 (1990). [Pg.1224]

Effect of storage on viscosity. Factors such as the method of storing undissolved nitrocellulose affect the viscosity of its solutions. It has been established (Kanamaru [73]) that nitrocellulose kept in a polar liquid, e.g. water, alcohol, and tested for viscosity at stated periods by dissolving samples in acetone, shows for the first few days a rather rapid increase in viscosity, which gradually becomes slower. If cellulose is stored in a non-polar liquid, such as carbon tetrachloride, or petroleum ether, then the viscosity of solutions remains unchanged or increases only very slightly. [Pg.267]

Second, the interfacial tensions of various polar test liquids with liquid hydrocarbons are determined. This is only possible with liquids that are immiscible with liquid hydrocarbons. It is assumed that the interaction between the polar liquid and the liquid hydrocarbon is only due to dispersive forces, and... [Pg.23]

A bsolute rate constants for electron transfer reactions of some aromatic molecules in solution have been reported in our earlier work (2) using the pulse radiolysis method. The transfer of an electron from various radical anions to a second aromatic compound in solution was observed directly. Of the rate constants for nine donor-acceptor pairs investigated, two were found to be lower than the diffusion controlled values, and a correlation with such parameters as the reduction potential difference of the pair was considered. These measurements have been extended to additional transfer pairs for which the reduction potential difference is small. The objective of this work, in addition to furnishing new data for electron transfer rates, is to provide an adequate test of theories of the rate of homogeneous electron transfer in polar liquids (10, 11,12,13, 14, 15,16,17). [Pg.375]

The initial contact angle value depends on the MDF cement surface hydrophilicity and liquid tested polarity. Glycerol with lower polarity compared to water leads to weaker interactions with the cement surface, and as consequence, higher contact angles have been obtained as shown also in Table 3. [Pg.69]

A In situ measurements from 76 test subjects 29 female and 47 male. Measurements made on teeth with intact pellicle (i.e., biofilm). 7/ only calculated from glycerol and thiodiglycol. t Average of 4 teeth from 2 subjects, calculated from non-polar liquids. [Pg.35]

Two approaches have been adopted for pC02 sensing, namely (1) wet sensors and (2) plastic (solid-state) sensors. A wet sensor consists of a pH-sensitive probe dissolved in aqueous bicarbonate buffer solution, which is separated from the gaseous or liquid test medium by a gas-permeable membrane [9]. In plastic sensors, a polar pH-probe is immobilised in a thin polymer film. The probe is usually ion-paired with a lipophilic base such as a tetra-alkyl ammonium hydroxide. This ion-pair combination facilitates compatibility between the two components, whilst simultaneously eliminating the need for aqueous buffers due to the associated water of hydration. This makes it possible for these sensors to maintain their sensitivity to CO2, although they may show some humidity dependence. The requisites of a CO2 probe are a suitable a significant change in absorption or emission characteristics upon... [Pg.411]

As the preceding sketches of developments in molecular theories of polar liquids are intended to suggest, the molecular models so far used are in most cases too simplified and idealized for the results to bear very close comparison with experimentally accessible properties of real fluids. One of the important uses of computer simulations is of course not only to do experiments giving such results for the assumed model but also to evaluate for comparison integrals correlation functions and the like treated approximately in the theories and not otherwise subject to direct experimental test. [Pg.80]

A medium Is required for cesium fluoride to react with either HPPO or OFIBO at room temperature. Tetraglyme (TG) was found to be the best of a number of polar and non-polar media tested. Initiation or ring opening by cesium fluoride In tetraglyme Is difficult because of the low solubility of the salt In either the solvent or the liquid monomers. Polymerization Is slow to Initiate, difficult to control and Is accompanied by a chain transfer reaction which yields only low molecular weight oligomers. [Pg.270]

Hence, the adduced above results have shown that polyethylenes samples fracture criterion in tests on cracking under stress in active mediums is polar liquid reaching of sample median plane. The stability to cracking is described correctly within the frameworks of fractal model of transport in polymers. The stability to cracking extreme growth cause is structural changes, which are due to high-disperse mixture Fe/FeO introduction and characterized by dimension D. ... [Pg.181]

The critical surface tension of a PSA cannot be determined directly, for when the test droplets of low polarity liquids are dissolved in the adhesive the contact angle is not defined. Therefore, this value was derived from those of chemically similar polymers, resulting in 33 mN/m for polyisobutylene and 35-36 mN/m for standard acrylic and rubber-rosin PSAs. [Pg.99]

The quantitative use of continuum models requires care. The absolute values of free energies of solvation depend on many parameters. The electrostatic contribution mainly depends on the shape and volume of the cavity. The most widely used shapes are defined by the molecular surface (Pascual-Ahuir and SiUa 1990 SUla et al. 1991) defined after the atomic radii (Bondi 1964) multiplied by a factor of the order of 1.3. A test for the choice of this parameter can be the comparison of the volume of the cavity with the apparent molecular volume of the solute (when known) in the liquid state or in the solution like in the Onsager s theory of the dielectric permittivity of pure polar liquids. [Pg.565]

Water was chosen as a polar, and di-iodomethane as a non-polar liquid to compare the surface properties of the hybrid polymer layers containing different commercially available long chain perfluoroalkyl silanes (1 mol% each) with those of other surfaces. The measured contact angles and the surface energy data of the solids calculated according to the Owens and Wendt equation [24] are given in Table 6.3. The increase in the contact angles as a measure for a clearly reduced wettability can be observed with both test substances. [Pg.113]

When a voltage is applied to a dielectric (insulator), a current passes that decays with time owing to various polarization mechanisms [ 133]. Conductivity is always time-dependent. This general time dependency affects conductivity measurement for nonconductive liquids, where the peak initial current is used to calculate conductivity. Test methods are given in 3-5.5 and... [Pg.15]

Because polarity is a dominant factor in solubility, phosphorus-containing anionic surfactants can be tested by solving them in a line of different liquids, e.g., heptane, toluene, propanone-2, ethanol, and water. From the behavior in those liquids the surfactants can be classified for an overall view on the solubility of phosphoric acid esters based on alcohols and ethoxylated alcohols in different surroundings. [Pg.591]


See other pages where Polar liquid, test is mentioned: [Pg.167]    [Pg.122]    [Pg.338]    [Pg.369]    [Pg.67]    [Pg.71]    [Pg.309]    [Pg.167]    [Pg.204]    [Pg.467]    [Pg.420]    [Pg.141]    [Pg.88]    [Pg.227]    [Pg.301]    [Pg.140]    [Pg.372]    [Pg.435]    [Pg.279]    [Pg.718]    [Pg.274]    [Pg.168]    [Pg.335]    [Pg.138]    [Pg.307]   
See also in sourсe #XX -- [ Pg.108 ]




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