Big Chemical Encyclopedia

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

Articles Figures Tables About

Fluorocarbon, 272 separation

The extensive use of the Young equation (Eq. X-18) reflects its general acceptance. Curiously, however, the equation has never been verified experimentally since surface tensions of solids are rather difficult to measure. While Fowkes and Sawyer [140] claimed verification for liquids on a fluorocarbon polymer, it is not clear that their assumptions are valid. Nucleation studies indicate that the interfacial tension between a solid and its liquid is appreciable (see Section K-3) and may not be ignored. Indirect experimental tests involve comparing the variation of the contact angle with solute concentration with separate adsorption studies [173]. [Pg.372]

Most LB-forming amphiphiles have hydrophobic tails, leaving a very hydrophobic surface. In order to introduce polarity to the final surface, one needs to incorporate bipolar components that would not normally form LB films on their own. Berg and co-workers have partly surmounted this problem with two- and three-component mixtures of fatty acids, amines, and bipolar alcohols [175, 176]. Interestingly, the type of deposition depends on the contact angle of the substrate, and, thus, when relatively polar monolayers are formed, they are deposited as Z-type multilayers. Phase-separated LB films of hydrocarbon-fluorocarbon mixtures provide selective adsorption sites for macromolecules, due to the formation of a step site at the domain boundary [177]. [Pg.560]

Organic fluorine as a separate industry that began in the late 1920s with the discovery by Midgle of fluorocarbons for use as refrigerants. Ammonia was unsuitable because of the hazard and unpleasant smell from minute leaks. Sulfur dioxide had similar problems. The best refrigerant was... [Pg.267]

Polyfluoroparafins, fluorocarbons, and other perfluoro denvatives show remarkable heat stability They are usually stable at temperatures below 300 C Thermal decomposition at 500-800 °C, however, causes all possible splits in the molecules and produces complex mixtures that are difficult to separate For preparative purposes, only pyrolyses that do not yield complicated mixtures of products are of interest [7] The pyrolytic reacpons of polyfluoro and perfluoro derivatives, when carried out at 500-11 Ofl °C, represent the most useful route to preparative generation of perfluoroolefins on the laboratory scale [7]... [Pg.918]

The high thermal and chemical stability of fluorocarbons, combined with their very weak intermolecular interactions, makes them ideal stationary phases for the separation of a wide variety of organic compounds, including both hydrocarbons and fluorine-containing molecules Fluonnated stationary phases include per-fluoroalkanes, fluorocarbon surfactants, poly(chlorotrifluoroethylene), polyfper-fluoroalkyl) ethers, and other functionalized perfluoro compounds The applications of fluonnated compounds as stationary phases in gas-liquid chroma... [Pg.1029]

Monde, T., Kamiusuki, T., Kuroda, T., Mikumo, K., Ohkawa, T., and Fukube, H., High-performance liquid chromatographic separation of phenols on a fluorocarbon-bonded silica gel column, /. Chromatogr. A, 722, 273, 1996. [Pg.51]

Williams, R. C., Vasta-Russell, J. F., Glajch, J. L., and Golebiowski, K., Separation of proteins on a polymeric fluorocarbon high-performance liquid chromatography packing, /. Chromatogr., 371, 63, 1986. [Pg.198]

In the present review, first we will describe how to fabricate artificial photosynthetic reaction center in nanometer scales by making use of phase separation in mixed monolayers of hydrocarbon (HC) and fluorocarbon (FC) amphiphiles [2,5,20-26] as shown in Fig. 2b [3]. The phase separated structures were studied by SPMs such as AFM, SSPM, and scanning near-field optical/atomic force microscopy (SNOAM) [27-33] as well as a conventional local surface analysis by SIMS [3,5], The model anionic and cationic HC amphiphilic... [Pg.194]

Parallel Synthesis m Separation m Fluorocarbon Bonded Silica Gel m Green Chemistry... [Pg.26]

Dinh is illustrative of the methods and their potential (Figure 4).1261 Hydrosilylation of enones like cydo-hexenone was conducted in two different ways. Under biphasic reaction conditions, an organic solvent like toluene containing the enone and phenyl-dimethyl silane was heated with a fluorocarbon solvent (perfluoromethylcyclohexane) containing a fluorous rhodium catalyst. The hydrosilylation reaction occurred over 10 h, and the reaction mixture was cooled and the phases were separated. Distillation of the residue from the organic phase gave the hydrosilylated products in excellent isolated yields... [Pg.29]

Despite the lack of solubility of 15 in fluorocarbon solvents, the huge retention differences between organic compounds (solvent front) and fluorous-tagged compounds (>30 min for the longer tags) translate into simple separations by solid... [Pg.34]

United States, See also American entries Army Corps of Engineers Atomic Energy Commission (AEC) Environmental Protection Agency (EPA) Federal entries Food and Drug Administration (FDA) Government entries National entries OSHA ozone exposure limits U.S. entries acrylic fiber consumption in, ll 220t acrylic fiber production in, 11 189 advanced materials research, 1 696 air separation industry in, 17 754 aliphatic fluorocarbon production in,... [Pg.984]

Most automotive fuel cells use a thin, fluorocarbon-based polymer to separate the electrodes. This is the proton exchange membrane (PEM) that gives this type of fuel cell its name. The polymer provides the electrolyte for charge transport as well as the physical barrier to block the mixing... [Pg.266]

These composites were prepared by mixing a fluorocarbon solution of the perfluorinated PPl dendrimers with an aqueous ethanolic solution of Pd, thereby forming an emulsion. After phase separation, the fluorous phase, which contains the dendrimer-encapsulated Pd +, was treated with a reducing agent yielding zero-valent Pd nanoclusters trapped within the dendrimer (Fig. 24). [Pg.123]


See other pages where Fluorocarbon, 272 separation is mentioned: [Pg.58]    [Pg.272]    [Pg.383]    [Pg.72]    [Pg.224]    [Pg.410]    [Pg.451]    [Pg.88]    [Pg.198]    [Pg.984]    [Pg.18]    [Pg.13]    [Pg.112]    [Pg.67]    [Pg.579]    [Pg.583]    [Pg.11]    [Pg.170]    [Pg.144]    [Pg.1688]    [Pg.451]    [Pg.50]    [Pg.348]    [Pg.1451]    [Pg.1453]    [Pg.192]    [Pg.28]    [Pg.32]    [Pg.203]    [Pg.14]    [Pg.505]    [Pg.293]    [Pg.282]    [Pg.54]    [Pg.393]    [Pg.203]    [Pg.300]   
See also in sourсe #XX -- [ Pg.74 ]




SEARCH



Fluorocarbon

© 2024 chempedia.info