Big Chemical Encyclopedia

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

Articles Figures Tables About

Crystalline phase distribution

The preparation and properties of a novel, commercially viable Li-ion battery based on a gel electrolyte has recently been disclosed by Bellcore (USA) [124]. The technology has, to date, been licensed to six companies and full commercial production is imminent. The polymer membrane is a copolymer based on PVdF copolymerized with hexafluoropropylene (HFP). HFP helps to decrease the crystallinity of the PVdF component, enhancing its ability to absorb liquid. Optimizing the liquid absorption ability, mechanical strength, and processability requires optimized amorphous/crystalline-phase distribution. The PVdF-HFP membrane can absorb plasticizer up to 200 percent of its original volume, especially when a pore former (fumed silica) is added. The liquid electrolyte is typically a solution of LiPF6 in 2 1 ethylene carbonate dimethyl car-... [Pg.517]

Crystallinity/phase purity lattice expansion due to Fe incorporation Absence of amorphous matter outside the crystalline phase distribution of Fe. [Pg.46]

Bragg-Brentano Powder Diffractometer. A powder diffraction experiment differs in several ways from a single-crystal diffraction experiment. The sample, instead of being a single crystal, usually consists of many small single crystals that have many different orientations. It may consist of one or more crystalline phases (components). The size of the crystaUites is usually about 1—50 p.m in diameter. The sample is usually prepared to have a fiat surface. If possible, the experimenter tries to produce a sample that has a random distribution of crystaUite orientations. [Pg.379]

Figure 4 Comparison of average distances from the bilayer center along the bilayer normal for deuterated methyl and methylene groups distributed throughout the DPPC molecule computed from constant-pressure MD calculations and neutron diffraction measurements on gel and liquid crystalline phase DPPC bilayers. Figure 4 Comparison of average distances from the bilayer center along the bilayer normal for deuterated methyl and methylene groups distributed throughout the DPPC molecule computed from constant-pressure MD calculations and neutron diffraction measurements on gel and liquid crystalline phase DPPC bilayers.
Figure 5 Electron density distributions along the bilayer normal from an MD simulation of a fully hydrated liquid crystalline phase DPPC bilayer. (a) Total, lipid, and water contributions (b) contributions of lipid components in the interfacial region. Figure 5 Electron density distributions along the bilayer normal from an MD simulation of a fully hydrated liquid crystalline phase DPPC bilayer. (a) Total, lipid, and water contributions (b) contributions of lipid components in the interfacial region.
Alloys are metallic materials prepared by mixing two or more molten metals. They are used for many purposes, such as construction, and are central to the transportation and electronics industries. Some common alloys are listed in Table 5.5. In homogeneous alloys, atoms of the different elements are distributed uniformly. Examples include brass, bronze, and the coinage alloys. Heterogeneous alloys, such as tin-lead solder and the mercury amalgam sometimes used to fill teeth, consist of a mixture of crystalline phases with different compositions. [Pg.324]

An increase indicates a broadening lifetime distribution. Gel-liquid-crystalline phase transition. [Pg.243]

The preparation of single crystals is difficult, but is successful in some case, so that we are well informed about the structures (1,6,17,21,22,23). The structures of the plastic phases are related to the well-known intermetallic phase Li3Bi, where the centres of the polycyclic P7 or Pn anions surround the positions of the Bi atoms in LisBi. The orientation of the polyanions is disordered (dynamically ). For these structures this orientation leads to a typical electron density distribution of a seemingly octahedral unit. In contrast the orientation of the anions is fixed for the crystalline phases. The symmetry of the unit cells as well as the distribution of cations and anions in these M3P7 and M3P11 type structures reflect the direct relationship to the structures of the plastic phases. [Pg.76]


See other pages where Crystalline phase distribution is mentioned: [Pg.52]    [Pg.170]    [Pg.241]    [Pg.76]    [Pg.77]    [Pg.31]    [Pg.52]    [Pg.170]    [Pg.241]    [Pg.76]    [Pg.77]    [Pg.31]    [Pg.86]    [Pg.1381]    [Pg.150]    [Pg.500]    [Pg.151]    [Pg.152]    [Pg.472]    [Pg.468]    [Pg.20]    [Pg.328]    [Pg.844]    [Pg.287]    [Pg.149]    [Pg.940]    [Pg.595]    [Pg.81]    [Pg.564]    [Pg.269]    [Pg.154]    [Pg.328]    [Pg.870]    [Pg.300]    [Pg.312]    [Pg.323]    [Pg.161]    [Pg.29]    [Pg.173]    [Pg.206]    [Pg.209]    [Pg.201]    [Pg.233]    [Pg.30]    [Pg.300]    [Pg.221]    [Pg.11]   


SEARCH



Crystalline Distribution

Crystalline phases

Distributive phase

Phase distribution

© 2024 chempedia.info