Search results for "Transform"
showing 10 items of 3975 documents
Effects of pressure and of thermal history on the structural phase transition of KCN
1992
The cubic-noncubic structural phase transition of a KCN single crystal is studied as a function of thermal history and of hydrostatic pressure up to 2 kbar. The standard sequence of phases is cubic-monoclinic-orthorhombic on cooling and orthorhombic-cubic on heating. The monoclinic phase is also absent in first cooling runs at low pressures (p≦250 bar). The width of the monoclinic field inp, T phase diagram is increased in second cooling runs. The effects are discussed in terms of a martensitic transformation behavior and random strain fields.
Study of interacting bands of silane: Analysis of infrared and Raman spectra
1990
Abstract The ν 1 ν 3 interacting bands of natural silane have been studied by Fourier transform spectroscopy and stimulated Raman spectroscopy, respectively, in the regions 2040–2320 and 2180–2187 cm−1. These data combined with available microwave observations have been analyzed using a reduced effective Hamiltonian developed through the fifth order for 28SiH4 and through the fourth order for 29SiH4 and 30SiH4. The observed infrared and Raman transitions have been very well reproduced with a standard deviation of about 0.0004 cm−1 for 28SiH4. Some anomalies in the Hamiltonian expansion have been found, but they did not perturb the analysis.
Dye-containing S∗cside-on/end-on copolymers
1995
Abstract Mesomorphic copolysiloxanes, which combine ‘normal’ end-on linked chiral mesogenic units inducing S∗c phases and side-on fixed chromophores were prepared. The interplay of the different orientational tendencies of these moieties, which are perpendicular (end-on linked mesogenic groups) or parallel (side-on fixed chromophores) to the polymer chain, lead to a strong destabilization of the S∗c phase. However, copolymers with up to about 10 mol % of chromophores still show a smectic C∗ phase. FTIR measurements show that both moieties orient parallel to each other and perpendicular to the polymer chains. These copolymers are interesting to consider as coloured guest-host S∗c materials f…
Covalently attached polymer mono- and multilayers on silanized glass substrates
1996
Abstract Applying grazing incidence FTIR and ellipsometry, the reaction of poly [(1-methyl-vinyl isocyanate)-alt-(maleic anhydride)](IAP) with amino-silanized glass and silicon oxide surfaces has been investigated. A reactive surface containing isocyanate and anhydride groups was formed after the adsorption of the polymer. The layer could be further functionalized using 2-aminoethanol. Multilayers could be built up by adsorbing a second layer of IAP onto an already reacted first layer of IAP.
Influence of plasticizers suggests role of topology in polymer solidification at high cooling rates
2012
Although solidification in processing deter- mines short- and long-term properties, methods for under- standing polymer crystallization mostly rely on real time experiments. Their evidences being drawn on time scales farther apart with respect to those experienced in process- ing. Nor significant outcomes have been so far drawn with approaches mimicking the typical processing times, the Continuous Cooling Transformation methods. Use of these techniques has indeed been limited to a heuristic interpretation of the structure developed under extreme solidification conditions without suggesting alternative routes to the understanding or even clues to the many open questions on polymer crystalliz…
Superhydrophobic TiO2/Fluorinated Polysiloxane Hybrid Coatings with Controlled Morphology for Solar Photocatalysis
2021
Abstract Technological applications of polysiloxane coatings have been influenced by their intrinsic low surface energy, which increases their water repellence. Accurate control of composition and interfacial properties through the introduction of perfluorinated moieties further lowers the polysiloxane surface energy, while mixing with metal oxide nanoparticles enhances roughness, resulting in a great potential in the development of superhydrophobic materials for photocatalysis. Herein, a series of hydrophobic and superhydrophobic hybrid coatings were prepared by dehydrocoupling and hydrosilylation reactions of polymethylhydrosiloxane with 1H,1H,2H,2H‐perfluorooctyltriethoxysilane and 1,3-d…
Carbon nitride as photocatalyst in organic selective transformations
2020
Abstract Graphitic carbon nitride (g-C3N4) is a metal-free conjugated polymer which has become a new research hotspot in photocatalysis. It can be used for solar energy exploitation like in solar energy organic synthesis, one of the most new and appealing green applications of heterogeneous photocatalysis. This chapter resumes the state-of-the-art and progresses in the application of heterogeneous visible light photocatalysis in organic selective transformations by using C3N4 as photocatalyst.
Martensitic phase transformation cubic-orthorhombic of NaCN and (NaCN)0.98 (KCN)0.02
1990
The ferroelastic cubic-orthorhombic transition of single crystals NaCN and (NaCN)0.98 (KCN)0.02 has been studied by x-ray diffraction. The domain configuration obtained is consistent with the Wechsler, Lieberman, Read-model for martensitic transformations.
Five-to-Six Membered Ring-rearrangements in the Reaction of 5-Perfluoroalkyl-1,2,4-oxadiazoles with Hydrazine and Methylhydrazine
2006
The hydrazinolysis reaction of 5-perfluoroalkyl-1,2,4-oxadiazoles with hydrazine or methylhydrazine as bidentate nucleophiles has been investigated. The reaction occurred through the addition of the bidentate nucleophile to the C(5)-N(4) double bond of the 1,2,4-oxadiazole followed by ring-opening and ring-closure (ANRORC) involving the second nucleophilic site of the reagent. This ring-closure step could involve either the original C(3) of the 1,2,4-oxadiazole (giving a five-to-five membered ring rearrangement) or an additional electrophilic center linked to it (exploiting a five-to-six membered ring rearrangement). An alternative initial nucleophilic attack may involve the additional elec…
Reduction of benzo(a)pyrene mutagenicity by dihydrodiol dehydrogenase
1979
THE enigma of how inert chemicals can exert potent mutagenic, carcinogenic, allergenic and cytotoxic effects has been much debated. It has been learned that such compounds are metabolically converted to chemically reactive species1. In the case of aromatic or olefinic compounds, monooxygenases located in the membranes of the cell can transform these compounds into epoxides2–5 which by virtue of electrophilic reactivity can bind chemically to cellular macromolecules such as DNA, RNA and proteins, thereby disturbing biochemical control mechanisms and leading to the above mentioned toxic effects. The same membranes in which such epoxides are produced possess an enzyme, epoxide hydratase, which…