Compounding montmorillonite (MMT) with polymorphic polyvinylidene fluoride (PVDF) by melt intercalation method can induce the crystal phase transformation of PVDF, which is of great significance to obtain the electroactive PVDF. In this research, PVDF/Organic‐Montmorillonite (OMMT) nanocomposites were prepared by a novel vane mixer, which was dominated by the elongational flow field in the whole plasticizing. The dispersion of OMMT, the crystal phase transformation of PVDF, and the resulting properties of nanocomposites were experimentally studied. The results of TEM and WAXD evidenced that homogeneous dispersion and desirable intercalation structure of OMMT were formed in the PVDF matrix under the effect of the elongational flow field. WAXD, FTIR, and DSC tests demonstrated that large amounts of β‐phase of PVDF was formed due to the introduction of OMMT. The intercalation structure of OMMT and the crystal transformation of PVDF increased the dielectric constant and piezoelectric properties of nanocomposites, while the dielectric loss still maintained at a very low level. Finally, the effect of unique ''double‐layer peeling'' mechanism of OMMT on the properties of nanocomposites was discussed.
Novel fluorine-containing polyimides were synthesized through copolymerization by using 2,3,3′,4′-biphenyltetracarboxylic dianhydride (α-BPDA) and 4,4′-(4,4′-isopropydenediphenox-y) bis-(phthalic anhydride) (BPADA) as dianhydrides and 4,4′-oxydianiline (ODA) and 2,2 - Bis [4-(4-aminophenoxy)phenyl]-hexafluoropropanane (HFBAPP) as diamines. Noncoplanar structure, flexible ether bond, and trifluoromethyl give the polyimide good thermoplastic, solubility, and heat resistance. The glass transition temperatures of polyimide films are 232.5°C∼262.2°C, the 5% weight loss temperatures are 521.5°C∼531.0°C, and the residual mass is more than 50% as heating to 800°C. With the increase of HFBAPP content in diamine, the dielectric constant of the material decreases from 3.21 to 2.78, and the dielectric loss decreases from 0.00962 to 0.00687 at 1 MHz, which greatly improves the dielectric properties of the material.
This work demonstrates a concept for improving rates of photocatalysis by mesoporous thin films of semiconducting oxide nanoparticles through manipulating the built-in electric field near the nominal free surface. The reaction rate increases via combinations of donor concentration and surface potential that yield wide space charge widths and correspondingly large regions encompassed by the built-in field. The field draws minority carriers generated deep within the film toward the nominal surface where the chemical reactant is most concentrated. In the photooxidation of aqueous methylene blue by anatase TiO 2 , optimization of the parameters increases the rate by nearly a factor of 3. The concept should extend to many photocatalytic materials and reactions.
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