The disclosure relates to a class of high and low phosphonated aliphatic fluoropolymer rubbers (pFKM) and perfluoropolymer rubbers (pFFKM) based on FKM and FFKM as well as the process for their preparation and their applications.

The present invention provides a vinyl alcohol-vinyl acetate copolymer having excellent solubility and a method for producing a vinyl alcohol-vinyl acetate copolymer. Provided is a vinyl alcohol-vinyl acetate copolymer including a unit of vinyl alcohol and a unit of vinyl acetate, the vinyl alcohol-vinyl acetate copolymer having a randomness value R of 0.5 or higher, the randomness value R being obtained using the following equation (1):

[00001]$\begin{array}{cc}R=\frac{1}{L_A}+\frac{1}{L_O}& \left(1\right)\end{array}$

where L.sub.O represents a mean chain length of the unit of vinyl alcohol and L.sub.A represents a mean chain length of the unit of vinyl acetate.

The present invention relates to a modifier represented by Formula 1, a method of preparing the same, a modified conjugated diene-based polymer having a high modification ratio which includes a modifier-derived functional group, and a method of preparing the polymer.

Aspects of the present invention relate to polymers, and particularly to farnesene polymers functionalized with one or more oxirane groups and, optionally, one or more hydroxyl groups. According to one aspect of the invention, provided is an epoxidized and optionally hydroxyl-functionalized polyfarnesene. The epoxidized farnesene polymer has at least one of a side chain or a main backbone functionalized with at least one oxirane group and, optionally, at least one terminal end functionalized with a hydroxyl group. In accordance with another aspect of the invention, a method is provided for preparing an epoxidized and optionally hydroxyl-functionalized polyfarnesene. The method includes epoxidizing a farnesene polymer, which may optionally contain one or more terminal hydroxyl groups, to functionalize at least one of a side chain or a main backbone of the farnesene polymer with an oxirane group.

Provided are an organic rare-earth solid micelle, a preparation method therefor, and a method for increasing the photoelectric conversion efficiency of a solar battery. A small organic conjugated ligand is taken as a first ligand, an amphiphilic diblock polymer is taken as a second ligand, and the first ligand and the second ligand are mixed and doped with a rare-earth chloride solution, and self-assembled to form an organic rare-earth solid micelle, whereby the fluorescence emission intensity and the fluorescence efficiency of the rare-earth element are improved. Next, the prepared organic rare-earth solid micelle is spin coated on an ITO layer of a solar battery, to prepare a solar battery with the organic rare-earth solid micelle. Therefore the sunlight absorption of a cell is increased, and the photoelectric conversion efficiency is improved. The preparation process is simple, low in cost, high in photoelectric conversion efficiency, and environmentally friendly.

A process for providing inorganic polymer ceramic-like materials. The process comprises providing a first material which comprises at least one non-oxide ceramic powder, and, at least one metal oxide, and providing a second material which comprises a caustic slurry composed of alkaline water and a solvent, and, combining the materials with stirring. There is also provided a composition of matter provided by the above-mentioned process which is a chemically bonded ceramic polymer comprising metal oxide and non-oxide ceramic bonds.

The anion exchange membranes exhibit enhanced chemical stability and ion conductivity when compared with traditional styrene-based alkaline anion exchange membranes. A copolymer backbone is polymerized from a reaction medium that includes a diphenylalkylene and an alkadiene. The copolymer includes a plurality of pendant phenyl groups. The diphenyl groups on the polymer backbone are functionalized with one or more haloalkylated precursor substrates. The terminal halide from the precursor substrate can then be substituted with a desired ionic group. The diphenylethylene-based alkaline anion exchange membranes lack the ?-hydrogens sharing tertiary carbons with phenyl groups from polystyrene or styrene-based precursor polymers, resulting in higher chemical stability. The ionic groups are also apart from each other by about 3 to 6 carbons in the polymer backbone, enhancing ion conductivity. These membrane are advantageous for use in fuel cells, electrolyzers employing hydrogen, ion separations, etc.

A universal adhesion promoter contains a compound based on polybutadiene having at least one repeat unit selected from the following divalent radicals: ##STR00001##

A sulfur-vulcanized rubber composition contains an ethylene-propylene copolymer rubber (A) as a main component and a vulcanization accelerator (B) and serves as a material of an innermost layer of a vehicle coolant transport hose. The vulcanization accelerator (B) includes at least one vulcanization accelerator selected from a group consisting of (B-1) to (B-3) below in a specific proportion. (B-1) A dithiocarbamate vulcanization accelerator having a molecular weight of 380 or greater. (B-2) A thiuram vulcanization accelerator having a molecular weight of 380 or greater. (B-3) A sulfenamide vulcanization accelerator.

Herein presented is a high electrical conductivity, uniform, material based on nanoparticles-Li.sup.+-polycarboxylate grafted few-layer graphene oxide including perovskite type nanoparticles for filler in polymeric matrices, in direct and reverse osmosis membranes, in lithium batteries, among others. The material is obtained by a method comprising the step of: preparation of a composite material having polymers with mono- or di-acid groups covalently bonded to graphene; optionally further comprising the preparation of a composite material with graphene covalently bonded to polymers having mono- or di-acid groups that have been replaced by lithium ion; and optionally further comprising the preparation of a composite material with graphene covalently bonded to polymers having mono- or di-acid groups that have been replaced by lithium ion in addition to grafted nanoparticles, including nanoparticles perovskite type.