Abstract: A copolymer of ethylene and of isoprene, which comprises from 10 to 35 mol % of isoprene units, at least 70% of which are in the 3,4 configuration and a portion of which is in the 1,2 configuration is provided. A copolymer of this type with a reduced crystallinity is synthesized with a much higher productivity than its homologues of ethylene and of butadiene, and also confers improved curing properties on rubber compositions.

Abstract: A heterophasic copolymer composition obtained by a process comprising polymerising in multiple steps and multiple polymerisation reactors propylene monomer and a comonomer selected from ethylene, alpha-olefins having 4 to 10 carbon atoms and their mixtures, in the presence of an olefin polymerisation catalyst comprising a solid catalyst component and a co-catalyst, wherein the solid catalyst component comprises titanium, magnesium, halogen and an internal donor of the formula (I): wherein R1 and R2 are the same or different being a linear or branched C1-C12-alkyl group and R is hydrogen or a linear, branched or cyclic C1 to C12-alkyl.

Abstract: A solution that can be used for trapping at least one toxic chemical agent, the solution comprising at least one protic solvent, at least one monomer comprising an (alkyl)acrylic, (alkyl)acrylate or (alkyl)acrylamide group, at least one crosslinking agent comprising at least two groups chosen from the (alkyl)acrylic, (alkyl)acrylate or (alkyl)acrylamide groups, at least one photopolymerization initiator, at least one thixotropic filler and at least one agent chosen from alkali metal halides, alkali metal phosphates, alkali metal sulfates and mixtures thereof.

Abstract: A composition that is easily applied, clear, well-bonded, and superhydrophobic is disclosed. In one aspect, the composition includes a hydrophobic fluorinated solvent, a binder comprising a hydrophobic fluorinated polymer, and hydrophobic fumed silica nanoparticles. Also disclosed is a structure including a substrate coated with the composition, as well as a method for making the composition and a method of coating a substrate with the composition.

Abstract: The invention relates to an anion-exchange membrane (AEM) having a multiblock copolymer including a hydrophilic norbornene-based monomer and a hydrophobic alkene-based or norbornene-based monomer. The hydrophilic norbornene-based monomers include one or more cationic head groups such as a quaternary ammonium ion, which can optionally be crosslinked with a crosslinking agent to increase the structural stability of the polymer. These AEMs can be employed in electrochemical devices such as fuel cells.

Abstract: A method for preparing an aqueous acrylic pressure-sensitive adhesive for clothing is provided, which maintains aging peel strength even when stored at a high temperature for a long time and has greatly improved residue properties when the adhesive is removed from clothing fabrics, and the like. An aqueous acrylic pressure-sensitive adhesive for clothing including the composition prepared as above is also provided.

Abstract: A particle-dispersed polyimide precursor solution contains a polyimide precursor having a unit represented by the following formula (I), particles, and a solvent, in which the particle-dispersed polyimide precursor solution satisfies both the following conditions (1) and (2), (in the formula (I), A represents a tetravalent organic group, and B represents a divalent organic group represented by any of the following formulas (B1) to (B4)), (in the formulas (B1) to (B4), Ar1, Ar10, and Ar11 each independently represent a trivalent aromatic group which may have a substituent, Ar2, Ar4, Ar5, Ar7 and Ar8 each independently represent a divalent aromatic group which may have a substituent, Ar3 and Ar6 each independently represent a tetravalent aromatic group which may have a substituent or a group represented by the following formula (II), Ar9 represents a divalent aromatic group which may have a substituent or a group represented by the following formula (III), X1 to X7 each independently represent N

Abstract: There are provided processes for recycling waste such as polystyrene thermoplastic polymer waste and/or polystyrene thermoplastic copolymer waste as well as recycled polystyrene thermoplastic polymer and/or recycled thermoplastic copolymer that may, for example, be obtained from such processes. The processes can comprise the use of a reducing agent.

Abstract: A latex composition for dip molding includes a carboxylic acid-modified nitrile-based copolymer latex and a cholate-based emulsifier, wherein the cholate-based emulsifier is included in an amount of 0.02 to 3 parts by weight based on a solid content with respect to a solid content of 100 parts by weight of the carboxylic acid-modified nitrile-based copolymer latex. A method of preparing the latex composition for dip molding and a molded article produced using the same are also provided.

Abstract: Provided herein are methods of making blended polymer compositions having enhanced elasticity. The present methods comprise the steps of producing a first polymer composition using a VTP catalyst system, producing a second polymer composition using a HMP catalyst system and combining the first polymer composition and the second polymer composition to make the blended polymer composition. The present methods include blending/combining the polymer compositions produced by different catalyst systems. One such catalyst system includes (i) a vinyl-terminated polymer (VTP) catalyst system comprising a VTP catalyst compound (referred to herein also as a “VTP catalyst”) and one or more activators. Another catalyst system includes a high molecular-weight polymer (HMP) catalyst system comprising a HMP catalyst compound (referred to herein also as a “HMP catalyst”) and one or more activators. The activators of these different catalyst systems can be the same or different in whole or in part.

Abstract: Provided herein are thioacetate isobutylene-based polymer compositions comprising thioalkylated functionalized polymer, and a sulfur donor and/or accelerator cure system. The thioalkylated functionalized polymer is produced via nucleophilic substitution reaction in solution. The present thioacetate functionalized isobutylene-based polymer compositions together with various accelerators and sulfur donors can form thermosets useful for pharmaceutical and tire applications without the use of zinc or a zinc oxide activator.

Abstract: There are provided a polyethylene capable of improving tensile strength while maintaining excellent processability and Mooney viscosity characteristics when preparing a chlorinated polyethylene compound by implementing a molecular structure having a low content of low molecular weight and a high content of high molecular weight, and a chlorinated polyethylene prepared using the same.

Abstract: The polyamide-based resin expanded beads are expanded beads including a polyamide-based resin as a base resin, in which the average value of bead weight of the expanded beads is 0.5 mg or more and 8 mg or less, the coefficient of variation of the bead weight of the expanded beads is 10% or less, and the average value of the ratio of a long diameter to a short diameter (a long diameter/a short diameter) of the expanded beads measured with a projection image photographing type bead size distribution analyzer is 1 or more and 1.5 or less, the coefficient of variation of the ratio (a long diameter/a short diameter) is 12% or less, the average value of the a short diameter is 1 mm or more and 4 mm or less, and the coefficient of variation of the a short diameter is 10% or less.

Abstract: An anion exchange membrane is made by mixing 2 trifluoromethyl ketone [nominal] (1.12 g, 4.53 mmol), 1 BiPhenyl (0.70 g, 4.53 mmol), methylene chloride (3.0 mL), trifluoromethanesulfonic acid (TFSA) (3.0 mL) to produce a pre-polymer. The pre-polymer is then functionalized to produce an anion exchange polymer. The pre-polymer may be functionalized with trimethylamamine in solution with water. The pre-polymer may be imbibed into a porous scaffold material, such as expanded polytetrafluoroethylene to produce a composite anion exchange membrane.

Abstract: Metal nanowires, such as silver nanowires coated on a substrate were sintered together to form fused metal nanowire networks that have greatly improved conductivity while maintaining good transparency and low haze. The method of forming such a fused metal nanowire networks are disclosed that involves exposure of metal nanowires to various fusing agents on a short timescale. The resulting sintered network can have a core-shell structure in which metal halide forms the shell. Additionally, effective methods are described for forming patterned structure with areas of sintered metal nanowire network with high conductivity and areas of un-sintered metal nanowires with low conductivity. The corresponding patterned films are also described.

Abstract: An anion exchange membrane is provided by converting carbon-carbon double bonds in the backbone of polystyrene-block-polybutadiene-block-polystyrene (SBS) into epoxide groups. Unmodified SBS is first partially hydrogenated to remove about 65% to about 90% of carbon-carbon double bonds. The remaining double bonds are then converted to epoxide groups to form an epoxidized SBS. UV-initiated ring opening reactions between the epoxidized SBS and haloalkyloxiranes are then employed to simultaneously functionalize and crosslink the epoxidized SBS. The halide groups in the crosslinked polymer network can be replaced via nucleophilic substitution to offer anion conductivity, e.g., via reaction with trimethylamine. Further ion exchange reactions can then be performed to make the membrane hydroxide conductive. The crosslinked membranes described herein exhibit a mechanical strength improvement of 200% compared to unmodified SBS, while maintaining high hydroxide conductivity.

Abstract: An infusible three-dimensional network of crosslinked acrylic-type polymer fibers, where the diameter of the fibers is between 0.1 and 1.5 ?m, the size of the interstices between the fibers is between 0.1 and 50 ?m2 and the stiffness of the network includes an elastic modulus between 0.01 and 10,000 kPa.

Abstract: The disclosure discloses an aerogel-modified polypropylene and a preparation method thereof, and ultralight thermal-insulating melt-blown non-woven fabric containing the aerogel-modified polypropylene and a preparation method thereof. The preparation method for the aerogel-modified polypropylene includes the following steps: before or during a polymerization reaction, adding aerogel to blend with reaction materials with low viscosities. thereby implementing uniform dispersion of the aerogel to prepare the aerogel-modified polypropylene; herein the reaction materials include a propylene monomer, a catalyst, and an additive, and the aerogel has a granularity falling within a range from 20 nm to 100 ?m, a porosity falling within a range from 40% to 99.9%, a stacking density falling within a range from to 500 g/L, and, a volume fraction being 20-60% of a volume of the ultralight thermal-insulating melt-blown non-woven fabric prepared from the aerogel-modified polypropylene.

Abstract: An organic electroluminescence device of an embodiment includes a first electrode, a second electrode, and an emission layer between the first electrode and the second electrode, and the emission layer includes a compound represented by Formula 1 below, and thus the organic electroluminescence device may exhibit high luminous efficiency characteristics and improved service life characteristics.

Abstract: Embodiments of this disclosure are directed to ethylene-based polymers. The ethylene-based polymer are polymerized units derived from ethylene, diene, and optionally, one or more C3-C12 ?-olefins. The ethylene-based polymer includes a melt viscosity ratio (V0.1/V100) at 190 C greater than 20. The V0.1 is the viscosity of the ethylene-based polymer at 190 C at a frequency of 0.1 radians/second, and the V100 is the viscosity of the ethylene-based polymer at 190 C at a frequency of 100 radians/second. Additionally, the ethylene-based polymer includes an average g greater than 0.86, where the average g? is an intrinsic viscosity ratio determined by gel permeation chromatography using a triple detector.