Abstract: A process for the production of high compressive strength microspheres of cured phenolic resins are disclosed. Specifically, the microspheres formed by this process exhibit excellent viscoelastic properties in that the microspheres retain their shape even after applying a load of at least 4 GPa at 2.5 percent strain, and exhibit high hardness of at least about 0.3 GPa.

Abstract: This invention discloses the use of sulfite salts as catalysts to make polyurethane polymers. In particular, this invention discloses the use of metal salts such as alkali metal salts as well as alkyl ammonium salts such as tetralkyl ammonium salts as catalysts to make polyurethane polymers. The sulfite salts are useful to make a wide variety of polyurethane polymers and polyurethane foam polymer products such as flexible polyurethane foam polymers, rigid foam polyurethane polymers, semi-rigid polyurethane polymer, microcellular polyurethane polymer, and spray foam polyurethane polymer as well as any polymeric material that requires the assistance of catalysts to promote the formation of urethane and urea bonds such as those found in polyurethane emusions for paints, coatings, protective coatings, lacquer, etc as well as other polyurethane or polyurethane containing materials such as thermoplastic polymers, thermoplastic polyurethane polymers, elastomers, adhesives, sealants, etc.

Abstract: The present invention provides a co-polymer polyol which has an ABA block structure wherein each A block comprises a plurality of hydroxy-carboxylic acid residues and the B block comprises at least one dimer fatty residue selected from a dimer fatty diacid residue, a dimer fatty diol residue and a dimer fatty diamine residue, wherein the co-polymer polyol comprises at least two hydroxyl end groups. The invention also provides a method of making the co-polymer polyol and a polyurethane comprising the co-polymer polyol.

Abstract: Novel polyurea prepolymer and quasi-prepolymer compositions are contemplated, the compositions being the reaction products of an isocyanate component and a secondary diamine component. Specifically, a an isocyanate component comprising uretonimine-modified 4,4? methylene diphenyl diisocyanates are reacted with various polyamines to form prepolymers or quasi-prepolymers. The isocyanate component may additionally comprise one or more other isocyanates, including pure MDI, aliphatic HDI trimer, HDI allophanate, and aliphatic HDI biuret.

Abstract: Disclosed are an epoxy compound having an alkoxysilyl group, a composite of which exhibits good heat resistant properties and/or a cured product of which exhibits good flame retardant properties, a method of preparing the same, a composition comprising the same, and a cured product and a use of the composition. An alkoxysilylated epoxy compound comprising at least one of Chemical Formula S1 substituent and at least two epoxy groups in a core, a method of preparing the epoxy compound by an allylation, a claisen rearrangement, an epoxidation and an alkoxysilylation, an epoxy composition comprising the epoxy compound, and a cured product and a use of the composition are provided. The composite of the disclosed exhibits improved chemical bonding, good heat resistant properties, a low CTE, a high glass transition temperature or Tg-less. The cured product of the composition exhibits good flame retardant properties.

Abstract: This invention provides, among others, curing agents of Formula II, methods for preparing these curing agents, prepreg materials, degradable cross-linked polymers and reinforced composites made from these curing agents and epoxy resins, and methods for degrading and/or recycling the degradable polymers and reinforced composites.

Abstract: A self-healing hydrophobic epoxy resin composition is provided. The self-healing epoxy resin composition comprises an epoxy resin component and a hardener component, the hardener component comprises at least 0.1 weight % of a modified epoxy resin hardener. The modified epoxy resin hardener is a reaction product of an amino modified oligomericsiloxane and a carboxylic acid anhydride. A process for preparing the modified epoxy resin hardener is also disclosed.

Abstract: The polyester resin according to the present invention is a polyester resin containing a diol unit and a dicarboxylic acid unit, wherein 50 to 95% by mol of the diol unit is a unit derived from pentacyclopentadecane dimethanol represented by a predetermined formula (I) and/or a unit derived from pentacyclopentadecane dimethanol represented by a predetermined formula (II), 50 to 100% by mol of the dicarboxylic acid unit is a unit derived from an aromatic dicarboxylic acid, and both of predetermined conditions (1) and (2) are satisfied.

Abstract: Biodegradable polyesters are made by synthesizing copolymers derived from biodegradable hydroxyacid monomers as well as from hydroxyacid monomers containing a functional group such as an azide group, a halogen group, a thioacetate group, and the like. Preferably, the functionalized biodegradable polyester copolymers are derived from a functionalized hydroxyacid such as a homolog of lactic acid and/or glycolic acid with the copolyester thus containing functional groups on the backbone thereof. These biodegradable polyesters can be utilized wherever biodegradable polyesters are currently used, and also serve as a polymer to which various medical and drug delivery systems can be attached.

Abstract: The invention provides a method for producing polyester comprising: a step for preparing an oligomer comprising a dicarboxylic acid diester by an esterification reaction or a transesterification reaction between a dicarboxylic acid or an ester-forming derivative thereof and a glycol, and then a step for subjecting the oligomer to melt-polycondensation to provide polyester as melt-polycondensate, wherein at least in the step of subjecting the oligomer to melt-polycondensation of the two steps, the oligomer is subjected to melt-polycondensation in the presence of titanium nitride and, as a polycondensation catalyst, particles of a solid base having a coating layer of titanic acid on the surfaces, thereby to provide polyester as melt-polycondensate.

Abstract: Provided is an ultraviolet-absorbing polycarbonate which exhibits excellent heat resistance as well as excellent weather resistance without showing a reduction in its performance or contaminating a processing facility during processing.

Abstract: The present invention relates to a process for preparing branched polyether carbonate polyols, comprising the step of reacting an alkylene oxide and carbon dioxide with an H-functional starter compound in the presence of a catalyst, wherein the reaction is additionally conducted in the presence of a branching compound comprising a functional group polymerizable by ring-opening and an H-functional group. The branching compound is added during the reaction in such a way that the proportion of the branching compound in the reaction mixture obtained, at any time during the addition, is <=7.5% by weight, based on the amount of H-functional starter compound, alkylene oxide and branching compound added at this time. The invention further relates to a polyether carbonate polyol preparable by the process according to the invention, and to crosslinked polyether carbonate polymers based thereon.

Abstract: The present invention relates to methods for producing polyaspartic acids with a weight-average molecular weight (Mw) of from 6,000 to 15,000 g/mol. The invention also relates to polyaspartic acids which can be obtained by the method according to the invention, to a composition containing the polyaspartic acids, and to the use thereof as scale inhibitors, dispersants and as an additive in dishwashing agents, detergents or cleaning agents.

Abstract: Poly(benzoxazine) polymer are prepared by heating a benzoxazine compound in the presence of a (meth)acrylate copolymer having pendent tosylate groups, resulting in an interpenetrating polymer network of a poly(benzoxazine) and a crosslinked (meth)acrylate copolymer.

Abstract: A photoalignment agent includes a polyimide and a capping terminal connected to a main chain end terminal of the polyimide. The capping terminal includes an alkylene group (—CmH2m—, m is a natural number) and a core stereo unit in a dendrimer format. A liquid crystal display includes a first substrate, a thin film transistor disposed on the first substrate, a first electrode connected to the thin film transistor, and a first alignment layer disposed on the first electrode. The first alignment layer includes a polyimide and a capping terminal connected to a main chain end terminal of the polyimide. The capping terminal includes an alkylene group (—CmH2m-, m is a natural number) and a core stereo unit in a dendrimer format.

Abstract: Organosilica materials, which are a polymer of at least one independent monomer of Formula [Z1OZ2OSiCH2]3 (I), wherein each Z1 and Z2 independently represent a hydrogen atom, a C1-C4 alkyl group or a bond to a silicon atom of another monomer and at least one other trivalent metal oxide monomer are provided herein. Methods of preparing and processes of using the organosilica materials, e.g., for catalysis etc., are also provided herein.

Abstract: The present invention provides a fluorine-containing silicon compound represented by the general formula (1), wherein each R1 independently represents a hydrocarbon group having 1 to 6 carbon atoms; each R2 independently represents a hydrogen atom or a hydrocarbon group having 1 to 6 carbon atoms; and n is an integer satisfying 0?n?2. There can be provided a fluorine-containing silicon compound having good storage stability and useful as a raw material of a composition for forming a silicon-containing intermediate film and a silicon-containing photoresist composition used for a fine processing in the manufacturing process of a semiconductor device.

Abstract: The present invention is: a curable composition comprising a component (A) and a component (B) in a mass ratio (component (A):component (B)) of 100:0.3 to 100:90, the component (A) being a silane compound polymer that is represented by a formula (a-1), wherein R1 is a group selected from an alkyl group having 1 to 20 carbon atoms, a cycloalkyl group having 3 to 10 carbon atoms, and a substituted or unsubstituted aryl group having 6 to 20 carbon atoms, Z is a hydroxyl group, an alkoxy group having 1 to 10 carbon atoms, or a halogen atom, m is a positive integer, and n and o are independently 0 or a positive integer, provided that a plurality of R1 are either identical or different, and a plurality of Z are either identical or different, and the component (B) being a silane coupling agent that comprises an isocyanurate skeleton in its molecule.

Abstract: The present invention relates to a silicone chain extender, more particularly a chain extender for silicone polymers and copolymers, to a chain extended silicone polymer or copolymer and to a functionalized chain extended silicone polymer or copolymer, to a method for the preparation thereof and the use thereof.

Abstract: The present invention aims to provide a polyrotaxane-containing composition having excellent transparency. The present invention relates to a polyrotaxane-containing composition including: a polyrotaxane that has a cyclic molecule, a linear molecule threading through a cavity of the cyclic molecule in a skewered manner, and capping groups capping both ends of the linear molecule; and an alkyl (meth) acrylate that has a C4-C18 alkyl group, the polyrotaxane having at least one cyclic molecule that has a C4-C18 alkyl group.

Abstract: This disclosure relates to rotomolded articles, having a wall structure, where the wall structure contains at least one layer containing an ethylene interpolymer product, or a blend containing an ethylene interpolymer product, where the ethylene interpolymer product has: a Dilution Index (Yd) greater than ?1.0; total catalytic metal ?3.0 ppm; ?0.03 terminal vinyl unsaturations per 100 carbon atoms. The ethylene interpolymer products have a melt index from about 0.5 to about 15 dg/minute, a density from about 0.930 to about 0.955 g/cm3, a polydispersity (Mw/Mn) from about 2 to about 6 and a CDBI50 from about 50% to about 98%. Further, the ethylene interpolymer products are a blend of at least two ethylene interpolymers; where one ethylene interpolymer is produced with a single-site catalyst formulation and at least one ethylene interpolymer is produced with a heterogeneous catalyst formulation.

Abstract: A handling film to be applied to an adhesive, wherein the handling film comprises a polyhydroxyamino ether thermoplastic, a monofunctional epoxy, and a carboxylated nitrile butadiene elastomer.

Abstract: Hydrophobic breathable film based on a polymer mixture of A) at least one hydrophilic elastomer block copolymer made of at least one polyamide block and at least one polyalkylene oxide block and B) at least one thermoplastic polymer, which regulates the steam-permeability of the breathable film.

Abstract: Disclosed herein are ethylene-based polymers having low densities and narrow molecular weight distributions, but high melt strengths for blown film processing. Such polymers can be produced by peroxide-treating a metallocene-catalyzed resin.

Abstract: In at least some implementations, a foam product includes 50% to 75% by weight thermoset, between 1% and 10% by weight colorant, between 1% and 3% by weight blowing agent, and one or more fire retardant additives embedded in the foam. Such a foam product may be used, for example, as a board, tile, shingle, shake, or other component for an interior or exterior portion of a residential or commercial structure. In the examples of shingles, shakes, tiles and the like, the foam product may be used on a roof or any other desired portion of a structure, and it may be used for decoration, protection and/or insulation of the structure.

Abstract: Asymmetric organic-inorganic films and methods for forming and using such films. For example, the films are used as membranes for selective separation applications. The methods combine co-assembly of block copolymer (BCP) and inorganic nanoparticles (NPs), such as, for example, titanium dioxide (TiO2), with non-solvent induced phase separation. The resulting films exhibit structural asymmetry. For example, the films have a thin nanoporous surface layer on top of a macroporous finger-like support layer. Parameters that may dictate membrane morphology include the fraction of inorganic nanoparticles used and the length of time allowed for surface layer development. In filtration tests, the resulting membranes show both desirable selectivity and permeability. The synthesis methods for hybrid membranes provide a new self-assembly platform upon which multi-functional and high-performance organic-inorganic membranes can be formed.

Abstract: Extruded polymer foams are made from a polymer composition that includes an unbrominated styrenic polymer, a brominated vinyl aromatic/butadiene flame retardant, and an unbrominated vinyl aromatic/butadiene polymer. The unbrominated vinyl aromatic/butadiene polymer improves the cell homogeneity.

Abstract: Carbon black-containing composite resin pre-expanded particles comprising 100 to 400 parts by mass of a polystyrene-based resin with respect to 100 parts by mass of a carbon black-containing polyolefin-based resin; having a carbon black content of 0.5 to 5.0% by mass and a bulk density of 0.015 to 0.25 g/cm3; and having an outermost layer of 30 to 80 pm after undergoing the following tests: (a) one of the carbon black-containing composite resin pre-expanded particles is sliced into a 1-mm slice in such a way that cross-section surfaces of cells are exposed on both surfaces of the slice; (b) the obtained slice is immersed in toluene at 25° C. for 24 hours to extract a polystyrene-based resin component as described above; (c) the cross-section surface of the slice is then subjected to magnified photographing by a microscope; (d) the obtained microscope image is observed.

Abstract: Compositions for the formation of heat resistant foams are disclosed. The invention also relates to a process for the production of polymeric foams containing amide groups with foaming substantially accomplished by elimination of carbon dioxide by reaction of polyfunctional isocyanates, carboxylic acids, and polyols in the presence of a catalyst system composition comprises a catalyst compound having a cation of a metal, in a salt or ligand, which metal is selected from the group consisting of magnesium, cobalt, manganese, yttrium, Lanthanide Series metals, and combinations thereof, resulting in formation of amide groups in the polymer.

Abstract: A method for generating a microstructure that includes microcellular bubbles, in a material that includes molecules of a thermoplastic polymer, comprises: determining a size-index for the material that represents an average size of the thermoplastic polymer molecules included in the material, and in response to the determined size-index, setting a parameter of a process to generate a microstructure in the material that includes microcellular bubbles. The process to generate a microstructure in the material includes: 1) infusing into the material, during a first period, a gas that does not react with the material, 2) making the gas-infused material thermodynamically unstable.

Abstract: In foamable polystyrene resin particles that are obtained by granulating a polystyrene resin containing a flame retardant and a foaming agent, the flame retardant has a bromine atom in a molecule, contains less than 70% by mass of bromine, has a benzene ring in a molecule, and has a 5% by mass decomposition temperature in a range of from 200° C. to 300° C., the flame retardant is the sole source of bromine in the foamable polystyrene resin particles, a ratio (B/A) between (A) a % by mass of the flame retardant contained in the total foamable polystyrene resin particles and (B) a % by mass of the flame retardant contained in the surface of the resin particles is in a range of from 0.8/1 to 1.2/1, and the amount of the flame retardant added is in a range of from 0.5% by mass to 5.0% by mass, based on 100 parts by mass of the resin fraction in the foamable polystyrene resin particles.

Abstract: The present invention relates to mouldings and processes for producing the same. In particular, the invention relates to foam mouldings and methods of making the same comprising providing a first amount of expandable foam particles and providing a second amount of expandable foam particles and preparing a physical mixture on the basis of the first and second amount of foam particles and introducing the mixture into a mould and sintering under pressure and heat, for example, where the chemical origin of the first amount of expandable foam particles differs from the chemical origin of the second amount of foam particles, and optionally further comprising the presence of a coating in the mixture before the introduction of the mixture into the mould.

Abstract: The present invention relates to a process for producing aerogels, which comprises reacting at least one polyfunctional isocyanate with at least one polyfunctional aromatic amine in the presence of at least one carboxylate as catalyst and a solvent. The invention further relates to the aerogels which can be obtained in this way and to the use of the aerogels as insulation material, in particular for applications in the building sector and in vacuum insulation panels.

Abstract: Polymeric porous particles have a continuous organic solid phase and at least two sets of discrete pores that are isolated from each other within the continuous phase and that have different average sizes. One set of discrete pores has a larger average size than another set of discrete pores by at least 50%. At least one set of discrete pores is free of detectably different marker materials. There porous particles can be prepared using evaporative limited coalescence techniques with especially chosen discrete pore stabilizing hydrocolloids to protect the pores during formation and to provide the different average sizes. The resulting porous particles can be incorporated into articles of various types and having various shapes.

Abstract: Syntactic polyurethane elastomers are made using a non-mercury catalyst. The elastomer is made from a reaction mixture containing a prepolymer made from a polyether polyol and a polyisocyanate, a chain extender, a polyisocyanate and microspheres. The elastomer adheres well to itself, which makes it very useful as thermal insulation for pipelines and other structures that have a complex geometry.

Abstract: An object of the present invention is to provide a method for efficiently degrading a biodegradable resin. In particular, the present invention relates to a method for degrading a biodegradable resin, the method comprising degrading the biodegradable resin in a buffer solution containing a biodegradable resin-degrading enzyme having an optimum pH of 7.5 or higher, wherein no anion derived from a buffer component is present on one side of an equilibrium equation of buffering of the buffer solution, and a pH of the buffer solution is adjusted within a pH range which gives conditions for shifting the equilibrium towards the side on which no anion is present.

Abstract: A process for producing a polyester polyol comprising reacting a recycle stream selected from recycled PET carpet, carpet fiber, containers, textiles, articles or mixtures thereof, with a glycol in a reactor, thereby forming a digested product stream comprising polyols, and an undigested stream; and then reacting the digested product stream with a hydrophobe selected from dimer fatty acids, trimer fatty acids, oleic acid, ricinoleic acid, tung oil, corn oil, canola oil, soybean oil, sunflower oil, bacterial oil, yeast oil, algae oil, castor oil, triglycerides or alkyl carboxylate esters having saturated or unsaturated C6-C36 fatty acid units, saturated or unsaturated C6-C36 fatty acids, alkoxylated castor oil, saturated or unsaturated C9-C18 dicarboxylic acids or diols, cardanol-based products, recycled cooking oil, branched or linear C6-C36 fatty alcohols, hydroxy-functional materials derived from epoxidized, ozonized, or hydroformylated fatty esters or acids, or mixtures thereof.

Abstract: A process for producing a polyester polyol comprising reacting a recycle stream selected from recycled PET carpet, carpet fiber, containers, textiles, articles or mixtures thereof, with a glycol in a reactor, thereby forming a digested product stream comprising polyols, and an undigested stream; and then reacting the digested product stream with a hydrophobe selected from dimer fatty acids, trimer fatty acids, oleic acid, ricinoleic acid, tung oil, corn oil, canola oil, soybean oil, sunflower oil, bacterial oil, yeast oil, algae oil, castor oil, triglycerides or alkyl carboxylate esters having saturated or unsaturated C6-C36 fatty acid units, saturated or unsaturated C6-C36 fatty acids, alkoxylated castor oil, saturated or unsaturated C9-C18 dicarboxylic acids or diols, cardanol-based products, recycled cooking oil, branched or linear C6-C36 fatty alcohols, hydroxy-functional materials derived from epoxidized, ozonized, or hydroformylated fatty esters or acids, or mixtures thereof.

Abstract: A process for producing a polyester polyol comprising reacting a recycle stream selected from recycled PET carpet, carpet fiber, containers, textiles, articles or mixtures thereof, with a glycol in a reactor, thereby forming a digested product stream comprising polyols, and an undigested stream; and then reacting the digested product stream with a hydrophobe selected from dimer fatty acids, trimer fatty acids, oleic acid, ricinoleic acid, tung oil, corn oil, canola oil, soybean oil, sunflower oil, bacterial oil, yeast oil, algae oil, castor oil, triglycerides or alkyl carboxylate esters having saturated or unsaturated C6-C36 fatty acid units, saturated or unsaturated C6-C36 fatty acids, alkoxylated castor oil, saturated or unsaturated C9-C18 dicarboxylic acids or diols, cardanol-based products, recycled cooking oil, branched or linear C6-C36 fatty alcohols, hydroxy-functional materials derived from epoxidized, ozonized, or hydroformylated fatty esters or acids, or mixtures thereof.

Abstract: A silicone gel composition including: an organopolysiloxane shown by the following general formula: RaR1bSiO(4-a-b)/2, having one or more alkenyl groups bound to a silicon atom in one molecule, wherein the amount is 100 parts by mass; an organohydrogenpolysiloxane shown by the following general formula: R2cHdSiO(4-c-d)/2, having two or more hydrogen atoms bound to a silicon atom in one molecule, wherein the amount is such that 0.6 to 3 hydrogen atoms bound to a silicon atom is contained relative to one alkenyl group bound to a silicon atom in the component; a platinum-based catalyst, wherein the amount is an effective amount; and a carbon nanotube, wherein the amount is 0.01 to 3 parts by mass. This provides a silicone gel composition which can be a silicone gel cured product with low elastic modulus, low stress, and excellent heat resistance at 230° C., when it is cured.

Abstract: A shaped part that is formed from a polymer composition that contains a liquid crystalline polymer and a black pigment is provided. By selectively controlling the type and relative concentration of these components, the polymer composition and shaped parts formed therefrom can have a dark black appearance, and yet still exhibit good thermal and mechanical properties at high temperatures.

Abstract: Provided herein is a translucent white polymer composition suitable for use as a safety glass interlayer. The translucent white polymer composition comprises a pigment and a polymeric resin that comprises an ionomer of an ethylene acid copolymer. Alumina (Al2O3) and alumina trihydrate (Al(OH)3; “ATH”) are preferred pigments. The translucent white polymer composition is useful in various molded articles. The translucent white polymer composition is particularly useful as an interlayer in glass laminates, including safety glass laminates and structural glass laminates. Further provided herein are methods of making the translucent white polymer composition, the articles and the glass laminates.

Abstract: A thermoplastic polymer composition comprises a thermoplastic polymer and a compatibilizing agent comprising a fulvene moiety or a fulvene-derived moiety. A heterophasic polymer composition comprises a propylene polymer phase, an ethylene polymer phase, and a compatibilizing agent comprising a fulvene moiety or a fulvene-derived moiety.

Abstract: Provided is a thermoformed container having a superior appearance as a result of inhibition of coloring and generation of defects during the melt molding, having sufficient strength, and further having a self-purge feature in a production process. The thermoformed container includes an EVOH layer (A) containing an ethylene-vinyl alcohol copolymer (I) as a principal component, wherein the EVOH layer (A) contains a carbonyl compound (II), the carbonyl compound (II) is an unsaturated aldehyde (II-1), a saturated aldehyde (II-2), a saturated ketone (II-3) or a combination thereof, and the content of the carbonyl compound (II) in the EVOH layer (A) is 0.01 ppm or greater and 100 ppm or less. The carbonyl compound (II) is preferably an unsaturated aldehyde (II-1), and the unsaturated aldehyde (II-1) is preferably an unsaturated aliphatic aldehyde.

Abstract: The present disclosure relates to oxygen scavenging molecules, compositions comprising the molecules, and articles made from the compositions.

Abstract: The present invention relates to the use of NOR-HALS compounds in flame retardant polymer compositions. These compositions are especially useful for the manufacture of flame retardant compositions based on thermoplastic polymers, especially polyolefin homo- and copolymers, polycondensates, such as polyamines or polyesters and duroplastic polymers, such as polyepoxides.

Abstract: A thermosetting resin composition comprising a thermosetting resin, an inorganic filler, and an organomolybdenum compound is disclosed. The thermosetting resin composition may be used for preparing a resin vanish and a prepreg, wherein the prepreg is used for laminates and printed circuit boards.

Abstract: Dark colored polycarbonate compositions and exterior automotive parts produced therefrom with infrared resistance additives are disclosed. The dark colored polycarbonate compositions and parts impart enhanced thermal management and reduce intrinsic heat up of darker materials by incorporation of an improved infrared resistance additive. The dark polycarbonate compositions and automotive parts may be used in various exterior applications including automotive glazing applications.

Abstract: A sulfur-crosslinkable rubber mixture includes from 40 to 100 phr of at least one natural and/or synthetic polyisoprene, and 15 phr or more of at least one hydrocarbon resin which is built up to the extent of 50 to 100 wt. % from aliphatic C5 monomers and to the extent of 0 to 50 wt. % from further monomers, where the hydrocarbon resin according to formula I) has a Q of from 0.015 [° C.·mol/g] to 0.050 [° C.·mol/g]. Formula I) is defined as Q=softening point [° C.]/centrifuge average Mc [g/mol]. In some aspects, the sulfur-crosslinkable rubber mixture includes 15 to 300 phr of the hydrocarbon resin, or even from 36 to 100 phr of the hydrocarbon resin. The further monomer(s) is or are selected from the group of unsaturated compounds, which can be polymerized cationically, which includes aromatics and/or unsaturated terpenes and/or alkenes and/or cycloalkenes.

Abstract: The present invention relates to a polyethylene composition comprising-a base resin comprising (A) a first ethylene homo- or copolymer component having a melt flow rate MFR2 (2.16 kg, 190° C.) of equal to or more than 150 g/10 min to equal to or less than 300 g/10 min, determined according to ISO 1133, and (B) a second ethylene homo- or copolymer component, -optional carbon black, -optional further polymer component(s) different to the first ethylene homo- or copolymer components (A) and (B), and -optional additive(s); wherein the first ethylene homo- or copolymer component (A) has a lower weight average molecular weight as the second ethylene homo- or copolymer component (B), and the weight ratio of the first ethylene homo- or copolymer component (A) to the second ethylene homo- or copolymer component (B) is from 40:60 to 47:53; the polyethylene composition has a melt flow rate MFRS (5 kg, 190° C.) of equal to or more than 0.35 g/10 min to equal to or less than 0.