High strength biomedical materials and processes for making the same are disclosed. Included in the disclosure are nanoporous hydrophilic solids that can be extruded with a high aspect ratio to make high strength medical catheters and other devices with lubricious and biocompatible surfaces. Polymers may be entrapped in pores of materials to provide a durable modification of the materials.

Methods of manufacturing a fire-retardant treated OSB to avoid press build-up issues with prior art fire retardants such as boric acid when subjected to normal heat and pressure used in forming an OSB panel. In one embodiment, the press temperature is reduced to below the melting point or softening temperature of the boric acid and/or prior art fire retardants, with a fast-cure adhesive system used in the mat to provide sufficient bonding and integrity while using a lower press temperature. Alternatively, a zinc borate or calcium borate dispersion, with melting points higher than normal press temperatures, is applied to the wood strands prior to pressing. The zinc borate and/or calcium borate are not melted or softened during the OSB manufacturing process, thereby avoiding the press build-up issues with boric acid.

The present invention relates to a polyamide moulding compound consisting of A 33-79.4 wt% of a polymer mixture consisting of wherein the sum of A1 and A2 is 100 wt% of A; A1 55 to 85 wt% of at least one semi-crystalline, aliphatic polyamide selected from the group PA 6, PA 46, PA 56, PA 66, PA 66/6, PA 610, PA 612, PA 6/12, PA 1010, PA 11, PA 12, PA 1012, PA 1212 and mixtures thereof; A2 15 to 45 wt% of at least one semi-aromatic polyamide selected from the group PA 6l, PA 5l/5T, PA 6l/6T, PA 10l/10T, PA 10T/6T, PA 6T/BACT/66/BAC6, PA MXD6, PA MXD6/MXDl and mixtures thereof; B 20 to 60 wt% of a reinforcing fibre; C 0.6 to 2.0 wt% metal borate, wherein the molar ratio of metal to boron is in the range from 0.5 to 4; D 0 to 5.0 wt% additives, different from A, B and C; wherein the sum of the components A to D is 100 wt% and wherein the moulding compound comprises neither copper halides nor metal phosphinates.

Flame retardant mixtures, flame-retardant polymer compositions, cables endowed therewith and use thereof What are described are flame retardant mixtures comprising a) salt of a phosphinic acid of the formula (I) in which R.sub.1 and R.sub.2 are independently alkyl, cycloalkyl, aryl or aralkyl that are optionally substituted, M is an m-valent cation, and m is 1 to 4, b) salt of a phosphinic acid of the formula (II) that differs from component a) in which R.sub.3 is optionally substituted alkyl, cycloalkyl, cycloalkylalkyl, aryl or aralkyl, preferably with alkyl radicals as substituents, R.sub.4 is alkyl with an even number of carbon atoms, with the proviso that, if R.sub.1 and/or R.sub.2 are alkyl, R.sub.4 has twice, three times or four times the number of carbon atoms of R.sub.1 or R.sub.2, M is an n-valent cation, and n is 1 to 4, c) organylphosphonate, d) phosphite, e) silicate, alumosilicate and/or silicon dioxide which is solid at 25° C., f) a representative selected from the group of triazine complex, polyphosphate, hypophosphite, nitrogen-containing diphosphate, organophosphate, phosphazene and/or polyphosphonate, g) optionally a representative selected from the group of metal hydroxide, metal carbonate, metal borate, zinc stannate and/or intumescent additive, and h) optionally pigment. The mixtures can be used for production of flame-retardant polymer compositions comprising thermoplastic and elastomeric polymers that are of excellent suitability for production of cable sheaths or cable insulations.

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Provided are: a gas barrier resin composition having sufficient long-run workability and superior gas barrier properties which compare favorably to those of fossil fuel-derived resins, while containing a biomass-derived raw material; a multilayer structure in which the gas barrier resin is used; and a method for producing such a gas barrier resin composition. The gas barrier resin composition contains at least one type of saponified ethylene-vinyl ester copolymer, wherein of ethylene and a vinyl ester, which are raw materials of the at least one type of saponified ethylene-vinyl ester copolymer, a part is derived from biomass, and a remainder is derived from a fossil fuel.

An asphaltic sheet comprising an asphaltic component including an asphalt binder and expandable graphite.

A ceramic bonding material including at least one fibrous material, a flux agent and a thickening agent wherein the ceramic bonding material fired at a set temperature to bond the two adjacent substrate faces.

A formulation for a photopolymer composite material for a 3D printing system includes an acrylate oligomer, an inorganic hydrate, a reinforcing filler, and an ultraviolet (UV) initiator. In the formulation the acrylate oligomer may be found in the range between about 20.0-60.0 w % of the formulation. The inorganic hydrate may be found in the range between about 20.0-50.0 w % of the formulation. The reinforcing filler may be found in the range between about 5.0-60.0 w % of the formulation, and the UV initiator may be found in the range between about 0.001-0.5 w % of the formulation. A method of generating a formulation of a photopolymer composite material for use in a 3D printing system includes using an acrylate oligomer, an inorganic hydrate, a reinforcing filler, and an ultraviolet (UV) initiator.

The invention relates to a mixture containing as component A at least one organic phosphinic acid salt and as component B at least one alkali metal stannate (M′.sub.2SnO.sub.3), alkali metal hydroxyl stannate (M′.sub.2Sn(OH).sub.6), alkaline earth metal stannate (M″SnO.sub.3) and/or alkaline earth metal hydroxy stannate (M″Sn(OH).sub.6). The invention relates also to the use of such a mixture.

Some variations provide a multiphase polymer composition comprising a first polymer material and a second polymer material that are chemically distinct, wherein the first polymer material and the second polymer material are microphase-separated on a microphase-separation length scale from about 0.1 microns to about 500 microns, wherein the multiphase polymer composition comprises first solid functional particles selectively dispersed within the first polymer material, and wherein the first solid functional particles are chemically distinct from the first polymer material and the second polymer material. Some embodiments provide an anti-corrosion composition comprising first corrosion-inhibitor particles or precursors selectively dispersed within the first polymer material, wherein the multiphase polymer composition optionally further comprises second corrosion-inhibitor particles or precursors selectively dispersed within the second polymer material. These multiphase polymer compositions may be used for other applications, such as self-cleaning, self-healing, or flame-retardant coatings. Methods of making and using these multiphase polymer compositions are disclosed.