Abstract: A method of manufacturing a tufted surface covering includes incorporating tuft fiber into a backing to form the tufted surface covering, wherein the tufted surface covering includes an underside and a pile surface; coating the underside with a colloidal latex coating, wherein the colloidal latex coating has an exposed surface; wetting the exposed surface with an anti-blistering agent; and heating at least the underside to cure the colloidal latex coating into a solid latex coating.

Abstract: A multiwall sheet comprises a sheet, comprising walls, wherein the walls comprise a first wall; a second wall; and an outermost rib extending between the first wall and the second wall, wherein the first wall extends longitudinally past the outermost rib to a first wall end and wherein the second wall extends longitudinally past the outermost rib to a second wall end; and an end cap comprising a top wall having a top wall end, a bottom wall having a bottom wall end, and a connecting wall disposed between the top wall end and the bottom wall end; wherein the end cap is disposed over the first wall end and the second wall end and wherein the top wall and the bottom wall extend longitudinally along the first wall and the second wall past the outermost rib.

Abstract: The invention provides for a method of manufacturing artificial turf (1000). The method comprising the steps of: creating (100) a polymer mixture (100, 400, 500), wherein the polymer mixture is at least a three-phase system, wherein the polymer mixture comprises a first polymer (402), a second polymer (404), and a compatibiiizer (406), wherein the first polymer and the second polymer are immiscible, wherein the first polymer forms polymer beads (408) surrounded by the compatibiiizer within the second polymer; extruding (102) the polymer mixture into a monofilament (606); quenching (104) the monofilament; reheating (106) the monofilament; stretching (108) the reheated monofilament to deform the polymer beads into threadlike regions (800) and to form the monofilament into an artificial turf fiber (1004); incorporating (110) the artificial turf fiber into an artificial turf carpet (1002).

Abstract: A method of manufacturing artificial turf includes the steps of: creating a polymer mixture including at least one polymer and a nucleating agent for crystallizing the at least one polymer, extruding the polymer mixture into a monofilament; quenching the monofilament; reheating the monofilament; stretching the reheated monofilament to form the monofilament into an artificial turf fiber, wherein during the stretching the nucleating agent boosts the creation of crystalline portions of the polymer within the monofilament; incorporating the artificial turf fiber into an artificial turf backing, thereby mechanically fixing the monofilaments of the arranged artificial turf fibers in the artificial turf backing.

Abstract: In an embodiment, a method of making an article comprises: co-extruding a core layer formed from a core composition comprising a core thermoplastic polymer and a first cap layer formed from a first cap composition comprising an intumescent flame retardant material to form the article; and thermoforming the article. In an embodiment, a multilayer sheet, comprises: an extruded first cap layer formed from a first cap composition comprising an intumescent flame retardant material; and a co-extruded core layer formed from a core composition comprising a thermoplastic polymer, wherein the first cap layer is disposed upon and in intimate contact with a surface of the core layer; wherein the first cap layer and the second cap layer have an adhesion test value of greater than 2 as measured according to ASTM D3359-02 before thermoforming the first cap layer and the second cap layer.

Abstract: A multiwall sheet comprises a sheet, comprising walls, wherein the walls comprise a first wall; a second wall; and an outermost rib extending between the first wall and the second wall, wherein the first wall extends longitudinally past the outermost rib to a first wall end and wherein the second wall extends longitudinally past the outermost rib to a second wall end; and an end cap comprising a top wall having a top wall end, a bottom wall having a bottom wall end, and a connecting wall disposed between the top wall end and the bottom wall end; wherein the end cap is disposed over the first wall end and the second wall end and wherein the top wall and the bottom wall extend longitudinally along the first wall and the second wall past the outermost rib.

Abstract: Disclosed herein is a foam that includes a polysiloxane block copolymer; the polysiloxane block copolymer including a first block that comprises a polysiloxane block and a second block that includes an organic polymer; the second block not containing a polysiloxane; the polysiloxane block being about 5 to about 45 repeat units; the foam having average pore sizes of less than or equal to about 100 nanometers.

Abstract: Disclosed herein is a foam that includes a polysiloxane block copolymer; the polysiloxane block copolymer including a first block that comprises a polysiloxane block and a second block that includes an organic polymer; the second block not containing a polysiloxane; the polysiloxane block being about 5 to about 45 repeat units; the foam having average pore sizes of less than or equal to about 100 nanometers.

Abstract: A method of increasing the branching and polydispersity of a polycarbonate includes the steps of: (a) including in the polycarbonate at least one species of an alkyl substituted monomer, and (b) treating the polycarbonate at an elevated temperature and for a sufficient time to increase the branching and polydispersity relative to an otherwise equivalent polycarbonate without alkyl substituents.

Abstract: An isosorbide-containing polycarbonate composition is provided. The composition contains a polycarbonate having repeat units derived from isosorbide, a polycarbonate-property-modifying additive, and a pH stabilizer. When a solution containing 10 wt. % of the composition dissolved in dichloromethane is prepared the solution has a non-aqueous pH in a range of equal to or between 0.8 below and 0.5 above the pH of the dichloromethane.

Abstract: A method of making polycarbonate includes the steps of forming polycarbonate by a melt transesterification method using an activated diaryl carbonate, and compounding the polycarbonate with a phosphorus-containing compound that has an abstractable proton or hydrolyzable group. The phosphorus-containing compound is compounded with the polycarbonate in an amount sufficient to result in an improvement in the color properties of the polycarbonate as compared to pellets formed from the same polycarbonate without addition of the phosphorus-containing compound.

Abstract: A downwell packer assembly includes a tubular member and a packer element mounted on the tubular member. The packer element comprises a composition that includes a polymer. The packer element includes micropores (typically created via a blowing agent). When the packer element is exposed to a swelling fluid, such as water or hydrocarbon, the micropores can help to control and, in some instances, increase the rate of swelling. Such swelling enables the packer element to form a seal against the walls of the wellbore.

Abstract: A packer system for a wellbore includes a tubular member and a packer element having an inner layer that circumferentially overlies the tubular member and an outer layer that circumferentially overlies the inner layer. The inner layer includes an elastomer that swells upon contact with a swelling fluid. The outer layer includes a material that provides at least a partial barrier to the swelling fluid.

Abstract: A method for preparing a molded article includes the steps of (a) obtaining a polycarbonate resin and (b) molding the polycarbonate resin. The polycarbonate resin is made by a transesterification reaction using an activated diaryl carbonate such that the polycarbonate is susceptible to the formation of internal ester linkages (IEL). The method occurs with the proviso that the polycarbonate resin, the molding conditions or both are selected to control the amount of IEL formed during the molding process to a level of less than 0.4 mol %.

Abstract: Polycarbonates incorporating terminal carbonate groups derived from ester-substituted activated carbonates in a transesterification process have unfavorable properties with respect to color, hydrolytic stability and thermal stability, particularly when the polycarbonate containing such end groups is molded. The number of activated carbonate end groups formed during the melt transesterification formation of polycarbonate can be reduced by reacting a dihydroxy compound with an activated diaryl carbonate in the presence of an esterification catalyst to produce a polycarbonate, in the presence of a monohydroxy chainstopper such as para-cumyl phenol in an amount that results in 35 to 65 mol % of the end groups being derived from the monohydroxy chainstopper. Suitably, the reactants are provided such that the molar ratio of activated diaryl carbonate to the total of dihydroxy compound plus ½ the chainstopping reagent that is less than 1.

Abstract: Polycarbonates incorporating terminal carbonate groups derived from ester-substituted activated carbonates, for example terminal methyl salicyl carbonate (TMSC) derived from the use of BMSC as the activated carbonate in a transesterification process, have unfavorable properties with respect to color, hydrolytic stability and thermal stability, particularly when the polycarbonate containing such end groups is molded. The number of activated carbonate end groups formed during the melt transesterification formation of polycarbonate can be reduced, however, without sacrificing the benefits of using an activated diaryl carbonate, and without requiring a separate reaction or additional additives by reacting a dihydroxy compound with an activated diaryl carbonate in the presence of an esterification catalyst to produce a polycarbonate, wherein the molar ratio of activated diaryl carbonate to dihydroxy compound is less than 1 when expressed to at least three decimal places, for example 0.996 or less.

Abstract: Polycarbonates incorporating terminal carbonate groups derived from ester-substituted activated carbonates, for example terminal methyl salicyl carbonate (TMSC) derived from the use of BMSC as the activated carbonate in a transesterification process, have unfavorable properties with respect to color, hydrolytic stability and thermal stability, particularly when the polycarbonate containing such end groups is molded. The number of activated carbonate end groups formed during the melt transesterification formation of polycarbonate can be reduced, however, without sacrificing the benefits of using an activated diaryl carbonate, and without requiring a separate reaction or additional additives by reacting a dihydroxy compound with an activated diaryl carbonate in the presence of an esterification catalyst to produce a polycarbonate, wherein the molar ratio of activated diaryl carbonate to dihydroxy compound is less than 1 when expressed to at least three decimal places, for example 0.996 or less.

Abstract: A method of making polycarbonate includes the steps of forming polycarbonate by a melt transesterification method using an activated diaryl carbonate, and compounding the polycarbonate with a phosphorus-containing compound that has an abstractable proton or hydrolyzable group. The phosphorus-containing compound is compounded with the polycarbonate in an amount sufficient to result in an improvement in the color properties of the polycarbonate as compared to pellets formed from the same polycarbonate without addition of the phosphorus-containing compound.

Abstract: A method of increasing the branching and polydispersity of a polycarbonate includes the steps of: (a) including in the polycarbonate at least one species of an alkyl substituted monomer, and (b) treating the polycarbonate at an elevated temperature and for a sufficient time to increase the branching and polydispersity relative to an otherwise equivalent polycarbonate without alkyl substituents.

Abstract: Polycarbonates incorporating terminal carbonate groups derived from ester-substituted activated carbonates in a transesterification process have unfavorable properties with respect to color, hydrolytic stability and thermal stability, particularly when the polycarbonate containing such end groups is molded. The number of activated carbonate end groups formed during the melt transesterification formation of polycarbonate can be reduced by reacting a dihydroxy compound with an activated diaryl carbonate in the presence of an esterification catalyst to produce a polycarbonate, in the presence of a monohydroxy chainstopper such as para-cumyl phenol in an amount that results in 35 to 65 mol % of the end groups being derived from the monohydroxy chainstopper. Suitably, the reactants are provided such that the molar ratio of activated diaryl carbonate to the total of dihydroxy compound plus ½ the chainstopping reagent that is less than 1.