Abstract: Metal coated molded polymer articles are described made from a polyoxymethylene polymer. In accordance with the present disclosure, the molded articles are produced from a polymer composition containing a functionalized polyoxymethylene polymer combined with a metal pigment. The functionalized polyoxymethylene polymer may comprise a polyoxymethylene polymer that has a significant amount of hydroxyl groups present in the terminal positions. The terminal positions can be on the end of the polymer chain or on the side of the polymer chain. In one embodiment, the metal coating is applied to the molded article using an electrolytic plating process. Electrolytic coatings applied to substrates made in accordance with the present disclosure have displayed excellent peel strengths.

Abstract: An overmolded composite structure that contains a metal component and a resinous component adhered to a surface thereof is provided. The resinous component is formed from a thermoplastic composition that contains at least one polyarylene sulfide and at least one mineral filler. The present inventors have discovered that the nature and relative concentration of the polyarylene sulfides, mineral fillers, and/or other materials in the thermoplastic composition can be selectively tailored so that the resulting resinous component has a coefficient of linear thermal expansion and/or color that is similar to the metal component.

Abstract: Melt processed polyarylene sulfide compositions are described as are methods of forming the melt processed polyarylene sulfide compositions. The melt processed polyarylene sulfide compositions are formed according to a melt processing method that includes melt processing a mixture that includes a starting polyarylene sulfide, a disulfide compound and a filler. The melt processed polyarylene sulfide compositions may provide low chlorine content products having excellent strength characteristics.

Abstract: Polyarylene sulfide/liquid crystal polymer alloys are described as are methods of forming the polyarylene sulfide/liquid crystal polymer alloys. The polyarylene sulfide/liquid crystal polymer alloys are formed according to a melt processing method that includes melt processing a polyarylene sulfide with a reactively functionalized disulfide compound and a liquid crystal polymer in a one or two step process. The reactively functionalized disulfide compound is added in a stoichiometric amount to react with a portion of the polyarylene sulfide. The melt processing forms a polyarylene sulfide/liquid crystal polymer copolymer that is a compatibilizer in the alloy. The polyarylene sulfide/liquid crystal polymer alloys may provide low chlorine content products having excellent strength characteristics.

Abstract: Methods for forming a low chlorine content washed polyarylene sulfide are described. Methods include washing a polyarylene sulfide that includes aryl halide endgroups with a solution that includes a disulfide compound. The solution can also include a catalyst and an organic solvent. During the disulfide wash, a nucleophilic substitution reaction occurs between the disulfide compound and aryl halides endgroups of the polyarylene sulfide. The nucleophilic substitution reaction is carried out at conditions to prevent chain scission of the polyarylene sulfide that includes the aryl halide endgroups. Compositions and products formed with the low chlorine content disulfide washed polyarylene sulfide are also described.

Abstract: A molded part having a predetermined shape is provided. The molded part may be formed by casting a liquid crystalline polymer composition into a mold cavity at a relatively low shear rate. Due to the use of a relatively low shear rate, the polymer composition does not generally undergo extensive shear orientation, which can allow the resulting part to be further processed using standard finishing techniques. The ability to use relatively low shear rates during casting is achieved in the present invention through the use of an aromatic amide oligomer. More particularly, the present inventors have discovered that the aromatic amide oligomer can serve as a flow aid by altering intermolecular polymer chain interactions, thereby lowering the overall viscosity of the polymer matrix to “ultralow” levels without having a significant impact on the mechanical properties.

Abstract: A thermotropic liquid crystalline polymer melt polymerized in the presence of a viscosity modifier that can help increase the “low shear” viscosity of the resulting composition is provided. The increased “low shear” viscosity can minimize drooling of the polymer composition during processing and also allow it to possess a greater melt strength, which facilitates its ability to be processed in a wide variety of applications without losing its physical integrity. Despite having a relatively high “low shear” viscosity, the present inventors have discovered that the viscosity modifier does not substantially increase the “high shear” melt viscosity of the polymer composition. In this regard, the ratio of the “low shear” viscosity to the melt viscosity is generally very high, such as within a range of from about 50 to about 1000.

Abstract: A polymer composition that contains a thermotropic liquid crystalline polymer, fibrous filler (e.g., glass fibers), and a flow aid is provided. The flow aid is in the form of an aromatic amide oligomer which, due to its unique nature and properties, has the ability to dramatically reduce melt viscosity with only a minimal degree of blending with the polymer. More particularly, the fibrous filler is supplied to an extruder in conjunction with the polymer and/or at a location downstream thereof so that the polymer is still in a solid or solid-like state when it initially contacts the filler. In this manner, the fibrous filler and polymer are allowed to mix together while the composition still has a relatively high melt viscosity, which helps to uniformly disperse the fibrous filler within the polymer matrix. After a certain period of time, the aromatic amide oligomer is then supplied to the extruder at a location downstream from the fibrous filler to reduce the melt viscosity of the composition.

Abstract: A method for forming a high molecular weight liquid crystalline polymer is provided. The method include melt polymerizing two or more precursor monomers (e.g., acetylated or non-acetylated) in the presence of an aromatic amide oligomer. The present inventors have discovered that such an oligomer can lower the melt viscosity of the viscous polymer as it is formed. The ability to lower melt viscosity in situ during melt polymerization enables the formation of high molecular weight polymers that display low melt viscosity and can still be removed from the reactor vessel without solidifying therein. This not only improves the ease of processing, but also allows molecular weights to be reached that are even higher than conventionally practical.

Abstract: A liquid crystalline polymer composition that contains a liquid crystalline polymer and an aromatic amide oligomer is provided. The oligomer can serve as a flow aid by altering intermolecular polymer chain interactions, thereby lowering the overall viscosity of the polymer matrix under shear. The oligomer is also not easily volatized or decomposed during compounding, molding, and/or use, which minimizes off-gassing and the formation of blisters that would otherwise impact the final mechanical properties of a part made from the polymer composition. While providing the benefits noted, the aromatic amide oligomer does not generally react with the polymer backbone of the liquid crystalline polymer to any appreciable extent so that the mechanical properties of the polymer are not adversely impacted.

Abstract: An aromatic amide compound having the following general formula (I) is provided: wherein, X1 and X2 are independently C(O)HN or NHC(O); G1, G2 and G3 are independently hydrogen, C(O)HN-phenyl, or NHC(O)-phenyl, wherein at least one of G1, G2 and G3 is C(O)HN-phenyl or NHC(O)-phenyl; Q1, Q2, and Q3 are independently hydrogen, C(O)HN-phenyl, or NHC(O)-phenyl, wherein at least one of Q1, Q2, and Q3 is C(O)HN-phenyl or NHC(O)-phenyl; R5 is halo, haloalkyl, alkyl, alkenyl, aryl, heteroaryl, cycloalkyl, or heterocyclyl; and m is from 0 to 4.

Abstract: A liquid crystalline polymer composition that contains a liquid crystalline polymer and an aromatic amide oligomer is provided. The oligomer can serve as a flow aid by altering intermolecular polymer chain interactions, thereby lowering the overall viscosity of the polymer matrix under shear. The oligomer is also not easily volatized or decomposed during compounding, molding, and/or use, which minimizes off-gassing and the formation of blisters that would otherwise impact the final mechanical properties of a part made from the polymer composition. While providing the benefits noted, the aromatic amide oligomer does not generally react with the polymer backbone of the liquid crystalline polymer to any appreciable extent so that the mechanical properties of the polymer are not adversely impacted.

Abstract: A thermotropic liquid crystalline polymer composition capable of exhibiting both a low melting temperature and good heat resistance without the use of conventional naphthenic acids is provided. The melting temperature may, for example, range from about 250° C. to about 400° C. Even at such low melting temperatures, the present inventors have surprisingly discovered that the ratio of the deflection temperature under load (“DTUL”), a measure of short term heat resistance, to the melting temperature may remain relatively high. The specific DTUL values may range from about 200° C. to about 300° C. The ability to form a polymer composition with the properties noted above may be achieved, at least in part, by the use of an aromatic amide oligomer.

Abstract: A method for lowering melt viscosity of a liquid crystalline polymer as it is formed in a reactor vessel. More particularly, a reaction mixture is initially supplied to the reactor vessel that contains two or more precursor monomers (e.g., acetylated or non-acetylated). The reaction mixture is heated to an elevated temperature under agitation to initiate formation of the polymer. After a certain period of time, an aromatic amide oligomer is added to the reaction mixture. Among other things, the present inventors have discovered that such an oligomer can serve as a flow aid by altering intermolecular polymer chain interactions, thereby lowering the overall viscosity of the polymer matrix under shear. This minimizes the likelihood of “freeze off” of the polymer within the reactor vessel and limits the impact of process disruptions on the production of the liquid crystalline polymer.

Abstract: A method for forming a high molecular weight thermotropic liquid crystalline polymer is provided. The method includes melt polymerizing two or more monomers in the presence of a unique aromatic amide oligomer to form a prepolymer, and then solid-state polymerizing the prepolymer to achieve a target molecular weight. The present inventors have discovered that a unique aromatic amide oligomer can be employed to help increase the “low shear” complex viscosity of the resulting solid-state polymerized composition. This allows for the attainment of higher than conventional “low shear” complex viscosity values and/or a substantial reduction in the solid-state polymerization time needed to achieve a target complex viscosity. In addition, the oligomeric flow aid can also accelerate the extent to which the “high shear” melt viscosity is increased during solid-state polymerization, which may also contribute to a substantial reduction in the solid-state polymerization time needed to achieve a certain molecular weight.

Abstract: A melt-extruded substrate that can be readily thermoformed into a shaped, three-dimensional article is provided. The substrate is formed from a polymer composition that contains a thermotropic liquid crystalline polymer and a unique aromatic amide oligomer. The present inventors have discovered that the oligomer can help increase the “low shear” complex viscosity of the resulting polymer. The ability to achieve enhanced low shear viscosity values can lead to polymer compositions with an increased melt strength, which allows the resulting substrate to better maintain its shape during thermoforming without exhibiting a substantial amount of sag. Due to its relatively high degree of melt strength, the polymer composition is particularly well suited for forming thin extruded substrates for use in thermoforming processes.

Abstract: A polyethylene powder has a molecular weight in the range of about 300,000 g/mol to about 2,000,000 g/mol as determined by ASTM-D 4020, an average particle size, D50, between about 300 and about 1500 ?m, and a bulk density between about 0.25 and about 0.5 g/ml. On sintering, the polyethylene powder produces a porous article having a porosity of at least 45% and a pressure drop less than 5 mbar. The porous article is useful in, for example, wastewater aeration and capillary and filtration applications.

Abstract: The present invention relates to a new molding powder comprising polyethylene polymer particles. The molecular weight of the polyethylene polymer is within the range of from about 600,000 g/mol to about 2,700,000 g/mol as determined by ASTM 4020. The average particle size of the particles of the polyethylene polymer is within the range of from about 5 microns to about 1000 microns and the polyethylene has a powder bulk density in the range of from about 0.10 to about 0.30 g/cc. Also disclosed is a process for molding a shape from a molding powder comprising the inventive polyethylene polymer particles, as well as porous articles made in accordance with the process. The articles have excellent porosity and good strength for porous and porous filtration applications.

Abstract: The invention relates to polyester compositions comprising a) a poly(cyclohexylene-dimethylene)terephthalate (PCT) resin, b) at least one copolyester elastomer and c) at least three ethylene copolymers chosen among c1) one or more ethylene alkyl-(meth)acrylate copolymers; c2) one or more ethylene acid copolymers and/or ionomers thereof; and c3) one or more ethylene epoxide copolymers. The disclosed polyester compositions are particularly well suited for manufacturing articles that maintain good mechanical properties against long-term high temperature exposure, i.e. for high temperature applications.