Abstract: A polyamide composition comprising from 15-70 wt % of a first polyamide; from 5-40 wt % of a second polyamide; from 0.01-10 wt % of a stabilizer comprising a lanthanoid-based compound; from 0.01-10 wt % of a first stabilizer comprising a copper-based compound; from 0.01-10 wt % of a second stabilizer comprising a copper-based compound; and from 20-65 wt % filler.

Abstract: A polyamide composition comprising from 25 wt % to 90 wt % of a first polyamide comprising a non-aromatic polyamide formed from 50 wt % to 90 wt % PA66; from 10-50 wt % of a second polyamide comprising a polyamide copolymer; from 0.01-10 wt % of a first stabilizer comprising a lanthanoid-based compound; from 0.01-10 wt % of a second stabilizer comprising a copper-based compound; and from 0-65 wt % filler.

Abstract: Provided herein is a polymer composition comprising an aromatic polyamide comprising terephthalic units and isophthalic units or a 6T/DT copolymer and having an overall high aromaticity, with a heat stabilizer and/or a lubricant. The polymer composition demonstrates improved electrical performance in terms of volume resistivity and dielectric strength.

Abstract: Polyamide resin that comprise one or more polyamides and a stabilizer component containing an copper complex and a copper salt is disclosed for improving the heat age performance for an article. The combination of a copper complex and a copper salt retains the mechanical properties of the article.

Abstract: An impact-modified polyamide composition comprising from 5 wt % to 85 wt % of polyamide polymer; from 10 wt % to 60 wt % glass fiber; from 3 wt % to 30 wt % of an impact modifier; and a melt stabilizer at a concentration less than 5 wt %; wherein the weight ratio of the impact modifier to the melt stabilizer ranges from 1.0:1 to 100:1; and wherein the polyamide composition demonstrates an un-notched Charpy impact energy loss at 23° C. that is greater than 80 kJ/m2 and a tensile strength greater than 135 MPa.

Abstract: A hydrolysis resistant polyamide composition comprising from 50 wt % to 80 wt % polyamide polymer having a theoretical amine end group content of at least 55 ?eq/gram; and from 25 wt % to 60 wt % glass fibers. The weight ratio of polyamide polymer to glass fibers ranges from 0.5:1 to 4.0:1. The polyamide composition comprises less than 0.06 wt % copper; and/or from 1 ppb to 0.24 wt % non-copper metal halide compound. The polyamide composition, when hydrolysis aged for 500 hours at 130° C., demonstrates an impact resilience greater than 40 kJ/m2, as measured at 23° C.

Abstract: The present disclosure relates to polyamide compositions and resulting injection-molded articles that can be plated, e.g., metal coated, to form aesthetic injection-molded articles. The polyamide compositions may include from 45 wt. % to 75 wt. % of an polyamide, from 2 wt. % to 40 wt. % of an etchable filler, from 10 wt. % to 40 wt. % of a semi-structural mineral, and optionally from 0.1 wt. % to 13 wt. % of additive. The polyamide composition imparts very good surface appearance to injection-molded articles that are substantially free of visual defects.

Abstract: The present disclosure relates to polyamide compositions and resulting injection-molded articles that can be plated, e.g., metal coated, to form structurally aesthetic injection-molded articles. The polyamide compositions may include from 40 wt. % to 80 wt. % of a polyamide, from 0.5 wt. % to 40 wt. % of an etchable filler, from 5 wt. % to 30 wt. % of glass fiber, optionally less than 40 wt. % of a semi-structural mineral, and optionally from 0.1 wt. % to 13 wt. % of additive. The polyamide composition imparts very good surface appearance and excellent mechanical properties to injection-molded articles that are substantially free of visual defects.

Abstract: A polyamide composition comprising from 45 wt % to 95 wt % of polyamide polymer and from 5 wt % to 55 wt % of a modifier comprising a C18-44 dimer acid or a C18-44 dimer amine or a combination thereof. A number average molecular weight of the polyamide polymer is less than 30,000 g/mol. The polyamide composition has a chemical resistance, as measured by exposure to HCl (10%) for 14 days at 58° C., resulting in a weight loss of less than 3.0 wt %; and a moisture uptake of less than about 2.0 wt % moisture at 95% RH. A process for preparing the polyamide composition is also disclosed.

Abstract: Provided herein are polyamide compositions including one or more semi-crystalline polyamides and either an amorphous polyamide or a semi-crystalline copolyamide such as PA66/6. The provided compositions are particularly useful as vibration isolators more effective at high-temperature noise and harshness damping than conventional polyamide compositions. Also provided are methods for making the provided compositions, and articles that include the provided compositions.

Abstract: A polymer composition for molded products having antimicrobial and/or antiviral properties comprising from 50 wt. % to 99.9 wt. % of a polymer, from 0.01 wt % to 10 wt % zinc, optionally from a zinc compound, less than 1 wt % of a phosphorus compound, and from 0 wt % to 20 wt % molding additives, wherein a molded product formed from the polymer composition demonstrates a Staphylococcus aureus log reduction greater than 1.0, as determined via ISO 22196:2011.

Abstract: A hydrolysis resistant polyamide composition comprising from 50 wt % to 80 wt % polyamide polymer having a theoretical amine end group content of at least 55 ?eq/gram; and from 25 wt % to 60 wt % glass fibers. The weight ratio of polyamide polymer to glass fibers ranges from 0.5:1 to 4.0:1. The polyamide composition comprises less than 0.06 wt % copper; and/or from 1 ppb to 0.24 wt % non-copper metal halide compound. The polyamide composition, when hydrolysis aged for 500 hours at 130° C., demonstrates an impact resilience greater than 40 kJ/m2, as measured at 23° C.

Abstract: A heat-stabilized polyamide composition comprising from 25 wt % to 99 wt % of an amide polymer having an amine end group level greater than 50 ?eq/gram; a first stabilizer comprising a lanthanoid-based compound; a second stabilizer; and from 0 wt % to 65 wt % filler; wherein, when heat aged for 3000 hours over a temperature range of from 190° C. to 220° C., the polyamide composition demonstrates a tensile strength retention of greater than 51%, as measured at 23° C.

Abstract: An impact-modified polyamide composition comprising from 5 wt % to 85 wt % of polyamide polymer; from 10 wt % to 60 wt % glass fiber; from 3 wt % to 30 wt % of an impact modifier; and a melt stabilizer at a concentration less than 5 wt %; wherein the weight ratio of the impact modifier to the melt stabilizer ranges from 1.0:1 to 100:1; and wherein the polyamide composition demonstrates an un-notched Charpy impact energy loss at 23° C. that is greater than 80 kJ/m2 and a tensile strength greater than 135 MPa.

Abstract: A method and apparatus that includes isolating a sample having a known volume and obtained near a reservoir that has a reserve; extracting hydrocarbons from the sample; and identifying data associated with the hydrocarbons. The data may include the volume of the extracted hydrocarbons. The method also includes using the data to estimate the reserve of the reservoir. The method can also include pulverizing the sample to release additional hydrocarbons.

Abstract: The present disclosure relates to polyamide compositions and resulting injection-molded articles that can be plated, e.g., metal coated, to form aesthetic injection-molded articles. The polyamide compositions may include from 45 wt. % to 75 wt. % of an polyamide, from 2 wt. % to 40 wt. % of an etchable filler, from 10 wt. % to 40 wt. % of a semi-structural mineral, and optionally from 0.1 wt. % to 13 wt. % of additive. The polyamide composition imparts very good surface appearance to injection-molded articles that are substantially free of visual defects.

Abstract: The present disclosure relates to polyamide compositions and resulting injection-molded articles that can be plated, e.g., metal coated, to form structurally aesthetic injection-molded articles. The polyamide compositions may include from 40 wt. % to 80 wt. % of a polyamide, from 0.5 wt. % to 40 wt. % of an etchable filler, from 5 wt. % to 30 wt. % of glass fiber, optionally less than 40 wt. % of a semi-structural mineral, and optionally from 0.1 wt. % to 13 wt. % of additive. The polyamide composition imparts very good surface appearance and excellent mechanical properties to injection-molded articles that are substantially free of visual defects.

Abstract: A heat-stabilized polyamide composition comprising from 25 wt % to 90 wt %% of an amide polymer from 0.01 wt % to 10 wt % of a cerium-based heat stabilizer, a second heat stabilizer, a halide additive, and less than 0.3 wt % of a stearate additive. A weight ratio of halide additive to stearate additive is less than 45.0.

Abstract: The present invention relates to compositions for treatment of subterranean formations including a curable resin that is amine-curable and a curing agent having a structure including at least one primary amine and at least one secondary amine, and methods of using the same. In various embodiments, the present invention provides a method of treating a subterranean formation. The method can include obtaining or providing a composition including a curable resin that is amine-curable and a curing agent having a structure including at least one primary amine and at least one secondary amine. The method can include placing the composition in a subterranean formation downhole.

Abstract: A treatment fluid is described suitable for use in subterranean formations comprising an aqueous phase, a carboxymethyl hydroxyethyl cellulose, and a breaker. The aqueous phase comprises water having at least 1,000 ppm total dissolved inorganic salts and at least one of: a sulfate concentration of about 4,000 ppm or greater, a phosphate concentration of about 100 ppm or greater, a carbonate concentration of about 100 ppm or greater, or a barium concentration of about 37,000 ppm or greater. The carboxymethyl hydroxyethyl cellulose has a carboxymethyl degree of substitution in the range of about 0.3 to about 0.45 per glucopyranose unit in the carboxymethyl hydroxyethyl cellulose polymer; and a hydroxyethyl molecular substitution in the range of about 2.1 to about 2.9 per glucopyranose unit in the carboxymethyl hydroxyethyl cellulose polymer; The treatment fluid is substantially free of any crosslinker.