4 results match your criteria: "Research Institute of Petroleum Progressing[Affiliation]"

Preparation of an Antibacterial Branched Polyamide 6 via Hydrolytic Ring-Opening Co-Polymerization of ε-Caprolactam and Lysine Derivative.

Polymers (Basel)

July 2024

State Key Laboratory of catalytic Material and Reaction Engineering, Research Institute of Petroleum Progressing, SINOPEC, 18th Xueyuan Road, Haidian District, Beijing 100083, China.

In this study, we successfully realized the hydrolytic ring-opening co-polymerization of ε-caprolactam (CPL) and lysine derivative. A novel antibacterial modified polyamide 6 with a branched structure was obtained after the quaternization of the co-polymers. The co-polymers exhibited a significant increase in zero shear viscosity, melt index and storage modulus at the low frequency region.

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Preparation of a Novel Branched Polyamide 6 (PA6) via Co-Polymerization of ε-Caprolactam and α-Amino-ε-Caprolactam.

Polymers (Basel)

June 2024

State Key Laboratory of Catalytic Material and Reaction Engineering, Research Institute of Petroleum Progressing, SINOPEC, 18th Xueyuan Road, Haidian District, Beijing 100083, China.

In this study, a novel branched polyamide 6 has been synthesized via the hydrolytic ring-opening co-polymerization of ε-caprolactam (CPL) and α-Amino-ε-caprolactam (ACL). The NMR characterization proves the existence of a branched chain structure. The rheological test determines that there is a remarkable increase in the melt index (MFR), zero shear rate viscosity, and storage modulus in the low-frequency region.

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Propylene is an important raw material in the chemical industry that needs new routes for its production to meet the demand. The CO-assisted oxidative dehydrogenation of propane (CO-ODHP) represents an ideal way to produce propylene and uses the greenhouse gas CO. The design of catalysts with high efficiency is crucial in CO-ODHP research.

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Functional polymers of nylon-6, particularly those with sustained antibacterial functions, have many practical applications. However, the development of functional ε-caprolactam monomers for the subsequent ring-opening copolymerization (ROCOP) formation of these materials remains a challenge. Here we report a -BuP-mediated ROCOP of dimethyl-protected cyclic lysine with ε-caprolactam, followed by quaternization, affording antibacterial nylon-6 polymers bearing quaternary ammonium functionality with high molecular weight (up to 77.

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