Chen, 2003 - Google Patents
Novel polymers with thermally controlled covalent cross-linkingChen, 2003
- Document ID
- 9302661875734271800
- Author
- Chen X
- Publication year
External Links
Snippet
The exploration of re-mending and self-healing of polymeric materials has become increasingly more exciting in the recent past. However, no highly cross-linked polymeric material could be healed in the absence of additional ingredients such as a catalyst …
- 229920000642 polymer 0 title description 215
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G73/00—Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
- C08G73/06—Polycondensates having nitrogen-containing heterocyclic rings in the main chain of the macromolecule
- C08G73/0622—Polycondensates containing six-membered rings, not condensed with other rings, with nitrogen atoms as the only ring hetero atoms
- C08G73/0638—Polycondensates containing six-membered rings, not condensed with other rings, with nitrogen atoms as the only ring hetero atoms with at least three nitrogen atoms in the ring
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G73/00—Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
- C08G73/06—Polycondensates having nitrogen-containing heterocyclic rings in the main chain of the macromolecule
- C08G73/10—Polyimides; Polyester-imides; Polyamide-imides; Polyamide acids or similar polyimide precursors
- C08G73/1003—Preparatory processes
- C08G73/1007—Preparatory processes from tetracarboxylic acids or derivatives and diamines
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/30—Low-molecular-weight compounds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G83/00—Macromolecular compounds not provided for in groups C08G2/00 - C08G81/00
- C08G83/002—Dendritic macromolecules
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G61/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
- C08G61/12—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G2261/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G75/00—Macromolecular compounds obtained by reactions forming a linkage containing sulfur with or without nitrogen, oxygen, or carbon in the main chain of the macromolecule
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Ratwani et al. | Self-healing by Diels-Alder cycloaddition in advanced functional polymers: A review | |
Tian et al. | A thermally remendable epoxy resin | |
Heo et al. | Self-healing polymers and composites for extreme environments | |
Kuang et al. | Facile fabrication of fast recyclable and multiple self‐healing epoxy materials through diels‐alder adduct cross‐linker | |
Heo et al. | Self‐healing polyurethanes with shape recovery | |
Burattini et al. | Healable polymeric materials: a tutorial review | |
Ishida et al. | Handbook of benzoxazine resins | |
Wilson et al. | Shape memory polymers based on uniform aliphatic urethane networks | |
Du et al. | Synthesis of linear polyurethane bearing pendant furan and cross-linked healable polyurethane containing Diels–Alder bonds | |
Fan et al. | Recyclable Diels–Alder furan/maleimide polymer networks with shape memory effect | |
Zhong et al. | Polyether–maleimide‐based crosslinked self‐healing polyurethane with Diels–Alder bonds | |
Bai et al. | Investigation of the thermal self-healing mechanism in a cross-linked epoxy system | |
Miao et al. | Eugenol-derived reconfigurable high-performance epoxy resin for self-deployable smart 3D structures | |
Wang et al. | Synthesis and Preparation of Bio‐Based ROMP Thermosets from Functionalized Renewable Isosorbide Derivative | |
Wang et al. | Design and synthesis of thermal contracting polymer with unique eight-membered carbocycle unit | |
Feng et al. | Tunable properties of novel tetra-functional fluorene-based benzoxazines from mixed amines: Synthesis, characterization and curing kinetics | |
Deng et al. | Insights into the Correlation of Cross‐linking Modes with Mechanical Properties for Dynamic Polymeric Networks | |
Hombunma et al. | Shape memory polymers from bio-based benzoxazine/epoxidized natural oil copolymers | |
Li et al. | Liquid crystalline networks based on photo-initiated thiol–ene click chemistry | |
Xu et al. | Formation of poly (ε-caprolactone) networks via supramolecular hydrogen bonding interactions | |
Xie et al. | High performance poly (methyl methacrylate) via hindered urea bond crosslinking | |
Zhao et al. | Synthesis and properties of strong and tough Diels–Alder self-healing crosslinked polyamides | |
Rashid et al. | A vanillin-derived hardener for recyclable, degradable and self-healable high-performance epoxy vitrimers based on transimination | |
Klein et al. | Reprocessable Vanillin‐Based Schiff Base Vitrimers: Tuning Mechanical and Thermomechanical Properties by Network Design | |
Chen | Novel polymers with thermally controlled covalent cross-linking |