Fernández‐García et al., 2001 - Google Patents
Glass Transition Temperatures of Poly [(methyl methacrylate)‐co‐(butyl acrylate)] s Synthesized by Atom‐Transfer Radical PolymerizationFernández‐García et al., 2001
- Document ID
- 5469933997445613249
- Author
- Fernández‐García M
- de la Fuente J
- Fernández‐Sanz M
- Madruga E
- Publication year
- Publication venue
- Macromolecular Rapid Communications
External Links
Snippet
Glass transition temperatures Tg of methyl methacrylate/butyl acrylate copolymers obtained by means of atom‐transfer radical polymerization are measured using differential scanning calorimetry. Due the nature of this polymerization method an increase in molecular weight is …
- 239000011521 glass 0 title abstract description 29
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/10—Esters
-
- 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
- C08G61/122—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule derived from five- or six-membered heterocyclic compounds, other than imides
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F297/00—Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer
- C08F297/06—Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer using a catalyst of the coordination type
- C08F297/08—Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer using a catalyst of the coordination type polymerising mono-olefins
- C08F297/083—Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer using a catalyst of the coordination type polymerising mono-olefins the monomers being ethylene or propylene
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F297/00—Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer
- C08F297/02—Macromolecular compounds obtained by successively polymerising different monomer systems using a catalyst of the ionic or coordination type without deactivating the intermediate polymer using a catalyst of the anionic type
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F226/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a single or double bond to nitrogen or by a heterocyclic ring containing nitrogen
- C08F226/06—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a single or double bond to nitrogen or by a heterocyclic ring containing nitrogen by a heterocyclic ring containing nitrogen
- C08F226/10—N-Vinyl-pyrrolidone
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F293/00—Macromolecular compounds obtained by polymerisation on to a macromolecule having groups capable of inducing the formation of new polymer chains bound exclusively at one or both ends of the starting macromolecule
- C08F293/005—Macromolecular compounds obtained by polymerisation on to a macromolecule having groups capable of inducing the formation of new polymer chains bound exclusively at one or both ends of the starting macromolecule using free radical "living" or "controlled" polymerisation, e.g. using a complexing agent
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F210/00—Copolymers of unsaturated aliphatic hydrocarbon having only one carbon-to-carbon double bond
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F224/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a heterocyclic ring containing oxygen
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Simon et al. | Hyperbranched methacrylates by self‐condensing group transfer polymerization | |
Jayakumar et al. | Studies on copolymers of 2-(N-phthalimido) ethyl methacrylate with methyl methacrylate | |
Fernández-Garcıa et al. | Free radical copolymerization of 2-hydroxyethyl methacrylate with butyl methacrylate: determination of monomer reactivity ratios and glass transition temperatures | |
Fernández–García et al. | Glass transition temperatures of butyl acrylate–methyl methacrylate copolymers | |
Guo et al. | Tailor-made compositional gradient copolymer by a many-shot RAFT emulsion polymerization method | |
Yang et al. | Equilibrium constants and predictions of miscibility windows and maps for polymer blends involving p-(hexafluoro-2-hydroxy-2-propyl) styrene with methacrylate and acetoxy groups | |
Driva et al. | Radical copolymerization of 2-vinyl pyridine and oligo (ethylene glycol) methyl ether methacrylates: Monomer reactivity ratios and thermal properties | |
Kowalczuk-Bleja et al. | Core-shell polyacrylate and polystyrene-block-polyacrylate stars | |
Fernández‐García et al. | Glass Transition Temperatures of Poly [(methyl methacrylate)‐co‐(butyl acrylate)] s Synthesized by Atom‐Transfer Radical Polymerization | |
Li et al. | Living cationic random copolymerization of β-pinene and isobutylene with 1-phenylethyl chloride/TiCl4/Ti (OiPr) 4/nBu4NCl | |
Godwin et al. | Homopolymer of 4-propanoylphenyl methacrylate and its copolymers with glycidyl methacrylate: synthesis, characterization, reactivity ratios and application as adhesives | |
Fernández-Garcı́a et al. | Preparation of poly (tert-butyl acrylate-g-styrene) as precursors of amphiphilic graft copolymers. 1. Kinetic study and thermal properties | |
Stergiou et al. | Radical copolymerization of styrene and alkyl methacrylates: monomer reactivity ratios and thermal properties | |
Su et al. | Syntheses and properties of poly (B-vinylborazine) and poly (styrene-co-B-vinylborazine) copolymers | |
Jedliński et al. | Anionic block polymerization of β‐lactones initiated by potassium solutions, 1. Synthesis of poly (4‐methyl‐2‐oxetanone‐block‐2‐oxetanone) | |
Gunaydin et al. | Copolymers of glycidyl methacrylate with 3-methylthienyl methacrylate: synthesis, characterization and reactivity ratios | |
Balaji et al. | Copolymerization of 3-methoxy-4-methacryloyloxybenzal phenylimine with methyl methacrylate | |
Sannigrahi et al. | Copolymerization of methyl methacrylate with lauryl methacrylate using group transfer polymerization | |
Madruga et al. | High conversion copolymerization of di-n-butyl itaconate with methyl methacrylate in benzene solution | |
Karra et al. | Radical copolymerization of 2-vinyl pyridine with functional methacrylates: monomer reactivity ratios and thermal properties | |
París et al. | Gelation-free synthesis of poly (allyl methacrylate-co-butyl acrylate) copolymers by atom transfer radical polymerization | |
Matsumoto et al. | Poly (N‐n‐butylitaconimide). Preparation and characterization | |
Makrikosta et al. | Statistical copolymers of styrene and 2-vinylpyridine with trimethylsilyl methacrylate and trimethylsilyloxyethyl methacrylate | |
Senthilkumar et al. | Synthesis, characterization and reactivity ratios of phenylethyl acrylate/methacrylate copolymers | |
Percec et al. | Intramolecular Charge Transfer Complexes. 4. Poly (N-(2-hydroxyethyl) carbazolyl Acrylate-co-Picryl Methacrylate) |