[go: up one dir, main page]
More Web Proxy on the site http://driver.im/

Liu et al., 2010 - Google Patents

Non‐isothermal crystallization kinetics of poly (L‐lactide)

Liu et al., 2010

View PDF
Document ID
10043305670601373130
Author
Liu Y
Wang L
He Y
Fan Z
Li S
Publication year
Publication venue
Polymer International

External Links

Snippet

The non‐isothermal crystallization kinetics of poly (l‐lactide)(PLLA) in comparison with a polylactide stereocopolymer (PLA98) containing 98% l‐lactyl and 2% d‐lactyl units were investigated using differential scanning calorimetry to examine the effect of the …
Continue reading at hal.science (PDF) (other versions)

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G63/00Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
    • C08G63/02Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
    • C08G63/06Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from hydroxycarboxylic acids
    • C08G63/08Lactones or lactides
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G63/00Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
    • C08G63/91Polymers modified by chemical after-treatment
    • C08G63/912Polymers modified by chemical after-treatment derived from hydroxycarboxylic acids

Similar Documents

Publication Publication Date Title
Liu et al. Non‐isothermal crystallization kinetics of poly (L‐lactide)
Di Lorenzo Calorimetric analysis of the multiple melting behavior of poly (L‐lactic acid)
Kim et al. Structural effect of linear and star‐shaped poly (L‐lactic acid) on physical properties
He et al. DSC analysis of isothermal melt-crystallization, glass transition and melting behavior of poly (l-lactide) with different molecular weights
Papageorgiou et al. Crystallization kinetics of biodegradable poly (butylene succinate) under isothermal and non‐isothermal conditions
Kai et al. Fast crystallization of poly (3‐hydroxybutyrate) and poly (3‐hydroxybutyrate‐co‐3‐hydroxyvalerate) with talc and boron nitride as nucleating agents
Pan et al. Polymorphous crystallization and multiple melting behavior of poly (L-lactide): molecular weight dependence
Gunaratne et al. Multiple melting behaviour of poly (3-hydroxybutyrate-co-hydroxyvalerate) using step-scan DSC
Chan et al. Crystallization and melting behavior of poly (3‐hydroxybutyrate)‐based blends
Rahaman et al. Isothermal crystallization and spherulite growth behavior of stereo multiblock poly (lactic acid) s: effects of block length
Davachi et al. Synthesis and characterization of a novel terpolymer based on L‐lactide, glycolide, and trimethylene carbonate for specific medical applications
Luo et al. The effect of molecular weight on the lamellar structure, thermal and mechanical properties of poly (hydroxybutyrate-co-hydroxyvalerates)
Henricks et al. Crystallization kinetics and structure evolution of a polylactic acid during melt and cold crystallization
Furuhashi et al. Stereocomplexation of solvent‐cast poly (lactic acid) by addition of non‐solvents
Jalali et al. Effect of molecular weight on the nucleation efficiency of poly (lactic acid) crystalline phases
Xu et al. Crystallization kinetics and morphology of biodegradable poly (butylene succinate‐co‐propylene succinate) s
Park et al. Crystallization behaviour of poly (butylene succinate) copolymers
Cai et al. Miscibility and crystallization of biodegradable poly (3‐hydroxybutyrate‐co‐3‐hydroxyhexanoate)/poly (vinyl phenol) blends
Yang et al. Nonisothermal crystallization behavior of the poly (ethylene glycol) block in poly (l‐lactide)–poly (ethylene glycol) diblock copolymers: Effect of the poly (l‐lactide) block length
Andjelić et al. Crystallization study on absorbable poly (p‐dioxanone) polymers by differential scanning calorimetry
Blumer et al. Crystallinity and Property Enhancements in Neat Polylactic Acid by Chilled Extrusion: Solid‐State Shear Pulverization and Solid‐State/Melt Extrusion
Chae et al. Effect of methyl substitution of the ethylene unit on the physical properties of poly (butylene succinate)
Wei et al. Thermophysical properties of bacterial poly (3‐hydroxybutyrate): Characterized by TMA, DSC, and TMDSC
Huang et al. Isothermal crystallization behavior of poly (l‐lactide) in poly (l‐lactide)‐block‐poly (ethylene glycol) diblock copolymers
Ravari et al. Non-isothermal cold crystallization behavior and kinetics of poly (l-lactide): effect of l-lactide dimer