Ratio of the glass transition temperature to the melting point in polymers

1970 ◽  
Vol 2 (1) ◽  
pp. 73-80 ◽  
Author(s):  
W. A. Lee ◽  
G. J. Knight
Keyword(s):  
Glass Transition ◽  
Transition Temperature ◽  
Glass Transition Temperature ◽  
Melting Point

Elastomer Structures and ‘Cold Crystallization’

1979 ◽  
Vol 52 (1) ◽  
pp. 207-212 ◽  
Author(s):  
M. Bruzzone ◽  
E. Sorta
Keyword(s):  
Glass Transition ◽  
Transition Temperature ◽  
Glass Transition Temperature ◽  
Melting Point ◽  
Natural Rubber ◽  
Crystallization Rate ◽  
Cold Crystallization ◽  
Structural Defects ◽  
Strain Induced Crystallization ◽  
Induced Crystallization

Abstract In a great number of applications an ideal elastomer should satisfy, to a certain extent, both of the following requirements: (1) nearly instantaneous crystallization upon application of strain (strain induced crystallization) and (2) slow or no crystallization when cooled at the temperature of maximum crystallization rate (cold induced crystallization). A noteworthy case of (2) is elastomer crystallization in a strained state. The connection between the points (1) and (2) has not been clearly understood up to now, but it is known that some crystallizable elastomers fulfil the requirements of both (1) and (2) better than others. From an experimental point of view, cold induced crystallization kinetics are substantially easier to measure than those of very fast strain induced crystallization. The phenomenon of cold induced crystallization in natural rubber, NR, has been known since the very beginning of elastomer technology and the tendency of natural rubber to crystallize by cooling has been overcome by crosslinking it with sulphur (vulcanization) without impairing its ability to crystallize by stretching (Goodyear, 1836). The synthesis of cis-polyisoprenes (IR) and cis-polybutadiene (BR) of different microstructural purity (different cis content) gave the possibility of changing the crystallization rate. It has also been reported that the very fast cold crystallization of trans-polypentenamer (TPA) could be reduced by lowering the trans content. The same fact had been observed earlier for trans-polychloroprene. There is a general agreement in postulating that the reduction of the crystallization rate, obtained either by cross-linking or by chain regularity reduction, can be linked with the lowering of the melting point. In both cases the low level of structural defects introduced in the chains does not affect the glass transition temperature in such a way as to vary the crystallization rate. The aim of this paper is to emphasize the importance of the variations of the glass transition temperature and melting point on the elastomeric cold crystallization rate and the way these may be used in planning new elastomer structures.

Determination of the Melting Point and Glass Transition Temperature of Polymers with the Lattice Model

2005 ◽  
Vol 37 (1) ◽  
pp. 31-34 ◽  
Author(s):  
V. F. Skorodumov ◽  
A. V. Motavkin ◽  
E. M. Pokrovskii
Keyword(s):  
Glass Transition ◽  
Transition Temperature ◽  
Glass Transition Temperature ◽  
Melting Point ◽  
Lattice Model

scholarly journals Predicting the influence of particle size on the glass transition temperature and viscosity of secondary organic material

2020 ◽  
Vol 10 (1) ◽  
Author(s):  
Markus Petters ◽  
Sabin Kasparoglu
Keyword(s):  
Particle Size ◽  
Glass Transition ◽  
Transition Temperature ◽  
Glass Transition Temperature ◽  
Melting Point ◽  
Critical Role ◽  
Particle Diameter ◽  
Cloud Formation ◽  
Melting Point Depression ◽  
Wide Range

Abstract Atmospheric aerosols can assume liquid, amorphous semi-solid or glassy, and crystalline phase states. Particle phase state plays a critical role in understanding and predicting aerosol impacts on human health, visibility, cloud formation, and climate. Melting point depression increases with decreasing particle diameter and is predicted by the Gibbs–Thompson relationship. This work reviews existing data on the melting point depression to constrain a simple parameterization of the process. The parameter $$\xi $$ ξ describes the degree to which particle size lowers the melting point and is found to vary between 300 and 1800 K nm for a wide range of particle compositions. The parameterization is used together with existing frameworks for modeling the temperature and RH dependence of viscosity to predict the influence of particle size on the glass transition temperature and viscosity of secondary organic aerosol formed from the oxidation of $$\alpha $$ α -pinene. Literature data are broadly consistent with the predictions. The model predicts a sharp decrease in viscosity for particles less than 100 nm in diameter. It is computationally efficient and suitable for inclusion in models to evaluate the potential influence of the phase change on atmospheric processes. New experimental data of the size-dependence of particle viscosity for atmospheric aerosol mimics are needed to thoroughly validate the predictions.

Thermal Properties of Hyperbranched Polymer/HTPB-PU IPN

2013 ◽  
Vol 575-576 ◽  
pp. 76-80
Author(s):  
Xue Jing Song ◽  
Yun Jun Luo
Keyword(s):  
Differential Scanning Calorimetry ◽  
Glass Transition ◽  
Thermal Properties ◽  
Transition Temperature ◽  
Glass Transition Temperature ◽  
Melting Point ◽  
Hyperbranched Polymer ◽  
Isophorone Diisocyanate ◽  
Scanning Calorimetry

Hyperbranched polymer/HTPB-PU IPNs were prepared, when HTPB (hydroxyl-terminated polybutadiene) and IPDI (isophorone diisocyanate) were cured into polyurethane (HTPB-PU) at the existence of hyperbranched polymer. Differential scanning calorimetry (DSC) was adopted to study the influence of hyperbranched polymer on thermal properties of HTPB-PU, while IPNs were formed. The result shows that the existance of hyperbranched polymer makes glass transition temperature of HTPB-PU reduces by around 2°C and that HTPB-PU lowers the melting point of hyperbranched polymer. Hyperbranched polymer plays a role of internal plasticization on HTPB-PU, and HTPB-PU influences crystallization of hyperbranched polymer in return.

scholarly journals Biosynthesis and Biodegradation of 3-Hydroxypropionate- Containing Polyesters

2010 ◽  
Vol 76 (15) ◽  
pp. 4919-4925 ◽  
Author(s):  
Bj�rn Andree�en ◽  
Alexander Steinb�chel
Keyword(s):  
Glass Transition ◽  
Transition Temperature ◽  
Glass Transition Temperature ◽  
Melting Point ◽  
Physical Properties ◽  
Chemical Industry

ABSTRACT 3-Hydroxypropionate (3HP) is an important compound in the chemical industry, and the polymerized 3HP can be used as a bioplastic. In this review, we focus on polyesters consisting of 3HP monomers, including the homopolyester poly(3-hydroxypropionate) and copolyesters poly(3-hydroxybutyrate-co-3-hydroxypropionate), poly(3-hydroxypropionate-co-3-hydroxybutyrate-co-3-hydroxyhexanoate-co-3-hydroxyoctanoate), poly(4-hydroxybutyrate-co-3-hydroxypropionate-co-lactate), and poly(3-hydroxybutyrate-co-3-hydroxypropionate-co-4-hydroxybutyrate-co-lactate). Homopolyesters like poly(3-hydroxybutyrate) are often highly crystalline and brittle, which limits some of their applications. The incorporation of 3HP monomers reduces the glass transition temperature, the crystallinity, and also, at up to 60 to 70 mol% 3HP, the melting point of the copolymer. This review provides a survey of the synthesis and physical properties of different polyesters containing 3HP.

Effect of Temperature and Catalyst Concentrations on the Thermal Properties of Polyamide Adhesives at Low Operating Pressure

2010 ◽  
Vol 5 (1) ◽  
Author(s):  
Nayef M. Ghasem
Keyword(s):  
Weight Loss ◽  
Glass Transition ◽  
Thermal Properties ◽  
Transition Temperature ◽  
Glass Transition Temperature ◽  
Melting Point ◽  
Reaction Temperature ◽  
Catalyst Concentration ◽  
Sample Weight ◽  
Sample Weight Loss

The polyamides used for hot-melt adhesives were synthesized from C36 dimer fatty acids and ethylenediamine under 200 mmHg and atmospheric pressures. The kinetics of the reaction rate at low pressure and the effect on the thermal properties of the produced polyamide adhesive were experimentally investigated. The effects of reaction temperature and catalyst concentration on polyamide melting point, glass transition temperature, sample weight loss and foaming height were studied. The kinetic rate constants were obtained for polymerization reaction carried out at three different reaction temperatures, 115, 120, and 135 °C, fixed mixing rate of 100 rpm and low operation pressure of 200 mmHg. Polymers produced at atmospheric pressure and reaction temperatures 140, 170, 180, and 190 °C where used to investigate the polyamide thermal properties using thermal gravimetric analysis (TGA) and differential scanning calorimetry (DSC). Thermal properties such as melting point, glass transition temperature and the temperature at which 5% and 10% weight loss were recorded by TGA at a heating rate of 10 C/min in N2 atmosphere. The effect of foaming height as a function of reaction temperature and catalyst concentration was measured. The analysis makes known that the reaction temperature and catalyst concentration has a noteworthy impact on the glass transition temperature, foam height and melting point and insignificant effect on the sample weight loss.

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