Photoinduced plasticizing effect of the addition of azobenzene on the glass transition temperature and mechanical properties of polycarbonate

2022 ◽  
Author(s):  
Mai Maeda ◽  
Shogo Nobukawa ◽  
Katsuhiro Inomata
Keyword(s):  
Mechanical Properties ◽  
Glass Transition ◽  
Transition Temperature ◽  
Glass Transition Temperature

scholarly journals Studies on the Modification of Commercial Bisphenol-A-Based Epoxy Resin Using Different Multifunctional Epoxy Systems

2021 ◽  
Vol 2 (2) ◽  
pp. 419-430
Author(s):  
Ankur Bajpai ◽  
James R. Davidson ◽  
Colin Robert
Keyword(s):  
Mechanical Properties ◽  
Glass Transition ◽  
Transition Temperature ◽  
Glass Transition Temperature ◽  
Bisphenol A ◽  
Epoxy Resin ◽  
Tensile Fracture ◽  
Chemical Structures ◽  
Amino Phenol ◽  
Epoxy Systems

The tensile fracture mechanics and thermo-mechanical properties of mixtures composed of two kinds of epoxy resins of different chemical structures and functional groups were studied. The base resin was a bi-functional epoxy resin based on diglycidyl ether of bisphenol-A (DGEBA) and the other resins were (a) distilled triglycidylether of meta-amino phenol (b) 1, 6–naphthalene di epoxy and (c) fluorene di epoxy. This research shows that a small number of multifunctional epoxy systems, both di- and tri-functional, can significantly increase tensile strength (14%) over neat DGEBA while having no negative impact on other mechanical properties including glass transition temperature and elastic modulus. In fact, when compared to unmodified DGEBA, the tri-functional epoxy shows a slight increase (5%) in glass transition temperature at 10 wt.% concentration. The enhanced crosslinking of DGEBA (90 wt.%)/distilled triglycidylether of meta-amino phenol (10 wt.%) blends may be the possible reason for the improved glass transition. Finally, the influence of strain rate, temperature and moisture were investigated for both the neat DGEBA and the best performing modified system. The neat DGEBA was steadily outperformed by its modified counterpart in every condition.

scholarly journals Synthesis, Properties, and Biodegradability of Thermoplastic Elastomers Made from 2-Methyl-1,3-propanediol, Glutaric Acid and Lactide

Life ◽  
2021 ◽  
Vol 11 (1) ◽  
pp. 43
Author(s):  
Lamya Zahir ◽  
Takumitsu Kida ◽  
Ryo Tanaka ◽  
Yuushou Nakayama ◽  
Takeshi Shiono ◽  
...  
Keyword(s):  
Mechanical Properties ◽  
Glass Transition ◽  
Transition Temperature ◽  
Glass Transition Temperature ◽  
Glutaric Acid ◽  
Triblock Copolymers ◽  
Tensile Tests ◽  
Thermoplastic Elastomers ◽  
Proteinase K ◽  
Synthesis Properties

An innovative type of biodegradable thermoplastic elastomers with improved mechanical properties from very common and potentially renewable sources, poly(L-lactide)-b-poly(2-methyl-1,3-propylene glutarate)-b-poly(L-lactide) (PLA-b-PMPG-b-PLA)s, has been developed for the first time. PLA-b-PMPG-b-PLAs were synthesized by polycondensation of 2-methyl-1,3-propanediol and glutaric acid and successive ring-opening polymerization of L-lactide, where PMPG is an amorphous central block with low glass transition temperature and PLA is hard semicrystalline terminal blocks. The copolymers showed glass transition temperature at lower than −40 °C and melting temperature at 130–152 °C. The tensile tests of these copolymers were also performed to evaluate their mechanical properties. The degradation of the copolymers and PMPG by enzymes proteinase K and lipase PS were investigated. Microbial biodegradation in seawater was also performed at 27 °C. The triblock copolymers and PMPG homopolymer were found to show 9–15% biodegradation within 28 days, representing their relatively high biodegradability in seawater. The macromolecular structure of the triblock copolymers of PLA and PMPG can be controlled to tune their mechanical and biodegradation properties, demonstrating their potential use in various applications.

Plasticization of poly(vinyl butyral) by water: Glass transition temperature and mechanical properties

2018 ◽  
Vol 136 (12) ◽  
pp. 47230 ◽  
Author(s):  
Marlène Desloir ◽  
Cyril Benoit ◽  
Amine Bendaoud ◽  
Pierre Alcouffe ◽  
Christian Carrot
Keyword(s):  
Mechanical Properties ◽  
Glass Transition ◽  
Transition Temperature ◽  
Glass Transition Temperature ◽  
Water Glass ◽  
Vinyl Butyral

scholarly journals INFLUENCE OF ENVIRONMENTAL FACTORS ON PHYSICAL-MECHANICAL PROPERTIES OF POLYDIMETHYL ETHER OF NORBORENE -2;3-DICARBOXYLIC ACID

2017 ◽  
Vol 60 (5) ◽  
pp. 68 ◽  
Author(s):  
Galina S. Bozhenkova ◽  
Alexandra N. Tarakanovskaya ◽  
Oksana D. Tarnovskaya ◽  
Roman V. Ashirov
Keyword(s):  
Mechanical Properties ◽  
Glass Transition ◽  
Transition Temperature ◽  
Glass Transition Temperature ◽  
Hydrochloric Acid ◽  
Environmental Factors ◽  
Dicarboxylic Acid ◽  
Uv Radiation ◽  
Accelerated Aging ◽  
The Impact

The article is devoted to the production of polymer by metathesis ring-opening polymerization under the influence of ruthenium initiator of type of Hoveyda-Grubbs II generation. The monomer used the mixture of dimethyl ether norbornene-2;3-dicarboxylic acid. The monomer was prepared by the Diels-Alder reaction of dicyclopentadiene and dimethyl maleate. The polymer was prepared in bulk of the monomer mixture. In this paper we have studied the physical and mechanical properties polydimethyl ether of norbornene-2;3-dicarboxylic acid; and assessed the impact of environmental factors on the change in properties of the polymer. As environmental factors; light; UV radiation; water; 0.1 M hydrochloric acid were applied; and accelerated aging conditions; which were held in a climate chamber. During performance we found that maintaining the polymer samples in the UV light chamber led to the slight increase in flexural modulus. In contrast; the polymer storage in water and in a hydrochloric acid solution for two months resulted in a slight decrease in the modulus of elasticity in bending index. These factors did not affect the change in the glass transition temperature of the polymer. Under the conditions of accelerated aging conducted for 1; 2 and 6 days after two cycles we observed the drop in modulus for bending of 8.5%; after 6 cycles of 13%. The glass transition temperature of polydimethyl ether of norbornene-2;3-dicarboxylic acid after 6 cycles decreased by only 3.4% in the climatic chamber. Studies have shown that the resulting polymer is resistant to water; hydrochloric acid; light and UV radiation; as well as it saves properties at a sufficient level for operation at conditions of accelerated aging. It should be noted that the tested polymer was prepared without additives; stabilizers and antioxidants. The proposed polymer can be used as a structural material for machine parts; including bulky.For citation:Bozhenkova G.S.; Tarakanovskaya A.N.; Tarnovskaya O.D.; Ashirov R.V. Influence of environmental factors on physical-mechanical properties of polydimethyl ether of norborene -2;3-dicarboxylic acid. Izv. Vyssh. Uchebn. Zaved. Khim. Khim. Tekhnol. 2017. V. 60. N 5. P. 68-73

scholarly journals SiO2 particles effect on the mechanical properties of the starch/PVA blends

2018 ◽  
Vol 16 (36) ◽  
pp. 153-171
Author(s):  
Nahida J. H.
Keyword(s):  
Mechanical Properties ◽  
Glass Transition ◽  
Transition Temperature ◽  
Glass Transition Temperature ◽  
Ultimate Strength ◽  
Thermo Gravimetric Analysis ◽  
Polymer System ◽  
Optical Microscope ◽  
Gravimetric Analysis ◽  
Ratio Increase

The present work studies the mechanical properties of SiO2 μPs, and NPs in St/PVA blends. The samples were prepared by casting method as PVA, St/PVA blends at different concentrations (30, 40, 50, and 60 %). DSC and TGA tests were carried out to the samples evolved. The result showed a single glass transition temperature (Tg) for all St /PVA blends that was attributed to the good miscibility of the blends involved. It was found that (Tg) decrease with starch ratio increase. It was seen that (PVA) of (Tg=105 oC); The glass transition temperature which was decrease with starch ratio that was attributed to glass transition relaxation process due to micro-Brownian motion of the main chain back bond. The endothermic peak at 200 oC was attributed to melting point of (PVA). Thermal properties of PVA; and St /PVA blends at different concentration (30, 40, 50, and 60 %) were evaluated by thermo gravimetric analysis (TGA). The analyses were carried out from 20 to 600 oC at 10 oC)/min heating rate in air oxygen atmosphere. The weight loss stages depended on polymer system. The starch addition causing shifting in the second degradation temperature to the higher temperature; which result in overlapping between the two main degradation steps, these result was attributed to the St/ PVA blend compatibility. The mechanical properties results showed a decrease in ultimate strength with starch ratio increase. The ultimate strength of (PVA) was (47 MPa), whereas the ultimate strength of 60 %St/PVA was (11 MPa) and for 30 %St/PVA was the highest ultimate strength of blends involved (26 MPa). SiO2μPs (753.7 nm), and NPs (263.1 nm) were added at different concentrations (1.5, 2, and 2.5 %). 1.5% SiO2μPs, and NPs of the best ultimate strength (69 MPa), (86 MPa) respectively then it was decreased by SiO2μPs, and NPs increase. Optical microscope of the samples involved was investigated. It was concluded the prepared samples were suggested to be used as packaging materials for agriculture application and its ultimate strength could be controlled by SiO2μPs, and NPs addition.

The Effects of Chemical Resistance for Nanocomposite Materials via Nano-Silica Addition into Glass Fiber/Epoxy

2013 ◽  
Vol 853 ◽  
pp. 28-33
Author(s):  
Huey Ling Chang ◽  
Chih Ming Chen ◽  
Kung Liang Lin ◽  
Bor Kae Chang
Keyword(s):  
Mechanical Properties ◽  
Glass Transition ◽  
Transition Temperature ◽  
Glass Transition Temperature ◽  
Glass Fiber ◽  
Epoxy Resin ◽  
Storage Modulus ◽  
Chemical Resistance ◽  
Dynamic Mechanical Properties ◽  
Silica Nanopowder

Nanocomposite samples containing epoxy resin, glass fiber and 0~2 wt.% SiO2 nanopowder are prepared. The effects of SiO2 addition on the chemical resistance, glass transition temperature (Tg) and dynamic mechanical properties of the various samples are then observed. The chemical resistance of the nanocomposite specimens is compared with that of pure glass fiber/epoxy composite specimens when tested in acetone. The results show that the addition of 2 wt.% SiO2 increases the value of storage modulus by 1646MPa compared to that of the sample containing no silica nanopowder. Following immersion in acetone, all the nanocomposite specimen storage modulus decreased, but the addition of SiO2 reduced the decline, where the 2 wt. % samples decrease from 11.76% reduction to 0.84% and no significant change in the Tg compared to that of the sample with no silica nanopowder. Therefore, the experimental results indicate that 2 wt.% SiO2 addition is beneficial in improving chemical resistance, glass transition temperature, and dynamic mechanical properties of epoxy resin / glass fiber nanocomposites.

scholarly journals Frost-Resistant Epoxy-Urethane Binders Containing Diglycidyl Urethane

2019 ◽  
Vol 2019 ◽  
pp. 1-7 ◽  
Author(s):  
Vladimir N. Strel’nikov ◽  
Valeriy Yu. Senichev ◽  
Alexey I. Slobodinyuk ◽  
Anna V. Savchuk ◽  
Elena R. Volkova
Keyword(s):  
Mechanical Properties ◽  
Glass Transition ◽  
Transition Temperature ◽  
Glass Transition Temperature ◽  
Elastic Materials ◽  
Novel Method

A novel method for developing frost-resistant epoxy-urethane binders is proposed that is based on mixtures of epoxy-urethane oligomers and diglycidyl urethane formed during synthesis. The microheterogeneous elastic materials obtained by curing these mixtures by the cycloaliphatic amines have a low glass transition temperature and high mechanical properties.

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