scholarly journals Thermal characterization of novel aliphatic polyesters with ether and thioether linkages

e-Polymers ◽  
2010 ◽  
Vol 10 (1) ◽  
Author(s):  
M. Soccio ◽  
N. Lotti ◽  
L. Finelli ◽  
A. Munari

AbstractSeveral novel ether or thioether linkage containing aliphatic polyesters and poly(alkylene dicarboxylate)s were synthesized for comparison and characterized in terms of chemical structure and molecular weight. The thermal behavior was examined by thermogravimetric analysis and differential scanning calorimetry. All the polymers showed a good thermal stability, even though lower for the ether or thioether linkage-containing polyesters. The decrement of the thermal stability appears to be more relevant in the case of the presence of sulphur atoms. At room temperature the samples appeared semicrystalline, except PTTDG and PDEDG, which were viscous oils; the effect of the introduction of ether or thioether group was an increment of the Tgvalue, a decrement of the melting temperature and a significant decrease of the crystallization rate. The entity of the variations was found to be affected by the kind of group introduced, and the trend observed can be explained on the basis of atom electronegativity and dimensions

e-Polymers ◽  
2011 ◽  
Vol 11 (1) ◽  
Author(s):  
M. Soccio ◽  
N. Lotti ◽  
L. Finelli ◽  
A. Munari

AbstractSeveral novel ether or thioether linkage containing aliphatic polyesters and poly(alkylene dicarboxylate)s for comparison were synthesized and characterized in terms of chemical structure and molecular weight. The thermal behavior was examined by thermogravimetric analysis and differential scanning calorimetry. All the polymers showed a good thermal stability, even though lower for the ether or thioether linkage-containing polyesters. The decrement of the thermal stability appears to be more relevant in the case of presence of sulphur atoms. At room temperature the samples appeared semicrystalline, except PTTDG and PDEDG, which were viscous oils; the effect of the introduction of ether or thioether group was an increment of the Tg value, a decrement of the melting temperature and a significant decrease of the crystallization rate. The entity of the variations was found to be affected by the kind of group introduced, and the trend observed can be explained on the basis of atom electronegativity and dimensions.


2020 ◽  
pp. 095400832097759
Author(s):  
Ke Li ◽  
Hua Yin ◽  
Kun Yang ◽  
Pei Dai ◽  
Ling Han ◽  
...  

Designing novel low-melting, high-rigidity phthalonitrile resin is of great significance in the current context of development. In this study, rigid spirocycle acetal structure was introduced into phthalonitrile to reduce the melting point and maintain their thermal stability. The chemical structure of resins was confirmed by nuclear magnetic resonance (NMR) spectrometry, matrix-assisted laser desorption/ionization time of flight (MALDI-TOF) mass spectrometry and Fourier-transform infrared (FTIR) spectroscopy. The curing behaviors were studied by differential scanning calorimetry (DSC). Thermal stability and mechanical properties of the cured resins were investigated by dynamic mechanical thermal analysis (DMTA) and thermogravimetric analysis (TGA). The processability was studied by rheological analysis. The results indicated the three monomers had a low melting temperature, wide processing windows and low viscosities. These polymers did not exhibit Tg from room temperature to 400°C, exhibited superb dynamic mechanical property and thermal stability.


2012 ◽  
Vol 727-728 ◽  
pp. 1552-1556
Author(s):  
Renata Barbosa ◽  
Dayanne Diniz Souza ◽  
Edcleide Maria Araújo ◽  
Tomás Jefférson Alves de Mélo

Studies of degradation have verified that the decomposition of some quaternary ammonium salts can begin to be significant at the temperature of about 180 ° C and like most thermoplastics are processed at least around this temperature, the thermal stability of the salt in clay should always be considered. Some salts are more stable than others, being necessary to study the degradation mechanisms of each case. In this work, four quaternary ammonium salts were characterized by differential scanning calorimetry (DSC) and thermogravimetry (TG). The results of DSC and TG showed that the salts based chloride (Cl-) anion begin to degrade at similar temperatures, while the salt based bromide (Br-) anion degrades at higher temperature. Subsequently, a quaternary ammonium salt was chosen to be used in organoclays, depending on its chemical structure and its thermal behavior.


2013 ◽  
Vol 1453 ◽  
Author(s):  
Sofía Vazquez-Rodriguez ◽  
Gloria E. Rodríguez-Vázquez ◽  
Selene Sepulveda-Guzman ◽  
Martín E. Reyes-Melo ◽  
Aaron Morelos-Gomez ◽  
...  

ABSTRACTUltra-high molecular weight polyethylene/graphite nanocomposites were prepared by high-energy cryogenic milling followed by syntering. Microstructure changes shows that graphite was reduced to graphite nanoplatelets by high-energy cryomilling and partial exfoliation of graphite to few layered graphene nanoplatelets occurred in a small extent. The resulting nanocomposites revealed high electrical conductivity and good mechanical performance. Thermal characterization of the nanocomposites was also carried out by differential scanning calorimetry.


2019 ◽  
Vol 52 (6) ◽  
pp. 483-494 ◽  
Author(s):  
Wenzheng Zhang ◽  
Ning Jiang ◽  
Tingting Zhang

The sustainable biomass cardanol grafting onto neoprene (CR) rubber was carried out successfully at room temperature by covalently binding to CR via click chemistry to realize the internal plasticization of CR rubber. The structure of the synthesized product was characterized by Fourier transform infrared spectroscopy and proton nuclear magnetic resonance, and differential scanning calorimetry and thermogravimetric analysis demonstrate a lowering of the glass transition temperature of the CR-propargyl ether cardanol as compared to CR. This confirms the plasticization effect of the cardanol when grafted onto CR. The cardanol as an internal plasticizer also has a good thermal stability and almost near-zero migration.


2003 ◽  
Vol 15 (3) ◽  
pp. 301-318 ◽  
Author(s):  
Vasile Cozan ◽  
Mitica Sava ◽  
Luminita Marin ◽  
Maria Bruma

Six new bismaleimides (BMIs) having arylidene or cardo cycloaliphatic internal moieties were prepared by reacting 4-maleimidobenzoyl chloride with various arylidene or cardo bisphenols. The structures of BMIs were confirmed using elemental analysis data and spectroscopic (IR, 1H-NMR) characterizations. Two poly(aminoaspartimide)s (PAAs) were synthesized to exemplify one of the post-reaction abilities of the BMIs. Thermotropic liquid crystalline behavior was observed by differential scanning calorimetry and polarized light microscopy. The thermal stability of BMIs and PAAs was determined by thermogravimetric analysis and they showed good thermal stability except BMI 10, containing a cyclopentanone unit, which decomposed around 235°C. In this paper, we discuss the synthesis and characterization of these materials.


e-Polymers ◽  
2006 ◽  
Vol 6 (1) ◽  
Author(s):  
N. Lotti ◽  
L. Finelli ◽  
M. Messori ◽  
A. Munari

AbstractPoly(thiodiethylene terephthalate) (PSDET), poly(thiodiethylene adipate) (PSDEA), poly(diethylene terephthalate) (PDET) and poly(diethylene adipate) (PDEA) for comparison were synthesized and characterized in terms of chemical structure and molecular weight. The thermal behavior was examined by thermo gravimetric analysis and differential scanning calorimetry. All the polymers showed a good thermal stability, even though lower for the sulfur-containing polyesters. At room temperature they appeared as semicrystalline materials, except PDEA, which was an oil; the effect of substitution of ether oxygen atoms with sulfur ones was a lowering in the Tg value, an increment of melting temperature and an increase of crystallization rate. The results were explained as due to the presence of flexible C-S-C bonds in the polymeric chain.


e-Polymers ◽  
2008 ◽  
Vol 8 (1) ◽  
Author(s):  
Corrado Berti ◽  
Annamaria Celli ◽  
Elisabetta Marianucci ◽  
Micaela Vannini

AbstractNew telechelic poly(butylene terephthalate) (PBT) ionomers, characterized by the presence of some aliphatic sulfonated chain ends, were prepared by reaction with the 1,4-butane sultone. Two methods of synthesis were compared and the final polymers, containing different percentages of ionic groups, were characterized, with particular attention to the thermal properties. Thermogravimetric analysis shows that the presence of ionic groups does not modify the thermal stability of PBT. The differential scanning calorimetry indicates that the crystalline phase and the crystallinity degree of PBT do not change in the presence of ionic chain ends, whereas the crystallization rate was found to be strongly modified. The ionomers crystallize at very high rate, due to the nucleating effect of the ionic aggregations formed in the melt.


2019 ◽  
pp. 089270571987822
Author(s):  
Saud Aldajah ◽  
Mohammad Y Al-Haik ◽  
Waseem Siddique ◽  
Mohammad M Kabir ◽  
Yousef Haik

This study reveals the enhancement of mechanical and thermal properties of maleic anhydride-grafted polypropylene (PP- g-MA) with the addition of nanocrystalline cellulose (NCC). A nanocomposite was manufactured by blending various percentages of PP, MA, and NCC nanoparticles by means of a twin-screw extruder. The influence of varying the percentages of NCC on the mechanical and thermal behavior of the nanocomposite was studied by performing three-point bending, nanoindentation, differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), scanning electron microscopy (SEM), and Fourier-transform infrared (FTIR) spectroscopy tests. The novelty of this study stems on the NCC nanoparticles and their ability to enhance the mechanical and thermal properties of PP. Three-point bending and nanoindentation tests revealed improvement in the mechanical properties in terms of strength, modulus, and hardness of the PP- g-MA nanocomposites as the addition of NCC increased. SEM showed homogeneity between the mixtures which proved the presence of interfacial adhesion between the PP- g-MA incorporated with NCC nanoparticles that was confirmed by the FTIR results. DSC and TGA measurements showed that the thermal stability of the nanocomposites was not compromised due to the addition of the coupling agent and reinforced nanoparticles.


Author(s):  
Ignazio Blanco ◽  
Traian Zaharescu

AbstractA series of ethylene-propylene-diene-terpolymer (EPDM)/polyhedral oligomeric silsesquioxane (POSS) composites at different percentage of POSS were prepared and subjected to γ-irradiation. Both irradiated and non-irradiated EPDM and composites were investigated by the means of thermal analysis to verify if the presence of POSS molecules is able to reduce the oxidation level of free radicals generated during the degradation and to evaluate the effects of the irradiation. EPDM composites at 1, 3 and 5 mass% of POSS were thus degraded in a thermogravimetric (TG) balance in dynamic heating conditions (25–700 °C), in both inert and oxidative atmosphere by flowing nitrogen and air respectively. Thermal characterization was then completed by carrying out Differential Scanning Calorimetry (DSC) analysis from sub-ambient to better highlight the melting of the polymer and polymer composites occurring just above the room temperature. FTIR spectroscopy was also performed for the prepared samples to check the presence of the molecular filler in the composites and for the TG’s residue at 700 °C, in order to evaluate its nature. DSC and TGA parameters were detected and discussed to have information about the effect of the degradation’s environment, the effect of irradiation on polymer stabilization and the effect of POSS content in the polymer matrix.


Sign in / Sign up

Export Citation Format

Share Document