scholarly journals Effect of E-Beam Irradiation on Thermal and Mechanical Properties of Ester Elastomers Containing Multifunctional Alcohols

Polymers ◽  
2020 ◽  
Vol 12 (5) ◽  
pp. 1043 ◽  
Author(s):  
Marta Piątek-Hnat ◽  
Kuba Bomba ◽  
Jakub Pęksiński ◽  
Agnieszka Kozłowska ◽  
Jacek G. Sośnicki ◽  
...  
Keyword(s):  
Mechanical Properties ◽  
Chemical Properties ◽  
Sebacic Acid ◽  
Gel Permeation Chromatography ◽  
Tensile Tests ◽  
Synthesis Process ◽  
Resonance Spectroscopy ◽  
Thermal And Mechanical Properties ◽  
Scanning Calorimetry ◽  
Water Contact

The aim of this work was to investigate the thermal and mechanical properties of novel, electron beam-modified ester elastomers containing multifunctional alcohols. Polymers tested in this work consist of two blocks: sebacic acid–butylene glycol block and sebacic acid–sugar alcohol block. Different sugar alcohols were utilized in the polymer synthesis: glycerol, sorbitol, xylitol, erythritol, and mannitol. The polymers have undergone an irradiation procedure. The materials were irradiated with doses of 50 kGy, 100 kGy, and 150 kGy. The expected effect of using ionizing radiation was crosslinking process and improvement of the mechanical properties. Additionally, a beneficial side effect of the irradiation process is sterilization of the affected materials. It is also worth noting that the materials described in this paper do not require either sensitizers or cross-linking agent in order to perform radiation modification. Radiation-modified poly(polyol sebacate-co-butylene sebacate) elastomers have been characterized in respect to the mechanical properties (quasi-static tensile tests), cross-link density, thermal properties (Differential Scanning Calorimetry (DSC)), chemical properties: Fourier transform infrared spectroscopy (FTIR), and wettability (water contact angle). Poly(polyol sebacate-co-butylene sebacate) preopolymers were characterized with nuclear magnetic resonance spectroscopy (1H NMR and 13C NMR) and gel permeation chromatography (GPC). Thermal stability of cross-linked materials (directly after synthesis process) was tested with thermogravimetric analysis (TGA).

scholarly journals Tailoring the Physico-Chemical Properties of Poly(xylitol-dicarboxylate-co-butylene dicarboxylate) Polyesters by Adjusting the Cross-Linking Time

Polymers ◽  
2020 ◽  
Vol 12 (7) ◽  
pp. 1493
Author(s):  
Marta Piątek-Hnat ◽  
Paulina Sładkiewicz ◽  
Kuba Bomba ◽  
Jakub Pęksiński ◽  
Agnieszka Kozłowska ◽  
...  
Keyword(s):  
Chemical Properties ◽  
Sebacic Acid ◽  
Dicarboxylic Acids ◽  
Tensile Tests ◽  
Cross Linking ◽  
Resonance Spectroscopy ◽  
Aliphatic Chain ◽  
Scanning Calorimetry ◽  
The Cross

Determining the cross-linking time resulting in the best achievable properties in elastomers is a very important factor when considering their mass production. In this paper, five biodegradable polymers were synthesized—poly(xylitol-dicarboxylate-co-butylene dicarboxylate) polymers, based on xylitol obtained from renewable sources. Five different dicarboxylic acids with even numbers of carbon atoms in the aliphatic chain were used: succinic acid, adipic acid, suberic acid, sebacic acid, and dodecanedioic acid. Samples were taken directly after polycondensation (prepolymer samples) and at different stages of the cross-linking process. Physiochemical properties were determined by a gel fraction test, differential scanning calorimetry (DSC), Fourier-transform infrared spectroscopy (FTIR), quasi-static tensile tests, nuclear magnetic resonance spectroscopy (1H NMR and 13C NMR), and an in vitro biodegradation test. The best cross-linking time was determined to be 288h. Properties and degradation time can be tailored for specific applications by adjusting the dicarboxylic acid chain length.

Influence of lignin modification on the mechanical properties of lignin/PEO blends

2016 ◽  
Vol 7 (6) ◽  
pp. 762-772 ◽  
Author(s):  
Stavros C. Anagnou ◽  
Eleni G. Milioni ◽  
Costas S. Mpalias ◽  
Ioannis A. Kartsonakis ◽  
Elias P. Koumoulos ◽  
...  
Keyword(s):  
Mechanical Properties ◽  
Tensile Tests ◽  
Mechanical And Thermal Properties ◽  
Thermal And Mechanical Properties ◽  
Scanning Calorimetry ◽  
Content Type ◽  
Poly Ethylene Oxide ◽  
Poly Ethylene ◽  
Modified Lignin ◽  
Softwood Kraft Lignin

Purpose The purpose of this paper is to focus on the investigation of mechanical and thermal properties of lignin/poly (ethylene oxide) (PEO) blends, intended to be used as carbon fiber precursor. Design/methodology/approach Softwood kraft lignin was modified via esterification using phthalic anhydride and then blended with PEO. The final lignin/PEO ratios blends were (w/w) 20/80, 50/50 and 80/20 for both unmodified and modified lignin. The structural, thermal and mechanical properties of the blends were investigated by Fourier transform infrared, differential scanning calorimetry and tensile tests, respectively. Findings The results revealed that modified lignin/PEO blend (20/80) exhibited enhanced elongation. Originality/value The structural analysis as well as thermal and mechanical properties of the produced blends are clearly demonstrated.

scholarly journals Phase Structure and Properties of Ternary Polylactide/Poly(methyl methacrylate)/Polysilsesquioxane Blends

Polymers ◽  
2021 ◽  
Vol 13 (7) ◽  
pp. 1033
Author(s):  
Anna Kowalewska ◽  
Agata S. Herc ◽  
Joanna Bojda ◽  
Maria Nowacka ◽  
Mariia Svyntkivska ◽  
...  
Keyword(s):  
Mechanical Properties ◽  
Methyl Methacrylate ◽  
Chemical Properties ◽  
Tensile Tests ◽  
Elastic Behaviour ◽  
Structure And Properties ◽  
Depth Sensing ◽  
Scanning Calorimetry ◽  
Poly Methyl Methacrylate ◽  
Solution Blending

Ternary blends of polylactide (PLA, 90 wt.%) and poly(methyl methacrylate) (PMMA, 10 wt.%) with functionalized polysilsesquioxanes (LPSQ-R) were obtained by solution blending. R groups in LPSQ containing hydroxyethyl (LPSQ-OH), methylglycolic (LPSQ-COOMe) and pentafluorophenyl (LPSQ-F5) moieties of different chemical properties were designed to modify PLA blends with PMMA. The effect of the type of LPSQ-R and their content, 1–3 wt.%, on the structure of the blends was studied with scanning electron microscopy (SEM) combined with energy dispersive spectroscopy (SEM-EDS), dynamic mechanical thermal analysis (DMTA) and Raman spectroscopy. Differential scanning calorimetry (DSC) and tensile tests also showed various effects of LPSQ-R on the thermal and mechanical properties of the blends. Depth-sensing indentation was used to resolve spatially the micro- and nano-scale mechanical properties (hardness and elastic behaviour) of the blends. The results showed clearly that LPSQ-R modulate the structure and properties of the blends.

scholarly journals Effects of Inorganic Fillers on the Thermal and Mechanical Properties of Poly(lactic acid)

2014 ◽  
Vol 2014 ◽  
pp. 1-8 ◽  
Author(s):  
Xingxun Liu ◽  
Tongxin Wang ◽  
Laurence C. Chow ◽  
Mingshu Yang ◽  
James W. Mitchell
Keyword(s):  
Mechanical Properties ◽  
Molecular Weight ◽  
Gel Permeation Chromatography ◽  
Mechanical Analysis ◽  
Poly Lactic Acid ◽  
Inorganic Filler ◽  
Homogeneous Distribution ◽  
Thermal And Mechanical Properties ◽  
Scanning Calorimetry ◽  
Tensile Tester

Addition of filler to polylactic acid (PLA) may affect its crystallization behavior and mechanical properties. The effects of talc and hydroxyapatite (HA) on the thermal and mechanical properties of two types of PLA (one amorphous and one semicrystalline) have been investigated. The composites were prepared by melt blending followed by injection molding. The molecular weight, morphology, mechanical properties, and thermal properties have been characterized by gel permeation chromatography (GPC), scanning electron microscope (SEM), instron tensile tester, thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), and dynamic mechanical analysis (DMA). It was found that the melting blending led to homogeneous distribution of the inorganic filler within the PLA matrix but decreased the molecular weight of PLA. Regarding the filler, addition of talc increased the crystallinity of PLA, but HA decreased the crystallinity of PLA. The tensile strength of the composites depended on the crystallinity of PLA and the interfacial properties between PLA and the filler, but both talc and HA filler increased the toughness of PLA.

scholarly journals Mechanical, Thermal and Rheological Properties of Polyethylene-Based Composites Filled with Micrometric Aluminum Powder

Materials ◽  
2020 ◽  
Vol 13 (5) ◽  
pp. 1242
Author(s):  
Olga Mysiukiewicz ◽  
Paulina Kosmela ◽  
Mateusz Barczewski ◽  
Aleksander Hejna
Keyword(s):  
Mechanical Properties ◽  
Melt Flow Index ◽  
Tensile Tests ◽  
Mechanical Analysis ◽  
Flow Index ◽  
Scanning Calorimetry ◽  
Metal Composites ◽  
Pre Treatment ◽  
The Impact ◽  
Properties Of Composites

Investigations related to polymer/metal composites are often limited to the analysis of the electrical and thermal conductivity of the materials. The presented study aims to analyze the impact of aluminum (Al) filler content (from 1 to 20 wt%) on the rarely investigated properties of composites based on the high-density polyethylene (HDPE) matrix. The crystalline structure, rheological (melt flow index and oscillatory rheometry), thermal (differential scanning calorimetry), as well as static (tensile tests, hardness, rebound resilience) and dynamic (dynamical mechanical analysis) mechanical properties of composites were investigated. The incorporation of 1 and 2 wt% of aluminum filler resulted in small enhancements of mechanical properties, while loadings of 5 and 10 wt% provided materials with a similar performance to neat HDPE. Such results were supported by the lack of disturbances in the rheological behavior of composites. The presented results indicate that a significant content of aluminum filler may be introduced into the HDPE matrix without additional pre-treatment and does not cause the deterioration of composites’ performance, which should be considered beneficial when engineering PE/metal composites.

Enhancing the Thermal and Mechanical Characteristics of Polyvinyl Alcohol (PVA)-Hemp Protein Particles (HPP) Composites

2021 ◽  
Vol 36 (2) ◽  
pp. 137-143
Author(s):  
S. A. Awad
Keyword(s):  
Mechanical Properties ◽  
Elevated Temperatures ◽  
Composite Films ◽  
Tensile Tests ◽  
Mechanical Analysis ◽  
Decomposition Temperature ◽  
Scanning Calorimetry ◽  
Solution Casting Method ◽  
Protein Particles

Abstract This paper aims to describe the thermal, mechanical, and surface properties of a PVA/HPP blend whereby the film was prepared using a solution casting method. The improvements in thermal and mechanical properties of HPP-based PVA composites were investigated. The characterization of pure PVA and PVA composite films included tensile tests, thermogravimetric analysis (TGA), and differential scanning calorimetry (DSC). The results of TGA and DSC indicated that the addition of HPP increased the thermal decomposition temperature of the composites. Mechanical properties are significantly improved in PVA/HPP composites. The thermal stability of the PVA composite increased with the increase of HPP filler content. The tensile strength increased from 15.74 ± 0.72 MPa to 27.54 ± 0.45 MPa and the Young’s modulus increased from 282.51 ± 20.56 MPa to 988.69 ± 42.64 MPa for the 12 wt% HPP doped sample. Dynamic mechanical analysis (DMA) revealed that at elevated temperatures, enhanced mechanical properties because of the presence of HPP was even more noticeable. Morphological observations displayed no signs of agglomeration of HPP fillers even in composites with high HPP loading.

Physico Chemical Characterization of Nanofibrous Poly(Ε-Caprolactone) Electrospun Templates for Cell Adhesion

MRS Advances ◽  
2017 ◽  
Vol 2 (49) ◽  
pp. 2689-2694
Author(s):  
Karla A. Gaspar-Ovalle ◽  
Juan V. Cauich-Rodriguez ◽  
Armando Encinas
Keyword(s):  
Mechanical Properties ◽  
Differential Scanning Calorimetry ◽  
Cell Adhesion ◽  
Tensile Modulus ◽  
Chemical Characterization ◽  
Mechanical Analysis ◽  
Scanning Calorimetry ◽  
Water Contact ◽  
Physico Chemical ◽  
Static Water

ABSTRACTNanofibrous mats of poly ε-caprolactone (PCL) were fabricated by electrospinning. The nanofiber structures were investigated and characterized by scanning electron microscope, differential scanning calorimetry, thermogravimetric analysis, dynamic mechanical analysis, static water-contact-angle analysis and mechanical properties. The results showed that the nanofibrous PCL is an ideal biopolymer for cell adhesion, owing to its biocompatibility, biodegradability, structural stability and mechanical properties. Differential scanning calorimetry results showed that the fibrous structure of PCL does not alter its crystallinity. Studies of the mechanical properties, wettability and degradability showed that the structure of the electrospun PCL improved the tensile modulus, tensile strength, wettability and biodegradability of the nanotemplates. To evaluate the nanofibrous structure of PCL on cell adhesion, osteoblasts cells were seeded on these templates. The results showed that both adhesion and proliferation of the cells is viable on these electrospun PCL membranes. Thus electrospinning is a relatively inexpensive and scalable manufacturing technique for submicron to nanometer diameter fibers, which can be of interest in the commodity industry.

Initial properties and ageing behaviour of pineapple leaf and palm fibre as reinforcement for polypropylene

2016 ◽  
Vol 30 (2) ◽  
pp. 174-195 ◽  
Author(s):  
Rungsima Chollakup ◽  
Haroutioun Askanian ◽  
Florence Delor-Jestin
Keyword(s):  
Mechanical Properties ◽  
Cost Effective ◽  
Tensile Tests ◽  
Natural Fibre ◽  
Thermal Ageing ◽  
Second Step ◽  
Scanning Calorimetry ◽  
Ultraviolet Exposure ◽  
Palm Fibre

In the furniture, automotive and contruction industries, there is increased demand for cost-effective and lightweight biocomposites. The objective of this work was to develop new natural fibre-based composites with specific properties. Palm and pineapple leaf fibres were chosen in association with polypropylene (PP). The first step was to investigate the effect of these natural fibres as reinforcement for PP. The evolution of chemical structure and crystallinity was proposed with infrared spectroscopy measurements and differential scanning calorimetry thermograms, respectively. The assessments of mechanical properties with tensile tests and melt viscoelastic behaviour were also investigated. The study enabled to distinguish the influence of fibre content. The second step in our work was to assess the composite durability after ultraviolet exposure or thermal ageing. The oxidation level was calculated. The long-term evolution of thermal and mechanical properties was also proposed. As a result, the PP/pineapple leaf composite revealed a promising biocomposite.

Phase Stability and Mechanical Properties of Ti(Ni, Ru) Alloys

2002 ◽  
Vol 753 ◽  
Author(s):  
Masahiro Tsuji ◽  
Hideki Hosoda ◽  
Kenji Wakashima ◽  
Yoko Yamabe-Mitarai
Keyword(s):  
Mechanical Properties ◽  
Phase Transformation ◽  
Phase Stability ◽  
Hot Forging ◽  
Tensile Tests ◽  
Lattice Parameter ◽  
Solid Solution Hardening ◽  
Scanning Calorimetry ◽  
Arc Melting ◽  
Transmission Electron

ABSTRACTEffects of ruthenium (Ru) substitution on constituent phases, phase transformation temperatures and mechanical properties were investigated for Ti-Ni shape memory alloys. Ti50Ni50-XRuX alloys with Ru contents (X) from 0mol% (binary TiNi) to 50mol% (binary TiRu) were systematically prepared by Ar arc-melting followed by hot-forging at temperatures from 1173K to 1673K depending on chemical composition. Phase stability was assessed by DSC (differential scanning calorimetry), XRD (X-ray diffractometry) and TEM (transmission electron microscopy). Mechanical properties were investigated using hardness and tensile tests at room temperature. With increasing Ru content, it was found that the lattice parameter of B2 phase increases, the martensitic transformation temperature slightly decreases, and the melting temperature increases monotonously. Besides, R-phase appears for Ti-Ni alloys containing 3mol% and 20mol%Ru but no diffusionless phase transformation is seen in Ti-Ni alloy containing 5mol%Ru. Vickers hardness shows the maximum at an intermediate composition (HV1030 at 30mol%Ru); this suggests that large solid solution hardening is caused by Ru substitution for the Ni-sites in TiNi.

The Structure and Mechanical Properties of Plastically Consolidated Al-Ni Alloy

2016 ◽  
Vol 682 ◽  
pp. 245-251 ◽  
Author(s):  
Grzegorz Włoch ◽  
Tomasz Skrzekut ◽  
Jakub Sobota ◽  
Antoni Woźnicki ◽  
Justyna Cisoń
Keyword(s):  
Mechanical Properties ◽  
Vickers Hardness ◽  
Tensile Tests ◽  
Mechanical Analysis ◽  
Intermetallic Phases ◽  
Scanning Calorimetry ◽  
Porosity Formation ◽  
X Ray ◽  
Ni Alloy ◽  
Thermal Stability Of

Mixed and preliminarily consolidated powders of aluminium and nickel (90 mass % Al and 10 mass % Ni) were hot extruded. As results the rod, 8 mm in diameter, was obtained. As-extruded material was subjected to the microstructural investigations using scanning electron microscopy (SEM/EDS) and X-ray analysis (XRD). The differential scanning calorimetry (DSC) and thermo-mechanical analysis (TMA) were also performed. The mechanical properties of as extruded material were determined by the tensile test and Vickers hardness measurements. In order to evaluate the thermal stability of PM alloy, samples were annealed at the temperature of 475 and 550 °C. After annealing Vickers hardness measurements and tensile tests were carried out. The plastic consolidation of powders during extrusion was found to be very effective, because no pores or voids were observed in the examined material. The detailed microstructural investigations and XRD analyses did not reveal the presence of the intermetallic phases in the as-extruded material. During annealing, the Al3Ni intermetallic compound was formed as the result of chemical reaction between the alloy components. The hardness of the alloy after annealing at the temperature of 475°C was found to be comparable to the hardness in as-extruded state. Annealing of the material at the temperature of 550°C results in hardness decreasing by about 50%, as the consequence of porosity formation and Al3Ni cracking.

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