scholarly journals The crystallization and mechanical properties of poly(4-methyl-1-pentene) hard elastic film with different melt draw ratios

e-Polymers ◽  
2021 ◽  
Vol 21 (1) ◽  
pp. 930-938
Author(s):  
Liangdong Yin ◽  
Ruijie Xu ◽  
Jiayi Xie ◽  
Caihong Lei ◽  
Qi Cai
Keyword(s):  
Mechanical Properties ◽  
Mechanical Test ◽  
Elastic Recovery ◽  
Amorphous Region ◽  
Structure Evolution ◽  
Scanning Calorimetry ◽  
Entanglement Density ◽  
X Ray Scattering ◽  
Elastic Film ◽  
Platelet Structure

Abstract To study the effect of the melt-draw ratios (MDRs) on the structure and properties of the poly(4-methyl-1-pentene) (PMP) film, the crystal structure evolution and mechanical properties of the PMP film with an MDR of 40–160 were characterized using scanning electron microscopy, differential scanning calorimetry, wide-angle X-ray scattering, and mechanical test. The results show that with the increase of MDR, the spherulite to platelet transition occurs in the PMP. When the MDR exceeds 100, a parallel platelet structure appears. Due to the side chains, with the increase of MDR, the distribution density of tie chains in PMP decreases and the entanglement density of amorphous chains increases. This leads to a decrease in the yield strength and the strain hardening becomes noticeable. Although the crystalline network becomes loose due to the decrease in tie chain density, the elastic recovery (ER) value still increases with the increase of MDR. This result indicates that the entanglement density of the amorphous region greatly contributes to the ER.

scholarly journals Poly(Glycerol Succinate) as an Eco-Friendly Component of PLLA and PLCL Fibres towards Medical Applications

Polymers ◽  
2020 ◽  
Vol 12 (8) ◽  
pp. 1731
Author(s):  
Dorota Kolbuk ◽  
Oliwia Jeznach ◽  
Michał Wrzecionek ◽  
Agnieszka Gadomska-Gajadhur
Keyword(s):  
Mechanical Properties ◽  
In Vitro Study ◽  
Medical Applications ◽  
Crystal Formation ◽  
Scanning Calorimetry ◽  
Chain Mobility ◽  
X Ray Scattering ◽  
Crystallisation Behaviour ◽  
Main Component

This study was conducted as a first step in obtaining eco-friendly fibres for medical applications using a synthesised oligomer poly(glycerol succinate) (PGSu) as an additive for synthetic poly(L-lactic acid) (PLLA) and poly (L-lactide-co-caprolactone) (PLCL). The effects of the oligomer on the structure formation, morphology, crystallisation behaviour, and mechanical properties of electrospun bicomponent fibres were investigated. Nonwovens were investigated by means of scanning electron microscopy (SEM), wide angle X-ray scattering (WAXS), differential scanning calorimetry (DSC), and mechanical testing. The molecular structure of PLLA fibres is influenced by the presence of PGSu mainly acting as an enhancer of molecular orientation. In the case of semicrystalline PLCL, chain mobility was enhanced by the presence of PGSu molecules, and the crystallinity of bicomponent fibres increased in relation to that of pure PLCL. The mechanical properties of bicomponent fibres were influenced by the level of PGSu present and the extent of crystal formation of the main component. An in vitro study conducted using L929 cells confirmed the biocompatible character of all bicomponent fibres.

scholarly journals Microstructural Changes of Aramid Fiber Due to Reaction with Toluene 2,4-diisocyanate under Tension in scCO2

Polymers ◽  
2019 ◽  
Vol 11 (7) ◽  
pp. 1110 ◽  
Author(s):  
Haijuan Kong ◽  
Qian Xu ◽  
Muhuo Yu
Keyword(s):  
Mechanical Properties ◽  
High Temperature ◽  
High Strength ◽  
Amorphous Region ◽  
Aramid Fiber ◽  
Crosslinking Reaction ◽  
X Ray Scattering ◽  
Rigid Molecule ◽  
Rigid Segment ◽  
Orientation Structure

High modulus aramid fiber, such as Kevlar 49, is conventionally prepared by the heat annealing of high strength aramid fiber under a suitable tension at high temperature, especially higher than 500 °C. This enables the mobility of a rigid molecule chain to be rearranged into a more perfect crystalline or orientation structure under tension. However, annealing decreases the tensile strength, since the thermal degradation of the molecular chain at high temperature cannot be avoided. Kevlar 49 fibers treated in supercritical carbon dioxide (scCO2) under tension could improve their mechanical properties at a low temperature. The effects of the tension on the mechanical properties and structure of the Kevlar 49 fibers were studied by mechanical testing, wide-angle and small-angle X-ray scattering (WAXS, SAXS), and scanning electron microscopy (SEM). The results show that the mechanical properties, crystallinity and orientation of the fiber can be improved when the tension is less than 0.6 cN/dtex, which may be due to the increasing of the mobility of a rigid segment with the help of the plasticization of scCO2 and re-arrangement of macromolecular chain into crystalline and orientation structure under tension. What’s more, the amorphous region also was enhanced by crosslinking reaction of toluene 2,4-diisocyanate (TDI) with the chain end groups of the macromolecules in the amorphous regions. However, a decrease of tenacity was found when the tension was higher than 0.6 cN/dtex, which is because the tension was so high that the microfibril was broken. The results indicated that treating the Kevlar 49 fiber in scCO2 under a suitable tension with TDI as a crosslink agent can simultaneously improve both the tenacity and modulus of the fiber.

Structure Evolution of Thermotropic Polymers by Thermal Annealing. A Light and X-Ray Scattering Study

2015 ◽  
Vol 1765 ◽  
pp. 65-70
Author(s):  
Adriana Reyes-Mayer ◽  
Angel Romo-Uribe ◽  
Michael Jaffe
Keyword(s):  
Mechanical Properties ◽  
Heat Treatment ◽  
Thermal Treatment ◽  
Structure Evolution ◽  
Wide Angle ◽  
Extrusion Axis ◽  
X Ray ◽  
X Ray Scattering ◽  
Extruded Films ◽  
Ray Scattering

ABSTRACTSmall-angle light scattering (SALS) and wide-angle X-ray scattering (WAXS) were used to study the influence of heat treatment on the texture and microstructure of extruded films of high-performance thermotropic liquid crystal polymers (LCPs). The microstructure was correlated with tensile mechanical properties. LCPs based on random units of hydroxybenzoic acid (B), hydroxynaphthoic acid (N), terephthalic acid (TA) and biphenol (BP) were supplied by the former Hoechst Celanese Corp. as 50 μm thick extruded films. The LCPs, denoted B-N, COTBP and RD1000, have B and N as common co-monomers and vary the other co-monomers. Thus, this study also enabled the investigation of the influence of monomer composition on microstructure and mechanical properties. Heat treatments were carried out at temperatures close to the solid-to-nematic transition (Ts→n) for periods up to 5 h, under dry air conditions. The thermal treatment produced either two endotherms or a small increase of Ts→n (B-N and RD1000), or Ts→n increased significantly (COTBP). Moreover, when heat treatment was carried out approximately 40°C below the respective Ts→n, the mechanical Young’s modulus, E, along the extrusion axis increased for all LCPs. Strikingly, for COTBP, E increased over 100% relative to the as-extruded film. The results also showed that the optimum treatment time for improving the Young modulus was between 3 and 4 h. Wide-angle X-ray scattering showed a significant sharpening of crystalline reflections and concentration of the 002 meridional reflection as a result of thermal treatment, suggesting the elimination of defects and a better alignment of the molecular chains along the extrusion axis. This would explain the increase in tensile modulus.

Role of Multiwalled Carbon Nanotube on Mechanical Reinforcement of High-Density Polyethylene

2013 ◽  
Vol 652-654 ◽  
pp. 15-24 ◽  
Author(s):  
Xia Ran Miao ◽  
Yuan Jiang Qi ◽  
Xiao Yun Li ◽  
Yu Zhu Wang ◽  
Xiao Long Li ◽  
...  
Keyword(s):  
Mechanical Properties ◽  
Carbon Nanotubes ◽  
High Density Polyethylene ◽  
High Density ◽  
Scanning Calorimetry ◽  
Melt Mixing ◽  
Multiwalled Carbon ◽  
Mechanical Reinforcement ◽  
Multi Wall Carbon Nanotubes ◽  
X Ray Scattering

The high density polyethylene (HDPE) nanocomposites were prepared by melt mixing HDPE with multi-wall carbon nanotubes (MWCNTs). In this work, the morphological, nucleation, crystallization and mechanical properties of the HDPE nanocomposites were studied by scanning electron microscopy, different scanning calorimetry, small-angle X-ray scattering and tensile testing. It was found that the tensile strength and Young’s modulus is increased by 42.4% and 116.5% at 3.wt% MWCNT loading compared to the pure HDPE. According to SEM results combined with SAXS, well-defined nanohybird shish-kebab (NHSK) entities exist in the composites, and in the shish-kebab structures fibrillous carbon nanotubes (MWCNTs) act as shish while HDPE lamellae act as kebab. The crystallization behavior, probed by DSC, suggests that MWCNTs have strong nucleation ability and shear stress plays an important role in polymer crystallization process. The mechanical properties demonstrated that the formation of the Shish-kebab structures improved the interfacial adhesion and brought obvious mechanical enhancement for the HDPE/MWCNTs nanocomposites.

Crystallization, Morphology and Mechanical Properties of PLA/PBAT/CaCO3 Composites

2012 ◽  
Vol 602-604 ◽  
pp. 768-771 ◽  
Author(s):  
Nan Shi ◽  
Jun Cai ◽  
Qiang Dou
Keyword(s):  
Electron Microscopy ◽  
Mechanical Properties ◽  
Scanning Electron Microscopy ◽  
Crystallization Behavior ◽  
Mechanical Test ◽  
Poly Lactic Acid ◽  
Scanning Calorimetry ◽  
Crystallization Morphology ◽  
Morphology And Mechanical Properties ◽  
Scanning Electron

The melting, crystallization behavior, morphology and mechanical properties of poly(lactic acid) (PLA)/poly(butylene adipate-co-terephthalate) (PBAT)/calcium carbonate (CaCO3) composites were investigated by means of differential scanning calorimetry (DSC), scanning electron microscopy(SEM), and mechanical test. It is shown that PBAT decreases the crystallinity, while CaCO3 increases the crystallinity of the composites. A synergistic toughening effect is obtained by the combination of CaCO3 and PBAT. The optimum mechanical properties can be achieved in case of the composite (PLA: PBAT: CaCO3=60: 20: 20).

Effect of Ultrasound and Strain Rate on Tensile Behavior of Neat Thermoplastic Polyurethane Thin Films

2010 ◽  
Author(s):  
Anandh Balakrishnan ◽  
Mrinal C. Saha
Keyword(s):  
Thin Films ◽  
Mechanical Properties ◽  
Strain Rate ◽  
Mechanical Test ◽  
Thermoplastic Polyurethane ◽  
Optical Element ◽  
Mechanical Tests ◽  
Primary Objective ◽  
Scanning Calorimetry ◽  
Rate Dependent

Thermoplastic Polyurethane (TPU) thin films have many applications in engineering and biomedical fields. Examples include moisture sensors, load cells, optical element and biocompatible stens. The TPU is a block copolymer naturally phase segregates into thermodynamically incompatible hard- and soft-segments. The size of the segments and their spatial distribution can significantly affect the microstructure and mechanical properties of the TPU. In this paper, we propose to investigate the effect of ultrasound energy on mechanical properties of TPU thin films fabricated via a solution route utilizing Tetra Hydro Furan (THF) as a solvent. The times of sonication was fixed at 60 minutes whilst all films were fabricated at average thickness of 20+/-5 um. The primary objective of the study was to understand the influence of ultrasound and strain rates on the material microstructure and the resulting mechanical properties. Mechanical tests have been conducted at two different displacement rates, namely 5 and 10 mm/min. Our preliminary results indicate that ultrasound improves the strength of the neat TPU films. We also see that strain hardening is displacement or strain rate dependent. We attribute these results to changes in the hard (H) and soft (S) domain structure. To further understand these microstructural variations, we propose to conduct Differential Scanning Calorimetry (DSC). The data has been interpreted in conjunction with our mechanical test data.

Effects of Ultrasound and Strain Rate on Tensile Mechanical Behavior of Thermoplastic Poly Urethane Thin Films

2011 ◽  
Vol 133 (4) ◽  
Author(s):  
Anandh Balakrishnan ◽  
Mrinal C. Saha
Keyword(s):  
Thin Films ◽  
Mechanical Properties ◽  
Mechanical Test ◽  
Film Formation ◽  
Mechanical Tests ◽  
Scanning Calorimetry ◽  
Film Properties ◽  
Differential Scanning Calorimetry Scan ◽  
The Times ◽  
Specific Heat Capacities

Thermoplastic poly urethane (TPU) is a diblock copolymer which naturally phase segregates into thermodynamically incompatible hard (H) and soft (S) segments. The size of the segments and their spatial distribution can significantly affect the microstructure and mechanical properties of the material. In this paper, we investigated the effect of duration of exposure to ultrasound on the solution prior to film formation on the final film properties. The response variable for the study was primarily mechanical properties of the TPU thin films fabricated via a solution route utilizing tetra hydro furan as a solvent. The times of sonication were varied between 30 min and 90 min, while all films were fabricated at average thickness of 20 ± 5 μm. The mechanical tests have been conducted at two different displacement rates of 5 and 10 mm/min. Our results indicated that (relative to untreated TPU) ultrasound tends not to deteriorate the fracture strength, strain and yet improve the fracture toughness. We attribute these results to subtle events at the H and S segment/domain levels. To further understand these microstructural variations, we conducted differential scanning calorimetry scan tests between 25 °C and 200 °C at 5 °C/min on untested and tested TPU samples of all types. This data showed a delicate sonication time dependent trend and has been interpreted in conjunction with our mechanical test data. Transition temperatures, enthalpies, and specific heat capacities have been computed for these cases.

Studies on Mechanical Properties and Structure of LLDPE/Nano-Montmorillonite Composites

2012 ◽  
Vol 510 ◽  
pp. 579-584
Author(s):  
Yu Xin Liu ◽  
Qi Yang ◽  
Fang Yang ◽  
Yong Fei Zhu ◽  
Xian Zhong Mo
Keyword(s):  
Mechanical Properties ◽  
Mechanical Test ◽  
Linear Low Density Polyethylene ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Melting Method ◽  
X Ray ◽  
Small Angle Light Scattering ◽  
The Impact ◽  
Scanning Electron

Linear low-density polyethylene (LLDPE)/nano-montmorillonite (nano-MMT) composites were prepared by melting method. Mechanical test, scanning electron microscope (SEM), X-ray diffraction (XRD), differential scanning calorimetry (DSC) and small angle light scattering (SALS) measurements were used to characterize the mechanical properties and structure of the LLDPE composite. The results indicated that the impact strength of LLDPE decreased with the increase of nano-MMT content. However, the tensile strength firstly increased and then decreased. The aggregation of nano-MMT in LLDPE happened at larger content. The spherulite size and crystallinity of LLDPE reduced with the addition of nano-MMT. Furthermore, it was found that the structure of the spherulite was destroyed by the nano-MMT. The microcrystal size of LLDPE also decreased with the increase of nano-MMT content.

Star-shaped arylacetylene resins derived from silicon

2020 ◽  
Vol 40 (8) ◽  
pp. 676-684
Author(s):  
Niping Dai ◽  
Junkun Tang ◽  
Manping Ma ◽  
Xiaotian Liu ◽  
Chuan Li ◽  
...  
Keyword(s):  
High Performance ◽  
Room Temperature ◽  
Mechanical Test ◽  
Flexural Modulus ◽  
Mechanical Analysis ◽  
Reinforced Composites ◽  
Scanning Calorimetry ◽  
Chemical Structures ◽  
Structures And Properties ◽  
High Performance Resin

AbstractStar-shaped arylacetylene resins, tris(3-ethynyl-phenylethynyl)methylsilane, tris(3-ethynyl-phenylethynyl) phenylsilane, and tris (3-ethynyl-phenylethynyl) silane (TEPHS), were synthesized through Grignard reaction between 1,3-diethynylbenzene and three types of trichlorinated silanes. The chemical structures and properties of the resins were characterized by means of nuclear magnetic resonance, fourier-transform infrared spectroscopy, Haake torque rheomoter, differential scanning calorimetry, dynamic mechanical analysis, mechanical test, and thermogravimetric analysis. The results show that the melt viscosity at 120 °C is lower than 150 mPa⋅s, and the processing windows are as wide as 60 °C for the resins. The resins cure at the temperature as low as 150 °C. The good processabilities make the resins to be suitable for resin transfer molding. The cured resins exhibit high flexural modulus and excellent heat-resistance. The flexural modulus of the cured TEPHS at room temperature arrives at as high as 10.9 GPa. Its temperature of 5% weight loss (Td5) is up to 697 °C in nitrogen. The resins show the potential for application in fiber-reinforced composites as high-performance resin in the field of aviation and aerospace.

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