Synthesis of Cyclic Polysulfides and their Properties as Curing Agents

2004 ◽  
Vol 77 (2) ◽  
pp. 380-390
Author(s):  
Wonmun Choi ◽  
Tomoyuki Matsumura
Keyword(s):  
Mechanical Properties ◽  
Molecular Weight ◽  
Tensile Strength ◽  
High Molecular Weight ◽  
Mass Spectra ◽  
Elongation At Break ◽  
Molecular Weights ◽  
Aging Properties ◽  
Curing Agents ◽  
Polysulfide Polymer

Abstract The reactions of dichloroalkanes and sodium tetra-sulfide (Na2S4) were carried out in a mixture of water and toluene to produce corresponding cyclic polysulfides and polysulfide polymer. The low molecular weights of cyclic sulfides were obtained by the reaction at 90 °C, while the high molecular weight of polysulfide polymer was obtained by the reaction at 50 °C. GPC chromatograms and Mass spectra revealed that the structures of cyclic polysulfide were 1:1, 2:2, and 3:3 adducts of dichloroalkane and sodium tetra-sulfide. The mechanical properties of vulcanized NR at 148 °C with cyclic sulfides were similar to that with sulfur. However, both tensile strength and elongation at break of vulcanized NR at 170 °C with cyclic sulfides are much higher than that with sulfur. The aging properties of vulcanized NR at 148 °C or 170 °C with cyclic polysulfides indicate better stability.

scholarly journals Melt- vs. Non-Melt Blending of Complexly Processable Ultra-High Molecular Weight Polyethylene/Cellulose Nanofiber Bionanocomposite

Polymers ◽  
2021 ◽  
Vol 13 (3) ◽  
pp. 404
Author(s):  
Nur Sharmila Sharip ◽  
Hidayah Ariffin ◽  
Tengku Arisyah Tengku Yasim-Anuar ◽  
Yoshito Andou ◽  
Yuki Shirosaki ◽  
...  
Keyword(s):  
Mechanical Properties ◽  
Molecular Weight ◽  
Tensile Strength ◽  
Yield Strength ◽  
Young’S Modulus ◽  
High Molecular Weight ◽  
Melt Processing ◽  
Cellulose Nanofiber ◽  
Melt Blending ◽  
Ultra High Molecular Weight

The major hurdle in melt-processing of ultra-high molecular weight polyethylene (UHMWPE) nanocomposite lies on the high melt viscosity of the UHMWPE, which may contribute to poor dispersion and distribution of the nanofiller. In this study, UHMWPE/cellulose nanofiber (UHMWPE/CNF) bionanocomposites were prepared by two different blending methods: (i) melt blending at 150 °C in a triple screw kneading extruder, and (ii) non-melt blending by ethanol mixing at room temperature. Results showed that melt-processing of UHMWPE without CNF (MB-UHMWPE/0) exhibited an increment in yield strength and Young’s modulus by 15% and 25%, respectively, compared to the Neat-UHMWPE. Tensile strength was however reduced by almost half. Ethanol mixed sample without CNF (EM-UHMWPE/0) on the other hand showed slight decrement in all mechanical properties tested. At 0.5% CNF inclusion, the mechanical properties of melt-blended bionanocomposites (MB-UHMWPE/0.5) were improved as compared to Neat-UHMWPE. It was also found that the yield strength, elongation at break, Young’s modulus, toughness and crystallinity of MB-UHMWPE/0.5 were higher by 28%, 61%, 47%, 45% and 11%, respectively, as compared to the ethanol mixing sample (EM-UHMWPE/0.5). Despite the reduction in tensile strength of MB-UHMWPE/0.5, the value i.e., 28.4 ± 1.0 MPa surpassed the minimum requirement of standard specification for fabricated UHMWPE in surgical implant application. Overall, melt-blending processing is more suitable for the preparation of UHMWPE/CNF bionanocomposites as exhibited by their characteristics presented herein. A better mechanical interlocking between UHMWPE and CNF at high temperature mixing with kneading was evident through FE-SEM observation, explains the higher mechanical properties of MB-UHMWPE/0.5 as compared to EM-UHMWPE/0.5.

The effect of simultaneous fiber surface treatment and matrix modification on mechanical properties of unidirectional ultra-high molecular weight polyethylene fiber/epoxy/nanoclay nanocomposites

2018 ◽  
Vol 52 (21) ◽  
pp. 2961-2972 ◽  
Author(s):  
Mohammad Mohammadalipour ◽  
Mahmood Masoomi ◽  
Mojtaba Ahmadi ◽  
Zahra Kazemi
Keyword(s):  
Mechanical Properties ◽  
Molecular Weight ◽  
Tensile Strength ◽  
High Molecular Weight ◽  
Glycidyl Methacrylate ◽  
Interfacial Adhesion ◽  
Fiber Surface ◽  
Cohesive Failure ◽  
Polyethylene Fiber ◽  
Ultra High Molecular Weight

Nonpolar structure of ultra-high molecular weight polyethylene fiber leads to a weak interfacial adhesion in ultra-high molecular weight polyethylene fiber reinforced epoxy composite. Herein, synchronized fiber and matrix modifications were utilized so as to improve the interfacial adhesion, resulting in promoting mechanical properties of these composites. For this purpose, the surface of ultra-high molecular weight polyethylene fiber was chemically treated with glycidyl methacrylate and the epoxy resin was modified through incorporation of different contents of nanoclay. The mechanical properties results showed that individual modification, either fiber or matrix, can just lead to improvements around 36.74% and 10.54% in tensile strength as well as 14.28% and 4.27% in tensile modulus, respectively. However, the ultimate outcome of the study revealed that much higher improvement can be achieved in synergistic attitude. The highest enhancement around 48.31% and 26.76% in tensile strength and modulus were seen for the sample containing glycidyl methacrylate-treated ultra-high molecular weight polyethylene fibers as reinforcement and nano epoxy modified with 1 wt.% of nanoclay. Such observation could be attributed to the mechanical interlocking and chemical reaction which were arising from incorporation of nanoclay in matrix and chemical treatment of fiber surface, correspondingly. In this regard, fiber roughness and chemical bonds formed between treated fiber and modified matrix play a key role in improving interfacial adhesion. Moreover, the fractured surface of such composites studied by scanning electron microscope confirmed the mechanical results and showed that much more matrix was adhered to the fiber surface after treatment, indicating cohesive failure.

scholarly journals Ultra-high molecular weight elastomeric polyethylene using an electronically and sterically enhanced nickel catalyst

2017 ◽  
Vol 8 (41) ◽  
pp. 6416-6430 ◽  
Author(s):  
Qaiser Mahmood ◽  
Yanning Zeng ◽  
Erlin Yue ◽  
Gregory A. Solan ◽  
Tongling Liang ◽  
...  
Keyword(s):  
Molecular Weight ◽  
Tensile Strength ◽  
High Molecular Weight ◽  
Nickel Catalyst ◽  
High Tensile Strength ◽  
Elongation At Break ◽  
Highly Active ◽  
High Elongation ◽  
Ultra High Molecular Weight ◽  
Shape Fixity

Highly active para-t-Bu-containing 1,2-bis(imino)acenaphthene-Ni(ii) catalysts are disclosed which afford hyper-branched PEs with Mw's up to 3.1 × 106 g mol−1; high tensile strength, excellent shape fixity as well as high elongation at break are a feature.

Mechanical and Dynamic Mechanical Properties of Degradable Polyurethane Foams with PEG/PCL Mixed Soft Segments

2011 ◽  
Vol 183-185 ◽  
pp. 1611-1615 ◽  
Author(s):  
Jian Hua Wang ◽  
Shuen Liang ◽  
Yan Yan Wang ◽  
Chun Rong Tian ◽  
Xiu Li Zhao
Keyword(s):  
Mechanical Properties ◽  
Molecular Weight ◽  
Tensile Strength ◽  
Compressive Strain ◽  
Dynamic Mechanical Properties ◽  
Polyurethane Foams ◽  
Elongation At Break ◽  
Dynamic Mechanical ◽  
Soft Segments ◽  
And Storage

Polyurethane (PU) with mixed poly(ethylene glycol) / poly(ε-caprolactone) (PEG/PCL) soft segments is a representatively kind of degradable polyurethane material. Polyurethane foams (PUF) with mixed PEG/PCL soft segments were synthesized by using one pot method, and their mechanical and dynamic mechanical properties were investigated. Influences of PEG/PCL weight ratio and molecular weight of soft segments on PUF's mechanical and dynamic mechanical properties were studied. The results showed that: with increasing content of PCL, PUF's tensile strength, elongation at break, stress at certain tensile/compressive strain and storage modulus increased gradually; with increasing molecular weight of soft segment, PUF's elongation at break increased, but tensile strength, stress at certain tensile/compressive strain and storage modulus all decreased accordingly; glass transition temperature (Tg) of PUF with various soft segments decreased according to the following sequence: PEG-400, PCL-210N, PEG-1000 and PTMG1000; loss factor of PUF with PEG/PCL mixed soft segments was higher than that of PUF with individual PEG or PCL soft segments.

Effect of Polyethylene Glycol (PEG) on Molten Plasticized Cellulose Acetate (CA)

2013 ◽  
Vol 830 ◽  
pp. 172-175
Author(s):  
Cheng Zhi Chuai ◽  
Zhi Zhang
Keyword(s):  
Mechanical Properties ◽  
Molecular Weight ◽  
Tensile Strength ◽  
Polyethylene Glycol ◽  
Flexural Strength ◽  
Cellulose Acetate ◽  
Flexural Modulus ◽  
Degree Of Polymerization ◽  
Maximum Elongation ◽  
Elongation At Break

Ethylene glycol (EG) and polyethylene glycol (PEG) were added as plasticizers to improve the processing performance of cellulose acetate (CA). The CA with 30% plasticizers were melted by HAAKE at 200 °C. The effects of EG and PEG (degree of polymerization in 200-800) on rheological properties and mechanical properties of CA were investigated. The results show that the plasticizing time, equilibrium torque and melt viscosity of the plasticizing system increase with the increase of PEG molecular weight, while the processing performance decreased. The tensile strength of the system decrease as the PEG molecular weight increased. The plasticizing system which contents 30% PEG-200(degree of polymerization is 200) shows the maximum elongation at break. The minimum values appeared in both flexural strength and flexural modulus in the CA/PEG-200 system.

scholarly journals Effect of Different Molecular Weight and Concentration of Polyethylene Glycol (PEG) on Tensile and Morphology of Sago Starch Film

2021 ◽  
Vol 16 ◽  
pp. 1-10
Author(s):  
Norzita Yacob
Keyword(s):  
Molecular Weight ◽  
Tensile Strength ◽  
Polyethylene Glycol ◽  
Tensile Stress ◽  
Sago Starch ◽  
Elongation At Break ◽  
Molecular Weights ◽  
Peg 4000 ◽  
Starch Films ◽  
Ftir Technique

Sago starch is a seasonal based plantation and widely found in Asia country. Its application mainly in cooking such as biscuits and as a thickener in jellies. To further utilize its application, bioplastic from sago starch was developed. In this study, sago starch films were prepared through a blending and casting method using polyethylene glycol (PEG) as a plasticizer by varying its molecular weights and concentrations. The interaction between starch and PEG in the blend was studied using FTIR technique. The effect on transparency, tensile stress, Young’s modulus as well as elongation percentages of the films was also examined. The results suggested that the addition of low molecular weight PEG (400 g.mol-1) increased the tensile stress of sago films from 33.51 MPa up to 39.11 MPa. Nevertheless, incorporation of high molecular weight of PEG (4000 g.mol-1) decreased the tensile strength of the film. Tensile strength and elongation at break of sago films increased with increasing of PEG concentration up to 2% and decreased with further increased of PEG content. Results indicated that there was a miscibility between these two components.

Effect of Different Fillers on Microstructure and Mechanical Properties of Ultrahigh Molecular Weight Polyethylene Composite

2009 ◽  
Vol 79-82 ◽  
pp. 23-26 ◽  
Author(s):  
Xu Ran ◽  
Di Zhang ◽  
You Quan Xia ◽  
Jing He Liu
Keyword(s):  
Mechanical Properties ◽  
Molecular Weight ◽  
Tensile Strength ◽  
Wear Resistance ◽  
Impact Strength ◽  
Glass Bead ◽  
Ultrahigh Molecular Weight Polyethylene ◽  
Elongation At Break ◽  
Polyethylene Composite ◽  
Ultrahigh Molecular Weight

Three fillers i.e. micro glass bead, nano-montmorillonite and graphite at 8wt% were respectively filled into ultrahigh molecular weight polyethylene (UHMWPE). The microstructure, mechanical properties were investigated. The results indicated that: The performances of three kinds of composites, such as morphology, tensile strength, impact strength, elongation at break and fraction wear, were in great difference. The bonding of interface between glass bead and UHMWPE was not firm, but nano-montmorillonite and graphite as filler dispersed in matrix evenly and coupling tight. Due to filling the filler, the tensile strength, impact strength and elongation at break decreased in varying degree compared with that of simple UHMWPE, but impact strengths reduced only a few; however the wear resistance of composite filled by graphite was improved obviously.

Nanoarchitectonics Composites of Thermoplastic Starch and Montmorillonite Modified with Low Molecular Weight Polylactic Acid

2020 ◽  
Vol 20 (5) ◽  
pp. 2955-2963
Author(s):  
Peixian Li ◽  
Huimin Guo ◽  
Kaixiong Yang ◽  
Xiaoyan Yu ◽  
Xiongwei Qu ◽  
...  
Keyword(s):  
Mechanical Properties ◽  
Molecular Weight ◽  
Tensile Strength ◽  
Polylactic Acid ◽  
Composite Films ◽  
Thermoplastic Starch ◽  
Nanocomposite Films ◽  
Low Molecular Weight ◽  
Elongation At Break ◽  
Starch Films

Nano montmorillonite (MMT) was modified by low molecular weight polylactic acid (PLA), then, the PLA modified MMT and raw MMT were added into thermoplastic starch (TPS) to prepare biodegradable nanocomposite films, respectively. For both nanocomposite films with raw MMT and modified MMT, the Tmax of degradation was enhanced and the mechanical properties were improved. The composite films containing 4 wt.% MMT displayed tensile strength of 5.06 MPa, approximately 1.4 times of that for the pure TPS films. The tensile strength of composite films containing 4 wt.% modified MMT is 6.74 MPa approximately 2 times of those for pure starch films. On the other hand, the composite film containing 4 wt.% modified MMT displayed elongation at break as high as 34.25%, which is 1.3 times of that of the pure starch film, while the composite films containing raw MMT had reduced elongation at break. This study showed that the MMT modified with PLA could significantly enhance the mechanical properties of TPS, and provides a new method to prepare fully biodegradable starch-based nanocomposites.

scholarly journals The Structure and Mechanical Properties of Hemp Fibers-Reinforced Poly(ε-Caprolactone) Composites Modified by Electron Beam Irradiation

2021 ◽  
Vol 11 (12) ◽  
pp. 5317
Author(s):  
Rafał Malinowski ◽  
Aneta Raszkowska-Kaczor ◽  
Krzysztof Moraczewski ◽  
Wojciech Głuszewski ◽  
Volodymyr Krasinskyi ◽  
...  
Keyword(s):  
Mechanical Properties ◽  
Tensile Strength ◽  
Electron Beam ◽  
Impact Strength ◽  
Flexural Modulus ◽  
Natural Fibers ◽  
High Energy ◽  
Electron Radiation ◽  
Elongation At Break ◽  
Hemp Fibers

The need for the development of new biodegradable materials and modification of the properties the current ones possess has essentially increased in recent years. The aim of this study was the comparison of changes occurring in poly(ε-caprolactone) (PCL) due to its modification by high-energy electron beam derived from a linear electron accelerator, as well as the addition of natural fibers in the form of cut hemp fibers. Changes to the fibers structure in the obtained composites and the geometrical surface structure of sample fractures with the use of scanning electron microscopy were investigated. Moreover, the mechanical properties were examined, including tensile strength, elongation at break, flexural modulus and impact strength of the modified PCL. It was found that PCL, modified with hemp fibers and/or electron radiation, exhibited enhanced flexural modulus but the elongation at break and impact strength decreased. Depending on the electron radiation dose and the hemp fibers content, tensile strength decreased or increased. It was also found that hemp fibers caused greater changes to the mechanical properties of PCL than electron radiation. The prepared composites exhibited uniform distribution of the dispersed phase in the polymer matrix and adequate adhesion at the interface between the two components.

scholarly journals Effect of Moisture Content on the Processing and Mechanical Properties of a Biodegradable Polyester

Polymers ◽  
2021 ◽  
Vol 13 (10) ◽  
pp. 1616
Author(s):  
Vincenzo Titone ◽  
Antonio Correnti ◽  
Francesco Paolo La Mantia
Keyword(s):  
Mechanical Properties ◽  
Tensile Strength ◽  
Moisture Content ◽  
Mechanical Testing ◽  
Hydrolytic Degradation ◽  
Slight Reduction ◽  
Biodegradable Polyester ◽  
Molding Process ◽  
Elongation At Break ◽  
Effect Of Moisture

This work is focused on the influence of moisture content on the processing and mechanical properties of a biodegradable polyester used for applications in injection molding. The pellets of the biodegradable polyester were exposed under different relative humidity conditions at a constant temperature before being compression molded. The compression-molded specimens were again placed under the above conditions before the mechanical testing. With all these samples, it is possible to determine the effect of moisture content on the processing and mechanical properties separately, as well as the combined effect of moisture content on the mechanical properties. The results obtained showed that the amount of absorbed water—both before processing and before mechanical testing—causes an increase in elongation at break and a slight reduction of the elastic modulus and tensile strength. These changes have been associated with possible hydrolytic degradation during the compression molding process and, in particular, with the plasticizing action of the moisture absorbed by the specimens.

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