| 1. |
- Liu, Xiaohui, et al.
(författare)
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Non-isothermal crystallization behaviors of polyamide 6/clay nanocomposites
- 2002
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Ingår i: European Polymer Journal. - 0014-3057 .- 1873-1945. ; 38:7, s. 1383-1389
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Tidskriftsartikel (refereegranskat)abstract
- The non-isothermal crystallization behaviors of polyamide 6/clay nanocomposite (PA6CN) were investigated by differential scanning calorimetry (DSC) and X-ray diffraction (XRD). DSC results showed that the nanometric silicate layers in PA6CN acted as effective nucleation agents. The addition of silicate layers influenced the mechanism of nucleation and the growth of PA6 crystallites. The DSC results also implied an unusual phenomenon, in contrast to PA6, the crystallinity degree of PA6CN increased with increasing cooling rate. XRD results verified this phenomenon and indicated that the addition of silicate layers favored the formation of the γ crystalline form.
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| 2. |
- Mathew, Aji P., et al.
(författare)
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Effect of initiating system, blend ratio and crosslink density on the mechanical properties and failure topography of nano-structured full-interpenetrating polymer networks from natural rubber and polystyrene
- 2001
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Ingår i: European Polymer Journal. - 0014-3057 .- 1873-1945. ; 37:9, s. 1921-1934
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Tidskriftsartikel (refereegranskat)abstract
- The mechanical performance of full-interpenetrating polymer networks (IPNs) based on natural rubber/polystyrene (NR/PS) system has been studied in detail. The IPNs were prepared using different initiators viz., benzoyl peroxide (BPO), azo-bis-isobutyronitrile (AIBN), and dicumyl peroxide (DCP) and the effect of initiating systems on the properties was studied. It was observed that in all cases the IPNs initiated using DCP showed a superior property compared to BPO and AIBN initiated ones. The crosslink density of the IPN was varied by varying the percent of divinyl benzene (crosslinking agent of PS) and the effect of crosslink density on the properties has been studied. The stress-strain behaviour, tensile strength, Young's modulus, elongation at break, tear strength, tension set and tensile set were determined. The effects of strain rate on tensile properties were analysed. The studies on the morphology using scanning electron microscopy showed an increase in phase mixing on increasing the PS content and PS crosslinking. However, high level of PS content and PS crosslinking lead to a decrease in phase mixing. The morphology studies using TEM revealed the interesting fact that NR/PS IPN system was nano-structured. The fracture surfaces of tensile and tear specimens were studied using scanning electron microscopy, to get a clear picture of the mechanism of failure.
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| 3. |
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| 4. |
- Alipour, Nazanin, et al.
(författare)
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Structure and properties of polyethylene-based and EVOH-based multilayered films with layer thicknesses of 150 nm and greater
- 2015
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Ingår i: European Polymer Journal. - : Elsevier BV. - 0014-3057 .- 1873-1945. ; 64, s. 36-51
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Tidskriftsartikel (refereegranskat)abstract
- This paper presents the structure and properties of two multilayered systems where polymers in adjacent layers were either miscible or immiscible. The miscible system consisted of 2, 17, 18, 24 and nominally 288 layers of alternating low-density (LDPE) and low-density/linear-low density (mPE) polyethylene layers with observed thicknesses ranging from 150 nm to 20 urn. The immiscible system consisted of 5 and 19 layer films with a combination of poly(ethylene-co-vinyl alcohol) (EVOH) (thickness: 9 and 1 gm, respectively), LDPE (17 and 7 gm) and a polyethylene adhesive (3 and 1 gm). The purpose of the multi-layering was to increase the crack growth resistance and, in the EVOH-based system, to decrease the oxygen transmission rate. Indeed, the crack growth resistance, as measured on tensile-tested notched films, increased with increasing number of layers. The thinnest polyethylene and polyethylene adhesive layers showed a clear ductile failure when fractured even in liquid nitrogen. Simultaneous synchrotron wide-angle/small-angle X-ray scattering and tensile testing indicated no new deformation features with changes in the layer thickness. The oxygen permeability was the same in the 5- and 19-layer EVOH-based films, but the uptake of n-hexane was strongly reduced in the 19-layer films, demonstrating the effective protective role of the EVOH layers. The n-hexane desorption data of the 2-layer LDPE/mPE film was successfully modeled using the diffusivities and solubilities of the single layers. Crystallization was slower and more confined in the films with thinner layers. The interlayer mixing in the melt (measured by isothermal crystallization from melts of initially layered polyethylene-based systems) was, as expected, significantly faster in the 24- and 288-multilayer films than in the 2-layer film.
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| 5. |
- Andersson, Mattias, 1985, et al.
(författare)
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Dielectric strength of γ-radiation cross-linked, high vinyl-content polyethylene
- 2015
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Ingår i: European Polymer Journal. - : Elsevier BV. - 0014-3057. ; 64, s. 101-107
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Tidskriftsartikel (refereegranskat)abstract
- We explore γ-radiation cross-linking of high vinyl-content low-density polyethylene (LDPE) and its potential use as a high-voltage insulation material. Of the three investigated resins containing 1, 0.5 and 0.17 vinyl groups per 1000 carbons, respectively, only the highest vinyl-content material featured a sufficiently high gel content of more than 70% and hot-set elongation below 175%, when cross-linked with a γ-radiation dose of at least 68 kGy. Differential scanning calorimetry (DSC) and small-angle X-ray scattering (SAXS) reveal that neither the crystallinity nor the lamellar thickness of the highest vinyl-content LDPE are negatively affected by γ-radiation cross-linking. As a result, we find that the dielectric strength, as characterized by electrical tree initiation experiments, can be maintained upon γ-radiation cross-linking.
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| 6. |
- Andriani, Fika, et al.
(författare)
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Statistical enchainment of ester/ether and carbonate cleavable bonds to control copolymers? : erosion rate and trigger environment-specific degradation
- 2022
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Ingår i: European Polymer Journal. - : Elsevier BV. - 0014-3057 .- 1873-1945. ; 178, s. 111457-
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Tidskriftsartikel (refereegranskat)abstract
- Polymers containing ester bonds undergo abiotic degradation independently from the surrounding environment as long as the hydrolytic conditions are provided. The hydrolysis of the ester bonds leads a bulk degradation of the polymeric matrix which, contrary to surface erosion, is unpredictable. The enchainment of diverse degradability functions was sought to expand the scope of the degradation mechanism and achieve a more predictable profile of the mass loss.The copolymerization of trimethylene carbonate and p-dioxanone enabled the synthesis of one class of copolymers with controllable erosion rate and susceptible to three degradation pathways depending on the surrounding environment. The synthetic strategy used organocatalysts and allowed the synthesis at room temperature of both random and block copolymers in high yield and with molar mass, Mn, in the range 12-22 kg mol- 1. The composition and microstructure of the random copolymers were regulated by varying the monomers' ratio. Diverse cleavable groups, i.e., ester/ether and carbonate bonds, were statistically incorporated along the same polymer chain to yield materials able to degrade under hydrolytic, oxidative and enzymatic conditions. Bulk degradation was the mechanism that took place under hydrolytic conditions, while the oxidative and enzymatic environments lead to surface erosion. The rate of mass loss of the random copolymers was regulated by varying the composition. These results showed how the statistical incorporation of different degradable bonds could pave the way to diverse and more predictable degradation pathways than simple hydrolysis by taking advantages of the surrounding environment to trigger surface erosion.
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| 7. |
- Badia, J. D., et al.
(författare)
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Assessing the MALDI-TOF MS sample preparation procedure to analyze the influence of thermo-oxidative ageing and thermo-mechanical degradation on poly (Lactide)
- 2011
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Ingår i: European Polymer Journal. - : Elsevier BV. - 0014-3057 .- 1873-1945. ; 47:7, s. 1416-1428
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Tidskriftsartikel (refereegranskat)abstract
- Multiple processing by means of successive injection cycles was used to simulate the thermo-mechanical degradation effects on the oligomeric distribution of PLA under mechanical recycling. Likewise, an accelerated thermal ageing over PLA glass transition was performed in order to simulate its service life. MALDI-TOF MS was used for the analysis and the sample preparation procedure was assessed by means of a statistical Design of Experiments (DoE). The quality effects in use for the analysis were signal-to-noise ratio and Resolution. Different matrixes, analyte/matrix proportions and the use of NaTFA as cationization agent were considered. A deep inspection of the statistical results provided a better understanding of the influence of the different factors, individually or in combination, to the signal. The application of DoE for the improvement of the MALDI measurement of PLA stated that the best combination of factors (levels) was the following: matrix (s-DHB), proportion analyte/matrix (1/5 V/V), and no use of cationization agent. Degradation primarily affected the initially predominant cyclic [LA(C)](n) and linear H-[LA(L)](n)-OH species, where LA stands for a PLA repeating unit. Intramolecular and intermolecular transesterifications as well as hydrolytic and homolytic reactions took place during the formation and disappearance of oligomeric species. In both degradation mechanisms induced by thermal ageing and thermo-mechanical degradation, the formation of H-[LA(L)](n)-O-CH(3) by intermolecular transesterifications was highlighted.
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| 8. |
- Bakare, Fatimat, et al.
(författare)
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Synthesis and characterization of unsaturated lactic acid based thermoset bio-resins
- 2014
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Ingår i: European Polymer Journal. - : Pergamon Press. - 0014-3057 .- 1873-1945. ; 67, s. 570-582
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Tidskriftsartikel (refereegranskat)abstract
- Bio-based thermoset resins have been synthesized using lactic acid oligomers, which were functionalized with carbon–carbon double bonds, in order to allow their crosslinking by a free radical mechanism. Two different resin structures were synthesized. One resin was composed of an allyl alcohol terminated lactic acid oligomer, which was end-functionalized with methacrylic anhydride (MLA resin). The second resin was a mixture of the same allyl alcohol-lactic acid oligomer, and penthaerythritol. This mixture was end-functionalized with methacrylic anhydride, in order to get a methacrylate functionalized lactic acid oligomer, and methacrylate functionalized penthaerythritol (PMLA resin). The synthesized resins were characterized using FT-IR, 1H NMR and 13C NMR spectroscopy, differential scanning calorimetry as well as dynamic mechanical analysis to confirm the resin structure and reactivity. The flow viscosities were also measured in order to evaluate the suitability of the resins to be used as a matrix in composite applications. The results showed that the PMLA resin has better mechanical, thermal and rheological properties than the MLA resin, and both had properties which were comparable with a commercial unsaturated polyester resin. The high biobased content of 90% and the high glass transition temperature at 100 °C for the PMLA resin makes it an attractive candidate for composite applications where crude oil based unsaturated polyester resins are normally used.
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| 9. |
- Bargathulla, Ibrahim, et al.
(författare)
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Pegylated bis-indolyl polyurethane dendrimer : Empty drug carrier with prominent anticancer activity
- 2021
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Ingår i: European Polymer Journal. - : Elsevier BV. - 0014-3057. ; 153
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Tidskriftsartikel (refereegranskat)abstract
- Blocked isocyanate-terminated, bioactive bis-indole based polyurethane dendrimers of generation G0 – G3 were subjected to urethane interchange reaction with poly(ethylene glycol) monomethyl ether; the reactions yielded corresponding PEGylated dendrimers. The structures of the PEGylated dendrimers were confirmed using spectroscopic and SEC-MALS techniques. The PDI of the polymers were found between 1.24 and 1.49 and these values were on par with 1.46 of poly(ethylene glycol) monomethyl ether used. All the PEGylated dendrimers were found to have a prominent cytotoxicity in human breast (MDA MB-231) and lung (A549) cancer cells. Based on the MTT, AO/EtBr staining and ROS assay results, PEGylated G2 and G3 dendrimers were further subjected to determination of apoptosis using protein markers; the pro-apoptotic markers BaX and caspase-3 were found up regulated and the anti-apoptotic marker Bcl-2 was down regulated. The results confirmed that the PEGylated bis-indolyl G3 polyurethane dendrimer – an empty drug carrier – itself had strong tendency to activate apoptosis type cell death in human cancer cells.
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| 10. |
- Barreto, C., et al.
(författare)
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Multiwall carbon nanotube/PPC composites: Preparation, structural analysis and thermal stability
- 2013
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Ingår i: European Polymer Journal. - : Elsevier BV. - 0014-3057 .- 1873-1945. ; 49:8, s. 2149-2161
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Tidskriftsartikel (refereegranskat)abstract
- The focus of this report concerns the preparation nanocomposites from poly(propylene carbonate) (PPC) and multiwall carbon nanotubes (MWNTs). A solvent route using tetrahydrofuran, ethoxylated non- ionic surfactants combined with sonication was found to be successful in deagglomerating and dispersing the nanotubes. Transmission electron microscopy revealed highly disentangled and dispersed nanotubes and was supported by the qualitative stability evaluations. The morphology and molecular mobility of the prepared nanocomposites (0.5, 3.0 and 5.0 wt% of nanotubes) were characterized by rheology, microscopy, low-field solid-state nuclear magnetic resonance, and electrical conductivity. The networking of nanotubes was highest with a stearyl alcohol ethoxylate surfactant, and was found to improve with the sonication time. Nanotube percolation was established, both rheologically and electrically, from a filler content of approximately 0.5 wt%. A higher tendency toward particle agglomeration was observed at higher MWNT loadings. Only minor changes in the glass transition temperature were measured presumably due to the presence of solvent and surfactant residues. The thermal stability was marginally improved by increasing the loading and dispersion of the nanotubes, and appeared to be modified by solvent and surfactant residues.
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