| 1. |
- Andersson, Mattias, 1985, et al.
(författare)
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Additive-like amounts of HDPE prevent creep of molten LDPE: Phase-behavior and thermo-mechanical properties of a melt-miscible blend
- 2017
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Ingår i: Journal of Polymer Science, Part B: Polymer Physics. - : Wiley. - 1099-0488 .- 0887-6266. ; 55:2, s. 146-156
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Tidskriftsartikel (refereegranskat)abstract
- Low-density polyethylene (LDPE) is the preferred type of polyolefin for many medical and electrical applications because of its superior purity and cleanliness. However, the inferior thermo-mechanical properties as compared to, for example, high-density polyethylene (HDPE), which arise because of the lower melting temperature of LDPE, constitute a significant drawback. Here, we demonstrate that the addition of minute amounts of HDPE to a LDPE resin considerably improves the mechanical integrity above the melting temperature of LDPE. A combination of dynamic mechanical analysis and creep experiments reveals that the addition of as little as 1 to 2 wt% HDPE leads to complete form stability above the melting temperature of LDPE. The investigated LDPE/HDPE blend is found to be miscible in the melt, which facilitates the formation of a solid-state microstructure that features a fine distribution of HDPE-rich lamellae. The absence of creep above the melting temperature of LDPE is rationalized with the presence of tie chains and trapped entanglements that connect the few remaining crystallites.
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| 2. |
- Andersson, S. Peter
(författare)
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Pressure and volume dependence of thermal conductivity and isothermal bulk modulus up to 1 GPa for poly(isobutylene)
- 1998
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Ingår i: Journal of Polymer Science Part B. - : John Wiley & Sons. - 0887-6266 .- 1099-0488. ; 36:10, s. 1781-1792
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Tidskriftsartikel (refereegranskat)abstract
- The thermal conductivity λ and heat capacity per unit volume ρcp of poly(isobutylene)s, one 2.8 in weight average molecular weight and one 85 kg mol-1 in viscosity average molecular weight (PIB-2800 and PIB-85000), have been measured in the temperature range 170-450 K at pressures up to 2 GPa using the transient hot-wire method. At 297 K and atmospheric pressure, λ = 0.115 W m-1 K-1 for PIB-2800 and λ = 0.120 W m-1 K-1 for PIB-85000. The bulk modulus BT has been measured in the temperature range 170-297 K up to 1 GPa. At atmospheric pressure, the room temperature bulk moduli BT are 2.0 GPa for PIB-2800 and 2.5 GPa for PIB-85000 with dBT/dp = 10 for both. These data were used to calculate the volume dependence of λ,g = -(∂λ/λ / ∂V/V)T.At room temperature and atmospheric pressure (liquid phase) we find g = 3.4 for PIB-2800 and g = 3.9 for PIB-85000, but g depends strongly on temperature for both molecular weights. The difference in g between the glassy state and liquid phase is small and just outside the inaccuracy of g of about 8%. The best predictions for g are given by the theoretical model of Horrocks and McLaughlin. We have found that PIE exhibits two relaxations, where one is associated with the glass transition. The value for dTg/dp at atmospheric pressure (for the main glass transition) is about 0.21 K MPa-1 for both molecular weights.
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| 3. |
- Andersson, S. Peter, et al.
(författare)
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Volume dependence of thermal conductivity and bulk modulus for poly(propylene glycol)
- 1998
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Ingår i: Journal of Polymer Science Part B. - : John Wiley & Sons. - 0887-6266 .- 1099-0488. ; 36:2, s. 345-355
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Tidskriftsartikel (refereegranskat)abstract
- The thermal conductivity λ and heat capacity per unit volume of poly(propylene glycol) PPG (0.4 and 4.0 kg.mol-1 in number-average molecular weight) have been measured in the temperature range 150-295 K at pressures up to 2 GPa using the transient hot-wire method. At 295 K and atmospheric pressure, λ = 0.147 W m-1K-1 for PPG (0.4 kg.mol-1) and λ = 0.151 W m-1K-1 for PPG (4.0 kg.mol-1). The temperature dependence of λ is less than 4 x 10-4 W m-1K-2 for both molecular weights. The bulk modulus has been measured in the temperature range 215-295 K up to 1.1 GPa. At atmospheric pressure, the room temperature bulk moduli are 1.97 GPa for PPG(0.4 kg.mol-1) and 1.75 GPa for PPG (4.0 kg.mol-1). These data were used to calculate the volume dependence of λ, g = -((∂λ/λ)/(∂V/V))T. At room temperature and atmospheric pressure (liquid phase) we find g = 2.79 for PPG (0.4 kg.mol-1) and g = 2.15 for PPG (4.0 kg.mol-1). The volume dependence of g, (∂g /∂ log V)T varies between -19 to -10 for both molecular weights. Under isochoric conditions, g is nearly independent of temperature. The difference in g between the glassy state and liquid phase is small and just outside the inaccuracy of g of about 8%. The theoretical model for λ by Horrocks and McLaughlin yields an overestimate of g by up to 120%.
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| 4. |
- Andersson, S. Peter, et al.
(författare)
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Volume dependence of thermal conductivity and isothermal bulk modulus up to 1 GPa for poly(vinyl acetate)
- 1998
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Ingår i: Journal of Polymer Science Part B. - : John Wiley & Sons. - 0887-6266 .- 1099-0488. ; 36:9, s. 1451-1463
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Tidskriftsartikel (refereegranskat)abstract
- The thermal conductivity λ and heat capacity per unit volume of poly(vinyl acetate) (260 kg mol-1 in weight average molecular weight) have been measured in the temperature range 150-450 K at pressures up to 1 GPa using the transient hot-wire method, which yielded λ = 0.19 W m-1 K-1 at atmospheric pressure and room temperature. The bulk modulus K has been measured in the temperature range 150-353 K up to 1 GPa. At atmospheric pressure and room temperature, K = 4.0 GPa and (∂K/∂p)T = 8.3. The volume data were used to calculate the volume dependence of λ,g = -((∂λ/λ)/(∂V/V))T.The values for g of the liquid and glassy states were 3.0 and 2.7, respectively, and g of the latter was almost independent of volume and temperature. Theoretical models can predict the value for g of the glassy state to within 25%.
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| 5. |
- Anselmo, Ana Sofia, 1980-, et al.
(författare)
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Molecular Orientation and Composition at the Surface of Spin-Coated Polyfluorene:Fullerene Blend Films
- 2013
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Ingår i: Journal of Polymer Science Part B. - Hoboken, New Jersey : John Wiley & Sons. - 0887-6266 .- 1099-0488. ; 51:3, s. 176-182
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Tidskriftsartikel (refereegranskat)abstract
- The surface composition in spin-coated films of polyfluorene:fullerene blends was determined quantitatively by near-edge X-ray absorption fine structure (NEXAFS) spectroscopy. By comparing partial and total electron yield spectra, we found vertical compositional differences in the surface region. Furthermore, the orientation of the polymer chains was investigated by variable-angle NEXAFS. Blend films of poly[(9,9-dioctylfluorenyl-2,7-diyl)-co-5,5-(4′,7′-di-2-thienyl-2′,1′,3′-benzothiadiazole] with [6,6]-phenyl-C61-butyric acid methyl ester in two different blend ratios were studied. Results showed polymer enrichment of the surfaces for films with a polymer:fullerene weight ratio of 20:80 and of 50:50, spin-coated from both chlorobenzene and chloroform solutions. The angular dependence of the NEXAFS spectra of the pure polymer films showed a preferential plane-on orientation, which was slightly stronger in the subsurface region than at the surface. In blend films, this orientational preference was less pronounced and the difference between surface and subsurface vanished
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| 6. |
- Arge, Tummas Napoleon, et al.
(författare)
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Measuring structural inhomogeneity of a helical conjugated polymer at high pressure and temperature
- 2019
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Ingår i: Journal of Polymer Science, Part B: Polymer Physics. - : Wiley. - 0887-6266. ; 57:7, s. 392-396
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Tidskriftsartikel (refereegranskat)abstract
- We report on X-ray scattering measurements of helical poly[9,9-bis(2-ethylhexyl)-fluorene-2,7-diyl] by mapping the sample with 10 μm spatial resolution from 0.3 GPa to 36 GPa. We follow the strongest 00l reflection, which moves toward higher scattering angles with pressure indicating planarization of helical polyfluorene. Lateral inhomogeneity is increased for >10 GPa concomitant with the solidification of the pressure transmitting medium (a 4:1 mixture of methanol and ethanol). We also follow the 00l reflection with increasing temperature at the constant pressure of 4.3 GPa in neon. We observe a sharp shift toward higher scattering angles indicative of a phase transition at 167–176 °C.
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| 7. |
- Asad Ayoubi, Mehran, et al.
(författare)
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Morphological Investigation of Polydisperse Asymmetric Block Copolymer Systems of Poly(styrene) and Poly(methacrylic acid) in the Strong Segregation Regime
- 2013
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Ingår i: Journal of Polymer Science. Part B, Polymer Physics. - : Wiley. - 0887-6266. ; 51:23, s. 1657-1671
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Tidskriftsartikel (refereegranskat)abstract
- Samples of compositionally (highly) asymmetric diblock copolymers and, also, mixtures of diblock and triblock copolymers (the latter obtained as end-coupling products of two diblock molecules of the mixture), composed of (a) monodisperse majority block(s) of poly(styrene) (PS) and a polydisperse minority block of poly(methacrylic acid) (PMAA), microphase separate into spherical PMAA microdomains, either in disordered liquid-like state or body-centered-cubic (BCC) arrangement, at various annealing temperatures T, in the strong segregation regime SSR. We found that (i) the microphase separated state is favored over an anticipated molecularly homogenous state, (ii) the spherical microdomain morphology (with BCC symmetry) is favored over an anticipated hexagonally packed cylindrical morphology, (iii) the extent of the dissolution of short PMAA blocks in the PS material can be quantified, (iv) the spherical microdomains are dilated, and (v) despite molecular-weight (and architectural) polydispersity, well-ordered BCC structures can be obtained. (c) 2013 Wiley Periodicals, Inc.
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| 8. |
- Aurand, Bastian, et al.
(författare)
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Preparation and characterization of nanometer-thin freestanding polymer foils for laser-ion acceleration
- 2013
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Ingår i: Journal of Polymer Science. Part B, Polymer Physics. - : Wiley. - 0887-6266. ; 51:18, s. 1355-1360
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Tidskriftsartikel (refereegranskat)abstract
- We report on the production and characterization of polymer-based ultra-thin (sub 10 nm) foils suited for experiments on laser-ion acceleration in the regime of radiation pressure acceleration. Beside the remarkable mechanical stability compared with commonly used diamond-like-carbon foils, a very homogeneous layer thickness and a small surface roughness have been achieved. We describe the technical issues of the production process as well as detailed studies of the mechanical stability and surface roughness tests. The capability of producing uniform targets of large area is essential for advanced laser-ion acceleration projects which are dealing with high repetition rate and extended measurement series, but might also be useful for other applications which require ultra-thin and freestanding substrates of high quality. (c) 2013 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2013, 51, 1355-1360
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| 9. |
- Aziz, Shazed, et al.
(författare)
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Controlled and scalable torsional actuation of twisted nylon 6 fiber
- 2016
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Ingår i: Journal of Polymer Science Part B. - : John Wiley & Sons. - 0887-6266 .- 1099-0488. ; 54:13, s. 1278-1286
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Tidskriftsartikel (refereegranskat)abstract
- Large‐scale torsional actuation occurs in twisted fibers and yarns as a result of volume change induced electrochemically, thermally, photonically, and other means. A quantitative relationship between torsional actuation (stroke and torque) and volume change is here introduced. The analysis is based on experimental investigation of the effects of fiber diameter and inserted twist on the torsional stroke and torque measured when heating and cooling nylon 6 fibers over the temperature range of 26–62 °C. The results show that the torsional stroke depends only on the amount of twist inserted into the fiber and is independent of fiber diameter. The torque generated is larger in fibers with more inserted twist and with larger diameters. These results are successfully modeled using a single‐helix approximation of the twisted fiber structure
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| 10. |
- Backman, Anna, et al.
(författare)
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Transport properties of uniaxially oriented aliphatic polyketone
- 2004
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Ingår i: Journal of Polymer Science Part B. - : Wiley. - 0887-6266 .- 1099-0488. ; 42:6, s. 947-955
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Tidskriftsartikel (refereegranskat)abstract
- The oxygen, carbon dioxide, and water-transport properties of a uniaxially oriented aliphatic polyketone were determined. The polyketone was drawn to 5-10 times its original length. The transport properties were related to changes in crystallinity estimated by differential scanning calorimetry and density measurements and by changes in the molecular and crystal orientation assessed by, respectively, infrared and X-ray spectroscopy. The film structures were characterized by confocal scanning laser microscopy and scanning electron microscopy. Stress-strain tests on the drawn specimens enabled the impacts of orientation on the transport and mechanical properties to be compared. A draw-induced increase in crystallinity and molecular orientation yielded permeabilities at a draw ratio of 10 that were 30-40% of the original value, and the percentage decrease was basically independent of the type of gas/vapor molecule. Also, the diffusivities of oxygen and carbon dioxide decreased by an order of magnitude. The fact that the amorphous permeability was peaking at a draw ratio of about 5 was a consequence of a peak in amorphous solubility, which was very high for oxygen and absent for water. It was suggested that the peak in solubility was mainly caused by the destruction of the polymer hydrogen-bond network during drawing and crystal reorientation. The impact of structural reorganization within the polymer and presence of surface valleys seemed to have less impact on the mechanical properties than on the transport properties. This suggested that transport data are more sensitive than mechanical data in probing material defects and changes in molecular packing and morphology.
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