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Träfflista för sökning "AMNE:(NATURAL SCIENCES Chemical Sciences Polymer Chemistry) srt2:(2010-2014)"

Sökning: AMNE:(NATURAL SCIENCES Chemical Sciences Polymer Chemistry) > (2010-2014)

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1.
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2.
  • Nicholls, Ian A., et al. (författare)
  • Rational design of biomimetic molecularly imprinted materials : theoretical and computational strategies for guiding nanoscale structured polymer development
  • 2011
  • Ingår i: Analytical and Bioanalytical Chemistry. - : Springer Science and Business Media LLC. - 1618-2642 .- 1618-2650. ; 400:6, s. 1771-1786
  • Forskningsöversikt (refereegranskat)abstract
    • In principle, molecularly imprinted polymer science and technology provides a means for ready access to nano-structured polymeric materials of predetermined selectivity. The versatility of the technique has brought it to the attention of many working with the development of nanomaterials with biological or biomimetic properties for use as therapeutics or in medical devices. Nonetheless, the further evolution of the field necessitates the development of robust predictive tools capable of handling the complexity of molecular imprinting systems. The rapid growth in computer power and software over the past decade has opened new possibilities for simulating aspects of the complex molecular imprinting process. We present here a survey of the current status of the use of in silico-based approaches to aspects of molecular imprinting. Finally, we highlight areas where ongoing and future efforts should yield information critical to our understanding of the underlying mechanisms sufficient to permit the rational design of molecularly imprinted polymers.
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3.
  • Wiklander, Jesper G., 1974-, et al. (författare)
  • Towards a synthetic avidin mimic
  • 2011
  • Ingår i: Analytical and Bioanalytical Chemistry. - : Springer Science and Business Media LLC. - 1618-2642 .- 1618-2650. ; 400:5, s. 1397-1404
  • Tidskriftsartikel (refereegranskat)abstract
    • A series of streptavidin-mimicking molecularly imprinted polymers has been developed and evaluated for their biotin binding characteristics. A combination of molecular dynamics and NMR spectroscopy was used to examine potential polymer systems, in particular with the functional monomers methacrylic acid and 2-acrylamidopyridine. The synthesis of copolymers of ethylene dimethacrylate and one or both of these functional monomers was performed. A combination of radioligand binding studies and surface area analyses demonstrated the presence of selectivity in polymers prepared using methacrylic acid as the functional monomer. This was predicted by the molecular dynamics studies showing the power of this methodology as a prognostic tool for predicting the behavior of molecularly imprinted polymers.
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4.
  • Younesi, Reza, et al. (författare)
  • Li-O-2 Battery Degradation by Lithium Peroxide (Li2O2): A Model Study
  • 2013
  • Ingår i: Chemistry of Materials. - : American Chemical Society (ACS). - 1520-5002 .- 0897-4756. ; 25:1, s. 77-84
  • Tidskriftsartikel (refereegranskat)abstract
    • The chemical stability of the Li-O-2 battery components (cathode and electrolyte) in contact with lithium peroxide (Li2O2) was investigated using X-ray photoelectron spectroscopy (XPS). XPS is a versatile method to detect amorphous as well as crystalline decomposition products of both salts and solvents. Two strategies were employed. First, cathodes including carbon, alpha-MnO2 catalyst, and Kynar binder (PVdF-HFP) were exposed to Li2O2 and LiClO4 in propylene carbonate (PC) or tetraethylene glycol dimethyl ether (TEGDME) electrolytes. The results indicated that Li2O2 degrades TEGDME to carboxylate containing species and that the decomposition products, in turn, degraded the Kynar binder. The alpha-MnO2 catalyst was unaffected. Second, Li2O2 model surfaces were kept in contact with different electrolytes to investigate the chemical stability and also the resulting surface layer on Li2O2. Further, the XPS experiments revealed that the Li salts such as LiPF6, LiBF4, and LiC!
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5.
  • Tan, Semra, et al. (författare)
  • Poly(ether amine) and cross-linked poly(propylene oxide) diacrylate thin-film polymer electrolyte for 3D-microbatteries
  • 2010
  • Ingår i: Electrochemistry communications. - : Elsevier BV. - 1388-2481 .- 1873-1902. ; 12:11, s. 1498-1500
  • Tidskriftsartikel (refereegranskat)abstract
    • This paper presents a novel thin-film electrolyte of a 2:1 blend of polyetheramine (glyceryl poly(oxypropylene)) and cross-linked oligomeric poly(propylene oxide) diacrylate with LiTFSI. The polyetheramine acts as a surfactant, and can thereby be applied as a conformal coating on complex surfaces-here demonstrated for porous LiFePO4 cathodes-making it useful for 3D-microbatteries. The poly(propylene oxide) diacrylate blends with the surfactant and is easily UV cross-linked, thereby ensuring good mechanical stability. Electrolytes, ∼ 2 μm thick, were casted onto LiFePO 4 cathodes and cycled against metallic lithium, displaying stable discharge capacities of ∼ 8 mAh/g at room temperature and ∼ 120 mAh/g at 60 °C. The electrolyte showed conductivities of 3.45 × 10 - 6 and 5.80 × 10- 5 S cm- 1 at room temperature and 60 °C, respectively.
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6.
  • Börjesson, Karl, 1982, et al. (författare)
  • Conjugated anthracene dendrimers with monomer-like fluorescence
  • 2014
  • Ingår i: RSC Advances. - : Royal Society of Chemistry (RSC). - 2046-2069. ; 4:38, s. 19846-19850
  • Tidskriftsartikel (refereegranskat)abstract
    • Two generations of highly emissive conjugated anthracene dendrimers containing up to 9 anthracene units are presented. In these dendrimers, anthracene-like absorption and emission properties are preserved due to the relatively weak electronic coupling between the anthracene units, while evidence of fast crosstalk within the molecular framework is still observed.
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7.
  • Höglund, Odd, et al. (författare)
  • A new resorbable device for ligation of blood vessels - A pilot study
  • 2011
  • Ingår i: Acta Veterinaria Scandinavica. - : Springer Science and Business Media LLC. - 0044-605X .- 1751-0147. ; 53, s. 47-
  • Tidskriftsartikel (refereegranskat)abstract
    • Background: During surgery, controlled haemostasis to prevent blood loss is vital for a successful outcome. It can be difficult to ligate vessels located deep in the abdomen. A device that is easy to use and enables secure ligatures could be beneficial. Cable ties made of nylon have been used for ligation but the non-resorbable material caused tissue reactions. The objective of this study was to use a resorbable material to construct a device with a self-locking mechanism and to test its mechanical strength and ligation efficiency. Methods: The device was manufactured by injection moulding of polydioxanone, a resorbable polymer used for suture materials. Polydioxanone with inherent viscosities of 1.9 dL/g and 1.3 dL/g were tested. The device consisted of a perforated flexible band which could be pulled through a case with a locking mechanism. After a first version of the device had been tested, some improvements were made. The locking case was downsized, corners were rounded off, the band was made thicker and the mould was redesigned to produce longer devices. Tensile tests were performed with the second version. The first version of the device was used to ligate the ovarian pedicle in a euthanized dog and to test echogenicity of the device with ultrasound. Compression of vessels of the ovarian pedicle was examined by histology. Both versions of the device were tested for haemostasis of and tissue grip on renal arteries in six anaesthetised pigs. Results: The tensile strength of the flexible band of the devices with inherent viscosity of 1.9 dL/g was 50.1 +/- 5.5 N (range 35.2-62.9 N, n = 11) and the devices with inherent viscosity of 1.3 dL/g had a tensile strength of 39.8 +/- 8.1 N (range 18.6-54.2 N, n = 11). Injection moulding of the polymer with lower inherent viscosity resulted in a longer flow distance. Both versions of the device had an effective tissue grip and complete haemostasis of renal arteries was verified. The device attached to the ovarian pedicle could be seen with ultrasound, and vessel compression and occlusion were verified by histology. Conclusions: Tests of functionality of the device showed complete haemostasis and good tissue grip. Devices with a band of sufficient length were easily applied and tightened in tissue.
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8.
  • Martinez-Sanz, Elena, et al. (författare)
  • Bone reservoir : Injectable hyaluronic acid hydrogel for minimal invasive bone augmentation
  • 2011
  • Ingår i: Journal of Controlled Release. - : Elsevier BV. - 0168-3659 .- 1873-4995. ; 152:2, s. 232-240
  • Tidskriftsartikel (refereegranskat)abstract
    • A strategy has been designed to develop hyaluronic acid (HA) hydrogel for in vivo bone augmentation using minimal invasive technique. A mild synthetic procedure was developed to prepare aldehyde modified HA by incorporating an amino-glycerol side chain via amidation reaction and selective oxidation of the pendent group. This modification, upon mixing with hydrazide modified HA formed hydrazone-crosslinked hydrogel within 30 s that was stable at physiological pH. In vitro experiments showed no cytotoxicity of hydrogel with the controlled release of active bone morphogenic protein-2 (BMP-2). In vivo evaluation of this gel as a BMP-2 carrier was performed by injecting gels over the rat calvarium and showed bone formation in 8 weeks in correlation with the amount of BMP-2 loaded (0, 1 and 30 pig) within the gel. Furthermore, hydrogels with 30 Kg of BMP-2 induced less bone formation upon subcutaneous injection in comparison with subperiosteal implantation. Histological examination showed newly formed bone with a high expression of osteocalcin, osteopontin and with angiogenic bone marrow when higher BMP-2 concentration was employed. Our result suggests that novel HA hydrogels could be used as a BMP-2 carrier and can promote bone augmentation for potential orthopedic applications.
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9.
  • Londero, Elisa, 1982, et al. (författare)
  • Desorption of n-alkanes from graphene: a van der Waals density functional study
  • 2012
  • Ingår i: Journal of Physics Condensed Matter. - : IOP Publishing. - 0953-8984 .- 1361-648X. ; 24:42, s. 424212-
  • Tidskriftsartikel (refereegranskat)abstract
    • A recent study of temperature-programmed desorption (TPD) measurements of small linear alkane molecules (n-alkanes, with formula CNH2N+2) from C(0001) deposited on Pt(111) shows a linear relationship of the desorption energy with increasing n-alkane chain length N. We here present a van der Waals density functional study of the desorption barrier energy of the ten smallest n-alkanes (of carbon chain length N = 1–10) from graphene. We find linear scaling with N, including a non-zero intercept with the energy axis, i.e. an offset at the extrapolation to N = 0. This calculated offset is quantitatively similar to the results of the TPD measurements. From further calculations of the polyethylene polymer we offer a suggestion for the origin of the offset.
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10.
  • Bylin, Susanne, 1982 (författare)
  • Mechanisms of Biopolymer Solvation: Development of a two-component ionic liquid solvent system
  • 2014
  • Licentiatavhandling (övrigt vetenskapligt/konstnärligt)abstract
    • Ionic liquids are of potential interest in the processing of lignocellulosic biomass, and/or its components, for the purpose of producing renewable and value-added biomaterials. An understanding of how solvation can be achieved and the way in which the feedstock biopolymers are affected, however, needs to be gained prior to a viable implementation. In this thesis, the solvation of the wood biopolymers cellulose, xylan and lignin in the ionic liquid (IL) 1-ethyl-3-methylimidazolium acetate (EMIMAc) in a novel combination with the second system component 1-methylimidazole (MIM) have been investigated:The solvation of dissolving pulp, beech xylan and LignoBoost lignin model materials, was studied using FBRM (focused beam reflectance measurements) particle characterization in combination with microscopic analysis (cellulose and xylan), determination of molecular weights (xylan and lignin) and 13C- and 31P-NMR (nuclear magnetic resonance spectroscopy) of lignin.It was concluded that the most efficient solvation of cellulose and xylan occurred using 3-4% and 9% IL (n/n anhydroglucose units and n/n anhydroxylose Units), respectively, while polymer integrity was maintained. Cellulose solvation was found to be greatly dependent on the IL to AGU ratio whereas xylan solvation varied greatly with temperature. Moreover, a theoretical model was developed for the solvation of cellulose in the present system. The solvation of lignin was achieved at ~20% lignin loading (w/w), in any combination of MIM/EMIMAc. Regeneration of lignin resulted in two sets of fractions; one exhibiting a general and higher apparent molecular weight (Mw) along with an enrichment of condensed/aliphatic ether linkages and aliphatic hydroxyls, and the other exhibiting a lower apparent Mw and an enrichment of carboxylic and phenolic groups. The knowledge of biopolymer solvation gained in the present solvent system provides future opportunities of tuning extraction and/or fractionation processes to suite the specifications of a particular biomass-derived product.
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