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Hard Segments (hard + segment)
Selected AbstractsSegmented Block Copolymers with Monodisperse Hard Segments: The Influence of H-Bonding on Various PropertiesMACROMOLECULAR MATERIALS & ENGINEERING, Issue 8 2009Gerard J. E. Biemond Abstract The properties of segmented-copolymer-based H-bonding and non-H-bonding crystallisable segments and poly(tetramethylene oxide) segments were studied. The crystallisable segments were monodisperse in length and the non-hydrogen-bonding segments were made of tetraamidepiperazineterephthalamide (TPTPT). The polymers were characterised by DSC, FT-IR, SAXS and DMTA. The mechanical properties were studied by tensile, compression set and tensile set measurements. The TPTPT segmented copolymers displayed low glass transition temperatures (Tg, ,70,°C), good low-temperature properties, moderate moduli (G,,,,10,33 MPa) and high melting temperatures (185,220,°C). However, as compared to H-bonded segments, both the modulus and the yield stress were relatively low. [source] Synthesis and characterization of novel polyurethanes based on N1,N4 -bis[(4-hydroxyphenyl)methylene]succinohydrazide hard segment,JOURNAL OF APPLIED POLYMER SCIENCE, Issue 4 2008A. V. Raghu Abstract This article deals with the synthesis and characterization of novel polyurethanes (PUs) by the reaction between two aromatic diisocyanates (4,4,-diphenylmethane diisocyanate and tolylene 2,4-diisocyanate) and two aliphatic diisocyanates (isophorone diisocyanate and hexamethylene diisocyanate) with N1,N4 -bis[(4-hydroxyphenyl)methylene]succinohydrazide, which acted as hard segment. UV,vis, FTIR, 1H NMR, 13C NMR, and DSC/TGA analytical technique has been used to determine the structural characterization and thermal properties of the hard segmented PUs. X-ray diffraction revealed that PUs contained semicrystalline and amorphous regions that varied depending upon the nature of the backbone structures. PUs were soluble in polar aprotic solvents. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 [source] Studies on thermoplastic polyurethanes based on new diphenylethane-derivative diols.JOURNAL OF APPLIED POLYMER SCIENCE, Issue 3 2008Abstract Two series of poly(ether urethane)s and one series of poly(ester urethane)s were synthesized, containing, respectively, poly(oxytetramethylene) diol (PTMO) of Mn = 1000 and 2000 and poly(,-caprolactone) diol of Mn = 2000 as soft segments. In each series the same hard segment, i.e., 4,4,-(ethane-1,2-diyl)bis(benzenethiohexanol)/hexane-1,6-diyl diisocyanate, with different content (, 14,72 wt %) was used. The polymers were prepared by a one-step melt polymerization in the presence of dibutyltin dilaurate as a catalyst, at the molar ratio of NCO/OH = 1 (in the case of the polymers from PTMO of Mn = 1000 also at 1.05). For all polymers structures (by FTIR and X-ray diffraction analysis) and physicochemical, thermal (by differential scanning calorimetry and thermogravimetric analysis), and tensile properties as well as Shore A/D hardness were determined. The resulting polymers were thermoplastic materials with partially crystalline structures (except the polymer with the highest content of PTMO of Mn = 2000). It was found that the poly(ether urethane)s showed lower crystallinity, glass-transition temperature (Tg), and hardness as well as better thermal stability than the poly(ester urethane)s. Poly(ether urethane)s also exhibited higher tensile strength (up to 23.5 MPa vs. 20.3 MPa) and elongation at break (up to , 1950% vs. 1200%) in comparison with the corresponding poly(ester urethane)s. Among the poly(ether urethane)s an increase in soft-segment length was accompanied by an increase in thermal stability, tensile strength, and elongation at break, as well as a decrease in Tg, crystallinity, and hardness. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008 [source] Solid polymer electrolytes III: Preparation, characterization, and ionic conductivity of new gelled polymer electrolytes based on segmented, perfluoropolyether-modified polyurethaneJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 4 2002Chi-Chang Chen Abstract New segmented polyurethanes with perfluoropolyether (PFPE) and poly(ethylene oxide) blocks were synthesized from a fluorinated macrodiol mixed with poly(ethylene glycol) (PEG) in different ratios as a soft segment, 2,4-toluene diisocyanate as a hard segment, and ethylene glycol as a chain extender. Fourier transform infrared, NMR, and thermal analysis [differential scanning calorimetry and thermogravimetric analysis (TGA)] were used to characterize the structures of these copolymers. The copolymer films were immersed in a liquid electrolyte (1 M LiClO4/propylene carbonate) to form gel-type electrolytes. The ionic conductivities of these polymer electrolytes were investigated through changes in the copolymer composition and content of the liquid electrolyte. The relative molar ratio of PFPE and PEG in the copolymer played an important role in the conductivity and the capacity to retain the liquid electrolyte solution. The copolymer with a 50/50 PFPE/PEG ratio, having the lowest decomposition temperature shown by TGA, exhibited the highest ionic conductivity and lowest activation energy for ion transportation. The conductivities of these systems were about 10,3 S cm,1 at room temperature and 10,2 S cm,1 at 70 °C; the films immersed in the liquid electrolyte with an increase of 70 wt % were homogenous with good mechanical properties. © 2002 John Wiley & Sons, Inc. J Polym Sci Part A: Polym Chem 40: 486,495, 2002; DOI 10.1002/pola.10119 [source] Influence of TiO2 Nanoparticles Incorporated into Elastomeric Polyesters on their Biocompatibility In Vitro and In VivoADVANCED ENGINEERING MATERIALS, Issue 11 2009Miroslawa El-Fray Abstract Fibroblasts proliferation and apoptosis as well as tissue response after implantation of elastomers containing nanocrystalline TiO2 were investigated in the present in vitro and in vivo study. Materials investigated were soft poly(aliphatic/aromatic-ester) multiblock thermoplastic elastomers with poly(ethylene terephthalate) (PET) hard segments and dimerized linoleic acid (DLA) soft segments, respectively, containing 0.2,wt% TiO2 nanoparticles. An investigation of the influence of TiO2 nanoparticles incorporated into polymeric material on in vitro biocompatibility revealed enhanced cell proliferation and diminished number of necrotic and apoptotic cells as compared to nanoparticles-free polymer. Implantation tests indicated that the observed tissue changes were similar to those observed with medical-grade silicone elastomer, no evidence of contact necrosis being observed. The unchanged morphology of rat liver hepatocytes and the lack of parenchymal necrosis also indicated that exposure to the material containing TiO2 nanoparticles, did not cause any cytotoxic reactions. The present study, thus, showed that elastomeric polyester containing TiO2 nanoparticles are interesting biomimetic constructs for improved tissue regeneration. [source] Structure and properties of cross-linked polyurethane copolymersADVANCES IN POLYMER TECHNOLOGY, Issue 3 2009S. Oprea Abstract Polyurethane elastomers based on polyester diols and aromatic or aliphatic diisocyanates can be used as vibration dampers and isolation materials. Two series of cross-linked polyurethanes with various hard segment structures and different amounts were prepared and thermomechanical properties of these materials were studied. Cross-linked polyurethane copolymers composed of poly(ethylene adipate)diol as soft segment and 4,4,-methylenebis(phenylisocyanate), 1,6-hexamethylene diisocyanate, and diols glycerin, 1,4-butanediol, and 1,6-hexanediol as hard segments were synthesized by a two-step process. The networks have been prepared by end-linking a mixture of the bifunctional precursor chains with trifunctional cross-linkers at off-stoichiometric ratios. The results show that the cross-link and the polyurethane hard segment interaction play a special role in the interconnected chain density and its magnitude is revealed by the mechanical properties. Of most importance, maximum stress, tensile modulus, and elongation at break increased significantly at the 22 wt % composition of hard segment content. Interchain cross-linking improves thermal stability, which was measured by thermogravimetric analysis and differential scanning calorimetry. Cross-linked polyurethane behaves as an elastomer and is useful for shock, noise, and vibration control. © 2009 Wiley Periodicals, Inc. Adv Polym Techn 28:165,172, 2009; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/adv.20155 [source] Surface properties of poly(ethylene oxide)-based segmented block copolymers with monodisperse hard segmentsJOURNAL OF APPLIED POLYMER SCIENCE, Issue 2 2009D. Husken Abstract The surface properties of segmented block copolymers based on poly(ethylene oxide) (PEO) segments and monodisperse crystallizable tetra-amide segments were studied. The monodisperse crystallizable segments (T6T6T) were based on terephthalate (T) and hexamethylenediamine (6). Due to the crystallinity of T6T6T being high (, 85%), the amount of amorphous T6T6T dissolved in the polyether phase was limited. The length of the PEO segments was varied (between 600 and 4600 g/mol) and effect of extending the PEO segments with terephthalic groups was investigated. Studied was the hydrophilicity of the surface by contact angle measurements and of the bulk copolymers by water absorption measurements The results were compared with data of PEO-poly(butylene terephthalate) (PEO-PBT) copolymers. For a given hydrophilicity of the bulk copolymer, the surface hydrophilicity decreased in the order PEO-PBT, PEO-T6T6T, and (PEO-T)-T6T6T. The use of short monodisperse hard segments resulted in low contact angles, with a lowest observed value of , 29°. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009 [source] Synthesis, characterization, and acoustic properties of new soluble polyurethanes based on 2,2,-[1,4-phenylenebis(nitrilomethylylidene)diphenol and 2,2,-[4,4,-methylene-di-2-methylphenylene-1,1,-bis(nitrilomethylylidene)]diphenol,JOURNAL OF APPLIED POLYMER SCIENCE, Issue 1 2007A. V. Raghu Abstract Eight novel polyurethanes based on 2,2,-[1,4-phenylenebis(nitrilomethylylidene)]diphenol and 2,2,-[4,4,-methylene-di-2-methylphenylene-1,1,-bis(nitrilomethylylidene)]diphenol acting as hard segments with two aromatic and two aliphatic diisocyanates (4,4,-diphenylmethane diisocyanate, toluene 2,4-diisocyanate, isophorone diisocyanate, and hexamethylene diisocyanate) were prepared and characterized with Fourier transform infrared, UV spectrophotometry, fluorescence spectroscopy, 1H-NMR and 13C-NMR spectroscopy, thermogravimetric analysis, and differential thermal analysis. All the polyurethanes contained domains of semicrystalline and amorphous structures, as indicated by X-ray diffraction. The acoustic properties and solubility parameters were calculated with the group contribution method. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 2007 [source] Synthesis, characterization, and molecular modeling studies of novel polyurethanes based on 2,2,-[ethane-1,2-diylbis(nitrilomethylylidene)]diphenol and 2,2,-[hexane-1,6-diylbis(nitrilomethylylidene)] diphenol hard segments,JOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 20 2006A. V. Raghu Abstract Novel polyurethanes (PUs) based on 2,2,-[ethane-1,2-diylbis(nitrilomethylylidene)]diphenol and 2,2,-[hexane-1,6-diylbis(nitrilomethylylidene)]diphenol as hard segments containing four aromatic diisocyanates (4,4,-diphenylmethane diisocyanate, toluene 2,4-diisocyanate, isophorone diisocyanate, and hexamethylene diisocyanate) have been prepared. Fourier transform infrared, UV spectrophotometry, fluorescence spectroscopy, 1H NMR and 13C NMR spectroscopy, thermogravimetric analysis, and differential thermal analysis have been used to determine the structural characterization and thermal properties of the segmented PUs. All the PUs contain domains of both semicrystalline and amorphous structures, as indicated by X-ray diffraction. The acoustic properties have been calculated with the group contribution method. Molecular dynamics simulations have been performed on all the PUs to estimate the cohesive energy density and solubility parameter values, which compare well with the values calculated with the group contribution method. Furthermore, the simulation protocols have been applied to the PUs to produce X-ray diffraction plots to determine the phase morphology of the PUs. The surface properties of the PUs have been estimated from the simulation protocols. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 6032,6046, 2006 [source] Synthesis and characterization of polyurethane,urea nanoparticles containing methylenedi- p -phenyl diisocyanate and isophorone diisocyanateJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 17 2004In Woo Cheong Abstract Water-based polyurethane,urea (WPUU) nanoparticles containing 4,4,-methylenedi- p -phenyl diisocyanate (MDI) and isophorone diisocyanate (IPDI) were synthesized by a stepwise prepolymer mixing process, that is, the consecutive formation of hydroxyl-terminated and isocyanate-terminated polyurethane prepolymers. The reaction behavior, chemical structure, and consequent morphology of the polyurethane prepolymers and WPUU were investigated with Fourier transform infrared (FTIR), gel permeation chromatography, and NMR techniques with MDI concentrations ranging from 0 (pure IPDI) to 50% with respect to the total moles of isocyanate. Wide-angle X-ray diffraction and differential scanning calorimetry patterns showed that the crystallinity of WPUU, which mostly originated from crystallizable poly(tetramethylene adipate) polyol, was significantly affected by the MDI content. Both the crystallinity and melting temperature of WPUU decreased as the MDI content increased. Deconvoluted relative peak areas of the carbonyl region in the FTIR spectrum revealed that the effect of hydrogen bonding among the hard segments became favorable as the MDI content increased, whereas the hydrogen bonding of the soft segments significantly decreased. © 2004 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 4353,4369, 2004 [source] Low-temperature route to thermoplastic polyamide elastomers,JOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 6 2004Gouher Rabani Abstract Thermoplastic polyamide elastomers were obtained by polymerization of aminobenzoyl-substituted telechelics derived from poly(tetrahydrofuran)-diols (number-average molecular weight: 1400 or 2000 g mol,1) with several diacid dichlorides (terephthaloyl dichloride, 4,4,-biphenyldicarbonyl dichloride, or 2,6-naphthalenedicarbonyl dichloride) and chlorotrimethylsilane in N,N -dimethylacetamide at 0,20 °C. The as-prepared polymers had melting temperatures above 190 °C and exhibited elastic properties at room temperature, as evidenced by dynamic mechanical analysis and stress,strain measurements. The polymer with 2,6-naphthalenedicarboxamide hard segments had the widest rubbery plateau within the series, the highest extension at break, and good recovery properties. © 2004 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 1449,1460, 2004 [source] The Structure of Water in PEO-Based Segmented Block Copolymers and its Effect on Transition TemperaturesMACROMOLECULAR CHEMISTRY AND PHYSICS, Issue 9 2008Debby Husken Abstract The effect of water on block copolymers that contain hydrophilic PEO flexible segments is studied. The polyether phase consisted of either PEO or mixtures of PEO and hydrophobic PTMO, monodisperse crystallisable T6T6T was used as hard segments. Water absorption as a function of relative humidity and PEO content were studied. The PEO melting temperature and crystallinity were strongly reduced when the copolymer absorbed water, while the PTMO phase remained unaffected by its presence. Freezing water was present in the PEO-based copolymers when the PEO phase contained ,30 vol.-% water, its relative amount being almost independent of PEO concentration and molecular weight and the presence of hydrophobic PTMO segments. [source] Segmented Block Copolymers with Monodisperse Aramide End-SegmentsMACROMOLECULAR CHEMISTRY AND PHYSICS, Issue 8 2008Araichimani Arun Abstract Segmented block copolymers were synthesized using monodisperse diaramide (T,T) as hard segments and PTMO with a molecular weight of 2,900 g,·,mol,1 as soft segments. The aramide: PTMO segment ratio was increased from 1:1 to 2:1 thereby changing the structure from a high molecular weight multi-block copolymer to a low molecular weight end-block copolymer. The thermal and thermal-mechanical properties were studied by DSC and DMA. Also studied were the tensile and the elastic properties as well as the melt rheological behavior as a function of frequency. The crystallinity of aramide in the end-block copolymers was found to be higher than in the multi-block copolymer. [source] Effect of Functionalized Carbon Nanotubes on Molecular Interaction and Properties of Polyurethane CompositesMACROMOLECULAR CHEMISTRY AND PHYSICS, Issue 19 2006Nanda Gopal Sahoo Abstract Summary: Functionalized MWNTs were incorporated into PU by solution mixing to improve the mechanical and thermal properties of composites. A homogeneous dispersion of MWNTs was successfully achieved in PU matrix as evidenced by scanning electron microscopy. It may be attributed to the hydrogen bonds existing between CO groups of hard segments of PU chains and COOH groups of the MWNT-COOH. The incorporation of the MWNTs effectively enhanced the crystallization of the PU matrix through heterogeneous nucleation, and the nucleation effect was more evident at 10 wt.-% functionalized MWNTs as compared to other composite systems. Mechanical properties of the PU-MWNTs composites were assessed as a function of MWNT concentration and dispersion of MWNT in PU matrix. The most significant improvement in mechanical properties was obtained, e.g., 740% increase in modulus and 180% increase in tensile strength over pure PU with 20% MWNT content. The thermal stability of composites due to thermal gravimetric measurements was significantly improved. A possible interaction of H-bonding existed between PU chain and MWNT-COOH. [source] Novel Dynamic Viscoelastic Measurements of Polyurethane Copolymer Melts and Their Implication to Tack ResultsMACROMOLECULAR MATERIALS & ENGINEERING, Issue 10 2006Sonia Florez Abstract Summary: A series of polyurethane multiblock copolymers with different proportions of hard segments (urethane) to soft segments (polyadipate of hexane-1,6-diol), are investigated. Dynamic viscoelastic functions of homogeneous melts in the terminal zone are determined. For the first time, entanglement modulus values of such copolymers are reported, which allows estimation of the packing length. These parameters do not vary with changing the hard-to-soft segment ratio, a result that is explained by a compensating effect of the chain architecture. For samples of similar molecular weight, the relaxation time of the terminal zone increases as the hard-to-soft segment ratio augments. The adhesives obtained from PUR solutions show a correlation between the elastic modulus and the debonding stress-strain curves in tack experiments. The storage modulus of the adhesives as a function of frequency at 70,°C. [source] Shape Memory Effect of Bacterial Poly[(3-hydroxybutyrate)- co -(3-hydroxyvalerate)],MACROMOLECULAR RAPID COMMUNICATIONS, Issue 13 2005Young Baek Kim Abstract Summary: A bacterial poly[(3-hydroxybutyrate)- co -(3-hydroxyvalerate)] biosynthesized by Pseudomonas sp. HJ-2 was found to be a shape memory polymer. Permanent shapes were set by annealing at room temperature the samples that had been pre-treated above 95,°C in specified shapes. The temporary shapes were set by stretching and holding the elongated samples. Thermal shrinkage began at 45,°C and stopped at 75,°C to recover to their permanent shapes. Apparently, the orientation induced the formation of hard segments that were responsible for setting the temporary shapes. The shape memory effect of this polymer was explained based on the DSC and XRD results at different phases. The recovery of a coil shape upon heating a strip of HJ-2 PHB35V, demonstrating the polymers shape memory effect. [source] Preparation and properties of transparent thermoplastic segmented polyurethanes derived from different polyolsPOLYMER ENGINEERING & SCIENCE, Issue 5 2007Da-Kong Lee Various segmented polyurethanes of different soft segment structure with hard segment content of about 50 wt% were prepared from 4,4,-diphenylmethane diisocyanate (MDI), 1,4-butanediol and different polyols with a Mn of 2000 by a one-shot, hand-cast bulk polymerization method. The polyols used were a poly(tetramethylene ether)glycol, a poly(tetramethylene adipate)glycol, a polycaprolactonediol and two polycarbonatediols. The segmented polyurethanes were characterized by gel permeation chromatography (GPC), UV-visible spectrometry, differential scanning calorimetry (DSC), dynamic mechanical analysis (DMA), X-ray diffraction, and their tensile properties and Shore A hardness were determined. The DSC and DMA data indicate that the miscibility between the soft segments and the hard segments of the segmented polyurethanes is dependent on the type of the soft segment, and follows the order: polycarbonate segments > polyester segments > polyether segments. The miscibility between the soft segments and the hard segments plays an important role in determining the transparency of the segmented polyurethanes. As the miscibility increases, the transparency of the segmented polyurethanes increases accordingly. The segmented polyurethanes exhibit high elongation and show ductile behavior. The tensile properties are also affected by the type of the soft segment to some extent. POLYM. ENG. SCI., 47:695,701, 2007. © 2007 Society of Plastics Engineers. [source] Preparation and characterization of polyurethane,gold nanocomposites prepared using encapsulated gold nanoparticlesPOLYMER INTERNATIONAL, Issue 7 2010Chao-Ching Chang Abstract Gold nanoparticles (GNPs) have been widely studied due to their unique properties. Although many research groups have developed the synthesis of GNPs using various polymers as stabilizing or reducing agents, the effects of GNPs on the structures and properties of polymer matrices have been less reported. We propose a new design for the preparation of polyurethane,gold (PU,Au) nanocomposites. 11-Mercapto-1-undecanol-coated GNPs acted as the chain extenders and reacted with isocyanates to form covalent bonds between PU and GNPs. PU,Au nanocomposites were successfully synthesized, and the effects of multifunctional GNPs on the structures, morphology and properties of poly(ester urethane) were investigated. Scanning electron microscopy images suggested the GNPs can be dispersed uniformly in the PU matrix. Maltese-cross of spherical crystals was observed in the PU,Au nanocomposites, and the size of the crystals decreased with an increase in gold content. As the gold content increased, the thermal decomposition temperature and the temperature of the maximum decomposition rate increased. The glass transition temperature, crystal melting temperature and melting enthalpy of the soft segment also increased progressively. The results showed that multifunctional GNPs concentrated hard segments and resulted in an increase of heterogeneous nucleation, phase separation and elasticity. Copyright © 2010 Society of Chemical Industry [source] Copolymers based on poly(butylene terephthalate) and polycaprolactone- block -polydimethylsiloxane- block -polycaprolactonePOLYMER INTERNATIONAL, Issue 6 2010Vesna V Anti Abstract A series of novel thermoplastic elastomers, based on poly(butylene terephthalate) (PBT) and polycaprolactone- block -polydimethylsiloxane- block -polycaprolactone (PCL-PDMS-PCL), with various mass fractions, were synthesized through melt polycondensation. In the synthesis of the poly(ester-siloxane)s, the PCL blocks served as a compatibilizer for the non-polar PDMS blocks and the polar comonomers dimethyl terephthalate and 1,4-butanediol. The introduction of PCL-PDMS-PCL soft segments resulted in an improvement of the miscibility of the reaction mixture and therefore in higher molecular weight polymers. The content of hard PBT segments in the polymer chains was varied from 10 to 80 mass%. The degree of crystallinity of the poly(ester-siloxane)s was determined using differential scanning calorimetry and wide-angle X-ray scattering. The introduction of PCL-PDMS-PCL soft segments into the polymer main chains reduced the crystallinity of the hard segments and altered related properties such as melting temperature and storage modulus, and also modified the surface properties. The thermal stability of the poly(ester-siloxane)s was higher than that of the PBT homopolymer. The inclusion of the siloxane prepolymer with terminal PCL into the macromolecular chains increased the molecular weight of the copolymers, the homogeneity of the samples in terms of composition and structure and the thermal stability. It also resulted in mechanical properties which could be tailored. Copyright © 2010 Society of Chemical Industry [source] Poly(hydroxyether of bisphenol A) -alt -polydimethylsiloxane: a novel thermally crosslinkable alternating block copolymerPOLYMER INTERNATIONAL, Issue 2 2009Lei Wang Abstract BACKGROUND: An important strategy for making polymer materials with combined properties is to prepare block copolymers consisting of well-defined blocks via facile approaches. RESULTS: Poly(hydroxyether of bisphenol A)- block -polydimethylsiloxane alternating block copolymers (PH- alt -PDMS) were synthesized via Mannich polycondensation involving phenolic hydroxyl-terminated poly(hydroxyether of bisphenol A), diaminopropyl-terminated polydimethylsiloxane and formaldehyde. The polymerization was carried out via the formation of benzoxazine ring linkages between poly(hydroxyether of bisphenol A) and polydimethylsiloxane blocks. Differential scanning calorimetry and small-angle X-ray scattering show that the alternating block copolymers are microphase-separated. Compared to poly(hydroxyether of bisphenol A), the copolymers displayed enhanced surface hydrophobicity (dewettability). In addition, subsequent crosslinking can occur upon heating the copolymers to elevated temperatures owing to the existence of benzoxazine linkages in the microdomains of hard segments. CONCLUSION: PH- alt -PDMS alternating block copolymers were successfully obtained. The subsequent self-crosslinking of the PH- alt -PDMS alternating block copolymers could lead to these polymer materials having potential applications. Copyright © 2008 Society of Chemical Industry [source] Surface tension of poly(ester urethane)s and poly(ether urethane)sPOLYMER INTERNATIONAL, Issue 3 2007Mihaela Lupu Abstract The correlation between the surface tension parameters and the chemical composition of poly(ester urethane) and poly(ether urethane) thin films with different soft and hard segments, both before and after plasma treatment, was investigated. Calculations are based on the geometric mean approach of Owens and Wendt (Owens DK and Wendt RC, J Appl Polym Sci13:1741 (1969)), Rabel (Rabel W, Physikalische Blätter33:151 (1977)) and Kälble (Kälble DH, J Adhesion1:102 (1969)), on the Lifshitz,van der Waals acid/base approach of van Oss and co-workers (van Oss CJ, Good RJ and Chaudhury MK, Langmuir4:884 (1988); van Oss CJ, Ju L, Chaudhury MK and Good RJ, Chem Rev88:927 (1988); van Oss CJ, Interfacial Forces in Aqueous Media. Marcel Dekker, New York (1994)) and on the theoretical methods involving quantitative structure,property relationships (Bicerano J, JMS Rev Macromol Chem PhysC36:161 (1996)). For all investigated films, the polar terms contribute significantly to the total surface tensions, as due to the large electron donor, , interactions. Plasma treatment alters the surface energy of samples by changing their surface polarity and hydrophilicity. The hydrophilicity trends for polyurethanes were also studied by means of the free energy of hydration between compounds and water. Preliminary blood contact tests of the selected polyurethane sample with higher hydrophilicity were developed for biomedical applications. Copyright © 2006 Society of Chemical Industry [source] Novel Segmented Thermoplastic Polyurethanes Elastomers Based on Tetrahydrofuran Ethylene Oxide Copolyethers as High Energetic Propellant BindersPROPELLANTS, EXPLOSIVES, PYROTECHNICS, Issue 1 2003Fu-Tai Chen Abstract Novel thermoplastic polyurethane (TPU) elastomers based on copolyether (tetrahydrofuran ethylene oxide) as soft segments, isophorone diisocyanate and 1,4-butanediol as hard segments were synthesized for the purpose of using as propellant binders. In order to increase the miscibility of thermoplastic polyurethane elastomers with nitrate ester, polyethylene glycol (PEG) is incorporated in the co-polyether (tetrahydrofuran ethylene oxide) as soft segment. When the molecular weight and content of polyethylene glycol are controlled to 4000 and 6% of soft segments, respectively, the properties of thermoplastic polyurethane elastomers are most perfect. If plasticizing ratio of nitrate ester to thermoplastic polyurethane elastomers exceeds 4 no crystallinities are determined at room temperature. The propellant samples were prepared by a conventional absorption-rolling extrusion process and the mechanical and combustion properties evaluated afterwards. The maximum impulse reaches up to 265,270 s which is a little bit higher than that of a HTPB propellant. The measured results reveal a promising TPE propellant candidate which shows good processing temperature (<393,K) and excellent mechanical properties. An attracting feature which can be pointed out is that the burning rate pressure exponent reaches as low as 0.36 without the addition of burning rate catalysts. This enables an easy control of propellant combustion. [source] | |||||||||||||