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1.
Core–shell type multi‐arm azide polymers based on hyperbranched copolyether as potential energetic materials in solid propellants
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A series of novel multi‐arm azide copolymers (POGs) with the same hyperbranched poly[3‐ethyl‐3‐(hydroxymethyl)oxetane] core (PEHO‐c) and different content of linear glycidyl azide polymer shell (GAP‐s) have been synthesized by sequential cationic ring‐opening polymerization and azidation. Detailed structural information of these copolyethers was deduced from Fourier transform infrared, 1H NMR and inverse gated decoupled 13C NMR spectroscopies, matrix‐assisted laser desorption ionization time‐of‐flight mass spectrometry, gel permeation chromatography and elemental analysis. The molecular weight of POG having GAP‐s and PEHO‐c with a molar ratio 14.95:1 (Rs/c) was around 31 000 g mol?1, far above that of linear GAP (around 4000 g mol?1). The apparent viscosity and glass transition temperature (?51 to ?23 °C) decreased first and then slightly increased with increasing molecular weight. Thermal analysis revealed that all the obtained POGs exhibited excellent resistance to thermal decomposition up to 220 °C. Moreover, the energetic properties, investigated using oxygen bomb calorimetric measurements, indicated that the enthalpy of formation of the POGs was higher than that of general linear GAP, but similar to that of branched GAP under reasonable Rs/c. The compatibilities of the POGs with common materials used in solid propellants were studied using differential scanning calorimetry and the results indicated that the POGs had good compatibility with these materials. © 2017 Society of Chemical Industry 相似文献
2.
Sasidhara K. Reshmi K. P. Vijayalakshmi Deepthi Thomas E. Arunan C. P. ReghunadhanNair 《Propellants, Explosives, Pyrotechnics》2013,38(4):525-532
Glycidyl azide polymer (GAP) was cured through “click chemistry” by reaction of the azide group with bispropargyl succinate (BPS) through a 1,3‐dipolar cycloaddition reaction to form 1,2,3‐triazole network. The properties of GAP‐based triazole networks are compared with the urethane cured GAP‐systems. The glass transition temperature (Tg), tensile strength, and modulus of the system increased with crosslink density, controlled by the azide to propargyl ratio. The triazole incorporation has a higher Tg in comparison to the GAP‐urethane system (Tg−20 °C) and the networks exhibit biphasic transitions at 61 and 88 °C. The triazole curing was studied using Differential Scanning Calorimetry (DSC) and the related kinetic parameters were helpful for predicting the cure profile at a given temperature. Density functional theory (DFT)‐based theoretical calculations implied marginal preference for 1,5‐addition over 1,4‐addition for the cycloaddition between azide and propargyl group. Thermogravimetic analysis (TG) showed better thermal stability for the GAP‐triazole and the mechanism of decomposition was elucidated using pyrolysis GC‐MS studies. The higher heat of exothermic decomposition of triazole adduct (418 kJ ⋅ mol−1) against that of azide (317 kJ ⋅ mol−1) and better mechanical properties of the GAP‐triazole renders it a better propellant binder than the GAP‐urethane system. 相似文献
3.
Polyurethanes (PUs) are the most widely used polymers because of their biocompatibility, tunable mechanical properties, and chemical versatility. In this study, a two‐step condensation polymerization of polycaprolactone diol and hexamethylene diisocyanate was carried out, and a glutamic acid ester derivative, (2S)‐bis(2‐hydroxypropyl) 2‐aminopentane dioate (HPAP), was used as a new chain extender to accelerate the biodegradation properties of PU. HPAP was synthesized by the Fischer esterification of l ‐glutamic acid. The chemical structure of HPAP was confirmed by high‐resolution mass spectroscopy and m/z (EI) was found to be 264.1447 [calculated value = 264.1443 for C11H21NO6 (M+)]. The Berry plot of static light‐scattering measurements showed that PU–HPAP had a weight‐average molecular weight and radius of gyration of 33,100 g/mol and 1420 nm, respectively. The presence of HPAP in the PU structure facilitated hydrogen bonding between the polymer chains and increased the glass‐transition temperature from ?56 °C (PU) to ?50 °C (PU–HPAP). PU–HPAP showed the highest hydrophilicity and surface free energy among all of samples, and this accelerated the in vitro biodegradation period via surface erosion. In addition, PU–HPAP did not show any cytotoxic effects on the L929 cells. A new biodegradable and biocompatible PU–HPAP was obtained as candidate for tissue engineering applications. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 45764. 相似文献
4.
Yang Zhang Juan Zhao Pan Yang Shangjin He Hengjian Huang 《Polymer Engineering and Science》2012,52(4):768-773
Energetic block copolymer of polyglycidylazide‐b‐poly (azidoethyl methacrylate) (GAP‐b‐PAEMA) was synthesized and characterized. Macroinitiator PECH‐Br prepared via the reaction of 2‐bromoisobutyryl bromide with hydroxyl‐terminated polyepichlorohydrin (PECH‐OH) was used to initiate the atom transfer radical polymerization (ATRP) of chloroethyl methacrylate (CEMA). After azidation of the resulting copolymer, energetic copolymer GAP‐b‐PAEMA was obtained. Increase in the molecular weight determined by gel permeation chromatograph (GPC) is in agreement with the formation of block copolymer. Fourier transform infrared spectroscopy (FTIR) shows that the chlorine groups in the block copolymer can be substituted by azide group easily. Thermogravimetric analysis (TGA) shows that degradation of GAP‐b‐PAEMA involves two steps: the instantaneous decomposition of the azide groups followed by progressive scission of the polymer backbone. From differential scanning calorimetry (DSC) analysis, the GAP‐b‐PAEMA copolymer exhibits two glass transition temperatures (Tg) at ?18 and 36°C, suggesting that the synthesized copolymer is a thermoplastic elastomer. This research provides a new method for the synthesis of energetic polymer. POLYM. ENG. SCI., 2011. © 2011 Society of Plastics Engineers 相似文献
5.
Phenolic‐epoxy matrix curable by click chemistry—synthesis,curing, and syntactic foam composite properties
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Alkyne functional phenolic resin was cured by azide functional epoxy resins making use of alkyne‐azide click reaction. For this, propargylated novolac (PN) was reacted with bisphenol A bisazide (BABA) and azido hydroxy propyloxy novolac (AHPN) leading to triazole‐linked phenolic‐epoxy networks. The click cure reaction was initiated at 40–65°C in presence of Cu2I2. Glass transition temperature (Tg) of the cured networks varied from 70°C to 75°C in the case of BABA‐PN and 75°C to 80°C in the case of AHPN‐PN. DSC and rheological studies revealed a single stage curing pattern for both the systems. The cured BABA‐PN and AHPN‐PN blends showed mass loss above 300°C because of decomposition of the triazole rings and the novolac backbone. Silica fiber‐reinforced syntactic foam composites derived from these resins possessed comparable mechanical properties and superior impact resistance vis‐a‐vis their phenolic resin analogues. The mechanical properties could be tuned by regulating the reactant stoichiometry. These low temperature addition curable resins are suited for light weight polymer composite for related applications. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 41254. 相似文献
6.
Differential scanning calorimetry (DSC) and thermal gravimetric analysis (TGA) were used to investigate the thermal behavior of glycidyl azide polymer (GAP) and GAP‐based binders, which are of potential interest for the development of high‐performance energetic propellants. The glass transition temperature (Tg) and decomposition temperature (Td) of pure GAP were found to be −45 and 242°C, respectively. The energy released during decomposition (ΔHd) was measured as 485 cal/g. The effect of the heating rate on these properties was also investigated. Then, to decrease its Tg, GAP was mixed with the plasticizers dioctiladipate (DOA) and bis‐2,2‐dinitropropyl acetal formal (BDNPA/F). The thermal characterization results showed that BDNPA/F is a suitable plasticiser for GAP‐based propellants. Later, GAP was crosslinked by using the curing agent triisocyanate N‐100 and a curing catalyst dibuthyltin dilaurate (DBTDL). The thermal characterization showed that crosslinking increases the Tg and decreases the Td of GAP. The Tg of cured GAP was decreased to sufficiently low temperatures (−45°C) by using BDNPA/F. The decomposition reaction‐rate constants were calculated. It can be concluded that the binder developed by using GAP/N‐100/BDNPA/F/DBTDL may meet the requirements of the properties that makes it useful for future propellant formulations. © 2000 John Wiley & Sons, Inc. J Appl Polym Sci 77: 538–546, 2000 相似文献
7.
The purpose of this study was to investigate the effects of polyol on glycidyl azide polyol (GAP)‐based energetic thermoplastic polyurethane elastomers (ETPEs). Briefly, a series of GAP/polyol‐based ETPEs (GAP/polyol ETPEs) with different copolyol ratios and hard segment contents were synthesized using GAP‐diol with common polyol and 4,4‐methylenebis(phenylisocyanate)‐extended 1,5‐pentanediol as soft and hard segments, respectively, by solution polymerization in dimethylformamide. The three types of polyols used were poly(tetramethylene ether) glycol (PTMG), polycarbonate‐diol (PCL‐diol) and polycaprolactone‐diol (PCD‐diol). The synthesized GAP/polyol ETPEs were identified and characterized using Fourier transform infrared and 1H NMR spectroscopy, differential scanning calorimetry (DSC), dynamic mechanical analysis (DMA) and rheometric mechanical spectrometry. For GAP/PCL ETPEs with lower hard segment content, DSC results showed that the GAP segment failed to interact with either the PCL segment or PCL melting. In addition, the results of DMA showed that the presence of PCL segments in ETPEs improved the storage modulus below the melting temperature of the PCL block. Further, the crystalline PCL segments were attributed to reinforcing the ETPEs in a manner similar to that of the hard domain. As the hard segment content increased in the GAP/polyol ETPEs, both GAP/PTMG ETPEs and GAP/PCL ETPEs exhibited microphase separation transitions, while rheological experiments demonstrated a sudden decrease in complex viscosity in neighboring microphase separation transitions. © 2012 Society of Chemical Industry 相似文献
8.
Mingyang Ma Yechen Shen Younghwan Kwon Chanhong Chung Jin Seuk Kim 《Propellants, Explosives, Pyrotechnics》2016,41(4):746-756
Reactive energetic plasticizers (REPs) for use in glycidyl azido polymer (GAP) based polyurethane (PU) energetic binders were investigated. These REPs consisted of an activated terminal alkyne group that was expected to give rise to Huisgen azide‐alkyne 1,3‐dipolar cycloaddition within the specific pot life for a PU formulation to prevent the migration of plasticizers, and with a gem‐dinitro group as an energy resource. A quantitative miscibility investigation between the plasticizers and uncured GAP showed that REPs exhibited better miscibility than conventional energetic plasticizers. The plasticization effect of the REPs on the GAP prepolymer with respect to the reduction of the viscosity illustrated REPs can effectively reduce the viscosity of the GAP prepolymer from 6,015 cP to 150–240 cP at the processing temperature when 50 wt‐% of REP was added. A comparison of the click reactivity and activation energies (Ea) of REPs and GAP prepolymer elucidated that the reactivity of azide‐alkyne cycloaddition depended on the dipolarophilicity of REPs which could be controlled by adjusting the length of methylene spacer between electron‐withdrawing groups (EWG) and neighboring alkynes in REPs. Thermogravimetric analysis manifested REP/GAP‐based PU binders maintained the thermal stability of the control GAP‐based PU binder. The mechanical properties and impact insensitivity of the GAP‐based PU binders were also improved by the incorporation of REPs. 相似文献
9.
Structure and mechanical properties of fluorine‐containing glycidyl azide polymer‐based energetic binders
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Minghui Xu Zhongxue Ge Xianming Lu Hongchang Mo Yueping Ji Huaiming Hu 《Polymer International》2017,66(9):1318-1323
A novel energetic polymer, fluorine‐containing glycidyl azide polymer (FGAP ), was developed via an initial cationic copolymerization of epichlorohydrin and 1,1,1‐trifluoro‐2,3‐epoxypropane, followed by azidation. The structure of FGAP was confirmed using Fourier transform infrared, 1H NMR and 13C NMR spectroscopies. The molecular weight and the thermal behavior of FGAP were characterized using gel permeation chromatography, differential scanning calorimetry and thermogravimetric analysis. FGAP had a molecular weight of 2845 g mol?1, and the glass transition temperature and decomposition temperature were found to be ?47.8 and 253 °C, respectively. FGAP ‐based polyurethane networks were further prepared using triphenylmethane‐4,4,4‐triisocyanate as the crosslinking agent. In comparison with GAP , FGAP ‐based polyurethane networks exhibited better mechanical behaviors (a tensile strength of 1.5 MPa and an elongation at break of 81.6%). The results demonstrated that FGAP might be a promising polymeric binder for future propellant formulations. © 2017 Society of Chemical Industry 相似文献
10.
The grafting of hydroxy telechelic polybutadienes (HTPBD) by 2‐mercaptoethanol to saturate 1,2‐double bonds which enabled an increase of the OH functionality of HTPBD is presented. The functionalities of the virgin and grafted HTPBD were characterized both by 1H‐NMR after silylation of the hydroxy end groups and the consumption of the mercaptan was determined by iodine titration. The radical addition of 2‐mercaptoethanol to HTPBD was not complete, which is not acceptable for an industrial application. Hence, the excess of mercaptan was reacted to allyl alcohol, leading to a new short telechelic diol able to be incorporated in the polyurethane (PU) network as a chain extender. This PU was prepared by addition of hexamethylene diisocyanate to both these diols. The thermal (glass transition, Tg, and decomposition temperatures), physical (gel time and viscosity), and mechanical (Shore hardness) properties were assessed. It was noted that the higher the hydroxyl functionality, the greater the Shore hardness, the viscosity, and the modulus but the lower the gel time and the break elongation. However, no improvement of the thermal stability was observed with the use of grafted HTPBD in PU resins. Their Tg's were observed to undergo a slight increase (of 4°C) in the case of PU prepared from Poly BD R45 HT® in contrast to that noted from Poly BD 20 LM® (20°C), showing a lower phase segregation in that latter case. © 2000 John Wiley & Sons, Inc. J Appl Polym Sci 75: 1655–1666, 2000 相似文献
11.
Sarawut Rimdusit Chalinee Liengvachiranon Sunan Tiptipakorn Chanchira Jubsilp 《应用聚合物科学杂志》2009,113(6):3823-3830
Copolymers of polybenzoxazine (BA‐a) and urethane elastomer (PU) with three different structures of isocyanates [i.e., toluene diisocyanate (TDI), diphenylmethane diisocyanate, and isophorone diisocyanate], were examined. The experimental results reveal that the enhancement in glass transition temperature (Tg) of BA‐a/PU copolymers was clearly observed [i.e., Tg of the BA‐a/PU copolymers in 60 : 40 BA‐a : PU system for all isocyanate types (Tg beyond 230°C) was higher than those of the parent resins (165°C for BA‐a and ?70°C for PU)]. It was reported that the degradation temperature increased from 321°C to about 330°C with increasing urethane content. Furthermore, the flexural strength synergism was found at the BA‐a : PU ratio of 90 : 10 for all types of isocyanates. The effect of urethane prepolymer based on TDI rendered the highest Tg, flexural modulus, and flexural strength of the copolymers among the three isocyanates used. The preferable isocyanate of the binary systems for making high processable carbon fiber composites was based on TDI. The flexural strength of the carbon fiber‐reinforced BA‐a : PU based on TDI at 80 wt % of the fiber in cross‐ply orientation provided relatively high values of about 490 MPa. The flexural modulus slightly decreased from 51 GPa for polybenzoxazine to 48 GPa in the 60 : 40 BA‐a : PU system. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009 相似文献
12.
Polyurethanes based on 2,2‐Dinitropropane‐1,3‐diol and 2,2‐bis(azidomethyl)propane‐1,3‐diol as potential energetic binders
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On the base of 2,2‐bis(azidomethyl)propane‐1,3‐diol (BAMP) and 2,2‐dinitropropane‐1,3‐diol (DNPD) four different polyurethanes were synthesized in a polyaddition reaction using hexamethylene diisocyanate (HMDI) and diisocyanato ethane (DIE). The obtained prepolymers were mainly characterized using vibrational spectroscopy (IR) and elemental analysis. For determination of low and high temperature behavior, differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA) were used. Investigations concerning friction and impact sensitivities were carried out using a BAM drop hammer and friction tester. The energetic properties of the polymers were determined using bomb calorimetric measurements and calculated with the EXPLO5 V6.02 computer code. The obtained values were compared with the glycidyl azide polymer (GAP). The compounds turned out to be insensitive toward friction (>360 N) and less sensitive toward impact (40 J). The good physical stabilities, along with their sufficient thermal stability (170–210 °C) and moderate energetic properties renders these polymers into potential compounds for applications as binders in energetic formul;ations. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43991. 相似文献
13.
Epoxy composite foams with excellent electromagnetic interference shielding and heat‐resistance performance
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Epoxy composite foams with improved heat‐resistant property and efficient electromagnetic interference shielding effectiveness (EMI SE) were fabricated through a two‐step foaming technique. A sort of novel and untraditional expandable microspheres was adopted to reduce the density of prepared materials. A multiscale conductive network system composed of multiwalled carbon nanotubes (MWCNTs) and nickel‐plated carbon fibers (NiCFs) was introduced in these foams. Benefitting from the synergistic effect between NiCFs and MWCNTs, the multiscale epoxy foam with best comprehensive performance achieved a greatly enhanced Tg at 178.3 °C and an exceptional specific EMI SE ranging from 52.8 to 72.6 dB cm3 g?1 in X band (8.2–12.4 GHz) at low filler loading. These properties are greatly better than original epoxy foam with a Tg of 157.8 °C and specific EMI SE of 1.0–6.4 dB cm3 g?1. Their shielding mechanisms were discussed and the results showed that reflection is dominating. The effects of microspheres content, foaming temperature, NiCFs content, and length were investigated. In general, we provided a feasible, convenient and cost‐effective method to fabricate light‐weight, heat‐resistant thermosetting epoxy foams with sufficient EMI shielding performance which has a potential to be applied in aerospace or electronic devices. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 46013. 相似文献
14.
Poly(N‐phenyl acrylamide) (PPA) and poly(N‐phenyl methacrylamide) (PPMA) were prepared by using N‐phenyl acrylamide and N‐phenyl methacrylamide as monomer, respectively, in tetrahydrofuran using azobisisobutyronitrile as initiator. FT‐IR, 1H‐NMR, and GPC were used to characterize their molecular structure. The PPA obtained exhibited higher molecular weight and wider molecular weight distribution than that of PPMA. Their thermal degradation and kinetics were systematically investigated in two atmospheres of nitrogen and air from room temperature to 800°C by thermogravimetric analysis at 10°C/min. Based on the thermal decomposition reactions in nitrogen and air, it is shown that a three‐step degradation process in nitrogen and a four‐step degradation process for two polymers were observed in this investigation. The initial thermal degradation temperature was lower than 190°C. Under two atmospheres, PPA exhibits higher degradation temperature, higher temperature at the maximum weight‐loss rate, faster maximum weight‐loss rates, and larger weight loss for the first‐stage decomposition, as well as higher char yield at 500°C than those of PPMA. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 88: 1065–1071, 2003 相似文献
15.
A diol‐based refined, bleached, and deodorized (RBD) palm kernel oil polyol was prepared. It was found that the polyurethane foam produced only gives a good compressive strength property at a 45 kg/m3 molded density. The combination of sorbitol into the polyol system resulted in a better dimensional stability and improved thermal conductivity as well as enhanced compressive strength. These were obtained by increasing the functionality of the polyol (functionality of 4.5) through introduction of a high molecular weight and branching polyhidric compound. Direct polycondensation and transesterification methods were used for the syntheses. The hydroxyl value, TLC, and FTIR were used to study the completion of the reaction. A comparative study of the mechanical properties and morphological behavior was carried out with a diol‐based polyol. From the water‐blown molded foam (zero ODP) with a density of about 44.2 kg/m3 and a closed‐cell content of 93%, a compressive strength of 222 kPa and a dimensional stability of 0.09, 0.10, and 0.12% at the length, width, and thickness of the foam, respectively, conditioned at ?15°C for 24 h, were obtained. The thermal conductivity improved to an initial value of 0.00198 W/mK, tested at 0°C. © 2001 John Wiley & Sons, Inc. J Appl Polym Sci 81: 384–389, 2001 相似文献
16.
Yinglei Wang Kangzhen Xu Fengqi Zhao Yueping Ji Jianhua Yi Siyu Xu Fulei Gao Bin Chen 《Propellants, Explosives, Pyrotechnics》2013,38(5):644-650
The energetic material, 3‐nitro‐1,5‐bis(4,4′‐dimethyl azide)‐1,2,3‐triazolyl‐3‐azapentane (NDTAP), was firstly synthesized by means of Click Chemistry using 1,5‐diazido‐3‐nitrazapentane as main material. The structure of NDTAP was confirmed by IR, 1H NMR, and 13C NMR spectroscopy; mass spectrometry, and elemental analysis. The crystal structure of NDTAP was determined by X‐ray diffraction. It belongs to monoclinic system, space group C2/c with crystal parameters a=1.7285(8) nm, b=0.6061(3) nm, c=1.6712(8) nm, β=104.846(8)°, V=1.6924(13) nm3, Z=8, μ=0.109 mm−1, F(000)=752, and Dc=1.422 g cm−3. The thermal behavior and non‐isothermal decomposition kinetics of NDTAP were studied with DSC and TG‐DTG methods. The self‐accelerating decomposition temperature and critical temperature of thermal explosion are 195.5 and 208.2 °C, respectively. NDTAP presents good thermal stability and is insensitive. 相似文献
17.
《Propellants, Explosives, Pyrotechnics》2017,42(4):386-393
Bis‐propargylhydroquinone (BPHQ) is an alkyne functionalized isocyanate‐free curing agent for hydroxyl terminated azido polymers. Conventionally, glycidyl azide polymer (GAP) is cured by isocyanate based curatives, which are toxic and hygroscopic in nature. The reaction between hydroxyl end group of GAP and isocyanate is highly sensitive to moisture causing voids in the propellant, leading to poor mechanical properties. Herein, an alternate approach was adapted to exploit 1,3‐dipolar cycloaddition reaction between azido group of GAP and the triple bond (–C≡CH) of BPHQ without catalyst at 50 °C forming triazole crosslinked polymer. The curing behavior of GAP‐BPHQ system was studied by rheological method and based on the results the gel time was determined. In addition, the reaction between GAP and BPHQ was carried out with various GAP/BPHQ ratios (0.9 to 2.5) and effects on mechanical properties of resulting triazole polymers were investigated. Post curing hardness of GAP‐BPHQ binder system was tested by surface Shore‐A hardness measurement. The compatibility of BPHQ with energetic oxidizers such as ammonium dinitramide (ADN) and hydrazinium nitroformate (HNF) were also studied by differential scanning calorimetery (DSC) technique and showed good compatibility. The activation energy (E a) of cured GAP‐BPHQ binder was evaluated by DSC using Ozawa and Kissinger methods and are found to be 33.55 and 33.16 kcal mol–1, respectively. The advantage of this curing system between GAP and BPHQ is unaffected by moisture as compared to isocyanate based urethane systems and also no need to control humidity during the processing of propellant. The experimental results reveal that triazole crosslinked polymer system could be a better choice to develop novel energetic binder systems for explosives as well as propellants composition with improved performance and eco‐friendly nature. 相似文献
18.
Poly(urethane‐benzoxazine)/clay hybrid nanocomposites (PU/Pa–OMMTs) were prepared from an in situ copolymerization of a polyurethane (PU) prepolymer and a monofunctional benzoxazine monomer, 3‐phenyl‐3,4‐dihydro‐2H‐1,3‐benzoxazine (Pa), in the presence of an organophilic montmorillonite (OMMT), by solvent method using DMAc. OMMT was made from cation‐exchange of Na‐montmorillonite (MMT) with dodecyl ammonium chloride. The formation of the exfoliated nanocomposite structures of PU/Pa‐OMMT was confirmed by XRD from the disappearance of the peak due to the basal diffraction of the layer‐structured clay found in both MMT and OMMT. DSC showed that, in the presence of OMMT, the curing temperature of PU/Pa lowered by ca. 60°C for the onset and ca. 20°C for the maximum. After curing at 190°C for 1 h, the exothermic peak on DSC disappeared. All the obtained films of PU/Pa–OMMT were deep yellow and transparent. As the content of OMMT increased, both the tensile modulus and strength of PU/Pa–OMMT films increased, while the elongation decreased. The characteristics of the PU/Pa–OMMT films changed from plastics to elastomers depending on OMMT content and PU/Pa ratio. PU/Pa–OMMT films also exhibited excellent resistance to the solvents such as tetrahydrofuran, N,N‐dimethylformamide and N‐methyl‐2‐pyrrolidinone. The thermal stability of PU/Pa were enhanced remarkably even with small amount of OMMT. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 90: 4075–4083, 2003 相似文献
19.
This paper describes the mechanical and thermal characterisation of cross‐linked glycidyl azide polymer (GAP) and GAP–hydroxyl terminated polybutadiene (HTPB) networks. Cross‐linked GAP and GAP–HTPB networks were prepared by reacting GAP diol and GAP–HTPB diol mixture with different diisocyanates. The physical and mechanical characteristics were found to be influenced by the type of isocyanate curing agents, [NCO]/[OH] equivalent ratios and concentration of GAP. For all the three types of curing agents, GAP–HTPB blends of 50 : 50 to 30 : 70 ratios show higher mechanical strength over the virgin networks of GAP or HTPB. Thermal decomposition of cross‐linked GAP–HTPB networks was evaluated by thermogravimetric analysis (TGA). The kinetic parameters for the decomposition of GAP–HTPB blends were found to be dependant on the concentration of GAP and HTPB in the blend. The cross‐linked GAP–HTPB blends were subjected to dynamic mechanical analysis (DMA). The glass transition characteristics of the blends were evaluated by DMA and it was found that blends prepared with GAP content up to 30% showed single transition in the loss tangent trace indicating no phase separation in the cured network. 相似文献
20.
Sulfonated poly(sulfone‐pyridine‐amide)/sulfonated polystyrene/multiwalled carbon nanotube‐based fuel cell membranes
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Ayesha Kausar Muhammad Khurram Muhammad Siddiq 《Polymer Engineering and Science》2015,55(8):1776-1786
In this study, aromatic sulfonated poly(sulfone‐pyridine‐amide) (S‐PSPA) has been prepared via polycondensation of sulfonated monomer 1‐(4‐thiocarbamoylaminophenyl‐sulfonylphenyl)thiourea and 2,6‐pyridinedicarboxylic acid at high temperature. Mechanically robust and thermally stable hybrid membranes were prepared using non‐functional and functional multiwalled carbon nanotube (MWCNT) i.e., S‐PS/S‐PSPA/MWCNT‐NF and S‐PS/S‐PSPA/MWCNT via solution blending. Field emission scanning electron microscopy exhibited porous membrane structure for 0.1–0.5 wt% nanotube loading, whereas well‐aligned functional MWCNT were observed in 1 wt% loaded sample. Increasing the functional nanotube content from 0.1 to 1 wt% increased tensile strength of functional S‐PS/S‐PSPA/MWCNT hybrids from 62.19 to 65.29 MPa compared with non‐functional hybrid (53.34 MPa) and neat S‐PS/S‐PSPA. 10% decomposition temperature of S‐PS/S‐PSPA/MWCNT 0.1–1 was in the range 491–502°C, while S‐PS/S‐PSPA/MWCNT‐NF showed relatively lower thermal stability (T10 489°C). Glass transition temperature of functional S‐PS/S‐PSPA/MWCNT was also higher (201–243°C) relative to S‐PS/S‐PSPA/MWCNT‐NF (194°C). Furthermore, functional MWCNT‐based membranes had higher ion exchange capacity (IEC) 3.2–3.6 mmol/g and lower activation energies (95–36 kJ/mol). Novel functional membranes also revealed high proton conductivity 1.68–2.55 S/cm in a wide range of humidity at 80°C higher than that of perfluorinated Nafion® membrane (1.1 ×10?1 S/cm) at 80°C (94% RH). POLYM. ENG. SCI., 55:1776–1786, 2015. © 2014 Society of Plastics Engineers 相似文献