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Sample records for hybrid sulfonated polyether

  1. Sulfonated poly(ether ether ketone)/mesoporous silica hybrid membrane for high performance vanadium redox flow battery

    Science.gov (United States)

    Li, Zhaohua; Dai, Wenjing; Yu, Lihong; Xi, Jingyu; Qiu, Xinping; Chen, Liquan

    2014-07-01

    Hybrid membranes of sulfonated poly(ether ether ketone) (SPEEK) and mesoporous silica SBA-15 are prepared with various mass ratios for vanadium redox flow battery (VRB) application and investigated in detail. The hybrid membranes are dense and homogeneous with no visible hole as the SEM and EDX images shown. With the increasing of SBA-15 mass ratio, the physicochemical property, VO2+ permeability, mechanical property and thermal stability of hybrid membranes exhibit good trends, which can be attributed to the interaction between SPEEK and SBA-15. The hybrid membrane with 20 wt.% SBA-15 (termed as S/SBA-15 20) shows the VRB single cell performance of CE 96.3% and EE 88.1% at 60 mA cm-2 due to its good balance of proton conductivity and VO2+ permeability, while Nafion 117 membrane shows the cell performance of CE 92.2% and EE 81.0%. Besides, the S/SBA-15 20 membrane shows stable cell performance of highly stable efficiency and slower discharge capacity decline during 120 cycles at 60 mA cm-2. Therefore, the SPEEK/SBA-15 hybrid membranes with optimized mass ratio and excellent VRB performance can be achieved, exhibiting good potential usage in VRB systems.

  2. Dihydrogenimidazole modified silica-sulfonated poly(ether ether ketone) hybrid materials as electrolyte membranes for direct ethanol fuel cells

    Energy Technology Data Exchange (ETDEWEB)

    Roelofs, Kimball S.; Hirth, Thomas [Fraunhofer Institute for Interfacial Engineering and Biotechnology, Nobelstr. 12, 70569 Stuttgart (Germany); Schiestel, Thomas, E-mail: Thomas.Schiestel@igb.fraunhofer.de [Fraunhofer Institute for Interfacial Engineering and Biotechnology, Nobelstr. 12, 70569 Stuttgart (Germany)

    2011-05-25

    The present study reports on dihydrogenimidazole modified inorganic-organic mixed matrix membranes for possible application as a proton exchange membrane in direct ethanol fuel cells. The polymeric phase consisted mainly of sulfonated poly(ether ether ketone) (sPEEK) with a sulfonation degree of 55%. The inorganic phase was built up from hydrophilic fumed silica particles interconnected with partially hydrolyzed and condensed tetraethoxysilane with a total inorganic loading of 27.3%. This inorganic phase was further modified with N-(3-triethoxysilylpropyl)-4,5-dihydroimidazole (DHIM), which consists of an hydrolyzable inorganic part and a functional organic group. The influence of the modifier on the mixed matrix system was studied by means of various modifier concentrations in various aqueous-ethanolic systems (water, 2 M and 4 M ethanol). Modifier concentration and ethanol concentration of the ethanol-water mixture exhibited significant but opposite effects on the liquid uptake of the mixed matrix membranes. The proton conductivity as well as the proton diffusion coefficient as a function of modifier content showed a linear decrease. The proton conductivity as a function of temperature showed Arrhenius behavior and the activation energy of the mixed matrix membranes was 43.9 {+-} 2.6 kJ mol{sup -1}. High selectivity of proton diffusion coefficient to ethanol permeability coefficient was obtained with high modifier concentrations. At low modifier concentrations, this selectivity was dominated by ethanol permeation and at high modifier concentrations by proton diffusion. The main electrolyte properties can be optimized by setting the DHIM content in mixed matrix membrane. With this approach, tailor-made membranes can be prepared for possible application in direct ethanol fuel cells.

  3. Fabrication of sulfonated poly(ether ether ketone)-based hybrid proton-conducting membranes containing carboxyl or amino acid-functionalized titania by in situ sol-gel process

    Science.gov (United States)

    Yin, Yongheng; Xu, Tao; He, Guangwei; Jiang, Zhongyi; Wu, Hong

    2015-02-01

    Functionalized titania are used as fillers to modify the sulfonated poly(ether ether ketone) (SPEEK) membrane for improved proton conductivity and methanol barrier property. The functionalized titania sol which contains proton conductive carboxylic acid groups or amino acid groups are derived from a facile chelation method using different functional additives. Then the novel SPEEK/carboxylic acid-functionalized titania (SPEEK/TC) and SPEEK/amino acid-functionalized titania (SPEEK/TNC) hybrid membranes are fabricated via in situ sol-gel method. The anti-swelling property and thermal stability of hybrid membranes are enhanced owing to the formation of electrostatic force between SPEEK and titania nanoparticles. The hybrid membranes exhibit higher proton conductivity than plain SPEEK membrane because more proton transfer sites are provided by the functionalized titania nanoparticles. Particularly, the proton conductivity of SPEEK/TNC membrane with 15% filler content reaches up to 6.24 × 10-2 S cm-1, which is 3.5 times higher than that of the pure SPEEK membrane. For methanol permeability, the SPEEK/TNC membranes possess the lowest values because the acid-base interaction between sulfonic acid groups in SPEEK and amino groups in functionalized titania leads to a more compact membrane structure.

  4. Synthesis and characterization of sulfonated poly(ether sulfone)s containing mesonaphthobifluorene for polymer electrolyte membrane fuel cell.

    Science.gov (United States)

    Lim, Youngdon; Seo, Dongwan; Lee, Soonho; Hossain, Md Awlad; Lim, Jinseong; Lee, Sangyoung; Hong, Taehoon; Kim, Whangi

    2014-10-01

    The novel sulfonated poly(ether sulfone)s containing mesonaphthobifluorene (MNF) moiety were synthesized and characterized their properties. The prepared polymers have highly conjugated aromatic structure due to the MNF group which is an allotrope of carbon and one atom thick planar sheets of sp2-bonded carbon atoms. Poly(ether sulfone)s bearing tetraphenylethylene on polymer backbone were synthesized by polycondensation and followed intra-cyclization from tetraphenylethylene to form MNF by Friedel-craft reaction with Lewis acid (FeCl3). The sulfonation was performed selectively on MNF units with conc. sulfuric acid. The structural properties of the sulfonated polymers were investigated by 1H-NMR spectroscopy. The membranes were studied by ion exchange capacity (IEC), water uptake, and proton conductivity. The synthesized polymer electrolyte membranes showed better thermal and dimensional stabilities owing to the inducted highly conjugated aromatic structure in the polymer backbone. The water uptake of the synthesized membranes ranged from 23-52%, compared with 32.13% for Nafion 211 at 80 degrees C. The synthesized membranes exhibited proton conductivities (80 degrees C, RH 90%) of 74.6-100.4 mS/cm, compared with 102.7 mS/cm for Nafion 211.

  5. Surface modification of carbon fibers by a polyether sulfone emulsion sizing for increased interfacial adhesion with polyether sulfone

    Energy Technology Data Exchange (ETDEWEB)

    Yuan, Haojie [National Engineering Laboratory for Carbon Fiber Technology, Institute of Coal Chemistry, Chinese Academy of Sciences, Taiyuan 030001 (China); University of Chinese Academy of Sciences, Beijing 100049 (China); Zhang, Shouchun, E-mail: zschun@sxicc.ac.cn [National Engineering Laboratory for Carbon Fiber Technology, Institute of Coal Chemistry, Chinese Academy of Sciences, Taiyuan 030001 (China); Lu, Chunxiang [National Engineering Laboratory for Carbon Fiber Technology, Institute of Coal Chemistry, Chinese Academy of Sciences, Taiyuan 030001 (China)

    2014-10-30

    Highlights: • A polyether sulfone emulsion (PES) sizing was prepared for the first time. • The sizing enhanced the surface activity and wettability of carbon fibers. • Compared to the original sizing, the PES emulsion sizing resulted in an 18.4% increase in the interlaminar shear strength of carbon fiber/PES composites. • Important influences of emulsifier on the fiber surface and composite interface were demonstrated. • The reinforcing mechanisms are the improved fiber surface wettability and interfacial compatibility in composites. - Abstract: Interests on carbon fiber-reinforced thermoplastic composites are growing rapidly, but the challenges with poor interfacial adhesion have slowed their adoption. In this work, a polyether sulfone (PES) emulsion sizing was prepared successfully for increased interfacial adhesion of carbon fiber/PES composites. To obtain a high-quality PES emulsion sizing, the key factor, emulsifier concentration, was studied by dynamic light scattering technique. The results demonstrated that the suitable weight ratio of PES to emulsifier was 8:3, and the resulting PES emulsion sizing had an average particle diameter of 117 nm and Zeta potential of −52.6 mV. After sizing, the surface oxygen-containing functional groups, free energy and wettability of carbon fibers increased significantly, which were advantageous to promote molecular-level contact between carbon fiber and PES. Finally, short beam shear tests were performed to evaluate the interfacial adhesion of carbon fiber/PES composites. The results indicated that PES emulsion sizing played a critical role for the enhanced interfacial adhesion in carbon fiber/PES composites, and a 26% increase of interlaminar shear strength was achieved, because of the improved fiber surface wettability and interfacial compatibility between carbon fiber and PES.

  6. Molecular sieve/sulfonated poly(ether ketone ether sulfone) composite membrane as proton exchange membrane

    Science.gov (United States)

    Changkhamchom, Sairung; Sirivat, Anuvat

    2012-02-01

    A proton exchange membrane (PEM) is an electrolyte membrane used in both polymer electrolyte membrane fuel cells (PEMFC) and direct methanol fuel cells (DMFCs). Currently, PEMs typically used for PEMFCs are mainly the commercially available Nafion^ membranes, which is high cost and loss of proton conductivity at elevated temperature. In this work, the Sulfonated poly(ether ketone ether sulfone), (S-PEKES), was synthesized by the nucleophilic aromatic substitution polycondensation between bisphenol S and 4,4'-dichlorobenzophenone, and followed by the sulfonation reaction with concentrated sulfuric acid. The molecular sieve was added in the S-PEKES matrix at various ratios to form composite membranes to be the candidate for PEM. Properties of both pure sulfonated polymer and composite membranes were compared with the commercial Nafion^ 117 membrane from Dupont. S-PEKES membranes cast from these materials were evaluated as a polymer electrolyte membrane for direct methanol fuel cells. The main properties investigated were the proton conductivity, methanol permeability, thermal, chemical, oxidative, and mechanical stabilities by using a LCR meter, Gas Chromatography, Thermogravimetric Analysis, Fourier Transform Infrared Spectroscopy, Fenton's reagent, and Universal Testing Machine. The addition of the molecular sieve helped to increase both the proton conductivity and the methanol stability. These composite membranes are shown as to be potential candidates for use as a Proton Exchange Membrane (PEM).

  7. Thin sulfonated poly(ether ether ketone) films for the dehydration of compressed carbon dioxide

    NARCIS (Netherlands)

    Koziara, B.T.

    2015-01-01

    In this thesis, the properties of thin films from highly sulfonated poly(ether ether ketone) (SPEEK) have been investigated within the context of their application as membranes for the dehydration of compressed carbon dioxide. Spectroscopic ellipsometry has been used as the predominant measurement t

  8. Optical anisotropy, molecular orientations, and internal stresses in thin sulfonated poly(ether ether ketone) films

    NARCIS (Netherlands)

    Koziara, Beata; Nijmeijer, Dorothea C.; Benes, Nieck Edwin

    2015-01-01

    The thickness, the refractive index, and the optical anisotropy of thin sulfonated poly(ether ether ketone) films, prepared by spin-coating or solvent deposition, have been investigated with spectroscopic ellipsometry. For not too high polymer concentrations (B5 wt%) and not too low spin speeds

  9. Optical anisotropy, molecular orientations, and internal stresses in thin sulfonated poly(ether ether ketone) films

    NARCIS (Netherlands)

    Koziara, B.T.; Nijmeijer, D.C.; Benes, N.E.

    2015-01-01

    The thickness, the refractive index, and the optical anisotropy of thin sulfonated poly(ether ether ketone) films, prepared by spin-coating or solvent deposition, have been investigated with spectroscopic ellipsometry. For not too high polymer concentrations (B5 wt%) and not too low spin speeds (C20

  10. Hyperbranched-linear poly(ether sulfone) blend films for proton exchange membranes

    Energy Technology Data Exchange (ETDEWEB)

    Grunzinger, Stephen J.; Watanabe, Masatoshi; Fukagawa, Kiyotaka; Kikuchi, Ryohei; Tominaga, Yoichi; Hayakawa, Teruaki; Kakimoto, Masa-aki [Department of Organic and Polymeric Materials, Tokyo Institute of Technology, 2-12-1 O-okayama, Meguro-ku, Tokyo 152-8552 (Japan)

    2008-01-03

    Hyperbranched poly(ether sulfone) polymers having sulfonyl chloride end-groups is blended at up to 30 w% with linear poly(ether ether ether sulfone)s and a two-phase system is generated via spinodal decomposition upon drying from a DMAc solution. Conversion of the end-groups from sulfonyl chloride to sulfonic acid is accomplished using 16 M H{sub 2}SO{sub 4} that is also believed to introduce additional sulfonic acid groups at the interface of the linear polymer. The blend films before and after conversion to sulfonic acid have similar tensile strengths as films composed of solely linear polymer (yield stress >40 MPa and Young's modulus >3 GPa m). These films are designed to test the viability of hyperbranched polymers as fuel cell membranes. Proton conductivities of up to 0.03 S cm{sup -1} are observed at 80 C and 90% R.H indicating a good potential for use of hyperbranched polymers as a proton conduction material. (author)

  11. Proton Conducting Composite Membranes from Sulfonated Polyether Ether Ketone and SiO2

    Institute of Scientific and Technical Information of China (English)

    ZHANG Gaowen; ZHOU Zhentao; LI Chunqing; CHU Heng

    2009-01-01

    Proton conducting composite membranes from sulfonated polyether ether ketone and SiO2 for direct methanol fuel cell (DMFC) application were prepared with sulfonated polyether ether ketone(SPEEK) and tetracethoxy silane(TEOS) by sol-gel method. The covalent crosslinking structure was formed between -SO3H of SPEEK via SiO2. The SEM images show that the interfacial compatibility of SPEEK and SiO2 is improved obviously and SiO2 disperses uniformly in the polymer matrix and the particle diameter of SiO2 does not exceed 40 nm. The proton conductivity of composite membranes decreases slightly compared with the SPEEK membrane while the methanol permeability and swelling of composite membrane are improved remarkablely owing to covalent cross-linking between -SO3H and SiO2 .

  12. Conductivity enhancement of sulfonated poly(ether ketone ketone) blends using electric field structuring techniques

    Science.gov (United States)

    Gasa, Jeffrey V.; Shaw, Montgomery T.

    2004-03-01

    Binary blends composed of an ion-containing polymer and a secondary component were cast under an applied elec. field to produce membranes with anisotropic morphologies. The ion-containing polymer was sulfonated poly(ether ketone ketone) (SPEKK) and the secondary component was either poly(ether imide) (PEI) or styrene-acrylonitrile (SAN) copolymer. A range of compositions and sulfonation levels were studied using this blend system. Optical and SEM micrographs of the resulting membranes showed columnar structures that were oriented along the direction of the field. It was found that electric field alignment only occurs when SPEKK is the dispersed phase but not when it is the matrix. The results show that the conductivities of the membranes that were cast under an electric field were significantly higher than those of the membranes cast without electric field. The conductivity measurements were interpreted in terms of a composite equation with structure-dependent parameters.

  13. Mass transport of direct methanol fuel cell species in sulfonated poly(ether ether ketone) membranes

    Energy Technology Data Exchange (ETDEWEB)

    Silva, V.S.; Boaventura, M.; Mendes, A.M.; Madeira, L.M. [LEPAE, Chemical Engineering Department, Faculty of Engineering, University of Porto, Rua Dr. Roberto Frias, 4200-465 Porto (Portugal); Ruffmann, B.; Vetter, S.; Nunes, S.P. [GKSS Research Centre, Max-Planck Str., 21502 Geesthacht (Germany)

    2006-05-05

    Homogeneous membranes based on sulfonated poly(ether ether ketone) (sPEEK) with different sulfonation degrees (SD) were prepared and characterized. In order to perform a critical analysis of the SD effect on the polymer barrier and mass transport properties towards direct methanol fuel cell species, proton conductivity, water/methanol pervaporation and nitrogen/oxygen/carbon dioxide pressure rise method experiments are proposed. This procedure allows the evaluation of the individual permeability coefficients in hydrated sPEEK membranes with different sulfonation degrees. Nafion{sup (R)} 112 was used as reference material. DMFC tests were also performed at 50{sup o}C. It was observed that the proton conductivity and the permeability towards water, methanol, oxygen and carbon dioxide increase with the sPEEK sulfonation degree. In contrast, the SD seems to not affect the nitrogen permeability coefficient. In terms of selectivity, it was observed that the carbon dioxide/oxygen selectivity increases with the sPEEK SD. In contrast, the nitrogen/oxygen selectivity decreases. In terms of barrier properties for preventing the DMFC reactants loss, the polymer electrolyte membrane based on the sulfonated poly(ether ether ketone) with SD lower or equal to 71%, although having slightly lower proton conductivity, presented much better characteristics for fuel cell applications compared with the well known Nafion{sup (R)} 112. In terms of the DMFC tests of the studied membranes at low temperature, the sPEEK membrane with SD=71% showed to have similar performance, or even better, as that of Nafion{sup (R)} 112. However, the highest DMFC overall efficiency was achieved using sPEEK membrane with SD=52%. (author)

  14. IONIC CONDUCTIVITY IN THE COMPLEXES OF COMB-SHAPED POLYETHER WITH LITHIUM AROMATIC SULFONATE

    Institute of Scientific and Technical Information of China (English)

    ZHANG Shengshui; QIU Weihua; XUE Dacui; LIU Qingguo

    1993-01-01

    Complexes of comb-shaped polyether and lithium aromatic sulfonates bearing different negative charge number were prepared by in situ thermal polymerization. Their conductivity depends deeply on salt content, ambient temperature and negative charge number of the added salts. Results show that anions can be partly immobilized by increasing their negative charges at lower temperature.Against discharge time the short circuit current of the battery (Li/complex film/Lix V3O8) is stabilized by increasing the anionic charge number of the complex.

  15. Highly charged proton-exchange membrane. Sulfonated poly(ether sulfone)-silica polyelectrolyte composite membranes for fuel cells

    Energy Technology Data Exchange (ETDEWEB)

    Shahi, Vinod K. [Electro-Membrane Processes Division, Central Salt and Marine Chemicals Research Institute, Bhavnagar-364002, Gujarat (India)

    2007-01-15

    Sulfonation of poly(ether sulfone) was carried out with chlorosulphonic acid in chloroform and its composite proton-exchange membrane was prepared using aminopropyltriethoxysilane as inorganic precursor by sol-gel in acidic medium. These membranes were further subjected to phosphorylation with phosphorous acid for introducing phosphonic acid functionality at inorganic segment. Extent of sulphonation was estimated by {sup 1}H-NMR spectroscopy while introduction of phosphonic acid groups was confirmed by FTIR spectroscopy and ion-exchange capacity studies. Different membranes, with varied silica content without and with phosphorylation, were characterized for their thermal and mechanical stabilities, physicochemical and electrochemical properties using thermogravimetric analysis (TGA), dynamic mechanical analysis (DMA), scanning electron microscopy (SEM), aq. methanol uptake studies, proton conductivity and methanol permeability measurements. The silica content in the membrane matrix and effect of phosphorylation was optimized as a function of membrane properties. Activation energy required for the proton transport across the membrane was also estimated and found to be comparable with Nafion 117 membrane. From the frictional interpretation and estimation of selectivity parameter it was observed that SPS-Si composite phosphorylated membrane with 20% silica content (SPS-Si(P)/20) resulted in the best proton-exchange membrane, which exhibited quite higher selectivity parameter in comparison to Nafion 117 for direct methanol fuel cell applications. Also, current-voltage polarization characteristics of SPS-Si(P)/20 membrane measured in direct methanol fuel cell, were found to be comparable to the Nafion 117 membrane. (author)

  16. The Effects of Sulfonated Poly(ether ether ketone Ion Exchange Preparation Conditions on Membrane Properties

    Directory of Open Access Journals (Sweden)

    Rebecca S. L. Yee

    2013-08-01

    Full Text Available A low cost cation exchange membrane to be used in a specific bioelectrochemical system has been developed using poly(ether ether ketone (PEEK. This material is presented as an alternative to current commercial ion exchange membranes that have been primarily designed for fuel cell applications. To increase the hydrophilicity and ion transport of the PEEK material, charged groups are introduced through sulfonation. The effect of sulfonation and casting conditions on membrane performance has been systematically determined by producing a series of membranes synthesized over an array of reaction and casting conditions. Optimal reaction and casting conditions for producing SPEEK ion exchange membranes with appropriate performance characteristics have been established by this uniquely systematic experimental series. Membrane materials were characterized by ion exchange capacity, water uptake, swelling, potential difference and NMR analysis. Testing this extensive membranes series established that the most appropriate sulfonation conditions were 60 °C for 6 h. For mechanical stability and ease of handling, SPEEK membranes cast from solvent casting concentrations of 15%–25% with a resulting thickness of 30–50 µm were also found to be most suitable from the series of tested casting conditions. Drying conditions did not have any apparent impact on the measured parameters in this study. The conductivity of SPEEK membranes was found to be in the range of 10−3 S cm−1, which is suitable for use as a low cost membrane in the intended bioelectrochemical systems.

  17. Preparation of new proton exchange membranes using sulfonated poly(ether sulfone) modified by octylamine (SPESOS)

    Energy Technology Data Exchange (ETDEWEB)

    Mabrouk, W. [Societe ERAS Labo, 222 RN 90, 38330, St Nazaire Les Eymes, Grenoble (France); Laboratoire des Materiaux Industriels, Conservatoire National des Arts et Metiers de Paris 75003, Paris (France); Laboratoire de Chimie Analytique et Electrochimie, Faculte des Sciences de Tunis, Campus Universitaire 1092, Tunis (Tunisia); Ogier, L. [Societe ERAS Labo, 222 RN 90, 38330, St Nazaire Les Eymes, Grenoble (France); Matoussi, F. [Laboratoire de Chimie Analytique et Electrochimie, Faculte des Sciences de Tunis, Campus Universitaire 1092, Tunis (Tunisia); Sollogoub, C., E-mail: cyrille.sollogoub@cnam.fr [Laboratoire des Materiaux Industriels, Conservatoire National des Arts et Metiers de Paris 75003, Paris (France); Vidal, S. [Societe ERAS Labo, 222 RN 90, 38330, St Nazaire Les Eymes, Grenoble (France); Dachraoui, M. [Laboratoire de Chimie Analytique et Electrochimie, Faculte des Sciences de Tunis, Campus Universitaire 1092, Tunis (Tunisia); Fauvarque, J.F. [Laboratoire des Materiaux Industriels, Conservatoire National des Arts et Metiers de Paris 75003, Paris (France)

    2011-08-15

    Highlights: {yields} New, simple and cheap way to synthesize a membrane. {yields} The membranes combine good proton conductivities with good mechanical properties. {yields} The membrane performances in a fuel cell are similar to the Nafion 117. - Abstract: Sulfonated poly(arylene ether sulfone) (SPES) has received considerable attention in membrane preparation for proton exchange membrane fuel cell (PEMFC). But such membranes are brittle and difficult to handle in operation. We investigated new membranes using SPES grafted with various degrees of octylamine. Five new materials made from sulfonated polyethersulfone sulfonamide (SPESOS) were synthetized with different grades of grafting. They were made from SPES, with initially an ionic exchange capacity (IEC) of 2.4 meq g{sup -1} (1.3 H{sup +} per monomer unit). Pristine SPES with that IEC is water swelling and becomes soluble at 80 deg. C, its proton conductivity is in the range of 0.1 S cm{sup -1} at room temperature in aqueous H{sub 2}SO{sub 4} 1 M, similar to that of Nafion. After grafting with various amounts of octylamine, the material is water insoluble; membranes are less brittle and show sufficient ionic conductivity. Proton transport numbers were measured close to 1.

  18. Poly(vinylbenzyl sulfonic acid)-grafted poly(ether ether ketone) membranes

    Energy Technology Data Exchange (ETDEWEB)

    Hwang, Mi-Lim; Choi, Jisun; Woo, Hyun-Su; Kumar, Vinod; Sohn, Joon-Yong; Shin, Junhwa, E-mail: shinj@kaeri.re.kr

    2014-02-15

    Highlights: • PEEK-g-PVBSA, a polymer electrolyte membrane was prepared by a radiation grafting technique. • Poly(ether ether ketone) (PEEK), an aromatic hydrocarbon polymer was used as a grafting backbone film. • The water uptake, proton conductivity, and methanol permeability of the membranes were evaluated. • PEEK-g-PVBSA membranes show considerably lower methanol permeability compared to a Nafion membrane. -- Abstract: In this study, an aromatic hydrocarbon based polymer electrolyte membrane, poly(vinylbenzyl sulfonic acid)-grafted poly(ether ether ketone) (PEEK-g-PVBSA), has been prepared by the simultaneous irradiation grafting of vinylbenzyl chloride (VBC) monomer onto a PEEK film and subsequent sulfonation. Each chemical conversion was monitored by FT-IR and SEM–EDX instruments. The physicochemical properties including IEC, water uptake, proton conductivity, and methanol permeability of the prepared membranes were also investigated and found that the values of these properties increase with the increase of degree of grafting. It was observed that the IEC values of the prepared PEEK-g-PVBSA membranes with 32%, 58%, and 80% DOG values were 0.50, 1.05, and 1.22 meq/g while the water uptakes were 14%, 20%, and 21%, respectively. The proton conductivities (0.0272–0.0721 S/cm at 70 °C) were found to be somewhat lower than Nafion 212 (0.126 S/cm at 70 °C) at a relative humidity of 90%. However, the prepared membranes showed a considerably lower methanol permeability (0.61–1.92 × 10{sup −7} cm{sup 2}/s) compared to a Nafion 212 membrane (5.37 × 10{sup −7} cm{sup 2}/s)

  19. Electrospun sulfonated poly(ether ketone) nanofibers as proton conductive reinforcement for durable Nafion composite membranes

    Science.gov (United States)

    Klose, Carolin; Breitwieser, Matthias; Vierrath, Severin; Klingele, Matthias; Cho, Hyeongrae; Büchler, Andreas; Kerres, Jochen; Thiele, Simon

    2017-09-01

    We show that the combination of direct membrane deposition with proton conductive nanofiber reinforcement yields highly durable and high power density fuel cells. Sulfonated poly(ether ketone) (SPEK) was directly electrospun onto gas diffusion electrodes and then filled with Nafion by inkjet-printing resulting in a 12 μm thin membrane. The ionic membrane resistance (30 mΩ*cm2) was well below that of a directly deposited membrane reinforced with chemically inert (PVDF-HFP) nanofibers (47 mΩ*cm2) of comparable thickness. The power density of the fuel cell with SPEK reinforced membrane (2.04 W/cm2) is 30% higher than that of the PVDF-HFP reinforced reference sample (1.57 W/cm2). During humidity cycling and open circuit voltage (OCV) hold, the SPEK reinforced Nafion membrane showed no measurable degradation in terms of H2 crossover current density, thus fulfilling the target of 2 mA/cm2 of the DOE after degradation. The chemical accelerated stress test (100 h OCV hold at 90 °C, 30% RH, H2/air, 50/50 kPa) revealed a degradation rate of about 0.8 mV/h for the fuel cell with SPEK reinforced membrane, compared to 1.0 mV/h for the PVDF-HFP reinforced membrane.

  20. Morphology Effect on Proton Dynamics in Nafion® 117 and Sulfonated Polyether Ether Ketone

    Science.gov (United States)

    Leong, Jun Xing; Diño, Wilson Agerico; Ahmad, Azizan; Daud, Wan Ramli Wan; Kasai, Hideaki

    2016-09-01

    We report results of our experimental and theoretical studies on the dynamics of proton conductivity in Nafion® 117 and self-fabricated sulfonated polyether ether ketone (SPEEK) membranes. Knowing that the presence of water molecules in the diffusion process results in a lower energy barrier, we determined the diffusion barriers and corresponding tunneling probabilities of Nafion® 117 and SPEEK system using a simple theoretical model that excludes the medium (water molecules) in the initial calculations. We then propose an equation that relates the membrane conductivity to the tunneling probability. We recover the effect of the medium by introducing a correction term into the proposed equation, which takes into account the effect of the proton diffusion distance and the hydration level. We have also experimentally verified that the proposed equation correctly explain the difference in conductivity between Nafion® 117 and SPEEK. We found that membranes that are to be operated in low hydration environments (high temperatures) need to be designed with short diffusion distances to enhance and maintain high conductivity.

  1. Modified nanocrystal cellulose/fluorene-containing sulfonated poly(ether ether ketone ketone) composites for proton exchange membranes

    Science.gov (United States)

    Wei, Yingcong; Shang, Yabei; Ni, Chuangjiang; Zhang, Hanyu; Li, Xiaobai; Liu, Baijun; Men, Yongfeng; Zhang, Mingyao; Hu, Wei

    2017-09-01

    Highly sulfonated poly(ether ether ketone ketone)s (SFPEEKKs) with sulfonation degrees of 2.34 (SFPEEKK5) and 2.48 (SFPEEKK10) were synthesized through the direct sulfonation of a fluorene-containing poly(ether ether ketone ketone) under a relatively mild reaction condition. Using the solution blending method, sulfonated nanocrystal cellulose (sNCC)-enhanced SFPEEKK composites (SFPEEKK/sNCC) were successfully prepared for investigation as proton exchange membranes. Transmission electron microscopy showed that sNCC was uniformly distributed in the composite membranes. The properties of the composite membranes, including thermal stability, mechanical properties, water uptake, swelling ratio, oxidative stability and proton conductivity were thoroughly evaluated. Results indicated that the insertion of sNCC could contribute to water management and improve the mechanical performance of the membranes. Notably, the proton conductivity of SFPEEKK5/sNCC-5 was as high as 0.242 S cm-1 at 80 °C. All data proved the potential of SFPEEKK/sNCC composites for proton exchange membranes in medium-temperature fuel cells.

  2. Hydrophilic modification of poly(ether sulfone) ultrafiltration membrane surface by self-assembly of TiO 2 nanoparticles

    Science.gov (United States)

    Luo, Ming-Liang; Zhao, Jian-Qing; Tang, Wu; Pu, Chun-Sheng

    2005-08-01

    Membrane fouling is one of the major obstacles for reaching the ultimate goal, which realizes high flux over a prolonged period of ultrafiltration (UF) operation. In this paper, TiO 2 nanoparticles of a quantum size (40 nm or less) in anatase crystal structure were prepared from the controlled hydrolysis of titanium tetraisopropoxide and characterized by X-ray diffraction (XRD) analysis and transmission electron microscopy (TEM). The hydrophilic modification of poly(ether sulfone) UF membrane was performed by self-assembly of the hydroxyl group of TiO 2 nanoparticle surface and the sulfone group and ether bond in poly(ether sulfone) structure through coordination and hydrogen bond interaction, which was ascertained by X-ray photoelectron spectroscopy (XPS). The morphology and hydrophilicity were characterized by scanning electron microscopy (SEM) and contact angle test, respectively. The composite UF membrane was also characterized in terms of separation behavior for polyethylene glycol-5000 solute. The experimental results show that the composite UF membrane has good separation performance and offers a strong potential for possible use as a new type of anti-fouling UF membrane.

  3. Electrochemical investigation of sulfonated poly(ether ether ketone)/clay nanocomposite membranes for moderate temperature fuel cell applications

    Energy Technology Data Exchange (ETDEWEB)

    Hasani-Sadrabadi, Mohammad Mahdi [Polymer Engineering Department, Amirkabir University of Technology, Tehran (Iran); Biomedical Engineering Department, Amirkabir University of Technology, Tehran (Iran); Dashtimoghadam, Erfan; Sarikhani, Kaveh [Polymer Engineering Department, Amirkabir University of Technology, Tehran (Iran); Majedi, Fatemeh S. [Biomedical Engineering Department, Amirkabir University of Technology, Tehran (Iran); Khanbabaei, Ghader [Polymer Science and Technology Division, Research Institute of Petroleum Industry, Tehran (Iran)

    2010-05-01

    In the present study, polyelectrolyte membranes based on partially sulfonated poly(ether ether ketone) (sPEEK) with various degrees of sulfonation are prepared. The optimum degree of sulfonation is determined according to the transport properties and hydrolytic stability of the membranes. Subsequently, various amounts of the organically modified montmorillonite (MMT) are introduced into the sPEEK matrices via the solution intercalation technique. The proton conductivity and methanol permeability measurements of the fabricated composite membranes reveal a high proton to methanol selectivity, even at elevated temperatures. Membrane based on sPEEK and 1 wt% of MMT, as the optimum nanoclay composition, exhibits a high selectivity and power density at the concentrated methanol feed. Moreover, it is found that the optimum nanocomposite membrane not only provides higher performance compared to the neat sPEEK and Nafion {sup registered} 117 membranes, but also exhibits a high open circuit voltage (OCV) at the elevated methanol concentration. Owing to the high proton conductivity, reduced methanol permeability, high power density, convenient processability and low cost, sPEEK/MMT nanocomposite membranes could be considered as the alternative membranes for moderate temperature direct methanol fuel cell applications. (author)

  4. Sulfonated poly(ether sulfone) (SPES)/boron phosphate (BPO{sub 4}) composite membranes for high-temperature proton-exchange membrane fuel cells

    Energy Technology Data Exchange (ETDEWEB)

    Wen, Sheng [Faculty of Chemistry and Material Science, Xiaogan University, Xiaogan, Hubei 432100 (China); Ministry of Education, Key Laboratory for the Green, Preparation and Application of Functional Materials, Institute of Composite Materials, Faculty of Materials Science and Engineering, Hubei University, Wuhan 430062 (China); Gong, Chunli [Faculty of Chemistry and Material Science, Xiaogan University, Xiaogan, Hubei 432100 (China); Tsen, Wen-Chin; Shu, Yao-Chi [Department of Polymer Materials, Vanung University, Tao-Yuan, Taiwan 32045 (China); Tsai, Fang-Chang [Ministry of Education, Key Laboratory for the Green, Preparation and Application of Functional Materials, Institute of Composite Materials, Faculty of Materials Science and Engineering, Hubei University, Wuhan 430062 (China)

    2009-11-15

    A new series of sulfonated poly(ether sulfone) (SPES)/boron phosphate (BPO{sub 4}) composite membranes for proton-exchange membrane fuel cells (PEMFCs) applications, with a BPO{sub 4} content up to 40 wt%, were prepared by a sol-gel method using tripropylborate and phosphoric acid as precursors. Compared to a pure SPES membrane, BPO{sub 4} doping in the membranes led to a higher thermal stability and glass-transition temperature (T{sub g}) as revealed by TGA-FTIR, DSC and DMTA. Water uptake and oxidative stability were significantly increased by increasing the content of BPO{sub 4}. At both operating temperature conditions, namely 20 C and 100 C, the tensile strength of all the composite membranes were lower than that of the SPES membrane. However, even when the content of BPO{sub 4} was as high as 30%, the composite membrane still possessed strength similar to the Nafion 112 membrane. SEM-EDX indicated that the BPO{sub 4} particles were uniformly embedded throughout the SPES matrix, which may facilitate proton transport. Proton conductivities increased from 0.0065 to 0.022 S cm{sup -1} at room temperature as BPO{sub 4} increased from 0 to 40%. The conductivities also increased with the temperature. The SPES/BPO{sub 4} composite membrane is a promising candidate for PEMFCs applications, especially at higher temperatures. (author)

  5. Effect of degree of sulfonation and casting solvent on sulfonated poly(ether ether ketone) membrane for vanadium redox flow battery

    Science.gov (United States)

    Xi, Jingyu; Li, Zhaohua; Yu, Lihong; Yin, Bibo; Wang, Lei; Liu, Le; Qiu, Xinping; Chen, Liquan

    2015-07-01

    The properties of sulfonated poly(ether ether ketone) (SPEEK) membranes with various degree of sulfonation (DS) and casting solvent are investigated for vanadium redox flow battery (VRFB). The optimum DS of SPEEK membrane is firstly confirmed by various characterizations such as physicochemical properties, ion selectivity, and VRFB single-cell performance. Subsequently the optimum casting solvent is selected for the optimum DS SPEEK membrane within N,N‧-dimethylformamide (DMF), N,N‧-dimethylacetamide (DMAc), N-methyl-2-pyrrolidone (NMP), and dimethylsulfoxide (DMSO). The different performance of SPEEK membranes prepared with various casting solvents can be attributed to the different interaction between solvent and -SO3H group of SPEEK. In the VRFB single-cell test, the optimum SPEEK membrane with DS of 67% and casting solvent of DMF (S67-DMF membrane) exhibits higher VRFB efficiencies and better cycle-life performance at 80 mA cm-2. The investigation of various DS and casting solvent will be effective guidance on the selection and modification of SPEEK membrane towards VRFB application.

  6. Highly stable ionic-covalent cross-linked sulfonated poly(ether ether ketone) for direct methanol fuel cells

    Science.gov (United States)

    Lei, Linfeng; Zhu, Xingye; Xu, Jianfeng; Qian, Huidong; Zou, Zhiqing; Yang, Hui

    2017-05-01

    A novel ionic cross-linked sulfonated poly(ether ether ketone) containing equal content of sulfonic acid and pendant tertiary amine groups (TA-SPEEK) has been initially synthesized for the application in direct methanol fuel cells (DMFCs). By adjusting the ratio of p-xylene dibromide to tertiary amine groups of TA-SPEEK, a series of ionic-covalent cross-linked membranes (C-SPEEK-x) with tunable degree of cross-linking are prepared. Compared with the pristine membrane, the ionic and ionic-covalent cross-linked proton exchange membranes (PEMs) exhibit reduced methanol permeability and improved mechanical properties, dimensional and oxidative stability. The proton conductivity and methanol selectivity of protonated TA-SPEEK and C-SPEEK-x at 25 °C is up to 0.109 S cm-1 and 3.88 × 105 S s cm-3, respectively, which are higher than that of Nafion 115. The DMFC incorporating C-SPEEK-25 exhibits a maximum power density as high as 35.3 mW cm-2 with 4 M MeOH at 25 °C (31.8 mW cm-2 for Nafion 115). Due to the highly oxidative stability of the membrane, no obvious performance degradation of the DMFC is observed after more than 400 h operation, indicating such cost-effective ionic-covalent cross-linked membranes have substantial potential as alternative PEMs for DMFC applications.

  7. Friedel-Crafts Crosslinked Highly Sulfonated Polyether Ether Ketone (SPEEK) Membranes for a Vanadium/Air Redox Flow Battery.

    Science.gov (United States)

    Merle, Géraldine; Ioana, Filipoi Carmen; Demco, Dan Eugen; Saakes, Michel; Hosseiny, Seyed Schwan

    2013-12-30

    Highly conductive and low vanadium permeable crosslinked sulfonated poly(ether ether ketone) (cSPEEK) membranes were prepared by electrophilic aromatic substitution for a Vanadium/Air Redox Flow Battery (Vanadium/Air-RFB) application. Membranes were synthesized from ethanol solution and crosslinked under different temperatures with 1,4-benzenedimethanol and ZnCl2 via the Friedel-Crafts crosslinking route. The crosslinking mechanism under different temperatures indicated two crosslinking pathways: (a) crosslinking on the sulfonic acid groups; and (b) crosslinking on the backbone. It was observed that membranes crosslinked at a temperature of 150 °C lead to low proton conductive membranes, whereas an increase in crosslinking temperature and time would lead to high proton conductive membranes. High temperature crosslinking also resulted in an increase in anisotropy and water diffusion. Furthermore, the membranes were investigated for a Vanadium/Air Redox Flow Battery application. Membranes crosslinked at 200 °C for 30 min with a molar ratio between 2:1 (mol repeat unit:mol benzenedimethanol) showed a proton conductivity of 27.9 mS/cm and a 100 times lower VO2+ crossover compared to Nafion.

  8. Friedel–Crafts Crosslinked Highly Sulfonated Polyether Ether Ketone (SPEEK Membranes for a Vanadium/Air Redox Flow Battery

    Directory of Open Access Journals (Sweden)

    Géraldine Merle

    2013-12-01

    Full Text Available Highly conductive and low vanadium permeable crosslinked sulfonated poly(ether ether ketone (cSPEEK membranes were prepared by electrophilic aromatic substitution for a Vanadium/Air Redox Flow Battery (Vanadium/Air-RFB application. Membranes were synthesized from ethanol solution and crosslinked under different temperatures with 1,4-benzenedimethanol and ZnCl2 via the Friedel–Crafts crosslinking route. The crosslinking mechanism under different temperatures indicated two crosslinking pathways: (a crosslinking on the sulfonic acid groups; and (b crosslinking on the backbone. It was observed that membranes crosslinked at a temperature of 150 °C lead to low proton conductive membranes, whereas an increase in crosslinking temperature and time would lead to high proton conductive membranes. High temperature crosslinking also resulted in an increase in anisotropy and water diffusion. Furthermore, the membranes were investigated for a Vanadium/Air Redox Flow Battery application. Membranes crosslinked at 200 °C for 30 min with a molar ratio between 2:1 (mol repeat unit:mol benzenedimethanol showed a proton conductivity of 27.9 mS/cm and a 100 times lower VO2+ crossover compared to Nafion.

  9. Friedel–Crafts Crosslinked Highly Sulfonated Polyether Ether Ketone (SPEEK) Membranes for a Vanadium/Air Redox Flow Battery

    Science.gov (United States)

    Merle, Géraldine; Ioana, Filipoi Carmen; Demco, Dan Eugen; Saakes, Michel; Hosseiny, Seyed Schwan

    2014-01-01

    Highly conductive and low vanadium permeable crosslinked sulfonated poly(ether ether ketone) (cSPEEK) membranes were prepared by electrophilic aromatic substitution for a Vanadium/Air Redox Flow Battery (Vanadium/Air-RFB) application. Membranes were synthesized from ethanol solution and crosslinked under different temperatures with 1,4-benzenedimethanol and ZnCl2 via the Friedel–Crafts crosslinking route. The crosslinking mechanism under different temperatures indicated two crosslinking pathways: (a) crosslinking on the sulfonic acid groups; and (b) crosslinking on the backbone. It was observed that membranes crosslinked at a temperature of 150 °C lead to low proton conductive membranes, whereas an increase in crosslinking temperature and time would lead to high proton conductive membranes. High temperature crosslinking also resulted in an increase in anisotropy and water diffusion. Furthermore, the membranes were investigated for a Vanadium/Air Redox Flow Battery application. Membranes crosslinked at 200 °C for 30 min with a molar ratio between 2:1 (mol repeat unit:mol benzenedimethanol) showed a proton conductivity of 27.9 mS/cm and a 100 times lower VO2+ crossover compared to Nafion. PMID:24957118

  10. State of the water in crosslinked sulfonated poly(ether ether ketone). Two-dimensional differential scanning calorimetry correlation mapping

    Energy Technology Data Exchange (ETDEWEB)

    Al Lafi, Abdul G. [Department of Chemistry, Atomic Energy Commission, Damascus, P.O. Box 6091 (Syrian Arab Republic); Hay, James N., E-mail: cscientific9@aec.org.sy [The School of Metallurgy and Materials, College of Physical Sciences and Engineering, University of Birmingham, Edgbaston, Birmingham B15 2TT (United Kingdom)

    2015-07-20

    Highlights: • 2D-DSC mapping was applied to analyze the heat flow responses of hydrated crosslinked sPEEK. • Two types of loosely bond water were observed. • The first was bond to the sulfonic acid groups and increased with ion exchange capacity. • The second was attributed to the polar groups introduced by ions irradiation and increased with crosslinking degree. • DSC combined with 2D mapping provides a powerful tool for polymer structural determination. - Abstract: This paper reports the first application of two-dimensional differential scanning calorimetry correlation mapping, 2D-DSC-CM to analyze the heat flow responses of sulphonated poly(ether ether ketone), sPEEK, films having different ion exchange capacity and degrees of crosslinks. With the help of high resolution and high sensitivity of 2D-DSC-CM, it was possible to locate two types of loosely bound water within the structure of crosslinked sPEEK. The first was bound to the sulfonic acid groups and dependent on the ion exchange capacity of the sPEEK. The second was bound to other polar groups, either introduced by irradiation with ions and dependent on the crosslinking degree or present in the polymer such as the carbonyl groups or terminal units. The results suggest that the ability of the sulfonic acid groups in the crosslinked sPEEK membranes to adsorb water molecules is increased by crosslinking, probably due to the better close packing efficiency of the crosslinked samples. DSC combined with 2D correlation mapping provides a fast and powerful tool for polymer structural determination.

  11. Dielectric Properties of Polyether Sulfone/Bismaleimide Resin Composite Based on Nanolumina Modified by Super-Critical Ethanol

    Science.gov (United States)

    Chen, Yufei; Li, Zhichao; Teng, Chengjun; Li, Fangliang; Han, Yang

    2016-11-01

    Nano-alumina was chemically modified with super-critical ethanol enabling a surface active coating. Modified nano-alumina was incorporated in polymer blends based on thermoplastic polyether sulfone and thermosetting bismaleimide resin to produce novel nanocomposites designated as SCE-Al2O3/PES-MBAE. In the SCE-Al2O3/PES-MBAE nano-composites, the matrix was originally formed from 4,4'-diamino diphenyl methane bismaleimide (MBMI) using the diluents of 3,3'-diallyl bisphenol A (BBA) and bisphenol-A diallyl ether (BBE), while polyether sulfone (PES) was used as toughening agent along with super-critically modified nano-alumina (SCE-Al2O3) as filler material. The content of SCE-Al2O3 was varied from 0 wt.% to 6 wt.%. The nano-composites were characterized for their morphological, spectroscopic and dielectric properties. Fourier transform infrared spectroscopy (FT-IR) indicated that ethanol molecules had adhered to the surface of the nano-Al2O3 in super-critical state. A reaction between MBMI and allyl compound occurred and SCE-Al2O3 was doped into the polymer matrix. Volume resistivity of the composite initially increased and then decreased. The modification due to SCE-Al2O3 could overcome the undesirable impact of PES by using a bare minimum level of SCE-Al2O3. The dielectric constant ( ɛ) and dielectric loss (tan δ) as in the case of volume resistivity were initially increased and then decreased with the content of SCE-Al2O3 in the composite. The dielectric constant, dielectric loss and dielectric strength of SCE-Al2O3 (4 wt.%)/PES (5 wt.%)-MBAE nano-composite were 3.53 (100 Hz), 1.52 × 10-3 (100 Hz) and 15.66 kV/mm, respectively, which indicated that the dielectric properties of the composite fulfilled the basic requirements of electrical and insulating material. It was evident from the morphological analysis that the SCE-Al2O3 was evenly dispersed at the nanoscale; for example, the size of SCE-Al2O3 in SCE-Al2O3 (4 wt.%)/PES (5 wt.%)-MBAE measured less than 50 nm.

  12. IMMOBILIZATION OF POTENTIALLY BIOACTIVE MOIETIES ONTO POLYETHER WITH POLY(ETHYLENE GLYCOL)-SULFONATE SPACER

    Institute of Scientific and Technical Information of China (English)

    JI Jian; FENG Linxian; QIU Yongxin; YU Xiaojie; YANG Shilin

    1997-01-01

    A new reactive graft copolymer, poly(tetramethylene glycol)-graft-ω-propyl sodium sulfonate-poly(ethylene glycol) (PTMG-g-PEG-CH2CH2CH2SO-3Na+), was synthesized by the cationic polymerization of α-ω-bifunctional PEG macromonomer ((o)CH2-PEG--CH2CH2CH2SO3Na ) and THF. The obtained copolymer exhibits the expected structure as indicated by the result of characterization. Two amino acids (L-arginine, L-tyrosine) were covalently attached to the copolymer after converting the sulfonate group to sulfonyl chloride. So the new reactive graft copolymer (PTMG-g-PEG-CH2CH2CH2SO-3Na+) is expected to be very useful in attachment of potentially bioactive moieties to polymer via a hydrophilic PEG spacer.

  13. Sulfonated poly(ether ether ketone)/zirconium tricarboxybutylphosphonate composite proton-exchange membranes for direct methanol fuel cells

    Institute of Scientific and Technical Information of China (English)

    Qijun GAO; Mianyan HUANG; Yuxin WANG; Yuquan CAI; Li XU

    2008-01-01

    Sulfonated poly(ether ether ketone) (SPEEK) is a very promising alternative membrane material for direct methanol fuel cells. However, with a fairly high degree ofsulfonation (DS), SPEEK membranes can swell excessively and even dissolve at high temperature. This restricts mem-branes from working above a high tolerable temperature to get high proton conductivity. To deal with this contra-dictory situation, insolvable zirconium tricarboxybutyl-phosphonate (Zr(PBTC)) powder was employed to make a composite with SPEEK polymer in an attempt to improve temperature tolerance of the membranes. SPEEK/Zr(PBTC) composite membranes were obtained by casting a homogeneous mixture of Zr(PBTC) and SPEEK in N,N-dimethylacetamide on a glass plate and then evaporating the solvent at 60℃. Many characteristics were investigated, including thermal stability, liquid uptake, methanol permeability and proton conductivity. Results showed significant improvement not only in tem-perature tolerance, but also in methanol resistance of the SPEEK/Zr(PBTC) composite membranes. The mem-branes containing 30 wt-%~40 wt-% of Zr(PBTC) had their methanol permeability around 10-7 cm2·S-1 at room temperature to 80℃, which was one order of magnitudelower than that of Nafion 115. High proton conductivity of the composite membranes, however, could also be achieved from higher temperature applied. At 100% rela-tive humidity, above 90℃ the conductivity of the compo-site membrane containing 40 wt-% of Zr(PBTC) exceeded that of the Nafion 115 membrane and even reached a high value of 0.36 S·cm-1 at 160℃. Improved applicable tem-perature and high conductivity of the composite membrane indicated its promising application in DMFC operations at high temperature.

  14. Photochemical modification of poly(ether sulfone) ultrafiltration membranes by UV-assisted graft polymerization for the prevention of biofouling

    Science.gov (United States)

    Pieracci, John Paul

    Membranes are widely used by the biotechnology industry in the separation and recovery of proteins from biological solutions. Fouling of membrane surfaces by irreversible protein adsorption during ultrafiltration causes loss of membrane permeability and can reduce membrane selectivity and lead to significant product loss through denaturation. In this work, low fouling poly(ether sulfone) (PES) ultrafiltration membranes were produced by ultraviolet (UV) assisted graft polymerization of hydrophilic vinyl monomers using a newly developed photochemical dip modification technique. This technique was developed to make the UV modification process more easily adaptable to continuous membrane manufacturing processes. A method was also developed to measure and track the degree of polymer grafting on the membrane surface using attenuated total reflection Fourier transform infrared spectroscopy (FTIR/ATR). Grafting the hydrophilic monomer N-vinyl-2-pyrrolidinone (NVP) onto the membrane surface increased surface wettability and produced membranes with the high wettability of regenerated cellulose membranes. The enhanced surface wettability significantly decreased irreversible adsorptive fouling during the filtration of the protein bovine serum albumin (BSA). In order to maintain the rejection of BSA after modification, PES chain scission was tightly controlled by regulating the UV wavelength range and the light intensity used. The UV reactor system was operated with 300 nm UV lamps and a benzene filter used to remove high energy wavelengths below 275 nm that were determined to cause severe loss of BSA rejection due to pore enlargement from extensive chain scission. Dip modification caused membrane permeability to decrease due to the grafted chains blocking the membrane pores. The use of a chain transfer agent during modification followed by ethanol cleaning increased modified membrane permeability, but BSA rejection was severely decreased. The resultant membranes produced by

  15. Crosslinked poly(vinyl alcohol)/sulfonated poly(ether ether ketone) blend membranes for fuel cell applications - Surface energy characteristics and proton conductivity

    Energy Technology Data Exchange (ETDEWEB)

    Kanakasabai, P.; Vijay, P.; Deshpande, Abhijit P.; Varughese, Susy [Department of Chemical Engineering, Indian Institute of Technology Madras, Chennai 600 036 (India)

    2011-02-01

    Ionic polymers, their blends and composites are considered potential candidates for application as electrolytes in fuel cells. While developing new materials for membranes, it is important to understand the interactions of these electrolytic materials with electrodes/catalysts and with reactants/products. Some of these interactions can be understood by estimating the surface energy and wettability of the membrane materials. In this work, polyvinyl alcohol with varying degrees of sulfonation and its blend with sulfonated poly(ether ether ketone) are prepared and studied for their wettability characteristics using goniometry. The surface energy and its components are estimated using different approaches and compared. Properties such as the ion-exchange capacity, the proton conductivity and the water sorption/desorption behaviour are also investigated to understand the relationship with wettability and surface energy and its components. Among the different methods, the van Oss acid-base and the modified Berthelot approaches yield comparable estimates for the total surface energy. (author)

  16. Sulfonated polystyrene fiber network-induced hybrid proton exchange membranes.

    Science.gov (United States)

    Yao, Yingfang; Ji, Liwen; Lin, Zhan; Li, Ying; Alcoutlabi, Mataz; Hamouda, Hechmi; Zhang, Xiangwu

    2011-09-01

    A novel type of hybrid membrane was fabricated by incorporating sulfonated polystyrene (S-PS) electrospun fibers into Nafion for the application in proton exchange membrane fuel cells. With the introduction of S-PS fiber mats, a large amount of sulfonic acid groups in Nafion aggregated onto the interfaces between S-PS fibers and the ionomer matrix, forming continuous pathways for facile proton transport. The resultant hybrid membranes had higher proton conductivities than that of recast Nafion, and the conductivities were controlled by selectively adjusting the fiber diameters. Consequently, hybrid membranes fabricated by ionomers, such as Nafion, incorporated with ionic-conducting nanofibers established a promising strategy for the rational design of high-performance proton exchange membranes.

  17. Influence of Silica/Sulfonated Polyether-Ether Ketone as Polymer Electrolyte Membrane for Hydrogen Fueled Proton Exchange Membrane Fuel Cells

    Directory of Open Access Journals (Sweden)

    Sri Handayani

    2011-12-01

    Full Text Available The operation of non-humidified condition of proton exchange membrane fuel cell (PEMFC using composite sPEEK-silica membrane is reported. Sulfonated membrane of PEEK is known as hydrocarbon polyelectrolyte membrane for PEMFC and direct methanol fuel cell (DMFC. The state of the art of fuel cells is based on the perluorosulfonic acid membrane (Nafion. Nafion has been the most used in both PEMFC and DMFC due to good performance although in low humidified condition showed poor current density. Here we reported the effect of silica in hydrocarbon sPEEK membrane that contributes for a better water management system inside the cell, and showed 0.16 W/cm2 of power density which is 78% higher than that of non-silica modified [Keywords: composite membrane, polyether-ether ketone, silica, proton exchange membrane fuel cell].

  18. Acid-base blend membranes based on 2-amino-benzimidazole and sulfonated poly(ether ether ketone) for direct methanol fuel cells

    Energy Technology Data Exchange (ETDEWEB)

    Fu, Yongzhu; Manthiram, Arumugam [Materials Science and Engineering Program, The University of Texas at Austin, Austin, TX 78712 (United States); Guiver, Michael D. [Institute for Chemical Process and Environmental Technology, National Research Council of (Canada)

    2007-05-15

    Direct methanol fuel cells (DMFC) are attractive for portable and automobile power needs, but their commercialization is hampered by high methanol permeability and the high cost of the currently used Nafion membrane. We report here a novel, low-cost blend membrane consisting of polysulfone-2-amide-benzimidazole (a basic polymer) and sulfonated poly(ether ether ketone) (an acidic polymer), which facilitates proton conduction through acid-base interactions while preserving excellent chemical and mechanical stabilities. The blend membrane exhibits performance in DMFC much higher than that of Nafion 115 and similar to that of Nafion 112, but with a remarkably superior long-term performance than Nafion 112 due to significantly reduced methanol crossover, enhancing the commercialization prospects of DMFC. (author)

  19. Partially Fluorinated Sulfonated Poly(ether amide Fuel Cell Membranes: Influence of Chemical Structure on Membrane Properties

    Directory of Open Access Journals (Sweden)

    Chulsung Bae

    2011-01-01

    Full Text Available A series of fluorinated sulfonated poly (ether amides (SPAs were synthesized for proton exchange membrane fuel cell applications. A polycondensation reaction of 4,4’-oxydianiline, 2-sulfoterephthalic acid monosodium salt, and tetrafluorophenylene dicarboxylic acids (terephthalic and isophthalic or fluoroaliphatic dicarboxylic acids produced SPAs with sulfonation degrees of 80–90%. Controlling the feed ratio of the sulfonated and unsulfonated dicarboxylic acid monomers afforded random SPAs with ion exchange capacities between 1.7 and 2.2 meq/g and good solubility in polar aprotic solvents. Their structures were characterized using NMR and FT IR spectroscopies. Tough, flexible, and transparent films were obtained with dimethylsulfoxide using a solution casting method. Most SPA membranes with 90% sulfonation degree showed high proton conductivity (>100 mS/cm at 80 °C and 100% relative humidity. Among them, two outstanding ionomers (ODA-STA-TPA-90 and ODA-STA-IPA-90 showed proton conductivity comparable to that of Nafion 117 between 40 and 80 °C. The influence of chemical structure on the membrane properties was systematically investigated by comparing the fluorinated polymers to their hydrogenated counterparts. The results suggest that the incorporation of fluorinated moieties in the polymer backbone of the membrane reduces water absorption. High molecular weight and the resulting physical entanglement of the polymers chains played a more important role in improving stability in water, however.

  20. Properties investigation of sulfonated poly(ether ether ketone)/polyacrylonitrile acid-base blend membrane for vanadium redox flow battery application.

    Science.gov (United States)

    Li, Zhaohua; Dai, Wenjing; Yu, Lihong; Liu, Le; Xi, Jingyu; Qiu, Xinping; Chen, Liquan

    2014-11-12

    Acid-base blend membrane prepared from sulfonated poly(ether ether ketone) (SPEEK) and polyacrylonitrile (PAN) was detailedly evaluated for vanadium redox flow battery (VRFB) application. SPEEK/PAN blend membrane exhibited dense and homogeneous cross-section morphology as scanning electron microscopy and energy-dispersive X-ray spectroscopy images show. The acid-base interaction of ionic cross-linking and hydrogen bonding between SPEEK and PAN could effectively reduce water uptake, swelling ratio, and vanadium ion permeability, and improve the performance and stability of blend membrane. Because of the good balance of proton conductivity and vanadium ion permeability, blend membrane with 20 wt % PAN (S/PAN-20%) showed higher Coulombic efficiency (96.2% vs 91.1%) and energy efficiency (83.5% vs 78.4%) than Nafion 117 membrane at current density of 80 mA cm(-2) when they were used in VRFB single cell. Besides, S/PAN-20% membrane kept a stable performance during 150 cycles at current density of 80 mA cm(-2) in the cycle life test. Hence the SPEEK/PAN acid-base blend membrane could be used as promising candidate for VRFB application.

  1. A new strategy for designing high-performance sulfonated poly(ether ether ketone) polymer electrolyte membranes using inorganic proton conductor-functionalized carbon nanotubes

    Science.gov (United States)

    Gong, Chunli; Zheng, Xuan; Liu, Hai; Wang, Guangjin; Cheng, Fan; Zheng, Genwen; Wen, Sheng; Law, Wing-Cheung; Tsui, Chi-Pong; Tang, Chak-Yin

    2016-09-01

    Remarkable progress has been made on the use of polymer electrolyte membranes (PEMs) for renewable-energy-related research. In particular, carbon nanotubes (CNTs) have emerged as versatile nanomaterials to modify PEMs. However, the inert ionic conduction ability and possible short-circuiting risk are the two major obstacles to their further development. In this work, CNTs are firstly functionalized with an inorganic proton conductor, boron phosphate (BPO4), using a facile polydopamine-assisted sol-gel method to yield BPO4@CNTs. This new additive is then used to modify sulfonated poly(ether ether ketone) (SPEEK). Polydopamine coating layer can act as an extraordinary glue to homogeneously adhere BPO4 nanoparticles on CNTs, thereby not only reducing the risk of short-circuiting, but also fabricating new proton-conducting pathways in the composite membranes. A comprehensive characterization reveals that the thermal stability, tensile properties, and dimensional stability of PEMs are significantly improved. Compared with pure SPEEK, the proton conductivity of SPEEK/BPO4@CNTs-2 is improved by 45% and 150% at 20 °C and at 80 °C, respectively. Furthermore, the H2/O2 cell performance of SPEEK/BPO4@CNTs-2 membrane exhibits a peak power density of 340.7 mW cm-2 at 70 °C, which is significantly better than that of pure SPEEK (254.2 mW cm-2), demonstrating the great potential of proton conductors-functionalized CNTs in PEMs.

  2. Characterization of sulfonated poly(ether ether ketone)/poly(vinylidene fluoride-co-hexafluoropropylene) composite membrane for vanadium redox flow battery application

    Science.gov (United States)

    Li, Zhaohua; Liu, Le; Yu, Lihong; Wang, Lei; Xi, Jingyu; Qiu, Xinping; Chen, Liquan

    2014-12-01

    Sulfonated poly(ether ether ketone) (SPEEK) and poly(vinylidene fluoride-co-hexafluoropropylene) (P(VDF-co-HFP)) composite membranes are prepared and investigated in detail for vanadium redox flow battery (VRFB) application. With the high hydrophobicity and stability of P(VDF-co-HFP), the properties of composite membranes such as mechanical property and vanadium ion permeability are effectively improved, showing good trends with the increasing of P(VDF-co-HFP) mass ratio. The VRFB single cell assembled with the composite membrane of 15 wt.% P(VDF-co-HFP) (SPEEK-15% membrane) exhibits higher coulombic efficiency (CE, 95.4%) and energy efficiency (EE, 83.8%) than that assembled with Nafion 117 membrane (CE 91.1% and EE 78.4%) at the current density of 80 mA cm-2. Furthermore, the SPEEK-15% membrane maintains a stable performance during 100 cycles at the current density of 80 mA cm-2. Therefore the SPEEK/P(VDF-co-HFP) composite membrane could be used as low-cost and high-performance membrane for VRFB application.

  3. Proton Conduction in Sulfonated Organic-Inorganic Hybrid Monoliths with Hierarchical Pore Structure.

    Science.gov (United States)

    von der Lehr, Martin; Seidler, Christopher F; Taffa, Dereje H; Wark, Michael; Smarsly, Bernd M; Marschall, Roland

    2016-09-28

    Porous organic-inorganic hybrid monoliths with hierarchical porosity exhibiting macro- and mesopores are prepared via sol-gel process under variation of the mesopore size. Organic moieties in the pore walls are incorporated by substituting up to 10% of the silicon precursor tetramethylorthosilicate with bisilylated benzene molecules. After functionalization with sulfonic acid groups, the resulting sulfonated hybrid monoliths featuring a bimodal pore structure are investigated regarding proton conduction depending on temperature and relative humidity. The hierarchical pore system and controlled mesopore design turn out to be crucial for sulfonation and proton conduction. These sulfonated hybrid hierarchical monoliths containing only 10% organic precursor exhibit higher proton conduction at different relative humidities than sulfonated periodic mesoporous organosilica made of 100% bisilylated precursors exhibiting solely mesopores, even with a lower concentration of sulfonic acid groups.

  4. Salinomycin Hydroxamic Acids: Synthesis, Structure, and Biological Activity of Polyether Ionophore Hybrids.

    Science.gov (United States)

    Borgström, Björn; Huang, Xiaoli; Chygorin, Eduard; Oredsson, Stina; Strand, Daniel

    2016-06-09

    The polyether ionophore salinomycin has recently gained attention due to its exceptional ability to selectively reduce the proportion of cancer stem cells within a number of cancer cell lines. Efficient single step strategies for the preparation of hydroxamic acid hybrids of this compound varying in N- and O-alkylation are presented. The parent hydroxamic acid, salinomycin-NHOH, forms both inclusion complexes and well-defined electroneutral complexes with potassium and sodium cations via 1,3-coordination by the hydroxamic acid moiety to the metal ion. A crystal structure of an cationic sodium complex with a noncoordinating anion corroborates this finding and, moreover, reveals a novel type of hydrogen bond network that stabilizes the head-to-tail conformation that encapsulates the cation analogously to the native structure. The hydroxamic acid derivatives display down to single digit micromolar activity against cancer cells but unlike salinomycin selective reduction of ALDH(+) cells, a phenotype associated with cancer stem cells was not observed. Mechanistic implications are discussed.

  5. Quantum dots-hyperbranched polyether hybrid nanospheres towards delivery and real-time detection of nitric oxide

    DEFF Research Database (Denmark)

    Liu, Shuiping; Gu, Tianxun; Fu, Jiajia;

    2014-01-01

    In this work, novel hybrid nanosphere vehicles were synthesized for nitric oxide (NO) donating and real-time detection. The hybrid nanosphere vehicles consist of cadmium selenide quantum dots (CdSe QDs) as NO fluorescent probes, and the modified hyperbranched polyether (mHP)-based diazeniumdiolat...... mechanism. The low cell-toxicity of QDs-mHP-NO nanospheres was verified by means of MTT assay on L929 cells viability. The QDs-mHP-NO nanospheres provide perspectives for designing a new class of biocompatible NO donating and imaging systems....

  6. Nuclear Magnetic Resonance Investigation of Dynamics in Poly(Ethylene Oxide) Based Lithium Polyether-ester-sulfonate Ionomers

    Energy Technology Data Exchange (ETDEWEB)

    Roach, David J.; Dou, Shichen; Colby, Ralph H.; Mueller, Karl T.

    2012-01-07

    Nuclear magnetic resonance (NMR) spectroscopy has been utilized to investigate the dynamics of poly(ethylene oxide)-based lithium sulfonate ionomer samples that have low glass transition temperatures. 1H and 7Li spin-lattice relaxation times (T1) of the bulk polymer and lithium ions, respectively, were analyzed in samples with a range of ion contents. The temperature dependence of T1 values along with the presence of minima in T1 enabled correlation times and activation energies to be obtained for both the segmental motion of the polymer backbone and the hopping motion of lithium cations. Similar activation energies of both the polymer and lithium ions in the lower ion content samples indicate that the polymer segmental motion and lithium ion hopping motion are correlated even though their respective correlation times differ significantly. A divergent trend is observed for correlation times and activation energies of the highest ion content sample due to the presence of ionic aggregation. Details about the polymer and cation dynamics on the nanosecond timescale are discussed and complement the findings of X-ray scattering and Quasi Elastic Neutron Scattering experiments.

  7. Quantum dots-hyperbranched polyether hybrid nanospheres towards delivery and real-time detection of nitric oxide

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Shuiping; Gu, Tianxun; Fu, Jiajia [Key Laboratory of Eco-Textiles, Ministry of Education (Jiangnan University), Wuxi 214122 (China); College of Textile and Clothing, Jiangnan University, Wuxi 214122 (China); Li, Xiaoqiang, E-mail: leecaiwei@163.com [Key Laboratory of Eco-Textiles, Ministry of Education (Jiangnan University), Wuxi 214122 (China); College of Textile and Clothing, Jiangnan University, Wuxi 214122 (China); Technical University of Denmark, DTU Food, Søltofts plads, B227, 2800 Kgs. Lyngby (Denmark); Chronakis, Ioannis S. [Technical University of Denmark, DTU Food, Søltofts plads, B227, 2800 Kgs. Lyngby (Denmark); Ge, Mingqiao [Key Laboratory of Eco-Textiles, Ministry of Education (Jiangnan University), Wuxi 214122 (China); College of Textile and Clothing, Jiangnan University, Wuxi 214122 (China)

    2014-12-01

    In this work, novel hybrid nanosphere vehicles were synthesized for nitric oxide (NO) donating and real-time detection. The hybrid nanosphere vehicles consist of cadmium selenide quantum dots (CdSe QDs) as NO fluorescent probes, and the modified hyperbranched polyether (mHP)-based diazeniumdiolates as NO donors, respectively. The nanospheres have spherical outline with dimension of ∼ 127 nm. The data of systematic characterization demonstrated that the mHP-based hybrid nanosphere vehicles (QDs-mHP-NO) can release and real-time detect NO with the low limit of 25 nM, based on fluorescence quenching mechanism. The low cell-toxicity of QDs-mHP-NO nanospheres was verified by means of MTT assay on L929 cells viability. The QDs-mHP-NO nanospheres provide perspectives for designing a new class of biocompatible NO donating and imaging systems. - Highlights: • QDs-mHP-NO fluorescent probe was prepared. • The QDs-mHP-NO probe is capable of releasing NO. • The QDs-mHP-NO probe can quantitatively detecting the release of NO in real time. • The low cell-toxicity of QDs-mHP-NO nanospheres was verified.

  8. 高磺化度芳香聚醚醚酮的合成与表征%Synthesis and Characterization of a Series of High Sulfonated Poly(ether ether ketone)s

    Institute of Scientific and Technical Information of China (English)

    刘盛洲; 王烽; 陈天禄

    2001-01-01

    A series of high sulfonated poly(ether ether ketone)s were prepared by copolymerization of sodium 5,5-carbonylbis(2-fluorobenzenesulfonate)(2), 4,4-difluorobenzophenone(1) and bisphenol A(3) in the presence of potassium carbonate in dimethylsulfoxide. The copolymers were characterized by IR and DSC. The influence of degree of sulfonation on the properties of copolymers, such as component, thermal stability, solubility and filming ability, was studied.%用3,3-二磺酸钠基-4,4-二氟二苯酮合成了具有高磺化度的荷电聚醚醚酮. 用红外吸收光谱及DSC对其进行了表征. 研究了共聚物的组成、 热稳定性、 溶解性、 成膜性及磺化度对共聚物性能的影响.

  9. Molecular modeling of the morphology and transport properties of two direct methanol fuel cell membranes: phenylated sulfonated poly(ether ether ketone ketone) versus Nafion

    Energy Technology Data Exchange (ETDEWEB)

    Devanathan, Ramaswami; Idupulapati, Nagesh B.; Dupuis, Michel

    2012-08-14

    We have used molecular dynamics simulations to examine membrane morphology and the transport of water, methanol and hydronium in phenylated sulfonated poly ether ether ketone ketone (Ph-SPEEKK) and Nafion membranes at 360 K for a range of hydration levels. At comparable hydration levels, the pore diameter is smaller, the sulfonate groups are more closely packed, the hydronium ions are more strongly bound to sulfonate groups, and the diffusion of water and hydronium is slower in Ph-SPEEKK relative to the corresponding properties in Nafion. The aromatic carbon backbone of Ph-SPEEKK is less hydrophobic than the fluorocarbon backbone of Nafion. Water network percolation occurs at a hydration level ({lambda}) of {approx}8 H{sub 2}O/SO{sub 3}{sup -}. At {lambda} = 20, water, methanol and hydronium diffusion coefficients were 1.4 x 10{sup -5}, 0.6 x 10{sup -5} and 0.2 x 10{sup -5} cm{sup 2}/s, respectively. The pore network in Ph-SPEEKK evolves dynamically and develops wide pores for {lambda} > 20, which leads to a jump in methanol crossover and ion transport. This study demonstrates the potential of aromatic membranes as low-cost challengers to Nafion for direct methanol fuel cell applications and the need to develop innovative strategies to combat methanol crossover at high hydration levels.

  10. Ion Exchange and Antibiofouling Properties of Poly(ether sulfone) Membranes Prepared by the Surface Immobilization of Brønsted Acidic Ionic Liquids via Double-Click Reactions.

    Science.gov (United States)

    Yi, Zhuan; Liu, Cui-Jing; Zhu, Li-Ping; Xu, You-Yi

    2015-07-28

    Brønsted acidic ionic liquids (BAILs) are unique ionic liquids that display chemical structures similar to zwitterions, and they were typically used as solvents and catalysts. In this work, an imidazole-based BAIL monolayer was fabricated onto poly(ether sulfone) (PES) membranes via surface clicking reactions, and the multifunctionality, including ion exchange and biofouling resistance to proteins and bacteria, was demonstrated, which was believed to be one of few works in which BAIL had been considered to be a novel fouling resistance layer for porous membranes. The successful immobilization of the BAILs onto a membrane surface was confirmed by X-ray photoelectron spectroscopy analysis, contact angle measurement, and ζ potential determination. The results from Raman spectroscopy showed that, as a decisive step prior to zwitterion, the BAIL was deprotonated in aqueous solution, and biofouling resistance to proteins and bacteria was found. However, BAIL displayed ion exchange ability at lower pH, and surface hydrophilicity/hydrophobicity of membranes could be tuned on purpose. Our results have demonstrated that the BAIL grafted onto membranes will not only act as an antibiofouling barrier like zwitterions but also provide a platform for surface chemical tailoring by ion exchange, the property of which will become especially important in acidic solutions where the fouling resistance performances of zwitterions are greatly weakened.

  11. Preparation of main-chain-type and side-chain-type sulfonated poly(ether ether ketone) membranes for direct methanol fuel cell applications

    Science.gov (United States)

    Tsai, Jie-Cheng; Lin, Chien-Kung

    Novel main-chain-type and side-chain-type sulphonated poly(ether ether ketone)s (MS-SPEEKs) are synthesised by reacting the sulphonic acid groups of pristine SPEEKs with 2-aminoethanesulphonic acid to improve the nano-phase separated morphology of the material. 1H NMR and FT-IR spectroscopy are employed to determine the structure and composition of main-chain-type and side-chain-type sulphonated polymers. Flexible and tough membranes with reasonable thermal properties are obtained. The MS-SPEEKs show good hydrolytic stability, and water uptake values ranging from 15% to 30% are observed. Compared to Nafion 117 ®, the methanol permeability of the MS-SPEEKs is dramatically reduced to 8.83 × 10 -8 cm 2 s -1 to 3.31 × 10 -7 cm 2 s -1. The proton conductivity increases with increasing temperature, reaching 0.013-0.182 S cm -1. A maximum power density and open circuit voltage of 115 mW cm -2 and 0.830 V are obtained at 80 °C, respectively, which is significantly greater than the values generated with Nafion 117 ®. The introduction of pendent side-chain-type sulphonic acid groups increases the single-cell performance by more than approximately 20%; thus, the lower water diffusivity, methanol permeability, electro-osmotic drag coefficient and high cell performance indicated that MS-SPEEK is a promising candidate for DMFC applications.

  12. Proton-exchange sulfonated poly(ether ether ketone)(SPEEK)/SiOx-s composite membranes in direct methanol fuel cells%DMFCs用SPEEK/SiOx-S复合质子交换膜

    Institute of Scientific and Technical Information of China (English)

    高启君; 王宇新; 许莉; 卫国强; 王志涛

    2009-01-01

    A sulfonated poly(ether ether ketone)(SPEEK)membrane with a fairly high degree of SUl fonation (DS)can swell excessively and even dissolve at high temperature.To solve these problems,insolvable functionalized silica powder with suIlbnic acid groups(SiOx-S)was added into the SPEEK matrix(DS=55.1%) to prepare SPEEK/SiOx-S composite membranes.The decrease in both the swelling degree and the methanol permeability of the membranes was a dose-dependent result of addition of the SiOx-S powder.Pure SPEEK membrane swelled 52.6%at 80°C,whereas the SPEEK/SiOx-S(1 5%,by mass)membrane swelled only 27.3%at the same temperature.From room temperature to 80℃,all SPEEK/SPEEK/SiOx-S composite membranes had methanol petea-bility of about one order of magnitude lower than that of Nafion r 115.Compared with pure SPEEK membranes,the addition of the SiOx-S powder not only leads to higher proton conductivity,but also increascs the dimensional stability at higher temperatures,and grcater proton conductivity can bc achieved at higher temperature.The SPEEK/SiOx-S(20%,by mass)membrane could withstand temperature up to 145°C,at which in 100%relative humidity(RH) its proton branc dissolved at 90°C.The SPFEk/SiOx-S composite membranes are promising for use in direct methanol fuel cells because of their good dimensional stability,high proton conductivity,and low methanol permeability.

  13. Preparation of sulfonated poly(ether ether ketone)s containing amino groups/epoxy resin composite membranes and their in situ crosslinking for application in fuel cells

    Energy Technology Data Exchange (ETDEWEB)

    Guo, Meimei; Liu, Baijun; Li, Long; Liu, Chang; Wang, Lifeng; Jiang, Zhenhua [Alan G. MacDiarmid Institute, Jilin University, 2699 Qianjin Street, Changchun 130012 (China)

    2010-01-01

    A series of amino-containing sulfonated poly(aryl ether ketone)/4,4'-diglycidyl(biphenyl) epoxy resin (DGBP) composite membranes for proton exchange membranes fuel cells (PEMFCs) are prepared by solution blending and casting. The reaction kinetics and the effects of introduction of DGBP content on the properties of the composite membranes are thoroughly investigated. The crosslinked composite membranes after treatment at either 120 C or 200 C have improved oxidative and dimensional stability than those without crosslinking. Despite the fact that crosslinked membranes generally have lower proton conductivity in comparison with the original ones, the proton conductivities of the membranes treated at 120 C are above 2.22 x 10{sup -2} S cm{sup -1} at room temperature and 9.42 x 10{sup -2} S cm{sup -1} at 100 C. Even for the samples treated at 200 C, their proton conductivities are still higher than 1.26 x 10{sup -2} S cm{sup -1} at room temperature and higher than 8.67 x 10{sup -2} S cm{sup -1} at 100 C, which are well satisfied with elementary requirement of fuel cells. In addition, all the evaluated membranes have low methanol permeability. For example, the methanol permeability of AP6FSPEEK/DGBP1 cured at 200 C is 0.33 x 10{sup -6} cm{sup 2} s{sup -1}, which is an order magnitude lower than Nafion 117. Therefore, these novel crosslinked composite membranes could be potential usage in fuel cells. (author)

  14. Organic-inorganic crosslinked and hybrid membranes derived from sulfonated poly(arylene ether sulfone)/silica via sol-gel process

    Science.gov (United States)

    Feng, Shaoguang; Shang, Yuming; Wang, Yingzi; Xie, Xiaofeng; Mathur, V. K.; Xu, Jingming

    A series of covalently crosslinkable organic-inorganic hybrid membranes have been prepared from sulfonated poly(arylene ether sulfone) (SPAES) with pendant propenyl moiety and various amounts of vinyl substituted silica via sol-gel process which are then thermally crosslinked in the presence of benzoyl peroxide (BPO) initiator. The obtained membranes are characterized in terms of oxidative stability, thermal property, ion exchange capacity (IEC), water uptake, swelling ratio in methanol aqueous solution, proton conductivity, and methanol permeability coefficient. The results indicate that the oxidative stability and thermal stability of the hybrid membranes are improved. Moreover, introduction of silica reduces the water uptake and methanol swelling of membranes. The swelling ratio of membranes in 2 mol L -1 methanol aqueous solution at 80 °C slowly decreases from 26 to 19% with the increase of SiO 2 content from 0 to 12 wt.%. Furthermore, with the increase in silica content, the methanol permeability coefficient of the hybrid membranes decreases at first and then increases. When the silica content reaches 8 wt.%, the methanol permeability coefficient is at the minimum of 6.02 × 10 -7 cm 2 s -1, a 2.64-fold decrease compared with that of the pristine SPAES membrane. Moreover, the proton conductivity is found to be at about 95% of that of pristine polymer at that silica content.

  15. Organic-inorganic crosslinked and hybrid membranes derived from sulfonated poly(arylene ether sulfone)/silica via sol-gel process

    Energy Technology Data Exchange (ETDEWEB)

    Feng, Shaoguang; Shang, Yuming; Wang, Yingzi; Xie, Xiaofeng; Xu, Jingming [Institute of Nuclear and New Energy Technology, Tsinghua University, Beijing 100084 (China); Mathur, V.K. [Department of Chemical Engineering, University of New Hampshire, NH 03824 (United States)

    2010-05-01

    A series of covalently crosslinkable organic-inorganic hybrid membranes have been prepared from sulfonated poly(arylene ether sulfone) (SPAES) with pendant propenyl moiety and various amounts of vinyl substituted silica via sol-gel process which are then thermally crosslinked in the presence of benzoyl peroxide (BPO) initiator. The obtained membranes are characterized in terms of oxidative stability, thermal property, ion exchange capacity (IEC), water uptake, swelling ratio in methanol aqueous solution, proton conductivity, and methanol permeability coefficient. The results indicate that the oxidative stability and thermal stability of the hybrid membranes are improved. Moreover, introduction of silica reduces the water uptake and methanol swelling of membranes. The swelling ratio of membranes in 2 mol L{sup -1} methanol aqueous solution at 80 C slowly decreases from 26 to 19% with the increase of SiO{sub 2} content from 0 to 12 wt.%. Furthermore, with the increase in silica content, the methanol permeability coefficient of the hybrid membranes decreases at first and then increases. When the silica content reaches 8 wt.%, the methanol permeability coefficient is at the minimum of 6.02 x 10{sup -7} cm{sup 2} s{sup -1}, a 2.64-fold decrease compared with that of the pristine SPAES membrane. Moreover, the proton conductivity is found to be at about 95% of that of pristine polymer at that silica content. (author)

  16. Synthesis of novel disulfide and sulfone hybrid scaffolds as potent β-glucuronidase inhibitor.

    Science.gov (United States)

    Taha, Muhammad; Ismail, Nor Hadiani; Imran, Syahrul; Wadood, Abdul; Rahim, Fazal; Al Muqarrabin, Laode Muhammad Ramadhan; Zaki, Hamizah Mohd; Ahmat, Norizan; Nasir, Abdul; Khan, Fahad

    2016-10-01

    Novel series of disulfide and sulfone hybrid analogs (1-20) were synthesized and characterized through EI-MS and (1)H NMR and evaluated for β-glucuronidase inhibitory potential. All synthesized analogs except 13 and 15 showed excellent β-glucuronidase inhibitory potential with IC50 value ranging in between 2.20-88.16μM as compared to standard d-saccharic acid 1,4 lactone (48.4±1.25μM). Analogs 19, 16, 4, 1, 17, 6, 10, 3, 18, 2, 11, 14 and 5 showed many fold potent activity against β-glucuronidase inhibitor. Structure activity relationship showed that substitution of electron withdrawing groups at ortho as well as para position on phenyl ring increase potency. Electron withdrawing groups at meta position on phenyl ring showed slightly low potency as compared to ortho and para position. The binding interactions were confirmed through molecular docking studies.

  17. Synthesis,crystal structure and properties of inorganic-organic hybrid polymers based on 8-hydroxylquinoline-5-sulfonic acid

    Institute of Scientific and Technical Information of China (English)

    2009-01-01

    Two new inorganic-organic hybrid polymers, Mn(QS)(H2O) (1) and Co(QS)(H2O)2 (2) (H2QS=8-hydroxyl-quinoline-5-sulfonic acid), based on 8-hydroxylquinoline-5-sulfonate ligand, have been synthesized under solvothermal conditions and their structures were solved by single-crystal X-ray diffraction analysis. Compound 1 is a three-dimensional open framework with rutile topology structure, and compound 2 is a three-dimensional supramolecular structure. These compounds were characterized by powder XRD, infrared spectroscopy, thermogravimetric analysis, fluorescence properties and magnetism properties.

  18. Synthesis, crystal structure and properties of inorganic-organic hybrid polymers based on 8-hydroxylquinoline-5-sulfonic acid

    Institute of Scientific and Technical Information of China (English)

    WANG Ying; XUE Ming; XU JiaNing; ZHU GuangShan; QIU ShiLun

    2009-01-01

    Two new inorganic-organic hybrid polymers, Mn(QS)(H_2O) (1) and Co(QS)(H_2O)2 (2) (H2QS=8-hydroxylquinoline-5-sulfonic acid), based on 8-hydroxylquinoline-5-sulfonate ligand, have been synthesized under solvothermal conditions and their structures were solved by single-crystal X-ray diffraction analysis. Compound 1 is a three-dimensional open framework with rutile topology structure, and compound 2 is a three-dimensional supramolecular structure. These compounds were characterized by powder XRD, infrared spectroscopy, thermogravimetric analysis, fluorescence properties and magnetism properties.

  19. Preparation and characterization of sulfonated amine-poly(ether sulfone)s for proton exchange membrane fuel cell

    Energy Technology Data Exchange (ETDEWEB)

    Seo, Dong-Wan; Lim, Young-Don; Lee, Soon-Ho; Jeong, Young-Gi; Kim, Whan-Gi [Department of Applied Chemistry/RIC-ReSEM, Konkuk University, Chungju-si, Chungbuk 380-701 (Korea, Republic of); Hong, Tae-Whan [Department of Materials Sci and Engineering/RIC-ReSEM, Chungju National University, Chungju, Chungbuk (Korea, Republic of)

    2010-12-15

    Sulfonated amine-poly(ether sulfone)s (S-APES)s were prepared by nitration, reduction and sulfonation of poly(ether sulfone) (ultrason {sup registered} -S6010). Poly(ether sulfone) was reacted with ammonium nitrate and trifluoroacetic anhydride to produce the nitrated poly(ether sulfone), and was followed by reduction using tin(II)chloride and sodium iodide as reducing agents to give the amino-poly(ether sulfone). The S-APES was obtained by reaction of 1,3-propanesultone and the amino-poly(ether sulfone) (NH{sub 2}-PES) with sodium methoxide. The different degrees of nitration and reduction of poly(ether sulfone) were successfully synthesized by an optimized process. The reduction of nitro group to amino was done quantitatively, and this controlled the contents of the sulfonic acid group. The films were converted from salt to acid forms with dilute hydrochloric acid. Different contents of sulfonated unit of the S-APES were studied by FT-IR, {sup 1}H NMR spectroscopy, differential scanning calorimetry (DSC), and thermo gravimetric analysis (TGA). Sorption experiments were conducted to observe the interaction of sulfonated polymers with water and methanol. The ion exchange capacity (IEC), a measure of proton conductivity, was evaluated. The S-APES membranes exhibit conductivities (25 C) from 1.05 x 10{sup -3} to 4.83 x 10{sup -3} S/cm, water swell from 30.25 to 66.50%, IEC from 0.38 to 0.82 meq/g, and methanol diffusion coefficients from 3.10 x 10{sup -7} to 4.82 x 10{sup -7} cm{sup 2}/S at 25 C. (author)

  20. Thermal stability and thermodynamic properties of hybrid proton-conducting polyaryl etherketones.

    Science.gov (United States)

    Marani, D; Di Vona, M L; Traversa, E; Licoccia, S; Beurroies, I; Llewellyn, P L; Knauth, P

    2006-08-17

    The thermal and structural stability of sulfonated cross-linked PEEK (polyether ether ketone) and its silicon-containing class II hybrid derivatives were characterized by combination of mass spectrometry, infrared spectroscopy, X-ray diffraction, thermogravimetric analysis, and differential scanning calorimetry. Thermodynamic properties of the hybrids were determined, including glass-transition temperature, degree of crystallinity, and thermal stability. The decomposition processes of the hybrid polymers could be consistently interpreted and their energetics quantitatively determined. The introduction of inorganic silanol moieties improves the thermal stability compared to sulfonated products.

  1. Synthesis and properties of poly(methyl methacrylate-2-acrylamido-2-methylpropane sulfonic acid)/PbS hybrid composite

    Energy Technology Data Exchange (ETDEWEB)

    Preda, N., E-mail: nicol@infim.ro [National Institute of Materials Physics, Multifunctional Materials and Structures Laboratory, P.O. Box MG-7, 77125 Bucharest (Romania); Rusen, E. [University Politehnica Bucharest, Department of Polymer Science, Calea Victoriei No. 71101, Bucharest (Romania); Musuc, A. [Institute of Physical Chemistry, 060021 Bucharest (Romania); Enculescu, M.; Matei, E. [National Institute of Materials Physics, Multifunctional Materials and Structures Laboratory, P.O. Box MG-7, 77125 Bucharest (Romania); Marculescu, B. [University Politehnica Bucharest, Department of Polymer Science, Calea Victoriei No. 71101, Bucharest (Romania); Fruth, V. [Institute of Physical Chemistry, 060021 Bucharest (Romania); Enculescu, I. [National Institute of Materials Physics, Multifunctional Materials and Structures Laboratory, P.O. Box MG-7, 77125 Bucharest (Romania)

    2010-08-15

    The synthesis of a new hybrid composite based on PbS nanoparticles and poly(methyl methacrylate-2-acrylamido-2-methylpropane sulfonic acid) [P(MMA-AMPSA)] copolymer is reported. The chemical synthesis consists in two steps: (i) a surfactant-free emulsion copolymerization between methyl methacrylate and 2-acrylamido-2-methylpropane sulfonic acid and (ii) the generation of PbS particles in the presence of the P(MMA-AMPSA) latex, from the reaction between lead nitrate and thiourea. The composite was studied by scanning electron microscopy (SEM), X-ray diffraction, FTIR spectroscopy, thermogravimetric analysis and differential scanning calorimetry. The microstructure observed using SEM proves that the PbS nanoparticles are well dispersed in the copolymer matrix. The X-ray diffraction measurements demonstrate that the PbS nanoparticles have a cubic rock salt structure. It was also found that the inorganic semiconductor nanoparticles improve the thermal stability of the copolymer matrix.

  2. Hyperbranched polyether hybrid nanospheres with CdSe quantum dots incorporated for selective detection of nitric oxide

    DEFF Research Database (Denmark)

    Liu, Shuiping; Jin, Lanming; Chronakis, Ioannis S.

    2014-01-01

    In this work, hybrid nanosphere vehicles consisting of cadmium selenide quantum dots (CdSe QDs) were synthesized for nitric oxide (NO) donating and real-time detecting. The nanospheres with QDs being encapsulation have spherical outline with dimension of ~127 nm. The fluorescence properties...

  3. DNA-树状聚脂肪醚杂化体的合成及组装性能研究%Synthesis and Self-Assembly of DNA-Aliphatic Polyether Dendron Hybrids

    Institute of Scientific and Technical Information of China (English)

    赵智勇; 吴芬; 杨忠强; 刘冬生; 范青华

    2013-01-01

    A new kind of amphiphilic DNA-aliphatic polyether dendron hybrids consisting of a flexible hydrophobic polyether dendron and a single stranded DNA are synthesized, which are characterized by MALDI-TOF mass spectroscopy, HPLC and polyacrylamide gel electrophoresis (PAGE). In aqueous solution, as DNA length shortens from 24 mer to 18 mer, to 12 mer, to 6 mer, the hydrophilic DNA content in the DNA-aliphatic polyether dendron hybrid decreases, the morphology of the aggregates change from spherical micelles to nanofibers, and to irregular clusters. These different assemblies from DNA-aliphatic polyether dendron hybrids in aqueous solution are depended on the hydrophobic/hydrophilic ratio between the polyether dendron skeleton and DNA strand. However, when adding 1/10 (V/V) organic solvents such as dichloromethane (DCM), diethyl ether (EtOEt) or tetrahydrofuran (THF) into aqueous solution and after the assembling process that the sample solution is heated to 90 ℃ for 30 min and subsequently cooled to room temperature overnight, the third generation dendron conjugated 18 mer DNA hybrid could assemble into nanofibers. Meanwhile, in the THF/H2O (1:10, V/V) mixed solvents, with the same assembling process, as different dendron generations (the second or third generation) and different DNA lengths (6 mer, 12 mer, 18 mer or 24 mer) in the hybrids, all these hybrids could assemble into long nanofibers. The assembled structures have been characterized by transmission electron microscopy (TEM), atomic force microscope (AFM), dynamic light scattering (DLS) and fluorescent experiments. Subsequently, we verified the assembling mechanism that the spherical micelles and nanofibers contain a hydrophobic dendron core and a hydrophilic DNA shell by hydrophobic fluorescent molecule Nile Red encapsulation experiment and precise DNA hybridization to load gold nanoparticles at a size of 10 nm. The hybridization property of DNA at the shell associated with the encapsulation ability of

  4. Novel sulfonated polyimide/zwitterionic polymer-functionalized graphene oxide hybrid membranes for vanadium redox flow battery

    Science.gov (United States)

    Cao, Li; Kong, Lei; Kong, Lingqian; Zhang, Xingxiang; Shi, Haifeng

    2015-12-01

    Hybrid membranes (SPI/ZGO) composed of sulfonated polyimide (SPI) and zwitterionic polymer-functionalized graphene oxide (ZGO) are fabricated via a solution-casting method for vanadium redox flow battery (VRB). Successful preparation of ZGO fillers and SPI/ZGO hybrid membranes are demonstrated by FT-IR, XPS and SEM, indicating that ZGO fillers is homogeneously dispersed into SPI matrix. Through controlling the interfacial interaction between SPI matrix and ZGO fillers, the physicochemical properties, e.g., vanadium ion barrier and proton transport pathway, of hybrid membranes are tuned via the zwitterionic acid-base interaction in the hybrid membrane, showing a high ion selectivity and good stability with the incorporated ZGO fillers. SPI/ZGO-4 hybrid membrane proves a higher cell efficiencies (CE: 92-98%, EE: 65-79%) than commercial Nafion 117 membrane (CE: 89-94%, EE: 59-70%) for VRB application at 30-80 mA cm-2. The assembled VRB with SPI/ZGO-4 membrane presents a stable cycling charge-discharge performance over 280 times, which demonstrates its excellent chemical stability under the strong acidic and oxidizing conditions. SPI/ZGO hybrid membranes show a brilliant perspective for VRB application.

  5. Sulfonated macro-RAFT agents for the surfactant-free synthesis of cerium oxide-based hybrid latexes.

    Science.gov (United States)

    Garnier, Jérôme; Warnant, Jérôme; Lacroix-Desmazes, Patrick; Dufils, Pierre-Emmanuel; Vinas, Jérôme; van Herk, Alex

    2013-10-01

    Three types of amphiphatic macro-RAFT agents were employed as compatibilizers to promote the polymerization reaction at the surface of nanoceria for the synthesis of CeO2-based hybrid latexes. Macro-RAFT copolymers and terpolymers were first synthesized employing various combinations of butyl acrylate as a hydrophobic monomer and acrylic acid (AA) and/or 2-acrylamido-2-methylpropane sulfonic acid (AMPS) as hydrophilic monomers. After characterizing the adsorption of these macro-RAFT agents at the cerium oxide surface by UV-visible spectrometry, emulsion copolymerization reactions of styrene and methyl acrylate were then carried out in the presence of the surface-modified nanoceria. Dynamic Light Scattering and cryo-Transmission Electron Microscopy were employed to confirm the hybrid structure of the final CeO2/polymer latexes, and proved that the presence of acrylic acid units in amphiphatic macro-RAFT agents enabled an efficient formation of hybrid structures, while the presence of AMPS units, when combined with AA units, resulted in a better distribution of cerium oxide nanoclusters between latex particles.

  6. Organic-inorganic hybrid protonic polymeric electrolytes grafted by sulfonic acid/sulfonamide moieties

    Energy Technology Data Exchange (ETDEWEB)

    Depre, L.; Poinsignon, C.; Popall, M.

    2000-07-01

    Thin proton conducting membranes of an organic-inorganic polymer electrolyte bearing sulphonamide and sulfonic groups are prepared by sol-gel process. Polycondensation of alkoxysilanes provides the inorganic silicate backbone whereas the organic network is formed from reactive functional groups R{prime}(({minus}DH{sub 2}){sub 3}-SO{sub 3}H) and [({minus}CH{sub 2}){sub 3}-SO{sub 2}NH{sub 2}] of alkoxysilanes of R{prime}Si[OR{sub 3}] type. Proton conductivity measured in the dry and wet state under controlled Temperature and Relative Humidity increases from 10{sup {minus}4} S/cm under vacuum to 6 10{sup {minus}2} S/cm at 70 C and 96% RH. Conductivity dependence on temperature and associated conduction mechanisms are discussed in both states.

  7. Organotin Polyethers as Biomaterials

    Directory of Open Access Journals (Sweden)

    Michael R. Roner

    2009-10-01

    Full Text Available Organotin polyethers are easily synthesized employing interfacial polymerization systems involving the reaction of hydroxyl-containing Lewis bases and organotin halides. A wide variety of organotin-containing polymeric products have been synthesized including those derived from natural and synthetic polymers such as lignin, xylan, cellulose, dextran, and poly(vinyl alcohol. Others have been synthesized employing known drug diols such as dicumarol, DES, and dienestrol and a wide variety of synthetic diols. Included in these materials are the first water soluble organotin polymers. The organotin polyethers exhibit a wide range of biological activities. Some selectively inhibit a number of unwanted bacteria, including Staph. MRSA, and unwanted yeasts such as Candida albicans. Some also inhibit a variety of viruses including those responsible for herpes infections and smallpox. Others show good inhibition of a wide variety of cancer cell lines including cell lines associated with ovarian, colon, lung, prostrate, pancreatic and breast cancer. The synthesis, structural characterization, and biological characterization of these materials is described in this review.

  8. Polyether-polyester graft copolymer

    Science.gov (United States)

    Bell, Vernon L. (Inventor)

    1987-01-01

    Described is a polyether graft polymer having improved solvent resistance and crystalline thermally reversible crosslinks. The copolymer is prepared by a novel process of anionic copolymerization. These polymers exhibit good solvent resistance and are well suited for aircraft parts. Previous aromatic polyethers, also known as polyphenylene oxides, have certain deficiencies which detract from their usefulness. These commercial polymers are often soluble in common solvents including the halocarbon and aromatic hydrocarbon types of paint thinners and removers. This limitation prevents the use of these polyethers in structural articles requiring frequent painting. In addition, the most popular commercially available polyether is a very high melting plastic. This makes it considerably more difficult to fabricate finished parts from this material. These problems are solved by providing an aromatic polyether graft copolymer with improved solvent resistance and crystalline thermally reversible crosslinks. The graft copolymer is formed by converting the carboxyl groups of a carboxylated polyphenylene oxide polymer to ionic carbonyl groups in a suitable solvent, reacting pivalolactone with the dissolved polymer, and adding acid to the solution to produce the graft copolymer.

  9. Morphology and properties of amine terminated poly(arylene ether ketone) and poly(arylene ether sulfone) modified epoxy resin systems

    Science.gov (United States)

    Cecere, J. A.; Mcgrath, J. E.; Hedrick, J. L.

    1986-01-01

    Epoxy resin networks cured with DDS were modified by incorporating tough ductile thermoplastics such as the amine terminated polyether sulfones and amine terminated polyether ketones. Both linear copolymers were able to significantly improve the fracture toughness values at the 15 and 30 weight percent concentrations examined. These improvements in fracture toughness were achieved without any significant change in the flexural modulus.

  10. Synthesis and Characterization of Ion-exchange Sulfonated Poly (ether sulfone)

    Institute of Scientific and Technical Information of China (English)

    2006-01-01

    N,N'-Bis(3-hydroxyphenyl)-1,8,4,5-naphthalenetetracarboxylic bisimide was prepared from the reaction of 1,8,4,5-naphthalenetetrcarboxylic acid dianhydride and 2-aminophenol in N,N-dimethylformamide. Polymerization of this bisimide with 4,4'-difluorodiphenylsulfone and disodium 3,3'-disulfonate4,4'-difluorodiphenylsulfone gave ion-exchange sulfonated poly(ether sulfone). The structure of the title compound was characterized with 1H-NMR and its polymer was characterized with FT-IR.

  11. Thermal and Dielectric Behavior Studies of Poly(Arylene Ether Sulfones with Sulfonated and Phosphonated Pendants

    Directory of Open Access Journals (Sweden)

    Shimoga D. Ganesh

    2016-01-01

    Full Text Available The present paper discusses the aspects of the synthesizing valeric acid based poly(ether sulfones with active carboxylic acid pendants (VALPSU from solution polymerization technique via nucleophilic displacement polycondensation reaction among 4,4′-dichlorodiphenyl sulfone (DCDPS and 4,4′-bis(4-hydroxyphenyl valeric acid (BHPA. The conditions necessary to synthesize and purify the polymer were investigated in some detail. The synthesized poly(ether sulfones comprise sulfone and ether linkages in addition to reactive carboxylic acid functionality; these active carboxylic acid functional groups were exploited to hold the phenyl sulphonic acid and phenyl phosphonic acid pendants. The phenyl sulphonic acid pendants in VALPSU were easily constructed by altering active carboxylic acid moieties by sulfanilic acid using N,N′-dicyclohexylcarbodiimide (DCC mediated mild synthetic route, whereas the latter one was built in two steps. Initially, polyphosphoric acid condensation with VALPSU by 4-bromoaniline and next straightforward palladium catalyzed synthetic route, in both of which acidic pendants are clenched by polymer backbone via amide linkage. Without impairing the primary polymeric backbone modified polymers were prepared by varying the stoichiometric ratios of respective combinations. All the polymers were physicochemically characterized and pressed into tablets; electrical contacts were established to study the dielectric properties. Finally, the influence of the acidic pendants on the dielectric properties was examined.

  12. Polyethism in a colony of artificial ants

    CERN Document Server

    Marriott, Chris

    2011-01-01

    We explore self-organizing strategies for role assignment in a foraging task carried out by a colony of artificial agents. Our strategies are inspired by various mechanisms of division of labor (polyethism) observed in eusocial insects like ants, termites, or bees. Specifically we instantiate models of caste polyethism and age or temporal polyethism to evaluated the benefits to foraging in a dynamic environment. Our experiment is directly related to the exploration/exploitation trade of in machine learning.

  13. Food contaminant analysis at ultra-high mass resolution: application of hybrid linear ion trap - orbitrap mass spectrometry for the determination of the polyether toxins, azaspiracids, in shellfish.

    LENUS (Irish Health Repository)

    2010-10-30

    The biotoxins, azaspiracids (AZAs), from marine phytoplankton accumulate in shellfish and affect human health by causing severe gastrointestinal disturbance, diarrhea, nausea and vomiting. Specific and sensitive methods have been developed and validated for the determination of the most commonly occurring azaspiracid analogs. An LTQ Orbitrap mass spectrometer is a hybrid instrument that combines linear ion trap (LIT) mass spectrometry (MS) with high-resolution Fourier transform (FT) MS and this was exploited to perform simultaneous ultra-high-resolution full-scan MS analysis and collision-induced dissociation (CID) tandem mass spectrometry (MS\\/MS). Using the highest mass resolution setting (100,000 FWHM) in full-scan mode, the methodology was validated for the determination of six AZAs in mussel (Mytilus galloprovincialis) tissue extracts. Ultra-high mass resolution, together with a narrow mass tolerance window of ±2 mDa, dramatically improved detection sensitivity. In addition to employing chromatographic resolution to distinguish between the isomeric azaspiracid analogs, AZA1\\/AZA6 and AZA4\\/AZA5, higher energy collisionally induced dissociation (HCD) fragmentation on selected precursor ions were performed in parallel with full-scan FTMS. Using HCD MS\\/MS, most precursor and product ion masses were determined within 1 ppm of the theoretical m\\/z values throughout the mass spectral range and this enhanced the reliability of analyte identity.For the analysis of mussels (M. galloprovincialis), the method limit of quantitation (LOQ) was 0.010 µg\\/g using full-scan FTMS and this was comparable with the LOQ (0.007 µg\\/g) using CID MS\\/MS. The repeatability data were; intra-day RSD% (1.8-4.4%; n = 6) and inter-day RSD% (4.7-8.6%; n = 3). Application of these methods to the analysis of mussels (M. edulis) that were naturally contaminated with azaspiracids, using high-resolution full-scan Orbitrap MS and low-resolution CID MS\\/MS, produced

  14. Enhancement of Hybrid SPEEK Based Polymer–Cyclodextrin-Silica Inorganic Membrane for Direct Methanol Fuel Cell Application

    Directory of Open Access Journals (Sweden)

    Tutuk Djoko Kusworo

    2017-06-01

      Keywords: Direct Methanol Fuel Cell, Poly(ether ether ketone, cyclodextrin-silica, sulfonation, ionic conductivity. Article History: Received January 18th 2017; Received in revised form April 21st 2017; Accepted June 22nd 2017; Available online How to Cite This Article: Kusworo, T.D., Hakim, M.F. and Hadiyanto, H. (2017 Enhancement of Hybrid SPEEK Based Polymer–Cyclodextrin-Silica Inorganic Membrane for Direct Methanol Fuel Cell Application. International Journal of Renewable Energy Development, 6(2, 165-170. https://doi.org/10.14710/ijred.6.2.165-170

  15. Polymer Materials for Fuel Cell Membranes :Sulfonated Poly(ether sulfone) for Universal Fuel Cell Operations

    Institute of Scientific and Technical Information of China (English)

    Hyoung-Juhn Kim

    2005-01-01

    @@ 1Introduction Polymer electrolyte fuel cells (PEFCs) have been spotlighted because they are clean and highly efficient power generation system. Proton exchange membrane fuel cells (PEMFCs), which use reformate gases or pure H2 for a fuel, have been employed for automotives and residential usages. Also, liquid-feed fuel cells such as direct methanol fuel cell (DMFC) and direct formic acid fuel cell (DFAFC) were studied for portable power generation.

  16. Preparation of poly(ether ether ketone)-based polymer electrolytes for fuel cell membranes using grafting technique

    Energy Technology Data Exchange (ETDEWEB)

    Hasegawa, Shin; Suzuki, Yasuyuki [Conducting Polymer Materials Group, Environment and Industrial Materials Research Division, Quantum Beam Science Directorate, Japan Atomic Energy Agency (JAEA), 1233 Watanuki, Takasaki, Gunma 370 1292 (Japan); Maekawa, Yasunari [Conducting Polymer Materials Group, Environment and Industrial Materials Research Division, Quantum Beam Science Directorate, Japan Atomic Energy Agency (JAEA), 1233 Watanuki, Takasaki, Gunma 370 1292 (Japan)], E-mail: maekawa.yasunari@jaea.go.jp

    2008-05-15

    Poly(ether ether ketone) (PEEK)-based polymer electrolyte membranes (PEMs) was successfully prepared by radiation grafting of a styrene monomer into PEEK films and the consequent selective sulfonation of the grafting chains in the film state. Using milder sulfonation, the sulfonation reactions proceeded at the grafted chains in preference to the phenylene rings of PEEK main chains; as a result, the grafted films could successfully transform to a PEM with conductivity of more than 0.1 S/cm. The ion exchange capacity (IEC) and conductivity of the grafted PEEK electrolyte membranes were controlled to the ranges of 1.2-2.9 mmol/g and 0.03-0.18 S/cm by changing the grafting degree. It should be noted that this is the first example of directly transforming super-engineering plastic films into a PEM using radiation grafting.

  17. 40 CFR 721.7500 - Nitrate polyether polyol (generic name).

    Science.gov (United States)

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Nitrate polyether polyol (generic name... Substances § 721.7500 Nitrate polyether polyol (generic name). (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance nitrate polyether polyol (PMN P88-2540)...

  18. EPOXY RESINS TOUGHENED WITH CARBOXYL TERMINATED POLYETHERS

    Institute of Scientific and Technical Information of China (English)

    YU Yunchao; LI Yiming

    1983-01-01

    Carboxyl terminated polyethers, the adducts of hydroxyl terminated polytetrahydrofuran and maleic anhydride, were used as toughener for epoxy resins. The morphology of the toughened resins was investigated by means of turbidity measurement, dynamic mechanical testing and scanning electron microscope observation. It turned out that the molecular weight and the carboxyl content of the polyether and the cure conditions are important factors, which affect the particle size of the polyether-rich domains and, in turn, the mechanical properties of the cured resin. Carboxyl terminated polytetrahydrofurans have a low glass transition temperature, and in appropriate amount they do not affect the thermal resistance of the resin. These advantages make them preferable as toughener for epoxy resins.

  19. Polyether matrices for lithium generators; Matrices polyethers pour generateurs au lithium

    Energy Technology Data Exchange (ETDEWEB)

    Alloin, F.; Sanchez, J.Y. [Laboratoire d`Electrochimie et de Physicochimie des Materiaux et des Interfaces, 38 - Saint-Martin-d`Heres (France)

    1996-12-31

    The use of solvating polymers of polyether type is an interesting solution for the manufacturing of high capacity lithium batteries with lithium metal anodes and which can operate at T > 50 deg. C. These operating conditions are perfectly compatible with electric-powered vehicle and stationary battery applications. In order to improve the ionic conductivity of polymer electrolytes, new aprotic and amorphous polyether lattices have been synthesized having a good conductivity but also good thermal, mechanical and electrochemical stabilities. Two type of 3-D polyether lattices obtained by reticulation of linear pre-polymers have been selected as host polymers: unsaturated poly-condensate and unsaturated co-polyethers. (J.S.) 18 refs.

  20. Synthesis and Application of the Polyether Modified Organic Silicone

    Institute of Scientific and Technical Information of China (English)

    TONG Dong-feng; LIU Jie; ZHAO Chuan-jun

    2014-01-01

    Polyether modified organic silicone was successfully prepared from Eight methyl siloxane, tetramethyl dihydro two siloxane and UPEO. The chemical structure of the Polyether modified organic silicone was characterized by FT-IR. The wettability of treated cotton fabrics was increased. And the softness was improved significantly.

  1. Synthesis and Process Optimization of Electrospun PEEK-Sulfonated Nanofibers by Response Surface Methodology

    Directory of Open Access Journals (Sweden)

    Carlo Boaretti

    2015-07-01

    Full Text Available In this study electrospun nanofibers of partially sulfonated polyether ether ketone have been produced as a preliminary step for a possible development of composite proton exchange membranes for fuel cells. Response surface methodology has been employed for the modelling and optimization of the electrospinning process, using a Box-Behnken design. The investigation, based on a second order polynomial model, has been focused on the analysis of the effect of both process (voltage, tip-to-collector distance, flow rate and material (sulfonation degree variables on the mean fiber diameter. The final model has been verified by a series of statistical tests on the residuals and validated by a comparison procedure of samples at different sulfonation degrees, realized according to optimized conditions, for the production of homogeneous thin nanofibers.

  2. Tunable, antibacterial activity of silicone polyether surfactants.

    Science.gov (United States)

    Khan, Madiha F; Zepeda-Velazquez, Laura; Brook, Michael A

    2015-08-01

    Silicone surfactants are used in a variety of applications, however, limited data is available on the relationship between surfactant structure and biological activity. A series of seven nonionic, silicone polyether surfactants with known structures was tested for in vitro antibacterial activity against Escherichia coli BL21. The compounds varied in their hydrophobic head, comprised of branched silicone structures with 3-10 siloxane linkages and, in two cases, phenyl substitution, and hydrophilic tail of 8-44 poly(ethylene glycol) units. The surfactants were tested at three concentrations: below, at, and above their Critical Micelle Concentrations (CMC) against 5 concentrations of E. coli BL21 in a three-step assay comprised of a 14-24h turbidometric screen, a live-dead stain and viable colony counts. The bacterial concentration had little effect on antibacterial activity. For most of the surfactants, antibacterial activity was higher at concentrations above the CMC. Surfactants with smaller silicone head groups had as much as 4 times the bioactivity of surfactants with larger groups, with the smallest hydrophobe exhibiting potency equivalent to sodium dodecyl sulfate (SDS). Smaller PEG chains were similarly associated with higher potency. These data link lower micelle stability and enhanced permeability of smaller silicone head groups to antibacterial activity. The results demonstrate that simple manipulation of nonionic silicone polyether structure leads to significant changes in antibacterial activity.

  3. Positively charged and bipolar layered poly(ether imide) nanofiltration membranes for water softening applications

    Science.gov (United States)

    Gassara, S.; Abdelkafi, A.; Quémener, D.; Amar, R. Ben; Deratani, A.

    2015-07-01

    Poly(ether imide) (PEI) ultrafiltration membranes were chemically modified with branched poly(ethyleneimine) to obtain nanofiltration (NF) membrane Cat PEI with a positive charge in the pH range below 9. An oppositely charged polyelectrolyte layer was deposited on the resulting membrane surface by using sodium polystyrene sulfonate (PSSNa) and sodium polyvinyl sulfonate (PVSNa) to prepare a bipolar layered membrane NF Cat PEI_PSS and Cat PEI_PVS having a negatively charged surface and positively charged pores. Cat PEI exhibited good performance to remove multivalent cations (more than 90% of Ca2+) from single salt solutions except in presence of sulfate ions. Adding an anionic polyelectrolyte layer onto the positively charged surface resulted in a significant enhancement of rejection performance even in presence of sulfate anions. Application of the prepared membranes in water softening of natural complex mixtures was successful for the different studied membranes and a large decrease of hardness was obtained. Moreover, Cat PEI_PSS showed a good selectivity for nitrate removal. Fouling experiments were carried out with bovine serum albumin, as model protein foulant. Cat PEI_PSS showed much better fouling resistance than Cat PEI with a quantitative flux recovery ratio.

  4. PRECISION OF STONE MODEL MOULDING ACCORDING TO THE POLYETHER IMPRESSION

    Directory of Open Access Journals (Sweden)

    Mona IONAŞ

    2015-03-01

    Full Text Available Polyethers represent imprinting materials largely used on the market due to their precision in reproducing the prosthetic field. The present study aims at evaluating the linear dimensional variations of the models of dental stone following imprinting with polyethers by the technique of monophasic impression. The obtained results show no significant dimensional differences between the models of dental stone gypsum moulded 24 hours or 7 days after imprinting. The conclusion to be drawn is that the imprinting materials containing polyethers, applied by the monophasic technique, permit realization of high-precision models even 7 days after imprinting.

  5. Structures and Properties of Naturally Occurring Polyether Antibiotics

    Directory of Open Access Journals (Sweden)

    Jacek Rutkowski

    2013-01-01

    Full Text Available Polyether ionophores represent a large group of natural, biologically active substances produced by Streptomyces spp. They are lipid soluble and able to transport metal cations across cell membranes. Several of polyether ionophores are widely used as growth promoters in veterinary. Polyether antibiotics show a broad spectrum of bioactivity ranging from antibacterial, antifungal, antiparasitic, antiviral, and tumour cell cytotoxicity. Recently, it has been shown that some of these compounds are able to selectively kill cancer stem cells and multidrug-resistant cancer cells. Thus, they are recognized as new potential anticancer drugs. The biological activity of polyether ionophores is strictly connected with their molecular structure; therefore, the purpose of this paper is to present an overview of their formula, molecular structure, and properties.

  6. Thermally curable fluorinated main chain benzoxazine polyethers via Ullmann coupling

    OpenAIRE

    Demirel, A. Levent; Latthe, Sanjay S.; Demir, Kubra Dogan ; Kışkan, Barış; Yağcı, Yusuf

    2013-01-01

    Fluorinated main chain benzoxazine polyethers were prepared by Ullmann coupling of fluorinated benzoxazines in the presence of a nano-copperoxide catalyst. Various parameters such as the monomer structure, temperature, and the effect of catalyst on the polymerization were studied. The benzoxazine groups present in the polyether structure were shown to readily undergo thermally activated ring-opening polymerization in the absence of an added catalyst forming cross-linked networks. The thermal ...

  7. A rare allergy to a polyether dental impression material.

    Science.gov (United States)

    Mittermüller, Pauline; Szeimies, Rolf-Markus; Landthaler, Michael; Schmalz, Gottfried

    2012-08-01

    Polyether impression materials have been used in dentistry for more than 40 years. Allergic reactions to these materials such as reported in the 1970s ceased after replacement of a catalyst. Very recently, however, patients have started to report symptoms that suggest a new allergic reaction from polyether impression materials. Here, we report on the results of allergy testing with polyether impression materials as well as with its components. Eight patients with clinical symptoms of a contact allergy (swelling, redness or blisters) after exposure to a polyether impression material were subjected to patch tests, two of them additionally to a prick test. A further patient with atypical symptoms of an allergy (nausea and vomiting after contact with a polyether impression material in the oral cavity) but with a history of other allergic reaction was also patch tested. The prick tests showed no immediate reactions in the two patients tested. In the patch tests, all eight patients with typical clinical symptoms showed positive reactions to the mixed polyether impression materials, to the base paste or to a base paste component. The patient with the atypical clinical symptoms did not show any positive patch test reactions. Polyether impression materials may evoke type IV allergic reactions. The causative agent was a component of the base paste. In consideration of the widespread use of this impression material (millions of applications per year) and in comparison to the number of adverse reactions from other dental materials, the number of such allergic reactions is very low. In very scarce cases, positive allergic reactions to polyether impression materials are possible.

  8. Sulfonated Polyetherimide and Its Membranes

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    Polyetherimide (PEI) was sulfonated by chlorosulfonic acid for the first time. The sulfonated products were characterized by FT-IR, DSC, ion exchange capacity and water sorption measurement. The hydrophilicity of PEI was improved by the sulfonation. The PEI was blended with the sodium salt form of sulfonated PEI (SPEI) to prepare microporous membranes. The morphologies of the membranes were studied with Scanning Electron Microscope (SEM).

  9. Non-linear Shear and Uniaxial Extensional Rheology of Polyether-Ester-Sulfonate Copolymer Ionomer Melts

    DEFF Research Database (Denmark)

    Shabbir, Aamir; Huang, Qian; P. Baeza, Guilhem

    2017-01-01

    (ethylene oxide) (PEO) along the backbone in the coionomer with poly ( tetramethylene glycol) PTMO, increases the maximum Hencky strain at fracture thus adding ductility to the brittle PTMO-Na ionomer. As a result, the coionomer deforms much more compared to PTMO-Na but both fracture eventually...... to formation of strong ionic aggre-gates. These ionomer melts exhibit viscoelastic properties similar to well-entangled melts with an extended rubbery plateau. To evaluate the effects of nonlinear deforma-tion, the rheology of these ionomers was investigated using uniaxial extension and shear. The measurements...

  10. Analytical methodology for sulfonated lignins

    NARCIS (Netherlands)

    Brudin, S.; Schoenmakers, P.

    2010-01-01

    There is a significant need to characterize and classify lignins and sulfonated lignins. Lignins have so far received a good deal of attention, whereas this is not true for sulfonated lignins. There is a clear demand for a better understanding of sulfonated lignins on a chemical as well as physical

  11. Analytical methodology for sulfonated lignins

    NARCIS (Netherlands)

    Brudin, S.; Schoenmakers, P.

    2010-01-01

    There is a significant need to characterize and classify lignins and sulfonated lignins. Lignins have so far received a good deal of attention, whereas this is not true for sulfonated lignins. There is a clear demand for a better understanding of sulfonated lignins on a chemical as well as physical

  12. Nanoclay reinforced thermoplastic toughened epoxy hybrid syntactic foam: Surface morphology, mechanical and thermo mechanical properties

    Energy Technology Data Exchange (ETDEWEB)

    Asif, A. [Propellants and Special Chemicals Group, Propellants Polymers Chemicals and Materials Entity, Vikram Sarabhai Space Centre, Trivandrum 695022 (India); Rao, V. Lakshmana, E-mail: rao_vl@yahoo.co.in [Propellants and Special Chemicals Group, Propellants Polymers Chemicals and Materials Entity, Vikram Sarabhai Space Centre, Trivandrum 695022 (India); Ninan, K.N. [Propellants and Special Chemicals Group, Propellants Polymers Chemicals and Materials Entity, Vikram Sarabhai Space Centre, Trivandrum 695022 (India)

    2010-09-15

    Epoxy hybrid syntactic foams were prepared with diglycidyl ether of bisphenol A (DGEBA) epoxy resin, diamino diphenyl sulfone (DDS), hydroxyl terminated polyether ether ketone having pendant methyl group (PEEKMOH), microballoon and nanoclay. The density of the foam was maintained between 0.6 and 0.72 g/cc for all compositions. Fracture toughness, tensile, flexural and compressive properties of the foam were evaluated with respect to clay and PEEKMOH concentrations. Morphology by X-ray diffraction revealed that the clay particles within the epoxy resin were intercalated for all the compositions of the syntactic foam. Fracture toughness and mechanical properties of the syntactic foam were significantly improved by the addition of nanoclay. A further enhancement in fracture toughness and mechanical properties was observed by the addition of PEEKMOH. The hybrid epoxy syntactic foam thus prepared exhibited 58%, 77% and 38% improvement in compressive strength, percentage elongation and fracture toughness, respectively, compared to the neat epoxy syntactic foam. The specific mechanical properties were found to be higher for the epoxy hybrid syntactic foam containing 3 wt% nanoclay and 3 wt% of PEEKMOH combination. The storage and loss modulus of the syntactic foam were also increased by the addition of nanoclay and PEEKMOH. A marginal improvement in T{sub g} was observed with clay incorporated syntactic foam. SEM analysis revealed that increased microcracking, crack path deflection, matrix deformation, plastic deformation, rupture of microballoons and debonded microspheres influencing on fracture toughness and mechanical properties of epoxy hybrid syntactic foam.

  13. Anticancer Activity of Polyether Ionophore-Salinomycin.

    Science.gov (United States)

    Antoszczak, Michał; Huczyński, Adam

    2015-01-01

    Since the discovery of unusual anti-tumor activity of natural polyether antibiotic - Salinomycin, this compound, along with its derivatives, has been intensively studied against different human cancer cells, both in vivo and in vitro. Salinomycin has shown strong inhibition activity against the proliferation process of many different cancer cells, including multi-drug resistance (MDR) cancer cells, as well as cancer stem cells (CSCs), i.e. leukemic stem cells, colon carcinoma stem cells, prostate cancer stem cells and many others. Additionally, the application of Salinomycin has been proved to enhance the anti-cancer effect of radio- and chemotherapy. Preliminary clinical studies have shown tumor regression and only transient acute side effects after application of Salinomycin. Up to now, major efforts have been devoted to elucidate the biological mechanisms of anti-tumor activity of Salinomycin and it is expected that the results may provide new therapeutic strategies based on biological modulation of Salinomycin activity. This review is focused on and describes the possible role of Salinomycin in cancer therapy and gives an overview of its properties.

  14. Salinomycin, a polyether ionophoric antibiotic, inhibits adipogenesis

    Energy Technology Data Exchange (ETDEWEB)

    Szkudlarek-Mikho, Maria; Saunders, Rudel A. [Department of Medicine, Biochemistry and Cancer Biology, Center for Diabetes and Endocrine Research, College of Medicine, University of Toledo, Toledo, OH 43614 (United States); Yap, Sook Fan [Faculty of Medicine and Health Sciences, Department of Pre-Clinical Sciences, University of Tunku Abdul Rahman (Malaysia); Ngeow, Yun Fong [Department of Medical Microbiology, Faculty of Medicine, University of Malaya, Kuala Lumpur 50603 (Malaysia); Chin, Khew-Voon, E-mail: khew-voon.chin@utoledo.edu [Department of Medicine, Biochemistry and Cancer Biology, Center for Diabetes and Endocrine Research, College of Medicine, University of Toledo, Toledo, OH 43614 (United States)

    2012-11-30

    Highlights: Black-Right-Pointing-Pointer Salinomycin inhibits preadipocyte differentiation into adipocytes. Black-Right-Pointing-Pointer Salinomycin inhibits transcriptional regulation of adipogenesis. Black-Right-Pointing-Pointer Pharmacological effects of salinomycin suggest toxicity in cancer therapy. -- Abstract: The polyether ionophoric antibiotics including monensin, salinomycin, and narasin, are widely used in veterinary medicine and as food additives and growth promoters in animal husbandry including poultry farming. Their effects on human health, however, are not fully understood. Recent studies showed that salinomycin is a cancer stem cell inhibitor. Since poultry consumption has risen sharply in the last three decades, we asked whether the consumption of meat tainted with growth promoting antibiotics might have effects on adipose cells. We showed in this report that the ionophoric antibiotics inhibit the differentiation of preadipocytes into adipocytes. The block of differentiation is not due to the induction of apoptosis nor the inhibition of cell proliferation. In addition, salinomycin also suppresses the transcriptional activity of the CCAAT/enhancer binding proteins and the peroxisome proliferator-activated receptor {gamma}. These results suggest that the ionophoric antibiotics can be exploited as novel anti-obesity therapeutics and as pharmacological probes for the study of adipose biology. Further, the pharmacological effects of salinomycin could be a harbinger of its toxicity on the adipose tissue and other susceptible target cells in cancer therapy.

  15. Hydroxyalkylation and polyether polyol grafting of graphene tailored for graphene/polyurethane nanocomposites.

    Science.gov (United States)

    Appel, Anna-Katharina; Thomann, Ralf; Mülhaupt, Rolf

    2013-08-01

    Graphene functionalization by hydroxyalkylation and grafting with polyether polyols enables polyurethane (PU) nanocomposites formation by in situ polymerization with isocyanates combined with effective covalent interfacial coupling. Functionalized graphene (FG) hydroxylation is achieved either by alkylation, transesterification, or grafting of thermally reduced graphite oxide. In the presence of K2 CO3 as catalyst the reaction of FG-OH with ethylene carbonate at 180 °C affords hydroxyethylated FG, whereas transesterification with castor oil produces riconoleiate-modified FG polyols. In the "grafting-from" process, FG-alkoholate macro initiators initiate the graft polymerization of propylene oxide to produce hybrid FG polyols containing 38 and 59 wt% oligopropylene oxide. In the "grafting-to" process 3-ethyl-3-hydroxymethyl-oxetane is cationically polymerized onto FG-OH, producing novel hyperbranched FG-based polyether polyols. Whereas hydroxylation and grafting of FG greatly improve FG dispersion in organic solvents, polyols and even PU, as confirmed by transmission electron microscopy, matrix reinforcement of FG/PU is impaired by increasing alkyl chain length and polyol graft copolymer content. © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  16. STUDIES ON THE OXIDATION AND GRAFT COPOLYMERIZATION OF POLYETHERS

    Institute of Scientific and Technical Information of China (English)

    SUN Yanhui; QIU Kunyuan; FENG Xinde VOONG Sing-tuh

    1984-01-01

    Polyethers could form hydroperoxide under air-oxidation or photo-oxidation in the presence of H2O2. The scission of ether linkage induced by moderate oxidation was prevented by controlling the reaction time and hydroperoxide concentration. The oxidation rate was affected by the end groups of polyethers. The decreasing order of oxidation rate for various poly(tetramethylene ether) glycol derivatives having different end groups are as follows: poly(tetramethylene ether) glycol (PTMG)> poly(tetramethylene ether)acetate (PTMGAC) > poly(tetramethylene ether) phenyl carbamate (PTMGPC). The urethane end groups in PTMGPC increase the resistance toward oxidation. Polyether hydroperoxide reacts with ferrous ion or N,N-dimethyl toluidine (DMT) to form polymericoxy radical which then initiates the graft copolymerization of vinyl monomers at low temperature,and was devoid of homopolymerization. The copolymer after separation and purification was proved to be a graft one by IR analysis and elemental analysis.

  17. 磺酸化石墨烯掺杂的离子交换聚合物电致动器%Electro-actuators of sulfonated graphene hybrid ion-exchange polymer

    Institute of Scientific and Technical Information of China (English)

    焦战士; 何青松; 郭东杰; 戴振东

    2012-01-01

    合成了磺酸化石墨烯单分子膜, 并按不同质量分数浇注了约200 μm厚的石墨烯/全氟磺酸杂化膜, 全反射衰减红外光谱验证了全部合成和掺杂过程; 对影响杂化膜电致动性能的相关物理参数进行了测试。 利用化学还原沉积技术在杂化膜两侧嵌入Pt纳米颗粒, 制成石墨烯/全氟磺酸-金属复合材料, 并进行了扫描电子显微镜观测。引入低频正弦电信号, 得到聚合物电致动器, 利用力和位移传感器测试其电致动性能。结果表明: 石墨烯掺杂后, 离子交换膜的柔韧性、 离子交换能力、 含水量均得到了一定程度的提高。金属Pt纳米电极表面平整; 颗粒较精细、 均匀; 电极与基底膜结合紧密。杂化膜具有高度的电致形变性能; 相同条件下, 最大输出位移可增加2.38倍。%Sulfonated graphene mono-molecular film was synthesized and doped into perfluorosulfonic acid solution to prepare around 200 μm thick hybrid membranes with varying mass ratios. Those processes were monitored and demonstrated by attenuated total reflectance Fourier transform infrared spectroscopy. The physical performances related to electromechanical properties were detected. To make ion exchange polymer-metal composites, two Pt nano sheets were sandwiched on both sides of the resultant membranes, which was observed by SEM. Inputted the sinusoidal wave with a low frequency for fabricating electro-active actuator, detections of force and displacement sensors were taken. The results show that the flexibilities, ionic exchange capacities, and water contents of hybrid membranes increase in a degree. The Pt nano particles are relatively fine and uniform, the electrodes planes are relatively flat, and the bonding between electrode and hybrid membrane is firm. The hybrid membrane has a high electrostrictive strain, and the maximum displacement is 2.38 times higher than that of the pure perfluorosulfonic acid membrane under

  18. Nanostructured membranes and electrodes with sulfonic acid functionalized carbon nanotubes

    KAUST Repository

    Tripathi, Bijay Prakash

    2011-02-01

    Herein we report the covalent functionalization of multiwall carbon nanotubes by grafting sulfanilic acid and their dispersion into sulfonated poly(ether ether ketone). The nanocomposites were explored as an option for tuning the proton and electron conductivity, swelling, water and alcohol permeability aiming at nanostructured membranes and electrodes for application in alcohol or hydrogen fuel cells and other electrochemical devices. The nanocomposites were extensively characterized, by studying their physicochemical and electrochemical properties. They were processed as self-supporting films with high mechanical stability, proton conductivity of 4.47 × 10 -2 S cm-1 at 30 °C and 16.8 × 10-2 S cm-1 at 80 °C and 100% humidity level, electron conductivity much higher than for the plain polymer. The methanol permeability could be reduced to 1/20, keeping water permeability at reasonable values. The ratio of bound water also increases with increasing content of sulfonated filler, helping in keeping water in the polymer in conditions of low external humidity level. © 2010 Elsevier B.V.

  19. Nanostructured membranes and electrodes with sulfonic acid functionalized carbon nanotubes

    Energy Technology Data Exchange (ETDEWEB)

    Tripathi, Bijay P. [Electro-Membrane Processes Division, Central Salt and Marine Chemicals Research Institute, Council of Scientific and Industrial Research (CSIR), G.B. Marg, Bhavnagar 364002, Gujarat (India); Department of Membranes for Sustainable Energy, GKSS Research Centre Geesthacht GmbH, Max Planck Str. 1, D-21502 Geesthacht (Germany); Schieda, M. [Department of Membranes for Sustainable Energy, GKSS Research Centre Geesthacht GmbH, Max Planck Str. 1, D-21502 Geesthacht (Germany); Shahi, Vinod K. [Electro-Membrane Processes Division, Central Salt and Marine Chemicals Research Institute, Council of Scientific and Industrial Research (CSIR), G.B. Marg, Bhavnagar 364002, Gujarat (India); Nunes, Suzana P. [King Abdullah University of Science and Technology, Thuwal 23955-6900 (Saudi Arabia)

    2011-02-01

    Herein we report the covalent functionalization of multiwall carbon nanotubes by grafting sulfanilic acid and their dispersion into sulfonated poly(ether ether ketone). The nanocomposites were explored as an option for tuning the proton and electron conductivity, swelling, water and alcohol permeability aiming at nanostructured membranes and electrodes for application in alcohol or hydrogen fuel cells and other electrochemical devices. The nanocomposites were extensively characterized, by studying their physicochemical and electrochemical properties. They were processed as self-supporting films with high mechanical stability, proton conductivity of 4.47 x 10{sup -2} S cm{sup -1} at 30 C and 16.8 x 10{sup -2} S cm{sup -1} at 80 C and 100% humidity level, electron conductivity much higher than for the plain polymer. The methanol permeability could be reduced to 1/20, keeping water permeability at reasonable values. The ratio of bound water also increases with increasing content of sulfonated filler, helping in keeping water in the polymer in conditions of low external humidity level. (author)

  20. Nanostructured membranes and electrodes with sulfonic acid functionalized carbon nanotubes

    Science.gov (United States)

    Tripathi, Bijay P.; Schieda, M.; Shahi, Vinod K.; Nunes, Suzana P.

    Herein we report the covalent functionalization of multiwall carbon nanotubes by grafting sulfanilic acid and their dispersion into sulfonated poly(ether ether ketone). The nanocomposites were explored as an option for tuning the proton and electron conductivity, swelling, water and alcohol permeability aiming at nanostructured membranes and electrodes for application in alcohol or hydrogen fuel cells and other electrochemical devices. The nanocomposites were extensively characterized, by studying their physicochemical and electrochemical properties. They were processed as self-supporting films with high mechanical stability, proton conductivity of 4.47 × 10 -2 S cm -1 at 30 °C and 16.8 × 10 -2 S cm -1 at 80 °C and 100% humidity level, electron conductivity much higher than for the plain polymer. The methanol permeability could be reduced to 1/20, keeping water permeability at reasonable values. The ratio of bound water also increases with increasing content of sulfonated filler, helping in keeping water in the polymer in conditions of low external humidity level.

  1. Sulfonated carbon black-based composite membranes for fuel cell applications

    Indian Academy of Sciences (India)

    Hacer Doǧan; Emel Yildiz; Metin Kaya; Tülay Y Inan

    2013-08-01

    Two different commercial grade carbon black samples, Cabot Regal 400R (C1) and Cabot Mogul L (C2), were sulfonated with diazonium salt of sulfanilic acid. The resultant sulfonated carbon black samples (S–C) were characterized by Fourier transform infrared spectroscopy (FTIR) and thermal gravimetric analysis (TGA). Composite membranes were then prepared using S–C as fillers and sulfonated poly(ether ether ketone) (SPEEK) as polymer matrix with three different sulfonation degrees (DS = 60, 70 and 82%). Structure and properties of the composite membranes were characterized by FTIR, TGA, scanning electron microscopy, proton conduction, water uptake, ion exchange capacity and chemical stability. Incorporation of S–C particles above 0.25 wt% caused decrease in chemical stability. Pristine and composite membranes prepared from SPEEK82 decomposed completely in <1 h, which is undesirable for fuel cell applications. SPEEK60 membrane having wt% of 0.25–0.5 with S–C particles led to higher proton conductivity than that of pristine membrane. No positive effect was observed on the properties of the composite membranes with the addition of S–C particles at high concentrations due to the agglomeration problems and decrease in the content of conductive polymer matrix.

  2. New bromotriterpene polyethers from the Indian alga Chondria armata

    Digital Repository Service at National Institute of Oceanography (India)

    Ciavatta, M.L.; Wahidullah, S.; DeSouza, L.; Scognamiglio, G.; Cimino, G.

    Six new bromotriterpene polyethers, armatol A-F (1-6), with a rearranged carbon skeleton, were isolated from the Indian Ocean red alga Chondria armata. The structures were characterized by spectroscopic techniques, in particular 1D- and 2D-NMR...

  3. 21 CFR 177.2430 - Polyether resins, chlorinated.

    Science.gov (United States)

    2010-04-01

    ...) FOOD FOR HUMAN CONSUMPTION (CONTINUED) INDIRECT FOOD ADDITIVES: POLYMERS Substances for Use Only as... producing, manufacturing, packing, processing, preparing, treating, packaging, transporting, or holding food... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Polyether resins, chlorinated. 177.2430 Section...

  4. Chemodiversity of Ladder-Frame Prymnesin Polyethers in Prymnesium parvum

    DEFF Research Database (Denmark)

    Rasmussen, Silas Anselm; Meier, Sebastian; Andersen, Nikolaj Gedsted;

    2016-01-01

    Blooms of the microalga Prymnesium parvum cause devastating fish kills worldwide, which are suspected to be caused by the supersized ladder-frame polyether toxins prymnesin-1 and -2. These toxins have, however, only been detected from P. parvum in rare cases since they were originally described two...

  5. Photodegradation of poly(ether sulphone). Part 2

    DEFF Research Database (Denmark)

    Norrman, K.; Krebs, Frederik C

    2004-01-01

    The photodegradation of poly(ether sulphone) (PES) was investigated systematically by time-of-flight SIMS (ToF-SIMS) and x-ray photoelectron spectroscopy (XPS). The effect of varying the irradiation dose, wavelength and the atmosphere was studied along with mechanistic photooxidation studies using...

  6. Resin Catalyst Hybrids

    Institute of Scientific and Technical Information of China (English)

    S. Asaoka

    2005-01-01

    @@ 1Introduction: What are resin catalyst hybrids? There are typically two types of resin catalyst. One is acidic resin which representative is polystyrene sulfonic acid. The other is basic resin which is availed as metal complex support. The objective items of this study on resin catalyst are consisting of pellet hybrid, equilibrium hybrid and function hybrid of acid and base,as shown in Fig. 1[1-5].

  7. PHOTOPHYSICAL STUDY OF SULFONATED POLYSTYRENE

    Institute of Scientific and Technical Information of China (English)

    ZHANG Jixiang; LI Hexian; WANG Guochang; WANG Yuexi; HE Binglin

    2004-01-01

    The photophysical properties of a series of sulfonated micromolecule (paratoluenesulfonic acid, HPTS) and macromolecules (linear and crosslinked polystyrene) have been studied by steady-state fluorescence spectra. The results indicate that the ground sulfonated ring associations can form in both the micromolecules and the macromolecules. The fluorescence spectra of the sulfonated crosslinked copolymers appear a red-shift when the copolymers change from hydrogen-type to sodium-type, and some new emission bands appear in the long-wavelength region. These results are explained in terms of synergetic effect of hydrogen bond, π-π interaction and crosslinking effect.

  8. The effect of polyether functional polydimethylsiloxane on surface and thermal properties of waterborne polyurethane

    Science.gov (United States)

    Zheng, Guikai; Lu, Ming; Rui, Xiaoping

    2017-03-01

    Waterborne polyurethanes (WPU) modified with polyether functional polydimethylsiloxane (PDMS) were synthesized by pre-polymerization method using isophorone diisocyanate (IPDI) and 1,4-butanediol (BDO) as hard segments and polybutylene adipate glycol (PBA) and polyether functional PDMS as soft segments. The effect of polyether functional PDMS on phase separation, thermal properties, surface properties including surface composition, morphology and wettability were investigated by FTIR, contact angle measurements, ARXPS, SEM-EDS, AFM, TG and DSC. The results showed that the compatibility between urethane hard segment and PDMS modified with polyether was good, and there was no distinct phase separation in both bulk and surface of WPU films. The degradation temperature and low temperature flexibility increased with increasing amounts of polyether functional PDMS. The enrichment of polyether functional PDMS with low surface energy on the surface imparted excellent hydrophobicity to WPU films.

  9. Aliphatic Polyethers: Classical Polymers for the 21st Century.

    Science.gov (United States)

    Klein, Rebecca; Wurm, Frederik R

    2015-06-01

    Polyethers-polymers with the structural element (R'-O-R)n in their backbone--are an old class of polymers which were already used at the time of the ancient Egyptians. However, still today these materials are highly important with applications in all areas of our life, reaching from the automotive and paper industry to cosmetics and biomedical applications. In this Review, different aliphatic polyethers like poly(epoxide)s, poly(oxetane)s, and poly(tetrahydrofuran) are discussed. Special emphasis is placed on the history, the polymerization techniques (industrially and in academia), the properties, the applications as well as recent developments of these materials. © 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  10. POLYETHER POLYURETHANE FROM MODIFIED WHEAT STRAW OXYGEN-ALKALINE LIGNIN

    Institute of Scientific and Technical Information of China (English)

    QuanxiaoLiu; HuaiyuZhan; BeihaiHe; ShuhuiYang; JianhuaLiu; JianluLiu(1); ZhenxingPang

    2004-01-01

    Polyether polyurethane was synthesized from modified wheat straw oxygen-alkaline lignin, polyethylene glycol and two different diisocyanates (diphenylemethane-4, 4'-diisocyanate, tolulene diisocyanate) by solution casting method, its properties were investigated. The results show that modified wheat straw oxygen-alkaline lignin can substitute part of polyethylene glycol to react with diisocyanate to synthesize polyurethane. The molar ratio of NCO to OH and modified wheat straw oxygen-alkaline lignin content affect the properties of lignin-based polyether polyurethane respectively. The addition of plasticizer in the polyurethane synthesis process improves the properties of synthesized polyurethane, especially the elasticity of polyurethane. The synthesized polyurethane from modified wheat straw oxygen-alkali lignin can be used as both engineering plastic and hard foam plastic in future.

  11. POLYETHER POLYURETHANE FROM MODIFIED WHEAT STRAW OXYGEN-ALKALINE LIGNIN

    Institute of Scientific and Technical Information of China (English)

    Quanxiao Liu; Huaiyu Zhan; Beihai He; Shuhui Yang; Jianhua Liu; Jianlu Liu; Zhenxing Pang

    2004-01-01

    Polyether polyurethane was synthesized from modified wheat straw oxygen-alkaline lignin,polyethylene glycol and two different diisocyanates (diphenylemethane-4, 4′-diisocyanate, tolulene diisocyanate) by solution casting method, its properties were investigated. The results show that modified wheat straw oxygen-alkaline lignin can substitute part of polyethylene glycol to react with diisocyanate to synthesize polyurethane. The molar ratio of NCO to OH and modified wheat straw oxygen-alkaline lignin content affect the properties of lignin-based polyether polyurethane respectively. The addition of plasticizer in the polyurethane synthesis process improves the properties of synthesized polyurethane, especially the elasticity of polyurethane. The synthesized polyurethane from modified wheat straw oxygen-alkali lignin can be used as both engineering plastic and hard foam plastic in future.

  12. Solvent-Induced Crystallization of Poly(ether ether ketone)

    OpenAIRE

    McPeak, Jennifer Lynne

    1999-01-01

    The purpose of this study was learn how the diffusion, swelling, and crystallization processes are coupled during solvent-induced crystallization of poly(ether ether ketone) (PEEK). Unoriented amorphous PEEK films were immersed in aprotic organic liquids at ambient temperature and bulk properties or characteristics were monitored as a function of immersion time. The sorption behavior, Tg and Tm° suppression, crystallinity, and dynamic mechanical response were correlated as a function of sol...

  13. Synthesis of Telechelic Polyisobutylenes and Polyethers and Their Characterization

    Institute of Scientific and Technical Information of China (English)

    Sándor Kéki; Miklós Nagy; Gy(o)rgy Deák; László Orosz; Miklós Zsuga

    2005-01-01

    @@ 1Introduction Telechelic polymers have attained great consideration as building blocks in the synthesis of block copolymers and networks. Telechelic polymers with various endgroups are also widely used materials for the preparation of polymeric prodrugs. Several methods have been reported to obtain functionalized polymers from the corresponding polyisobutylene (PIB) and polyether derivatives. In this presentation, we will demonstrate very versatile and powerful synthetic methods to obtain telechelic polymers.

  14. Novel Polyethers Doped with Nanoscale Insulating oxides for Lithium Battery Elec Project

    Data.gov (United States)

    National Aeronautics and Space Administration — Novel polyethers doped with insulating oxides are used to prepare solid polymer electrolytes for high energy density lithium batteries. The electrolytes are...

  15. 40 CFR Table 4 to Subpart Ppp of... - Known Organic HAP From Polyether Polyol Products

    Science.gov (United States)

    2010-07-01

    ... CATEGORIES National Emission Standards for Hazardous Air Pollutant Emissions for Polyether Polyols Production...-Hexane (110543) Methanol (67561) Propylene Oxide (75569) Toluene (108883) CAS No. = Chemical Abstracts...

  16. Mechanical properties and chemical stability of pivalolactone-based poly(ether ester)s

    NARCIS (Netherlands)

    Tijsma, E.J.; Does, van der L.; Bantjes, A.; Vulic, I.

    1994-01-01

    The processing, mechanical and chemical properties of poly(ether ester)s, prepared from pivalolactone (PVL), 1,4-butanediol (4G) and dimethyl terephthalate (DMT), were studied. The poly(ether ester)s could easily be processed by injection moulding, owing to their favourable rheological and thermal p

  17. Lignin Sulfonation - A different Approach

    DEFF Research Database (Denmark)

    Bjørkmann, Anders

    2001-01-01

    . It was found that lignin is very reactive, that is why the sulfonation chemistry alone does not necessarily determine its dissolution rate. It became evident that the ultrastructure dispersion of lignin in wood is beneficial for its dissolution. For W, the rate was much higher at pH 1.5 than at 6. MW lignin...... and MWL dissolved (after extraction of the "immediate" lignin) at higher rates than W lignin. For MWL, the rate difference between pH 1.5 and 6 was moderate, compared to W lignin. Borohydride reduction did not affect the lignin dissolution from W, but gave a large decrease of sulfonation rate for MWL...

  18. Chemodiversity of Ladder-Frame Prymnesin Polyethers in Prymnesium parvum

    DEFF Research Database (Denmark)

    Rasmussen, Silas Anselm; Meier, Sebastian; Andersen, Nikolaj Gedsted;

    2016-01-01

    Blooms of the microalga Prymnesium parvum cause devastating fish kills worldwide, which are suspected to be caused by the supersized ladder-frame polyether toxins prymnesin-1 and -2. These toxins have, however, only been detected from P. parvum in rare cases since they were originally described two......-HRMS) of 10 strains of P. parvum collected worldwide showed that only one strain produced the original prymnesin-1 and -2, whereas four strains produced the novel B-type prymnesin. In total 13 further prymnesin analogues differing in their core backbone and chlorination and glycosylation patterns could...

  19. Nanofiber poly ether sulfone as adipose derived stem cell holding scaffold with or without growth factor on wound healing in rat

    Directory of Open Access Journals (Sweden)

    Mohammd Javad Fatemi

    2017-03-01

    Full Text Available Background: Acute and chronic wound healing has always been problematic. Stem cells with or without the scaffold carrying these cells have been proposed as new methods in the treatment of wounds. In this case study we have tried to examine the effect of scaffold made of polyether sulfone (PES alone, with stem cells and along with stem cell and growth factor on wound healing in rats. Methods: This experimental study was conducted in Animal Laboratory of Hazrat Fatemeh Hospital in 2012. In this study, 48 rats were randomly divided into four groups. A wound created on the back of each rat at the size of 3×3 cm. The surface of the wound in the first group is covered with PES seeded with adipose-derived stem cell (ASC and growth factor (GF, in the second group with polyether Sulfone seeded with ASC, in the third group only with PEWS, and in the fourth group (control with Vaseline gauze. On 20th and 35th days, the surface of the wound was assessed by photography in order to understand the process of healing. In addition, on days 20 and 45, the histopathology characteristics of the samples were studied with a biopsy of the wounds. Results: The Results of wound healing in the control group was better than the other groups and its statistical difference between others was meaningful. (P=0.008, P=0.013, P=0.001 On day 20, by examining histopathological characteristics including epithelialization, the number of inflammatory cells, the amount of angiogenesis and collagen synthesis in control group, we gained better results. (P=0.000, But on day 45, the results in different parameters were not equal. Conclusion: polyether sulfone scaffold alone or with adipose-derived stem cells couldn’t improve the process of wound healing. Also adding vascular endothelial growth factor (VEGF did not change the results significantly.

  20. Computational and experimental investigations of one-step conversion of poly(carbonate)s into value-added poly(aryl ether sulfone)s.

    Science.gov (United States)

    Jones, Gavin O; Yuen, Alexander; Wojtecki, Rudy J; Hedrick, James L; García, Jeannette M

    2016-07-12

    It is estimated that ∼2.7 million tons poly(carbonate)s (PCs) are produced annually worldwide. In 2008, retailers pulled products from store shelves after reports of bisphenol A (BPA) leaching from baby bottles, reusable drink bottles, and other retail products. Since PCs are not typically recycled, a need for the repurposing of the PC waste has arisen. We report the one-step synthesis of poly(aryl ether sulfone)s (PSUs) from the depolymerization of PCs and in situ polycondensation with bis(aryl fluorides) in the presence of carbonate salts. PSUs are high-performance engineering thermoplastics that are commonly used for reverse osmosis and water purification membranes, medical equipment, as well as high temperature applications. PSUs generated through this cascade approach were isolated in high purity and yield with the expected thermal properties and represent a procedure for direct conversion of one class of polymer to another in a single step. Computational investigations performed with density functional theory predict that the carbonate salt plays two important catalytic roles in this reaction: it decomposes the PCs by nucleophilic attack, and in the subsequent polyether formation process, it promotes the reaction of phenolate dimers formed in situ with the aryl fluorides present. We envision repurposing poly(BPA carbonate) for the production of value-added polymers.

  1. New functional polyether binders for low vulnerability propellants; Nouveaux liants polyethers fonctionnels pour propergols a faible vulnerabilite

    Energy Technology Data Exchange (ETDEWEB)

    Moreau-Friot, C.; Eck, G.; Jacob, G.; Chevalier, S.; Golfier, M.; Guengant, Y. [Groupe SNPE Propulsion/ Centre de Recherches du Boucher, 91 - Vert le Petit (France)

    2002-09-01

    HTPB propellants are widely used in solid rocket propellants. Their slow cook-off behaviour has to be improved because they lead to reactions type IV or V in the MURAT scale. Some work on propellants with polyether binders has shown that they lead to moderate reactions at slow cook-off tests. Work is based on the synthesis of functional polyethers. The objective consists in preparing a hydroxyl terminated polymer with a molecular weight between 1000 and 4000 g.mol{sup -1}, a low viscosity and a correct functionality. The binder, which is composed of a polymer, a plasticizer and a curing system, will be able to give mechanical properties in the use field (between -40 and +60 deg C). The polymer chosen to answer all those characteristics is composed of tetrahydrofuran and ethylene oxide. It is synthesised by cationic ring opening polymerisation in the presence of a diol and an adapted catalyst (BF{sub 3}OEt{sub 2}, HBF{sub 4}, SnCl{sub 4}/AT-..). First polymerizations were carried out of laboratory scale (from 30 g to 200 g). The study consists in varying the nature of catalysts the temperature, the solvent the purification methods and so on. The selected copolymer is chosen from many analysis results of the structure, particularly the average number molecular weight the hydroxyl rate, and the best alternative between a high molecular weight and a correct functionality. The behaviour of the propellant is also important because it will allow a widely scale synthesis or complementary laboratory work. A transfer has permitted to obtain a 10 kg scale. Its characteristics are the same that those of the product obtained at a laboratory scale. Propellants with polyether binder have been tested. The correct viscosity allows a high charge rate, which means energetic propellants. It also has to be noted that the binder does not crystallize. Those propellants have a good mechanistic behaviour in a large field of temperature. They also have a good behaviour at slow cook-off. The

  2. Coarse graining of polystyrene sulfonate

    Science.gov (United States)

    Perahia, Dvora; Agrawal, Anupriya; Grest, Gary S.

    2015-03-01

    Capturing large length scales in soft matter while retaining atomistic properties is imperative to computational studies. Here we develop a new coarse-grained model for polystyrene sulfonate (PSS) that often serves as a model system because of its narrow molecular weight distribution and defined degree of sulfonation. Four beads are used to represent polymer where the backbone, the phenyl group, and the sulfonated group are each represented by a different bead and the fourth one represents counterion, which is sodium in our case. Initial atomistic simulations of PSS melt with sulfonation levels of 2-10%, with a dielectric constant ɛ = 1 revealed a ``locked'' phase where motion of the polymer is limited. Dielectric constant of ɛ = 5 was used to accelerate the dynamics. Bonded interactions were obtained using Boltzmann inversion on the bonded distributions extracted from atomistic simulation. Non-bonded interaction of polystyrene monomer was taken from our previous work and potential of mean force was used as the initial guess for interaction of the ionic beads. This set of potential was subsequently iterated to get a good match with radial distribution functions. This potential and its transferability across dielectric constants and temperatures will be presented. Grant DE-SC007908.

  3. Parasite infection accelerates age polyethism in young honey bees.

    Science.gov (United States)

    Lecocq, Antoine; Jensen, Annette Bruun; Kryger, Per; Nieh, James C

    2016-02-25

    Honey bees (Apis mellifera) are important pollinators and their health is threatened worldwide by persistent exposure to a wide range of factors including pesticides, poor nutrition, and pathogens. Nosema ceranae is a ubiquitous microsporidian associated with high colony mortality. We used lab micro-colonies of honey bees and video analyses to track the effects of N. ceranae infection and exposure on a range of individual and social behaviours in young adult bees. We provide detailed data showing that N. ceranae infection significantly accelerated the age polyethism of young bees, causing them to exhibit behaviours typical of older bees. Bees with high N. ceranae spore counts had significantly increased walking rates and decreased attraction to queen mandibular pheromone. Infected bees also exhibited higher rates of trophallaxis (food exchange), potentially reflecting parasite manipulation to increase colony infection. However, reduction in queen contacts could help bees limit the spread of infection. Such accelerated age polyethism may provide a form of behavioural immunity, particularly if it is elicited by a wide variety of pathogens.

  4. Synthesis and characterization of sulfonated cardo poly(arylene ether sulfone)s for fuel cell proton exchange membrane application

    Energy Technology Data Exchange (ETDEWEB)

    Islam, M.M.; Jang, H.H.; Lim, Y.D.; Seo, D.W.; Kim, W.G. [Department of Applied Chemistry, Konkuk University, Chungju, Chungbuk (Korea, Republic of); Kim, T.H.; Hong, Y.T. [Energy Material Research Center, Korea Research Institute of Chemical Technology, Daejeon (Korea, Republic of); Kim, D.M. [Material Engineering and Science, Hongik Univ, Jochiwon-eup, Yeongi-gun, Chungnam (Korea, Republic of)

    2012-12-15

    Sulfonated cardo poly(arylene ether sulfone)s (SPPA-PES) with various degrees of sulfonation (DS) were prepared by post-sulfonation of synthesized phenolphthalein anilide (PPA; N-phenyl-3,3'-bis(4-hydroxyphenyl)-1-isobenzopyrolidone) poly(arylene ether sulfone)s (PPA-PES) by using concentrated sulfuric acid. PPA-PES copolymers were synthesized by direct polycondensation of PPA with bis-(4-fluorophenyl)-sulfone and 4,4'-sulfonyldiphenol. The DS was varied with different mole ratios of PPA (24, 30, 40, 50 mol.%) in the polymer. The structure of the resulting SPPA-PES copolymers and the different contents of the sulfonated unit were studied by Fourier transform infrared (FT-IR) spectroscopy, {sup 1}H NMR spectroscopy, and thermogravimetric analysis (TGA). Sorption experiments were conducted to observe the interaction of sulfonated polymer with water. The ion exchange capacity (IEC) and proton conductivity of SPPA-PES were evaluated according to the increase of DS. The water uptake (WU) of the resulting SPPA-PES membranes was in the range of 20-72%, compared with 28% for Nafion 211 registered. The SPPA-PES membranes showed proton conductivities of 23-82 mS cm{sup -1}, compared with 194 mS cm{sup -1} for Nafion 211 registered, under 100% relative humidity (RH) at 80 C. (Copyright copyright 2012 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  5. The effect of polyether on the separation of pentlandite and serpentine

    Directory of Open Access Journals (Sweden)

    Xiaowen Zhou

    2015-10-01

    Full Text Available The effect of polyether on the separation of pentlandite from serpentine has been studied. In addition to flotation and sedimentation tests, electrophoresis and adsorption tests have been conducted. The flotation and sedimentation results show that serpentine impairs flotation performance of pentlandite, by adhering to the pentlandite particles. Addition of the polyether could promote the dispersion of the mixed sample of pentlandite and serpentine in alkaline conditions and significantly reduce adverse effects of serpentine on the pentlandite flotation. The electrophoresis and adsorption tests show that polyether can selectively adsorb onto pentlandite surface through hydrophobic reaction and remove serpentine slime particles from pentlandite surfaces by steric hindrance effect.

  6. A Durable Alternative for Proton-Exchange Membranes: Sulfonated Poly(Benzoxazole Thioether Sulfone)s

    Energy Technology Data Exchange (ETDEWEB)

    Zhao, Dan; Li, Jin Hui; Song, Min Kyu; Yi, Baolian; Zhang, Huamin; Liu, Meilin

    2011-02-24

    To develop a durable proton-exchange membrane (PEM) for fuel-cell applications, a series of sulfonated poly(benzoxazole thioether sulfone)s ( SPTESBOs) are designed and synthesized, with anticipated good dimensional stability (via acid–base cross linking), improved oxidative stability against free radicals (via incorporation of thioether groups), and enhanced inherent stability (via elimination of unstable end groups) of the backbone. The structures and the degree of sulfonation of the copolymers are characterized using Fourier-transform infrared spectroscopy, and nuclear magnetic resonance spectroscopy ({sup 1}H NMR and {sup 19}F NMR). The electrochemical stabilities of the monomers are examined using cyclic voltammetry in a typical three-electrode cell configuration. The physicochemical properties of the membranes vital to fuel-cell performance are also carefully evaluated under conditions relevant to fuel-cell operation, including chemical and thermal stability, proton conductivity, solubility in different solvents, water uptake, and swelling ratio. The new membranes exhibit low dimensional change at 25°C to 90°C and excellent thermal stability up to 250°C. Upon elimination of unstable end groups, the co-polymers display enhanced chemical resistance and oxidative stability in Fenton's test. Further, the SPTESBO-HFB-60 (HFB-60=hexafluorobenzene, 60 mol% sulfone) membrane displays comparable fuel-cell performance to that of an NRE 212 membrane at 80°C under fully humidified condition, suggesting that the new membranes have the potential to be more durable but less expensive for fuel-cell applications.

  7. A durable alternative for proton-exchange membranes: sulfonated poly(benzoxazole thioether sulfone)s

    Energy Technology Data Exchange (ETDEWEB)

    Zhao, Dan [Center for Innovative Fuel Cell and Battery Technologies, School of Materials Science and Engineering, Georgia Institute of Technology, Atlanta, GA 30332-0245 (United States); Lab of PEMFC Key Materials and Technologies, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, 457 Zhongshan Road, Liaoning, Dalian 116023 (China); Graduate School of the Chinese Academy of Sciences, Beijing 100039 (China); Li, Jinhuan [Center for Innovative Fuel Cell and Battery Technologies, School of Materials Science and Engineering, Georgia Institute of Technology, Atlanta, GA 30332-0245 (United States); College of Materials Science and Technology, Nanjing University of Aeronautics and Astronautics, Nanjing 210016 (China); Song, Min-Kyu; Liu, Meilin [Center for Innovative Fuel Cell and Battery Technologies, School of Materials Science and Engineering, Georgia Institute of Technology, Atlanta, GA 30332-0245 (United States); Yi, Baolian; Zhang, Huamin [Lab of PEMFC Key Materials and Technologies, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, 457 Zhongshan Road, Liaoning, Dalian 116023 (China)

    2011-03-18

    To develop a durable proton-exchange membrane (PEM) for fuel-cell applications, a series of sulfonated poly(benzoxazole thioether sulfone)s (SPTESBOs) are designed and synthesized, with anticipated good dimensional stability (via acid-base cross linking), improved oxidative stability against free radicals (via incorporation of thioether groups), and enhanced inherent stability (via elimination of unstable end groups) of the backbone. The structures and the degree of sulfonation of the copolymers are characterized using Fourier-transform infrared spectroscopy, and nuclear magnetic resonance spectroscopy ({sup 1}H NMR and {sup 19}F NMR). The electrochemical stabilities of the monomers are examined using cyclic voltammetry in a typical three-electrode cell configuration. The physicochemical properties of the membranes vital to fuel-cell performance are also carefully evaluated under conditions relevant to fuel-cell operation, including chemical and thermal stability, proton conductivity, solubility in different solvents, water uptake, and swelling ratio. The new membranes exhibit low dimensional change at 25 C to 90 C and excellent thermal stability up to 250 C. Upon elimination of unstable end groups, the co-polymers display enhanced chemical resistance and oxidative stability in Fenton's test. Further, the SPTESBO-HFB-60 (HFB-60=hexafluorobenzene, 60 mol% sulfone) membrane displays comparable fuel-cell performance to that of an NRE 212 membrane at 80 C under fully humidified condition, suggesting that the new membranes have the potential to be more durable but less expensive for fuel-cell applications. (Copyright copyright 2011 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  8. Polymerization-induced phase separation in polyether-sulfone modified epoxy resin systems: effect of curing reaction mechanism

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    Polyethersulfone (PES)-modified epoxy systems with stepwise reaction were studied throughout the entire curing process by using optical microscopes, time-resolved light scattering (TRLS), and a rheolometry instrument compared with that of chainwise polymerization. The results suggested that the phase separation process is mainly controlled by the diffusion of epoxy oligomers for stepwise mechanism system and by that of epoxy monomers for chainwise mechanism system. In case of high PES content (SPES-20%) light-scattering results showed a viscoelastic phase separation and the characteristic relaxation time of phase separation can be described well by the WLF equation. However, in the case of low PES content (SPES-14%) secondary phase separation phenomenon was observed by Optical Microscope and further demonstrated by rheological study.

  9. Degradation mechanism of sulfonated poly(ether ether ketone) (SPEEK) ion exchange membranes under vanadium flow battery medium.

    Science.gov (United States)

    Yuan, Zhizhang; Li, Xianfeng; Hu, Jinbo; Xu, Wanxing; Cao, Jingyu; Zhang, Huamin

    2014-10-07

    The degradation mechanism of hydrocarbon ion exchange membranes under vanadium flow battery (VFB) medium was investigated and clarified for the first time. This work will be highly beneficial for improving the chemical stability of hydrocarbon ion exchange membranes, which is one of the most challenging issues for VFB application.

  10. Characterization of sulfonated poly(ether ether ketone)/silane nanocomposite membrane for high temperature polymer electrolyte membrane fuel cells.

    Science.gov (United States)

    Ghil, Lee-Jin; Kim, Chang-Kyeom; Park, Na-Ri; Rhee, Hee-Woo

    2011-01-01

    The perfluorosulfonic acid polymer membrane is most widely used in PEMFCs. However, its some major drawbacks like high cost and performance limitation at high temperature are obstacles of its commercialization. The goal of this study was to develop low cost membranes which have good conductivity in the range of PEMFCs operating temperature. We fabricated new sPEEK/3-APTES nanocomposite membrane where inorganic particles were chemically bonded to sulfuric acid group of sPEEK. PEEK is a thermally stable, mechanically tough and very cheap polymer. And the addition of 3-APTES and phosphorous acid increased the proton conductivity of composite membranes at high temperatures. This nanocomposite membranes maintained good conductivity at 110 degrees C.

  11. Lignin Sulfonation - A different Approach

    DEFF Research Database (Denmark)

    Bjørkmann, Anders

    2001-01-01

    . It was found that lignin is very reactive, that is why the sulfonation chemistry alone does not necessarily determine its dissolution rate. It became evident that the ultrastructure dispersion of lignin in wood is beneficial for its dissolution. For W, the rate was much higher at pH 1.5 than at 6. MW lignin....... Methylation had also a small rate effect for W, but again a large decrease for MWL....

  12. Surface Heparinization of Poly(ether ether ketone)

    Institute of Scientific and Technical Information of China (English)

    SUN Hui; CHEN Rui-chao; LIU Shu; XU Guo-zhi

    2012-01-01

    Photo-grafting of hydrophilic monomer and space arms was used to enhance the hydrophilicity of poly(ether ether ketone)(PEEK) with the aim of extending its application to biological fields.PEEK films were surface modified by UV grafting of acrylic acid(AA) to introduce-COOH on PEEK surface.Adipic amine was used as a.space ann to introduce heparin on PEEK surface based on the condensation reaction between -NH2 and -COOH.The modified PEEK(PEEK-COOH,PEEK-NH2 and PEEK-Hep) was characterized by energy-disperse spectroscopy (EDS),X-ray photoelectron spectroscopy(XPS) and water contact angle measurements,which show that heparin was grafted on PEEK surface.The contact angles of modified PEEK films were lower than those of original films,demonstrating a significant improvement of surface hydrophilicity.

  13. Parasite infection accelerates age polyethism in young honey bees

    DEFF Research Database (Denmark)

    Lecocq, Antoine; Jensen, Annette Bruun; Kryger, Per

    2016-01-01

    Honey bees (Apis mellifera) are important pollinators and their health is threatened worldwide by persistent exposure to a wide range of factors including pesticides, poor nutrition, and pathogens. Nosema ceranae is a ubiquitous microsporidian associated with high colony mortality. We used lab...... micro-colonies of honey bees and video analyses to track the effects of N. ceranae infection and exposure on a range of individual and social behaviours in young adult bees. We provide detailed data showing that N. ceranae infection significantly accelerated the age polyethism of young bees, causing...... them to exhibit behaviours typical of older bees. Bees with high N. ceranae spore counts had significantly increased walking rates and decreased attraction to queen mandibular pheromone. Infected bees also exhibited higher rates of trophallaxis (food exchange), potentially reflecting parasite...

  14. Helical peptide-polyamine and -polyether conjugates as synthetic ionophores.

    Science.gov (United States)

    Benincasa, Monica; Francescon, Marco; Fregonese, Massimo; Gennaro, Renato; Pengo, Paolo; Rossi, Paola; Scrimin, Paolo; Tecilla, Paolo

    2015-12-01

    Two new synthetic ionophores in which the hydrophobic portion is represented by a short helical Aib-peptide (Aib=α-amino-isobutyric acid) and the hydrophilic one is a poly-amino (1a) or a polyether (1b) chain have been prepared. The two conjugates show a high ionophoric activity in phospholipid membranes being able to efficiently dissipate a pH gradient and, in the case of 1b, to transport Na(+) across the membrane. Bioactivity evaluation of the two conjugates shows that 1a has a moderate antimicrobial activity against a broad spectrum of microorganisms and it is able to permeabilize the inner and the outer membrane of Escherichia coli cells.

  15. In Situ Preparation of Polyether Amine Functionalized MWCNT Nanofiller as Reinforcing Agents

    Directory of Open Access Journals (Sweden)

    Ayber Yıldrım

    2014-01-01

    Full Text Available In situ preparation of polyether amine functionalized cross-linked multiwalled carbon nanotube (MWCNT nanofillers may improve the thermal and mechanical properties of the composites in which they are used as reinforcing agents. The reduction and functionalization of MWCNT using ethylenediamine in the presence of polyether amine produced stitched MWCNT's due to the presence of two amine (–NH2 functionalities on both sides of the polymer. Polyether amine was chosen to polymerize the carboxylated MWCNT due to its potential to form bonds with the amino groups and carboxyl groups of MWCNT which produces a resin used as polymeric matrix for nanocomposite materials. The attachment of the polyether amine (Jeffamine groups was verified by TGA, FT-IR, XRD, SEM, and Raman spectroscopy. The temperature at which the curing enthalpy is maximum, observed by DSC, was shifted to higher values by adding functionalized MWCNT. SEM images show the polymer formation between MWCNT sheets.

  16. Characterization of the P. Brevis Polyether Neurotoxin Binding Component in Excitable Membranes

    Science.gov (United States)

    1991-09-14

    International Conference on Ciguatera . (T. R. Tosteson and D. Ballantyne, Eds.) in press. Baden, D.G. (1991) The Polyether Brevetoxins and Site Five of the...Confomrations and Potency Correlations. Third Intl. Conf. Ciguatera , Puerto Rico 1990. Tosteson, T.R., and Baden, D.G. Polyether Dinoflagellate Toxins...and Caribbean Ciguatera : Correlation of Fish Toxins with Standard Toxins Third International Conference on Ciguatera , Peurto Rico 1990. Baden, D.G

  17. Ion-polyether coordination complexes: crystalline ionic conductors for clean energy storage.

    Science.gov (United States)

    Bruce, Peter G

    2006-03-21

    Ion-polyether complexes are the solid state analogues of crown ether and cryptand complexes. They represent a fascinating class of coordination compounds in their own right, with the ability to support ionic conductivity and the potential to be used as electrolytes in all-solid-state rechargeable lithium batteries. Here the recent discovery of ionic conductivity in crystalline ion-polyether complexes, when for 30 years such materials were considered to be insulators, is described, along with their closely related structural chemistry.

  18. Overbased Calcium sulfonate Detergent Technology Overview

    Institute of Scientific and Technical Information of China (English)

    MA Qing-gao; MUIR Ronald J.

    2009-01-01

    Overbased calcium sulfonate is used widely as detergent in automotive and marine lubricants, as well as various industrial oil applications. In this paper, the process to produce overbased calcium sulfonate is overviewed. The sulfonate structure and molecular weight and its molecular weight distribution, the enclosed calcium carbonate nanoparticle size and crystalline structure, properties of the carrier oil, all influence its properties, such as stability, viscosity, and detergency of the system.

  19. Study of distillation and degradation of perfluoro polyether; Estudo da destilacao e degradacao do perfluoropolieter

    Energy Technology Data Exchange (ETDEWEB)

    Lopergolo, Lilian Cristine

    1997-07-01

    Perfluoro-polyethers, PFPE, were first synthesised by Sianesi and collaborators giving rise to a new lubricant oils and greases classes with several applications. Perfluoro polyethers have excellent properties, for instance: high chemical stability and thermal stability, high density, high radiation resistance and excellent lubricating properties. FOMBLIN-Y oil is one of the perfluoro polyethers used as a lubricant in vacuum systems applied in the UF{sub 6} enrichment installations. Due to its excellent properties and for its applications in the nuclear field, IPEN-CNEN/S P had the interest to dominate its production technology with the aim to substitute the commercial FOMBLIN-Y oil used in the national consumption. The FOMBLIN-Y oil synthesis method, adopted in IPEN-CNEN/S P, made by the photooxidation of the hexa fluoro propylene. In this work we study the fraction separation of the national available production with restricted an increased molecular weights which was obtained by fraction distillation in a vacuum according to the ASTM D-1160 norm. We also study the catalytic effect of metals on the thermal stability of perfluoro polyethers. The inertness of perfluoro polyethers at temperatures higher than 300 deg C is strongly affected by presence of some metals. Al and Ti alloys cause fluid degradation at 250 deg C. This degradation is very important because it has a yield increase of the perfluoro polyethers production. (author)

  20. Properties of polypyrrole doped with alkylbenzene sulfonates

    DEFF Research Database (Denmark)

    Bay, Lasse; Skaarup, Steen; West, Keld

    2001-01-01

    -standing 10 mu m thick film is prepared electrochemically at a constant current from an aqueous solution of pyrrole and sodium alkylbenzene sulfonate. The mechanical properties of the film (tensile strength and Young's modulus) and the reversible linear elongation between the oxidised and reduced states...... are measured. Alkylbenzene sulfonates with alkyl chain lengths between 1 and 22 carbon atoms are used as dopant anion. The films made with the different anions have highly different properties and are here compared to outline the influence of the size of the anion. A maximum in linear elongation is found for p......-(n-octyl)benzene sulfonate and in conductivity for p-(n-butyl)benzene sulfonate....

  1. Copolymers of fluorinated polydienes and sulfonated polystyrene

    Science.gov (United States)

    Mays, Jimmy W.; Gido, Samuel P.; Huang, Tianzi; Hong, Kunlun

    2009-11-17

    Copolymers of fluorinated polydienes and sulfonated polystyrene and their use in fuel cell membranes, batteries, breathable chemical-biological protective materials, and templates for sol-gel polymerization.

  2. Polystyrene-supported Selenomethyl-sulfonates:Efficient Reagents for Stereocontrolled Synthesis of Substituted Vinyl Sulfones

    Institute of Scientific and Technical Information of China (English)

    Wei Ming XU; Lu Ling WU; Xian HUANG

    2004-01-01

    Polystyrene-supported selenomethyl-sulfonates have been prepared. These novel reagents were treated with LDA to produce selenium stabilized carbanions, which reacted with alkyl halide and epoxides, followed by selenoxide syn-elimination, to give E-vinyl sulfones and γ-hydroxy-substituted-E-vinyl sulfones respectively.

  3. SYNTHESIS OF A HYPERBRANCHED POLYETHER EPOXY THROUGH ONESTEP PROTON TRANSFER POLYMERIZATION AND ITS APPLICATION AS A TOUGHENER FOR EPOXY RESIN DGEBA

    Institute of Scientific and Technical Information of China (English)

    Jian-yong Lv; Yan Meng; Li-fan He; Xiao-yu Li; Hai-qiao Wang

    2012-01-01

    A novel liquid hyperbranched polyether epoxy (HBPEE) based on commercially available hydroquinone (HQ) and 1,1,1-trihydroxymethylpropane triglycidyl ether (TMPGE) was synthesized through an A2 + B3 one-step proton transfer polymerization.In order to improve the toughness,the synthesized HBPEE was mixed with diglycidyl ether of bisphenol A (DGEBA) in different ratios to form hybrids and cured with triethylenetetrarnine (TETA).Thermal and mechanical properties of the cured hybrids were evaluated.Results show that addition of HBPEE can improve the toughness of cured hybrids remarkably at < 20 wt% loading,without compromising the tensile strength.However,the glass transition temperature (Tg) of the cured hybrids decreases with increasing HBPEE content.Fracture surface images from scanning electron microscope show oriented fibrils in hybrids containing HBPEE.The formation and orientation of the fibrils can absorb energy under impact and lead to an improvement of toughness.Furthermore,based on the morphology of fractured surfaces and the single Tg in each hybrid,no sign of phase separation was found in the cured hybrid systems.As a result,the toughening mechanism could be explained by in situ homogeneous toughening mechanism rather than phase separation mechanism.

  4. 4-Aminopyridinium-3-sulfonate monohydrate

    Directory of Open Access Journals (Sweden)

    Zhi-Biao Zhu

    2011-02-01

    Full Text Available The reaction of 4-aminopyridine and oleum yielded the title hydrated zwitterion, C5H6N2O3S·H2O. There are two formula units in the asymmetric unit. The H and non-H atoms of both zwitterions lie on a mirror plane except for one sulfonate O atom. The water molecules are also situated on a mirror plane. In the crystal, the zwitterions and water molecules are linked by O—H...O and N—H...O hydrogen bonds, generating a three-dimensional network.

  5. Computational screening of oxetane monomers for novel hydroxy terminated polyethers.

    Science.gov (United States)

    Sarangapani, Radhakrishnan; Ghule, Vikas D; Sikder, Arun K

    2014-06-01

    Energetic hydroxy terminated polyether prepolymers find paramount importance in search of energetic binders for propellant applications. In the present study, density functional theory (DFT) has been employed to screen the various novel energetic oxetane derivatives, which usually construct the backbone for these energetic polymers. Molecular structures were investigated at the B3LYP/6-31G* level, and isodesmic reactions were designed for calculating the gas phase heats of formation. The condensed phase heats of formation for designed compounds were calculated by the Politzer approach using heats of sublimation. Among the designed oxetane derivatives, T4 and T5 possess condensed phase heat of formation above 210 kJ mol(-1). The crystal packing density of the designed oxetane derivatives varied from 1.2 to 1.6 g/cm(3). The detonation velocities and pressures were evaluated using the Kamlet-Jacobs equations, utilizing the predicted densities and HOFCond. It was found that most of the designed oxetane derivatives have detonation performance comparable to the monomers of benchmark energetic polymers viz., NIMMO, AMMO, and BAMO. The strain energy (SE) for the oxetane derivatives were calculated using homodesmotic reactions, while intramolecular group interactions were predicted through the disproportionation energies. The concept of chemical hardness is used to analyze the susceptibility of designed compounds to reactivity and chemical transformations. The heats of formation, density, and predicted performance imply that the designed molecules are expected to be candidates for polymer synthesis and potential molecules for energetic binders.

  6. Yessotoxins, a Group of Marine Polyether Toxins: an Overview

    Directory of Open Access Journals (Sweden)

    José J. Fernández

    2008-05-01

    Full Text Available Yessotoxin (YTX is a marine polyether toxin that was first isolated in 1986 from the scallop Patinopecten yessoensis. Subsequently, it was reported that YTX is produced by the dinoflagellates Protoceratium reticulatum, Lingulodinium polyedrum and Gonyaulax spinifera. YTXs have been associated with diarrhetic shellfish poisoning (DSP because they are often simultaneously extracted with DSP toxins, and give positive results when tested in the conventional mouse bioassay for DSP toxins. However, recent evidence suggests that YTXs should be excluded from the DSP toxins group, because unlike okadaic acid (OA and dinophyisistoxin-1 (DTX-1, YTXs do not cause either diarrhea or inhibition of protein phosphatases . In spite of the increasing number of molecular studies focused on the toxicity of YTX, the precise mechanism of action is currently unknown. Since the discovery of YTX, almost forty new analogues isolated from both mussels and dinoflagellates have been characterized by NMR or LC-MS/MS techniques. These studies indicate a wide variability in the profile and the relative abundance of YTXs in both, bivalves and dinoflagellates. This review covers current knowledge on the origin, producer organisms and vectors, chemical structures, metabolism, biosynthetic origin, toxicological properties, potential risks to human health and advances in detection methods of YTXs.

  7. Trace Level Determination of Polyether Ionophores in Feed

    Directory of Open Access Journals (Sweden)

    Mervi Rokka

    2013-01-01

    Full Text Available A liquid chromatography-mass spectrometric method was developed and validated to determine six polyether ionophores (lasalocid sodium, monensin sodium, salinomycin sodium, narasin, maduramicin ammonium alpha, and semduramicin sodium in feed samples. The method developed was very straightforward, involving extraction with 84% acetonitrile of the coccidiostats from the feed samples and filtration of the raw extract prior to chromatographic analysis. Method validation included the determination of selectivity, linearity, specificity, repeatability, the limit of detection, limit of quantification, decision limit (CCα, detection capability (CCβ, and recovery. Feed samples from the Finnish national feed control programme and suspected carry-over samples from a feed manufacturer were analysed in parallel with an existing liquid chromatography method coupled with ultraviolet detection. All feed control samples were negative in LC-UV, but with the developed MS method, monensin, salinomycin, and narasin were detected at concentrations of <0.025–0.73 mg/kg, <0.025–0.027 mg/kg, and <0.025–1.6 mg/kg, respectively. In suspected carry-over samples after an output of 2.0 tonnes of unmedicated feed in the pelletizer line, the concentrations of monensin, salinomycin, and narasin varied from undetected to 16 mg/kg. In the mixer line, after 3.2 tonnes of unmedicated feed output, the concentrations of monensin, salinomycin, and narasin varied from undetected to 2.4 mg/kg.

  8. High Resolution Mass Spectrometry of Polyfluorinated Polyether-Based Formulation

    Science.gov (United States)

    Dimzon, Ian Ken; Trier, Xenia; Frömel, Tobias; Helmus, Rick; Knepper, Thomas P.; de Voogt, Pim

    2016-02-01

    High resolution mass spectrometry (HRMS) was successfully applied to elucidate the structure of a polyfluorinated polyether (PFPE)-based formulation. The mass spectrum generated from direct injection into the MS was examined by identifying the different repeating units manually and with the aid of an instrument data processor. Highly accurate mass spectral data enabled the calculation of higher-order mass defects. The different plots of MW and the nth-order mass defects (up to n = 3) could aid in assessing the structure of the different repeating units and estimating their absolute and relative number per molecule. The three major repeating units were -C2H4O-, -C2F4O-, and -CF2O-. Tandem MS was used to identify the end groups that appeared to be phosphates, as well as the possible distribution of the repeating units. Reversed-phase HPLC separated of the polymer molecules on the basis of number of nonpolar repeating units. The elucidated structure resembles the structure in the published manufacturer technical data. This analytical approach to the characterization of a PFPE-based formulation can serve as a guide in analyzing not just other PFPE-based formulations but also other fluorinated and non-fluorinated polymers. The information from MS is essential in studying the physico-chemical properties of PFPEs and can help in assessing the risks they pose to the environment and to human health.

  9. A research on polyether glycol replaced APCP rocket propellant

    Science.gov (United States)

    Lou, Tianyou; Bao, Chun Jia; Wang, Yiyang

    2017-08-01

    Ammonium perchlorate composite propellant (APCP) is a modern solid rocket propellant used in rocket vehicles. It differs from many traditional solid rocket propellants by the nature of how it is processed. APCP is cast into shape, as opposed to powder pressing it with black powder. This provides manufacturing regularity and repeatability, which are necessary requirements for use in the aerospace industry. For traditional APCP, ingredients normally used are ammonium peroxide, aluminum, Hydroxyl-terminated polybutadiene(HTPB), curing agency and other additives, the greatest disadvantage is that the fuel is too expensive. According to the price we collected in our country, a single kilogram of this fuel will cost 200 Yuan, which is about 35 dollars, for a fan who may use tons of the fuel in a single year, it definitely is a great deal of money. For this reason, we invented a new kind of APCP fuel. Changing adhesive agency from cross-linked htpb to cross linked polyether glycol gives a similar specific thrust, density and mechanical property while costs a lower price.

  10. Bitemark analysis: Use of polyether in evidence collection, conservation, and comparison

    Directory of Open Access Journals (Sweden)

    Gabriel M Fonseca

    2009-01-01

    Full Text Available Background: While bitemarks are categorical identification evidence, the dynamics of biting, the anatomical location of the bite, and failures in wound records can introduce distorted images and mislead crime investigation. Materials and Methods: In this study, 20 bitemarks were performed on dead pig skin and subsequently photographed, excised, conserved, and analyzed using digital comparison (Adobe Photoshop™ 8.0, following the standard procedures (ABFO; physical comparison was also done using polyether (Impregum™; 3M casts. Study plaster casts of the upper and lower jaws of each subject were taken using type IV yellow densite stone. Polyether was used as impression material to obtain bitemarks, and casts were made from densite stone and polyether. Results: Because of its elasticity, polyether casts can compensate for primary or secondary distortions, so that there is a better degree of match when positioning the subject′s dental cast. Conclusion: Polyether is an alternative impression material and is an excellent option for creating positive casts of the wound for physical dynamic comparison.

  11. Preparation and characterization of monovalent ion selective cation exchange membranes based on sulphonated poly(ether ether ketone)

    NARCIS (Netherlands)

    Balster, J.H.; Krupenko, O.; Krupenko, O.; Punt, Ineke G.M.; Stamatialis, Dimitrios; Wessling, Matthias

    2005-01-01

    This paper analyses the separation properties of various commercial cation exchange membranes (CEMs) and tailor made membranes based on sulphonated poly(ether ether ketone) and poly(ether sulphone) for binary electrolyte solutions containing protons and calcium ions. All membranes are thoroughly

  12. Preparation and characterisation of monovalent ion selective cation exchange membranes based on sulphonated poly(ether ether ketone)

    NARCIS (Netherlands)

    Balster, J.; Krupenko, O.; Punt, I.G.M.; Stamatialis, D.; Wessling, M.

    2005-01-01

    This paper analyses the separation properties of various commercial cation exchange membranes (CEMs) and tailor made membranes based on sulphonated poly(ether ether ketone) and poly(ether sulphone) for binary electrolyte solutions containing protons and calcium ions. All membranes are thoroughly cha

  13. Polyether ionophores: broad-spectrum and promising biologically active molecules for the control of drug-resistant bacteria and parasites

    Science.gov (United States)

    Kevin, Dion A; Meujo, Damaris AF; Hamann, Mark T

    2016-01-01

    Background As multidrug-resistant (MDR) pathogens continue to emerge, there is a substantial amount of pressure to identify new drug candidates. Carboxyl polyethers, also referred to as polyether antibiotics, are a unique class of compounds with outstanding potency against a variety of critical infectious disease targets including protozoa, bacteria and viruses. The characteristics of these molecules that are of key interest are their selectivity and high potency against several MDR etiological agents. Objective Although many studies have been published about carboxyl polyether antibiotics, there are no recent reviews of this class of drugs. The purpose of this review is to provide the reader with an overview of the spectrum of activity of polyether antibiotics, their mechanism of action, toxicity and potential as drug candidates to combat drug-resistant infectious diseases. Conclusion Polyether ionophores show a high degree of promise for the potential control of drug-resistant bacterial and parasitic infections. Despite the long history of use of this class of drugs, very limited medicinal chemistry and drug optimization studies have been reported, thus leaving the door open to these opportunities in the future. Scifinder and PubMed were the main search engines used to locate articles relevant to the topic presented in the present review. Keywords used in our search were specific names of each of the 88 compounds presented in the review as well as more general terms such as polyethers, ionophores, carboxylic polyethers and polyether antibiotics. PMID:23480512

  14. Ammonium Y zeolite applied as a thermochemolysis reagent for identification of polyethers and polyesters.

    Science.gov (United States)

    Blazsó, Marianne; Bozi, János

    2013-01-04

    A potential thermochemolysis reagent has been tested for the pyrolysis gas chromatographic identification of polyether, polyester and polyether- or polyester-based thermoplastic polyurethane. The main advantage of ammonium Y zeolite over liquid reagents is that it does not react prior to pyrolysis, and its reactions have no incomplete products. The procedure of the thermochemolysis is as simple as running a pyrolysis-GC/MS analysis sampling a powder mixture of roughly equal mass of polymer and ammonium Y zeolite. The GC/MS chromatograms obtained show that the products of thermochemolysis are specific to the diol and dicarboxylic units of the polymer. It was observed that ethanal or 1,4-dioxane forms from ethylene oxide components of polyethers and polyesters, tetrahydrofuran from butylene oxide units, hexanedinitrile from adipate groups, and benzodinitrile from terephthalate groups.

  15. Compression-induced transformation of aldehydes into polyethers: a first-principles molecular dynamics study.

    Science.gov (United States)

    Mosey, Nicholas J

    2010-04-07

    First-principles molecular dynamics simulations are used to investigate the behavior of bulk acetaldehyde (MeCHO) under conditions of increasing pressure. The results demonstrate that increasing pressure causes the aldehydes to polymerize, yielding polyethers through a process involving the rapid formation of C-O bonds between multiple neighboring MeCHO molecules. Attempts to induce polyether formation at different densities through the application of geometric constraints show that polymerization occurs only once a critical density of approximately 1.7 g/cm(3) has been reached. The results of simulations performed at several different temperatures are also consistent with a process that is induced by reaching a critical density. The origins of this effect are rationalized in terms of the structural requirements for the formation of C-O bonds between multiple MeCHO molecules in rapid succession. Specifically, the collective formation of C-O bonds requires the typical distance between the sp(2) carbon atoms and oxygen atoms in neighboring MeCHO molecules to reach a value of approximately 2.5 A. Radial distribution functions calculated at different densities show that this structural requirement is reached when the density is near the observed threshold. The observed reaction may be useful in the context of lubrication, with polyethers being effective lubricants and the extreme conditions experienced in sliding contacts providing the ability to reach the high densities needed to induce the reaction. In this context, the calculations indicate that polyether formation is associated with significant energy dissipation, while energy dissipation is minimal once the polyethers are formed. Furthermore, the polyethers are stable with respect to multiple compression/decompression cycles and pressures of at least 60 GPa.

  16. Chemodiversity of Ladder-Frame Prymnesin Polyethers in Prymnesium parvum.

    Science.gov (United States)

    Rasmussen, Silas Anselm; Meier, Sebastian; Andersen, Nikolaj Gedsted; Blossom, Hannah Eva; Duus, Jens Øllgaard; Nielsen, Kristian Fog; Hansen, Per Juel; Larsen, Thomas Ostenfeld

    2016-09-23

    Blooms of the microalga Prymnesium parvum cause devastating fish kills worldwide, which are suspected to be caused by the supersized ladder-frame polyether toxins prymnesin-1 and -2. These toxins have, however, only been detected from P. parvum in rare cases since they were originally described two decades ago. Here, we report the isolation and characterization of a novel B-type prymnesin, based on extensive analysis of 2D- and 3D-NMR data of natural as well as 90% (13)C enriched material. B-type prymnesins lack a complete 1,6-dioxadecalin core unit, which is replaced by a short acyclic C2 linkage compared to the structure of the original prymnesins. Comparison of the bioactivity of prymnesin-2 with prymnesin-B1 in an RTgill-W1 cell line assay identified both compounds as toxic in the low nanomolar range. Chemical investigations by liquid chromatography high-resolution mass spectrometry (LC-HRMS) of 10 strains of P. parvum collected worldwide showed that only one strain produced the original prymnesin-1 and -2, whereas four strains produced the novel B-type prymnesin. In total 13 further prymnesin analogues differing in their core backbone and chlorination and glycosylation patterns could be tentatively detected by LC-MS/HRMS, including a likely C-type prymnesin in five strains. Altogether, our work indicates that evolution of prymnesins has yielded a diverse family of fish-killing toxins that occurs around the globe and has significant ecological and economic impact.

  17. 磺酸盐封端聚醚及其聚合物的阻垢应用%Sulfate-capped polyether and their copolymers applied as inhibitors

    Institute of Scientific and Technical Information of China (English)

    符嫦娥; 仓理; 陈健

    2011-01-01

    Amidosulfonic acid has been used as sulfonating agent for synthesizing macro-monomer polyether sulfate (APES) ,and APES and AA have been used as monomer for synthesizing block copolymer AA-b-APES in aqueous solutions. APES and AA-b-APES are characterized by bromine value,hydroxyl value,element analysis, thermo-gravimetric analysis and FT-IR. Transmission electron microscope (TEM) images show that the application of AA-b -APES significantly decreases the size of calcium phosphate solid granules. The research indicates that the sulfonating rate of APES is approximately 90% and calcium phosphate inhibiting rate is 92% ,when the dosage of AA-b-APES is 6 mg/L. Therefore, AA-b-APES is a kind of non-phosphorus scale inhibitor for inhibiting calcium phosphate scale, superior to commercial scale inhibitors.%以氨基磺酸为磺化剂合成了具有聚乙烯氧基长链的大分子单体聚醚磺酸盐(APES),并以APES和丙烯酸(AA)为单体水相合成了嵌段共聚物AA-b-APES.通过红外光谱、溴值、羟值、元素分析和热重分析对APES和AA-b-APES进行了表征.透射电镜表明,AA-b-APES减小了磷酸钙固体颗粒尺寸.研究表明,APES的磺化率约为90%,AA-b-APES在6mg/L时的阻磷酸钙垢率为92%,是一种优于商业阻垢剂的阻磷酸钙垢的无磷阻垢剂.

  18. An investigation of the preparation of high molecular weight perfluorocarbon polyethers

    Science.gov (United States)

    Watts, R. O.; Tarrant, P.

    1972-01-01

    High molecular weight perfluorocarbon polyether gums were obtained by photolysis of perfluorodienes and discyl fluorides containing a perfluorocarbon polyether backbond. The materials obtained are represented by chemical formulas. A method was developed whereby reactive acyl fluoride and trifluorovinyl end groups are converted into inert structures. In order to investigate the possible preparation of difunctional molecules which may be useful in polymer synthesis, the reactions of hexafluoropropene oxide (HFPO) with Grignard and organolithium reagents have been studied. Reactions of various nucleophilic reagents with HFPO were also investigated.

  19. Synthesis and Characterization of Poly(ether amide)s Containing Bisphthalazinone and Ether Linkages

    Institute of Scientific and Technical Information of China (English)

    Cheng LIU; Shou Hai ZHANG; Ming Jing WANG; Qi Zhen LIANG; Xi Gao JIAN

    2005-01-01

    A novel aromatic diacid, 4, 4'-bis[2-(4-carboxyphenyl)phthalazin-1-one-4-yl]-bisphenyl ether Ⅲ, containing bisphthalazinone and ether linkages was prepared from nucleophilic substitution of p-chlorobenzonitrile with the bisphenol-like monomer Ⅰ, followed by alkaline hydrolysis of the intermediate dinitrile Ⅱ. A series of poly(ether amide)s containing bisphthalazinone and ether linkages derived from diacid Ⅲ and aromatic diamines were synthesized by one-step solution condensation polymerization using triphenyl phosphite and pyridine as condensing agents. Moreover, the properties of poly(ether amide)s including thermal stability,solubility and crystallinity were also studied.

  20. A thin film degradation study of a fluorinated polyether liquid lubricant using an HPLC method

    Science.gov (United States)

    Morales, W.

    1986-01-01

    A High Pressure Liquid Chromatography (HPLC) separation method was developed to study and analyze a fluorinated polyether fluid which is promising liquid lubricant for future applications. This HPLC separation method was used in a preliminary study investigating the catalytic effect of various metal, metal alloy, and ceramic engineering materials on the degradation of this fluid in a dry air atmosphere at 345 C. Using a 440 C stainless steel as a reference catalytic material it was found that a titanium alloy and a chromium plated material degraded the fluorinated polyether fluid substantially more than the reference material.

  1. STUDY ON SOME PROPERTIES OF Si-CONTAINING POLYESTER-POLYETHER MULTIBLOCK COPOLYMERS

    Institute of Scientific and Technical Information of China (English)

    LI Zhenyi; ZHU Jin

    1997-01-01

    Some physical properties of the polyester-polyether multiblock copolymers with Si-containing hard segment were further examined by a series of physical methods. The hydrophobicity of the copolymers was improved with the incorporation of increasing amount of orgauosilicone, XPS test proved that silicon element was enriched at the surface of the Si-containing polyester-polyether copolymers. It was also found that their heat resistance and gas permeability for O2 and N2 were greatly improved. The study on semipermeability of films made of the Si-containing copolymers was also followed with interest.

  2. Chlorine resistant desalination membranes based on directly sulfonated poly(arylene ether sulfone) copolymers

    Science.gov (United States)

    McGrath, James E.; Park, Ho Bum; Freeman, Benny D.

    2011-10-04

    The present invention provides a membrane, kit, and method of making a hydrophilic-hydrophobic random copolymer membrane. The hydrophilic-hydrophobic random copolymer membrane includes a hydrophilic-hydrophobic random copolymer. The hydrophilic-hydrophobic random copolymer includes one or more hydrophilic monomers having a sulfonated polyarylsulfone monomer and a second monomer and one or more hydrophobic monomers having a non-sulfonated third monomer and a fourth monomer. The sulfonated polyarylsulfone monomer introduces a sulfonate into the hydrophilic-hydrophobic random copolymer prior to polymerization.

  3. Comparison of Properties among Dendritic and Hyperbranched Poly(ether ether ketone)s and Linear Poly(ether ketone)s.

    Science.gov (United States)

    Morikawa, Atsushi

    2016-02-16

    Poly(ether ether ketone) dendrimers and hyperbranched polymers were prepared from 3,5-dimethoxy-4'-(4-fluorobenzoyl)diphenyl ether and 3,5-dihydroxy-4'-(4-fluorobenzoyl)diphenyl ether through aromatic nucleophilic substitution reactions. 1-(tert-Butyldimethylsiloxy)-3,5-bis(4-fluorobenzoyl)benzene was polycondensed with bisphenols, followed by cleavage of the protective group to form linear poly(ether ketone)s having the same hydroxyl groups in the side chains as the chain ends of the dendrimer and hyperbranched polymers. Their properties, such as solubilities, reduced viscosities, and thermal properties, were compared with one another. Similar comparisons were also carried out among the corresponding methoxy group polymers, and the size of the molecules was shown to affect the properties.

  4. Preparation of Overbased Calcium Alkylbenzene Sulfonate for Formulating Complex Sulfonate Grease

    Institute of Scientific and Technical Information of China (English)

    Liu Yinong

    2015-01-01

    Six kinds of alkylbenzene sulfonic acids were selected to prepare the sulfonates S1—S6. Among them, the sul-fonates S3, S4, and S6 could be incorporated into lubricating grease with good performance in comparison with the grease produced from commercial sulfonates T106-1 and T106-2. The optimized conditions for synthesis of the sulfonates S3, S4, and S6were explored by using different mass ratios of methanol, water and the type of copromoters. It was found out that the appropriate conditions for synthesis of the sulfonate S3 included a methanol to M (M is the total mass of alkylbenzene sulfonic acid and base oil) mass ratio of 16%, a water to M mass ratio of 4%, and a copromoter A to M mass ratio of 2%; the appropriate conditions for synthesis of the sulfonate S4 included a methanol to M mass ratio of 24%, a water to M mass ratio of 2%, a copromoter B to M mass ratio of 2%; and the optimized conditions for synthesis of the sulfonate S6 included a methanol/ M mass ratio of 8%, a water/M mass ratio of 4% and a copromoter B/M mass ratio of 2%. The new sulfonates S3, S4, and S6 produced under the optimized conditions exhibited higher TBN and better antiwear property in camparison with the previous products. Grease samples G9, G10, and G11 were prepared with new sulfonates S3, S4, and S6 successfully and exhibited improved water stability and high temperature performance.

  5. Preparation and antibacterial properties of hybrid-zirconia films with silver nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Azocar, Ignacio, E-mail: manuel.azocar@usach.cl [Departamento de Quimica de los Materiales, Facultad de Quimica y Biologia, Universidad de Santiago de Chile, USACH, Avenida Bernardo O' Higgins 3363, Casilla 40, Correo 33, Santiago (Chile); Vargas, Esteban [Facultad de Ingenieria, Departamento de Metalurgia, Universidad de Santiago de Chile, USACH (Chile); Duran, Nicole [Departamento de Quimica de los Materiales, Facultad de Quimica y Biologia, Universidad de Santiago de Chile, USACH, Avenida Bernardo O' Higgins 3363, Casilla 40, Correo 33, Santiago (Chile); Arrieta, Abel [Departamento de Biologia, Facultad de Quimica y Biologia, Universidad de Santiago de Chile, USACH (Chile); Gonzalez, Evelyn [Departamento de Quimica de los Materiales, Facultad de Quimica y Biologia, Universidad de Santiago de Chile, USACH, Avenida Bernardo O' Higgins 3363, Casilla 40, Correo 33, Santiago (Chile); Facultad de Ingenieria, Departamento de Metalurgia, Universidad de Santiago de Chile, USACH (Chile); Departamento de Biologia, Facultad de Quimica y Biologia, Universidad de Santiago de Chile, USACH (Chile); Departamento de Quimica Farmacologica y Toxicologica, Facultad de Ciencias Quimicas, Universidad de Chile, Sergio Livingstone Polhammer 1007, Santiago (Chile); and others

    2012-11-15

    The antimicrobial effect of incorporating silver nanoparticles (AgNps) into zirconia matrix-polyether glycol was studied. AgNps of 4-6 nm in size were synthesized using the inverse micelles method, and different doses of metallic nanoparticles were incorporated into zirconia-polyether glycol mixtures during the ageing procedure. Atomic force microscopy (AFM) of the modified hybrid film showed a homogenous distribution of 20-80 nm diameter AgNps, indicating agglomeration of these structures during film modification; such agglomerations were greater when increasing the dosage of the colloidal system. The AgNps-hybrid films showed higher antimicrobial activity against Gram-positive bacteria than for Gram-negative bacteria. Hybrid films prepared with dioctyl sodium sulfosuccinate (AOT) stabilized AgNps presented enhanced antibacterial activity compared to that obtained through the addition of a high AgNO{sub 3} concentration (0.3 wt%). -- Graphical abstract: Atomic Force Micrographs, top and cross section view, showing silver nanoparticles embedded in a zirconia-polyether glycol hybrid film. Highlights: Black-Right-Pointing-Pointer Antibacterial activity of films (zirconia-polyether glycol) modified with silver nanoparticles. Black-Right-Pointing-Pointer Biofilm formation is prevented. Black-Right-Pointing-Pointer High sensibility against gram positive bacteria.

  6. Sulfonation of vulcanized ethylene-propylene-diene terpolymer membranes

    Energy Technology Data Exchange (ETDEWEB)

    Barroso-Bujans, F. [Instituto de Ciencia y Tecnologia de Polimeros, CSIC, Juan de la Cierva 3, 28006 Madrid (Spain)], E-mail: fbarroso@ictp.csic.es; Verdejo, R.; Lozano, A. [Instituto de Ciencia y Tecnologia de Polimeros, CSIC, Juan de la Cierva 3, 28006 Madrid (Spain); Fierro, J.L.G. [Instituto de Catalisis y Petroleoquimica, CSIC, Marie Curie 2, Cantoblanco, 28049 Madrid (Spain); Lopez-Manchado, M.A. [Instituto de Ciencia y Tecnologia de Polimeros, CSIC, Juan de la Cierva 3, 28006 Madrid (Spain)

    2008-10-15

    In the present work, sulfonation of previously vulcanized ethylene propylene diene terpolymer (EPDM) membranes was developed in a swelling solvent with acetyl sulfate. This procedure avoids the need to pre-dissolve the raw polymer. The reaction conditions were optimized in terms of solvent type, reaction time, acetyl sulfate concentration and film thickness to obtain the maximum degree of sulfonation of the polymer. The sulfonation procedure presented in this study yields a degree of sulfonation comparable to the chlorosulfonic acid procedure. Sulfonic acid groups were detected by X-ray photoelectron spectroscopy and Fourier transform infrared spectroscopy, and quantified by titrations. Proton conductivity and water uptake were measured by means of impedance spectroscopy and swelling measurements, respectively, and were correlated with the degree of sulfonation. Tensile strength and Young's modulus of sulfonated EPDM increased with the degree of sulfonation, while elongation at break remained constant. Thermal stability of the sulfonated EPDM was studied by simultaneous thermogravimetry-mass spectroscopy.

  7. Polyether ether ketone implants achieve increased bone fusion when coated with nano-sized hydroxyapatite

    DEFF Research Database (Denmark)

    Johansson, Pär; Jimbo, Ryo; Naito, Yoshihito

    2016-01-01

    Polyether ether ketone (PEEK) possesses excellent mechanical properties similar to those of human bone and is considered the best alternative material other than titanium for orthopedic spine and trauma implants. However, the deficient osteogenic properties and the bioinertness of PEEK limit its...

  8. IONIC CONDUCTIVITIES OF SEGMENTED POLYETHER POLYURETHANEUREA COMPLEXES WITH LiClO4

    Institute of Scientific and Technical Information of China (English)

    GU Qingchao; XU Weizheng; YE Wenwen; MO Tianlin

    1991-01-01

    Ionic conductivity values for segmented polyether polyurethaneurea (PEUU) complexes with VTF (Vogel-Tamman-Fulcher) equation and WLF (Williams-Landel-Ferry) type equation. Values have been estimated for the "apparent" activation energies of ion transport from VTF equation and they lie in the range 2.70- 5.53 kJ·mol-1.

  9. Synthesis of Amine-Terminated Polyether%端氨基聚醚的合成

    Institute of Scientific and Technical Information of China (English)

    张金龙

    2011-01-01

    High pressure catalytic animation of polyether to amine-terminated polyether was studied in the presence of modified Raney Ni catalyst, polyether and liquid ammonia. The reaction factors, including temperature, the amount of catalyst, ratio of ammonia to hydroxyl and ratio of hydrogen to hydroxyl were investigated. The optimized conditions were obtained by experiment. The best process condition was temperature 220 ℃, the ratio of ammonia to hydroxyl 10 ~ 12, the ratio of hydrogen to hydroxyl 0. 6 ~0. 8, the catalyst content 7% ~11% and the reaction time 4 ~ 5 h. The conversion of polyether could be up to 97%.%研究了以改性雷尼镍为催化剂、聚醚和液氨为原料,临氢高压催化氨化制备端氨基聚醚的工艺路线,考察了反应温度、催化剂用量、氨醇比、氢醇比对反应的影响.结果表明,温度220℃、氨醇摩尔比10 ~ 12、氢醇摩尔比0.6~0.8、催化剂质量分数为7%~11%、反应时间4~5h时,聚醚氨化制备端氨基聚醚的转化率大于97%.

  10. SEPARATION OF OCTYLPHENOL POLYETHER ALCOHOLS SURFACTANTS BY CAPILLARY COLUMN SFC AND HPLC

    Science.gov (United States)

    Separation of nonionic octylphenol polyether alcohols (OPA) by supercritical fluid chromatography (SFC) and HPLC is described. Using a density programming and a 50-μm i.d. capillary column, a total of 18 group oligomers was separated. The effects of the operating parameters, such...

  11. Effects of poly-ether B on proteome and phosphoproteome expression in biofouling Balanus amphitrite cyprids

    KAUST Repository

    Dash, Swagatika

    2012-04-01

    Biofouling is ubiquitous in marine environments, and the barnacle Balanus amphitrite is one of the most recalcitrant and aggressive biofoulers in tropical waters. Several natural antifoulants that were claimed to be non-toxic have been isolated in recent years, although the mechanism by which they inhibit fouling is yet to be investigated. Poly-ether B has shown promise in the non-toxic inhibition of larval barnacle attachment. Hence, in this study, multiplex two-dimensional electrophoresis (2-DE) was applied in conjunction with mass spectrometry to investigate the effects of poly-ether B on barnacle larvae at the molecular level. The cyprid proteome response to poly-ether B treatment was analyzed at the total proteome and phosphoproteome levels, with 65 protein and 19 phosphoprotein spots found to be up- or down-regulated. The proteins were found to be related to energy-metabolism, oxidative stress, and molecular chaperones, thus indicating that poly-ether B may interfere with the redox-regulatory mechanisms governing the settlement of barnacle larvae. The results of this study demonstrate the usefulness of the proteomic technique in revealing the working mechanisms of antifouling compounds. © 2012 Copyright Taylor and Francis Group, LLC.

  12. GRAFT COPOLYMERIZATION OF ACRYLAMIDE ONTO THE UV-RAY IRRADIATED FILM OF POLYESTER-POLYETHER

    Institute of Scientific and Technical Information of China (English)

    CHEN Chuanfu; LI Xuefen; LI Zhifen

    1988-01-01

    In this paper the Ce(Ⅳ) salt initiated graft copolymerization of acrylamide onto the film of polyester-polyether block copolymer irradiated by UV-ray was reported. The UV-irradiation of the film and its graft process have been investigated by UV spectrum, ESR and ESCA and the influence of other factors on the graft copolymerization has been discussed.

  13. Poly(ether ester) Ionomers as Water-Soluble Polymers for Material Extrusion Additive Manufacturing Processes.

    Science.gov (United States)

    Pekkanen, Allison M; Zawaski, Callie; Stevenson, André T; Dickerman, Ross; Whittington, Abby R; Williams, Christopher B; Long, Timothy E

    2017-04-12

    Water-soluble polymers as sacrificial supports for additive manufacturing (AM) facilitate complex features in printed objects. Few water-soluble polymers beyond poly(vinyl alcohol) enable material extrusion AM. In this work, charged poly(ether ester)s with tailored rheological and mechanical properties serve as novel materials for extrusion-based AM at low temperatures. Melt transesterification of poly(ethylene glycol) (PEG, 8k) and dimethyl 5-sulfoisophthalate afforded poly(ether ester)s of sufficient molecular weight to impart mechanical integrity. Quantitative ion exchange provided a library of poly(ether ester)s with varying counterions, including both monovalent and divalent cations. Dynamic mechanical and tensile analysis revealed an insignificant difference in mechanical properties for these polymers below the melting temperature, suggesting an insignificant change in final part properties. Rheological analysis, however, revealed the advantageous effect of divalent countercations (Ca(2+), Mg(2+), and Zn(2+)) in the melt state and exhibited an increase in viscosity of two orders of magnitude. Furthermore, time-temperature superposition identified an elevation in modulus, melt viscosity, and flow activation energy, suggesting intramolecular interactions between polymer chains and a higher apparent molecular weight. In particular, extrusion of poly(PEG8k-co-CaSIP) revealed vast opportunities for extrusion AM of well-defined parts. The unique melt rheological properties highlighted these poly(ether ester) ionomers as ideal candidates for low-temperature material extrusion additive manufacturing of water-soluble parts.

  14. Synthesis of polyether-based block copolymers based on poly(propylene oxide) and terephthalates

    NARCIS (Netherlands)

    van der Schuur, J.M.; Feijen, Jan; Gaymans, R.J.

    2005-01-01

    Poly(propylene oxide) (PPO) is a low reactive telechelic polyether and the synthesis of high molecular weight poly(propylene oxide)-based block copolymers was studied. The poly(propylene oxide) used was end capped with 20 wt % ethylene oxide and had a molecular weight of 2300 g/mol (ultra-low monol

  15. Primary biodegradation of linear alkyltoluene and alkylbenzene sulfonates.

    Science.gov (United States)

    Singh, M; Satish, S

    1989-01-01

    Studies on the primary biodegradation of linear dodecylbenzene sulfonate, linear dodecyltoluene sulfonate, linear C(10-14) benzene sulfonate, linear C(10-14) toluene sulfonate, commercial samples of linear C(10-14) benzene sulfonate and branched dodecylbenzene sulfonate (DDBS) were carried out using a microbial culture developed from garden soil. Results show that linear alkyl toluene (LAT) is as degradable as linear alkylbenzene (LAB) in 7 days. However, a slower rate of degradation was noted with LAT. Various distributions of the positional isomers of the phenyl ring in the alkane chain of C(10-14) LAB showed no change in the pattern of primary biodegradation.

  16. Reactive phase inversion for manufacture of asymmetric poly (ether imide sulfone) membranes

    KAUST Repository

    Jalal, Taghreed

    2014-12-01

    Poly (ether imide sulfone) membranes were manufactured by combining phase inversion and functionalization reaction between epoxy groups and amine modified polyether oligomers (Jeffamine) or TiO2 nanoparticles. Polysilsesquioxanes containing epoxy functionalities were in-situ grown in the casting solution and made available for further reaction with amines in the coagulation/annealing baths. The membranes were characterized by field emission scanning electron microscopy, porosimetry and water flux measurements. Water permeances up to 1500 l m-2 h-1 bar-1 were obtained with sharp pore size distribution and a pore diameter peak at 66 nm, confirmed by porosimetry, which allowed 99.2% rejection of γ-globulin. Water flux recovery of 77.5% was achieved after filtration with proteins. The membranes were stable in 50:50 dimethylformamide/water, 50:50 N-methyl pyrrolidone/water and 100% tetrahydrofuran. The possibility of using similar concept for homogeneous and stable attachment of nanoparticles on the membrane surface was demonstrated.

  17. Fluorescent Polystyrene Sulfonate for Polyelectrolyte Studies

    Science.gov (United States)

    Huberty, Wayne; Tong, Xiaowei; Balamurugan, Sreelatha; Zhang, Donghui; Russo, Paul

    2012-02-01

    The slow-mode decay found by dynamic light scattering for polyelectrolytes in low-salt conditions has perplexed investigators since its first observation. Many characterization methods have suggested temporary or transient aggregation, although there is still no consensus on the cause. Many different polyelectrolytes demonstrate the slow-mode decay, but the sodium salt of polystyrene sulfonate (NaPSS) is the most popular choice for study. Commercially available NaPSS may have hydrophobic patches due to incomplete sulfonation leading to associations apart from any putative ionic mechanisms. Therefore, essentially full sulfonation, or ``patchless'', NaPSS should be synthesized. To facilitate fluorescence measurements, which can provide new insights to the slow-mode phenomenon, the material must be rendered fluorescent (F-NaPSS). Several approaches to F-NaPSS have appeared; some labeled a previously synthesized NaPSS without concern for its hydrophobic patches. Other strategies include a free radical copolymerization of styrene sulfonate and a vinyl amine to provide side chains viable for labeling. This method is successful, but yields only small amounts of nearly monodisperse polymer after fractionation. In this presentation, a high-yield synthesis of fully sulfonated, low-polydispersity, fluorescently tagged polymer will be discussed.

  18. Susceptibility of Candida albicans to new synthetic sulfone derivatives.

    Science.gov (United States)

    Staniszewska, Monika; Bondaryk, Małgorzata; Ochal, Zbigniew

    2015-02-01

    The influence of halogenated methyl sulfones, i.e. bromodichloromethyl-4-chloro-3-nitrophenyl sulfone (named halogenated methyl sulfone 1), dichloromethyl-4-chloro-3-nitrophenyl sulfone (halogenated methyl sulfone 2), and chlorodibromomethyl-4-hydrazino-3-nitrophenyl sulfone (halogenated methyl sulfone 3), on cell growth inhibition, aspartic protease gene (SAP4-6) expression, adhesion to epithelium, and filamentation was investigated. Antifungal susceptibility of the halogenated methyl sulfones was determined with the M27-A3 protocol in the range of 16-0.0313 µg/mL. Adherence to Caco-2 cells was performed in 24-well plates; relative quantification was normalized against ACT1 in cells after 18 h of growth in YEPD and on Caco-2 cells. SAP4-6 expression was analyzed using RT-PCR. Structure-activity relationship studies suggested that halogenated methyl sulfone 1 containing bromodichloromethyl or dichloromethyl function at C-4 (halogenated methyl sulfone 2) of the phenyl ring showed the best activity (100% cell inhibition at 0.5 µg/mL), while hydrazine at C-1 (halogenated methyl sulfone 3) reduced the sulfone potential (100% = 4 µg/mL). SAP4-6 were up- or down-regulated depending on the strains' genetic background and the substitutions on the phenyl ring. Halogenated methyl sulfone 2 repressed germination and affected adherence to epithelium (P ≤ 0.05). The tested halogenated methyl sulfones interfered with the adhesion of Candida albicans cells to the epithelial tissues, without affecting their viability after 90 min of incubation. The mode of action of the halogenated methyl sulfones was attributed to the reduced virulence of C. albicans. SAP5 and SAP6 contribute to halogenated methyl sulfones resistance. Thus, halogenated methyl sulfones can inhibit biofilm formation due to their interference with adherence and with the yeast-to-hyphae transition.

  19. Interaction of apo cytochrome c with sulfonated polystyrene nanoparticles.

    Science.gov (United States)

    Liang, Li; Yao, Ping; Gong, Jie; Jiang, Ming

    2004-04-13

    Stable nanoparticle dispersion in aqueous solutions was obtained with partially sulfonated polystyrene. The hydrophobic association of the backbone chains and phenyl groups is balanced by the electrostatic repulsion of the sulfonate groups on the particle surface. The size distribution of the sulfonated polystyrene particles in relation to concentration, degree of sulfonation and chain length, and pH was characterized by dynamic laser light-scattering. The structure and morphology of the particles were characterized with fluorescence and atom force microscopy. Highly sulfonated polystyrene particles can form large complex particles with positively charged protein, apo cytochrome c. Dynamic laser light-scattering and atom force microscopy studies show that the size and distribution of the complex particles depend on the relative amount of apo cytochrome c and sulfonated polystyrene. When sulfonated polystyrene is in excess, apo cytochrome c interacts with sulfonated polystyrene particles forming stable complexes and excessive sulfonated polystyrene particles bind to the periphery of the complexes preventing them from further aggregation. When apo cytochrome c is in excess, apo cytochrome c links the complexes forming much larger particles. Fluorescence study demonstrates that the hydrophobicity/hydrophility of the complex particles is relative to the ratio of apo cytochrome c and sulfonated polystyrene, degree of sulfonation, and pH. Apo cytochrome c not only can neutralize the negative charges on the surface of sulfonated polystyrene particles, but may also insert into the cores disrupting the original structure of sulfonated polystyrene particles.

  20. Reinforced films based on cross-linked water-soluble sulfonated carbon nanotubes with sulfonated polystyrene.

    Science.gov (United States)

    Dai, Ying; Haiping, Hong; Guiver, Michael; Welsh, Jeffry S

    2009-09-01

    Reinforced films based on sulfonated polystyrene cross-linked with water-soluble sulfonated carbon nanotubes were fabricated using a free-standing film-making method. Transmission and scanning electron microscopy (TEM and SEM), and X-ray photoelectron spectroscopy (XPS) were used to verify the cross-linking reaction. The mechanical properties of these films demonstrated that the tensile strength increases with an increase in the sulfonated nanotube concentration. At 5 wt% nanotube loading, the tensile strength increased 84% compared with polymer containing no nanotube loading. The relationships between structure and mechanical properties are discussed and a possible direction for making ultra thin and ultra lightweight film is proposed.

  1. Reinforced membrane based on crosslink reaction between water soluble sulfonated carbon nanotubes and sulfonated polystyrene

    Science.gov (United States)

    Dai, Ying; Hong, Haiping; Welsh, Jeffry S.

    2008-08-01

    Reinforced films based on sulfonated polystyrene cross-linked with water-soluble sulfonated carbon nanotubes were fabricated using a free-standing film-making method. Transmission and scanning electron microscopy, X-ray photoelectron spectroscopy, and thermo-gravimetric analysis were used to verify the cross-linking reaction. The mechanical properties of these films demonstrated that the tensile strength increases with an increase in the sulfonated nanotube concentration. At 5 wt% nanotube loading, the tensile strength increased 84% compared with polymer containing no nanotube loading. The relationships between structure and mechanical properties are discussed and a possible direction for making ultra thin and ultra lightweight film is proposed

  2. Anaerobic degradation of linear alkylbenzene sulfonate

    DEFF Research Database (Denmark)

    Mogensen, Anders Skibsted; Haagensen, Frank; Ahring, Birgitte Kiær

    2003-01-01

    Linear alkylbenzene sulfonate (LAS) found in wastewater is removed in the wastewater treatment facilities by sorption and aerobic biodegradation. The anaerobic digestion of sewage sludge has not been shown to contribute to the removal. The concentration of LAS based on dry matter typically...... increases during anaerobic stabilization due to transformation of easily degradable organic matter. Hence, LAS is regarded as resistant to biodegradation under anaerobic conditions. We present data from a lab-scale semi-continuously stirred tank reactor (CSTR) spiked with linear dodecylbenzene sulfonate (C...

  3. Properties of polypyrrole doped with alkylbenzene sulfonates

    DEFF Research Database (Denmark)

    Bay, Lasse; Skaarup, Steen; West, Keld;

    2001-01-01

    -standing 10 mu m thick film is prepared electrochemically at a constant current from an aqueous solution of pyrrole and sodium alkylbenzene sulfonate. The mechanical properties of the film (tensile strength and Young's modulus) and the reversible linear elongation between the oxidised and reduced states...... are measured. Alkylbenzene sulfonates with alkyl chain lengths between 1 and 22 carbon atoms are used as dopant anion. The films made with the different anions have highly different properties and are here compared to outline the influence of the size of the anion. A maximum in linear elongation is found for p...

  4. The facile insertion of β-keto sulfones to arynes: The direct preparation of polysubstituted ortho-keto benzyl sulfones

    Institute of Scientific and Technical Information of China (English)

    Jian Xue; Lu Ling Wu; Xian Huang

    2008-01-01

    One novel carbon-carbon bond insertion reaction of arynes has been developed. By this reaction β-keto sulfones can insert the triple bond of arynes to prepare polysubstituted ortho-keto benzyl sulfones.

  5. 21 CFR 177.2500 - Polyphenylene sulfone resins.

    Science.gov (United States)

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Polyphenylene sulfone resins. 177.2500 Section 177... Components of Articles Intended for Repeated Use § 177.2500 Polyphenylene sulfone resins. The polyphenylene sulfone resins (CAS Reg. No. 31833-61-1) identified in paragraph (a) of this section may be safely used...

  6. Mouse determinant lethal and bone marrow micronucleus studies on methyl vinyl sulfone and divinyl sulfone

    OpenAIRE

    1991-01-01

    Artículo científico-- Instituto de Investigaciones en Salud-- 1991. La revista no permite distribuir la versión final del documento. Methyl vinyl sulfone and divinyl sulfone were tested for the induction of dominant lethal mutations and micronucleated bone-marrow erythrocytes in male mice. These chemicals were chosen for study because of their similarities in structure and chemical reactivity to acrylamide which is known to induce both effects. Following administration of the test...

  7. Fate and biodegradability of sulfonated aromatic amines

    NARCIS (Netherlands)

    Tan, N.C.G.; Leeuwen, van A.; Voorthuizen, van E.M.; Slenders, P.; Prenafeta, F.X.; Temmink, H.; Lettinga, G.; Field, J.A.

    2005-01-01

    Ten sulfonated aromatic amines were tested for their aerobic and anaerobic biodegradability and toxicity potential in a variety of environmental inocula. Of all the compounds tested, only two aminobenzenesulfonic acid (ABS) isomers, 2- and 4-ABS, were degraded. The observed degradation occurred only

  8. Carbon dioxide sensing with sulfonated polyaniline

    NARCIS (Netherlands)

    Doan, D.C.T.; Ramaneti, R.; Baggerman, J.; Bent, van der J.; Marcelis, A.T.M.; Tong, H.D.; Rijn, van C.J.M.

    2012-01-01

    The use of polyaniline and especially sulfonated polyaniline (SPAN) is explored for sensing carbon dioxide (CO2) at room temperature. Frequency-dependent AC measurements were carried out to detect changes in impedance of the polymer, drop casted on interdigitated electrodes, when exposed to CO2 gas.

  9. Fate and biodegradability of sulfonated aromatic amines

    NARCIS (Netherlands)

    Tan, N.C.G.; Leeuwen, van A.; Voorthuizen, van E.M.; Slenders, P.; Prenafeta, F.X.; Temmink, H.; Lettinga, G.; Field, J.A.

    2005-01-01

    Ten sulfonated aromatic amines were tested for their aerobic and anaerobic biodegradability and toxicity potential in a variety of environmental inocula. Of all the compounds tested, only two aminobenzenesulfonic acid (ABS) isomers, 2- and 4-ABS, were degraded. The observed degradation occurred only

  10. Properties of polypyrrole doped with alkylbenzene sulfonates

    Science.gov (United States)

    Bay, Lasse; Skaarup, Steen; West, Keld; Mazur, Tanja; Joergensen, Ole; Rasmussen, Helle D.

    2001-07-01

    Conducting polymers such as polypyrrole (PPy) doped with large anionic detergents have high stability in aqueous systems. PPy can be reversibly oxidised and reduced electrochemically. The redox change of PPy is accompanied by a change in volume of the polymer. This is partly ascribed to take-up of ions and solvent molecules. This volume change can be used as a polymer actuator (artificial muscle) working in a narrow voltage range (less than 1 V). The properties of the PPy polymer are largely determined by the dopant ions and also by the deposition conditions and the substrate. A free-standing 10 micrometers thick film is prepared electrochemically at a constant current from an aqueous solution of pyrrole and sodium alkylbenzene sulfonate. The mechanical properties of the film (tensile strength and Young's modulus) and the reversible linear elongation between the oxidised and reduced states are measured. Alkylbenzene sulfonates with alkyl chain lengths between 1 and 22 carbon atoms are used as dopant anion. The films made with the different anions have highly different properties and are here compared to outline the influence of the size of the anion. A maximum in linear elongation is found for p-(n-octyl)benzene sulfonate and in conductivity for p-(n-butyl)benzene sulfonate.

  11. Anaerobic degradation of linear alkylbenzene sulfonate

    DEFF Research Database (Denmark)

    Mogensen, Anders Skibsted; Haagensen, Frank; Ahring, Birgitte Kiær

    2003-01-01

    increases during anaerobic stabilization due to transformation of easily degradable organic matter. Hence, LAS is regarded as resistant to biodegradation under anaerobic conditions. We present data from a lab-scale semi-continuously stirred tank reactor (CSTR) spiked with linear dodecylbenzene sulfonate (C...

  12. Research on Preparation and Properties of Coated Polyether Silicone Microencapsulation Based on Polystyrene

    Directory of Open Access Journals (Sweden)

    Ren Shuiyun

    2015-01-01

    Full Text Available By the method of interfacial polymerization, the novel microcapsules were prepared with polystyrene as wall material and polyether silicone as core material. In order to demonstrate the morphologies, particle size distribution and properties of microcapsules, scanning electron microscopy (SEM, laser particle size analysis and infrared spectroscopy (FTIR are also applied in the experiments, and the thermal stability of microcapsules is obtained by thermal gravimetric (TG and differential scanning calorimetry (DSC. The material ratio (core to wall in weight of microcapsules and stirring rate ratio are discussed. The results show that under the optimum process conditions of a material ratio (core to wall in weight which is 4:10 and agitating rate of 500r·min‒1, the synthesized polyether silicone microcapsules have a higher yield and the coating and densification properties; their average size is 210μm, and the thermal stability temperature can reach up to 390°C.

  13. XPS investigations on the UV-laser ablation mechanism of poly(ether imide)

    Energy Technology Data Exchange (ETDEWEB)

    Wambach, J.; Kunz, T.; Schnyder, B.; Koetz, R.; Wokaun, A. [Paul Scherrer Inst. (PSI), Villigen (Switzerland)

    1999-08-01

    UV-Laser ablated samples of poly(ether imide) [Kapton{sup TM}] were studied with small-spot XPS. Applying fluences above the threshold level (0.167 J/cm{sup 2}) resulted in the expected behaviour of a decline of both nitrogen and oxygen. Below the threshold level a hint for an altered ablation mechanism was found. (author) 1 fig., 5 refs.

  14. EPR character of gadolinium complexes with noncyclic polyether Schiff bases and its solvent effects

    Institute of Scientific and Technical Information of China (English)

    姚克敏; 陈德余; 王晓南; 邓宁

    1996-01-01

    EPR characters of three new gadolinium complexes with noncydic polyether Schiff bases in powder or organic solvents, including various oxyethylene chain lengths and different substituting groups in ligands, are investigated respectively. Some regularities are summed up. The difference of EPR character in various solvents, particularly at different temperatures, has been examined. The ’single peak effect’ due to THF solvent at low temperature is observed for the first time. This phenomenon is explicated.

  15. Cloning and Characterization of the Polyether Salinomycin Biosynthesis Gene Cluster of Streptomyces albus XM211

    OpenAIRE

    Jiang, Chunyan; Wang, Hougen; Kang, Qianjin; Jing LIU; Bai, Linquan

    2012-01-01

    Salinomycin is widely used in animal husbandry as a food additive due to its antibacterial and anticoccidial activities. However, its biosynthesis had only been studied by feeding experiments with isotope-labeled precursors. A strategy with degenerate primers based on the polyether-specific epoxidase sequences was successfully developed to clone the salinomycin gene cluster. Using this strategy, a putative epoxidase gene, slnC, was cloned from the salinomycin producer Streptomyces albus XM211...

  16. UV-Surface Treatment of Fungal Resistant Polyether Polyurethane Film-Induced Growth of Entomopathogenic Fungi

    Directory of Open Access Journals (Sweden)

    Gabriela Albara Lando

    2017-07-01

    Full Text Available Synthetic polymers are the cause of some major environmental impacts due to their low degradation rates. Polyurethanes (PU are widely used synthetic polymers, and their growing use in industry has produced an increase in plastic waste. A commercial polyether-based thermoplastic PU with hydrolytic stability and fungus resistance was only attacked by an entomopathogenic fungus, Metarhiziumanisopliae, when the films were pre-treated with Ultraviolet (UV irradiation in the presence of reactive atmospheres. Water contact angle, Fourier transform infrared spectroscopy in attenuated total reflection mode (FTIR-ATR, scanning electron microscopy (SEM, and profilometer measurements were mainly used for analysis. Permanent hydrophilic PU films were produced by the UV-assisted treatments. Pristine polyether PU films incubated for 10, 30, and 60 days did not show any indication of fungal growth. On the contrary, when using oxygen in the UV pre-treatment a layer of fungi spores covered the sample, indicating a great adherence of the microorganisms to the polymer. However, if acrylic acid vapors were used during the UV pre-treatment, a visible attack by the entomopathogenic fungi was observed. SEM and FTIR-ATR data showed clear evidence of fungal development: growth and ramifications of hyphae on the polymer surface with the increase in UV pre-treatment time and fungus incubation time. The results indicated that the simple UV surface activation process has proven to be a promising alternative for polyether PU waste management.

  17. Sulindac Sulfide, but Not Sulindac Sulfone, Inhibits Colorectal Cancer Growth

    Directory of Open Access Journals (Sweden)

    Christopher S. Williams

    1999-06-01

    Full Text Available Sulindac sulfide, a metabolite of the nonsteroidal antiinflammatory drug (NSAID sulindac sulfoxide, is effective at reducing tumor burden in both familial adenomatous polyposis patients and in animals with colorectal cancer. Another sulindac sulfoxide metabolite, sulindac sulfone, has been reported to have antitumor properties without inhibiting cyclooxygenase activity. Here we report the effect of sulindac sulfone treatment on the growth of colorectal carcinoma cells. We observed that sulindac sulfide or sulfone treatment of HCA-7 cells led to inhibition of prostaglandin E2 production. Both sulindac sulfide and sulfone inhibited HCA-7 and HCT-116 cell growth in vitro. Sulindac sulfone had no effect on the growth of either HCA-7 or HCT-116 xenografts, whereas the sulfide derivative inhibited HCA-7 growth in vivo. Both sulindac sulfide and sulfone inhibited colon carcinoma cell growth and prostaglandin production in vitro, but sulindac sulfone had no effect on the growth of colon cancer cell xenografts in nude mice.

  18. Dynamic Viscosity for HFC-134a + Polyether Mixtures up to 373.15 K and 140 MPa at Low Polyether Concentration. Measurements and Modeling

    CERN Document Server

    Comuñas, Maria J P; Boned, Christian; Fernandez, Josefa

    2008-01-01

    This paper reports viscosity data for mixtures containing a refrigerant (HFC-134a) and a lubricant (triethylene glycol dimethyether, TriEGDME, or tetraethylene glycol dimethyl ether, TEGDME), at 12% of TriEGDME or 14% mass fraction of TEGDME. The measurements (140 data points) were obtained at various pressures (between 10 and 140 MPa) in the monophasic liquid state from 293.15 to 373.15 K. Because HFC-134a and the polyethers are not in the same single phase at normal pressure and temperature (the refrigerant is a gas, whereas the polyethers are liquids), accurate measurements of their mixtures require specific procedures for preparation of the samples and filling of the apparatus. A specially designed isobaric-transfer falling-body viscometer is used in this work. The viscosities of the mixtures are, on average, 40% higher than that of the pure refrigerant, and this increase is more noticeable at low temperatures. The experimental viscosities have been used to check the predictive and correlation ability of ...

  19. Synthesis and Properties of Terminated Polyether%封端聚醚的合成及性能研究

    Institute of Scientific and Technical Information of China (English)

    程亮; 张东恒

    2015-01-01

    Alkyl terminated polyether was prepared in high yield by using sodium methoxide as alkaline reagent and methyl chloride as alkyl terminated reagent. The structures of the products were characterized by means of infrared spectroscopy ( IR) , nuclear magnetic resonance ( NMR) and gel permeation chromatography ( GPC) . Compared the physical and chemi-cal properties of the alkyl terminated polyether with unsealed polyether, it was found that the alkyl terminated polyether has lower viscosity and higher viscosity index. The anti-oxidation performances of the two kinds of polyether were investigated by rotary oxygen bomb test method ( ROBT) . By the study of the suitability of different antioxidants in two kinds of poly-ether, the antioxidant suitable for alkyl terminated polyether was developed, which can make the ROBT reach to 1950 mi-nutes.%以甲醇钠作为碱性试剂,一氯甲烷为封端试剂,高产率制备了烷基封端聚醚. 并通过红外光谱( IR)、核磁共振( NMR)和凝胶渗透色谱( GPC)对其进行表征. 对比了两种聚醚的指标变化,结果发现,封端聚醚具有更低的黏度、更高的黏度指数. 利用旋转氧弹测试方法考察了封端聚醚与未封端聚醚的抗氧化性能,通过考察不同抗氧剂在两种聚醚中的适应性,开发了适合封端聚醚的抗氧体系,该抗氧体系可以使封端聚醚的旋转氧弹时间达到1950 min.

  20. Highly branched sulfonated poly(fluorenyl ether ketone sulfone)s membrane for energy efficient vanadium redox flow battery

    Science.gov (United States)

    Yin, Bibo; Li, Zhaohua; Dai, Wenjing; Wang, Lei; Yu, Lihong; Xi, Jingyu

    2015-07-01

    A series of highly branched sulfonated poly (fluorenyl ether ketone sulfone)s (HSPAEK) are synthesized by direct polycondensation reactions. The HSPAEK with 8% degree of branching is further investigated as membrane for vanadium redox flow battery (VRFB). The HSPAEK membrane prepared by solution casting method exhibits smooth, dense and tough morphology. It possesses very low VO2+ permeability and high ion selectivity compared to those of Nafion 117 membrane. When applied to VRFB, this novel membrane shows higher coulombic efficiency (CE, 99%) and energy efficiency (EE, 84%) than Nafion 117 membrane (CE, 92% and EE, 78%) at current density of 80 mA cm-2. Besides, the HSPAEK membrane shows super stable CE and EE as well as excellent discharge capacity retention (83%) during 100 cycles life test. After being soaked in 1.5 mol L-1 VO2+ solution for 21 days, the weight loss of HSPAEK membrane and the amount of VO2+ reduced from VO2+ are only 0.26% and 0.7%, respectively, indicating the superior chemical stability of the membrane.

  1. Photolytic treatment of aqueous linear alkylbenzene sulfonate.

    Science.gov (United States)

    Venhuis, Sarah Hatfield; Mehrvar, Mehrab

    2005-01-01

    Treatment of a model detergent compound, linear alkylbenzene sulfonate (LAS), using photolytic processes was studied. In the photolytic degradation of LAS, both ultraviolet (UV) light at 254 nm wavelength and its combination with hydrogen peroxide (H2O2) were investigated. Based on first-order rate constants, it was shown that 5000 mg/L of H2O2 for degradation of a 100-mg/L solution of linear alkylbenzene sulfonate was optimum. Addition of H2O2 at different illumination times with UV light at 254 nm did not improve first-order rate constants compared with the addition of H2O2 at the start of illumination. Degradation rates of the model compound (LAS) with three detergents were compared.

  2. STUDY ON LIGHTLY SULFONATED SYNDIOTACTIC POLYSTYRENE IONOMERS

    Institute of Scientific and Technical Information of China (English)

    Jin Wang; Fang-ming Zhu; Jin-cheng Lui; Hua-ming Li; Shang-an Lin

    2001-01-01

    ulfonated syndiotactic polystyrene ionomers (SsPS) with 1.8 mol% degree of sulfonation have been studied.SWAXD shows that the crystallinity of SsPS ionomers was decreased with increasing diameter size of the counter ions and sPS > SsPS-H > SsPS-K > SsPS-Zn. Moreover, SsPS ionomers only have α crystal form, while original sPS has two crystal forms: α and β crystal form. TGA shows that the thermal stability of SsPS ionomers is higher than that of the original sPS and SsPS-Zn > SsPS-K > SsPS-H. DSC shows that all the glass transition temperatures (Tg) of SsPS ionomers are higher than that of the neat sPS and SsPS-Zn > SsPS-Na > SsPS-K > SsPS-H. However, the melting temperature (Tm) and crystallization peak temperature (Tp) of SsPS ionomers are lower and SsPS-H > SsPS-Zn > SsPS-K > SsPS-Na, while the crystallinity (Xc) of SsPS-Zn is the lowest. Nonisothermal crystallization kinetics shows that the Avrami index of sPS and SsPS-H are both about 4, suggesting the nucleation growth of SsPS-H with lower degree of sulfonation still keeps its threedimension form. FTIR spectra of SsPS ionomers show a splitting absorption band for asymmetric stretching vibration of sulfonation group. The CH in-plane bending vibration of benzene ring shifted to higher wavenumber and the symmetric stretching vibration of sulfonation group changed slightly with different counter ion neutralized SsPS ionomers.

  3. Poly-ethers from Winogradskyella poriferorum: Antifouling potential, time-course study of production and natural abundance

    KAUST Repository

    Dash, Swagatika

    2011-08-01

    A sponge-associated bacterium, Winogradskyella poriferorum strain UST030701-295T was cultured up to 100l for extraction of antifouling bioactive compounds. Five poly-ethers were isolated and partially characterized based on nuclear magnetic resonance (NMR) spectroscopy and mass spectrometry (MS); two of them showed inhibitory effects on biofilm formation of marine bacteria and larval settlement of macro-foulers but did not produce any adverse effects on the phenotypes of zebra fish embryos at a concentration of 5μgml -1. The effect of culture duration on the production of the poly-ethers and the bioactivity of the relevant extracts was monitored over a period of 12days. The total crude poly-ether production increased from day 2 to day 5 and the highest bioactivity was observed on day 3. The poly-ethers were found to be localized in the cellular fraction of the extracts, implying their natural occurrence. The potent bioactivity of these poly-ethers together with their high natural abundance in bacteria makes them promising candidates as ingredients in antifouling applications. © 2011 Elsevier Ltd.

  4. The Effect of Sulfonation and Neutralization on the Dynamics of Zn Neutralized Sulfonated Polystyrene Ionomers

    Science.gov (United States)

    Castagna, Alicia; Wang, Wenqin; Winey, Karen I.; Runt, James

    2011-03-01

    The effect of sulfonation and neutralization levels on structure and dynamics of Zn neutralized sulfonated polystyrene (SPS) ionomers were investigated using scanning transmission electron microscopy (STEM), X-ray scattering, and dielectric relaxation spectroscopy. STEM and X-ray scattering revealed the presence of spherical aggregates 2 nm in diameter. Successful fitting of the scattering data to the Kinning-Thomas modified hard sphere model revealed that aggregate size is independent of degree of sulfonation and neutralization level, and that aggregate composition becomes increasingly ionic with increasing neutralization. Two segmental relaxations were identified in dielectric loss spectra corresponding to cooperative motion of chain segments in the unrestricted matrix and motions of chain segments restricted by aggregates. A Maxwell-Wagner-Sillars interfacial polarization process was revealed, with relaxation times that were in good agreement with predictions from a simple model of dispersed ionic spheres.

  5. SULFONATION OF A NEW POLYETHERETHERKETONE PREPARED FROM PHENOLPHTHALEIN

    Institute of Scientific and Technical Information of China (English)

    CHEN Tianlu; YUAN Yagui; ZHANG Manhua; CHEN Zhongqing; XU Jiping

    1990-01-01

    A novel polyetheretherketone (PEK-C) prepared from phenolphthalein has been synthesized. In order to improve some of its properties for application in high performance membrane, the PEK-C has been sulfonated with concentrated sulfuric acid. Degree of sulfonation can be regulated by controlling the temperature and time of sulfonation. The characterization of the sulfonated PEK-C in sodium salt form has been made by IR, 1H NMR and 13C NMR etc. It is shown that the sulfonation appears to take place exclusively in the ortho position to phenolic ether of phenolphthalein unit. The result is in agreement with theoretical deduction. Some properties of the sulfonated PEK-C, such as solubility, transition temperature, thermal degradation and hydrophilicity have also been discussed.

  6. Phosphorus-containing sulfonated polyimides for proton exchange membranes

    OpenAIRE

    2008-01-01

    Synthesis and characterization of the novel sulfonated BAPPO monomer and its use in the synthesis of a new phosphine oxide-based sulfonated polyimide are described. BTDA, 6FDA, and DDS were used as monomers in the polyimide synthesis. Sulfonated polyimide membranes were obtained by a solution thermal imidization method. The thermal behavior of the polymers was investigated by DSC and TGA. The morphological structure of the membranes was investigated by tapping-mode AFM. The proton conductivit...

  7. Preparation of Sulfonated Poly(aryl ether sulfone) Electrospun Mat/Phosphosilicate Composite Proton Exchange Membrane

    Science.gov (United States)

    Wang, Limei; Dou, Liyan; Guan, Guoying

    2017-03-01

    Side-chain-type sulfonated poly(aryl ether sulfone) (SPES) was synthesized and then electrospun into mats. Phosphosilicate glass (PS) via in situ sol-gel synthesis was enclosed in the mats to form a new reinforced composite membrane. The SPES/PS composite membranes showed satisfactory dimensional change behavior with varying humidity. Especially, the composite membrane exhibits excellent proton conductivity at harsh measurement conditions of low humidity at 80°C. The composite membrane with outstanding combined properties has potential applications for high temperature polymer electrolyte membrane fuel cells.

  8. Preparation of Sulfonated Poly(aryl ether sulfone) Electrospun Mat/Phosphosilicate Composite Proton Exchange Membrane

    Science.gov (United States)

    Wang, Limei; Dou, Liyan; Guan, Guoying

    2017-01-01

    Side-chain-type sulfonated poly(aryl ether sulfone) (SPES) was synthesized and then electrospun into mats. Phosphosilicate glass (PS) via in situ sol-gel synthesis was enclosed in the mats to form a new reinforced composite membrane. The SPES/PS composite membranes showed satisfactory dimensional change behavior with varying humidity. Especially, the composite membrane exhibits excellent proton conductivity at harsh measurement conditions of low humidity at 80°C. The composite membrane with outstanding combined properties has potential applications for high temperature polymer electrolyte membrane fuel cells.

  9. Hydrolysis of p-Nitrophenyl Picolinate Catalyzed by Mono-and Binuclear Transition Metal Complexes with Polyether Bridged Dihydroxamic Acid

    Institute of Scientific and Technical Information of China (English)

    李建章; 李鸿波; 冯发美; 谢家庆; 李慎新; 周波; 秦圣英

    2005-01-01

    Two polyether bridged dihydroxamic acids and their mono-and binuclear manganese(Ⅱ), zinc(Ⅱ) complexes have been synthesized and employed as models to mimic hydrolase in catalytic hydrolysis of p-nitrophenyl picolinate (PNPP). The reaction kinetics and the mechanism of hydrolysis of PNPP have been investigated. The kinetic mathematical model for PNPP cleaved by the complexes has been proposed. The effects of the different central metal ion, mono-and binuclear metal, the pseudo-macrocyclic polyether constructed by polyethoxy group of the complexes, and reactive temperature on the rate for catalytic hydrolysis of PNPP have been examined. The results showed that the transition metal dthydroxamates exhibited high catalytic activity to the hydrolysis of PNPP, the catalytic activity of binuclear complexes was higher than that of mononuclear ones, and the pseudo-macrocyclic polyether might synergetically activate H20 coordinated to metal ion with central metal ion together and promote the catalytic hydrolysis of PNPP.

  10. Polymerization behaviour of butyl bis(hydroxymethyl)phosphine oxide: Phosphorus containing polyethers for Li-ion conductivity

    Indian Academy of Sciences (India)

    Heeralal Vignesh Babu; Billakanti Srinivas; Khevath Praveen Kumar Naik; Krishnamurthi Muralidharan

    2015-04-01

    Synthesis of phosphorus containing polyethers and their lithium-ion conductivities for the potential use as solid polymer electrolyte (SPE) in high-energy density lithium-ion batteries have been described. Co-polymerization of butyl bis(hydroxymethyl)phosphine oxide with three different dibromo monomers were carried out to produce three novel phosphorous containing polyethers (P1–P3). These polymers were obtained via nucleophilic substitution reactions and were characterized by 1H, 31P NMR spectral data and gel permeation chromatography. SPEs were prepared using polyethers (P1 and P2) with various amounts of lithium bis(trifluoromethanesulfonyl)imide (LiTFSI). The lithium-ion conductivity of SPE2 containing 40 wt% of LiTFSI was 2.1 × 10−5 S cm−1 at room temperature and 3.7 × 10−4 S cm−1 at 80°C.

  11. Langmuir and Langmuir-Blodgett films of multifunctional, amphiphilic polyethers with cholesterol moieties.

    Science.gov (United States)

    Reuter, Sascha; Hofmann, Anna M; Busse, Karsten; Frey, Holger; Kressler, Jörg

    2011-03-01

    Langmuir films of multifunctional, hydrophilic polyethers containing a hydrophobic cholesterol group (Ch) were studied by surface pressure-mean molecular area (π-mmA) measurements and Brewster angle microscopy (BAM). The polyethers were either homopolymers or diblock copolymers of linear poly(glycerol) (lPG), linear poly(glyceryl glycidyl ether) (lPGG), linear poly(ethylene glycol) (lPEG), or hyperbranched poly(glycerol) (hbPG). Surface pressure measurements revealed that the homopolymers lPG and hbPG did not stay at the water surface after spreading and solvent evaporation, in contrast to lPEG. Because of the incorporation of the Ch group in the polymer structure, stable Langmuir films were formed by Ch-lPG(n), Ch-lPGG(n), and Ch-hbPG(n). The Ch-hbPG(n), Ch-lPEG(n), Ch-lPEG(n)-b-lPG(m), Ch-lPEG(n)-b-lPGG(m), and Ch-lPEG(n)-b-hbPG(m) systems showed an extended plateau region assigned to a phase transition involving the Ch groups. Typical hierarchically ordered morphologies of the LB films on hydrophilic substrates were observed for all Ch-initiated polymers. All LB films showed that Ch of the Ch-initiated homopolymers is able to crystallize. This strong tendency of self-aggregation then triggers further dewetting effects of the respective polyether entities. Fingerlike morphologies are observed for Ch-lPEG(69), since the lPEG(69) entity is able to undergo crystallization after transfer onto the silicon substrate.

  12. Accelerated simulations of aromatic polymers: application to polyether ether ketone (PEEK)

    Science.gov (United States)

    Broadbent, Richard J.; Spencer, James S.; Mostofi, Arash A.; Sutton, Adrian P.

    2014-10-01

    For aromatic polymers, the out-of-plane oscillations of aromatic groups limit the maximum accessible time step in a molecular dynamics simulation. We present a systematic approach to removing such high-frequency oscillations from planar groups along aromatic polymer backbones, while preserving the dynamical properties of the system. We consider, as an example, the industrially important polymer, polyether ether ketone (PEEK), and show that this coarse graining technique maintains excellent agreement with the fully flexible all-atom and all-atom rigid bond models whilst allowing the time step to increase fivefold to 5 fs.

  13. An olefin metathesis-iodoetherification-dehydroiodination strategy for spiroketal subunits of the polyether antibiotics

    Science.gov (United States)

    Tony, Kurissery A.; Dabideen, Darrin; Li, Jialiang; Díaz-Hernández, Maria Dolores; Jiménez-Barbero, Jesús; Mootoo, David R.

    2012-01-01

    The convergent synthesis of two pentacyclic analogs of the polyether monensin A is described. Although different with respect to the configuration of the alcohol at the 3 position of the six membered ring of the spiroketal subunit, the configuration at the acetal center in both structures is unchanged and is consistent with the anomeric effect. The key synthetic steps are the coupling of two complex segments via an olefin metathesis, and the subsequent conversion of a dihydroxyalkene to the spiroketal through an iodoetherification-dehydroiodination sequence. The compatibility of these transformations with a variety of functional groups makes the overall strategy appropriate for highly substituted frameworks. PMID:19813766

  14. Dispersion of Co-poly Carboxylate Superplasticizer Containing Polyether Side Chain

    Institute of Scientific and Technical Information of China (English)

    2006-01-01

    Free radical co-polymerization was employed to synthesize co-poly carboxylate (PC) superplasticizers with different amount of carboxyl and methyl polyethylene glycol (MPEG) side chain.Dispersion ability and retention of PC were compared with one another. The results show that increase of side chain is advantageous to dispersion, but it decreases when amount of MPEG is beyond a certain value which is different with the proportion of carboxyl. If the amount of carboxyl increases, the influence of side chain in copolymer on dispersion diminishes. Polyether side chain is advantageous to retention. And the author explained the mechanism of PC using the theory of steric repulsive force.

  15. SYNTHESIS AND CHARACTERIZATION OF Si-CONTAINING POLYESTER-POLYETHER MULTIBLOCK COPOLYMERS

    Institute of Scientific and Technical Information of China (English)

    LI Zhenyi; ZHU Jin

    1996-01-01

    A series of Si-containing polyester-polyether multiblock copolymers were synthesized by transesterification and melt copolycondensation of organosilicon monomers [1, 1, 3, 3-tetramethyl-1, 3-bis (p-carbomethoxyphenyl) disiloxane] (I) or dimethyl bis (p-carbomethoxyphenyl) silane] (II) and dimethyl terephthalate (DMT), with 1, 4-butanediol, polytetramethylene glycol (PTMG) respectively. The organosilicon monomers were prepared by Grinard reaction, oxidation and esterification. The structures of the above monomers (Ⅰ), (Ⅱ) and the copolymers were characterized by MS anal. and 1H-NMR.

  16. SYNTHESES OF POLYSTYRENE RESINS CONTAINING POLYETHER OLIGOMERS AND THEIR EXTRACTION FOR GOLD (Ⅲ)

    Institute of Scientific and Technical Information of China (English)

    DONG Shihua; LIU Shi; XU Yuwu

    1994-01-01

    Three polystyrene resins containing polyether oligomers as extractants were synthesized and their extraction properties were studied. Gold (Ⅲ) ion could be extracted rapidly by the resins (T1/2<1min.)with high efficiency and capacity (for LS-B resin that were 99.8% and 95.8mg/gR respectively) from aqueous solution but most of the co-existing metal ions such as Pd (Ⅱ),Cu(Ⅱ), Zn (Ⅱ), Pb (Ⅱ) and Cd (Ⅱ) were remained. The extraction capacity and stripping percentage for gold (Ⅲ) remained unchanged in four extraction-stripping cycles. The resins also showed good column extraction-elution properties.

  17. Binding of alkali metal ions by cyclic polyethers: significance in ion transport processes.

    Science.gov (United States)

    Izatt, R M; Rytting, J H; Nelson, D P; Haymore, B L; Christensen, J J

    1969-04-25

    Values for the formation constant (log K), the change in enthalpy (triangle upH degrees ), and the change in entropy (triangle upS degrees ) have been determined for the interaction of lithium, sodium, potassium, rubidium, and cesium ions with the two isomers of the cyclic polyether, 2,5,8,15,18,21-hexaoxatricyclo[20.4.0.0(9,14)] hexacosane. The stability order of these metal ions with either isomer is identical to the permeability order for these same metal ions with the structurally related antibiotics, valinomycin and monactin.

  18. Pore size and concentration effect of mesoporous silica nanoparticles on the coefficient of thermal expansion and optical transparency of poly(ether sulfone) films.

    Science.gov (United States)

    Vo, Nhat Tri; Patra, Astam K; Kim, Dukjoon

    2017-01-18

    Mesoporous silica nanoparticles (MSNs) with uniform size (thermal expansion (CTE) without sacrificing optical transparency. Here, both CTE and optical transparency of the MSN/PES nanocomposite films gradually decreased with increasing MSN concentration. The PES films containing MSNs with larger pores showed the best performance in CTE and optical transparency. While the CTE decreased by 32.3% with increasing MSN content up to 0.5 wt%, the optical transparency decreased by only less than 6.9% because of the small and uniform particle size of less than 50 nm, which minimizes light scattering. This pore size effect is more clearly observed via an annealing process, which enables the polymer chains to slowly move and fill in the free volume in the pores of the MSN, and thus restricts the thermal motion. The effect of the silica nanoparticles was investigated not only on the thermal stability but also on the mechanical stability. We expect the MSNs synthesized in this study to be used as a promising filler to enhance the thermal and mechanical stability of the PES substrate without sacrificing its optical transparency.

  19. Solid State Nuclear Magnetic Resonance Investigation of Polymer Backbone Dynamics in Poly(Ethylene Oxide) Based Lithium and Sodium Polyether-ester-sulfonate Ionomers

    Energy Technology Data Exchange (ETDEWEB)

    Roach, David J.; Dou, Shichen; Colby, Ralph H.; Mueller, Karl T.

    2013-01-01

    Polymer backbone dynamics of single ion conducting poly(ethylene oxide) (PEO)-based ionomer samples with low glass transition temperatures (Tg) have been investigated using solid-state nuclear magnetic resonance (NMR). Experiments detecting 13C with 1H decoupling under magic angle spinning (MAS) conditions identified the different components of the polymer backbone (PEO spacer and isophthalate groups) and their relative mobilities for a suite of lithium- and sodium-containing ionomer samples with varying cation contents. Variable temperature (203-373 K) 1H-13C cross-polarization MAS (CP-MAS) experiments also provided qualitative assessment of the differences in the motions of the polymer backbone components as a function of cation content and identity. Each of the main backbone components exhibit distinct motions, following the trends expected for motional characteristics based on earlier Quasi Elastic Neutron Scattering and 1H spin-lattice relaxation rate measurements. Previous 1H and 7Li spin-lattice relaxation measurements focused on both the polymer backbone and cation motion on the nanosecond timescale. The studies presented here assess the slower timescale motion of the polymer backbone allowing for a more comprehensive understanding of the polymer dynamics. The temperature dependences of 13C linewidths were used to both qualitatively and quantitatively examine the effects of cation content and identity on PEO spacer mobility. Variable contact time 1H-13C CP-MAS experiments were used to further assess the motions of the polymer backbone on the microsecond timescale. The motion of the PEO spacer, reported via the rate of magnetization transfer from 1H to 13C nuclei, becomes similar for T ≳ 1.1 Tg in all ionic samples, indicating that at similar elevated reduced temperatures the motions of the polymer backbones on the microsecond timescale become insensitive to ion interactions. These results present an improved picture, beyond those of previous findings, for the dependence of backbone dynamics on cation density (and here, cation identity as well) in these amorphous PEO-based ionomer systems.

  20. Blending of styrene-block-butadiene-block-styrene copolymer with sulfonated vinyl aromatic polymers

    OpenAIRE

    Ruggeri, Giacomo; Passaglia, Elisa; Giorgi, Ivan; Picchioni, Francesco; Aglietto, Mauro

    2001-01-01

    Different polymers containing sulfonic groups attached to the phenyl rings were prepared by sulfonation of polystyrene (PS) and styrene-block-(ethylene-co-1-butene)-block-styrene (SEBS). The sulfonation degree (SD) was varied between 1 and 20 mol% of the styrene units. Polyphase materials containing sulfonated units were prepared by blending styrene-block-butadiene-block-styrene (SBS), with both sulfonated PS and sulfonated SEBS in a Brabender mixer. Such a procedure was performed as an alter...

  1. Lithiated and sulphonated poly(ether ether ketone) solid state electrolyte films for supercapacitors

    Energy Technology Data Exchange (ETDEWEB)

    Chiu, K.-F.; Su, S.-H., E-mail: minimono42@gmail.com

    2013-10-01

    Poly(ether ether ketone) (PEEK) films have been synthesised and used as solid-state electrolytes for supercapacitors. In order to increase their ion conductivity, the PEEK films were sulphonated by sulphuric acid, and various amounts of LiClO{sub 4} were added. The solid-state electrolyte films were characterised by Fourier transform infrared spectroscopy, scanning electron microscopy, energy-dispersive X-ray spectroscopy, and thermogravimetric analysis. The ionic conductivities of the electrolyte films were analysed by performing electrochemical impedance spectroscopy. The obtained electrolyte films can be sandwiched or directly coated on activated carbon electrodes to form solid-state supercapacitors. The electrochemical characteristics of these supercapacitors were investigated by performing cyclic voltammetry and charge–discharge tests. Under an optimal content of LiClO{sub 4}, the supercapacitor can provide a capacitance as high as 190 F/g. After 1000 cycles, the supercapacitors show almost no capacitance fading, indicating high stability of the solid-state electrolyte films. - Highlights: • Poly(ether ether ketone) (PEEK) films have been used as solid-state electrolytes. • LiClO4 addition can efficiently improve the ionic conductivity. • Supercapacitors using PEEK electrolyte films deliver high capacitance.

  2. Isocyanate-terminated Polyethers Toughened Epoxy Resin: Chemical Modification, Thermal Properties, and Mechanical Strength

    Institute of Scientific and Technical Information of China (English)

    CAI Haopeng; WANG Jun; WANG Xiang; XU Renxin

    2007-01-01

    The toughening of the diglycidyl ether of bisphenol A epoxy resin with isocyanateterminated polyethers (ITPE) was investigated. The progress of the reaction and the structural changes during modification process were studied using FTIR spectroscopy. The studies support the proposition that TDI (tolylene diisocyanate) acts as a coupling agent between the epoxy and polyethers, forming a urethane linkage with the former and the latter, respectively. Me THPA-cured ER/ITPs blends were characterized using dynamic mechanical analysis (DMA) and thermogravimetric analysis (TGA). It is indicated the glass transition temperature (Tg) of systems was lower than the Tg of pure epoxy resin and overfull ITPE separated from the modified epoxy resin and formed another phase at an ITPE-content of more than 10wt%. The thermal stability was decreased by the introduction of ITPE. The impact strength and the flexural strength of the cured modifiedepoxy increased with increasing the ITPE content and a maximum plateau value of about 24.03 kJ/m2 and 130.56 MPa was measured in 10wt% ITPE. From scanning electron microscopy (SEM) studies of the fractrue surfaces of ER/ITPE systems, the nature of the micromechanisms responsible for the increases in toughness of the systems was identified.

  3. Assessment of Physical Stability and Antioxidant Activity of Polysiloxane Polyalkyl Polyether Copolymer-Based Creams

    Directory of Open Access Journals (Sweden)

    Atif Ali

    2013-01-01

    Full Text Available The purpose of the present work was to investigate the changes on physical stability (color, creaming, liquefaction, pH, conductivity, centrifugation, viscosity and rheological parameters by non-ionic surfactant polysiloxane polyalkyl polyether copolymer based creams following inclusion of plant extract containing phenolic compounds. The antioxidant activity of the plant extract alone and after addition in the cream was assessed using the stable free radical 1,1-diphenyl-2-picrylhydrazyl (DPPH assay. Physical stability was assessed by submitting the creams to storage at 8°C, 25°C, 40°C, and at 40°C with 70% RH (relative humidity for a period of two months. Physical characteristics of polysiloxane polyalkyl polyether copolymer based creams, that is, color, creaming, liquefaction, centrifugation and pH were noted at various intervals for 2 months. The viscosities and rheological behavior of creams were determined using a rotational rheometer. Data were analyzed by using Brookfield Software Rheocalc version (2.6 with IPC Paste and Power Law (PL math models. Cream with plant extract showed pseudo plastic behaviour with decreasing on viscosity. The Acacia nilotica (AN extract alone and the cream containing this extract showed great antioxidant and free radical scavenging activities. Power Law and IPC analysis were found to fit all the rheograms.

  4. Polyether precursors of molecular recognition systems based on the 9,10-anthraquinone moiety

    Science.gov (United States)

    Wcisło, Anna; Cirocka, Anna; Zarzeczańska, Dorota; Niedziałkowski, Paweł; Nakonieczna, Sandra; Ossowski, Tadeusz

    2015-02-01

    A series of novel polyether derivatives of 9,10-anthraquinone (AQ) was synthesized and characterized by means of UV-Vis spectroscopy, acid-base titration and complexometric titration. The results were compared with 1-NEt2AQ and 1-NHEtAQ - model compounds of alkylaminoanthraquinones. Acetonitrile and methanol were used as solvents for determination of spectroscopic and acid-base properties. Complexometric titrations were carried out exclusively in acetonitrile. Spectral characteristic of these compounds strongly depends on pH. Addition of acid causes the decrease of absorption intensity and in some cases also a shift of the visible range band. The weakest base is the compound (2), and the strongest - compound (1), both in methanol and acetonitrile solution. The introduction of an additional substituent in the position 8 of the anthraquinone compound increases its basicity. The presence of metal ions causes changes in intensity of absorption (decrease for compounds (2) and (3) and increase with bathochromic shift for (1) and (4)). For the determination of the coordination properties aluminum (III) ions were chosen. The highest complex stability constant with Al (III) ions is observed for compound (1), and the weakest for compound (3). The elongation of the polyether chain decreases the stability of the complex formed.

  5. Salinomycin and other polyether ionophores are a new class of antiscarring agent.

    Science.gov (United States)

    Woeller, Collynn F; O'Loughlin, Charles W; Roztocil, Elisa; Feldon, Steven E; Phipps, Richard P

    2015-02-06

    Although scarring is a component of wound healing, excessive scar formation is a debilitating condition that results in pain, loss of tissue function, and even death. Many tissues, including the lungs, heart, skin, and eyes, can develop excessive scar tissue as a result of tissue injury, chronic inflammation, or autoimmune disease. Unfortunately, there are few, if any, effective treatments to prevent excess scarring, and new treatment strategies are needed. Using HEK293FT cells stably transfected with a TGFβ-dependent luciferase reporter, we performed a small molecule screen to identify novel compounds with antiscarring activity. We discovered that the polyether ionophore salinomycin potently inhibited the formation of scar-forming myofibroblasts. Salinomycin (250 nm) blocked TGFβ-dependent expression of the cardinal myofibroblast products α smooth muscle actin, calponin, and collagen in primary human fibroblasts without causing cell death. Salinomycin blocked phosphorylation and activation of TAK1 and p38, two proteins fundamentally involved in signaling myofibroblast and scar formation. Expression of constitutively active mitogen activated kinase kinase 6, which activates p38 MAPK, attenuated the ability of salinomycin to block myofibroblast formation, demonstrating that salinomycin targets the p38 kinase pathway to disrupt TGFβ signaling. These data identify salinomycin and other polyether ionophores as novel potential antiscarring therapeutics.

  6. Cloning and characterization of the polyether salinomycin biosynthesis gene cluster of Streptomyces albus XM211.

    Science.gov (United States)

    Jiang, Chunyan; Wang, Hougen; Kang, Qianjin; Liu, Jing; Bai, Linquan

    2012-02-01

    Salinomycin is widely used in animal husbandry as a food additive due to its antibacterial and anticoccidial activities. However, its biosynthesis had only been studied by feeding experiments with isotope-labeled precursors. A strategy with degenerate primers based on the polyether-specific epoxidase sequences was successfully developed to clone the salinomycin gene cluster. Using this strategy, a putative epoxidase gene, slnC, was cloned from the salinomycin producer Streptomyces albus XM211. The targeted replacement of slnC and subsequent trans-complementation proved its involvement in salinomycin biosynthesis. A 127-kb DNA region containing slnC was sequenced, including genes for polyketide assembly and release, oxidative cyclization, modification, export, and regulation. In order to gain insight into the salinomycin biosynthesis mechanism, 13 gene replacements and deletions were conducted. Including slnC, 7 genes were identified as essential for salinomycin biosynthesis and putatively responsible for polyketide chain release, oxidative cyclization, modification, and regulation. Moreover, 6 genes were found to be relevant to salinomycin biosynthesis and possibly involved in precursor supply, removal of aberrant extender units, and regulation. Sequence analysis and a series of gene replacements suggest a proposed pathway for the biosynthesis of salinomycin. The information presented here expands the understanding of polyether biosynthesis mechanisms and paves the way for targeted engineering of salinomycin activity and productivity.

  7. Isopropyl Myristate-Modified Polyether-Urethane Coatings as Protective Barriers for Implantable Medical Devices

    Directory of Open Access Journals (Sweden)

    Pankaj Vadgama

    2009-06-01

    Full Text Available Polyurethane films have potential applications in medicine, especially for packaging implantable medical devices. Although polyether-urethanes have superior mechanical properties and are biocompatible, achieving water resistance is still a challenge. Polyether based polyurethanes with two different molecular weights (PTMO1000, PTMO2000 were prepared from 4,4’-diphenylmethane diisocyanate and poly(tetra-methylene oxide. Polymer films were introduced using different concentrations (0.5-10 wt % of isopropyl myristate lipid (IPM as a non-toxic modifying agent. The physical and mechanical properties of these polymers were characterised using physical and spectroscopy techniques (FTIR, Raman, DSC, DMA, tensile testing. Water contact angle and water uptake of the membranes as a function of IPM concentration was also determined accordingly. The FTIR and Raman data indicate that IPM is dispersed in polyurethane at ≤ 2wt% and thermal analysis confirmed this miscibility to be dependent on soft segment length. Modified polymers showed increased tensile strength and failure strain as well as reduced water uptake by up to 24% at 1-2 wt% IPM.

  8. Molecular dynamics simulations to calculate glass transition temperature and elastic constants of novel polyethers.

    Science.gov (United States)

    Sarangapani, Radhakrishnan; Reddy, Sreekantha T; Sikder, Arun K

    2015-04-01

    Molecular dynamics simulations studies are carried out on hydroxyl terminated polyethers that are useful in energetic polymeric binder applications. Energetic polymers derived from oxetanes with heterocyclic side chains with different energetic substituents are designed and simulated under the ensembles of constant particle number, pressure, temperature (NPT) and constant particle number, volume, temperature (NVT). Specific volume of different amorphous polymeric models is predicted using NPT-MD simulations as a function of temperature. Plots of specific volume versus temperature exhibited a characteristic change in slope when amorphous systems change from glassy to rubbery state. Several material properties such as Young's, shear, and bulk modulus, Poisson's ratio, etc. are predicted from equilibrated structures and established the structure-property relations among designed polymers. Energetic performance parameters of these polymers are calculated and results reveal that the performance of the designed polymers is comparable to the benchmark energetic polymers like polyNIMMO, polyAMMO and polyBAMO. Overall, it is worthy remark that this molecular simulations study on novel energetic polyethers provides a good guidance on mastering the design principles and allows us to design novel polymers of tailored properties.

  9. Bisphenol A sulfonation is impaired in metabolic and liver disease

    Science.gov (United States)

    Yalcin, Emine B.; Kulkarni, Supriya R.; Slitt, Angela L.; King, Roberta

    2016-01-01

    Background Bisphenol A (BPA) is a widely used industrial chemical and suspected endocrine disruptor to which humans are ubiquitously exposed. Liver metabolizes and facilitates BPA excretion through glucuronidation and sulfonation. The sulfotransferase enzymes contributing to BPA sulfonation (detected in human and rodents) is poorly understood. Objectives To determine the impact of metabolic and liver disease on BPA sulfonation in human and mouse livers. Methods The capacity for BPA sulfonation was determined in human liver samples that were categorized into different stages of metabolic and liver disease (including obesity, diabetes, steatosis, and cirrhosis) and in livers from ob/ob mice. Results In human liver tissues, BPA sulfonation was substantially lower in livers from subjects with steatosis (23%), diabetes cirrhosis (16%), and cirrhosis (18%), relative to healthy individuals with non-fatty livers (100%). In livers of obese mice (ob/ob), BPA sulfonation was lower (23%) than in livers from lean wild-type controls (100%). In addition to BPA sulfonation activity, Sult1a1 protein expression decreased by 97% in obese mouse livers. Conclusion Taken together these findings establish a profoundly reduced capacity of BPA elimination via sulfonation in obese or diabetic individuals and in those with fatty or cirrhotic livers versus individuals with healthy livers. PMID:26712468

  10. 40 CFR 721.1625 - Alkylbenzene sulfonate, amine salt.

    Science.gov (United States)

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Alkylbenzene sulfonate, amine salt... Substances § 721.1625 Alkylbenzene sulfonate, amine salt. (a) Chemical substance and significant new uses... salt (PMN P-90-456) is subject to reporting under this section for the significant new use described in...

  11. Controlling Structure in Sulfonated Block Copolymer Membranes

    Science.gov (United States)

    Truong, Phuc; Stein, Gila; Strzalka, Joe

    2015-03-01

    In many ionic block copolymer systems, the strong incompatibility between ionic and non-ionic segments will trap non-equilibrium structures in the film, making it difficult to engineer the optimal domain sizes and transport pathways. The goal of this work is to establish a framework for controlling the solid-state structure of sulfonated pentablock copolymer membranes. They have ABCBA block sequence, where A is poly(t-butyl styrene), B is poly(hydrogenated isoprene), and C is poly(styrene sulfonate). To process into films, the polymer is dissolved in toluene/n-propanol solvent mixtures, where the solvent proportions and the polymer loading were both varied. Solution-state structure was measured with small angle X-ray scattering (SAXS). We detected micelles with radii that depend on the solvent composition and polymer loading. Film structure was measured with grazing-incidence SAXS, which shows (i) domain periodicity is constant throughout film thickness; (ii) domain periodicity depends on solvent composition and polymer loading, and approximately matches the micelle radii in solutions. The solid-state packing is consistent with a hard sphere structure factor. Results suggest that solid-state structure can be tuned by manipulating the solution-state self-assembly.

  12. Anaerobic degradation of linear alkylbenzene sulfonate.

    Science.gov (United States)

    Mogensen, Anders S; Haagensen, Frank; Ahring, Birgitte K

    2003-04-01

    Linear alkylbenzene sulfonate (LAS) found in wastewater is removed in the wastewater treatment facilities by sorption and aerobic biodegradation. The anaerobic digestion of sewage sludge has not been shown to contribute to the removal. The concentration of LAS based on dry matter typically increases during anaerobic stabilization due to transformation of easily degradable organic matter. Hence, LAS is regarded as resistant to biodegradation under anaerobic conditions. We present data from a lab-scale semi-continuously stirred tank reactor (CSTR) spiked with linear dodecylbenzene sulfonate (C12 LAS), which show that C12 LAS was biodegradable under methanogenic conditions. Sorption of C12 LAS on sewage sludge was described with a Freundlich isotherm. The C12 LAS sorption was determined with different concentrations of total solids (TS). In the semi-continuously stirred tank reactor, 18% of the added C12 LAS was bioavailable and 20% was biotransformed when spiking with 100 mg/L of C12 LAS and a TS concentration of 14.2 mg/L. Enhanced bioavailability of C12 LAS was obtained in an upflow anaerobic sludge blanket (UASB) reactor inoculated with granular sludge and sewage sludge. Biodegradation under thermophilic conditions was 37% with LAS as sole carbon source. Benzaldehyde was produced in the UASB reactor during LAS transformation.

  13. Influence of disinfection with peracetic acid and hypochlorite in dimensional alterations of casts obtained from addition silicone and polyether impressions.

    Science.gov (United States)

    Queiroz, Daher Antonio; Peçanha, Marcelo Massaroni; Neves, Ana Christina Claro; Frizzera, Fausto; Tonetto, Mateus Rodrigues; Silva-Concílio, Laís Regiane

    2013-11-01

    Dental impressions disinfection is important to reduce the risk of cross contamination but this process may produce dimensional distortions. Peracetic acid is a disinfectant agent with several favorable characteristics yet underutilized in Dentistry. The aim of this paper is to compare the dimensional stability of casts obtained from addition silicone and polyether impressions that were immersed for 10 minutes in a solution of 0.2% peracetic acid or 1% sodium hypochlorite. Sixty samples in type IV gypsum were produced after a master cast that simulated a full crown preparation of a maxillary premolar. Samples were divided in 6 groups (n = 10) according to the impression material and disinfection agent: Group AC--addition silicone control (without disinfectant); Group APA--addition silicone + 0.2% peracetic acid; Group AH--addition silicone + 1% sodium hypochlorite; Group PC--polyether control (without disinfectant); Group PPA--polyether + 0.2% peracetic acid; Group PH--polyether + 1% sodium hypochlorite. Cast height, base and top diameter were measured and a mean value was obtained for each sample and group all data was statistically analyzed (ANOVA, p peracetic acid could be considered a reliable material to disinfect dental molds.

  14. Ion conducting solid polymer electrolytes based on polypentafluorostyrene-b-polyether-b-polypentafluorostyrene prepared by atom transfer radical polymerization

    DEFF Research Database (Denmark)

    Jankova, Katja; Jannasch, P.; Hvilsted, Søren

    2004-01-01

    .3. The bromoisobutyrate functionalized polyether macroinitiators with molecular masses (M-n) of approx. 10 000 enabled the addition of between 15 and 39 wt.% flanking PFS as found by H-1 NMR. In a similar fashion monomethoxy PEG ( MPEG, Mn 5 000) was added 50 wt.% PFS. Polymer electrolytes were prepared by complexing...

  15. Rh-Catalyzed Asymmetric Hydrogenation of α-Substituted Vinyl Sulfones: An Efficient Approach to Chiral Sulfones.

    Science.gov (United States)

    Shi, Liyang; Wei, Biao; Yin, Xuguang; Xue, Peng; Lv, Hui; Zhang, Xumu

    2017-03-03

    Rh/(S)-(+)-DTBM-Segphos complex catalyzed asymmetric hydrogenation of α-substituted vinyl sulfones has been achieved, furnishing the desired products in high yields and excellent enantioselectivities (>90% yield, up to 99% ee). This method provided an efficient approach to α-substituted chiral sulfones under mild conditions and has potential applications in organic synthesis.

  16. Pengaruh Rasio Mol Reaktan dan Lama Sulfonasi terhadap Karakteristik Methyl Ester Sulfonic (MES) dari Metil Ester Minyak Sawit (Effects of Mol Ratio and Sulfonation Time on Methyl Ester Sulfonic (MES) Characteristics from Methyl Ester of Palm Oil)

    OpenAIRE

    Sri Hidayati; Pudji Permadi; Hestuti Eni

    2017-01-01

    An experiment of sulfonation process of methyl ester to produce methyl ester sulfonates (MES) was caried out using methyl ester palm oil in factorial design and NaHSO as sulfonating agent with variation of ratio mol NaHSO : methyl ester (1:1.25, 1:1.5, 1:1.75 and 1:2 ) and sulfonation time (3 hour (L1), 4.5 hour (L2) and 6 hour (L3). The result showed that the best sulfonation condition present in 1:1,5 mol ratio and sulfonation time of 4,5 hour. The best characteristic of MES was produced em...

  17. Synthesis and characterization of polymer blends of sulfonated polyethersulfone and sulfonated polyethersulfone octylsulfonamide for PEMFC applications

    Energy Technology Data Exchange (ETDEWEB)

    Mabrouk, W. [ERAS Labo, St Nazaire Les Eymes, Grenoble (France); Laboratoire des Materiaux Industriels, Conservatoire National des Arts et Metiers de Paris, 75003 Paris (France); Laboratoire de Chimie Analytique et Electrochimie, Faculte des Sciences de Tunis, Campus Universitaire, 1092 Tunis (Tunisia); Ogier, L.; Vidal, S. [ERAS Labo, St Nazaire Les Eymes, Grenoble (France); Sollogoub, C.; Fauvarque, J.F. [Laboratoire des Materiaux Industriels, Conservatoire National des Arts et Metiers de Paris, 75003 Paris (France); Matoussi, F.; Dachraoui, M. [Laboratoire de Chimie Analytique et Electrochimie, Faculte des Sciences de Tunis, Campus Universitaire, 1092 Tunis (Tunisia)

    2012-04-15

    Our goal in the present work was to synthesize a new proton exchange membrane that could be used in proton exchange membrane fuel cell (PEMFC), based on a blend of sulfonated polyethersulfone (S-PES) and sulfonated polyethersulfone octylsulfonamide (S-PESOS). Five blends, using S-PESOS with different grafting ratios of sulfonamide groups, have been elaborated, characterized, and tested in a PEMFC. The similar chemical structure between these two polymers favored their compatibility. The synthesized membranes showed a high water swelling capacity and an ionic conductivity equivalent to that of Nafion registered (0.1 S cm{sup -1}) in the same conditions. (Copyright copyright 2012 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  18. Cd(II and Pb(II complexes of the polyether ionophorous antibiotic salinomycin

    Directory of Open Access Journals (Sweden)

    Tanabe Makoto

    2011-09-01

    Full Text Available Abstract Background The natural polyether ionophorous antibiotics are used for the treatment of coccidiosis in poultry and ruminants. They are effective agents against infections caused by Gram-positive microorganisms. On the other hand, it was found that some of these compounds selectively bind lead(II ions in in vivo experiments, despite so far no Pb(II-containing compounds of defined composition have been isolated and characterized. To assess the potential of polyether ionophores as possible antidotes in the agriculture, a detailed study on their in vitro complexation with toxic metal ions is required. In the present paper we report for the first time the preparation and the structure elucidation of salinomycin complexes with ions of cadmium(II and lead(II. Results New metal(II complexes of the polyether ionophorous antibiotic salinomycin with Cd(II and Pb(II ions were prepared and structurally characterized by IR, FAB-MS and NMR techniques. The spectroscopic information and elemental analysis data reveal that sodium salinomycin (SalNa undergoes a reaction with heavy metal(II ions to form [Cd(Sal2(H2O2] (1 and [Pb(Sal(NO3] (2, respectively. Abstraction of sodium ions from the cavity of the antibiotic is occurring during the complexation reaction. Salinomycin coordinates with cadmium(II ions as a bidentate monoanionic ligand through the deprotonated carboxylic moiety and one of the hydroxyl groups to yield 1. Two salinomycin anions occupy the equatorial plane of the Cd(II center, while two water molecules take the axial positions of the inner coordination sphere of the metal(II cation. Complex 2 consists of monoanionic salinomycin acting in polydentate coordination mode in a molar ratio of 1: 1 to the metal ion with one nitrate ion for charge compensation. Conclusion The formation of the salinomycin heavy metal(II complexes indicates a possible antidote activity of the ligand in case of chronic/acute intoxications likely to occur in the stock

  19. Hydroquinone based sulfonated poly (arylene ether sulfone copolymer as proton exchange membrane for fuel cell applications

    Directory of Open Access Journals (Sweden)

    V. Kiran

    2015-12-01

    Full Text Available Synthesis of sulfonated poly (arylene ether sulfone copolymer by direct copolymerization of 4,4'-bis(4-hydroxyphenyl valeric acid, benzene 1,4-diol and synthesized sulfonated 4,4'-difluorodiphenylsulfone and its characterization by using FTIR (Fourier Transform Infrared and NMR (Nuclear Magnetic Resonance spectroscopic techniques have been performed. The copolymer was subsequently cross-linked with 4, 4!(hexafluoroisopropylidenediphenol epoxy resin by thermal curing reaction to synthesize crosslinked membranes. The evaluation of properties showed reduction in water and methanol uptake, ion exchange capacity, proton conductivity with simultaneous enhancement in oxidative stability of the crosslinked membranes as compared to pristine membrane. The performance of the membranes has also been evaluated in terms of thermal stability, morphology, mechanical strength and methanol permeability by using Thermo gravimetric analyzer, Differential scanning calorimetery, Atomic force microscopy, XPERT-PRO diffractometer, universal testing machine and diffusion cell, respectively. The results demonstrated that the crosslinked membranes exhibited high thermal stability with phase separation, restrained crystallinity, acceptable mechanical properties and methanol permeability. Therefore, these can serve as promising proton exchange membranes for fuel cell applications.

  20. Sulfonated poly (fluorenyl ether ketone) membrane with embedded silica rich layer and enhanced proton selectivity for vanadium redox flow battery

    Science.gov (United States)

    Chen, Dongyang; Wang, Shuanjin; Xiao, Min; Han, Dongmei; Meng, Yuezhong

    A series of novel organic-inorganic hybrid membranes with special microstructure, based on sulfonated poly (fluorenyl ether ketone) ionomer (SFPEK, IEC = 1.92 mequiv. g -1) and SiO 2 or sulfonic acid group containing SiO 2 (SiO 2-SO 3H), has been successfully designed and prepared for vanadium redox flow battery (VRB) application. The SiO 2-SO 3H is synthesized by co-condensation of tetraethoxysilane and γ-propyl mercaptotrimethoxysilane via sol-gel process to control the same IEC with neat SPFEK. The hybrid membranes are prepared by simply adding the inorganic particles into the SPFEK solution in N, N‧-dimethylacetamide, followed by ultrasonic dispersion, casting and profiled temperature drying process. The morphology is examined by SEM-EDX which is applied to the top surface, bottom surface and cross-section of the hybrid membranes. The water uptake, oxidative stability, thermal property, mechanical property, proton conductivity, VO 2+ permeability and single cell performance are investigated in detail in order to understand the relationship between morphology and property of the membranes. All the hybrid membranes show dramatically improved proton selectivity at 20 °C and 40 °C when compared with Nafion117. The VRB assembled with the SPFEK/3%SiO 2 and SPFEK/9%SiO 2 membranes exhibit higher coulombic efficiency and average discharge voltage than the VRB assembled with the SPFEK membrane at all the tested current densities.

  1. Boiling significantly promotes photodegradation of perfluorooctane sulfonate.

    Science.gov (United States)

    Lyu, Xian-Jin; Li, Wen-Wei; Lam, Paul K S; Yu, Han-Qing

    2015-11-01

    The application of photochemical processes for perfluorooctane sulfonate (PFOS) degradation has been limited by a low treatment efficiency. This study reports a significant acceleration of PFOS photodegradation under boiling condition compared with the non-boiling control. The PFOS decomposition rate increased with the increasing boiling intensity, but declined at a higher hydronium level or under oxygenation. These results suggest that the boiling state of solution resulted in higher effective concentrations of reactants at the gas-liquid interface and enhanced the interfacial mass transfer, thereby accelerating the PFOS decomposition. This study broadens our knowledge of PFOS photodegradation process and may have implications for development of efficient photodegradation technologies. Copyright © 2015 Elsevier Ltd. All rights reserved.

  2. Sulfonated polystyrene as a new gradient-index medium for light-focusing elements.

    Science.gov (United States)

    Jung, S D; Hwang, W Y; Song, S H; Lee, el-H; Lee, J I; Shim, H K

    1995-06-01

    We have discovered that the sulfonation of polystyrene can form a gradient-index medium useful for lightfocusing purposes. We found that the refractive index of sulfonated polystyrene varies with the degree of sulfonation and that the refractive index of the fully sulfonated polystyrene decreased by approximately 0.06 at 0.633 microm from that of pure polystyrene.

  3. Thermally stable hyperbranched polyether-based polymer electrolyte for lithium-ion batteries

    Science.gov (United States)

    Wu, Feng; Feng, Ting; Wu, Chuan; Bai, Ying; Ye, Lin; Chen, Junzheng

    2010-01-01

    A thermally stable polymer matrix, comprising hyperbranched polyether PHEMO (poly(3-{2-[2-(2-hydroxyethoxy) ethoxy] ethoxy}methyl-3'-methyloxetane)) and PVDF-HFP (poly(vinylidene fluoride-hexafluoropropylene)), has been successfully prepared for applications in lithium-ion batteries. This type of polymer electrolyte has been made by adding different amounts of lithium bis(oxalate)borate (LiBOB) to the polymer matrix. Its thermal and structural properties were measured using differential scanning calorimetry and x-ray diffraction. Experimental results show that the polymer electrolyte system possesses good thermal stability, with a decomposition temperature above 420 °C. The ionic conductivity of the polymer electrolyte system is dependent on the lithium salt content, reaching a maximum of 1.1 × 10-5 S cm-1 at 30 °C and 2.3 × 10-4 S cm-1 at 80 °C when doped with 10 wt% LiBOB.

  4. Influence of technique and pouring time on dimensional stability of polyvinyl siloxane and polyether impressions.

    Science.gov (United States)

    Gomez-Polo, Miguel; Celemin, Alicia; del Rio, Jaime; Sanchez, Andres

    2012-01-01

    This study aimed to determine how impression technique and pouring time affect casts obtained using polyvinyl siloxane (PVS) and polyether (PE) impressions. A total of 480 impressions were taken using three techniques: single-step (SS), two-step (TS), and two-step with a spacer (TSS). Impressions were poured after 1 and 24 hours and 7 and 14 days. Significant differences (P < .01) were found between the TS technique and the SS and TSS methods as well as between PE and PVS (P < .01) in terms of the effects of pouring time. SS and TSS yielded similar dimensional results, while greater dimensional change was induced with TS. PE impressions had to be poured no later than 7 days after preparation to ensure dimensional stability.

  5. Ciguatoxins: Cyclic Polyether Modulators of Voltage-gated Iion Channel Function

    Directory of Open Access Journals (Sweden)

    Richard J. Lewis

    2006-04-01

    Full Text Available Ciguatoxins are cyclic polyether toxins, derived from marine dinoflagellates, which are responsible for the symptoms of ciguatera poisoning. Ingestion of tropical and subtropical fin fish contaminated by ciguatoxins results in an illness characterised by neurological, cardiovascular and gastrointestinal disorders. The pharmacology of ciguatoxins is characterised by their ability to cause persistent activation of voltage-gated sodium channels, to increase neuronal excitability and neurotransmitter release, to impair synaptic vesicle recycling, and to cause cell swelling. It is these effects, in combination with an action to block voltage-gated potassium channels at high doses, which are believed to underlie the complex of symptoms associated with ciguatera. This review examines the sources, structures and pharmacology of ciguatoxins. In particular, attention is placed on their cellular modes of actions to modulate voltage-gated ion channels and other Na+-dependent mechanisms in numerous cell types and to current approaches for detection and treatment of ciguatera.

  6. Modification of Poly(ether ether ketone Polymer for Fuel Cell Application

    Directory of Open Access Journals (Sweden)

    Devesh Shukla

    2013-01-01

    Full Text Available Polyelectrolyte membrane (PEM is an important part of PEM fuel cell. Nafion is a commercially known membrane which gives the satisfactory result in PEM fuel cell operating at low temperature. Present research paper includes functionalization of Poly(ether ether ketone (PEEK polymer with phosphonic acid group. The functionalization was done with the help of nickel-based catalyst. Further, the polymer was characterized by the FTIR, EDAX, DSC, TGA, and 1H NMR, and it was found that PEEK polymer was functionalized with phosphonic acid group with good thermal stability in comparison to virgin PEEK. Finally, the thin films of functionalized polymer were prepared by solution casting method, and proton conductivity of film samples was measured by impedance spectra whose value was found satisfactory with good thermal stability in comparison to commercially available Nafion membrane.

  7. Evaluation of Stabilization Performances of Antioxidants in Poly(ether ether ketone)

    Institute of Scientific and Technical Information of China (English)

    ZHOU Zheng; ZHOU Fu-gui; ZHANG Shu-ling; MU Jian-xin; YUE Xi-gui; WANG Gui-bin

    2012-01-01

    Two types of antioxidants(a primary antioxidant and a secondary antioxidant) were used to improve the stability of poly(ether ether ketone)(PEEK).The effects of the antioxidants on the properties of PEEK and the stabilization mechanism were investigated by some characterization methods,such as rheometer,thermogravinetric analysis(TGA),universal tester and electron spin resonance(ESR).The results indicate that the efficiency of the phosphorous antioxidant(DS) in improving the stability of PEEK was better than that of the phenolic antioxidant(DN) in both melting stability and thermal stability,and the thermal stability of PEEK sample containing 0.07%(mass fraction) DS was the best among all the samples due to the decrease of the free radicals density,as proven by ESR measurement.Additionally,no obvious changes could be observed in mechanical properties of PEEK containing antioxidants compared to those of virgin PEEK.

  8. The Thermoplastic Polyether-imide%热塑性聚醚酰亚胺

    Institute of Scientific and Technical Information of China (English)

    张露; 张雯; 张凯

    2001-01-01

    Polyether-imide (PEI)is a new amorphous thermoplastic polyimide.It has good processing behavior with typical thermoplastic processing and forming equipment to manufacture a lot of products.It possesses heat resistance,dimensional stability and excellent flame retardancy.In this paper,the properties and application of PEI are briefly introduced.%聚醚酰亚胺(PEI)是一种新型热塑性聚酰亚胺,具有很好的成型加工性能,可用一般热塑性塑料成型加工工艺和设备制造多种制品。产品具有高的长期耐热性、尺寸稳定性及突出的阻燃性。本文介绍了近年来PEI的生产、应用和开发情况。

  9. Study on EPR Spectra of Three Gadolinium Complexes With Noncyclic Polyether Schiff Bases

    Institute of Scientific and Technical Information of China (English)

    陈德余; 姚克敏; 封子先; 蔡乐真; 周佩芬; 薛祺

    1994-01-01

    The EPR spectra of three new gadolinium complexes with noncyclic polyether Schiff bases in powder and those of these complexes in organic solvents were investigated at different temperatures. It was observed that EPR spectra of nine and four peaks of Gd(Ⅲ) complexes in polycrystalline powder and freezing samples appeared at low temperature respectively for the first time. The interpretations of these results obtained on the basis of spin Hamiltonian of s = 7/2 system are satisfactory. The correlations of EPR feature between crystal-field strength in complexes and local symmetry around Gd3+ ions were revealed. The crystal-field parameters b20 and the asymmetry parameters λ’ of complexes were estimated. A series of interesting regularity and new results were obtained.

  10. Synthesis and antimicrobial activity of amide derivatives of polyether antibiotic-salinomycin.

    Science.gov (United States)

    Huczyński, Adam; Janczak, Jan; Stefańska, Joanna; Antoszczak, Michał; Brzezinski, Bogumil

    2012-07-15

    For the first time a direct and practical approach to the synthesis of eight amide derivatives of polyether antibiotic-salinomycin is described. The structure of allyl amide (3a) has been determined using X-ray diffraction. Salinomycin and its amide derivatives have been screened for their in vitro antimicrobial activity against the typical gram-positive cocci, gram-negative rods and yeast-like organisms, as well as against a series of clinical isolates of methicillin-resistant Staphylococcus aureus and methicillin-sensitive S. aureus. Amides of salinomycin have been found to show a wide range of activities, from inactive at 256 μg/mL to active with MIC of 2 μg/mL, comparable with salinomycin. As a result, phenyl amide (3b) was found to be the most active salinomycin derivative against gram-positive bacteria, MRSA and MSSA.

  11. Analysis of Percolation Behavior of Electrical Conductivity of the Systems Based on Polyethers and Carbon Nanotubes

    Directory of Open Access Journals (Sweden)

    E.A. Lysenkov

    2016-03-01

    Full Text Available The basic theoretical models of electrical conductivity of polymer nanocomposites and their accordance to experimental results are analysed for the systems based on polyethers and carbon nanotubes using the methods of mathematical simulation. It is set that models which are based on the effective medium approximation do not take into account existence of percolation threshold and can’t be using for exact definition of experimental data. It is discovered that the Fourier model demonstrats a good accordance with an experiment, however it is applicable only for the systems in which a large increase of conductivity under reaching the percolation threshold is observed, that systems with low own conductivity. It is set that the best accordance to experimental data was shown by the Kirkpatrick model and the generalized McLachlan model, which, except for the percolation threshold, structural descriptions of clusters which are formed from carbon nanotubes take into account.

  12. Synthesis of Polyethers Containing Triazole Units in the Backbone by Click Chemistry in a Tricomponent Reaction

    Directory of Open Access Journals (Sweden)

    Moslem Mansour Lakouraj

    2013-01-01

    Full Text Available A series of linear aromatic polyethers containing triazole units were synthesized via the direct click reaction of dibromide and bisethynyl compounds in the presence of sodium azide as one pot reaction. The structures of polymers were approved by using IR and 1H NMR techniques. The solubility experiments showed that polymers have good solubility in polar aprotic solvents such as DMSO, DMF, and NMP at higher temperatures. Thermal stability of the polymers was measured using thermogravimetric analysis (TGA and differential scanning calorimetry (DSC which indicated that they possessed good thermal stability ( up to 558°C and high (191.7–260°C under N2 atmosphere. All the polymers were amorphous according to the DSC and X-ray diffraction. These polymers exhibited strong UV-vis absorption maxima near to 400 nm and up to 500 nm in DMSO solution.

  13. Fully Aromatic Block Copolymers for Fuel Cell Membranes with Densely Sulfonated Nanophase Domains

    DEFF Research Database (Denmark)

    Takamuku, Shogo; Jannasch, Patrick; Lund, Peter Brilner

    Two multiblock copoly(arylene ether sulfone)s with similar block lengths and ion exchange capacities (IECs) were prepared by a coupling reaction between a non-sulfonated precursor block and a highly sulfonated precursor block containing either fully disulfonated diarylsulfone or fully...... tetrasulfonated tetraaryldisulfone segments. The latter two precursor blocks were sulfonated via lithiation-sulfination reactions whereby the sulfonic acid groups were exclu- sively placed in ortho positions to the many sulfone bridges, giving these locks IECs of 4.1 and 4.6 meqg1, respectively. Copolymer...

  14. Ion atmosphere relaxation controlled electron transfers in cobaltocenium polyether molten salts.

    Science.gov (United States)

    Harper, Amanda S; Leone, Anthony M; Lee, Dongil; Wang, Wei; Ranganathan, Srikanth; Williams, Mary Elizabeth; Murray, Royce W

    2005-10-13

    A room-temperature redox molten salt for the study of electron transfers in semisolid media, based on combining bis(cyclopentadienyl)cobalt with oligomeric polyether counterions, [Cp2Co](MePEG350SO3), is reported. The transport properties of the new molten salt can be varied (plasticized) by varying the polyether content. The charge transport rate during voltammetric reduction of the ionically conductive [Cp2Co](MePEG350SO3) molten salt exceeds the actual physical diffusivity of [Cp2Co]+ because of rapid [Cp2Co](+/0) electron self-exchanges. The measured [Cp2Co](+/0) electron self-exchange rate constants (k(EX)) are proportional to the diffusion coefficients (D(CION)) of the counterions in the melt. The electron-transfer activation barrier energies are also close to those of ionic diffusion but are larger than those derived from optical intervalent charge-transfer results. Additionally, the [Cp2Co](+/0) rate constant results are close to those of dissimilar redox moieties in molten salts where D(CION) values are similar. All of these characteristics are consistent with the rates of electron transfers of [Cp2Co](+/0) (and the other donor-acceptor pairs) being controlled not by the intrinsic electron-transfer rates but by the rate of relaxation of the ion atmosphere around the reacting pair. In the low driving force regime of mixed-valent concentration gradients, the ion atmosphere relaxation is competitive with electron transfer. The results support the generality of the recently proposed model of ionic atmosphere relaxation control of electron transfers in ionically conductive, semisolid materials.

  15. Quantitative analysis of oleic acid and three types of polyethers according to the number of hydroxy end groups in Polysorbate 80 by hydrophilic interaction chromatography at critical conditions.

    Science.gov (United States)

    Zhang, Rui; Wang, Yu; Ji, Yu; Shi, Bei-jia; Zhang, Zai-ping; Zhang, Hai-yan; Yang, Ming; Wang, Yong-mei

    2013-01-11

    A quantitative characterization of Polysorbate 80 is crucial for its many applications. In this paper we report a quick RP-HPLC method for the quantitative determination of Polysorbate 80. The hydrolysis of Polysorbate 80 to release oleic acid and three types of polyethers was first carried out. A chromatographic method based on liquid chromatography at critical conditions (LCCC) was then developed for an endgroup-based separation of low-molecular-mass polyether. With this method the polyether, irrespective of its molecular-mass, is separated according to endgroups (functionality) due to interactions of the polar endgroups with the hydrophilic stationary phase. The different types of polyethers and oleic acid were identified using on-line electrospray ionization mass spectrometry and quantified by evaporative light scattering detection.

  16. Synthesis of Poly(phthalazinone ether ketone) Containing Sodium Sulfonate Groups via Direct Polymerization

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    1, 2-Dihydro-4-(4-hydroxyphenyl)(2H)phthalazin-1-one(DHPZ) was sulfonated in con- centrated sulfuric acid. Poly(phthalazinone ether ketone) containing pendant sodium sulfonate group was synthesized from sulfonated and pure 1,2-dihydro-4-(4-hydroxyphenyl)(2H)phthalazin- 1-one, and 4,4(-difluorodiphenylketone. The sulfonated monomer and sulfonated polymer were characterized with FT-IR and 1H-NMR.

  17. Ionomeric membranes based on partially sulfonated poly(styrene): synthesis, proton conduction and methanol permeation

    OpenAIRE

    Picchioni, F.; Tricoli,V.; Carretta, N.

    2000-01-01

    Homogeneuosly sulfonated poly(styrene) (SPS) was prepared with various concentration of sulfonic acid groups in the base polymer. Membranes cast from these materials were investigated in relation to proton conductivity and methanol permeability in the temperature range from 20°C to 60°C. It was found that both these properties increase as the polymer is increasingly sulfonated, with abrupt jumps occurring at a concentration of sulfonic acid groups of about 15 mol%. The most extensively sulfon...

  18. Synthesis in pilot plant scale and physical properties of sulfonated polystyrene

    OpenAIRE

    Martins, Cristiane R.; Ruggeri,Giacommo; Paoli,Marco-A. De

    2003-01-01

    The homogenous sulfonation of polystyrene was developed in a pilot plant scale producing polymers with different sulfonation degrees (18 to 22 mole % of sulfonated styrene units). The reaction yield depends chiefly on the concentration ratio of acetyl sulfate and polystyrene. The morphological and thermal properties of the sulfonated polystyrene obtained by homogeneous sulfonation were studied by means of scanning electron microscopy, differential scanning calorimetry and thermogravimetry. Th...

  19. Room temperature synthesis of biodiesel using sulfonated graphitic carbon nitride

    Science.gov (United States)

    Sulfonation of graphitic carbon nitride (g-CN) affords a polar and strongly acidic catalyst, Sg-CN, which displays unprecedented reactivity and selectivity in biodiesel synthesis and esterification reactions at room temperature.

  20. Affinity labelling enzymes with esters of aromatic sulfonic acids

    Science.gov (United States)

    Wong, Show-Chu; Shaw, Elliott

    1977-01-01

    Novel esters of aromatic sulfonic acids are disclosed. The specific esters are nitrophenyl p- and m-amidinophenylmethanesulfonate. Also disclosed is a method for specific inactivation of the enzyme, thrombin, employing nitrophenyl p-amidinophenylmethanesulfonate.

  1. Tracer Diffusion of Polystyrene in Lightly Sulfonated Polystyrene

    Science.gov (United States)

    Xu, Chen; Zhou, Nancy; Burghardt, Wesley; Winey, Karen; Composto, Russell

    2005-03-01

    The tracer diffusion coefficient D^* of deuterated polystyrene (d-PS) (Mw = 65,900 g/mol) in lightly sulfonated polystyrene (P(S-SSx)) (Mw = 65,000 g/mol) as a function of sulfonation mole fraction (x) was measured by forward recoil spectrometry (FRES). For x sulfonation, according to D^* = Do exp(-0.14 Ns), where Ns is the number of sulfuric acid groups per chain. This slowing-down is attributed to an increase in the monomeric friction coefficient which increases with sulfonation. The diffusion mechanism includes both reptation and constraint release. The monomeric friction coefficient for d-PS in P(S-SSx) is compared with the coefficient for P(S-SSx) measured by rheology.

  2. Room temperature synthesis of biodiesel using sulfonated graphitic carbon nitride

    Science.gov (United States)

    Baig, R. B. Nasir; Verma, Sanny; Nadagouda, Mallikarjuna N.; Varma, Rajender S.

    2016-12-01

    Sulfonation of graphitic carbon nitride (g-CN) affords a polar and strongly acidic catalyst, Sg-CN, which displays unprecedented reactivity and selectivity in biodiesel synthesis and esterification reactions at room temperature.

  3. Sulfonated hydrocarbon graft architectures for cation exchange membranes

    DEFF Research Database (Denmark)

    Nielsen, Mads Møller; Jankova Atanasova, Katja; Hvilsted, Søren

    2013-01-01

    A synthetic strategy to hydrocarbon graft architectures prepared from a commercial polysulfone and aimed as ion exchange membrane material is proposed. Polystyrene is grafted from a polysulfone macroinitiator by atom transfer radical polymerization, and subsequently sulfonated with acetyl sulfate...

  4. The Snail-Induced Sulfonation Pathway in Breast Cancer Metastasis

    Science.gov (United States)

    2014-09-01

    AD_________________ Award Number: W81XWH-11-1-0494   TITLE: The Snail -Induced Sulfonation... Snail -Induced Sulfonation Pathway in Breast Cancer Metastasis 5b. GRANT NUMBER W81XWH-11-1-0494 5c. PROGRAM ELEMENT NUMBER 6. AUTHOR(S) Dr...provided funding for a 3-year project that has resulted in fundamental new insights into how the transcription factor Snail can control gene

  5. Oil recovery with vinyl sulfonic acid-acrylamide copolymers

    Energy Technology Data Exchange (ETDEWEB)

    Norton, C.J.; Falk, D.O.

    1973-12-18

    An aqueous polymer flood containing sulfomethylated alkali metal vinyl sulfonate-acrylamide copolymers was proposed for use in secondary or tertiary enhanced oil recovery. The sulfonate groups on the copolymers sustain the viscosity of the flood in the presence of brine and lime. Injection of the copolymer solution into a waterflooded Berea core, produced 30.5 percent of the residual oil. It is preferred that the copolymers are partially hydrolyzed.

  6. PREPARATION AND PROPERTIES OF SPAES-TiO_2 HYBRID MEMBRANES FOR DIRECT METHANOL FUEL CELL

    Institute of Scientific and Technical Information of China (English)

    刘惠玲

    2009-01-01

    Sulfonated poly(arylene ether sulfone)(SPAES) copolymer with degree of sulfonation of 1.0 was synthesized and characterized.A series of SPAES-TiO_2 hybrid membranes with various contents of nano-sized TiO_2 particles were prepared and characterized through sol-gel reactions.Scanning electron microscopy(SEM) images indicated the TiO_2 particles were well dispersed within polymer matrix.These composite membranes were evaluated for proton exchange membranes(PEMs) in direct methanol fuel cell(DMFC).These mem...

  7. Synthesis and Water Uptake of Sulfonated Poly (phthalazinone ether sulfone ketone)/Polyacrylic Acid Proton Exchange Membranes

    Institute of Scientific and Technical Information of China (English)

    Xue Mei WU; Gao Hong HE; Lin GAO; Shuang GU; Zheng Wen HU; Ping Jing YAO

    2006-01-01

    Novel SPPESK/PAA composite proton exchange membranes with semi-interpenetrating polymer network (sIPN) structure have been synthesized through the in-situ polymerization of acrylic acid (AA) in the presence of sulfonated poly (phthalazinone ether sulfone ketone) (SPPESK). The composite membranes were identified by FT-IR analysis. Water uptake of the composite membranes was as high as 89.7% at 90℃, nearly one time higher than that of the corresponding SPPESK membrane.

  8. SORPTION OF Ga (III ON FLEXIBLE OPEN CELL POLYURETHANE FOAM OF POLYETHER TYPE IMPREGNATED WITH TRI-N-BUTHYL PHOSPATE

    Directory of Open Access Journals (Sweden)

    Lavinia Tofan

    2007-06-01

    Full Text Available The obtained results concerning the Ga (III ion retention on flexible open cell polyurethane foam of polyether type pretreated with tri-n-butyl phosphate are presented. The influence of solution acidity, phases contact time, Ga (III concentration and solution temperature have been investigated. The parameters of Ga (III batch sorption have been optimized. On the basis of Langmuir isotherms, the sorption constants and the thermodynamic parameters, ∆G, ∆Η and ∆S have been calculated.

  9. Improvement of the water selectivity of ULTEM poly(ether imide) pervaporation films by an allylamine-plasma-polymerized layer

    OpenAIRE

    Kaba, Meriyam; Raklaoui, Nabil; Guimon, Marie Françoise; Mas, André

    2005-01-01

    International audience; The wettability and surface energy of extruded ULTEM poly(ether imide) films strongly increased (the water contact angle varied from 75 to 38° and the surface energy varied from 45.3 to 59.5 mJ m-2, respectively) with the deposition of an allylamine-plasma-polymerized layer and were characterized with X-ray photoelectron spectroscopy, scanning electron microscopy, and atomic force microscopy according to the experimental parameters. Pervaporation tests for dehydrating ...

  10. Fibronectin fibrillogenesis on sulfonated polystyrene surfaces.

    Science.gov (United States)

    Pernodet, Nadine; Rafailovich, Miriam; Sokolov, Jonathan; Xu, D; Yang, Nan-Loh; McLeod, Kenneth

    2003-03-15

    Extracellular matrix (ECM) protein adsorption and organization serves as a critical first step in the development and organization of tissues. Advances in tissue engineering, therefore, will depend on the ability to control the rate and pattern of ECM formation. Fibronectin is a prominent component of the ECM, which undergoes fibrillogenesis in the presence of cells. Using sulfonated polysyrene surfaces, we showed that fibronectin undergoes a transition from monolayer to multilayer adsorption at calculated surface charge densities above 0.03 Coulombs (C)/m(2). At charge densities above approximately 0.08 C/m(2), distinct fibronectin fibrillar networks are observed to form with a fibril morphology similar to those observed to form in situ on cell surfaces. This self-organization process is time dependent, with the fibrils achieving dimensions of 30-40 microm in length and 1 microm in height after 72 h of incubation. We suggest that the polarization of charge domains on the polyampholytic fibronectin molecules near high charge density surfaces is sufficient to initiate the multilayer adsorption and the organization of these fibrillar structures. These results suggest that the nonlinear dependence of adsorption on surface charge density may play an important role in the self-organization of many matrix components.

  11. Nanoscale Morphology of Sulfonated Polystyrene Ionomers

    Science.gov (United States)

    Zhou, Nancy C.; Winey, Karen I.

    2007-03-01

    We have applied our scanning transmission electron microscopy (STEM) methods to investigate the size, shape and spatial distribution of the ionic, nanoscale aggregates in poly(styrene-ran-styrene sulfonate) (P(S-SSx)) ionomers. This analytical electron microscopy method minimizes phase contrast that can obscure nano-scale features and accentuates differences in atomic number. We recently reported quantitative agreement between STEM and X-ray scattering results in a Cu-neutralized poly(styrene-ran-methacrylic acid) (SMAA) ionomer with respect to the size of the ionic aggregates and their number density. For this study, P(S-SSx) ionomers were prepared by solution neutralizing with metal acetates, solution casting, and annealing. Initial STEM results from P(S-SS0.019) fully neutralized with Zn indicate a uniform distribution of monodisperse spherical aggregates. Combining direct imaging and X-ray scattering of P(S-SSx) ionomers, we will investigate the effect of cation type and level of neutralization.

  12. Ion Exchange Formation via Sulfonated Bicomponent Nonwovens

    Science.gov (United States)

    Stoughton, Hannah L.

    For many years ion exchange resins were used to: remove heavy metals from water, recover materials from wastewater, and eliminate harmful gases from the air. While use of these resin beads dominates the ion exchange industry, the beads have limitations that should be considered when decisions are made to employ them. For instance, officials must balance the inherent zero sum surface area and porosity of the materials. This series of studies investigates the use of bicomponent nonwovens as a base substrate for producing high surface area ion exchange materials for the removal of heavy metal ions. Functionalized materials were produced in a two-step process: (1) PET/PE spunbond bicomponent fibers were fractured completely, producing the high surface area nonwoven to be used as the base ion exchange material, and (2) the conditions for functionalizing the PET fibers of the nonwoven webs were investigated where an epoxy containing monomer was grafted to the surface followed by sulfonation of the monomer. The functionalization reactions of the PET fibers were monitored based on: weight gain, FTIR, TOF-SIMS, and SEM. Ion exchange properties were evaluated using titration and copper ion removal capacity from test solutions. The relationship between web structure and removal efficiency of the metal ions was defined through a comparison of the bicomponent and homocomponent nonwovens for copper ion removal efficiency. The investigation revealed that utilizing the high surface area, fractured bicomponent nonwoven ion exchange materials with capacities comparable to commercially available ion exchange resins could be produced.

  13. Multiblock copolymers with highly sulfonated blocks containing di- and tetrasulfonated arylene sulfone segments for proton exchange membrane fuel cell applications

    Energy Technology Data Exchange (ETDEWEB)

    Takamuku, Shogo; Jannasch, Patric [Polymer and Materials Chemistry, Department of Chemistry, Lund University (Sweden)

    2012-01-15

    Multiblock copoly(arylene ether sulfone)s with different block lengths and ionic contents are tailored for durable and proton-conducting electrolyte membranes. Two series of fully aromatic copolymers are prepared by coupling reactions between non-sulfonated hydrophobic precursor blocks and highly sulfonated hydrophilic precursor blocks containing either fully disulfonated diarylsulfone or fully tetrasulfonated tetraaryldisulfone segments. The sulfonic acid groups are exclusively introduced in ortho positions to the sulfone bridges to impede desulfonation reactions and give the blocks ion exchange capacities (IECs) of 4.1 and 4.6 meq. g{sup -1}, respectively. Solvent cast block copolymer membranes show well-connected hydrophilic nanophase domains for proton transport and high decomposition temperatures above 310 C under air. Despite higher IEC values, membranes containing tetrasulfonated tetraaryldisulfone segments display a markedly lower water uptake than the corresponding ones with disulfonated diarylsulfone segments when immersed in water at 100 C, presumably because of the much higher chain stiffness and glass transition temperature of the former segments. The former membranes have proton conductivities in level of a perfluorosulfonic acid membrane (NRE212) under fully humidified conditions. A membrane with an IEC of 1.83 meq. g{sup -1} reaches above 6 mS cm{sup -1} under 30% relative humidity at 80 C, to be compared with 10 mS cm{sup -1} for NRE212 under the same conditions. (Copyright copyright 2012 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  14. Intercalation of sulfonated melamine formaldehyde polycondensates into a hydrocalumite LDH structure

    Science.gov (United States)

    von Hoessle, F.; Plank, J.; Leroux, F.

    2015-05-01

    A series of sulfonated melamine formaldehyde (SMF) polycondensates possessing different anionic charge amounts and molecular weights was synthesized and incorporated into a hydrocalumite type layered double hydroxide structure using the rehydration method. For this purpose, tricalcium aluminate was dispersed in water and hydrated in the presence of these polymers. Defined inorganic-organic hybrid materials were obtained as reaction products. All SMF polymers tested intercalated readily into the hydrocalumite structure, independent of their different molecular weights (chain lengths) and anionic charge amounts. X-ray diffraction revealed typical patterns for weakly ordered, highly polymer loaded LDH materials which was confirmed via elemental analysis and thermogravimetry. IR spectroscopy suggests that the SMF polymers are interleaved between the [Ca2Al(OH)6]+ main sheets via electrostatic interaction, and that no chemical bond between the host matrix and the guest anion is formed. The SMF polymers well ensconced within the LDH structure exhibit significantly slower thermal degradation.

  15. Synthesis in pilot plant scale and physical properties of sulfonated polystyrene

    Directory of Open Access Journals (Sweden)

    Martins Cristiane R.

    2003-01-01

    Full Text Available The homogenous sulfonation of polystyrene was developed in a pilot plant scale producing polymers with different sulfonation degrees (18 to 22 mole % of sulfonated styrene units. The reaction yield depends chiefly on the concentration ratio of acetyl sulfate and polystyrene. The morphological and thermal properties of the sulfonated polystyrene obtained by homogeneous sulfonation were studied by means of scanning electron microscopy, differential scanning calorimetry and thermogravimetry. The glass transition temperature of sulfonated polystyrene increases in relation to pure polystyrene and DCp was evaluated in order to confirm the strong interactions among the ~SO3H groups.

  16. Perfluoroalkyl sulfonates cause alkyl chain length-dependent hepatic steatosis and hypolipidemia mainly by impairing lipoprotein production in APOE*3-leiden CETP mice

    NARCIS (Netherlands)

    Bijland, S.; Rensen, P.C.N.; Pieterman, E.J.; Maas, A.C.E.; Hoorn, J.W. van der; Erk, M.J. van; Havekes, L.M.; Dijk, K.W. van; Chang, S.C.; Ehresman, D.J.; Butenhoff, J.L.; Princen, H.M.G.

    2011-01-01

    Perfluorobutane sulfonate (PFBS), perfluorohexane sulfonate (PFHxS), and perfluorooctane sulfonate (PFOS) are stable perfluoroalkyl sulfonate (PFAS) surfactants, and PFHxS and PFOS are frequently detected in human biomonitoring studies. Some epidemiological studies have shown modest positive correla

  17. Miscibility of Polystyrene and Lighted Sulfonated Polystyrene Blends

    Science.gov (United States)

    Zhou, N. C.; Burghardt, W. R.; Composto, R. J.

    2005-03-01

    The blend miscibility of deuterated polystyrene (dPS) and lighted sulfonated poly(styrene-ran-sulfonated polystyrene) (P (S-SS)) has been examined by forward recoil spectrometry (FRES). Equilibrium coexistence compositions were determined for dPS:P(S-SSx) blends where x is the mole percent of sulfonation.At x = 0.2%, the blends are fully miscible at 150°C to 190°C, while at x = 2.6% the system fully immiscible at the same temperatures. Intermediate levels of sulfonation (0.7, 1.0 and 1.2%) are partially miscible and exhibit an upper critical solution temperature (UCST). This behavior is attributed to the dilution of repulsive intra-molecular interaction between the ionic and non-ionic groups in the copolymer due to favorable interactions with the non-ionic group of the homopolymer PS. Estimates using the Flory-Huggins and the copolymer effect theories found a large ( 20) positive monomer-monomer interaction parameter between styrene and styrene sulfonate. This large interaction parameter might drive phase separation within a compositionally disperse random copolymers sample.

  18. Thermally stable hyperbranched polyether-based polymer electrolyte for lithium-ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Wu Feng; Feng Ting; Wu Chuan; Bai Ying; Chen Junzheng [School of Chemical Engineering and Environment, Beijing Institute of Technology, Beijing 10081 (China); Ye Lin, E-mail: chuanwu@bit.edu.c [School of Materials Science and Engineering, Beijing Institute of Technology, Beijing 10081 (China)

    2010-01-27

    A thermally stable polymer matrix, comprising hyperbranched polyether PHEMO (poly(3-{l_brace}2-[2-(2-hydroxyethoxy) ethoxy] ethoxy{r_brace}methyl-3'-methyloxetane)) and PVDF-HFP (poly(vinylidene fluoride-hexafluoropropylene)), has been successfully prepared for applications in lithium-ion batteries. This type of polymer electrolyte has been made by adding different amounts of lithium bis(oxalate)borate (LiBOB) to the polymer matrix. Its thermal and structural properties were measured using differential scanning calorimetry and x-ray diffraction. Experimental results show that the polymer electrolyte system possesses good thermal stability, with a decomposition temperature above 420 {sup 0}C. The ionic conductivity of the polymer electrolyte system is dependent on the lithium salt content, reaching a maximum of 1.1 x 10{sup -5} S cm{sup -1} at 30 {sup 0}C and 2.3 x 10{sup -4} S cm{sup -1} at 80 {sup 0}C when doped with 10 wt% LiBOB.

  19. Zinc ion conducting polymer electrolytes based on oligomeric polyether/PVDF-HFP blends

    Science.gov (United States)

    Ye, Hui; Xu, Jun John

    Here we report novel zinc ion conducting polymer electrolytes based on oligomeric polyether/PVDF-HFP blends with or without the incorporation of a small amount of organic carbonates. Their thermal properties, ionic conductivity and electrochemical properties are characterized and the effect of different Zn salts and incorporation of a small amount of organic carbonates are investigated. These polymer electrolyte membranes exhibit essentially no or very low volatility, high thermal stability, high ionic conductivity, wide electrochemical stability window, acceptable interfacial resistance with zinc, and the capability for reversible Zn plating/stripping. Particularly promising are electrolyte systems based on the combination of low lattice energy zinc imide salt and a special co-solvent of oligomeric poly(ethylene glycol) dimethyl ether (PEGDME) mixed with a small amount of ethylene carbonate (EC), dimensionally stabilized with PVDF-HFP. Such novel polymer electrolyte membranes could lead to the development of new kinds of electrochemical energy storage devices based on zinc electrochemistry, including solid-state, thin-film rechargeable zinc/air cells envisaged.

  20. Zinc ion conducting polymer electrolytes based on oligomeric polyether/PVDF-HFP blends

    Energy Technology Data Exchange (ETDEWEB)

    Ye, Hui; Xu, Jun John [Department of Materials Science and Engineering, Rutgers, the State University of New Jersey, Piscataway, NJ 08854 (United States)

    2007-03-20

    Here we report novel zinc ion conducting polymer electrolytes based on oligomeric polyether/PVDF-HFP blends with or without the incorporation of a small amount of organic carbonates. Their thermal properties, ionic conductivity and electrochemical properties are characterized and the effect of different Zn salts and incorporation of a small amount of organic carbonates are investigated. These polymer electrolyte membranes exhibit essentially no or very low volatility, high thermal stability, high ionic conductivity, wide electrochemical stability window, acceptable interfacial resistance with zinc, and the capability for reversible Zn plating/stripping. Particularly promising are electrolyte systems based on the combination of low lattice energy zinc imide salt and a special co-solvent of oligomeric poly(ethylene glycol) dimethyl ether (PEGDME) mixed with a small amount of ethylene carbonate (EC), dimensionally stabilized with PVDF-HFP. Such novel polymer electrolyte membranes could lead to the development of new kinds of electrochemical energy storage devices based on zinc electrochemistry, including solid-state, thin-film rechargeable zinc/air cells envisaged. (author)

  1. Adsorption capacity of poly(ether imide) microparticles to uremic toxins.

    Science.gov (United States)

    Tetali, Sarada D; Jankowski, Vera; Luetzow, Karola; Kratz, Karl; Lendlein, Andreas; Jankowski, Joachim

    2016-01-01

    Uremia is a phenomenon caused by retention of uremic toxins in the plasma due to functional impairment of kidneys in the elimination of urinary waste products. Uremia is presently treated by dialysis techniques like hemofiltration, dialysis or hemodiafiltration. However, these techniques in use are more favorable towards removing hydrophilic than hydrophobic uremic toxins. Hydrophobic uremic toxins, such as hydroxy hipuric acid (OH-HPA), phenylacetic acid (PAA), indoxyl sulfate (IDS) and p-cresylsulfate (pCRS), contribute substantially to the progression of chronic kidney disease (CKD) and cardiovascular disease. Therefore, objective of the present study is to test adsorption capacity of highly porous microparticles prepared from poly(ether imide) (PEI) as an alternative technique for the removal of uremic toxins. Two types of nanoporous, spherically shaped microparticles were prepared from PEI by a spraying/coagulation process.PEI particles were packed into a preparative HPLC column to which a mixture of the four types of uremic toxins was injected and eluted with ethanol. Eluted toxins were quantified by analytical HPLC. PEI particles were able to adsorb all four toxins, with the highest affinity for PAA and pCR. IDS and OH-HPA showed a partially non-reversible binding. In summary, PEI particles are interesting candidates to be explored for future application in CKD.

  2. Influence of nanoporous poly(ether imide) particle extracts on human aortic endothelial cells (HAECs).

    Science.gov (United States)

    Kumar, Reddi K; Basu, Sayantani; Lemke, Horst-Dieter; Jankowski, Joachim; Kratz, Karl; Lendlein, Andreas; Tetali, Sarada D

    2016-01-01

    Accumulated uremic toxins like indoxyl sulphate, hippuric acid and p-cresyl sulphates in renal failure patients stimulate proinflammatory effects, and consequently kidney and cardiovascular diseases. Low clearance rate of these uremic toxins from the blood of uremic patients by conventional techniques like hemodialysis is due to their strong covalent albumin binding (greater than 95%) and hydrophobic nature, which led to alternatives like usage of hydrophobic adsorber's in removing these toxins from the plasma of kidney patients. Polymers like polyethylene, polyurethane, polymethylmethacrylate, cellophane and polytetrafluoroethylene were already in use as substitutes for metal devices as dialysis membranes. Among new synthetic polymers, one such ideal adsorber material are highly porous microparticles of poly(ether imide) (PEI) with diameters in the range from 50-180μm and a porosity around 88±2% prepared by a spraying and coagulation process.It is essential to make sure that these synthetic polymers should not evoke any inflammatory or apoptotic response during dialysis. Therefore in our study we evaluated in vitro effect of PEI microparticle extracts in human aortic endothelial cells (HEACs) concerning toxicity, inflammation and apoptosis. No cell toxicity was observed when HAECs were treated with PEI extracts and inflammatory/apoptotic markers were not upregulated in presence of PEI extracts. Our results ensure biocompatibility of PEI particles and further hemocompatibility of particles will be tested.

  3. Research on Influence Factors of Surfactivity of Polyester Polyether Block Copolymer

    Institute of Scientific and Technical Information of China (English)

    WU Ming-hua; LIN He-ming

    2008-01-01

    Polyester polyether block copolymer (PPBC) was synthesized by ester-exchange and polycodensation reactions using dimethyl terephthalate (DMT), ethylene glycol (EG) and polyethylene glycol (PEG) as monomer. The effects of PEG molecular weight, mol ratio of DMT to PEG (nDMT/nPEG), temperature and time of polycondensation reaction and vacuum degree in the reaction system on the surface tension and critical micelle concentration (CMC) of PPBC aqueous solution were studied. It was found that both the molecular weight and the concentration of PEG can affect PPBC'S surface activity obviously, and the optimum synthesis condition of PPBC used as surfactant is as follows: PEG molecular weight is 1500, mol ratio of DMT to PEG is 3, temperature and time of polycondensation reaction is 260°C×1h, vacuum degree of condensation reaction is 0.03-0.05 MPa. It was proved by surface tension measurement of PPBC aqueous solution that the PPBC synthesized in this condition is a good surfactant with excellent surfactivity.

  4. In Vitro Evaluation of Bioactivity of Chemically Deposited Hydroxyapatite on Polyether Ether Ketone

    Directory of Open Access Journals (Sweden)

    D. Almasi

    2015-01-01

    Full Text Available Polyether ether ketone (PEEK is considered the best alternative material for titanium for spinal fusion cage implants due to its low elasticity modulus and radiolucent property. The main problem of PEEK is its bioinert properties. Coating with hydroxyapatite (HA showed very good improvement in bioactivity of the PEEK implants. However the existing methods for deposition of HA have some disadvantages and damage the PEEK substrate. In our previous study a new method for deposition of HA on PEEK was presented. In this study cell proliferation of mesenchymal stem cell and apatite formation in simulated body fluid (SBF tests were conducted to probe the effect of this new method in improvement of the bioactivity of PEEK. The mesenchymal stem cell proliferation result showed better cells proliferation on the treated layer in comparison with untreated PEEK. The apatite formation results showed the growth of the HA on the treated PEEK but there was not any sight of the growth of HA on the untreated PEEK even after 2 weeks. The results showed the new method of the HA deposition improved the bioactivity of the treated PEEK in comparison with the bare PEEK.

  5. UV-induced Self-initiated Graft Polymerization of Acrylamide onto Poly(ether ether ketone)

    Institute of Scientific and Technical Information of China (English)

    CHEN Rui-chao; SUN Hui; LI Ang; XU Guo-zhi

    2012-01-01

    Photo-grafting of hydrophilic monomer was used to enhance the hydrophilicity of poly(ether ether ketone)(PEEK) with the aim of extending its applications to biological fields.PEEK sheets were surface modified by grafting of acrylamide(AAm) with ultraviolet(UV) irradiation in the presence or absence of benzophenone(BP).The effects of BP,irradiation time and monomer concentration on the surface wettability of PEEK were investigated.Characterization of modified PEEK using scanning electron microscopy(SEM),energy-disperse spectrometer(EDS) and water contact angle measurements shows that AAm was successfully grafted on PEEK surface both in presence and absence of BP.With the increase in irradiation time and monomer concentration,contact angles decrease to as low as 30°,demonstrating a significant improvement of surface hydrophilicity.In agreement with the decrease in contact angle,under identical conditions,the nitrogen concentration increases,suggesting the increase in grafting degree of the grafting polymerization.This investigation demonstrates a self-initiation of PEEK due to its BP-like structure in the backbone of the polymer.Though the graft polymerization proceeds more readily in the presence of BP,the self-initiated graft polymerization is clearly observed.

  6. Preparation of composite poly(ether block amide) membrane for CO2 capture

    Institute of Scientific and Technical Information of China (English)

    Lianjun Wang; Yang Li; Shuguang Li; Pengfei Ji; Chengzhang Jiang

    2014-01-01

    In this study, a poly(ether block amide) (Pebax 1657) composite membrane applied for CO2 capture was prepared by coating Pebax 1657 solution on polyacrylonitrile (PAN) ultrafiltration membrane. Ethanol/water mixture was used as the solvent of Pebax and the effects of ethanol/water mass ratios and Pebax concentration on the permeation properties of composite membrane were studied. To enhance the com-posite membrane permeance, the gutter layer, made from reactive amino silicone crosslinking with polydimethylsiloxane (PDMS), was de-signed. The influence of crosslinking degree of the gutter layer on membrane performance was investigated. As a result, a Pebax/amino-PDMS/PAN multilayer membrane with hexane resistance was developed, showing CO2 permeance of 350 GPU and CO2/N2 selectivity over 50. The blend of polyethylene glycol dimethyl ether (PEG-DME) with Pebax as coating material was studied to further improve the membrane performance. After being combined with PEG-DME additive, CO2 permeance of the final Pebax-PEG-DME/amino-PDMS/PAN composite membrane reached 400 GPU above with CO2/N2 selectivity over 65.

  7. Crosslinked poly(ether block amide) composite membranes for organic solvent nanofiltration applications

    KAUST Repository

    Aburabie, Jamaliah

    2016-10-01

    Poly(ether block amide) – Pebax® – based membranes are well described for gas separation applications. But only a few publications exist for their application in pressure driven liquid applications like ultrafiltration and nanofiltration. Here we use the commercially available Pebax® 1657 for the preparation of membranes for the filtration of organic solvents. Porous polyacrylonitrile membranes were coated with Pebax® 1657 which was then crosslinked. Toluene diisocyanate (TDI) was used as a crosslinker agent for the coating. Reaction time and crosslinker concentration were optimized for the aimed application. The Pebax® coating and the impact of the TDI on the resulting crosslinked membranes were investigated by Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM) and differential scanning calorimetry (DSC). SEM analysis shows a uniform thin coating of the PEBAX that covers the pores of the PAN membranes. FTIR and DSC analysis confirm the crosslinking reaction. Crosslinked Pebax® membranes show high stability toward ethanol propanol, acetone and even dimethylformamide (DMF). In the case of DMF applications, the standard PAN was replaced by crosslinked PAN developed in our laboratory. In order to increase the membranes permeances, graphene oxide (GO) nanosheets were incorporated in the Pebax® coating. These GO containing membranes showed strongly increased permeances for selected solvents. © 2016 Elsevier B.V.

  8. Synthesis, cytotoxicity and antibacterial activity of new esters of polyether antibiotic - salinomycin.

    Science.gov (United States)

    Antoszczak, Michał; Popiel, Katarzyna; Stefańska, Joanna; Wietrzyk, Joanna; Maj, Ewa; Janczak, Jan; Michalska, Greta; Brzezinski, Bogumil; Huczyński, Adam

    2014-04-09

    A series of 12 novel ester derivatives of naturally occurring polyether antibiotic - salinomycin were synthesized, characterised by spectroscopic method and evaluated for their in vitro antibacterial activity and cytotoxicity. The new esters were demonstrated to form complexes with monovalent and divalent metal cation of 1:1 stoichiometry in contrast to the salinomycin which forms only complexes with monovalent cations. All the obtained compounds show potent antiproliferative activity against human cancer cell lines and a good selectivity index for cancer versus mammalian cells. Additionally, 3 compounds showed higher antiproliferative activity against the drug-resistant cancer cells and lower toxicity towards normal cells than those of unmodified salinomycin and standard anticancer drugs such as cisplatin and doxorubicin. Some of the synthesized compounds showed good inhibitory activity against Staphylococcus strains and clinical isolates of methicillin-resistant Staphylococcus aureus (MRSA) and Staphylococcus epidermidis (MRSE). These studies show that salinomycin esters are interesting scaffolds for the development of novel anticancer and Gram-positive antibacterial agents.

  9. Toughening polylactide with polyether-block-amide and thermoplastic starch acetate: Influence of starch esterification degree.

    Science.gov (United States)

    Zhou, Linyao; Zhao, Guiyan; Feng, Yulin; Yin, Jinghua; Jiang, Wei

    2015-01-01

    Native corn starch was esterified with acetic anhydride and plasticized with glycerol to give the thermoplastic starch acetate (TPSA). TPSA was blended with polylactide (PLA) and polyether-block-amide-graft-glycidyl methacrylate (PEBA-g-GMA) to obtain biodegradable PLA/PEBA-g-GMA/TPSA blends with high notched impact resistance and low cost. Compared with PLA/PEBA-g-GMA blends, as much as 9 wt% expensive PEBA-g-GMA elastomer could be substituted by the slightly acetylated thermoplastic starch while retaining high impact strength. The mechanical properties depended on the esterification degree of starch acetate. The impact strength, tensile strength and elongation at break increased to the peak value with increasing the esterification degree from 0 to 0.04, thereafter they decreased on further increasing the esterification degree. The morphological results showed that the TPSA particles were smaller and more uniform at the optimum esterification degree of 0.04, leading to the peak value of the mechanical properties. Copyright © 2015 Elsevier Ltd. All rights reserved.

  10. An SEM and EDS study of the microstructure of nitrate ester plasticized polyether propellants

    Directory of Open Access Journals (Sweden)

    YONG LIU

    2010-03-01

    Full Text Available To probe the microstructures of nitrate ester plasticized polyether (NEPE composite propellants and observe the morphology of each constitute in the propellant, the microstructure and elemental constitutes of NEPE propellants were investigated using scanning electron microscopy and energy dispersive X-ray spectroscopy. The ammonium perchlorate (AP grains had a scraggy surface and were difficult to disperse uniformly. The compatibility between the AP grains and the polymer binder was poor, especially for large grains. The size distribution range of the AP and octogen (HMX grains in propellants varied from several to several hundreds μm for the former while for the latter from several to several tens μm. Contrasting images before and after dissolution the propellant in trichloromethane showed that the degree of crosslinking of the polymer binder was low since non-crosslinked binder on the surface areas was easily removed by the solvent, and that the plasticizer was near the HMX grains and contributed more O to the element analysis of HMX.

  11. Comparative study to evaluate the accuracy of polyether occlusal bite registration material and occlusal registration wax as a guide for occlusal reduction during tooth preparation

    Directory of Open Access Journals (Sweden)

    Niranjan Joshi

    2013-01-01

    Objective: The objective of this study was to compare and evaluate the reliability of the most commonly used occlusal registration wax that with polyether bite registration material as a guide for occlusal reduction required during tooth preparations. Materials and Methods: For the purpose of this study, 25 abutment teeth requiring tooth preparation for fixed prosthesis were selected and tooth preparations carried out. Modeling wax strips of specific dimensions were placed onto the cast of prepared tooth, which was mounted on maximum intercuspation on the articulator and the articulator was closed. The thickness of the wax registration was measured at three zones namely two functional cusps and central fossa. Similar measurements were made using the polyether bite registration material and prosthesis at the same zones. The data was tabulated and was subjected to statistical analysis using anova test and Tukey honestly significant difference test. Results: The differences in thickness between wax record and prosthesis by 0.1346 mm, whereas the difference between polyether and prosthesis was 0.02 mm with a P value of 0.042, which is statistically significant. This means that the wax record was 8.25% larger than the prosthesis while polyether was just 1.27% larger than the prosthesis. Conclusion: The clinical significance of the above analysis is that Ramitec polyether bite registration material is most suitable material when compared with commonly used modeling wax during the tooth preparation.

  12. Final Report for "Solid State Voltammetry and Other Experiments in Molecular Melts" Semi-Solid Nanoparticles, and Biomolecule Polyether Hybrids"

    Energy Technology Data Exchange (ETDEWEB)

    Royce W. Murray

    2005-07-27

    Since the technical progress report of the previous renewal proposal, my students and I have published or have in press 13 papers (5 in JACS). Another is under review; several others are in draft form. This Final Report is an updated version of the Performance Report submitted with the renewal proposal for this project.

  13. Surface Sulfonation of Polyvinyl Chloride by Plasma for Antithrombogenicity

    Institute of Scientific and Technical Information of China (English)

    刘鹏; 陈亚芍

    2004-01-01

    To enhance the blood compatibility of Polyvinyl Chloride (PVC) film, the film was modified by SO2/O2 gas plasma treatment. The effect of surface sulfonation of PVC treated by various SO2/O2 gas plasma depended on the volume ratio O2/(SO2 + 02). When the volumeratio was 0.5, the effect of sulfonation was the best. Sulfonic acid groups were specifically and efficiently introduced onto the PVC surface, which was proved by X-ray photoelectron spectroscopy (XPS) and Attenuated Total Reflectance Fourier Transfer Infrared (ATR-FTIR) spectroscopy. The surface microstructure of modified PVC film was studied with scanning electron microscopy (SEM).The antithrombogenicity of the samples was determined by the activated partial thromboplastin time (APTT), prothrombin time (PT), thrombin time (TT) and plasma recalcification time (PRT)tests and platelet adhesion experiment. The results indicated that the antithrombogenicity of modified PVC was improved remarkably.

  14. Phase Behavior and Structural Transitions in Sodium Dodecyl Sulfonate Microemulsions

    Institute of Scientific and Technical Information of China (English)

    杨根生; 施介华; 等

    2002-01-01

    The forming mechanism of microemulsion of sodium dodecyl sulfonate.alcohols,water and isooctane was studied,with particular emphasis on the effect of molecular weight and concentration of alocohols.Phase diagram of the four components,alcohol, sodium dodecyl sulfonate,water and isooctane,was used as a means of study,through which the microemulsion regions were determined.Phase diagram of sodium dodecyl sulfonate/n-pentanol/isooctane/water system at km=2(km=Wn-pentanol/WSDS)is presented. The variation of conductivities of different microemulsion samples with water was measured.From the conductivities we investigated a change in structure from water droplets in oil(W/O)at low water content to liquid crystal at intermediate water content and a structure of oil droplets in water(O/W)at high water content.

  15. Dynamics of Sulfonated Polystyrene Ionomers by Dielectric Relaxation Spectroscopy

    Science.gov (United States)

    Castagna, Alicia; Wang, Wenqin; Winey, Karen; Runt, James

    2010-03-01

    Broadband dielectric spectroscopy was used to investigate the dynamics of sulfonated polystyrene (SPS) ionomers, in both the acid and neutralized form. This study seeks to elucidate the role of counter ion type (Zn, Na, and Cs), degree of sulfonation (9 and 6%), and ion cluster morphology on the relaxation phenomena of SPS. Degree of neutralization and ion type have been found to significantly impact the breadth and time scale of the segmental relaxation process. High temperature relaxation processes, tentatively proposed to arise from Maxwell-Wagner-Sillars interfacial polarization and a hydrogen bonding relaxation, have also been identified. Bands in the sulfonate stretching region of FTIR spectra reveal information about ion coordination in the local aggregate environment. A combination of scanning transmission electron microscopy imaging and X-ray scattering confirmed the presence of homogeneously distributed, nearly monodisperse spherical ionic aggregates in the polymer matrix.

  16. Julia Olefination as a General Route to Phenyl (alpha-Fluoro)vinyl Sulfones.

    Science.gov (United States)

    He, Maggie; Ghosh, Arun K; Zajc, Barbara

    2008-04-01

    Mild and efficient synthesis of phenyl (alpha-fluoro)vinyl sulfones via condensation of aldehydes and a ketone with a novel benzothiazolyl based bis-sulfone reagent is reported and this proceeds with moderate to good Z-stereoselectivity.

  17. Ruthenium-catalyzed meta sulfonation of 2-phenylpyridines.

    Science.gov (United States)

    Saidi, Ourida; Marafie, Jameel; Ledger, Araminta E W; Liu, Po Man; Mahon, Mary F; Kociok-Köhn, Gabriele; Whittlesey, Michael K; Frost, Christopher G

    2011-12-07

    A selective catalytic meta sulfonation of 2-phenylpyridines was found to occur in the presence of (arene)ruthenium(II) complexes upon reaction with sulfonyl chlorides. The 2-pyridyl group facilitates the formation of a stable Ru-C(aryl) σ bond that induces a strong para-directing effect. Electrophilic aromatic substitution proceeds with the sulfonyl chloride to furnish a sulfone at the position meta to the chelating group. This new catalytic process offers access to atypical regioselectivity for reactions involving chelation-assisted cyclometalation.

  18. Sulfur and Hydrogen Isotope Anomalies in Meteorite Sulfonic Acids

    Science.gov (United States)

    Cooper, George W.; Thiemens, Mark H.; Jackson, Teresa L.; Chang, Sherwood

    1997-01-01

    Intramolecular carbon, hydrogen, and sulfur isotope ratios were measured on a homologous series of organic sulfonic acids discovered in the Murchison meteorite. Mass-independent sulfur isotope fractionations were observed along with high deuterium/hydrogen ratios. The deuterium enrichments indicate formation of the hydrocarbon portion of these compounds in a low-temperature environment that is consistent with that of interstellar clouds. Sulfur-33 enrichments observed in methanesulfonic acid could have resulted from gas-phase ultraviolet irradiation of a precursor, carbon disulfide. The source of the sulfonic acid precursors may have been the reactive interstellar molecule carbon monosulfide.

  19. Conjugate Additions of Secondary Amines and Water to Allenyl Perfluoroalkyl Sulfones

    Institute of Scientific and Technical Information of China (English)

    WANG Xiao-Jin; LIN Yun; LIU Jin-Tao

    2006-01-01

    Preparation of allenyl perfluoroalkyl sulfones from perfluoroalkyl sulfinyl chlorides and their reactions with secondary amines and water were studied. At room temperature secondary amines reacted readily with allenyl perfluoroalkyl sulfones to give the corresponding enamine adducts, which underwent rearrangement to afford conjugate enamines in refluxing toluene. Good diastereoslectivities were observed in the addition of diethylamine to γ-ethyl-γ-methylallenyl perfluoroalkyl sulfones. In refluxing acetonitrile, water could also undergo the similar addition with allenyl perfluoroalkyl sulfones.

  20. Miscibility of Methylmethacrylate-co-methacrylic Acid Polymer with Magnesium, Zinc, and Manganese Sulfonated Polystyrene Ionomers

    OpenAIRE

    ALKAN, Cemil; YURTSEVEN, Nebahat; ARAS, Leyla

    2005-01-01

    The miscibility of methyl methacrylate-co-methacrylic acid polymer (MMA-MAA) with metal neutralized sulfonated polystyrene ionomers was investigated by viscometry, differential scanning calorimetry (DSC), and Fourier transform infrared radiation spectroscopy (FTIR) techniques. Polystyrene (PS) was sulfonated by acetic anhydride and sulfuric acid and the sulfonation degree was found to be 2.6 mole percent, and 2.6 mole percent sulfonated polystyrene was neutralized by Mg, Zn, and Mn sa...

  1. Phase behavior of a pure alkyl aryl sulfonate surfactant. [Sodium 8-phenyl-n-hexadecyl-p-sulfonate

    Energy Technology Data Exchange (ETDEWEB)

    Franses, E.I.; Davis, H.T.; Miller, W.G.; Scriven, L.E.

    1978-03-01

    Specctroturbidimetry, visual and microscopic observations, ultracentrifugation and ultrafiltration, conductimetry, and /sup 13/C NMR were used to study the phase behavior of pure sodium 8-phenyl-n-hexadecyl-p-sulfonate in water--NaCl, decane, and water--decane. Solubility of the sulfonate in water is 0.06 wt % at 25/sup 0/C and 0.7 wt % at 90/sup 0/C, and it drops to 0.0002 wt % in 3 wt % NaCl (25/sup 0/C). A liquid crystalline phase in equilibrium with aqueous solution contains 25 wt % water. Nucleation of supersaturated solutions is slow. Dispersability of the sulfonate is high, but NaCl has an adverse effect. 39 references, 13 figs., 5 tables. (DLC)

  2. 40 CFR 721.5425 - α-Olefin sulfonate, potassium salts.

    Science.gov (United States)

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false α-Olefin sulfonate, potassium salts... Substances § 721.5425 α-Olefin sulfonate, potassium salts. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified as an α-olefin sulfonate, potassium salt...

  3. Blending of styrene-block-butadiene-block-styrene copolymer with sulfonated vinyl aromatic polymers

    NARCIS (Netherlands)

    Ruggeri, Giacomo; Passaglia, Elisa; Giorgi, Ivan; Picchioni, Francesco; Aglietto, Mauro

    2001-01-01

    Different polymers containing sulfonic groups attached to the phenyl rings were prepared by sulfonation of polystyrene (PS) and styrene-block-(ethylene-co-1-butene)-block-styrene (SEBS). The sulfonation degree (SD) was varied between 1 and 20 mol% of the styrene units. Polyphase materials containing

  4. Enchansing the Ionic Purity of Hydrophilic Channels by Blending Fully Sulfonated Graft Copolymers with PVDF Homopolymer

    DEFF Research Database (Denmark)

    Nielsen, Mads Møller; Ching-Ching Yang, Ami; Jankova Atanasova, Katja

    2013-01-01

    The influence of tuning the ionic content of membranes by blending, as opposed to varying the degree of sulfonation, is evaluated. Membranes of fully sulfonated poly(vinylidene fluoride-co-chlorotrifluoroethylene)-g-poly(styrene sulfonic acid) blended with PVDF were prepared and investigated...

  5. 40 CFR 721.9620 - Aromatic sulfonic acid compound with amine.

    Science.gov (United States)

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Aromatic sulfonic acid compound with... Specific Chemical Substances § 721.9620 Aromatic sulfonic acid compound with amine. (a) Chemical substance... aromatic sulfonic acid compound with amine (PMN P-93-832) is subject to reporting under this section...

  6. Chemical Agent Performance of Sulfonated Ionomeric Membranes for Chem/Bio Applications

    Science.gov (United States)

    2008-12-01

    Polyisobutylene ( PIB ) Chemically Modified IB Sulfonic Acid Counter-ion (Ba, Mg, Ca, Zn, Cs)Block Copolymer Morphology Sulfonic acid...Mauritz, K., 2000: Diffusion of Alcohols Through Sulfonated PS/ PIB /PS Block Copolymers Using FTIR-ATR Spectroscopy, Polymer Materials: Engineering

  7. Blending of styrene-block-butadiene-block-styrene copolymer with sulfonated vinyl aromatic polymers

    NARCIS (Netherlands)

    Ruggeri, Giacomo; Passaglia, Elisa; Giorgi, Ivan; Picchioni, Francesco; Aglietto, Mauro

    2001-01-01

    Different polymers containing sulfonic groups attached to the phenyl rings were prepared by sulfonation of polystyrene (PS) and styrene-block-(ethylene-co-1-butene)-block-styrene (SEBS). The sulfonation degree (SD) was varied between 1 and 20 mol% of the styrene units. Polyphase materials containing

  8. 40 CFR 721.5450 - α-Olefin sulfonate, sodium salt.

    Science.gov (United States)

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false α-Olefin sulfonate, sodium salt. 721... Substances § 721.5450 α-Olefin sulfonate, sodium salt. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as α-olefin sulfonate, sodium salt...

  9. Survey of sulfonated polyimide membrane as a good candidate for nafion substitution in fuel cell

    Energy Technology Data Exchange (ETDEWEB)

    Akbarian-Feizi, Leila; Mehdipour-Ataei, Shahram; Yeganeh, Hamid [Iran Polymer and Petrochemical Institute, P.O. Box 14965/115, Tehran (Iran)

    2010-09-15

    Studies in fuel cell membranes show that modification of polyimides by introduction of aliphatic linkages in the structure of sulfonated copolyimides, synthesis of branched/crosslinked sulfonated polyimides, and semi and fully interpenetrating polymer networks of sulfonated polyimides restrain suitable potential for Nafion substitution. (author)

  10. Moisture effect on polyether and polyvinylsiloxane dimensional accuracy and detail reproduction.

    Science.gov (United States)

    Walker, Mary P; Petrie, Cynthia S; Haj-Ali, Reem; Spencer, Paulette; Dumas, Chris; Williams, Karen

    2005-09-01

    This investigation evaluated and compared the dimensional accuracy and surface detail reproduction of two hydrophilic polyvinylsiloxane (PVS) and two polyether (PE) impression materials when used under dry and moist conditions. Impressions were made of stainless steel dies as described in ANSI/ADA specification no. 19, with two vertical and three horizontal lines inscribed on the die superior surface. Impressions were made under dry and moist conditions (17 impressions per condition for each material). Dimensional accuracy was measured by comparing the average length of the middle horizontal line in each impression with the same line on the metal die using a measuring microscope with an accuracy of 0.001 mm. Surface detail reproduction was evaluated by using criteria similar to ADA specification no. 19: continuous replication of at least two of the three horizontal lines. The mean percent dimensional change and SD values ranged from -0.135% (0.035) to 0.053% (0.031). A two-way analysis of variance (ANOVA) indicated that moisture did not cause significant adverse effects on the dimensional accuracy of any material (p > 0.05); however, significant differences were found between the materials (p Aquasil and Genie Ultra PVS impressions produced satisfactory detail reproduction, while 100% of Permadyne Garant and Impregum Penta Soft PE impressions still met the surface detail criteria. Although moisture may not adversely affect the dimensional accuracy of either PE or hydrophilic PVS material, the evidence suggests that PE material is more likely to produce impressions with superior detail reproduction in the presence of moisture.

  11. Synthesis, characterization and properties of yellow-light-emitting polyethers containing bis(styryl)anthracene units

    Energy Technology Data Exchange (ETDEWEB)

    Gioti, M., E-mail: mgiot@physics.auth.gr; Pitsalidis, C., E-mail: mgiot@physics.auth.gr; Tzounis, L.; Logothetidis, S., E-mail: logot@auth.gr [Laboratory for Thin Films-Nanosystems and Nanometrology (LTFN), Physics Department, Aristotle University of Thessaloniki, GR-54124 Thessaloniki (Greece); Andreopoulou, A. K.; Kallitsis, J. K. [Department of Chemistry, University of Patras, University Campus, Rio-Patras GR26504, Greece and Foundation for Research and Technology Hellas, Institute of Chemical Engineering Sciences (FORTH/ICE-HT), Platani Str., Patras GR26504 (Greece); Mparmpoutsis, E. [Department of Chemistry, University of Patras, University Campus, Rio-Patras GR26504 (Greece)

    2015-02-17

    Aromatic aliphatic polyethers containing bis(styryl)anthracene units in the main chain separated by flexible spacer of 11 (AND52) or 12 (AND53) methylene units, were synthesized and characterized aiming to be applied as emitting materials in polymer light emitting diode (PLED) devices. The polymers are soluble in common organic solvents and have average molecular weight of about 15kDa. Differentiations owing to an odd-even number of methylene units (χ=11 vs χ=12) are observed in their optical properties in solid state. Thin films as well as PLED devices were fabricated via conventional spin-coating process. Initially, various parameters have been investigated concerning the solubility of the polymers, the effect of film thickness on the electrical properties, and their thermal stability. The optical properties of the two polymers were investigated by NIR-Vis-far UV spectroscopic ellipsometry (SE). The accurate determination of the thickness and the optical constants (refractive index and dielectric function as a function of wavelength) were derived. These provide substantial insights into the final design of the optimum final multi-layer structure of the PLEDs, if we take into account that the external quantum efficiency (EQE) of electroluminescence (EL) strongly depends on the optical interference of the beams of emitted light that have been multiply reflected from the layer interfaces. The morphological characterization of the AND52 and AND53 polymeric thin films was carried out using atomic force microscopy (AFM), while current density-voltage (J-V) characteristics of the devices were studied by electrical measurements. The single PLED devices were switched on at relatively low operation voltages, showing the potential as backplanes for active matrix PLED applications. In this perspective, it can be assumed that further studies of the presented materials will enable the development of flexible PLEDs with the possibility to scale up their dimensions for bigger

  12. Synthesis and Characterization of a New Network Polymer Electrolyte Containing Polyether in the Main Chains and Side Chains

    Institute of Scientific and Technical Information of China (English)

    Wang; Cheng-chien; Chen; Chuh-yung

    2007-01-01

    1 Results A new network polymer electrolyte matrix with polyether in the side chains and main chains was synthesized by the azo-macroinitiator method and urethane reaction.The macroinitiator,polymer and network polymer were confirmed by Fourier-transform infrared (FT-IR) spectroscopy and 1H NMR.FT-IR was also used to study the environment of lithium ions doped in these network polymer electrolytes.Three important groups are considered: N-H,carbonyl,and ether groups.The thermal properties of the polymer ...

  13. Di-ureasil hybrids doped with LiBF4 : spectroscopic study of the ionic interactions and hydrogen bonding

    OpenAIRE

    Fernandes, Mariana; Barbosa, P. C.; Silva,Maria Manuela; Smith, Michael John; Zea Bermudez, V. de

    2011-01-01

    In the present work Fourier Transform infrared and Raman spectroscopy were used to characterize the cation/polymer, cation/cross-link, cation/anion and hydrogen bonding interactions in hybrid electrolytes composed of lithium tetrafluoroborate (LiBF4) and di-urea cross-linked poly(oxyethylene) (POE)/siloxane hybrid networks (di-ureasils) designated as d-(2000) and d-U(600) and incorporating polyether chains with ca. 40.5 and 8.5 oxyethylene repeat units, respectively. Samples with ∞ > n ≥ 2.5 ...

  14. Synthesis and properties of poly(sulfone-arylate) copolymers

    NARCIS (Netherlands)

    Stephen, Ranimol; Gibon, Cécile M.; Weber, Martin; Gaymans, Reinoud J.

    2009-01-01

    Poly(sulfone-arylate) was synthesized in a reaction between dihydroxy polysulfone prepolymers and either diphenyl terephthalate or terephthaloyl chloride. The dihydroxy polysulfone prepolymers had molecular weights of 2000 and 4000 g/mol. The polymerization with diphenyl terephthalate was carried ou

  15. Amperometric urea biosensors based on sulfonated graphene/polyaniline nanocomposite

    Directory of Open Access Journals (Sweden)

    Das G

    2015-08-01

    Full Text Available Gautam Das, Hyon Hee Yoon Department of Chemical and Biological Engineering, Gachon University, Seongnam, Gyeonggi-do, South Korea Abstract: An electrochemical biosensor based on sulfonated graphene/polyaniline nanocomposite was developed for urea analysis. Oxidative polymerization of aniline in the presence of sulfonated graphene oxide was carried out by electrochemical methods in an aqueous environment. The structural properties of the nanocomposite were characterized by Fourier-transform infrared, Raman spectroscopy, X-ray photoelectron spectroscopy, and scanning electron microscopy techniques. The urease enzyme-immobilized sulfonated graphene/polyaniline nanocomposite film showed impressive performance in the electroanalytical detection of urea with a detection limit of 0.050 mM and a sensitivity of 0.85 µA·cm-2·mM-1. The biosensor achieved a broad linear range of detection (0.12–12.3 mM with a notable response time of approximately 5 seconds. Moreover, the fabricated biosensor retained 81% of its initial activity (based on sensitivity after 15 days of storage at 4°C. The ease of fabrication coupled with the low cost and good electrochemical performance of this system holds potential for the development of solid-state biosensors for urea detection. Keywords: electrochemical deposition, sulfonated graphene oxide, urease

  16. Sodium dimercaptopropane sulfonate as antidote against non-metallic pesticides

    Institute of Scientific and Technical Information of China (English)

    Zhi-kang CHEN; Zhong-qiu LU

    2004-01-01

    @@ INTRODUCTION With the advent of World War II, dimercaptol was first developed in England as an effective antidote against arsenical agents. In 1950' s, scientists from the Soviet Union developed a water-soluble compound, sodium dimercaptopropane sulfonate (Na-DMPS) named as Unithiol (or Unitiol), which was able to chelate heavy metals and metalloids.

  17. Sulfonated polyimides containing triphenylphosphine oxide for proton exchange membranes

    Energy Technology Data Exchange (ETDEWEB)

    Mandal, Arun Kumar; Bera, Debaditya; Banerjee, Susanta, E-mail: susanta@matsc.iitkgp.ernet.in

    2016-09-15

    A series of sulfonated co-polyimides (co-SPI) were prepared by one pot polycondensation reaction of a combination of diamines namely; 4,4′-diaminostilbene-2,2′-disulfonic acid (DSDSA) and prepared non-sulfonated diamine (DATPPO) containing triphenylphosphine oxide with 1,4,5,8-naphthalenetetracarboxylic dianhydride (NTDA). All these soluble co-SPI gave flexible membranes with high thermal stability and showed good mechanical property. Transmission electron microscopy (TEM) analysis revealed the microphase separated morphology with well-dispersed hydrophilic (cluster size in the range of 5–55 nm) domains. The co-SPI membranes showed high oxidative and hydrolytic stability with higher proton conductivity. All these co-SPI membranes exhibited low water uptake and swelling ratio. The co-SPI membrane TPPO-60 (60% degree of sulfonation) with IEC{sub W} = 1.84 mequiv g{sup −1} showed high proton conductivity (99 mS cm{sup −1} at 80 °C and 107 mS cm{sup −1} at 90 °C) in water with high oxidative (20 h) and hydrolytic stability (only 5% degradation in 24 h). - Highlights: • Triphenylphosphine oxide containing sulfonated polyimides (SPIs) was synthesized. • The SPIs showed good oxidative and hydrolytic stability and high proton conductivity. • TEM analysis revealed well separated morphology of the SPIs.

  18. Intrinsic and Ionic Conduction in Humidity-Sensitive Sulfonated Polyaniline

    NARCIS (Netherlands)

    Doan, D.C.T.; Ramaneti, R.; Baggerman, J.; Tong, H.D.; Marcelis, A.T.M.; Rijn, van C.J.M.

    2014-01-01

    The influence of humidity on the conductivity of sulfonated polyaniline (SPANI) and polyaniline (PANI) is investigated with electrochemical impedance spectroscopy (EIS). Separation of intrinsic (q) and ionic charge (i) mobility was observed using combination of ac and dc impedance measurements at

  19. Homolytic C-O cleavage in phosphates and sulfonates.

    Science.gov (United States)

    Ding, Lanlan; Zheng, Wenrui; Wang, Yingxing

    2015-04-09

    The C-O homolytic bond dissociation enthalpies(BDEs) were calculated by high-level ab initio including G4, G3B3, G3, CBS-QB3 and a series of density function theory (DFT) methods. It is found that the wB97 method gave the most reliable C-O BDEs and the root-mean-square deviation (RMSD) is 7.6 kJ/mol. Therefore, the C(sp(2))-O BDE predictions and the substituent effects of alkenyl phosphates/sulfonates and aryl phosphates/sulfonates were investigated in detail by using the wB97 method. Interestingly, there exist different substituent effects in α- and β-substituted alkenyl phosphates/sulfonates. Excellent linear relationships between the C-O BDEs of β-substituted alkenyl phosphates/sulfonates with substituent constant σp(+) were found. In addition, the NBO analysis further disclosed the essence of the substituent effects on C-O BDEs.

  20. Response of weeping willows to linear alkylbenzene sulfonate

    DEFF Research Database (Denmark)

    Yu, X.; Trapp, Stefan; Zhou, P.

    2006-01-01

    Linear alkylbenzene sulfonate (LAS) is the most commonly used anionic surfactant in laundry detergents and cleaning agents. LAS compounds are found in surface waters and soils. The short-term acute toxicity of LAS to weeping willows (Salix babylonica L.) was investigated. Willow cuttings were grown...

  1. Electronic Conductivity of Polypyrrole−Dodecyl Benzene Sulfonate Complexes

    DEFF Research Database (Denmark)

    West, Keld; Bay, Lasse; Nielsen, Martin Meedom

    2004-01-01

    The electronic conductivity of the electroactive polymer polypyrrole-dodecyl benzene sulfonate (PPy-DBS) has been characterized as function of the redox level. The polymer was synthesized with different isomers of the dopant anions: the common mixed DBS tenside and three well-defined synthetic...

  2. Production of sulfonated cation-exchangers from petroleum asphaltites

    Energy Technology Data Exchange (ETDEWEB)

    Pokonova, Yu.V.; Pol' kin, G.B.; Proskuryakov, V.A.; Vinogradov, M.V.

    1982-02-10

    Continuing our studies of the preparation of products of practical value from asphaltite, a new by-product of oil refining, we obtained sulfonated cation-exchangers from a mixture of asphaltite and acid tar. It is shown that these cation-exchangers have good kinetic properties and are superior in thermal and thermohydrolytic stability to the commercial cation-exchange resin KU-2.

  3. Wetting behavior of lightly sulfonated polystyrene ionomers on silica surfaces.

    Science.gov (United States)

    Zhai, Xiaowen; Weiss, R A

    2008-11-18

    The wetting/dewetting behavior of thin films of lightly sulfonated low molecular weight polystyrene (SPS) ionomers spin-coated onto silica surfaces were studied using atomic force microscopy (AFM), contact angle measurements, and electron microscopy. The effects of the sulfonation level, the choice of the cation, the solvent used to spin-coat the films, and the molecular weight of the ionomer were investigated. Small angle X-ray scattering was used to determine the bulk microstructure of the films. The addition of the sulfonate groups suppressed the dewetting behavior of the PS above its glass transition temperature, e.g. no dewetting occurred even after 240 h of annealing at 120 degrees C. Increasing the sulfonation level led to more homogeneous and smoother surfaces. The choice of the cation used affected the wetting properties, but not in a predictable manner. When tetrahydrofuran (THF) or a THF/methanol mixed solvent was used for spin-casting, a submicron-textured surface morphology was produced, which may be a consequence of spinodal decomposition of the film surface during casting. Upon annealing for long times, the particles coalesced into a coherent, nonwetted film.

  4. Epoxy-crosslinked sulfonated poly (phenylene) copolymer proton exchange membranes

    Science.gov (United States)

    Hibbs, Michael; Fujimoto, Cy H.; Norman, Kirsten; Hickner, Michael A.

    2010-10-19

    An epoxy-crosslinked sulfonated poly(phenylene) copolymer composition used as proton exchange membranes, methods of making the same, and their use as proton exchange membranes (PEM) in hydrogen fuel cells, direct methanol fuel cell, in electrode casting solutions and electrodes, and in sulfur dioxide electrolyzers. These improved membranes are tougher, have higher temperature capability, and lower SO.sub.2 crossover rates.

  5. Fate of linear alkylbenzene sulfonate (LAS) in activated sludge plants

    NARCIS (Netherlands)

    Temmink, B.G.; Klapwijk, A.

    2004-01-01

    Monitoring data were collected in a pilot-scale municipal activated sludge plant to assess the fate of the C12-homologue of linear alkyl benzene sulfonate (LAS-C12). The pilot-plant was operated at influent LAS-C12 concentrations between 2 and 12 mg/l and at sludge retention times of 10 and 27 days<

  6. Thermoanalytical Investigation of Some Sulfone-Containing Drugs

    OpenAIRE

    2012-01-01

    The thermal behavior of some sulfone-containing drugs, namely, dapsone (DDS), dimethylsulfone (MSM), and topiramate (TOP) in drug substances, and products were investigated using different thermal techniques. These include thermogravimetry (TGA), derivative thermogravimetry (DTG), differential thermal analysis (DTA), and differential scanning calorimetry (DSC). The thermogravimetric data allowed the determination of the kinetic parameters: activation energy (E a ), frequency factor (A), and r...

  7. Waterborne Polyurethane-Polyacrylic Ester Hybrid Dispersion Modified by Hexamethylene Diisocyanate Trimer%Waterborne Polyurethane-Polyacrylic Ester Hybrid Dispersion Modified by Hexamethylene Diisocyanate Trimer

    Institute of Scientific and Technical Information of China (English)

    2011-01-01

    A self-emulsifying waterborne polyurethane dispersion was synthesized with both hexamethylene diisocyanate (HDI) trimer and toluene diisoeyanate (TDI), polyether diols N220, 1,4- butanediol(BDO), 2-hydroxymethyl-propionic acid(DMPA) and epoxy resin E-20 as main raw materials with acetone-based method. The dispersion was further modified by methyl methacrylate (MMA) to form a kind of nuclear-shell hybrid dispersion, in which the hydrophobic nuclear was the polymethyl methacrylate and the hydrophilic shell was the self-emulsifying waterborne polyurethane dispersion modified by HDI trimer.

  8. Aligned electrospun nanofibers as proton conductive channels through thickness of sulfonated poly (phthalazinone ether sulfone ketone) proton exchange membranes

    Science.gov (United States)

    Gong, Xue; He, Gaohong; Wu, Yao; Zhang, Shikai; Chen, Bo; Dai, Yan; Wu, Xuemei

    2017-08-01

    A novel approach is proposed to fabricate sulfonated poly (phthalazinone ether sulfone ketone) (SPPESK) proton exchange membranes with ordered through-plane electrospinning nanofibers, which provide nano-scale through-plane proton conductive channels along the thickness direction of the membranes, aiming to satisfy the challenging requirement of high through-plane proton conductivity in fuel cell operations. Induced by electrostatic attraction of strong electric field, the negatively charged sulfonic acid groups tend to aggregate towards surface of the electrospun fibers, which is evidenced by TEM and SAXS and further induces aggregation of the sulfonic acid groups in the SPPESK inferfiber voids filler along the surface of the nanofibers. The aligned electrospun nanofibers carries long-range ionic clusters along the thickness direction of the membrane and results in much higher total through-plane conductivity in the thickness aligned electrospun membranes, nearly twice as much as that of the cast SPPESK membrane. With smooth treatment, the thickness aligned electrospun SPPESK membranes exhibit higher single cell power density and tensile strength as compared with Nafion 115 (around 1.2 and 1.5 folds, respectively). Such a design of thickness aligned nano-size proton conductive channels provide feasibility for high performance non-fluorinated PEMs in fuel cell applications.

  9. Dimensional Stability of Polyether, Alginate, and Silicone Impression Materials After Disinfection With 2% Sanosil Through the Immersion Technique

    Directory of Open Access Journals (Sweden)

    Izadi

    2014-10-01

    Full Text Available Background To prevent diseases transmission, infection control in dental offices without reducing the accuracy and dimensional stability of impression materials is very important. Objectives The aim of this study was to evaluate the effects of Sanosil disinfectants on the dimensional stability of some usual impression materials. Materials and Methods Three types of impression material, namely, alginate, condensational silicone, and polyether, were used in this study. Impressions were obtained from the master steel model. Fifteen impressions of each material (control group were immersed in water for ten minutes and impressions of study groups were disinfected by immersion in 2% Sanosil for ten minutes. Then impressions were poured by type III gypsum according to the manufacture's instruction. Dimensions of casts in the two anterior dimensions, i.e. interval between the anterior abutments and interval between anterior-posterior abutments, were recorded by a digital caliper with the accuracy of 0.01 mm. Data were analyzed with SPSS through two-way ANOVA test. Results The results showed that there was no significant difference in the mean dimension of casts prepared by different impression materials in anterior and anterior-posterior dimensions in comparison to the original model after disinfection with Sanosil. Conclusions The study revealed that disinfection with 2% Sanosil has no significant effect on casts dimensions of alginate, silicone, and polyether impression and dimensional stability is maintained.

  10. Characterization of a poly(ether urethane)-based controlled release membrane system for delivery of ketoprofen

    Energy Technology Data Exchange (ETDEWEB)

    Macocinschi, Doina, E-mail: eradro2002@yahoo.com [Department of Physical Chemistry of Polymers, ' Petru Poni' Institute of Macromolecular Chemistry, Aleea Gr. Ghica Voda 41 A, 700487 Iasi (Romania); Filip, Daniela; Vlad, Stelian; Oprea, Ana Maria [Department of Physical Chemistry of Polymers, ' Petru Poni' Institute of Macromolecular Chemistry, Aleea Gr. Ghica Voda 41 A, 700487 Iasi (Romania); Gafitanu, Carmen Anatolia [Faculty of Pharmacy, ' Gr. T. Popa' University of Medicine and Pharmacy, Universitatii 16, 700115 Iasi (Romania)

    2012-10-15

    Highlights: Black-Right-Pointing-Pointer Ketoprofen incorporation in poly(ether urethane) microporous membrane. Black-Right-Pointing-Pointer Moisture sorption properties of as-cast membrane. Black-Right-Pointing-Pointer Drug release mechanisms in function of pH and composition of membranes. - Abstract: A poly(ether urethane) based on polytetrahydrofuran containing hydroxypropyl cellulose for biomedical applications was tested for its biocompatibility. Ketoprofen was incorporated (3% and 6%) in the polyurethane matrix as an anti-inflammatory drug. Kinetic and drug release mechanisms were studied. The pore size and pore size distribution of the polyurethane membranes were investigated by scanning electron microscopy. Surface tension characteristics as well as moisture sorption properties such as diffusion coefficients and equilibrium moisture contents of the membrane material were studied. It was found that kinetics and release mechanisms are in function of medium pH, composition of polymer-drug system, pore morphology and pore size distribution. Prolonged nature of release of ketoprofen is assured by low amount of drug in polyurethane membrane and physiological pH.

  11. Cloud Points of Water—soluble Polyether Phosphites and Their Application in the Biphasic Hydroformylation of Higher Olefins

    Institute of Scientific and Technical Information of China (English)

    LIU,Xiao-Zhong; WANG,Yan-Hua; KONG,Fan-Zhi; JIN,Zi-Lin

    2003-01-01

    Wate-soluble polyether phosphites alkyl polyethylene glycol ophenylene phosphite(APGPPS)were alcoholysis of phosphorus chloride with plyoxyethylene alkyl ether.With appropriate HLB(hydrophile-lypophile balance),the phosphites possess clear cloud points below 100℃,Addition of some inorganic salts decreases cloud points of the phosphites.When the phosphiites have long polyether chain binding to short-chain alkyl group,their cloud points could be extrapolated from figure of dependece of cloud points on addition of inorganic salts.Utilizing octylpolyglycol-phenylene-phosphite(OPGPP)(APGPP,R:Octyl)/Rh complex formed in situ as catalyst,over 90% conversion of 1-decene was obtained ,avoiding the limitation of water insolubility of substrates.Preliminary results indicated that micellar catalysis and thermoregulated phase-transfer catalysis(TRPTC)coexist in the reaction system.Below cloud point,micellar catalysis induced by plyether phosphites may be existed.When temperature is increased to above cloud point of the phosphies,this reaction works mainly in TRPTC.The catalysts could be easily spearated by simple decantation,but followed by considerable loss in activity after three successive reaction runs.Preliminary results indicated hydrolysis of OPGPP happened during the reaction.which may explain for the bad loss in activity.The catalyst was reused up to seven times with-out clear decrease in activity when OPGPP/Rh ratio was increased to 50.

  12. Patterns of venom production and temporal polyethism in workers of Jerdon's jumping ant, Harpegnathos saltator.

    Science.gov (United States)

    Haight, Kevin L

    2012-12-01

    Ants are chemical factories, and among their more noticeable products are their venoms. Though many studies have addressed the properties and activities of ant venoms, basic venom-related physiological questions, such as how venom production and replacement may vary with age, are rarely addressed. The answers to these questions are fundamental to understanding the physiological capabilities of these organisms, as well as the parameters within which potential optimization of their investment in venom production must take place. The only previous investigation into venom production in ants found it to be limited to early life in workers of the fire ant, Solenopsis invicta (Haight and Tschinkel, 2003). Because similar studies have not been conducted for comparison, it is unclear whether or not this is a common physiological pattern in ants. As a parsimonious way to address this question, and, more generally, to increase the currently scant information available regarding the venom-producing capabilities of ants, the longevity, temporal polyethism, age-related venom production, and age-related venom replacement capabilities of workers of Jerdon's jumping ant, Harpegnathos saltator were investigated. Longevity varied from 10 days to nearly 2 years, with a median lifespan of 206 days. Workers remained in the nest when young, transitioned to outside work (foraging) after 50 days of age, and reached a plateau in their tendency to be outside the nest at 74 days of age. They eclosed with empty venom sacs, filled them by about 57 days of age, and were able to replace venom at all three ages tested (though at a higher rate when aged 100 days than 30 and 206). So, venom-production ability is not limited to early life in H. saltator workers, and aspects of venom physiology and exploratory behavior appear to coincide in a manner likely to result in foraging efficiency benefits; venom sacs reach fullness around the age workers begin their foraging careers, and venom replacement

  13. Isotopic Measurements of Organic Sulfonates From The Murchison Meteorite

    Science.gov (United States)

    Cooper, G. W.; Chang, S.; DeVincenzi, Donald L. (Technical Monitor)

    1995-01-01

    Organic sulfonates and phosphonates have been extracted from the Murchison meteorite for stable isotope measurements. Preliminary stable isotope measurements of individual alkyl sulfonates, R-SO3H (R=C(sub n)H(sub 2n+l)), are shown. These compounds were found in aqueous extracts of Murchison. Both groups show trends similar to other homologous series of organic compounds indigenous to Murchison. Molecular abundances decrease with increasing carbon number, and all possible isomers at each carbon number (through C-4) are present. Carbon isotope measurements of the sulfonates show a decrease in the C-13/C-12 ratio with increasing carbon number. The overall objectives of this project are to obtain dime element carbon, hydrogen, and sulfur - intramolecular isotopic analyses of individual sulfonates, and isotopic measurement of carbon and hydrogen of the phosphonates as a group. The Murchison meteorite is the best characterized carbonaceous chondrite with respect to organic chemistry. The finding of organic sulfonates and phosphonates in Murchison is of interest because they are the first well-characterized series of sulfur and phosphorus containing organic compounds found in meteorites. Also, meteorites, comets, and interplanetary dust particles may have been involved in chemical evolution on the early Earth. Because of the critical role of organic phosphorus and sulfur in all living systems, it is particularly interesting to see examples of abiotic syntheses of these classes of compounds. The study of the isotopic composition of the sulfonates and phosphonates can yield insight into their possible interstellar origin as well as their mechanisms of synthesis in the early solar system. Previous isotopic analyses of other classes of organic compounds indigenous to meteorites, e.g., amino acids, carboxylic acids, and hydrocarbons indicate the possibility that interstellar molecules were incorporated into meteorite parent bodies. In these compounds the ratios of heavy to

  14. Synthesis, morphology and properties of segmented poly(ether ester amide)s comprising uniform glycine or β-alanine extended bisoxalamide hard segments

    NARCIS (Netherlands)

    Sijbrandi, N.J.; Kimenai, A.J.; Mes, E.P.C.; Broos, R.; Bar, G.; Rosenthal, M.; Odarchenko, Y.; Ivanov, D.A.; Feijen, J.; Dijkstra, P.J.

    2012-01-01

    Segmented poly(ether ester amide)s comprising glycine or β-alanine extended bisoxalamide hard segments are highly phase separated thermoplastic elastomers with a broad temperature independent rubber plateau. These materials with molecular weights, Mn, exceeding 30 × 103 g mol−1 are conveniently prep

  15. The importance of orientation in proton transport of a polymer film based on an oriented self-organized columnar liquid-crystalline polyether

    Energy Technology Data Exchange (ETDEWEB)

    Tylkowski, Bartosz; Castelao, Nuria [Departament d' Enginyeria Quimica, Universitat Rovira i Virgili, Av. Paiesos Catalans, 26, E-43007, Tarragona (Spain); Giamberini, Marta, E-mail: marta.giamberini@urv.net [Departament d' Enginyeria Quimica, Universitat Rovira i Virgili, Av. Paiesos Catalans, 26, E-43007, Tarragona (Spain); Garcia-Valls, Ricard [Departament d' Enginyeria Quimica, Universitat Rovira i Virgili, Av. Paiesos Catalans, 26, E-43007, Tarragona (Spain); Reina, Jose Antonio [Departament de Quimica Analitica i Quimica Organica, Universitat Rovira i Virgili, Carrer Marcel.li Domingo s/n, E-43007, Tarragona (Spain); Gumi, Tania [Departament d' Enginyeria Quimica, Universitat Rovira i Virgili, Av. Paiesos Catalans, 26, E-43007, Tarragona (Spain)

    2012-02-01

    We prepared membranes based on a liquid-crystalline side-chain polyether obtained by chemical modification of commercial poly(epichlorohydrin) (PECH) with dendrons. This polymer exhibited a columnar structure, which could form an ion channel in the inner part. The columns were successfully oriented by taking advantage of surface interactions between the polymer and hydrophilic substrates, as confirmed by X-ray diffraction analysis (XRD), environmental scanning electron microscopy (ESEM) and optical microscopy between crossed polars (POM). Column orientation was found to be crucial for effective transport: the oriented membranes exhibited proton transport comparable to that of Nafion Registered-Sign N117 and no water uptake. An increase in sodium ion concentration in the feed phase suggested a proton/cation antiport. On the contrary, no proton transport was detected on unoriented membranes based on the same liquid-crystalline side-chain polyether or on unmodified PECH. - Highlights: Black-Right-Pointing-Pointer We prepared oriented membranes based on a liquid crystalline columnar polyether. Black-Right-Pointing-Pointer In this structure, the inner polyether chain could work as an ion channel. Black-Right-Pointing-Pointer We obtained membranes by casting a chloroform solution in the presence of water. Black-Right-Pointing-Pointer Membranes showed good proton permeability due to the presence of oriented channels.

  16. Hybrid Baryons

    CERN Document Server

    Page, P R

    2003-01-01

    We review the status of hybrid baryons. The only known way to study hybrids rigorously is via excited adiabatic potentials. Hybrids can be modelled by both the bag and flux-tube models. The low-lying hybrid baryon is N 1/2^+ with a mass of 1.5-1.8 GeV. Hybrid baryons can be produced in the glue-rich processes of diffractive gamma N and pi N production, Psi decays and p pbar annihilation.

  17. FY08 MEMBRANE CHARACTERIZATION REPORT FOR HYBRID SULFUR ELECTROLYZER

    Energy Technology Data Exchange (ETDEWEB)

    Hobbs, D; Hector Colon-Mercado, H; Mark Elvington, M

    2008-09-01

    This report summarizes results from all of the membrane testing completed to date at the Savannah River National Laboratory (SRNL) for the sulfur dioxide-depolarized electrolyzer (SDE). Several types of commercially-available membranes have been analyzed for ionic resistance and sulfur dioxide transport including perfluorinated sulfonic acid (PFSA), sulfonated polyether-ketone-ketone (SPEKK), and polybenzimidazole membranes (PBI). Of these membrane types, the poly-benzimidazole membrane, Celtec-L, exhibited the best combination of characteristics for use in an SDE. Several experimental membranes have also been analyzed including hydrated sulfonated Diels-Alder polyphenylenes (SDAPP) membranes from Sandia National Laboratory, perfluorosulfonimide (PFSI) and sulfonated perfluorocyclobutyl aromatic ether (S-PFCB) prepared by Clemson University, hydrated platinum-treated PFSA prepared by Giner Electrochemical Systems (GES) and Pt-Nafion{reg_sign} 115 composites prepared at SRNL. The chemical stability, SO{sub 2} transport and ionic conductivity characteristics have been measured for several commercially available and experimental proton-conducting membranes. Commercially available PFSA membranes such as the Nafion{reg_sign} series exhibited excellent chemical stability and ionic conductivity in sulfur dioxide saturated sulfuric acid solutions. Sulfur dioxide transport in the Nafion{reg_sign} membranes varied proportionally with the thickness and equivalent weight of the membrane. Although the SO{sub 2} transport in the Nafion{reg_sign} membranes is higher than desired, the excellent chemical stability and conductivity makes this membrane the best commercially-available membrane at this time. Initial results indicated that a modified Nafion{reg_sign} membrane incorporating Pt nanoparticles exhibited significantly reduced SO{sub 2} transport. Reduced SO{sub 2} transport was also measured with commercially available PBI membrane and several experimental membranes produced

  18. 二苯砜-3磺酸钾的合成及表征%SYNTHESIS AND CHARACTERIZATION OF POTASSIUM-DIPHENYL SULFONE SULFONATE

    Institute of Scientific and Technical Information of China (English)

    弋冰; 王德义; 李泽军

    2001-01-01

    Potassium-diphenyl sulfone sulfonate,a kind of effective flame retardant,was synthesized by two steps from benzene,benzenesulfony chloride and chlorosulfonic acid.The structure of the product was analyzed by MS,FT-IR and 1HNMR techniques.

  19. Dual-mode fluorescence switching induced by self-assembly of well-defined poly(arylene ether sulfone)s containing pyrene and amide moieties.

    Science.gov (United States)

    Park, Jeyoung; Kim, Jisung; Seo, Myungeun; Lee, Jinhee; Kim, Sang Youl

    2012-11-04

    A new class of fluorescent organogelators, pyrene-containing poly(arylene ether sulfone)s, showed two fluorescence switching modes in different gelation solvents. The THF gel exhibited excimer emission due to dimerization of the pyrene groups. In contrast, excimer emission was quenched after gelation in MC because of stacking among the pyrene groups.

  20. Mortar modified with sulfonated polystyrene produced from waste plastic cups

    Directory of Open Access Journals (Sweden)

    L. A. C. MOTTA

    Full Text Available Abstract In this work, we studied the addition of sulfonated polystyrene produced from waste plastic cups as an admixture for mortars. Mortars were analyzed with polystyrene content of 0.0; 0.2; 0.6; 1.0 and 1.4% in relation to the cement mass. The influence of polystyrene on the mortars' properties was evaluated by the consistency index, water retention, water absorption, porosity, elasticity modulus, compressive strength, flexural strength, bond tensile strength and microscopy. The increase in the sulfonated polystyrene content decreased the elasticity modulus of the mortar and, despite higher porosity, there was a reduction of water absorption by capillarity. In relation to mortar without admixture, the modified mortar showed an increase in water retention and consistency index, and a large increase in flexural strength and bond tensile strength. The significant increase of bond tensile strength (214% with admixture 1% highlights the potential of the produced material as an adhesive mortar.

  1. Proton conductive membranes based on doped sulfonated polytriazole

    Energy Technology Data Exchange (ETDEWEB)

    Boaventura, M.; Brandao, L.; Mendes, A. [Laboratorio de Engenharia de Processos, Ambiente e Energia (LEPAE), Faculdade de Engenharia da Universidade do Porto, Rua Roberto Frias, 4200-465 Porto (Portugal); Ponce, M.L.; Nunes, S.P. [GKSS Research Centre Geesthacht GmbH, Max Planck Str. 1, D-21502, Geesthacht (Germany)

    2010-11-15

    This work reports the preparation and characterization of proton conducting sulfonated polytriazole membranes doped with three different agents: 1H-benzimidazole-2-sulfonic acid, benzimidazole and phosphoric acid. The modified membranes were characterized by scanning electron microscopy (SEM), infrared spectra, thermogravimetric analysis (TGA), dynamical mechanical thermal analysis (DMTA) and electrochemical impedance spectroscopy (EIS). The addition of doping agents resulted in a decrease of the glass transition temperature. For membranes doped with 85 wt.% phosphoric acid solution proton conductivity increased up to 2.10{sup -3} S cm{sup -1} at 120 C and at 5% relative humidity. The performance of the phosphoric acid doped membranes was evaluated in a fuel cell set-up at 120 C and 2.5% relative humidity. (author)

  2. Preparation of sulfonated cation exchangers from petroleum asphaltites

    Energy Technology Data Exchange (ETDEWEB)

    Pokonova, Yu.V.; Pol' kin, G.B.; Proskuryakov, V.A.

    1980-01-01

    It was established that the reaction of petroleum asphaltite sulfonation is determined in the first step by the chemical reaction rate, and in the last --- by diffusion factors. The kinetic constants were found for each reaction step. Sulfonated cation exchangers were obtained having the characteristics: specific volume of the swollen cation exchanger 3.30 mL/g, bulk density of the air-dry product 0.58 g/mL., moisture content 23.4%, swelling in water 41.6%, mechanical strength 80.0%, static exchange capacity with respect to 0.1N NaOH solution 2.76 mg equiv/g, dynamic exchange capacity with respect to 0.0035N CaC1/sub 2/ solution for a specific load of 10 L/L.h 465 mg equiv/L.

  3. Dynamics and Morphology of Sulfonated Polystyrene Ionomers by Dielectric Spectroscopy

    Science.gov (United States)

    Castagna, Alicia; Wang, Wenqin; Winey, Karen I.; Runt, James

    2009-03-01

    The dynamics of sulfonated polystyrene (SPS) ionomers, in both the acid and neutralized forms, were investigated using broadband dielectric spectroscopy. The influences of acid content, counterion type (Zn, Na and Cs), degree of neutralization, and microphase separated morphology on segmental and local dynamics, as well as on Maxwell -- Wagner -- Sillars interfacial polarization, were examined. Ionomers prepared from SPS containing 1.9 mol% sulfonic acid species exhibit a broader segmental process indicative of a considerably broader distribution of local environments, as compared to those in unneutralized SPS. Moreover, multiple segmental relaxations were identified in the dielectric spectra of Zn and Na neutralized SPS (1.9 mol%) ionomers, likely indicating two distinct environments arising from ion clustering. A combination of STEM imaging and X-ray scattering confirmed the presence of monodisperse spherical ionic aggregates that were homogeneously distributed in the polymer matrix.

  4. SULFONATED POLYIMIDES CONTAINING PYRIDINE GROUPS AS PROTON EXCHANGE MEMBRANE MATERIALS

    Institute of Scientific and Technical Information of China (English)

    Rui Lei; Chuan-qing Kang; Yun-jie Huang; Xue-peng Qiu; Xiang-ling Ji; Wei Xing; Lian-xun Gao

    2011-01-01

    A series of sulfonated polyimides (SPIs) containing pyridine groups were prepared by direct polycondensation from 1,4,5,8-naphthalenetetracarboxylic dianhydride (NTDA),4,4′-diaminodiphenyl ether-2,2′-disulfonic acid (ODADS) and 4-(4-methoxy)phenyl-2,6-bis(4-aminophenyl)pyridine (DAM).The resulting copolymers displayed good solubility in common organic solvents.Flexible,transparent,tough membranes were obtained via solution casting.All the films showed high thermal stability with desulfonation temperature over 300℃.They exhibited prominent mechanical properties with Young's modulus around 2.0 GPa.High proton conductivity (0.23 S/em at 100% RH) was also observed.More importantly,the new materials exhibited low water uptake (30 wt%-75 wt% at 80℃) and improved water stability,which were attributed to the acid-base interaction between sulfonic acid and pyridine functional groups.

  5. Permselectivity and conductivity of membranes based on sulfonated naphthalenic copolyimides.

    Science.gov (United States)

    Guo, Xiaoxia; Zhai, Fengxia; Fang, Jianhua; Laguna, Maria Fe; López-Gonzalez, Mar; Riande, Evaristo

    2007-12-13

    A series of sulfonated diamines were synthesized which were further used to obtain relevant sulfonated naphthalenic copolyimides. Tough and ductile membranes were cast from solutions of the copolyimides in dimethylsulfoxide, which exhibit high ion-exchange capacity and high water uptake. The protonic conductivity of the membranes equilibrated with water lies in the range 1.0-8.6 S/m, at 25 degrees C, being of the same order of magnitude as that reported for perfluorinated acidic membranes. The values of the transport number of protons and sodium ions are close to the unit for very dilute electrolyte solutions, but they lie in the range 0.80-0.90 for moderate concentrations. The membranes exhibit rather high electroosmotic permeability. The similarity of the diffusion coefficients of protons and water in the membranes suggests that the Grottus mechanism governs the protonic conductive process in the acidic membranes equilibrated with water.

  6. New Fluorinated and Sulfonated Block Copolymers Final Report

    Science.gov (United States)

    2009-04-23

    serves as a plasticizer even in the hydrophobic FI domain. Similar glass transition reduction effects observed in other ionomer systems have been...Sulfonated Ionomer : Thermal Annealing and Solvent Effects.” American Physical Society National Meeting. Los Angeles, CA. March 21, 2005. 4. Akinbode...optimizing morphology and ultimately properties, membranes have been cast from relatively inexpensive block-copolymer ionomers of fluorinated poly

  7. Regioselective synthesis of chiral dimethyl-bis(ethylenedithiotetrathiafulvalene sulfones

    Directory of Open Access Journals (Sweden)

    Flavia Pop

    2015-07-01

    Full Text Available Enantiopure (R,R and (S,S-dimethyl-bis(ethylenedithiotetrathiafulvalene monosulfones have been synthesized by the aerial oxidation of the chiral dithiolates generated from the propionitrile-protected precursors. Both enantiomers crystallize in the orthorhombic chiral space group P212121. They show a boat-type conformation of the TTF moiety, a rather rigid dithiin sulfone ring and the methyl groups in a bisequatorial conformation. Cyclic voltammetry measurements indicate fully reversible oxidation in radical cation and dication species.

  8. Inhibition of the anaerobic digestion process by linear alkylbenzene sulfonates

    DEFF Research Database (Denmark)

    Gavala, Hariklia N.; Ahring, Birgitte Kiær

    2002-01-01

    of the anaerobic digestion process should be seriously taken into consideration when wastewater from a surfactant producing industry is to be treated biologically or enter a municipal wastewater treatment plant that employs anaerobic technology. The upper allowable biomass specific LAS concentration should be 14......Linear Alkylbenzene Sulfonates (LAS) are the most widely used synthetic anionic surfactants. They are anthropogenic, toxic compounds and are found in the primary sludge generated in municipal wastewater treatment plants. Primary sludge is usually stabilized anaerobically and therefore...

  9. Anaerobic degradation of linear alkylbenzene sulfonate in fluidized bed reactor

    OpenAIRE

    2010-01-01

    An anaerobic fluidized bed reactor was used to assess the degradation of the surfactant linear alkylbenzene sulfonate (LAS). The reactor was inoculated with sludge from an UASB reactor treating swine wastewater and was fed with a synthetic substrate supplemented with LAS. Sand was used as support material for biomass immobilization. The reactor was kept in a controlled temperature chamber (30±1 ºC) and operated with a hydraulic retention time (HRT) of 18 h. The LAS concentration was gradually...

  10. Amperometric urea biosensors based on sulfonated graphene/polyaniline nanocomposite

    Science.gov (United States)

    Das, Gautam; Yoon, Hyon Hee

    2015-01-01

    An electrochemical biosensor based on sulfonated graphene/polyaniline nanocomposite was developed for urea analysis. Oxidative polymerization of aniline in the presence of sulfonated graphene oxide was carried out by electrochemical methods in an aqueous environment. The structural properties of the nanocomposite were characterized by Fourier-transform infrared, Raman spectroscopy, X-ray photoelectron spectroscopy, and scanning electron microscopy techniques. The urease enzyme-immobilized sulfonated graphene/polyaniline nanocomposite film showed impressive performance in the electroanalytical detection of urea with a detection limit of 0.050 mM and a sensitivity of 0.85 (μA · cm−2·mM−1. The biosensor achieved a broad linear range of detection (0.12–12.3 mM) with a notable response time of approximately 5 seconds. Moreover, the fabricated biosensor retained 81% of its initial activity (based on sensitivity) after 15 days of storage at 4°C. The ease of fabrication coupled with the low cost and good electrochemical performance of this system holds potential for the development of solid-state biosensors for urea detection. PMID:26346240

  11. Amperometric urea biosensors based on sulfonated graphene/polyaniline nanocomposite.

    Science.gov (United States)

    Das, Gautam; Yoon, Hyon Hee

    2015-01-01

    An electrochemical biosensor based on sulfonated graphene/polyaniline nanocomposite was developed for urea analysis. Oxidative polymerization of aniline in the presence of sulfonated graphene oxide was carried out by electrochemical methods in an aqueous environment. The structural properties of the nanocomposite were characterized by Fourier-transform infrared, Raman spectroscopy, X-ray photoelectron spectroscopy, and scanning electron microscopy techniques. The urease enzyme-immobilized sulfonated graphene/polyaniline nanocomposite film showed impressive performance in the electroanalytical detection of urea with a detection limit of 0.050 mM and a sensitivity of 0.85 (μA · cm(-2)·mM(-1). The biosensor achieved a broad linear range of detection (0.12-12.3 mM) with a notable response time of approximately 5 seconds. Moreover, the fabricated biosensor retained 81% of its initial activity (based on sensitivity) after 15 days of storage at 4°C. The ease of fabrication coupled with the low cost and good electrochemical performance of this system holds potential for the development of solid-state biosensors for urea detection.

  12. Thermally stimulated depolarization current studies of sulfonated polystyrene ionomers

    Science.gov (United States)

    Carvalho, Antonio José Felix; Viana, Vicente Galber Freitas; Faria, Roberto Mendonça

    2009-12-01

    A detailed study of thermally stimulated depolarization current (TSDC) was carried out to investigate dipolar relaxation and the charge storage phenomenon in films of sulfonated polystyrene (SPS) ionomers having lithium or potassium as counterions. Differential scanning calorimetry measurements were also applied as a complementary technique, mainly to follow the change of the glass transition temperature with the amount of sulfonated groups. It was observed that, since the glass transition does not change significantly with the amount of sulfonated groups, a cluster of multiplets is expected not to be formed in the range used in this work. TSDC of SPS samples polarized at temperatures higher than the glass transition temperature showed three peaks: one at lower temperature (peak β), an intermediate peak (peak α), and a third that appeared at a temperature coincident with the polarization temperature (peak ρ). Quantitative information about trapping-detrapping and dipolar relaxation and their corresponding activation energies was determined by fittings of the deconvoluted peaks with kinetic relaxation processes.

  13. Thermally stimulated depolarization current studies of sulfonated polystyrene ionomers

    Energy Technology Data Exchange (ETDEWEB)

    Carvalho, Antonio Jose Felix [Universidade Federal de Sao Carlos, Laboratory of Polymers and Renewable Materials, Sorocaba, SP (Brazil); Viana, Vicente Galber Freitas [Universidade Federal do Piaui, Centro de Ciencias da Natureza, Teresina, PI (Brazil); Faria, Roberto Mendonca [USP, Instituto de Fisica de Sao Carlos, SP (Brazil)

    2009-12-15

    A detailed study of thermally stimulated depolarization current (TSDC) was carried out to investigate dipolar relaxation and the charge storage phenomenon in films of sulfonated polystyrene (SPS) ionomers having lithium or potassium as counterions. Differential scanning calorimetry measurements were also applied as a complementary technique, mainly to follow the change of the glass transition temperature with the amount of sulfonated groups. It was observed that, since the glass transition does not change significantly with the amount of sulfonated groups, a cluster of multiplets is expected not to be formed in the range used in this work. TSDC of SPS samples polarized at temperatures higher than the glass transition temperature showed three peaks: one at lower temperature (peak {beta}), an intermediate peak (peak {alpha}), and a third that appeared at a temperature coincident with the polarization temperature (peak {rho}). Quantitative information about trapping-detrapping and dipolar relaxation and their corresponding activation energies was determined by fittings of the deconvoluted peaks with kinetic relaxation processes. (orig.)

  14. Composite plasma polymerized sulfonated polystyrene membrane for PEMFC

    Energy Technology Data Exchange (ETDEWEB)

    Nath, Bhabesh Kumar; Khan, Aziz; Chutia, Joyanti, E-mail: jchutiaiasst@gmail.com

    2015-10-15

    Highlights: • Methyl methane sulfonate (MMS) is used as the sulfonating agent. • The proton conductivity of the membrane is found to be 0.141 S cm{sup −1}. • Power density of fuel cell with styrene/MMS membrane is 0.5 W cm{sup −2}. • The membrane exhibits thermal stability up to 140 °C. - Abstract: This work presents the introduction of an organic compound methyl methane sulfonate (MMS) for the first time in fabrication of polystyrene based proton exchange membrane (PEM) by plasma polymerization process. The membrane is fabricated by co-polymerizing styrene and MMS in capacitively coupled continuous RF plasma. The chemical composition of the plasma polymerized polymer membrane is investigated using Fourier Transform Infrared Spectroscopy which reveals the formation of composite structure of styrene and MMS. The surface morphology studied using AFM and SEM depicts the effect of higher partial pressure of MMS on surface topography of the membrane. The proton transport property of the membrane studied using electrochemical impedance spectroscopy shows the achievement of maximum proton conductivity of 0.141 S cm{sup −1} which is comparable to Nafion 117 membrane. Fuel cell performance test of the synthesized membrane shows a maximum power density of 500 mW cm{sup −2} and current density of 0.62 A cm{sup −2} at 0.6 V.

  15. The silica-doped sulfonated poly(fluorenyl ether ketone)s membrane using hydroxypropyl methyl cellulose as dispersant for high temperature proton exchange membrane fuel cells

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Y.F.; Wang, S.J.; Xiao, M.; Bian, S.G.; Meng, Y.Z. [State Key Laboratory of Optoelectronic Materials and Technologies, Institute of Optoelectronic and Functional Composite Materials, Sun Yat-sen University, Xingangxi Road, Guangzhou 510275 (China)

    2009-05-15

    The sulfonated poly(fluorenyl ether ketone)s (SPFEK) membranes doped with SiO{sub 2} and dispersed by hydroxypropyl methyl cellulose (HPMC) were prepared and investigated for polymer electrolyte membrane fuel cells (PEMFCs) used at high temperature and low relative humidity (RH). The above membrane was prepared by solution dispersion of SPFEK and SiO{sub 2} using HPMC as dispersant. The physio-chemical properties of the hybrid membrane were studied by means of scanning electron microscope (SEM), ion-exchange capacity (IEC), proton conductivity, and single cell performance tests. The hybrid membranes dispersed by HPMC were well dispersed when compared with common organic/inorganic hybrid membranes. The hybrid membranes showed superior characteristics as a proton exchange membrane (PEM) for PEMFC application, such as high ionic exchange content (IEC) of 1.51 equiv/g, high temperature operation properties, and the satisfactory ability of anti-H{sub 2} crossover. The single cell performances of the hybrid membranes were examined in a 5 cm{sup 2} commercial single cell at both 80 C and 120 C under different relative humidity (RH) conditions. The hybrid membrane dispersed by HPMC gave the best performance of 260 mW/cm{sup 2} under conditions of 0.4 V, 120 C, 50% RH and ambient pressure. The results demonstrated HPMC being an efficient dispersant for the organic/inorganic hybrid membrane used for PEM fuel cell. (author)

  16. Sulfonate-containing Copolymers Prepared by Semi-Continuous Emulsion Copolymerizaiton of Styrene and Sodium Styrene Sulfonate

    Institute of Scientific and Technical Information of China (English)

    Shiming HUANG; Wei XIE; Chengyou KAN; Yajie LI; Deshan LIU

    2005-01-01

    @@ 1Introduction Soap-free emulsion copolymerization of styrene (St) and sodium sulfonate styrene (NaSS) could yield homodisperse sulfonate-containing particles with clean surface. But the incorporation of NaSS could never be increased beyond 2.6 % by weight in the conventional batch and seeded emulsion copolymerization in the absence of emulsifier because large amounts of soluble polyelectrolyte would unstablize the reaction system if excessive amount of NaSS was used[1]. In our work, semi-continuous copolymerizations were carried out in the presence of mixed emulsifiers, and a new method to purify the latex polymer was developed. The influences of the NaSS mole ratio in the total monomers and the monomer addition time on the S content in the purified copolymer were investigated by elemental analysis.

  17. Sulfonation and characterization of styrene-indene copolymers for the development of proton conducting polymer membranes

    Directory of Open Access Journals (Sweden)

    Cristiane M. Becker

    2012-01-01

    Full Text Available The aim of this work is to obtain polymer precursors based on styrene copolymers with distinct degrees of sulfonation, as an alternative material for fuel cell membranes. Acetyl sulfate was used to carry out the sulfonation and the performance of the polyelectrolyte was evaluated based on the content of acid polar groups incorporated into the macromolecular chain. Polymeric films were produced by blending the sulfonated styrene-indene copolymer with poly(vinylidene fluoride. The degree of sulfonation of the polymer was strongly affected by the sulfonation reaction parameters, with a direct impact on the ionic exchange capacity and the ionic conductivity of the sulfonated polymers and the membranes obtained from them. The films produced with the blends showed more suitable mechanical properties, although the conductivity of the membranes was still lower than that of commercially available membranes used in fuel cells.

  18. Temperature effects on the rheological properties of current polyether and polysiloxane impression materials during setting.

    Science.gov (United States)

    Berg, John C; Johnson, Glen H; Lepe, Xavier; Adán-Plaza, Sergio

    2003-08-01

    Rheological tests of elastomeric impression materials during setting have been most often conducted at room temperature rather than at intraoral temperature. Because temperature may affect properties and the setting kinetics, clinically relevant inferences may not be accurate with studies conducted at room temperature. The purpose of this study was to determine the viscoelastic properties of new low- and medium-viscosity elastomeric impression materials during setting at 33 degrees C and to evaluate the medium-viscosity materials at 3 additional temperatures. The impression materials investigated at 33 degrees C were 2 polyvinylsiloxanes (PVS) (Aquasil Deca and Aquasil LV) and 5 polyethers (PE) (Impregum Penta, Impregum Penta Soft H, Impregum Penta Soft L, Impregum Garant Soft L, and Permadyne Garant L). Three impression materials (Aquasil Deca, Impregum Penta, and Impregum Penta Soft H) were also investigated at 25 degrees, 29 degrees, and 37 degrees C. Time-dependent oscillatory rheometry was carried out on these materials (n=3) with a rheometer with a 25-mm diameter parallel plate cell. The storage modulus (G') and the loss tangent (tandelta) were determined as functions of time over a period from 0 seconds to 900 seconds, commencing 40 seconds after mixing. Induction time (t(ind)) or initial setting time and tandelta, the relative liquidlike behavior, were also computed. A single-factor analysis of variance (ANOVA) was used for the properties determined at 33 degrees C and a 2-factor ANOVA was used for the temperature studies, with hypothesis testing at alpha=.05. The G'(t) curves for all materials displayed the expected sigmoidal shape with time, with the solid-like behavior rising slowly, then more rapidly, and again slowly to final set. The initial setting time (t(ind)) was found to be approximately 2.8 minutes for the PVS materials and for Impregum Penta and Impregum Penta Soft H, but was significantly longer for the remaining 3 PE low viscosity materials

  19. A STUDY OF THE HEAT OF HYDRATION OF SULFONIC ACID RESINS

    Institute of Scientific and Technical Information of China (English)

    XURongnan; JIJunyan; 等

    1992-01-01

    The heat of hydration of dry sulfonic acid resin in different comcentrations of sulfuric acid has been determined. The heat of hydration of the resin in H2O is 143.4J/g(resin). The greater the concentration of sulfuric acid,the less the heat will be released.The hydrate formed from three sulfonic acid groups and one water molecule is the most stable one of all the hydrates of sulfonic acid resin and water.

  20. Study on the generation of perfluorooctane sulfonate from the aqueous film-forming foam.

    Science.gov (United States)

    Kishi, Takahiro; Arai, Mitsuru

    2008-11-15

    Perfluorooctane sulfonate (C(8)HF(17)SO(3)) and perfluorooctane acid (C(8)HF(15)O(2)) are artificial chemicals and have been used all over the world, mainly as water repellent agents, fluorochemical surfactants, coating agents, etc. However, perfluorooctane sulfonate and perfluorooctane acid are environmental contaminants because of their stability, bio-accumulativeness, and long-term persistence in the ecological environment. At the present day, they are diffused all over the world. Lately, this diffusion is viewed with suspicion and there is a movement towards their restriction, even if the environmental fate of them is still under investigation. Fluorochemical surfactants are key compounds in the aqueous film-forming foam (AFFF) formulations. AFFFs are used for massive conflagration such as industrial fire and petroleum fire because of their efficient fire control. On the other hand, a lot of AFFFs are used in case of massive conflagration and most of them enter ocean and groundwater. Actually, perfluorooctane sulfonate and perfluorooctane sulfonate related substances were detected from the fire-fighting facility of US forces. Therefore, there is the possibility of generating perfluorooctane sulfonate and perfluorooctane sulfonate related substances from fluorochemical surfactants in the AFFFs. In this study, activated sludge added AFFF were analyzed for perfluorooctane sulfonate and perfluorooctane acid with time. And the perfluorooctane sulfonate was directly detected after 2 days using LC-MS. This shows that AFFF can be decomposed perfluorooctane sulfonate by microorganisms easily. However, perfluorooctane sulfonate would not decompose at all. Additionally, activated sludge added N-polyoxyethylene-N-propyl perfluorooctane sulfonamide which is one of the fluorochemical surfactants used in the AFFF was analyzed for perfluorooctane sulfonate and perfluorooctane acid with time and the perfluorooctane sulfonate was detected too.

  1. The synthesis, structure and photoluminescence property of a novel 3D supramolecular compound based on mixed ligands of 8-hydroxy-quionline-5-sulfonate and ethylenediamine

    Directory of Open Access Journals (Sweden)

    Wang Ying

    2011-01-01

    Full Text Available A new organic-inorganic hybrid coordination compound ZnQS (en•2H2O (1 in which two different organic ligands, ethylenediamine (en and 8-hydroxy-quinoline-5-sulfonic acid (H2QS coordinate with zinc ions, has been synthesized via the evaporation method and characterized by single crystal X-ray diffraction analysis, IR spectroscopy and thermogravimetric analysis (TGA. The structure solution showed that compound 1 displays a three-dimensional supramolecular network by synergic linkage of hydrogen and coordinated bonds. Moreover, compound 1 exhibits intense photoluminescence at 513 nm excited at 396 nm in the solid state at room temperature.

  2. Effect of cervical relining of acrylic resin copings on the accuracy of stone dies obtained using a polyether impression material

    Directory of Open Access Journals (Sweden)

    André Tomazini Gomes de Sá

    2008-02-01

    Full Text Available The purpose of this study was to evaluate the accuracy of the respective dies after polyether elastomeric procedure in the presence or absence of cervical contact of the acrylic resin shell with the cervical region, establishing a comparison to dies obtained with stock trays. This study consisted of three groups with 10 specimens each: 1 acrylic copings without cervical contact, (cn; 2 acrylic copings with cervical contact (cc; 3 perforated stock tray, (st. The accuracy of the resulting dies was verified with the aid of a master crown, precisely fit to the master steel die. ANOVA test found statistically significant differences among groups (p<0.001. Tukey's test found that the smallest discrepancy occurred in group cn, followed by cc, while the st group presented the highest difference (cc x cn: p=0.007; st x cn: p<0.001; st x cc: p<0.001.

  3. Expression of the Foraging Gene Is Associated with Age Polyethism, Not Task Preference, in the Ant Cardiocondyla obscurior

    Science.gov (United States)

    Oettler, Jan; Nachtigal, Anna-Lena; Schrader, Lukas

    2015-01-01

    One of the fundamental principles of social organization, age polyethism, describes behavioral maturation of workers leading to switches in task preference. Here we present a system that allows for studying division of labor (DOL) by taking advantage of the relative short life of Cardiocondyla obscurior workers and thereby the pace of behavioral transitions. By challenging same-age young and older age cohorts to de novo establish DOL into nurse and foraging tasks and by forcing nurses to precociously become foragers and vice versa we studied expression patterns of one of the best known candidates for social insect worker behavior, the foraging gene. Contrary to our expectations we found that foraging gene expression correlates with age, but not with the task foraging per se. This suggests that this nutrition-related gene, and the pathways it is embedded in, correlates with physiological changes over time and potentially primes, but not determines task preference of individual workers. PMID:26650238

  4. Rheological and electrical percolation in melt-processed poly(ether ether ketone)/multi-wall carbon nanotube composites

    Science.gov (United States)

    Bangarusampath, D. S.; Ruckdäschel, Holger; Altstädt, Volker; Sandler, Jan K. W.; Garray, Didier; Shaffer, Milo S. P.

    2009-11-01

    Multi-wall carbon nanotubes were dispersed homogeneously throughout a poly(ether ether ketone) matrix by melt processing. The influence of nanotube content on both rheological and electrical properties was analysed. The dynamic storage modulus, G', shows a characteristic solid-like behavior above 1 wt% nanotubes. A sharp transition from an electrically insulating to a conductive composite was observed between 1 and 1.5 wt%. By applying a power-law relation, the rheological and electrical percolation thresholds were found to be 0.9 wt%, and 1.3 wt%, respectively. Considering this data, Guth's filler reinforcement theory provides a valuable estimation of the aspect ratio of the nanotubes after processing and indicates substantial length degradation during the dispersion process.

  5. Characterization of a poly(ether urethane)-based controlled release membrane system for delivery of ketoprofen

    Science.gov (United States)

    Macocinschi, Doina; Filip, Daniela; Vlad, Stelian; Oprea, Ana Maria; Gafitanu, Carmen Anatolia

    2012-10-01

    A poly(ether urethane) based on polytetrahydrofuran containing hydroxypropyl cellulose for biomedical applications was tested for its biocompatibility. Ketoprofen was incorporated (3% and 6%) in the polyurethane matrix as an anti-inflammatory drug. Kinetic and drug release mechanisms were studied. The pore size and pore size distribution of the polyurethane membranes were investigated by scanning electron microscopy. Surface tension characteristics as well as moisture sorption properties such as diffusion coefficients and equilibrium moisture contents of the membrane material were studied. It was found that kinetics and release mechanisms are in function of medium pH, composition of polymer-drug system, pore morphology and pore size distribution. Prolonged nature of release of ketoprofen is assured by low amount of drug in polyurethane membrane and physiological pH.

  6. Expression of the Foraging Gene Is Associated with Age Polyethism, Not Task Preference, in the Ant Cardiocondyla obscurior.

    Science.gov (United States)

    Oettler, Jan; Nachtigal, Anna-Lena; Schrader, Lukas

    2015-01-01

    One of the fundamental principles of social organization, age polyethism, describes behavioral maturation of workers leading to switches in task preference. Here we present a system that allows for studying division of labor (DOL) by taking advantage of the relative short life of Cardiocondyla obscurior workers and thereby the pace of behavioral transitions. By challenging same-age young and older age cohorts to de novo establish DOL into nurse and foraging tasks and by forcing nurses to precociously become foragers and vice versa we studied expression patterns of one of the best known candidates for social insect worker behavior, the foraging gene. Contrary to our expectations we found that foraging gene expression correlates with age, but not with the task foraging per se. This suggests that this nutrition-related gene, and the pathways it is embedded in, correlates with physiological changes over time and potentially primes, but not determines task preference of individual workers.

  7. Expression of the Foraging Gene Is Associated with Age Polyethism, Not Task Preference, in the Ant Cardiocondyla obscurior.

    Directory of Open Access Journals (Sweden)

    Jan Oettler

    Full Text Available One of the fundamental principles of social organization, age polyethism, describes behavioral maturation of workers leading to switches in task preference. Here we present a system that allows for studying division of labor (DOL by taking advantage of the relative short life of Cardiocondyla obscurior workers and thereby the pace of behavioral transitions. By challenging same-age young and older age cohorts to de novo establish DOL into nurse and foraging tasks and by forcing nurses to precociously become foragers and vice versa we studied expression patterns of one of the best known candidates for social insect worker behavior, the foraging gene. Contrary to our expectations we found that foraging gene expression correlates with age, but not with the task foraging per se. This suggests that this nutrition-related gene, and the pathways it is embedded in, correlates with physiological changes over time and potentially primes, but not determines task preference of individual workers.

  8. Studies on microdomain structure in segmented polyether polyurethaneureas by positron annihilation lifetime and small—angle X—ray scattering

    Institute of Scientific and Technical Information of China (English)

    YinChuan-Yuan; GuQing-Chao; 等

    1997-01-01

    The microdomain structure of segmented polyether polyurethaneureas is investigated by means of positron annihilation lifetime spectroscopy,small-angle X-ray scattering and differential scanning calorimetry.The experimental results show that the decrease in the domain volume and free volume results from the increase in the hard segment (polyurethaneurea segment)contents as the number-average molecular weight Mn of the soft segments (polyethylene glycol segments)is the same,and that the increase in domain volume and free volume result from the increase in the Mn of the soft segments when the hard segment content is the same or nearly the same.These results demonstrate that positron annihilation lifetime spectroscopy is a sensitive technique to probe the microdomain structure in polymers.

  9. A study on the microstructure of a nitrate ester plasticized polyether propellant dissolved in HCl and KOH solutions

    Directory of Open Access Journals (Sweden)

    YONG LIU

    2010-07-01

    Full Text Available Understanding of how the properties and performance of nitrate ester plasticized polyether (NEPE propellants relate to microstructure is complicated by numerous components that have different characteristics. One approach to alleviating these complications is to observe a microstructure that has lost one or several components. This article examines the dissolution process, mass loss and change of the ion concentration of propellants in acid and alkali solutions. A scanning electron microscope was used to observe the dissolved residual of the propellants. The results revealed that the main constituents of NEPE propellant have different dissolving properties in solutions of HCl and KOH. By monitoring the dissolution process of NEPE propellant in HCl and KOH solutions, it was found that the microstructure of the propellant is generally compact and the polymer binder not only binds all the other components, but also protects the inner part of the propellant in solution.

  10. Direct electrochemical DNA detection originated from the self-redox signal of sulfonated polyaniline enhanced by graphene oxide in neutral solution.

    Science.gov (United States)

    Yang, Tao; Meng, Le; Wang, Xinxing; Wang, Longlong; Jiao, Kui

    2013-11-13

    In this paper, a type of direct DNA impedance detection using the self-redox signal change of sulfonated polyaniline (SPAN) enhanced by graphene oxide (GNO) was reported, here SPAN is a copolymer obtained from aniline and m-aminobenzenesulfonic acid. The resulting nanocomposite was characterized by scanning electron microscopy, transmission electron microscopy, Fourier transform infrared spectroscopy, cyclic voltammetry, and electrochemical impedance spectroscopy. The π-π planar structure of GNO and the carboxyl groups on the surface of GNO ensured it could act as an excellent substrate for adsorption and polymerization of aniline monomer. Because of the existence of GNO, the electrochemical activities of SPAN were enhanced obviously. Because of abundant sulfonic acid groups, the resulting nanocomposite showed obvious self-redox signal even at physiological pH, which is beneficial for biosensing field. DNA probes with amine groups could be covalently attached to the modified electrode surface through the acyl chloride cross-linking reaction of sulfonic groups and amines. When the flexible probe DNA was successfully grafted, the electrode was coated and electron transfer between electrode and buffer was restrained. Thus, the inner impedance value of SPAN (rather than using outer classic EIS probe, [Fe(CN)6](3-/4-)) increased significantly. After hybridization, the rigid helix opened the electron channel, which induced impedance value decreased dramatically. As an initial application of this system, the PML/RARA fusion gene sequence formed from promyelocytic leukemia (PML) and retinoic acid receptor alpha (RARA) was successfully detected.

  11. A comparison of the accuracy of polyether, polyvinyl siloxane, and plaster impressions for long-span implant-supported prostheses.

    Science.gov (United States)

    Hoods-Moonsammy, Vyonne J; Owen, Peter; Howes, Dale G

    2014-01-01

    The purpose of this study was to compare the capacity of different impression materials to accurately reproduce the positions of five implant analogs on a master model by comparing the resulting cast with the stainless steel master model. The study was motivated by the knowledge that distortions can occur during impression making and the pouring of casts and that this distortion may produce inaccuracies of subsequent restorations, especially long-span castings for implant superstructures. The master model was a stainless steel model with five implant analogs. The impression materials used were impression plaster (Plastogum, Harry J Bosworth), a polyether (Impregum Penta, 3M ESPE), and two polyvinyl siloxane (PVS) materials (Aquasil Monophase and Aquasil putty with light-body wash, Dentsply). Five impressions were made with each impression material and cast in die stone under strictly controlled laboratory conditions. The positions of the implants on the master model, the impression copings, and the implant analogs in the subsequent casts were measured using a coordinate measuring machine that measures within 4 μm of accuracy. Statistical analyses indicated that distortion occurred in all of the impression materials, but inconsistently. The PVS monophase material reproduced the master model most accurately. Although there was no significant distortion between the impressions and the master model or between the impressions and their casts, there were distortions between the master model and the master casts, which highlighted the cumulative effects of the distortions. The polyether material proved to be the most reliable in terms of predictability. The impression plaster displayed cumulative distortion, and the PVS putty with light body showed the least reliability. Some of the distortions observed are of clinical significance and likely to contribute to a lack of passive fit of any superstructure. The inaccuracy of these analog materials and procedures suggested

  12. Expression patterns of a circadian clock gene are associated with age-related polyethism in harvester ants, Pogonomyrmex occidentalis

    Directory of Open Access Journals (Sweden)

    Ingram Krista K

    2009-04-01

    Full Text Available Abstract Background Recent advances in sociogenomics allow for comparative analyses of molecular mechanisms regulating the development of social behavior. In eusocial insects, one key aspect of their sociality, the division of labor, has received the most attention. Age-related polyethism, a derived form of division of labor in ants and bees where colony tasks are allocated among distinct behavioral phenotypes, has traditionally been assumed to be a product of convergent evolution. Previous work has shown that the circadian clock is associated with the development of behavior and division of labor in honeybee societies. We cloned the ortholog of the clock gene, period, from a harvester ant (Pogonomyrmex occidentalis and examined circadian rhythms and daily activity patterns in a species that represents an evolutionary origin of eusociality independent of the honeybee. Results Using real time qPCR analyses, we determined that harvester ants have a daily cyclic expression of period and this rhythm is endogenous (free-running under dark-dark conditions. Cyclic expression of period is task-specific; foragers have strong daily fluctuations but nest workers inside the nest do not. These patterns correspond to differences in behavior as activity levels of foragers show a diurnal pattern while nest workers tend to exhibit continuous locomotor activity at lower levels. In addition, we found that foragers collected in the early fall (relative warm, long days exhibit a delay in the nightly peak of period expression relative to foragers collected in the early spring (relative cold, short days. Conclusion The association of period mRNA expression levels with harvester ant task behaviors suggests that the development of circadian rhythms is associated with the behavioral development of ants. Thus, the circadian clock pathway may represent a conserved 'genetic toolkit' that has facilitated the parallel evolution of age-related polyethism and task allocation in

  13. Sulfonated phenolic material and its use in post primary oil recovery

    Energy Technology Data Exchange (ETDEWEB)

    Pardue, J. E.; Stapp, P. R.

    1984-09-04

    Sulfonated phenolic compounds as well as sulfomethylated phenolic compounds, surfactant systems containing such compound and the use of such surfactant systems in post primary oil recovery are disclosed.

  14. Quinone-mediated decolorization of sulfonated azo dyes by cells and cell extracts from Sphingomonas xenophaga

    Institute of Scientific and Technical Information of China (English)

    JIAO Ling; LU Hong; ZHOU Jiti; WANG Jing

    2009-01-01

    The effects of various quinone compounds on the decolorization rates of sulfonated azo dyes by Sphingomonas xenophaga QYY were investigated. The results showed that anthraquinone-2-sulfonate (AQS) was the most effective redox mediator and AQS reduction was the rate-limited step of AQS-mediated decolorization of sulfonated azo dyes. Based on AQS biological toxicity tests, it was assumed that AQS might enter the cells to kill them. In the cytoplasmic extracts from strain QYY, AQS effectively increased decolorization rates of sulfonated azo dyes than other quinone compounds. In addition, we found a NADH/FMN-dependent AQS reductase using nondenaturing polyacrylamide gel electrophoresis (Native-PAGE).

  15. A facile synthesis of a novel optoelectric material: a nanocomposite of SWCNT/ZnO nanostructures embedded in sulfonated polyaniline

    Directory of Open Access Journals (Sweden)

    Rajesh K. Agrawalla

    2014-07-01

    Full Text Available Functionalized single-walled carbon nanotubes (f-SWCNTs hybridized with freshly prepared zinc oxide (ZnO nanocrystals have been found to be good luminescent material with tuned emission properties. A three-phase nanocomposite of sulfonated polyaniline embedded with such SWCNT/ZnO nanostructures has been prepared by a simple solution mixing chemical process and characterized by using high-resolution transmission electron microscopy, X-ray diffractometry, Raman spectroscopy, Fourier transform infrared spectroscopy, and thermogravimetric analysis. The study of UV-visible absorption and photoluminescence spectroscopies reveal that the ternary polymer nanocomposite is a luminescent material with enhanced emission intensity. Also an increase in DC conductivity indicates that the nanocomposite is also a good conductive material, satisfying Mott’s variable range hopping model for a two-dimensional conduction. Such a three-phase nanocomposite may find extensive application in dye-sensitized solar cells, sensors, and supercapacitors.

  16. Hybrid vehicles

    Energy Technology Data Exchange (ETDEWEB)

    West, J.G.W. [Electrical Machines (United Kingdom)

    1997-07-01

    The reasons for adopting hybrid vehicles result mainly from the lack of adequate range from electric vehicles at an acceptable cost. Hybrids can offer significant improvements in emissions and fuel economy. Series and parallel hybrids are compared. A combination of series and parallel operation would be the ideal. This can be obtained using a planetary gearbox as a power split device allowing a small generator to transfer power to the propulsion motor giving the effect of a CVT. It allows the engine to run at semi-constant speed giving better fuel economy and reduced emissions. Hybrid car developments are described that show the wide range of possible hybrid systems. (author)

  17. Hydronium 4-oxo-1,4-dihydropyridine-3-sulfonate dihydrate

    Directory of Open Access Journals (Sweden)

    Zhi-Biao Zhu

    2009-11-01

    Full Text Available 2-Hydroxypyridine when treated with concentrated sulfuric acid is sulfonated at the 3-position to yield the title hydrated salt, H3O+·C5H4NO3S−·2H2O. In the crystal structure, the cations, anions and uncoordinated water molecules are linked by extensive O—H...O and N—H...O hydrogen bonds into a three-dimensional network. The crystal studied is a non-merohedral twin with a twin component of 36%.

  18. Properties of sulfonated cation-exchangers made from petroleum asphaltites

    Energy Technology Data Exchange (ETDEWEB)

    Pokonova, Yu.V.; Pol' kin, G.B.; Proskuryakov, V.A.

    1982-01-10

    The use of ion-exchangers in radiochemical technology is accompanied by changes of their properties under the influence of ionizing radiation. The rate of development of these processes depends on the nature and structure of the matrix and on the nature and amount of ionic groups. We have proposed a method of synthesis of ion-exchangers resistant to ..gamma.. radiation from petroleum asphaltites. Continuing these investigations, we prepared cation-exchangers by sulfonation of a mixture of petroleum asphaltites and acid asphalt. An investigation of their radiation resistance is described in this paper.

  19. [Hygienic assessment of biologically rigid linear alkylbenzene sulfonates].

    Science.gov (United States)

    Bocharov, V V; Ryzhkova, O A

    2010-01-01

    It has been found that there are both biologically rigid and biologically soft homologues in the homologous series of linear alkylbenzene sulfonates (LABS). It is shown that absorption of LABS molecules from aqueous to activated sludge phase may serve as a determinant that should be used to refer a homologue to as rigid or soft surfactants. The biodegradability, detergency, and toxicity of LABS were ascertained to be related to the size of molecular alkyl molecular substitute. It has established that the fractional compositions of linear alkobenzenes should be changed for the synthesis of LABS that have the maximum detergency, a high biodegradability rate, and a low toxicity.

  20. Electrooxidation of Linear Alkyl Benzene Sulfonate (LAS) on Pt Electrodes

    OpenAIRE

    1999-01-01

    The electrochemical behaviour of linear alklybenzene sulfonate (LAS) on Pt electrodes was investigated in 0.05M Na2SO4 and in 0.1M NaCl at pH=8 by the potentiokinetic method and by electrolysis. The anodic and cathodic semilogarithmic current-potential curves were obtained between -1.6V - +1.6V. The experimental discharge potentials were determined by means of current-potential-curves obtained by electrolysis between 0-3V. The percentages of surface active material remaining in the so...

  1. Inhibition of the anaerobic digestion process by linear alkylbenzene sulfonates

    DEFF Research Database (Denmark)

    Gavala, Hariklia N.; Ahring, Birgitte Kiær

    2002-01-01

    it is important to investigate the effect of these xenobiotic compounds on an anaerobic environment. The inhibitory effect of Linear Alkylbenzene Sulfonates (LAS) on the acetogenic and methanogenic step of the anaerobic digestion process was studied. LAS inhibit both acetogenesis from propionate...... of the anaerobic digestion process should be seriously taken into consideration when wastewater from a surfactant producing industry is to be treated biologically or enter a municipal wastewater treatment plant that employs anaerobic technology. The upper allowable biomass specific LAS concentration should be 14...

  2. Synthesis and characterization of polyether urethane acrylate -LiCF{sub 3}SO{sub 3}-based polymer electrolytes by UV-curing in lithium batteries

    Energy Technology Data Exchange (ETDEWEB)

    Kim, Cheon Soo; Kim, Bo Hyun; Kim, Keon [Korea Univ., Seoul (Korea). Dept. of Chemistry

    1999-11-01

    The prepolymers of polyether urethane acrylate (PEUA) were synthesized from polyether polyol (polyethylene glycol (PEG) or polypropylene glycol (PPG)), diisocyanate (hexamethylene diisocyanate (HMDI) or toluene, 2,4-diisocyanate (TDI)), and the caprolactone-modified hydroxyethyl acrylate (FA2D) using the catalyst (dibutyltin dilaurate (DBTDL)) by stepwise addition reaction. Lithium triflate (LiCF{sub 3}SO{sub 3}) was dissolved in PEUA prepolymers, and plasticizer (propylene carbonate (PC)) was added into prepolymer and salt mixtures. Then photoinitiator (Irgacure 184) was also dissolved in the mixtures. Thin films were prepared by casting on the glass plate, and then by curing the plasticized prepolymer and salt mixtures under UV radiation. Electrochemical and electrical properties of PEUA-LiCF{sub 3}SO{sub 3}-based polymer electrolytes were evaluated and discussed to be used in lithium batteries. (orig.)

  3. Synthesis and characterization of polyether urethane acrylate-LiCF 3SO 3-based polymer electrolytes by UV-curing in lithium batteries

    Science.gov (United States)

    Kim, Cheon-Soo; Kim, Bo-Hyun; Kim, Keon

    The prepolymers of polyether urethane acrylate (PEUA) were synthesized from polyether polyol (polyethylene glycol (PEG) or polypropylene glycol (PPG)), diisocyanate (hexamethylene diisocyanate (HMDI) or toluene 2,4-diisocyanate (TDI)), and the caprolactone-modified hydroxyethyl acrylate (FA2D) using the catalyst (dibutyltin dilaurate (DBTDL)) by stepwise addition reaction. Lithium triflate (LiCF 3SO 3) was dissolved in PEUA prepolymers, and plasticizer (propylene carbonate (PC)) was added into prepolymer and salt mixtures. Then photoinitiator (Irgacure 184) was also dissolved in the mixtures. Thin films were prepared by casting on the glass plate, and then by curing the plasticized prepolymer and salt mixtures under UV radiation. Electrochemical and electrical properties of PEUA-LiCF 3SO 3-based polymer electrolytes were evaluated and discussed to be used in lithium batteries.

  4. Ionomeric membranes based on partially sulfonated poly(styrene) : synthesis, proton conduction and methanol permeation

    NARCIS (Netherlands)

    Picchioni, F.; Tricoli, V.; Carretta, N.

    2000-01-01

    Homogeneuosly sulfonated poly(styrene) (SPS) was prepared with various concentration of sulfonic acid groups in the base polymer. Membranes cast from these materials were investigated in relation to proton conductivity and methanol permeability in the temperature range from 20°C to 60°C. It was foun

  5. APPLICATION OF THE SULFONATE ESTER GROUP AS A LINKER FOR SOLID PHASE ORGANIC SYNTHESIS

    Institute of Scientific and Technical Information of China (English)

    SUN Weimin; LUO Juntao; HUANG Wenqiang; ZHU Xiaoxia

    2001-01-01

    A use of Sulfonate ester as a linker in synthesis of ω-aminoalkanols was reported. Diols were tethered onto polystyryl sulfonyl chloride resin, yielding sulfonate resins (2). After cleaved by diethyl amine, diisopropylamine and propylamine respectively, three ω-aminoalkanols were obtained.

  6. Sulfonated polyetherketone (SPEK-C) films investigated by positron annihilation lifetime spectroscopy and atomic force microscopy

    Institute of Scientific and Technical Information of China (English)

    Htwe Htwe Yin; YIN Ze-Jie; TANG Shi-Biao; HUANG Huan; ZHU Da-Ming

    2005-01-01

    The characterization of sulfonated polyetherketone (SPEK-C) films was investigated by using positron annihilation lifetime spectroscopy (PALS) and atomic force microscopy (AFM). It was found that free volume radius and intensity depend on the variation of sulfonation degree and solvent evaporation time of the films. Pore size and distribution determined from PALS and AFM measurements showed reasonable agreement.

  7. APPLICATION OF THE SULFONATE ESTER GROUP AS A LINKER FOR SOLID PHASE ORGANIC SYNTHESIS

    Institute of Scientific and Technical Information of China (English)

    SUNWeimin; ZHUXiaoxia; 等

    2001-01-01

    A use of sulfonate ester as a linker in synthesis of w-aminoalkanols was reporte.Diols were tethered onto polystyryl sulfonyl chloride resin,yielding sulfonate resins(2).After cleaved by diethyl amine,diisopropylamine and propylamine respectively,three w-aminoalkanlos were obtained.

  8. Coating of Sulfonic Silica onto Magnetite from Marina Beach Iron sand, Semarang, Indonesia

    Science.gov (United States)

    Azmiyawati, C.; Suyati, L.; Taslimah; Anggraeni, R. D.

    2017-02-01

    The mineral iron oxide is the main component of sand iron that are abundant in nature. Mineral iron oxide not yet widely applied into more useful products. The main component of iron ore is magnetite. Magnetite can be used as a basic ingredient in the manufacture of magnetite-modified silica adsorbent sulfonate. In this research, the adsorbent made from sulfonic functionalized silica-coated magnetic particle has been successfully produced, with the magnetite was obtained from iron sand at Marina Beach, Semarang Indonesia. This adsorbent was then used as a metal ion preconcentration media. From the research that it was found that the sulfonic has been bound to the silica marked by the emergence of element S on EDX. Whilst, the evidence that silica has coated on the magnetite could be seen from the SEM images which showed the morphology of sulfonic functionalized silica-coated magnetic particles were larger than the sulfonic functionalized silica without magnetite. From the DSC results showed that the addition of magnetite on sulfonic functionalized silica did not change the heat resistance of the sulfonic functionalized silica. Based on the XRD patterns show that magnetite sulfonate silica was formed.

  9. Cationic and radical intermediates in the acid photorelease from aryl sulfonates and phosphates.

    Science.gov (United States)

    Terpolilli, Marco; Merli, Daniele; Protti, Stefano; Dichiarante, Valentina; Fagnoni, Maurizio; Albini, Angelo

    2011-01-01

    The irradiation of a series of phenyl sulfonates and phosphates leads to the quantitative release of acidity with a reasonable quantum yield (≈0.2). Products characterization, ion chromatography analysis and potentiometric titration are consistent with the intervening of two different paths in this reaction, viz. cationic with phosphates and (mainly) radical with sulfonates.

  10. Colonic necrosis due to calcium polystyrene sulfonate (Kalimate) not suspended in sorbitol.

    Science.gov (United States)

    Castillo-Cejas, María Dolores; de-Torres-Ramírez, Inés; Alonso-Cotoner, Carmen

    2013-04-01

    Cation-exchange resins are used in the management of hyperkalemia, particularly in patients with end-stage renal disease. These resins were associated with gastrointestinal tract lesions, especially sodium polystyrene sulfonate (Kayexalate) mixed with sorbitol. We present a case of colonic necrosis after the administration of calcium polystyrene sulfonate (Kalimate) not suspended in sorbitol.

  11. Colonic necrosis due to calcium polystyrene sulfonate (Kalimate) not suspended in sorbitol

    OpenAIRE

    María Dolores Castillo-Cejas; Inés de Torres-Ramírez; Carmen Alonso-Cotoner

    2013-01-01

    Cation-exchange resins are used in the management of hyperkalemia, particularly in patients with end-stage renal disease. These resins were associated with gastrointestinal tract lesions, especially sodium polystyrene sulfonate (Kayexalate) mixed with sorbitol. We present a case of colonic necrosis after the administration of calcium polystyrene sulfonate (Kalimate) not suspended in sorbitol.

  12. 78 FR 62443 - Perfluoroalkyl Sulfonates and Long-Chain Perfluoroalkyl Carboxylate Chemical Substances; Final...

    Science.gov (United States)

    2013-10-22

    ... AGENCY 40 CFR Parts 9 and 721 RIN 2070-AJ95 Perfluoroalkyl Sulfonates and Long-Chain Perfluoroalkyl... new use rule (SNUR) for perfluoroalkyl sulfonate (PFAS) chemical substances to add PFAS chemical.... EPA is also finalizing a SNUR for long-chain perfluoroalkyl carboxylate (LCPFAC) chemical...

  13. Ionomeric membranes based on partially sulfonated poly(styrene) : synthesis, proton conduction and methanol permeation

    NARCIS (Netherlands)

    Picchioni, F.; Tricoli, V.; Carretta, N.

    2000-01-01

    Homogeneuosly sulfonated poly(styrene) (SPS) was prepared with various concentration of sulfonic acid groups in the base polymer. Membranes cast from these materials were investigated in relation to proton conductivity and methanol permeability in the temperature range from 20°C to 60°C. It was foun

  14. 40 CFR 721.10045 - Diazotized substituted heteromonocycle coupled with naphthalene sulfonic acid derivative, nickel...

    Science.gov (United States)

    2010-07-01

    ... coupled with naphthalene sulfonic acid derivative, nickel complex, alkaline salt (generic). 721.10045... derivative, nickel complex, alkaline salt (generic). (a) Chemical substance and significant new uses subject... heteromonocycle coupled with naphthalene sulfonic acid derivative, nickel complex, alkaline salt (PMN P-02-737)...

  15. Colonic necrosis due to calcium polystyrene sulfonate (Kalimate not suspended in sorbitol

    Directory of Open Access Journals (Sweden)

    María Dolores Castillo-Cejas

    2013-04-01

    Full Text Available Cation-exchange resins are used in the management of hyperkalemia, particularly in patients with end-stage renal disease. These resins were associated with gastrointestinal tract lesions, especially sodium polystyrene sulfonate (Kayexalate mixed with sorbitol. We present a case of colonic necrosis after the administration of calcium polystyrene sulfonate (Kalimate not suspended in sorbitol.

  16. Julia Olefination as a General Route to Phenyl (α-Fluoro)vinyl Sulfones

    Science.gov (United States)

    He, Maggie; Ghosh, Arun K.; Zajc, Barbara

    2009-01-01

    Mild and efficient synthesis of phenyl (α-fluoro)vinyl sulfones via condensation of aldehydes and a ketone with a novel benzothiazolyl based bis-sulfone reagent is reported and this proceeds with moderate to good Z-stereoselectivity. PMID:19888442

  17. Evaluation of surface detail reproduction, dimensional stability and gypsum compatibility of monophase polyvinyl-siloxane and polyether elastomeric impression materials under dry and moist conditions

    OpenAIRE

    Vadapalli, Sriharsha Babu; Atluri, Kaleswararao; Putcha, Madhu Sudhan; Kondreddi, Sirisha; Kumar, N. Suman; Tadi, Durga Prasad

    2016-01-01

    Objectives: This in vitro study was designed to compare polyvinyl-siloxane (PVS) monophase and polyether (PE) monophase materials under dry and moist conditions for properties such as surface detail reproduction, dimensional stability, and gypsum compatibility. Materials and Methods: Surface detail reproduction was evaluated using two criteria. Dimensional stability was evaluated according to American Dental Association (ADA) specification no. 19. Gypsum compatibility was assessed by two crit...

  18. Mass spectrometric composition and structural studies of petroleum sulfonates and petroleum sulfonate components for utilization in tertiary petroleum production

    Energy Technology Data Exchange (ETDEWEB)

    Belafi, L.; Decsy, Z.; Kerenyi, E.; Lukacs, J.

    1984-01-01

    A separation and mass spectrometric analytical method was developed for the separation and characterization of the monosulfonate fractions of petroleum sulfonate products. The technique is based on distillation and preparative column and thin-layer chromatography. The structure and carbon number distributions of monosulfonate fractions transformed to metilesters were measured based on their low resolution molecular mass spectra. The conditions of an actual petroleum container were simulated and the measurement of the effluent composition during its discharge revealed no change in the composition of monosulfonates.

  19. Radiation-chemical synthesis of polypropylene fabrics with sulfonic acid functional groups

    Energy Technology Data Exchange (ETDEWEB)

    Cho, Hyun Kug; Park, Jung Soo; Han, Do Hung, E-mail: dhhan@yumail.ac.kr; Bondar, Iuliia, E-mail: juliavad@yahoo.co

    2011-04-01

    A sorption-active material carrying sulfonic acid groups was synthesized by the radiation-induced graft polymerization of styrene monomer onto the surface of non-woven polypropylene fabric, followed by sulfonation of the grafted polystyrene chains. The effect of the main experimental parameters (absorbed dose, monomer concentration, reaction time) on the styrene degree of grafting was investigated. The sulfonation process with 5% chlorosulfonic acid at room temperature was investigated in detail and the optimal sulfonation conditions for the samples with a medium degree of grafting (70-140%) were determined. Densities of 3.5-5 meq/g were obtained by applying those sorption-active PP fabrics with a sulfonic acid group.

  20. Selective sorption of perfluorooctane sulfonate on molecularly imprinted polymer adsorbents

    Institute of Scientific and Technical Information of China (English)

    Shubo DENG; Danmeng SHUAI; Qiang YU; Jun HUANG; Gang YU

    2009-01-01

    Perfluorooctane sulfonate (PFOS), as a potential persistent organic pollutant, has been widely detected in water environments, and has become a great concern in recent years. PFOS is very stable and difficult to decompose using conventional techniques. Sorption may be an attractive method to remove it from water. In this study, the molecularly imprinted polymer (MIP) adsorbents were prepared through the polymerization of 4-vinylpyridine under different preparation conditions in order to remove perfluorooctane sulfonate (PFOS) from water. The MIP adsorbents using perfluorooctanoic acid (PFOA) as the template had good imprinting effects and could selectively remove PFOS from aqueous solution. The sorption behaviors including sorption kinetics,isotherms, and effect of pH, salt, and competitive anions were investigated. Experimental results showed that the sorption of PFOS On the MIP adsorbents was very fast, pH-dependent, and highly selective. The achieved fast sorption equilibrium within 1 h was attributed to the surface sorption on the fine adsorbents. The sorption isotherms showed that the sorption selectivity of PFOS on the MIP adsorbents decreased at high PFOS concentrations, which may be due to the double-layer sorption and the formation of PFOS micelles on the sorbent surface. The sorption of PFOS on the MIP adsorbents was mainly dominated by the electrostatic interaction between the protonated vinylpyridine on the adsorbent surface and the anionic PFOS. The prepared MIP adsorbents can potentially be applied in water and wastewater treatment for selective removal of PFOS.

  1. Polyaniline synthesized with functionalized sulfonic acids for blends manufacture

    Directory of Open Access Journals (Sweden)

    Mara Joelma Raupp Cardoso

    2007-12-01

    Full Text Available Polyaniline (PAni, an electronic conductive polymer, has poor mechanical properties, such as low tensile, compressive and flexural strength that render PAni a non-ideal material to be processed for practical applications. Desired properties of polyaniline can be enhanced by mixing it with a polymer that has good mechanical properties. In this work, PAni was synthesised using functionalized sulfonic acids like camphorsulfonic acid (CSA and dodecilbenzene sulfonic acid (DBSA in order to promote PAni doping and improve its solubility, making possible conductive blends manufacture. The different forms of PAni were characterized by infra-red spectroscopy, thermal analysis, scanning electron microscopy and conductivity measurements. A conductive blend composed of PAni/DBSA and lower density polyethylene (LDPE was obtained via solubilization method and its thermal, morphological and electrical properties were investigated. Concentrations as low as 5 wt. (% of PAni was able to lead to electrical conductivities of PAni/LDPE blends in the range of 10-3 S.cm-1, showing great potential to be used in antistatic packing, electromagnetic shielding, anti-corrosion shielding or as a semiconductor.

  2. Sulfonated Poly(styrene) Chains Grafted on Magnetic Nanoparticles

    Science.gov (United States)

    Jiao, Yang; Yevelev, Anton; Parra, Javier; Akcora, Pinar; Stevens Institute of Technology Team

    2014-03-01

    Iron oxide nanoparticles functionalized with poly(styrene) (PS) chains at various grafting densities and loadings present stable and ordered nanostructures for tuning the mechanical and conductive properties in polymer composites. Strings, spherical and anisotropic clusters and well-dispersed particles are achieved with PS-grafted Fe3O4 nanoparticles in PS matrices upon varying the system parameters. In this work, we report the effect of sulfonic group locations on the aggregation state of polymer-grafted nanoparticles. Structures formed by the random and diblock copolymers of PS-poly(styrene sulfonate) (PSS) grafted particles will be discussed with small-angle x-ray scattering (SAXS) measurements in solution and melts. The conformational changes in PS-grafted chains and ion-containing grafts will be also presented in small-angle neutron-scattering (SANS) results to understand the role of polymer on the assembly of particles at the low grafting density. We acknowledge support by NSF-CAREER-DMR (#1048865).

  3. Anisotropic Ionic Conductivity of Lithium-Doped Sulfonated PBI.

    Science.gov (United States)

    Spry, R. J.; Arnold, F. E.; Dean, D. R.; Alexander, M. D., Jr.; Bai, S. J.; Dang, T. D.; Price, G. E.; Solomon, J. S.

    1997-03-01

    We report the conductivity study results of lithium-doped sulfonated PBI, a conjugated rigid rod polymer, poly[(1,7-dihydrobenzo[1,2-d:4,5-d']dimidazole-2,6-diyl)-2-(2-sulfo)-p- phenylene], derivatized with pendants of propane sulfonate Li^+ ionomer. The DC four-probe conductivity parallel to the surface of cast films was as large as 8.3× 10-3 S/cm. Similar measurements in an eight-probe configuration showed no difference between bulk and surface conductivity. The ionic nature of the conductivity was indicated by constant voltage depletion experiments and by secondary ion mass spectroscopy measurements of the residues near the electrodes. Both the AC and DC two-probe conductivities measured transverse to the sample surface were ~ 10-8 S/cm. Electron microscopy indicated that the films has a layered structure parallel to the surfaces. This structural anisotropy was confirmed by refractive index values obtained from wave-guide experiments. The polymer morphology was also investigated by X-ray scattering.

  4. Photocatalytic treatment of linear alkylbenzene sulfonate (LAS) in water.

    Science.gov (United States)

    Mehrvar, Mehrab; Venhuis, Sarah Hatfield

    2005-01-01

    The photocatalytic degradation of aqueous linear alkylbenzene sulfonate (LAS) was studied. Two different photocatalysts, Degussa P25 TiO2 and Hombikat UV 100 TiO2, were used to degrade aqueous linear alkylbenzene sulfonate in slurry batch photoreactors. For a 100 mg/L LAS solution based on first-order rate constants, the optimum photocatalyst loading for Degussa P25 TiO2 was 4.0 g/L, while for Hombikat UV 100 TiO2 it was 2.0 g/L. The photoactivity of Degussa P25 TiO2 it was higher than that of Hombikat UV 100 TiO2 for the treatment of LAS. A mixture of both photocatalysts did not improve the LAS degradation rates in batch experiments. Combination of Degussa P25 TiO2 and 600 mg/L H2O2 along with irradiation with UV light at either 254 or 365 nm did not improve the LAS degradation rates over the photocatalytic or photolytic processes individually.

  5. Sulfonated PEEK and fluorinated polymer based blends for fuel cell applications: Investigation of the effect of type and molecular weight of the fluorinated polymers on the membrane's properties

    Energy Technology Data Exchange (ETDEWEB)

    Inan, Tuelay Y.; Dogan, Hacer; Unveren, Elif E. [The Scientific and Technological Research Council of Turkey (TUBITAK), Marmara Research Center, Chemistry Institute, 41470 Gebze, Kocaeli (Turkey); Eker, Ersoy [Tuerk Demirdoekuem Fabrikalari A.S., 11300 Bozueyuek, Bilecik (Turkey)

    2010-11-15

    This work clearly demonstrates the effect of the type and molecular weight of the fluorinated polymer of SPEEK/Fluorinated polymer blends for low temperature (<80 C) Fuel Cell Applications. Comparisons with trademarks (e.g., Nafion {sup registered}) suggests that the membranes we have prepared in this study have good compatibility in all application respects. Membranes were prepared by solution casting method from four different fluorinated polymers; poly (vinylidene fluoride) with three different molecular weights (PVDF, M{sub w}: 180.000, M{sub w}: 275.000, M{sub w}: 530.000); Poli(vinylidene fluoride-co-Hexafluoro propylen) (PVDF-HFP M{sub n}:130.000) and sulfonated poly(ether ether ketone) (SPEEK) with sulfonation degree (SD) of 70. The sulfonation degree (SD) of SPEEK was determined by FTIR, {sup 1}H NMR and ion exchange capacity (IEC) measurements. Thermo-oxidative stability and proton conductivity of the membranes were determined by using thermal gravimetric analysis (TGA) and BT-512 BekkTech membrane test systems, respectively. Chemical degradation of SPEEK membranes was investigated via Fenton test. The morphology of the membranes were examined by scanning electron microscopy (SEM) and transmission electron microscopy (TEM). Water uptake and proton conductivity values decreased with the addition of fluorinated polymers (PVDF, PVDF-HFP) as expected, but proton conductivity values were still comparable to that of Nafion 117 {sup registered} membrane. Addition of fluorinated polymers improved chemical degradation of the blend membranes in all ratios while addition of PVDF-HFP to the SPEEK70 caused phase separations in all ratios. Methanol permeability value of SPEEK70/PVDF(M{sub w} = 275.000) blend membrane (3.13E-07 (cm{sup 2}/s)) was much lower than Nafion 117 {sup registered} (1.21E-06 (cm{sup 2}/s)). PVDF addition to the SPEEK polymers caused increase in elongation of the membranes. Increase in the molecular weight of the PVDF did not show any effect on

  6. 40 CFR 417.140 - Applicability; description of the neutralization of sulfuric acid esters and sulfonic acids...

    Science.gov (United States)

    2010-07-01

    ... neutralization of sulfuric acid esters and sulfonic acids subcategory. 417.140 Section 417.140 Protection of... MANUFACTURING POINT SOURCE CATEGORY Neutralization of Sulfuric Acid Esters and Sulfonic Acids Subcategory § 417.140 Applicability; description of the neutralization of sulfuric acid esters and sulfonic acids...

  7. Coupling hydrogen separation with butanone hydrogenation in an electrochemical hydrogen pump with sulfonated poly (phthalazinone ether sulfone ketone) membrane

    Science.gov (United States)

    Huang, Shiqi; Wang, Tao; Wu, Xuemei; Xiao, Wu; Yu, Miao; Chen, Wei; Zhang, Fengxiang; He, Gaohong

    2016-09-01

    This work reports the novel work of coupling H2/CO2 separation with biomass-derived butanone hydrogenation in non-fluorinated sulfonated poly (phthalazinone ether sulfone ketone) (SPPESK) electrochemical hydrogen pump (EHP) reactor. Due to higher resistance to swelling, SPPESK-based EHP reactor exhibits more excellent reaction rate in elevated temperature (60 °C) and higher butanone concentration (2 M) as 270, 260 nmol cm-2 s-1, respectively, higher than 240, 200 nmol cm-2 s-1of Nafion-based EHP reactors. Also, the SPPESK-based EHP reactor remains 90% of initial hydrogenation rate after 4 batches, better than that of Nafion-based EHP reactors, which is only 62%. The energy efficiency of EHP separator reaches 40% under H2/CO2 mixture feed mode, and electricity of about 0.3 kWh is consumed per Nm3 H2 product, being superior to energy consumption compared with alternative processes like PSA and electrolysis of water. In addition, SPPESK-based EHP exhibits better hydrogenation stability due to lower CO2 permeation than Nafion. With increasing CO2 content in H2 feed, hydrogenation rate almost keeps constant at around 210 nmol cm-2 s-1 in SPPESK-based EHP reactor while decreases fast to 50 nmol cm-2 s-1 in Nafion/PTFE-based EHP reactor. These results show integration of gas separation with hydrogenation reactor is feasible in SPPESK-based EHP reactor.

  8. 含氟聚醚多元醇的研究进展%The Research Progress of Fluorine-Containing Polyether Polyol

    Institute of Scientific and Technical Information of China (English)

    张英强; 徐微; 李烨

    2012-01-01

    Compared with conventional hydroxyl-terminated polyethers, the fluorine-containing polyether polyols can be used to prepare polymers with better performances, such as water repellent and oil repellent, self-cleaning, self-lubricating, and resistant to heat, UV light, weathering, corrosion, chemical, solvent and so on. Therefore it has a wide range of potential applications and development prospects. In this article, preparation technical approaches and chemical structure features of fluorine-containing polyether polyols at home and abroad have been reviewed in detail. Research progresses on fluorine-containing polyether polyol used in polyurethane elastmers, coatings and other application areas are briefly introduced. It is pointed out that the main directions of fluorine-containing polyether polyols for the future research and development should focus on lowering products costs, developing green high performance technical process, simplifying preparation techniques, optimizing the process conditions, and developing new products.%与常规羟基聚醚相比,含氟聚醚多元醇可被用来制备具有耐热、耐UV光、耐候、耐腐蚀、耐化学品、耐溶剂、拒油拒水、自清洁、自润滑等优良性能的高分子,因此具有多种潜在应用领域和发展前景。本文综述了国内外含氟聚醚多元醇的制备技术途径、结构类型特点,并阐述了其在聚氨酯弹性体、涂料及其它应用领域的研究进展。指出降低成本、开发绿色高效的制备技术、简化工艺路线、优化工艺条件、研发新产品为未来发展含氟聚醚多元醇的主要研发方向。

  9. Red electroluminescence of ruthenium sensitizer functionalized by sulfonate anchoring groups.

    Science.gov (United States)

    Shahroosvand, Hashem; Abbasi, Parisa; Mohajerani, Ezeddin; Janghouri, Mohammad

    2014-06-28

    We have synthesized five novel Ru(ii) phenanthroline complexes with an additional aryl sulfonate ligating substituent at the 5-position [Ru(L)(bpy)2](BF4)2 (1), [Ru(L)(bpy)(SCN)2] (2), [Ru(L)3](BF4)2 (3), [Ru(L)2(bpy)](BF4)2 (4) and [Ru(L)(BPhen)(SCN)2] (5) (where L = 6-one-[1,10]phenanthroline-5-ylamino)-3-hydroxynaphthalene 1-sulfonic, bpy = 2,2'-bipyridine, BPhen = 4,7-diphenyl-1,10-phenanthroline), as both photosensitizers for oxide semiconductor solar cells (DSSCs) and light emitting diodes (LEDs). The absorption and emission maxima of these complexes red shifted upon extending the conjugation of the phenanthroline ligand. Ru phenanthroline complexes exhibit broad metal to ligand charge transfer-centered electroluminescence (EL) with a maximum near 580 nm. Our results indicated that a particular structure (2) can be considered as both DSSC and OLED devices. The efficiency of the LED performance can be tuned by using a range of ligands. Device (2) has a luminance of 550 cd m(-2) and maximum efficiency of 0.9 cd A(-1) at 18 V, which are the highest values among the five devices. The turn-on voltage of this device is approximately 5 V. The role of auxiliary ligands in the photophysical properties of Ru complexes was investigated by DFT calculation. We have also studied photovoltaic properties of dye-sensitized nanocrystalline semiconductor solar cells based on Ru phenanthroline complexes and an iodine redox electrolyte. A solar energy to electricity conversion efficiency (η) of 0.67% was obtained for Ru complex (2) under standard AM 1.5 irradiation with a short-circuit photocurrent density (Jsc) of 2.46 mA cm(-2), an open-circuit photovoltage (Voc) of 0.6 V, and a fill factor (ff) of 40%, which are all among the highest values for ruthenium sulfonated anchoring groups reported so far. Monochromatic incident photon to current conversion efficiency was 23% at 475 nm. Photovoltaic studies clearly indicated dyes with two SCN substituents yielded a higher Jsc for the

  10. Surface modification of poly(ether ether ketone) with methacryloyl-functionalized phospholipid polymers via self-initiation graft polymerization.

    Science.gov (United States)

    Kawasaki, Yoshihiro; Iwasaki, Yasuhiko

    2014-01-01

    To improve blood compatibility of poly(ether ether ketone) (PEEK), surface modification with methacryloyl-functionalized phospholipid polymers was performed through self-initiation graft polymerization. The copolymers (PMA) of 2-methacryloyloxyethyl phosphorylcholine (MPC) and 2-aminoethyl methacrylate hydrochloride were synthesized by conventional free radical polymerization. The PMA was then immobilized with pentafluorophenyl methacrylate to obtain methacryloyl-functionalized MPC polymers (PMAMA). The degree of substitution of the methacryloyl group into the copolymer was nearly completed. The PMAMA was dissolved in 1-butanol and the solution was dropped on PEEK. UV light (350±50 nm) was subsequently irradiated on PEEK for various periods. Elemental analysis of the PEEK surface was performed by X-ray photoelectron spectroscopy and phosphorus and nitrogen signals due to the MPC units on PEEK were observed. The surface wettability of PEEK was also improved by immobilization of PMAMA. Plasma protein adsorption was effectively reduced on the PMAMA-immobilized surface regardless of the type of protein. Furthermore, PMAMA immobilization was also useful in reducing platelet adhesion on PEEK. In conclusion, methacryloyl-functionalized MPC polymers could be immobilized on PEEK by simple photo-irradiation, resulting in significant improvement in blood compatibility.

  11. Macromolecular Engineering: New Routes Towards the Synthesis of Well-??Defined Polyethers/Polyesters Co/Terpolymers with Different Architectures

    KAUST Repository

    Alamri, Haleema

    2016-05-18

    The primary objective of this research was to develop a new and efficient pathway for well-defined multicomponent homo/co/terpolymers of cyclic esters/ethers using an organocatalytic approach with an emphasis on the macromolecular engineering aspects of the overall synthesis. Macromolecular engineering (as discussed in the first chapter) of homo/copolymers refers to the specific tailoring of these materials for achieving an easy and reproducible synthesis that results in precise molecular characteristics, i.e. molecular weight and polydispersity, as well as specific structure and end?group choices. Precise control of these molecular characteristics will provide access to new materials that can be used for pre-targeted purposes such as biomedical applications. Among the most commonly used engineering materials are polyesters (biocompatible and biodegradable) and polyethers (biocompatible), either as homopolymers or when or copolymers with linear structures. The ability to create non-linear structures, for example stars, will open new horizons in the applications of these important polymeric materials. The second part of this thesis describes the synthesis of aliphatic polyesters, particularly polycaprolactone and polylactide, using a metal-free initiator/catalyst system. A phosphazene base (t?BuP2) was used as the catalyst for the ring-opening copolymerization of ?-aprolactone (??CL) and L,Lactide (LLA) at room temperature with a variety of protic initiators in different solvents. These studies provided important information for the design of a metal-free route toward the synthesis of polyester?based (bio) materials. The third part of the thesis describes a novel route for the one?pot synthesis of polyether-b polyester block copolymers with either a linear or a specific macromolecular architecture. Poly (styrene oxide)?b?poly(caprolactone)?b?poly(L,lactide) was prepared using this method with the goal of synthesizing poly(styrene oxide)-based materials since this

  12. Shape Memory Composites Based on Electrospun Poly(vinyl alcohol) Fibers and a Thermoplastic Polyether Block Amide Elastomer.

    Science.gov (United States)

    Shirole, Anuja; Sapkota, Janak; Foster, E Johan; Weder, Christoph

    2016-03-01

    The present study aimed at developing new thermally responsive shape-memory composites, that were fabricated by compacting mats of electrospun poly(vinyl alcohol) (PVA) fibers and sheets of a thermoplastic polyether block amide elastomer (PEBA). This design was based on the expectation that the combination of the rubber elasticity of the PEBA matrix and the mechanical switching exploitable through the reversible glass transition temperature (Tg) of the PVA filler could be combined to create materials that display shape memory characteristics as an emergent effect. Dynamic mechanical analyses (DMA) show that, upon introduction of 10-20% w/w PVA fibers, the room-temperature storage modulus (E') increased by a factor of 4-5 in comparison to the neat PEBA, and they reveal a stepwise reduction of E' around the Tg of PVA (85 °C). This transition could indeed be utilized to fix a temporary shape and recover the permanent shape. At low strain, the fixity was 66 ± 14% and the recovery was 98 ± 2%. Overall, the data validate a simple and practical strategy for the fabrication of shape memory composites that involves a melt compaction process and employs two commercially available polymers.

  13. Celecoxib influences steroid sulfonation catalyzed by human recombinant sulfotransferase 2A1.

    Science.gov (United States)

    Ambadapadi, Sriram; Wang, Peter L; Palii, Sergiu P; James, Margaret O

    2015-08-01

    Celecoxib has been reported to switch the human SULT2A1-catalyzed sulfonation of 17β-estradiol (17β-E2) from the 3- to the 17-position. The effects of celecoxib on the sulfonation of selected steroids catalyzed by human SULT2A1 were assessed through in vitro and in silico studies. Celecoxib inhibited SULT2A1-catalyzed sulfonation of dehydroepiandrosterone (DHEA), androst-5-ene-3β, 17β-diol (AD), testosterone (T) and epitestosterone (Epi-T) in a concentration-dependent manner. Low μM concentrations of celecoxib strikingly enhanced the formation of the 17-sulfates of 6-dehydroestradiol (6D-E2), 17β-dihydroequilenin (17β-Eqn), 17β-dihydroequilin (17β-Eq), and 9-dehydroestradiol (9D-E2) as well as the overall rate of sulfonation. For 6D-E2, 9D-E2 and 17β-Eqn, celecoxib inhibited 3-sulfonation, however 3-sulfonation of 17β-Eq was stimulated at celecoxib concentrations below 40 μM. Ligand docking studies in silico suggest that celecoxib binds in the substrate-binding site of SULT2A1 in a manner that prohibits the usual binding of substrates but facilitates, for appropriately shaped substrates, a binding mode that favors 17-sulfonation.

  14. Sulfonated chitosan and dopamine based coatings for metallic implants in contact with blood.

    Science.gov (United States)

    Campelo, Clayton S; Chevallier, Pascale; Vaz, Juliana M; Vieira, Rodrigo S; Mantovani, Diego

    2017-03-01

    Thrombosis and calcification constitute the main clinical problems when blood-interacting devices are implanted in the body. Coatings with thin polymer layers represent an acknowledged strategy to modulate interactions between the material surface and the blood environment. To ensure the implant success, at short-term the coating should limit platelets adhesion and delay the clot formation, and at long-term it should delay the calcification process. Sulfonated chitosan, if compared to native chitosan, shows the unique ability to reduce proteins adsorption, decrease thrombogenic properties and limit calcification. In this work, stainless steel surfaces, commonly used for cardiovascular applications, were coated with sulfonated chitosan, by using dopamine and PEG as anchors, and the effect of these grafted surfaces on platelet adhesion, clot formation as well as on calcification were investigated. Surface characterization techniques evidenced that the coating formation was successful, and the sulfonated chitosan grafted sample exhibited a higher roughness and hydrophilicity, if compared to native chitosan one. Moreover, sulfonated surface limited platelet activation and the process of clot formation, thus confirming its high biological performances in blood. Calcium deposits were also lower on the sulfonated chitosan sample compared to the chitosan one, thus showing that calcification was minimal in presence of sulfonate groups. In conclusion, this sulfonated-modified surface has potential to be as blood-interacting material. Copyright © 2016. Published by Elsevier B.V.

  15. Sulfonated polyvinyl chloride fibers for cation-exchange microextraction.

    Science.gov (United States)

    Xu, Li; Lee, Hian Kee

    2009-09-18

    Polyvinyl chloride (PVC) fiber was derivatized by concentrated sulfuric acid to yield sulfonated PVC (PVC-SO3H). The PVC-SO3H fiber had dual properties as a sorbent, based on cation-exchange and hydrophobicity. In the present study, the novel fiber was used directly as an individual device for extraction purposes in the cation-exchange microextraction of anaesthetics, followed by high-performance liquid chromatography-UV analysis. The results demonstrated that this PVC-SO3H fiber-based microextraction afforded convenient operation and cost-effective application to basic analytes. The limits of detection for four anaesthetics ranged from 1.2 to 6.0 ng/mL. No carryover (because of its disposable usage), and no loss of sorbent phase (which normally occurs in stir-bar sorptive extraction) during extraction were observed.

  16. Mouse model of ulcerative colitis using trinitrobenzene sulfonic acid

    Directory of Open Access Journals (Sweden)

    Irfan Ahmad Rather

    2015-12-01

    Full Text Available Animal model of intestinal inflammation is of paramount significance that aids in discerning the pathologies underlying ulcerative colitis and Crohn’s disease, the two clinical presentations of inflammatory bowel disease. The 2,4,6-trinitrobenzene sulfonic acid (TNBS colitis model represents one such intestinal inflammation-prototype that is generated in susceptible strains of mice through intra-rectal instillation of compound TNBS. In this paper, we demonstrate the experimental induction of TNBS-mediated colitis in a susceptible strain of ICR mice. This can be done by the following steps: a acclimation, b induction and c observation. TNBS-mouse model provides the information in shortest possible time and simultaneously represents a cost effective and highly reproducible model method of studying the pathogenesis of inflammatory bowel disease.

  17. Chemoselective allylation of ketones in ionic liquids containing sulfonate anions.

    Science.gov (United States)

    Galletti, Paola; Moretti, Fabio; Samorì, Chiara; Tagliavini, Emilio

    2009-01-01

    The chemoselective addition of tetraallyltin to dialkyl, alkenyl-alkyl, and alkynyl-alkyl ketones can be performed with high yields in N-methyl-N-butylpyrrolidinium trifuoromethansulfonate (MBP-Tf). Other room temperature ionic liquids (RTILs) can also be successfully employed if some sulfonic acid is added. The reaction is very sensitive to the electronic properties of the substrate. Aryl alkyl ketones bearing electron-withdrawing substituents behave like dialkyl ketones and react promptly; on the contrary, electron-rich aryl alkyl ketones react sluggishly, which allows selective competitive allylation of dialkyl substrates to occur. The ionic liquid solvent can be easily recycled, which meets the green chemistry principles of selectivity and reuse of chemicals. NMR spectroscopic data support the formation of tin-triflate catalysts in situ.

  18. Characteristics of polyaniline electropolymerized in camphor sulfonic acid

    Energy Technology Data Exchange (ETDEWEB)

    Santos, J.R. Jr. [Instituto de Quimica de Sao Carlos/DFQ/USP, C.P. 369, 13560-970, Sao Carlos, SP (Brazil); Malmonge, J.A. [Instituto de Fisica de Sao Carlos/DFCM/USP, C.P. 369, 13560-970, Sao Carlos, SP (Brazil); Conceicao Silva, A.J.G. [Instituto de Fisica de Sao Carlos/DFCM/USP, C.P. 369, 13560-970, Sao Carlos, SP (Brazil); Motheo, A.J. [Instituto de Quimica de Sao Carlos/DFQ/USP, C.P. 369, 13560-970, Sao Carlos, SP (Brazil); Mascarenhas, Y.P. [Instituto de Fisica de Sao Carlos/DFCM/USP, C.P. 369, 13560-970, Sao Carlos, SP (Brazil); Mattoso, L.H.C. [Instituto de Fisica de Sao Carlos/DFCM/USP, C.P. 369, 13560-970, Sao Carlos, SP (Brazil)

    1995-03-01

    Polyaniline was electropolymerized by cyclic voltammetry in the presence of camphor sulfonic acid (CSA), and the resulting film was characterized by solubility tests, UV-Vis absorption, electron microscopy, X-ray diffraction and conductivity measurements. The use of the functionalized acid - CSA - made it possible to obtain the as-electropolymerized polymer (in the doped state) soluble in organic solvents such as m-cresol and chloroform. The UV-Vis spectra of PAni-CSA in m-cresol presented a free-carrier tail commencing at 1000nm which may be attributed to secondary doping due to conformational changes of the polymer chains. After treatment with m-cresol the film exhibited an increase of conductivity reaching ca. 100S/cm. (orig.)

  19. Anaerobic degradation of linear alkylbenzene sulfonate in fluidized bed reactor

    Directory of Open Access Journals (Sweden)

    L. L. Oliveira

    2010-12-01

    Full Text Available An anaerobic fluidized bed reactor was used to assess the degradation of the surfactant linear alkylbenzene sulfonate (LAS. The reactor was inoculated with sludge from an UASB reactor treating swine wastewater and was fed with a synthetic substrate supplemented with LAS. Sand was used as support material for biomass immobilization. The reactor was kept in a controlled temperature chamber (30±1 ºC and operated with a hydraulic retention time (HRT of 18 h. The LAS concentration was gradually increased from 8.2±1.3 to 45.8±5.4 mg.L-1. The COD removal was 91%, on average, when the influent COD was 645±49 mg.L-1. The results obtained by chromatographic analysis showed that the reactor removed 93% of the LAS after 270 days of operation.

  20. Radiation-induced crosslinking of poly(styrene–butadiene–styrene) block copolymers and their sulfonation

    Energy Technology Data Exchange (ETDEWEB)

    Lee, Sun-Young [Advanced Radiation Technology Institute, Korea Atomic Energy Research Institute, 29 Geumgu-gil, Jeongeup-si, Jeollabuk-do 580-185 (Korea, Republic of); Department of Chemical and Biomolecular Engineering, Yonsei University, 50 Yonsei-ro, Seodaemun-gu, Seoul 120-749 (Korea, Republic of); Song, Ju-Myung; Sohn, Joon-Yong [Advanced Radiation Technology Institute, Korea Atomic Energy Research Institute, 29 Geumgu-gil, Jeongeup-si, Jeollabuk-do 580-185 (Korea, Republic of); Shul, Yong-Gun [Department of Chemical and Biomolecular Engineering, Yonsei University, 50 Yonsei-ro, Seodaemun-gu, Seoul 120-749 (Korea, Republic of); Shin, Junhwa, E-mail: shinj@kaeri.re.kr [Advanced Radiation Technology Institute, Korea Atomic Energy Research Institute, 29 Geumgu-gil, Jeongeup-si, Jeollabuk-do 580-185 (Korea, Republic of)

    2013-12-01

    Highlights: • The c-SBS films were prepared using a gamma ray or electron beam. • The crosslinking degree of the c-SBS films were increased with the irradiation dose. • The prepared c-SBS films were sulfonated with various concentration of CSA. • The sulfonation of the c-SBS film is largely dependent on the concentration of CSA. • The sulfonation process is progressed from the surface to the inner part of c-SBS film. -- Abstract: Several crosslinked poly(styrene–butadiene–styrene) (c-SBS) block copolymer films were prepared using a gamma ray or electron beam with various irradiation doses and the prepared c-SBS film was then subjected to sulfonation using a chlorosulfonic acid (CSA) solution to introduce a sulfonic acid group. To estimate the degree of crosslinking, the gel fractions and FT-IR spectra of the c-SBS films were used and the results indicate that the degree of crosslinking is increased with an increase in the radiation dose. The surface morphology and mechanical property of the c-SBS films were observed using SEM and UTM instruments, respectively. The sulfonated c-SBS films were investigated by measuring the ion exchange capacity (IEC) and by observing the cross-sectional distribution patterns of sulfonic acid group using an SEM-EDX instrument. The IEC and SEM-EDX studies indicate that the sulfonated c-SBS membranes can be successfully prepared through the radiation crosslinking of the SBS film and the subsequent sulfonation with a diluted CSA solution.

  1. Diffusion Coefficient of Tin(II) Methanesulfonate in Ionic Liquid and Methane Sulfonic Acid (MSA) Solvent

    Science.gov (United States)

    Yang, Kok Kee; Mahmoudian, M. R.; Ebadi, Mehdi; Koay, Hun Lee; Basirun, Wan Jeffrey

    2011-12-01

    Voltammetry and chronoamperometry for the electrodeposition of tin from Tin(II) methane sulfonate mixed with ionic liquid and methane sulfonate acid at room temperature was studied. Cyclic voltammetry shows redox waves of Tin(II), which proves that the electrodeposition of tin from Tin(II) methane sulfonate is a diffusion-controlled process. The diffusion coefficient of Tin(II) ions in the solvent mixture showed good agreement from both voltammetry and chronoamperometry results. The diffusion coefficient of Tin(II) in the mixture was much smaller than in aqueous solution, and it depends on the anion of the ionic liquid.

  2. Synthesis and characterization of quaternized poly(phthalazinone ether sulfone ketone) for anion-exchange membrane

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    Chloromethylated poly(phthalazinone ether sulfone ketone) (CMPPESK) was prepared from poly(phthalazinone ether sulfone ketone) (PPESK) using chloromethyl octyl ethers (CMOE) with lower toxicity as chloromethylated regent. CMPPESK was soluble in N-methyl-2-pyrrolidone (NMP), N,N-dimethylacetamide (DMAc) and chloroform. Quatemized poly(phthalazinone ether sulfone ketone) (QAPPESK) was prepared from CMPPESK by quaternization. QAPPESK had excellent solvent resistance,which was only partly soluble in sulfuric acid (98%) and swollen in N,N-dimethylformamide (DMF). The vanadium redox flow battery (V-RFB) using QAPPESK anion-exchange membrane had better performance with 88.3% of overall energy efficiency.

  3. Sterically Stabilized Poly(3,4-ethylenedioxythiophene) Colloidal Dispersions Doped with Different Sulfonic Acids

    Institute of Scientific and Technical Information of China (English)

    Tie Jun WANG; Ping CHEN; Xiu Jie HU; Shu Yun ZHOU

    2006-01-01

    The preparation of sterically stabilized poly(3, 4-ethylenedioxythiophene)(PEDOT)colloidal dispersions doped with different sulfonic acids is described. Three different sulfonic acids, i.e., p-toluenesulfonic acid, β-naphthalenesuffonic acid and D-camphor-10-sulfonic acid are used, facilitating the preparation of sterically stable PEDOT colloidal particles. The influences of the dopants and concentration of polymeric stabilizer on the yields, morphologies and electrical properties of the resultant colloidal particles were investigated. The colloidal particles with the size ranging from 172 to 334 nm have been obtained in good yields. The compressed pellet conductivity was as high as 4.5 Scm-1.

  4. Laser photolysis of interaction of poly-guanylic acid (5′) with anthraquinone-2-sulfonate

    Institute of Scientific and Technical Information of China (English)

    马建华; 林维真; 王文峰; 韩镇辉; 姚思德; 林念芸

    2002-01-01

    The electron transfer reaction between triplet anthraquinone-2-sulfonate and poly- guanylic acid (5′) in CH3CN-H2O (97:3) has been investigated by 248 nm (KrF) laser flash photolysis. The transient absorption spectra and kinetics obtained from the interaction of triplet anthraquinone-2-sulfonate and poly[G] demonstrate that the primary ionic radical pair, radical cation of poly[G] and radical anion of anthraquinone-2-sulfonate have been detected simultaneously. The free energy changes in the process of the electron transfer were also calculated.

  5. Laser photolysis of interaction of poly-guanylic acid (5’) with anthraquinone-2-sulfonate

    Institute of Scientific and Technical Information of China (English)

    马建华; 韩镇辉; 林维真; 姚思德; 王文峰; 林念芸

    2002-01-01

    The electron transfer reaction between triplet anthraquinone-2-sulfonate and poly-guanylic acid (5’) in CH3CN-H2O (97 : 3) has been investigated by 248 nm (KrF) laser flash photolysis. The transient absorption spectra and kinetics obtained from the interaction of triplet anthraquinone-2-sulfonate and poly[G] demonstrate that the primary ionic radical pair, radical cation of poly[G] and radical anion of anthraquinone-2-sulfonate have been detected simultaneously. The free energy changes in the process of the electron transfer were also calculated.

  6. Derivatives of phenyl tribromomethyl sulfone as novel compounds with potential pesticidal activity

    Directory of Open Access Journals (Sweden)

    Krzysztof M. Borys

    2012-02-01

    Full Text Available A halogenmethylsulfonyl moiety is incorporated in numerous active herbicides and fungicides. The synthesis of tribromomethyl phenyl sulfone derivatives as novel potential pesticides is reported. The title sulfone was obtained by following three different synthetic routes, starting from 4-chlorothiophenol or 4-halogenphenyl methyl sulfone. Products of its subsequent nitration were subjected to the SNAr reactions with ammonia, amines, hydrazines and phenolates to give 2-nitroaniline, 2-nitrophenylhydrazine and diphenyl ether derivatives. Reduction of the nitro group of 4-tribromomethylsulfonyl-2-nitroaniline yielded the corresponding o-phenylenediamine substrate for preparation of structurally varied benzimidazoles.

  7. Degradation and contamination of perfluorinated sulfonic acid membrane due to swelling-dehydration cycles

    DEFF Research Database (Denmark)

    Andersen, Shuang Ma; Morgen, Per; Skou, Eivind Morten

    Formation of sulfonic anhydride S-O-S (from the condensation of sulfonic acids) was known one of the important degradation mechanisms [i] for Nafion membrane under hydrothermal aging condition, which is especially critical for hydrogen fuel cells. Similar mechanism would also have be desirable...... to the membrane degradation in direct methanol fuel cells (DMFCs), where liquid water has direct contact with the electrolyte. An ex-situ experiment was established with swelling-dehydration cycles on the membrane. However, formation of sulfonic anhydride was not detected during the entire treatment; instead...

  8. Hybrid Metaheuristics

    CERN Document Server

    2013-01-01

    The main goal of this book is to provide a state of the art of hybrid metaheuristics. The book provides a complete background that enables readers to design and implement hybrid metaheuristics to solve complex optimization problems (continuous/discrete, mono-objective/multi-objective, optimization under uncertainty) in a diverse range of application domains. Readers learn to solve large scale problems quickly and efficiently combining metaheuristics with complementary metaheuristics, mathematical programming, constraint programming and machine learning. Numerous real-world examples of problems and solutions demonstrate how hybrid metaheuristics are applied in such fields as networks, logistics and transportation, bio-medical, engineering design, scheduling.

  9. PREPARATION AND PROPERTIES OF SPAES-TiO_2 HYBRID MEMBRANES FOR DIRECT METHANOL FUEL CELL

    Institute of Scientific and Technical Information of China (English)

    Ni Zhang; Hui-ling Liu; Jun-jing Li; Zhi Xia

    2009-01-01

    Sulfonated poly(arylene ether sulfone) (SPAES) copolymer with degree of sulfonation of 1.0 was synthesized and characterized. A series of SPAES-TiO_2 hybrid membranes with various contents of nano-sized TiO_2 particles were prepared and characterized through sol-gel reactions. Scanning electron microscopy (SEM) images indicated the TiO_2 particles were well dispersed within polymer matrix. These composite membranes were evaluated for proton exchange membranes (PEMs) in direct methanol fuel cell (DMFC). These membranes showed good thermal stability and mechanical properties. It was found that the water uptake of these membranes increased with the increase of the TiO_2 contents in the hybrid membranes. Meanwhile, the introduction of inorganic particles increased the proton conductivity and reduced the methanol permeability. The proton conductivities (0.118-0.162 S/cm) of SPAES-TiO_2 hybrid membranes with 8% TiO_2 particles are much higher than those of Nation 117 membrane (0.095-0.117 S/cm) and pure SPAES membrane (0.100-0.124 S/cm) with degree of sulfonation of 1.0 at all temperatures (25-100℃). Especially, the methanol diffusion coefficient (8.4×10~(-7) cm~2/s) of SPAES-TiO_2 hybrid membranes with 8% TiO_2 is much lower than that of Nation 117 membrane (2.1 ×10~(-6) cm~2/s). SPAES-TiO_2 hybrid membranes were therefore proposed as candidates of material for PEM in DMFC.

  10. Hybrid intermediaries

    OpenAIRE

    Cetorelli, Nicola

    2014-01-01

    I introduce the concept of hybrid intermediaries: financial conglomerates that control a multiplicity of entity types active in the "assembly line" process of modern financial intermediation, a system that has become known as shadow banking. The complex bank holding companies of today are the best example of hybrid intermediaries, but I argue that financial firms from the "nonbank" space can just as easily evolve into conglomerates with similar organizational structure, thus acquiring the cap...

  11. Hybrid composites

    CSIR Research Space (South Africa)

    Jacob John, Maya

    2009-04-01

    Full Text Available effect was observed for the elongation at break of the hybrid composites. The impact strength of the hybrid composites increased with the addition of glass fibres. The tensile and impact properties of thermoplastic natural rubber reinforced short... panels made from conventional structural materials. Figure 3 illustrates the performance of cellular biocomposite panels against conventional systems used for building and residential construction, namely a pre- cast pre-stressed hollow core concrete...

  12. Synthesis of sulfonated oxindoles by potassium iodide catalyzed arylsulfonylation of activated alkenes with sulfonylhydrazides in water.

    Science.gov (United States)

    Li, Xiaoqing; Xu, Xiangsheng; Hu, Peizhu; Xiao, Xuqiong; Zhou, Can

    2013-07-19

    A catalytic system consisting of KI, 18-crown-6, and TBHP for arylsulfonylation of activated alkenes with sulfonylhydrazides as sulfonyl precursor is described. This protocol provides a practical and environmentally benign method for the construction of sulfonated oxindoles in water.

  13. Sulfonyl Imidazoles as Reagents for the Preparation of Sulfonates and Sulfonamides

    Institute of Scientific and Technical Information of China (English)

    2008-01-01

    Several new sulfonates and sulfonamides were synthesized with sulfonyl imidazoles as reagents. These compounds were characterized by 1H NMR. The melting points of all solids synthesized were obtained on Fisher-Johns Melting Point Apparatus.

  14. Preparation of a Sulfonated Carbonaceous Material from Lignosulfonate and Its Usefulness as an Esterification Catalyst

    Directory of Open Access Journals (Sweden)

    Duckhee Lee

    2013-07-01

    Full Text Available Sulfonated carbonaceous material useful as a solid acid catalyst was prepared from lignosulfonate, a waste of the paper-making industry sulfite pulping process, and characterized by 13C-NMR, FT-IR, TGA, SEM and elemental analysis, etc. The sulfonic acid group density and total density of all acid groups in the sulfonated carbonaceous material was determined by titration to be 1.24 mmol/g and 5.90 mmol/g, respectively. Its catalytic activity in the esterification of cyclohexanecarboxylic acid with anhydrous ethanol was shown to be comparable to that of the ionic exchange resin Amberlyst-15, when they were used in the same amount. In the meantime, the sulfonic acid group was found to be leached out by 26%–29% after it was exposed to hot water (95 °C for 5 h. The catalytic usefulness of the prepared carbonaceous material was investigated by performing esterifications.

  15. Photoinduced Electron Transfer Reaction between Poly-guanylic Acid (5`) with Anthraquinone-2-sulfonate

    Institute of Scientific and Technical Information of China (English)

    2000-01-01

    The electron transfer reaction between triplet anthraquinone-2-sulfonate with poly-guanylic acid (5) (poly[G]) in acetonitrile-H2O has been investigated by 248 nm laser flash photolysis. The transient absorption spectra of radical cation of poly[G] and radical anion of anthraqunione-2-sulfonate(AQS) arising from electron transfer reaction has been observed simultaneously for the first time. The formation processes of radical cation of poly[G] and radical anion of anthraquinone-2-sulfonate as well as the decay processes of triplet anthraquinone-2-sulfonate have also been observed, the apparent rate constants for the formation and decay of transient species have been determined. The free energy changes in the process of the electron transfer was also calculated.

  16. Synthesis and characterization of novel sulfonated polyimide containing phthalazinone moieties as PEM for PEMFC

    Institute of Scientific and Technical Information of China (English)

    Hai Yan Pan; Yong Fang Liang; Xiu Ling Zhu; Xi Gao Jian

    2007-01-01

    A novel sulfonated diamine monomer, 1,2-dihydro-2-(3-sulfonic-4-aminophenyl)-4-[4-(4-aminophenoxy)-phenyl]phthalazin1-one (S-DHPZDA), was successfully synthesized by direct sulfonation of diamine 1,2-dihydro-2-(4-aminophenyl)-4-[4-(4-aminophenoxy)-phenyl]-phthalazin- 1-one (DHPZDA). A series of sulfonated polyimides (SPIs), which can be used as the material of the proton exchange membrane (PEM) for the proton exchange membrane fuel cell (PEMFC), were prepared from 1,4,5,8-naphthalenetetracarboxylic dianhydride (NTDA), S-DHPZDA, and nonsulfonated diamines DHPZDA. The structure of the monomer and polymers were characterized by FT-IR and 1H NMR. The solubility of the S-DHPZDA-based SPIs has been improved due to the induction of the phthalazione moiety. The SPIs membranes have high thermo-stability, predominant swelling resistance with high ion exchange capacity.

  17. Nonaqueous preparation of stable silver nano particles dispersions from organic sulfonic acids.

    Directory of Open Access Journals (Sweden)

    Valentina Glushko

    2016-05-01

    Full Text Available The conditions for stable silver nano particles dispersions synthesis from organic sulfonic acids in an anhydrous medium of ethylene glycol and its methyl ester were studied. Ascorbic acid and potassium citrate were used as reducing agents.

  18. Utilization of common ditch vegetation in the reduction of fipronil and its sulfone metabolite

    Science.gov (United States)

    Fipronil, a phenylpyrazole insecticide and its oxidative sulfone metabolite are two potential nonpoint source pollutants from treated rice and cotton production. A consequence of these pollutants occurring in surface runoff is degradation of downstream aquatic ecosystems. Utilization of primary inte...

  19. Derivatization of enolic OH of piroxicam: a comparative study on esters and sulfonates

    Energy Technology Data Exchange (ETDEWEB)

    Jayaselli, J.; Cheemala, J. Manila Sagar; Geetha Rani, D.P.; Pal, Sarbani [MNR Post Graduate College, Kukatpally, Hyderabad (India). Dept. of Chemistry]. E-mail: sarbani277@yahoo.com

    2008-07-01

    A number of ester and sulfonate derivatives of piroxicam were prepared via acylation/sulfonation of the enolic OH of piroxicam. All the compounds were evaluated for their chemical stability and cyclooxygenase inhibiting properties. Data suggested that esters could be useful for the development of potential prodrugs. The sulfonate derivatives prepared for the first time were found to be stable. One of them showed a moderately selective COX-2 inhibition over COX-1 and would have lower gastrointestinal side effects than piroxicam due to the masked enolic OH group. A plausible mechanism for the acylation/sulfonation process has been proposed that involves participation of the pyridine moiety of piroxicam. Molecular structure of one of the ester was established for the first time by the crystal structure analysis from X-ray powder data. (author)

  20. Nanoscale Organic−Inorganic Hybrid Lubricants

    KAUST Repository

    Kim, Daniel

    2011-03-15

    Silica (SiO2) nanoparticles densely grafted with amphiphilic organic chains are used to create a family of organic-inorganic hybrid lubricants. Short sulfonate-functionalized alkylaryl chains covalently tethered to the particles form a dense corona brush that stabilizes them against aggregation. When these hybrid particles are dispersed in poly-α-olefin (PAO) oligomers, they form homogeneous nanocomposite fluids at both low and high particle loadings. By varying the volume fraction of the SiO2 nanostructures in the PAO nanocomposites, we show that exceptionally stable hybrid lubricants can be created and that their mechanical properties can be tuned to span the spectrum from simple liquids to complex gels. We further show that these hybrid lubricants simultaneously exhibit lower interfacial friction coefficients, enhanced wear and mechanical properties, and superior thermal stability in comparison with either PAO or its nanocomposites created at low nanoparticle loadings. Profilometry and energy dispersive X-ray spectroscopic analysis of the wear track show that the enhanced wear characteristics in PAO-SiO2 composite lubricants originate from two sources: localization of the SiO2 particles into the wear track and extension of the elastohydrodynamic lubrication regime to Sommerfeld numbers more than an order of magnitude larger than for PAO. © 2011 American Chemical Society.

  1. Asymmetrical Self-assembly From Fluorinated and Sulfonated Block Copolymers in Aqueous Media

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Xiaojun [ORNL; Hong, Kunlun [ORNL; Baskaran, Durairaj [University of Tennessee, Knoxville (UTK); Goswami, Monojoy [ORNL; Sumpter, Bobby G [ORNL; Mays, Jimmy [ORNL

    2011-01-01

    Block copolymers of fluorinated isoprene and partially sulfonated styrene form novel tapered rods and ribbon-like micelles in aqueous media due to a distribution of sulfonation sites and a large Flory-Huggins interaction parameter. A combination of microscopy, light scattering, and simulation demonstrates the presence of these unique nanostructures. This study sheds light on the micellization behavior of amphiphilic block polymers by revealing a new mechanism of self-assembly.

  2. Unusual Cycloadducts from the Dipolar Cycloaddition of Allenyl Perfluoroalkyl Sulfones to Nitrones

    Institute of Scientific and Technical Information of China (English)

    WANG,Xiao-Jin; LIU,Jin-Tao

    2007-01-01

    The dipolar cycloaddition reaction of allenyl perfluoroalkyl sulfones (1) to nitrones (2) was described. Unlike nonfluorine-containing allenyl sulfones, 1 reacted readily with 2 in ether at room temperature and unusual zwitterionic cycloadducts (3) were obtained in good yields due to the strong electron-withdrawing effect of perfluoroalkyl groups. The structure of 3 was characterized by spectral analyses and X-ray crystallography.

  3. Colonic necrosis and perforation due to calcium polystyrene sulfonate in a uraemic patient: a case report

    OpenAIRE

    Akagun, Tulin; Yazici, Halil; Gulluoglu, Mine G.; Yegen, Gulcin; Turkmen, Aydin

    2011-01-01

    Sodium or calcium polystyrene sulfonate (Kayexalate or analog) is an ion-exchange resin commonly used to treat hyperkalaemia in patients with chronic kidney disease. It is known to cause digestive complications, such as nausea, vomiting and constipation. Although rare, colonic necrosis and perforation are very severe complications associated with the medication. In this case report, we present a case of calcium polystyrene sulfonate-induced colonic necrosis and perforation to remind clinician...

  4. Efficiency of conventional activated sludge in the removal of linear alkylbenzene sulfonate from municipal sewage

    OpenAIRE

    2014-01-01

    Background: Linear Alkylbenzene Sulfonate (LAS) is an anionic detergent that is abundantly produced in different countries and discharged into natural environment through wastewater collection systems. Wastewater treatment systems play an important role in the removal of this contaminant. The purpose of this study was to determine the efficiency of a conventional activated sludge system in removing linear alkylbenzene sulfonate from wastewater in Kermanshah. Methods: This cross-sectional d...

  5. Activated-sludge nitrification in the presence of linear and branched-chain alkyl benzene sulfonates.

    Science.gov (United States)

    Baillod, C R; Boyle, W C

    1968-01-01

    The effects of biodegradable linear alkyl benzene sulfonate and branched-chain alkyl benzene sulfonate detergents on activated-sludge nitrification were investigated by administering a synthetic waste containing up to 23 mg of each detergent per liter to eight bench-scale, batch, activated-sludge units. It was found that both detergents tended to promote complete oxidation of ammonia to nitrate, whereas control units produced approximately equal amounts of nitrite and nitrate. Various hypotheses are offered to explain the phenomenon.

  6. Synthesis, structure, theoretical calculations and biological activity of sulfonate active ester new derivatives

    Science.gov (United States)

    Ghazzali, Mohamed; Khattab, Sherine A. N.; Elnakady, Yasser A.; Al-Mekhlafi, Fahd A.; Al-Farhan, Khalid; El-Faham, Ayman

    2013-08-01

    A series of naphthyl and tolyl sulfonate ester were synthesized and characterized by H NMR. X-ray single crystal diffraction experiments established the molecular structure of three new sulfonate esters derivatives, and spectral data agree with these in solution. The observed hydrogen bonding is discussed on the basis of crystal structural analyses and DFT/MP2 geometry optimization quantum calculations. Antimicrobial activities were screened for selected compounds against three human cancer cell lines and Mosquito Culex pipiens larvae.

  7. Composite proton exchange membrane based on sulfonated organic nanoparticles

    Science.gov (United States)

    Pitia, Emmanuel Sokiri

    As the world sets its sight into the future, energy remains a great challenge. Proton exchange membrane (PEM) fuel cell is part of the solution to the energy challenge because of its high efficiency and diverse application. The purpose of the PEM is to provide a path for proton transport and to prevent direct mixing of hydrogen and oxygen at the anode and the cathode, respectively. Hence, PEMs must have good proton conductivity, excellent chemical stability, and mechanical durability. The current state-of-the-art PEM is a perfluorosulfonate ionomer, Nafion®. Although Nafion® has many desirable properties, it has high methanol crossover and it is expensive. The objective of this research was to develop a cost effective two-phase, composite PEM wherein a dispersed conductive organic phase preferentially aligned in the transport direction controls proton transport, and a continuous hydrophobic phase provides mechanical durability to the PEM. The hypothesis that was driving this research was that one might expect better dispersion, higher surface to volume ratio and improved proton conductivity of a composite membrane if the dispersed particles were nanometer in size and had high ion exchange capacity (IEC, = [mmol sulfonic acid]/gram of polymer). In view of this, considerable efforts were employed in the synthesis of high IEC organic nanoparticles and fabrication of a composite membrane with controlled microstructure. High IEC, ~ 4.5 meq/g (in acid form, theoretical limit is 5.4 meq/g) nanoparticles were achieved by emulsion copolymerization of a quaternary alkyl ammonium (QAA) neutralized-sulfonated styrene (QAA-SS), styrene, and divinylbenzene (DVB). The effects of varying the counterion of the sulfonated styrene (SS) monomer (alkali metal and QAA cations), SS concentration, and the addition of a crosslinking agent (DVB) on the ability to stabilize the nanoparticles to higher IECs were assessed. The nanoparticles were ion exchanged to acid form. The extent of ion

  8. Viscoelastic Behavior of Low Molecular Weight Sulfonated Polystyrene Ionomers

    Science.gov (United States)

    Zhao, Hongying

    Ionomers are those hydrophobic polymers having small amounts of bonded ionic groups. The introduction of the ionic groups into polymer chain produces large changes in the physical, mechanical and rheological properties of the parent polymer. Characterization of the effect of the ionic interactions on the rheology is complicated by the difficulty in separating effects due to molecular entanglements and the ionic interactions. In this study, low molecular weight (Mw=4000) sulfonated polystyrene (SPS) was used to study the dynamic and steady shear rheology of SPS ionomers. The polymer chain length used was far below the entanglement molecular weight of polystyrene and effects of molecular entanglements will be absent. Any polymer chain entanglements or lengthening behavior on the melt rheology should be due to the ionic interactions. Random SPS ionomers with two sulfonation levels were examined, 2.5 and 4.8 mol%, which corresponded, respectively, to one and two sulfonate groups per chain on average. The metal counterions was varied across the alkali metal series of the periodic table. Morphology of the ionomer was characterized by using small angle x-ray scattering (SAXS) analysis, and dynamic and steady shear measurements were performed to investigate rheological behavior of the ionomers. Glass transition temperatures of the ionomers increased with increasing ion concentration but were insensitive to cation used. The scattering peak in SAXS indicates the existence of the nanophase separated ionic clusters. The strong ionic nanophase persist up to very high temperatures and is not sensitive to the external stress. Time-temperature superposition (TTS) of G' worked reasonably well while TTS of G" failed for most ionomers. Ionic interactions increased the terminal relaxation time of the melts as much as seven orders of magnitude greater than the unentangled PS melt. The zero shear viscosity and first normal stress coefficients scaled with cq/a, where c was the

  9. Accuracy of implant transfer and surface detail reproduction with polyether and polyvinyl siloxane using closed-tray impression technique

    Directory of Open Access Journals (Sweden)

    Marzieh Alikhasi

    2013-10-01

    Full Text Available   Background and Aims: Making accurate impressions of prepared teeth when they are adjacent to dental implants is of great importance. In these situations, disregarding the selection of appropriate impression material and technique, not only can affect accuracy of transferring of the 3-dimentional spatial status of implant, but also can jeopardize the accurate recording of tooth. In the present study, the accuracy of two impression materials with taper impression copings for recording implant position and surface details was evaluated.   Materials and Methods: One metal reference model with 2 implants (Implantium and a preparation of three grooves on a tooth according to ADA no. 19 standard was fabricated. 10 medium- consistency polyEther (PE impressions using custom trays and 10 polyVinyl Siloxane (PVS putty wash impressions using prefabricated trays with conical impression coping were made. Impressions were poured with ADA type IV stone. A Coordinate Measuring Machine (CMM evaluated x, y and angular displacement of the implant analog heads and also accuracy of groove reproduction were measured using a Video Measuring Machine (VMM. These measurements were compared to the ones from reference model. Data were analyzed using one-way ANOVA and T-test.   Results: Putty wash PVS had less linear discrepancy compared with reference model (P > 0.001. There was no significant difference in the surface detail reproduction (P = 0.15.   Conclusion: Putty wash PVS had better results for linear displacement compared with medium consistency PE. There was no significant difference in surface detail reproduction between the two impression materials.

  10. Synthesis and properties of aromatic polyethers containing poly(ethylene oxide) side chains as polymer electrolytes for lithium ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Vöge, Andrea, E-mail: andreavoege@online.de [Department of Chemistry, University of Patras, 26500 Patras (Greece); Deimede, Valadoula, E-mail: deimede@upatras.gr [Department of Chemistry, University of Patras, 26500 Patras (Greece); Paloukis, Fotis; Neophytides, Stylianos G. [Foundation of Research and Technology – Hellas, Institute of Chemical Engineering Sciences (FORTH/ICE-HT), Patras 26504 (Greece); Kallitsis, Joannis K. [Department of Chemistry, University of Patras, 26500 Patras (Greece)

    2014-11-14

    Polymer electrolytes consisting of polar pyridine units in the backbone and poly(ethylene oxide) (PEO) side chains are designed for possible application in lithium ion batteries. In particular, aromatic polyethers bearing PEO side chains with varying length are synthesized either by copolymerization of the corresponding PEO based diols with different arylfluorides or by modification of dihydroxyl functionalized precursor polymers with poly(ethylene oxide) methyl ether tosylate. The formation of free standing films is dependent on the PEO content, polymers' composition as well as on the different monomers used. The mechanical properties study shows that the glass transition temperature can be controlled by varying the PEO content. Thermal stability is also influenced by the PEO length: the shorter the PEO side chain, the higher the stability. XRD analysis gives information about the desired amorphous character of these polymers, which is independent of the PEO content. Solid polymer electrolytes prepared by blending the PEO-based polymers with lithium salt and PEO 2000 (used as plasticizer) show ambient temperature conductivities in the range of 10{sup −6} S/cm. To further improve conductivity doping of PEO-based polymers in liquid electrolyte (1 M LiPF{sub 6} in EC/DMC 1/1) in some cases results in high conductivities in the range of 10{sup −3} S cm{sup −1} at 80 °C. - Highlights: • Polymer electrolytes bearing PEO side chains of varying lengths were designed. • DMA and TGA show that T{sub g} and T{sub d} can be controlled by varying the PEO content. • XRD confirms polymers amorphous character, independent of the PEO content. • Membranes doped in liquid electrolyte have high conductivities (10{sup −3} S cm{sup −1}, 80 °C)

  11. Single-step synthesis of sulfonated polyoxadiazoles and their use as proton conducting membranes

    Science.gov (United States)

    Gomes, Dominique; Roeder, Jerusa; Ponce, Mariela L.; Nunes, Suzana P.

    A single-step approach for the synthesis of sulfonated polyoxadiazoles from hydrazine sulfate was developed using non-sulfonated diacids in polyphosphoric acid. The post-sulfonation conditions were optimized by varying reaction time, medium and reagent concentrations in sulfuric acid, oleum and/or their mixtures. For the first time, a series of sulfonated polyoxadiazoles with ion exchange capacity (IEC) ranging from 1.26 to 2.7 meqiv. g -1 and high molecular weight (about 40,0000 g mol -1) were synthesized. The structures of the polymers were characterized by elemental analysis, 1H NMR, and FTIR. Sulfonated polyoxadiazole membranes with high thermal stability indicated by observed glass-transition temperatures (T g) ranging from 364 to 442 °C in sodium salt form and from 304 to 333 °C in acid form and with high mechanical properties (storage modulus about 3 GPa at 300 °C) have been prepared. The membrane stability to oxidation was investigated by soaking the film in Fenton's reagent at 80 °C for 1 h. The sulfonated polyoxadiazole membranes exhibited high oxidative stability, retaining 98-100% of their weight after the test. Proton conductivity values with the order of magnitude of 10 -1 to 10 -2 S cm -1 at 80 °C and with relative humidity ranging from 100% to 20% were obtained.

  12. Morphogenetic control of calcite crystal growth in sulfonic acid based hydrogels.

    Science.gov (United States)

    Grassmann, Olaf; Löbmann, Peer

    2003-03-17

    In this paper the mineralization of CaCO(3) in various hydrogel matrices is presented. Sulfonic acid based hydrogels were prepared by introduction of sulfonate-containing monomers into a polyacrylamide network. The sulfonate content of polyacrylamide-co-vinylsulfonate and polyacrylamide-co-allylsulfonate decreases during elution of the copolymers in demineralized water, indicating insufficient linking of the sulfonate-bearing monomers within the hydrogel. In contrast to this, acrylamidomethylpropanesulfonate (AMPS) effectively copolymerizes with acrylamide (AAm) monomers. To study the influence of spatial arrangement of ionic functional groups within hydrogel networks on the mineralization of CaCO(3), AMPS copolymers with different degrees of AMPS cross-linking were synthesized. For the mineralization experiments the copolymers were placed into a double-diffusion arrangement. Calcite as the thermodynamically stable modification of CaCO(3) was obtained with a particular morphology. The pseudocubic habitus resembles aggregates obtained by mineralization in pure polyacrylamide. However, closer examination of the aggregates by scanning electron microscopy (SEM) shows that the crystal growth in the AMPS copolymers is different from that observed in polyacrylamide. Whereas the morphology of the calcite aggregates could be fine-tuned by using copolymers with different sulfonate content, the spatial distribution of the ionic functional groups alters the course of crystallization. Calcium ions are locally accumulated due to the heterogeneous distribution of functional sulfonate groups within the copolymer network. Thereby the nucleation of calcite is triggered, resulting in enhanced mineralization.

  13. Radiation-induced crosslinking of poly(styrene-butadiene-styrene) block copolymers and their sulfonation

    Science.gov (United States)

    Lee, Sun-Young; Song, Ju-Myung; Sohn, Joon-Yong; Shul, Yong-Gun; Shin, Junhwa

    2013-12-01

    Several crosslinked poly(styrene-butadiene-styrene) (c-SBS) block copolymer films were prepared using a gamma ray or electron beam with various irradiation doses and the prepared c-SBS film was then subjected to sulfonation using a chlorosulfonic acid (CSA) solution to introduce a sulfonic acid group. To estimate the degree of crosslinking, the gel fractions and FT-IR spectra of the c-SBS films were used and the results indicate that the degree of crosslinking is increased with an increase in the radiation dose. The surface morphology and mechanical property of the c-SBS films were observed using SEM and UTM instruments, respectively. The sulfonated c-SBS films were investigated by measuring the ion exchange capacity (IEC) and by observing the cross-sectional distribution patterns of sulfonic acid group using an SEM-EDX instrument. The IEC and SEM-EDX studies indicate that the sulfonated c-SBS membranes can be successfully prepared through the radiation crosslinking of the SBS film and the subsequent sulfonation with a diluted CSA solution.

  14. Semiquantitative evaluation of fibronectin adsorption on unmodified and sulfonated polystyrene, as related to cell adhesion.

    Science.gov (United States)

    Kowalczyńska, Hanna M; Nowak-Wyrzykowska, Małgorzata; Kołos, Robert; Dobkowski, Jacek; Kamiński, Jarosław

    2008-12-15

    The process of human fibronectin (FN) adsorption on nonsulfonated and sulfonated polystyrene surfaces was studied in relation to mechanisms of L1210 cell adhesion. Radioisotope assays directed towards FN, as well as ELISA measurements of adsorbed FN and bovine serum albumin (BSA) were carried out. (125)I radioisotope assays led to linear FN adsorption isotherms. When combined to ELISA measurements for FN, they revealed the multilayer adsorption. Results indicated a large difference in the saturating first-layer surface density of FN adsorbed on sulfonated and nonsulfonated polystyrene surfaces: significantly (ca. factor of 5) less FN molecules are necessary to complete a monolayer on sulfonated than on nonsulfonated polystyrene. This suggests an unfolded conformation of FN on sulfonated polystyrene, and a more compact one on the nonsulfonated polymer. Significant conformational changes of FN are also indicated by the following: (1) early phase of cell adhesion to FN adsorbed on sulfonated polystyrene surfaces is significantly (ca. factor of 6) higher than to FN on nonsulfonated surfaces, and in the former case adhesion proceeds mostly via alpha(5)beta(1) integrins; (2) RGD, the crucial fragment within central cell binding domain, seems to be partially hidden in the protein structure adopted on nonsulfonated surfaces; (3) patterns of F-actin organization differ in cells adhering to FN on sulfonated and nonsulfonated surfaces. The ELISA study directed against BSA (this protein always present on the surface after the adsorption of FN), showed the importance of "free area," uncovered by both proteins, which influence the cell adhesion processes.

  15. 油溶性聚醚的制备及其抗氧化性能考察%PREARATION AND ANTIOXIDANT CHARACTERISTICS OF OIL-SOLUCLE POLYETHER

    Institute of Scientific and Technical Information of China (English)

    程亮; 李洪伟; 孔令杰; 张东恒

    2014-01-01

    以氢氧化钾作为催化剂,环氧丙烷与环氧丁烷共聚制备了分别符合黏度级别 OSP-18,OSP-46, OSP-150要求的油溶性聚醚,并通过红外光谱(IR)、核磁共振(NMR)和凝胶渗透色谱(GPC)对其进行表征。利用旋转氧弹测试方法考察了油溶性聚醚的抗氧化性能,结果表明油溶性聚醚本身的抗氧化性能较差。通过考察不同抗氧剂与油溶性聚醚的互配性,开发了α-苯胺与氨基甲酸酯组成的复合抗氧剂,该复合抗氧剂与油溶性聚醚有较好的互配性,可使油溶性聚醚的旋转氧弹时间达到1200 min,复合抗氧剂可使油溶性聚醚在不同配方体系中得到应用。%Oil-soluble polyether (OSP)was prepared by the copolymerization of propylene oxide and butylene oxide using KOH as a catalyst.The viscosity grades of the prepared oil-soluble polyether are OSP-18,OSP-46,OSP-150,respectively.The structures of the products were defined by means of infra-red spectroscopy (IR),nuclear magnetic resonance (NMR)and gel permeation chromatography (GPC). The anti-oxidation performance of OSPs were investigated by rotary oxygen bomb test method (ROBT).The results indicate that the oil-soluble polyether is poor in anti-oxidation with short induc-tion period.However,the performance of the oil-soluble polyether is greatly improved by addition of the composite antioxidant,composed of α-aniline (AOA-4 )and carbamate (AOL-1 ). The ROBT can reach to 1 200 minutes.The performance of this composite antioxidant makes OSP the best application in different formulations.

  16. SYNTHESES OF RESINS IMPREGNATED WITH POLYETHER OR POLYTHIOETHER OLIGOMERS AND THEIR EXTRACTION FOR GOLD(Ⅲ) and palladium(Ⅱ)

    Institute of Scientific and Technical Information of China (English)

    DONGShihua; LIUShi; 等

    1992-01-01

    Six novel resins impregnated with polyether or polythioether oligomers have been synthesized and their extraction properties have also been investigated.Gold(Ⅲ) and /or palladium (Ⅱ) coulld be extracted repidly by the resins with high percentage and capacities from aqueous solution but most of the co-existing base metal ions were remained.The extraction capacities and stripping percentage were approximately unchanged after four extraction-elution cycles and the resins also showed excellent column extraction-elution properties.

  17. Amitriptyline, clomipramine, and doxepin adsorption onto sodium polystyrene sulfonate

    Science.gov (United States)

    2014-01-01

    Purpose of the study Comparative in vitro studies were carried out to determine the adsorption characteristics of 3 drugs on activated charcoal (AC) and sodium polystyrene sulfonate (SPS). Activated charcoal (AC) has been long used as gastric decontamination agent for tricyclic antidepressants (TCA). Methods Solutions containing drugs (amitriptyline, clomipramine, or doxepin) and variable amount of AC or SPS were incubated for 30 minutes. Results At pH 1.2 the adsorbent: drug mass ratio varied from 2 : 1 to 40 : 1 for AC, and from 0.4 : 1 to 8 : 1 for SPS. UV–VIS spectrophotometer was used for the determination of free drug concentrations. The qmax of amitriptyline was 0.055 mg/mg AC and 0.574 mg/mg SPS, qmax of clomipramine was 0.053 mg/mg AC and 0.572 mg/mg SPS, and qmax of doxepin was 0.045 mg/mg AC and 0.556 mg/mg SPS. The results of adsorption experiments with SPS revealed higher values for the qmax parameters in comparison with AC. Conclusion In vitro gastric decontamination experiments for antidepressant amitriptyline, clomipramine, and doxepin showed that SPS has higher qmax values than the corresponding experiments with AC. Therefore, we suggest SPS is a better gastric decontaminating agent for the management of acute TCA intoxication. PMID:24450391

  18. Chronic perfluorooctane sulfonate (PFOS) exposure induces hepatic steatosis in zebrafish

    Energy Technology Data Exchange (ETDEWEB)

    Cheng, Jiangfei; Lv, Suping; Nie, Shangfei; Liu, Jing; Tong, Shoufang; Kang, Ning; Xiao, Yanyan; Dong, Qiaoxiang [Zhejiang Provincial Key Laboratory for Technology and Application of Model Organisms (China); Institute of Environmental Safety and Human Health, Wenzhou Medical University, Wenzhou, 325035 (China); Huang, Changjiang, E-mail: cjhuang5711@163.com [Zhejiang Provincial Key Laboratory for Technology and Application of Model Organisms (China); Institute of Environmental Safety and Human Health, Wenzhou Medical University, Wenzhou, 325035 (China); Yang, Dongren, E-mail: yangdongren@yahoo.com [Zhejiang Provincial Key Laboratory for Technology and Application of Model Organisms (China); Institute of Environmental Safety and Human Health, Wenzhou Medical University, Wenzhou, 325035 (China)

    2016-07-15

    Highlights: • PFOS chronic exposure induces sex-dependent hepatic steotosis in zebrafish. • PFOS interferes with β-oxidation, lipid synthesis, and lipid hepatic export process. • Zebrafish could be used as an alternative model for PFOS chronic toxicity screening. - Abstract: Perfluorooctane sulfonate (PFOS), one persistent organic pollutant, has been widely detected in the environment, wildlife and human. Currently few studies have documented the effects of chronic PFOS exposure on lipid metabolism, especially in aquatic organisms. The underlying mechanisms of hepatotoxicity induced by chronic PFOS exposure are still largely unknown. The present study defined the effects of chronic exposure to low level of PFOS on lipid metabolism using zebrafish as a model system. Our findings revealed a severe hepatic steatosis in the liver of males treated with 0.5 μM PFOS as evidenced by hepatosomatic index, histological assessment and liver lipid profiles. Quantitative PCR assay further indicated that PFOS significantly increase the transcriptional expression of nuclear receptors (nr1h3, rara, rxrgb, nr1l2) and the genes associated with fatty acid oxidation (acox1, acadm, cpt1a). In addition, chronic PFOS exposure significantly decreased liver ATP content and serum level of VLDL/LDL lipoprotein in males. Taken together, these findings suggest that chronic PFOS exposure induces hepatic steatosis in zebrafish via disturbing lipid biosynthesis, fatty acid β-oxidation and excretion of VLDL/LDL lipoprotein, and also demonstrate the validity of using zebrafish as an alternative model for PFOS chronic toxicity screening.

  19. Differential toxicity between perfluorooctane sulfonate (PFOS) and perfluorooctanoic acid (PFOA).

    Science.gov (United States)

    Tsuda, Shuji

    2016-01-01

    Perfluoroalkyl substances (PFASs) are persistent environmental contaminants. Perfluorooctane sulfonate (PFOS) and Perfluorooctanoic acid (PFOA) are representatives of PFASs. Recently, the U.S. Environmental Protection Agency (US EPA) set the health advisory level as 70 parts per trillion for lifetime exposure to PFOS and PFOA from drinking water, based on the EPA's 2016 Health Effects Support Documents. Then, a monograph on PFOA was made available online by the International Agency for Research on Cancer, where the agency classified PFOA as "possibly carcinogenic to humans" (Group 2B). The distinction between PFOS and PFOA, however, may not be easily understood from the above documents. This paper discussed differential toxicity between PFOS and PFOA focusing on neurotoxicity, developmental toxicity and carcinogenicity, mainly based on these documents. The conclusions are as follows: Further mechanistic studies may be necessary for ultrasonic-induced PFOS-specific neurotoxicity. To support the hypothesis for PFOS-specific neonatal death that PFOS interacts directly with components of natural lung surfactant, in vivo studies to relate the physicochemical effects to lung collapse may be required. PFOA-induced DNA damage secondary to oxidative stress may develop to mutagenicity under the condition where PFOA-induced apoptosis is not sufficient to remove the damaged cells. A study to find whether PFOA induces apoptosis in normal human cells may contribute to assessment of human carcinogenicity. Studies for new targets such as hepatocyte nuclear factor 4α (HNF4α) may help clarify the underlying mechanism for PFOA-induced carcinogenicity.

  20. Toxicity of perfluorononanoic acid and perfluorooctane sulfonate to Daphnia magna

    Institute of Scientific and Technical Information of China (English)

    Guang-hua Lu; Jian-chao Liu; Li-sha Sun; Lu-jin Yuan

    2015-01-01

    In order to study toxicological effects of perfluorononanoic acid (PFNA), perfluorooctane sulfonate (PFOS), and their mixtures (PFNA/PFOS) on Daphnia magna (D. magna), a suite of comprehensive toxicity tests were conducted, including a 48-h acute toxicity test, a 21-day chronic test, a feeding experiment, and a biomarker assay. D. magna were exposed to aqueous solutions of PFNA and PFOS (alone and in combination) at concentrations ranging from 0.008 to 5 mg/L. The survival, growth, and reproduction of D. magna were monitored over a 21-day life cycle. The biomarkers, including acetylcholinesterase (AChE), superoxide dismutase (SOD), and catalase (CAT) activities, were determined after seven days of exposure. PFOS was more toxic than PFNA based on the results of the acute toxicity test. Perfluorinated compounds (PFCs) inhibited both growth and reproduction of D. magna during the testing period. The ingestion rates and the biomarkers, including AChE, SOD, and CAT activities, were significantly inhibited by PFCs in most cases. Moreover, the combined effects related to the growth and reproduction showed the antagonistic effects of PFCs.

  1. Phase behaviour of tertiary recovery sulfonates - petroleum fractions - aqueous systems

    Energy Technology Data Exchange (ETDEWEB)

    Ghoniem, S.A.; Darwish, T.A.; Salamah, A.O.

    1988-02-01

    The phase behaviour of tertiary recovery sulfonates having commercial names TRS-10, TRS-16 and TRS-40 with aqueous phase and light petroleum fractions (non polar kerosene and gasoline) was studied at 20, 40 and 60/sup 0/C. The adopted pseudo components of the ternary diagram are hydrocarbon, surfactant and aqueous phase. The aqueous phase was composed of bidistilled water in addition to different proportions of pure alcohols and sodium chloride. The tested alcohols included methanol, ethanol, iso-propanol, n-butanol and n-pentanol. Thus, the best alcohol type and concentration in addition to optimum salinity, which correspond to maximum single phase region, were established for each surfactant at the various tested temperatures. It was shown that higher the affinity of the tested surfactant for hydrocarbon phase, the greater is the solubility of the corresponding optimum co-surfactant in water. The variation of optimum alcohol concentration with temperature, the effect of salt on the single phase region and the effect of hydrocarbon phase on the observed phenomena were discussed and found to agree with the previously established theories.

  2. Sorption and desorption of dyes by sulfonated coal

    Energy Technology Data Exchange (ETDEWEB)

    Mittal, A.K. (Motilal Nehru Regional Coll. of Engineering, Allahabad (India)); Venkobachar, C. (Indian Inst. of Tech., Kanpur (India))

    Wastewaters from dye-manufacturing factories and textile, paper, and pulp industries are highly colored. Their discharge into river waters make the water inhibitory to aquatic life, aside from causing, visible pollution. Dyes have a tendency to sequester metals, thus causing microtoxicity to fish and other aquatic organisms. A wide variety of low-cost materials such as flyash, clay minerals, coal, tire chippings, coconut shell powder and biosorbents are being tried as viable substitutes for activated carbon to remove different pollutants such as pesticides, heavy metals, and dyes. The removal of dyes depends upon their physical and chemical characteristics, as well as the properties of the selected sorbents. To understand the nature of the chemical bonding between dyes and sorbents during the sorption process, it is essential to conduct desorption studies. The reversibility of adsorption of dyes can also be determined by a simple mathematical equation. These studies provide information on whether or not the sorbent material can be regenerated after exhaustion. The present study focuses on sorption-desorption of dyes by sulfonated coal, whose dye sorption potential was established by Mittal and Venkobachar (1990).

  3. Perfluorooctane sulfonate (PFOS) and perfluorooctanoic acid (PFOA) contamination from textiles.

    Science.gov (United States)

    Supreeyasunthorn, Phenpimuk; Boontanon, Suwanna K; Boontanon, Narin

    2016-01-01

    The goals of this study were to determine the concentrations of perfluorooctane sulfonate (PFOS) and perfluorooctanoic acid (PFOA) in textiles and to determine PFOS and PFOA contamination in textile washing water. Quantification analysis was performed by high performance liquid chromatography coupled with tandem mass spectrometry. Analysis of 32 textile samples by methanol extraction revealed that the average concentrations of PFOS and PFOA were 0.18 µg m(-2) (0.02 to 0.61 µg m(-2)) and 2.74 µg m(-2) (0.31 to 14.14 µg m(-2)), respectively. Although the average concentration of PFOS found in textile samples was below European Union (EU) Commission regulations (textile samples had PFOA concentrations exceeding 1 µg m(-2). Thus, based on these results, the concentration of PFOA in products should also be regulated. Experiments on PFOS and PFOA leaching into washing water were conducted. The maximum concentrations of PFOS and PFOA were measured after the first washing; the concentrations gradually decreased with each subsequent washing. PFOS and PFOA migrated from textiles and were released into the environment, with disappearance percentages of 29.8% for PFOS and 99% for PFOA. The data presented in this study showed that textiles could be a significant direct and indirect source of PFOS and PFOA exposure for both humans and the environment.

  4. Perfluorooctane sulfonate (PFOS) induced embryotoxicity and disruption of cardiogenesis.

    Science.gov (United States)

    Cheng, Wei; Yu, Zhuo; Feng, Lixin; Wang, Yan

    2013-08-01

    Prenatal exposure to perfluorooctane sulfonate (PFOS) is correlated with birth defects and adverse health effects. However, the mechanisms remain largely unknown. In current study, the embryonic stem cell test (EST) was performed to evaluate the embryotoxicity of PFOS, and embryonic stem cells (ESCs)-derived cardiomyocytes were used as a model of the early stages of heart development to determine the developmental toxicity of PFOS. One validated endpoint and three molecular endpoints were observed to ensure accurate evaluation of toxicity. According to the criteria of the EST, PFOS was classified as weak embryotoxic. In addition, a cascade of genes related to normal cardiac development was examined at three different time points to monitor cardiogenesis. We found that PFOS significantly interfered with gene expression during cardiogenesis, especially on Nkx2.5 and Myl4. Further, PFOS reduced ATP production in ESCs-derived cardiomyocytes, together with PFOS induced apoptosis, could explain the reduction in beating ability. PFOS-induced reactive oxygen species (ROS) accumulated within cells, which was accompanied by an interfering expression of apoptosis-related genes, ultimately leading to apoptosis. In conclusion, PFOS altered the expression of crucial genes, reduced ATP production, induced ROS, and stimulated apoptosis during the early stages of cardiogenesis; these effects may result in poor developmental outcomes.

  5. Kinetics of low frequency sonodegradation of linear alkylbenzene sulfonate solutions.

    Science.gov (United States)

    Abu-Hassan, Mohd A; Kim, Jung K; Metcalfe, Ian S; Mantzavinos, Dionissios

    2006-02-01

    The decomposition of sodium dodecylbenzene sulfonate (SDBS) in water by means of ultrasound irradiation at 20kHz was investigated. Experiments were conducted at surfactant concentrations of 175, 260 and 350 mg l(-1), liquid volumes of 120, 170 and 220 ml, temperatures of 20, 30 and 45 degrees C and applied power of 40, 80 and 125 W. The extent of degradation was followed monitoring substrate and organic carbon concentrations, while hydrogen peroxide concentration was also measured; the latter is a product of water sonolysis due to hydroxyl radical recombination. 80% SDBS conversion was achieved after 120 min of sonication at 125 W and 30 degrees C; nonetheless, SDBS and its degradation intermediates proved difficult to oxidise as only about 20-25% of the initial carbon content was transformed to carbon dioxide. At the initial stages of the reaction, degradation rate appears to be only weakly dependent on the substrate concentration with the rate increasing from 3.1 to 4 mg l(-1)min(-1) with increasing concentration from 175 to 350 mg l(-1). Degradation appears to occur at the bubble-liquid interface through hydroxyl radical-mediated reactions whose role was established by performing experiments in the presence of radical scavengers, namely potassium bromide and sodium benzoate. Degradation rates increased with increasing power and decreasing temperature and volume.

  6. Response of weeping willows to linear alkylbenzene sulfonate.

    Science.gov (United States)

    Yu, Xiaozhang; Trapp, Stefan; Zhou, Puhua; Peng, Xiaoying; Cao, Xi

    2006-06-01

    Linear alkylbenzene sulfonate (LAS) is the most commonly used anionic surfactant in laundry detergents and cleaning agents. LAS compounds are found in surface waters and soils. The short-term acute toxicity of LAS to weeping willows (Salix babylonica L.) was investigated. Willow cuttings were grown in hydroponic solution spiked with LAS at 24.0+/-1 degrees C for 192 h. The normalized relative transpiration of plants was used to determine toxicity. Severe reduction of the transpiration was only found for high doses of LAS (240 mgl(-1)). Chlorophyll contents in leaves of treated plants varied with the dose of LAS, but there was no significant linear correlation. The activities of the enzymes superoxide dismutases (SOD), catalase (CAT), and peroxidase (POD) were quantified at the end of experiments. At higher concentrations of LAS (240 mgl(-1)), the activities of SOD and CAT were decreased. The correlation between the dose of LAS and the POD activity in leaf cells was the highest of all enzyme assays (R(2)=0.5). EC(50) values for a 50% inhibition of the transpiration of the trees were estimated to 374 mgl(-1) (72 h) and 166 mgl(-1) (192 h). Results from this experiment indicated that phytotoxic effects of LAS on willow trees are not expected for normal environmental conditions.

  7. Toxicity of perfluorononanoic acid and perfluorooctane sulfonate to Daphnia magna

    Directory of Open Access Journals (Sweden)

    Guang-hua LU

    2015-01-01

    Full Text Available In order to study toxicological effects of perfluorononanoic acid (PFNA, perfluorooctane sulfonate (PFOS, and their mixtures (PFNA/PFOS on Daphnia magna (D. magna, a suite of comprehensive toxicity tests were conducted, including a 48-hour acute toxicity test, a 21-day chronic test, a feeding experiment, and a biomarker assay. D. magna were exposed to aqueous solutions of PFNA and PFOS (alone and in combination at concentrations ranging from 0.008 to 5 mg/L. The survival, growth, and reproduction of D. magna were monitored over a 21-day life cycle. The biomarkers, including acetylcholinesterase (AChE, superoxide dismutase (SOD, and catalase (CAT activities, were determined after seven days of exposure. PFOS was more toxic than PFNA based on the results of the acute toxicity test. Perfluorinated compounds (PFCs inhibited both growth and reproduction of D. magna during the testing period. The ingestion rates and the biomarkers, including AChE, SOD, and CAT activities, were significantly inhibited by PFCs in most cases. Moreover, the combined effects related to the growth and reproduction showed the antagonistic effects of PFCs.

  8. Alginate-Poly(ethylene glycol) Hybrid Microspheres for Primary Cell Microencapsulation

    OpenAIRE

    Redouan Mahou; Meier, Raphael P H; Bühler, Léo H.; Christine Wandrey

    2014-01-01

    The progress of medical therapies, which rely on the transplantation of microencapsulated living cells, depends on the quality of the encapsulating material. Such material has to be biocompatible, and the microencapsulation process must be simple and not harm the cells. Alginate-poly(ethylene glycol) hybrid microspheres (alg-PEG-M) were produced by combining ionotropic gelation of sodium alginate (Na-alg) using calcium ions with covalent crosslinking of vinyl sulfone-terminated multi-arm poly...

  9. PEMFC performance of MEAS based on Nafion{sup R} and sPSEBS hybrid membranes

    Energy Technology Data Exchange (ETDEWEB)

    Fernandez-Carretero, F.J.; Compan, V. [Univ, Politecnica de Valencia, Valencia (Spain). Dept. Termodinamica Aplicada; Suarez, K.; Solorza, O. [Inst. Politecnico Nacional, Centro de Investigacion y de Estudios Avanzados, Mexico City (Mexico). Dept. de Quimica; Riande, E. [Inst. de Ciencia y Tecnologia de Polimeros, Madrid (Spain)

    2010-07-15

    Important scientific, technical and economic problems must be solved before widespread commercialization of polymer electrolyte membrane fuel cells (PEMFC). The main issues facing the development of commercial low temperature fuel cells are the synthesis of efficient solid electrolytes separating the anode from the cathode as well as the development of cheaper catalysts for fuel oxidation. This study involved the preparation of hybrid membranes based on Nafion 117 and sulfonated Calprene H6120 containing partially sulfonated inorganic fillers such as silica, SBA-15 and sepiolite. The feasibility of using the membranes as polyelectrolytes for low temperature fuel cells was then evaluated. The water uptake of Nafion hybrid membranes is 1/3 to 1/4 of that in composite membranes based on sulfonated Calprene H6120. The proton conductivity of Nafion 117 hybrid membranes-electrode assemblies is nearly 1/5 of the pristine Nafion membrane assembly. Sulfonated Calprene H6120 hybrid membranes typically have better proton conductivity than the Nafion 117 composites. The performance of fuel cells containing different MEAs was examined by measuring their polarization curves in different operating conditions. The kinetic parameters governing the voltage dependence on current density were also estimated. It was concluded that the superior performance of the fuel cells with MEAs of NAF-SEP, sPSEBS-SIL and sPSEBS-SBA is not due to the membranes themselves, but to the kinetic processes that occur at the electrodes, which in this study were less efficient for fuel cells with the Nafion MEA. 34 refs., 3 tabs., 9 figs.

  10. SYNTHESIS AND PROPERTIES OF SULFONATED POLY(ARYLENE ETHER) CONTAINING TRIPHENYL METHANE MOIETIES FROM ISOCYNATE MASKED BISPHENOL

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    A novel sulfonated poly(arylene ether) containing triphenylmethane moieties was synthesized by the sulfonation of a designed parent polymer using chlorosulfonic acid as sulfonation agent. The sulfonation took place at the para position of the pendant phenyl rings because of the specially designed parent polymer. The position and degree of sulfonation were characterized by 1H-NMR and elemental analysis. The sulfonated polymers are highly soluble in common organic solvents, such as dimethylsulfoxide, N,N'-dimethylacetamide, dimethylformamide, ethylene glycol monomethyl ether, and can be readily cast into tough and smooth films from solutions. The films showed good thermal and hydrolysis stabilities. Moreover, Fenton's reagent test revealed that the films exhibited superior stability to oxidation. The proton conductivities of the films were comparable with Nation 117 under same conditions. The membrane electrode assembly (MEA) prepared with the asmade film (706 EW, 100 μm dry thickness) shows better cell performance than Nation 115-MEA in the whole current density range.

  11. An investigation of proton conductivity of binary matrices sulfonated polysulfone/polyvinyltriazole after doping with inorganic acids

    Indian Academy of Sciences (India)

    Serkan Sevinç; Sevim Ünügür Çelik; Ayhan Bozkurt

    2015-04-01

    As anhydrous proton conductive membranes, sulfonated polysulfone (SPSU) and polyvinyl triazole were studied as binary matrices. The sulfonation of polysulfone was performed with trimethylsilylchlorosulfonate and high degree of sulfonation (140%) was obtained. Ion exchange capacity of SPSU was determined as 3.05 mmol−1/g. The polymer electrolyte membranes were prepared by blending of sulfonated polysulfone with polyvinyl triazole and phosphoric acid. Fourier transform infrared spectroscopy confirmed the sulfonation of the polysulfone and the ionic interaction between sulfonic acid and triazole units. Thermogravimetric analysis showed that the polymer electrolyte membranes are thermally stable up to at least 150° C. Scanning electron microscopy analysis indicated the homogeneity of the ternary composites. The maximum proton conductivity has been measured as 3.63 × 10−4S cm−1 at 150° C.

  12. Characterization of hybrids between bovine (MDBK) and mouse (L-cell) cell lines.

    Science.gov (United States)

    Chinchar, V G; Floyd, A D; Chinchar, G D; Taylor, M W

    1979-02-01

    Hypoxanthine-guanine phosphoribosyltransferase (HGPRT)-deficient mutants of a bovine kidney cell line (MDBK) were selected following mutagenesis with ethylmethane sulfonate or ICR-170G. MDBK mutants were hybridized to thymidine kinase-deficient L cells and selected in HAT medium. Parental and hybrid cells were characterized for isozyme patterns of lactic dehydrogenase malate dehydrogenase, glucose-6-phosphate dehydrogenase, and glutamate oxalate transaminase. Chromosomes of MDBK can be distinguished from mouse L cells by configuration and by fluorescent staining with Hoechst 33-258 stain. Hybrid cells contained both MDBK and L-cell chromosomes and had elevated DNA content. MDBK cells are normally restrictive for mengovirus replication. Both permissive and restrictive hybrids were found. Our data indicate that there was preferential loss of MDBK chromosomes in the hybrid cell lines.

  13. Nitric Acid Dehydration Using Perfluoro Carboxylate and Mixed Sulfonate/Carboxylate Membranes

    Energy Technology Data Exchange (ETDEWEB)

    Ames, Richard L. [Colorado School of Mines, Golden, CO (United States)

    2004-09-01

    Perfluoro ionomer membranes are tetrafluoro ethylene-based materials with microheterogeneous structures consisting of a hydrophobic polymer backbone and a hydrophilic side-chain cluster region. Due to the ionomer cluster morphology, these films exhibit unique transport properties. Recent investigations with perfluoro sulfonate and perfluoro sulfonate/carboxylate composite polymers have demonstrated their value in the dehydration of nitric acid and they show potential as an alternative to conventional, energy intensive unit operations in the concentration of acid feeds. As a result, investigations were conducted to determine the feasibility of using pure perfluoro carboxylate and mixed perfluoro sulfonate/carboxylate films for the dehydration of nitric acid because of the speculation of improved water selectivity of the carboxylate pendant chain. During the first phase of these investigations the effort was focused on generating a thin, solution cast perfluoro carboxylate ionomer film, to evaluate the general, chemical and physical characteristics of the polymer, and to assess the material's aqueous transport performance (flux and nitrate separation efficiencies) in pervaporation and high-pressure environments. Results demonstrated that generating robust solution-cast films was difficult yet a number of membranes survived high trans-membrane pressures up to 700 psig. General characterization of the solution cast product showed reduced ion exchange capacities when compared with thicker, ''as received'' perfluoro carboxylate and similar sulfonate films. Small angle x-ray scattering analysis results suggested that the solution cast carboxylate films contained a small fraction of sulfonate terminated side-chains. Aqueous transport experimentation showed that permeate fluxes for both pure water and nitric acid were approximately two orders of magnitude smaller for the carboxylate solution cast membranes when compared to their sulfonate

  14. Role of Modular Polyketide Synthases in the Production of Polyether Ladder Compounds in Ciguatoxin-producing Gambierdiscus polynesiensis and G.excentricus (Dinophyceae).

    Science.gov (United States)

    Kohli, Gurjeet S; Campbell, Katrina; John, Uwe; Smith, Kirsty F; Fraga, Santiago; Rhodes, Lesley L; Murray, Shauna A

    2017-02-17

    Gambierdiscus, a benthic dinoflagellate, produces ciguatoxins that cause the human illness Ciguatera. Ciguatoxins are polyether ladder compounds that have a polyketide origin, indicating that polyketide synthases (PKS) are involved in their production. We sequenced transcriptomes of G. excentricus and G. polynesiensis and found 264 contigs encoding single domain ketoacyl synthases (KS; G. excentricus: 106, G. polynesiensis: 143) and ketoreductases (KR; G. excentricus: 7, G. polynesiensis: 8) with sequence similarity to type I PKSs, as reported in other dinoflagellates. Additionally, 24 contigs (G. excentricus: 3, G. polynesiensis: 21) encoding multiple PKS domains (forming typical type I PKSs modules) were found. The proposed structure produced by one of these megasynthases resembles a partial carbon backbone of a polyether ladder compound. Seventeen contigs encoding single domain KS, KR, s-malonyltransacylase, dehydratase and enoyl-reductase with sequence similarity to type II fatty acid synthases (FAS) in plants were found. Type I PKS and type II FAS genes were distinguished based on the arrangement of domains on the contigs and their sequence similarity and phylogenetic clustering with known PKS/FAS genes in other organisms. This differentiation of PKS and FAS pathways in Gambierdiscus is important, as it will facilitate approaches to investigating toxin biosynthesis pathways in dinoflagellates. This article is protected by copyright. All rights reserved.

  15. Cationic Copolymerization of 3,3-Bis(hydroxymethyl)oxetane and Glycidol: Biocompatible Hyperbranched Polyether Polyols with High Content of Primary Hydroxyl Groups.

    Science.gov (United States)

    Christ, Eva-Maria; Hobernik, Dominika; Bros, Matthias; Wagner, Manfred; Frey, Holger

    2015-10-12

    The cationic ring-opening copolymerization of 3,3-bis(hydroxymethyl)oxetane (BHMO) with glycidol using different comonomer ratios (BHMO content from 25 to 90%) and BF3OEt2 as an initiator has been studied. Apparent molecular weights of the resulting hyperbranched polyether copolymers ranged from 1400 to 3300 g mol(-1) (PDI: 1.21-1.48; method: SEC, linear PEG standards). Incorporation of both comonomers is evidenced by MALDI-TOF mass spectroscopy. All hyperbranched polyether polyols with high content of primary hydroxyl groups portray good solubility in water, which correlates with an increasing content of glycerol units. Detailed NMR characterization was employed to elucidate the copolymer microstructures. Kinetic studies via FTIR demonstrated a weak gradient-type character of the copolymers. MTT assays of the copolymers (up to 100 μg mL(-1)) on HEK and fibroblast cell lines (3T3, L929, WEHI) as well as viability tests on the fibroblast cells were carried out to assess the biocompatibility of the materials, confirming excellent biocompatibility. Transfection efficiency characterization by flow cytometry and confocal laser microscopy demonstrated cellular uptake of the copolymers. Antiadhesive properties of the materials on surfaces were assessed by adhesion assays with fibroblast cells.

  16. Intermediates in monensin biosynthesis: A late step in biosynthesis of the polyether ionophore monensin is crucial for the integrity of cation binding

    Directory of Open Access Journals (Sweden)

    Wolfgang Hüttel

    2014-02-01

    Full Text Available Polyether antibiotics such as monensin are biosynthesised via a cascade of directed ring expansions operating on a putative polyepoxide precursor. The resulting structures containing fused cyclic ethers and a lipophilic backbone can form strong ionophoric complexes with certain metal cations. In this work, we demonstrate for monensin biosynthesis that, as well as ether formation, a late-stage hydroxylation step is crucial for the correct formation of the sodium monensin complex. We have investigated the last two steps in monensin biosynthesis, namely hydroxylation catalysed by the P450 monooxygenase MonD and O-methylation catalysed by the methyl-transferase MonE. The corresponding genes were deleted in-frame in a monensin-overproducing strain of Streptomyces cinnamonensis. The mutants produced the expected monensin derivatives in excellent yields (ΔmonD: 1.13 g L−1 dehydroxymonensin; ΔmonE: 0.50 g L−1 demethylmonensin; and double mutant ΔmonDΔmonE: 0.34 g L−1 dehydroxydemethylmonensin. Single crystals were obtained from purified fractions of dehydroxymonensin and demethylmonensin. X-ray structure analysis revealed that the conformation of sodium dimethylmonensin is very similar to that of sodium monensin. In contrast, the coordination of the sodium ion is significantly different in the sodium dehydroxymonensin complex. This shows that the final constitution of the sodium monensin complex requires this tailoring step as well as polyether formation.

  17. 聚醚嵌段改性硅油的合成与应用%Synthesis and Application of Polyether Block Modified Amino Silicone Oil

    Institute of Scientific and Technical Information of China (English)

    刘瑞云; 缪瑶生; 蒋英妹

    2012-01-01

    将端含氢硅油与烯丙基聚氧烷乙基环氧基醚进行加成反应,再使用端氨基聚醚对其进行氨化反应,得到聚醚嵌段改性硅油.并用于全棉织物、涤棉织物的整理.结果表明:经聚醚嵌段改性硅油整理后的织物具有良好的亲水性、手感、白度等.%Side hydrogen silicone oil was reacted with polyoxyethylene alkyl allyl ether through hydrosily-lation and the product was then aminated with an amino-terminated polyoxypropylene, to afford a polyether block modified amino silicone oil, which was used for the finishing of cotton and polyester fabric. Results showed that the fabric treated with polyether-block modified silicone oil BW has a good performance of hydro-philicity, feel and whiteness.

  18. Intermediates in monensin biosynthesis: A late step in biosynthesis of the polyether ionophore monensin is crucial for the integrity of cation binding

    Science.gov (United States)

    Spencer, Jonathan B; Leadlay, Peter F

    2014-01-01

    Summary Polyether antibiotics such as monensin are biosynthesised via a cascade of directed ring expansions operating on a putative polyepoxide precursor. The resulting structures containing fused cyclic ethers and a lipophilic backbone can form strong ionophoric complexes with certain metal cations. In this work, we demonstrate for monensin biosynthesis that, as well as ether formation, a late-stage hydroxylation step is crucial for the correct formation of the sodium monensin complex. We have investigated the last two steps in monensin biosynthesis, namely hydroxylation catalysed by the P450 monooxygenase MonD and O-methylation catalysed by the methyl-transferase MonE. The corresponding genes were deleted in-frame in a monensin-overproducing strain of Streptomyces cinnamonensis. The mutants produced the expected monensin derivatives in excellent yields (ΔmonD: 1.13 g L−1 dehydroxymonensin; ΔmonE: 0.50 g L−1 demethylmonensin; and double mutant ΔmonDΔmonE: 0.34 g L−1 dehydroxydemethylmonensin). Single crystals were obtained from purified fractions of dehydroxymonensin and demethylmonensin. X-ray structure analysis revealed that the conformation of sodium dimethylmonensin is very similar to that of sodium monensin. In contrast, the coordination of the sodium ion is significantly different in the sodium dehydroxymonensin complex. This shows that the final constitution of the sodium monensin complex requires this tailoring step as well as polyether formation. PMID:24605157

  19. Synthesis and Characterization of Macrocyclic Polyether N,N′-Diallyl-7,16-diaza-1,4,10,13-tetraoxa-dibenzo-18-crown-6

    Directory of Open Access Journals (Sweden)

    Julius Toeri

    2016-01-01

    Full Text Available In this study an efficient and direct production procedure for a macrocyclic polyether N,N′-diallyl-7,16-diaza-1,4,10,13-tetraoxa-dibenzo-18-crown-6 from the reaction of catechol and N,N-bis(2-chloroethylprop-2-en-1-amine in n-butanol in the presence of a strong base is reported. The synthesis involves a two-step addition of sodium hydroxide to enhance the cyclization process, and at the end of the reaction, the reaction mixture is neutralized and the solvent replaced with water in-situ through distillation to afford a relatively pure precipitate that is easily recrystallized from acetone. The yield of the macrocycle was 36%–45% and could be scaled-up to one-mole quantities. The structure and purity of this compound was verified on the basis of elemental analysis, IR, UV-Vis, 1H-, 13C-NMR, 2D-NMR, mass spectroscopy, and thermal analysis. The white crystalline compound has a sharp melting point of 124 °C and a crystallization temperature of 81.4 °C determined by differential scanning calorimetry. Our motivation behind the synthesis of the bibracchial lariat azacrown polyether ligand was to examine its possible applications in ion-selective polymer-supported materials.

  20. Molecular dynamics simulation of nanoscale distribution and mobility of water and dimethylmethylphosphonate in sulfonated polystyrene.

    Science.gov (United States)

    Vishnyakov, Aleksey; Neimark, Alexander V

    2008-11-27

    The interest in a better understanding of the specific interactions of phosphor-organic compounds and water with sulfonated polystyrene (sPS) is motivated by the use of block copolymers as protective membranes against chemical warfare agents. Using classical molecular dynamics simulations, we explored the nanoscale segregation and diffusion of water and nerve gas simulant dimethylmethylphosphonate (DMMP) in sPS neutralized with calcium counterions at different sulfonation and hydration levels. The water content was varied from 15 to 54% of dry polymer weight, and the DMMP content was varied from 0 to 100 wt %. We found that, in the 40% sulfonated polystyrene, water forms well defined aggregates, which grow in size as the hydration increases, reaching approximately 20 A at the maximum water content. In the 100% sulfonated polystyrene, the overall structure of hydrated polymer is more uniform with smaller water aggregates. Diffusion of water at the same number of water molecules per sulfonate group is faster at a lower sulfonation level. The solvation of sPS in water-DMMP binary mixtures was found to differ substantially from Nafion, where DMMP forms a layer between the hydropholic and hydrophobic subphases. In sPS with divalent Ca(2+) counterions, DMMP and water compete for the solvation of the sulfonate group. At high water and DMMP contents, the diffusion of DMMP turned out to be rather fast with a diffusion coefficient of ca. 30% of that of water. At the same time, water diffusion slows down as the DMMP concentration increases. This observation suggests that although sPS is permeable for both solvents, water and DMMP are partially segregated on the scale of 1-2 nm and have different pathways through the system. The nonuniform nanoscale distribution of water and DMMP in sPS is confirmed by analyses of different pair correlation functions. This feature may significantly affect the perm-selective properties of sPS-contained block copolymer membranes.

  1. Randomized Clinical Trial of Sodium Polystyrene Sulfonate for the Treatment of Mild Hyperkalemia in CKD.

    Science.gov (United States)

    Lepage, Laurence; Dufour, Anne-Claude; Doiron, Jessica; Handfield, Katia; Desforges, Katherine; Bell, Robert; Vallée, Michel; Savoie, Michel; Perreault, Sylvie; Laurin, Louis-Philippe; Pichette, Vincent; Lafrance, Jean-Philippe

    2015-12-07

    Hyperkalemia affects up to 10% of patients with CKD. Sodium polystyrene sulfonate has long been prescribed for this condition, although evidence is lacking on its efficacy for the treatment of mild hyperkalemia over several days. This study aimed to evaluate the efficacy of sodium polystyrene sulfonate in the treatment of mild hyperkalemia. In total, 33 outpatients with CKD and mild hyperkalemia (5.0-5.9 mEq/L) in a single teaching hospital were included in this double-blind randomized clinical trial. We randomly assigned these patients to receive either placebo or sodium polystyrene sulfonate of 30 g orally one time per day for 7 days. The primary outcome was the comparison between study groups of the mean difference of serum potassium levels between the day after the last dose of treatment and baseline. The mean duration of treatment was 6.9 days. Sodium polystyrene sulfonate was superior to placebo in the reduction of serum potassium levels (mean difference between groups, -1.04 mEq/L; 95% confidence interval, -1.37 to -0.71). A higher proportion of patients in the sodium polystyrene sulfonate group attained normokalemia at the end of their treatment compared with those in the placebo group, but the difference did not reach statistical significance (73% versus 38%; P=0.07). There was a trend toward higher rates of electrolytic disturbances and an increase in gastrointestinal side effects in the group receiving sodium polystyrene sulfonate. Sodium polystyrene sulfonate was superior to placebo in reducing serum potassium over 7 days in patients with mild hyperkalemia and CKD. Copyright © 2015 by the American Society of Nephrology.

  2. Highly Efficient Biomimetic Oxidation of Sulfide to Sulfone by Hydrogen Peroxide in the Presence of Manganese meso-Tetraphenylporphyrin

    Institute of Scientific and Technical Information of China (English)

    ZHOU,Xian-Tai; JI,Hong-Bing; YUAN,Qiu-Lan; XU,Jian-Chang; PEI,Li-Xia; WANG,Le-Fu

    2008-01-01

    Low amount of manganese meso-tetraphenyl porphyrin [Mn(TPP)] was used for highly efficient selective oxidation of sulfide to sulfone by hydrogen peroxide at room temperature.Sulfones were produced directly with yields generally around 90% while the catalyst concentration was only 4 ×10-5 mol·L-1.In a large-scale experiment of thioanisole oxidation,the isolated yield of sulfone (87%) was obtained and the turnover number (TON) reached up to 8×106,which is the highest TON for the oxidation systems of sulfide to sulfone catalyzed by metalloporphyrins.

  3. Synthesis and characterization of sulfonated polyesters derived from glycerol; Sintese e caracterizacao de poliesteres sulfonados obtidos a partir do glicerol

    Energy Technology Data Exchange (ETDEWEB)

    Fiuza, R.A.; Jose, N.M.; Boaventura, J.S. [Universidade Federal da Bahia (IQ/UFBA), Salvador, BA (Brazil). Inst. de Quimica; Fiuza, R.P. [Universidade Federal da Bahia (EP/UFBA), Salvador, BA (Brazil). Escola Politecnica. Curso de Mestrado em Engenharia Quimica

    2010-07-01

    In this work were synthesized polyesters from glycerol and acid sulfonated phthalic previously. The materials were characterized by DSC, TGA, FTIR, SEM, XRD and XRF. The results showed effective sulfonation of phthalic acid. The presence of sulfonic groups promoted strong changes in the crystallinity of the new material makes the lens. The polyesters made from phthalic acid sulfonated combine characteristics such as heat resistance and groups that drivers potentiate the electrolyte for application in fuel cells proton exchange membrane and also for gas separation. (author)

  4. Phosphoric Acid-Mediated Synthesis of Vinyl Sulfones through Decarboxylative Coupling Reactions of Sodium Sulfinates with Phenylpropiolic Acids.

    Science.gov (United States)

    Rong, Guangwei; Mao, Jincheng; Yan, Hong; Zheng, Yang; Zhang, Guoqi

    2015-08-07

    A novel phosphoric acid -mediated synthesis of vinyl sulfones through decarboxylative coupling reactions of sodium sulfinates with phenylpropiolic acids is described. This transformation is efficient and environmentally friendly.

  5. Neurotoxicity of perfluorooctane sulfonate to hippocampal cells in adult mice.

    Directory of Open Access Journals (Sweden)

    Yan Long

    Full Text Available Perfluorooctane sulfonate (PFOS is a ubiquitous pollutant and found in the environment and in biota. The neurotoxicity of PFOS has received much concern among its various toxic effects when given during developing period of brain. However, little is known about the neurotoxic effects and potential mechanisms of PFOS in the mature brain. Our study demonstrated the neurotoxicity and the potential mechanisms of PFOS in the hippocampus of adult mice for the first time. The impairments of spatial learning and memory were observed by water maze studies after exposure to PFOS for three months. Significant apoptosis was found in hippocampal cells after PFOS exposure, accompanied with a increase of glutamate in the hippocampus and decreases of dopamine (DA and 3,4-dihydrophenylacetic acid (DOPAC in Caudate Putamen in the 10.75 mg/kg PFOS group. By two-dimensional fluorescence difference in gel electrophoresis (2D-DIGE analysis, seven related proteins in the hippocampus that responded to PFOS exposure were identified, among which, Mib1 protein (an E3 ubiquitin-protein ligase, Herc5 (hect domain and RLD 5 isoform 2 and Tyro3 (TYRO3 protein tyrosine kinase 3 were found down-regulated, while Sdha (Succinate dehydrogenase flavoprotein subunit, Gzma (Isoform HF1 of Granzyme A precursor, Plau (Urokinase-type plasminogen activator precursor and Lig4 (DNA ligase 4 were found up-regulated in the 10.75 mg/kg PFOS-treated group compare with control group. Furthermore, we also found that (i increased expression of caspase-3 protein and decreased expression of Bcl-2, Bcl-XL and survivin proteins, (ii the increased glutamate release in the hippocampus. All these might contribute to the dysfunction of hippocampus which finally account for the impairments of spatial learning and memory in adult mice.

  6. Fate of linear alkylbenzene sulfonate (LAS) in activated sludge plants.

    Science.gov (United States)

    Temmink, H; Klapwijk, Bram

    2004-02-01

    Monitoring data were collected in a pilot-scale municipal activated sludge plant to assess the fate of the C12-homologue of linear alkyl benzene sulfonate (LAS-C12). The pilot-plant was operated at influent LAS-C12 concentrations between 2 and 12 mg l(-1) and at sludge retention times of 10 and 27 days. Effluent and waste sludge concentrations varied between 5 and 10 microg l(-1) and between 37 and 69 microg g(-1) VSS, respectively. In the sludge samples only 2-8% was present as dissolved LAS-C12, whereas the remaining 92-98% was found to be adsorbed to the sludge. In spite of this high degree of sorption, more than 99% of the LAS-C12 load was removed by biodegradation, showing that not only the soluble fraction but also the adsorbed fraction of LAS-C12 is readily available for biodegradation. Sorption and biodegradation of LAS-C12 were also investigated separately. Sorption was an extremely fast and reversible process and could be described by a linear isotherm with a partition coefficient of 3.2 l g(-1) volatile suspended solids. From the results of biodegradation kinetic tests it was concluded that primary biodegradation of LAS-C12 cannot be described by a (growth) Monod model, but a secondary utilisation model should be used instead. The apparent affinity of the sludge to biodegrade LAS-C12 increased when the sludge was loaded with higher influent concentrations of LAS-C12.

  7. Mechanisms for selective toxicity of fipronil insecticide and its sulfone metabolite and desulfinyl photoproduct.

    Science.gov (United States)

    Hainzl, D; Cole, L M; Casida, J E

    1998-12-01

    Fipronil, an N-phenylpyrazole with a trifluoromethylsulfinyl substituent, initiated the second generation of insecticides acting at the gamma-aminobutyric acid (GABA) receptor to block the chloride channel. The first generation includes the polychlorocycloalkanes alpha-endosulfan and lindane. In this study, we examine the mechanisms for selective toxicity of the sulfoxide fipronil and its sulfone metabolite and desulfinyl photoproduct relative to their target site interactions in vitro and ex vivo and the importance in fipronil action of biooxidation to the sulfone. Differences in GABA receptor sensitivity, assayed by displacement of 4'-ethynyl-4-n-[2, 3-3H2]propylbicycloorthobenzoate ([3H]EBOB) from the noncompetitive blocker site, appear to be a major factor in fipronil being much more toxic to the insects (housefly and fruit fly) than to the vertebrates (humans, dogs, mice, chickens, quail, and salmon) examined; in insects, the IC50s range from 3 to 12 nM for fipronil and its sulfone and desulfinyl derivatives, while in vertebrates, the IC50 average values are 1103, 175, and 129 nM for fipronil, fipronil sulfone, and desulfinyl fipronil, respectively. The insect relative to the vertebrate specificity decreases in the following order: fipronil > lindane > desulfinyl fipronil > fipronil sulfone > alpha-endosulfan. Ex vivo inhibition of [3H]EBOB binding in mouse brain is similar for fipronil and its sulfone and desulfinyl derivatives at the LD50 dose, but surprisingly, at higher doses fipronil can be lethal without detectably blocking the [3H]EBOB site. The P450 inhibitor piperonyl butoxide, acting in houseflies, increases the metabolic stability and effectiveness of fipronil and the sulfone but not those of the desulfinyl compound, and in mice it completely blocks the sulfoxide to sulfone conversion without altering the poisoning. Thus, the selective toxicity of fipronil and fipronil-derived residues is due in part to the higher potency of the parent compound at

  8. 新型汽车密封胶用聚醚多元醇的合成及其应用%The Synthesis and Application of a New Polyether Polyol Used in Automobile Sealant

    Institute of Scientific and Technical Information of China (English)

    王丙龙; 刘小会; 董立红; 张成; 刘茂炟

    2015-01-01

    以丙二醇和甘油为混合起始剂,合成了一种新型汽车密封胶用聚醚多元醇,并与二苯基甲烷二异氰酸酯反应合成了聚氨酯预聚体密封胶,探讨了催化剂、温度等因素对聚醚多元醇及预聚体的影响。结果表明,此聚醚多元醇反应活性比传统三官能度聚醚更稳定,降低了预聚体的聚釜风险,并提高制品的拉伸强度和断裂伸长率。%A novel polyether polyol for automobile sealant was synthesized using propylene glycol and glycerol mixture as initiator. The prepolymer for sealant were prepared by using this polyether polyol reacted with diphenyl⁃methane diisocyanate. The influence of catalyst and temperature on the novel polyether polyol and its prepolymer was discussed. The results showed that the polyol was more stable than the conventional trifunctional polyether, the risk of prepolymer gelation in the reactor was reduced, the tensile strength and elongation at break of products were improved.

  9. Polymer electrolyte membranes from fluorinated polyisoprene-block-sulfonated polystyrene: Membrane structure and transport properties

    Energy Technology Data Exchange (ETDEWEB)

    Sodeye, Akinbode [Department of Polymer Science and Engineering, University of Massachusetts; Huang, Tianzi [University of Tennessee, Knoxville (UTK); Gido, Samuel [University of Massachusetts, Amherst; Mays, Jimmy [ORNL

    2011-01-01

    With a view to optimizing morphology and ultimately properties, membranes have been cast from relatively inexpensive block copolymer ionomers of fluorinated polyisoprene-block-sulfonated polystyrene (FISS) with various sulfonation levels, in both the acid form and the cesium neutralized form. The morphology of these membranes was characterized by transmission electron microscopy and ultra-small angle X-ray scattering, as well as water uptake, proton conductivity and methanol permeability within the temperature range from 20 to 60 C. Random phase separated morphologies were obtained for all samples except the cesium sample with 50 mol% sulfonation. The transport properties increased with increasing degree of sulfonation and temperature for all samples. The acid form samples absorbed more water than the cesium samples with a maximum swelling of 595% recorded at 60 C for the acid sample having 50 mol% sulfonation. Methanol permeability for the latter sample was more than an order of magnitude less than for Nafion 112 but so was the proton conductivity within the plane of the membrane at 20 C. Across the plane of the membrane this sample had half the conductivity of Nafion 112 at 60 C.

  10. The host cell sulfonation pathway contributes to retroviral infection at a step coincident with provirus establishment.

    Directory of Open Access Journals (Sweden)

    James W Bruce

    2008-11-01

    Full Text Available The early steps of retrovirus replication leading up to provirus establishment are highly dependent on cellular processes and represent a time when the virus is particularly vulnerable to antivirals and host defense mechanisms. However, the roles played by cellular factors are only partially understood. To identify cellular processes that participate in these critical steps, we employed a high volume screening of insertionally mutagenized somatic cells using a murine leukemia virus (MLV vector. This approach identified a role for 3'-phosphoadenosine 5'-phosphosulfate synthase 1 (PAPSS1, one of two enzymes that synthesize PAPS, the high energy sulfate donor used in all sulfonation reactions catalyzed by cellular sulfotransferases. The role of the cellular sulfonation pathway was confirmed using chemical inhibitors of PAPS synthases and cellular sulfotransferases. The requirement for sulfonation was mapped to a stage during or shortly after MLV provirus establishment and influenced subsequent gene expression from the viral long terminal repeat (LTR promoter. Infection of cells by an HIV vector was also shown to be highly dependent on the cellular sulfonation pathway. These studies have uncovered a heretofore unknown regulatory step of retroviral replication, have defined a new biological function for sulfonation in nuclear gene expression, and provide a potentially valuable new target for HIV/AIDS therapy.

  11. One Step Preparation of Sulfonated Solid Catalyst and Its Effect in Esterification Reaction

    Institute of Scientific and Technical Information of China (English)

    康世民; 常杰; 范娟

    2014-01-01

    A carbon-based sulfonated catalyst was prepared by direct sulfonation and carbonization (in moderate conditions:200 °C, 12 h) of red liquor solids, a by-product of paper-making process. The prepared sulfonated cata-lyst (SC) had aromatic structure, composed of carbon enriched inner core, and oxygen-containing (SO3H, COOH, OH) groups enriched surface. The SO3H, COOH, OH groups amounted to 0.74 mmol·g-1, 0.78 mmol·g-1, 2.18 mmol·g-1, respectively. The fresh SC showed much higher catalytic activity than that of the traditional solid acid catalysts (strong-acid 732 cation exchange resin, hydrogen type zeolite socony mobile-five (HZSM-5), sulfated zir-conia) in esterification of oleic acid. SC was deactivated during the reactions, through the mechanisms of leaching of sulfonated species and formation of sulfonate esters. Two regeneration methods were developed, and the catalytic activity can be mostly regenerated by regeneration Method 1 and be fully regenerated by regeneration Method 2, respectively.

  12. EFFECT OF SOLVENT COMPOSITION ON THE SULFONATION DEGREE OF OLY(PHENYLENE OXIDE) (PPO)

    Institute of Scientific and Technical Information of China (English)

    Tong-wen Xu; Wei-hua Yang; Bing-lin He

    2002-01-01

    This paper investigates the possibility of attaining sulphonated poly(phenylene oxide) (SPPO) with a relatively higher sulfonation degree. To achieve this aim, the approach we adopt is to improve the solubility of the final product in the mixed solvent so that the sulfonation may take place between the bulk solutions and PPO powders even at higher sulfonation degree. It is shown that the addition of a proper amount of dimethyl formide (DMF) to the conventional PPO-chloroform system can actually enhance the sulfonation effect. The solvent composition is then correlated with the sulfonation degree based on the solubility parameters. It is interesting to find that solubility parameters between the mixed solvent and the precipitated products keep an approximately unchanged value at about 4.9, which is just equal to that when pure chloroform is used, though the solubility parameters of both solvents increase with the content of DMF in solution. This may be the main reason why the addition of DMF can reduce the precipitation and improve the ion exchange capacity (IEC) of SPPO polymer.

  13. Preparation of Sulfonated PVA-TMSP Membranes for Direct Methanol Fuel Cell

    Directory of Open Access Journals (Sweden)

    Haryadi

    2012-08-01

    Full Text Available Novel preparation and characterization of sulfonated polyvinyl alcohol (PVA–trimethoxysilyl propanethiol (TMSP membranes for direct methanol fuel cell (DMFC application have been investigated. Preparation of sulfonated PVA-TMSP membrane was conducted by crosslinking steps using sol-gel method and a catalyst of concentrated HCl. TMSP concentrations were varied from 1% to 3%. The gel solution was cast on to the membrane metal plate to obtain membrane sheets. The membrane was then oxidized in H2O2 concentrations of (10-30% to convert the mercapto groups into sulfonate group. Investigations of the cross-linking process and the existence of sulfonate group were conducted by infrared spectroscopy as shown for frequencies at 1140–1200/cm and 1200–1145/cm respectively. The scanning electron microscope–energy dispersive X-rays (SEM–EDX of the membranes indicated that the distribution of silica particles from sol–gel reaction products was uneven due to the fast exchange rate of condensation. The degree of swelling decreased as methanol concentrations increase for sulfonated PVA–TMSP membrane which opposed toward the value of commercial Nafion membrane. The maximum value of ion exchange capacity of the membrane was 1.82 mmol/g whereas the highest proton conductivity was 3.9 x 10-4 S/cm. Therefore it can be concluded that the membrane was a potential candidate for application in DMFC.

  14. Highly Sulfonated Diamine Synthesized Polyimides and Protic Ionic Liquid Composite Membranes Improve PEM Conductivity

    Directory of Open Access Journals (Sweden)

    Bor-Kuan Chen

    2015-06-01

    Full Text Available A novel sulfonated diamine was synthesized from 1,4-bis(4-aminophenoxy benzene [pBAB]. Sulfonated polyimides (SPIs were synthesized from sulfonated pBAB, 1,4-bis(4-aminophenoxy-2-sulfonic acid benzenesulfonic acid [pBABTS], various diamines and aromatic dianhydrides. Composite proton exchange membranes (PEMs made of novel SPIs and a protic ionic liquid (PIL 1-vinyl-3-H-imidazolium trifluoromethanesulfonate [VIm][OTf] showed substantially increased conductivity. We prepared an SPI/PIL composite PEM using pBABTS, 4,4′-(9-fluorenylidene dianiline (9FDA as diamine, 3,3′,4,4′-diphenylsulfone tetracarboxylic dianhydride (DSDA as dianhydride and 40 wt % [VIm][OTf] with a high conductivity of 16 mS/cm at 120 °C and anhydrous condition. pBABTS offered better conductivity, since the chemical structure had more sulfonated groups that provide increased conductivity. The new composite membrane could be a promising anhydrous or low-humidity PEM for intermediate or high-temperature fuel cells.

  15. Sodium polystyrene sulfonate (kayexalate) aspiration: histologic appearance and infrared microspectrophotometric analysis of two cases.

    Science.gov (United States)

    Fenton, J J; Johnson, F B; Przygodzk, R M; Kalasinsky, V F; Al-Dayel, F; Travis, W D

    1996-10-01

    Sodium polystyrene sulfonate (kayexalate) is a cation-exchange resin given enterally for the treatment of hyperkalemia. Aspiration of this material is a rare occurrence, but when visualized in the alveolus, it has a characteristic microscopic appearance that is virtually diagnostic. In two cases, recognition of the characteristic morphology of the foreign material raised the question of sodium polystyrene sulfonate. We used infrared spectroscopy to demonstrate the presence of this material in lung biopsies of two patients by identifying foreign body particles. Histories of the patients were reviewed for exposure to sodium polystyrene sulfonate. Two lung specimens were referred to the Armed Forces Institute of Pathology with an unknown foreign material identified within the air spaces. The lung biopsies were from two children, one postterm female infant who died at 3 days of life and a 4-year-old girl who underwent lung biopsy during surgical repair for tetralogy of Fallot. Both patients had received sodium polystyrene sulfonate previously for control of hyperkalemia. The lung specimens showed characteristic basophilic, amorphous foreign material in airspaces on histologic sections. The identity of this material was confirmed by Fourier transform infrared microspectrophotometry. To our knowledge, we report the first two cases of sodium polystyrene sulfonate aspiration in children. This material has a distinctive morphologic appearance on histologic sections, and its identity can be confirmed by Fourier transform infrared microspectrophotometry.

  16. The host cell sulfonation pathway contributes to retroviral infection at a step coincident with provirus establishment.

    Directory of Open Access Journals (Sweden)

    James W Bruce

    2008-11-01

    Full Text Available The early steps of retrovirus replication leading up to provirus establishment are highly dependent on cellular processes and represent a time when the virus is particularly vulnerable to antivirals and host defense mechanisms. However, the roles played by cellular factors are only partially understood. To identify cellular processes that participate in these critical steps, we employed a high volume screening of insertionally mutagenized somatic cells using a murine leukemia virus (MLV vector. This approach identified a role for 3'-phosphoadenosine 5'-phosphosulfate synthase 1 (PAPSS1, one of two enzymes that synthesize PAPS, the high energy sulfate donor used in all sulfonation reactions catalyzed by cellular sulfotransferases. The role of the cellular sulfonation pathway was confirmed using chemical inhibitors of PAPS synthases and cellular sulfotransferases. The requirement for sulfonation was mapped to a stage during or shortly after MLV provirus establishment and influenced subsequent gene expression from the viral long terminal repeat (LTR promoter. Infection of cells by an HIV vector was also shown to be highly dependent on the cellular sulfonation pathway. These studies have uncovered a heretofore unknown regulatory step of retroviral replication, have defined a new biological function for sulfonation in nuclear gene expression, and provide a potentially valuable new target for HIV/AIDS therapy.

  17. CHARACTERIZATION OF SULFONATED SYNDIOTACTIC POLYSTYRENE%磺化间规聚苯乙烯的表征

    Institute of Scientific and Technical Information of China (English)

    王进; 祝方明; 刘金成; 黎华明; 林尚安

    2001-01-01

    The effect of different sulfonation degree on properties of sulfonated syndiotactic polystyrene(SsPS) was investigated by 1H-NMR,13C-NMR,FTIR,DSC and WAXD.The results of 13C-NMR showed that a peak at δ=145.5 appeared in all SsPS spectra,which proved that the syndiotactic structure of syndiotactic polystyrene(sPS) still existed in SsPS.With increasing degree of sulfonition,the chemical shifts of C-1 and C\\|3 for sulfonated benzene ring turned out to be wider.1H-NMR spectra showed that C\\|3 for sulfonated benzene ring had a chemical shift of 7.66.FTIR spectra showed that sulfonic acid groups were introduced on the para position of benzene rings and with increasing sulfonation degree,the absorption strength of 612/1600 cm-1,834/1600cm-1 increased,but the absorption strength of 1078/1600cm-1 decreased.The absorption of ~1030cm-1,~1179cm-1,~1217cm-1 appeared when the sulfonation degree was higher that 6%.sPS and SsPS-H-2.2 had absorption at 975 and 943cm-1 and also had double peaks around ~1175cm-1;DSC showed that with increasing sulfonation degree, the glass transition temperature increased, the melt temperature,crystallization temperature and crystallization degree decreased;SsPS couldn't crystallize when sulfonation degree was higher that 6mol%;WAXD proved that sPS had the α and β crystal types, however,SsPS with 2.2% sulfonation degree only had the β crystal type, and SsPS with 6.1% sulfonation degree didn't crystallize.

  18. Synthesis and Promising in Vitro Antiproliferative Activity of Sulfones of a 5-Nitrothiazole Series

    Directory of Open Access Journals (Sweden)

    Nadine Azas

    2012-12-01

    Full Text Available  The synthesis in water of new sulfone derivatives under microwave irradiation is described. This eco-friendly process leads to the expected products in good yields by reaction of various substituted sulfinates (commercially available or obtained by reduction of the corresponding sulfonyl chlorides with 4-chloromethyl-2-methyl-5-nitro-1,3-thiazole. In order to evaluate the antiproliferative effect of these compounds, several sulfone derivatives are also dichlorinated on the Cα next to the sulfonyl group. An evaluation on different cancer cell lines reveals promising selective in vitro antiproliferative activity toward HepG2 human cell lines by dihydrogenated sulfones, suggesting further research should be to explore their anticancer potential in the treatment of liver cancer.

  19. Polymer electrolyte membranes from fluorinated polyisoprene-block-sulfonated polystyrene: Structural evolution with hydration and heating

    Energy Technology Data Exchange (ETDEWEB)

    Sodeye, Akinbode [Department of Polymer Science and Engineering, University of Massachusetts; Huang, Tianzi [University of Tennessee, Knoxville (UTK); Gido, Samuel [University of Massachusetts, Amherst; Mays, Jimmy [ORNL

    2011-01-01

    Small-angle neutron scattering (SANS) and ultra-small-angle X-ray scattering (USAXS) have been used to study the structural changes in fluorinated polyisoprene/sulfonated polystyrene (FISS) diblock copolymers as they evolved from the dry state to the water swollen state. A dilation of the nanometer-scale hydrophilic domains has been observed as hydration increased, with greater dilation occurring in the more highly sulfonated samples or upon hydration at higher temperatures. Furthermore, a decrease in the order in these phase separated structures is observed upon swelling. The glass transition temperatures of the fluorinated blocks have been observed to decrease upon hydration of these materials, and at the highest hydration levels, differential scanning calorimetry (DSC) has shown the presence of tightly bound water. A precipitous drop in the mechanical integrity of the 50% sulfonated materials is also observed upon exceeding the glass transition temperature (Tg), as measured by dynamic mechanical analysis (DMA).

  20. Periodic Mesoporous Organosilica Functionalized with Sulfonic Acid Groups as Acid Catalyst for Glycerol Acetylation

    Directory of Open Access Journals (Sweden)

    Pascal Van Der Voort

    2013-08-01

    Full Text Available A Periodic Mesoporous Organosilica (PMO functionalized with sulfonic acid groups has been successfully synthesized via a sequence of post-synthetic modification steps of a trans-ethenylene bridged PMO material. The double bond is functionalized via a bromination and subsequent substitution obtaining a thiol functionality. This is followed by an oxidation towards a sulfonic acid group. After full characterization, the solid acid catalyst is used in the acetylation of glycerol. The catalytic reactivity and reusability of the sulfonic acid modified PMO material is investigated. The catalyst showed a catalytic activity and kinetics that are comparable with the commercially available resin, Amberlyst-15, and furthermore our catalyst can be recycled for several subsequent catalytic runs and retains its catalytic activity.