Sample records for diglycidyl resorcinol ether

  1. Synthesis of New Liquid Crystalline Diglycidyl Ethers

    Issam Ahmed Mohammed


    Full Text Available The phenolic Schiff bases I–VI were synthesized by condensation reactions between various diamines, namely o-dianisidine, o-tolidine and ethylenediamine with vanillin or p-hydroxybenzaldehyde and subsequent reactions between these phenolic Schiff bases and epichlorohydrin to produce new diglycidyl ethers Ia–VIa. The structures of these compounds were confirmed by CHN, FT-IR, 1H-NMR, and 13C-NMR spectroscopy. Their thermotropic liquid crystalline behavior was studied using differential scanning calorimetry (DSC and polarizing optical microscopy (POM. All the diglycidyl ethers prepared exhibit nematic mesophases, except for Va and VIa, which did not show any transition mesophases, but simply flow to liquids.

  2. 40 CFR 721.10017 - Amine terminated bisphenol A diglycidyl ether polymer (generic).


    ... diglycidyl ether polymer (generic). 721.10017 Section 721.10017 Protection of Environment ENVIRONMENTAL... ether polymer (generic). (a) Chemical substances and significant new uses subject to reporting. (1) The chemical substances identified generically as amine terminated bisphenol A diglycidyl ether polymer (PMNs P...

  3. Thermal and Mechanical Properties Curing Kinetics of Resorcinol Diglycidyl Ether/m-Xylylene Diamine%间苯二酚缩水甘油醚/间苯二甲胺体系的热机械性能和固化动力学

    杨庆旭; 肖斐


    利用热分析技术对具有高温快速固化性能的间苯二酚缩水甘油醚/间苯二甲胺体系的热机械性能和表观固化反应动力学进行了研究。热机械性能分析(DMA和TMA)结果表明,间苯二酚缩水甘油醚/间苯二甲胺固化产物的玻璃化转变温度为83℃,室温下储能模量为2600 MPa,玻璃态热膨胀系数(α1)为54.9×10-6℃-1,橡胶态的线性热膨胀系数(α2)为177.9×10-6℃-1。通过恒温和非恒温模式差示扫描量热(DSC)测试得到体系的表观反应活化能为62.7 kJ/mol,由此估算出固化反应在160℃时仅需数秒即可完成。%The thermal and mechanical properties of a fast curing system,resorcinol diglycidyl ether/m-xylylene diamine(RDGE/XDA),were investigated by means of thermal analysis techniques.The results of dynamic mechanical analysis(DMA) and thermo-mechanical analysis(TMA) show that the glass transition temperature of RDGE/XDA is 83 ℃,and the storage modulus at room temperature is 2600 MPa.The coefficients of thermal expansion corresponding to the glassy and rubbery state is 54.9×10-6 ℃-1 and 177.9×10-6 ℃-1,respectively.The apparent activation energy obtained through isothermal and non-isothermal differential scanning calorimetry(DSC) measurement is 62.7 kJ/mol.Thus,the curing process of RDGE/XDA takes only a few seconds at 160 ℃ estimated from the curing rate at lower temperature and the apparent activation energy.

  4. Crosslinking and modification of dermal sheep collagen using 1,4-butanediol diglycidyl ether

    Zeeman, R; Dijkstra, PJ; van Wachem, PB; van Luyn, MJA; Hendriks, M; Cahalan, PT; Feijen, J


    Crosslinking of dermal sheep collagen (DSC) was accomplished using 1,4-butanediol diglycidyl ether (BDDGE). At pH values > 8.0, epoxide groups of BDDGE will react with amine groups of collagen. The effects of BDDGE concentration, pH, time, and temperature were studied. Utilization of a 4-wt % BDDGE

  5. Occurrence of bisphenol-F-diglycidyl ether (BFDGE) in fish canned in oil.

    Theobald, A; Simoneau, C; Hannaert, P; Roncari, P; Roncari, A; Rudolph, T; Anklam, E


    The levels of bisphenol-F-diglycidyl ether (BFDGE) were quantified as part of a European survey on the migration of residues of epoxy resins into oil from canned fish. The contents of BFDGE in cans, lids and fish collected from all 15 Member States of the European Union and Switzerland were analysed in 382 samples. Cans and lids were separately extracted with acetonitrile. The extraction from fish was carried out with hexane followed by re-extraction with acetonitrile. The analysis was performed by reverse phase HPLC with fluorescence detection. BFDGE could be detected in 12% of the fish, 24% of the cans and 18% of the lids. Only 3% of the fish contained BFDGE in concentrations considerably above 1 mg/kg. In addition to the presented data, a comparison was made with the levels of BADGE (bisphenol-A-diglycidyl ether) analysed in the same products in the context of a previous study.

  6. Bio-based alternative to the diglycidyl ether of bisphenol A with controlled materials properties.

    Maiorana, Anthony; Spinella, Stephen; Gross, Richard A


    A series of biobased epoxy monomers were prepared from diphenolic acid (DPA) by transforming the free acid into n-alkyl esters and the phenolic hydroxyl groups into diglycidyl ethers. NMR experiments confirmed that the diglycidyl ethers of diphenolates (DGEDP) with methyl and ethyl esters have 6 and 3 mol % of glycidyl ester. Increasing the chain length of DGEDP n-alkyl esters from methyl to n-pentyl resulted in large decreases in epoxy resin viscosity (700-to-11 Pa·s). Storage modulus of DPA epoxy resins, cured with isophorone diamine, also varied with n-alkyl ester chain length (e.g., 3300 and 2100 MPa for the methyl and n-pentyl esters). The alpha transition temperature of the cured materials showed a linear decrease from 158 to 86 °C as the ester length increases. The Young's modulus and tensile strengths were about 1150 and 40 MPa, respectively, for all the cured resins tested (including DGEBA) and varied little as a function of ester length. Degree of cure for the different epoxy resins, determined by FTIR and DSC, closely approached the theoretical maximum. The result of this work demonstrates that diglycidyl ethers of n-alkyl diphenolates represent a new family of biobased liquid epoxy resins that, when cured, have similar properties to those from DGEBA.

  7. Reaction kinetics and modeling of photoinitiated cationic polymerization of an alicyclic based diglycidyl ether

    Harikrishna, R., E-mail: [Polymer Science and Engineering Division, National Chemical Laboratory, Pune 411008 (India); Ponrathnam, S. [Polymer Science and Engineering Division, National Chemical Laboratory, Pune 411008 (India); Tambe, S.S. [Chemical Engineering and Process Development Division, National Chemical Laboratory, Pune 411008 (India)


    Highlights: • Photocationic polymerization of alicyclic based diglycidyl ether was carried out. • Kinetic parameters were influenced by gelation and diffusional restrictions. • Applicability of autocatalytic model was established by nonlinear regression. • System showed higher activation energy than cycloaliphatic and aromatic diepoxides. -- Abstract: Photoinitiated cationic polymerization of cycloaliphatic diepoxides had received tremendous attention, while studies with lesser polymerizable diglycidyl ethers are comparatively less reported. The present work deals with the photoinitiated cationic polymerization of cyclohexane dimethanol diglycidyl ether followed by estimation of kinetic parameters. The effects of concentration of photoinitiator and temperature on curing performance were studied using photo differential scanning calorimeter or photo DSC with polychromatic radiation. It was observed that the rate of polymerization as well as ultimate conversion increased with increasing concentration of photoinitiator and temperature. The influences of gelation as well as diffusional restrictions have remarkable effect on cure performance. The kinetic parameters as per autocatalytic kinetic model were studied by Levenberg–Marquardt nonlinear regression method instead of conventional linear method for obtaining more accurate values of apparent rate constant. It was observed that the model fits with data from initial stages to almost towards the end of the reaction. The activation energy was found to be higher than the values reported for more reactive cycloaliphatic diepoxides. The value of pre-exponential factor increased with increase in activation energy showing influence of gelation at early stages of reaction.

  8. Determination of the diglycidyl ether of bisphenol A and its derivatives in canned foods.

    Biles, J E; White, K D; McNeal, T P; Begley, T H


    Migration of the diglycidyl ether of bisphenol A (DGEBA) to food from can enamels and can pull-top seals is reported. Derivatives of DGEBA are also determined in some foods. Levels of DGEBA in the foods surveyed in this study range from nondetected (DGEBA in water, acid, and saline solutions show conversion to the hydrolysis products and chloro adducts occurs readily. The presence of DGEBA derivatives in food demonstrates that analysis for DGEBA migration alone is not a good indicator of total migration from can coatings to foods.

  9. Bisphenol diglycidyl ethers and bisphenol A and their hydrolysis in drinking water.

    Lane, R F; Adams, C D; Randtke, S J; Carter, R E


    Epoxy coatings are commonly used to protect the interior (and exterior) surfaces of water mains and storage tanks and can be used on the interior surfaces of water pipes in homes, hospitals, hotels, and other buildings. Common major components of epoxies include bisphenols, such as bisphenol A (BPA) or bisphenol F (BPF), and their reactive prepolymers, bisphenol A diglycidyl ether (BADGE) and bisphenol F diglycidyl ether (BFDGE), respectively. There currently are health concerns about the safety of BPA and BPF due to known estrogenic effects. Determination of key bisphenol leachates, development of a hydrolysis model, and identification of stable hydrolysis products will aid in assessment of human bisphenol exposure through ingestion of drinking water. Liquid chromatography/mass spectrometry (LC/MS/MS) was used for quantitation of key analytes, and a pseudo-first order kinetic approach was used for modeling. In fill-and-dump studies on epoxy-coated pipe specimens, BADGE and a BPA-like compound were identified as leachates. The BADGE hydrolysis model predicts BADGE half-lives at pH 7 and 15, 25, 35, and 40 °C to be 11, 4.6, 2.0, and 1.4 days respectively; the BFDGE half-life was 5 days at pH 7 and 25 °C. The two identified BADGE hydrolysis products are BADGE-H2O and BADGE 2H2O, with BADGE 2H2O being the final end product under the conditions studied.

  10. Synthesis of a Novel UV-curable Prepolymer Polypropyleneglycol Diglycidyl Ether Diacrylate

    HUANG Biwu; HUANG Bofen; DU Guoping; CHEN Weiqing


    A novel UV-curable prepolymer polypropyleneglycol diglycidyl ether diacrylate(PPGGEA) was synthesized by utilizing polypropyleneglycol diglycidyl ether(PPGGE)and acrylic acid(AA)as starting materials,N,N-dimethylbenzylamine as catalyst and p-hydroxyanisole as inhibitor.The optimum synthetic conditions were in the following:the concentration of N,N-dimethylbenzylamine was 0.80 wt% of reactants,the concentration of p-hydroxyanisole was 0.3 wt%of reactants.the reaction temperature was 90-110℃,and the molar ratio of PPGGE to AA was 1:2.2.Meanwhile,1-hydroxycyclOhexyl phenyl ketone of a UV-cured initiator was added to the synthesized PPGGEA to prepare a kind of UV-cured coating.The mechanical properties of the UV-cured films were determined,giving 29.99 MPa of tensile strength,834.27 MPa of the Young'S modulus and 5.66%of elongation at tear.

  11. Analysis of reaction products of food contaminants and ingredients: Bisphenol A diglycidyl ether (BADGE) in canned foods

    Coulier, L.; Bradley, E.L.; Bas, R.C.; Verhoeckx, K.C.M.; Driffield, M.; Harmer, N.; Castle, L.


    Bisphenol A diglycidyl ether (BADGE) is an epoxide that is used as a starting substance in the manufacture of can coatings for food-contact applications. Following migration from the can coating into food, BADGE levels decay and new reaction products are formed by reaction with food ingredients. The

  12. Monitoring of bisphenol-A-diglycidyl-ether (BADGE) in canned fish in oil.

    Simoneau, C; Theobald, A; Hannaert, P; Roncari, P; Roncari, A; Rudolph, T; Anklam, E


    A survey at the European levels was initiated on the quantification of bisphenol-A-diglycidyl-ether (BADGE) in canned fish in oil in order to assess the exposure of BADGE. A total of 382 canned fish sample were collected from all 15 Member States and Switzerland and analysed for BADGE in fish. The fish was extracted first with hexane and reextracted with acetonitrile, followed by a membrane filtration and reverse phase HPLC analysis with fluorescence detection. The analysis of the fish showed that about 3% of the samples contained BADGE at a level above 1 mg/kg. The samples exceeding the limit by a larger margin were mostly from anchovy cans and cans manufactured in 1991-1995.

  13. Immediate and delayed allergy from epoxy resins based on diglycidyl ether of bisphenol A.

    Kanerva, L; Jolanki, R; Tupasela, O; Halmepuro, L; Keskinen, H; Estlander, T; Sysilampi, M L


    This case report presents two patients with immediate and delayed allergy to epoxy resins based on diglycidyl ether of bisphenol A (DGEBA). In patch testing, the epoxy resin (DGEBA-based) of the standard series gave allergic reactions. Both patients had a prick test reaction of histamine size or larger to the human serum albumin (HSA) conjugate of DGEBA-based epoxy resins. One had been occupationally exposed to methyl tetrahydrophthalic anhydride (MTHPA) and had a histamine-size prick test reaction to the HSA conjugate of MTHPA; the other did not react to the conjugate. Determinations of specific immunoglobulin E were carried out with HSA-DGEBA conjugates, two DGEBA-based epoxy resins, and phthalic anhydrides. The first patient had positive tests to DGEBA, the DGEBA-based epoxy resins, and two phthalic anhydrides, and the second to DGEBA and the DGEBA-based epoxy resins, but not to the phthalic anhydrides.

  14. Survey of the occurrence of 1,6-hexanediol diglycidyl ether in food contact materials

    This project is a survey of the occurence of 1,6-hexanediol diglycidyl ether (HDDGE) specifically in food contact material on the Danish market This survey clarifies that HDDGE is listed on an inventory for possible use in printing inks food contact materials, but that is not used by European...... producers and importers. The substance is not allowed for use in plastic materials for food contact. One Danish company reported a possible use of HDDGE in coating of drinking tanks and pipelines. This is the only use of HDDGE confirmed in relation to food contact materials in Denmark. The project...... is following up on a previous survey under the Danish EPA’s LOUS-review (Environmental Project no. 1472)....

  15. Synthesis of a novel UV-curable prepolymer neopentyl glycol diglycidyl ether diacrylate and its cured film tensile property

    HUANG Bi-wu; HUANG Bo-fen; CHEN Wei-qing; OUYANG Zhi-qiang


    A novel UV-curable prepolymer neopentyl glycol diglycidyl ether diacrylate(NPGGEA)was synthesized by using neopentyl glycol diglycidyl ether(NPGGE)and acrylic acid(AA)as starting materials, N, N-dimethylbenzylamine as catalyst and p-hydroxyanisole as inhibitor. The optimum synthetic conditions were taken as follows: The concentration of N,N-dimethylbenzylamine, 0.80% of reactants; the concentration of p-hydroxyanisole, 0.3% of reactants; the reaction temperature, 90-110℃; the molar ratio of NPGGE to AA, 1:2.2. Meanwhile, 1-hydroxycyclohexyl phenyl ketone of a UV-cured initiator was added to the synthesized NPGGEA to prepare a kind of UV-cured coating. Mechanical properties of the UV-cured films were determined, giving 28.75 MPa of tensile strength, 923.82 MPa of Young's modulus and 5.51% of elongation at tear.

  16. Synthesis of a Novel UV-curable Prepolymer Hexanediol Diglycidyl Ether Diacrylate and Its Cured Film Tensile Property

    HUANG Biwu; CHEN Weiqing; YANG Zhihong; JIANG Ankun; WENG Zixiang


    A novel UV-curable prepolymer hexanediol diglycidyl ether diacrylate (HDGEA)was synthesized by utilizing hexanediol diglycidyl ether (HDGE) and acrylic acid (AA) as starting materials, N, N-dimethylbenzylamine as catalyst and p-hydroxyanisole as inhibitor. The optimal synthetic conditions were that the concentration of N, N-dimethylbenzylamine was 0.80 wt% of reactants, the concentration of p-hydroxyanisole was 0.3 wt% of reactants, the reaction temperature was 90-110 ℃, and the molar ratio of HDGE to AA was 1 ∶ 2.2. Meanwhile, 1-hydroxycyclohexyl phenyl ketone of a UV-curing initiator was added to the synthesized HDGEA to prepare a kind of UV-curing coating. The mechanical properties of the UV-cured films were determined, giving 31.87 MPa of tensile strength, 871.88 MPa of Young's modulus and 6.77% of elongation at tear.

  17. Luminescence spectroscopy applied to a study of the curing process of diglycidyl-ether of bisphenol-A (DGEBA)

    Rita de Cássia Mendonça Sales; Deborah Dibbern Brunelli


    This work involved the application of luminescence spectroscopy under steady-state conditions to study the curing process of the epoxy resin diglycidyl-ether of bisphenol-A (DGEBA) using the curing agents 4,4'-diaminodiphenylmethane (DDM) and 4,4'-diaminodiphenylsulfone (DDS). Two fluorescence methods were employed: the intrinsic method related to the polymeric matrix and the extrinsic method, using the molecular probe 9-anthroic acid (9-AA). Stoichiometric mixtures, with and without 9-AA, we...

  18. A New Flexible Soy-Based Adhesive Enhanced with Neopentyl Glycol Diglycidyl Ether: Properties and Application

    Jing Luo


    Full Text Available Soy-based adhesives inherently possess low water resistance and brittleness, which limit their application on plywood fabrication. This investigation involves using a long chain cross-linker, neopentyl glycol diglycidyl ether (NGDE, to produce an intrinsic toughening effect to reduce the brittleness and improve the water resistance of a soybean meal–based adhesive. The solids content, viscosity, functional groups, fracture surface micrographs, and thermal stability of the adhesives were measured. Three-layer plywood was fabricated using the resultant adhesive, and the tensile shear strength of the plywood was measured. All adhesive properties were compared with a soybean meal/polyamidoamine-epichlorohydrin (PAE adhesive and commercial melamine urea formaldehyde resin. The results showed that adding 6 g NGDE improved the water resistance of the soybean meal-based adhesive by 12.5%. This improvement is attributed to the following reasons: (1 a dense cross-linked network is formed by the chemical reaction between NGDE and protein molecules; (2 the toughness of the adhesive increases and a smooth and homogeneous fracture surface is created, which effectively prevents moisture intrusion; (3 the addition of NGDE increases the thermostability of the cured adhesive. The tensile shear strength of the plywood bonded with the soybean meal-based adhesive with 6 g NGDE was 286.2% higher than that without NGDE and attained 1.12 MPa, which was attributed to the reduction in the adhesive’s viscosity, and the improvement in the water resistance and toughness of the adhesive. The tensile shear strength of the plywood bonded with 6 g NGDE was 19.1% higher than that with 6 g PAE and was similar to the MUF resin, which validated the novel adhesive being suitable for use as an industrial plywood adhesive.

  19. [Determination of eight bisphenol diglycidyl ethers in water by solid phase extraction-high performance liquid chromatography-tandem mass spectrometry].

    Zhang, Haijing; Lin, Shaobin


    A solid phase extraction coupled with high performance liquid chromatography-tandem mass spectrometry (SPE-HPLC-MS/MS) method was developed for the determination of eight bisphenol diglycidyl ethers, including bisphenol A diglycidyl ether (BADGE), bisphenol A (3-chloro-2-hydroxypropyl) glycidyl ether (BADGE x HCl), bisphenol A bis (3-chloro-2-hydroxypropyl) ether (BADGE x 2HCl), bisphenol A (2, 3-dihydroxypropyl) glycidyl ether (BADGE x H2O), bisphenol A bis(2,3-dihydroxypropyl) ether (BADGE x 2H2O), bisphenol A (3-chloro-2-hydroxypropyl) (2,3-dihydroxypropyl) ether (BADGE x HCl x H2O), bisphenol F diglycidyl ether (BFDGE) and bisphenol F bis (3-chloro-2-hydroxypropyl) ether (BFDGE 2HCl) in water. A total of ten samples were collected from the leaching of the coatings for drinking water supply system. Then, 200 mL exposure water was preconcentrated on C18 solid-phase extraction cartridge. The eight compounds were analyzed by liquid chromatography-tandem mass spectrometry method on a C18 column by the gradient elution with methanol, water and 5 mmol/L ammonium acetate as mobile phases in the multiple reaction monitoring (MRM) scan mode. The external matrix standard solutions were used for the quantitative determination and the calibration curves of the eight compounds showed good linearity in the range of 0.007-5.00 microg/L with the correlation coefficients more than 0.999 0. The limits of quantification (LOQs) of the method were 7-91 ng/L. The spiked recoveries ranged from 79.1% to 101% with the relative standard deviations of 4.0% - 12%. The method is sensitive and accurate, and is applicable to the determination of bisphenol diglycidyl ethers in water.

  20. Novel Finding of Widespread Occurrence and Accumulation of Bisphenol A Diglycidyl Ethers (BADGEs) and Novolac Glycidyl Ethers (NOGEs) in Marine Mammals from the United States Coastal Waters.

    Xue, Jingchuan; Kannan, Kurunthachalam


    Bisphenol A diglycidyl ether (BADGE)- and bisphenol F diglycidyl ether (BFDGE)-based epoxy resins have a broad range of applications, including serving as inner coatings of food and beverage cans and as protective coatings in marine construction. Prior to this study, no studies had examined the occurrence and bioaccumulation of BADGEs or BFDGEs in aquatic organisms. In this study, BADGE, BFDGE, and nine of their derivatives were determined in 121 tissue (liver, kidney, blubber, and brain) samples from eight species of marine mammals collected from the U.S. coastal waters of Florida, California, Washington, and Alaska. BADGE·2HCl was the predominant compound found in the majority (78.5%) of the marine mammal tissues analyzed, at concentrations of up to 2950 ng/g (wet weight (wt)) found in the liver of a sea otter from Kachemak Bay, Alaska. The measured concentrations of BADGE·2HCl in marine mammals were on the order of hundreds of nanograms per gram tissue, which are some of the highest concentrations ever reported for this compound in biota. Males contained greater concentrations of BADGE·2HCl than did females. BADGE·2HCl also was found in the brain tissues of sea otters. Trace levels of BADGE·2HCl were found in the livers of polar bears from Alaska, which suggested that BADGEs are widely distributed in the oceanic environment.

  1. Effects of Different Montmorillonite Nanoclay Loading on Cure Behavior and Properties of Diglycidyl Ether of Bisphenol A Epoxy

    Alfred Tcherbi-Narteh


    Full Text Available The primary focus of this study was to understand the effects of different amounts of montmorillonite nanoclay (MMT loading on viscosity, cure behavior, reaction mechanism, and properties of diglycidyl ether of bisphenol A (DGEBA epoxy composites. Influence of 1–3 wt.% MMT on rheological and subsequent cure behavior of SC-15 epoxy resin was studied using nonisothermal and isothermal rheometry and differential scanning calorimetry (DSC. Rheological properties were influenced by different amounts of MMT at lower shear rates prior to and during curing. Cure reaction mechanism was unaffected by different MMT concentration; however heat and activation energy of reactions increased with increasing MMT loading. Samples with 2 wt.% MMT showed highest reaction rate constant, indicative of catalytic behavior. X-ray diffraction (XRD and transmission electron microscope (TEM revealed mainly intercalated microstructure throughout the MMT infused epoxy composite samples irrespective of the percent loading.

  2. Luminescence spectroscopy applied to a study of the curing process of diglycidyl-ether of bisphenol-A (DGEBA

    Rita de Cássia Mendonça Sales


    Full Text Available This work involved the application of luminescence spectroscopy under steady-state conditions to study the curing process of the epoxy resin diglycidyl-ether of bisphenol-A (DGEBA using the curing agents 4,4'-diaminodiphenylmethane (DDM and 4,4'-diaminodiphenylsulfone (DDS. Two fluorescence methods were employed: the intrinsic method related to the polymeric matrix and the extrinsic method, using the molecular probe 9-anthroic acid (9-AA. Stoichiometric mixtures, with and without 9-AA, were heated to 120 °C at a 5 °C/min heating rate. These samples were then cured at 120 °C for a further 2 hours and allowed to cool to room temperature for 20 minutes. The results obtained by the two methods indicate that the cross-linking reaction can be monitored by analyzing the spectral changes of the emission bands of DGEBA, curing agents and 9-AA.

  3. Effects of Surface Treatments of Montmorillonite Nanoclay on Cure Behavior of Diglycidyl Ether of Bisphenol A Epoxy Resin

    Alfred Tcherbi-Narteh


    Full Text Available Diglycidyl ether of Bisphenol A (DGEBA based SC-15 epoxy resin was modified with three different commercially available montmorillonite (MMT nanoclay: Nanomer I.28E and Cloisite 10A and 30B. Cure behavior of nanocomposites was studied using a variety of techniques. Primary focus of this study was to investigate influence of different surface modifications of MMT nanoclay on rheological properties and cure behavior of SC-15 epoxy resin. By adding MMT to SC-15 epoxy resin, chemistry of the epoxy is altered leading to changes in rheological properties and ultimately enthalpy and activation energy of reactions. Addition of Nanomer I.28E delayed gelation, while Cloisite 10A and 30B accelerated gelation, regardless of the curing temperature. Activation energy of reaction was lower with the addition of Nanomer I.28E and Cloisite 10A and higher for Cloisite 30B compared to neat SC-15 epoxy composite.

  4. Analogues of the epoxy resin monomer diglycidyl ether of bisphenol F: effects on contact allergenic potency and cytotoxicity.

    O'Boyle, Niamh M; Delaine, Tamara; Luthman, Kristina; Natsch, Andreas; Karlberg, Ann-Therese


    Diglycidyl ethers of bisphenol A (DGEBA) and bisphenol F (DGEBF) are widely used as components in epoxy resin thermosetting products. They are known to cause occupational and nonoccupational allergic contact dermatitis. The aim of this study is to investigate analogues of DGEBF with regard to contact allergy and cytotoxicity. A comprehensive knowledge of the structural features that contribute to the allergenic and cytotoxic effects of DGEBF will guide the development of future novel epoxy resin systems with reduced health hazards for those coming into contact with them. It was found that the allergenic effects of DGEBF were dependent on its terminal epoxide groups. In contrast, it was found that the cytotoxicity in monolayer cell culture was dependent not only on the presence of epoxide groups but also on other structural features.

  5. New chemically reworkable epoxy coatings obtained by the addition of polyesters with star topologies to diglycidyl ether of bisphenol A resins

    Tomuta, Adrian Marius; Ramis Juan, Xavier; Fernández Francos, Xavier; Ferrando Piera, Francesc; Serra Albet, Àngels


    A new multiarm star with hyperbranched aromatic–aliphatic polyester core and poly(ɛ-caprolactone) arms (HBPCL) was synthesized and characterized. Mixtures of diglycidyl ether of bisphenol A (DGEBA) resin and different proportions of this star type modifier were cured using a thermal cationic curing agent, Yb(OTf)3. The HBPCL prepared has hydroxyl groups as chain ends, which are capable of chemically incorporating to the epoxy matrix by means of the monomer activated mechanism. This, together ...

  6. Estimation of intake of bisphenol-A-diglycidyl-ether (BADGE) from canned fish consumption in Europe and migration survey.

    Simoneau, C; Theobald, A; Wiltschko, D; Anklam, E


    The exposure to bisphenol-A-diglycidyl-ether (BADGE) from canned fish in oil was assessed from consumption data collected for each Member State of the European Union and Switzerland, and migration data from a European survey on 382 samples. Trade figures were used when no consumption data were available. The average consumption of canned fish in Europe was 2.3 kg per person per year, with values ranging from 0.2 kg per person per year in the United Kingdom to 5.1 kg per person per year in Denmark. The exposure to BADGE was calculated as microgram per person per day. The data indicated that exposure to BADGE was in the range below 4 mg per person per year, i.e. 9 micrograms per person per day, hence a fairly low exposure in part due to the fact that canned fish is a relatively minor dietary item. An approximation assuming the general figure of a 60 kg adult, would thus be 0.15 microgram/kg body weight per day. This is a fairly limited exposure considering the provisional limit in food had been set a 1 mg/kg and assumed 1 kg of food ingested. In countries for which increased exposure was found, the reason was mainly caused by one individual sample exhibiting a high concentration rather than a larger number of samples with mildly elevated concentrations.

  7. 双酚A二缩水甘油醚的合成%Synthesis of diglycidyl ether of bisphenol A

    赵洪池; 马双霞; 王耀辉; 李江涛; 陈世辉; 王苗苗


    以双酚A(BPA)和环氧氯丙烷(ECH)为原料,在NaOH作催化剂的条件下合成了双酚A二缩水甘油醚(DGEBA).考察了w(NaOH)、反应温度、反应时间、n(ECH)/n(BPA)对DGEBA产率的影响.DGEBA的熔点为47.5℃.提高w(NaOH)和n(ECH)/n(BPA),延长反应时间,DGEBA的产率均呈现先增大后减小的趋势;DGEBA产率随着反应温度的升高而降低;当n(ECH)/n(BPA)为10∶1,w(NaOH)为30%,反应温度为75℃,反应时间为170 min时,DGEBA产率可达到80.1%.%Diglycidyl ether of bisphenol A (DGEBA) was prepared by using bisphenol A (BPA) and epichlo-rohydrin (ECH) as raw materials in the catalysis of sodium hydroxide. The effects of the mass fraction of sodium hydroxide, reaction temperature and time as well as molar ratio of ECH to BPA on DGEBA yield were investigated. The melting point of DGEBA was 47.5 ℃. The DGEBA yield had a tendency to increase first and then decrease with increasing the mass fraction of sodium hydroxide, molar ratio of ECH to BPA and reaction time, while the yield decreased with the rise in the reaction temperature. The yield of DGEBA reached 80.1% when the molar ratio of ECH to BPA was10 : 1, mass fraction of sodium hydroxide was 30%, reaction temperature was 75 ℃ and reaction time was 170 min.

  8. The utilization of the mesoporous Ti-SBA-15 catalyst in the epoxidation of allyl alcohol to glycidol and diglycidyl ether in the water medium

    Wróblewska Agnieszka


    Full Text Available This work presents the studies on the optimization the process of allyl alcohol epoxidation over the Ti-SBA-15 catalyst. The optimization was carried out in an aqueous medium, wherein water was introduced into the reaction medium with an oxidizing agent (30 wt% aqueous solution of hydrogen peroxide and it was formed in the reaction medium during the processes. The main investigated technological parameters were: the temperature, the molar ratio of allyl alcohol/hydrogen peroxide, the catalyst content and the reaction time. The main functions the process were: the selectivity of transformation to glycidol in relation to allyl alcohol consumed, the selectivity of transformation to diglycidyl ether in relation to allyl alcohol consumed, the conversion of allyl alcohol and the selectivity of transformation to organic compounds in relation to hydrogen peroxide consumed. The analysis of the layer drawings showed that in water solution it is best to conduct allyl alcohol epoxidation in direction of glycidol (selectivity of glycidol 54 mol% at: the temperature of 10–17°C, the molar ratio of reactants 0.5–1.9, the catalyst content 2.9–4.0 wt%, the reaction time 2.7–3.0 h and in direction of diglycidyl ether (selectivity of diglycidyl ether 16 mol% at: the temperature of 18–33°C, the molar ratio of reactants 0.9–1.65, the catalyst content 2.0–3.4 wt%, the reaction time 1.7–2.6 h. The presented method allows to obtain two very valuable intermediates for the organic industry.

  9. Unexpected differences between thermal and photoinitiated cationic curing of a diglycidyl ether of bisphenol A modified with a multiarm star poly(styrene-b-poly(ε-caprolactone polymer

    J. M. Morancho


    Full Text Available The effect of adding a multiarm star poly(styrene-b-poly(ε-caprolactone polymer on the cationic thermal and photoinitiated curing of diglycidyl ether of bisphenol A was studied. This star-polymer decelerated the thermal curing of diglycidyl ether of bisphenol A and modified the final structure of the epoxy matrix. The photocuring was influenced significantly by the addition of the multiarm star. When the proportion of this modifier added was 5%, much more time was necessary for complete photocuring (160 min at 40ºC. In the presence of 10% of modifier, the degree of photocuring reached was very low (0.196 at 120°C. A subsequent thermal post-curing was necessary to cure completely the system. During photocuring in presence of poly(styrene-b-poly(ε-caprolactone, the formation of dormant species, which are reactivated when the temperature increases, takes places. The kinetics of the thermal curing and the photocuring was analyzed using an isoconversional method due to the complexity of the reactive process. Applying this method, it has been confirmed the dependence of activation energy on the degree of conversion. The fracture morphology analyzed by scanning electron microscopy exhibited a second phase originated during photocuring by the presence of the modifier.

  10. 40 CFR 721.7260 - Polymer of poly-ethylene-polyamine and alkanediol di-gly-cidyl ether.


    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Polymer of poly-ethylene-polyamine and... New Uses for Specific Chemical Substances § 721.7260 Polymer of poly-ethylene-polyamine and alkanediol... chemical substance identified generically as polymer of polyethylenepolyamine and alkanediol diglycidyl...

  11. Curing Kinetics and Thermal Stability of Diglycidyl Ether of Bisphenol-A Using Mixtures of Heterocyclic Derivatives of Stannanes and 4,4'-Diaminodiphenylsulfone

    SINGH Vikram; DEEP Gagan; NARULA Anudeep Kumar


    Curing kinetics of diglycidyl ether of bisphenol-A (DGEBA) in the presence of varying molar ratios of derivafives of stannanes to 4,4'-diaminodiphenylsulfone (DDS) was investigated by the dynamic differential scanning calorimetry. The derivatives were synthesized by reacting 1 mole of biguanide (B) with 1 mole of phenylethyltindihydride (PETH) or phenylmethyltindihydride (PMTH) or phenylbutyltindihydride (PBTH) and designated as BPETH or BPMTH or BPBTH respectively. These derivatives were characterized by elemental analysis and spectroscopic techniques such as IR, 1H NMR, 13C NMR and 119Sn NMR. The mixtures of these derivatives to DDS at of epoxy resins. The thermal stability of the isothermally cured resins was also evaluated using dynamic thermogravimetry in a nitrogen atmosphere.

  12. Effect of heat processing and storage time on migration of bisphenol A (BPA) and bisphenol A-diglycidyl ether (BADGE) to aqueous food simulant from Mexican can coatings.

    Munguia-Lopez, E M; Soto-Valdez, H


    Effects of heat processing and storage time (up to 70 days) on migration of bisphenol A (BPA) and bisphenol A-diglycidyl ether (BADGE) from can coatings into an aqueous food simulant were determined. Distilled water was canned in two types of Mexican cans: for tuna and for jalapeño peppers. Results showed that there is an effect of heat treatment on migration of both compounds. Storage time did not show any effect in BPA migration from tuna cans. There was an effect of storage time on BPA migration from jalapeño pepper cans. Results for BADGE migration were affected by its susceptibility to hydrolyze in aqueous simulants. BADGE concentration decreased, or was not detected, during storage in both types of cans. Migration levels for BPA and BADGE were within 0.6-83.4 and Mercosur legislation limits. Other migrating compounds were detected, although no identification was performed.

  13. Widespread occurrence of bisphenol A diglycidyl ethers, p-hydroxybenzoic acid esters (parabens), benzophenone type-UV filters, triclosan, and triclocarban in human urine from Athens, Greece.

    Asimakopoulos, Alexandros G; Thomaidis, Nikolaos S; Kannan, Kurunthachalam


    Biomonitoring of human exposure to bisphenol A diglycidyl ethers (BADGEs; resin coating for food cans), p-hydroxybenzoic acid esters (parabens; preservatives), benzophenone-type UV filters (BP-UV filters; sunscreen agents), triclosan (TCS; antimicrobials), and triclocarban (TCC; antimicrobials) has been investigated in western European countries and North America. Nevertheless, little is known about the exposure of Greek populations to these environmental chemicals. In this study, 100 urine samples collected from Athens, Greece, were analyzed by liquid chromatography-tandem mass spectrometry (HPLC-MS/MS) for the determination of total concentrations of five derivatives of BADGEs, six parabens and their metabolite (ethyl-protocatechuate), five derivatives of BP-UV filters, TCS, and TCC. Urinary concentrations of BADGEs, parabens, ethyl-protocatechuate, BP-UV filters, TCS and TCC (on a volume basis) ranged 0.3-20.9 (geometric mean: 0.9), 1.6-1010 (24.2), paraben (100%), bisphenol A bis (2,3-dihydroxypropyl) ether (90%), ethyl paraben (87%), 2,4-dihydroxybenzophenone (78%), propyl paraben (72%), and TCS (71%). Estimated daily intakes (EDIurine), calculated on the basis of the measured urinary concentrations, ranged from 0.023 μg/kg bw/day for Σ5BADGEs to 31.4 μg/kg bw/day for Σ6Parabens.

  14. Matrix effect on leaching of Bisphenol A diglycidyl ether (BADGE) from epoxy resin based inner lacquer of aluminium tubes into semi-solid dosage forms.

    Lipke, Uwe; Haverkamp, Jan Boris; Zapf, Thomas; Lipperheide, Cornelia


    To study the impact of different semi-solid dosage form components on the leaching of Bisphenol A (BPA) and Bisphenol A diglycidyl ether (BADGE) from the epoxy resin-based inner lacquer of aluminium tubes, the tubes were filled with different matrix preparations and stored at an elevated temperature. Despite compliance with the European Standards EN 15348 and EN 15766 on porosity and polymerisation of internal coatings of aluminium tubes, the commercially available tubes used in the study contained an increased amount of polymerisation residues, such as unbound BPA, BADGE and BADGE derivatives in the lacquer, as determined by acetonitrile extraction. Storage of Macrogol ointments in these tubes resulted in an almost quantitative migration of the unbound polymerisation residues from the coating into the ointment. In addition, due to alterations observed in the RP-HPLC chromatograms of the matrix spiked with BADGE and BADGE derivatives it is supposed that the leachates can react with formulation components. The contamination of the medicinal product by BPA, BADGE and BADGE derivatives can be precluded by using aluminium tubes with an internal lacquer with a low degree of unbound polymerisation residues. Copyright © 2015 The Authors. Published by Elsevier B.V. All rights reserved.

  15. Effect of Chitosan Loading on the Morphological, Thermal, and Mechanical Properties of Diglycidyl Ether of Bisphenol A/Hexamethylenediamine Epoxy System

    B. Satheesh


    Full Text Available The effect of chitosan filled diglycidyl ether of bisphenol A (DGEBA epoxy system were investigated using the thermal, mechanical, and morphological properties. The mixing ratio of resin/hardener was kept constant while the chitosan of 1.0, 2.5, 5.0, 7.5, and 10 weight percentage (wt% was incorporated into the system. The thermal stability and the transition behaviour of the chitosan filled epoxy system were analysed through a differential scanning calorimetry (DSC, thermogravimetric analysis (TGA, and Fourier transform infrared spectroscopy (FTIR while atomic force microscope (AFM and scanning electron microscopy (SEM were used to investigate the morphology. It was observed that the additive tends to agglomerate, with the formation of clear phase separation, when the chitosan content increases above 5 wt%. At lower chitosan loading (2.5 wt% and below, relatively uniform dispersion of the additive can be achieved. The thermal stability of the system increases with chitosan loading while the mechanical tensile strength is compromised.

  16. Occurrence of phthalate diesters (phthalates), p-hydroxybenzoic acid esters (parabens), bisphenol A diglycidyl ether (BADGE) and their derivatives in indoor dust from Vietnam: Implications for exposure.

    Tran, Tri Manh; Minh, Tu Binh; Kumosani, Taha A; Kannan, Kurunthachalam


    Phthalate diesters (phthalates), esters of p-hydroxybenzoic acid (parabens), and bisphenol A diglycidyl ether (BADGE) are used in personal care products, food packages, household products, or pharmaceuticals. These compounds possess endocrine-disrupting potentials and have been reported to occur in the environment. Nevertheless, no previous studies have reported the occurrence of these compounds in indoor dust from Vietnam. In this study, nine phthalates, six parabens, and four BADGEs were determined in indoor dust samples collected from Hanoi, Hatinh, Hungyen, and Thaibinh, in Vietnam. Total concentrations of phthalates, parabens, and BADGEs in indoor dust ranged from 3440 to 106,000 ng/g (median: 22,600 ng/g), 40-840 ng/g (median: 123 ng/g), and 23 to 1750 ng/g (median: 184 ng/g), respectively. Based on the measured median concentration of phthalates, parabens, and BADGEs in indoor dust, we estimated human exposure doses to these compounds through indoor dust ingestion for various age groups. The exposure doses to phthalates, parabens, and BADGEs decreased with age and ranged from 19.4 to 90.4 ng/kg-bw/d, 0.113-0.528 ng/kg-bw/d, and 0.158-0.736 ng/kg-bw/d, respectively. This is the first study on the occurrence and human exposure of phthalates, parabens, and BADGEs in indoor dust from Vietnam.

  17. Chemical modification of wheat protein-based natural polymers: grafting and cross-linking reactions with poly(ethylene oxide) diglycidyl ether and ethyl diamine.

    Kurniawan, Lusiana; Qiao, Greg G; Zhang, Xiaoqing


    Mobile poly(ethylene oxide) diglycidyl ether (PEODGE) segments were chemically grafted onto a soluble wheat protein (WP), and different network structures were formed via coupling reactions with ethyl diamine (EDA) in different PEODGE/EDA (PE) ratios. When the PE ratio was 1:1, linear PEs were the predominant segments grafted onto WP chains and the whole WP-PEODGE-EDA (WPE) system was still soluble with an increased molecular weight. Reducing the amount of EDA in the systems produced insoluble cross-linked WPE networks. The broad distribution of network structures and chain mobility resulted in a broad glass transition for the WPE materials. However, the glass transition started at lower temperatures, and the materials became flexible at room temperature. The PE segments were present in all rigid, intermediate, and mobile phases in WPE networks, while the proportion of mobile WP chains was increased as a result of the plasticization effect from the mobile PE segments. The mobility of the most mobile component lipid was also restricted to some extent when forming the cross-linked WPE networks. The study demonstrated that the formation of different network structures with PE segments could significantly improve the flexibility of WP materials, vary the solubility, and modify the mechanical performance of WP-based natural polymer materials.


    Darshana; Priti Malhotra; A.K.Narula


    The curing behavior of diglycidyl ether of bisphenol-A(DGEBA)with aromatic diamide-diimide-diamines having aryl ether,sulfone and methylene linkages was studied by differential scanning calorimetry(DSC).Nine diamide-diimide diamines of varying structure were synthesized by reacting 1 mole of dianhydride with 2 moles of L-cysteine(S)in a mixture of acetic acid and pyridine(3:2 V/V)followed by activation with thionyl chloride(SOCl2)and then condensation with excess of diamines.Structural characterization of diamide-diimide-diamines was done by using FTIR,1H-NMR,13C-NMR spectroscopy and elemental analysis.The peak exotherm temperature(Tp)was lowest in DGEBA cured using EPSM and highest in DGEBA cured using ENSS.Thermal stability of the isothermally cured DGEBA with diamide-diimide-diamines was investigated using dynamic thermogravimetry(TGA)in nitrogen atmosphere,and it was found that NTDA based diamide-diimide-diamines provided good stability to DGEBA.The char yield was highest for resin cured with ENSE which might be due to the presence of more compact structure i.e.naphthalene.

  19. 羟乙基化双酚A环氧树脂的合成与性能研究%Synthesis and properties of diglycidyl ether of ethoxylated bisphenol-A

    何佩佩; 杨欣; 黄伟


    A low viscosity epoxy resin named diglycidyl ether of ethoxylated bisphenol-A (DGEBAEO-2.25)was synthesized by one-step method using solid sodium hydroxide as catalyst.The structure of DGEBAEO-2.25 was characterized by FT-IR,1H-NMR,and GPC.The DGEBAEO-2.25 was cured by 4,4'-diamino diphenyl sulfone (DDS).The viscosity,curing reactivity,thermal and mechanical properties of the DGEBAEO-2.25 system were investigated by comparison with the diglycidyl ether of bisphenol-A (DGEBA,epoxy value 0.51) system.The results showed that DGEBAEO-2.25 had lower viscosity which was one seventh of DGEBA and the curing reactivity and glass transition temperature were lower than that of DGEBA.The toughness of the cured product was significantly improved and the impact strength was two times higher than that of DGEBA.The tensile,flexural strength and modulus were essentially unchanged.%使用固体NaOH为催化剂,通过一步法合成了低粘度的羟乙基化双酚A环氧树脂(DGEBAEO-2.25),并利用FT-IR,1H-NMR,GPC对产物的结构进行了表征.采用4,4’-二氨基二苯砜(DDS)固化DGEBAEO-2.25,通过与双酚A环氧树脂(DGEBA,环氧值0.51)体系的比较,研究了DGEBAEO-2.25体系的粘度、固化活性、热性能及力学性能.结果表明,DGEBAEO-2.25的粘度仅为DGEBA的1/7;固化活性及玻璃化温度降低;固化物韧性明显提高,冲击强度提高2倍多,且拉伸、弯曲强度和模量基本保持不变.

  20. Occurrence and human exposure of p-hydroxybenzoic acid esters (parabens), bisphenol A diglycidyl ether (BADGE), and their hydrolysis products in indoor dust from the United States and three East Asian countries.

    Wang, Lei; Liao, Chunyang; Liu, Fang; Wu, Qian; Guo, Ying; Moon, Hyo-Bang; Nakata, Haruhiko; Kannan, Kurunthachalam


    p-Hydroxybenzoic acid esters (parabens) and bisphenol A diglycidyl ether (BADGE) are widely present in personal care products, food packages, and material coatings. Nevertheless, little is known about the occurrence of these compounds in indoor dust. In this study, we collected 158 indoor dust samples from the U.S., China, Korea, and Japan and determined the concentrations of 11 target chemicals, viz., six parabens and their common hydrolysis product, 4-hydroxybenzoic acid (4-HB), as well as BADGE and its three hydrolysis products (BADGE·H(2)O, BADGE·2H(2)O, and BADGE·HCl·H(2)O). All of the target compounds were found in dust samples from four countries. Concentrations of sum of six parabens in dust were on the order of several hundred to several thousands of nanogram per gram. Geometric mean concentrations of BADGEs in dust ranged from 1300 to 2890 ng/g among four countries. Methyl paraben (MeP), propyl paraben (PrP), BADGE·2H(2)O, and BADGE·HCl·H(2)O were the predominant compounds found in dust samples. This is the first report of BADGE and its hydrolysis products (BADGEs) in indoor dust samples and of parabens in indoor dust from Asian countries. On the basis of the measured concentrations of target chemicals, we estimated the daily intake (EDI) via dust ingestion. The EDIs of parabens via dust ingestion were 5-10 times higher in children than in adults. Among the four countries studied, the EDIs of parabens (5.4 ng/kg-bw/day) and BADGEs (6.5 ng/kg-bw/day) through dust ingestion were the highest for children in Korea and Japan.

  1. 超支化聚苯醚对双酚A型环氧树脂的低介电改性%Low dielectric constant modification of bisphenol A diglycidyl ether with hyperbranched poly (phenylene oxide)

    吕健勇; 孟焱; 何立凡; 邱藤; 李效玉; 王海侨


    自制了一种反应型端环氧基超支化聚苯醚(EHPPO),将其添加到双酚A型环氧树脂中进行改性并用酸酐固化剂固化,表征了固化样品的热性能、力学性能和介电性能.此外还使用分子主链结构相同、端基为非反应型苄基的超支化聚苯醚(CHPPO)进行了对比改性研究.结果表明,两种不同的改性剂对双酚A型环氧树脂的改性效果各有优势,其中,使用EHPPO改性得到的环氧树脂具有更加优异的热性能和拉伸强度,而由CHPPO改性的环氧树脂介电常数相对更低.%A reactive epoxidized hyperbranched poly(phenylene oxide) (EHPPO) was added to the diglycidyl ether of bisphenol A (DGEBA) to form a hybrid which was cured with methyl-5-norbornene-2,3-dicarboxylic anhydride (methyl nadic anhydride) in order to improve its thermal and dielectric properties.The thermal and dielectric properties of the cured hybrid were investigated.In addition,as a non-reactive modifier,benzyl-capped hyperbranched poly (phenylene oxide) (CHPPO) was prepared and added to DGEBA for comparison.The results showed that addition of EHPPO and CHPPO can improve both thermal and dielectric properties of DGEBA.Hybrids with EHPPO have much higher glass transition temperature and better thermal stability than those with CHPPO,whereas,DGEBA/CHPPO hybrids have lower dielectric constants than DGEBA/EHPPO hybrids.

  2. A multi-class bioanalytical methodology for the determination of bisphenol A diglycidyl ethers, p-hydroxybenzoic acid esters, benzophenone-type ultraviolet filters, triclosan, and triclocarban in human urine by liquid chromatography-tandem mass spectrometry.

    Asimakopoulos, Alexandros G; Wang, Lei; Thomaidis, Nikolaos S; Kannan, Kurunthachalam


    A liquid-liquid extraction (LLE; ethyl acetate) protocol, followed by liquid chromatography-electrospray ionization tandem mass spectrometry (LC-ESI-MS/MS) methodology, was developed for the determination of 19 compounds, including bisphenol A diglycidyl ethers (BADGEs; industrial ethers), benzophenone-type UV filters (BP-UV filters; precursors and metabolites), p-hydroxybenzoic acid esters (parabens; preservatives), triclosan (TCS) and triclocarban (TCC) in human urine. Urine specimens were enzymatically deconjugated with β-glucuronidase (from Helix pomatia) and extracted by a LLE procedure for the measurement of total concentrations (i.e., free+conjugated forms) of target analytes. Absolute recoveries of BADGEs, BP-UV filters, parabens, TCS and TCC ranged 25-135%, 84-125%, 52-126%, 75-118% and 90-124%, respectively. Method precision (absolute values; N=5 replicate analyses at the fortification level of 10 ng, k=5 days) ranged from 5.8 (ethyl paraben) to 24.0% (TCS). The limits of quantification (LOQs) varied depending on the target compound and generally ranged from 0.2 to 2.0 ng/mL. The matrix effects ranged from +11 (2,3,4-trihydroxybenzophenone) to -86% (2,4-dihydroxybenzophenone). A total of 30 urine specimens collected from Athens, Greece, were analyzed for the 19 target compounds to demonstrate the applicability of the developed method. The concentrations of target chemicals in urine were presented on volume-, specific gravity (SG)-, and creatinine-normalization bases. MeP, EtP, PrP, OH-EtP, BADGE·2H2O, BP-1 and TCS were found frequently in urine at concentrations in the range of 2.7-436 ng/mL, <0.5-25.4 ng/mL, <0.5-575 ng/mL, <2-18.4 ng/mL, <0.5-13.8 ng/mL, <1-14.6 ng/mL and <0.5-95.3 ng/mL, respectively. Copyright © 2013 Elsevier B.V. All rights reserved.

  3. Caracterização do sistema éter diglicidílico do bisfenol A / poliaminas alifáticas Characterization of diglycidyl ether of bisphenol A / aliphatic polyamines systems

    Filiberto González-Garcia


    Full Text Available O sistema epoxídico constituído pelo éter diglicidílico do bisfenol A (DGEBA, produto DER 331 com endurecedor 24 comercializados pela Dow Química do Brasil foi caracterizado por métodos espectroscópicos, calorimétricos e de determinação de grupos funcionais. O endurecedor 24 é constituído por trietilenotetramina (60 % molar e uma mistura de etilenoaminas polifuncionais com estruturas lineares, ramificadas e cíclicas. O equivalente epoxídico da resina resultou de 187 g eq-1. A funcionalidade média, o equivalente de amina, e a concentração do endurecedor que satisfaz a estequiometria, corresponde a 5,54, 27,5 g eq-1, e 14,7 phr, respectivamente. O sistema epoxídico manifestou uma entalpia de reação de 486 J g-1 (106,6 kJ eq-1, e uma temperatura de transição vítrea (Tg¥ de 124 ºC. O trabalho apresenta ainda um programa de cura em duas etapas onde se alcança a conversão máxima, e se apresenta o diagrama de transformações conversão vs temperatura (CTT.Diglycidyl ether of the bisphenol A (DGEBA, product DER 331 and hardener 24 system marketed by Chemical Dow of Brazil were characterized by spectroscopic, calorimetric and determination of functional groups methods. The hardener 24 is constituted by triethylenetetramine (60 % molar and a mixture of ethylene polyfunctional amines with linear, ramified and cyclic structures. The epoxy equivalent of the resin corresponds to 187 g eq-1. The functionality average, equivalent amine, and the concentration of the hardener that satisfy the stoichiometry corresponds to 5.54, 27.5 g eq-1, and 14.7 phr, respectively. The epoxy system displayed an enthalpy of reaction of 486 J g-1 (106.6 kJ eq-1, and a glass transition temperature (Tg¥ of 124 ºC. Also presented in this work is a cure program in two stages where the maximum conversion was reached.

  4. Determination of bisphenol diglycidyl ether residues in canned foodstuffs by high performance liquid chromatographytandem mass spectrometry%高效液相色谱-串联质谱法同时测定肉类罐头中双酚-二缩水甘油醚

    赵晓亚; 付晓芳; 王鹏; 李晶; 胡小钟


    An accurate quantitative determination and confirmative method for bisphenol diglycidyl ether residues, bisphenol A diglycidyl ether ( BADGE) , bisphenol F diglycidyl ether (BFDGE), bisphenol A (2,3-dihydroxypropyl)glycidyl ether (BADGE -H2O) , bisphenol A bis (2,3-dihydroxypropyl) ether (BADGE -2H2O) , bisphenol A (3-chloro-2-hydroxy propyl) (2,3-dihydroxypropyl) ether (BADGE -H2O -HC1) , bisphenol A (3-chloro-2-hydroxypropyl)glycidyl ether (BADGE -HC1) , bisphenol A bis(3-chloro-2-hydroxypropyl) ether (BADGE -2HC1) , bisphenol F bis ( 2, 3-dihydroxypropyl) ether (BFDGE -2H2O), bisphenol F bis ( 3-chloro-2-hydroxypropyl) ether ( BFDGE -2HC1) in canned foodstuffs by high performance liquid chroma-tography-tandem mass spectrometry ( HPLC-MS/MS) has been established. The sample was extracted with teri-butylmethyl ether and the extract was cleaned-up and concentrated on a Waters Oasis HLB column. The target compounds were analyzed by HPLC-MS/MS on a C18column by the gradient elution with methanol and 5 mmol/L ammonium acetate containing 0. 1 % formic acid in a multiple reaction monitoring (MRM) scan mode. External matrix standard solutions were used for the quantitative determination and the calibration curves showed good linearity in the concentration range of 10. 0 -2 000. 0 μg/L for the nine target compounds. The limits of quantification of the nine compounds were 10.0 jxg/kg (S/N≥10). The average recoveries of the nine compounds ranged from 79. 6% to 100. 9% at the spiked levels of 10. 0, 100. 0, 1 000. 0 μg/kg with the relative standard deviations (RSDs) of 6. 3% - 12. 1%. The method is sensitive, accurate, and suitable for the rapid determination of bisphenol diglycidyl ether residues in canned foodstuffs.%建立了同时测定肉类罐头中双酚A-二缩水甘油醚(BADGE)、双酚F-二缩水甘油醚(BFDGE)及其衍生物双酚A-(2,3-二羟丙基)甘油醚(BADGE·H2O)、双酚A-双(2,3-二羟丙基)醚(BADGE·2H2O)、双酚A-(3-氯-2-羟丙基)(2,3-

  5. Rapid Determination of Bisphenol Diglycidyl Ethers and Its Migration Regulations in Interior Coating of Food Cans%食品罐内壁涂料中双酚-二缩水甘油醚的快速检测和迁移规律

    曹国洲; 陈少鸿; 肖道清; 朱晓艳; 马明; 刘在美


    A rapid and simple ultra performance liquid chromatographic method for determination the specific migration of bisphenol A diglycidyl ether ( BADGE ) , bisphenol F diglycidyl ether ( BFDGE ) and their derivatives in food simulants was developed. Water, 3% acetic acid, 10% ethanol and sunflower oil were used as food simulants to simulate the specific migration of bisphenol diglycidyl ethers from interior coating of food cans after 10 days storage at 60℃. After the migration period, the aqueous food simulants were directly measured without any further purification, while the sunflower oil simulant was extracted by acetonitrile followed by cleaning up using solid phase extraction. Among the migration process, BADGE and bisphenol A (3-chloro-2-hydroxypropyl)glycidyl ether (BADGE·HCl) migrated into aqueous simulants were hydrolysed into bisphenol A bis ( 2, 3-dihydroxypropyl ) ether ( BADGE · 2H2 O ) and bisphenol A ( 3-chloro-2-hydroxypropyl) (2,3-dihydroxypropyl) ether (BADGE·H2O·HCl), respectively. However, BADGE and BADGE·HCl migrated into sunflower oil were not hydrolysed. The calibrating curves showed a good linearity from 0. 05 to 10 mg/L for all the 9 target compounds. The detection limits of the method for aqueous food simulants and sunflower oil stimulant were 5μg/L and 20μg/kg, respectively. The method was applied to the determination of bisphenol diglycidyl ethers migrated from 10 kinds of food cans which were intended to contact with food. The results indicate that BADGE and its derivatives were detected at 5 of the cans, and the specific migration of BADGE(or BADGE·2H2O)and BADGE·HCl(or BADGE·H2O·HCl)in 1 cans even exceed the responding limitation regulated in EC/1895/2005 .%建立了快速、简便的超高效液相色谱法同时测定食品模拟物中双酚A-二缩水甘油醚( BADGE)、双酚F-二缩水甘油醚( BFDGE)及其衍生物特定迁移量的方法。采用水、3%乙酸、10%乙醇和葵花籽油4种食品模拟物在60℃、10

  6. Separação de fases induzida por meio de reação química no sistema éter diglicidílico do bisfenol A e piperidina com poli(metacrilato de metila Phase separation induced by chemical reaction in the system of diglycidyl ether of bisphenol A and piperidine with poly(methyl methacrylate

    Filiberto González Garcia


    Full Text Available O comportamento da separação de fases e da gelificação do sistema epoxídico, constituído pelo éter diglicidílico do bisfenol A (DGEBA e a piperidina, modificado com poli(metacrilato de metila (PMMA, foi estudado na faixa de temperatura de 60 °C - 120 °C. A concentração de PMMA e a temperatura de cura causam mudanças significativas na morfologia gerada. A massa molecular de PMMA provoca ligeiras mudanças para a observação da separação de fases e não afeta a velocidade da reação. O sistema modificado com PMMA mostra o efeito de retardação cinético e a velocidade de separação de fases é maior que a velocidade de polimerização.The phase separation and gelification behavior of epoxy system based on diglycidyl ether of bisphenol-A (DGEBA and piperidine modified with poly(methyl methacrylate (PMMA were studied in the range between 60 °C and 120 °C. The morphology is influenced by the PMMA content in the blend and also by the cure temperature. The molecular weight of PMMA provokes slight changes on cloud point and does not affect the reaction rate. The systems modified by PMMA exhibited kinetic retardation effect but the cloud point rate was higher than the polymerization rate.

  7. 超高效液相色谱-串联质谱法同时测定鱼、肉类罐头食品中的BADGE、NOGE及其衍生物%Determination of Bisphenol a Diglycidyl Ether (BADGE), Novolac Glycidyl Ethers(NOGE) and Its Derivatives in Canned Fish and Meat by Ultra-performance Liquid Chromatography with Tandem Mass Spectrometry

    林赛君; 陈思; 薛鸣; 张虹


    An ultra-performance liquid chromatography with tandem mass spectrometry method for determination of bisphenol A diglycidyl ether (BADGE) , novolac glycidyl ether (NOGE) and its derivatives from canned food has been developed. The proposed method includes microwave-assisted extraction followed by puri? cation by solid phase extraction (SPE). After separation by BEH Cls ( column 100 mm ×2.1 mm, 1.7 μm), the sample was detected by API 4000 - QTRAP mass spectrometry under positive electrospray ionization mode, with acetonitrile and 0.2% aqueous formic acid as mobile phase. The detection limits were 0. 010 2 - 0. 197 2 ng/g, and recoveries at three different concentrations ranged from 65.7% to 99. 1%. This method was successfully applied to canned fish and meat, the highest total contents of 3 -6 R-NOGE reached 209.03 mg/6 dm2.%建立了一种罐头食品中的BADGE(bisphenol A diglycidyl ether,双酚A-二环氧甘油醚)、NOGE(novolac glycidyl ether,酚醛清漆甘油醚)及其衍生物含量的超高效液相色谱-串联质谱检测法。前处理包括正己烷/丙酮微波辅助萃取,Varain-PS-DVB固相萃取柱净化等。样品经BEH C18色谱柱(100mm×2.1mm,1.7μm)分离,以乙腈和0.2%甲酸水为流动相,进行梯度洗脱,在API4000-Q TRAP质谱仪电喷雾正离子、多反应监测(MRM)模式下进行检测。分析物检出限达到0.0102ng/g到0.1972ng/g,三水平加标回收率在65.7%~99.1%。

  8. 40 CFR 721.3465 - Stilbene diglycidyl ether.


    ... section, manufacturers, importers, and processors of this substance may follow the terms of the new..., commercial, and consumer activities. Requirements as specified in § 721.80(q). (b) Specific requirements. The... (i) are applicable to manufacturers, importers, and processors of this substance. (2) Limitations...

  9. Crosslinking in the diglycidyl ether oligoepichlorhydrin-piperazine

    Konstantyn E. Varlan


    Full Text Available The possibility of acquiring film material from a mixture of oligoepichlorhydrin diglycidylether and piperazyne discussed. The process involves elongation of the chain by means of reaction of the oligomer terminal oxyran cycles with piperazine aminogrups, and the subsequent formation of crosslinked by tertiary amine alongthe chainsalkylation whis chlorometyl dand groups of macromolecules. With this purpose, the model system investigated: epichlorohydrin−piperidine, epichlorohydrin−piperazine, oligoetylenglikol glicidyl ether−piperazine. The possibility of regulating the contributions of reactions of epoxy group and alkylation on crosslinking primary stage is disclosed, as well as material properties. Taking into account the found regularities receive elastic film structured materials with quaternary nitrogen atoms in the nodes. The ratio of tertiary and quaternary structure of nitrogen depends on the process conditions. Films swell in polar solvents and has ion-exchange properties.

  10. Biodegradation of resorcinol by Pseudomonas sp.

    Nader Hajizadeh


    Full Text Available Objective: To investigate the ability of Pseudomonas sp. isolated from East Azarbaijan, Iran in bioremediation of resorcinol. Methods: Resorcinol biodegradation was evaluated using spectrophotometry and confirmed by gas chromatography-mass spectroscopy. Results: This isolate was able to remove up to 37.12% of resorcinol from contaminated water. Reusability experiments had confirmed the biodegradation process which produced seven intermediate compounds. These intermediates were characterized by gas chromatographymass spectroscopy technique. The products of resorcinol biodegradation were apparently 1, 4-cyclohexadiene, nonadecene, 2-heptadecanone, 1-isopropyl-2-methoxy-4-methylbenzene, hexadecanoic acid, 9-octadecenoic acid, phenol and 5-methyl-2-(1-methylethyl. Conclusions: The findings revealed that Pseudomonas sp. is able to degrade resorcinol. Because of being an indigenous organism, this isolate is more compatible with the climate of the northwest region of Iran and possibly will be used for degradation of other similar aromatic compounds.

  11. Biodegradation of resorcinol byPseudomonas sp.

    Nader Hajizadeh; Najibeh Shirzad; Ali Farzi; Mojtaba Salouti; Azra Momeni


    ABSTRACT Objective:To investigate the ability ofPseudomonas sp. isolated from East Azarbaijan, Iran in bioremediation of resorcinol. Methods: Resorcinol biodegradation was evaluated using spectrophotometry and confirmed by gas chromatography-mass spectroscopy. Results:This isolate was able to remove up to 37.12% of resorcinol from contaminated water. Reusability experiments had confirmed the biodegradation process which produced seven intermediate compounds. These intermediates were characterized by gas chromatography-mass spectroscopy technique. The products of resorcinol biodegradation were apparently 1, 4-cyclohexadiene, nonadecene, 2-heptadecanone, 1-isopropyl-2-methoxy-4-methylbenzene, hexadecanoic acid, 9-octadecenoic acid, phenol and 5-methyl-2-(1-methylethyl). Conclusions: The findings revealed thatPseudomonas sp. is able to degrade resorcinol. Because of being an indigenous organism, this isolate is more compatible with the climate of the northwest region of Iran and possibly will be used for degradation of other similar aromatic compounds.

  12. Modificação de polímeros termorrígidos por separação de fases induzida por reação química: Sistema éter diglicidílico do Bisfenol-A e trietilenotetramina com copolímeros acrílicos Modification of thermosetting polymers by induced phase separation by chemical reaction: Diglycidyl ether of Bisphenol-A and triethylenetetramine with acrylic copolymers

    Garcia Filiberto González


    Full Text Available O comportamento da separação de fases e da gelificação do sistema do éter diglicidílico do Bisfenol-A com trietilenotetramina modificado com diferentes copolímeros acrílicos foi estudado. As massas moleculares e as concentrações de grupos carboxílicos nos copolímeros provocaram mudanças significativas na morfologia e provocaram ligeiras mudanças para a observação da separação de fases. Contudo, não mudaram de maneira significativa os tempos de gelificação e não afetaram a velocidade da reação. O sistema modificado com os copolímeros acrílicos mostrou o efeito de retardação cinética. A morfologia foi relacionada com a aderência ao cisalhamento, em juntas de aço-aço, através de ensaios de resistência mecânica usando juntas de cisalhamento simples, as que foram produzidas com o sistema modificado com os copolímeros acrílicos segundo a norma ASTM D 1002. Amostras com a fase dispersa apresentando morfologia com partículas de diâmetro médio menor que 0,10 µm mostraram o melhor desempenho de aderência ao cisalhamento para as massas moleculares dos copolímeros estudadas. Entretanto, um melhor comportamento mecânico para as concentrações de grupos carboxílicos nos copolímeros acrílicos foi observado para a morfologia com distribuição de tamanhos de partículas na faixa de 0,20 a 0,52 µm.The cloud point and the gel time behavior of an epoxy system based on diglycidyl ether of Bisphenol-A with triethylenetetramine modified with different acrylic copolymers were studied. The molecular weights and the concentration of carboxyl groups in the copolymers affected the morphology and the cloud point, but did not affect the gel times and reaction rates significantly. The system modified with the acrylic copolymers exhibited kinetic retardation effects. The morphology was related to adherence to the lap shear in steel-steel joints, through mechanical resistance essays using a single-lap-joint, which was produced

  13. Antidermatophytic Action of Resorcinol Derivatives: Ultrastructural Evidence of the Activity of Phenylethyl Resorcinol against Microsporum gypseum

    Carlo Romagnoli


    Full Text Available In this work, we evaluated the antidermatophytic activities of three resorcinol derivatives that have a history of use in dermo-cosmetic applications to discover molecules with multiple dermatological activities (i.e., multi-target drugs, thereby reducing the cost and time necessary for new drug development. The antidermatophytic activities of the three skin lighteners were evaluated relative to the known antifungal drug fluconazole on nine dermatophytes responsible for the most common dermatomycoses: Microsporum gypseum, Microsporum canis, Trichophyton violaceum, Arthroderma cajetani, Trichophyton mentagrophytes, Epidermophyton floccosum, Nannizzia gypsea, Trichophyton rubrum and Trichophyton tonsurans. Among the three tested resorcinols, only two showed promising properties, with the ability to inhibit the growth of all tested dermatophytes; additionally, the IC50 values of these two resorcinols against the nine dermatophytes confirmed their good antifungal activity, particularly for phenylethyl resorcinol against M. gypseum. Ultrastructural alterations exhibited by the fungus were observed using scanning electron microscopy and transmission electron microscopy and reflected a dose-dependent response to treatment with the activation of defence and self-preservation strategies.

  14. Antidermatophytic Action of Resorcinol Derivatives: Ultrastructural Evidence of the Activity of Phenylethyl Resorcinol against Microsporum gypseum.

    Romagnoli, Carlo; Baldisserotto, Anna; Vicentini, Chiara B; Mares, Donatella; Andreotti, Elisa; Vertuani, Silvia; Manfredini, Stefano


    In this work, we evaluated the antidermatophytic activities of three resorcinol derivatives that have a history of use in dermo-cosmetic applications to discover molecules with multiple dermatological activities (i.e., multi-target drugs), thereby reducing the cost and time necessary for new drug development. The antidermatophytic activities of the three skin lighteners were evaluated relative to the known antifungal drug fluconazole on nine dermatophytes responsible for the most common dermatomycoses: Microsporum gypseum, Microsporum canis, Trichophyton violaceum, Arthroderma cajetani, Trichophyton mentagrophytes, Epidermophyton floccosum, Nannizzia gypsea, Trichophyton rubrum and Trichophyton tonsurans. Among the three tested resorcinols, only two showed promising properties, with the ability to inhibit the growth of all tested dermatophytes; additionally, the IC50 values of these two resorcinols against the nine dermatophytes confirmed their good antifungal activity, particularly for phenylethyl resorcinol against M. gypseum. Ultrastructural alterations exhibited by the fungus were observed using scanning electron microscopy and transmission electron microscopy and reflected a dose-dependent response to treatment with the activation of defence and self-preservation strategies.

  15. Synthesis and Analysis of Resorcinol-Acetone Copolymer

    Gen-ichi Konishi


    Full Text Available Synthesis and characterization of resorcinol-acetone copolymer is described. The polymer was prepared by trifluoroacetic acid-catalyzed polymerization of resorcinol with acetone. According to the 1H-NMR, 13C-NMR, and MALDI-TOF Mass spectra data, the obtained polymer had three types of repeating units: isopropylidene bridged-resorcinol, chromane ring, and spiro-shaped double chromane ring, indicating that polymerization proceeded via simultaneous addition-condensation and cyclization of resorcinol with acetone. The obtained polymer can be useful not only for the development of plastic materials such as thermosets, adhesives, and coatings but also for the synthesis of biomaterials such as antimicrobial agents, pesticides, and medicines.

  16. Alkyl resorcinols in grains from plants from the family Gramineae

    Grzegorz Kubus


    Full Text Available 5-n-alkylresorcinols were found in 22 of the 27 studied species of grasses. In Agropyron caninum and Bromus macrostachys only the content of alkyl resorcinols was determined, in Agropyron repens, Bromus mollis and Elymus arenarius the composition of alkyl resorcinol homologues was also established. When calculated per gram of dry mass of air-dried grains, the content of alkyl resorcinols was found to be: in the genus Agropyron - approximately 715 µg, in the genus Bromus approximately 60 µg and in Elymus arenarius, 272 µg. The homologues of alkyl resorcinods in the studied genera of grasses differ from the homologues found in wheat or rye by their greater content of long-chain fractions.

  17. Boron complexing with H-resorcinol and acidic hydroxyxanthene dyes

    Nazarenko, V.A.; Flyantikova, G.V.; Chekirda, T.N. (AN Ukrainskoj SSR, Odessa. Fiziko-Khimicheskij Inst.)


    Complex formation of boron with H-resorcinol (hr; 2,4-dihydroxybenzene-azo -8-hydroxynaphtalene-3,6-disulfonic acid) and acidic hydroxyxanthene dyes (hxd: fluorescein, eosine, erathrosine). Mixed-ligand complexes with a ratio of r:hr:hxd=1:1:1 are formed at pH=5-6. The chemism of the complex formation of boron with H-resorcinol and fluorescein has been studied. The stability constant of the complex is 1.12x10/sup 21/, the conditional molar absorptivitis 1.80x10/sup 0/. This complex formation reaction was used for photometric determination of boron in natural water.

  18. Beads on a Chain (BOC) Polymers Formed from the Reaction of NH2PhSiO1.5]x[PhSiO1.5]10-x and [NH2PhSiO1.5]x[PhSiO1.5]12-x Mixtures (x = 2-4) with the Diglycidyl Ether of Bisphenol A

    Jung, Jae Hwan [Univ. of Michigan, Ann Arbor, MI (United States); Laine, Richard M. [Univ. of Michigan, Ann Arbor, MI (United States)


    We recently reported that catalytic amounts of F cause rapid rearrangement of silsesquioxane (SQ) T₈ cages in THF at room temperature. These rearrangements lead primarily to the T₁₀ and T₁₂ cages as long as the Fis trapped for example using CaCl₂ to form insoluble CaF₂ in situ. In this report, we use this approach to make di- and triaminophenyl, phenyl silsesquioxane T₁₀ and T₁₂ mixtures: (NH2Ph)2xPh10/12–x(SiO1.5)10/12. Thereafter, we isolate the fraction that consists primarily of x = 2–3 via column chromatography. We then explore the reaction of this fraction (fraction 3) with the diglycidyl ether of bisphenol A (DGEBA) to form a soluble epoxy resin wherein the cage SQs are contained in the chain backbone. We call these products beads on a chain (BoC) polymers. The use of 1:1 mole ratios of [epoxide]:[NH2Ph] of DGEBA and (NH2Ph)2xPh10/12–x(SiO1.5)10/12 leads to insoluble products. However, the reaction of 0.8:1 mole ratio of [epoxide]:[NH2Ph] provides a soluble but bimodal distribution of products (after 24 h reaction at 90 °C in THF). The low MW component is much more soluble in THF than the higher MW component, allowing simple separation. The low MW polymer has a Mn of 6000 Da with a PDI of 1.6. The higher MW material has an Mn of 21 000 000 Da with a PDI of 21. Both components offer similar ceramic yields (to SiO₂) of 32 ± 1%, indicating that the relative contents of cages are identical. They also exhibit very similar FTIR spectra, suggesting that they are the same material. Two explanations are possible for the bimodal size distribution. One is that the positioning of the NH₂ groups on the cage leads to cyclic trimers given that the average monomer unit will mass ≈1700–1900 Da, which represents the low MW fraction. Alternately and more

  19. An improved assay with 4-(2-thiazolylazo)-resorcinol for non-esterified fatty acids in biological fluids.

    Bergmann, S R; Carlson, E; Dannen, E; Sobel, B E


    A simple and rapid colorimetric assay for non-esterified fatty acids (NEFA) was developed employing extraction of samples with 0.1 mol/l glycine (pH 2.7) and methoxyethanol : butyl ether, and formation of a copper-fatty acid soap detected with 4-(2-thiazolylazo)-resorcinol. The method developed is sensitive enough to detect as little as 11 nmol/0.25 ml sample. Results are not affected by marked molar excesses of phospholipids, cholesterol, cholesterol esters, triglycerides, bilirubin, or lactate. Recovery of palmitate in the extract averages 94.2 +/- 3.2% (S.D.) and other long chain fatty acids are recovered equally. The copper-NEFA-indicator complex formed is stable. Extracted samples can be stored for as long as 2 weeks without appreciable changes in measured NEFA content. The method developed is suitable for both manual and semi-automated procedures for determining NEFA content in biological fluids.

  20. Solar photocatalytic degradation of resorcinol a model endocrine disrupter in water using zinc oxide

    Pardeshi, S.K. [Department of Chemistry, University of Pune, Ganeshkhind, Pune 411007 (India)], E-mail:; Patil, A.B. [Department of Chemistry, University of Pune, Ganeshkhind, Pune 411007 (India)


    Photocatalytic degradation (PCD) of resorcinol a potent endocrine disrupting chemical in aqueous medium was investigated by ZnO under sunlight irradiation in a batch photoreactor. The influence of various parameters such as photocatalyst amount, initial concentration of resorcinol and pH was examined for maximum PCD of resorcinol. A considerable influence of pH upon the chemical oxygen demand (COD) disappearance was observed. In general, neutral or basic pH is favorable for COD removal of resorcinol. PCD intermediates were identified using FTIR and GC/MS. Two of the initial oxidation intermediates detected were 1,2,4-trihydroxy-benzene and 1,2,3-trihydroxy-benzene. FTIR studies revealed 1,2,4-trihydroxy-benzene as the major PCD intermediate. A working photodegradation mechanism is also suggested for PCD of resorcinol. This work envisages the great potential that sunlight mediated photocatalysis has in the removal of resorcinol from waste water.

  1. Characterization of the action of tyrosinase on resorcinols.

    Garcia-Jimenez, Antonio; Teruel-Puche, Jose Antonio; Berna, José; Rodriguez-Lopez, José Neptuno; Tudela, Jose; Garcia-Ruiz, Pedro Antonio; Garcia-Canovas, Francisco


    The action of tyrosinase on resorcinol and some derivatives (4-ethylresorcinol, 2-methylresorcinol and 4-methylresorcinol) was investigated. If the catalytic cycle is completed with a reductant such as ascorbic acid or an o-diphenol such as 4-tert-butylcatechol, these compounds act as substrates of tyrosinase in all cases. The reaction can also be carried out, adding hydrogen peroxide to the medium. All the above compounds were characterized as substrates of the enzyme and their kinetic constants, KM (Michaelis constant) and kcat (catalytic constant) were determined. Measurement of the activity of the enzyme after pre-incubation with resorcinol, 4-ethylresorcinol or 4-methylresorcinol points to an apparent loss of activity at short times, which could correspond to an enzymatic inactivation process. However, if the measurements are extended over longer times, a burst is observed and the enzymatic activity is recovered, demonstrating that these compounds are not suicide substrates of the enzyme. These effects are not observed with 2-methylresorcinol. The docking results indicate that the binding of met-tyrosinase with these resorcinols occurs in the same way, but not with 2-methylresorcinol, due to steric hindrance.

  2. Cosmic Ether

    Tomaschitz, R


    A prerelativistic approach to particle dynamics is explored in an expanding Robertson-Walker cosmology. The receding galactic background provides a distinguished frame of reference and a unique cosmic time. In this context the relativistic, purely geometric space-time concept is criticized. Physical space is regarded as a permeable medium, the cosmic ether, which effects the world-lines of particles and rays. We study in detail a Robertson-Walker universe with linear expansion factor and negatively curved, open three-space; we choose the permeability tensor of the ether in such a way that the semiclassical approximation is exact. Galactic red-shifts depend on the refractive index of the ether. In the local Minkowskian limit the ether causes a time variation of mass, which scales inversely proportional to cosmic time. In the globally geodesic rest frames of galactic observers the ether manifests itself in an unbounded speed of signal transfer, in bifurcations of world-lines, and in time inversion effects.

  3. Permeability changes of erythrocytes and liposomes by 5-(n-alk(en)yl) resorcinols from rye

    Kozubek, A.; Demel, R.A.


    5-(n-Alk(en)yl) resorcinols can induce potassium release from liposomes and erythrocytes. The results suggest that 5-(n-pentyl)resorcinol can induce a specific permeability to protons as well as to potassium and other small molecules. The highest permeability changes were found in the presence of 5-

  4. Synthesis of resorcinolic lipids bearing structural similarities to cytosporone A

    Edson dos Anjos dos Santos


    Full Text Available Inspired by the structure and biological activities of resorcinolic lipids and, particularly cytosporone A- a potent inhibitor of plantule germination and growth, we have performed the synthesis of the analogs 3-heptyl-3-hydroxy-5,7-dimethoxy-2-benzofuran-1(3H-one (1 and 3-heptyl-3-hydroxy-4,6-dimethoxy-2-benzofuran-1(3H-one (2. The intermediates and products were submitted to allelopathic test using Lactuca sativa L. seeds. Target compound 1 showed an inhibitory effect on germination and growth of hypocotyl and radicle in milimolar range.

  5. Synthesis of resorcinolic lipids bearing structural similarities to cytosporone A

    Santos, Edson dos Anjos dos; Beatriz, Adilson; Lima, Denis Pires de [Universidade Federal Mato Grosso do Sul (UFMS), Campo Grande, MS (Brazil). Centro de Ciencias Exatas e Tecnologia. Dept. de Quimica], e-mail:; Marques, Maria Rita; Leite, Carla Braga [Universidade Federal Mato Grosso do Sul (UFMS), Campo Grande, MS (Brazil). Centro de Ciencias Biologicas. Dept. de Morfofisiologia


    Inspired by the structure and biological activities of resorcinolic lipids and, particularly cytosporone A- a potent inhibitor of plantule germination and growth, we have performed the synthesis of the analogs 3-heptyl-3-hydroxy-5,7-dimethoxy-2-benzofuran-1(3H)-one (1) and 3-heptyl-3-hydroxy-4,6-dimethoxy-2-benzofuran-1(3H)-one (2). The intermediates and products were submitted to allelopathic test using Lactuca sativa L. seeds. Target compound 1 showed an inhibitory effect on germination and growth of hypocotyl and radicle in millimolar range. (author)


    King, W; Fernando Fondeur, F; Bill Wilmarth, B; Myra Pettis, M; Shirley Mccollum, S


    Solid-state infrared spectroscopy, differential scanning calorimetry, and elemental analysis have been used to evaluate the reactivity of resorcinol formaldehyde resin with nitric acid and characterize the solid product. Two distinct reactions were identified within the temperature range 25-55 C. The first reaction is primarily associated with resin nitration, while the second involves bulk oxidation and degradation of the polymer network leading to dissolution and off-gassing. Reaction was confirmed with nitric acid concentrations as low as 3 M at 25 C applied temperature and 0.625 M at 66 C. Although a nitrated resin product can be isolated under appropriate experimental conditions, calorimetry testing indicates no significant hazard associated with handling the dry material.

  7. Reactivity of Resorcinol Formaldehyde Resin with Nitric Acid

    King, William D.; Fondeur, Fernando F.; Wilmarth, William R.; Pettis, Myra E.


    Solid-state infrared spectroscopy, differential scanning calorimetry, and elemental analysis have been used to evaluate the reactivity of resorcinol formaldehyde resin with nitric acid and characterize the solid product. Two distinct reactions were identified within the temperature range 25-55 C. The first reaction is primarily associated with resin nitration, while the second involves bulk oxidation and degradation of the polymer network leading to dissolution and off-gassing. The threshold conditions promoting reaction have been identified. Reaction was confirmed with nitric acid concentrations as low as 3 M at 25 C applied temperature and 0.625 M at 66 C. Although a nitrated resin product can be isolated under appropriate experimental conditions, calorimetry testing indicates no significant hazard associated with handling the dry material.

  8. Spherical Resorcinol-Formaldehyde Synthesis by Inverse Suspension Polymerization

    Ray, Robert J.; Scrivens, Walter A.; Nash, Charles


    Base catalyzed sol-gel polycondensation of resorcinol (1,3-dihydroxybenzene) with formaldehyde by inverse suspension polymerization leads to the formation of uniform, highly cross-linked, translucent, spherical gels, which have increased selectivity and capacity for cesium ion removal from high alkaline solutions. Because of its high selectivity for cesium ion, resorcinol-formaldehyde (R-F) resins are being considered for process scale column radioactive cesium removal by ion-exchange at the Waste Treatment and Immobilization Plant (WTP), which is now under construction at the Hanford site. Other specialty resins such as Superlig{reg_sign} 644 have been ground and sieved and column tested for process scale radioactive cesium removal but show high pressure drops across the resin bed during transition from column regeneration to loading and elution. Furthermore, van Deemter considerations indicate better displacement column chromatography by the use of spherical particle beads rather than irregularly shaped ground or granular particles. In our studies batch contact equilibrium experiments using a high alkaline simulant show a definite increase in cesium loading onto spherical R-F resin. Distribution coefficient (Kd) values ranged from 777 to 429 mL/g in the presence of 0.1M and 0.7M potassium ions, respectively. Though other techniques for making R-F resins have been employed, to our knowledge no one has made spherical R-F resins by inverse suspension polymerization. Moreover, in this study we discuss the data comparisons to known algebraic isotherms used to evaluate ion-exchange resins for WTP plant scale cesium removal operations.


    ZHUANG Yinfeng; Stanley McCool; G. Paul Willhite; Don W. Green


    Factors affecting the gelation of resorcinol-formaldehyde systems have been examined over variable ranges applicable to oilfield use. Gelation of resorcinol-formaldehyde (RF)system was sensitive to pH,salinity and hardness. Generally,this gel system could be used in fresh water or low salinity brine at pH higher than about 9. The application would require careful monitoring of injection fluids to avoid premature gelation or prolonged shut-in times ,especially under conditions of low salinity and high pH. Salinity and hardness compatibilities of the system were improved by sulfomethylation of resorcinol. Aqueous sulfomethylated resorcinol formaldehyde (SMRF)system could be used in brine with higher salinity and hardness and at a wider pH range of 5-10.

  10. Reaction of pyrocatechol and resorcinol with styrene in the presence of aluminum phenolate

    Kozlikovskii, Y.B.; Butov, S.A.; Koshchii, V.A.


    The alkylation of pyrocatechol and resorcinol with styrene in the presence of aluminum phenolate leads to a mixture of isomeric (..cap alpha..-methylbenzyl)dihydroxybenzenes, in which the ortho-alkylation products as a rule predominate.

  11. 40 CFR 721.9480 - Resorcinol, formaldehyde substituted carbomonocycle resin (generic).


    ... carbomonocycle resin (generic). 721.9480 Section 721.9480 Protection of Environment ENVIRONMENTAL PROTECTION... carbomonocycle resin (generic). (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as resorcinol, formaldehyde substituted carbomonocycle resin...

  12. Growth-induced incommensurability observed in the organic co-crystal hexamethylenetetramine resorcinol.

    Rodriguez, Soraya Maria Belluga; Palatinus, Lukás; Petrícek, Václav; Chapuis, Gervais


    Co-crystals of hexamethylenetetramine and resorcinol were investigated by X-ray diffraction. The structure was refined in the superspace group Xmcm(0beta0)s0s, X=(1/2 1/2 0 1/2). In the average structure the resorcinol molecules are disordered between two orientations. The main effect of the modulation in the structure is a harmonic modulation of the occupation probabilities of the two orientations of the resorcinol molecule. However, the modulated order is not perfect and the resorcinol molecules remain partially disordered. Below 270 K the crystal undergoes a phase transition to a commensurately modulated structure with modulation vector q=(0 1/2 1/4) and superspace group X2/m(0betagamma)0s. The structure of the low-temperature phase could not be determined owing to the poor quality of the crystals affected by the reconstructive phase transition.

  13. Cure Studies and Cured Properties of Diglycidyl Ether of 4- Methylolresorcinol (A Rapid-Gelling Epoxy Resin)


    potassium iodide method. A resin sample of were determined by the 1.0 to 1.5 g was weighed Erlenmeyer flask, mixture was then To the held at...bromophenol blue in 99.9 g n-propanol) and 3.0 g of potassium iodide in 5 ml of distilled water were added rapidly. The titrated with 1 N...increase its shelf life , the resin should therefore be stored at lower temperatures. At -14"C ាF), no viscosity increase was noticed over 6 months

  14. Resorcinol degradation by a Penicillium chrysogenum strain under osmotic stress: mono and binary substrate matrices with phenol.

    Guedes, Sumaya Ferreira; Mendes, Benilde; Leitão, Ana Lúcia


    A phenol-degrading Penicillium chrysogenum strain previously isolated from a salt mine was able to grow at 1,000 mg l(-1) of resorcinol on solid medium. The aerobic degradation of resorcinol by P. chrysogenum CLONA2 was studied in batch cultures in minimal mineral medium with 58.5 g l(-1) of sodium chloride using resorcinol as the sole carbon source. The fungal strain showed the ability to degrade up to 250 mg l(-1) of resorcinol. Resorcinol and phenol efficiency degradation by P. chrysogenum CLONA2 was compared. This strain removes phenol faster than resorcinol. When phenol and resorcinol were in binary substrate matrices, phenol enhanced resorcinol degradation, and organic load decreased with respect to the mono substrate matrices. The acute toxicity of phenol and resorcinol, individually and in combination, to Artemia franciscana larvae has been verified before and after the bioremediation process with P. chrysogenum CLONA2. The remediation process was effective in mono and binary substrate systems.

  15. Bimodal activated carbons derived from resorcinol-formaldehyde cryogels

    Szczurek, Andrzej; Amaral-Labat, Gisele; Fierro, Vanessa; Celzard, Alain [Institut Jean Lamour-UMR CNRS 7198, CNRS-Nancy-Universite-UPV-Metz, Departement Chimie et Physique des Solides et des Surfaces. ENSTIB, 27 rue Philippe Seguin, BP 1041, 88051 Epinal cedex 9 (France); Pizzi, Antonio, E-mail: [ENSTIB-LERMAB, Nancy-Universite, 27 rue Philippe Seguin, BP1041, 88051 Epinal cedex 9 (France)


    Resorcinol-formaldehyde cryogels prepared at different dilution ratios have been activated with phosphoric acid at 450 deg. C and compared with their carbonaceous counterparts obtained by pyrolysis at 900 deg. C. Whereas the latter were, as expected, highly mesoporous carbons, the former cryogels had very different pore textures. Highly diluted cryogels allowed preparation of microporous materials with high surface areas, but activation of initially dense cryogels led to almost non-porous carbons, with much lower surface areas than those obtained by pyrolysis. The optimal acid concentration for activation, corresponding to stoichiometry between molecules of acid and hydroxyl groups, was 2 M l{sup -1}, and the acid-cryogel contact time also had an optimal value. Such optimization allowed us to achieve surface areas and micropore volumes among the highest ever obtained by activation with H{sub 3}PO{sub 4}, close to 2200 m{sup 2} g{sup -1} and 0.7 cm{sup 3} g{sup -1}, respectively. Activation of diluted cryogels with a lower acid concentration of 1.2 M l{sup -1} led to authentic bimodal activated carbons, having a surface area as high as 1780 m{sup 2} g{sup -1} and 0.6 cm{sup 3} g{sup -1} of microporous volume easily accessible through a widely developed macroporosity.

  16. Adsorbent for resorcinol removal based on cellulose functionalized with magnetic poly(dopamine).

    Ding, Chaofan; Sun, Yuanling; Wang, Yanhui; Li, Jianbo; Lin, Yanna; Sun, Weiyan; Luo, Chuannan


    A simple chemical bonding method to synthesize magnetic cellulose-poly(dopamine) (Fe3O4@CMC@PDA) was reported. The adsorption behaviors of resorcinol in aqueous solution on Fe3O4@CMC@PDA were systematically investigated. As the results shown that, with the advantage of high surface area, abundant hydroxyl and amino groups of Fe3O4@CMC@PDA, and the magnetic property of Fe3O4, the resorcinol can be easily and rapidly extracted from the water by magnetic attraction under investigation. The adsorption equilibrium of Fe3O4@CMC@PDA for resorcinol corresponded with Freundlich isotherm, and the novel adsorbent exhibited better resorcinol removal efficiency in solutions with low pH. It was found that the resorcinol adsorption performance of Fe3O4@CMC@PDA strongly depends on their surface charge concentration and specific surface area. These results provide evidences for estimating and optimizing the removal of phenols from the wastewater by using of Fe3O4@CMC@PDA composites in the future. Copyright © 2017 Elsevier B.V. All rights reserved.

  17. Solution-state NMR analysis of hydroxymethylated resorcinol cured in the presence of crude milled-wood lignin from Acer saccharum

    Daniel J. Yelle


    Resorcinol-formaldehyde adhesives can reinforce stress fractures that appear from wood surface preparation. Researchers have found that applying the resorcinol-formaldehyde prepolymer, hydroxymethylated resorcinol is thought to plasticize lignin components and stabilize stress fractures through reactions with lignin subunits and hemicelluloses in wood. In this study, a...

  18. Spectrophotometric determination of tetrazene in primers and primer mixes by use of resorcinol.

    Norwitz, G; Keliher, P N


    A spectrophotometric method is proposed for the determination of tetrazene (tetracene) in primers and primer mixes that involves treatment of the tetrazene with resorcinol solution and measurement of the intensity of the yellow colour of the diazo-dye produced. In the application of the method, lead styphnate and barium nitrate are first removed by extraction with ammonium acetate solution and then nitrocellulose and PETN are removed by extraction with acetone. The insoluble matter containing the tetrazene is boiled with resorcinol reagent, the solution filtered, and the absorbance measured at 400 nm. Conditions for optimum colour development are studied and the nature of the reaction is considered.

  19. An Engineering Evaluation of Spherical Resorcinol Formaldehyde Resin

    Birdwell Jr, Joseph F [ORNL; Lee, Denise L [ORNL; Taylor, Paul Allen [ORNL; Collins, Robert T [ORNL; Hunt, Rodney Dale [ORNL


    A small column ion exchange (SCIX) system has been proposed for removal of cesium from caustic, supernatant, and dissolved salt solutions stored or generated from high-level tank wastes at the US Department of Energy (DOE) Hanford Site and Savannah River Sites. In both instances, deployment of SCIX systems, either in-tank or near-tank, is a means of expediting waste pretreatment and dispositioning with minimal or no new infrastructure requirements. Conceptually, the treatment approach can utilize a range of ion exchange media. Previously, both crystalline silicotitanate (CST), an inorganic, nonelutable sorbent, and resorcinol-formaldehyde (RF), an organic, elutable resin, have been considered for cesium removal from tank waste. More recently, Pacific Northwest National Laboratory (PNNL) evaluated use of SuperLig{reg_sign} 644, an elutable ion exchange medium, for the subject application. Results of testing indicate hydraulic limitations of the SuperLig{reg_sign} resin, specifically a high pressure drop through packed ion exchange columns. This limitation is likely the result of swelling and shrinkage of the irregularly shaped (granular) resin during repeated conversions between sodium and hydrogen forms as the resin is first loaded then eluted. It is anticipated that a similar flow limitation would exist in columns packed with conventional, granular RF resin. However, use of spherical RF resin is a likely means of mitigating processing limitations due to excessive pressure drop. Although size changes occur as the spherical resin is cycled through loading and elution operations, the geometry of the resin is expected to effectively mitigate the close packing that leads to high pressure drops across ion exchange columns. Multiple evaluations have been performed to determine the feasibility of using spherical RF resin and to obtain data necessary for design of an SCIX process. The work performed consisted of examination of radiation effects on resin performance


    Nash, C.; Duignan, M.


    This report presents characterization data for two spherical resorcinol-formaldehyde (sRF) resin beds that had processed cesium in non-radioactive and radioactive cycles. All column cycle operations for the resin beds including loading, displacements, elution, regeneration, breakthroughs, and solution analyses are reported in Nash and Duignan, 2009a. That report covered four ion exchange (IX) campaigns using the two {approx}11 mL beds in columns in a lead-lag arrangement. The first two campaigns used Savannah River Site (SRS) Tank 2F nonradioactive simulant while the latter two were fed with actual dissolved salt in the Savannah River National Laboratory (SRNL) Shielded Cells. Both radioactive cycles ran to cesium breakthrough of the lead column. The resin beds saw in excess of 400 bed volumes of feed in each cycle. Resin disposal plans in tank farm processing depend on characterizations of resin used with actual tank feed. Following a final 30 bed volume (BV) elution with nitric acid, the resin beds were found to contain detectable chromium, barium, boron, aluminum, iron, sodium, sulfur, plutonium, cesium, and mercury. Resin affinity for plutonium is important in criticality safety considerations. Cesium-137 was found to be less than 10E+7 dpm/g of resin, similar to past work with sRF resin. Sulfur levels are reasonably consistent with other work and are expected to represent sulfur chemistry used in the resin manufacture. There were low but detectable levels of technetium, americium, and curium. Toxicity Characteristic Leaching Procedure (TCLP) work on the used (eluted) resin samples showed significant contents of mercury, barium, and chromium. One resin sample exceeded the TCLP level for mercury while the other metals were below TCLP levels. TCLP organics measurements indicated measurable benzene in one case, though the source was unknown. Results of this work were compared with other work on similar sRF resin characterizations in this report. This is the first

  1. Synthesis and characterization of resorcinol-formaldehyde resin chars doped by zinc oxide

    Gun'ko, Vladimir M.; Bogatyrov, Viktor M.; Oranska, Olena I.; Urubkov, Iliya V.; Leboda, Roman; Charmas, Barbara; Skubiszewska-Zięba, Jadwiga


    Polycondensation polymerization of resorcinol-formaldehyde (RF) mixtures in water with addition of different amounts of zinc acetate and then carbonization of dried gels are studied to prepare ZnO doped chars. Zinc acetate as a catalyst of resorcinol-formaldehyde polycondensation affects structural features of the RF resin (RFR) and, therefore, the texture of chars prepared from Zn-doped RFR. The ZnO doped chars are characterized using thermogravimetry, low temperature nitrogen adsorption/desorption, Raman spectroscopy, X-ray diffraction (XRD), scanning electron microscopy (SEM), and high resolution transmission electron microscopy (HRTEM). At a relatively high content of zinc acetate (1 mol per 10-40 mol of resorcinol) in the reaction mixture, the formation of crystallites of ZnO (zincite) occurs in a shape of straight nanorods of 20-130 nm in diameter and 1-3 μm in length. At a small content of zinc acetate (1 mol per 100-500 mol of resorcinol), ZnO in composites is XRD amorphous and does not form individual particles. The ZnO doped chars are pure nanoporous at a minimal ZnO content and nano-mesoporous or nano-meso-macroporous at a higher ZnO content.

  2. Sol-gel coating of inorganic nanostructures with resorcinol-formaldehyde resin.

    Li, Na; Zhang, Qiao; Liu, Jian; Joo, Jibong; Lee, Austin; Gan, Yang; Yin, Yadong


    A general sol-gel process has been developed to form a coating of resorcinol-formaldehyde (RF) resin on inorganic nanostructures of various compositions and morphologies. The RF shell can be conveniently converted into carbon through high temperature carbonization under an inert atmosphere.

  3. Application of an easily water-compatible hypercrosslinked polymeric adsorbent for efficient removal of catechol and resorcinol in aqueous solution

    Huang Jianhan, E-mail: [College of Chemistry and Chemical Engineering, Central South University, Changsha 410083 (China); Huang Kelong; Yan Cheng [College of Chemistry and Chemical Engineering, Central South University, Changsha 410083 (China)


    An easily water-compatible hypercrosslinked resin HJ-1 was developed for adsorbing catechol and resorcinol in aqueous solution in this study. Its adsorption performances for catechol and resorcinol were investigated in aqueous solution by using the commercial Amberlite XAD-4 as a reference. The adsorption dynamic curves were measured and the adsorption obeyed the pseudo-second-order rate equation of Boyer and Hsu. The adsorption isotherms were scaled and Freundlich isotherm model characterized the adsorption better. The adsorption thermodynamic parameters were calculated and the adsorption was an exothermic, favorable, and more ordered process. The fact that the adsorption capacity of catechol was larger than resorcinol and the adsorption enthalpy of catechol was more negative than resorcinol can be explained in terms of the solubility and the polarity of two adsorbates.

  4. Solvent mediated stabilisation of dissolution at the resorcinol-water interface

    Hussain, M.; Sahudin, S. [Faculty of Pharmacy, Universiti Kebangsaan Malaysia, Jalan Raja Muda Abdul Aziz, 50300 Kuala Lumpur (Malaysia)


    Experimental evidence suggests dissolution along the polar c-axis of {alpha}-resorcinol in water preferentially occurs at the {l_brace}011{r_brace} surface. In an attempt to understand the mechanism by which solvent influences this process, dissolution at the resorcinol {l_brace}011{r_brace} and {l_brace}011{r_brace} surfaces has been studied using molecular dynamics simulations. Our computations indicate dissolution at the two faces is dependent upon solvent behaviour at the crystal surface, where strong water-crystal interactions serve to stabilise the crystal surface and retard dissolution. (copyright 2010 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)


    Eghe A. Oyedoh


    Full Text Available The adsorption of chromium(VI metal ion in aqueous solutions by activated carbon resorcinol formaldehyde xerogels (ACRF was investigated. The results showed that pore structure, surface area and the adsorbent surface chemistry are important factors in the control of the adsorption of chromium(VI metal ions. The isotherm parameters were obtained from plots of the isotherms and from the application of Langmuir and Freundlich Isotherms. Based on regression analysis, the Langmuir isotherm model was the best fit. The maximum adsorption capacity of ACRF for chromium (VI was 241.9 mg/g. The pseudo-second-order kinetic model was the best fit to the experimental data for the adsorption of chromium metal ions by activated carbon resorcinol formaldehyde xerogels. The thermodynamics of Cr(VI ions adsorption onto ACRF was a spontaneous and endothermic process.

  6. Vinyl ether silicones

    Herzig, C.; Dauth, J.; Deubzer, B.; Weis, J. [Wacker-Chemie GmbH, Burghausen (Germany)


    Siloxanes with vinyl ether groups are prepared by hydrosilylation reaction of dihydrosiloxanes with divinyl ethers in excess. Different stoichiometry, produces linear copolymers of different viscosities and double bond concentrations always with an active vinyl ether group at each chain end. Polymerisations triggered by UV light were done with mixtures of these compounds and a series of onium salts. Very fast cure is observed even with low doses at 290 nm. V.E. silicones are found to cure essentially quantitative. The comparison with other highly reactive cationic monomers revealed that compounds are among the fastest curing prepolymers in cationic chemistry.

  7. Catalytic oxidation of dimethyl ether

    Zelenay, Piotr; Wu, Gang; Johnston, Christina M.; Li, Qing


    A composition for oxidizing dimethyl ether includes an alloy supported on carbon, the alloy being of platinum, ruthenium, and palladium. A process for oxidizing dimethyl ether involves exposing dimethyl ether to a carbon-supported alloy of platinum, ruthenium, and palladium under conditions sufficient to electrochemically oxidize the dimethyl ether.

  8. Chemical derivatization to enhance chemical/oxidative stability of resorcinol-formaldehyde resin

    Hubler, T. [Pacific Northwest National Laboratory, Richland, WA (United States)


    The purpose of this work is to develop modified resorcinol-formaldehyde (R-F) resin with enhanced chemical/oxidative stability in conditions typically encountered in the remediation of radioactive waste tanks. R-F resin is a regenerable organic ion-exchanger developed at Savannah River Technology Center that is being considered for use in the selective removal of radioactive cesium from alkaline waste tank supernates at both the Hanford and Savannah River sites.

  9. Inorganic layered double hydroxides as a 4-hexyl resorcinol delivery system for topical applications

    Mosangi, Damodar


    Full Text Available inhibitors to control pigmentation byRSC Adv., 2016, 6, 77709–77716 | 77709 Fig. 1 Chemical structure of 4-hexyl resorcinol. RSC Advances Paperaffecting the transcription and activity of pigmentary enzymes are peroxidase, tyrosinase, tyrosinase...-related protein-1 (Tyrp-1), tyrosinase-related protein-2 (Tyrp-2), methimazole, ellagic acid and hydroquinone.34–36 Among the different skin lightening agents, hydroquinone has been the most frequently used in numerous even tone formulations for more than 5...

  10. Lawps ion exchange column gravity drain of spherical resorcinol formaldehyde resin

    Duignan, M. R. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Herman, D. T. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Restivo, M. L. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Burket, P. R. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL)


    Experiments at several different scales were performed to understand the removal of spherical resorcinol formaldehyde (sRF) ion exchange resin using a gravity drain system with a valve located above the resin screen in the ion exchange column (IXC). This is being considered as part of the design for the Low Activity Waste Pretreatment System (LAWPS) to be constructed at the DOE Hanford Site.

  11. Chemical derivatization to enhance chemical/oxidative stability of resorcinol-formaldehyde resin

    Hubler, T.L. [Pacific Northwest National Lab., Richland, WA (United States)


    The goal of this task is to develop modified resorcinol-formaldehyde (R-F) resin to improve the chemical/oxidative stability of the resin. R-F resin is a regenerable organic ion-exchange resin that is selective for cesium ion in highly alkaline, high ionic-strength solutions. R-F resin tends to undergo chemical degradation, reducing its ability to remove cesium ion from waste solutions; the mechanistic details of these decomposition reactions are currently unknown. The approach used for this task is chemical modification of the resin structure, particularly the resorcinol ring unit of the polymer resin. This approach is based on prior characterization studies conducted at Pacific Northwest National Laboratory (PNNL) that indicated the facile chemical degradation of the resin is oxidation of the resorcinol ring to the para-quinone structure, with subsequent loss of ion-exchange sites for cesium ion. R-F resin represents an important alternative to current radiocesium remediation technology for tank wastes at both the Hanford and Savannah River sites, particularly if regenerable resins are needed.

  12. Theoretical Study on Reaction Pathways Leading to CO and CO2 in the Pyrolysis of Resorcinol.

    Furutani, Yuki; Kudo, Shinji; Hayashi, Jun-Ichiro; Norinaga, Koyo


    Possible pathways for the pyrolysis of resorcinol with the formation of CO and CO2 as final products were proposed and evaluated using ab initio calculations. Our experimental study revealed that large quantities of CO2 are generated in the pyrolysis of 1,3-dihydroxybenzene (resorcinol), while the pyrolysis of the dihydroxybenzene isomers 1,2-dihydroxybenzene (catechol) and 1,4-dihydroxybenzene (hydroquinone) produces little CO2. The fate of oxygen atoms in catechol and hydroquinone was essentially the formation of CO. In the proposed pathways, the triplet ground state m-benzoquinone was generated initially from simultaneous cleavage of the two O-H bonds in resorcinol. Subsequently, the direct cleavage of a C-C bond of the m-benzoquinone diradical yields 2-oxidanylcyclopenta-2,4-dien-1-yl-methanone, which can be converted via two channels: release of CO from the aldehyde radical group and combination of the ketone radical and carbon atom in the aldehyde radical group to form the 6-oxabicyclo[3.2.0]hepta-2,4-dien-7-one, resulting in the release of CO2. Potential energy surfaces along the proposed reaction pathways were calculated employing the CBS-QB3 method, and the rate constants at the high-pressure limit were also evaluated based on transition-state theory to assess the feasibility of the proposed reaction pathways.

  13. Simultaneous Quantification of Dexpanthenol and Resorcinol from Hair Care Formulation Using Liquid Chromatography: Method Development and Validation

    Amit Kumar De


    Full Text Available The current study presents the simultaneous quantification of dexpanthenol and resorcinol from marketed hair care formulation. Dexpanthenol is often present as an active ingredient in personal care products for its beautifying and invigorating properties and restorative and smoothing properties. On the other hand resorcinol is mainly prescribed for the treatment of seborrheic dermatitis of scalp. The toxic side effects of resorcinol limit its use in dermatological preparations. Therefore an accurate quantification technique for the simultaneous estimation of these two components can be helpful for the formulation industries for the accurate analysis of their product quality. In the current study a high performance liquid chromatographic technique has been developed using a C18 column and a mobile phase consisting of phosphate buffer of pH = 2.8 following a gradient elution. The mobile phase flow rate was 0.6 mL per minute and the detection wavelength was 210 nm for dexpanthenol and 280 nm for resorcinol. The linearity study was carried out using five solutions having concentrations ranging between 10.34 μg·mL−1 and 82.69 μg·mL−1 (r2=0.999 for resorcinol and 10.44 μg·mL−1 and 83.50 μg·mL−1 (r2=0.998 for dexpanthenol. The method has been validated as per ICH Q2(R1 guidelines. The ease of single step sample preparation, accuracy, and precision (intraday and interday study presents the method suitable for the simultaneous quantification of dexpanthenol and resorcinol from any personal care product and dermatological preparations containing these two ingredients.

  14. Induction of apoptosis on human hepatocarcinoma cell lines by an alkyl resorcinol isolated from Lithraea molleoides

    Luciana Barbini; Paula Lopez; Julieta Ruffa; Virginia Martino; Graciela Ferraro; Rodolfo Campos; Lucia Cavallaro


    AIM: To study the mechanism of cytotoxicity of a new active 5-alkyl resorcinol [1, 3-dihydroxy-5- (tridec-4', 7'-dienyl) benzene] isolated from Lithraea molleoides leaves on liver tumor cells.METHODS: Human hepatocarcinoma cell lines (HepG2and Hep3B) in culture were treated with inhibitory concentrations, 50% of the compound, for 24 h. The induction of apoptosis was detected in treated cells by analysis of DNA fragmentation, DNA content, and acridine orange and propidium iodide staining.RESULTS: After 24 h of 5-alkyl resorcinol treatment,both cell lines showed: (1) the typical morphological alterations of apoptosis; (2) DNA fragmentation, detected by laddering and appearance of a subG0 population by flow cytometry; and (3) condensed and fragmented nuclei by acridine orange-propidium iodide staining.CONCLUSION: Based on the results, this compound exerts its cytotoxic effect in both hepatocellular cell lines through apoptotic cell death. For Hep3B, cells with mutated p53 and Fas, apoptosis would proceed by p53-or Fas-independent pathways.

  15. Induction of apoptosis on human hepatocarcinoma cell lines by an alkyl resorcinol isolated from Lithraea molleoides

    Barbini, Luciana; Lopez, Paula; Ruffa, Julieta; Martino, Virginia; Ferraro, Graciela; Campos, Rodolfo; Cavallaro, Lucia


    AIM: To study the mechanism of cytotoxicity of a new active 5-alkyl resorcinol [1, 3-dihydroxy-5- (tridec-4’, 7’-dienyl) benzene] isolated from Lithraea molleoides leaves on liver tumor cells. METHODS: Human hepatocarcinoma cell lines (HepG2 and Hep3B) in culture were treated with inhibitory concentrations, 50% of the compound, for 24 h. The induction of apoptosis was detected in treated cells by analysis of DNA fragmentation, DNA content, and acridine orange and propidium iodide staining. RESULTS: After 24 h of 5-alkyl resorcinol treatment, both cell lines showed: (1) the typical morphological alterations of apoptosis; (2) DNA fragmentation, detected by laddering and appearance of a subG0 population by flow cytometry; and (3) condensed and fragmented nuclei by acridine orange-propidium iodide staining. CONCLUSION: Based on the results, this compound exerts its cytotoxic effect in both hepatocellular cell lines through apoptotic cell death. For Hep3B, cells with mutated p53 and Fas, apoptosis would proceed by p53- or Fas-independent pathways. PMID:17009393

  16. Concentrating cesium-137 from seawater using resorcinol-formaldehyde resin for radioecological monitoring

    Egorin, Andrei; Tokar, Eduard; Tutov, Mikhail; Avramenko, Valentin [Institute of Chemistry FEBRAS, Vladivostok (Russian Federation); Far Eastern Federal Univ., Vladivostok (Russian Federation); Palamarchuk, Marina; Marinin, Dmitry [Institute of Chemistry FEBRAS, Vladivostok (Russian Federation)


    A method of preconcentrating cesium-137 from seawater using a resorcinol-formaldehyde resin, which enables one to optimize the ecological monitoring procedure, has been suggested. Studies of sorption of cesium-137 from seawater by resorcinol-formaldehyde resin have been performed, and it has been demonstrated that the cation exchanger is characterized by high selectivity with respect to cesium-137. It was found that the selectivity depended on the temperature of resin solidification and the seawater pH value. The maximal value of the cesium-137 distribution coefficient is equal to 4.1-4.5 x 10{sup 3} cm{sup 3} g{sup -1}. Under dynamic conditions, the ion-exchange resin capacity is 310-910 bed volumes depending on the seawater pH, whereas the efficiency of cesium removal exceeds 95%. The removal of more than 95% of cesium-137 has been attained using 1-3 M solutions of nitric acid: here, the eluate volume was 8-8.4 bed volumes. Application of 3 M solution of nitric acid results in resin degradation with the release of gaseous products.

  17. Wet air oxidation of resorcinol as a model treatment for refractory organics in wastewaters from the wood processing industry.

    Weber, Bernd; Chavez, Alma; Morales-Mejia, Julio; Eichenauer, Sabrina; Stadlbauer, Ernst A; Almanza, Rafael


    Wastewater treatment systems are important tools to enhance sustainability in terms of reducing environmental impact and complying with sanitary requirements. This work addresses the wet air oxidation (WAO) process for pre-treatment of phenolic wastewater effluents. The aim was to increase biodegradability prior to a subsequent anaerobic stage. In WAO laboratory experiments using a micro-autoclave, the model compound resorcinol was degraded under different oxygen availability regims within the temperature range 150 °C-270 °C. The activation energy was determined to be 51.5 kJ/mol. Analysis of the products revealed that after 3 h of reaction at 230 °C, 97.5% degradation of resorcinol was achieved. At 250 °C and the same reaction time complete removal of resorcinol was observed. In this case the total organic carbon content was reduced down to 29%, from 118.0 mg/L down to 34.4 mg/L. Under these process conditions, the pollutant was only partially mineralized and the ratio of the biological oxygen demand relative to the chemical oxygen demand, which is 0.07 for resorcinol, was increased to a value exceeding 0.5. The main by-product acetic acid, which is a preferred compound for methanogenic bacteria, was found to account for 33% of the total organic carbon.

  18. Surface grafting of resorcinol onto polyethylene film%PE膜表面接枝间苯二酚

    程珏; 郑义; 杨万泰


    Low density polyethylene film surface-grafted resorcinol was prepared by a sequential process.Firstly, acrylic acid was grafted to the surface of low density polyethylene by UV photografting.Secondly, the carboxylic groups in poly(acrylic acid) chains were transferred to acyl chloride groups by the reaction of carboxylic groups with thionyl chloride.The stability of acyl chloride groups in several solvents(alcohol, water, acetone, aqueous NaOH and in N2 atmosphere) was investigated, and N2 atmosphere and acetone were appropriate media to protect acyl chloride groups from side reaction.Finally, resorcinol monomer reacted with acyl chloride to append to the poly(acrylic acid)chains at room temperature.FT-IR-ATR was used to characterize the change of carbonyl groups during each step of the grafting process.Furthermore, by the experimental data of gravimetric analysis the grafted resorcinol monomer on the surface of low density polyethylene film was verified to have undergone condensation with acetone further in the resorcinol/acetone solution at 56℃, which might be a useful feature for synthesizing a thermoplastic/thermosetting composition.

  19. Performance of CTBN(carboxyl-terminated poly (butadiene-co-acrylonitrile))-EP(diglycidyl ether of bisphenol-A(DGEBA)) Prepolymers and CTBN-EP/polyetheramine (PEA) System

    SHI Minxian; HUANG Zhixiong; LI Yaming; YANG Guorui


    CTBN-EP prepolymers were synthesized from CTBN and epoxy resin under the catalysis of HTMAB.FTIR analyses indicate the formation of ester group between the carboxyl group of CTBN and the oxirane group of epoxy resin.The viscosity of modified prepolymer increases with CTBN content increasing,but the epoxy value of the prepolymer decreases greatly.DSC analyses verify that CTBN affects the curing process of CTBN-EP/PEA system.Mechanical testing presents the improved toughness of CTBN-EP/PEA curings for the decrease of tensile strength,flexural strength and compressive strength,and increase of impact strength and elongation-at-break with the CTBN content increasing.SEM micrographs show the rubber phase with many holes in diameter about 0.5-1.5μm is formed when CTBN content is lower than 10 phr.However,the pattern of SEM graph shows some stalactite-like strips when CTBN content is higher than 15 phr.Furthermore,the SEM image of 25 phr CTBN sample forms a kind of co-continuous structure.

  20. Synthesis and Properties of Diglycidyl Ether of Tetrabromobisphenol-A%四溴双酚A二缩水甘油醚的合成与表征

    贾修伟; 房晓敏; 丁涛; 刘治国; 徐元清


    通过探索温度、加碱方式、碱用量等因素对合成四溴双酚A二缩水甘油醚(DGEBA)的影响,优化出较好的合成条件.较理想的合成条件如下:两步加碱,第一步为催化剂量的碱,先于70 ℃醚化0.5 h,然后升温至100~105 ℃醚化1.5 h;第二步增加碱用量,闭环反应3 h.采用FT-IR、1H-NMR和热分析等对之进行表征.分析结果显示:产品纯度较高,没有未反应的TBBPA,环氧端基的特征吸收峰十分明显;热稳定性较高,热分解温度高于300 ℃.

  1. Nanosheet Graphene Composite Carbon Aerogels from Resorcinol-Formaldehyde via an Adsorption-Assembly Polymerization Method .

    Qiu, Jielong; Zhang, Shuting; Mai, Jiawen; Wu, Fangjun; Liu, Wei


    An adsorption-assembly sol-gel polymerization between graphene oxide (GO) sheets and resorcinol-formaldehyde aqueous solution was investigated as a method to form graphene composite carbon aerogels (GCAs) with cross-linked nanosheet structure and a surface area as high as 489 m2/g. By adjusting the amount of GO and the catalyst of hexamethylenetetramine (HMTA) in the precursor mixture, aerogels with little drying shrinkage under ambient pressure condition could be obtained. Benefiting from the attendance of graphene oxide, the obtained GCAs showed a regular nanosheets structure with countless nano-size particles on the sheet surface, which is quite different from the conventional carbon aerogels. The electrochemical performance of the GCAs were evaluated, they displayed small internal resistance and outstanding electrochemical specific capacitance (131 F/g), as well as a stable cycle performance (no capacitance loss after 5000 cycles).

  2. Study on efficient removal of clopyralid from water using resorcinol-formaldehyde carbon cryogel

    Momčilović Milan Z.


    Full Text Available Resorcinol-formaldehyde carbon cryogel has been prepared, characterized and used for the removal of commonly used herbicide clopyralid from the aqueous solutions under varying experimental conditions. Carbon has shown a relatively high specific surface area, significant mesoporosity and an amorphous structure. A set of the following isotherm models has been used to interpret the equilibrium data: Langmuir, Freundlich, Temkin, Dubinin-Radushkevich, Jovanović, Hurkins-Jura, and Helsey model. Several models have fitted well although the calculated values for qmax poorly correlate with the data obtained experimentally. The kinetic models of the pseudo-first and pseudo-second-order, the models of Elovich, Bangham and the intraparticle diffusion model have been used for fitting the kinetic data. The rate of the process is fast in the beginning while adsorption equilibrium is attained not until 24 hours. Adsorption was found to be pH dependent and favored in acidic solutions.

  3. An investigation of the radiolytic stability of a resorcinol-formaldehyde ion exchange resin

    Crawford, C.L.; Bibler, N.E.


    Developing and demonstrating waste separations technologies are the principal objectives of the Underground Storage Tank -Integrated Demonstration (UST-ID) Program carried out by Pacific Northwest Laboratories (PNL) at the DOE Hanford site. One planned separation technique utilizes ion exchange for removal of cesium and strontium from high-level liquid supernates. A resorcinol-formaldehyde resin, which is a polycondensation-type cation exchange resin for cesium removal, has been developed at the Savannah River Technology Center (SRTC) and has demonstrated superlative performance in testing at SRS, Oak Ridge and PNL. Advantages of this resin relative to other media for cesium removal are its high capacity for cesium and its compatibility with the high pH and aluminum and sodium concentrations of both Hanford and SRS high-level liquid wastes.

  4. Evaluations of Mechanisms for Pu Uptake and Retention within Spherical Resorcinol-Formaldehyde Resin Columns

    Delegard, Calvin H. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Levitskaia, Tatiana G. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Fiskum, Sandra K. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States)


    The unexpected uptake and retention of plutonium (Pu) onto columns containing spherical resorcinol-formaldehyde (sRF) resin during ion exchange testing of Cs (Cs) removal from alkaline tank waste was observed in experiments at both the Pacific Northwest National Laboratory (PNNL) and the Savannah River National Laboratory (SRNL). These observations have raised concern regarding the criticality safety of the Cs removal unit operation within the low-activity waste pretreatment system (LAWPS). Accordingly, studies have been initiated at Washington River Protection Solutions (WRPS), who manages the operations of the Hanford Site tank farms, including the LAWPS, PNNL, and elsewhere to investigate these findings. As part of these efforts, PNNL has prepared the present report to summarize the laboratory testing observations, evaluate these phenomena in light of published and unpublished technical information, and outline future laboratory testing, as deemed appropriate based on the literature studies, with the goal to elucidate the mechanisms for the observed Pu uptake and retention.

  5. Cesium Isotherm Testing with Spherical Resorcinol-Formaldehyde Resin at High Sodium Concentrations

    Russell, Renee L. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Fiskum, Sandra K. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Smoot, Margaret R. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Rinehart, Donald E. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States)


    Washington River Protection Solutions (WRPS) is developing a Low-Activity Waste Pretreatment System (LAWPS) to provide low-activity waste (LAW) directly to the Hanford Tank Waste Treatment and Immobilization Plant (WTP) Low-Activity Waste Facility for immobilization. The pretreatment that will be conducted on tank waste supernate at the LAWPS facility entails filtration to remove entrained solids and cesium (Cs) ion exchange to remove Cs from the product sent to the WTP. Currently, spherical resorcinol-formaldehyde (sRF) resin (Microbeads AS, Skedsmokorset, Norway) is the Cs ion exchange resin of choice. Most work on Cs ion exchange efficacy in Hanford tank waste has been conducted at nominally 5 M sodium (Na). WRPS is examining the possibility of processing supernatant at high Na concentrations—up to 8 M Na—to maximize processing efficiency through the LAWPS. Minimal Cs ion exchange work has been conducted at 6 M and 8 M Na concentrations..

  6. Comparative study on pore structures of mesoporous ZSM-5 from resorcinol-formaldehyde aerogel and carbon aerogel templating.

    Tao, Yousheng; Hattori, Yoshiyuki; Matumoto, Akihiko; Kanoh, Hirofumi; Kaneko, Katsumi


    Resorcinol-formaldehyde aerogels and carbon aerogels of different mesoporosities have been used as templates for preparing bimodal zeolites of mesopores. Samples were thoroughly characterized with X-ray diffraction, field emission scanning electron microscopy, thermogravimetric analysis, X-ray photoelectron spectroscopy, N(2) adsorption at 77 K, as well as FT-IR spectroscopy and (29)Si nuclear magnetic resonance spectroscopy. The mesoporous ZSM-5 zeolites have additional mesopores of 9-25 nm in widths and 0.07-0.2 cm(3)/g in volumes, besides their perfect inherent micropores. Experimental results show the mesoporous systems of the finally obtained zeolites can be influenced by proper preparation of resorcinol-formaldehyde aerogels and carbon aerogels through solution chemistry. Consequently, zeolites of tunable mesoporosities can be prepared with this unique methodology.

  7. Preparation of alpha-bisabolol and phenylethyl resorcinol/TiO2 hybrid composites for potential applications in cosmetics.

    Leong, H J; Jang, I; Hyun, K-S; Jung, S-K; Hong, G-H; Jeong, H-A; Oh, S-G


    Bifunctional alpha-bisabolol and phenylethyl resorcinol/TiO2 hybrids were prepared to apply in cosmetic fields, particularly in anti-ageing and hyperpigmentation treatment. The synergistic effect of combined antioxidant and UV filtering properties was achieved through functionalization of TiO2 particles with skin-lightening materials such as alpha-bisabolol and phenylethyl resorcinol. TiO2 microspheres with a diameter of about 1 μm were synthesized through surfactant-assisted sol-gel method for use as supporting materials in the formation of hybrid composites. Carboxylation treatment was performed for surface modification of the TiO2 surface with carboxyl groups as chemical binders. Esterification reaction between carboxyl groups of carboxylated TiO2 and hydroxyl groups of alpha-bisabolol or phenylethyl resorcinol was performed. The hybrids were characterized using various techniques such as FE-SEM, DLS, EDS, ATR-FTIR, XPS and TGA. For application of prepared TiO2 composites in the field of cosmetics, the anti-radicular antioxidant abilities were evaluated using ABTS and DPPH colorimetric antioxidant assay. Organic/inorganic hybrid composites were successfully formed using esterification reaction between the carboxyl groups at TiO2 surface and the hydroxyl groups of the skin-lightening materials. The results demonstrate that both functionalized microspheres show scavenging ability towards the ABTS(•) and DPPH(•) radicals. Specifically, the phenylethyl resorcinol/TiO2 composites exhibited the highest antioxidant ability among the prepared samples owing to the presence of phenolic groups to scavenge free radicals. Using this strategy, it could be possible to prepare not only inorganic UV filter but also hybrid organic/inorganic materials with multifunctions and advantages which would be in a great demand for cosmetic applications. © 2016 Society of Cosmetic Scientists and the Société Française de Cosmétologie.

  8. Direct Dimethyl Ether Synthesis

    Takashi Ogawa; Norio Inoue; Tutomu Shikada; Yotaro Ohno


    Dimethyl ether (DME) is a clean and economical alternative fuel which can be produced from natural gas through synthesis gas. The properties of DME are very similar to those of LP gas. DME can be used for various fields as a fuel such as power generation, transportation, home heating and cooking,etc. It contains no sulfur or nitrogen. It is not corrosive to any metal and not harmful to human body. An innovative process of direct synthesis of DME from synthesis gas has been developed. Newly developed catalyst in a slurry phase reactor gave a high conversion and high selectivity of DME production. One and half year pilot scale plant (5 tons per day) testing, which was supported by METI, had successfully finished with about 400 tons DME production.

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

    McPeak, Jennifer Lynne


    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...


    Feng Chen


    Full Text Available Lignin can be used as a cheap natural raw material to prepare organic aerogels based upon gelation and supercritical drying in ethanol. The aerogels were prepared from a mixture of the raw materials with lignin (L, resorcinol (R, and formaldehyde (F, followed by a reaction catalyzed by NaOH(C. The effect of the preparation conditions, such as the LRF concentration, the mass ratio of LR to NaOH (LR/C, the mole ratio of LR to F (LR/F, and the gelation temperature, on the gelation ability and the bulk density were studied. The results showed that the density of LRF aerogels increased with increasing reactant concentration and catalyst content. The microstructure of the porous carbon aerogels was investigated by SEM and TEM. The specific surface area and pore size distribution of LRF and RF aerogels were studied by nitrogen adsorption-desorption analysis. The pore width of LRF aerogels ranged from 1 nm to 100 nm. Most of the pores were about 50 nm wide, as is typical for mesoporous materials.

  11. Fire Safety Tests for Spherical Resorcinol Formaldehyde Resin: Data Summary Report

    Kim, Dong-Sang; Peterson, Reid A.; Schweiger, Michael J.


    A draft safety evaluation of the scenario for spherical resorcinol-formaldehyde (SRF) resin fire inside the ion exchange column was performed by the Hanford Tank Waste Treatment and Immobilization Plant (WTP) Fire Safety organization. The result of this draft evaluation suggested a potential change of the fire safety classification for the Cesium Ion Exchange Process System (CXP) emergency elution vessels, equipment, and piping, which may be overly bounding based on the fire performance data from the manufacturer of the ion exchange resin selected for use at the WTP. To resolve this question, the fire properties of the SRF resin were measured by Southwest Research Institute (SwRI), following the American Society for Testing and Materials (ASTM) standard procedures, through a subcontract managed by Pacific Northwest National Laboratory (PNNL). For some tests, the ASTM standard procedures were not entirely appropriate or practical for the SRF resin material, so the procedures were modified and deviations from the ASTM standard procedures were noted. This report summarizes the results of fire safety tests performed and reported by SwRI. The efforts by PNNL were limited to summarizing the test results provided by SwRI into one consolidated data report. All as-received SwRI reports are attached to this report in the Appendix. Where applicable, the precision and bias of each test method, as given by each ASTM standard procedure, are included and compared with the SwRI test results of the SRF resin.

  12. Effect of Fiber Treatment and Fiber Loading on Mechanical Properties of Luffa-Resorcinol Composites

    Chhatrapati Parida


    Full Text Available Tensile and compressive behaviour of resorcinol-formaldehyde (RF matrix and its composites reinforced with fibers of Luffa cylindrica (LC have been studied. LC fibers were subjected to chemical treatments such as alkali activation by NaOH followed by bleaching and acid hydrolysis in order to improve fiber-matrix adhesion. Both treated and untreated LC fibers are modified with calcium phosphate. The presence of hydroxy apatite, a polymorph of calcium phosphate and a major constituent of vertebrate bone and teeth, was confirmed from XRD peak of treated LC fiber. XRD analysis of the treated LC fiber has confirmed the crystalline nature of the chemically treated LC fiber by its crystallinity index. The effects of fiber loading of chemically treated and untreated LC fiber on ultimate stress, yield strength, breaking stress, and modulus of the composites were analyzed. The tensile and compressive modulus of the composites were increased with incorporation of both treated and untreated LC fibers into the RF matrix. The modulus of composites with treated LC fiber was enhanced compared to that of the untreated fiber composites. Furthermore the values of ultimate stress, yield stress, and breaking stress were increased with the incorporation of treated LC fiber in the composites.

  13. Gelation mechanism of resorcinol-formaldehyde gels investigated by dynamic light scattering.

    Taylor, Stewart J; Haw, Mark D; Sefcik, Jan; Fletcher, Ashleigh J


    Xerogels and porous materials for specific applications such as catalyst supports, CO2 capture, pollutant adsorption, and selective membrane design require fine control of pore structure, which in turn requires improved understanding of the chemistry and physics of growth, aggregation, and gelation processes governing nanostructure formation in these materials. We used time-resolved dynamic light scattering to study the formation of resorcinol-formaldehyde gels through a sol-gel process in the presence of Group I metal carbonates. We showed that an underlying nanoscale phase transition (independent of carbonate concentration or metal type) controls the size of primary clusters during the preaggregation phase; while the amount of carbonate determines the number concentration of clusters and, hence, the size to which clusters grow before filling space to form the gel. This novel physical insight, based on a close relationship between cluster size at the onset of gelation and average pore size in the final xerogel results in a well-defined master curve, directly linking final gel properties to process conditions, facilitating the rational design of porous gels with properties specifically tuned for particular applications. Interestingly, although results for lithium, sodium, and potassium carbonate fall on the same master curve, cesium carbonate gels have significantly larger average pore size and cluster size at gelation, providing an extended range of tunable pore size for further adsorption applications.

  14. Simultaneous Determination of Hydroquinone, Catechol and Resorcinol at Graphene Doped Carbon Ionic Liquid Electrode

    Li Ma


    Full Text Available A new composite electrode has been prepared with doping graphene into the paste consisting graphite and ionic liquid, n-octyl-pyridinum hexafluorophosphate (OPFP. This electrode shows an excellent electrochemical activity for the redox of hydroquinone (HQ, catechol (CC, and resorcinol (RS. In comparison with bare paste electrode, the redox peaks of three isomers of dihydroxybenzene can be obviously, simultaneously observed at graphene doping paste electrode. Under the optimized condition, the simultaneous determination of HQ, CC, and RS in their ternary mixture can be carried out with a differential pulse voltammetric technique. The peak currents are linear to the concentration of HQ, CC, and RS in the range form 1×10−5 to 4×10−4, 1×10−5 to 3×10−4, and 1×10−6 to 1.7×10−4 mol L−1, respectively. The limits of detection are 1.8×10−6 mol L−1 for HQ, 7.4×10−7 mol L−1 for CC, and 3.6×10−7 M for RS, respectively.

  15. Spectrophotometric Determination of Gallium(III with 4-(2-Pyridylazo-resorcinol and Nitron

    Petya Vassileva Racheva


    Full Text Available The formation and liquid-liquid extraction of ion-association complex between gallium(III − 4-(2-pyridylazo-resorcinol (PAR – 1,4-diphenyl-3-(phenylamino-1H-1,2,4-triazole (nitron, Nt, water and chloroform were studied. The optimum conditions for gallium(III extraction as an ion-association complex, (NtH+[Ga3+(PAR2]-, were found: pH, concentration of the reagents and shaking time. The following key constants were calculated: constant of extraction (logKex = 6.28 ± 0.07, constant of association (logβ = 4.98 ± 0.05, constant of distribution (logKD = 1.30 ± 0.02 and recovery factor (R / % = 95.17 ± 0.02. Beerʼs law is obeyed for Ga(III concentration up to 0.8 μg cm-3 with apparent molar absorptivity of (10.3 ± 0.4×104 dm-3 mol-1 cm-1 at λmax = 510 nm. Some additional characteristics, such as limit of detection (LOD = 0.072 μg cm-3, limit of quantification (LOQ = 0.24 μg cm-3 and Sandellʼs sensitivity (SS = 0.000675 ng cm-2 were estimated as well.

  16. Ion Exchange Modeling Of Cesium Removal From Hanford Waste Using Spherical Resorcinol-Formaldehyde Resin

    Aleman, S. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Hamm, L. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Smith, F. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL)


    This report discusses the expected performance of spherical Resorcinol-Formaldehyde (RF) ion exchange resin for the removal of cesium from alkaline Hanford radioactive waste. Predictions of full scale column performance in a carousel mode are made for the Hot Commissioning, Envelope B, and Subsequent Operations waste compositions under nominal operating conditions and for perturbations from the nominal. Only the loading phase of the process cycle is addressed in this report. Pertinent bench-scale column tests, kinetic experiments, and batch equilibrium experiments are used to estimate model parameters and to benchmark the ion-exchange model. The methodology and application presented in this report reflect the expected behavior of spherical RF resin manufactured at the intermediate-scale (i.e., approximately 100 gallon batch size; batch 5E-370/641). It is generally believed that scale-up to production-scale in resin manufacturing will result in similarly behaving resin batches whose chemical selectivity is unaffected while total capacity per gram of resin may vary some. As such, the full-scale facility predictions provided within this report should provide reasonable estimates of production-scale column performance.

  17. Fire Safety Tests for Cesium-Loaded Spherical Resorcinol Formaldehyde Resin: Data Summary Report

    Kim, Dong-Sang; Schweiger, Michael J.; Peterson, Reid A.


    A draft safety evaluation of the scenario for spherical resorcinol formaldehyde (SRF) resin fire inside the ion exchange column was performed by the Hanford Tank Waste Treatment and Immobilization Plant (WTP) Fire Safety organization. The result of this draft evaluation suggested a potential change of the fire safety classification for the Cesium Ion Exchange Process System (CXP) emergency elution vessels, equipment, and piping. To resolve this question, the fire properties of the SRF resin were measured by Southwest Research Institute (SwRI) through a subcontract managed by Pacific Northwest National Laboratory (PNNL). The results of initial fire safety tests on the SRF resin were documented in a previous report (WTP-RPT-218). The present report summarizes the results of additional tests performed by SwRI on the cesium-loaded SRF resin. The efforts by PNNL were limited to summarizing the test results provided by SwRI into one consolidated data report. The as-received SwRI report is attached to this report in the Appendix A. Where applicable, the precision and bias of each test method, as given by each American Society for Testing and Materials (ASTM) standard procedure, are included and compared with the SwRI test results of the cesium-loaded SRF resin.

  18. Equation-of-State Measurements of Resorcinol Formaldehyde Foam Using Imaging X-Ray Thomson Spectrometer

    Belancourt, Patrick; Theobald, W.; Keiter, P. A.; Collins, T. J. B.; Bonino, M. J.; Kozlowski, P.; Drake, R. P.


    Understanding the equation of state of materials under shocked conditions is important for laboratory astrophysics and high-energy-density physics experiments. This talk will focus on experiments dedicated to developing a platform for measuring the equation of state of shocked foams on OMEGA EP. The foam used in the development of this platform is resorcinol formaldehyde foam with an initial density of 0.34 g/cc. One OMEGA EP beam drives a shock into the foam, while the remaining three beams irradiate a nickel foil to create the x-ray backlighter. The primary diagnostic for this platform, the imaging x-ray Thomson spectrometer (IXTS), spectrally resolves the scattered x-ray beam while imaging in one spatial dimension. The IXTS is ideally suited to measure plasma conditions upstream, downstream and at the shock front in the foam. Preliminary results from these experiments will be shown. This material is based upon work supported by the Department of Energy National Nuclear Security Administration under Award Number DE-NA0001944, the NNSA-DS and SC-OFES Joint Program in High-Energy-Density Laboratory Plasmas DE-NA0001840, and by the National Laser User Facility Program DE-NA0000850.

  19. Fabrication of Graphene/polydopamine Modified Electrode and Simultaneous Determination of Hydroquinone, Catechol and Resorcinol

    QI; Ya’e; SONG; Hai; REN; Xuefeng; XU; Li


    Graphite oxide(GO) prepared by an improved Hummers method was reduced to graphene(Gr) by a hydrothermal method with Na BH4 as a reductant. Gr sample was characterized by scanning electron microscopy, X-ray diffraction and BET specific surface area analysis, respectively. The Gr-PDA modified glass carbon electrode(Gr-PDA/GCE) was designed and constructed for the simultaneous determination of hydroquinone(HQ), catechol(CC) and resorcinol(RC). The electrochemical behaviors of HQ, CC and RC on the Gr-PDA/GCE were investigated by cyclic voltammetry(CV) and differential pulse voltammetry(DPV) techniques. The results show that there are the three detections with a high peak current on the modified electrode duo to the synergetic effects of Gr and PDA, the linear response ranges for HQ and CC are 40.2–1559.6 and 24.7–1105.0 μM and the detection limits(S/N=3) are 13.4 and 8.2 μM, respectively.

  20. Glyceryl guaiacol ether – review

    Massone, Flávio; Universidade Estadual Paulista; Luna, Stélio Pacca Loureiro; Universidade Estadual Paulista; Castro, Gladys Bastos; Universidade Estadual Paulista


    The history, physical and chemical properties, pharmacodynamics, pharmacokinetics, adverse effects, toxicity, clinical use in wild and domestic species and drug interactions with glyceryl guaiacol ether, an a-glyceryt ether, is presented. Guaiphenesin produces muscle relaxation without affecting diaphragmatic function. Besides muscle relaxation, the drug produces hypocholesterolemia, hypouricemia and has antitussive and expectorant actions, among others. It is a safe agent, but can produce th...

  1. Rearrangements of Cycloalkenyl Aryl Ethers

    Mercedesz Törincsi


    Full Text Available Rearrangement reactions of cycloalkenyl phenol and naphthyl ethers and the acid-catalyzed cyclization of the resulting product were investigated. Claisen rearrangement afforded 2-substituted phenol and naphthol derivatives. Combined Claisen and Cope rearrangement resulted in the formation of 4-substituted phenol and naphthol derivatives. In the case of cycloocthylphenyl ether the consecutive Claisen and Cope rearrangements were followed by an alkyl migration. The mechanism of this novel rearrangement reaction is also discussed.

  2. Ether: Bitcoin's competitor or ally?

    Bouoiyour, Jamal; Selmi, Refk


    Although Bitcoin has long been dominant in the crypto scene, it is certainly not alone. Ether is another cryptocurrency related project that has attracted an intensive attention because of its additional features. This study seeks to test whether these cryptocurrencies differ in terms of their volatile and speculative behaviors, hedge, safe haven and risk diversification properties. Using different econometric techniques, we show that a) Bitcoin and Ether are volatile and relatively more resp...

  3. Hair dyes resorcinol and lawsone reduce production of melanin in melanoma cells by tyrosinase activity inhibition and decreasing tyrosinase and microphthalmia-associated transcription factor (MITF) expression.

    Lee, Shu-Mei; Chen, Yi-Shyan; Lin, Chih-Chien; Chen, Kuan-Hung


    Hair coloring products are one of the most important cosmetics for modern people; there are three major types of hair dyes, including the temporary, semi-permanent and permanent hair dyes. The selected hair dyes (such as ammonium persulfate, sodium persulfate, resorcinol and lawsone) are the important components for hair coloring products. Therefore, we analyzed the effects of these compounds on melanogenesis in B16-F10 melanoma cells. The results proved that hair dyes resorcinol and lawsone can reduce the production of melanin. The results also confirmed that resorcinol and lawsone inhibit mushroom and cellular tyrosinase activities in vitro. Resorcinol and lawsone can also downregulate the protein levels of tyrosinase and microphthalmia-associated transcription factor (MITF) in B16-F10 cells. Thus, we suggest that frequent use of hair dyes may have the risk of reducing natural melanin production in hair follicles. Moreover, resorcinol and lawsone may also be used as hypopigmenting agents to food, agricultural and cosmetic industry in the future.

  4. Hair Dyes Resorcinol and Lawsone Reduce Production of Melanin in Melanoma Cells by Tyrosinase Activity Inhibition and Decreasing Tyrosinase and Microphthalmia-Associated Transcription Factor (MITF Expression

    Shu-Mei Lee


    Full Text Available Hair coloring products are one of the most important cosmetics for modern people; there are three major types of hair dyes, including the temporary, semi-permanent and permanent hair dyes. The selected hair dyes (such as ammonium persulfate, sodium persulfate, resorcinol and lawsone are the important components for hair coloring products. Therefore, we analyzed the effects of these compounds on melanogenesis in B16-F10 melanoma cells. The results proved that hair dyes resorcinol and lawsone can reduce the production of melanin. The results also confirmed that resorcinol and lawsone inhibit mushroom and cellular tyrosinase activities in vitro. Resorcinol and lawsone can also downregulate the protein levels of tyrosinase and microphthalmia-associated transcription factor (MITF in B16-F10 cells. Thus, we suggest that frequent use of hair dyes may have the risk of reducing natural melanin production in hair follicles. Moreover, resorcinol and lawsone may also be used as hypopigmenting agents to food, agricultural and cosmetic industry in the future.


    Adamson, D.


    Savannah River National Laboratory (SRNL) performed pilot-scale hydraulic/chemical testing of spherical resorcinol formaldehyde (RF) ion exchange (IX) resin for the River Protection Project-Hanford Tank Waste Treatment & Immobilization Plant (WTP) Project. The RF resin hydraulic cycle testing was conducted in two pilot-scale IX columns, 1/4 and 1/2 scale. A total of twenty-three hydraulic/chemical cycles were successfully completed on the spherical RF resin. Sixteen of these cycles were completed in the 24-inch IX Column (1/2 scale column). Hydraulic testing showed that the permeability of the RF resin remained essentially constant, with no observed trend in the reduction of the permeability as the number of cycles increased. The permeability during the pilot-scale testing was 3 times better than the design requirements of the WTP full-scale IX system. The RF resin bed showed no tendency to form fissures or pack more densely as the number of cycles increased. Particle size measurements of the RF resin showed no indication of particle size change (for a given chemical) with cycles and essentially no fines formation. The permeability of the resin bed was uniform with respect to changes in bed depth. Upflow Regeneration and Simulant Introduction in the IX columns revealed another RF resin benefit; negligible radial pressures to the column walls from the swelling of resin beads. The hydraulic and chemical performance of the spherical RF resin during cycle testing was found to be superior to all other tested IX resins. The pilot-scale testing indicates that the RF resin is durable and should hold up to many hydraulic cycles in actual radioactive Cesium (Cs) separation.

  6. Storage and Aging Effects on Spherical Resorcinol-Formaldehyde Resin Ion Exchange Performance

    Fiskum, Sandra K.; Arm, Stuart T.; Edwards, Matthew K.; Steele, Marilyn J.; Thomas, Kathie K.


    Bechtel National, Inc. (BNI) is evaluating the alternate Cs ion exchanger, spherical resorcinol-formaldehyde (RF), for use in the River Protection Project-Waste Treatment Plant (RPP-WTP).( ) Previous test activities with spherical RF indicate that it has adequate capacity, selectivity, and kinetics to perform in the plant according to the flowsheet needs. It appears to have better elution and hydraulic properties than the existing alternatives: ground-gel RF and SuperLig® 644 (SL 644).( ) To date, the spherical RF performance testing has been conducted on freshly manufactured resin (within ~2 months of manufacture). The ion exchange resins will be manufactured and shipped to the WTP up to 1 year before being used in the plant. Changes in the resin properties during storage could reduce the capacity of the resin to remove Cs from low-activity waste solutions. Active sites on organic SL-644 resin have been shown to degrade during storage (Arm et al. 2004). Additional testing was needed to study the effects of storage conditions and aging on spherical RF ion exchange performance. Variables that could have a significant impact on ion exchange resins during storage include storage temperature, medium, and time. Battelle—Pacific Northwest Division (PNWD) was contracted to test the effects of various storage conditions on spherical RF resin. Data obtained from the testing will be used by the WTP operations to provide direction for suitable storage conditions and manage the spherical RF resin stock. Storage test conditions included wet and dry resin configurations under nitrogen at three temperatures. Work was initially conducted under contract number 24590-101-TSA-W000-00004 satisfying the needs defined in Appendix C of the Research and Technology Plan( ) TSS A-219 to evaluate the impact of storage conditions on RF resin performance. In February 2007, the contract mechanism was switched to Pacific Northwest National Laboratory (PNNL) Operating Contract DE-AC05-76RL

  7. Mixture Design Approach on the Physical Properties of Lignin-Resorcinol-Formaldehyde Xerogels

    Chris D. Castro


    Full Text Available Organic xerogels were functionalized by incorporating sugarcane bagasse lignin from soda pulping black liquor, not used so far in this materials, with the aim of introducing new functional groups on traditional gels that could improve its adsorptive capacity. Two mixing designs were applied to identify the reactive combinations that allow a well gel formation and to adjust models that predict physical properties. The designs study five components: resorcinol (R, 0.04–0.3, lignin (L, 0.004–0.14, formaldehyde (F, 0.08–0.17, water (W, 0.45–0.8, and NaOH (C, 0.0003–0.0035. The first experimental design was an extreme vertices design and its results showed shrinkage between 4.3 and 59.7 and a bulk density from 0.54 to 1.3; a mass ratio LR/F near 1.5 was required for gel formation. In the second design a D-Optimal was used to achieve better adjusted coefficients and incorporate the largest possible amount of lignin in the gels. Bulk density varies from 0.42 to 0.9, shrinkage varies from 3.42 to 25.35, and specific surface area reaches values of 451.86 m2/g with 13% lignin and 270 m2/g with 27% lignin. High catalyst content improves lignin dissolution and increase shrinkage and bulk density of xerogels and bulk density. Lignin contributes to reducing shrinkage and specific surface area due to his compact and rigid structure.

  8. Epoxidation of allyl-glycidyl ether with hydrogen peroxide over Ti-SBA-15 catalyst and in methanol medium

    Walasek Marika


    Full Text Available This work presents the studies on the epoxidation of allyl-glycidyl ether (AGE over the Ti-SBA-15 catalyst. In these studies an aqueous hydrogen peroxide was used as an oxidizing agent and as a solvent methanol was applied. The studies on the influence the following parameters: temperature (20–80°C, molar ratio of AGE/H2O2 (1:1.5–5:1, methanol concentration (10–90 wt%, catalyst content (1–9 wt% and reaction time (15–240 min. were carried out and the most favourable values of these parameters were chosen (temperature 80°C, molar ratio of AGE/H2O2 = 5:1, methanol concentration 30 wt%, catalyst content 3 wt% and the reaction time 240 min.. At these conditions the functions describing the process reached the following values: the selectivity of diglycidyl ether (DGE 9.2 mol%, the conversion of AGE 13.9 mol% and the efficiency of H2O2 conversion 89.9 mol%.

  9. Simultaneous Detection and Estimation of Catechol, Hydroquinone, and Resorcinol in Binary and Ternary Mixtures Using Electrochemical Techniques.

    Hossain, Md Uzzal; Rahman, Md Toufiqur; Ehsan, Md Qamrul


    Cyclic voltammetry (CV) and differential pulse voltammetry (DPV) were performed with a glassy carbon electrode (GCE) modified with polyglutamic acid (PGA) on the three dihydroxybenzene isomers, catechol (CT), hydroquinone (HQ), and resorcinol (RS). At bare GCE, these isomers exhibited voltammograms with highly overlapped redox peaks that impeded their simultaneous detection in binary and ternary mixtures. On the contrary, at PGA modified GCE binary and ternary mixtures of the dihydroxybenzene isomers showed well-resolved redox peaks in both CV and DPV experiments. This resolving ability of PGA modified GCE proves its potential to be exploited as an electrochemical sensor for the simultaneous detection of these isomers.

  10. Simultaneous Detection and Estimation of Catechol, Hydroquinone, and Resorcinol in Binary and Ternary Mixtures Using Electrochemical Techniques

    Md. Uzzal Hossain


    Full Text Available Cyclic voltammetry (CV and differential pulse voltammetry (DPV were performed with a glassy carbon electrode (GCE modified with polyglutamic acid (PGA on the three dihydroxybenzene isomers, catechol (CT, hydroquinone (HQ, and resorcinol (RS. At bare GCE, these isomers exhibited voltammograms with highly overlapped redox peaks that impeded their simultaneous detection in binary and ternary mixtures. On the contrary, at PGA modified GCE binary and ternary mixtures of the dihydroxybenzene isomers showed well-resolved redox peaks in both CV and DPV experiments. This resolving ability of PGA modified GCE proves its potential to be exploited as an electrochemical sensor for the simultaneous detection of these isomers.

  11. Luminescent Lariat Aza-Crown Ether

    Burkhard König


    Full Text Available Lariat ethers are interesting recognition motifs in supramolecular chemistry. The synthesis of a luminescent lariat ether with triglycol chain by azide–alkyne (Huisgen cycloaddition is presented.

  12. Exogenous ether lipids predominantly target mitochondria.

    Lars Kuerschner

    Full Text Available Ether lipids are ubiquitous constituents of cellular membranes with no discrete cell biological function assigned yet. Using fluorescent polyene-ether lipids we analyzed their intracellular distribution in living cells by microscopy. Mitochondria and the endoplasmic reticulum accumulated high amounts of ether-phosphatidylcholine and ether-phosphatidylethanolamine. Both lipids were specifically labeled using the corresponding lyso-ether lipids, which we established as supreme precursors for lipid tagging. Polyfosine, a fluorescent analogue of the anti-neoplastic ether lipid edelfosine, accumulated to mitochondria and induced morphological changes and cellular apoptosis. These data indicate that edelfosine could exert its pro-apoptotic power by targeting and damaging mitochondria and thereby inducing cellular apoptosis. In general, this study implies an important role of mitochondria in ether lipid metabolism and intracellular ether lipid trafficking.

  13. Synthesis of a series of aromatic benziporphyrins and heteroanalogues via tripyrrane-like intermediates derived from resorcinol and 2-methylresorcinol.

    Lash, Timothy D; Miyake, Kae; Xu, Linlin; Ferrence, Gregory M


    Tripyrrane analogues were prepared by reacting resorcinol or 2-methylresorcinol with 2 equiv of an acetoxymethylpyrrole in the presence of p-toluenesulfonic acid and calcium chloride. Following removal of the benzyl ester protective groups, the resorcinol-derived benzitripyrrane was reacted with a pyrrole dialdehyde to give an aromatic hydroxyoxybenziporphyrin. However, furan and thiophene dialdehydes gave highly insoluble products that could not be fully characterized. The methylresorcinol-derived tripyrrane analogue reacted with pyrrole, furan, thiophene, and selenophene dialdehydes to give unstable porphyrinoids that were further oxidized with [bis(trifluoroacetoxy)iodo]benzene to give stable benziporphyrin derivatives. These oxidized benziporphyrins showed strongly diatropic properties by proton NMR spectroscopy where the differences in chemical shifts (Δδ) were >18 ppm in some cases. The selenophene-derived system was further characterized by X-ray crystallography, and these results showed that one of the pyrrole subunits in this crowded structure was tilted by 21° relative to the mean macrocyclic plane. The tripyrrolic system reacted with silver(I) acetate to give the corresponding silver(III) organometallic complex. Regioselective alkylation with methyl or ethyl iodide and potassium carbonate gave diastereomeric mixtures of N-alkyl derivatives, and the N-ethyl substitution products showed highly diastereotopic characteristics.

  14. The Nitrite-Scavenging Properties of Catechol, Resorcinol, and Hydroquinone: A Comparative Study on Their Nitration and Nitrosation Reactions.

    Lu, Yunhao; Dong, Yanzuo; Li, Xueli; He, Qiang


    The nitration and nitrosation reactions of catechol, resorcinol, and hydroquinone (0.05 mmol/L) with sodium nitrite (0.05 mmol/L) at pH 3 and 37 °C were studied by using liquid chromatography and mass spectrometry (LC-MS) and atom charge analysis, which was aimed to provide chemical insight into the nitrite-scavenging behavior of polyphenols. The 3 benzenediols showed different mechanisms to scavenge nitrite due to their differences in hydroxyl position. Catechol was nitrated with 1 NO2 group at the hydroxyl oxygen, and resorcinol was nitrosated with 2 NO groups at the C2 and C4 (or C6 ) positions of the benzene ring. Hydroquinone could scavenge nitrite through both nitration and nitrosation mechanisms. The nitrated hydroquinone had 1 NO2 group at the hydroxyl oxygen in the molecule, while the nitrosated 1 containing 2 NO groups at the benzene ring might have 3 structure probabilities. The results may provide a structure-activity understanding on the nitrite-scavenging property of polyphenols, so as to promote their application in the food industry for the removal of possibly toxic nitrites found in many vegetables and often in processed meat products. © 2016 Institute of Food Technologists®.


    Adu-Wusu, K.; Pennebaker, F.


    Small-column ion exchange (SCIX) units installed in high-level waste tanks to remove Cs-137 from highly alkaline salt solutions are among the waste treatment plans in the DOE-complex. Spherical Resorcinol-Formaldehyde (sRF) is the ion exchange resin selected for use in the Hanford Waste Treatment and Immobilization Plant (WTP). It is also the primary ion exchange material under consideration for SCIX at the Hanford site. The elution step of the multi-step ion exchange process is typically done with 0.5 M nitric acid. An acid eluant is a potential hazard in the event of a spill, leak, etc. because the high-level waste tanks are made of carbon steel. Corrosion and associated structural damage may ensue. A study has been conducted to explore non-acid elution as an alternative. Batch contact sorption equilibrium screening tests have been conducted with 36 potential non-acid eluants. The sorption tests involve equilibrating each cesium-containing eluant solution with the sRF resin for 48 hours at 25 C in a shaker oven. In the sorption tests, an eluant is deemed to have a high cesium elution potential if it minimizes cesium sorption onto the sRF resin. The top candidates (based on lowest cesium sorption distribution coefficients) include ammonium carbonate, ammonium carbonate/ammonium hydroxide, ammonium bicarbonate, rubidium carbonate, ammonium acetate, ammonium acetate/ammonium hydroxide, ammonium bicarbonate/ammonium hydroxide, calcium chloride, and magnesium chloride. A select few of the top candidate eluants from the screening tests were subjected to actual sorption (loading) and elution tests to confirm their elution ability. The actual sorption (loading) and elution tests mimicked the typical sRF-cesium ion exchange process (i.e., sorption or loading, caustic wash, water rinse, and elution) via batch contact sorption and quasi column caustic wash/water rinse/elution. The eluants tested included ammonium carbonate, ammonium acetate, calcium acetate, magnesium

  16. Bis(imino)pyridine (BIMP) Fe(II) catalyses one-pot green condensation of resorcinol, malononitrile, aromatic aldehydes and cyclohexanone

    Saman Damavandi; Reza Sandaroos


    A novel, efficient and green approach for the synthesis of pyranopyridine derivatives through one-pot, four-component reaction of resorcinol, malononitrile, aromatic aldehydes and cyclohexanone using bis(imino)pyridine (BIMP) Fe(II) catalyst under solvent-free and ultrasonic irradiation is described.

  17. Solution of Azelaic Acid (20%), Resorcinol (10%) and Phytic Acid (6%) Versus Glycolic Acid (50%) Peeling Agent in the Treatment of Female Patients with Facial Melasma.

    Faghihi, Gita; Taheri, Azam; Shahmoradi, Zabihollah; Nilforoushzadeh, Mohammad Ali


    Melasma, a common acquired disorder of hyperpigmentation, especially in women, is often resistant to therapy. This study was aimed to evaluate the efficacy and safety of azelaic acid, resorcinol and phytic acid solution in chemical peeling of melasma in comparison to 50% glycolic acid. This clinical trial was performed, on 42 female patients with bilateral melasma. Severity of melasma was assessed by melasma area and severity index (MASI). Combination of (20% azelaic acid + 10% resorcinol + 6% phytic acid) was used as a new peeling agent on the right side of the face and 50% glycolic acid on the left side every 2 weeks for 6 times. Follow-up was carried out for 3 months after the last session. Any decrease in MASI score and unwanted complications following peeling were evaluated and compared during the trial. Patients showed marked improvement as calculated with MASI score before and after treatment in both sides of the face. The efficacy of combination formula (azelaic acid, resorcinol and phytic acid) was similar to glycolic acid, but with fewer complications. There was no statistically difference in improvement between two groups (P > 0.05). However, the patient's discomfort following procedures was significantly lower with azelaic acid, resorcinol and phytic compared with the glycolic acid peels (P glycolic acid peel.


    Thalita S. Taiariol


    Full Text Available Resorcinol-formaldehyde (RF organic gels have been extensively used to produce carbon aerogels. The organic gel synthesis parameters greatly affect the structure of the resulting aerogel. In this study, the influence of the catalyst quantity on the polymeric solution sol-gel process was investigated. Sodium carbonate was used as a basic catalyst. RF gels were synthesized with a resorcinol to formaldehyde molar ratio of 0.5, a resorcinol to catalyst (R/C molar ratio equal to 50 or 300, and a resorcinol to solvent ratio of 0.1 g mL-1. The sol-gel process was evaluated in situ by Fourier transform infrared spectroscopy using a universal attenuated total reflectance sensor and measurements of the kinematic viscosity. The techniques showed the evolution of the sol-gel process, and the results showed that the lower catalyst quantity induced a higher gel point, with a lower viscosity at the gel point. Differential scanning calorimetry was used to investigate the thermal behavior of the RF dried gel, and results showed that the exothermic event related to the curing process was shifted to higher temperatures for solutions containing higher R/C ratios.

  19. Surface Heparinization of Poly(ether ether ketone)

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


    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 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.

  20. ETG举办针对EtherCAT产品提供商的EtherCAT培训



  1. On the synthesis and structure of resorcinol-formaldehyde polymeric networks – Precursors to 3D-carbon macroassemblies

    Lewicki, James P.; Fox, Christina A.; Worsley, Marcus A.


    With the new impetus towards the development of hierarchical graphene and CNT macro-assemblies for application in fields such as advanced energy storage, catalysis and electronics; there is much renewed interest in organic carbon-based sol–gel processes as a synthetically convenient and versatile means of forming three dimensional, covalently bonded organic/inorganic networks. Such matrices can act as highly effective precursors, scaffolds or molecular ‘glues’ for the assembly of a wide variety of functional carbon macro-assemblies. However, despite the utility and broad use of organic sol–gel processes – such as the ubiquitous resorcinol-formaldehyde (RF) reaction, there are details of the reaction chemistries of these important sol–gel processes that remain poorly understood at present. It is therefore both timely and necessary to examine these reactions in more detail using modern analytical techniques in order to gain a more rigorous understanding of the mechanisms by which these organic networks form. The goal of such studies is to obtain improved and rational control over the organic network structure, in order to better direct and tailor the architecture of the final inorganic carbon matrix. In this study we have investigated in detail, the mechanism of the organic sol–gel network forming reaction of resorcinol and formaldehyde from a structural and kinetic standpoint, by using a combination of real-time high field solution state nuclear magnetic resonance (NMR), low field NMR relaxometry and differential scanning calorimetry (DSC). These investigations have allowed us to track the network formation processes in real-time, gain both detailed structural information on the mechanisms of the RF sol–gel process and a quantitative assessment of the kinetics of the global network formation process. It has been shown that the mechanism, by which the RF organic network forms, proceeds via an initial exothermic step correlated to the formation of a


    Adu-Wusu, K.; Nash, C.; Pennebaker, F.


    Ion Exchange column loading and elution of cesium from spherical resorcinol-formaldehyde resin have been conducted for two potential non-acid eluants -(NH{sub 4}){sub 2}CO{sub 3} and CH{sub 3}COONH{sub 4}. The results revealed encouraging cesium elution performance. 100% elution was achieved in at most 22 hours ({approx}28 bed volumes) of elution. Elution performance was fairly high at 6 hours ({approx}8 bed volumes) of elution for some of the eluants and also practically comparable to the benchmark acid eluant (HNO{sub 3}). Hence, it is quite possible 100% percent elution will be closer to the 6th hour than the 22nd hour. Elution is generally enhanced by increasing the concentration and pH of the eluants, and combining the eluants.


    C. C. Lobo

    Full Text Available Abstract In this work the aerobic degradation of phenol (PH, catechol (CA, resorcinol (RE, hydroquinone (HY and of the binary mixtures PH+CA, PH+RE, PH+HY by phenol-acclimated activated sludge was studied. Single substrate experiments show a Haldane-type dependence of the respiration rate on PH, RE and HY, while CA corresponded to the Monod model. Binary substrate experiments demonstrated that the presence of a second substrate only affected the kinetics, but not the stoichiometry of the oxidation of the compounds tested. While CA inhibited the oxidation of PH, PH inhibited the oxidation of RE and HY. A mathematical model was developed to represent the aerobic biodegradation of the phenolic compounds tested. The agreement between the proposed model and the experimental data indicates that the proposed model can be useful for predicting substrate and dissolved oxygen concentrations in bioreactors treating phenolic wastewaters.

  4. 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

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


    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)

  5. Properties of epoxy-amine networks containing nanostructured ether-crosslinked domains

    Hsu, Ying-Gev, E-mail: [Department of Material Science and Engineering, National Taiwan University of Science and Technology, Taipei 106, Taiwan (China); Lin, Kuan-Hung; Lin, Tse-Yu; Fang, Yi-Lung [Department of Material Science and Engineering, National Taiwan University of Science and Technology, Taipei 106, Taiwan (China); Chen, Su-Chen; Sung, Yi-Ching [Department of Raw Materials and Yarns, Taiwan Textile Research Institute, New Taipei, Taiwan (China)


    Highlights: Black-Right-Pointing-Pointer The epoxy-amine networks with nanostructured ether-crosslinked domains (NECDs) was obtained. Black-Right-Pointing-Pointer The morphology of the networks dispersed with 10-30-nm-sized NECDs was investigated by AFM. Black-Right-Pointing-Pointer The molecular-level cavity in the matrix was inferred by a molecular-size simulation. Black-Right-Pointing-Pointer The fracture toughness of the networks were reinforced up to 1.35 times that of neat epoxy. Black-Right-Pointing-Pointer The networks were more thermostable than the neat epoxy because of higher cross-linking. - Abstract: Epoxy-amine networks with a nanodomain toughener-soft nanostructured ether-crosslinked domains (NECDs), which could increase the fracture and tensile toughness of the networks, were simply obtained when a mixture of diglycidyl ether bisphenol A (DGEBA) epoxy resin and 4,4 Prime -methylene dianiline (MDA) hardener was heat-cured in the presence of varying amounts of the imidazole derivatives (called imidazoles)-1-methylimidazole (1-MI) or 2-methylimidazole (2-MI). Under these conditions, the epoxide groups in DGEBA underwent not only polyaddition with the aromatic amine of the MDA to form a hard epoxy-amine networked matrix but also anionic ring-opening polymerization by itself to build soft NECDs connected to the epoxy-amine matrix. The curing chemistry of the DGEBA/MDA mixture, both with and without the imidazoles, was studied using differential scanning calorimetry (DSC) and Fourier transform infrared spectroscopy (FTIR). The morphology of the networks dispersed with 5-30-nm-sized NECDs was investigated by atomic force microscopy (AFM). When the optimum amount ({approx}0.15-0.30 wt%) of imidazoles was added, the NECDs were effective in significantly increasing the tensile and fracture toughness and the thermal stability of the epoxy-amine networks without markedly sacrificing the glass transition temperature (T{sub g}). The novel toughening mechanism and

  6. Generation of a Focused Poly(amino ether Library: Polymer-mediated Transgene Delivery and Gold-Nanorod based Theranostic Systems

    Lucas Vu, James Ramos, Thrimoorthy Potta, Kaushal Rege


    Full Text Available A focused library of twenty-one cationic poly(amino ethers was synthesized following ring-opening polymerization of two diglycidyl ethers by different oligoamines. The polymers were screened in parallel for plasmid DNA (pDNA delivery, and transgene expression efficacies of individual polymers were compared to those of 25 kDa polyethylenimine (PEI, a current standard for polymer-mediated transgene delivery. Seven lead polymers that demonstrated higher transgene expression than PEI in pancreatic and prostate cancer cells lines were identified from the screen. All seven lead polymers showed highest transgene expression at a polymer:pDNA weight ratio of 5:1 in the MIA PaCa-2 pancreatic cancer cell line. Among the conditions studied, transgene expression efficacy correlated with minimal polymer cytotoxicity but not polyplex sizes. In addition, this study indicated that methylene spacing between amine centers in the monomers, amine content, and molecular weight of the polymers are all significant factors and should be considered when designing polymers for transgene delivery. A lead effective polymer was employed for coating gold nanorods, leading to theranostic nanoassemblies that possess combined transgene delivery and optical imaging capabilities, leading to potential theranostic systems.

  7. Can simultaneous contact allergies to phenyl glycidyl ether and epoxy resins of the bisphenol A/F-types be explained by contamination of the epoxy resins?

    Pontén, Ann; Zimerson, Erik; Bruze, Magnus


    Simultaneous contact allergies to epoxy resins based on diglycidyl ether of bisphenol A (DGEBA-R) or epoxy resins of the bisphenol F-type and the reactive diluent phenyl glycidyl ether (PGE) have been reported. The reason might be cross-reactivity, exposure to an epoxy resin system with PGE as a component, or contamination by PGE in the epoxy resin. To study contamination by PGE, 20 commercial epoxy resins were analysed for the presence of PGE. To study contact allergy to PGE and its relation to epoxy resins by inserting PGE in the standard series. Among 2227 patients, 7 reacted to PGE. Of 23 (30%) patients, 7 with contact allergy to DGEBA-R and 7/19 (37%) with contact allergy to an epoxy resin of the bisphenol F-type reacted to PGE. All 7 patients with contact allergy to PGE reacted both to the DGEBA-R and to the epoxy resin of the bisphenol F-type. PGE was found in 90% of the investigated resins. The amounts of PGE ranged between 0.004% w/w and 0.18% w/w. Most probably, the presence of PGE as a contaminant in epoxy resins is of minor importance for the sensitization, but possibly the contamination of PGE might elicit contact dermatitis in individuals with a high reactivity to PGE.

  8. Enhancement in Mode II Interlaminar Fracture Toughness at Cryogenic Temperature of Glass Fiber/Epoxy Composites through Matrix Modification by Carbon Nanotubes and n-Butyl Glycidyl Ether

    Yu Liu


    Full Text Available A typical diglycidyl ether of bisphenol-F (DGEBF/diethyl toluene diamine (DETD epoxy system modified by multiwalled carbon nanotubes (MWCNTs and a reactive aliphatic diluent named n-butyl glycidyl ether (BGE was used as the matrix for glass fiber composites. The glass fiber (GF reinforced composites based on the unmodified and modified epoxy matrices were prepared by the hand lay-up hot-press process. Mode II interlaminar fracture toughness at both room temperature (RT and cryogenic temperature (77 K of the GF reinforced epoxy composites was investigated to examine the effect of the matrix modification. The result showed that the introduction of MWCNTs and BGE at their previously reported optimal contents led to the remarkable enhancement in mode II interlaminar fracture toughness of the composites. Namely, the 22.9% enhancement at RT and the 31.4% enhancement at 77 K were observed for mode II interlaminar fracture toughness of the fiber composite based on the optimally modified epoxy matrix by MWCNTs and BGE compared to the unmodified case.

  9. The viscosity of dimethyl ether

    Sivebæk, Ion Marius; Jakobsen, Jørgen


    Dimethyl ether (DME) has been recognised as an excellent fuel for diesel engines for over one decade now. Engines fuelled by DME emit virtually no particulate matter even at low NOx levels. This is only possible in the case of diesel oil operation if expensive and efficient lowering particles...... for pressurisation in these methods. The results of the VFVM are consolidated by measurements of the viscosities of propane and butane: these agree with the outcome of measurements using a quartz crystal microbalance (QCM) a method that is supposedly less sensible than the Reynolds number....

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

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


    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.

  11. Synthesis of Disperse Dyes from Pyridone and Resorcinol Coupled to Diazotized 2-Amino-4-chloro-5-formylthiazole and Application to Polyester

    Yusuf Y. Lams


    Full Text Available The aim of this study was to synthesize disperse dyes in the derivative of 2-amino-4-chloro-5-formylthiazole by conventional diazotization and couplings with pyridone and resorcinol. The dyes were characterized by visible absorption spectroscopy, IR spectral studies, and 1H and 13C NMR. The pyridone and resorcinol substituted dyes exhausted well with good depth on 100% polyester fabrics with a shade of brown and purple colours, respectively. The heteroatom and the intrinsic conjugation in the thiazole structure results in high bathochromic shifts and lead to brightness of shades. The dyed fabrics showed very good to excellent wash fastness and moderate to good light and perspiration fastness properties.

  12. 27 CFR 21.108 - Ethyl ether.


    ... 27 Alcohol, Tobacco Products and Firearms 1 2010-04-01 2010-04-01 false Ethyl ether. 21.108 Section 21.108 Alcohol, Tobacco Products and Firearms ALCOHOL AND TOBACCO TAX AND TRADE BUREAU, DEPARTMENT....108 Ethyl ether. (a) Odor. Characteristic odor. (b) Specific gravity at 15.56 °/15.56 °C. Not...

  13. Differential effects of bisphenol A diglicydyl ether on bone quality and marrow adiposity in ovary-intact and ovariectomized rats.

    Li, Guanwu; Xu, Zheng; Hou, Lingmi; Li, Xuefeng; Li, Xin; Yuan, Wei; Polat, Maki; Chang, Shixin


    Bisphenol A diglycidyl ether (BADGE), a PPARγ2 antagonist, has been shown to inhibit marrow adipogenesis and promote bone formation in intact animals. We investigated the impact of BADGE on a new and more clinically relevant physiological model, the ovariectomized (OVX) rat model. Forty female Wistar rats were divided into four treatment groups for 12 wk (n = 10/group): sham+vehicle, sham+BADGE, OVX+vehicle, and OVX+BADGE. Postmortem analyses included MRI, micro-CT, serological test, histomorphometry, biomechanical tests, RT-PCR, and Western blot. Overall, OVX induced a sequential marrow fat expansion accompanied by bone deterioration. Compared with OVX controls, BADGE reduced fat fraction of the distal femur by 36.3%, adipocyte density by 33.0%, adipocyte size by 28.6%, adipocyte volume percentage by 57.8%, and adipogenic markers PPARγ2 and C/EBPα by ∼50% in OVX rats. Similar results were observed in sham rats vs. vehicle. BADGE could promote bone quality in sham rats; however, BADGE did not significantly improve trabecular microarchitecture, biomechanical strength, and dynamic histomorphometric parameters except for trabecular separation in OVX rats. We concluded that early BADGE treatment at a dose of 30 mg/kg attenuates marrow adiposity in ovary-intact and OVX rats and stimulates bone formation in ovary-intact rats but does not significantly rescue bone quality in OVX rats. Copyright © 2016 the American Physiological Society.

  14. 间苯二酚催化加氢反应产物的分析及精制%Analysis and Purification of Hydrogenation Products of Resorcinol

    李杏花; 魏作君; 刘迎新; 孟令富


    1,3-cyclohexanedione (CHD) has generally been industrially produced from the hydrogenation of resorcinol (RES). In this paper, the analysis and purification of the resorcinol hydrogenation products were studied by GC-MS. A gas chromatography method was established to quantitatively analyze the resorcinol and 1,3-cyclohexanedione. The stability of resorcinol and 1,3-cyclohexanedione in several organic solvents were studied by GC-MS, the results show that the acetonitrile is the most favorable solvent for the extraction and post processing. Then the acetonitrile was used as recrystalization solvent for 1,3-cyclohexanedione and a higher purity was obtained.%间苯二酚催化加氢法是目前生产l,3-环己二酮的主流方法.今采用气相色谱-质谱法对间苯二酚催化加氢反应产物的分析及精制进行研究,建立了间苯二酚及1,3-环己二酮的气相色谱定量分析方法.通过气相色谱-质谱法对该体系在有机溶剂中的稳定性研究表明,丙酮、乙醇和乙酸乙酯均不适合作为该反应体系后处理的溶剂,而乙腈符合选择的要求.用乙腈对反应产物进行重结晶,得到了高纯度的1,3-环己二酮产品.

  15. An expedient synthesis of linden ether.

    Serra, Stefano; Cominetti, Alessandra A


    We here describe a comprehensive study on the preparation of the intensive flavor 3,9-epoxy-p-mentha-1,4(8)-diene (1). Key steps of the presented synthesis are the selective addition of MeLi to the keto-ester 7, the regioselective cyclization of the obtained triol to give the ethers 4 and 8 and the selective dehydration of ether 4 through the use of POCI3 and pyridine. It is worth noting that the presented synthesis represents the first expedient and reliable entry to ether 1. Being present in linden honey, 1 is also known as linden ether and it has been regarded as a potential marker for the authentication of the linden honey origin. Therefore, ether 1 can be used as a useful reference standard for the analysis of the natural flavors, as we demonstrated by means of its identification in a sample ofunifloral linden honey.

  16. A new alternative to expandable pedicle screws: Expandable poly-ether-ether-ketone shell.

    Demir, Teyfik


    Screw pullout is a very common problem in the fixation of sacrum with pedicle screws. The principal cause of this problem is that the cyclic micro motions in the fixation of sacrum are higher than the other regions of the vertebrae that limit the osteo-integration between bone and screw. In addition to that, the bone quality is very poor at sacrum region. This study investigated a possible solution to the pullout problem without the expandable screws' handicaps. Newly designed poly-ether-ether-ketone expandable shell and classical pedicle screws were biomechanically compared. Torsion test, pullout tests, fatigue tests, flexion/extension moment test, axial gripping capacity tests and torsional gripping capacity tests were conducted in accordance with ASTM F543, F1798 and F1717. Standard polyurethane foam and calf vertebrae were used as embedding medium for pullout tests. Classical pedicle screw pullout load on polyurethane foam was 564.8 N compared to the failure load for calf vertebrae's 1264 N. Under the same test conditions, expandable poly-ether-ether-ketone shell system's pullout loads from polyurethane foam and calf vertebrae were 1196.3 and 1890 N, respectively. The pullout values for expandable poly-ether-ether-ketone shell were 33% and 53% higher than classical pedicle screw on polyurethane foam and calf vertebrae, respectively. The expandable poly-ether-ether-ketone shell exhibited endurance on its 90% of yield load. Contrary to poly-ether-ether-ketone shell, classical pedicle screw exhibited endurance on 70% of its yield load. Expandable poly-ether-ether-ketone shell exhibited much higher pullout performance than classical pedicle screw. Fatigue performance of expandable poly-ether-ether-ketone shell is also higher than classical pedicle screw due to damping the micro motion capacity of the poly-ether-ether-ketone. Expandable poly-ether-ether-ketone shell is a safe alternative to all other expandable pedicle screw systems on mechanical perspective

  17. 含芳醚芴二胺/环氧树脂固化反应动力学及性能研究%Curing kinetics and properties of epoxy resins/fluorene diamine containing aryl ether linkage

    刘文彬; 王军; 李国兵; 郝永昌; 黎亚明


    以9,9-双[4-4-氨基苯氧基苯基]芴(BAOFL)作为固化剂,采用非等温DSC技术,研究了BAOFL/环氧树脂(E-51、TDE-85和芴基环氧树脂)体系的固化反应动力学,利用动态热机械分析仪(DMA)和热重分析仪(TGA)测试了固化树脂的力学性能和热稳定性。结果表明,固化反应活化能与环氧树脂和固化剂的结构密切相关,芳醚的引入提高了氨基与环氧基的反应性,固化树脂呈现出优良的热性能和力学性能,其玻璃化转变温度(T )达到206~248℃,贮能模量为2.54~2.94 GPa,初始热分解温度312~375℃,700℃g时的残炭率达到15.2%~31.7%。%In this study,the curing kinetics of 9,9-bis[4-(4-aminophenoxy)phenyl]fluorene (BAOFL) with different epoxy resins including diglycidyl ether of bisphenol A (E-51),cycloaliphatic epoxy resin (TDE-85) and diglycidyl ether of bisphenol fluorene (DGEBF) was investigated using nonisothermal differential scanning calorimetry (DSC) by Kissinger and Ozawa methods.The thermal properties of obtained polymers were evaluated by dynamic mechanical thermal analysis (DMA) and thermogravimetric analysis (TGA).The results showed that the values of activation energy (Ea) werea strongly dependent on the structures of epoxy resin and curing agent.The curing reactivity between amino groups and epoxy groups in the epoxy system was improved by introduction of the flexible aryl ether linkages into the chain backbone.The cured polymers exhibited higher glass transition temperature (Tg),lower rigidity and better thermal stability compared tog those of the corresponding epoxy resins/fluorenyl diamine without aryl ether linkages.The cured product of epoxy resin/BAOFL has a Tg of and a 206-248 storage modulus of 2.54-2.94 GPa.The thermal decomposition temperatureg℃weight loss and the char yield at 700 of the cured polymer were 312-375℃ and 15.2%-31.7%,respectively.

  18. Immobilization of complexes of some heavy metals with a 2-(4-pyridylazo)-resorcinol 'PAR' on Algerian hydrothermal clay

    Bendjeffal, H.; Guerfi, K.; Bouhedja, Y.; Rebbani, N.


    The immobilization of the complexes of some heavy metals such as Co(II) and Ni(II) with a 2-(4-pyridylazo)-resorcinol 'PAR' from aqueous solution is studied using a natural and activated kaolin of Hameme Edbegh-Guelma (East of Algeria). The sorption of these metals complexes on kaolin from aqueous medium through the process of adsorption is studied under a set of variables such as concentration of metal complex, amount of kaolin, time and temperature of interaction. The suitability of the adsorbent was tested by fitting the adsorption data with Langmuir and Freundlich isotherms. The sorption of these complexes conformed to linear form of Langmuir adsorption equation. Langmuir qm constants for each metal complex were found as 0.391-0.493 mg/g (NiII-PAR2), 0.129-0.168 mg/g (CoII-PAR2) at 30 ∘C, respectively also, kinetic and thermodynamic parameters such as enthalpy (ΔH), free energy (ΔG) and entropy (ΔS) were calculated and these values show that adsorption of Co(II) and Ni(II) complex on kaolin was an exothermic.

  19. One-pot synthesis of interpenetrating inorganic/organic networks of CuO/resorcinol-formaldehyde aerogels: nanostructured energetic materials.

    Leventis, Nicholas; Chandrasekaran, Naveen; Sadekar, Anand G; Sotiriou-Leventis, Chariklia; Lu, Hongbing


    For many applications ranging from catalysis to sensors to energetic materials, it is desirable to produce intimate mixtures of nanoparticles. For instance, to improve the reaction rates of energetic materials, the oxidizing agent and the fuel need to be mixed as intimately as possible, ideally at the nanoscopic level. In this context, the acidity of a hydrated CuCl(2) solution reacting toward a network of CuO nanoparticles (a good oxidant) is used to induce one-pot cogelation of a nanostructured network of a resorcinol-formaldehyde resin (RF, the fuel). The resulting wet gels are dried to aerogels, and upon pyrolysis under Ar, the interpenetrating CuO/RF network undergoes a smelting reaction toward metallic Cu. Upon ignition in the open air, pure RF aerogels do not burn, while CuO/RF composites, even with substoichiometric CuO, sustain combustion, burning completely leaving only a solid residue of CuO whose role then has been that of a redox mediator through the smelting reaction.

  20. Simultaneous determination of hydroquinone, catechol and resorcinol by voltammetry using graphene screen-printed electrodes and partial least squares calibration.

    Aragó, Miriam; Ariño, Cristina; Dago, Àngela; Díaz-Cruz, José Manuel; Esteban, Miquel


    Catechol (CC), resorcinol (RC) and hydroquinone (HQ) are dihydroxybenzene isomers that usually coexist in different samples and can be determined using voltammetric techniques taking profit of their fast response, high sensitivity and selectivity, cheap instrumentation, simple and timesaving operation modes. However, a strong overlapping of CC and HQ signals is observed hindering their accurate analysis. In the present work, the combination of differential pulse voltammetry with graphene screen-printed electrodes (allowing detection limits of 2.7, 1.7 and 2.4µmolL(-1) for HQ, CC and RC respectively) and the data analysis by partial least squares calibration (giving root mean square errors of prediction, RMSEP values, of 2.6, 4.1 and 2.3 for HQ, CC and RC respectively) has been proposed as a powerful tool for the quantification of mixtures of these dihydroxybenzene isomers. The commercial availability of the screen-printed devices and the low cost and simplicity of the analysis suggest that the proposed method can be a valuable alternative to chromatographic and electrophoretic methods for the considered species. The method has been applied to the analysis of these isomers in spiked tap water.

  1. Removal and Recovery of Some From Simulated Nuclear Waste Radionuclides Using Amberlite XAD-16-Pyridylazo Resorcinol (AXAD-PR) Composite

    Akçağlar, Sevil


    In this study, Amberlite XAD-16-Pyridylazo resorcinol composite (AXAD-PR) were developed under laboratory conditions to detect the removals and recoveries of U(IV) and Am(III) from simulated nuclear wastes by adsorption and desorption processes. The effects of contacting time (5, 15, 25 and 200 min), of AXAD-PR concentrations (5, 25, 50 and 100 mg/l), of temperatures (15, 30 and 45°C), increasing U(IV) and Am(III) concentrations (1, 5, 10, 15, 20, 30 and 40) and pH levels (acidic, basic and neutral conditions) on the removals and recoveries of U(IV) and Am(III) radionuclides were investigated. The data obtained showed that the maximum adsorption yields of U(IV) and Am(III) were found to be 96% and 95%, respectively, after 25 min using 25 mg/l AXAD-PR at 30°C at an acidic pH of 5. The adsorption kinetic of radionuclides to AXAD-PR isotherm was in accordance with Langmuir. The AXAD-PR can be reused and can be used again. The regeneration of the composite is possible and can be attained a desorption efficiency of 99% using 0.4 M HNO3 acid solution from 25 mg/l prepared AXAD-PR.

  2. Photopolymerization of Glycerin Triglycidyl Ether Based Systems

    HUANG Biwu; CHEN Yiwang; DENG Qilan


    Photopolymerization process of glycerin triglycidyl ether based systems was studied by an FT-IR spectrometer.An increase in the rate of polymerization for glycerin triglycidyl ether was evident when 3,4-epoxycyclohexylmethyl-3',4'-epoxycyclohexanecarboxylate was added to it.Its copolymerization mechanism was confirmed by using DSC analysis.The effect of ethoxylated trimethyol propane triacrylate on the rate of polymerization for glycerin triglycidyl ether was also studied,and the formation of interpenetrating network tightly cross-link was proposed.

  3. A transferable force field to predict phase equilibria and surface tension of ethers and glycol ethers.

    Ferrando, Nicolas; Lachet, Véronique; Pérez-Pellitero, Javier; Mackie, Allan D; Malfreyt, Patrice; Boutin, Anne


    We propose a new transferable force field to simulate phase equilibrium and interfacial properties of systems involving ethers and glycol ethers. On the basis of the anisotropic united-atom force field, only one new group is introduced: the ether oxygen atom. The optimized Lennard-Jones (LJ) parameters of this atom are identical whatever the molecule simulated (linear ether, branched ether, cyclic ether, aromatic ether, diether, or glycol ether). Accurate predictions are achieved for pure compound saturated properties, critical properties, and surface tensions of the liquid-vapor interface, as well as for pressure-composition binary mixture diagrams. Multifunctional molecules (1,2-dimethoxyethane, 2-methoxyethanol, diethylene glycol) have also been studied using a recently proposed methodology for the calculation of the intramolecular electrostatic energy avoiding the use of additional empirical parameters. This new force field appears transferable for a wide variety of molecules and properties. It is furthermore worth noticing that binary mixtures have been simulated without introducing empirical binary parameters, highlighting also the transferability to mixtures. Hence, this new force field gives future opportunities to simulate complex systems of industrial interest involving molecules with ether functions.

  4. 基于FPGA的EtherCAT从站节点开发%FPGA- based Development of EtherCAT Slave Node

    李昆; 杨建武


    随着实时工业以太网技术在工业自动化领域的发展和应用,德国倍福公司推出的EtherCAT技术尤其备受瞩目.EtherCAT技术的核心在于EtherCAT通信机制、EtherCAT主站和EtherCAT从站节点.EtherCAT从站节点通常是采用EtherCAT从站控制芯片和从站控制微处理器来设计实现的,对此提出了一种使用FPGA技术开发实现EtherCAT从站节点功能的方法,并验证了方法的可行性.%With the development and application of the real - time industrial Ethernet technology in industrial automation, EtherCAT technology introduced by Beckhoff is especially well received. The core of EtherCAT technology is the EtherCAT communication mechanisms, EtherCAT Master and EtherCAT Slave Node. EtherCAT slave node is usually designed by using EtherCAT slave controller chip and slave control microprocessor chip to achieve its function, this paper presents a method which is using FPGA technology to develop the EtherCAT slave node, and verifies the feasibility of it.

  5. Vacuum condensates and `ether-drift' experiments

    Consoli, M.; Pagano, A.; Pappalardo, L.


    The idea of a `condensed' vacuum state is generally accepted in modern elementary particle physics. We argue that this should motivate a new generation of precise `ether-drift' experiments with present-day technology.

  6. Activity relationships for aromatic crown ethers

    Wilson, M J


    This thesis involves an investigation of aromatic crown ethers and a study of their binding constants for alkali metals. The study was motivated by the current needs of the semiconductor industry to improve the scavenging of mobile ions from fabricated circuits. A number of aromatic crown ethers have been sulphonated in an attempt to improve their water solubility and cation binding activity. These materials have been extensively studied and their binding activity determined. In collaboration with a molecular modelling study, the effect of ionisable sulphonate groups on the macrocycles' behaviour has been investigated. The broader issue of the effect of substituents in aromatic crown ethers has also been studied with the preparation of a wide range of substituted crown ethers. The cation binding activity of these materials has been found to bear a simple relationship to the electron withdrawing nature of the aromatic substituents. This relationship can be accurately monitored using electronic charge densities...

  7. Exogenous ether lipids predominantly target mitochondria

    Kuerschner, Lars; Richter, Doris; Hannibal-Bach, Hans Kristian


    Ether lipids are ubiquitous constituents of cellular membranes with no discrete cell biological function assigned yet. Using fluorescent polyene-ether lipids we analyzed their intracellular distribution in living cells by microscopy. Mitochondria and the endoplasmic reticulum accumulated high......, accumulated to mitochondria and induced morphological changes and cellular apoptosis. These data indicate that edelfosine could exert its pro-apoptotic power by targeting and damaging mitochondria and thereby inducing cellular apoptosis. In general, this study implies an important role of mitochondria...


    Aleman, S.; Hamm, L.; Smith, F.


    The current strategy for removal of cesium from the Hanford waste stream is ion-exchange using spherical Resorcinol-Formaldehyde (sRF) resin. The original resin of choice was granular SuperLig 644 resin and during testing of this resin several operational issues were identified. For example, the granular material had a high angle of internal friction resulting in fragmentation of resin particles along its edges during cycling and adverse hydraulic performance. Efforts to replace SuperLig 644 were undertaken and one candidate was the granular Resorcinol-Formaldehyde (RF) resin where experience with this cation exchanger dates back to the late 1940's. To minimize hydraulic concerns a spherical version of RF was developed and several different chemically produced batches were created. The 5E-370/641 batch of sRF was selected and for the last decade numerous studies have been performed (e.g., batch contact tests, column loading and elution tests). The Waste Treatment Plant (WTP) flowsheet shows that the aqueous phase waste stream will have a wide range of ionic concentrations (e.g., during the loading step 0-3 M free OH, 5+ M Na, 0-1 M K, 0-3 M NO{sub 3}). Several steps are required in the ion-exchange process to achieve the required Cs separation factors: loading, displacement, washing, elution, and regeneration. The sRF resin will be operated over a wide range in pH (i.e., pH of 12-14 during the loading step and pH of 0.01-1 during the elution step). During some of these steps very high levels of counter-ions and co-ions will be present within the aqueous phase. Alternative process feeds are under consideration as well (e.g., sodium levels as high as 8 M and column operation up to 45 C during loading, reduced and recycled HNO{sub 3} during elution). In order to model the performance of sRF resin through an entire ion-exchange cycle, a more robust isotherm model is required. To achieve this more robust isotherm model requires knowledge of the numbers and kinds of

  9. Development and validation of an ultraviolet-visible spectrophotometric method for determination of phenylethyl resorcinol in new topical nanoemulsions.

    Hong, L; Han, D; Li, M-X; Zhang, P; Liu, C-G


    To develop a rapid, simple and efficient ultraviolet-visible (UV-vis) spectrophotometric method for the quantification of phenylethyl resorcinol (PR), a potent skin-lightening agent, incorporated into new topical nanoemulsions, and to validate this method according to International Commission for Harmonization (ICH) guidelines. UV-vis spectrophotometric method for quantification of PR in new topical nanoemulsions was developed and validated in terms of specificity, linearity, sensitivity, precision and accuracy. The method was applied to determine PR content (extraction recoveries) in the nanoemulsions and entrapment efficiencies. The calibration curve for PR was linear in the range of 10-60 μg mL(-1) , with a determination coefficient (r(2) ) which is higher than 0.999. The limit of detection (LOD) and limit of quantitation (LOQ) were 1.55 and 4.69 μg mL(-1) , respectively. The method was shown to be specific, precise [intraday, interday and reproducibility levels relative standard deviation < 3%] and accurate (between 91.90 ± 1.28% and 104.73 ± 0.60%). The extraction recoveries of PR in nanoemulsions were 97.07%, 96.64% and 103.54% at concentrations of 3, 6 and 9 mg mL(-1) , respectively. The entrapment efficiencies were nearly 100%, which agrees with the oil core location of PR in nanoemulsions. This developed method was confirmed to be rapid, simple, cost-effective, specific, precise, accurate and suitable for determination of PR content in nanoemulsions and entrapment efficiencies. © 2016 Society of Cosmetic Scientists and the Société Française de Cosmétologie.

  10. Development of a nanostructured lipid carrier formulation for increasing photo-stability and water solubility of Phenylethyl Resorcinol

    Fan, Hengfeng; Liu, Guoqing; Huang, Yiqing; Li, Yan; Xia, Qiang


    The Phenylethyl Resorcinol loaded nanostructured lipid carrier (PR-NLC) was developed by hot high-pressure homogenization method. The freshly prepared PR-NLC showed a spherical morphology under transmission electron microscope, and the particle size was 218.3 ± 9.2 nm. The value of the zeta potential of PR-NLC decreased from -30.2 ± 1.9 mV to -64.9 ± 1.3 mV when the dilution times reach 10. The loading amount of PR encapsulated in NLC was 2.94 ± 0.03%, and the average entrapment efficiencies of PR-NLC determinated by size exclusion chromatography and ultrafiltration were 90.2 ± 0.6% and 98.3 ± 0.3%. Lyophilization was proved feasible for the storage of NLC dispersion. Fourier transform infrared spectra (FTIR) was exploited to investigate the possible drug-lipid complex formation. Advancements in water solubility of PR were demonstrated by NLC using a contact angle measurement. The hemolysis percentage of the NLC was less than 1.3% in a certain range of concentration. In 90 days' storage, 88.6 ± 2.8% of PR remained unchanged in PR-NLC under natural daylight. In vitro release studies revealed a sustained drug release, and in vitro penetration studies showed an increase of retention amount of PR in the skin, when applying PR-NLC. Therefore, the NLC might be a potential delivery vehicle in cosmetic dermal products.

  11. Development of a nanostructured lipid carrier formulation for increasing photo-stability and water solubility of Phenylethyl Resorcinol

    Fan, Hengfeng; Liu, Guoqing; Huang, Yiqing; Li, Yan; Xia, Qiang, E-mail:


    The Phenylethyl Resorcinol loaded nanostructured lipid carrier (PR-NLC) was developed by hot high-pressure homogenization method. The freshly prepared PR-NLC showed a spherical morphology under transmission electron microscope, and the particle size was 218.3 ± 9.2 nm. The value of the zeta potential of PR-NLC decreased from −30.2 ± 1.9 mV to −64.9 ± 1.3 mV when the dilution times reach 10. The loading amount of PR encapsulated in NLC was 2.94 ± 0.03%, and the average entrapment efficiencies of PR-NLC determinated by size exclusion chromatography and ultrafiltration were 90.2 ± 0.6% and 98.3 ± 0.3%. Lyophilization was proved feasible for the storage of NLC dispersion. Fourier transform infrared spectra (FTIR) was exploited to investigate the possible drug–lipid complex formation. Advancements in water solubility of PR were demonstrated by NLC using a contact angle measurement. The hemolysis percentage of the NLC was less than 1.3% in a certain range of concentration. In 90 days’ storage, 88.6 ± 2.8% of PR remained unchanged in PR-NLC under natural daylight. In vitro release studies revealed a sustained drug release, and in vitro penetration studies showed an increase of retention amount of PR in the skin, when applying PR-NLC. Therefore, the NLC might be a potential delivery vehicle in cosmetic dermal products.

  12. Study on Phthalic Anhydride Cured Diglycidyl Ether of Bisphenol A Decomposed by Tetramethyl Ammonium Hydroxide%四甲基氢氧化铵降解苯酐固化双酚A型环氧树脂的研究

    姜坤; 罗炎



  13. A Dft Analysis of the Vibrational Spectra of Bisphenol A Diglycidyl Ether and Bispheonl A%双酚A和双酚A二缩水甘油醚振动谱的理论和实验比较分析

    王玉芳; 朱箭; 王斌; 曹学伟; 徐晓轩


    利用基于密度泛函理论的第一性原理计算,本文研究双酚A(BPA)和双酚A二缩水甘油醚(EDGE-BA)分子的结构和振动性质,分析了两种分子红外活性和拉曼活性特征振动的频率和对称性.计算结果表明,BPA分子的拉曼散射峰基本归属于对位取代苯的骨架振动,500~1600 cm-1红外强度较强;对于DGEBA分子环氧基团指纹区的特征振动频率为860,930,1123,1260 cm-1,其红外光谱强度较大,可用于DGEBA类树脂固化反应过程监控;1260 cm1附近的振动模,其拉曼散射强度较高,可成为拉曼光谱研究固化反应过程的特征振动.而1160 cm-1附近的振动属于芳香环的特征振动,强度基本不变.

  14. Migration of Bisphenol A Diglycidyl Ether and Its Derivatives into Canned Meat and Fish%肉类罐头食品中双酚A二缩水甘油醚及其衍生物的迁移

    罗生亮; 吴少林; 张朝晖; 周光漪; 高洋洋; 李晶


    本实验应用高效液相色谱-电喷雾串联质谱法分析检测肉类罐头食品中双酚A二缩水甘油醚(BADGE)及其衍生物的残留,重点研究了肉类罐头中的内容物、存储时间(6个月、9个月、12个月)以及存储温度(4、20、100℃)对双酚A二缩水甘油醚(BADGE)及其衍生物的迁移量的影响,单因素方差分析(One-way ANOVA)检验实验结果表明,不同内容物罐头中从内壁涂层迁移至样品的BADGE及其衍生物存在显著性差异(p<0.05),Student-NewmanKeuls 法检验表明存储12个月后目标化合物的迁移量与6个月、9个月存在显著性差异,存储温度为4、20℃时化合物迁移量没有显著差异,但是罐头加热到100℃后目标化合物迁移量是最大的.

  15. Purification of Tetrabromobisphenol A Diglycidyl Ether of the Reactive Flame Retardant%反应型阻燃剂四溴双酚A双缩水甘油醚的精制

    贾修伟; 刘治国; 丁涛; 房晓敏; 徐元清



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

    Koziara, B.T.


    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

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

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


    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

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

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


    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

  19. I(+1) transfer from diiodomalonic acid to malonic acid and a complete inhibition of the CO and CO2 evolution in the Briggs-Rauscher reaction by resorcinol.

    Onel, Lavinia; Bourceanu, Gelu; Wittmann, Maria; Noszticzius, Zoltán; Szabó, Gabriella


    A recent report on an intense CO 2 and CO evolution in the Briggs-Rauscher (BR) reaction revealed that iodination of malonic acid (MA) is not the only important organic reaction in the classical BR oscillator. To disclose the source of the gas evolution, iodomalonic (IMA) and diiodomalonic (I2MA) acids were prepared by iodinating MA with nascent iodine in a semibatch reactor. The nascent iodine was generated by an iodide inflow into the reactor, which contained a mixture of MA and acidic iodate. Some CO2 and a minor CO production was observed during these iodinations. It was found that in an aqueous acidic medium the produced I2MA is not stable but decomposes slowly to diiodoacetic acid and CO2. The first-order rate constant of the I 2MA decarboxylation at 20 degrees C was found to be k1 = 9 x 10(-5) s(-1), which is rather close to the rate constant of the analogous decarboxylation of dibromomalonic acid under similar conditions (7 x 10(-5)s(-1)). From the rate of the CO2 evolution, the I2MA concentration can be calculated in a MA-IMA-I2MA mixture as only I2MA decarboxylates spontaneously but MA and IMA are stable. Following CO2 evolution rates, it was proven that I2MA can react with MA in the reversible reaction I2MA + MA 2 IMA. The equilibrium constant of this reaction was calculated as K = 380 together with the rate constants of the forward k 2 = 6.2 x 10 (-2) M (-1)s(-1) and backward k-2 = 1.6 x 10(-4) M(-1)s(-1) reactions. The probable mechanism of the reaction is I(+1) transfer from I2MA to MA. The presence of I(+1) in a I2MA solution is demonstrated by its reduction with ascorbic acid. To estimate the fraction of CO2 coming from the decarboxylation of I2MA in an oscillatory BR reaction, the oscillations were inhibited by resorcinol. Unexpectedly, all CO2 and CO evolution was interrupted for more than one hour after injecting a small amount of resorcinol (10(-5) M initial concentration in the reactor). Finally, some implications of the newly found I(+1

  20. Thermodynamic equilibrium calculations of dimethyl ether steam reforming and dimethyl ether hydrolysis

    Semelsberger, Troy A.; Borup, Rodney L.

    The production of a hydrogen-rich fuel-cell feed by dimethyl ether (DME) steam reforming was investigated using calculations of thermodynamic equilibrium as a function of steam-to-carbon ratio (0.00-4.00), temperature (100-600 °C), pressure (1-5 atm), and product species. Species considered were acetone, acetylene, carbon dioxide, carbon monoxide, dimethyl ether, ethane, ethanol, ethylene, formaldehyde, formic acid, hydrogen, isopropanol, methane, methanol, methyl-ethyl ether, n-propanol and water. Thermodynamic equilibrium calculations of DME steam reforming indicate complete conversion of dimethyl ether to hydrogen, carbon monoxide and carbon dioxide at temperatures greater than 200 °C and steam-to-carbon ratios greater than 1.25 at atmospheric pressure ( P = 1 atm). Increasing the operating pressure shifts the equilibrium toward the reactants; increasing the pressure from 1 to 5 atm decreases the conversion of dimethyl ether from 99.5 to 76.2%. The trend of thermodynamically stable products in decreasing mole fraction is methane, ethane, isopropyl alcohol, acetone, n-propanol, ethylene, ethanol, methyl-ethyl ether and methanol-formaldehyde, formic acid, and acetylene were not observed. Based on the equilibrium calculations, the optimal processing conditions for dimethyl ether steam reforming occur at a steam-to-carbon ratio of 1.50, a pressure of 1 atm, and a temperature of 200 °C. These thermodynamic equilibrium calculations show dimethyl ether processed with steam will produce hydrogen-rich fuel-cell feeds—with hydrogen concentrations exceeding 70%. The conversion of dimethyl ether via hydrolysis (considering methanol as the only product) is limited by thermodynamic equilibrium. Equilibrium conversion increases with temperature and steam-to-carbon ratio. A maximum dimethyl ether conversion of 62% is achieved at a steam-to-carbon ratio of 5.00 and a processing temperature of 600 °C.

  1. EtherCAT协议分析



    <正>EtherCAT协议是德国倍福自动化有限公司(Beckhoff Automation GmbH)于2003年提出,并于2005年被定为IEC标准62407;2007年,IEC把EtherCAT协议加到工业现场总线标准61158。一、协议概述为提高通信效率以及实时性,EtherCAT协议的主要思想有两方面。简化协议,协议兼容以太网的MAC层协议,并由纯硬件完成解析,提高处理速度;而其他协议由软件

  2. Limonene ethers from tire pyrolysis oil

    Stanciulescu, Maria; Ikura, Michio [CANMET Energy Technology Centre, Natural Resources Canada, 1 Haanel Drive, Ottawa, ON (Canada)


    Tire pyrolysis oil was produced by EnerVision Inc., Halifax, Canada using the continuous ablative reactor (CAR) system. The tire oil was separated by distillation into several fractions. Naphtha and limonene enriched naphtha were reacted with methanol over different catalysts. Batch experiments were carried out to separate limonene as methyl limonene ethers. Whole tire pyrolysis oil was distilled and the resulting distillates were redistilled to separate the limonene (bp about 176{sup o}C). Vacuum distillation yielded on average 25.5wt% naphtha containing 16.3wt% limonene (average). Redistillation increased the limonene concentration to approximately 32-37wt%. The conversion of limonene (mono-terpene) to limonene ethers (terpenoides) shifted the boiling point of the limonene derivatives out of the naphtha boiling range (IBP -190{sup o}C). This allowed the separation of fragrant limonene ethers from foul smelling naphtha. Alkoxylation reactions were performed mostly using methanol and acidic catalysts. The methyl ether [1-methyl-4-({alpha}-methoxy-isopropyl)-1-cyclohexene] has a boiling point of about 198{sup o}C which is higher than the end boiling point of the naphtha cut. Five heterogeneous catalysts (four zeolites and one ion exchange resin) were tested in a batch reactor. {beta}-Zeolite produced excellent results. The reaction of R-(+)-limonene with methanol in the presence of activated {beta}-zeolite yielded methyl ether, 87.5% at selectivity 89.7% with a maximum of 2h reaction time. Limonene conversion from whole naphtha to ethers was also high. (author)

  3. Synthesis, characterization, thermal behavior, and DNA-cleaving studies of cyano-bridged nickel(II)-copper(II) complexes of 4-(pyridin-2-ylazenyl)resorcinol.

    Karipcin, Fatma; Ozmen, Ismail; Cülü, Burcin; Celikoğlu, Umut


    We present here the syntheses of a mononuclear Cu(II) complex and two polynuclear Cu(II)-Ni(II) complexes of the azenyl ligand, 4-(pyridin-2-ylazenyl)resorcinol (HL; 1). The reaction of HL (1) and copper(II) perchlorate with KCN gave a mononuclear complex [CuL(CN)] (4). Using 4, one pentanuclear complex, [{CuL(NC)}(4) Ni](ClO(4))(2) (5) and one trinuclear complex, [{CuL(CN)}(2) NiL]ClO(4) (6), were prepared and characterized by elemental analyses, magnetic susceptibility, molar conductance, IR, and thermal analysis. Stoichiometric and spectral results of the mononuclear Cu(II) complex indicated that the metal/ligand/CN ratio was 1 : 1 : 1, and the ligand behaved as a tridentate ligand forming neutral metal chelates through the pyridinyl and azenyl N-, and resorcinol O-atom. The interaction between the compounds (the ligand 1, its Ni(II) and Cu(II) complexes without CN, i.e., 2 and 3, and its complexes with CN, 4-6) and DNA has also been investigated by agarose gel electrophoresis. The pentanuclear Cu(4) Ni complex (5) with H(2) O(2) as a co-oxidant exhibited the strongest DNA-cleaving activity.

  4. Molecular, spectroscopic and thermal studies on catechol, 4,5-dibromocatechol, resorcinol, hydroquinone and 4-4‧-dihydroxybiphenyl derivatives armed with benzothiazole moieties

    Alshargabi, Arwa; Yeap, Guan-Yeow; Mahmood, Wan Ahmad Kamil; Samikannu, Rakesh


    A new series of catechol, 4,5-dibromocatechol, resorcinol, hydroquinone and 4-4'-dihydroxybiphenyl derivatives possessing two benzothiazole moieties at respective positions of 1,2, 1,3, 1,4 and/or 4,4' has successfully been synthesized. The molecular structures were fully elucidated by spectroscopic techniques (1H NMR, 13C NMR and two dimensional COSY, HMBC, HMQC, DEPT-135 and DEPT-90). The connectivity study between the cause of using different core systems in the target compounds and the anisotropic behavior as inferred from phase transition temperature and relevant morphology studies has led to some unique features arising from this series. Compounds with ortho substituent exhibit enantiotropic N and SmA phases. The analogues containing resorcinol and 4,4'-disubstituentbiphenyl show enanotiotropic nematic behavior while the hydroquinone derivative induces the formation of monotropic nematogen. An extensive study to further substantiate the relationship between the stability of the nematic phase and associated transition temperatures due to different core systems is also reported.

  5. Study of transport properties and conduction mechanism of pure and composite resorcinol formaldehyde aerogel doped with Co-ferrite

    Attia, S.M., E-mail: [Physics Department, Faculty of Science, Kafrelsheikh University, Kafr El-Sheikh (Egypt); Physics Department, College of Applied Sciences, Umm Al-Qura University, PB 7296, Makkah 21955 (Saudi Arabia); Sharshar, T. [Physics Department, Faculty of Science, Kafrelsheikh University, Kafr El-Sheikh (Egypt); Physics Department, Faculty of Science, Taif University, Taif, 888 Hawiya (Saudi Arabia); Abd-Elwahed, A.R. [Physics Department, Faculty of Science, Kafrelsheikh University, Kafr El-Sheikh (Egypt); Tawfik, A. [Physics Department, Faculty of Science, Tanta University, Tanta (Egypt)


    Highlights: • A novel composite RF aerogels with Co-ferrite were prepared by sol–gel process. • RF aerogels exhibit a semiconducting behavior. • The dielectric constant of RF aerogel is very low (4 times as that of air) and can be controlled by adding Co-ferrite. • Large overlapping polaron (OLP) was found to be the preferred conduction mechanism in these materials. -- Abstract: A series of resorcinol formaldehyde aerogels (RF aerogels) composite with nanoparticles of CoFe{sub 2}O{sub 4} have been prepared by sol–gel method. Four samples of pure RF aerogels were prepared at different concentrations of Na{sub 2}CO{sub 3} as catalyst (0.02, 0.025, 0.03, and 0.04 wt.%) and four samples of composite RF aerogels were prepared at different concentration of doped CoFe{sub 2}O{sub 4} (0.075, 0.1, 0.125, and 0.15 wt.%; Na{sub 2}CO{sub 3} concentration = 0.03 wt.%). DC electrical conductivity as a function of temperature was studied in the temperature range 25 °C–200 °C for all samples. AC electrical conductivity and dielectric properties were determined using RLC Bridge in the frequency range 100 Hz–1 MHz at different temperature (25–200 °C). The pore size of the samples was determined using positron annihilation lifetime spectroscopy (PALS). RF aerogels are found to exhibit a semiconducting behavior and characterized by two transition temperatures T{sub 1} and T{sub 2}. Also σ{sub DC} increases with increase of Co-ferrite contents. Pure RF aerogels posses a very low dielectric constant, where the lowest value of ε′ is ∼4 times as that of air. ε′ decreases with increase of frequency, and increases with increase of temperature. Large overlapping polaron (OLP) is found to be the preferred conduction mechanism in these materials. The results of PALS show that there are two types of pore size in these samples; the first ranges from 1.9 to 2.5 nm, while the second ranges from 3.2 to 5.3 nm.

  6. Finkelstein Reaction in Functionalized Crown-ether Ionic Liquids

    Xiao Hua WANG; Han Zhi WANG; Hui LIU; Yuan KOU


    Functional crown-ether ionic liquids were used as catalytic green solvents of Finkelstein reaction of 1-bromooctane and iodide. The rate and yield of the reaction were obvious improved compared with that using crown ether in water. No free crown ether loss was observed after reaction.

  7. 40 CFR 721.3435 - Butoxy-substituted ether alkane.


    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Butoxy-substituted ether alkane. 721... Substances § 721.3435 Butoxy-substituted ether alkane. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as butoxy-substituted ether...

  8. 46 CFR 151.50-42 - Ethyl ether.


    ... 46 Shipping 5 2010-10-01 2010-10-01 false Ethyl ether. 151.50-42 Section 151.50-42 Shipping COAST... LIQUID HAZARDOUS MATERIAL CARGOES Special Requirements § 151.50-42 Ethyl ether. (a)(1) Gravity tanks... liquid. (g) Precautions shall be taken to prevent the contamination of ethyl ether by strong...

  9. Preparation and properties of cardanol glycidyl ether%腰果酚基缩水甘油醚的制备及其性能研究

    张俊珩; 闪洁; 秦小玉; 赵婷婷


    Reports on the synthesis of cardanol glycidyl ether( CGE )and the hybrid composite of CGE and diglycidyl ether of bisphenol-A( DGEBA). Studied was shown that,the mechanical performance of the CGE/DGEBA blends had maximum with the increase of CGE content. The tensile strength,flexural strength and impact strength of the cured system with 15% CGE can be enhanced respectively about 35 . 4%,43 . 3% and 109 . 5%. The toughness mechanism is the micro-phase separation during curing and sea-island microstructure appearing on the fractured surface.%以腰果酚、环氧氯丙烷为主要原料,制备腰果酚基缩水甘油醚( CGE ),并研究 CGE/双酚 A型环氧树脂( DGEBA)固化物的性能。研究表明,在CGE用量达15%时,环氧树脂固化物的机械性能达到最大值。与纯DGEBA的性能相比,复合材料的拉伸强度、弯曲强度、冲击强度分别提高了35.4%,43.3%和109.5%。随着CGE含量的增加,材料的玻璃化转变温度降低。固化微观相分离和断面出现“海岛”结构是腰果酚基缩水甘油醚的增韧机理。

  10. Impact of a heteroatom in a structure-activity relationship study on analogues of phenyl glycidyl ether (PGE) from epoxy resin systems.

    Niklasson, Ida B; Delaine, Tamara; Luthman, Kristina; Karlberg, Ann-Therese


    Epoxy resins are among the most common causes of occupational contact dermatitis. They are normally used in so-called epoxy resin systems (ERS). These commercial products are combinations of epoxy resins, curing agents, modifiers, and reactive diluents. The most frequently used resins are diglycidyl ethers based on bisphenol A (DGEBA) and bisphenol F (DGEBF). In this study, we have investigated the contact allergenic properties of a series of analogues to the reactive diluent phenyl glycidyl ether (PGE), all with similar basic structures but with varying heteroatoms or with no heteroatom present. The chemical reactivity of the compounds in the test series toward the hexapeptide H-Pro-His-Cys-Lys-Arg-Met-OH was investigated. All epoxides were shown to bind covalently to both cysteine and proline residues. The percent depletion of nonreacted peptide was also studied resulting in ca. 60% depletion when using either PGE, phenyl 2,3-epoxypropyl sulfide (2), or N-(2,3-epoxypropyl)aniline (3), and only 15% when using 1,2-epoxy-4-phenylbutane (4) at the same time point. The skin sensitization potencies of the epoxides using the murine local lymph node assay (LLNA) were evaluated in relation to the observed physicochemical and reactivity properties. To enable determination of statistical significance between structurally closely related compounds, a nonpooled LLNA was performed. It was found that all investigated compounds containing a heteroatom in the α-position to the epoxide were strong sensitizers, congruent with the reactivity data, indicating that the impact of a heteroatom is crucial for the sensitizing capacity for this type of epoxides.

  11. Orphan enzymes in ether lipid metabolism.

    Watschinger, Katrin; Werner, Ernst R


    Ether lipids are an emerging class of lipids which have so far not been investigated and understood in every detail. They have important roles as membrane components of e.g. lens, brain and testis, and as mediators such as platelet-activating factor. The metabolic enzymes for biosynthesis and degradation have been investigated to some extent. As most involved enzymes are integral membrane proteins they are tricky to handle in biochemical protocols. The sequence of some ether lipid metabolising enzymes has only recently been reported and other sequences still remain obscure. Defined enzymes without assigned sequence are known as orphan enzymes. One of these enzymes with uncharacterised sequence is plasmanylethanolamine desaturase, a key enzyme for the biosynthesis of one of the most abundant phospholipids in our body, the plasmalogens. This review aims to briefly summarise known functions of ether lipids, give an overview on their metabolism including the most prominent members, platelet-activating factor and the plasmalogens. A special focus is set on the description of orphan enzymes in ether lipid metabolism and on the successful strategies how four previous orphans have recently been assigned a sequence. Only one of these four was characterised by classical protein purification and sequencing, whereas the other three required alternative strategies such as bioinformatic candidate gene selection and recombinant expression or development of an inhibitor and multidimensional metabolic profiling.


    Polybrominated diphenyl ethers (PBDEs) are used as flame retardants in a wide variety of consumer products. Concerns surrounding these compounds are primarily due do their ubiquitous presence in the environment as well as in human tissue, such as milk, coupled with evidence indi...

  13. Ether, Luminosity and Galactic Source Counts

    Tomaschitz, R


    An interpretation of the cosmological redshift in terms of a cosmic ether is given. We study a Robertson-Walker cosmology in which the ether is phenomenologically defined by a homogeneous and isotropic permeability tensor. The speed of light becomes so a function of cosmic time like in a dielectric medium. However, the cosmic ether is dispersion free, it does not lead to a broadening of spectral lines. Locally, in Euclidean frames, the scale factors of the permeability tensor get absorbed in the fundamental constants. Mass and charge scale with cosmic time, and so do atomic energy levels. This substantially changes the interpretation of the cosmological redshift as a Doppler shift. Photon frequencies are independent of the expansion factor; their time scaling is determined by the permeability tensor. The impact of the ether on the luminosity-distance, on the distance-redshift relation, and on galactic number counts is discussed. The Hubble constant is related to the scale factors of the metric and the permeab...

  14. Biosynthesis of archaeal membrane ether lipids

    Jain, Samta; Caforio, Antonella; Driessen, Arnold J. M.


    A vital function of the cell membrane in all living organism is to maintain the membrane permeability barrier and fluidity. The composition of the phospholipid bilayer is distinct in archaea when compared to bacteria and eukarya. In archaea, isoprenoid hydrocarbon side chains are linked via an ether

  15. Based Design EtherCAT Slave%基于EtherCAT的从站设计



    Fieldbus has become an important part of the automatic control technology, through a large number of practical experiments and testing, now widely applied. EtherCAT has good real-time capability to adapt to the small amount of data communications, and affordable, the industrial control has been widely used. However, due to EtherCAT Slave design must use a special chip, leading from the station complex hardware design, commissioning difficulties, increasing costs. In this paper, AM3358 Cortex A8 processor plus Ethernet physical layer transceiver (PHY) program, due to the integrated chip inside AM3358 Industrial communications subsystem (PRU-ICSS) EtherCAT protocol can be achieved, so long as the external PHY can become EtherCAT Slave ..%现场总线已经成为自动化控制技术重要组成部分,通过大量的实践实验与测试,如今已经获得广泛的应用。EtherCAT具有良好的实时能力,适应小数据量通信,并且价格经济,在工业控制上得到广泛的应用。但由于EtherCAT从站设计必须使用专门的芯片,导致从站的硬件设计复杂、调试困难、成本增加。文章采用AM3358 Cortex A8处理器外加以太网物理层收发器(PHY)的方案,由于AM3358片内集成工业用通信子系统(PRU-ICSS)可以实现EtherCAT协议,因此只要外加PHY就可以成为EtherCAT从站。

  16. Synthesis of poly(vinyl ether)s with perfluoroalkyl pendant groups

    Höpken, Jens; Möller, Martin; Lee, Myongsoo; Percec, Virgil


    2-Perfluoro(alkyl)ethyl vinyl ethers, F(CF2)nCH2CH2OCHCH2, (n = 6 or 8), were synthesized and polymerized by means of cationic initiators (HI/ZnI2 and CF3SO3H/(CH3)2S). The perfluorohexyl-substituted poly(vinyl ether) is completely amorphous. The polymer with perfluorooctyl segments shows side chain

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

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


    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

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

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


    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

  19. Tween as a Substitute for Diethyl Ether in the Formalin-Ether Sedimentation Technique

    NA Ahmadi


    Full Text Available Background: Tween as a substitute for diethyl ether in the formalin-ether sedimentation technique was evaluated for para­site detection.Methods: Fresh fecal material free of parasites with 10% formalin to prepare standardized specimen was thoroughly pooled. This specimen was divided into 5 equal portions; one was without infection, and each of the others was individually seeded with Entamoeba coli, and Giardia lamblia cysts, ova of Ascaris lumbericoides, and Hymenolepis nana. Six hundred and eighty four slides including 228 stool samples for each of formalin-tween, formalin-ether and direct wet mount proce­dures were examined.Results: The sensitivity of above mentioned procedures were computed 72.1%, 55% and 30 %; their negative predictive value were 69.3%, 58.3% and 47.3%; and their false negative error rate were 27.9%, 45% and 70%, respectively. There were no false-positive results among the 264 specimens previously identified as negative for the presence of intestinal para­sites. Therefore, specificity for each technique was 100%.Conclusion: In the range of our study, formalin-tween method proved to be equivalent to or better than formalin-ether tech­nique in concentrating parasite eggs, and cysts, as well as in maintaining characteristic morphology. Tween is more stable, safer, cheaper, and less flammable than that of ether; and promises to be a useful alternative to ether.

  20. Inhibition of diethyl ether degradation in Rhodococcus sp. strain DEE5151 by glutaraldehyde and ethyl vinyl ether.

    Kim, Yong-Hak; Engesser, Karl-Heinrich


    Alkyl ether-degrading Rhodococcus sp. strain DEE5151, isolated from activated sewage sludge, has an activity for the oxidation of a variety of alkyl ethers, aralkyl ethers and dibenzyl ether. The whole cell activity for diethyl ether oxidation was effectively inhibited by 2,3-dihydrofurane, ethyl vinyl ether and glutaraldehyde. Glutaraldehyde of less than 30 microM inhibited the activity by a competitive manner with the inhibition constant, K(I) of 7.07+/-1.36 microM. The inhibition type became mixed at higher glutaraldehyde concentrations >30 microM, probably due to the inactivation of the cell activity by the Schiff-base formation. Structurally analogous ethyl vinyl ether inhibited the diethyl ether oxidation activity in a mixed manner with decreasing the apparent maximum oxidation rate, v(max)(app), and increasing the apparent Michaelis-Menten constant, K(M)(app). The mixed type inhibition by ethyl vinyl ether seemed to be introduced not only by the structure similarity with diethyl ether, but also by the reactivity of the vinyl ether with cellular components in the whole cell system.

  1. A direct spectrophotometric method for the simultaneous determination of zinc and cobalt in metalloproteins using 4-(2-pyridylazo)resorcinol.

    Säbel, Crystal E; Shepherd, Jeffrey L; Siemann, Stefan


    An assay involving the direct and simultaneous determination of low micromolar concentrations (1-10 microM) of both zinc and cobalt ions suitable for metal content analyses of metalloproteins is described. The procedure exploits differences in the visible absorption spectra of the chromophoric chelator 4-(2-pyridylazo)resorcinol (PAR) resulting from its complexation to Zn2+ and/or Co2+ ions and is based on the fit of experimental spectra to a linear addition of Beer-Lambert law. The method eliminates the need for separating or masking one of the metal ions prior to their quantification and could prove to be particularly useful in studies on Co2+-substituted zinc proteins.

  2. Complex Formation in a Liquid-Liquid Extraction System Containing Co(II), 4-(2-Thiazolylazo)resorcinol and Monotetrazolium Salt.

    Divarova, Vidka; Stojnova, Kirila; Racheva, Petya; Lekova, Vanya


    The ion-associated complex formed between anionic chelate of Co(II)-4-(2-Thiazolylazo)resorcinol (TAR) with the monotetrazolium cation of 2-(4-Iodophenyl)-3-(4-nitrophenyl)-5-phenyl-2H-tetrazolium chloride (INT) in the liquid-liquid extraction system Co(II)-TAR-INT-H(2)O-CHCl(3) was studied by the spectrophotometric method. The optimum extraction conditions of Co(II) were found. The extraction equilibria were studied. The equilibrium constants, the recovery factor and some analytical characteristics were calculated. The validity of Beer's law was checked. The molar ratio of the components in the ternary ion-associated complex Co(II)-TAR-INT was determined. The general formula of the complex was suggested. The effect of various foreign ions and reagents on the process of complex formation in the liquid-liquid extraction system was studied.

  3. Emergent gravity and ether-drift experiments

    Consoli, M


    In principle, ether-drift experiments could distinguish phenomenologically emergent-gravity approaches, where an effective curvature emerges from hydrodynamic distortions of the same physical, flat-space vacuum, from the more conventional scenario where curvature is considered a fundamental property of space-time down to extremely small length scales and the speed of light represents a universal constant. From an experimental point of view, in this particular context, besides time modulations that might be induced by the Earth's rotation (and its orbital revolution), one should also consider the possibility of random fluctuations of the signal. These might reflect the stochastic nature of the underlying 'quantum ether' and be erroneously interpreted as mere instrumental noise. To test the present interpretation, we have extracted the mean amplitude of the signal from various experiments with different systematics, operating both at room temperature and in the cryogenic regime. They all give the same consisten...

  4. Fluoroalkylation of aryl ether perfluorocyclobutyl polymers

    Ligon, Clark; Ameduri, Bruno; Boutevin, Bernard; Smith, Dennis


    International audience; Post functionalization of aryl ether perfluorocyclobutyl (PFCB) polymers with fluoroalkyl side chains was accomplished with Umemoto's FITS reagents. The fluoroalkylated PFCB polymers (20 % functionalized) showed increases in both hydrophobicity and oleophobicity. Static contact angle for hexadecane was increased after fluoroalkylation from 0° to greater than 30° for the two PFCB polymers tested. Increased oil repellency makes these materials potential candidates for va...

  5. Catalytic intermolecular hydroamination of vinyl ethers.

    Pahadi, Nirmal K; Tunge, Jon A


    This manuscript details the development of a palladium-catalyzed hydroamination of vinyl ethers. It is proposed that palladium catalyzes the hydroamination via Bronsted base catalysis, where palladium is protonated by the relatively acidic sulfonamide to generate a palladium hydride as well as the active anionic sulfonamide nucleophile. Thus, this process is distinct from known palladium-catalyzed hydroaminations of styrene derivatives that utilize less acidic amines.

  6. Converting biogenic dimethyl ether into fuels

    Zimmermann, Michael; Otto, Thomas N.; Dinjus, Eckhard [Karlsruher Institut fuer Technologie (KIT), Eggenstein-Leopoldshafen (Germany). Inst. fuer Katalyseforschung und -technologie (IKFT)


    In the seventies, the MtG (''methanol-to-gasoline'') process was an alternative to the Fischer-Tropsch process developed in the thirties of the past century. The MtG process is performed with dimethyl ether (DME) as an intermediate. Hydrocarbons (C{sub 1}-C{sub 10}) directly synthesised via DME with the assistance of zeolites as catalysts offers considerable advantages over the MtG process. Zeolites play an important role in the production of biomass-based fuels from synthesis gas. Known and mature technologies exist for synthesis gas of fossil origin (coal, natural gas, petroleum). These established technologies may also be transferred to synthesis gas of biogenous origin. Dimethyl ether produced from biomass-based synthesis gas is a central intermediate product. In the MtG and DtG (''dimethyl ether-to-gasoline'') process H-ZSM-5 zeolites are of major significance. Modification of H-ZSM-5 catalysts is the basis of customized product synthesis. Hierarchic structures of zeolites change the diffusion properties of the crystals and can help to achieve a more selective range of products. (orig.)

  7. Nikola Tesla, the Ether and his Telautomaton

    Milar, Kendall


    In the nineteenth century physicists' understanding of the ether changed dramatically. New developments in thermodynamics, energy physics, and electricity and magnetism dictated new properties of the ether. These have traditionally been examined from the perspective of the scientists re-conceptualizing the ether. However Nikola Tesla, a prolific inventor and writer, presents a different picture of nineteenth century physics. Alongside the displays that showcased his inventions he presented alternative interpretations of physical, physiological and even psychical research. This is particularly evident in his telautomaton, a radio remote controlled boat. This invention and Tesla's descriptions of it showcase some of his novel interpretations of physical theories. He offered a perspective on nineteenth century physics that focused on practical application instead of experiment. Sometimes the understanding of physical theories that Tesla reached was counterproductive to his own inventive work; other times he offered new insights. Tesla's utilitarian interpretation of physical theories suggests a more scientifically curious and invested inventor than previously described and a connection between the scientific and inventive communities.

  8. From ether theory to ether theology: Oliver Lodge and the physics of immortality.

    Raia, Courtenay Grean


    This article follows the development of physicist Oliver Lodge's religio-scientific worldview, beginning with his reticent attraction to metaphysics in the early 1880s to the full formulation of his "ether theology" in the late 1890s. Lodge undertook the study of psychical phenomena such as telepathy, telekinesis, and "ectoplasm" to further his scientific investigations of the ether, speculating that electrical and psychical manifestations were linked phenomena that described the deeper underlying structures of the universe, beneath and beyond matter. For Lodge, to fully understand the ether was to force from the universe an ultimate Revelation, and psychical research, as the most modern and probatory science, was poised to replace religion as the means of that disclosure. (c) 2007 Wiley Periodicals, Inc.

  9. Synthesis of Diaryl Ethers, Diaryl Sulfides, Heteroaryl Ethers and Heteroaryl Sulfides under Microwave Heating

    LI,Feng; ZOU,Jiong; WANG,Quan-Rui; TAO,Feng-Gang


    @@ Diaryl ether moiety is found in a pool of naturally occurring and medicinally important compounds.[1] As a consequent, considerable efforts have been devoted to the assembly of this framework.[2] Recently, we have developed a microwave heating version of the synthesis of diaryl ethers as well as aryl sulfides. Under our conditions, even the extremely electron-poor 4-nitrophenol works well and its reaction with 1-halo-4-nitrobenzenes produces 4-(nitrophenoxy)-benzonitriles in satisfactory yield. The scope of the present protocol has been expanded to hydroxylated six-membered heterocycles as well as 2-pyrimidinethiol with mildly activated aryl halides, affording heteroaryl ethers and respectively sulfides. The advantages of the present method include the wide substrate scope, no use of any metal catalysts, the ease of product isolation and high yields.

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

    Morikawa, Atsushi


    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.

  11. 76 FR 38026 - Diethylene Glycol Mono Butyl Ether; Exemption From the Requirement of a Tolerance


    ... butyl ether, also a glycol ether differing in only one ethyl group from DEGBE. These data were used to... monobutyl ether, also a glycol ether differing only in one ethyl group. This data was used to assess the... AGENCY 40 CFR Part 180 Diethylene Glycol Mono Butyl Ether; Exemption From the Requirement of a...

  12. Azidated Ether-Butadiene-Ether Block Copolymers as Binders for Solid Propellants

    Cappello, Miriam; Lamia, Pietro; Mura, Claudio; Polacco, Giovanni; Filippi, Sara


    Polymeric binders for solid propellants are usually based on hydroxyl-terminated polybutadiene (HTPB), which does not contribute to the overall energy output. Azidic polyethers represent an interesting alternative but may have poorer mechanical properties. Polybutadiene-polyether copolymers may combine the advantages of both. Four different ether-butadiene-ether triblock copolymers were prepared and azidated starting from halogenated and/or tosylated monomers using HTPB as initiator. The presence of the butadiene block complicates the azidation step and reduces the storage stability of the azidic polymer. Nevertheless, the procedure allows modifying the binder properties by varying the type and lengths of the energetic blocks.

  13. Phenolic ethers in the organic polymer of the Murchison meteorite

    Hayatsu, R.; Winans, R. E.; Scott, R. G.; McBeth, R. L.; Moore, L. P.; Studier, M. H.


    Results of the oxidation of the organic polymer of the Murchison meteorite with alkaline cupric oxide, a mild-oxidant specific for cleaving ether linkages, are reported. Qualitative analyses by gas chromatography-mass spectrometry, solid-probe mass spectrometry and high-resolution mass spectrometry reveal the presence of large amounts of meta-hydroxybenzoic acid and 3-hydroxy-1,5-benzenedicarboxylic acid, along with seven phenolic acids, in the oxidized solution, indicating the presence of phenolic ethers and of aryl alkyl ethers having no nuclear hydroxy group in the meteorite. The formation of phenolic ethers in the solar nebula by Fischer-Tropsch type reactions is then discussed.

  14. Alcohol dehydration: Mechanism of ether formation using an alumina catalyst

    Shi, B.; Davis, B.H. [Univ. of Kentucky, Lexington, KY (United States)


    Ether formation during the dehydration of secondary alcohols, namely, 2-butanol, 3-pentanol, and 1-cyclopentylethanol, was investigated. Using the proper reaction conditions, the yield of di-2-butyl ether during the dehydration of 2-butanol on alumina can be as high as 40%. That ether is formed by adding an alcohol to the alkene is ruled out by the results from deuterium tracer studies. Results from experiments using S(+)- 2-butanol suggest that the formation of di-2-butyl ether occurs by a S{sub N}2-type mechanism. 33 refs., 5 figs., 3 tabs.

  15. Correlation of electronic transitions and redox potentials measured for pyrocatechol, resorcinol, hydroquinone, pyrogallol, and gallic acid with results of semi-empirical molecular orbital computations A useful interpretation tool

    Carter, Melvin Keith


    Cyclic voltammogram (CV) electrochemical measurements for pyrocatechol, resorcinol, hydroquinone, pyrogallol, and gallic acid in strong alkaline solution produced observable oxidation-reduction potentials for each hydroxy group present except for resorcinol. UV absorption spectra were also observed for the diluted solutions. Semi-empirical molecular orbital computations were conducted for these molecules of C2 v point group symmetry to determine the character and energies to aid interpretation of the experimental results. CV oxidation removed a π-electron by a radiationless π-π* transition followed by an electron shift from a negative oxygen to the positive aromatic π-system indicated by an observable σ-π* transition. Simple semi-empirical computations correlated with measured excited electronic states during electron transfer.

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

    Chiu, K.-F.; Su, S.-H., E-mail:


    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.

  17. Syntheses and GABA uptake properties of 6-ether- and 6-enol ether-substituted nipecotic acids.

    N'Goka, Victor; Bissantz, Caterina; Bisel, Philippe; Stenbøl, Tine B; Krogsgaard-Larsen, Povl; Schlewer, Gilbert


    6-aralkylether- and 6-arylenol-ether-substituted nipecotic acids were synthesized. These analogues are poor GABA uptake inhibitors. The electronegative region concept developed in the N-substituted nipecotic acid series cannot be transferred on the side chain of this series of 6-substituted analogues.

  18. Novel high T{sub g} high-strength poly(aryl ether)s

    Banerjee, S.; Maier, G. [Technische Univ. Muenchen, Garching (Germany). Lehrstuhl fuer Makromolekulare Stoffe


    A novel 2-perfluoroalkyl-activated bisfluoro monomer has been synthesized successfully using a Pd(0)-catalyzed cross-coupling reaction of 4-fluoro-3-trifluoromethyl phenyl boronic acid with 4,4{prime}-dibromodiphenylbenzene. This monomer was converted to novel poly(aryl ether)s by nucleophilic displacement of the fluorine atoms on the benzene ring with several bisphenols. The products obtained by displacement of the fluorine atoms exhibit weight average molar masses up to 1.06 {times} 10{sup 5} g/mol in GPC. These poly(aryl ether)s showed outstanding thermooxidative stability up to 534 C for 5% weight loss in TGA under synthetic air and high glass transition temperatures (T{sub g}) even up to 300 C in DSC and DMTA. These polymers are soluble in a wide range of organic solvents, e.g., CHCl{sub 3}, THF, NMP, DMF, toluene, etc., and are insoluble in DMSO and acetone. Transparent thin films of these polymers cast from DMF exhibited tensile strengths up to 115 MPa, moduli up to 2.59 GPa, and elongations up to 120% depending on their exact repeating unit structures. These values are comparable to those of high performance thermoplastic materials such as PEEK or Ultem PEI.

  19. Novel high T[sub g] high-strength poly(aryl ether)s

    Banerjee, S.; Maier, G. (Technische Univ. Muenchen, Garching (Germany). Lehrstuhl fuer Makromolekulare Stoffe)


    A novel 2-perfluoroalkyl-activated bisfluoro monomer has been synthesized successfully using a Pd(0)-catalyzed cross-coupling reaction of 4-fluoro-3-trifluoromethyl phenyl boronic acid with 4,4[prime]-dibromodiphenylbenzene. This monomer was converted to novel poly(aryl ether)s by nucleophilic displacement of the fluorine atoms on the benzene ring with several bisphenols. The products obtained by displacement of the fluorine atoms exhibit weight average molar masses up to 1.06 [times] 10[sup 5] g/mol in GPC. These poly(aryl ether)s showed outstanding thermooxidative stability up to 534 C for 5% weight loss in TGA under synthetic air and high glass transition temperatures (T[sub g]) even up to 300 C in DSC and DMTA. These polymers are soluble in a wide range of organic solvents, e.g., CHCl[sub 3], THF, NMP, DMF, toluene, etc., and are insoluble in DMSO and acetone. Transparent thin films of these polymers cast from DMF exhibited tensile strengths up to 115 MPa, moduli up to 2.59 GPa, and elongations up to 120% depending on their exact repeating unit structures. These values are comparable to those of high performance thermoplastic materials such as PEEK or Ultem PEI.

  20. 75 FR 28804 - An Exposure Assessment of Polybrominated Diphenyl Ethers (PBDEs)


    ... AGENCY An Exposure Assessment of Polybrominated Diphenyl Ethers (PBDEs) AGENCY: Environmental Protection...'s 2006 Polybrominated Diphenyl Ethers (PBDEs) Project Plan. This document ] provides an assessment of the exposure of Americans to polybrominated diphenyl ethers (PBDEs), a class of brominated...

  1. A new synthetic resorcinolic lipid 3-heptyl-3,4,6-trimethoxy-3H-isobenzofuran-1-one: evaluation of toxicology and ability to potentiate the mutagenic and apoptotic effects of cyclophosphamide.

    Navarro, Stephanie Dynczuki; Beatriz, Adilson; Meza, Alisson; Pesarini, João Renato; Gomes, Roberto da Silva; Karaziack, Caroline Bilhar; Cunha-Laura, Andréa Luiza; Monreal, Antônio Carlos Duenhas; Romão, Wanderson; Lacerda Júnior, Valdemar; Mauro, Mariana de Oliveira; Oliveira, Rodrigo Juliano


    Resorcinolic lipids have important biological actions, including anti-carcinogenic activity. Therefore, we evaluated the mutagenic, genotoxic, immunomodulatory and apoptotic potential and the biochemical and histopathological changes caused by the synthetic resorcinolic lipid 3-Heptyl-3,4,6-trimethoxy-3H-isobenzofuran-1-one, (AMS35AA; 10, 20 and 40 mg/kg) alone or in combination with cyclophosphamide (100 mg/kg) in Swiss mice. The results indicated that AMS35AA is not genotoxic or mutagenic and does not alter liver or kidney histology. However, the compound does cause an increase (p mutagenic damage (although the compound had anti-genotoxic activity), splenic phagocytosis, neutropenia and glutamic-oxaloacetic transaminase and creatinine levels (even in the absence of histological damage) and induced liver and kidney apoptosis. We conclude that this resorcinolic lipid may be an important chemotherapy adjuvant that can potentiate mutagenic damage and increase apoptosis caused by cyclophosphamide without causing adverse effects. In addition, the immunomodulatory activity of the compound should be noted, which counters reductions in lymphocyte number, a primary side effect of cyclophosphamide in cancer therapy.

  2. Short and stereoselective total synthesis of furano lignans (+/-)-dihydrosesamin, (+/-)-lariciresinol dimethyl ether, (+/-)-acuminatin methyl ether, (+/-)-sanshodiol methyl ether, (+/-)-lariciresinol, (+/-)-acuminatin, and (+/-)-lariciresinol monomethyl ether and furofuran lignans (+/-)-sesamin, (+/-)-eudesmin, (+/-)-piperitol methyl ether, (+/-)-pinoresinol, (+/-)-piperitol, and (+/-)-pinoresinol monomethyl ether by radical cyclization of epoxides using a transition-metal radical source.

    Roy, Subhas Chandra; Rana, Kalyan Kumar; Guin, Chandrani


    Intramolecular radical cyclization of suitably substituted epoxy ethers 4a-g using bis(cyclopentadienyl)titanium(III) chloride as the radical source resulted in trisubstituted tetrahydrofurano lignans and 2,6-diaryl-3,7-dioxabicyclo[3.3.0]octane lignans depending on the reaction conditions. The titanium(III) species was prepared in situ from commercially available titanocene dichloride and activated zinc dust in THF. Upon radical cyclization followed by acidic workup, epoxy olefinic ethers 4a-g afforded furano lignans dihydrosesamin 1a, lariciresinol dimethyl ether 1b, acuminatin methyl ether 1e, and sanshodiol methyl ether 1g directly and lariciresinol 1h, acuminatin 1i, and lariciresinol monomethyl ether 1j after removal of the benzyl protecting group by controlled hydrogenolysis of the corresponding cyclized products. The furofuran lignans sesamin 2a, eudesmin 2b, and piperitol methyl ether 2e were also prepared directly by using the same precursors 4a-f on radical cyclization followed by treatment with iodine and pinoresinol 2h, piperitol 2i, and pinoresinol monomethyl ether 2j after controlled hydrogenolysis of the benzyl protecting group of the corresponding cyclized products. Two naturally occurring acyclic lignans, secoisolariciresinol 5h and secoisolariciresinol dimethyl ether 5b, have also been prepared by exhaustive hydrogenolysis of 2h and 2b, respectively.

  3. Application of simplified PC-SAFT to glycol ethers

    Avlund, Ane Søgaard; Kontogeorgis, Georgios; Michelsen, Michael Locht


    The simplified PC-SAFT (sPC-SAFT) equation of state is applied for binary glycol ether-containing mixtures, and it is investigated how the results are influenced by inclusion of intramolecular association in the association theory. Three different glycol ethers are examined: 2-methoxyethanol, 2-e...

  4. Congenital malformations and maternal occupational exposure to glycol ethers

    Cordier, S; Bergeret, A; Goujard, J; Ha, MC; Ayme, S; Calzolari, E; DeWalle, HEK; KnillJones, R; Candela, S; Dale, [No Value; Dananche, B; deVigan, C; Fevotte, J; Kiel, G; Mandereau, L


    Glycol ethers are found in a wide range of domestic and industrial products, many of which are used in women's work environments. Motivated by concern about their potential reproductive toxicity, we have evaluated the risk of congenital malformations related to glycol ether exposure during preg nanc

  5. Characterization of Poly(ether)urethanes - High Resolution Thermogravimetric Analysis


    ether)urethanes.11 Table 5. Percent weight loss for steps in stepwise isothermal TGA analysis .......................... 14 viii DRDC Atlantic...Stepwise isothermal plots for the six poly(ether)urethanes. Table 5. Percent weight loss for steps in stepwise isothermal TGA analysis . SAMPLE/ % WT LOSS


    Diego Blanco


    Full Text Available Se estudia la adsorción de resorcinol, sobre carbones activados modificados, obtenidos a partir de un carbón activado comercial CarbochemTM –PS30, CAG, por medio de tratamiento químico con HNO3 7M, CAO y tratamiento térmico bajo flujo de H2, CAR; se analiza la influencia del pH de la solución, la reducción y oxidación de la superficie del carbón y se determina la entalpía de inmersión de los carbones activados en soluciones acuosas de resorcinol.La interacción sólido-solución se caracteriza por el análisis de las isotermas de adsorción a 298 K a los pHs de 7, 9 y 11 con el propósito de evaluar el sistema sobre y por debajo del valor de las pKa del resorcinol. La capacidad de adsorción de los carbones aumenta al disminuir el pH de la solución. La cantidad retenida aumenta en el carbón reducido al pH de máxima adsorción y disminuye en el carbón oxidado. Los resultados experimentales de las isotermas de adsorción se ajustaron a los modelos de Freundlich y Langmuir, obteniendo valores para el parámetro Qmáx del modelo de Langmuir en el CAG de 179, 156 y 44 mgg-1, para valores de pH de 7, 9 y 11 respectivamente. En el caso de los carbones modificados se obtienen valores de 233, 179 y 164 mgg-1, para el CAR, CAG y CAO a pH 7 respectivamente. Como tendencia general la adsorción de resorcinol aumenta en el siguiente orden CAR > CAG > CAO Similares conclusiones se obtienen de las entalpías de inmersión, cuyos valores se incrementan con la cantidad de soluto retenido. En el caso del CAG se obtienen entalpías de inmersión entre 25,8 a 40,9 Jg-1 para soluciones acuosas de resorcinol en un rango de 20 a 1500 mgL-1.

  7. Structural features of resorcinol-formaldehyde resin chars and interfacial behavior of water co-adsorbed with low-molecular weight organics

    Gun'ko, Vladimir M.; Bogatyrov, Viktor M.; Turov, Vladimir V.; Leboda, Roman; Skubiszewska-Zięba, Jadwiga; Urubkov, Iliya V.


    Products of resorcinol-formaldehyde resin carbonization (chars) are characterized by different morphology (particle shape and sizes) and texture (specific surface area, pore volume and pore size distribution) depending on water content during resin polymerization. At a low amount of water (Cw = 37.8 wt.%) during synthesis resulting in strongly cross-linked polymers, carbonization gives nonporous particles. An increase in the water content to 62.7 wt.% results in a nano/mesoporous char, but if Cw = 73.3 wt.%, a char is purely nanoporous. Despite these textural differences, the Raman spectra of all the chars are similar because of the similarity in the structure of their carbon sheets with a significant contribution of sp3 C atoms. However, the difference in the spatial organization of the carbon sheet stacks in the particles results in the significant differences in the textural and morphological characteristics and in the adsorption properties of chars with respect to water, methane, benzene, hydrogen, methylene chloride, and dimethylsulfoxide.

  8. Role of 2-hexyl, 5-propyl resorcinol production by Pseudomonas chlororaphis PCL1606 in the multitrophic interactions in the avocado rhizosphere during the biocontrol process.

    Calderón, Claudia E; de Vicente, Antonio; Cazorla, Francisco M


    Different bacterial traits can contribute to the biocontrol of soilborne phytopathogenic fungus. Among others, (1) antagonism, (2) competition for nutrients and niches, (3) induction of systemic resistance of the plants and (4) predation and parasitism are the most studied. Pseudomonas chlororaphis PCL1606 is an antagonistic rhizobacterium that produces the antifungal metabolite 2-hexyl, 5-propyl resorcinol (HPR). This bacterium can biologically control the avocado white root rot caused by Rosellinia necatrix. Confocal laser scanning microscopy of the avocado rhizosphere revealed that this biocontrol bacterium and the fungal pathogen compete for the same niche and presumably also for root exudate nutrients. The use of derivative mutants in the geners related to HPR biosynthesis (dar genes) revealed that the lack of HPR production by P. chlororaphis PCL1606 negatively influences the bacterial colonisation of the avocado root surface. Microscopical analysis showed that P. chlororaphis PCL1606 closely interacts and colonises the fungal hyphae, which may represent a novel biocontrol mechanism in this pseudomonad. Additionally, the presence of HPR-producing biocontrol bacteria negatively affects the ability of the fungi to infect the avocado root. HPR production negatively affects hyphal growth, leading to alterations in the R. necatrix physiology visible under microscopy, including the curling, vacuolisation and branching of hyphae, which presumably affects the colonisation and infection abilities of the fungus. This study provides the first report of multitrophic interactions in the avocado rhizosphere, advancing our understanding of the role of HPR production in those interactions.

  9. Simultaneous Electrochemical Determination of Hydroquinone, Catechol and Resorcinol at Nitrogen Doped Porous Carbon Nanopolyhedrons-multiwall Carbon Nanotubes Hybrid Materials Modified Glassy Carbon Electrode

    Liu, Wei; Wu, Liang; Zhang, Xiaohua; Chen, Jinhua [Hunan Univ., Changsha (China)


    The nitrogen doped porous carbon nanopolyhedrons (N-PCNPs)-multi-walled carbon nanotubes (MWCNTs) hybrid materials were prepared for the first time. Combining the excellent catalytic activities, good electrical conductivities and high surface areas of N-PCNPs and MWCNTs, the simultaneous determination of hydroquinone (HQ), catechol (CC) and resorcinol (RE) with good analytical performance was achieved at the N-PCNPs-MWCNTs modified electrode. The linear response ranges for HQ, CC and RE are 0.2-455 μM, 0.7-440 μM and 3.0-365 μM, respectively, and the detection limits (S/N = 3) are 0.03 μM, 0.11 μM and 0.38 μM, respectively. These results are much better than that obtained on some graphene or CNTs-based materials modified electrodes. Furthermore, the developed sensor was successfully applied to simultaneously detect HQ, CC and RE in the local river water samples.

  10. Electrochemical behavior of catechol, resorcinol and hydroquinone at graphene-chitosan composite film modified glassy carbon electrode and their simultaneous determination in water samples

    Yin Huanshun [College of Chemistry and Material Science, Shandong Agricultural University, Taian, 271018 Shandong (China); College of Resources and Environment, Shandong Agricultural University, Taian 271018, Shandong (China); Zhang Qingming [College of Resources and Environment, Shandong Agricultural University, Taian 271018, Shandong (China); College of Chemistry and Pharmaceutical Sciences, Qingdao Agriculture University, Qingdao 266109 (China); Zhou Yunlei [College of Life Science, Beijing Normal University, 100875 Beijing (China); Ma Qiang; Liu Tao [College of Chemistry and Material Science, Shandong Agricultural University, Taian, 271018 Shandong (China); Zhu Lusheng, E-mail: [College of Resources and Environment, Shandong Agricultural University, Taian 271018, Shandong (China); Ai Shiyun, E-mail: [College of Chemistry and Material Science, Shandong Agricultural University, Taian, 271018 Shandong (China)


    Graphene-chitosan composite film modified glassy carbon electrode was prepared and characterized. The fabricated electrode showed excellent electrochemical catalytic activities towards the oxidation of catechol (CT), resorcinol (RS) and hydroquinone (HQ). The oxidation overpotentials of CT, RS and HQ decreased significantly and the corresponding oxidation currents increased remarkably compared with those obtained at the bare GCE and chitosan modified GCE. Some kinetic parameters, such as the electron transfer number (n), proton transfer number (m), charge transfer coefficient ({alpha}) and the apparent heterogeneous electron transfer rate constant (k{sub s}), were calculated. Differential pulse voltammetry was used for the simultaneous determination of CT, RS and HQ in their ternary mixture. The peak-to-peak potential separations between CT and RS, RS and HQ, and HQ and CT were 0.388, 0.484 and 0.096 V, respectively. The calibration curves for CT, RS and HQ were obtained in the range of 1 x 10{sup -6} to 4 x 10{sup -4}, 1 x 10{sup -6} to 5.5 x 10{sup -4} and 1 x 10{sup -6} to 3 x 10{sup -4} mol L{sup -1}, respectively. The detection limits were 7.5 x 10{sup -7} mol L{sup -1} (S/N = 3).

  11. Ethylated Urea - Ether - Modified Urea - Formaldehyde Resins,

    Mathew Obichukwu EDOGA


    Full Text Available First, phenol - formaldehyde (PF and urea - formaldehyde (UFII resins were separately conventionally prepared in our laboratory. Also, UF resin synthesized from the acid modified synthesis procedure was synthesized in a purely acid medium of pH 1.0, FU molar ratio of 1.0 and at 50oC (one-stage acid modified-synthesis procedure. Subsequently, the UF resin II was modified during synthesis by incorporating ethylated urea-ether (EUER (i.e. UFIII and glycerol (GLYC (i.e. UFV cured with and without acid curing agent. The structural and physicochemical analyses of the various resin samples were carried out.The results showed that the unmodified UF resin (UF II synthesized in acid medium of pH 1.0, F/U molar ratio 1.0, and at 50oC, cured in absence of acid curing catalyst, showed features in their spectra which are consistent with a tri-, and/or tetra-substituted urea in the reaction to give a 3 - dimensional network cured UF resin. Modification of the UF resin(UF II with ethylated urea-ether and glycerol to produce UF resins III and respectively V prominently increased the absorbance of methylene and ether groups in the spectra which are consistent with increased hydrophobicity and improved hydrolytic stability. For the conventional UF resin (UF I, the only clear distinction between spectra for the UF resin II and UF resins (III/V is the presence of diminished peaks for methylene groups at 2.2 ppm. The relationship between the logarithmic viscosity of cured PF resin with time showed continuos dependence of viscosity with time during cure up to 70 minutes. Similar trends were shown by UF resins (III/V, cured in absence of acid catalyst. In contrast, the conventional UF resins I and UF IV (i.e. UF II cured with NH4CL showed abrupt discontinuity in viscosity with time just after about 20 minutes of cure.

  12. Polymeric 32-channel arrayed waveguide grating multiplexer using fluorinated poly (ether ether ketone)

    Fei Wang(王菲); Wei Sun(孙伟); Aize Li(李艾泽); Maobin Yi(衣茂斌); Zhenhua Jiang(姜振华); Daming Zhang(张大明)


    In wavelength division multiplexing (WDM) systems, an arrayed waveguide grating (AWG) multiplexer is a key component. A polymeric AWG multiplexer has recently attracted much attention due to its low cost processing and a potential of integration with other devices. Fluorinated poly (ether ether ketone)(FPEEK) is excellent material for fabrication of optical waveguides due to its low absorption loss at 1.55-μm wavelength and high thermal stability. A 32-channel AWG multiplexer has been designed based on the grating diffraction theory and fabricated using newly synthesized FPEEK. During the fabrication process of the Polymer/Si AWG device, spin coating, vaporizing, photolithographic patterning and reactive ion etching (RIE) are used. The AWG multiplexer measurement system is based on a tunable semiconductor laser, infrared camera and a Peltier-type heater. The device exhibits a wavelength channel spacing of 0.8nm and a center wavelength of 1548 nm in the room temperature.

  13. Origin of mechanical modifications in poly (ether ether ketone)/carbon nanotube composite

    Pavlenko, Ekaterina; Puech, Pascal; Bacsa, Wolfgang, E-mail: [CEMES-CNRS and University of Toulouse, 29 Jeanne Marvig, 31055 Toulouse (France); Boyer, François; Olivier, Philippe [Université de Toulouse, Institut Clément Ader, I.U.T. Université Paul Sabatier - 133C Avenue de Rangueil - B.P. 67701, 31077 Toulouse CEDEX 4 (France); Sapelkin, Andrei [School of Physics and Astronomy, Queen Mary, University of London, Mile End Road, E1 4NS London (United Kingdom); King, Stephen; Heenan, Richard [ISIS Facility, Rutherford Appleton Laboratory, Chilton, OX11 0QX Didcot (United Kingdom); Pons, François; Gauthier, Bénédicte; Cadaux, Pierre-Henri [AIRBUS FRANCE (B.E. M and P Toulouse), 316 Route de Bayonne, 31060 Toulouse (France)


    Variations in the hardness of a poly (ether ether ketone) beam electrically modified with multi-walled carbon nanotubes (MWCNT, 0.5%-3%) are investigated. It is shown that both rupture and hardness variations correlate with the changes in carbon nanotube concentration when using micro indentation and extended Raman imaging. Statistical analysis of the relative spectral intensities in the Raman image is used to estimate local tube concentration and polymer crystallinity. We show that the histogram of the Raman D band across the image provides information about the amount of MWCNTs and the dispersion of MWCNTs in the composite. We speculate that we have observed a local modification of the ordering between pure and modified polymer. This is partially supported by small angle neutron scattering measurements, which indicate that the agglomeration state of the MWCNTs is the same at the concentrations studied.

  14. Sulfonated poly(tetramethydiphenyl ether ether ketone) membranes for vanadium redox flow battery application

    Mai, Zhensheng; Bi, Cheng; Dai, Hua [PEMFC Key Materials and Technology Laboratory, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Zhongshan Road 457, Dalian 116023 (China); Graduate University of the Chinese Academy of Sciences, Beijing 100039 (China); Zhang, Huamin; Li, Xianfeng [PEMFC Key Materials and Technology Laboratory, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Zhongshan Road 457, Dalian 116023 (China)


    Sulfonated poly(tetramethydiphenyl ether ether ketone) (SPEEK) with various degree of sulfonation is prepared and first used as ion exchange membrane for vanadium redox flow battery (VRB) application. The vanadium ion permeability of SPEEK40 membrane is one order of magnitude lower than that of Nafion 115 membrane. The low cost SPEEK membranes exhibit a better performance than Nafion at the same operating condition. VRB single cells with SPEEK membranes show very high energy efficiency (>84%), comparable to that of the Nafion, but at much higher columbic efficiency (>97%). In the self-discharge test, the duration of the cell with the SPEEK membrane is two times longer than that with Nafion 115. The membrane keeps a stable performance after 80-cycles charge-discharge test. (author)

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

    Devesh Shukla


    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.

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

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


    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.

  17. Sulfonated poly(tetramethydiphenyl ether ether ketone) membranes for vanadium redox flow battery application

    Mai, Zhensheng; Zhang, Huamin; Li, Xianfeng; Bi, Cheng; Dai, Hua

    Sulfonated poly(tetramethydiphenyl ether ether ketone) (SPEEK) with various degree of sulfonation is prepared and first used as ion exchange membrane for vanadium redox flow battery (VRB) application. The vanadium ion permeability of SPEEK40 membrane is one order of magnitude lower than that of Nafion 115 membrane. The low cost SPEEK membranes exhibit a better performance than Nafion at the same operating condition. VRB single cells with SPEEK membranes show very high energy efficiency (>84%), comparable to that of the Nafion, but at much higher columbic efficiency (>97%). In the self-discharge test, the duration of the cell with the SPEEK membrane is two times longer than that with Nafion 115. The membrane keeps a stable performance after 80-cycles charge-discharge test.


    Jing-kun Xu; Wei-qiang Zhou; Jian Hou; Shou-zhi Pu; Jing-wu Wang; Liu-shui Yan


    High quality poly(5-cyanoindole) (P5CI) films were electrosynthesized by direct anodic oxidation of 5-cyanoindole on stainless steel sheet in the mixed electrolytes of boron trifluoride diethyl etherate (BFEE) and diethyl ether (EE) (by volume 1:1) + 0.05 mol L-1 Bu4NBF4. The film formed can be peeled off the electrode into freestanding films. The addition of EE into BFEE can improve the solubility of monomer. P5CI films obtained from this medium showed excellent electrochemical behavior with conductivity of 10-2 Scm-1. Structural studies showed that the polymerization of 5-cyanoindole occurred at the 2,3 position. As-formed P5CI films were thoroughly soluble in strong polar organic solvent dimethyl sulfoxide (DMSO) while partly soluble in tetrahydrofuran (THF) or acetone. Fluorescence spectral studies indicated that P5CI was a good blue-light emitter.

  19. Dielectric properties of poly (1,4-phenylene ether-ether-sulfone)

    Spasevska, H


    Dielectric properties of Poly (1,4-phenylene ether-ether-sulfone) are obtained from dielectric spectroscopy of the polymer pellet. The values of relative dielectric constant epsilon', dielectric losses epsilon sup , dielectric dissipation factor tan delta and complex impedance are obtained at temperature of 75 sup o C. The temperature dependence of these parameters is investigated for three frequencies (8x10 sup 4 Hz; 8x10 sup 5 Hz; 8x10 sup 6 Hz) of applied electric field. The specific conductivity sigma, which depends on temperature, is related to the ohmic resistance R, at temperature in the interval from 66 to 83 sup o C. Fitting the experimental data, the value of the activation energy U is obtained. (Original)

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

    Hwang, Mi-Lim; Choi, Jisun; Woo, Hyun-Su; Kumar, Vinod; Sohn, Joon-Yong; Shin, Junhwa, E-mail:


    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)

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

    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)


    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)

  2. Microwave Spectrum of the Ethylmethyl Ether Molecule

    Kojiro Takagi


    Full Text Available We have observed rotational transitions of ethylmethyl ether (CH3CH2OCH3 in the 24-110 GHz frequency range. We newly assigned the transitions of four Q-branch series for J=1-38 with Ka=0-5 and six R-branch series of b-type transitions for J=7-37 with Ka=0-3. All these assigned transitions were observed to be split into two or four components due to the internal rotations of the methyl groups. We analyzed the averaged frequencies of the split components on the basis of the Watson A-reduced Hamiltonian, neglecting the effect of the internal rotations. A total of 122 transitions were fitted to eight molecular parameters to a 1s standard deviation of 24 kHz. The parameters A, B, C and DJ were improved, and DJK, Dk, dJ and dK were determined for the first time.

  3. Molecular dynamics model of dimethyl ether

    Lin, B.; Halley, W.J. [Univ. of Minnesota, Minneapolis, MN (United States)


    We report a molecular dynamics model of the monomeric liquid dimethyl ether. The united atom approach is used to treat CH{sub 3} groups as point source centers. Partial charges are derived from the experimental dipole moment. Harmonic force constants are used for intramolecular interactions, and their values are so chosen that the model`s fundamental frequencies agree with experimental results. Because we are interested in solvation properties, the model contains flexible molecules, allowing molecular distortion and internal dynamical quantities. We report radial distribution functions and the static structure factors as well as some dynamical quantities such as the dynamical structure factor, infrared absorption, and Raman scattering spectra. Calculated results agree reasonably well with experimental and other simulation results. 25 refs., 8 figs., 1 tab.

  4. Thermolysis of phenethyl phenyl ether: A model of ether linkages in low rank coal

    Britt, P.F.; Buchanan, A.C. III; Malcolm, E.A.


    Currently, an area of interest and frustration for coal chemists has been the direct liquefaction of low rank coal. Although low rank coals are more reactive than bituminous coals, they are more difficult to liquefy and offer lower liquefaction yields under conditions optimized for bituminous coals. Solomon, Serio, and co-workers have shown that: in the pyrolysis and liquefaction of low rank coals, a low temperature cross-linking reaction associated with oxygen functional groups occurs before tar evolution. A variety of pretreatments (demineralization, alkylation, and ion-exchange) have been shown to reduce these retrogressive reactions and increase tar yields, but the actual chemical reactions responsible for these processes have not been defined. In order to gain insight into the thermochemical reactions leading to cross-linking in low rank coal, we have undertaken a study of the pyrolysis of oxygen containing coal model compounds. Solid state NMR studies suggest that the alkyl aryl ether linkage may be present in modest amounts in low rank coal. Therefore, in this paper, we will investigate the thermolysis of phenethyl phenyl ether (PPE) as a model of 0-aryl ether linkages found in low rank coal, lignites, and lignin, an evolutionary precursor of coal. Our results have uncovered a new reaction channel that can account for 25% of the products formed. The impact of reaction conditions, including restricted mass transport, on this new reaction pathway and the role of oxygen functional groups in cross-linking reactions will be investigated.

  5. Cationic Poly(benzyl ether)s as Self-Immolative Antimicrobial Polymers.

    Ergene, Cansu; Palermo, Edmund F


    Self-immolative polymers (SIMPs) are macromolecules that spontaneously undergo depolymerization into small molecules when triggered by specific external stimuli. We report here the first examples of antimicrobial SIMPs with potent, rapid, and broad-spectrum bactericidal activity. Their antibacterial and hemolytic activities were examined as a function of cationic functionality. Polymers bearing primary ammonium cationic groups showed more potent bactericidal activity against Escherichia coli, relative to tertiary and quaternary ammonium counterparts, whereas the quaternary ammonium polymers showed the lowest hemolytic toxicity. These antibacterial polycations undergo end-to-end depolymerization when triggered by an externally applied stimulus. Specifically, poly(benzyl ether)s end-capped with a silyl ether group and bearing pendant allyl side chains were converted to polycations by photoinitiated thiol-ene radical addition using cysteamine HCl. The intact polycations are stable in solution, but they spontaneously unzip into their component monomers upon exposure to fluoride ions, with excellent sensitivity and selectivity. Upon triggered depolymerization, the antibacterial potency was largely retained but the hemolytic toxicity was substantially reduced. Thus, we reveal the first example of a self-immolative antibacterial polymer platform that will enable antibacterial materials to spontaneously unzip into biologically active small molecules upon the introduction of a specifically designed stimulus.

  6. High temperature fuel cell membranes based on poly(arylene ether)s containing benzimidazole groups

    Kim, Dae Sik [Los Alamos National Laboratory; Kim, Yu Seung [Los Alamos National Laboratory; Lee, Kwan - Soo [Los Alamos National Laboratory; Boncella, James M [Los Alamos National Laboratory; Kuiper, David [Los Alamos National Laboratory; Guiver, Michael D [CANADA


    Development of new high-performance polymer membranes that retain their proton conductivity under low humidity conditions is one of the most critical requirements to commercialize PEMFC systems. Current sulfonated proton exchange membranes acquire proton conductivity by water that solvates ion and carries proton. Consequently, a loss of water under low RH conditions immediately results in a loss of proton conductivity. One approach to maintain proton conductivity under low RH conditions is to replace water with a less volatile proton solvent. Kreuer has pointed out the possibility to develop fully polymeric proton-conducting membranes based on nitrogen-containing heterocycles such as imidazole, benzimidazole, and pyrazole. We have attempted to blend those less volatile proton solvent with sulfonated copolymers such as polystyrene sulfonic acid, Nafion, poly(arylene ether sulfone, BPSH-xx). [Ref. DOE review meeting 2007 and 2008] However, we observed that imidazole was slowly sublimated out as temperature and humidity increases which could cause poisoning of electro-catalyst, corrosion and losing conductivity. In this presentation, we report the synthesis of novel poly(arylene ether sulfone)s containing benzimidazole groups These benzimidazole containing polymer was blended with sulfonated poly(arylene ether sulfone). In the blend system, benzimidazole group attached to the polysulfone acts as a medium through the basic nitrogen for transfer of protons between the sulfonic acid groups. Proton conductivity of the blend membranes was investigated as a function of water content at 80 C and compared the performance with water based proton conduction system.

  7. Formulating liquid ethers for microtubular SOFCs

    Kendall, Kevin; Slinn, Matthew; Preece, John

    One of the key problems of applying solid oxide fuel cells (SOFCs) in transportation is that conventional fuels like kerosene and diesel do not operate directly in SOFCs without prereforming to hydrogen and carbon monoxide which can be handled by the nickel cermet anode. SOFCs can internally reform certain hydrocarbon molecules such as methanol and methane. However, other liquid fuels usable in petrol or diesel internal combustion engines (ICEs) have not easily been reformable directly on the anode. This paper describes a search for liquid fuels which can be mixed with petrol or diesel and also injected directly into an SOFC without destroying the nickel anode. When fuel molecules such as octane are injected onto the conventional nickel/yttria stabilised zirconia (Ni/YSZ) SOFC fuel electrode, the anode rapidly becomes blocked by carbon deposition and the cell power drops to near zero in minutes. This degeneration of the anode can be inhibited by injection of air or water into the anode or by some upstream reforming just before entry to the SOFC. Some smaller molecules such as methane, methanol and methanoic acid produce a slight tendency to carbon deposition but not sufficient to prevent long term operation. In this project we have investigated a large number of molecules and now found that some liquid ethers do not significantly damage the anode when directly injected. These molecules and formulations with other components have been evaluated in this study. The theory put forward in this paper is that carbon-carbon bonds in the fuel are the main reason for anode damage. By testing a number of fuels without such bonds, particularly liquid ethers such as methyl formate and dimethoxy methane, it has been shown that SOFCs can run without substantial carbon formation. The proposal is that conventional fuels can be doped with these molecules to allow hybrid operation of an ICE/SOFC device.

  8. Vapor intrusion risk of fuel ether oxygenates methyl tert-butyl ether (MTBE), tert-amyl methyl ether (TAME) and ethyl tert-butyl ether (ETBE): A modeling study.

    Ma, Jie; Xiong, Desen; Li, Haiyan; Ding, Yi; Xia, Xiangcheng; Yang, Yongqi


    Vapor intrusion of synthetic fuel additives represents a critical yet still neglected problem at sites contaminated by petroleum fuel releases. This study used an advanced numerical model to investigate the vapor intrusion potential of fuel ether oxygenates methyl tert-butyl ether (MTBE), tert-amyl methyl ether (TAME), and ethyl tert-butyl ether (ETBE). Simulated indoor air concentration of these compounds can exceed USEPA indoor air screening level for MTBE (110μg/m(3)). Our results also reveal that MTBE has much higher chance to cause vapor intrusion problems than TAME and ETBE. This study supports the statements made by USEPA in the Petroleum Vapor Intrusion (PVI) Guidance that the vertical screening criteria for petroleum hydrocarbons may not provide sufficient protectiveness for fuel additives, and ether oxygenates in particular. In addition to adverse impacts on human health, ether oxygenate vapor intrusion may also cause aesthetic problems (i.e., odour and flavour). Overall, this study points out that ether oxygenates can cause vapor intrusion problems. We recommend that USEPA consider including the field measurement data of synthetic fuel additives in the existing PVI database and possibly revising the PVI Guidance as necessary.

  9. Characterization of Microsolvated Crown Ethers from Broadband Rotational Spectroscopy

    Perez, Cristobal; Schnell, Melanie; Blanco, Susana; Lopez, Juan Carlos


    Since they were first synthetized, crown ethers have been extensively used in organometallic chemistry due to their unparalleled binding selectivity with alkali metal cations. From a structural point of view, crown ethers are heterocycles containing oxygen and/or other heteroatoms, although the most common ones are formed from ethylene oxide unit. Crown ethers are conventionally seen as being hydrophilic inside and hydrophobic outside when the structures found for the metal cation complexes are considered. However, crown ethers are extremely flexible and in isolation may present a variety of stable conformations so that their structure may be easily adapted in presence of a strong ligand as an alkali metal cation minimize the energy of the resulting complex. Water can be considered a soft ligand which interacts with crown ethers through moderate hydrogen bonds. It is thus interesting to investigate which conformers are selected by water to form complexes, the preferred interaction sites and the possible conformational changes due to the presence of one or more water molecules. Previous studies identified microsolvated crown ethers but in all cases with a chromophore group attached to the structure. Here we present a broadband rotational spectroscopy study of microsolvated crown ethers produced in a pulsed molecular jet expansion. Several 1:1 and 1:2 crown ether:water aggregates are presented for 12-crown-4, 15-crown-5 and 18-crown-6. Unambiguous identification of the structures has been achieved using isotopic substitution within the water unit. The subtle changes induced in the structures of the crown ether monomer upon complexation and the hydrogen-bonding network that hold them together will be also discussed. F. Gámez, B. Martínez-Haya, S. Blanco,J. C. López and J. L. Alonso, Phys. Chem. Chem. Phys. 2014, 14 12912-12918 V. A. Shubert, C.W. Müller and T. Zwier, J. Phys. Chem. A 2009, 113 8067-8079

  10. 德国赫优讯EtherCAT新产品


    EtherCAT作为实时以太网协议之一,以其强大的性能和“On the fly”的速度,以及网络抖动小于1μs的同步功能.成为发展最快的实时网络协议。同时,EtherCAT全球组织在中国代表处的设立,表明了EtherCAT全球组织对中国市场的关心。

  11. Impact of cellulose ethers on the cement paste microstructure

    Pourchez, Jérémie; Grosseau, Philippe; Rouèche-Pourchez, Emilie; Debayle, Johan; Pinoli, Jean-Charles; Maire, Eric; Boller, Elodie; Parra-Denis, Estelle


    ISBN = 3-87264-022-4 7 pages; International audience; Complementary investigation tools (2D and 3D observations by optical microscopy and fast X-ray microtomography and then image analysis) were developed in order to examine the effects of cellulose ethers on the cement paste microstructure. The obtained results show that the presence of cellulose ether may induce an increase of both 50-250 µm-diameter air voids. The chemistry of the cellulose ethers appears as a main controlling factor of th...

  12. Synthesis and Adsorption Property of Dihydroxyl Azacrown Ether-Grafted Chitosan


    A novel dihydroxyl azacrown ether chitosan was synthesized by reacting dihydroxyl azacrown ether with epoxy activated chitosan. The adsorption property of the azacrown ether chitosan for Pb2+, Cr3+, and Ag+, were determined. The experimental results showed that the dihydroxyl azacrown ether grafted chitosan has high adsorption capacity and high selectivity for some metal ions.

  13. Evaluation of crystallization kinetics of poly (ether-ketone-ketone and poly (ether-ether-ketone by DSC

    Gibran da Cunha Vasconcelos


    Full Text Available The poly (aryl ether ketones are used as matrices in advanced composites with high performance due to its high thermal stability, excellent environmental performance and superior mechanical properties. Most of the physical, mechanical and thermodynamic properties of semi-crystalline polymers depend on the degree of crystallinity and morphology of the crystalline regions. Thus, a study on the crystallization process promotes a good prediction of how the manufacturing parameters affect the developed structure, and the properties of the final product. The objective of this work was to evaluate the thermoplastics polymers PEKK e PEEK by DSC, aiming to obtain the relationship between kinetics, content, nucleation and geometry of the crystalline phases, according to the parameters of the Avrami and Kissinger models. The analysis of the Avrami exponents obtained for the studied polymers indicates that both showed the formation of crystalline phases with heterogeneous nucleation and growth geometry of the type sticks or discs, depending on the cooling conditions. It was also found that the PEEK has a higher crystallinity than PEKK.

  14. Spatial trends of polybrominated diphenyl ether (PBDE) congeners

    National Oceanic and Atmospheric Administration, Department of Commerce — Spatial trends of polybrominated diphenyl ether (PBDE) congeners were analyzed in young of the year bluefish collected along the U.S. Atlantic coastline from...

  15. Fluorinated Alkyl Ether Epoxy Resin Compositions and Applications Thereof

    Wohl, Christopher J. (Inventor); Connell, John W. (Inventor); Smith, Joseph G. (Inventor); Siochi, Emilie J. (Inventor); Gardner, John M. (Inventor); Palmieri, Frank M. (Inventor)


    Epoxy resin compositions prepared using amino terminated fluoro alkyl ethers. The epoxy resin compositions exhibit low surface adhesion properties making them useful as coatings, paints, moldings, adhesives, and fiber reinforced composites.

  16. Molar absorption coefficients and stability constants of metal complexes of 4-(2-pyridylazo)resorcinol (PAR): Revisiting common chelating probe for the study of metalloproteins.

    Kocyła, Anna; Pomorski, Adam; Krężel, Artur


    4-(2-Pyridylazo)resorcinol (PAR) is one of the most popular chromogenic chelator used in the determination of the concentrations of various metal ions from the d, p and f blocks and their affinities for metal ion-binding biomolecules. The most important characteristics of such a sensor are the molar absorption coefficient and the metal-ligand complex dissociation constant. However, it must be remembered that these values are dependent on the specific experimental conditions (e.g. pH, solvent components, and reactant ratios). If one uses these values to process data obtained in different conditions, the final result can be under- or overestimated. We aimed to establish the spectral properties and the stability of PAR and its complexes accurately with Zn(2+), Cd(2+), Hg(2+), Co(2+), Ni(2+), Cu(2+), Mn(2+) and Pb(2+) at a multiple pH values. The obtained results account for the presence of different species of metal-PAR complexes in the physiological pH range of 5 to 8 and have been frequently neglected in previous studies. The effective molar absorption coefficient at 492 nm for the ZnHx(PAR)2 complex at pH7.4 in buffered water solution is 71,500 M(-1) cm(-1), and the dissociation constant of the complex in these conditions is 7.08×10(-13) M(2). To confirm these values and estimate the range of the dissociation constants of zinc-binding biomolecules that can be measured using PAR, we performed several titrations of zinc finger peptides and zinc chelators. Taken together, our results provide the updated parameters that are applicable to any experiment conducted using inexpensive and commercially available PAR.

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  18. Nickel-catalyzed direct synthesis of dialkoxymethane ethers



    A simple and efficient method for the preparation of dialkoxymethane ethers (oxymethylene ethers) from alcohols and paraformaldehyde in the presence of commercially available nickel(II) salt is described. The reaction proceeds readily under neutral, solvent-free conditions using paraformaldehyde as a C1 source. The present strategy has a broad substrate scope including aliphatic (both primary and secondary) and aromatic alcohols and provides a benign method for the preparation of symmetrical dialkoxymethanes in good yields (up to 89%).

  19. Imide/Arylene Ether Copolymers Containing Phosphine Oxide

    Jensen, Brian J.; Partos, Richard D.


    Phosphine oxide groups react with oxygen to form protective phosphate surface layers. Series of imide/arylene ether block copolymers containing phosphine oxide units in backbone synthesized and characterized. In comparison with commercial polyimide, these copolymers display better resistance to etching by oxygen plasma. Tensile strengths and tensile moduli greater than those of polyarylene ether homopolymer. Combination of properties makes copolymers attractive for films, coatings, adhesives, and composite matrices where resistance to atomic oxygen needed.

  20. Marine Sponge Dysidea herbacea revisited: Another Brominated Diphenyl Ether

    Bruce F. Bowden


    Full Text Available Abstract: A pentabrominated phenolic diphenyl ether (1 that has not previously been reported from marine sources has been isolated from Dysidea herbacea collected at Pelorus Island, Great Barrier Reef, Australia. The structure was determined by comparison of NMR data with those of known structurally-related metabolites. NMR spectral assignments for (1 are discussed in context with those of three previously reported isomeric pentabrominated phenolic diphenyl ethers.

  1. Effect of diethyl ether on the biliary excretion of acetaminophen.

    Watkins, J B; Siegers, C P; Klaassen, C D


    The biliary and renal excretion of acetaminophen and its metabolites over 8 hr was determined in rats exposed to diethyl ether by inhalation for 1 hr. Additional rats were anesthetized with urethane (1 g/kg ip) while control animals were conscious throughout the experiment (surgery was performed under hexobarbital narcosis: 150 mg/kg ip; 30-min duration). The concentration of UDP-glucuronic acid was decreased 80% in livers from ether-anesthetized rats but was not reduced in urethane-treated animals when compared to that in control rats. The concentration of reduced glutathione was not affected by either urethane or diethyl ether. Basal bile flow was not altered by the anesthetic agents. Bile flow rate after acetaminophen injection (100 mg/kg iv) was increased slightly over basal levels for 2 hr in hexobarbital-treated control rats, was unaltered in urethane-anesthetized animals, and was decreased throughout the 8-hr experiment in rats exposed to diethyl ether for 1 hr. In control and urethane-anesthetized animals, approximately 30-35% of the total acetaminophen dose (100 mg/kg iv) was excreted into bile in 8 hr, while only 16% was excreted in rats anesthetized with diethyl ether. Urinary elimination (60-70% of the dose) was not altered by exposure to ether. Separation of metabolites by reverse-phase high-pressure liquid chromatography showed that ether decreased the biliary elimination of unchanged acetaminophen and its glucuronide, sulfate, and glutathione conjugates by 47, 40, 49, and 73%, respectively, as compared to control rats. Excretion of unchanged acetaminophen and the glutathione conjugate into bile was depressed in urethane-anesthetized animals by 45 and 66%, respectively, whereas elimination of the glucuronide and sulfate conjugates was increased by 27 and 50%, respectively. These results indicate that biliary excretion is influenced by the anesthetic agent and that diethyl ether depresses conjugation with sulfate and glutathione as well as glucuronic

  2. Advanced hybrid fluoropolymers from the cycloaddition of aryl trifluorovinyl ethers

    Ligon, S. Clark, Jr.

    This dissertation discusses the synthesis of aryl trifluorovinyl ethers and their cycloaddition polymerization to give perfluorocyclobutyl (PFCB) polymers. To explore the stereochemistry of these polymers, simple monomfunctional aryl trifluorovinyl ethers were dimerized and the resultant cis and trans isomers were separated. Differences in structure help to improve understanding of the amorphous nature of the bulk PFCB polymeric material. To apply this knowledge, crown ether containing perfluorocyclobutyl (PFCB) polymers were synthesized for use in lithium ion battery applications. While poor solubility has hindered further development of these materials, slight modifications to structure may provide a solution. Also described is a fluorinated aryl vinyl ether and its attempted copolymerization with chlorotrifluoroethylene. While this copolymerization did not yield the desired materials, novel semifluorinated phenol precursors have been utilized in reactions with carboxylic acids to give polyesters and most recently with phosgene like species to give polycarbonates. Next, PFCB polymers were post functionalized with fluoroalkyl tethers to improve oleophobicity and hydrophobicity without decreasing thermal stability or optical clarity. In addition, various silica nanostructures were functionalized with aryl trifluorovinyl ethers. This includes the reaction of aryl silanes to give trifluorovinyl ether functional POSS and their polymerization to provide PFCB hybrid materials. Silane coupling agents were also used to functionalize colloidal silica and fumed silica nanoparticles. These procedures allow excellent dispersion of the silica nanoparticles throughout the fluoropolymer matrix. Finally, the reaction of aryl trifluorovinyl ether with nonfluorinated alkenes and alkynes was explored. In these reactions, the fluorinated olefin adds with the hydrocarbon olefin to give semifluorinated cyclobutanes (SFCB) and with the alkyne to give semifluorinated cyclobutene. The

  3. Effects of the ether phospholipid AMG-PC on mast cells are similar to that of the ether lipid AMG but different from that of the analogue hexadecylphosphocholine

    Grosman, Nina


    Farmakologi, ether phospholipid, hexacylphosphocholine, miltefosine, protein kinase C, AMG-PC(alkyl-methyl-glycero-phosphocholine), Histamine release, mast cell......Farmakologi, ether phospholipid, hexacylphosphocholine, miltefosine, protein kinase C, AMG-PC(alkyl-methyl-glycero-phosphocholine), Histamine release, mast cell...

  4. Review on Modification of Sulfonated Poly (-ether-ether-ketone Membranes Used as Proton Exchange Membranes

    Xiaomin GAO


    Full Text Available The proton exchange membrane fuel cell (PEMFC is a type of modern power, but the traditional proton exchange membranes (PEM of PEMFC are limited by high methanol permeability and water uptake. Poly-ether-ether-ketone (PEEK is a widely used thermoplastic with good cost-effective property. Sulfonated poly (-ether-ether-ketone (SPEEK has high electric conductivity and low methanol permeability, as well as comprehensive property, which is expected to be used as PEMs. However, the proton exchange ability, methanol resistance, mechanical property and thermal stability of SPEEK are closely related to the degree of sulfonation (DS of SPEEK membranes. Additionally, the proton conductivity, methanol permeability, and stability of SPEEK membranes applied in various conditions need to be further improved. In this paper, the research into modification of SPEEK membranes made by SPEEK and other polymers, inorganic materials are introduced. The properties and modification situation of the SPEEK and the composite membranes, as well as the advantages and disadvantages of membranes prepared by different materials are summarized. From the results we know that, the methanol permeability of SPEEK/PES-C membranes is within the order of magnitude, 10-7cm2/s. The proton conductivity of the SPPESK/SPEEK blend membrane reaches 0.212 S cm-1 at 80 °C. The cross-linked SPEEK membranes have raised thermal and dimensional stability. The non-solvent caused aggregation of the SPEEK ionomers. The proton conductivity of SPEEK/50%BMIMPF6/4.6PA membrane maintains stable as 2.0 x 10-2S cm-1 after 600 h at 160 °C. Incorporation of aligned CNT into SPEEK increases the proton conductivity and reduces the methanol permeability of the composite membranes. The PANI improves the hydrothermal stability. More proton transfer sites lead to a more compact structure in the composite membranes. According to the results, the proton exchange capacity, water uptake, and conductivity of

  5. Conversion of dimethyl ether on zeolite catalysts

    Abramova, A.V.; Kulumbegov, R.V.; Khadzhiev, S.N. [Russian Academy of Sciences, Moscow (Russian Federation). A.V. Topchiev Inst. of Petrochemical Synthesis


    Catalytic conversion of dimethyl ether to hydrocarbons was investigated using zeolite catalyst ZSM-5 type. 2% MexOy - 60% HZVM(analogue of ZSM-5)/Al{sub 2}O{sub 3}, (Me = Zn, Ga, Fe, Co, V, Ni) catalyst samples have been obtained. The reaction was carried out in a fixed bed reaction set-up at 350-400 C, pressure 3 MPa, gas mix (% vol.): 24 DME, 76 N{sub 2}, WHSV=1300 l/l-{sub kat.}h. Most effective catalysts of DME conversion are pentasil based catalysts with promoter metals zinc, iron and cobalt by totality DME-conversion, gas and liquid hydrocarbon selectivity, ethylene and propylene content in gas. The best work temperatures are 350 and 375 C, thereupon increasing of temperature to 400 C leads to considerable growth of methane in hydrocarbon gas. Liquid hydrocarbons have high content of aromatics and iso-paraffins. Liquid hydrocarbon product is characterized by high octane number (RON) 90-98. (orig.)

  6. Dimethyl ether (DME) as an alternative fuel

    Semelsberger, Troy A.; Borup, Rodney L.; Greene, Howard L.

    With ever growing concerns on environmental pollution, energy security, and future oil supplies, the global community is seeking non-petroleum based alternative fuels, along with more advanced energy technologies (e.g., fuel cells) to increase the efficiency of energy use. The most promising alternative fuel will be the fuel that has the greatest impact on society. The major impact areas include well-to-wheel greenhouse gas emissions, non-petroleum feed stocks, well-to-wheel efficiencies, fuel versatility, infrastructure, availability, economics, and safety. Compared to some of the other leading alternative fuel candidates (i.e., methane, methanol, ethanol, and Fischer-Tropsch fuels), dimethyl ether appears to have the largest potential impact on society, and should be considered as the fuel of choice for eliminating the dependency on petroleum. DME can be used as a clean high-efficiency compression ignition fuel with reduced NO x, SO x, and particulate matter, it can be efficiently reformed to hydrogen at low temperatures, and does not have large issues with toxicity, production, infrastructure, and transportation as do various other fuels. The literature relevant to DME use is reviewed and summarized to demonstrate the viability of DME as an alternative fuel.

  7. Polybrominated diphenyl ethers and novel flame retardants

    Frederiksen, Marie; Vorkamp, Katrin; Nielsen, Jesper Bo

    ,4,6-tribromophenyl ether (TBP-DBPE) and dechlorane plus (DDC-CO) have been detected in the same dust samples previously analysed for PBDEs and are currently being analysed in the corresponding human milk samples. [1] Stapleon H.M., Eagle S., Sjödin A., Webster T.F. (2012). Serum PBDEs in a North Carolina Toddler......, the objectives were to study whether i) the associations observed for plasma also existed for human milk, ii) the PBDE profiles in dust and milk could provide insights into the bioavailability and bioaccumulation of individual congeners, iii) NFRs were measurable in human milk, and iv) infants were exposed...... to significant amounts of NFRs via breast feeding. PBDEs were detected in all of the 40 milk samples analysed in this study. ΣPBDEtri-hepta ranged from 0.98-45.8 ng/g lw, with a median of 2.26 ng/g lw. The main congener in milk was BDE-153, accounting for 35% of ΣPBDEtri-hepta. This is much higher than in dust...

  8. Molecular Design of Crown Ethers.22.Synthesis of Benzocrown Ether Derivatives and Their Solvent Extraction with Univalent/Bivalent Metal Picrates

    YANG,Ying-Wei(杨英威); LI,Chun-Ju(李春举); ZHANG,Heng-Yi(张衡益); LIU,Yu(刘育)


    Three novel benzocrown ether derivatives have been synthesized and their cation binding behavior with uniand bi-valent metal ions was evaluated by the solvent extraction of aqueous metal picrates. The obtained results indicate that the size-fit of crown ether and metal cation, and electron effect of the side arm attached to benzocrown ethers affect their cation binding ability and selectivity.

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

    Rebecca S. L. Yee


    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.

  10. Evaluation of workers exposed to ethylene glycol monomethyl ether and ethylene glycol monomethyl ether acetate.

    Park, Jiyoung; Yoon, Chungsik; Byun, Hyaejeong; Kim, Yangho; Park, Donguk; Ha, Kwonchul; Lee, Sang man; Park, Sungki; Chung, Eunkyo


    Ethylene glycol monomethyl ether (EGME) and ethylene glycol monomethyl ether acetate (EGMEA) are widely used in industries as solvents for coatings, paint and ink, but exposure data are limited because they are minor components out of mixed solvents, as well as because of inconsistency in desorption solvent use. The objective of this study was to investigate the worker exposure profile of EGME and EGMEA. Our study investigated 27 workplaces from June to September 2008 and detected EGME and EGMEA in 20 and 13, respectively. Both personal and area sampling were conducted using a charcoal tube to collect EGME and EGMEA. Gas chromatography with a flame ionization detector was used to analyze these compounds after desorption using a mixture of methylene chloride and methanol. The arithmetic mean concentrations of EGME and EGMEA during periods of full work shifts were 2.59 ppm and 0.33 ppm, respectively. The exposure levels were lower than the Korean Ministry of Labor (MOL) OEL (5 ppm) but higher than the ACGIH TLV (0.1 ppm). In general, the working environments were poor and required much improvement, including the use of personal protective equipment. Only 50% of the workplaces had local exhaust ventilation systems in operation. The average capture velocity of the operating local exhaust ventilation systems was 0.27 m/s, which did not meet the legal requirement of 0.5 m/s. Educating workers to clearly understand the handling and use of hazardous chemicals and improving working conditions are strongly suggested.

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

    Changkhamchom, Sairung; Sirivat, Anuvat


    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).

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

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


    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.

  13. EtherCAT bus application in CNC system%EtherCAT总线在数控系统中的应用




  14. Biodegradation of ethyl t-butyl ether (ETBE), methyl t-butyl ether (MTBE) and t-amyl methyl ether (TAME) by Gordonia terrae.

    Hernandez-Perez, G; Fayolle, F; Vandecasteele, J P


    Gordonia terrae strain IFP 2001 was selected from activated sludge for its capacity to grow on ethyl t-butyl ether (ETBE) as sole carbon and energy source. ETBE was stoichiometrically degraded to t-butyl alcohol (TBA) and the activity was inducible. A constitutive strain, G. terrae IFP 2007, derived from strain IFP 2001, was also selected. Methyl t-butyl ether (MTBE) and t-amyl methyl ether (TAME) were not used as carbon and energy sources by the two strains, but cometabolic degradation of MTBE and TAME was demonstrated, to TBA and t-amyl alcohol (TAA) respectively, in the presence of a carbon source such as ethanol. No two-carbon compound was detected during growth on ETBE, but formate was produced during cometabolic degradation of MTBE or TAME. A monooxygenase was involved in the degradation of ethers, because no degradation of ETBE was observed under anaerobic conditions and the presence of a cytochrome P-450 was demonstrated in G. terrae IFP 2001 after induction by cultivation on ETBE.

  15. Role of hydrogen-bonding and photoinduced electron transfer (PET) on the interaction of resorcinol based acridinedione dyes with Bovine Serum Albumin (BSA) in water

    Kumaran, Rajendran, E-mail: [Department of Chemistry, Dwaraka Doss Goverdhan Doss, Vaishnav College (Autonomous), 833, Gokul Bagh, E.V.R. Periyar Road, Arumbakkam, Chennai 600106, Tamil Nadu (India); Vanjinathan, Mahalingam [Department of Chemistry, Dwaraka Doss Goverdhan Doss, Vaishnav College (Autonomous), 833, Gokul Bagh, E.V.R. Periyar Road, Arumbakkam, Chennai 600106, Tamil Nadu (India); Ramamurthy, Perumal [National Centre for Ultrafast Processes, University of Madras, Taramani Campus Chennai 600113, Tamil Nadu (India)


    Resorcinol based acridinedione (ADDR) dyes are a class of laser dyes and have structural similarity with purine derivatives, nicotinamide adenine dinucleotide (NADH) analogs. These dyes are classified into photoinduced electron transfer (PET) and non-photoinduced electron transfer dyes, and the photophysical properties of family of these dyes exhibiting PET behavior are entirely different from that of non-PET dyes. The PET process in ADDR dyes is governed by the solvent polarity such that an ADDR dye exhibits PET process through space in an aprotic solvent like acetonitrile and does not exhibit the same in protic solvents like water and methanol. A comparison on the fluorescence emission, lifetime and nature of interaction of various ADDR dyes with a large globular protein like Bovine Serum Albumin (BSA) was carried out in aqueous solution. The interaction of PET based ADDR dyes with BSA in water is found to be largely hydrophobic, but hydrogen-bonding interaction of BSA with dye molecule influences the fluorescence emission of the dye and shifts the emission towards red region. Fluorescence spectral studies reveal that the excited state properties of PET based ADDR dyes are largely influenced by the addition of BSA. The microenvironment around the dye results in significant change in the fluorescence lifetime and emission. Fluorescence enhancement with a red shift in the emission results after the addition of BSA to ADDR dyes containing free amino hydrogen in the 10th position of basic acridinedione dye. The amino hydrogen (N–H) in the 10th position of ADDR dye is replaced by methyl group (N–CH{sub 3}), a significant decrease in the fluorescence intensity with no apparent shift in the emission maximum was observed after the addition of BSA. The nature of interaction between ADDR dyes with BSA is hydrogen-bonding and the dye remains unbound even at the highest concentration of BSA. Circular Dichroism (CD) studies show that the addition of dye to BSA results in

  16. Crystal structures of bis[2-(diphenylphosphinothioylphenyl] ether and bis{2-[diphenyl(selanylidenephosphanyl]phenyl} ether

    Daron E. Janzen


    Full Text Available The title compounds, C36H28OP2S2, (1, and C36H28OP2Se2, (2, exhibit remarkably similar structures although they are not isomorphous. The whole molecule of compound (2 is generated by twofold symmetry, with the ether O atom located on the twofold axis. Both compounds have intramolecular π–π interactions between terminal phenyl rings with centroid–centroid distances of 3.6214 (16 and 3.8027 (14 Å in (1 and (2, respectively. In the crystal of (1, short C—H...S hydrogen bonds link the molecules, forming chains along [001], while in (2 there are no analogous C—H...Se interactions present.

  17. Stress shielding and fatigue limits of poly-ether-ether-ketone dental implants.

    Lee, Woo-Taek; Koak, Jai-Young; Lim, Young-Jun; Kim, Seong-Kyun; Kwon, Ho-Beom; Kim, Myung-Joo


    The poly-ether-ether-ketone (PEEK) polymer is of great interest as an alternative to titanium in orthopedics because of its biocompatibility and low elastic modulus. This study evaluated the fatigue limits of PEEK and the effects of the low elastic modulus PEEK in relation to existing dental implants. Compressive loading tests were performed with glass fiber-reinforced PEEK (GFR-PEEK), carbon fiber-reinforced PEEK (CFR-PEEK), and titanium rods. Among these tests, GFR-PEEK fatigue tests were performed according to ISO 14801. For the finite element analysis, three-dimensional models of dental implants and bone were constructed. The implants in the test groups were coated with a 0.5-mm thick and 5-mm long PEEK layer on the upper intrabony area. The strain energy densities (SED) were calculated, and the bone resorption was predicted. The fatigue limits of GFR-PEEK were 310 N and were higher than the static compressive strength of GFR-PEEK. The bone around PEEK-coated implants showed higher levels of SED than the bone in direct contact with the implants, and the wider diameter and stiffer implants showed lower levels of SED. The compressive strength of the GFR-PEEK and CFR-PEEK implants ranged within the bite force of the anterior and posterior dentitions, respectively, and the PEEK implants showed adequate fatigue limits for replacing the anterior teeth. Dental implants with PEEK coatings and PEEK implants may reduce stress shielding effects. Dental implant application of PEEK polymer-fatigue limit and stress shielding. Copyright © 2012 Wiley Periodicals, Inc.

  18. Influence of Cellulose Ethers on Hydration Products of Portland Cement

    MA Baoguo; OU Zhihua; JIAN Shouwei; XU Rulin


    Cellulose ethers are widely used to mortar formulations, and it is significant to understand the interaction between cellulose ethers and cement pastes. FT-IR spectra, thermal analysis and SEM are used to investigate hydration products in the cement pastes modified by HEMC and HPMC in this article. The results show that the hydration products in modified cement pastes were finally identical with those in the unmodified cement paste, but the major hydration products, such as CH (calcium hydroxide), ettringite and C-S-H, appeared later in the modified cement pastes than in the unmodified cement paste. The cellulose ethers decrease the outer products and increase inner products of C-S-H gels. Compared to unmodified cement pastes, no new products are found in the modified cement pastes in the present experiment. The HEMC and HPMC investigation shows almost the same influence on the hydration products of Portland cement.

  19. Synthesis and characterization of novel cellulose ether sulfates.

    Rohowsky, Juta; Heise, Katja; Fischer, Steffen; Hettrich, Kay


    The synthesis and characterization of novel cellulose sulfate derivatives was reported. Various cellulose ethers were prepared in a homogeneous reaction with common sulfating agents. The received product possess different properties in dependence on the reaction conditions like sulfating agent, solvent, reaction time and reaction temperature. The cellulose ether sulfates are all soluble in water, they rheological behavior could be determined by viscosity measurements and the determination of the sulfur content by elemental analysis lead to a resulting degree of substitution ascribed to sulfate groups (DSSul) of the product. A wide range of products from DSSul 0.1 to DSSul 2.7 will be obtained. Furthermore the cellulose sulfate ethers could be characterized by Raman spectroscopy.

  20. Spontaneous Generation of Chirality in Simple Diaryl Ethers.

    Lennartson, Anders; Hedström, Anna; Håkansson, Mikael


    We studied the spontaneous formation of chiral crystals of four diaryl ethers, 3-phenoxybenzaldehyde, 1; 1,3-dimethyl-2-phenoxybenzene, 2; di(4-aminophenyl) ether, 3; and di(p-tolyl) ether, 4. Compounds 1, 3, and 4 form conformationally chiral molecules in the solid state, while the chirality of 2 arises from the formation of supramolecular helices. Compound 1 is a liquid at ambient temperature, but 2-4 are crystalline, and solid-state CD-spectroscopy showed that they could be obtained as optically active bulk samples. It should be noted that the optical activity arise upon crystallization, and no optically active precursors were used. Indeed, even commercial samples of 3 and 4 were found to be optically active, giving evidence for the ease at which total spontaneous resolution may occur in certain systems.

  1. Highly efficient palladium-catalyzed hydrostannation of ethyl ethynyl ether.

    Andrews, Ian P; Kwon, Ohyun


    The palladium-catalyzed hydrostannation of acetylenes is widely exploited in organic synthesis as a means of forming vinyl stannanes for use in palladium-catalyzed cross-coupling reactions. Application of this methodology to ethyl ethynyl ether results in an enol ether that is challenging to isolate from the crude reaction mixture because of incompatibility with typical silica gel chromatography. Reported here is a highly efficient procedure for the palladium-catalyzed hydrostannation of ethyl ethynyl ether using 0.1% palladium(0) catalyst and 1.0 equiv of tributyltin hydride. The product obtained is a mixture of regioisomers that can be carried forward with exclusive reaction of the beta-isomer. This method is highly reproducible; relative to previously reported procedures, it is more economical and involves a more facile purification procedure.

  2. EtherCAT被纳入EUROMAP协议规范



  3. EtherCAT以太网现场总线



  4. ELMO驱动器获得EtherCAT审批



  5. Enzymatic network for production of ether amines from alcohols

    Palacio, Cyntia M.; Crismaru, Ciprian G.; Bartsch, Sebastian


    of the desired ether amines from the corresponding ether alcohols with inorganic ammonium as the only additional substrate. To examine conversion, individual and overall reaction equilibria were established. Using these data, it was found that the experimentally observed conversions of up to 60% observed...... for reactions containing 10mM alcohol and up to 280mM ammonia corresponded well to predicted conversions. The results indicate that efficient amination can be driven by high concentrations of ammonia and may require improving enzyme robustness for scale-up....

  6. Synthesis and biophysical characterization of chlorambucil anticancer ether lipid prodrugs.

    Pedersen, Palle J; Christensen, Mikkel S; Ruysschaert, Tristan; Linderoth, Lars; Andresen, Thomas L; Melander, Fredrik; Mouritsen, Ole G; Madsen, Robert; Clausen, Mads H


    The synthesis and biophysical characterization of four prodrug ether phospholipid conjugates are described. The lipids are prepared from the anticancer drug chlorambucil and have C16 and C18 ether chains with phosphatidylcholine or phosphatidylglycerol headgroups. All four prodrugs have the ability to form unilamellar liposomes (86-125 nm) and are hydrolyzed by phospholipase A(2), resulting in chlorambucil release. Liposomal formulations of prodrug lipids displayed cytotoxicity toward HT-29, MT-3, and ES-2 cancer cell lines in the presence of phospholipase A(2), with IC(50) values in the 8-36 microM range.

  7. Synthesis and Biophysical Characterization of Chlorambucil Anticancer Ether Lipid Prodrugs

    Pedersen, Palle Jacob; Christensen, Mikkel Stochkendahl; Ruysschaert, Tristan


    The synthesis and biophysical characterization of four prodrug ether phospholipid conjugates are described. The lipids are prepared from the anticancer drug chlorambucil and have C16 and C18 ether chains with phosphatidylcholine or phosphatidylglycerol headgroups. All four prodrugs have the ability...... to form unilamellar liposomes (86-125 nm) and are hydrolyzed by phospholipase A2, resulting in chlorambucil release. Liposomal formulations of prodrug lipids displayed cytotoxicity toward HT-29, MT-3, and ES-2 cancer cell lines in the presence of phospholipase A2, with IC50 values in the 8-36 μM range....

  8. Effects of dimethyl ether on n-butane oxidation

    Bekat, Tuğçe; İnal, Fikret


    Dimethyl ether (DME) is the simplest ether and it is used as an alternative fuel or fuel additive to reduce toxic emissions from combustion processes. The effects of DME on n-butane oxidation were investigated for two different concentrations of DME in the fuel mixture (i.e., 20% and 50%) and two different fuel-rich equivalence ratios (i.e., 2.6 and 3.0) using detailed chemical kinetic modeling. Reactor model was selected as atmospheric-pressure, adiabatic, tubular reactor, operated under lam...

  9. Diphytanyl and dibiphytanyl glycerol ether lipids of methanogenic archaebacteria

    Tornabene, T.G. (Colorado State Univ., Fort Collins); Langworthy, T.A.


    The lipids of nine different methanogenic bacterial strains are comprised of diphytanyl glycerol diethers, previously known only in extremely halophilic bacteria, as well as dibiphytanyl diglycerol tetraethers, known formerly only in the extremely thermoacidophilic bacteria Thermoplasma and Sulfolobus. Of the methanogens examined from four representative taxonomic groups, Methanobacterium and Methanospirillum contained both types of isopranyl ethers in nearly equal proportions, whereas the coccal forms, Methanosarcina and Methanococcus, possessed diphytanyl glycerol diethers, but with only a trace of or no dibiphytanyl diglycerol tetraethers. The occurrence of both types of isopranyl glycerol ethers in methanogenic bacteria supports the proposal that they have a close genealogical relationship to the extremely halophilic and thermoacidophilic bacteria.

  10. Environmental analysis of higher brominated diphenyl ethers and decabromodiphenyl ethane.

    Kierkegaard, Amelie; Sellström, Ulla; McLachlan, Michael S


    Methods for environmental analysis of higher brominated diphenyl ethers (PBDEs), in particular decabromodiphenyl ether (BDE209), and the recently discovered environmental contaminant decabromodiphenyl ethane (deBDethane) are reviewed. The extensive literature on analysis of BDE209 has identified several critical issues, including contamination of the sample, degradation of the analyte during sample preparation and GC analysis, and the selection of appropriate detection methods and surrogate standards. The limited experience with the analysis of deBDethane suggests that there are many commonalities with BDE209. The experience garnered from the analysis of BDE209 over the last 15 years will greatly facilitate progress in the analysis of deBDethane.

  11. IRIS Toxicological Review of Ethyl Tertiary Butyl Ether (ETBE) ...

    The IRIS Toxicological Review of Ethyl Tertiary Butyl Ether (ETBE) was released for external peer review in April 2017. EPA’s Science Advisory Board’s (SAB) Chemical Assessment Advisory Committee (CAAC) will conduct a peer review of the scientific basis supporting the ETBE assessment and release a final report of their review. Information regarding the peer review can be found on the SAB website. EPA is conducting an Integrated Risk Information System (IRIS) health assessment for Ethyl Tertiary Butyl Ether (ETBE). The outcome of this project is a Toxicological Review and IRIS Summary for ETBE that will be entered into the IRIS database.

  12. Acid Catalyzed Condensation of Phenylethanal Enol or Thiol Enol Ether to 2-Phenylnaphthalene

    CHANG, Yu-An


    Treatment of enol ether or thiol enol ether of phenylethanals with sulfuric or polyphosphoric acid in toluene or xylene gave 2-phenylnaphthalene in good yield. More importantly, a one-pot reaction has been developed.

  13. Aliphatic polycarbonates based on carbon dioxide, furfuryl glycidyl ether, and glycidyl methyl ether: reversible functionalization and cross-linking.

    Hilf, Jeannette; Scharfenberg, Markus; Poon, Jeffrey; Moers, Christian; Frey, Holger


    Well-defined poly((furfuryl glycidyl ether)-co-(glycidyl methyl ether) carbonate) (P((FGE-co-GME)C)) copolymers with varying furfuryl glycidyl ether (FGE) content in the range of 26% to 100% are prepared directly from CO2 and the respective epoxides in a solvent-free synthesis. All materials are characterized by size-exclusion chromatography (SEC), (1)H NMR spectroscopy, and differential scanning calorimetry (DSC). The furfuryl-functional samples exhibit monomodal molecular weight distributions with Mw/Mn in the range of 1.16 to 1.43 and molecular weights (Mn) between 2300 and 4300 g mol(-1). Thermal properties reflect the amorphous structure of the polymers. Both post-functionalization and cross-linking are performed via Diels-Alder chemistry using maleimide derivatives, leading to reversible network formation. This transformation is shown to be thermally reversible at 110 °C.

  14. Two Reaction Mechanisms via Iminium Ion Intermediates: The Different Reactivities of Diphenylprolinol Silyl Ether and Trifluoromethyl-Substituted Diarylprolinol Silyl Ether.

    Gotoh, Hiroaki; Uchimaru, Tadafumi; Hayashi, Yujiro


    The reactions of α,β-unsaturated aldehydes with cyclopentadiene in the presence of diarylprolinol silyl ethers as catalyst proceed via iminium cations as intermediates, and can be divided into two types; one involving a Michael-type reaction (type A) and one involving a cycloaddition (type B). Diphenylprolinol silyl ethers and trifluoromethyl-substituted diarylprolinol silyl ethers, which are widely used proline-type organocatalysts, have been investigated in this study. As the LUMO of the iminium ion derived from trifluoromethyl-substituted diarylprolinol silyl ether is lower in energy than that derived from diphenylprolinol silyl ether, as supported by ab initio calculations, the trifluoromethyl-substituted catalyst is more reactive in a type B reaction. The iminium ion from an α,β-unsaturated aldehyde is generated more quickly with diphenylprolinol silyl ether than with the trifluoromethyl-substituted diarylprolinol silyl ether. When the generation of the iminium ion is the rate-determining step, the diphenylprolinol silyl ether catalyst is the more reactive. Because acid accelerates the generation of iminium ions and reduces the generation of anionic nucleophiles in the Michael-type reaction (type A), it is necessary to select the appropriate acid for specific reactions. In general, diphenylprolinol silyl ether is a superior catalyst for type A reactions, whereas the trifluoromethyl-substituted diarylprolinol silyl ether catalyst is preferred for type B reactions.

  15. Sulfoalkyl ether-alkyl ether cyclodextrin derivatives, their synthesis, NMR characterization, and binding of 6alpha-methylprednisolone.

    Tongiani, Serena; Velde, David Vander; Ozeki, Tetsuya; Stella, Valentino J


    The objective of this study is to see if random alkyl ethers of various sulfoalkyl ether cyclodextrins can be synthesized and characterized. The purpose of the alkylation was to test the hypothesis that an increase in the "height" of a cyclodextrins cavity would help in the binding/complexation of larger more structurally complex molecules. The synthesis of new cyclodextrin derivatives comprising a mixture of sulfoalkyl ether and alkyl ether substituents on the same cyclodextrin ring was performed in aqueous alkaline solutions using various sultones and alkylsulfates. The method presented provided an easy and efficient way to modify cyclodextrins avoiding the use of organic solvents and high quantities of alkylating agents and could be carried out in either a two step or "one pot" single step process. Purification was by neutralization followed by ultrafiltration. The derivatives were characterized by 1D, ((1)H and (13)C), and a 2D NMR technique (HMQC, Heteronuclear Multiple Quantum Coherence). The combination of these techniques allowed an analysis of the degree of substitution and the site of substitution on the cyclodextrin (CD) nucleus. For both beta- and gamma-CD, sulfoakylation was preferred on the 2 > 3 > 6 hydroxyls while alkylation was preferred 6 > 2 > 3. Due to the simultaneous presence of short alkyl ether chains and negatively charged sulfoalkyl ether chains, these mixed water-soluble cyclodextrin derivatives, especially those of gamma-cyclodextrin, should be able to bind more complex drugs. The improved binding capacity of these new modified CDs with the model drug 6alpha-methylprednisolone is reported.

  16. Research of EtherCAT master based on Linux-RTAI%基于Linux-RTAI的EtherCAT主站研究

    张少勋; 郗晓田




    S. Guhan; N.Arun Kumar; D.Sangeetha


    Composite membranes with polyvinyl alcohol (PVA),sulphonated poly ether ether ketone (SPEEK) and phosphotungstic acid (PWA) were prepared using solvent casting method.The proton conductivities of such membranes were found to be in the order of 10-3 S/cm in the fully hydrated condition at room temperature as measured by impedance spectroscopy.The crystalline properties were studied by X-ray diffraction analysis.The thermal properties were determined by TGA and DSC techniques.The tensile strength and percentage elongation were obtained from UTM studies.Water and methanol uptake of these membranes were studied.

  18. EtherCAT技术协会宣布成立中国代表处


    在北京一年一度的自动化展会FA/PA2007的高峰论坛上。EtherCAT技术协会(EtherCAT Technology Group,ETG)主席Martin Rostan先生宣布了EtherCAT技术协会中国代表处的成立。

  19. 21 CFR 177.1970 - Vinyl chloride-lauryl vinyl ether copolymers.


    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Vinyl chloride-lauryl vinyl ether copolymers. 177... for Use as Basic Components of Single and Repeated Use Food Contact Surfaces § 177.1970 Vinyl chloride-lauryl vinyl ether copolymers. The vinyl chloride-lauryl vinyl ether copolymers identified in...

  20. Synthesis and Properties of New-type Troponoid Dithio-Crown Ethers


    Condensation of 3,7-dichloromethyl-5-isopropyl-2-methoxytropone 4 with bis (mer-captoethyl) ether 5a and mono, di, and tri-ethylene glycol bis(mercaptoethyl) ethers 5b-5d gave troponoid-annexed dithiocrown ethers 6a-6d. Compounds 6a-6d have selective and reversible mercury salt capturing ability.

  1. Selection and identification of bacterial strains with methyl-tert-butyl ether, ethyl-tert-butyl ether, and tert-amyl methyl ether degrading capacities.

    Purswani, Jessica; Pozo, Clementina; Rodríguez-Díaz, Marina; González-López, Jesús


    Nine bacterial strains isolated from two hydrocarbon-contaminated soils were selected because of their capacity for growth in culture media amended with 200 mg/L of one of the following gasoline oxygenates: Methyl-tert-butyl ether (MTBE), ethyl-tert-butyl ether (ETBE), and tert-amyl methyl ether (TAME). These strains were identified by amplification of their 16S rRNA gene, using fDl and rD1 primers, and were tested for their capacity to grow and biotransform these oxygenates in both mineral and cometabolic media. The isolates were classified as Bacillus simplex, Bacillus drentensis, Arthrobacter sp., Acinetobacter calcoaceticus, Acinetobacter sp., Gordonia amicalis (two strains), Nocardioides sp., and Rhodococcus ruber. Arthrobacter sp. (strain MG) and A. calcoaceticus (strain M10) consumed 100 (cometabolic medium) and 82 mg/L (mineral medium) of oxygenate TAME in 21 d, respectively, under aerobic conditions. Rhodococcus ruber (strain E10) was observed to use MTBE and ETBE as the sole carbon and energy source, whereas G. amicalis (strain T3) used TAME as the sole carbon and energy source for growth. All the bacterial strains transformed oxygenates better in the presence of an alternative carbon source (ethanol) with the exception of A. calcoaceticus (strain M10). The capacity of the selected strains to remove MTBE, ETBE, and TAME looks promising for application in bioremediation technologies.

  2. Dimethyl ether in diesel engines - progress and perspectives

    Sorenson, Spencer C


    A review of recent developments related to the use of dimethyl ether (DME) in engines is presented Research work discussed is in the areas of engine performance and emissions, fuel injection systems, spray and ignition delay, and detailed chemical kinetic modeling. DME's properties and safety...

  3. Ether lipids of planktonic archae in the marine water column

    Sinninghe Damsté, J.S.; Hoefs, M.J.L.; Schouten, S.; King, L.L.; Wakeham, S.G.; Leeuw, J.W. de


    Acyclic and cyclic biphytanes derived from the membrane ether lipids of archaea were found in water column particulate and sedimentary organic matter from several oxic and anoxic marine environments. Compound-specific isotope analyses of the carbon skeletons suggest that planktonic archaea utilize a

  4. The effect of gasses on the viscosity of dimethyl ether

    Sivebæk, Ion Marius; Jakobsen, Jørgen


    Dimethyl ether (DME) has been recognised as a clean substitute for diesel oil as it does not form soot during combustion. DME has a vapour pressure of 6 bar at 25 degrees C; so pressurisation is necessary to keep DME liquid at ambient temperature. Inert gases are good candidates as pressurising m...

  5. Conversion Excess Coal Gas to Dimethyl Ether in Steel Works


    With the technical progress of metallurgical industry, more excess gas will be produced in steel works. The feasibility of producing dimethyl ether by gas synthesis was discussed, which focused on marketing, energy balance, process design, economic evaluation, and environmental protection etc. DME was considered to be a new way to utilize excess coal gas in steel works.

  6. Synthesis of hydroxytyrosyl alkyl ethers from olive oil waste waters

    Juan Fernández-Bolaños; Mariana Trujillo; Guillermo Rodríguez; Raquel Mateos; Gema Pereira-Caro; Andrés Madrona; Espartero, José L.


    The preparation of a new type of derivatives of the naturally occurring antioxidant hydroxytyrosol is reported. Hydroxytyrosyl alkyl ethers were obtained in high yield by a three-step procedure starting from hydroxytyrosol isolated from olive oil waste waters. Preliminary results obtained by the Rancimat method have shown that these derivatives retain the high protective capacity of free hydroxytyrosol.

  7. Synthesis of Hydroxytyrosyl Alkyl Ethers from Olive Oil Waste Waters

    Juan Fernández-Bolaños


    Full Text Available The preparation of a new type of derivatives of the naturally occurring antioxidant hydroxytyrosol is reported. Hydroxytyrosyl alkyl ethers were obtained in high yield by a three-step procedure starting from hydroxytyrosol isolated from olive oil waste waters. Preliminary results obtained by the Rancimat method have shown that these derivatives retain the high protective capacity of free hydroxytyrosol.

  8. Antiknock evaluation of hydrocarbons and ethers as aviation fuel components

    Barnett, Henry C


    The results of a NACA investigation conducted over a period of several years to evaluate the anti-knock characteristics of organic compounds are summarized. Included are data for 18 branched paraffins and olefins, 27 aromatics, and 22 ethers. The factors of performance investigated were blending characteristics, temperature sensitivity, lead response, and relation between molecular structure and antiknock ratings. Four engines were used.

  9. Why do crown ethers activate enzymes in organic solvents?

    Unen, van Dirk-Jan; Engbersen, Johan F.J.; Reinhoudt, David N.


    One of the major drawbacks of enzymes in nonaqueous solvents is that their activity is often dramatically low compared to that in water. This limitation can be largely overcome by crown ether treatment of enzymes. In this paper, we describe a number of carefully designed new experiments that have im

  10. Anthracylmethyl Benzoazacrown Ether as Selective Fluorescence Sensors for Zn2+

    Li Hua JIA; Xiang Feng GUO; Yuan Yuan LIU; Xu Hong QIAN


    A new benzoazacrown ether fluorescence sensor was synthesized with 9-anthrylmethyl chloride and benzoaza-15-crown-5 in CH3CN, which particularly shows a strong affinity for Zn2+. Its fluorescence quantum yield increase more than one order of magnitude and a red shift could be noticed when passing from the apolar to the polar solvent.

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

    Norrman, K.; Krebs, Frederik C


    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...

  12. Functionalization of thiocrown ethers containing the thioacetal unit

    Buter, Jan; Meijer, Renzo H.; Kellogg, Richard M.; Meijer, H.C.


    Thiocrown ethers containing thioacetal units are readily prepared by reaction of the cesium salts of long chain dithiols with methylene dibromide. Preparation of the trimethylsilyl derivatives followed by condensation with aldehydes under basic conditions (Peterson reaction) leads to the expected ma

  13. Isotope effects of hafnium in solvent extraction using crown ethers

    Fujii, Toshiyuki; Moriyama, Hirotake [Research Reactor Institute, Kyoto University, Osaka (Japan); Hirata, Takafumi [Laboratory for Planetary Sciences, Tokyo Institute of Technology, Tokyo (Japan); Nishizawa, Kazushige [Department of Nuclear Engineering, Graduate School of Engineering, Osaka University, Osaka (Japan)


    Hafnium isotopes were fractionated in a liquid-liquid extraction system by using seven types of crown ethers, tributyl phosphate, or {omicron}-diethoxybenzene. The largest isotope effect was observed in the isotope pair of {sup 177}Hf-{sup 179}Hf with dibenzo-24-crown-8; the isotope enrichment factor was observed to be 0.0129{+-}0.0032. (author)

  14. Lithium air batteries having ether-based electrolytes

    Amine, Khalil; Curtiss, Larry A.; Lu, Jun; Lau, Kah Chun; Zhang, Zhengcheng; Sun, Yang-Kook


    A lithium-air battery includes a cathode including a porous active carbon material, a separator, an anode including lithium, and an electrolyte including a lithium salt and polyalkylene glycol ether, where the porous active carbon material is free of a metal-based catalyst.

  15. Study on the Multi-axis Motion Controller Based on EtherCAT%基于EtherCAT的多轴运动控制器研究

    刘艳强; 王健; 单春荣



  16. EtherCAT-Industrial Ethernet Fieldbus and Its Driver Design%工业以太网现场总线EtherCAT及驱动程序设计

    单春荣; 刘艳强; 郇极




    CHENYuanyin; MENGLingzhi; 等


    Network crown ether polymer with pendant sulfide side chain in the network structure units has been synthesized via ring-opening copolymerization of β-ethylthioethyl glycidyl ether and diethylene glycol bisglycidyl ether.A kind of active catalyst suitable for this reaction was suggested.The title polymer was found to be a good ligand for platinous chloride,and the platinous complex could catalyze the hydrosilylation of ole fins with triethoxysilane efficiently.

  18. Ether CAT总线在数控系统中的应用




  19. A mild and efficient procedure for the synthesis of ethers from various alkyl halides

    Mosstafa Kazemi


    Full Text Available A simple, mild and practical procedure has been developed for the synthesis of symmetrical and unsymmetrical ethers by using DMSO, TBAI in the presence of K2CO3. We extended the utility of Potassium carbonate as an efficient base for the preparation of ethers. A wide range of alkyl aryl and dialkyl ethers are synthezied from treatment of aliphatic alcohols and phenols with various alkyl halides in the prescence of efficient base Potassium carbonate. Secondary alkyl halides were easily converted to corresponding ethers in releatively good yields . This is a mild, simple and practical procedure for the preparation of ethers in high yields and suitable times under mild condition.

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

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


    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.

  1. Comparative photophysical behaviour of naphthalene-linked crown ethers and aza crown ethers of varying cavity dimensions

    Subhodip Samanta; Pinki Saha Sardar; Shyam Sundar Maity; Anirban Pal; Maitrayee Basu Roy; Sanjib Ghosh


    A comparative time-resolved emission studies of several naphtho-crown ethers I-V, where metal ions can be complexed in a predetermined orientation with respect to the naphthalene (Naph) - plane and naphthalene-linked aza crown ethers (L1 and L2) have been presented. In both the systems, crown ethers and aza crown ethers, naphthalene fluorescence gets quenched. In the systems I to V, the quenching is mainly due to efficient spin-orbit coupling (SOC) leading to greater population of the lowest triplet state of naphthalene. This SOC depends on the orientation of the crown ring with respect to the Naph--plane. However, in the systems L1 and L2, the quenching is due to photoinduced electron transfer (PET) from nitrogen lone pair of the aza crown ring to naphthalene moiety and consequent exciplex formation. The results have been interpreted using the time-resolved emission studies of all the compounds in various solvents, their alkali metal ion complexes, and protonated ligands.

  2. Designed poly(ether-imide)s and fluoro-copoly(ether-imide)s: Synthesis, characterization and their film properties

    Vora, Rohitkumar H. [Advanced Polymer Research and Technologies, 505 Cinder Road, Edison, NJ 08820 (United States)]. E-mail:; Goh, Suat Hong [Department of Chemistry, National University of Singapore, 10 Kent Ridge Crescent, Singapore 119260 (Singapore)


    Two series of amorphous fluoro-poly(ether-imide) (6F-PEI) and one series of fluoro-coploy(ether-imide) (6F-CoPEI) polymers based on 2,2'-bis(3,4-dicarboxyphenyl) hexafluropropane dianhydride (6FDA) and di-ether-containing diamines: 1,2'-bis(4-aminophenoxy)benzene (o-BAPOB) and 4,4'-bis(4-aminophenoxy)diphenyl sulfone (p-SED) were synthesized. The solution properties, chemical resistance, thermal stability, mechanical properties, thermo-oxidative and hydrolytic stability of selected 6F-PEIs and 6F-CoPEIs were studied. The dielectric constant ({epsilon}') values of 6F-PEI and 6F-CoPEI were estimated by additive group contribution calculation using mathematical equations defined by the Lorentz-Lorenz's theory and the Vogel's theory, and by Vora-Wang equations, respectively. These polymers not only showed excellent electrical properties but also excellent long-term thermo-oxidative stability and reduced water absorption relative to non-fluorinated polyimides. The estimated dielectric constant of these polymers ({epsilon}' < 3.15) were lower than those of commercially available poly(ether-imide) ULTEM[reg] 1000 and polyimides Kapton[reg] H, respectively at 1 kHz. The analytical results are summarized and discussed.

  3. Enhanced response of microbial fuel cell using sulfonated poly ether ether ketone membrane as a biochemical oxygen demand sensor

    Ayyaru, Sivasankaran; Dharmalingam, Sangeetha, E-mail:


    Graphical abstract: - Highlights: • Sulfonated poly ether ether ketone (SPEEK) membrane in SCMFC used to determine the BOD. • The biosensor produces a good linear relationship with the BOD concentration up to 650 ppm. • This sensing range was 62.5% higher than that of Nafion{sup ®}. • SPEEK exhibited one order lesser oxygen permeability than Nafion{sup ®}. • Nafion{sup ®} shows high anodic internal resistance (67 Ω) than the SPEEK (39 Ω). - Abstract: The present study is focused on the development of single chamber microbial fuel cell (SCMFC) using sulfonated poly ether ether ketone (SPEEK) membrane to determine the biochemical oxygen demand (BOD) matter present in artificial wastewater (AW). The biosensor produces a good linear relationship with the BOD concentration up to 650 ppm when using artificial wastewater. This sensing range was 62.5% higher than that of Nafion{sup ®}. The most serious problem in using MFC as a BOD sensor is the oxygen diffusion into the anode compartment, which consumes electrons in the anode compartment, thereby reducing the coulomb yield and reducing the electrical signal from the MFC. SPEEK exhibited one order lesser oxygen permeability than Nafion{sup ®}, resulting in low internal resistance and substrate loss, thus improving the sensing range of BOD. The system was further improved by making a double membrane electrode assembly (MEA) with an increased electrode surface area which provide high surface area for electrically active bacteria.

  4. Use of fluorinated polybrominated diphenyl ethers and simplified cleanup for the analysis of polybrominated diphenyl ethers in house dust

    A simple, cost-effective method is described for the analysis of polybrominated diphenyl ethers (PBDEs) in house dust using pressurized fluid extraction, cleanup with modified silica solid phase extraction tubes, and fluorinated internal standards. There are 14 PBDE congeners inc...

  5. Biodegradability of fuel-ethers in environment; Biodegradabilite des ethers-carburants dans l'environnement

    Fayolle-Guichard, F.


    Fuel ethers (methyl tert-butyl ether or MTBE, ethyl tert-butyl ether or ETBE and tert-amyl methyl ether or TAME have been used as gasoline additives since about twenty years in order to meet the requirements for the octane index and to limit the polluting emission in exhaust pipe gas (unburnt hydrocarbons and carbon monoxide). The high water solubility and the poor biodegradability of these compounds make them pollutants frequently encountered in aquifers. The present manuscript summarizes the knowledge concerning the biodegradability of fuel ethers obtained both at IFP and during collaborations with the Pasteur Institute (Paris), the Biotechnology Research Institute (Montreal, Canada) and the Center for Environmental Biotechnology (University of Tennessee, USA). Rhodococcus ruber IFP 2001 and Mycobacterium austroafricanum IFP 2012, two microorganisms isolated at IFP for their ability to grow, respectively, on ETBE and MTBE, were studied in order to determine the intermediates produced during MTBE and ETBE biodegradation and the enzymes required for each biodegradation step, thus allowing us to propose MTBE and ETBE catabolic pathways. A proteomic approach, from the protein induced during the degradation of ETBE or MTBE to the genes encoding these different enzymes, was carried out. The isolation of such genes is required:1) to use them for help in determining the bio-remediation capacities in polluted aquifers (DNA micro-arrays), 2) to monitor the microorganisms isolated for their degradative capacities during bio-remediation processes (fluorescent in situ hybridization or FISH) and 3) to create new tools for the detection and the quantification of ETBE or MTBE in contaminated aquifers (bio-sensor). The manuscript also describes the different ways for the adaptation of microorganisms to the presence of a xenobiotic compound. (author)

  6. Degradation of various alkyl ethers by alkyl ether-degrading Actinobacteria isolated from activated sludge of a mixed wastewater treatment.

    Kim, Yong-Hak; Cha, Chang-Jun; Engesser, Karl-Heinrich; Kim, Sang-Jong


    Various substrate specificity groups of alkyl ether (AE)-degrading Actinobacteria coexisted in activated sewage sludge of a mixed wastewater treatment. There were substrate niche overlaps including diethyl ether between linear AE- and cyclic AE-degrading strains and phenetole between monoalkoxybenzene- and linear AE-degrading strains. Representatives of each group showed different substrate specificities and degradation pathways for the preferred substrates. Determining the rates of initial reactions and the initial metabolite(s) from whole cell biotransformation helped us to get information about the degradation pathways. Rhodococcus sp. strain DEE5311 and Rhodococcus rhodochrous strain 117 both were able to degrade anisole and phenetole through aromatic 2-monooxygenation to form 2-alkoxyphenols. In contrast, diethyl ether-oxidizing strain DEE5311 capable of degrading a broad range of linear AE, dibenzyl ether and monoalkoxybenzenes initially transformed anisole and phenetole to phenol via direct O-dealkylation. Compared to this, cyclic AE-degrading Rhodococcus sp. strain THF100 preferred tetrahydrofuran (265 ± 35 nmol min(-1)mg(-1) protein) to diethyl ether (diethoxybenzene-degrading Rhodococcus sp. strain DEOB100 and Gordonia sp. strain DEOB200 transformed 1,3-/1,4-dialkoxybenzenes to 3-/4-alkoxyphenols by similar manners in the order of rates (nmol min(-1) mg(-1) protein): 1,4-diethoxybenzene (11.1 vs. 3.9)>1,4-dimethoxybenzene (1.6 vs. 2.6)>1,3-dimethoxybenzene (0.6 vs. 0.6). This study suggests that the AE-degrading Actinobacteria can orchestrate various substrate specificity responses to the degradation of various categories of AE pollutants in activated sludge communities.

  7. EtherCAT高性能从站的设计与实现%Design and implementation of EtherCAT high performance slave station

    任计羽; 范永坤; 熊皑


    The use of dedicated EtherCAT slave chip leads to high cost, low hardware integration, software complexity and difficulty in debugging, so a new hardware and software design method of EtherCAT slave station was presented. In the method, the AM3359 ARM chip was used, in which all functions including EtherCAT slave communication and application layer ware achieved, so the hardware cost was greatly reduced. A layered approach was used in software design, so it became simple and convenient to program and debug software. EtherCAT slave was implemented, at the same time, a EtherCAT network was designed to test and analyze the performance of EtherCAT slave. The EtherCAT slave station could work well.%针对使用专用芯片导致EtherCAT从站成本增加、硬件集成度下降、软件复杂、调试困难的问题,提出了新的EtherCAT从站软硬件设计方法。该方法使用AM3359 ARM芯片,在一块芯片内实现了EtherCAT从站通信功能和应用层功能,使硬件成本降低;使用分层的软件设计方法,软件编程简单,调试方便。通过搭建EtherCAT测试网络对所设计的从站功能进行测试,从站能够完好地工作。

  8. Biodegradation of the gasoline oxygenates methyl tert-butyl ether, ethyl tert-butyl ether, and tert-amyl methyl ether by propane-oxidizing bacteria.

    Steffan, R J; McClay, K; Vainberg, S; Condee, C W; Zhang, D


    Several propane-oxidizing bacteria were tested for their ability to degrade gasoline oxygenates, including methyl tert-butyl ether (MTBE), ethyl tert-butyl ether (ETBE), and tert-amyl methyl ether (TAME). Both a laboratory strain and natural isolates were able to degrade each compound after growth on propane. When propane-grown strain ENV425 was incubated with 20 mg of uniformly labeled [14C]MTBE per liter, the strain converted > 60% of the added MTBE to 14CO2 in production of nearly stoichiometric amounts of tert-butyl alcohol (TBA), while the initial oxidation of TAME resulted in the production of tert-amyl alcohol. The methoxy methyl group of MTBE was oxidized to formaldehyde and ultimately to CO2. TBA was further oxidized to 2-methyl-2-hydroxy-1-propanol and then 2-hydroxy isobutyric acid; however, neither of these degradation products was an effective growth substrate for the propane oxidizers. Analysis of cell extracts of ENV425 and experiments with enzyme inhibitors implicated a soluble P-450 enzyme in the oxidation of both MTBE and TBA. MTBE was oxidized to TBA by camphor-grown Pseudomonas putida CAM, which produces the well-characterized P-450cam, but not by Rhodococcus rhodochrous 116, which produces two P-450 enzymes. Rates of MTBE degradation by propane-oxidizing strains ranged from 3.9 to 9.2 nmol/min/mg of cell protein at 28 degrees C, whereas TBA was oxidized at a rate of only 1.8 to 2.4 nmol/min/mg of cell protein at the same temperature.


    Gagik Torosyan


    Full Text Available It has been established the possibility for phenol allylation on natural zeolites and them analogs. Here is demonstrated the synthesis of allyl phenol, which has wide industrial applications. The offered method in comparison with the traditional methods has more advantages – higher selectivity, smaller material and power resources consumption. It has been obtained the mixture of allylating phenols (30% in general with allyl phenyl ether (1 with 80% yields. At 600 K is obtained allylphenyl ether, at 700 K beginning the formation of allyl phenols, which is the result of direct C-allylation of the aromatic ring. It has been investigated the possibility of Claisen rearrangement in the same conditions. All of that are established by gas-liquid chromatography and liquid chromatography data.

  10. [Ethylene glycol and propylene glycol ethers - Reproductive and developmental toxicity].

    Starek-Świechowicz, Beata; Starek, Andrzej


    Both ethylene and propylene glycol alkyl ethers (EGAEs and PGAEs, respectively) are widely used, mainly as solvents, in industrial and household products. Some EGAEs demonstrate gonadotoxic, embriotoxic, fetotoxic and teratogenic effects in both humans and experimental animals. Due to the noxious impact of these ethers on reproduction and development of organisms EGAEs are replaced for considerably less toxic PGAEs. The data on the mechanisms of testicular, embriotoxic, fetotoxic and teratogenic effects of EGAEs are presented in this paper. Our particular attention was focused on the metabolism of some EGAEs and their organ-specific toxicities, apoptosis of spermatocytes associated with changes in the expression of various genes that code for oxidative stress factors, protein kinases and nuclear hormone receptors.

  11. Synthesis of hydroxylated and methoxylated polybrominated diphenyl ethers

    ZHENG Ke-wen; GAO Li-ping; CAO Jie; YU Hai-wen; ZHANG Zhang


    Hydroxylated/methoxylated polybrominated diphenyl ethers (OH/MeO-PBDEs) are not only detected as natural products, but also regarded as metabolites formed from polybrominated diphenyl ethers (PBDEs), which are widely used as flame-retardants in various materials. The aim of the present study was to synthesize authentic OH-PBDEs and MeO-PBDEs, as reference standards for environmental exploration. Twenty OH-PBDEs and their corresponding MeO-PBDEs containing three to six bromine atoms were synthesized via a trial of reactions including coupling, oxidation, bromination, methylation, etc. The products were characterized by GC-MS and 1H-NMR spectroscopy in the work. As results show, all compounds synthesized were up to 99% on purity and be reqarded as authentic standards for detecting the chemical pollutants in the emvironment.

  12. Synthesis of Ethers via Reaction of Carbanions and Monoperoxyacetals


    Although transfer of electrophilic alkoxyl (“RO+”) from organic peroxides to organometallics offers a complement to traditional methods for etherification, application has been limited by constraints associated with peroxide reactivity and stability. We now demonstrate that readily prepared tetrahydropyranyl monoperoxyacetals react with sp3 and sp2 organolithium and organomagnesium reagents to furnish moderate to high yields of ethers. The method is successfully applied to the synthesis of alkyl, alkenyl, aryl, heteroaryl, and cyclopropyl ethers, mixed O,O-acetals, and S,S,O-orthoesters. In contrast to reactions of dialkyl and alkyl/silyl peroxides, the displacements of monoperoxyacetals provide no evidence for alkoxy radical intermediates. At the same time, the high yields observed for transfer of primary, secondary, or tertiary alkoxides, the latter involving attack on neopentyl oxygen, are inconsistent with an SN2 mechanism. Theoretical studies suggest a mechanism involving Lewis acid promoted insertion of organometallics into the O–O bond. PMID:26560686


    Kamil Klier; Richard G. Herman; James G.C. Shen; Qisheng Ma


    A novel 1,2-ethanediol, bis(hydrogen sulfate), disodium salt precursor-based solid acid catalyst with a zirconia substrate was synthesized and demonstrated to have significantly enhanced activity and high selectivity in producing methyl isobutyl ether (MIBE) or isobutene from methanol-isobutanol mixtures. The precursor salt was synthesized and provided by Dr. T. H. Kalantar of the M.E. Pruitt Research Center, Dow Chemical Co., Midland, MI 48674. Molecular modeling of the catalyst synthesis steps and of the alcohol coupling reaction is being carried out. A representation of the methyl transfer from the surface activated methanol molecule (left) to the activated oxygen of the isobutanol molecule (right) to form an ether linkage to yield MIBE is shown.

  14. Structural Study of Mismatched Disila-Crown Ether Complexes

    Kirsten Reuter


    Full Text Available Mismatched complexes of the alkali metals cations Li+ and Na+ were synthesized from 1,2-disila[18]crown-6 (1 and 2 and of K+ from 1,2,4,5-tetrasila[18]crown-6 (4. In these alkali metal complexes, not all crown ether O atoms participate in the coordination, which depicts the coordination ability of the C-, Si/C-, and Si-bonded O atoms. Furthermore, the inverse case—the coordination of the large Ba2+ ion by the relatively small ligand 1,2-disila[15]crown-5—was investigated, yielding the dinuclear complex 5. This structure represents a first outlook on sandwich complexes based on hybrid crown ethers.

  15. Intrinsic Kinetics of Dimethyl Ether Synthesis from Syngas

    Zhaoguang Nie; Hongwei Liu; Dianhua Liu; Weiyong Ying; Dingye Fang


    The intrinsic kinetics of dimethyl ether (DME) synthesis from syngas over a methanol synthesis catalyst mixed with methanol dehydration catalyst has been investigated in a tubular integral reactor at 3-7 MPa and 220-260 ℃. The three reactions including methanol synthesis from CO and H2, CO2 and H2, and methanol dehydration were chosen as the independent reactions. The L-H kinetic model was presented for dimethyl ether synthesis and the parameters of the model were obtained by using simplex method combined with genetic algorithm. The model is reliable according to statistical analysis and residual error analysis. The synergy effect of the reactions over the bifunctional catalyst was compared with the effect for methanol synthesis catalyst under the same conditions based on the model. The effects of syngas containing N2 on the reactions were also simulated.

  16. A Facile Synthesis of Two Sesquiterpenes Methyl Ether

    DU Zhen-Ting; ZHANG Yan-Mei; WANG Zi-Kun; WU Tong-Xing; PAN Xin-Fu


    @@ Bisabolane sesquiterpenes are a big family of naturally occurring products with significantly biological activities most of which can be separated from Chinese traditional medicines. Parahigginone (1a) was firstly separated as a bisabolane by Shen Y. C. et al. from the Taiwan marine sponges in 1999, [1] it shows very promising antitumor activity.[1] As far as we know, there is no synthetic report on it. Curcuphenol (2a) was a cytotoxic sesquiterpene which was first discovered in Pseudopterogorgia rigida[2,3] which has been synthesized by Frank[2] and Tsutomu[4] before. In order to study the relationship between the structures and the activities, we have synthesized parahiggi none methyl ether (1) and curcuphenol methyl ether (2) in six steps successfully, and the stereoselective synthesis is carried out in progress.

  17. Numerical investigation on the effect of injection pressure on the internal flow characteristics for diethyl ether, dimethyl ether and diesel fuel injectors using CFD

    Vijayakumar Thulasi


    Full Text Available The spray characteristics of the diesel fuel are greatly affected by the cavitation formed inside the injector due to the high pressure differential across the nozzle. Many researchers across the globe are exploring the potential of using diethyl ether and dimethyl ether as an alternate for diesel fuel to meet the strict emission norms. Due to the variation in the fuel properties the internal flow characteristics in injectors for ether fuels are expected to be different from that of the diesel fuel. In this paper computational technique is used to study and compare the internal flow characteristics of diethyl ether, dimethyl ether and diesel fuel. The two phase flow model considering the fuel as a mixture of liquid and vapor is adopted for the simulation study. The injection pressure is varied from 100 to 400 bar and the flow characteristics of all three fuels are simulated and compared. Results indicate that all three fuels have distinct cavitating patterns owing to different property values. The dimethyl ether is found to be more cavitating than diesel and diethyl ether fuels as expected. The mass of fuel injected are found to be decreasing for the ether fuels when compared with diesel fuel at all injection pressures.


    CHEN Yuanyin; MENG Lingzhi; YIN Yihua; GENG Chengai


    The title polymer was prepared from 5-diethylamino-3-thia-pentyl glycidyl ether and diethylene glycol bisglycidyl ether via ring-opening copolymerization. It was found that this reaction could be catalyzed by sodium, but not Lewis acid. The obtained polymer can coordinate with platinum compound, and the platinum complex is a new kind of catalyst for the hydrosilylation of olefins with triethoxysilane.

  19. EL2595 EtherCAT端子模块



  20. Synthesis and adsorption properties of chitosan-crown ether resins

    彭长宏; 陈艺锋; 唐谟堂


    Two kinds of novel chitosan-crown ether resins, Schiff base type chitosan-benzo-15-crown-5 (CTS-B15)and chitosan-benzo-18-crown-6 (CTS-B18), were synthesized through the reaction between -NH2 in chitosan and -CHO in 4′-formyl benzo-crown ethers. Their structures were characterized by elemental analysis and FT-IR spectra analysis. The elemental analysis results show that the mass fractions of nitrogen in CTS-B15 and CTS-B18 are much lower than those of chitosan. The results of FT-IR spectra of CTS-B15 and CTS-B18 reveal that there exist characteristic peak of C= N, N-H and Ar, and characteristic peak of pyr anoside in the chain of chitosan-crown ether resins, showing that the structures of chitosan-crown ethers are as expected. The adsorption properties of CTS-B15 and CTS-B18 for Pd2+ , Cu2 + and Hg2+ were studied and the experimental results show that these adsorbents have both good adsorption characterization and especially high particular adsorption selectivity for Pd2+ when Cu2+ and Hg2+ are in coexistence, and the coefficients of selectivity of CTS-B15 and CTS-B18 for metal ions are KPd2+/cu2+ =7.56, KPd2+/Hg2+ = 68.00, Kcu2+/Hg2+ = 9.00 and KPd2+/cu2+ = 6.00, KPd2+/Hg2+ = 19. 00, Kcu2+/Hg2+ = 3.00, respectively.

  1. Patch test with ether extracts in salicaceae allergy

    Sawhney M


    Full Text Available A total of 23 cases suggestive of airborne contact dermatitis were patch tested with ether extracts of flowers and leaves of populus sp. and salix sp. in a study conducted in Ladakh at an altitude of 3445 meters above sea level. Overall positivity was found in 12 (52.17%, with populus sp. alone in 7 (30. 43%, salix sp. alone in 4 17.39% and to both in one (8.33%.

  2. Cross sections for electron collisions with dimethyl ether

    Sugohara, RT; Homem, MGP; Iga, I; de Souza, GLC; MACHADO, LE; Ferraz, JR; dos Santos, AS; Brescansin, LM; Lucchese, RR; Lee, MT


    We report a joint theoretical-experimental investigation of electron collision with dimethyl ether (DME) in the low- and intermediate-energy ranges. Experimental absolute differential, integral, and momentum-transfer cross sections for elastic e(-)-DME scattering are reported in the 100-1000 eV energy range. Our measurements were performed using a crossed electron-beam-molecular-beam geometry. The angular distribution of the scattered electrons was converted to absolute cross section using th...

  3. 12-Crown-4 Ether Improves Rechargeable Lithium Cells

    Nagasubramanian, Ganesan; Attia, Alan I.


    Experiments show addition of 12-crown-4 ether (12Cr4) to thin film of polyethylene oxide (PEO) and LiBF4 reduces charge-transfer resistance of film and enhances performance of electrochemical cell in which film is electrolyte, anode is lithium, and cathode is LixCoO2. By increasing conductivity of the electrolyte, 12Cr4 reduces polarization loss; enabling cell to sustain higher current. Result is new type of rechargeable lithium cell.

  4. 高速无线EtherNet/IP模块


    ProSoft Technology专为Control Logix平台设计的高速无线Ether Net/IP模块(MVI56-WA-ElP)使无线以太网连接和编程成为可能。无需打开工厂底层设备箱保护你的设备,并且减少由于弧光的危险带来的停工期。

  5. Study on Synergy Effect in Dimethyl Ether Synthesis from Syngas

    王志良; 刁杰; 王金福; 金涌


    Influence of reaction temperature, pressure and space velocity on the direct synthesis of dimethyl ether (DME) from syngas is studied in an isothermal fixed-bed reactor. The catalyst is a physical mixture of C30 copper-based methanol (MeOH) synthesis catalyst and ZSM-5 dehydration catalyst. The experimental results show that the chemical synergy between methanol synthesis reaction and methanol dehydration reaction is evident. The conversion of carbon monoxide is over 90%.

  6. Homogeneous Charge Compression Ignition Combustion of Dimethyl Ether

    Pedersen, Troels Dyhr; Schramm, Jesper


    This thesis is based on experimental and numerical studies on the use of dimethyl ether (DME) in the homogeneous charge compression ignition (HCCI) combustion process. The first paper in this thesis was published in 2007 and describes HCCI combustion of pure DME in a small diesel engine. The tests were designed to investigate the effect of engine speed, compression ratio and equivalence ratio on the combustion timing and the engine performance. It was found that the required compression ratio...

  7. Diethyl Ether Production Process with Various Catalyst Type



    Full Text Available Several H-zeolite and HZSM-5 catalysts was preparated and their characters have also been investigated. H-zeolit Catalyst was preparated from Natural Zeolite that obtained from Malang District and Gunung Kidul District. Diethyl ether was produced by Ethanol with concentration of 95%. This research use fixed bed reactor that 1 gram of catalyst as bed catalyst, atmospheric pressure and temperature 140oC as the operating condition. Ethanol vapor from vaporization tank was driven by 200 ml/min Nitrogen stream. The responds in this research is liquid product concentration; diethyl ether, ethanol, methanol and water concentration. The results showed that the largest ethanol conversion was produced by the use of 56.44% HZSM-5 and the largest yield of diethyl ether diethyl was produced by the use of alumina and H-zeolite catalyst. The larger ratio between natural zeolite with HCl solvent will produce the larger surface area of catalyst and ethanol conversion. The largest ethanol conversion was produced at reactan ratio 1:20.

  8. Thermolysis of surface-immobilized phenethyl phenyl ether

    Britt, P.F.; Buchanan, A.C. III; Hitsman, V.M.


    Our research has focused on modeling the constraints on free-radical reactions that might be imposed in coal as a consequence of its cross-linked macromolecular structure by covalently bonding diphenylalkanes to an inert silica surface. A surface-immobilized phenethyl phenyl ether ({approx}PhCH{sub 2}CH{sub 2}POh, or {approx}PPE-3) has been prepared as a model for ether linkages in lignin by the condensation of p-HOPhCH{sub 2}CH{sub 2}OPh with the surface hydroxyls of a high purity fumed silica. Thermolysis of {approx}PPE-3 at saturation surface coverage at 375{degree}C produces {approx}PhCH = CH{sub 2} and PhOH as the major products which are consistent with the proposed free-radical chain mechanism for the decomposition of fluid-phase phenethyl phenyl ether. However, significant quantities of {approx}PhCH{sub 3} and PhCHO (ca. 18% of the products) are produced indicating the emergence of a new reaction pathway on the surface. The mechanism for the decomposition of {approx}PPE-3 will be discussed in light of this new information. 18 refs., 1 fig.

  9. Radical addition-initiated domino reactions of conjugated oxime ethers.

    Ueda, Masafumi


    The application of conjugated oxime ethers to the synthesis of complex chemical scaffolds using domino radical reactions has been described in detail. The triethylborane-mediated hydroxysulfenylation reaction allows for the regioselective construction of a carbon-sulfur bond and a carbon-oxygen bond in a single operation for the formation of β-hydroxy sulfides. This reaction proceeds via a radical pathway involving regioselective thiyl addition and the subsequent trapping of the resulting α-imino radical with O₂, where the imino group enhances the stability of the intermediate radical. Hydroxyalkylation reactions that occur via a carbon radical addition reaction followed by the hydroxylation of the resulting N-borylenamine with O₂ have also been developed. We investigated sequential radical addition aldol-type reactions in detail to explore the novel domino reactions that occur via the generation of N-borylenamine. The radical reaction of a conjugated oxime ether with triethylborane in the presence of an aldehyde affords γ-butyrolactone via sequential processes including ethyl radical addition, the generation of N-borylenamine, an aldol-type reaction with an aldehyde, and a lactonization reaction. A novel domino reaction has also been developed involving the [3,3]-sigmatropic rearrangement of N-boryl-N-phenoxyenamine. The triethylborane-mediated domino reactions of O-phenyl-conjugated oxime ethers afforded the corresponding benzofuro[2,3-b]pyrrol-2-ones via a radical addition/[3,3]-sigmatropic rearrangement/cyclization/lactamization cascade.

  10. Preparation and antioxidant activity of tyrosyl and homovanillyl ethers.

    Madrona, A; Pereira-Caro, G; Bravo, L; Mateos, R; Espartero, J L


    Preparation of tyrosyl and homovanillyl lipophilic derivatives was carried out as a response to the food industry's increasing demand for new synthetic lipophilic antioxidants. Tyrosyl and homovanillyl ethers were synthesized in high yields by a three-step procedure starting from tyrosol (Ty) and homovanillic alcohol (HMV). The antioxidant activity of these new series of alkyl tyrosyl and homovanillyl ethers was evaluated by the Rancimat test in a lipophilic food matrix and by the FRAP, ABTS and ORAC assays and compared to free Ty and HMV as well as two antioxidants widely used in the food industry, butylhydroxytoluene (BHT) and α-tocopherol. The results pointed out the higher activity of homovanillyl series in comparison with tyrosyl series with all the assayed methods. However, while both synthetic series were less antioxidant than BHT and α-tocopherol in a lipophilic matrix after their Rancimat test evaluation, homovanillyl alkyl ethers showed the best reducing power and radical scavenging activity of all evaluated compounds. This batch of synthetic lipophilic compounds, derived from biologically active compounds such as Ty and HMV, provide interesting and potentially bioactive compounds.

  11. Enhanced response of microbial fuel cell using sulfonated poly ether ether ketone membrane as a biochemical oxygen demand sensor.

    Ayyaru, Sivasankaran; Dharmalingam, Sangeetha


    The present study is focused on the development of single chamber microbial fuel cell (SCMFC) using sulfonated poly ether ether ketone (SPEEK) membrane to determine the biochemical oxygen demand (BOD) matter present in artificial wastewater (AW). The biosensor produces a good linear relationship with the BOD concentration up to 650 ppm when using artificial wastewater. This sensing range was 62.5% higher than that of Nafion(®). The most serious problem in using MFC as a BOD sensor is the oxygen diffusion into the anode compartment, which consumes electrons in the anode compartment, thereby reducing the coulomb yield and reducing the electrical signal from the MFC. SPEEK exhibited one order lesser oxygen permeability than Nafion(®), resulting in low internal resistance and substrate loss, thus improving the sensing range of BOD. The system was further improved by making a double membrane electrode assembly (MEA) with an increased electrode surface area which provide high surface area for electrically active bacteria.

  12. Rheological and electrical percolation in melt-processed poly(ether ether ketone)/multi-wall carbon nanotube composites

    Bangarusampath, D. S.; Ruckdäschel, Holger; Altstädt, Volker; Sandler, Jan K. W.; Garray, Didier; Shaffer, Milo S. P.


    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.

  13. Poly (ether ether ketone) membranes for fuel cells; Membranas de poli (eter eter cetona) sulfonado para celulas a combustivel

    Marrero, Jacqueline C.; Gomes, Ailton de S.; Filho, Jose C.D., E-mail: [Universidade Federal do Rio de Janeiro (UFRJ), Rio de Janeiro, RJ (Brazil); Hui, Wang S. [Universidade de Sao Paulo (USP), Sao Paulo, SP (Brazil); Oliveira, Vivianna S. de [Escola Tecnica Rezende-Rammel, Rio de Janeiro, RJ (Brazil)


    Polymeric membranes were developed using a SPEEK polymer matrix (sulphonated poly (ether ether ketone)), containing hygroscopic particles of zirconia (Zr) (incorporated by sol-gel method), for use as electrolyte membranes in fuel cells. SPEEK with different sulfonation degrees were used: 63 and 86%. The thermal analysis (TGA and DSC) was carried out to characterize the membranes and electrochemical impedance spectroscopy (EIS) was carried out to evaluating the proton conductivity of the membranes. Additional analysis were underway in order to characterize these membranes, which include: X-ray diffraction (XRD), scanning electron microscopy (SEM) and transmission electron microscopy (TEM) in order to evaluate the influence of zirconia and sulfonation degree on the properties of the membranes. (author)

  14. An estimation of fatigue life for a carbon fibre/poly ether ether ketone hip joint prosthesis.

    Akay, M; Aslan, N


    A fracture mechanics approach was applied to estimate the life of a prosthesis injection moulded from short carbon fibre reinforced poly ether ether ketone. Flexural modulus and strength, fracture toughness, fatigue endurance limit, fatigue crack growth rate and threshold stress intensity factor were determined. The dimensions of the test pieces were selected to yield fibre orientation and fibre length distributions similar to those obtained in the prosthesis. Stress levels generated in the prosthesis under different activities were estimated by conducting three-dimensional finite element analysis. It was shown by a fracture mechanics approach that a fatigue failure due to the propagation of an embedded elliptical slit, under these stresses, would be unlikely for a crack length smaller than 1.85 mm. However, the cement would fail under the same conditions, irrespective of the type of the prosthesis employed.

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

    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:


    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.

  16. ETBE (ethyl tert butyl ether) and TAME (tert amyl methyl ether) affect microbial community structure and function in soils.

    Bartling, Johanna; Esperschütz, Jürgen; Wilke, Berndt-Michael; Schloter, Michael


    Ethyl tert butyl ether (ETBE) and tert amyl methyl ether (TAME) are oxygenates used in gasoline in order to reduce emissions from vehicles. The present study investigated their impact on a soil microflora that never was exposed to any contamination before. Therefore, soil was artificially contaminated and incubated over 6 weeks. Substrate induced respiration (SIR) measurements and phospholipid fatty acid (PLFA) analysis indicated shifts in both, microbial function and structure during incubation. The results showed an activation of microbial respiration in the presence of ETBE and TAME, suggesting biodegradation by the microflora. Furthermore, PLFA concentrations decreased in the presence of ETBE and TAME and Gram-positive bacteria became more dominant in the microbial community.

  17. Influence of the angle between two crown ether moieties on supramolecular copolymerization of bis(crown ether)s and bisparaquat homoditopic monomers


    Bis(crown ether) homoditopic monomers containing two bis(p-phenylene)-34-crown-10 moieties with different angles(180° for monomer 3,120°for monomer 4,and 60°for monomer 5) and a complementary bisparaquat homoditopic monomer(7) were designed and synthesized.The three bis(crown ether) monomers could organize into linear supramolecular polymers in concentrated solutions in CHCl3/CH3CN with the bisparaquat monomer 7,as demonstrated by 1 H NMR and viscosity studies. The pseudorotaxanes or supramolecular polymers formed from 3+7 and 4+7 had larger values of Ka,p,n,slope 1,and slope 2 than those of 5+7.This result was attributed to the greater steric hindrance of compound 5 than that of 3 and 4,which resulted in less effective formation of linear supramolecular polymers from 5 with compound 7 than those from compounds 3 and 4 with compound 7,as also demonstrated by UV-vis method.

  18. A facile synthesis of highly stable multiblock poly(arylene ether)s based alkaline membranes for fuel cells

    Jasti, Amaranadh; Shahi, Vinod K.


    Herein, we are disclosing simple route for the preparation of alkaline membranes (AMs) based on aminated multiblock poly(arylene ether)s (AMPEs) synthesized by nucleophilic substitution-poly condensation followed by quaternization and alkalization reactions. In this procedure, four quaternary ammonium groups are successfully introduced without use of carcinogenic reagents such as chloromethylmethyl ether (CMME). Hydrophilic/hydrophobic phase separation is responsible for their high hydroxide conductivity (∼150 mS cm-1 at 80 °C) due to development of interconnected ion transport pathway. AMs are exhibiting good alkaline stability due to the presence of two vicinal quaternary ammonium groups and avoid degradation such as Sommelet-Hauser rearrangement and Hofmann elimination. Vicinal quaternary ammonium groups also resist nucleophilic (OH-) attack and suppress the Stevens rearrangement as well as SN2 substitution reaction due to stearic hindrance. Optimized AM (AMPE-M20N15 (55% DCM)) exhibits about 0.95 V open circuit voltage (OCV) and 48.8 mW cm-2 power density at 65 °C in alkaline direct methanol fuel cell (ADMFC) operation. These results suggest promising begin for the preparation of stable and conductive AMs for ADMFC applications and useful for developing hydroxide conductive materials.

  19. Crystallization Kinetics and Melting Behavior of PA1010/Ether-based TPU Blends

    ZHANG Shu-ling; ZHAO Yan; SUN Xiao-bo; JIANG Zhen-hua; WU Zhong-wen; WANG Gui-Bin


    Polyamide 1010(PA1010)/thermoplastic poly(ether urethane) elastomer(ether-based TPU) blends were prepared via melt extrusion. The crystallization kinetics and melting behavior of PA1010/ether-based TPU blends were systematically investigated using differential scanning calorimetry. The crystallization kinetics results show that the addition of ether-based TPU hinders the crystallization of PA1010, and the hindrance effect increases with the increase of the concentration of ether-based TPU. Both pure PA1010 and PA1010/ether-based TPU blends exhibit double melting peaks in the process of nonisothermal crystallization. The double melting peaks change differently with the variation of cooling rate and blend composition. The cooling rate only influences the lower melting peak; however, the blend composition influences not only the lower melting peak but also the higher melting peak. The reason for the phenomenon must be the interaction between the two compositions.

  20. Antimutagenic effect of crown ethers on heavy metal-induced sister chromatid exchanges.

    Cai, M Y; Arenaz, P


    Macrocyclic polyethers (crown ethers) are a family of compounds that possess the ability to complex with and transport metal ions across membranes. Because of their unique ionophoric characteristic, they have wide application in industry and research, chemistry and biology. In the current investigation the relationship between heavy metal mutagenesis and crown ether co-mutagenicity and/or antimutagenicity in mammalian cells has been examined using sister chromatid exchange (SCE) as the cytogenetic end point. Chinese hamster ovary cells were treated with lead or cadmium, with and without selected crown ethers. Several genotoxic end points, including SCEs were scored and statistically compared. We report here that most of the crown ethers studied had little or no influence on lead- or cadmium-induced SCEs or chromosome aberrations. On the other hand, the substituted crown ether dicyclohexyl 21-crown-7 significantly decreased both spontaneous and metal-induced SCE frequencies, suggesting that this crown ether may possess antimutagenic activity.

  1. The Wireless Gateway Design of the Industrial Ethernet EtherCAT Network%工业以太网EtherCAT的无线网关设计

    魏亚鹏; 韩卫光


    The Real-time Ethernet technology is a hot issue in the industrial communication area,and the EtherCAT technology has a bright prospect in such field.The wireless sensor network ZigBee technology can bring forth the convenience of the transmission channel on the deployment and planning,which can reduce many costs and troubles of the network cabling construction.Making a gateway which connects the EtherCAT network with the ZigBee network can expand the range of the industrial communication networks.In this way,the EtherCAT master can achieve a perception of the change in the industrial manufacturing environment.On the basis of further study on these two protocols,an implementation scheme of ZigBee accessing EtherCAT is proposed,and a communication model of an EtherCAT-ZigBee gateway is designed,and the gateway which connects the EtherCAT network and the ZigBee network is designed and realized through using ARM Cortex-A8 and CC2530.After tests,it shows that the EtherCAT network and the ZigBee network can communicate with each other through the gateway,which is able to meet the needs of real-time collection of field data.%实时工业以太网技术是目前工业通信领域研究的热点,EtherCAT技术具有光明的应用前景.无线传感网ZigBee技术可以带来传输通道部署和规划上的便利,可以减少大量布线施工的代价与困扰.开发连接EtherCAT和ZigBee的网关可以拓展工业通信网络的范围,实现对工业制造现场的环境变化的感知.在对两种协议深入研究的基础上,提出了ZigBee接入EtherCAT的实现方案,设计了EtherCAT和ZigBee的网关通信模型,并且采用ARM Cortex-A8和CC2530设计并实现了连接EtherCAT与ZigBee的网关.经过测试表明,该网关实现了EtherCAT与ZigBee网络通信的协议转换功能,能够满足实时采集现场数据的需要.

  2. Thermodynamics of Hydrogen Production from Dimethyl Ether Steam Reforming and Hydrolysis

    T.A. Semelsberger


    The thermodynamic analyses of producing a hydrogen-rich fuel-cell feed from the process of dimethyl ether (DME) steam reforming were investigated as a function of steam-to-carbon ratio (0-4), temperature (100 C-600 C), pressure (1-5 atm), and product species: acetylene, ethanol, methanol, ethylene, methyl-ethyl ether, formaldehyde, formic acid, acetone, n-propanol, ethane and isopropyl alcohol. Results of the thermodynamic processing of dimethyl ether with steam indicate the complete conversion of dimethyl ether to hydrogen, carbon monoxide and carbon dioxide for temperatures greater than 200 C and steam-to-carbon ratios greater than 1.25 at atmospheric pressure (P = 1 atm). Increasing the operating pressure was observed to shift the equilibrium toward the reactants; increasing the pressure from 1 atm to 5 atm decreased the conversion of dimethyl ether from 99.5% to 76.2%. The order of thermodynamically stable products in decreasing mole fraction was methane, ethane, isopropyl alcohol, acetone, n-propanol, ethylene, ethanol, methyl-ethyl ether and methanol--formaldehyde, formic acid, and acetylene were not observed. The optimal processing conditions for dimethyl ether steam reforming occurred at a steam-to-carbon ratio of 1.5, a pressure of 1 atm, and a temperature of 200 C. Modeling the thermodynamics of dimethyl ether hydrolysis (with methanol as the only product considered), the equilibrium conversion of dimethyl ether is limited. The equilibrium conversion was observed to increase with temperature and steam-to-carbon ratio, resulting in a maximum dimethyl ether conversion of approximately 68% at a steam-to-carbon ratio of 4.5 and a processing temperature of 600 C. Thermodynamically, dimethyl ether processed with steam can produce hydrogen-rich fuel-cell feeds--with hydrogen concentrations exceeding 70%. This substantiates dimethyl ether as a viable source of hydrogen for PEM fuel cells.

  3. Integrated catalytic and electrocatalytic conversion of substituted phenols and diaryl ethers

    Song, Yang; Chia, Shao H.; Sanyal, Udishnu; Gutierrez, Oliver Y.; Lercher, Johannes A.


    Electrocatalytic hydrogenation and catalytic thermal hydrogenation of substituted phenols and diaryl ethers were studied on carbon-supported Rh. For electrocatalytic and catalytic thermal hydrogen addition reactions, the dominant reaction pathway is hydrogenation to cyclic alcohols and cycloalkyl ethers. The presence of substituting methyl or methoxy groups led to lower rates compared to unsubstituted phenol or diphenyl ether. Methoxy or benzyloxy groups, however, undergo C-O bond cleavage via hydrogenolysis and hydrolysis (minor pathway).

  4. Cure kinetics of diglycidyl ether of bisphenol-A/dicyandiamide system for copper clad laminates%覆铜箔层压板专用双酚A二缩水甘油醚/双氰胺体系的固化反应动力学

    汪晓东; 宁林坚; 张强



  5. 三羟基苯甲基氨基均三嗪与双酚A型环氧树脂的固化反应研究%Study on the curing behavior of 2, 4, 6-tri (hydroxylphenylamine)-s-triazine and diglycidyl ether of bisphenol A

    张兴宏; 黄丽华; 戚国荣


    采用等转化率法研究了2,4,6-三(羟基苯甲基氨基)-均三嗪(MFP)与双酚A型环氧树脂(DGEBA)在等温和非等温条件下的固化反应行为,两种条件下MFP/DGEBA固化反应的表观活化能(Eα)均随转化率(α)增加呈先减后增的趋势(α=0.25 时取得最小值).由于仲胺基和酚羟基对环氧基反应的不等活性,非等温固化反应时两种反应先后发生,形成Triazine-NCH2-CH(OH)-结构后,再形成ArO-CH2-CH(OH)-结构并产生交联,前后两阶段Eα分别为69.8、86.8 kJ·mol-1.对等温固化反应,由于起始反应温度高,仲胺基和酚羟基几乎同步与环氧基发生反应,两者的相互催化作用使反应前期Eα相对较低(59.1 kJ·mol-1),固化反应速度较快,引起体系粘度迅速增大,扩散控制反应提前,从而造成反应后期Eα(89.7 kJ·mol-1)相对较大.

  6. 聚醚链段长度对氨基聚醚-环氧树脂力学性能的影响%Influence of Polyether Segment Length on Mechanical Properties of Cured Epoxy Resins Based on Amino-terminated Poly(ethylene glycol) and Diglycidyl Ether of Bisphenol

    赵立英; 马会茹; 官建国


    增加韧性(包括冲击强度和拉伸韧性)、断裂应变和模量损耗因子; 另一方面也能提高固化产物在低温下的储存模量. 优化[AKM-9]PE可制备出在中低温下同时具有优异的拉伸强度、模量、断裂应变和冲击性能的BATPE-DGEBA环氧树脂.

  7. Determination of Bisphenol Diglycidyl Ethers in Fish Canned Foodstuffs by Solid-phase Extraction/HPLC-MS/MS%鱼肉类罐头中双酚-二环氧甘油醚的固相萃取/HPLC-MS/MS法检测

    张朝晖; 罗生亮; 吴少林; 赵鑫; 刘文涛; 云环


    建立了鱼肉类罐头中内分泌干扰物质双酚A二缩水甘油醚(BADGE)及其衍生物BADGE·H2O、BADGE·2H2O、BADGE·2HCl、BADGE·HCl·H2O和双酚F二缩水甘油醚(BFDGE)及其衍生物BFDGE·2H2O、BFDGE·2HCl 8种双酚-二环氧甘油醚的固相萃取/液相色谱-电喷雾串联质谱分析方法.以叔丁基甲醚为提取溶剂,采用超声波辅助溶剂萃取法萃取,萃取液用Waters Oasis HLB固相萃取柱进行净化浓缩.以Thermo Hypersil Gold C18色谱柱为分离柱,在正离子模式下以电喷雾电离串联质谱仪进行测定.考察了流动相组分和流动相添加剂对质谱离子化效率的影响,8种双酚-二环氧甘油醚在1.0 ~100.0 μg/L范围内线性关系良好(r≥0.99).在2.0、10.0和50.0 μg/kg的添加水平下,8种目标化合物的回收率为83% ~99%,相对标准偏差小于9.0%,方法的检出限为0.13 ~0.30 μg/kg.方法具有较高的灵敏度和准确度,能够满足鱼肉类罐头食品中双酚-二环氧甘油醚残留量的快速检测.

  8. EtherCAT主导运动控制通信技术



  9. Synthesis and characterization of quaternized poly(phthalazinone ether sulfone ketone) for anion-exchange membrane


    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.


    F. H. Chang ، C. R. Yang ، C. Y. Tsai ، W. C. Lin


    Full Text Available This study characterized the airborne exposure of students to thirty polybrominated diphenyl ether congeners inside and outside a computer classroom in a southern Taiwan college. Arithmetic mean values of total indoor and outdoor polybrominated diphenyl ether concentrations were 125.0 pg/m3 (89.8 to 203.9 pg/m3 and 110.3 pg/m3 (83.5 to 157.0 pg/m3, respectively. Total indoor polybrominated diphenyl ether concentrations were one order of magnitude lower than those detected in homes in Birmingham, United Kingdom and in Ottawa, Canada but were several times higher than those measured in the ambient air in Ottawa, Canada and from the Bohai Sea to the Arctic. The five highest indoor concentrations of polybrominated diphenyl ether congeners were decabromodiphenyl ether (23.0 pg/m3, 4,4’-dibromodiphenyl ether (15.9 pg/m3, 2,2’,3,4,4’,5,5’,6-octabromodiphenyl ether (10.6 pg/m3, 2,4-dibromodiphenyl ether (10.3 pg/m3 and 2,2’,3,4,4’,5’,6-heptabromodiphenyl ether (10.0 pg/m3. Although indoor and outdoor total polybrominated diphenyl ether concentrations did not significantly differ, the indoor concentrations of 2,4-dibromodiphenyl ether, 2,2’,4-tribromodiphenyl ether, 2,4,4’-tribromodiphenyl ether, 2,2’,4,5’-tetrabromodiphenyl ether and 2,3’,4’,6-tetrabromodiphenyl ether were significantly higher than their outdoor concentrations. This study suggests the following measures: 1 to increase the air exchange rate and open classroom doors and windows for several minutes before classes to reduce indoor PBDE concentrations; 2 to reduce polybrominated diphenyl ether emissions from new devices, it’s better to use computer-related products that meet the Restriction of Hazardous Substances Directive adopted by the European Union.

  11. Oxidation of ethyl ether on borate glass: chemiluminescence, mechanism, and development of a sensitive gas sensor.

    Hu, Jing; Xu, Kailai; Jia, Yunzhen; Lv, Yi; Li, Yubao; Hou, Xiandeng


    A gas sensor was developed by using the chemiluminescence (CL) emission from the oxidation of ethyl ether by oxygen in the air on the surface of borate glass. Theoretical calculation, together with experimental investigation, revealed the main CL reactions: ethyl ether is first oxidized to acetaldehyde and then to acetic acid, during which main luminous intermediates such as CH 3CO (*) are generated and emit light with a peak at 493 nm. At a reaction temperature of 245 degrees C, the overall maximal emission was found at around 460 nm, and the linear range of the CL intensity versus the concentration of ethyl ether was 0.12-51.7 microg mL (-1) ( R = 0.999, n = 7) with a limit of detection (3sigma) of 0.04 microg mL (-1). Interference from foreign substances including alcohol (methanol, ethanol and isopropanol), acetone, ethyl acetate, n-hexane, cyclohexane, dichloromethane, or ether ( n-butyl ether, tetrahydrofuran, propylene oxide, isopropyl ether and methyl tert-butyl ether) was not significant except a minimal signal from n-butyl ether (ethyl ether.

  12. Reliability Analysis of Mine Monitoring Network Based on Ether CAT%EtherCAT井下监控网络可靠性分析研究

    王玉梅; 张国治



  13. 工业以太网EtherCAT技术的原理及其实现%The principle of Industry Ethernet-EtherCAT and its implementation




  14. Polybrominated diphenyl ethers (PBDEs): new pollutants-old diseases.

    Siddiqi, Muhammad Akmal; Laessig, Ronald H; Reed, Kurt D


    Polybrominated diphenyl ethers (PBDEs) are a class of recalcitrant and bioaccumulative halogenated compounds that have emerged as a major environmental pollutant. PBDEs are used as a flame-retardant and are found in consumer goods such as electrical equipment, construction materials, coatings, textiles and polyurethane foam (furniture padding). Similar in structure to polychlorinated biphenyls (PCBs), PBDEs resist degradation in the environment. Less brominated PBDEs like tetra-, penta- and hexa- demonstrate high affinity for lipids and can accumulate in the bodies of animals and humans. Breast milk from North American women contained much higher amounts of PBDEs than levels in breast milk from Swedish women, indicating that North American exposures to PBDEs may be particularly high. Evidence to date suggests that tetra- and penta-BDEs are likely to be the more toxic and bioaccumulative of the PBDE compounds, compared to octa- and deca-congeners. PBDEs are sold as mixtures, under names such as "pentabromodiphenyl ether" and "octabromodiphenyl ether." The pentabromo product is a mixture of tetra-BDEs and penta-BDEs in approximately equal amounts. Pentabromo consists of PBDEs that are believed to be the most toxic. This mixture has been banned by the European Union, but is still used in North America. The United States is the leading producer and user of pentabromo. In August 2003, the State of California passed a bill to phase out the use of penta- and octa-PBDE by 2008. The toxicology of PBDEs is not well understood, but PBDEs have been associated with tumors, neurodevelopmental toxicity and thyroid hormone imbalance. The neurotoxic effects of PBDEs are similar to those observed for PCBs. Children exposed to PBDEs are prone to subtle but measurable developmental problems. It is presumed that PBDEs are endocrine disruptors, but research in this area is scant. Further studies are imperative in a multitude of health and environmental disciplines to determine the

  15. On the radiation stability of crown ethers in ionic liquids.

    Shkrob, I.; Marin, T.; Dietz, M. (Chemical Sciences and Engineering Division); (Benedictine Univ.); (Univ. of Wisconsin at Milwaukee)


    Crown ethers (CEs) are macrocyclic ionophores used for the separation of strontium-90 from acidic nuclear waste streams. Room temperature ionic liquids (ILs) are presently being considered as replacements for traditional molecular solvents employed in such separations. It is desirable that the extraction efficacy obtained with such solvents should not deteriorate in the strong radiation fields generated by decaying radionuclides. This deterioration will depend on the extent of radiation damage to both the IL solvent and the CE solute. While radiation damage to ILs has been extensively studied, the issue of the radiation stability of crown ethers, particularly in an IL matrix, has not been adequately addressed. With this in mind, we have employed electron paramagnetic resonance (EPR) spectroscopy to study the formation of CE-related radicals in the radiolysis of selected CEs in ILs incorporating aromatic (imidazolium and pyridinium) cations. The crown ethers have been found to yield primarily hydrogen loss radicals, H atoms, and the formyl radical. In the low-dose regime, the relative yield of these radicals increases linearly with the mole fraction of the solute, suggesting negligible transfer of the excitation energy from the solvent to the solute; that is, the solvent has a 'radioprotective' effect. The damage to the CE in the loading region of practical interest is relatively low. Under such conditions, the main chemical pathway leading to decreased extraction performance is protonation of the macrocycle. At high radiation doses, sufficient to increase the acidity of the IL solvent significantly, such proton complexes compete with the solvent cations as electron traps. In this regime, the CEs will rapidly degrade as the result of H abstraction from the CE ring by the released H atoms. Thus, the radiation dose to which a CE/IL system is exposed must be maintained at a level sufficiently low to avoid this regime.

  16. Microbial degradation of 4-monobrominated diphenyl ether with anaerobic sludge

    Shih, Yang-hsin, E-mail: [Department of Agricultural Chemistry, National Taiwan University, Taipei 106, Taiwan, ROC (China); Chou, Hsi-Ling [Department of Soil and Environmental Sciences, National Chung Hsing University, Taichung 407, Taiwan, ROC (China); Peng, Yu-Huei [Department of Agricultural Chemistry, National Taiwan University, Taipei 106, Taiwan, ROC (China)


    Highlights: Black-Right-Pointing-Pointer BDE-3 was degraded with two anaerobes in different rates. Black-Right-Pointing-Pointer Glucose addition augment the debromination efficiencies. Black-Right-Pointing-Pointer Hydrogen gas was detected and relative microbes were identified. Black-Right-Pointing-Pointer Extra-carbon source enhanced degradation partial due to H{sub 2}-generation bacteria. - Abstract: Polybrominated diphenyl ethers (PBDEs) are widely used flame retardant additives for many plastic and electronic products. Owing to their ubiquitous distribution in the environment, multiple toxicity to humans, and increasing accumulation in the environment, the fate of PBDEs is of serious concern for public safety. In this study, the degradation of 4-monobrominated diphenyl ether (BDE-3) in anaerobic sludge and the effect of carbon source addition were investigated. BDE-3 can be degraded by two different anaerobic sludge samples. The by-products, diphenyl ether (DE) and bromide ions, were monitored, indicating the reaction of debromination within these anaerobic samples. Co-metabolism with glucose facilitated BDE-3 biodegradation in terms of kinetics and efficiency in the Jhongsing sludge. Through the pattern of amplified 16S rRNA gene fragments in denatured gradient gel electrophoresis (DGGE), the composition of the microbial community was analyzed. Most of the predominant microbes were novel species. The fragments enriched in BDE-3-degrading anaerobic sludge samples are presumably Clostridium sp. This enrichment coincides with the H{sub 2} gas generation and the facilitation of debromination during the degradation process. Findings of this study provide better understanding of the biodegradation of brominated DEs and can facilitate the prediction of the fate of PBDEs in the environment.


    Kamil Klier; Richard G. Herman; Heock-Hoi Kwon; James G. C. Shen; Qisheng Ma; Robert A. Hunsicker; Andrew P. Butler; Scott J. Bollinger


    A tungstena-zirconia (WZ) catalyst has been investigated for coupling methanol and isobutanol to unsymmetrical ethers, i.e. methyl isobutyl ether (MIBE) and compared with earlier studied sulfated-zirconia (SZ) and Nafion-H catalysts. In all cases, the ether synthesis mechanism is a dual site S{sub N}2 process involving competitive adsorption of reactants on proximal acid sites. At low reaction temperatures, methylisobutylether (MIBE) is the predominant product. However, at temperatures >135 C the WZ catalyst is very good for dehydration of isobutanol to isobutene. The surface acid sites of the WZ catalyst and a Nafion-H catalyst were diagnosed by high resolution X-ray photoelectron spectroscopy (XPS) of N 1s shifts after adsorption of amines. Using pyridine, ethylenediamine, and triethylamine, it is shown that WZ has heterogeneous strong Broensted acid sites. Theoretical study located the transition state of the alcohol coupling reaction on proximal Broensted acid sites and accounted well for XPS core-level shifts upon surface acid-base interactions. While computations have not been carried out with WZ, it is shown that the SZ catalyst is a slightly stronger acid than CF{sub 3}SO{sub 3}H (a model for Nafion-H) by 1.3-1.4 kcal/mol. A novel sulfated zirconia catalyst having proximal strong Broensted acid sites was synthesized and shown to have significantly enhanced activity and high selectivity in producing MIBE or isobutene from methanol/isobutanol mixtures. The catalyst was prepared by anchoring 1,2-ethanediol bis(hydrogen sulfate) salt precursor onto zirconium hydroxide, followed by calcination to remove the -(CH{sub 2}CH{sub 2})- bridging residues.

  18. Green mechanochemical oxidative decomposition of powdery decabromodiphenyl ether with persulfate

    Huang, Aizhen; Zhang, Zhimin; Wang, Nan [College of Chemistry and Chemical Engineering, Huazhong University of Science and Technology, Wuhan 430074 (China); Zhu, Lihua, E-mail: [College of Chemistry and Chemical Engineering, Huazhong University of Science and Technology, Wuhan 430074 (China); Zou, Jing [School of Chemistry and Environmental Engineering, Wuhan Institute of Technology, Wuhan 430073 (China)


    Highlights: • MC process greatly enhanced the decomposition of PS into reactive sulfate radicals. • The mechanochemical (MC) activation of persulfate was applied to degrade BDE209. • This method could achieve a rapid and complete debromination and mineralization of BDE209. • No toxic low brominated polybrominated diphenyl ethers were produced and accumulated. • Sulfate radicals were the main oxidizing species for the decomposition of BDE209. - Abstract: A method was developed for efficiently degrading powdery decabromodiphenyl ether (BDE209) by using mechanochemical (MC) activation of persulfate (PS). Characteristic Raman spectra of BDE209 corresponding to C−Br and C−O bonds were decreased in intensity and finally disappeared as the MC reaction proceeded. The BDE209 removal was influenced by the molar ratio of PS to BDE209, the mass ratio of milling ball to reaction mixtures, the ball size, and the ball rotation speed. Under optimal conditions, the new method could achieve a complete degradation, debromination and mineralization of BDE209 within 3 h of milling. However, the degradation removal (or debromination efficiency) was decreased to only 51.7% (15.6%) and 67.8% (31.5%) for the use of CaO and peroxymonosulfate, respectively. The analyses of products demonstrated that once the degradation was initiated, BDE209 molecules were deeply debrominated and fully mineralized in the MC-PS system. The strong oxidizing ability of this system was due to the reactive sulfate radicals generated from the MC-enhanced activation of PS, which was confirmed with electron spin resonance spectroscopy. Because no toxic low brominated polybrominated diphenyl ethers were accumulated as byproducts, the proposed MC oxidative degradation method will have promising applications in the treatment of solid BDE209 at high concentrations.

  19. EtherCAT技术协会精彩亮相



  20. Degradation of β-Aryl Ether Bonds in Transgenic Plants

    Mnich, Ewelina

    of the monolignols coniferyl alcohol, p-coumaryl alcohol and sinapyl alcohol which during radical-mediated oxidative coupling bind together forming different linkage types. Lignin is the main obstacle in biofuel production as it forms a mechanical barrier limiting accessibility for polysaccharide hydrolyzing enzymes...... system to degrade lignin. An important step in this degradation is cleavage of the most abundant lignin linkage type, β-aryl ether. It is cleaved in a three step reaction catalyzed by a dehydrogenase, a glutathione S-transferase and a glutathione lyase. Due to the nature of the enzymatic reactions...

  1. Fluorescence properties of crown ethers with phenylbenzothiozole pendant group

    Kapoor, S.; Sapre, A. V.; Kumar, S.; Mashraqui, S. H.; Mukherjee, T.


    Photophysical characteristics of 2-phenylbenzothiazole (PBT) substituted crown ether (CRE-PBT) molecules have been investigated in various polar protic solvents. Large Stokes' and good solvatochromic shifts have been observed for CRE-PBT molecules. It is seen that in these molecules, the fluorescence lifetimes and quantum yields increase as compared to the pristine PBT molecule. Temperature-dependence studies have been carried out to understand the effect of CRE substitution and the role of C-C single bond rotation on the fluorescence quantum yield and lifetime.

  2. Developments of Catalysts for Hydrogen Production from Dimethyl Ether

    Kaoru; Takeishi


    1 Results Dimethyl ether (DME) is expected as a clean fuel of the 21st century.I have developed new catalysts for hydrogen production by steam reforming of DME.Cu-Zn/Al2O3 catalysts prepared by the sol-gel method produce large quantities of H2 and CO2 by DME steam reforming under lower reaction temperature[1].However,the sol-gel catalysts will be more expensive than general catalysts prepared by impregnation methods and coprecipitation methods,because the precursor,alkoxides are very expensive.For pract...

  3. Dimethyl ether production from methanol and/or syngas

    Dagle, Robert A; Wang, Yong; Baker, Eddie G; Hu, Jianli


    Disclosed are methods for producing dimethyl ether (DME) from methanol and for producing DME directly from syngas, such as syngas from biomass. Also disclosed are apparatus for DME production. The disclosed processes generally function at higher temperatures with lower contact times and at lower pressures than conventional processes so as to produce higher DME yields than do conventional processes. Certain embodiments of the processes are carried out in reactors providing greater surface to volume ratios than the presently used DME reactors. Certain embodiments of the processes are carried out in systems comprising multiple microchannel reactors.

  4. Synthesis of dimethyl ether from methane mediated by HBr

    Qin You; Zhen Liu; Wensheng Li; Xiaoping Zhou


    Dimethyl ether (DME) was synthesized from methane through a two-step process,in which CH_3 Br was prepared from the oxidative bromination reaction of methane in the presence of HBr and oxygen over a Rh-SiO_2 catalyst and then,in the second step,CH_3Br was hydrolyzed to DME over a silica supported metal chloride catalyst. 12 mol%ZnCl_2/SiO_2 catalyst was found to be the most active,but it deactivated because of Cl- losing.

  5. An aging study of wire chambers with dimethyl ether

    Jibaly, M.; Chrusch, P. Jr.; Hilgenberg, G.; Majewski, S.; Wojcik, R.; Sauli, F.; Gaudaen, J.


    The authors report results on the aging of different types of resistive and non-resistive wires in wire chambers filled with dimethyl ether (DME) of varying degrees of purity. Among the Freon impurities detected in our DME batches, only Freon-11 was found to contribute to the aging process. Of the resistive wires, Nicotin and Stablohm produced fast aging, whereas stainless steel withstood extended irradiation in purified DME (up to 1 C/cm) without any apparent damage. Gold-plated tungsten and molybdenum wires produced results comparable to those of the stainless steel.

  6. Electrochemical Study of Diphenyl Ether Derivatives Used as Herbicides

    Amira Zaouak


    Full Text Available The electrochemical behaviour of five nitro diphenyl ethers used as herbicides is investigated in acetonitrile. A detailed study by cyclic voltammetry and exhaustive electrolysis is carried out for the anodic oxidation of 2-Chloro-6-nitro-3-phenoxyaniline (aclonifen and shows that the major oxidation product is a dimeric compound. A mechanistic scheme involving a coupling process is postulated for the electrochemical oxidation of this compound. Furthermore, the use of differential pulse voltammetry on a glassy carbon electrode permits the selective determination of aclonifen. The limit of detection is 0.6 μg/mL.

  7. Direct dimethyl ether high temperature polymer electrolyte membrane fuel cells

    Vassiliev, Anton; Jensen, Jens Oluf; Li, Qingfeng

    and suffers from low DME solubility in water. When the DME - water mixture is fed as vapour miscibility is no longer a problem. The increased temperature is more beneficial for the kinetics of the direct oxidation of DME than of methanol. The Open Circuit Voltage (OCV) with DME operation was 50 to 100 m......A high temperature polybenzimidazole (PBI) polymer fuel cell was fed with dimethyl ether (DME) and water vapour mixture on the anode at ambient pressure with air as oxidant. A peak power density of 79 mW/cm2 was achieved at 200°C. A conventional polymer based direct DME fuel cell is liquid fed...

  8. Polybrominated diphenyl ethers (PBDEs) in house dust in Beijing, China.

    Li, K; Fu, S


    Eleven house dust samples were collected in Beijing to quantify 42 different polybrominated diphenyl ethers (PBDEs). Total PBDEs concentrations ranged from 140 to 1,300 ng g(-1). The dominant PBDEs congener identified was BDE 209, which made up more than 70% of all PBDEs congeners. Concentrations of PBDEs in Chinese house dust were lower than in other countries. The most polluted areas were electronics shops and households. It is likely that PBDEs exposure is a potential threat for Beijing residents, particularly toddlers.

  9. Density measurements of compressed-liquid dimethyl ether + pentane mixtures.

    Outcalt, Stephanie L; Lemmon, Eric W


    Compressed-liquid densities of three compositions of the binary mixture dimethyl ether (CAS No. 115-10-6) + pentane (CAS No. 109-66-0) have been measured with a vibrating U-tube densimeter. Measurements were made at temperatures from 270 K to 390 K with pressures from 1.0 MPa to 50 MPa. The overall combined uncertainty (k=2) of the density data is 0.81 kg·m(-3). Data presented here have been used to improve a previously formulated Helmholtz energy based mixture model. The newly derived parameters are given.

  10. Nucleophilic Addition of Organozinc Reagents to 2-Sulfonyl Cyclic Ethers

    Kim, Hyoungsu; Kasper, Amanda C.; Moon, Eui Jung; Park, Yongho; Wooten, Ceshea M.; Dewhirst, Mark W.; Hong, Jiyong


    A convergent route to the synthesis of manassantins A and B, potent inhibitors of HIF-1, is described. Central to the synthesis is a stereoselective addition of an organozinc reagent to a 2-benzenesulfonyl cyclic ether to achieve the 2,3-cis-3,4-trans-4,5-cis-tetrahydrofuran of the natural products. Preliminary structure—activity relationships suggested that the (R)-configuration at C-7 and C-7″′ is not critical for HIF-1 inhibition. In addition, the hydroxyl group at C-7 and C-7″′ can be replaced with carbonyl group without loss of activity. PMID:19111058

  11. Synthesis and Characterization of a Novel Cellulose Nonionic Ether

    SHAO Zi-qiang; XU Kun; TIAN Yong-sheng; WANG Fei-jun; WANG Ji-xun


    A kind of novel cellulose ether-trihydroxybutyl cellulose (THBC) was synthesized. The process includes the steam explosion treatment of cotton cellulose, alkalization, etherification and purification. Sweep electron microscope (SEM), Fourier transform infrared (FTIR) and X-ray diffraction were used to characterize the cellulose pretreated and the product. The effects of reaction conditions (temperature, time) on the molecular substitution (Sm) were discussed. To obtain a higher degree of molecular substitution, the reaction temperature is 80 ℃, and the reaction time is 4 h.

  12. Structure and Reactivity of Alkyl Ethers Adsorbed on CeO(2)(111) Model Catalysts

    Calaza, Florencia C [ORNL; Chen, Tsung-Liang [ORNL; Mullins, David R [ORNL; Overbury, Steven {Steve} H [ORNL


    The effect of surface hydroxyls on the adsorption of ether on ceria was explored. Adsorption of dimethyl ether (DME) and diethyl ether (DEE) on oxidized and reduced CeO{sub 2}(111) films was studied and compared with Ru(0001) using RAIRS and sXPS within a UHV environment. On Ru(0001) the ethers adsorb weakly with the molecular plane close to parallel to the surface plane. On the ceria films, the adsorption of the ethers was stronger than on the metal surface, presumably due to stronger interaction of the ether oxygen lone pair electrons with a cerium cation. This interaction causes the ethers to tilt away from the surface plane compared to the Ru(0001) surface. No pronounced differences were found between oxidized (CeO{sub 2}) and reduced (CeOx) films. The adsorption of the ethers was found to be perturbed by the presence of OH groups on hydroxylated CeOx. In the case of DEE, the geometry of adsorption resembles that found on Ru, and in the case of dimethyl ether DME is in between that one found on clean CeOx and the metal surface. Decomposition of the DEE was observed on the OH/CeOx surface following high DEE exposure at 300 K and higher temperatures. Ethoxides and acetates were identified as adsorbed species on the surface by means of RAIRS and ethoxides and formates by s-XPS. No decomposition of dimethyl ether was observed on the OH/CeOx at these higher temperatures, implying that the dissociation of the C-O bond from ethers requires the presence of {beta}-hydrogen.

  13. Anion exchangers with branched functional ion exchange layers of different hydrophilicity for ion chromatography.

    Shchukina, O I; Zatirakha, A V; Smolenkov, A D; Nesterenko, P N; Shpigun, O A


    Novel polystyrene-divinylbenzene (PS-DVB) based anion exchangers differing from each other in the structure of the branched functional ion exchange layer are prepared to investigate the role of linker and functional site on ion exchange selectivity. The proposed method of synthesis includes the obtaining of aminated PS-DVB particles by means of their acylation with following reductive amination with methylamine. Further modification of the obtained secondary aminogroups is provided by the alkylation with either 1,4-butanediol diglycidyl ether (1,4-BDDGE) or resorcinol diglycidyl ether (RDGE), which form the linkers of different hydrophobicity, and amination of terminal epoxide rings with trimethylamine (TMA), dimethylethanolamine (DMEA), methyldiethanolamine (MDEA) or triethanolamine (TEA). The variation of the structure and hydrophobicity of the linker and terminal quaternary ammonium sites in the functional layer allows the alteration of selectivity and separation efficiency of the obtained adsorbents. The ion exchange selectivity and separation efficiency of the anion exchangers are evaluated using the model mixtures of anions (F(-), HCOO(-), Cl(-), NO2(-), Br(-), NO3(-), HPO4(2-) and SO4(2-)) in potassium hydroxide eluents. The adsorbents show the decrease of selectivity with increasing the hydrophilicity of the terminal functional site. The anion exchangers having more flexible and hydrophilic 1,4-BDDGE linker provide smaller separation factors for most of the analytes as compared with RDGE-containing adsorbents with the same terminal ion exchange sites, but are characterized with higher column efficiencies and better peak symmetry for polarizable anions. In case of 1,4-BDDGE-modified anion exchangers of the particle size of 3.3μm functionalized with DMEA and MDEA the calculated values of column efficiencies for polarizable NO3(-) and Br(-) are up to 49,000 and 53,000N/m, respectively, which is almost twice higher than the values obtained for the RDGE

  14. Quantitative Determination of α-Arbutin, β-Arbutin, Kojic Acid, Nicotinamide, Hydroquinone, Resorcinol, 4-Methoxyphenol, 4-Ethoxyphenol, and Ascorbic Acid from Skin Whitening Products by HPLC-UV.

    Wang, Yan-Hong; Avonto, Cristina; Avula, Bharathi; Wang, Mei; Rua, Diego; Khan, Ikhlas A


    An HPLC-UV method was developed for the quantitative analysis of nine skin whitening agents in a single injection. These compounds are α-arbutin, β-arbutin, kojic acid, nicotinamide, resorcinol, ascorbic acid, hydroquinone, 4-methoxyphenol, and 4-ethoxyphenol. The separation was achieved on a reversed-phase C18 column within 30 min. The mobile phase was composed of water and methanol, both containing 0.1% acetic acid (v/v). The stability of the analytes was evaluated at different pH values between 2.3 and 7.6, and the extraction procedure was validated for different types of skin whitening product matrixes, which included two creams, a soap bar, and a capsule. The best solvent system for sample preparation was 20 mM NaH2PO4 containing 10% methanol at pH 2.3. The analytical method was validated for accuracy, precision, LOD, and LOQ. The developed HPLC-UV method was applied for the quantitation of the nine analytes in 59 skin whitening products including creams, lotions, sera, foams, gels, mask sheets, soap bars, tablets, and capsules.

  15. Determinação espectrofotométrica indireta de capsaicinoides em pimentas Capsicum a partir da reação com o complexo de Co(II com 4-(2-piridilazo resorcinol

    Patrícia Tonon de Souza


    Full Text Available Capsaicinoids (CAPS are substances responsible for pungency in Capsicum. It is important to quantify these types of compounds owing to their broad application in food, pharmaceuticals, cosmetics and chemical weapons. In this work, we developed an indirect spectrophotometric method based on the colorimetric reaction between CAPS, Co(II 3.10×10-5 mol L-1 and 4-(2-pyridylazo resorcinol (PAR 6.23×10-5 and, in cachaça:water 92:8v/v solutions, for quantification of total CAPS in Capsicum peppers. The product of the reaction is CoPAR2CAPS2 and its absorption in aquo-ethanolic solution at 510 nm is proportional to the total CAPS concentration from 0.60 to 17.94 mg L-1. The values of limit of detection and limit of quantification were 0.0004 and 0.001 mg of CAPS/g of pepper, respectively, with 4% relative standard deviation. The developed method yielded similar results to those obtained from high performance liquid chromatography, with 95% of confidence.

  16. Simultaneous preconcentration of copper, zinc, cadmium, and nickel in water samples by cloud point extraction using 4-(2-pyridylazo)-resorcinol and their determination by inductively coupled plasma optic emission spectrometry

    Silva, Edson Luiz, E-mail: [Centro de Energia Nuclear na Agricultura, Universidade de Sao Paulo, Av. Centenario, 303, CP 96, 13416-000 Piracicaba, SP (Brazil); Santos Roldan, Paulo dos [Universidade Federal de Alagoas, Campus A.C. Simoes, Av. Lourival Melo Mota, Tabuleiro do Martins, CEP: 57072-970 AL (Brazil); Gine, Maria Fernanda [Centro de Energia Nuclear na Agricultura, Universidade de Sao Paulo, Av. Centenario, 303, CP 96, 13416-000 Piracicaba, SP (Brazil)


    A procedure for simultaneous separation/preconcentration of copper, zinc, cadmium, and nickel in water samples, based on cloud point extraction (CPE) as a prior step to their determination by inductively coupled plasma optic emission spectrometry (ICP-OES), has been developed. The analytes reacted with 4-(2-pyridylazo)-resorcinol (PAR) at pH 5 to form hydrophobic chelates, which were separated and preconcentrated in a surfactant-rich phase of octylphenoxypolyethoxyethanol (Triton X-114). The parameters affecting the extraction efficiency of the proposed method, such as sample pH, complexing agent concentration, buffer amount, surfactant concentration, temperature, kinetics of complexation reaction, and incubation time were optimized and their respective values were 5, 0.6 mmol L{sup -1}, 0.3 mL, 0.15% (w/v), 50 deg. C, 40 min, and 10 min for 15 mL of preconcentrated solution. The method presented precision (R.S.D.) between 1.3% and 2.6% (n = 9). The concentration factors with and without dilution of the surfactant-rich phase for the analytes ranged from 9.4 to 10.1 and from 94.0 to 100.1, respectively. The limits of detection (L.O.D.) obtained for copper, zinc, cadmium, and nickel were 1.2, 1.1, 1.0, and 6.3 {mu}g L{sup -1}, respectively. The accuracy of the procedure was evaluated through recovery experiments on aqueous samples.

  17. Simultaneous preconcentration of copper, zinc, cadmium, and nickel in water samples by cloud point extraction using 4-(2-pyridylazo)-resorcinol and their determination by inductively coupled plasma optic emission spectrometry.

    Silva, Edson Luiz; Roldan, Paulo dos Santos; Giné, Maria Fernanda


    A procedure for simultaneous separation/preconcentration of copper, zinc, cadmium, and nickel in water samples, based on cloud point extraction (CPE) as a prior step to their determination by inductively coupled plasma optic emission spectrometry (ICP-OES), has been developed. The analytes reacted with 4-(2-pyridylazo)-resorcinol (PAR) at pH 5 to form hydrophobic chelates, which were separated and preconcentrated in a surfactant-rich phase of octylphenoxypolyethoxyethanol (Triton X-114). The parameters affecting the extraction efficiency of the proposed method, such as sample pH, complexing agent concentration, buffer amount, surfactant concentration, temperature, kinetics of complexation reaction, and incubation time were optimized and their respective values were 5, 0.6 mmol L(-1), 0.3 mL, 0.15% (w/v), 50 degrees C, 40 min, and 10 min for 15 mL of preconcentrated solution. The method presented precision (R.S.D.) between 1.3% and 2.6% (n=9). The concentration factors with and without dilution of the surfactant-rich phase for the analytes ranged from 9.4 to 10.1 and from 94.0 to 100.1, respectively. The limits of detection (L.O.D.) obtained for copper, zinc, cadmium, and nickel were 1.2, 1.1, 1.0, and 6.3 microg L(-1), respectively. The accuracy of the procedure was evaluated through recovery experiments on aqueous samples.

  18. Simultaneous preconcentration of vanadium(V/IV) species with palmitoyl quinolin-8-ol bonded to amberlite XAD 2 and their separate spectrophotometric determination with 4-(2-pyridylazo)-resorcinol using CDTA as masking agent

    Filik, Hayati; Berker, Kadriye Isil; Balkis, Nuray; Apak, Resat


    This paper reports the simultaneous preconcentration and separation of trace amounts of V species in synthetic solutions and seawater with palmitoyl quinolin-8-ol bonded amberlite XAD 2 copolymer resin column prior to simultaneous speciation analysis. Both V(IV) and V(V) species could be sorbed and preconcentrated by the resin. Both vanadium species were quantitatively eluted together from the resin column using HCl as stripping agent and used for speciation studies. For the speciation analysis of eluted V species, the selected route involved spectrophotometric determination of total vanadium with 4-(2-pyridylazo)-resorcinol (PAR) and vanadate estimation by masking vanadyl with 1,2 cyclohexanediaminetetraacetic acid (CDTA). The preconcentrated V species were assayed spectrophotometrically with PAR at 542 nm, and the results were compared with those of FAAS. The detection limits of V(V) with spectrophotometry and FAAS were 1.6 and 0.9 {mu}g l{sup -1}, respectively. The optimal experimental parameters such as pH, sample flow rate, desorption flow rate, redox behaviour of V(IV) and V(V) in resin and volume of eluent and sample were investigated. The values obtained for the preconcentration factor by the two methods were nearly consistent, and were in the range 150-fold. Analysis of certified reference material (IAEA-405) by the proposed method showed good agreement with the certified value. The established procedure was employed for preconcentrating the vanadium species from artificial and real seawater.

  19. Solid-phase extraction and preconcentration of copper in mineral waters with 4-(2-pyridyl-azo) resorcinol-loaded amberlite XAD-7 and flame atomic absorption spectrometry.

    Ince, Muharrem; Kaplan, Olcay; Yaman, Mehmet


    A simple, sensitive, accurate, and selective method for determination of ultratrace levels of copper is modified. The method is based on preconcentration of copper on the 4-(2-pyridyl-azo) resorcinol-loaded amberlite XAD-7 (non-ionic copoly[styrene-acrylic compound]) at pH 5.0 to 6.5 for contact time as low as 45 minutes. The adsorbed copper was eluted with concentrated nitric acid and measured by flame atomic absorption spectrometry. Recoveries of up to 90% were achieved. The optimized preconcentration method was applied to copper determination in various water samples. The detection limit was found to be 0.09 ng mL(-1). The relative standard deviation was found to be 9% using 300 mL of 5.0 ng mL(-1) for 10 replicate preconcentration procedures. Copper concentrations in the studied water samples were found to be in the ranges of 0.4 to 18.0 ng mL(-1).

  20. Sorption-desorption behavior of polybrominated diphenyl ethers in soils

    Olshansky, Yaniv; Polubesova, Tamara [Department of Soil and Water Sciences, Robert H. Smith Faculty of Agriculture, Food and Environment, Hebrew University of Jerusalem, P.O. Box 12, Rehovot 76100 (Israel); Vetter, Walter [Institute of Food Chemistry (170b), University of Hohenheim, Garbenstr. 28, D-70599 Stuttgart (Germany); Chefetz, Benny, E-mail: [Department of Soil and Water Sciences, Robert H. Smith Faculty of Agriculture, Food and Environment, The Hebrew University of Jerusalem, P.O. Box 12, Rehovot 76100 (Israel)


    Polybrominated diphenyl ethers (PBDEs) are flame retardants that are commonly found in commercial and household products. These compounds are considered persistent organic pollutants. In this study, we used 4,4'-dibromodiphenyl ether (BDE-15) as a model compound to elucidate the sorption and desorption behavior of PBDEs in soils. The organic carbon-normalized sorption coefficient (K{sub OC}) of BDE-15 was more than three times higher for humin than for bulk soils. However, pronounced desorption hysteresis was obtained mainly for bulk soils. For humin, increasing concentration of sorbed BDE-15 resulted in decreased desorption. Our data illustrate that BDE-15 and probably other PBDEs exhibit high sorption affinity to soils. Moreover, sorption is irreversible and thus PBDEs can potentially accumulate in the topsoil layer. We also suggest that although humin is probably a major sorbent for PBDEs in soils, other humic materials are also responsible for their sequestration. - Highlights: > BDE-15 exhibited pronounced desorption hysteresis. > BDE-15 sowed higher sorption affinity to humin as compared to the bulk soils. > Sequestration of PBDEs depends on soil organic matter constitutes other than humin. - Pronounced desorption hysteresis was observed for BDE-15 in natural soils.

  1. Alkali-crown ether complexes at metal surfaces

    Thontasen, Nicha; Deng, Zhitao; Rauschenbach, Stephan [Max Planck Institute for Solid State Research, Stuttgart (Germany); Levita, Giacomo [University of Trieste, Trieste (Italy); Malinowski, Nikola [Max Planck Institute for Solid State Research, Stuttgart (Germany); Bulgarian Academy of Sciences, Sofia (Bulgaria); Kern, Klaus [Max Planck Institute for Solid State Research, Stuttgart (Germany); EPFL, Lausanne (Switzerland)


    Crown ethers are polycyclic ethers which, in solution, selectively bind cations depending on the size of the ring cavity. The study of a single host-guest complex is highly desirable in order to reveal the characteristics of these specific interactions at the atomic scale. Such detailed investigation is possible at the surface where high resolution imaging tools like scanning tunneling microscopy (STM) can be applied. Here, electrospray ion beam deposition (ES-IBD) is employed for the deposition of Dibenzo-24-crown-8 (DB24C8)-H{sup +}, -Na{sup +} and -Cs{sup +} complexes on a solid surface in ultrahigh vacuum (UHV). Where other deposition techniques have not been successful, this deposition technique combines the advantages of solution based preparation of the complex ions with a highly clean and controlled deposition in UHV. Single molecular structures and the cation-binding of DB24C8 at the surface are studied in situ by STM and MALDI-MS (matrix assisted laser desorption ionization mass spectrometry). The internal structure of the complex, i.e. ring and cavity, is observable only when alkali cations are incorporated. The BD24C8-H{sup +} complex in contrast appears as a compact feature. This result is in good agreement with theoretical models based on density functional theory calculations.

  2. High octane ethers from synthesis gas-derived alcohols

    Klier, K.; Herman, R.G.; DeTavernier, S.; Johannson, M.; Kieke, M.; Bastian, R.D.


    The temperature dependence of ether synthesis, particularly unsymmetric methylisobutylether (MIBE), was carried out over the Nafion-H microsaddles (MS) catalyst. The principal product formed under the rather severe reaction conditions of 1100 psig pressure and temperatures in the range of 123--157{degree}C was the expected MIBE formed directly by coupling the methanol/isobutanol reactants. In addition, significantly larger quantities of the dimethylether (DME) and hydrocarbon products were observed than were obtained under milder reaction conditions. Deactivation of the Nafion-H MS catalyst was determined by periodically testing the catalyst under a given set of reaction conditions for the synthesis of MIBE and MTBE from methanol/isobutanol = 2/1, i.e. 123{degree}C, 1100 psig, and total GHSV = 248 mol/kg cat/hr. After carrying out various tests over a period of 2420 hr, with intermittant periods of standing under nitrogen at ambient conditions, the yields of MIBE and MTBE had decreased by 25% and 41%, respectively. In order to gain insight into the role of the surface acidity in promoting the selective coupling of the alcohols to form the unsymmetric ether, the strengths of the acid sites on the catalysts are still being probed by calorimetric titrations in non-aqueous solutions. 11 refs., 13 figs., 9 tabs.

  3. Evaluating the Swelling, Erosion and Compaction Properties of Cellulose Ethers.

    Ghori, Muhammad U; Grover, Liam M; Asare-Addo, Kofi; Smith, Alan M; Conway, Barbara R


    Swelling, erosion, deformation and consolidation properties can affect the performance of cellulose ethers, the most commonly used matrix former in hydrophilic sustained tablet formulations. The present study was designed to comparatively evaluate the swelling, erosion, compression, compaction and relaxation properties of the cellulose ethers in a comprehensive study using standardised conditions. The interrelationship between various compressional models and the inherent deformation and consolidation properties of the polymers on the derived swelling and erosion parameters are consolidated. The impact of swelling (Kw) on erosion rates (KE) and the inter-relationship between Heckel and Kawakita plasticity constants was also investigated. It is evident from the findings that the increases in both substitution and polymer chain length led to higher Kw, but a lower KE; this was also true for all particle size fractions regardless of polymer grade. Smaller particle size and high substitution levels tend to increase the relative density of the matrix but reduce porosity, yield pressure (Py), Kawakita plasticity parameter (b(-1)) and elastic relaxation. Both KW vs KE (R(2) = 0.949-0.980) and Py vs b(-1) correlations (R(2) = 0.820-0.934) were reasonably linear with regards to increasing hydroxypropyl substitution and molecular size. Hence, it can be concluded that the combined knowledge of swelling and erosion kinetics in tandem with the in and out-of-die compression findings can be used to select a specific polymer grade and further to develop and optimise formulations for oral controlled drug delivery applications.

  4. Developmental toxicity of diphenyl ether herbicides in nestling American kestrels

    Hoffman, D.J.; Spann, J.W.; LeCaptain, L.J.; Bunck, C.M.; Rattner, B.A.


    Beginning the day after hatching, American kestrel (Falco sparverius) nestlings were orally dosed for 10 consecutive days with 5 microliters/g of corn oil (controls) or one of the diphenyl ether herbicides (nitrofen, bifenox, or oxyfluorfen) at concentrations of 10, 50, 250, or 500 mg/kg in corn oil. At 500 mg/kg, nitrofen resulted in complete nestling mortality, bifenox in high (66%) mortality, and oxyfluorfen in no mortality. Nitrofen at 250 mg/kg reduced nestling growth as reflected by decreased body weight, crownrump length, and bone lengths including humerus, radiusulna, femur, and tibiotarsus. Bifenox at 250 mg/kg had less effect on growth than nitrofen, but crownrump, humerus, radiusulna, and femur were significantly shorter than controls. Liver weight as a percent of body weight increased with 50 and 250 mg/kg nitrofen. Other manifestations of impending hepatotoxicity following nitrofen ingestion included increased hepatic GSH peroxidase activity in all nitrofentreated groups, and increased plasma enzyme activities for ALT, AST, and LDHL in the 250mg/kg group. Bifenox ingestion resulted in increased hepatic GSH peroxidase activity in the 50and 250mg/kg groups. Nitrofen exposure also resulted in an increase in total plasma thyroxine (T4) concentration. These findings suggest that altricial nestlings are more sensitive to diphenyl ether herbicides than young or adult birds of precocial species.

  5. Molecular dynamics simulations of ether- and ester-linked phospholipids.

    Kruczek, James; Saunders, Matthew; Khosla, Meghna; Tu, Yicheng; Pandit, Sagar A


    Dissimilarities in the bulk structure of bilayers composed of ether- vs ester-linked lipids are well-established; however, the atomistic interactions responsible for these differences are not well known. These differences are important in understanding of why archaea have a different bilayer composition than the other domains of life and why humans have larger concentrations of plasmalogens in specialized membranes? In this paper, we simulate two lipid bilayers, the ester linked dipalmitoylphosphatidylcholine (DPPC) and the ether lined dihexadecylphosphatidylcholine (DHPC), to study these variations. The structural analysis of the bilayers reveals that DPPC is more compressible than DHPC. A closer examination of dipole potential shows DHPC, despite having a smaller dipole potential of the bilayer, has a higher potential barrier than DPPC at the surface. Analysis of water order and dynamics suggests DHPC has a more ordered, less mobile layer of water in the headgroup. These results seem to resolve the issue as to whether the decrease in permeability of DHPC is due to of differences in minimum area per lipid (A0) or diffusion coefficient of water in the headgroup region (Dhead) (Guler et al., 2009) since we have shown significant changes in the order and mobility of water in that region. Copyright © 2017 Elsevier B.V. All rights reserved.

  6. Photodissociation dynamics of ethyl ethynyl ether: A ketenyl radical precursor

    Krisch, Maria; Miller, Johanna; Butler, Laurie; Su, Hongmei; Bersohn, Richard; Shu, Jinian


    We investigate the photodissociation dynamics of ethyl ethynyl ether at 193.3 nm with crossed laser-molecular beam photofragment translational spectroscopy and laser-induced fluorescence. We establish ethyl ethynyl ether as the first clean precursor to the ketenyl radical, a key species in combustion reactions. One major bond fission channel was observed for the system, cleavage along the HCCO-C2H5 bond, leading to ground state C2H5 (ethyl) radicals and HCCO (ketenyl) radical products in two distinct electronic states. We observed neither cleavage of the other C-O bond nor molecular elimination to form C2H4 + CH2CO (ketene). Ketenyl radicals formed in the higher recoil kinetic energy channel could be either X(^2A") or Ã(^2A') state ketenyl radical. We assign the lower recoil kinetic energy channel to the spin forbidden ã(^4A") state of the ketenyl radical, reached through intersystem crossing. Laser-induced fluorescence from the ketenyl radical peaks after a 20 μs delay, indicating that it is formed with a significant amount of internal energy and subsequently relaxes to the lowest vibrational level of the ground electronic state, a result consistent with the product assignment.

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

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


    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

  8. Development and validation of a congener-specific photodegradation model for polybrominated diphenyl ethers

    Zeng, X.; Simonich, S.L.M.; Robrock, K.R.; Korytar, P.; Alvarez-Cohen, L.; Barofsky, D.F.


    With the phaseout of the manufacture of some polybrominated diphenyl ether ( PBDE) formulations, namely penta-brominated diphenyl ether (BDE) and octa-BDE, and the continued use of the deca-BDE formulation, it is important to be able to predict the photodegradation of the more highly brominated cong

  9. Effects of petroleum ether extract of Amorphophallus paeoniifolius tuber on central nervous system in mice

    Das S


    Full Text Available The central nervous system activity of the petroleum ether extract of Amorphophallus paeoniifolius tuber was examined in mice, fed normal as well as healthy conditions. The petroleum ether extract of Amorphophallus paeoniifolius tuber at the doses of 100, 300 and 1000 mg/kg showed significant central nervous system activity in mice.

  10. Crown Ether Complexes with H3O+ and NH4+: Proton Localization and Proton Bridge Formation

    Hurtado, P.; Gamez, F.; Hamad, S.; Martinez-Haya, B.; Steill, J. D.; Oomens, J.


    The complexes formed by crown ethers with hydronium and ammonium cations are of key relevance for the understanding of their supramolecular behavior in protic solvents. In this work, the complexes of the 15-crown-5 (15c5) and 18-crown-6 (18c6) ethers with H3O+ and NH4+ and their deuterated variants

  11. Direct dimethyl ether fueling of a high temperature polymer fuel cell

    Jensen, Jens Oluf; Vassiliev, Anton; Olsen, M.I.


    Direct dimethyl ether (DME) fuel cells suffer from poor DME–water miscibility and so far peak powers of only 20–40 mW cm−2 have been reported. Based on available literature on solubility of dimethyl ether (DME) in water at ambient pressure it was estimated that the maximum concentration of DME at...

  12. Oral 2-oleyl glyceryl ether improves glucose tolerance in mice through the GPR119 receptor

    Hassing, H A; Engelstoft, M S; Sichlau, R M


    abolished the hormone release. Similarly, in isolated primary colonic crypt cultures from WT mice, GPR119 was required for 2-OG-stimulated GLP-1 release while there was no response in crypts from KO mice. In vivo, gavage with 2-oleyl glyceryl ether ((2-OG ether), a stable 2-OG analog with a potency of 5.3 µ...

  13. 76 FR 69659 - Methacrylic Acid-Methyl Methacrylate-Polyethylene Glycol Monomethyl Ether Methacrylate Graft...


    ... AGENCY 40 CFR Part 180 Methacrylic Acid-Methyl Methacrylate-Polyethylene Glycol Monomethyl Ether... residues of methacrylic acid-methyl methacrylate- polyethylene glycol monomethyl ether methacrylate graft... permissible level for residues of methacrylic acid-methyl methacrylate-polyethylene glycol monomethyl...

  14. A convenient procedure for the synthesis of allyl and benzyl ethers from alcohols and phenols

    H Surya Prakash Rao; S P Senthilkumar


    Allyl and benzyl ethers of alcohols can be prepared conveniently and in high yield with allyl and benzyl bromide in the presence of solid potassium hydroxide without use of any solvent. Phenols can be converted to allyl ethers but are inert to benzylation under above conditions.

  15. Dimethylzinc-Initiated Radical Coupling of β-Bromostyrenes with Ethers and Amines

    Sølvhøj, Amanda Birgitte; Ahlburg, Andreas; Madsen, Robert


    A new coupling reaction has been developed in which β-bromostyrenes react with ethers and tertiary amines to introduce the styryl group in the α-position. The transformation is mediated by Me2Zn/O2 with 10 % MnCl2 and is believed to proceed by a radical addition-elimination mechanism. The ether...

  16. Characterization of the molecular degradation mechanism of diphenyl ethers by Cupriavidus sp. WS.

    Wang, Sheng; Bai, Naling; Wang, Bing; Feng, Zhuo; Hutchins, William C; Yang, Ching-Hong; Zhao, Yuhua


    Commonly used flame retardants, such as polybrominated diphenyl ethers, are extremely persistent in the environment, causing serious environmental risks. Certain strains of bacteria are able to degrade several low brominated congeners of PBDEs aerobically. However, the aerobic degradation pathway is not yet well understood, particularly at the genetic level. In this study, we isolated Cupriavidus sp. WS from the environment that could degrade diphenyl ether (DE), 4-bromodiphenyl ether, and 4,4'-bromodiphenyl ether. DE was completely degraded in 6 days without any detectable end-product. Using transposon mutagenesis, several DE degradation-deficient mutants were obtained. Knocking out bphA1, bphA2, and bphA3 eliminated the ability of the Cupriavidus sp. WS bacterium to degrade DE, indicating that the bph genes play a crucial role in DE degradation by this strain. The specific roles of bphA, bphB, and bphC were identified by systematically expressing these genes in Escherichia coli. The dihydrodiol product of BphA was dehydrogenated into 2,3-dihydroxydiphenyl ether by BphB. 2,3-Dihydroxydiphenyl ether was then decomposed into phenol and 2-pyrone-6-carboxylic acid by BphC. Thus, BphA, BphB, and BphC act sequentially in the aerobic degradation of DE, 4-bromodiphenyl ether, and 4,4'-dibromodiphenyl ether by the Cupriavidus sp. WS bacterium.

  17. Reaction Pathways and Energetics of Etheric C–O Bond Cleavage Catalyzed by Lanthanide Triflates

    Assary, Rajeev S.; Atesin, Abdurrahman C.; Li, Zhi; Curtiss, Larry A.; Marks, Tobin J.


    Efficient and selective cleavage of etheric C-O bonds is crucial for converting biomass into platform chemicals and liquid transportation fuels. In this contribution, computational methods at the DFT B3LYP level of theory are employed to understand the efficacy of lanthanide triflate catalysts (Ln(OTf)3, Ln = La, Ce, Sm, Gd, Yb, and Lu) in cleaving etheric C-O bonds. In agreement with experiment, the calculations indicate that the reaction pathway for C-O cleavage occurs via a C-H → O-H proton transfer in concert with weakening of the C-O bond of the coordinated ether substrate to ultimately yield a coordinated alkenol. The activation energy for this process falls as the lanthanide ionic radius decreases, reflecting enhanced metal ion electrophilicity. Details of the reaction mechanism for Yb(OTf)3-catalyzed ring opening are explored in depth, and for 1-methyl-d3-butyl phenyl ether, the computed primary kinetic isotope effect of 2.4 is in excellent agreement with experiment (2.7), confirming that etheric ring-opening pathway involves proton transfer from the methyl group alpha to the etheric oxygen atom, which is activated by the electrophilic lanthanide ion. Calculations of the catalytic pathway using eight different ether substrates indicate that the more rapid cleavage of acyclic versus cyclic ethers is largely due to entropic effects, with the former C-O bond scission processes increasing the degrees of freedom/particles as the transition state is approached.

  18. Crown ether activation of cross-linked subtilisin Carlsberg crystals in organic solvents

    Unen, van Dirk-Jan; Sakodinskaya, Inna K.; Engbersen, Johan F.J.; Reinhoudt, David N.


    The activity of cross-linked subtilisin Carlsberg crystals in the catalysis of peptide bond formation can be significantly enhanced by pretreatment of the enzyme crystals with crown ethers. Soaking of the enzyme crystals in a solution of crown ether in acetonitrile followed by evaporation of the sol


    Diphenyl methyl (DPM) ethers constitute important structural portion of some pharmaceutical entities and also as protective group for hydroxyl groups in synthetic chemistry. DPM ethers are normally prepared using concentrated acids or base as catalysts, which may result in the fo...

  20. 40 CFR 721.7000 - Polymer of disodium maleate, allyl ether, and ethylene oxide.


    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Polymer of disodium maleate, allyl... New Uses for Specific Chemical Substances § 721.7000 Polymer of disodium maleate, allyl ether, and... substance identified generically as a polymer of disodium maleate, allyl ether, and ethylene oxide (P-91...

  1. Glyceryl ether monooxygenase resembles aromatic amino acid hydroxylases in metal ion and tetrahydrobiopterin dependence.

    Watschinger, Katrin; Keller, Markus A; Hermetter, Albin; Golderer, Georg; Werner-Felmayer, Gabriele; Werner, Ernst R


    Glyceryl ether monooxygenase is a tetrahydrobiopterin-dependent membrane-bound enzyme which catalyses the cleavage of lipid ethers into glycerol and the corresponding aldehyde. Despite many different characterisation and purification attempts, so far no gene and primary sequence have been assigned to this enzyme. The seven other tetrahydrobiopterin-dependent enzymes can be divided in the family of aromatic amino acid hydroxylases - comprising phenylalanine hydroxylase, tyrosine hydroxylase and the two tryptophan hydroxylases - and into the three nitric oxide synthases. We tested the influences of different metal ions and metal ion chelators on glyceryl ether monooxygenase, phenylalanine hydroxylase and nitric oxide synthase activity to elucidate the relationship of glyceryl ether monooxygenase to these two families. 1,10-Phenanthroline, an inhibitor of non-heme iron-dependent enzymes, was able to potently block glyceryl ether monooxygenase as well as phenylalanine hydroxylase, but had no effect on inducible nitric oxide synthase. Two tetrahydrobiopterin analogues, N(5)-methyltetrahydrobiopterin and 4-aminotetrahydrobiopterin, had a similar impact on glyceryl ether monooxygenase activity, as has already been shown for phenylalanine hydroxylase. These observations point to a close analogy of the role of tetrahydrobiopterin in glyceryl ether monooxygenase and in aromatic amino acid hydroxylases and suggest that glyceryl ether monooxygenase may require a non-heme iron for catalysis.

  2. Synthesis of imide/arylene ether copolymers for adhesives and composite matrices

    Jensen, B. J.; Hergenrother, P. M.; Bass, R. G.


    A series of imide/arylene ether copolymers were prepared from the reaction of an amorphous arylene ether oligomer and a semi-crystalline imide oligomer. These copolymers were thermally characterized and mechanical properties were measured. One block copolymer was endcapped and the molecular weight was controlled to provide a material that displayed good compression moldability and attractive adhesion and composite properties.

  3. 46 CFR 151.50-40 - Additional requirements for carbon disulfide (carbon bisulfide) and ethyl ether.


    ... bisulfide) and ethyl ether. 151.50-40 Section 151.50-40 Shipping COAST GUARD, DEPARTMENT OF HOMELAND... disulfide (carbon bisulfide) and § 151.50-42 for ethyl ether shall also be observed. ... Special Requirements § 151.50-40 Additional requirements for carbon disulfide (carbon bisulfide) and...

  4. 40 CFR 721.6181 - Fatty acid, reaction product with substituted oxirane, formaldehyde-phenol polymer glycidyl ether...


    ... substituted oxirane, formaldehyde-phenol polymer glycidyl ether, substituted proplyamine and...-phenol polymer glycidyl ether, substituted proplyamine and polyethylenepolyamines (generic). (a) Chemical... as fatty acid, reaction product with substituted oxirane, formaldehyde-phenol polymer glycidyl...

  5. 伺服驱动器EtherCAT接口设计%Design of Servo Driver Communication Interface Based on EtherCAT Protocol

    李文虎; 李叶松; 王江城


    To apply the industrial ethernet technology in motion control filed, the EtherCAT protocol was generally introduced,mainly described the design procedures of realizing the EtherCAT communication interface on servo driver. It emphasized on the methods of combining the CANopen protocol with EtherCAT protocol and the design of application layer software of servo motion control, the basic frame,flow and points were given to build the software. Finally,practical operation results of this network-based servo drive system were given to verify the validity. The results show that EtherCAT can satisfy the strict requirements of motion control.%为将工业以太网技术应用于运动控制领域,简单介绍了EtherCAT协议,描述了实现伺服驱动器EtherCAT协议通讯接口的设计过程.重点分析了将CANopen相关行规映射到EtherCAT协议的基本方法和针对伺服运动控制的应用层软件设计,给出了软件实现的基本框架、流程和要点.最后给出了网络化伺服驱动系统的实际控制结果,运行结果表明EtherCAT能够很好地满足运动控制领域的高要求.

  6. Poly(aryl-ether-ether-ketone) as a Possible Metalized Film Capacitor Dielectric: Accurate Description of the Band Gap Through Ab Initio Calculation


    Poly(aryl-ether-ether-ketone) as a Possible Metalized Film Capacitor Dielectric: Accurate Description of the Band Gap Through Ab Initio...Possible Metalized Film Capacitor Dielectric: Accurate Description of the Band Gap Through Ab Initio Calculation Janet Ho and Marco Olguin Sensors...a Possible Metalized Film Capacitor Dielectric: Accurate Description of the Band Gap Through Ab Initio Calculation 5a. CONTRACT NUMBER 5b. GRANT

  7. Metabolism of methyl tert-butyl ether and other gasoline ethers in mouse liver microsomes lacking cytochrome P450 2E1.

    Hong, J Y; Wang, Y Y; Bondoc, F Y; Yang, C S; Gonzalez, F J; Pan, Z; Cokonis, C D; Hu, W Y; Bao, Z


    To reduce the production of pollutants in motor vehicle exhaust, methyl tert-butyl ether (MTBE) and other ethers such as ethyl tert-butyl ether (ETBE) and tert-amyl methyl ether (TAME) are added to gasoline as oxygenates for more complete combustion. Metabolism of these gasoline ethers is catalyzed by cytochrome P450 (P450) enzymes. P450 2E1, which metabolizes diethyl ether, was suggested to be an enzyme involved. The present study used 2E1 knock-out mice (2E1-/-) to assess the contribution of 2E1 to the metabolism of MTBE, ETBE and TAME. Liver microsomes prepared from the 2E1 knock-out mice lacked 2E1 activity (assayed as N-nitrosodimethylamine demethylation), but were still active in metabolizing all three gasoline ethers. The levels of ether-metabolizing activity (nmol/min per mg) in the liver microsomes from 7 week old female 2E1 knock-out mice were 0.54+/-0.17 for MTBE, 0.51+/-0.24 for ETBE and 1.14+/-0.25 for TAME at a 1 mM substrate concentration. These activity levels were not significantly different from those of the sex- and age-matched C57BL/6N and 129/Sv mice, which are the parental lineage strains of the 2E1 knock-out mice and are both 2E1+/+. Our results clearly demonstrate that 2E1 plays a negligible role in the metabolism of MTBE, ETBE and TAME in mouse livers.

  8. Oil recovery with sulfomethylated poly (lower alkyl vinyl ether/maleic anhydride)

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


    Lower alkyl vinyl ether e.g., methyl vinyl ether, propyl vinyl ether, isopropyl vinyl ether, hexyl vinyl ether, is copolymerized conventionally with maleic anhydride, the resulting copolymer is treated with ammonia or ammonium hydroxide to form the partial amide-ammonium salt, and this salt is in turn treated with formaldehyde and thereafter or simultaneously with ammonium or alkali metal salt sulfite (including bisulfites, etc.) to form an at least partially sulfomethylated copolymer. Aqueous solutions of the sulfomethylated copolymer are useful in increasing the viscosity of drive fluids used in the supplemented recovery of petroleum from subterranean formations. In general, enhancing the polyionic character of mobility control agents used in supplemented recovery of petroleum provides enhanced recovery. Achieving this enhancement of polyionic character through use of sulfonate groups provides a mobility control agent with good ability to sustain viscosity in the presence of brine and lime, usually present in the connate waters of petroleum-bearing formations. (7 claims)

  9. Sorbents based on crown ethers: preparation and application for the sorption of strontium

    Bezhin, N. A.; Dovhyi, I. I.


    The key approaches to the synthesis of crown ether-based sorbents, including immobilization both with and without covalent bonding, are reviewed. Examples of sorbent preparation using anodic oxidation, chemical modification of polymers, polycondensation reactions, chemical modification of inorganic supports and radiochemical synthesis for covalent bonding of crown ether moieties are considered. Immobilization methods without covalent bonding including support synthesis in the presence of crown ethers, impregnation of supports with a crown ether solution and the use of powdered crown ether as a sorbent are presented. The applications of sorbents for selective removal of strontium from solutions of radioactive waste and spent nuclear fuel, for radiochemical analysis (determination of strontium in water, soil and biological materials) and for separation of strontium and yttrium isotopes are discussed. The bibliography includes 114 references.

  10. Rational Design of Cesium-Selective Ionophores and Chemosensors: Dihydrocalix[4]arene Crown-6 Ethers

    Sachleben, Richard A.; Bryan, Jeffrey C.; Brown, Gilbert M.; Engle, Nancy L.; Haverlock, Tamara J.; Hay, Benjamin P.; Urvoas, Agathe; Moyer, Bruce A.


    Molecular mechanics calculations performed on calix[4]arene crown-6 ethers predict that the 1,3-dihydro derivatives will exhibit greater complementarity for potassium and cesium ions than the parent 1,3-dialkoxy calix crowns. The X-ray crystal structures of 1,3-alt bis-octyloxycalix[4]arene benzocrown-6 ether, dihydrocalix[4]arene benzocrown-6 ether, and the cesium nitrate complex of dihydrocalix[4]arene benzocrown-6 ether were determined. The cesium complex structure corresponds closely to the structure predicted by molecular mechanics. The dihydrocalix[4]arene crown-6 ethers exhibit enhanced cesium selectivity in the extraction of alkali metal salts and provide a platform for a highly sensitive and selective cesium chemosensor.

  11. Identification of oxygenated ions in premixed flames of dimethyl ether and oxygen

    Frøsig Østergaard, L.; Egsgaard, H.; Hammerum, S.


    dimethyl ether, (CH3)(2)OH+. The flame-ion m/z 61 is a mixture of the trimethyloxonium ion, (CH3)(3)O+ and lesser amounts of protonated methyl formate and/or protonated ethyl methyl ether. The viability of an ionic mechanism to soot formation for dimethyl ether-oxygen flames is discussed on the background......The structure of characteristic flame-ions in premixed flames of dimethyl ether and oxygen was studied by ion-molecule reactions with ammonia and collision activation with argon. The results obtained show that the flame-ions m/z 45 and m/z 47 are the methoxymethyl cation, CH3OCH2+, and protonated...... of ions present in the dimethyl ether flames and the reactivity of the ions....

  12. Design and Implementation of EtherCAT Master Based on ARM + FPGA%基于ARM+FPGA的EtherCAT主站设计及实现

    徐健; 唐小琦; 宋宝



  13. An Implementation of Open CNC Based on EtherCAT Network%一种基于EtherCAT网络的开放式CNC实现

    李欣; 张彩虹; 梁艺


    文章分析了EtherCAT工业以太网的特点、性能及主从站通信原理。在开放式CNC主站内核中嵌入帧处理函数,从而将EtherCAT与CNC联系起来,实现一种基于EtherCAT协议的开放式网络化CNC系统,为进一步提高CNC系统的开放性和可靠性,降低系统对硬件的依赖性和整机成本开辟了新的思路。%The features, functions and working principles of Ether CAT Network are analyzed. By inserting frame-processing function into the open CNC, EtherCAT is connected with CNC,an open network CNC system based on EtherCAT protocol was implemented. This work opened a new way for further enhancing the openness and reliability of the CNC system, reducing the reliance on hardware and saving the cost of CNC system.

  14. A method of communication between EPICS IOC and EtherCAT devices%EPICS IOC与EtherCAT设备通信的一种方法

    何泳成; 王春红; 吴煊


    EtherCAT (Ethemet Control Automation Technology)是一种用于工业自动化的实时以太网现场总线协议.通过使用OPC (Object Linking and Embedding for Process Control) Gateway驱动程序实现了EPICS(Experimental Physics and Industrial Control System) IOC (Input/Output Controller)与EtherCAT设备的通信,从而使EtherCAT成为加速器控制系统中对实时性要求很高的高速控制系统的一种解决方案.在简要介绍EPICS、EtherCAT、OPC及OPC Gateway的基础上,对使用OPC Gateway驱动程序实现EPICS IOC与EtherCAT设备通信进行了测试.结果表明,EPICS IOC可通过OPC Gateway驱动程序与EtherCAT设备正常通信.

  15. 3'-O-(5-fluoro-2,4-dinitrophenyl)ADP ether and ATP ether. Affinity reagents for labeling ATPases.

    Chuan, H; Wang, J H


    The affinity reagents 3'-O-(5-fluoro-2,4-dinitrophenyl)ADP ether (FDNP-ADP) and 3'-O-(5-fluoro-2,4-dinitrophenyl)ATP ether (FDNP-ATP) were synthesized and characterized. FDNP[14C]ADP was found to label the active site of mitochondrial F1-ATPase slowly at room temperature but with high specificity. F1 was effectively protected from the labeling reagent by ATP or ADP. An average number of 1.3 covalent label per F1 is sufficient for 100% inhibition of the ATPase. About 73% of the radioactive label was found covalently attached to beta subunits, 9% on alpha, practically none on gamma, delta, and epsilon. Cleavage of the labeled enzyme by pepsin and sequencing of the major radioactive peptide showed that the labeled amino acid residue in beta subunit was Lys beta 162. These results show that Lys beta 162 is indeed at the active site of F1 as assumed in the recently proposed models (Fry, D. C., Kuby, S. A., and Mildvan, A. S. (1986) Proc. Natl. Acad. Sci. U. S. A. 83, 907-911; Duncan, I. M., Parsonage, D., and Senior, A. E. (1986) FEBS Lett. 208, 1-6).

  16. Surface modification of poly(ether ether ketone) with methacryloyl-functionalized phospholipid polymers via self-initiation graft polymerization.

    Kawasaki, Yoshihiro; Iwasaki, Yasuhiko


    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.

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

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


    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.

  18. Effect of surface finishing on friction and wear of Poly-Ether-Ether-Ketone (PEEK under oil lubrication

    Thiago Fontoura de Andrade

    Full Text Available Abstract The tribological properties of poly-ether-ether-ketone (PEEK containing 30% of carbon fiber were studied in an oil-lubricated environment and different surface finishing of the metallic counterbody. Four different finishing processes, commonly used in the automotive industry, were chosen for this study: turning, grinding, honing and polishing. The test system used was tri-pin on disc with pins made of PEEK and counterbody made of steel; they were fully immersed in ATF Dexron VI oil. Some test parameters were held constant, such as the apparent pressure of 2 MPa, linear velocity of 2 m/s, oil temperature at 85 °C, and the time - 120 minutes. The lubrication regime for the apparent pressure of 1 MPa to 7 MPa range was also studied at different sliding speeds. A direct correlation was found between the wear rate, friction coefficient and the lubrication regime, wherein wear under hydrodynamic lubrication was, on average, approximately 5 times lower, and the friction coefficient 3 times lower than under boundary lubrication.

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

    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)


    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)

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

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


    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.

  1. Low-Temperature Oxidation of Dimethyl Ether to Polyoxymethylene Dimethyl Ethers over CNT-Supported Rhenium Catalyst

    Qingde Zhang


    Full Text Available Due to its excellent conductivity, good thermal stability and large specific surface area, carbon nano-tubes (CNTs were selected as support to prepare a Re-based catalyst for dimethyl ether (DME direct oxidation to polyoxymethylene dimethyl ethers (DMMx. The catalyst performance was tested in a continuous flow type fixed-bed reactor. H3PW12O40 (PW12 was used to modify Re/CNTs to improve its activity and selectivity. The effects of PW12 content, reaction temperature, gas hourly space velocity (GHSV and reaction time on DME oxidation to DMMx were investigated. The results showed that modification of CNT-supported Re with 30% PW12 significantly increased the selectivity of DMM and DMM2 up to 59.0% from 6.6% with a DME conversion of 8.9%; besides that, there was no COx production observed in the reaction under the optimum conditions of 513 K and 1800 h−1. The techniques of XRD, BET, NH3-TPD, H2-TPR, XPS, TEM and SEM were used to characterize the structure, surface properties and morphology of the catalysts. The optimum amount of weak acid sites and redox sites promotes the synthesis of DMM and DMM2 from DME direct oxidation.

  2. Polybrominated Diphenyl Ethers Alter Hepatic Phosphoenolpyruvate Carboxykinase Enzyme Kinetics in Male Wistar Rats: Implications for Lipid and Glucose Metabolism

    Polybrominated diphenyl ethers (PBDE) are a family of lipophilic brominated flame-retardants consisting of 209 possible congeners. Three PBDE commercially-produced mixtures are decabrominated diphenyl ether (e.g. deca-BDE or DE-83R); octabrominated diphenyl ether (e.g. octa-BDE o...

  3. Computational Approach to Diarylprolinol-Silyl Ethers in Aminocatalysis.

    Halskov, Kim Søholm; Donslund, Bjarke S; Paz, Bruno Matos; Jørgensen, Karl Anker


    Asymmetric organocatalysis has witnessed a remarkable development since its "re-birth" in the beginning of the millenium. In this rapidly growing field, computational investigations have proven to be an important contribution for the elucidation of mechanisms and rationalizations of the stereochemical outcomes of many of the reaction concepts developed. The improved understanding of mechanistic details has facilitated the further advancement of the field. The diarylprolinol-silyl ethers have since their introduction been one of the most applied catalysts in asymmetric aminocatalysis due to their robustness and generality. Although aminocatalytic methods at first glance appear to follow relatively simple mechanistic principles, more comprehensive computational studies have shown that this notion in some cases is deceiving and that more complex pathways might be operating. In this Account, the application of density functional theory (DFT) and other computational methods on systems catalyzed by the diarylprolinol-silyl ethers is described. It will be illustrated how computational investigations have shed light on the structure and reactivity of important intermediates in aminocatalysis, such as enamines and iminium ions formed from aldehydes and α,β-unsaturated aldehydes, respectively. Enamine and iminium ion catalysis can be classified as HOMO-raising and LUMO-lowering activation modes. In these systems, the exclusive reactivity through one of the possible intermediates is often a requisite for achieving high stereoselectivity; therefore, the appreciation of subtle energy differences has been vital for the efficient development of new stereoselective reactions. The diarylprolinol-silyl ethers have also allowed for novel activation modes for unsaturated aldehydes, which have opened up avenues for the development of new remote functionalization reactions of poly-unsaturated carbonyl compounds via di-, tri-, and tetraenamine intermediates and vinylogous iminium ions

  4. Single-walled carbon nanotubes as an effective adsorbent in solid-phase microextraction of low level methyl tert-butyl ether, ethyl tert-butyl ether and methyl tert-amyl ether from human urine.

    Rastkari, Noushin; Ahmadkhaniha, Reza; Yunesian, Masud


    Carbon nanotubes (CNTs) are a kind of new carbon-based nano-materials which have drawn great attention in many application fields. The potential single-walled carbon nanotubes (SWCNTs) as solid-phase microextraction (SPME) adsorbents for the preconcentration of environmental pollutants have been investigated in recent years. The goal of this work was to investigate the feasibility of SWCNTs used as adsorbents for solid-phase microextraction of methyl tert-butyl ether (MTBE), ethyl tert-butyl ether (ETBE) and tert-amyl methyl ether (TAME) in human urine. SWCNTs were attached onto a stainless steel wire through organic binder. Potential factors affecting the extraction efficiency were optimized, including extraction time, extraction temperature, desorption time, desorption temperature, and salinity. The developed method showed good performance according to the ICH performance criteria for bioanalytical methods. The calibration curves of the ethers were linear (r(2)>or=0.992) in the range from 10 to 5000 ng L(-1). The limits of detection at a signal-to-noise (S/N) ratio of 3 were 10 ng L(-1) for all the analytes. In addition, compared with the commercial carboxen/polydimethylsiloxane (CAR/PDMS) fiber, the SWCNT fiber showed better thermal stability (over 350 degrees C) and longer life span (over 150 times). The developed method was applied successfully to determine trace level of the ethers in urine of 10 healthy male volunteers.

  5. Hydrogen Production with Steam Reforming of Dimethyl Ether

    Kaoru TAKEISHI; Akane ARASE


    @@ 1Introduction Steam reforming of methanol and gasoline is actively researched and developed as hydrogen supply methods for the fuel cells of vehicles and so on. However, these materials have the problems such as the infrastructure, toxicity, difficulty of the reforming, and so forth. Dimethyl ether (DME) does not contain the poisonous substances, and is expected as a clean fuel of the next generation. DME is able to take the place of light oil and LPG, and its physical properties are similar to those of LPG. There is possibility that DME infrastructures will be settled more rapidly than those of hydrogen and methanol, because LPG infrastructures existing are able to use for DME. Then, we have been studying on steam reforming of DME for the hydrogen production.

  6. Homogeneous Charge Compression Ignition Combustion of Dimethyl Ether

    Pedersen, Troels Dyhr

    This thesis is based on experimental and numerical studies on the use of dimethyl ether (DME) in the homogeneous charge compression ignition (HCCI) combustion process. The first paper in this thesis was published in 2007 and describes HCCI combustion of pure DME in a small diesel engine. The tests...... a substantial combustion delay in HCCI operation with DME to achieve post TDC combustion. By adding methanol to the inlet port during HCCI combustion of DME, the engine reached 50 percent of its full DI CI load capability without engine knock at 1000 rpm and somewhat less at 1800 rpm. The engine also had EGR...... were designed to investigate the effect of engine speed, compression ratio and equivalence ratio on the combustion timing and the engine performance. It was found that the required compression ratio depended on the equivalence ratio used. A lower equivalence ratio requires a higher compression ratio...

  7. Study of expoxy resins modified by soluble poly (ether ether ketone) and poly (ether ether ketone)%可溶性聚醚醚酮改性环氧树脂的研究

    孙攀; 史翎; 张军营


    A series of epoxy resins modified soluble poly ( ether ether ketone) (s-PEEK) have been prepared by a hot-melt method. The resulting modified epoxy resins were compared with epoxy resins modified with poly ( ether ether ketone) (PEEK). The effect of the type of PEEK and its content on the gelation time, impact strength, flexural properties and fracture morphology of the resulting materials were studied and the glass transition temperatures (Tg) and thermal stabilities of the modified materials were compared. The experimental results showed that the impact properties, flexural properties, Tg and thermal stability were all improved by addition of both types of PEEK. The impact strength of the cured materials (with a mass ratio of epoxy resin to s-PEEK or PEEK of 100: 5) were 42.6 and 46.6 kJ/m2 , respectively, representing increases in the values for the pure epoxy resin of 69.1% and 85.6%, respectively. When the mass ratio of epoxy resin to s-PEEK was 100: 25, the value of Tg was about 179.1 ℃. Scanning electron microscopy showed that the s-PEEK-toughened epoxy resins were homogeneous systems, while the PEEK toughened epoxy resins were granule-enforced systems.%采用热熔法制备了一系列可溶性聚醚醚酮(s-PEEK)改性环氧树脂(EP),并与普通聚醚醚酮(PEEK)改性环氧体系进行比较,探讨了聚醚醚酮类型、用量对改性树脂固化体系的凝胶时间、冲击强度、弯曲性能和断裂形貌的影响,并对含s-PEEK树脂体系的玻璃化转变温度(Tg)和热稳定性进行了分析.结果表明,s-PEEK和PEEK可在提高环氧体系冲击性能的同时,提高材料的弯曲性能、玻璃化温度和热稳定性;当m(s-PEEK):m(E-51)和m(PEEK):m(E-51)均为5:100时,冲击强度达到42.6和46.6 kJ/m2,分别比未改性的环氧体系提高69.1%和85.6%;m(s-PEEK):m(E-51)=25:100时,Tg=179.1℃,比未改性环氧树脂提高20℃左右;且含s-PEEK的体系是均相体系,含s-PEEK的固化物是颗粒增强体系.

  8. Ether lipids from thermophilic archaea; Konetsusei kosaikin no eteru shishitsu

    Sugai, A. [Kitazato Univ., Kanagawa (Japan). Center of Liberal Arts and Sciences


    The lipids of the archaebacteria grown at ambient temperature are fundamentally archaeol in which sn-2 and sn-3 of glycerol are ether linked with C20 phytanol, while the lipids of the archaebacteria grown at high temperature are mainly caldarchaeol of a tetraether type with a structure in which two molecules of confronted diether lipid are linked by condensation of each hydrocarbon terminal or calditocaldarchaeol incorporating calditol instead of one of two glycerol moieties. The thermophilic archaea is classified into two types, i.e., those grown in a strongly acidic condition and others living around neutral condition. The former consists of tetraether type lipids without exception. Main lipids of the archaea belonging to family Sulfolobaceae are calditocaldarchaeol. This characteristic structure probably contribute to the acid resistance and thermal resistance of these archaea. The present status of the studies on the lipids from thermophilic archaea grown around neutral condition under high pressure are also outlined. 39 refs., 4 figs., 2 tabs.

  9. Calorimetric study of binding of some disaccharides with crown ethers

    Davydova, Olga I.; Lebedeva, Nataliya Sh.; Parfenyuk, Elena V


    Isothermal titration calorimetry has been applied to the determination of the thermodynamic parameters of binding of {beta}-lactose, {alpha},{alpha}-trehalose and sucrose with 15-crown-5 and 18-crown-6 in water at 298.15 K. The formation of 1:1 molecular associates has been found for the systems studied except 18-crown-6 and {beta}-lactose. The associates are preferentially or completely entropy stabilized. The most stable associate is formed between {alpha},{alpha}-trehalose and 18-crown-6. The obtained values of thermodynamic parameters of binding are discussed from the point of view of solute-solvent interactions as well as conformational and structural peculiarities of the disaccharides (DS) and crown ethers (CE)

  10. Fibril Formation and Phase Separation in Aqueous Cellulose Ethers

    Maxwell, Amanda; Schmidt, Peter; McAllister, John; Lott, Joseph; Bates, Frank; Lodge, Timothy

    Aqueous solutions of many cellulose ethers are known to undergo thermoreversible gelation and phase separation upon heating to form turbid hydrogels, but the mechanism and resulting structures have not been well understood. Turbidity, light scattering and small-angle neutron scattering (SANS) are used to show that hydroxypropyl methylcellulose (HPMC) chains are dissolved in water below 50 °C and undergo phase separation at higher temperatures. At 70 °C, at sufficiently high concentrations in water, HPMC orders into fibrillar structures with a well-defined radius of 18 +/- 2 nm, as characterized by cryogenic transmission electron microscopy and SANS. The HPMC fibril structure is independent of concentration and heating rate. However, HPMC fibrils do not form a percolating network as readily as is seen in methylcellulose, resulting in a lower hot-gel modulus, as demonstrated by rheology.

  11. New controllable premixed combustion for dimethyl ether engine


    A new concept of the controllable premixed combustion (CPC) system was proposed for dimethyl ether (DME) to explore a new approach to achieving ultra-low NOX emissions with the zero level of particulate matter exhaust emissions. The DME fuel was injected into the premix chamber by means of the electronically controlled low pressure injection system, then the mixture formation and combustion process were controlled with a control-valve set between the main chamber and the premix chamber. The test bench was constructed based on a single diesel engine. Preliminary studies demonstrated that ultra-low NOX emissions had been realized with zero particulate matter emissions under the optimum specifications of the DME engine, NOX emissions were less than 65 × 10-6. According to the engine combustion analysis, it was found that the control-valve played an important role in the pre-mixture formation and ignition timing.

  12. Time resolve study on isopropyl-ether porphyrindiol

    ZHANG; Lianwen; (张连文); YAO; Side; (姚思德); LIN; Weizhen; (林维真); CHEN; Zhilong; (陈志龙)


    A novel fat-soluble porphyrin derivative--isopropyl-ether porphyrindiol (IPEP) has been investigated using the nanosecond laser photolysis and pulse radiolysis. In acetonitrile, IPEP-excited triplet state shows two relative absorption areas peaking at 320 and 430 nm, molar extinction coefficients by energytransfer method (in benzene solution) are proved to be ε(315) = 1.07×105, ε(450) = 3.3×104 L3@mol-1@cm-1 and the excited triplet state quantum yield by comparative method is 0.18. Laser photolysis of IPEP in dGMP-containing solutionshows that the triplet state cannot excite/oxidize dGMP via the energy/electrontransfer process.

  13. Polybrominated diphenyl ethers in Mississippi River suspended sediment

    Raff, J.; Hites, R. [Indiana Univ., Bloomington, IN (United States)


    The Mississippi River Basin drains water from 41% of the conterminous U.S. and is a valuable resource that supplies food, transportation, and irrigation to more than 95 million people of the region. Discharge and runoff from industry, agriculture, and population centers have increased the loads of anthropogenic organic compounds in the river. There has been growing concern over the rising levels of polybrominated diphenyl ethers (PBDEs) in air, sediment, biota, and humans, but there have been no studies to measure the concentrations of these chemicals in North America's largest river system. The goal of this study was to investigate the occurrence of PBDEs (15 congeners including BDE-209) and to identify possible sources within the Mississippi River Basin. We found PBDEs to be widespread throughout the region, rivaling PCBs in their extent and magnitude of contamination. We have also calculated the total amount of PBDEs released to the Gulf of Mexico in 2002.

  14. Tiny pollutant emissions of a dimethyl ether fuelled engine

    LANG Jing; ZHANG Yu-sheng; ZHOU Xiao-song; WU Hong-wei


    Emissions of dimethyl ether (DME) fuelled engines were investigated by orthogonal experiments on a ZS195 diesel engine. The study mainly focused on the tiny pollutant emissions of formaldehyde (CH2O), methyl formate (CH3OCHO) and formic acid (HCOOH). The presence of CH2O, CH3OCHO and HCOOH are proved in the exhaust by gas chromatograph and Fourier transform infrared spectroscopy. The analysis of variance results indicate that the fuel delivery advance angle is the most important factor for CH2O emission. The fuel delivery advance angle and the interaction of injection pressure and nozzle diameter are considerable factors for unburned hydrocarbon (UHC) emission. The mechanism forming tiny pollutants, primarily through CH2O formation, is suggested to be similar to the mechanism forming UHC by DME partial oxidation existing in crevices and boundary zones, and is verified via DME combustion simulation of a multizone chemical kinetic model.

  15. Servo Making Wave Control System Based on EtherCAT%基于EtherCAT网络的伺服造波控制系统

    聂俊杰; 徐东亮; 王龙飞; 陈宗雨


    介绍了TwinCAT和EtherCAT的基本特性。阐述了构建EtherCAT网络伺服造波控制系统的硬件结构和软件流程。该系统采用安装德国 Beckhoff公司的TwinCAT软件的工控机作为主站、基于伦茨EtherCAT的数字伺服驱动器I700作从站、菲仕同步交流伺服电机U725.20.3作执行机构。对EtherCAT 的主从站进行了一系列的配置,编写 TwinCAT PLC 程序,结合驱动器的 PID 算法,实现了造波板的高精度同步。%Introduces the basic characteristics of TwinCAT and EtherCAT. And describes the hardware structure and software of the system. Using Beckoff company's TwinCAT software as soft master device, Lenze EtherCAT-based digital servo drive I700 as slave device, Phase synchronous AC servo motor U725. 20. 3 as actuator, formed the system. The EtherCAT master and slave station conducted a series of configu-ration, and write TwinCAT PLC program, and combined with PID algorithm of the drive, the wave-maker boards have a high-precision synchronization.

  16. Liquid/air partition coefficients of methyl and ethyl T-butyl ethers, T-amyl methyl ether, and T-butyl alcohol.

    Nihlen, A; Lof, A; Johanson, G


    Partition coefficients are essential to a description of the uptake and distribution of volatile substances in humans and in the development of physiologically based pharmacokinetic models. Liquid/air partition coefficients (lambda) of three ethers, methyl t-butyl ether (MTBE), ethyl t-butyl ether (ETBE), and t-amyl methyl ether (TAME) were determined in vitro by head space-gas chromatography. These ethers, and especially MTBE, are used in unleaded gasoline to enhance the oxygen and octane content, and to reduce the output of carbon monoxide during combustion. Partition coefficients of t-butyl alcohol (TBA), a metabolite of MTBE, were determined also. The liquids tested were fresh human blood, water (physiological saline), and olive oil. The (lambda)blood/air values were: 17.7 (95% confidence interval 17.0-18.4) for MTBE; 11.7 (11.3-12.1) for ETBE; and 17.9 (17.3-18.5) for TAME. Corresponding (lambda)water/air values were 15.2 (14.9-15.5), 8.39 (8.19-8.59), and 11.9 (11.7-12.1). The ethers have a higher affinity for oil, the values for (lambda)oil/air being 120 (114-125), 190 (183-197), and 337 (320-354), respectively. As expected, the (lambda)blood/air and (lambda)water/air for TBA were much higher than for the ethers, 462 (440-484) and 603 (590-617), respectively. The (lambda)oil/air was 168 (161-174) for TBA. The interindividual variability of the (lambda)blood/air (10 subjects) was calculated as the coefficient of variation, and estimated as: 14% for MTBE, 20% for ETBE, 20% for TAME, and 30% for TBA. No significant difference was seen in the (lambda)blood/air between the sexes.

  17. Searching for trans ethyl methyl ether in Orion KL(.)

    Tercero, B; Cernicharo, J; López, A; Brouillet, N; Kolesniková, L; Motiyenko, R A; Margulès, L; Alonso, J L; Guillemin, J-C


    We report on the tentative detection of trans ethyl methyl ether (tEME), t-CH3CH2OCH3, through the identification of a large number of rotational lines from each one of the spin states of the molecule towards Orion KL. We also search for gauche-trans-n-propanol, Gt-n-CH3CH2CH2OH, an isomer of tEME in the same source. We have identified lines of both species in the IRAM 30 m line survey and in the ALMA Science Verification data. We have obtained ALMA maps to establish the spatial distribution of these species. Whereas tEME mainly arises from the compact ridge component of Orion, Gt-n-propanol appears at the emission peak of ethanol (south hot core). The derived column densities of these species at the location of their emission peaks are ≤(4.0 ± 0.8) × 10(15) cm(-2) and ≤(1.0 ± 0.2)× 10(15) cm(-2) for tEME and Gt-n-propanol, respectively. The rotational temperature is ~100 K for both molecules. We also provide maps of CH3OCOH, CH3CH2OCOH, CH3OCH3, CH3OH, and CH3CH2OH to compare the distribution of these organic saturated O-bearing species containing methyl and ethyl groups in this region. Abundance ratios of related species and upper limits to the abundances of non-detected ethers are provided. We derive an abundance ratio N(CH3OCH3)/N(tEME) ≥ 150 in the compact ridge of Orion.

  18. Alternariol 9-methyl ether from the endophytic fungus Alternaria sp. Samif01 and its bioactivities

    Jingfeng Lou


    Full Text Available Abstract One bioactive compound, identified as alternariol 9-methyl ether, was isolated from the crude extract of the endophytic fungus Alternaria sp. Samif01 residing in the roots of Salvia miltiorrhiza Bunge. Alternariol 9-methyl ether was active against bacteria with minimum inhibitory concentration values ranging from 25 to 75 µg/mL and median inhibitory concentration (IC50 values ranging from 16.00 to 38.27 µg/mL. The IC50 value of alternariol 9-methyl ether against spore germination of Magnaporthe oryzae was 87.18 µg/mL. Alternariol 9-methyl ether also showed antinematodal activity against Bursaphelenchus xylophilus and Caenorhabditis elegans with IC50 values of 98.17 µg/mL and 74.62 µg/mL, respectively. This work is the first report on alternariol 9-methyl ether and its biological activities from the endophytic fungus Alternaria sp. Samif01 derived from S. miltiorrhiza Bunge. The results indicate the potential of Alternaria sp. Samif01 as a source of alternariol 9-methyl ether and also support that alternariol 9-methyl ether is a natural compound with high potential bioactivity against microorganisms.

  19. Alternariol 9-methyl ether from the endophytic fungus Alternaria sp. Samif01 and its bioactivities.

    Lou, Jingfeng; Yu, Ruiting; Wang, Xiaohan; Mao, Ziling; Fu, Linyun; Liu, Yang; Zhou, Ligang


    One bioactive compound, identified as alternariol 9-methyl ether, was isolated from the crude extract of the endophytic fungus Alternaria sp. Samif01 residing in the roots of Salvia miltiorrhiza Bunge. Alternariol 9-methyl ether was active against bacteria with minimum inhibitory concentration values ranging from 25 to 75μg/mL and median inhibitory concentration (IC50) values ranging from 16.00 to 38.27μg/mL. The IC50 value of alternariol 9-methyl ether against spore germination of Magnaporthe oryzae was 87.18μg/mL. Alternariol 9-methyl ether also showed antinematodal activity against Bursaphelenchus xylophilus and Caenorhabditis elegans with IC50 values of 98.17μg/mL and 74.62μg/mL, respectively. This work is the first report on alternariol 9-methyl ether and its biological activities from the endophytic fungus Alternaria sp. Samif01 derived from S. miltiorrhiza Bunge. The results indicate the potential of Alternaria sp. Samif01 as a source of alternariol 9-methyl ether and also support that alternariol 9-methyl ether is a natural compound with high potential bioactivity against microorganisms.

  20. Discrimination against diacylglycerol ethers in lipase-catalysed ethanolysis of shark liver oil.

    Fernández, Óscar; Vázquez, Luis; Reglero, Guillermo; Torres, Carlos F


    Lipase-catalysed ethanolysis of squalene-free shark liver oil was investigated. The mentioned shark liver oil was comprised mainly of diacylglycerol ether and triacylglycerols. In order to test discrimination against diacylglycerol ether, up to 10 different lipases were compared. The ratio of oil to ethanol and lipase stability were also evaluated. Surprisingly, lipase from Pseudomonas stutzeri was the fastest biocatalyst among all assayed, although poor discrimination against diacylglycerol ether was observed. The best results in terms of selectivity and stability were obtained with immobilised lipase from Candida antarctica (Novozym 435). Ethanolysis reaction after 24h in the presence of Novozym 435 produced total disappearance of triacylglycerol and a final reaction mixture comprised mainly of diacylglycerol ethers (10.6%), monoacylglycerol ethers (32.9%) and fatty acid ethyl esters (46.0%). In addition, when an excess of ethanol was used, diacylglycerol ethers completely disappeared after 15 h, giving a final product mainly composed of monoacylglycerol ethers (36.6%) and fatty acid ethyl esters (46.4%).

  1. Furfuryl ethyl ether: important aging flavor and a new marker for the storage conditions of beer.

    Vanderhaegen, Bart; Neven, Hedwig; Daenen, Luk; Verstrepen, Kevin J; Verachtert, Hubert; Derdelinckx, Guy


    Recently, it was reported that furfuryl ethyl ether is an important flavor compound indicative of beer storage and aging conditions. A study of the reaction mechanism indicates that furfuryl ethyl ether is most likely formed by protonation of furfuryl alcohol or furfuryl acetate followed by S(N)2-substitution of the leaving group by the nucleophilic ethanol. For the reaction in beer, a pseudo-first-order reaction kinetics was derived. A close correlation was found between the values predicted by the kinetic model and the actual furfuryl ethyl ether concentration evolution during storage of beer. Furthermore, 10 commercial beers of different types, aged during 4 years in natural conditions, were analyzed, and it was found that the furfuryl ethyl ether flavor threshold was largely exceeded in each type of beer. In these natural aging conditions, lower pH, darker color, and higher alcohol content were factors that enhanced furfuryl ethyl ether formation. On the other hand, sulfite clearly reduced furfuryl ethyl ether formation. All results show that the furfuryl ethyl ether concentration is an excellent time-temperature integrator for beer storage.

  2. Performance evaluation of the Switched EtherCAT networks with VLAN tagging

    Knežić Mladen


    Full Text Available EtherCAT technology is one of the most popular Real-Time Ethernet (RTE solutions present on the market at this time. Due to its communication efficiency, EtherCAT is particularly suitable for networks with a large number of devices which demand short cycle times. This paper reviews the application aspects and implementation issues of the Switched EtherCAT networks with VLAN tagging, including their limitations, and provides guidelines for engineering staff in selection of the optimal solution when designing a specific automation system.

  3. EtherCAT已来到中国-访ETG执行Rostan先生



  4. 欧姆龙选用EtherCAT作为运动控制总线


    EtherCAT技术协会(ETG)新闻发布会上,欧姆龙集团运动控制分部的总经理Eiji Ikeno先生宣布,欧姆龙决定选用EtherCAT作为其下一代运动控制总线系统。欧姆龙将在ETG日本和亚洲市场扮演更加活跃的会员角色,其用户可平稳无缝过渡到EtherCAT技术的应用上。

  5. 丰田选择EtherCAT作为其工业以太网技术



  6. EtherCAT技术协会盛装亮相SIAF2012



  7. Evaluation of thermal gelation behavior of different cellulose ether polymers by rheology

    Balaghi, S.; Edelby, Y.; Senge, B.


    Hydroxypropylmethylcellulose (HPMC) and Methylcellulose (MC) are cellulose ethers which can be dispersed in water and used as thickeners, emulsifiers, binders, film formers, and water-retention agents due to their hydrophilic and hydrophobic characteristics. In this study, various types of HPMCs, in comparison with two types of MCs were examined. The formed gels of the different cellulose ethers showed specific and various structural formation and network properties. The degree of methylation (Meth.) and hydroxypropylation (HyPr.) affected drastically the heat-induced gelation of the examined cellulose ethers.

  8. EDTA-type Polymer Based on Diazacrown Ether as the Solubilizer of Barium Sulfate to Water

    Bo ZHOU; Jian Zhang LI; Chun Hong HE; Sheng Ying QIN


    The EDTA dianhydride reacted with diazacrown ethers to obtain the water-soluble EDTA-diazacrown ether polymers 1~3. The effects of crown ether ring in the polymer chains including its cavity size on the solubilization of barium sulfate to water were investigated by comparison with the crown ring-free analogue 4. The result shows that the polymer 2 is the efficient solubilizer of BaSO4 and the highest solubilization efficiency of the BaSO4 to water is up to 72.5%.

  9. Kinetic studies on the etherification of C5-alkenes to fuel ether tame

    Pääkkönen, Päivi


    Tertiary ethers are formed in reactions between alcohols and alkenes and are used in reformulated gasoline as octane-enhancing agents. By blending ethers into the gasoline pool, less ground-level ozone is formed and combustion of the gasoline is more efficient as a result of the oxygen boost. The main goal of this research was to study the synthesis of TAME (tert-amyl methyl ether, 2-methoxy-2-methylbutane) and to formulate a kinetic model as precise as possible for process design purpose...

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

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


    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.

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

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


    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.

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

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


    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.

  13. Distributed Measurement and Control System Based on EtherCAT Bus%基于EtherCAT总线的分布式测控系统设计

    赵君; 刘卫国; 彭喆


    介绍一种EtherCAT实时工业以太网现场总线技术,研究EtherCAT工作原理,通信协议及主、从站实现方法;针对一般工业现场测控需求,利用EtherCAT总线技术,设计基于工控机的主站管理软件和基于FPGA的嵌人式从站软硬件;应用结果表明,该分布式测控系统运行稳定可靠,数据丢失率低,实时性好.%A more reliable distributed measurement and control system is introduced. Based on EtherCAT bus-, in this thesis. And They are introduced, the principle, technical characteristic and capability of EtherCAT. According to the most tasks demand of measuring and controU the design method was presented, the process of how to configuring the master node based on IPC and Slave node based on FPGA. And how to managing the system. The application results show that there are low data loss rate and more real-time, and the performance is stable and reliable in this system.

  14. EtherCAT协议芯片与单片机通信系统的研究%The research of communication system based EtherCAT and MCU

    康存锋; 杜斐斐; 马春敏; 黄旭东; 费仁元


    EtherCAT是基于标准的以太网技术,具有灵活的网络拓扑结构,系统配置简单,具有高速、高有效数据率等特点,其有效数据率可达90%以上.PIC系列单片机和EtherCAT协议芯片通过SPI串行通信方式进行连接,实现基于EtherCAT协议通信系统的基本通信功能,解决了传统以太网的介质访问控制方式不能满足工业现场实时性要求的问题.系统测试实验表明,系统通信准确,运行稳定,而且通过分析系统通信过程中的报文可知,系统的通信完全符合EthercAT 协议的要求.%EtherCAT based measured Ethernet technology has flexible framework of topology of network, simple of configure of system, and it has character of high speed and percentage of available date, which can reach ninety percent. It has solved problem of real time of Ethernet. The PIC series MCU was selected to communicated with EtherCAT by SPI connection. The result of experiment show that exact communication and stably system.

  15. Synthesis, Characterization and Performance Study of Phosphosilicate Gel-Sulfonated Poly (Ether Ether Ketone Nanocomposite Membrane for Fuel Cell Application

    S. Ganguly


    Full Text Available Phosphosilicate gel – SPEEK (Sulfonated Poly Ether Ether Ketone hybrid nanocomposite membranes are proposed for performance enhancement of polymer electrolyte fuel cell. The nanocomposite membranes are synthesized and characterized at 50 and 60 weight percent of inorganic loading. Phosphosilicate gel particles of varying size (sub micro to nanometer are synthesized using sol gel approach followed by grinding using planetary ball mill for different time. Transmission Electron Microscopy (TEM reveals less than 10 nm particle size for 20 hr grinding. Nano composite membrane having inorganic particles of size less than 10 nm exhibits higher values of proton conductivity, ion exchange capacity and water uptake compared to composite membrane comprising of larger (400 nm and above inorganic particles. The membrane is assembled with the electrode in the unit cell and the polarization characteristics are measured at different operating temperatures. Performance study reveals that between 70 to 80 C the membrane offers best performance in terms of peak power generation and of allowable load current. For the same conditions 40-50 % nano-enhancement of peak power generation is achieved by reducing the average gel particle size from sub micro to less than 10 nm. At medium temperature (between 70 to 80 C the nanocomposite membrane offers more than 100 enhancement of peak power generation compared to that generated by SPEEK membrane. Phosphosilicate gel – SPEEK (Sulfonated Poly Ether Ether Ketone hybrid nanocomposite membranes are proposed for performance enhancement of polymer electrolyte fuel cell. The nanocomposite membranes are synthesized and characterized at 50 and 60 weight percent of inorganic loading. Phosphosilicate gel particles of varying size (sub micro to nanometer are synthesized using sol gel approach followed by grinding using planetary ball mill for different time. Transmission Electron Microscopy (TEM reveals less than 10 nm

  16. 一种高速卷烟机EtherCAT从站设计%Design of EtherCAT Slave Station for High Speed Cigarette Machine

    李源源; 张旭



  17. Chemistry and properties of poly(arylene ether 1,3,4-oxadiazole)s and poly(arylene ether 1,2,4-triazole)s

    Connell, J. W.; Hergenrother, P. M.; Wolf, P.


    Poly(arylene ether)s containing l,3,4-oxadiazole and 1,2,4-triazole units were prepared by the aromatic nucleophilic displacement reaction of bisphenol oxadiazole and bisphenol triazole compounds with activated aromatic dihalides. The polymers exhibited glass transition temperatures (Tg) ranging from 182 to 242 C, and several polymers exhibited melting transitions (Tm) ranging from 265 to 390 C. Inherent viscosities ranged from 1.02 to 3.40 dl/g, indicating relatively high molecular weights. Thin films exhibited tensile strengths, moduli, and elongations at 23 C of 90-110 MPa, 2.7-3.6 GPa, and 4-7 percent, respectively. Titanium-to-titanium tensile shear specimens of a poly(arylene ether 1,3,4-oxadiazole) exhibited tensile shear strengths at 23 and 150 C of 22.1 and 17.9 MPa, respectively.

  18. EtherCAT中国巡回研讨会即将启动



  19. EtherCAT中国巡回研讨会即将启动



  20. EtherCAT技术协会举办研发培训活动



  1. Synthesis and biological evaluation of arctigenin ester and ether derivatives as activators of AMPK.

    Shen, Sida; Zhuang, Jingjing; Chen, Yijia; Lei, Min; Chen, Jing; Shen, Xu; Hu, Lihong


    A series of new arctigenin and 9-deoxy-arctigenin derivatives bearing different ester and ether side chains at the phenolic hydroxyl positions are designed, synthesized, and evaluated for activating AMPK potency in L6 myoblasts. Initial biological evaluation indicates that some alkyl ester and phenethyl ether arctigenin derivatives display potential activities in AMPK phosphorylation improvement. Further structure-activity relationship analysis shows that arctigenin ester derivatives 3a, 3h and 9-deoxy-arctigenin phenethyl ether derivatives 6a, 6c, 6d activate AMPK more potently than arctigenin. Moreover, the 2-(3,4-dimethoxyphenyl)ethyl ether moiety of 6c has been demonstrated as a potential functional group to improve the effect of AMPK phosphorylation. The structural optimization of arctigenin leads to the identification of 6c as a promising lead compound that exhibits excellent activity in AMPK activation.

  2. Degradation of the Alternaria mycotoxins alternariol, alternariol monomethyl ether, and altenuene upon bread baking.

    Siegel, David; Feist, Michael; Proske, Matthias; Koch, Matthias; Nehls, Irene


    The stability of the Alternaria mycotoxins alternariol, alternariol monomethyl ether, and altenuene upon bread baking was investigated by model experiments using a spiked wholemeal wheat flour matrix. For alternariol and alternariol monomethyl ether, but not for altenuene, degradation products, formed through a sequence of hydrolysis and decarboxylation, could be identified in pilot studies. The simultaneous quantification of alternariol, alternariol monomethyl ether, altenuene, and the degradation products was achieved by a newly developed high performance liquid chromatography tandem mass spectrometry (HPLC-MS/MS) multimethod. The obtained quantitative data indicate that the Alternaria mycotoxins are barely degraded during wet baking, while significant degradation occurs upon dry baking, with the stability decreasing in the order alternariol monomethyl ether>alternariol>altenuene. The novel degradation products could be detected after the wet baking of flour spiked with alternariol and in a sample survey of 24 commercial cereal based baking products.

  3. Miconidin and miconidin methyl ether from Primula obconica Hance: new allergens in an old sensitizer

    Paulsen, Evy; Christensen, Lars P; Andersen, Klaus Ejner


    of the individual primin reactions, and remained inexplicably negative while testing with miconidin in 96% ethanol and pet., while miconidin methyl ether elicited 7 positive reactions. Although both miconidin and miconidin methyl ether may be allergenic only due to their conversion to primin in the skin......Several chemical and clinical observations have suggested the presence of at least one more allergen in addition to primin in Primula obconica. The aim of this study was to investigate the allergenicity of the primin precursor miconidin and the related miconidin methyl ether, both isolated from P....... obconica. 12 primin-positive persons were patch tested with miconidin 0.01% petrolatum (pet.), miconidin in 96% ethanol incorporated into 0.01% pet., and miconidin methyl ether 1.0% pet. All persons were positive to miconidin 0.01% pet., with the strength of reactions very similar to those...

  4. Oxime Ethers of (E)-11-Isonitrosostrychnine as Highly Potent Glycine Receptor Antagonists

    Mohsen, Amal M Y; Mandour, Yasmine M; Sarukhanyan, Edita


    A series of (E)-11-isonitrosostrychnine oxime ethers, 2-aminostrychnine, (strychnine-2-yl)propionamide, 18-oxostrychnine, and N-propylstrychnine bromide were synthesized and evaluated pharmacologically at human α1 and α1β glycine receptors in a functional fluorescence-based and a whole-cell patch......-clamp assay and in [(3)H]strychnine binding studies. 2-Aminostrychnine and the methyl, allyl, and propargyl oxime ethers were the most potent α1 and α1β antagonists in the series, displaying IC50 values similar to those of strychnine at the two receptors. Docking experiments to the strychnine binding site...... of the crystal structure of the α3 glycine receptor indicated the same orientation of the strychnine core for all analogues. For the most potent oxime ethers, the ether substituent was accommodated in a lipophilic receptor binding pocket. The findings identify the oxime hydroxy group as a suitable attachment...

  5. IRIS Toxicological Review of Ethylene Glycol Mono-Butyl Ether (Egbe) (External Review Draft)

    EPA has conducted a peer review of the scientific basis supporting the human health hazard and dose-response assessment of ethylene glycol monobutyl ether that will appear on the Integrated Risk Information System (IRIS) database.

  6. A versatile pathway to end-functionalized cellulose ethers for click chemistry applications.

    Kamitakahara, Hiroshi; Suhara, Ryo; Yamagami, Mao; Kawano, Haruko; Okanishi, Ryoko; Asahi, Tomoyuki; Takano, Toshiyuki


    This paper describes a versatile pathway to heterobifunctional/telechelic cellulose ethers, such as tri-O-methyl cellulosyl azide and propargyl tri-O-methyl celluloside, having one free C-4 hydroxyl group attached to the glucosyl residue at the non-reducing end for the use in Huisgen 1,3-dipolar cycloaddition and copper(I)-catalyzed azide-alkyne cycloaddition (CuAAC). The one-step end-functionalization of cellulose ethers for molecular rod synthesis involves the introduction of two reactive groups at both ends of the cellulose molecule, and can afford linear triblock copolymers via CuAAC and further reactions. We were able to tailor the degree of polymerization of end-functionalized cellulose ethers with controlled amounts of a Lewis acid, namely SnCl4. Chemical structures of the above cellulose ethers and the reaction conditions for controlling molecular length are discussed.

  7. Cholesterol-containing liquid crystal dimmers with ether linkages between the spacer and mesogenic units

    Marcelis, A.T.M.; Koudijs, A.; Karczmarzyk, Z.; Sudhölter, E.J.R.


    Three series of chiral liquid crystalline dimers were investigated, having a cholesteryl and a cyanobiphenylyl, butoxybiphenylyl or hexyloxybiphenylyl group connected to a variable alkyl spacer through ether linkages. Their properties were compared with those of the corresponding ester derivatives.

  8. Cholesterol-containing liquid crystal dimmers with ether linkages between the spacer and mesogenic units

    Marcelis, A.T.M.; Koudijs, A.; Karczmarzyk, Z.; Sudhölter, E.J.R.


    Three series of chiral liquid crystalline dimers were investigated, having a cholesteryl and a cyanobiphenylyl, butoxybiphenylyl or hexyloxybiphenylyl group connected to a variable alkyl spacer through ether linkages. Their properties were compared with those of the corresponding ester derivatives.

  9. Elton Romeo Smilie, the not-quite discoverer of ether anesthesia.

    Stone, Martha E; Meyer, Marlene R; Alston, Theodore A


    Like William T.G. Morton, Elton Romeo Smilie (1819-1889) was raised in Massachusetts, attended medical school in New England, practiced dentistry there, strove for clinical invention, and moved to Boston. In October 1846, both announced that inhaled ethereal preparations achieved reversible insensibility in surgical patients. Smilie published a report in the Boston Med Surg J 3 wk before Bigelow used that forum to broadcast Morton's Ether Day. Smilie's preparation was an ethereal tincture of opium, and, as he mistakenly believed the opium to be volatile and important, he ceded priority to Morton for ether anesthesia. The two authors collaborated on chloroform, but Smilie soon headed off in the Gold Rush to California. It is tempting to speculate that Charles T. Jackson and Morton were indebted in part to Smilie.

  10. Fluorinated 5- and 7-membered carbacycle motifs by reaction of difluorocarbene with acetylene ethers.

    Chia, Poh Wai; Bello, Davide; Slawin, Alexandra M Z; O'Hagan, David


    The reaction of acetylene ethers with difluorocarbene (CF(2)), generated from the Ruppert-Prakash reagent, unexpectedly gave rise to co-produced fluorinated bicyclic [2.1.1]-hex-2-ene and cyclohepta-1,4-diene ring products.

  11. A Study on Antibacterial Activity and Chemical Composition of the Petroleum Ether Extract from Aspergillusniger Mycelia

    Yang; XIAO; Wujuan; LIU; Zhu; LI


    In order to develop natural antibacterial agents,the antibacterial activity of Aspergillusnigerxj was investigated.After being cultured in potato dextrose liquid medium liquid medium,mycelia was under heating reflux extraction with 90% ethanol.Removal of ethanol under reduced pressure gave a residue,to which water was added and then extracted with petroleum ether and ethyl acetate.In vacuo evaporation of the solvents yielded three crude extracts.Then the disc diffusion method was used to measure the antibacterial activity of these extracts.The petroleum ether extract with antibacterial activity was separated by silica gel column chromatography method,then separated and identified by GC-MS after been methyl esterified.At the concentration of 50 mg /mL,the petroleum ether extract of mycelia exhibited inhibitory effect against Staphylococcus aureus.The petroleum ether extract from Aspergillusnigerxj mycelia contained natural substances with antibacterial activity and fatty acids are the main constituents in it.

  12. Researh and Application of Industrial Ethernet Safety Based on EtherCAT%基于EtherCAT的工业以太网安全技术的研究∗

    刘才思; 刘峰; 郑飂默; 尹震宇


    在研究EtherCAT协议栈,以及EtherCAT的软、硬件结构特性和帧结构特点的基础上,分析了EtherCAT工业以太网存在的通信故障错误,及其对应的安全通信机制措施,建立了安全系统体系结构和安全通信协议模型,设计了EtherCAT功能安全通信过程,开发了安全协议层软件。经过试验测试表明,通过在EtherCAT应用层之上添加EtherCAT安全通信,并且对EtherCAT通信报文中用户数据单元进行扩展,来实现关键安全措施,满足了安全相关领域通信的要求,保障了EtherCAT系统的安全性和可靠性。%Under the study of EtherCAT protocol stack and the characteristics of software , hardware and frame of EtherCAT , we analyzed communication faults and errors in the industrial ethernet and the counter safety communication mechanism measures, established the safety system architecture and safety communi-cation protocol model, designed the EtherCAT safety communication process, and developed safety protocol layer software. As the result of experimental test shows, by adding EtherCAT safety layer upon application layer and safety measures into user data unit with some critical safety measures, we made the protocol meet the safety requirements of communication related fields and guarantee the EtherCAT system safety and relia-bility.

  13. Research of robot control bus scheme based on EtherCAT%基于EtherCAT的机器人控制总线方案研究

    刘冬; 闵华松; 杨杰


    In view of the higher demand of communication bandwidth, response speed, real time and other aspects in current robot network control, a robot control bus solution based on EtherCAT is proposed. In the analysis of the robot control requirements and the characteristics of EtherCAT, a research platform is built using a linear topological structure. In the slave STM32 and COMX module are used to design servo controller, while in the master Linux system and RTAI module to are used construct supporting platform, and EtherCAT protocol stack SOEM is transplanted, then combined with the network control model, the distributed control of the robot servo nodes is realized. Through the experiment the feasibility of this system is verified, and the composition of bus delay is analyzed.%针对当前机器人网络化控制对通信带宽、响应速度、实时性等方面的更高要求,提出了基于EtherCAT的机器人控制总线解决方案.通过分析机器人控制的需求和EtherCAT的特点,采用线性拓扑结构来构建研究平台.从站采用STM32和COMX模块设计伺服控制器;主站采用Linux系统和RTAI模块构建支撑平台,并移植EtherCAT协议栈SOEM,结合网络控制模型来实现机器人伺服节点的分布式控制.通过实验验证了方案的可行性,并分析了总线的延时组成.

  14. Pra Desain Pabrik Dimethyl Ether (DME dari Gas Alam

    Ajeng Puspitasari Yudiputri


    Full Text Available Berdasarkan data PT Pertamina (Persero, total konsumsi LPG 2008 mencapai 1,85 juta ton dan 600.000 ton di antaranya untuk program konversi. Pada 2009 kebutuhan LPG akan meningkat menjadi 3,67 juta ton dan 2 juta ton di antaranya untuk program konversi sampai akhir tahun. Namun, sumber pasokan LPG dari dalam negeri diperkirakan tidak akan beranjak dari angka 1,8 juta ton per tahun dalam beberapa tahun mendatang. Sehingga, Indonesia harus menutup kebutuhan dengan mengimpor LPG dalam jumlah cukup besar. Maka dari itu dibutuhkan bahan bakar gas lain yang mampu mengatasi permasalahan yang ditimbulkan tersebut. Dimethyl Ether (DME merupakan senyawa ether yang paling sederhana dengan rumus kimia CH3OCH3. Produksi DME dapat dihasilkan melalui sintesis gas alam. DME berbentuk gas yang tidak berwarna pada suhu ambien, zat kimia yang stabil, dengan titik didih -25,1oC. Tekanan uap DME sekitar 0,6 Mpa pada 25oC dan dapat dicairkan seperti halnya LPG. Viskositas DME 0,12-0,15 kg/ms, setara dengan viskositas propana dan butane (konstituen utama LPG, sehingga infrastruktur untuk LPG dapat juga digunakan untuk DME. Berdasarkan data Departemen ESDM pada Januari 2012, total cadangan gas alam Indonesia tercatat mencapai 150,70 Trillion Square Cubic Feet (TSCF. Berdasarkan jumlah tersebut, sebanyak 103,35 TSCF merupakan gas alam terbukti, sementara 47,35 TSCF sisanya masih belum terbukti. Berdasarkan hal tersebut, diketahui bahwa senyawa DME merupakan senyawa yang sesuai untuk bahan substitusi LPG. Dan ditinjau dari analisa ekonomi, didapatkan besar Investasi : $ 636,447,074.69 ; Internal Rate of Return\t: 20.51%; POT: 4.13 tahun; BEP : 37.36 %; dan NPV 10 year : $ 518,848,692. Dari ketiga parameter sensitifitas yaitu fluktuasi biaya investasi, harga bahan baku, dan harga jual dari produk, terlihat bahwa ketiganya tidak memberikan pengaruh yang cukup signifikan terhadap kenaikan atau penurunan nilai IRR pabrik. Sehingga pabrik DME dari Gas Alam ini layak untuk

  15. Searching for trans ethyl methyl ether in Orion KL⋆

    Tercero, B.; Cernicharo, J.; López, A.; Brouillet, N.; Kolesniková, L.; Motiyenko, R. A.; Margulès, L.; Alonso, J. L.; Guillemin, J.-C.


    We report on the tentative detection of trans ethyl methyl ether (tEME), t-CH3CH2OCH3, through the identification of a large number of rotational lines from each one of the spin states of the molecule towards Orion KL. We also search for gauche-trans-n-propanol, Gt-n-CH3CH2CH2OH, an isomer of tEME in the same source. We have identified lines of both species in the IRAM 30 m line survey and in the ALMA Science Verification data. We have obtained ALMA maps to establish the spatial distribution of these species. Whereas tEME mainly arises from the compact ridge component of Orion, Gt-n-propanol appears at the emission peak of ethanol (south hot core). The derived column densities of these species at the location of their emission peaks are ≤(4.0 ± 0.8) × 1015 cm-2 and ≤(1.0 ± 0.2) × 1015 cm-2 for tEME and Gt-n-propanol, respectively. The rotational temperature is ~100 K for both molecules. We also provide maps of CH3OCOH, CH3CH2OCOH, CH3OCH3, CH3OH, and CH3CH2OH to compare the distribution of these organic saturated O-bearing species containing methyl and ethyl groups in this region. Abundance ratios of related species and upper limits to the abundances of non-detected ethers are provided. We derive an abundance ratio N(CH3OCH3)/N(tEME) ≥ 150 in the compact ridge of Orion. This paper makes use of the following ALMA data: ADS/JAO.ALMA#2011.0.00009.SV. ALMA is a partnership of ESO (representing its member states), NSF (USA), and NINS (Japan) with NRC (Canada), NSC, and ASIAA (Taiwan), and KASI (Republic of Korea), in cooperation with the Republic of Chile. The Joint ALMA Observatory is operated by ESO, AUI/NRAO, and NAOJ. This work was also based on observations carried out with the IRAM 30-m telescope. IRAM is supported by INSU/CNRS (France), MPG (Germany), and IGN (Spain).Appendix A is available in electronic form at

  16. EtherCAT技术培训及Workshop课程在广州成功举办



  17. Modular construction of 2-substituted benzo[b]furans from 1,2-dichlorovinyl ethers.

    Geary, Laina M; Hultin, Philip G


    (E)-1,2-Dichlorovinyl ethers and amides are easily accessible from trichloroethylene via nucleophilic addition across in situ synthesized dichloroacetylene. A one-pot, sequential Suzuki-Miyaura coupling/intramolecular direct arylation between dichlorovinyl ethers and organoboronic acids provides easy access to a variety of benzofurans in only two steps from inexpensive commercially available compounds. The method is extendable to the preparation of indoles from the analogous dichlorovinyl amides.

  18. Contact angle measurements of a polyphenyl ether to 190 C on M-50 steel

    Jones, W. R., Jr.


    Contact angle measurements were performed for a polyphenyl ether on steel in nitrogen. A tilting plate and a sessile drop apparatus were used. Surface tension was measured with a maximum bubble pressure apparatus. Critical surface energies of spreading were found to be 30.1 and 31.3 dynes/cm. It was concluded that the polyphenyl ether is inherently autophobic and will not spread on its own surface film.

  19. The Experiment of Michelson and Morley: Experiment That Ruled Out Ether

    Amit Roy


    Light was assumed to propagate in a medium called etherwhich was all pervading and stationary. Earth’s motionthrough ether was expected to have an effect on the velocityof light in the direction of the relative motion by the law ofaddition of velocities. Michelson–Morley experiment used aninterferometric technique to detect this effect and got a nullresult, which was the first strong evidence against existenceof ether and eventually had a natural explanation in specialtheory of relativity.

  20. The action of certain antibiotics and ether on swine enzootic pneumonia.

    Huhn, R G


    The susceptibility of Mycoplasma hyopneumoniae to the action of three antibiotics and diethyl ether was determined. Infected swine were used in an in vivo sensitivity detection system. The parameter of susceptibility was lesion prophylaxis. In vivo, Mycoplasma hyopneumoniae appeared to be resistant to diethyl ether, tylosin tartrate, and erythromycin, but was susceptible to the action of chlortetracycline. Chlortetracycline was effective in preventing the development of lesions when given at levels which would be practical in commercial swine operations.