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Sample records for benzene sulfonic acid

  1. 40 CFR 721.9595 - Alkyl benzene sulfonic acids and alkyl sulfates, amine salts (generic).

    Science.gov (United States)

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Alkyl benzene sulfonic acids and alkyl... Significant New Uses for Specific Chemical Substances § 721.9595 Alkyl benzene sulfonic acids and alkyl...) The chemical substances identified generically as alkyl benzene sulfonic acids and alkyl...

  2. A STUDY ON THE DEGRADATION MECHANISM OF PHOTOCROSSLINKING PRODUCTS FORMED BY CYCLIZED POLYISOPRENE-DIAZIDE SYSTEM UNDER THE INFLUENCE OF ALKYL BENZENE SULFONIC ACIDS

    Institute of Scientific and Technical Information of China (English)

    HUANG Junlian; SUN Meng

    1989-01-01

    The degradation mechanism of photocrosslinking products formed by cyclized polyisoprene-diazide system under the influence of the different alkyl benzene sulfonic acids was studied. The effects ofalkyl chain length and the concentration of alkyl benzene sulfonic acids on the rate of degradation reaction were discussed. It was found that in the initial stage of degradation, the cyclicity ratio and the average fused ring number did not change considerably, but the percentage of uncyclized parts content varied significantly. The suitable mechanism was supposed.

  3. Crystal structure of 2-benzene-sulfon-amido-3-hy-droxy-propanoic acid.

    Science.gov (United States)

    Jabeen, Nabila; Mushtaq, Misbah; Danish, Muhammad; Tahir, Muhammad Nawaz; Raza, Muhammad Asam

    2015-11-01

    In the title compound, C9H11NO5S, the O=S=O plane of the sulfonyl group is twisted at a dihedral angle of 52.54 (16)° with respect to the benzene ring. The dihedral angle between the carb-oxy-lic acid group and the benzene ring is 49.91 (16)°. In the crystal, C-H⋯O, N-H⋯O and O-H⋯O hydrogen bonds link the mol-ecules into (001) sheets. PMID:26594589

  4. An Evaluation of a Teat Dip with Dodecyl Benzene Sulfonic Acid in Preventing Bovine Mammary Gland Infection from Experimental Exposure to Streptococcus agalactiae and Staphylococcus aureus

    OpenAIRE

    Barnum, D A; Johnson, R. E.; Brooks, B W

    1982-01-01

    The effectiveness of a teat dip with dodecyl benzene sulfonic acid (1.94%) for the prevention of intramammary infections was determined in cows experimentally challenged with Streptococcus agalactiae and Staphylococcus aureus. The infection rates with Streptococcus agalactiae and Staphylococcus aureus were 62.5% and 75% in undipped quarters, 12.5% and 21.5% in dipped quarters with a reduction rate of 80% and 71% respectively. The significance of some findings in relation to mastitis control a...

  5. Electrochemical detection of Hg(II in water using self-assembled single walled carbon nanotube-poly(m-amino benzene sulfonic acid on gold electrode

    Directory of Open Access Journals (Sweden)

    Gauta Gold Matlou

    2016-09-01

    Full Text Available This work reports on the detection of mercury using single walled carbon nanotube-poly (m-amino benzene sulfonic acid (SWCNT-PABS modified gold electrode by self-assembled monolayers (SAMs technique. A thiol containing moiety (dimethyl amino ethane thiol (DMAET was used to facilitate the assembly of the SWCNT-PABS molecules onto the Au electrode surface. The successfully assembled monolayers were characterised using atomic force microscopy (AFM. Cyclic voltammetric and electrochemical impedance spectroscopic studies of the modified electrode (Au-DMAET-(SWCNT-PABS showed improved electron transfer over the bare Au electrode and the Au-DMAET in [Fe (CN6]3−/4− solution. The Au-DMAET-(SWCNT-PABS was used for the detection of Hg in water by square wave anodic stripping voltammetry (SWASV analysis at the following optimized conditions: deposition potential of −0.1 V, deposition time of 30 s, 0.1 M HCl electrolyte and pH 3. The sensor showed a good sensitivity and a limit of detection of 0.06 μM with a linear concentration range of 20 ppb to 250 ppb under the optimum conditions. The analytical applicability of the proposed method with the sensor electrode was tested with real water sample and the method was validated with inductively coupled plasma – optical emission spectroscopy.

  6. Electronic Conductivity of Polypyrrole−Dodecyl Benzene Sulfonate Complexes

    DEFF Research Database (Denmark)

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

    2004-01-01

    The electronic conductivity of the electroactive polymer polypyrrole-dodecyl benzene sulfonate (PPy-DBS) has been characterized as function of the redox level. The polymer was synthesized with different isomers of the dopant anions: the common mixed DBS tenside and three well-defined synthetic...... dodecyl isomers (with the benzene group at positions 1, 2 and 6). The conductivity was measured both by van der Pauw measurements on PPy-DBS in the oxidized, dry state as function of temperature, and by electrochemical impedance spectroscopy as function of potential in 0.1 M NaCl aqueous electrolyte...

  7. 十二烷基苯磺酸木薯淀粉酯微波法制备工艺研究%Preparation technology of dodecyl benzene sulfonic acid cassava starch ester by microwave

    Institute of Scientific and Technical Information of China (English)

    张利伟; 薛行华; 赵法敏; 张永强; 李光

    2013-01-01

    Dodecyl benzene sulfonic acid cassava starch ester was prepared by microwave method with cassava starch as the raw material , sodium dodecyl benzene sulfonate as the esterification agent and sodium hydroxide as the catalyst .The effects of synthetic condition , such as molar ratio ( sodi-um dodecyl benzene sulfonate to glucose unit of cassava starch ) , reaction time , incubated tempera-ture and pH value , on the substitution degree were investigated .The best conditions by orthogonal design were the molar ratio of sodium dodecyl benzene sulfonate to cassava at 0.06 , reaction time 5 h and the incubated temperature 80 ℃, at which the degree of substitution was 0.010 0 .FT-IR and XRD revealed the changes in the structure of the esterified starch , and TG analysis also dis-played the decline of the hydrophilic and thermal stability of the esterified starch .%  以木薯淀粉为原料,十二烷基苯磺酸钠为酯化剂,NaOH为催化剂,采用微波法制备十二烷基苯磺酸木薯淀粉酯,并考察其合成的工艺条件。探讨了十二烷基苯磺酸钠与木薯淀粉葡萄糖单元的摩尔比、反应时间、反应温度和pH值对产物取代度的影响,用正交实验分析对制备工艺进行优化,并通过红外、X射线和热重分析表征了酯化淀粉的结构及其热稳定性。结果表明,在十二烷基苯磺酸钠与木薯淀粉葡萄糖单元摩尔比为0.06、反应时间5 h、反应温度80℃和pH为10的条件下制备的十二烷基苯磺酸酯淀粉的取代度最佳,取代度为0.0100。红外和X射线谱图证明了酯化淀粉结构的改变,热重分析表明酯化淀粉亲水性与热稳定性有所下降。

  8. Hydrazine-1,2-diium bis-(3-carb-oxy-4-hy-droxy-benzene-sulfonate) tetra-hydrate.

    Science.gov (United States)

    Selvaraju, Devipriya; Venkatesh, Ranjithkumar; Sundararajan, Vairam

    2011-05-01

    Reaction of 5-sulfosalicylic acid with hydrazine hydrate at pH = 1 results in the formation of the title hydrated salt, 0.5N(2)H(6) (2+)·C(7)H(5)O(6)S(-)·2H(2)O. The hydrazinium dications lie on centres of inversion. They are located between 3-carb-oxy-4-hy-droxy-benzene-sulfonate anions, forming inter-molecular N-H⋯O hydrogen bonds with sulfonate ions and water mol-ecules of crystallisation. Further intra- and inter-molecular O-H⋯O hydrogen bonds are observed in the crystal structure. PMID:21754532

  9. Preparation and characterization of proton exchange poly (ether sulfone)s membranes grafted propane sulfonic acid on pendant phenyl groups

    International Nuclear Information System (INIS)

    Poly(ether sulfone)s containing hexaphenyl (PHP) was prepared by 1,2-bis(4-hydroxyphenyl)-3,4,5,6-tetraphenylbenzene, 4,4-hydroxyphenylsulfone, and 4,4-fluorophenylsulfone, followed bromination on phenyl groups to produce brominated PHP (Br-PHP). Grafted sulfonated poly(ether sulfone)s containing hexaphenyl (GSPHP) were prepared from Br-PHP and 3-bromopropane sulfonic acid with potassium salt and copper powder. The salt form was converted to free acid using 1 M sulfuric acid solution. All these membranes were cast from dimethylacetamide (DMAc). The structural properties of the synthesized polymers were investigated by 1H-NMR spectroscopy. The membranes were studied with regard to ion exchange capacity (IEC), water uptake, Fenton test, and proton conductivity. These grafted polymer membranes were compared with normal sulfonated poly(ether sulfone)s and Nafion

  10. SOLVENT-FREE FACILE SYNTHESIS OF NOVEL α-TOSYLOXY β-KETO SULFONES USING [HYDROXY(TOSYLOXY)IODO]BENZENE

    Science.gov (United States)

    A facile, general and high yielding protocol for the synthesis of novel α-tosyloxy β-keto sulfones is described utilizing relatively non-toxic, [hydroxy(tosyloxy)iodo]benzene, under solvent-free conditions at room temperature.

  11. Interfacial assignment of branched-alkyl benzene sulfonates: A molecular simulation

    Science.gov (United States)

    Liu, Zi-Yu; Wei, Ning; Wang, Ce; Zhou, He; Zhang, Lei; Liao, Qi; Zhang, Lu

    2015-11-01

    A molecular dynamics simulation was conducted to analyze orientations of sodium branched-alkyl benzene sulfonates molecules at nonane/water interface, which is helpful to design optimal surfactant structures to achieve ultralow interfacial tension (IFT). Through the two dimensional density profiles, monolayer collapses are found when surfactant concentration continues to increase. Thus the precise scope of monolayer is certain and orientation can be analyzed. Based on the simulated results, we verdict the interfacial assignment of branched-alkyl benzene sulfonates at the oil-water interface, and discuss the effect of hydrophobic tail structure on surfactant assignment. Bigger hydrophobic size can slow the change rate of surfactant occupied area as steric hindrance, and surfactant meta hydrophobic tails have a stronger tendency to stretch to the oil phase below the collapsed concentration. Furthermore, an interfacial model with reference to collapse, increasing steric hindrance and charge repulsive force between interfacial surfactant molecules, responsible for effecting of surfactant concentration and structure has been supposed.

  12. Small-angle neutron scattering studies of sodium butyl benzene sulfonate aggregates in aqueous solution

    Indian Academy of Sciences (India)

    O R Pal; V G Gaikar; J V Joshi; P S Goyal; V K Aswal

    2004-08-01

    The aggregation behaviour of a hydrotrope, sodium -butyl benzene sulfonate (Na-NBBS), in aqueous solutions is investigated by small-angle neutron scattering (SANS). Nearly ellipsoidal aggregates of Na-NBBS at concentrations well above its minimum hydrotrope concentration were detected by SANS. The hydrotrope seems to form self-assemblies with aggregation number of 36–40 with a substantial charge on the aggregate. This aggregation number is weakly affected by the hydrotrope concentration.

  13. Interfacial assignment of branched-alkyl benzene sulfonates: A molecular simulation

    Directory of Open Access Journals (Sweden)

    Zi-Yu Liu

    2015-11-01

    Full Text Available A molecular dynamics simulation was conducted to analyze orientations of sodium branched-alkyl benzene sulfonates molecules at nonane/water interface, which is helpful to design optimal surfactant structures to achieve ultralow interfacial tension (IFT. Through the two dimensional density profiles, monolayer collapses are found when surfactant concentration continues to increase. Thus the precise scope of monolayer is certain and orientation can be analyzed. Based on the simulated results, we verdict the interfacial assignment of branched-alkyl benzene sulfonates at the oil-water interface, and discuss the effect of hydrophobic tail structure on surfactant assignment. Bigger hydrophobic size can slow the change rate of surfactant occupied area as steric hindrance, and surfactant meta hydrophobic tails have a stronger tendency to stretch to the oil phase below the collapsed concentration. Furthermore, an interfacial model with reference to collapse, increasing steric hindrance and charge repulsive force between interfacial surfactant molecules, responsible for effecting of surfactant concentration and structure has been supposed.

  14. Synthesis of dodecyl lauroyl benzene sulfonate and its application in enhanced oil recovery

    Energy Technology Data Exchange (ETDEWEB)

    Cui, Zhenggang; Wu, Le; Sun, Mingming; Jiang, Jian-zhong; Wang, Feng [Jiangnan Univ., Wuxi (China). School of Chemical and Material Engineering

    2011-09-15

    A new hydrophobic surfactant, dodecyl lauroyl benzene sulfonate (DLBS), was synthesized and its application in enhanced oil recovery by alkali-surfactant-polymer (ASP) flooding was studied. The results show that DLBS can be synthesized by reaction of industrial dodecyl benzene with lauroyl chloride in the presence of AlCl{sub 3}, followed by sulfonation with ClSO{sub 3}H and neutralization with NaOH. The lauroyl-group is confirmed to be connected to the para-position of the alkylbenzene by1HNMR spectrum. The synthesized DLBS is well soluble in pure water and reservoir (connate) water at 45 C. It is highly surface active which is indicated by its low CMC of 1.1 . 10{sup -5} mol/L, and its low surface tension, {gamma}{sub cmc} of 28.6 mN m{sup -1}. By mixing with heavy alkylbenzene sulfonates of relatively low average molar mass (387g mol{sup -1}) at a total surfactant concentration of 5 mM, DLBS can reduce the interfacial tension of Daqing crude oil/connate water to an order of 10{sup -3} mN/m at 45 C in the presence of 0.5-1.0 wt.% NaOH and 1000 mg L{sup -1} of polymer. If the NaOH was replaced by a gentle alkaline salt, Na{sub 2}CO{sub 3}, certain amounts of dodecyl dimethyl carboxy betaine were added and the concentration of Na{sub 2}CO{sub 3} was increased to 1.2-2.0 wt.%, the interfacial tension of Daqing crude oil/connate water can also be reduced to an ultralow value. Therefore DLBS is a good hydrophobic surfactant applicable in ASP flooding with either NaOH or Na{sub 2}CO{sub 3} as alkaline agents. (orig.)

  15. Methane sulfonic acid in the marine atmosphere

    OpenAIRE

    E. S. Saltzman; Savoie, D. L.; Zika, R. G; J. M. Prospero

    1983-01-01

    Methane sulfonic acid (MSA) is an oxidation product of the reaction of OH radical with dimethyl sulfide and, hence, should be an important constituent of marine air. MSA concentrations in marine aerosols ranged from 0.009 to 0.075 μg/m3 in samples from the Pacific and Indian oceans and Miami, Florida. In the samples from remote areas (Pacific and Indian oceans), MSA levels averaged 6.7% (S = 1.9) of the non-sea-salt (nss) SO4 =. In the Miami area, ratios were occasionally lower be...

  16. Extraction Behavior and Wastewater Treatment of Amino Sulfonic Acid with Alamine 336

    Institute of Scientific and Technical Information of China (English)

    秦炜; 李振宇; 汪敏; 戴猷元

    2004-01-01

    p-Amino benzene sulfonic acid (PABSA) is selected as the solute with amphoteric functional group, Lewis acid and Lewis base, to be separated from its dilute solutions. An aliphatic, straight chain amine, Alamine 336, is used as the extractant, and kerosene, 1-octanol, chloroform, butyl acetate and benzene as the diluent. The effects of pH value of solution, extractant concentration, salt and types of diluent on the distribution coefficient, D, are studied. There is a peak of D value with pH value of solution, the polar diluents are favorable for extracting PABSA, and the salt in aqueous phase reduces values of D apparently. The extraction equilibrium is described using the mass action law, and the calculated data according to the proposed model agree with the experimental data well. Further, the extraction behavior for other amino benzene sulfonic acids, 1-amino-8-naphtol-3,6-disulfonic acid (H acid) and 4,4′-diaminostilbene-2,2′-disulfonic acid (DSD acid), is investigated in a wide pH value region. Finally. H acid and DSD acid are successfully removed from wastewater by the extraction with Alamine 336.

  17. Optimization of Biodegradability and Toxicity Testing of Degradation Product from Linear Alkyl BenzeneSulfonate (LAS Surfactant as Cleaning Detergent Agent

    Directory of Open Access Journals (Sweden)

    Neera Khairani

    2009-11-01

    Full Text Available Optimization of Biodegradability and Toxicity Testing of Degradation Product from Linear Alkyl BenzeneSulfonate (LAS Surfactant as Cleaning Detergent Agent. Linear Alkyl Benzene Sulfonate (LAS is a surfactantused in laundry detergent as cleaning agent and toxic to aquatic organisms. Results shows, with the LAS concentrationused (20 ppm in medium, adaptation time and Acinetobacter sp. growth has shown better biodegradation ability thanthree other bacteria used Pseudomonas putida, Pseudomonas fluorescence, Bacillaria spp. Thus, Acinetobacter sp isused further for biodegradation process of LAS. Based on its biodegradation half-life using Acinetobacter sp, and withmixed culture (± 52.32% and ± 46.82% respectively could be achieved in 4 (four days, LAS could be categorized as abiodegradable compound. The toxicity assay is based on tetrazolium dye reduction with Rhizobium meliloti as indicatororganism. LAS is more toxic than its intermediate product from biodegradation, with IC50 = 34.35 ppm, and theintermediate product, Ac and Cm, has IC50 = 446.19 ppm and 111.28 ppm respectively. Identification of intermediateproducts using IR and LC-MS analysis shows that the degradation product contains chemicals compounds withfunctional group as follows: benzene, benzoic acid, hydroxyl, and aliphatic carbons with large molecule weight. Untilits half-time degradation time, LAS biodegradation process only occurs at the aliphatic carbon chain, and have not yetreached the stage of aromatic ring opening.

  18. Basic dye removal from aqueous solutions by dodecylsulfate- and dodecyl benzene sulfonate-intercalated hydrotalcite

    International Nuclear Information System (INIS)

    Dodecylsulfate- and dodecyl benzene sulfonate-hydrotalcites were prepared by calcination-rehydratation method. The surfactants intercalation in the interlayer space of hydrotalcite were checked by PXRD and FTIR spectroscopy where the resulting materials were found to be similar to those reported in the literature and were used to remove a basic dye (safranine) from aqueous solutions. The sorption kinetics data fitted the pseudo second order model. The isotherms were established and the parameters calculated. The sorption data fitted the Langmuir model with good values of the determination coefficient. The thermodynamic parameters calculated from Van't Hoff plots gave a low value of ΔGo (-1) indicating a spontaneous physisorption process. Two regeneration cycles were processed by acetone extraction leading to the same removal capacity of the obtained materials as the original surfactant-intercalated hydrotalcites. The UV-vis spectra of the recovered extracts were similar to the spectrum of safranine, which means that the dye was recovered without any modification

  19. Affinity labelling enzymes with esters of aromatic sulfonic acids

    Science.gov (United States)

    Wong, Show-Chu; Shaw, Elliott

    1977-01-01

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

  20. Fluorescence enhancement effect for the determination of curcumin with yttrium(III)-curcumin-sodium dodecyl benzene sulfonate system

    International Nuclear Information System (INIS)

    It is found that the fluorescence of curcumin is greatly enhanced by yttrium(III) (Y3+) in the presence of sodium dodecyl benzene sulfonate. Based on this, a sensitive fluorimetric method for the determination of curcumin in aqueous solution is proposed. In the potassium hydrogen phthalate (KHP) buffer, the fluorescence intensity of curcumin is proportional to the concentration of curcumin in the range of 7.37x10-4-0.18, 0.18-2.95 μg mL-1 and the detection limit is 0.1583 ng mL-1. The actual samples are satisfactorily determined. In addition, the interaction mechanism is also studied

  1. (E)-4-[4-(Diethyl-amino)-benzyl-idene-ammonio]-benzene-sulfonate.

    Science.gov (United States)

    Ruanwas, Pumsak; Chantrapromma, Suchada; Fun, Hoong-Kun

    2012-07-01

    The title compound, C(17)H(20)N(2)O(3)S, synthesised from sulfanilic acid and 4-diethyl-amino-benzaldehyde, crystallized out as a zwitterion with the central N atom protonated. The zwitterion exists in an E conformation with respect to the C=N double bond. The dihedral angle between the benzene rings is 37.57 (5)°. In the crystal, the zwitterions are linked into a tape along the a axis by N-H⋯O hydrogen bonds. The crystal structure is further stabilized by weak C-H⋯O inter-actions and π-π inter-actions with a centroid-centroid distance of 3.8541 (6) Å. An O⋯O [2.8498 (11) Å] short contact is present.

  2. 40 CFR 721.9620 - Aromatic sulfonic acid compound with amine.

    Science.gov (United States)

    2010-07-01

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

  3. Fluorescence enhancement effect for the determination of curcumin with yttrium(III)-curcumin-sodium dodecyl benzene sulfonate system

    Energy Technology Data Exchange (ETDEWEB)

    Wang Feng [Department of Chemistry, Zaozhuang University, Zaozhuang, 277160 (China)], E-mail: wf332@uzz.edu.cn; Huang Wei; Wang Yanwei [Department of Chemistry, Zaozhuang University, Zaozhuang, 277160 (China)

    2008-01-15

    It is found that the fluorescence of curcumin is greatly enhanced by yttrium(III) (Y{sup 3+}) in the presence of sodium dodecyl benzene sulfonate. Based on this, a sensitive fluorimetric method for the determination of curcumin in aqueous solution is proposed. In the potassium hydrogen phthalate (KHP) buffer, the fluorescence intensity of curcumin is proportional to the concentration of curcumin in the range of 7.37x10{sup -4}-0.18, 0.18-2.95 {mu}g mL{sup -1} and the detection limit is 0.1583 ng mL{sup -1}. The actual samples are satisfactorily determined. In addition, the interaction mechanism is also studied.

  4. High Bulk Modulus of Nanocrystal γ-Fe2O3 with Chemical Dodecyl Benzene Sulfonic Decoration Under High Pressure

    Institute of Scientific and Technical Information of China (English)

    ZHAO Jing; GUO Lin; LIU Jing; YANG Yang; CHE Rong-Zheng; ZHOU Lei

    2000-01-01

    Structural transformation in γ-Fe2O3 nanocrystals (about 1Onm) with dodecyl benzene sulfonic (DBS) coated is studied by using high-pressure energy dispersive x-ray diffraction of synchrotron radiation and high-resolution transmission electron microscopy (HRTEM). Relative to the bulk crystal, the transition pressure showed a decrease while the compressibility increases significantly up to 375 (±9 GPa). HRTEM picture confirmed that there is surface cladding surrounding nanocrystals due to DBS, which formed new special boundaries between nanocrystals and should be different from the ordinary grain boundaries. The experimental results imply that the surface layers of γ-Fe2O3 nanocrystals have strong effect on the compressibility.

  5. Toxicity of perfluorononanoic acid and perfluorooctane sulfonate to Daphnia magna

    OpenAIRE

    Lu, Guang-hua; Jian-chao LIU; Sun, Li-Sha; Lu-jin YUAN

    2015-01-01

    In order to study toxicological effects of perfluorononanoic acid (PFNA), perfluorooctane sulfonate (PFOS), and their mixtures (PFNA/PFOS) on Daphnia magna (D. magna), a suite of comprehensive toxicity tests were conducted, including a 48-hour acute toxicity test, a 21-day chronic test, a feeding experiment, and a biomarker assay. D. magna were exposed to aqueous solutions of PFNA and PFOS (alone and in combination) at concentrations ranging from 0.008 to 5 mg/L. The survival, growth, and rep...

  6. A STUDY OF THE HEAT OF HYDRATION OF SULFONIC ACID RESINS

    Institute of Scientific and Technical Information of China (English)

    XURongnan; JIJunyan; 等

    1992-01-01

    The heat of hydration of dry sulfonic acid resin in different comcentrations of sulfuric acid has been determined. The heat of hydration of the resin in H2O is 143.4J/g(resin). The greater the concentration of sulfuric acid,the less the heat will be released.The hydrate formed from three sulfonic acid groups and one water molecule is the most stable one of all the hydrates of sulfonic acid resin and water.

  7. Synergistic flame retardant effects of composites containing organic montmorillonite, Nylon 6 and 2-cyclic pentaerythritoloctahydrogen tetraphosphate-4,6-benzene sulfonic acid sodium ammion-triazine%新型单组份磷-氮膨胀型阻燃剂/OMMT对尼龙6热稳定性能的影响及其协同阻燃效果

    Institute of Scientific and Technical Information of China (English)

    王超; 李迎春; 胡国胜; 曹东豪

    2015-01-01

    A novel P-N containing intumescent flame retardant, 2-cyclic pentaerythritoloctahydrogen tetraphosphate-4,6-benzene sulfonic acid sodium ammion-triazine ( CTOB) was synthesized and used as an additive in intumescent flame retardant composites containing organic montmorillonite (OMMT) and Nylon 6. The thermal stability and flammability properties of Nylon 6, CTOB, OMMT and their composites were investigated by TGA, limiting oxygen index ( LOI) and cone calorimeter tests. Synergistic effects between CTOB and OMMT in the Nylon 6/CTOB/OMM composite were observed. A combination of CTOB and OMMT improved the thermal stability and the flammability properties of Nylon 6 and increased the LOI value to 28. 0%. The average and peak heat release rates of the ternary composite were reduced by about 65. 7 and 49. 3%, respectively, compared with those of Nylon 6. The residue generated after the cone calorimeter tests upon combustion of the ternary composite was a compact and dense char as revealed by SEM, which is critically important for an excellent flame retardant.%合成出新型单组份磷-氮膨胀型阻燃剂2-环季戊四醇磷酸酯-4,6-对氨基苯磺酸钠均三嗪(CTOB),通过FT-IR,1H NMR和31 P NMR对其结构进行表征。以CTOB与有机蒙脱土( OMMT)为原料,制备出阻燃型CTOB/ OMMT/ Nylon 6复合材料。热重分析表明:CTOB和OMMT的加入能有效提高尼龙6的热稳定性能和成炭性能,通过极限氧指数( LOI)、锥形量热、垂直燃烧实验(UL-94)和TGA对CTOB/ OMMT/ Nylon 6复合材料的阻燃性能进行研究。结果表明,CTOB和 OMMT在尼龙6中表现出良好的协同阻燃效果,CTOB/OMMT/ Nylon 6的氧指数可达28.0%,垂直燃烧性能达到UL-94 V-0级,阻燃后的尼龙6其PHRR 和 THR分别下降了65.7%和49.3%。 CTOB/ OMMT/ Nylon 6燃烧后,表面可生成致密性良好的膨胀炭层,膨胀炭层的形成是有效提高Nylon 6阻燃性能的关键因素。

  8. Modification of the cellulosic component of hemp fibers using sulfonic acid derivatives: Surface and thermal characterization.

    Science.gov (United States)

    George, Michael; Mussone, Paolo G; Bressler, David C

    2015-12-10

    The aim of this study was to characterize the surface, morphological, and thermal properties of hemp fibers treated with two commercially available, inexpensive, and water soluble sulfonic acid derivatives. Specifically, the cellulosic component of the fibers were targeted, because cellulose is not easily removed during chemical treatment. These acids have the potential to selectively transform the surfaces of natural fibers for composite applications. The proposed method proceeds in the absence of conventional organic solvents and high reaction temperatures. Surface chemical composition and signature were measured using gravimetric analysis, X-ray photoelectron spectroscopy (XPS) and Fourier transform infra-red spectroscopy (FTIR). XPS data from the treated hemp fibers were characterized by measuring the reduction in O/C ratio and an increase in abundance of the C-C-O signature. FTIR confirmed the reaction with the emergence of peaks characteristic of disubstituted benzene and amino groups. Grafting of the sulfonic derivatives resulted in lower surface polarity. Thermogravimetric analysis revealed that treated fibers were characterized by lower percent degradation between 200 and 300 °C, and a higher initial degradation temperature.

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

    Institute of Scientific and Technical Information of China (English)

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

    2006-01-01

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

  10. Adsorption mechanism of sodium dodecyl benzene sulfonate on carbon blacks by adsorption isotherm and zeta potential determinations.

    Science.gov (United States)

    Zhao, Yapei; Lu, Pei; Li, Caiting; Fan, Xiaopeng; Wen, Qingbo; Zhan, Qi; Shu, Xin; Xu, Tieliang; Zeng, Guangming

    2013-01-01

    Surfactant solutions were propounded to remove fine and hydrophobic carbon black particles from coal-fired flue gas. The adsorption mechanisms between sodium dodecyl benzene sulfonate (SDBS, an anionic surfactant) and carbon black particles in suspension were investigated. The influence of inorganic salt (NaCl) was also considered. As results showed, hydrophobic interactions contributed to the strong adsorption between SDBS and carbon black particles in the absence of NaCl, and adding NaCl affected the adsorption process. The adsorption amount of SDBS significantly increased when NaCl was added into the SDBS solution; however, when SDBS was in low concentration, the amount of adsorbed SDBS, which was responsible for the shift of zeta potentials, varied little under different concentrations of NaCl. This indicated that the adsorption of SDBS was mainly caused by hydrophobic interaction and Na+ could not change the adsorption of SDBS on adsorption site when SDBS was in low concentration. Moreover, the adsorbed SDBS and Na+ were retained in the Stern layer. PMID:23530331

  11. Impact of model perfume molecules on the self-assembly of anionic surfactant sodium dodecyl 6-benzene sulfonate.

    Science.gov (United States)

    Bradbury, Robert; Penfold, Jeffrey; Thomas, Robert K; Tucker, Ian M; Petkov, Jordan T; Jones, Craig; Grillo, Isabelle

    2013-03-12

    The impact of two model perfumes with differing degrees of hydrophobicity/hydrophilicity, linalool (LL) and phenylethanol (PE), on the solution structure of anionic surfactant sodium dodecyl 6-benzene sulfonate, LAS-6, has been studied by small angle neutron scattering, SANS. For both types of perfume molecules, complex phase behavior is observed. The phase behavior depends upon the concentration, surfactant/perfume composition, and type of perfume. The more hydrophilic perfume PE promotes the formation of more highly curved structures. At relatively low surfactant concentrations, small globular micelles, L1, are formed. These become perfume droplets, L(sm), stabilized by the surfactant at much higher perfume solution compositions. At higher surfactant concentrations, the tendency of LAS-6 to form more planar structures is evident. The more hydrophobic linalool promotes the formation of more planar structures. Combined with the greater tendency of LAS-6 to form planar structures, this results in the planar structures dominating the phase behavior for the LAS-6/linalool mixtures. For the LAS-6/linalool mixture, the self-assembly is in the form of micelles only at the lowest surfactant and perfume concentrations. Over most of the concentration-composition space explored, the structures are predominantly lamellar, L(α), or vesicle, L(v), or in the form of a lamellar/micellar coexistence. At low and intermediate amounts of LL, a significantly different structure is observed, and the aggregates are in the form of small, relatively monodisperse vesicles (i.e., nanovesicles), L(sv).

  12. Polyaniline synthesized with functionalized sulfonic acids for blends manufacture

    Directory of Open Access Journals (Sweden)

    Mara Joelma Raupp Cardoso

    2007-12-01

    Full Text Available Polyaniline (PAni, an electronic conductive polymer, has poor mechanical properties, such as low tensile, compressive and flexural strength that render PAni a non-ideal material to be processed for practical applications. Desired properties of polyaniline can be enhanced by mixing it with a polymer that has good mechanical properties. In this work, PAni was synthesised using functionalized sulfonic acids like camphorsulfonic acid (CSA and dodecilbenzene sulfonic acid (DBSA in order to promote PAni doping and improve its solubility, making possible conductive blends manufacture. The different forms of PAni were characterized by infra-red spectroscopy, thermal analysis, scanning electron microscopy and conductivity measurements. A conductive blend composed of PAni/DBSA and lower density polyethylene (LDPE was obtained via solubilization method and its thermal, morphological and electrical properties were investigated. Concentrations as low as 5 wt. (% of PAni was able to lead to electrical conductivities of PAni/LDPE blends in the range of 10-3 S.cm-1, showing great potential to be used in antistatic packing, electromagnetic shielding, anti-corrosion shielding or as a semiconductor.

  13. A Porous Aromatic Framework Constructed from Benzene Rings Has a High Adsorption Capacity for Perfluorooctane Sulfonate

    Science.gov (United States)

    Luo, Qin; Zhao, Changwei; Liu, Guixia; Ren, Hao

    2016-02-01

    A low-cost and easily constructed porous aromatic framework (PAF-45) was successfully prepared using the Scholl reaction. PAF-45 was, for the first time, used to remove perfluorooctane sulfonate (PFOS) from aqueous solution. Systematic experiments were performed to determine the adsorption capacity of PAF-45 for PFOS and to characterize the kinetics of the adsorption process. The adsorption of PFOS onto PAF-45 reached equilibrium in 30 min, and the adsorption capacity of PAF-45 for PFOS was excellent (5847 mg g-1 at pH 3). The amount of PFOS adsorbed by PAF-45 increased significantly as the cation (Na+, Mg2+, or Fe3+) concentration increased, which probably occurred because the cations enhanced the interactions between the negatively charged PFOS molecules and the positively charged PAF-45 surface. The cations Na+, Mg2+, and Fe3+ were found to form complexes with PFOS anions in solution. Density functional theory was used to identify the interactions between PFOS and Na+, Mg2+, and Fe3+. We expect that materials of the same type as PAF-45 could be useful adsorbents for removing organic pollutants from industrial wastewater and contaminated surface water.

  14. Inhibition of biogas production by alkyl benzene sulfonates (LAS) in a screening test for anaerobic biodegradability.

    Science.gov (United States)

    Garcia, M Teresa; Campos, Encarna; Dalmau, Manel; Illán, Patricia; Sánchez-Leal, Joaquin

    2006-02-01

    The effect of the inoculum source on the digestion of linear alkylbenzene sulfonates (LAS) under anaerobic conditions has been investigated. The potential for primary and ultimate LAS biodegradation of anaerobic sludge samples obtained from wastewater treatment plants (WWTPs) of different geographical locations was studied applying a batch test system. It was found that only 4-22% of the LAS added to the batch anaerobic digesters was primarily transformed suggesting a poor primary degradation of the LAS molecule in anaerobic discontinuous systems. Regarding ultimate biodegradation, the addition of LAS to the batch anaerobic digesters caused a reduction on the extent of biogas production. Significant differences in the inhibition extent of the biogas production were observed (4-26%) depending on the sludge used as inoculum. Effect of the surfactant on the anaerobic microorganisms was correlated with its concentration in the aqueous phase. Sorption of LAS on anaerobic sludge affects its toxicity by depletion of the available fraction of the surfactant. LAS content on sludge was related to the total amount of calcium and magnesium extractable ions. The presence of divalent cations promote the association of LAS with anaerobic sludge reducing its bioavailability and the extent of its inhibitory effect on the biogas production. PMID:16453170

  15. Periodic Mesoporous Organosilica Functionalized with Sulfonic Acid Groups as Acid Catalyst for Glycerol Acetylation

    Directory of Open Access Journals (Sweden)

    Pascal Van Der Voort

    2013-08-01

    Full Text Available A Periodic Mesoporous Organosilica (PMO functionalized with sulfonic acid groups has been successfully synthesized via a sequence of post-synthetic modification steps of a trans-ethenylene bridged PMO material. The double bond is functionalized via a bromination and subsequent substitution obtaining a thiol functionality. This is followed by an oxidation towards a sulfonic acid group. After full characterization, the solid acid catalyst is used in the acetylation of glycerol. The catalytic reactivity and reusability of the sulfonic acid modified PMO material is investigated. The catalyst showed a catalytic activity and kinetics that are comparable with the commercially available resin, Amberlyst-15, and furthermore our catalyst can be recycled for several subsequent catalytic runs and retains its catalytic activity.

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

    Science.gov (United States)

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

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

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2011-02-01

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

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

    KAUST Repository

    Tripathi, Bijay Prakash

    2011-02-01

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

  19. The Performance of Advanced Sequencing Batch Reactor in Wastewater Treatment Plant to Remove Organic Materials and Linear Alkyl Benzene Sulfonates

    Directory of Open Access Journals (Sweden)

    Eslami

    2015-07-01

    Full Text Available Background Linear alkyl benzene sulfonates (LAS are the most important ionic detergents that produce negative ions in the environment. These compounds enter surface waters through domestic and industrial wastewaters and cause environmental hazards. Objectives The present study was aimed at assessing the performance of advanced sequencing batch reactor (SBR in wastewater treatment plant of Yazd, Iran, to remove organic materials and detergents. Materials and Methods The present research was a descriptive longitudinal study conducted on 96 input and output samples of SBR system over eight months from October 2012 to June 2013. The studied parameters were biochemical oxygen demand 5 (BOD5, chemical oxygen demand (COD, and detergents (LAS, which were assessed through standard methods. Finally, the study data were analyzed through analysis of variance (ANOVA using software package for statistical analysis (SPSS. Results The mean inputs of BOD5, COD, and LAS to the SBR system were 292.40 ± 45.28, 597.15 ± 97.30, and 3.29 ± 0.92 mg/L, and the mean outputs were 20.59 ± 3.54, 59.34 ± 9.47, and 0.606 ± 0.09 mg/L, respectively. The removal efficiency of BOD5, COD and LAS were respectively 92.95%, 90.06% and 81.6%. The results of ANOVA indicated that there was a significant relationship between the mean inputs and outputs of BOD5, COD, and the detergents (P ≤ 0.001. Conclusions With the proper operation of wastewater the treatment plant and increasing the retention time, the removal efficiency of the detergents increased. In addition, according to the environmental standards for BOD5, COD and the detergents, the results of the present study indicated that the outputs of these parameters from the SBR system were appropriate for agricultural irrigation.

  20. Sterically Stabilized Poly(3,4-ethylenedioxythiophene) Colloidal Dispersions Doped with Different Sulfonic Acids

    Institute of Scientific and Technical Information of China (English)

    Tie Jun WANG; Ping CHEN; Xiu Jie HU; Shu Yun ZHOU

    2006-01-01

    The preparation of sterically stabilized poly(3, 4-ethylenedioxythiophene)(PEDOT)colloidal dispersions doped with different sulfonic acids is described. Three different sulfonic acids, i.e., p-toluenesulfonic acid, β-naphthalenesuffonic acid and D-camphor-10-sulfonic acid are used, facilitating the preparation of sterically stable PEDOT colloidal particles. The influences of the dopants and concentration of polymeric stabilizer on the yields, morphologies and electrical properties of the resultant colloidal particles were investigated. The colloidal particles with the size ranging from 172 to 334 nm have been obtained in good yields. The compressed pellet conductivity was as high as 4.5 Scm-1.

  1. Electrochemical study of benzene on Pt of various surface structures in alkaline and acidic solutions

    OpenAIRE

    Montilla Jiménez, Francisco; Morallón Núñez, Emilia; Vázquez Picó, José Luis

    2002-01-01

    The electrochemical behaviour of benzene on platinum electrodes (polycrystalline and single-crystal electrodes) has been studied in acidic and alkaline solutions. In acid solutions the reduction of benzene to cyclohexane takes place in all the platinum surface structure employed, however it does not occur in alkaline media (0.1 M NaOH). In this case, the hydrogen adsorption/desorption processes displace the adsorbed benzene from the electrode surface. The oxidation of benzene is also af...

  2. Nonaqueous preparation of stable silver nano particles dispersions from organic sulfonic acids.

    Directory of Open Access Journals (Sweden)

    Valentina Glushko

    2016-05-01

    Full Text Available The conditions for stable silver nano particles dispersions synthesis from organic sulfonic acids in an anhydrous medium of ethylene glycol and its methyl ester were studied. Ascorbic acid and potassium citrate were used as reducing agents.

  3. 2H NMR study of dynamics of benzene-d6 interacting with humic and fulvic acids.

    Science.gov (United States)

    Eastman, Margaret A; Brothers, Lucinda A; Nanny, Mark A

    2011-05-01

    Samples of three humic acids and one fulvic acid with 1% loading of benzene-d(6) in sealed glass tubes have been studied with solid-state deuterium quadrupole-echo nuclear magnetic resonance spectroscopy. Calculated spectra combining three motional models, two isotropic models and a third more restricted small-angle wobble (SAW) motional model, are fit to the experimental spectra. One isotropic motion (ISO(v)) is assigned to vaporous benzene-d(6) due to the small line width, short T(1), and the loss of this component by about -25 °C when the temperature is lowered. The remaining two motional components, ISO(s) and SAW, are sorbed by the humic or fulvic acid. Benzene-d(6) slowly interacts with the humic substances, progressively filling SAW sites as ISO(s) motion diminishes. Both the sorption and increase in percentage of SAW motion are for the most part complete within 200 days but continue to a lesser extent over a period of a few years. For the SAW motion there are at least two and most likely a series of T(1) values, indicating more than one adsorption environment. Enthalpies of sorption, obtained from application of the van't Hoff equation to the percentages of the different motional models derived from a series of variable temperature spectra, are comparable in magnitude to the enthalpy of vaporization of benzene. In Leonardite humic acid, ΔH and ΔS for the ISO(s) to SAW transition change from positive to negative values with age, implying a transition in the driving force from an entropic effect associated with expansion and deformation in the molecular structure of the humic substance to accommodate benzene-d(6) to an enthalpic effect of strong benzene-d(6)-humic substance interactions. In contrast, at advanced ages, Suwannee River humic and fulvic acids have small positive or near zero ΔH and positive ΔS for the ISO(s) to SAW transition. PMID:21456559

  4. Cytotoxic effects of sodium dodecyl benzene sulfonate on human keratinocytes are not associated with proinflammatory cytokines expression

    Institute of Scientific and Technical Information of China (English)

    Mu Zhanglei; Liu Xiaojing; Zhao Yan; Zhang Jianzhong

    2014-01-01

    Background Keratinocytes play a crucial role in the biological function of skin barrier.The relationship between sodium lauryl sulfate (SLS) and keratinocytes has been studied.However,the cytotoxicity and effects of sodium dodecyl benzene sulfonate (SDBS),a common detergent similar to SLS,on keratinocytes are still not known.This study aimed to investigate the effects of SDBS on cytotoxicity and expression of proinflammatory cytokines in cultured human keratinocytes.Methods This study was carried out using the keratinocytes cell line,HaCaT cells.The cytotoxicity of SDBS on HaCaT cells was evaluated with cell counting kit-8 (CCK-8) and phase-contrast microscopy.After exposure to different concentrations of SDBS,the total RNA of the HaCaT cells was extracted for evaluating the relative mRNA expression of IL-1α,IL-6,IL-8,and TNF-α by qPCR.The supernatants of cells were collected for measuring the levels of IL-6 and IL-8 by enzyme-linked immunosorbent assay (ELISA).Results SDBS at concentrations of 20 Jg/ml and over showed direct cytotoxicity and induced morphological changes of the HaCaT cells.The mRNA expressions of IL-1a,IL-6,IL-8,and TNF-α in different concentrations of SDBS at different time were comparable with that of controls.SDBS at concentrations of 5,10,and 15 μg/ml had no significant effects on IL-6 and IL-8 excretion from HaCaT cells after 24-hour exposure.Moreover,no significant effects on the IL-6 and IL-8 excretion were found after 10 and 15 μg/ml S DBS stimulations for 6,12,and 24 hours,respectively.Conclusion SDBS at higher concentrations had cytotoxicity on HaCaT cells but had no effects on the mRNA expression of IL-1α,IL-6,IL-8,and TNF-α,that was different from SLS.

  5. Imidazolium ionic liquid-supported sulfonic acids: Efficient and recyclable catalysts for esterification of benzoic acid

    Institute of Scientific and Technical Information of China (English)

    Yue Qin Cai; Guo Qiang Yu; Chuan Duo Liu; Yuan Yuan Xu; Wei Wang

    2012-01-01

    Several imidazolium ionic liquid (IL)-supported sulfonic acids with different anions,[C3SO3Hmim]HSO4,[C3SO3Hmim]BF4,[C3SO3Hmim]PF6,and [C3SO3Hmim]CF3SO3,were synthesized and applied as catalysts for esterification reaction of benzoic acid.The experimental results indicate that imidazolium IL-supported sulfonic acid containing anion of HSO4- shows the best catalytic activity.Only when less [C3SO3Hmim]HSO4 (0.3 equiv.) applied,was the product obtained with high yield of 97%.Furthermore,the produced esters could be separated by decantation,and the catalyst could be reused after the removal of water.

  6. Toxicity of perfluorononanoic acid and perfluorooctane sulfonate to Daphnia magna

    Directory of Open Access Journals (Sweden)

    Guang-hua LU

    2015-01-01

    Full Text Available In order to study toxicological effects of perfluorononanoic acid (PFNA, perfluorooctane sulfonate (PFOS, and their mixtures (PFNA/PFOS on Daphnia magna (D. magna, a suite of comprehensive toxicity tests were conducted, including a 48-hour acute toxicity test, a 21-day chronic test, a feeding experiment, and a biomarker assay. D. magna were exposed to aqueous solutions of PFNA and PFOS (alone and in combination at concentrations ranging from 0.008 to 5 mg/L. The survival, growth, and reproduction of D. magna were monitored over a 21-day life cycle. The biomarkers, including acetylcholinesterase (AChE, superoxide dismutase (SOD, and catalase (CAT activities, were determined after seven days of exposure. PFOS was more toxic than PFNA based on the results of the acute toxicity test. Perfluorinated compounds (PFCs inhibited both growth and reproduction of D. magna during the testing period. The ingestion rates and the biomarkers, including AChE, SOD, and CAT activities, were significantly inhibited by PFCs in most cases. Moreover, the combined effects related to the growth and reproduction showed the antagonistic effects of PFCs.

  7. Toxicity of perfluorononanoic acid and perfluorooctane sulfonate to Daphnia magna

    Institute of Scientific and Technical Information of China (English)

    Guang-hua Lu; Jian-chao Liu; Li-sha Sun; Lu-jin Yuan

    2015-01-01

    In order to study toxicological effects of perfluorononanoic acid (PFNA), perfluorooctane sulfonate (PFOS), and their mixtures (PFNA/PFOS) on Daphnia magna (D. magna), a suite of comprehensive toxicity tests were conducted, including a 48-h acute toxicity test, a 21-day chronic test, a feeding experiment, and a biomarker assay. D. magna were exposed to aqueous solutions of PFNA and PFOS (alone and in combination) at concentrations ranging from 0.008 to 5 mg/L. The survival, growth, and reproduction of D. magna were monitored over a 21-day life cycle. The biomarkers, including acetylcholinesterase (AChE), superoxide dismutase (SOD), and catalase (CAT) activities, were determined after seven days of exposure. PFOS was more toxic than PFNA based on the results of the acute toxicity test. Perfluorinated compounds (PFCs) inhibited both growth and reproduction of D. magna during the testing period. The ingestion rates and the biomarkers, including AChE, SOD, and CAT activities, were significantly inhibited by PFCs in most cases. Moreover, the combined effects related to the growth and reproduction showed the antagonistic effects of PFCs.

  8. Oil recovery with vinyl sulfonic acid-acrylamide copolymers

    Energy Technology Data Exchange (ETDEWEB)

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

    1973-12-18

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

  9. [New synthesis of the anticoagulant pentasaccharide idraparinux and preparation of its analogues containing sulfonic acid moieties].

    Science.gov (United States)

    Herczeg, Mihály

    2012-01-01

    Two novel synthetic pathways were elaborated for the preparation of idraparinux, a heparin-related fully O-sulfated, O-methylated anticoagulant pentasaccharide. Both methods based upon a [2+3] block synthesis utilizing the same trisaccharide acceptor which was coupled to either a uronic acid disaccharide donor or its nonoxidized precursor. Two bioisosteric sulfonic acid analogues of idraparinux were also prepared, in which two or three primary sulfate esters were replaced by sodium-sulfonatomethyl moieties. The sulfonic acid groups were formed on a monosaccharide level and the obtained carbohydrate sulfonic acid esters were found to be excellent donors and acceptors in the glycosylation reactions. The disulfonic-acid analogue was prepared in a [2+3] block synthesis by using a trisaccharide disulfonic acid as an acceptor and a glucuronide disaccharide as a donor. For the synthesis of the pentasaccharide trisulfonic acid, a more-efficient approach, which involved elongation of the trisaccharide acceptor with a non-oxidized precursor of the glucuronic acid followed by post-glycosidation oxidation at the tetrasaccharide level and a subsequent [1+4] coupling reaction, was elaborated. In vitro evaluation of the anticoagulant activity of the reference compound idraparinux and the new sulfonic acid derivatives revealed that the disulfonate analogue inhibited the blood-coagulation-proteinase factor Xa with outstanding efficacy; however, the introduction of the third sulfonic acid moiety resulted in a notable decrease in the anti-Xa activity. PMID:23230650

  10. Poly(p-Phenylene Sulfonic Acids). PEMs with frozen-in free volume

    Energy Technology Data Exchange (ETDEWEB)

    Litt, Morton [Case Western Reserve Univ., Cleveland, OH (United States)

    2016-01-21

    Early work with rigid rod aromatic polyelectrolytes implied that steric hindrance in packing of the rigid rods left unoccupied volumes that could absorb and hold water molecules strongly. We called this “frozen in free volume). It is illustrated and contrasted with the packing of flexible backbone polyelectrolytes (Reference 5 of this report). This was quantified for poly(biphenylene disulfonic acid) (PBDSA) and poly(phenylene disulfonic acid) (PPDSA). We found that PPDSA held three water molecules per acid group down to 11% relative humidity (RH) and had very high conductivity even at these low RHs. (Reference 1 of report.) The frozen-in free volume was calculated to be equivalent to a λ of 3.5. The work reported below concentrated on studying these polymers and their copolymers with biphenylene disulfonic acid. As expected, the polyelectrolytes are water soluble. Several approaches towards making water stable films were studied. Grafting alkyl benzene substituents on sulfonic acid groups had worked for PBPDSA (1) so it was tried with PPDSA and a 20%/80% copolymer of BPDSA and PDSA (B20P80). T-butyl, n-octyl and n-dodecyl benzene were grafted. Good films could be made. Water absorption and conductivity were studied as a function of RH and temperature (Reference 2). When less than 20% of the sulfonic acid groups were grafted, conductivity was much higher than that of Nafion NR212 at all RHs. At low graft levels, conductivity was ten times higher. Mechanical properties and swelling were acceptable below 90% RH. However, all the films were unstable in water and slowly disintegrated. The proposed explanation was that the molecules formed nano-aggregates in solution held together by hydrophobic bonding. Their cast films disintegrated when placed in water since hydrophobic bonding between the nano-aggregates was poor. We then shifted to crosslinking as a method to produce water stable films (References 3 and 4). Biphenyl could easily be reacted with the polymer

  11. Poly(p-Phenylene Sulfonic Acids). PEMs with frozen-in free volume

    Energy Technology Data Exchange (ETDEWEB)

    Litt, Morton [Case Western Reserve Univ., Cleveland, OH (United States)

    2016-01-21

    Early work with rigid rod aromatic polyelectrolytes implied that steric hindrance in packing of the rigid rods left unoccupied volumes that could absorb and hold water molecules strongly. We called this “frozen in free volume). It is illustrated and contrasted with the packing of flexible backbone polyelectrolytes (Reference 5 of this report). This was quantified for poly(biphenylene disulfonic acid) (PBDSA) and poly(phenylene disulfonic acid) (PPDSA). We found that PPDSA held three water molecules per acid group down to 11% relative humidity (RH) and had very high conductivity even at these low RHs. (Reference 1 of report.) The frozen-in free volume was calculated to be equivalent to a λ of 3.5. The work reported below concentrated on studying these polymers and their copolymers with biphenylene disulfonic acid. As expected, the polyelectrolytes are water soluble. Several approaches towards making water stable films were studied. Grafting alkyl benzene substituents on sulfonic acid groups had worked for PBPDSA (1) so it was tried with PPDSA and a 20%/80% copolymer of BPDSA and PDSA (B20P80). T-butyl, n-octyl and n-dodecyl benzene were grafted. Good films could be made. Water absorption and conductivity were studied as a function of RH and temperature (Reference 2). When less than 20% of the sulfonic acid groups were grafted, conductivity was much higher than that of Nafion NR212 at all RHs. At low graft levels, conductivity was ten times higher. Mechanical properties and swelling were acceptable below 90% RH. However, all the films were unstable in water and slowly disintegrated. The proposed explanation was that the molecules formed nano-aggregates in solution held together by hydrophobic bonding. Their cast films disintegrated when placed in water since hydrophobic bonding between the nano-aggregates was poor. We then shifted to crosslinking as a method to produce water stable films (References 3 and 4). Biphenyl could easily be reacted with the polymer

  12. Degradation and contamination of perfluorinated sulfonic acid membrane due to swelling-dehydration cycles

    DEFF Research Database (Denmark)

    Andersen, Shuang Ma; Morgen, Per; Skou, Eivind Morten

    to the membrane degradation in direct methanol fuel cells (DMFCs), where liquid water has direct contact with the electrolyte. An ex-situ experiment was established with swelling-dehydration cycles on the membrane. However, formation of sulfonic anhydride was not detected during the entire treatment; instead......Formation of sulfonic anhydride S-O-S (from the condensation of sulfonic acids) was known one of the important degradation mechanisms [i] for Nafion membrane under hydrothermal aging condition, which is especially critical for hydrogen fuel cells. Similar mechanism would also have be desirable...

  13. Laser photolysis of interaction of poly-guanylic acid (5’) with anthraquinone-2-sulfonate

    Institute of Scientific and Technical Information of China (English)

    马建华; 韩镇辉; 林维真; 姚思德; 王文峰; 林念芸

    2002-01-01

    The electron transfer reaction between triplet anthraquinone-2-sulfonate and poly-guanylic acid (5’) in CH3CN-H2O (97 : 3) has been investigated by 248 nm (KrF) laser flash photolysis. The transient absorption spectra and kinetics obtained from the interaction of triplet anthraquinone-2-sulfonate and poly[G] demonstrate that the primary ionic radical pair, radical cation of poly[G] and radical anion of anthraquinone-2-sulfonate have been detected simultaneously. The free energy changes in the process of the electron transfer were also calculated.

  14. 76 FR 52875 - 2-Propenoic Acid, Polymer With Ethenylbenzene and (1-methylethenyl) Benzene, Sodium Salt...

    Science.gov (United States)

    2011-08-24

    ... in this unit, no mammalian toxicity is anticipated from dietary, inhalation, or dermal exposure to 2... AGENCY 40 CFR Part 180 2-Propenoic Acid, Polymer With Ethenylbenzene and (1- methylethenyl) Benzene...-Propenoic acid, polymer with ethenylbenzene and (1-methylethenyl) benzene, sodium salt when used as an...

  15. Ag (I)-based 2D metal frameworks with helical structures decorated by the homochiral camphor-10-sulfonic acid

    Science.gov (United States)

    Guo, Peng; Wang, Jing; Wang, Jun; Pan, Daocheng; Xu, Guohai

    2010-12-01

    Two two-dimension homochiral Ag (I) metal frameworks constructed from enantiopure camphor-10-sulfonic acid and hexamethylenetetramine have been synthesized at the room temperature. These two complexes with (6, 3) topology decorated by the homochiral camphor-10-sulfonic acid possess the unique helical structures. The result of Circular Dichroism (CD) spectroscopy confirms that the bulk materials are homochiral and also indicates the handedness of the single crystals can be controlled by the chirality of the camphor-10-sulfonic acid.

  16. Lateral phase separation gives multiple lamellar phases in a "binary" surfactant/water system: the phase behavior of sodium alkyl benzene sulfonate/water mixtures.

    Science.gov (United States)

    Richards, Claire; Tiddy, Gordon J T; Casey, Siobhan

    2007-01-16

    We have examined the structure of the lamellar phase (Lalpha) that coexists with a micellar solution (L1) for a commercial sodium alkyl benzene sulfonate (LAS) mixed with water. The surfactant is a mixture containing C10-C13 alkyl chains, having all positional isomers of the benzene sulfonate group present except the 1-isomer. Unusually for ionic surfactants, the difference in compositions between the coexisting L1 and Lalpha phases is large (L1 = approximately 20 wt % LAS; Lalpha = approximately 65 wt %). The main technique employed was X-ray diffraction, supplemented by optical microscopy and differential scanning calorimetry (DSC). At ambient temperatures, the lamellar phase gives a single diffraction pattern with the main reflection (d) at approximately 32.5 A, whatever the composition. However, above 40 degrees C, the diffraction peak becomes broader and moves to higher d values. At higher temperatures still, several distinct and different diffraction peaks are observed, differing in detail according to composition. The largest d values (approximately 42-4 A) are observed for the lowest LAS concentrations, while the largest number of separate reflections (five) occurs for samples with approximately 44-50% LAS, both at the highest temperatures. Although there are some differences in the data between heating and cooling cycles, the d values return to the original value at low temperature. There are no observable transitions in DSC, nor is there any heterogeneity in the lamellar phase observable by microscopy. The data clearly indicate that there is some lateral separation of the different LAS isomers within the bilayers, which results in the formation of local lamellar regions having different surfactant compositions. This lateral phase separation may arise from the presence of an (electrostatic) attractive interaction, which gives rise to an upper consolute loop within the lamellar phase region of a pure LAS isomer. Similar mechanisms may occur in biological

  17. Anaerobic degradation of benzene by enriched consortia with humic acids as terminal electron acceptors

    Energy Technology Data Exchange (ETDEWEB)

    Cervantes, Francisco J., E-mail: fjcervantes@ipicyt.edu.mx [Division de Ciencias Ambientales, Instituto Potosino de Investigacion Cientifica y Tecnologica (IPICyT), Camino a la Presa San Jose 2055, Col. Lomas 4a. Seccion, San Luis Potosi, SLP, 78216 Mexico (Mexico); Mancilla, Ana Rosa; Toro, E. Emilia Rios-del [Division de Ciencias Ambientales, Instituto Potosino de Investigacion Cientifica y Tecnologica (IPICyT), Camino a la Presa San Jose 2055, Col. Lomas 4a. Seccion, San Luis Potosi, SLP, 78216 Mexico (Mexico); Alpuche-Solis, Angel G.; Montoya-Lorenzana, Lilia [Division de Biologia Molecular, Instituto Potosino de Investigacion Cientifica y Tecnologica (IPICyT), Camino a la Presa San Jose 2055, Col. Lomas 4a. Seccion, San Luis Potosi, SLP, 78216 Mexico (Mexico)

    2011-11-15

    Highlights: {yields} Enriched consortia were able to couple the anaerobic degradation of benzene to the reduction of humic acids. {yields} Electron-equivalents derived from anaerobic benzene oxidation were highly recovered as reduced humic acids. {yields} Several species from classes {beta}-, {delta}- and {gamma}-Proteobacteria were enriched during the anaerobic degradation of benzene. - Abstract: The anaerobic degradation of benzene coupled to the reduction of humic acids (HA) was demonstrated in two enriched consortia. Both inocula were able to oxidize benzene under strict anaerobic conditions when the humic model compound, anthraquinone-2,6-disulfonate (AQDS), was supplied as terminal electron acceptor. An enrichment culture originated from a contaminated soil was also able to oxidize benzene linked to the reduction of highly purified soil humic acids (HPSHA). In HPSHA-amended cultures, 9.3 {mu}M of benzene were degraded, which corresponds to 279 {+-} 27 micro-electron equivalents ({mu}Eq) L{sup -1}, linked to the reduction of 619 {+-} 81 {mu}Eq L{sup -1} of HPSHA. Neither anaerobic benzene oxidation nor reduction of HPSHA occurred in sterilized controls. Anaerobic benzene oxidation did not occur in soil incubations lacking HPSHA. Furthermore, negligible reduction of HPSHA occurred in the absence of benzene. The enrichment culture derived from this soil was dominated by two {gamma}-Proteobacteria phylotypes. A benzene-degrading AQDS-reducing enrichment originated from a sediment sample showed the prevalence of different species from classes {beta}-, {delta}- and {gamma}-Proteobacteria. The present study provides clear quantitative demonstration of anaerobic degradation of benzene coupled to the reduction of HA.

  18. Dual role of endogenous serotonin in 2,4,6-trinitrobenzene sulfonic acid-induced colitis

    Directory of Open Access Journals (Sweden)

    Alberto eRapalli

    2016-03-01

    Full Text Available Background and Aims: Changes in gut serotonin content have been described in Inflammatory Bowel Disease and in different experimental models of colitis: the critical role of this monoamine in the pathogenesis of chronic gastrointestinal inflammation is gradually emerging. Aim of the present study was to evaluate the contribution of endogenous serotonin through the activation of its specific receptor subtypes to the local and systemic inflammatory responses in an experimental model of Inflammatory Bowel Disease. Methods: Colitis was induced by intrarectal 2,4,6-TriNitroBenzene Sulfonic acid in mice subacutely treated with selective antagonists of 5-HT1A (WAY100135, 5-HT2A (Ketanserin, 5-HT3 (Ondansetron, 5-HT4 (GR125487, 5-HT7 (SB269970 receptors and with 5-HT1A agonist 8-Hydroxy-2-(di-n-propylaminotetralin. Results: Blockade of 5-HT1A receptors worsened TNBS-induced local and systemic neutrophil recruitment while 5-HT1A agonist delayed and mitigated the severity of colitis, counteracting the increase in colonic 5-HT content. On the contrary, blockade of 5-HT2A receptors improved global health conditions, reduced colonic morphological alterations, down-regulated neutrophil recruitment, inflammatory cytokines levels and colonic apoptosis. Antagonism of 5-HT3, 5-HT4 and 5-HT7 receptor sites did not remarkably affect the progression and outcome of the pathology or only slightly improved it.Conclusions: The prevailing deleterious contribution given by endogenous serotonin to inflammation in TNBS-induced colitis is seemingly mediated by 5-HT2A and, to a lesser extent, by 5-HT4 receptors and coexists with the weak beneficial effect elicited by 5-HT1A stimulation. These findings suggest how only a selective interference with 5-HT pro-inflammatory actions may represent an additional potential therapeutic option for intestinal inflammatory disorders.

  19. 40 CFR 721.1225 - Benzene, 1,2-dimethyl-, poly-propene derivatives, sulfonated, po-tas-sium salts.

    Science.gov (United States)

    2010-07-01

    ... releases of the substance are subject to an EPA Significant New Use Rule (SNUR) under 40 CFR part 721 which...) (where N = 25 ppb). The requirement of 40 CFR 721.91(a)(4) that the amount of the substance estimated to... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Benzene, 1,2-dimethyl-,...

  20. Nitric Acid Dehydration Using Perfluoro Carboxylate and Mixed Sulfonate/Carboxylate Membranes

    Energy Technology Data Exchange (ETDEWEB)

    R.L. Ames

    2004-09-01

    Perfluoro ionomer membranes are tetrafluoro ethylene-based materials with microheterogeneous structures consisting of a hydrophobic polymer backbone and a hydrophilic side-chain cluster region. Due to the ionomer cluster morphology, these films exhibit unique transport properties. Recent investigations with perfluoro sulfonate and perfluoro sulfonate/carboxylate composite polymers have demonstrated their value in the dehydration of nitric acid and they show potential as an alternative to conventional, energy intensive unit operations in the concentration of acid feeds. As a result, investigations were conducted to determine the feasibility of using pure perfluoro carboxylate and mixed perfluoro sulfonate/carboxylate films for the dehydration of nitric acid because of the speculation of improved water selectivity of the carboxylate pendant chain. During the first phase of these investigations the effort was focused on generating a thin, solution cast perfluoro carboxylate ionomer film, to evaluate the general, chemical and physical characteristics of the polymer, and to assess the material's aqueous transport performance (flux and nitrate separation efficiencies) in pervaporation and high-pressure environments. Results demonstrated that generating robust solution-cast films was difficult yet a number of membranes survived high trans-membrane pressures up to 700 psig. General characterization of the solution cast product showed reduced ion exchange capacities when compared with thicker, ''as received'' perfluoro carboxylate and similar sulfonate films. Small angle x-ray scattering analysis results suggested that the solution cast carboxylate films contained a small fraction of sulfonate terminated side-chains. Aqueous transport experimentation showed that permeate fluxes for both pure water and nitric acid were approximately two orders of magnitude smaller for the carboxylate solution cast membranes when compared to their sulfonate

  1. Tin Coatings Electrodeposited from Sulfonic Acid-Based Electrolytes: Tribological Behavior

    Science.gov (United States)

    Bengoa, L. N.; Tuckart, W. R.; Zabala, N.; Prieto, G.; Egli, W. A.

    2015-06-01

    A high efficiency methane sulfonic acid electrolyte used for tin electrodeposition was studied, and the properties of the resulting deposits were compared to those of tin coatings obtained from an industrial phenol sulfonic acid electrolyte. Cyclic voltammetry was used to study the effect of organic additives on the reduction process to define the composition of the electrolytic bath. Thick tin electrodeposits were obtained on rotating cylinder steel electrodes, and their surface morphology, preferred crystal orientation, surface roughness, micro hardness, and tribological behavior were measured. Smooth, adherent, and bright tin coatings were obtained from the methane sulfonic acid electrolyte, which differed in morphology and texture from tin electrodeposited from the industrial bath. Influence of organic additives on preferred crystal orientation of the coatings was found to be stronger than changing the supporting sulfonic acid type. Tribological tests showed that the two types of deposits have a similar coefficient of friction. However, tin coatings obtained from methane sulfonic electrolytes presented a lower wear resistance and underwent galling at lower loads.

  2. Nuclear Magnetic Resonance Identification of New Sulfonic Acid Metabolites of Chloroacetanilide Herbicides

    Science.gov (United States)

    Morton, M.D.; Walters, F.H.; Aga, D.S.; Thurman, E.M.; Larive, C.K.

    1997-01-01

    The detection of the sulfonic acid metabolites of the chloroacetanilide herbicides acetochlor, alachlor, butachlor, propachlor, and, more recently, metolachlor in surface and ground water suggests that a common mechanism for dechlorination exists via the glutathione conjugation pathway. The identification of these herbicides and their metabolites is important due to growing public awareness and concern about pesticide levels in drinking water. Although these herbicides are regulated, little is known about the fate of their metabolites in soil. The sulfonic acid metabolites were synthesized by reaction of the parent compounds with an excess of sodium sulfite. Acetochlor, alachlor, butachlor, metolachlor, and propachlor and their sulfonic acid metabolites were studied by nuclear magnetic resonance spectroscopy and fast atom bombardment mass spectrometry. This paper provides a direct method for the preparation and characterization of these compounds that will be useful in the analysis and study of chloracetanilide herbicides and their metabolites.

  3. Synthesis of sulfonated porous carbon nanospheres solid acid by a facile chemical activation route

    Energy Technology Data Exchange (ETDEWEB)

    Chang, Binbin, E-mail: changbinbin806@163.com; Guo, Yanzhen; Yin, Hang; Zhang, Shouren; Yang, Baocheng, E-mail: baochengyang@yahoo.com

    2015-01-15

    Generally, porous carbon nanospheres materials are usually prepared via a template method, which is a multi-steps and high-cost strategy. Here, we reported a porous carbon nanosphere solid acid with high surface area and superior porosity, as well as uniform nanospheical morphology, which prepared by a facile chemical activation with ZnCl{sub 2} using resorcinol-formaldehyde (RF) resins spheres as precursor. The activation of RF resins spheres by ZnCl{sub 2} at 400 °C brought high surface area and large volume, and simultaneously retained numerous oxygen-containing and hydrogen-containing groups due to the relatively low processing temperature. The presence of these functional groups is favorable for the modification of –SO{sub 3}H groups by a followed sulfonation treating with sulphuric acid and organic sulfonic acid. The results of N{sub 2} adsorption–desorption and electron microscopy clearly showed the preservation of porous structure and nanospherical morphology. Infrared spectra certified the variation of surface functional groups after activation and the successful modification of –SO{sub 3}H groups after sulfonation. The acidities of catalysts were estimated by an indirect titration method and the modified amount of –SO{sub 3}H groups were examined by energy dispersive spectra. The results suggested sulfonated porous carbon nanospheres catalysts possessed high acidities and –SO{sub 3}H densities, which endowed their significantly catalytic activities for biodiesel production. Furthermore, their excellent stability and recycling property were also demonstrated by five consecutive cycles. - Graphical abstract: Sulfonated porous carbon nanospheres with high surface area and superior catalytic performance were prepared by a facile chemical activation route. - Highlights: • Porous carbon spheres solid acid prepared by a facile chemical activation. • It owns high surface area, superior porosity and uniform spherical morphology. • It possesses

  4. Synthesis of sulfonated porous carbon nanospheres solid acid by a facile chemical activation route

    Science.gov (United States)

    Chang, Binbin; Guo, Yanzhen; Yin, Hang; Zhang, Shouren; Yang, Baocheng

    2015-01-01

    Generally, porous carbon nanospheres materials are usually prepared via a template method, which is a multi-steps and high-cost strategy. Here, we reported a porous carbon nanosphere solid acid with high surface area and superior porosity, as well as uniform nanospheical morphology, which prepared by a facile chemical activation with ZnCl2 using resorcinol-formaldehyde (RF) resins spheres as precursor. The activation of RF resins spheres by ZnCl2 at 400 °C brought high surface area and large volume, and simultaneously retained numerous oxygen-containing and hydrogen-containing groups due to the relatively low processing temperature. The presence of these functional groups is favorable for the modification of -SO3H groups by a followed sulfonation treating with sulphuric acid and organic sulfonic acid. The results of N2 adsorption-desorption and electron microscopy clearly showed the preservation of porous structure and nanospherical morphology. Infrared spectra certified the variation of surface functional groups after activation and the successful modification of -SO3H groups after sulfonation. The acidities of catalysts were estimated by an indirect titration method and the modified amount of -SO3H groups were examined by energy dispersive spectra. The results suggested sulfonated porous carbon nanospheres catalysts possessed high acidities and -SO3H densities, which endowed their significantly catalytic activities for biodiesel production. Furthermore, their excellent stability and recycling property were also demonstrated by five consecutive cycles.

  5. An investigation of proton conductivity of binary matrices sulfonated polysulfone/polyvinyltriazole after doping with inorganic acids

    Indian Academy of Sciences (India)

    Serkan Sevinç; Sevim Ünügür Çelik; Ayhan Bozkurt

    2015-04-01

    As anhydrous proton conductive membranes, sulfonated polysulfone (SPSU) and polyvinyl triazole were studied as binary matrices. The sulfonation of polysulfone was performed with trimethylsilylchlorosulfonate and high degree of sulfonation (140%) was obtained. Ion exchange capacity of SPSU was determined as 3.05 mmol−1/g. The polymer electrolyte membranes were prepared by blending of sulfonated polysulfone with polyvinyl triazole and phosphoric acid. Fourier transform infrared spectroscopy confirmed the sulfonation of the polysulfone and the ionic interaction between sulfonic acid and triazole units. Thermogravimetric analysis showed that the polymer electrolyte membranes are thermally stable up to at least 150° C. Scanning electron microscopy analysis indicated the homogeneity of the ternary composites. The maximum proton conductivity has been measured as 3.63 × 10−4S cm−1 at 150° C.

  6. Gene expression profiling identifies mechanisms of protection to recurrent trinitrobenzene sulfonic acid colitis mediated by probiotics

    NARCIS (Netherlands)

    Mariman, R.; Kremer, S.H.A.; Erk, M. van; Lagerweij, T.; Koning, F.; Nagelkerken, L.

    2012-01-01

    Background: Host-microbiota interactions in the intestinal mucosa play a major role in intestinal immune homeostasis and control the threshold of local inflammation. The aim of this study was to evaluate the efficacy of probiotics in the recurrent trinitrobenzene sulfonic acid (TNBS)-induced colitis

  7. Preparation and Reactions of Amino Acid Ester Sulfones as New Remote Asymmetrical Induced Reagents

    Institute of Scientific and Technical Information of China (English)

    ZHOU,Cheng-He; BAI,Xue; LI,Tan-Qing; WU,Jun; Alfred Hassner

    2004-01-01

    @@ The development of chiral auxiliary-controlled asymmetric synthesis has been receiving increasing interest in recent yearsfi,2] Various chiral auxiliary reagents have been observed[3] and a lot of results showed that variation of the chiral auxiliary could influence asymmetric induction. Recently, it has been reported the reaction of the aminated sulfones as a remote chiral auxiliary with α,β-unsaturated carbonyl compounds.[4] Here we would like to report the preparation of amino acid ester sulfones as new remote asymmetrical induced reagents and their reactions with α,β-unsaturated esters.

  8. Meso- and macroporous sulfonated starch solid acid catalyst for esterification of palm fatty acid

    Directory of Open Access Journals (Sweden)

    Ibrahim M. Lokman

    2016-03-01

    Full Text Available In the present work, a heterogeneous solid acid catalyst was successfully developed from starch. The catalyst was prepared by a significant two-step process; the initial step was incomplete carbonization of starch (ICS at 400 °C for 12 h and consequently followed by sulfonation process using concentrated H2SO4 to produce sulfonated-incomplete carbonized starch (ICS-SO3H. The characterization of the ICS-SO3H catalyst was done for chemical and physical properties such as X-ray diffraction (XRD, ammonia-temperature programmed desorption (NH3-TPD, surface area analysis, thermal gravimetric analysis (TGA, elemental analysis and morphology analysis by scanning electron microscope (SEM. BET results showed the structure of ICS-SO3H consists of meso- and macro-porous properties, which allowed high density of the SO3H group attached on its carbon networks. The catalytic activity of ICS-SO3H catalyst was determined by analyzing the catalyst performance to esterify palm fatty acid distillate (PFAD and sequentially produced methyl ester. The maximum free fatty acid (FFA conversion and FAME yield were as high as 94.6% and 90.4%, respectively, at 75 °C using 10:1 methanol-to-PFAD molar ratio and 2 wt.% of catalyst within 3 h. The catalyst has sufficient potential to recycle up to 6 reactions without reactivation step and any remarkable loss of catalytic activity. It revealed that the heterogeneous ICS-SO3H catalyst exhibits high stability, reusability and catalytic activity.

  9. Ag island film-enhanced rare earth co-luminescence effect of Tb-Gd-protein-sodium dodecyl benzene sulfonate system and sensitive detection of protein.

    Science.gov (United States)

    Sun, Chang Xia; Wu, Xia; Zhou, Hai Ping; Wang, Fei; Ding, Hong Hong; Zhao, Liang Liang; Yang, Jing He

    2008-09-15

    This paper reported the coupling technique of Ag island film-enhanced fluorescence with rare earth co-luminescence effect of Tb-Gd-sodium dodecyl benzene sulfonate (SDBS)-protein system. While the collagen is used as the separator between Ag island film and the fluorophore because it not only can decrease the fluorescence of the blank, but also can promote the adsorption of other proteins and change the conformation of the protein. The effects of Ag island film on both the fluorescence and resonance energy transfer process of Tb-Gd-SDBS-protein system are studied, finding that Ag island film can enhance the energy transfer efficiency of this system, resulting in fluorescence enhancement about tenfold compared with this system without Ag island film. Therefore, this technique is used for the detection of proteins as low as 0.72 ng/mL for BSA and 1.3 ng/mL for HSA. In addition, Ag island film can also change the energy transfer process of Tb-SDBS-protein system. PMID:18761153

  10. Absorption characteristic of paeoniflorin-6'-O-benzene sulfonate (CP-25) in in situ single-pass intestinal perfusion in rats.

    Science.gov (United States)

    Yang, Xiao-Dan; Wang, Chun; Zhou, Peng; Yu, Jun; Asenso, James; Ma, Yong; Wei, Wei

    2016-09-01

    1. Paeoniflorin-6'-O-benzene sulfonate (CP-25) was synthesized to improve the poor oral absorption of paeoniflorin (Pae). 2. This study was performed to investigate the absorptive behavior and mechanism of CP-25 in in situ single-pass intestinal perfusion in rats, using Pae as a control. 3. The results showed that intestinal absorption of CP-25 was neither segmental nor sex dependent. However, the main segment of intestine that absorbed Pae was the duodenum. Furthermore, passive transport was confirmed to be the main absorption pattern of CP-25. More importantly, the absorption of CP-25 was much higher than Pae in the small intestine. 4. Among the ABC transporter inhibitors, the absorption rate of Pae increased in the presence of P-gp inhibitors verapamil and GF120918, which indicated that Pae was a substrate of P-glycoprotein (P-gp), however, such was not observed in the presence of breast cancer resistance protein and multidrug resistance-associated protein 2. Finally, the ABC transporter inhibitors did not have any significant impact on CP-25 as demonstrated in the parallel studies. 5. CP-25 could improve the poor absorption of Pae, which may be attributed to both the lipid solubility enhancement and its resistance to P-gp-mediated efflux. PMID:26711120

  11. Assessment and influence of operational parameters on the TiO2 photocatalytic degradation of sodium benzene sulfonate under highly concentrated solar light illumination

    International Nuclear Information System (INIS)

    Sodium benzene sulfonate (BS) was decomposed in aqueous TiO2 dispersions under highly concentrated solar light illumination to examine the photocatalytic characteristics of a parabolic round concentrator (PRC) reactor to degrade the pollutant without visible light absorption. The effects of such operational parameters as initial concentration, volume of the aqueous BS solution, oxygen purging, and TiO2 loading on the kinetics of decomposition of BS were investigated. An effective photodegradation necessitates a suitable combination of initial volume and concentration of BS solution. Relative to atmospheric air, oxygen purging significantly accelerates the degradation process at high initial concentrations of BS (0.40 mM or 1.0 mM). Optimal TiO2 loading was 9 gl -1, greater than previously reported. Elimination of TOC (total organic carbon) followed pseudo first-order kinetics in the initial stages of the photodegradation process. The relative photonic efficiency for the photodegradation of BS is ζrel=1.0. (Author)

  12. Effects of sodium dodecyl benzene sulfonate on the crystal structures and photocatalytic performance of ZnO powders prepared by hydrothermal method

    Energy Technology Data Exchange (ETDEWEB)

    Hu, Limin; Dong, Shuying; Li, Qilu; Li, Yifan; Pi, Yunqing; Liu, Menglin; Han, Xiao; Sun, Jianhui, E-mail: sunjh@htu.cn

    2015-11-15

    A facile and efficient route for the controllable synthesis of ZnO nanostructures by hydrothermal method using sodium dodecyl benzene sulfonate (SDBS) as surfactant was reported. The obtained products were well characterized with the aid of various techniques to probe their crystallographic, morphological, chemical, electrochemical and optical properties. The prepared products were used as photocatalysts in the application of the degradation of metronidazole (MNZ)-contained wastewater under visible light irradiation. A 4.5-fold augmentation of degradation efficiency was in turn observed for optimal ZnO (ZO-0.75) photocatalyst compared with that of sample without SDBS addition (ZO) under the visible light irradiation. The effects of SDBS dosage on the crystal structures of prepared samples as well as the crystal growth mechanism were also probed. - Graphical abstract: ZnO photocatalysts were fabricated through a facile and efficient hydrothermal method using SDBS as structure-directing surfactant in a controllable manner. In particular, the sample with different SDBS dosage exhibited distinct crystal structure and photocatalytic performance. - Highlights: • A rod-like ZnO photocatalyst was facilely synthesized by using SDBS as surfactant. • The effect of SDBS dosage on the crystal structure of photocatalyst was probed. • The probably crystal growth mechanism of prepared photocatalyst was explored. • The optimal ZnO with 0.75 g SDBS dosage displayed the best photocatalytic activity.

  13. Determination of Protein by Fluorescence Enhancement of Curcumin in Lanthanum-Curcumin-Sodium Dodecyl Benzene Sulfonate-Protein System

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Feng [Zaozhuang University, People' s Republic of China; Huang, Wei [Zaozhuang University, People' s Republic of China; Zhang, Yunfeng [Zaozhuang University, People' s Republic of China; Wang, Mingyin [Zaozhuang University, People' s Republic of China; Sun, Lina [Zaozhuang University, People' s Republic of China; Tang, Bo [Shandong University, Jinan, China; Wang, Wei [ORNL

    2011-01-01

    We found that the fluorescence intensity of the lanthanum (La(3+))-curcumin (CU) complex can be highly enhanced by proteins in the presence of sodium dodecyl benzene sulphonate (SDBS). Based on this finding, a new fluorimetric method for the determination of protein was developed. Under optimized conditions, the enhanced intensities of fluorescence are quantitatively in proportion to the concentrations of proteins in the range 0.0080-20.0 g mL(-1) for bovine serum albumin (BSA) and 0.00080-20.0 g mL(-1) for human serum albumin (HSA) with excitation of 425 nm, and 0.00020-20.0 g mL(-1) for bovine serum albumin (BSA) and 0.00080-20.0 g mL(-1)for human serum albumin (HSA) with excitation of 280 nm, while corresponding qualitative detection limits (S/N 3) are as low as 5.368, 0.573, 0.049, 0.562 g mL(-1), respectively. Study on reaction mechanism reveals that proteins can bind with La(3+), CU and SDBS through self-assembling function with electrostatic attraction, hydrogen bonding, hydrophobic interaction and van der Waals forces, etc. The proteins form a supermolecular association with multilayer structure, in which La(3+)-CU is clamped between BSA and SDBS. The unique high fluorescence enhancement of CU is resulted through synergic effects of favorable hydrophobic microenvironment provided by BSA and SDBS, and efficient intermolecular energy transfer among BSA, SDBS and CU. In energy transfer process, La(3+) plays a crucial role because it not only shortens the distance between SDBS and CU, but also acts as a "bridge" for transferring the energy from BSA to CU.

  14. Three 2D Ag(I)-framework isomers with helical structures controlled by the chirality of camphor-10-sulfonic acid.

    Science.gov (United States)

    Guo, Peng

    2011-02-28

    Three 2D Ag(I)-framework isomers were constructed from enantiopure camphor-10-sulfonic acids or racemic camphor-10-sulfonic acids, together with achiral 4-aminobenzoic acids. In complex 1, (+)-camphor-10-sulfonic acids bridge the single left-handed helices that are made up of Ag ions and 4-aminobenzoic acids, generating a homochiral 2D layer. In such a structure, the interweaving of triple left-handed homohelices was also found. It is worth noting that the helicity of complex 2 could be controlled by the handedness of the camphor-10-sulfonic acid. In complex 2, there are right-handed helical structures, including single right-handed and triple right-handed helical structures connected by (-)-camphor-10-sulfonic acids. For a comparative study, (±)-camphor-10-sulfonic acids were utilized to synthesize complex 3, in which equal numbers of right-handed or left-handed double-helical chains are created. All the complexes were characterized by single-crystal X-ray structure determination, powder X-ray diffraction, IR, TGA and element analysis. Circular dichroism spectra of complexes 1 and 2 were been studied to confirm the fact that enantiopure bridging ligands do not racemize. PMID:21264423

  15. Adsorption behavior of perfluorinated sulfonic acid ionomer on highly graphitized carbon nanofibers and their thermal stabilities

    DEFF Research Database (Denmark)

    Andersen, Shuang Ma; Borghei, Maryam; Dhiman, Rajnish;

    2014-01-01

    isotherm), the ionomer has varying affinities for CNFs (Keq. = between 5 and 22) as compared to Vulcan (Keq. = 18), depending on surface treatments. However, the interactions are most likely governed by different adsorption mechanisms depending on hydrophilicity / hydrophobicity of the adsorbent carbon......A systematic adsorption study of perfluorinated sulfonic acid Nafion® ionomer on ribbon type highly graphitized carbon nanofibers (CNFs) was carried out using 19 fluorine nuclear magnetic resonance spectroscopy. Based on the values obtained for the equilibrium constant (Keq., derived from Langmuir....... The ionomer is probably adsorbed via the polar sulfonic group on hydrophilic Vulcan, whereas, it is adsorbed primarily via hydrophobic -CF2- backbone on the highly hydrophobic pristine CNFs. Ionomer adsorption behavior is gradually altered from apolar to polar group adsorption for the acid modified CNFs...

  16. Esterification of levulinic acid into ethyl levulinate catalysed by sulfonated hydrothermal carbons

    Institute of Scientific and Technical Information of China (English)

    Filoklis D. Pileidis; Maham Tabassum; Sam Coutts; Maria-Magdalena Ttitirici

    2014-01-01

    The synthesis of carbon-based, heterogeneous sulphonic catalysts for the production of levulinate esters. Hydrothermal treatment at moderated temperatures was employed to generate highly func-tional carbonaceous materials, referred to as hydrothermal carbons (HTCs), from both glucose, cellulose and rye straw. The products were sulfonated to generate solid acid-catalysts. Characterisa-tion of the as-synthesised materials as well as catalyst activity tests were performed. SEM images indicate the micrometre-sized particles present in both HTCs were largely unaffected by sulfona-tion, although cellulose-derived HTC displayed signs of inadequate hydrolysis. FT-IR spectroscopy and elemental analysis confirmed successful incorporation of sulphonic groups. 13C solid state NMR, in addition to TGA, elucidated the carbons’ structural composition and supported the common-ly-proposed hydrothermal carbonisation mechanism. Finally, the catalysts were tested via levulinic acid-ethanol esterification and gave high conversion and ester-selectivities (>90%).

  17. Reaction kinetics of free fatty acids esterification in palm fatty acid distillate using coconut shell biochar sulfonated catalyst

    Science.gov (United States)

    Hidayat, Arif; Rochmadi, Wijaya, Karna; Budiman, Arief

    2015-12-01

    Recently, a new strategy of preparing novel carbon-based solid acids has been developed. In this research, the esterification reactions of Palm Fatty Acid Distillate (PFAD) with methanol, using coconut shell biochar sulfonated catalyst from biomass wastes as catalyst, were studied. In this study, the coconut shell biochar sulfonated catalysts were synthesized by sulfonating the coconut shell biochar using concentrated H2SO4. The kinetics of free fatty acid (FFA) esterification in PFAD using a coconut shell biochar sulfonated catalyst was also studied. The effects of the mass ratio of catalyst to oil (1-10%), the molar ratio of methanol to oil (6:1-12:1), and the reaction temperature (40-60°C) were studied for the conversion of PFAD to optimize the reaction conditions. The results showed that the optimal conditions were an methanol to PFAD molar ratio of 12:1, the amount of catalyst of 10%w, and reaction temperature of 60°C. The proposed kinetic model shows a reversible second order reaction and represents all the experimental data satisfactorily, providing deeper insight into the kinetics of the reaction.

  18. Clean synthesis of biodiesel over solid acid catalysts of sulfonated mesopolymers

    Institute of Scientific and Technical Information of China (English)

    2010-01-01

    FDU-15-SO3H,a solid acid material prepared from the sulfonation of FDU-15 mesoporous polymer,has been demonstrated to serve as an efficient catalyst in the esterification of palmitic acid with methanol as well as in the transesterification of fatty acid-edible oil mixture.FDU-15-SO3H achieved an acid conversion of 99.0% when the esterification was carried out at 343 K with a methanol/palmitic acid molar ratio of 6:1 and 5 wt% catalyst loading.It was capable of giving 99.0% yield of fatty acid methyl esters (FAME) when the transesterification of soybean oil was performed at 413 K and the methanol/oil weight ratio of 1:1.FDU-15-SO3H was further applied to the transesterification/esterification of the oil mixtures with a varying ratio of soybean oil to palmitic acid,which simulated the feedstock with a high content of free fatty acids.The yield of FAME reached 95% for the oil mixtures containing 30 wt% palmitic acid.This indicated the sulfonated mesopolymer was a potential catalyst for clean synthesis of fuel alternative of biodiesel from the waste oil without further purification.

  19. Preparation and Characterization of Sulfonic Acid Functionalized Silica and Its Application for the Esterification of Ethanol and Maleic Acid

    Science.gov (United States)

    Sirsam, Rajkumar; Usmani, Ghayas

    2016-04-01

    The surface of commercially available silica gel, 60-200 mesh size, was modified with sulfonic acid through surface activation, grafting of 3-Mercaptopropyltrimethoxysilane, oxidation and acidification of 3-Mercaptopropylsilica. Sulfonic Acid Functionalization of Silica (SAFS) was confirmed by Fourier Transform Infra-red (FTIR) spectroscopy and thermal gravimetric analysis. Acid-base titration was used to estimate the cation exchange capacity of the SAFS. Catalytic activity of SAFS was judged for the esterification of ethanol with maleic acid. An effect of different process parameters viz. molar ratio, catalyst loading, speed of agitation and temperature were studied and optimized by Box Behnken Design (BBD) of Response Surface Methodology (RSM). Quadratic model developed by BBD-RSM reasonably satisfied an experimental and predicted values with correlation coefficient value R2 = 0.9504.

  20. Validation and optimization of experimental colitis induction in rats using 2, 4, 6-trinitrobenzene sulfonic acid

    OpenAIRE

    Motavallian-Naeini, A.; Andalib, S.; M Rabbani; Mahzouni, P.; Afsharipour, M.; Minaiyan, M.

    2012-01-01

    Trinitrobenzene sulfonic acid (TNBS)-induced colitis is one of the most common methods for studying inflammatory bowel disease in animal models. Several factors may, however, affect its reproducibility, rate of animal mortality, and macroscopic and histopathological outcomes. Our aim was to validate the main contributing factors to this method and compare the effects of different reference drugs upon remission of resultant colon injuries. TNBS was dissolved in 0.25 ml of ethanol (50% v/v) and...

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

    Science.gov (United States)

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

    2016-09-28

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

  2. 4-Benzene­sulfonamido­benzoic acid

    OpenAIRE

    Sharif, Hafiz Muhammad Adeel; Dong, Gui-Ying; Arshad, Muhammad Nadeem; Khan, Islam Ullah

    2009-01-01

    In the mol­ecule of the title sulfonamide compound, C13H11NO4S, the dihedral angle between the planes of the benzene ring and the carboxyl substituent group is 6.7 (4)°. The two aromatic rings are inclined at 45.36 (15)° to one another. In the crystal, adjacent mol­ecules are linked via classical inter­molecular N—H⋯O and O—H⋯O, and non-classical C—H⋯O hydrogen bonds, which stabilize the crystal structure.

  3. 4-Benzene­sulfonamido­benzoic acid

    Science.gov (United States)

    Sharif, Hafiz Muhammad Adeel; Dong, Gui-Ying; Arshad, Muhammad Nadeem; Khan, Islam Ullah

    2009-01-01

    In the mol­ecule of the title sulfonamide compound, C13H11NO4S, the dihedral angle between the planes of the benzene ring and the carboxyl substituent group is 6.7 (4)°. The two aromatic rings are inclined at 45.36 (15)° to one another. In the crystal, adjacent mol­ecules are linked via classical inter­molecular N—H⋯O and O—H⋯O, and non-classical C—H⋯O hydrogen bonds, which stabilize the crystal structure. PMID:21578816

  4. Production of biodiesel from palm fatty acid distillate using sulfonated-glucose solid acid catalyst:Characterization and optimization

    Institute of Scientific and Technical Information of China (English)

    Ibrahim M Lokman; Umer Rashid; Yun Hin Taufiq-Yap

    2015-01-01

    A palm fatty acid distillate (PFAD) has been used for biodiesel production. An efficient sulfonated-glucose acid catalyst (SGAC) was prepared by sulfonation to catalyze the esterification reaction. The effect of three variables i.e. methanol-to-PFAD molar ratio, catalyst amount and reaction time, on the yield of PFAD esters was studied by the response surface methodology (RSM). The optimum reaction conditions were:12.2:1 methanol-to-PFAD molar ratio, 2.9%catalyst concentration and 134 min of time as predicted by the RSM. The reaction under the optimum conditions resulted in 94.5%of the free fatty acid (FFA) conversion with 92.4%of the FAME yield. The properties of the PFAD esters were determined according to biodiesel standards.

  5. Vacuum thermal evaporation of polyaniline doped with camphor sulfonic acid

    Energy Technology Data Exchange (ETDEWEB)

    Boyne, Devon; Menegazzo, Nicola; Pupillo, Rachel C.; Rosenthal, Joel; Booksh, Karl S., E-mail: kbooksh@udel.edu [Department of Chemistry and Biochemistry, University of Delaware, Newark, Delaware 19716 (United States)

    2015-05-15

    Intrinsically conducting polymers belong to a class of organic polymers with intriguing electronic and physical properties specifically for electro-optical applications. Significant interest into doped polyaniline (PAni) can be attributed to its high conductivity and environmental stability. Poor dissolution in most solvents has thus far hindered the successful integration of PAni into commercial applications, which in turn, has led to the investigations of various deposition and acidic doping methods. Physical vapor deposition methods, including D.C. magnetron sputtering and vacuum thermal evaporation, have shown exceptional control over physical film properties (thickness and morphology). However, resulting films are less conductive than films deposited by conventional methods (i.e., spin and drop casting) due to interruption of the hyperconjugation of polymer chains. Specifically, vacuum thermal evaporation requires a postdoping process, which results in incorporation of impurities and oxidation of surface moieties. In this contribution, thermally evaporated films, sequentially doped by vacuum evaporation of an organic acid (camphorsulfonic acid, CSA) is explored. Spectroscopic evidence confirms the successful doping of PAni with CSA while physical characterization (atomic force microscopy) suggests films retain good morphology and are not damaged by the doping process. The procedure presented herein also combines other postpreparation methods in an attempt to improve conductivity and/or substrate adhesion.

  6. Sulfonic acid heterogeneous catalysts for dehydration of C6-monosaccharides to 5-hydroxymethylfurfural in dimethyl sulfoxide

    Institute of Scientific and Technical Information of China (English)

    Gabriel Morales; Juan A.Melero; Marta Paniagua; Jose Iglesias; Blanca Hernández; María Sanz

    2014-01-01

    Sulfonic acid-functionalized heterogeneous catalysts have been evaluated in the catalytic dehydra-tion of C6 monosaccharides into 5-hydroxymethylfurfural (HMF) using dimethyl sulfoxide (DMSO) as solvent. Sulfonic commercial resin Amberlyst-70 was the most active catalyst, which was as-cribed to its higher concentration of sulfonic acid sites as compared with the other catalysts, and it gave 93 mol%yield of HMF from fructose in 1 h. With glucose as the starting material, which is a much more difficult reaction, the reaction conditions (time, temperature, and catalyst loading) were optimized for Amberlyst-70 by a response surface methodology, which gave a maximum HMF yield of 33 mol%at 147°C with 23 wt%catalyst loading based on glucose and 24 h reaction time. DMSO promotes the dehydration of glucose into anhydroglucose, which acts as a reservoir of the substrate to facilitate the production of HMF by reducing side reactions. Catalyst reuse without a regeneration treatment showed a gradual but not very significant decay in catalytic activity.

  7. Nanocasting Design and Spatially Selective Sulfonation of Polystyrene-Based Polymer Networks as Solid Acid Catalysts.

    Science.gov (United States)

    Richter, Felix H; Sahraoui, Laila; Schüth, Ferdi

    2016-09-12

    Nanocasting is a general and widely applied method in the generation of porous materials during which a sacrificial solid template is used as a mold on the nanoscale. Ideally, the resulting structure is the inverse of the template. However, replication is not always as direct as anticipated, so the influences of the degree of pore filling and of potential restructuring processes after removal of the template need to be considered. These apparent limitations give rise to opportunities in the synthesis of poly(styrene-co-divinylbenzene) (PSD) polymer networks of widely varying porosities (BET surface area=63-562 m(2)  g(-1) ; Vtot =0.18-1.05 cm(3)  g(-1) ) by applying a single synthesis methodology. In addition, spatially selective sulfonation on the nanoscale seems possible. Together, nanocasting and sulfonation enable rational catalyst design. The highly porous nanocast and predominantly surface-sulfonated PSD networks approach the activity of the corresponding molecular catalyst, para-toluenesulfonic acid, and exceed those of commercial ion-exchange polymers in the depolymerization of macromolecular inulin.

  8. Synthesis of Rare Metal Yttrium of Camphor Sulfonic Acid%樟脑磺酸钇的合成

    Institute of Scientific and Technical Information of China (English)

    刘晓红; 柯春兰

    2015-01-01

    This paper studied the preparation of Yttrium of L-camphor sulfonic acid and Yttrium of D-cam-phor sulfonic acid. In this experiment,racemic camphor was uesd as the raw material,and through the sulfonation reaction,split,purification and separate,chiral camphor sulfonic acid was abtained,and it can react with Y2 O3 to get yttrium of chiral Camphor sulfonic acid. The optimal synthesis conditions were:Camphor sulfonic acid concentration was 12% -15%,reaction temperature was 90 ℃,reaction time was 0. 5-1 h,Y2 O3 excessed 50%. Tested by in-frared spectroscopy( IR)and XRD,it can be found that Yttrium of Rare Metal Camphor Sulfonic Acid are consist-ent with the standard compounds.%研究了左旋樟脑磺酸钇和右旋樟脑磺酸钇的制备。实验以合成樟脑粉为原料,经过磺化反应、拆分、纯化分离等步骤得到手性樟脑磺酸,稀土金属氧化钇与手性樟脑磺酸反应合成了稀土金属樟脑磺酸钇,合成条件:樟脑磺酸质量浓度12%~15%,反应温度90℃,反应时间0.5~1 h,氧化钇过量50%。得到的产品稀土金属樟脑磺酸钇经红外光谱( IR)、XRD分析,证明与目标产物一致。

  9. 4-[(E-(5-tert-Butyl-2-hydroxyphenyldiazenyl]benzoic acid benzene hemisolvate

    Directory of Open Access Journals (Sweden)

    Edward R. T. Tiekink

    2010-03-01

    Full Text Available The title benzene hemisolvate, C17H18N2O3·0.5C6H6, features an essentially planar (the r.m.s. deviation of the non-H atoms, excluding methyl-C, is 0.071 Å diazo molecule with an E conformation about the N=N bond, and a half-molecule of benzene disposed about a centre of inversion. The dihedral angle formed between the benzene rings of the diazo molecule is 7.69 (12°. In the crystal, centrosymmetrically related dimers associate via the eight-membered carboxylic acid dimer synthon, {...HOC(=O}2, and these are connected into a supramolecular chain along the b axis via C—H...O contacts.

  10. Mesoporous silica containing sulfonic acid groups as catalysts for alpha-pinene methoxylation

    OpenAIRE

    Castanheiro, J; Guerreiro, L; Fonseca, I.; Ramos, A.; Vital, J

    2008-01-01

    The methoxylation of a-pinene was studied over sulfonic acid-functionalized mesoporous silica (MCM-41, PMO) at 60ºC. The support functionalization was achieved by the introduction of 3-(mercaptopropyl)trimethoxysilane onto the surface of these materials either by grafting or by co-condensation. The thiol groups were oxidized to SO3H by treatment with H2O2. All the catalysts were active in the studied reaction being the PMO-SO3H-g the best one. Good values of selectivity to a-terpinyl methyl e...

  11. SYNTESIS OF THE COMPLEXES OF MACROPOROUS SULFONATED RESINS WITH FERRIC CHLORIDE AND THEIR CATALYTIC BEHAVIOR FOR SETERIFICATION OF ACETIC ACID WITH BUTANOL

    Institute of Scientific and Technical Information of China (English)

    HuangWenqiang; HouXin; 等

    1997-01-01

    The complex resins prepared from macroporous sulfonated resin D72(H+ form) with ferric chloride or ferric chloride hexahydrate have both sites of Bronsted acid and Lewis acid.In the catalysis of exterification of acetic acid with butanol the complex resins show to have much higher catalytic activity than that of its matrix.a conventional sulfonated cation exchange resin D72.

  12. Development and characterization of acid-doped polybenzimidazole/sulfonated polysulfone blend polymer electrolytes for fuel cells

    DEFF Research Database (Denmark)

    Hasiotis, C.; Li, Qingfeng; Deimede, V.;

    2001-01-01

    Polymeric membranes from blends of sulfonated polysulfones (SPSF) and polybenzimidazole (PBI) doped with phosphoric acid were developed as potential high-temperature polymer electrolytes for fuel cells and other electrochemical applications. The water uptake and acid doping of these polymeric...... membranes were investigated. Ionic conductivity of the membranes was measured in relation to temperature, acid doping level, sulfonation degree of SPSF, relative humidity, and blend composition. The conductivity of SPSF was of the order of 10/sup -3/ S cm/sup -1/. In the case of blends of PBI and SPSF...

  13. Physicochemical pretreatments and hydrolysis of furfural residues via carbon-based sulfonated solid acid.

    Science.gov (United States)

    Ma, Bao Jun; Sun, Yuan; Lin, Ke Ying; Li, Bing; Liu, Wan Yi

    2014-03-01

    Potential commercial physicochemical pretreatment methods, NaOH/microwave and NaOH/ultrasound were developed, and the carbon-based sulfonated solid acid catalysts were prepared for furfural residues conversion into reducing sugars. After the two optimum pretreatments, both the content of cellulose increased (74.03%, 72.28%, respectively) and the content of hemicellulose (94.11%, 94.17% of removal rate, respectively) and lignin (91.75%, 92.09% of removal rate, respectively) decreased in furfural residues. The reducing sugar yields of furfural residues with the two physicochemical pretreatments on coal tar-based solid acid reached 33.94% and 33.13%, respectively, higher than that pretreated via NaOH alone (27%) and comparable to that pretreated via NaOH/H2O2 (35.67%). The XRD patterns, IR spectra and SEM images show microwave and ultrasound improve the pretreatment effect. The results demonstrate the carbon-based sulfonated solid acids and the physicochemical pretreatments are green, effective, low-cost for furfural residues conversion.

  14. Silica Bonded S-Sulfonic Acid: A Recyclable Catalyst for the Synthesis of Quinoxalines at Room Temperature

    Directory of Open Access Journals (Sweden)

    Khodabakhsh Niknam

    2009-05-01

    Full Text Available The reaction of 3-mercaptopropylsilica (MPS and chlorosulfonic acid in chloroform afforded silica bonded S-sulfonic acid (SBSSA, which was used as a catalyst for the room temperature synthesis of quinoxaline derivatives from 1,2-diamino compounds and 1,2-dicarbonyl compounds. The catalyst could be recycled and reused several times without any loss of efficiency.

  15. Synthesis of a Sulfonated Two-Dimensional Covalent Organic Framework as an Efficient Solid Acid Catalyst for Biobased Chemical Conversion.

    Science.gov (United States)

    Peng, Yongwu; Hu, Zhigang; Gao, Yongjun; Yuan, Daqiang; Kang, Zixi; Qian, Yuhong; Yan, Ning; Zhao, Dan

    2015-10-12

    Because of limited framework stability tolerance, de novo synthesis of sulfonated covalent organic frameworks (COFs) remains challenging and unexplored. Herein, a sulfonated two-dimensional crystalline COF, termed TFP-DABA, was synthesized directly from 1,3,5-triformylphloroglucinol and 2,5-diaminobenzenesulfonic acid through a previously reported Schiff base condensation reaction, followed by irreversible enol-to-keto tautomerization, which strengthened its structural stability. TFP-DABA is a highly efficient solid acid catalyst for fructose conversion with remarkable yields (97 % for 5-hydroxymethylfurfural and 65 % for 2,5-diformylfuran), good chemoselectivity, and good recyclability. The present study sheds light on the de novo synthesis of sulfonated COFs as novel solid acid catalysts for biobased chemical conversion.

  16. Synthesis of a Sulfonated Two-Dimensional Covalent Organic Framework as an Efficient Solid Acid Catalyst for Biobased Chemical Conversion.

    Science.gov (United States)

    Peng, Yongwu; Hu, Zhigang; Gao, Yongjun; Yuan, Daqiang; Kang, Zixi; Qian, Yuhong; Yan, Ning; Zhao, Dan

    2015-10-12

    Because of limited framework stability tolerance, de novo synthesis of sulfonated covalent organic frameworks (COFs) remains challenging and unexplored. Herein, a sulfonated two-dimensional crystalline COF, termed TFP-DABA, was synthesized directly from 1,3,5-triformylphloroglucinol and 2,5-diaminobenzenesulfonic acid through a previously reported Schiff base condensation reaction, followed by irreversible enol-to-keto tautomerization, which strengthened its structural stability. TFP-DABA is a highly efficient solid acid catalyst for fructose conversion with remarkable yields (97 % for 5-hydroxymethylfurfural and 65 % for 2,5-diformylfuran), good chemoselectivity, and good recyclability. The present study sheds light on the de novo synthesis of sulfonated COFs as novel solid acid catalysts for biobased chemical conversion. PMID:26448524

  17. Alkyl sulfonic acide hydrazides: Synthesis, characterization, computational studies and anticancer, antibacterial, anticarbonic anhydrase II (hCA II) activities

    Science.gov (United States)

    O. Ozdemir, Ummuhan; İlbiz, Firdevs; Balaban Gunduzalp, Ayla; Ozbek, Neslihan; Karagoz Genç, Zuhal; Hamurcu, Fatma; Tekin, Suat

    2015-11-01

    Methane sulfonic acide hydrazide, CH3SO2NHNH2 (1), ethane sulfonic acide hydrazide, CH3CH2SO2NHNH2 (2), propane sulfonic acide hydrazide, CH3CH2CH2SO2NHNH2 (3) and butane sulfonic acide hydrazide, CH3CH2CH2CH2SO2NHNH2 (4) have been synthesized as homologous series and characterized by using elemental analysis, spectrophotometric methods (1H-13C NMR, FT-IR, LC-MS). In order to gain insight into the structure of the compounds, we have performed computational studies by using 6-311G(d, p) functional in which B3LYP functional were implemented. The geometry of the sulfonic acide hydrazides were optimized at the DFT method with Gaussian 09 program package. A conformational analysis of compounds were performed by using NMR theoretical calculations with DFT/B3LYP/6-311++G(2d, 2p) level of theory by applying the (GIAO) approach. The anticancer activities of these compounds on MCF-7 human breast cancer cell line investigated by comparing IC50 values. The antibacterial activities of synthesized compounds were studied against Gram positive bacteria; Staphylococcus aureus ATCC 6538, Bacillus subtilis ATCC 6633, Bacillus cereus NRRL-B-3711, Enterococcus faecalis ATCC 29212 and Gram negative bacteria; Escherichia coli ATCC 11230, Pseudomonas aeruginosa ATCC 15442, Klebsiella pneumonia ATCC 70063 by using the disc diffusion method. The inhibition activities of these compounds on carbonic anhydrase II enzyme (hCA II) have been investigated by comparing IC50 and Ki values. The biological activity screening shows that butane sulfonic acide hydrazide (4) has more activity than the others against tested breast cancer cell lines MCF-7, Gram negative/Gram positive bacteria and carbonic anhydrase II (hCA II) isoenzyme.

  18. Estimated pKa values for the environmentally relevant C1 through C8 perfluorinated sulfonic acid isomers.

    Science.gov (United States)

    Rayne, Sierra; Forest, Kaya

    2016-10-14

    In order to estimate isomer-specific acidity constants (pKa) for the perfluorinated sulfonic acid (PFSA) environmental contaminants, the parameterization method 6 (PM6) pKa prediction method was extensively validated against a wide range of carbon oxyacids and related sulfonic/sulfinic acids. Excellent pKa prediction performance was observed for the carbon oxyacids using the PM6 method, but this approach was found to have a severe positive bias for sulfonic/sulfinic acids. To overcome this obstacle, a correlation was developed between non-adjusted PM6 pKa values and the corresponding experimentally obtained/estimated acidity constants for a range of representative alkyl, aryl and halogen-substituted sulfonic acids. Application of this correction to the PM6 values allows for extension of this computational method to a new acid functional group. When used to estimate isomer-specific pKa values for the C1 through C8 PFSAs, the modified PM6 approach suggests an adjusted pKa range from -5.3 to -9.0, indicating that all members of this class of well-known environmental contaminants will be effectively completely dissociated in aquatic systems. PMID:27389973

  19. A study on the distribution of polystyrene sulfonic acid grafts over the cross-section of a PFA film

    International Nuclear Information System (INIS)

    In this study, the distribution behaviors of polystyrene sulfonic acid (PSSA) grafts over the cross-section of grafted PFA membranes (PFA-g-PSSA) were investigated by using SEM-EDX analysis. Membranes with various degrees of grafting (DOG) and thicknesses were prepared by a simultaneous radiation grafting of styrene and a subsequent sulfonation with chlorosulfonic acid. A SEM-EDX instrument was utilized to directly observe that the distribution behaviors of the PSSA grafts over the cross-section of grafted PFA membranes and the results showed that the distribution behaviors were largely affected by the grafting conditions such as the degree of grafting, monomer concentration, and film thickness.

  20. Effect of a sulfonated azo dye and sulfanilic acid on nitrogen transformation processes in soil.

    Science.gov (United States)

    Topaç, F Olcay; Dindar, Efsun; Uçaroğlu, Selnur; Başkaya, Hüseyin S

    2009-10-30

    Introduction of organic dyes into soil via wastewater and sludge applications has been of increasing concern especially in developing or under-developed countries where appropriate management strategies are scarce. Assessing the response of terrestrial ecosystems to organic dyes and estimating the inhibition concentrations will probably contribute to soil remediation studies in regions affected by the same problem. Hence, an incubation study was conducted in order to investigate the impact of a sulfonated azo dye, Reactive Black 5 (RB5) and sulfanilic acid (SA), a typical representative of aromatic sulfonated amines, on soil nitrogen transformation processes. The results apparently showed that nitrogen related processes in soil can be used as bioindicators of anthropogenic stress caused by organic dyes. It was found that urease activity, arginine ammonification rate, nitrification potential and ammonium oxidising bacteria numbers decreased by 10-20% and 7-28% in the presence of RB5 (> 20 mg/kg dry soil) and SA (> 8 mg/kg dry soil), respectively. Accordingly, it was concluded that organic dye pollution may restrict the nitrogen-use-efficiency of plants, thus further reducing the productivity of terrestrial ecosystems. Furthermore, the response of soil microbiota to SA suggested that inhibition effects of the organic dye may continue after the possible reduction of the parent dye to associated aromatic amines.

  1. Synthesis, characterization, antibacterial activity and quantum chemical studies of N'-Acetyl propane sulfonic acid hydrazide

    Science.gov (United States)

    Alyar, Saliha; Alyar, Hamit; Ozdemir, Ummuhan Ozmen; Sahin, Omer; Kaya, Kerem; Ozbek, Neslihan; Gunduzalp, Ayla Balaban

    2015-08-01

    A new N'-Acetyl propane sulfonic acid hydrazide, C3H7sbnd SO2sbnd NHsbnd NHsbnd COCH3 (Apsh, an sulfon amide compound) has been synthesized for the first time. The structure of Apsh was investigated using elemental analysis, spectral (IR, 1H/13C NMR) measurements. In addition, molecular structure of the Apsh was determined by single crystal X-ray diffraction technique and found that the compound crystallizes in monoclinic, space group P 21/c. 1H and 13C shielding tensors for crystal structure were calculated with GIAO/DFT/B3LYP/6-311++G(d,p) methods in CDCl3. The structure of Apsh is optimized using Density Functional Theory (DFT) method. The vibrational band assignments were performed at B3LYP/6-311++G(d,p) theory level combined with scaled quantum mechanics force field (SQMFF) methodology. The theoretical IR frequencies are found to be in good agreement with the experimental IR frequencies. Nonlinear optical (NLO) behaviour of Apsh is also examined by the theoretically predicted values of dipole moment (μ), polarizability (α0) and first hyperpolarizability (βtot). The antibacterial activities of synthesized compound were studied against Gram positive bacteria: Staphylococcus aureus ATCC 25923, Enterococcus faecalis ATCC 23212, Staphylococcus epidermidis ATCC 34384, Gram negative bacteria: Eschericha coli ATCC 25922, Pseudomonas aeruginosa ATCC 27853, Klebsiella pneumoniae ATCC 70063 by using microdilution method (as MICs) and disc diffusion method.

  2. Removal of 5-Amino-2-chlorotoluene-4-sulfonic and Chlorhydric Acids From Wastewater by Weakly Basic Resin: Equilibrium and Kinetics

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    To study the adsorption of 5-Amino-2-chlorotoluene-4-sulfonic (CLT) and chlorhydric (HCl) acids from wastewater by weakly basic resin.Methods The kinetics and isotherm were studied. Thermodynamic parameters for the adsorption of acids were calculated and discussed.Results The adsorption of CLT and HCl acids followed Langmuir isotherm and the first-order kinetics model.Conclusion The adsorptive affinity of the two acids on D301R is in the order of CLT acid > HCl acid. CLT and HCl acids can be separated.

  3. Mineralization of sulfonated azo dyes and sulfanilic acid by Phanerochaete chrysosporium and Streptomyces chromofuscus.

    Science.gov (United States)

    Paszczynski, A; Pasti-Grigsby, M B; Goszczynski, S; Crawford, R L; Crawford, D L

    1992-11-01

    Five 14C-radiolabeled azo dyes and sulfanilic acid were synthesized and used to examine the relationship between dye substitution patterns and biodegradability (mineralization to CO2) by a white-rot fungus and an actinomycete. 4-Amino-[U-14C]benzenesulfonic acid and 4-(3-sulfo-4-aminophenylazo)-[U-14C]benzenesulfonic acid were used as representative compounds having sulfo groups or both sulfo and azo groups. Such compounds are not known to be present in the biosphere as natural products. The introduction of lignin-like fragments into the molecules of 4-amino-[U-14C]benzenesulfonic acid and 4-(3-sulfo-4-aminophenylazo)-[U-14C]benzenesulfonic acid by coupling reactions with guaiacol (2-methoxyphenol) resulted in the formation of the dyes 4-(3-methoxy-4-hydroxyphenylazo)-[U-14C]benzenesulfonic acid and 4-(2-sulfo-3'-methoxy-4'-hydroxy-azobenzene-4-azo)-[U-14C]benzenesulf oni c acid, respectively. The synthesis of acid azo dyes 4-(2-hydroxy-1-naphthylazo)-[U-14C]benzenesulfonic acid and 4-(4-hydroxy-1-naphthylazo)-[U-14C]benzenesulfonic acid also allowed the abilities of these microorganisms to mineralize these commercially important compounds to be evaluated. Phanerochaete chrysosporium mineralized all of the sulfonated azo dyes, and the substitution pattern did not significantly influence the susceptibility of the dyes to degradation. In contrast, Streptomyces chromofuscus was unable to mineralize aromatics with sulfo groups and both sulfo and azo groups. However, it mediated the mineralization of modified dyes containing lignin-like substitution patterns. This work showed that lignocellulolytic fungi and bacteria can be used for the biodegradation of anionic azo dyes, which thus far have been considered among the xenobiotic compounds most resistant to biodegradation.(ABSTRACT TRUNCATED AT 250 WORDS)

  4. Synthesis of naphthoxazinone derivatives using silica-bonded -sulfonic acid as catalyst under solvent-free conditions

    Indian Academy of Sciences (India)

    Khodabakhsh Niknam; Parisa Abolpour

    2015-07-01

    Silica-bonded -sulfonic acid is employed as a recyclable catalyst for the synthesis of naphthoxazinone derivatives from the reaction of -naphthol, aromatic aldehydes and urea at 150°C under solvent-free conditions. The heterogeneous catalyst was recycled for five runs after the reaction of -naphthol, benzaldehyde and urea without losing its catalytic activity.

  5. Comparison of gene expression methods to identify genes responsive to perfluorooctane sulfonic acid.

    Science.gov (United States)

    Hu, Wenyue; Jones, Paul D; Decoen, Wim; Newsted, John L; Giesy, John P

    2005-01-01

    Genome-wide expression techniques are being increasingly used to assess the effects of environmental contaminants. Oligonucleotide or cDNA microarray methods make possible the screening of large numbers of known sequences for a given model species, while differential display analysis makes possible analysis of the expression of all the genes from any species. We report a comparison of two currently popular methods for genome-wide expression analysis in rat hepatoma cells treated with perfluorooctane sulfonic acid. The two analyses provided 'complimentary' information. Approximately 5% of the 8000 genes analyzed by the GeneChip array, were altered by a factor of three or greater. Differential display results were more difficult to interpret, since multiple gene products were present in most gel bands so a probabilistic approach was used to determine which pathways were affected. The mechanistic interpretation derived from these two methods was in agreement, both showing similar alterations in a specific set of genes. PMID:21783471

  6. Selective Preparation of Furfural from Xylose over Sulfonic Acid Functionalized Mesoporous Sba-15 Materials

    Directory of Open Access Journals (Sweden)

    Panpan Li

    2011-04-01

    Full Text Available Sulfonic acid functionalized mesoporous SBA-15 materials were prepared using the co-condensation and grafting methods, respectively, and their catalytic performance in the dehydration of xylose to furfural was examined. SBA-15-SO3H(C prepared by the co-condensation method showed 92–95% xylose conversion and 74% furfural selectivity, and 68–70% furfural yield under the given reaction conditions. The deactivation and regeneration of the SBA-15-SO3H(C catalyst for the dehydration of xylose was also investigated. The results indicate that the used and regeneration catalysts retained the SBA-15 mesoporous structure, and the S content of SBA-15-SO3H(C almost did not change. The deactivation of the catalysts is proposed to be associated with the accumulation of byproducts, which is caused by the loss reaction of furfural. After regeneration by H2O2, the catalytic activity of the catalyst almost recovered.

  7. SYNTHESIS, STRUCTURE AND PROPERTIES OF INTERPENETRATING SULFONIC ACID RESINS WITH HIGH CAPACITY

    Institute of Scientific and Technical Information of China (English)

    XU Hede; LI Guoming

    1989-01-01

    Two series of interpenetrating sulfonic acid resins (ISAR), 10 × n and n × 10 ,were prepared by means of the wet method, and the physicochemical, thermodynamic and kinetic properties of the ISAR were measured . The results show: 10 × n resins exhibit better properties than n × 10 ones ,mainly in higher apparent degree of crosslinking and larger conformational entropy effect, among which , 10 × 1 resin exhibits the best thermodynamic and kinetic properties. In the DTA graphs of n × 10 resins, there are two Tg and two Tox, but in those of 10 × n, only one Tg and one Tox . This result well supports the conclusion that 10 × n resins have much better interpenetrating structural aspects.

  8. Nanoscale Distribution of Sulfonic Acid Groups Determines Structure and Binding of Water in Nafion Membranes

    Science.gov (United States)

    Ling, Xiao; Bonn, Mischa

    2016-01-01

    Abstract The connection between the nanoscale structure of two chemically equivalent, yet morphologically distinct Nafion fuel‐cell membranes and their macroscopic chemical properties is demonstrated. Quantification of the chemical interactions between water and Nafion reveals that extruded membranes have smaller water channels with a reduced sulfonic acid head group density compared to dispersion‐cast membranes. As a result, a disproportionally large amount of non‐bulk water molecules exists in extruded membranes, which also exhibit larger proton conductivity and larger water mobility compared to cast membranes. The differences in the physicochemical properties of the membranes, that is, the chemical constitution of the water channels and the local water structure, and the accompanying differences in macroscopic water and proton transport suggest that the chemistry of nanoscale channels is an important, yet largely overlooked parameter that influences the functionality of fuel‐cell membranes. PMID:26895211

  9. THERMODYNAMIC STUDY ON ADSORPTION OF AROMATIC SULFONIC ACIDS ONTO MACROPOROUS WEAK BASE ANION EXCHANGER FROM AQUEOUS SOLUTIONS

    Institute of Scientific and Technical Information of China (English)

    Chao Long; Quan-xing Zhang; Ai-min Li; Jin-long Chen

    2004-01-01

    The adsorption equilibrium isotherms of three aromatic sulfonic acid compounds, 2-naphthalenesulfonic acid, ptoluenesulfonic acid and p-chlorobenzenesulfonic acid, from aqueous solutions by macroporous weak base anion exchanger within the temperature range of 293 K-313 K were obtained. Several isotherm equations were correlated with the equilibrium data, and the experimental data was found to fit the three-parameter Redlich-Peterson equation best within the entire range of concentrations. The study showed that the hydrophobicity of solute has distinct influence on adsorption capacity of the anion exchanger for the aromatic sulfonic acid. Moreover, estimations of the isosteric enthalpy, free energy,and entropy change of adsorption were also reported. The positive isosteric enthalpy and entropy change for adsorption indicate an endothermic and entropy driven process in the present study.

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

    Institute of Scientific and Technical Information of China (English)

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

    2009-01-01

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

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

    Institute of Scientific and Technical Information of China (English)

    2009-01-01

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

  12. A verapamil electrochemical sensor based on magnetic mobile crystalline material-41 grafted by sulfonic acid

    International Nuclear Information System (INIS)

    Graphical abstract: The Fe2O3-MCM-41-SO3H was characterized with TEM and used to investigate the electrochemical behavior of verapamil. The results indicated that Fe2O3-MCM-41-SO3H-CPE facilitate the determination of verapamil with good sensitivity. Highlights: ► Electrooxidation of verapamil was performed using Fe2O3-MCM-41-SO3H-CPE. ► Modified electrode shows many advantages as a verapamil sensor. ► Excellent electrocatalytic activity was obtained for verapamil oxidation. ► The response of the modified electrode is linear over the entire 50–160 and 160–350 nM. -- Abstract: Magnetic (Fe2O3) mobile crystalline material-41 (MCM-41) grafted by sulfonic acid (Fe2O3-MCM-41-SO3H) was prepared and characterized using transmission electron microscopy (TEM) and nitrogen adsorption–desorption techniques. Cyclic voltammetry (CV) and differential pulse voltammetry (DPV) and square wave voltametry (SQWV) used to investigate the electrochemical behavior of verapamil at the sulfonic acid functionalized magnetic mesoporous silica, which was modified through carbon paste electrode (Fe2O3-MCM-41-SO3H-CPE). The Fe2O3-MCM-41-SO3H-CPE showed better performance for the electrochemical oxidation of verapamil, when compared with bare carbon paste electrode (CPE) and Fe2O3-MCM-41-CPE. The experimental conditions influencing the determination of verapamil were optimized and under optimal conditions, the oxidation peak current was proportional to verapamil concentration in the range of 50–160 and 160–350 nmol dm−3, while the detection limit was 41 nmol dm−3 (S/N = 3). The proposed method was successfully applied to determine verapamil in human serum, yielding satisfactory results. The spiked recoveries were in the range of (94.5–104.1%)

  13. Chemical Mechanical Polishing of Glass Substrate with α-Alumina-g-Polystyrene Sulfonic Acid Composite Abrasive

    Institute of Scientific and Technical Information of China (English)

    LEI Hong; BU Naijing; ZHANG Zefang; CHEN Ruling

    2010-01-01

    Abrasive is the one of key influencing factors during chemical mechanical polishing(CMP) process. Currently, α-Alumina (α-Al2O3) particle, as a kind of abrasive, has been widely used in CMP slurries, but their high hardness and poor dispersion stability often lead to more surface defects. After being polished with composite particles, the surface defects of work pieces decrease obviously. So the composite particles as abrasives in slurry have been paid more attention. In order to reduce defect caused by pure α-Al2O3 abrasive, α-alumina-g-polystyrene sulfonic acid (α-Al2O3-g-PSS) composite abrasive was prepared by surface graft polymerization. The composition, structure and morphology of the product were characterized by Fourier transform infrared spectroscopy(FTIR), X-ray photoelectron spectroscopy(XPS), time-of-flight secondary ion mass spectroscopy(TOF-SIMS), and scanning electron microscopy(SEM), respectively. The results show that polystyrene sulfonic acid grafts onto α-Al2O3, and has well dispersibility. Then, the chemical mechanical polishing performances of the composite abrasive on glass substrate were investigated with a SPEEDFAM-16B-4M CMP machine. Atomic force microscopy(AFM) images indicate that the average roughness of the polished glass substrate surface can be decreased from 0.835 nm for pure α-Al2O3 abrasive to 0.583 nm for prepared α-Al2O3-g-PSS core-shell abrasive. The research provides a new and effect way to improve the surface qualities during CMP.

  14. Vapor-phase Nitration of Benzene to Nitrobenzene over Supported Sulfuric Acid Catalyst

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    Vapor-phase nitration of benzene over solid acid catalyst is expected to be a clean process with no sulfuric acid waste.We investigated this process over solid acidic catalysts utilizing diluted nitric acid (60-70%) as nitrating agent,and found that supported sulfuric acid catalyst exhibited a very high catalytic activity.Under the conditions of reaction temperature 160-170℃,space velocity (SV) 1200 h-1,the yield and the space-time yield (STY) of nitrobenzene (NB) based on HNO3 were more than 98% and 0.75 kg@kgcat-1@h-1 over 10% H2SO4/SiO2 (by weight) catalyst respectively.

  15. Direct Synthesis of Phenol from Benzene on an Activated Carbon Catalyst Treated with Nitric Acid

    Institute of Scientific and Technical Information of China (English)

    Cui-hong Chen; Jia-quan Xu; Ming-ming Jin; Gui-ying Li; Chang-wei Hu

    2011-01-01

    Commercially available coal-based activated carbon was treated by nitric acid with different concentrations and the resultant samples were used as catalysts for the direct hydroxylation of benzene to phenol in acetonitrile. Boehm titration, X-ray photoelectron spectroscopy,scanning electron microscope coupled with an energy dispersive X-ray microanalyzer, and Brunauer-Emmett-Teller method were used to characterize toe samples. The number of carboxyl groups on the surface was found to be the main factor affecting the catalytic activity. An optimum catalytic performance with a yield of 15.7% and a selectivity of 87.2% to phenol was obtained.

  16. 4-(4-Bromo­benzene­sulfonamido)benzoic acid

    OpenAIRE

    Islam Ullah Khan; Shahzad Sharif; Muhammad Shafiq; Muhammad Nadeem Arshad; Ghulam Mustafa

    2009-01-01

    The title compound, C13H10BrNO4S, belongs to the sulfonamide class of organic compounds. The two aromatic rings are inclined at 34.30 (15)° to one another, and the carboxyl substituent lies in the plane of the benzene ring to which it is bound (maximum deviation = 0.004 Å). In the crystal structure, charactersitic carboxylic acid dimers are formed through O—H...O hydrogen bonds. These dimers are linked into rows down a by N—H...O inter...

  17. Removal of free fatty acid in Palm Fatty Acid Distillate using sulfonated carbon catalyst derived from biomass wastefor biodiesel production

    Science.gov (United States)

    Hidayat, Arif; Rochmadi; Wijaya, Karna; Budiman, Arief

    2016-01-01

    In this research, the esterification of PFAD using the sulfonatedcoconut shell biochar catalyst was studied. Carbon solid catalysts were prepared by a sulfonation of carbonized coconut shells. The performances of the catalysts were evaluated in terms of the reaction temperatures, the molar ratios of methanol to PFAD, the catalyst loading and the reaction times. The reusability of the solid acid carbon catalysts was also studied in this work. The results indicated that the FFA conversion was significantly increased with increasing catalyst loading and reaction times. It can be concluded that the optimal conditions were an PFAD to methanol molar ratio of 1:12, the amount of catalyst of 10%w, and reaction temperature of 60oC.At this optimum condition, the conversion to biodieselreached 88%.

  18. Effect of time and temperature exposition in the crystallinity degree of sulfonated poly-(styrene acrylic acid) (PSAA-S)

    Energy Technology Data Exchange (ETDEWEB)

    Duarte, G.W.; Becker, E.B.; Silva, L.; Naspolini, A.M.; Consenso, E.C.; Paula, M.M.S.; Fiori, M.A., E-mail: glau_bn@hotmail.co [University of Extreme South of Santa Catarina Criciuma, SC (Brazil). Dept. of Materials Engineering; Silveira, F.Z. [Federal University of Santa Catarina (UFSC), Florianopolis, SC (Brazil). Dept. of Chemical Engineering

    2010-07-01

    Polymers with special properties have been increasingly applied in the development of technological devices. For example, polymeric materials with special electric properties, such as sulfonated poly-(styrene-acrylic acid) - PSAA-S, are of great interest for showing different conductivities depending on the environment where they are applied. The special properties of PSAA are obtained only after sulfonation step in acidic media. The present work aimed to evaluate the effect of time and temperature exposition in the crystallinity degree of PSAA-S, through a statistical experimental factorial planning. The samples of PSAA-S were submitted to FT-IR and DRX tests. The results showed that the temperature and the time of exposition are significant factors in the crystallinity degree of PSAA-S, considering that the crystal lattices created during the polymerization are damaged by the action of time and temperature at which the polymer is exposed. (author)

  19. Isonicotinic acid-ligated cobalt (II phthalocyanine-modified titania as photocatalyst for benzene degradation via fluorescent lamp

    Directory of Open Access Journals (Sweden)

    Joey Andrew A. Valinton

    2016-06-01

    Full Text Available The utilization of bis(isonicotinic acidphthalocyaninatocobalt (II [CoPc(isa2] incorporated on TiO2 has been studied as a photocatalyst to degrade benzene vapor under fluorescent lamp (indoor light conditions. The photocatalytic activity of [CoPc(isa2]-TiO2 compared to TiO2 showed an increase in the extent of degradation. The axial isonicotinic acid ligand attached to CoPc improved the degradation rate of benzene as compared with unligated CoPc-TiO2 which may be attributed to the enhancement of electronic structure in the complex due to the additional isonicotinic acid ligand and its possible attachment to the TiO2 surface through the carboxylic acid moiety. Therefore, covalently-linked CoPc(isa2 to TiO2 can enhance the extent of photodegradation of benzene and other common volatile organic compounds under indoor lighting conditions.

  20. Ag nanoparticle/melamine sulfonic acid supported on silica gel as an efficient catalytic system for synthesis of dihydropyrimidinthiones

    Directory of Open Access Journals (Sweden)

    Parya Nasehi

    2014-07-01

    Full Text Available 3,4-Dihydropyrimidin-2(1H-thiones were synthesized in the presence of Ag nanoparticle/melamine sulfonic acid (MSA supported on silica gel. The reactionwas carried out at 110 oC for 20 min under solvent free conditions. This method hassome advantages such as good yield, mild reaction conditions, ease of operation and work up, short reaction time and high product purity.

  1. Thermodynamics of the ethylene glycol pair interaction with some amino acids and benzene

    International Nuclear Information System (INIS)

    Highlights: • Thermodynamics of amino acid solutions in highly aqueous Eg was studied at 298 and 313 K. • The pair interaction parameters were computed using the virial expansion technique. • The results were discussed in terms of solute–Eg pair interactions. - Abstract: We have studied thermodynamics of interaction of benzene and some amino acids with ethylene glycol (Eg) which is a stabilizing agent for proteins in water using calorimetric and solubility data. Enthalpic, entropic and free energy parameters in highly diluted aqueous solutions have been computed at 298 and 313 K using the virial expansion technique and compared with available literature values. The results obtained are discussed in terms of solute–solute interactions and their relation to stability of macromolecules

  2. Spontaneous modification of graphite anode by anthraquinone-2-sulfonic acid for microbial fuel cells.

    Science.gov (United States)

    Tang, Xinhua; Li, Haoran; Du, Zhuwei; Ng, How Yong

    2014-07-01

    In this study, anthraquinone-2-sulfonic acid (AQS), an electron transfer mediator, was immobilized onto graphite felt surface via spontaneous reduction of the in situ generated AQS diazonium cations. Cyclic voltammetry (CV) and energy dispersive spectrometry (EDS) characterizations of AQS modified graphite demonstrated that AQS was covalently grafted onto the graphite surface. The modified graphite, with a surface AQS concentration of 5.37 ± 1.15 × 10(-9)mol/cm(2), exhibited good electrochemical activity and high stability. The midpoint potential of the modified graphite was about -0.248 V (vs. normal hydrogen electrode, NHE), indicating that electrons could be easily transferred from NADH in bacteria to the electrode. AQS modified anode in MFCs increased the maximum power density from 967 ± 33 mW/m(2) to 1872 ± 42 mW/m(2). These results demonstrated that covalently modified AQS functioned as an electron transfer mediator to facilitate extracellular electron transfer from bacteria to electrode and significantly enhanced the power production in MFCs.

  3. Use of anionic clays for photoprotection and sunscreen photostability: Hydrotalcites and phenylbenzimidazole sulfonic acid

    Science.gov (United States)

    Perioli, Luana; Ambrogi, Valeria; Rossi, Carlo; Latterini, Loredana; Nocchetti, Morena; Costantino, Umberto

    2006-05-01

    Layered double hydroxides of hydrotalcite (HTlc) type have many applications as matrices in pharmaceutical and cosmetic fields when intercalated with active species in anionic form. The aim of this work was to intercalate 2-phenyl-1H-benzimidazole-5-sulfonic acid (Eusolex 232) (EUS) as sunscreen molecule into hydrotalcites in order to obtain the sunscreen stabilization, the reduction of its photodegradation and the elimination of close contact between skin and filter. Hydrotalcites MgAl and ZnAl were used as hosts and the intercalation products obtained were characterized by TG, RX and DSC. They were also submitted to spectrophotometric assays in order to study the matrix influence on sunlight protection and on sunscreen photostability. These experiments showed that both MgAl and ZnAl HTlc intercalation products maintained the sunscreen properties and eusolex photodegradation was reduced. The in vitro EUS release from both formulations was almost negligible when compared with formulations containing free EUS. The EUS intercalation in HTlc and the respective formulations provided advantages in the maintenance of photoprotection efficacy, filter photostabilization and avoidance of a close contact between skin and filter, with consequent elimination of allergy problems and photocross reactions.

  4. Effect of Dodecylbenzene Sulfonic Acid Used as Additive on Residue Hydrotreating

    Institute of Scientific and Technical Information of China (English)

    Sun Yudong; Yang Chaohe

    2015-01-01

    The effect of additive—dodecylbenzene sulfonic acid (DBSA)—on residue hydrotreating was studied in the au-toclave. The results showed that the additive improved stabilization of the colloid system of residue, which could delay the aggregation and coke formation from asphaltenes on the catalyst, and make heavy components transformed into light oil. The residue conversion in the presence of this additive increased by 1.94%, and the yield of light oil increased by 1.53% when the reaction time was 90 min. The surface properties of the catalyst in the presence of this additive were better than that of the blank test within a very short time (30 min) and deteriorated rapidly after a longer reaction time due to higher conversion and coke deposition. Compared with the blank test, the case using the said additive had shown that the structure of hydrotreated asphaltene units was smaller and the condensation degrees were higher. The test results indicated that the additive could improve the hydrotreating reactivity of residue via permeation and depolymerization, the heavier components could be transformed into light oil more easily, and the light oil yield and residue conversion were higher for the case using the said additive in residue hydrotreating process.

  5. 脂肪酸甲酯磺酸盐%Fatty acid methyl ester sulfonate

    Institute of Scientific and Technical Information of China (English)

    韩建英

    2012-01-01

    Fatty acid methyl ester sulfonate(MES) is an anionic surfactant based on natural oils generated from plant and animal as raw materials. MES has good detergency, lime soap dispersing ability, hard water-resistance, emulsibility, water-solubility and biodegradability; besides, it can improve the solubility of soap in water. Because of the good performance of MES, it can be used in synthetic powder detergent, compound soap powder, composite soap, shampoo and personal care products. The present production situation, product forms, properties as well as applications of MES were related.%脂肪酸甲酯磺酸盐简称(MES)是以天然动植物油脂为原料制得的脂肪酸系阴离子表面活性剂。它具有良好的去污性、钙皂分散性、抗硬水性、乳化性、增溶性和生物降解性,并能改进肥皂的溶解性。由于MES性能优良,主要用于合成洗衣粉、复合皂粉、复合肥皂、香波以及个人清洁用品中。对MES的生产现状、产品形式、性能以及应用进行了概述。

  6. Removal of textile dyes and metallic ions using polyelectrolytes and macroelectrolytes containing sulfonic acid groups.

    Science.gov (United States)

    Caldera Villalobos, M; Peláez Cid, A A; Herrera González, Ana M

    2016-07-15

    This work reports the removal of textile dyes and metallic ions by means of adsorption and coagulation-flocculation using two polyelectrolytes and two macroelectrolytes containing sulfonic acid groups. The adsorption of textile dyes was studied in aqueous solutions containing cationic dyes and in wastewater containing a vat dye. Also, removal of vat and naphthol dyes was studied using the process of coagulation-flocculation. The results show these materials possess elevated adsorption capacity, and they accomplished removal rates above 97% in aqueous solutions. The removal of the vat dye improved the quality of the wastewater notably, and an uncolored effluent was obtained at the end of the treatment. The treatment using adsorption decreased the values for coloration, conductivity, suspended solids, and pH. The removal of vat and naphthol dyes by means of coagulation-flocculation was studied as well, and removal rates of 90% were obtained. The polyelectrolytes and macroelectrolytes also proved effective in the adsorption of metallic ions in wastewater. The treatment using adsorption accomplished high removal rates of metallic ions, and it showed greater selectivity towards Cu(2+), Fe(3+) and Pb(2+). A decrease in the content of solids as well as the values for COD and conductivity was observed in the wastewater as well. The analyses of FT-IR indicated that cationic dyes and metallic ions were chemisorbed by means of ionic exchange. PMID:27082258

  7. Crystal structure of benzene-1,3,5-tri-carb-oxy-lic acid-4-pyridone (1/3).

    Science.gov (United States)

    Staun, Selena L; Oliver, Allen G

    2015-11-01

    Slow co-crystallization of a solution of benzene-1,3,5-tri-carb-oxy-lic acid with a large excess of 4-hy-droxy-pyridine produces an inter-penetrating, three-dimensional, hydrogen-bonded framework consisting of three 4-pyridone and one benzene-1,3,5-tri-carb-oxy-lic acid mol-ecules, C9H6O6·3C5H5NO. This structure represents an ortho-rhom-bic polymorph of the previously reported C-centered, monoclinic structure [Campos-Gaxiola et al. (2014 ▸). Acta Cryst. E70, o453-o454]. PMID:26594492

  8. Sulfonated mesoporous silica–carbon composites and their use as solid acid catalysts

    OpenAIRE

    Valle Vigón, Patricia; Sevilla Solís, Marta; Fuertes Arias, Antonio Benito

    2012-01-01

    [EN] The synthesis of highly functionalized porous silica–carbon composites made up of sulfonic groups attached to a carbon layer coating the pores of three types of mesostructured silica (i.e. SBA-15, KIT-6 and mesocellular silica) is presented. The synthesis procedure involves the following steps: (a) removal of the surfactant, (b) impregnation of the silica pores with a carbon precursor, (c) carbonization and (d) sulfonation. The resulting silica–carbon composites contain ∼30 wt % of carbo...

  9. Chemical mechanical polishing of hard disk substrate with {alpha}-alumina-g-polystyrene sulfonic acid composite abrasive

    Energy Technology Data Exchange (ETDEWEB)

    Lei Hong, E-mail: hong_lei2005@yahoo.com.c [Research Center of Nano-science and Nano-technology, Shanghai University, Shanghai 200444 (China); Bu Naijing; Chen Ruling; Hao Ping [Research Center of Nano-science and Nano-technology, Shanghai University, Shanghai 200444 (China); Neng Sima; Tu Xifu; Yuen Kwok [Shenzhen Kaifa Magnetic Recording Co., LTD, Shenzhen, 518035 (China)

    2010-05-03

    {alpha}-Alumina-g-polystyrene sulfonic acid ({alpha}-Al{sub 2}O{sub 3}-g-PSS) composite abrasive was prepared by surface activation, graft polymerization and sulfonation, successively. The composition, dispersibility and morphology of the product were characterized by Fourier transformed infrared spectroscopy, laser particle size analysis and scanning electron microscopy, respectively. The chemical mechanical polishing (CMP) performances of the composite abrasive on hard disk substrate with nickel-phosphorous plating were investigated. The microscopy images of the polished surfaces show that {alpha}-Al{sub 2}O{sub 3}-g-PSS composite abrasive results in improved CMP and post-CMP cleaning performances than pure {alpha}-alumina abrasive under the same testing conditions.

  10. Toxicity of perfluorooctane sulfonic acid and perfluorooctanoic acid on freshwater macroinvertebrates (Daphnia magna and Moina macrocopa) and fish (Oryzias latipes).

    Science.gov (United States)

    Ji, Kyunghee; Kim, Younghee; Oh, Sorin; Ahn, Byeongwoo; Jo, Hyunye; Choi, Kyungho

    2008-10-01

    Because of their global distribution, persistence, and tendency to bioaccumulate, concerns about perfluorooctane sulfonic acid (PFOS) and perfluorooctanoic acid (PFOA) are growing. We determined the toxicity of PFOS and PFOA in several freshwater organisms, including two cladocerans, Daphnia magna and Moina macrocopa, and the teleost Oryzias latipes. In general, PFOS is approximately 10 times more toxic than PFOA in these organisms. In M. macrocopa, the median lethal concentration (LC50) was 17.95 mg/L for PFOS and 199.51 mg/L for PFOA. Moina macrocopa exhibited greater sensitivity than D. magna to both perfluorinated compounds in both acute and chronic exposures. In the 48-h acute toxicity test, M. macrocopa was approximately two times more sensitive than D. magna. In the 7-d chronic toxicity test, M. macrocopa showed significant reproductive changes at 0.31 mg/L for PFOS, which was approximately seven times lower than the effect concentrations observed over the 21-d exposure in D. magna. Two-generation fish toxicity tests showed that parental exposure to both compounds affected the performance of offspring. Unexposed progeny-generation (F1) fish exhibited elevated mortality and histopathological changes that were correlated with exposure in the parental generation (F0). Continuous exposure from F0 through F1 generations increased the extent of adverse effects. Considering the persistent nature of PFOS and PFOA, more research is required to determine potential consequences of long-term exposure to these compounds in aquatic ecosystems. PMID:18593212

  11. High-performance Liquid Chromatographic Determination of Urinary Trans, Trans-Muconic Acid Excreted by Workers Occupationally Exposed to Benzene

    Institute of Scientific and Technical Information of China (English)

    XIA-MIN HU; SHI-ZHEN SONG; FANG-LI YE; LI-WEN LIU

    2006-01-01

    To investigate the relationship between trans, trans-muconic acid (ttMA) as benzene metabolite of occupational workers and benzene concentration in air. Methods A rapid and sensitive high-performance liquid chromatography was developed to determine the level of urinary ttMA. ttMA was extrated from urinary samples in liquid-liquid phase a ODS (2) (5u) column (Φ4.6 mm× 150 mm) and detected at wavelength 264 nm in a UV detector using vanillic acid as an internal standard. The mobile phase was acetaticacid/tetrahydrofuran/methanol/water (v/v, 1:2:10:87). The method was validated with 56 urine samples collected from occupationally benzene-exposed individuals. Results A correlation coefficient (r = 0.9963 ) was found for ttMA ranging 0.10-10.00 μg/mL. The limit of detection was 0.10 μg/mL. The recovery and reproducibility were generally over 90%. There was a positive correlation between ttMA and benzene level in air. The equation was Y=0.859+0.108C (before work, r=-0.6200) or Y=1.980+0.179C (after work, r=0.7930). Conclusion This method can be used to determine and control the level of urinary ttMA in those who are occupationally exposed to benzene.

  12. 4-(4-Bromo­benzene­sulfonamido)benzoic acid

    Science.gov (United States)

    Khan, Islam Ullah; Mustafa, Ghulam; Arshad, Muhammad Nadeem; Shafiq, Muhammad; Sharif, Shahzad

    2009-01-01

    The title compound, C13H10BrNO4S, belongs to the sulfonamide class of organic compounds. The two aromatic rings are inclined at 34.30 (15)° to one another, and the carboxyl substituent lies in the plane of the benzene ring to which it is bound (maximum deviation = 0.004 Å). In the crystal structure, charactersitic carboxylic acid dimers are formed through O—H⋯O hydrogen bonds. These dimers are linked into rows down a by N—H⋯O inter­actions. Additional C—H⋯O contacts further stabilize the structure, and a close Br⋯Br(x, −y + 1, −z + 1) contact of 3.5199 (9) Å is also observed. PMID:21583888

  13. Crystal Structure and Characterization of Salicylic Acid-benzene Azimide Cocrystal

    Institute of Scientific and Technical Information of China (English)

    DUAN Jiong; GUO Ping; PAN Qing-Qing; WU You; WU Xiao-Qing; LI Hui

    2013-01-01

    A new single crystal of 1∶1 salicylic acid-benzene azimide was determined and characterized.It belongs to space group P21/n with a =13.8085(13),b =5.3846(4),c =16.7063(13) (A)and β =102.331(9)°.Crystals of the title compound,C7H6O3·C6H5N3,were obtained by cocrystallization.FT-IR,Raman spectroscopy and TGA-DTA were applied to characterize the title compound as supplemental evidence to prove the formation of the crystal.Our work describes the solubility of the crystal by considering the equilibria between the crystal,components,and solution mixture.

  14. Comparative Study on Single-Molecule Junctions of Alkane- and Benzene-Based Molecules with Carboxylic Acid/Aldehyde as the Anchoring Groups

    Science.gov (United States)

    Chen, Fang; Peng, Lin-Lu; Hong, Ze-Wen; Mao, Jin-Chuan; Zheng, Ju-Fang; Shao, Yong; Niu, Zhen-Jiang; Zhou, Xiao-Shun

    2016-08-01

    We have measured the alkane and benzene-based molecules with aldehyde and carboxylic acid as anchoring groups by using the electrochemical jump-to-contact scanning tunneling microscopy break junction (ECSTM-BJ) approach. The results show that molecule with benzene backbone has better peak shape and intensity than those with alkane backbone. Typically, high junction formation probability for same anchoring group (aldehyde and carboxylic acid) with benzene backbone is found, which contributes to the stronger attractive interaction between Cu and molecules with benzene backbone. The present work shows the import role of backbone in junction, which can guide the design molecule to form effective junction for studying molecular electronics.

  15. Occurrence of Perfluorooctanoic Acid and Perfluorooctane Sulfonate in Milk and Yogurt and Their Risk Assessment

    Directory of Open Access Journals (Sweden)

    Zhenni Xing

    2016-10-01

    Full Text Available Although perfluorooctanoic acid (PFOA and perfluorooctane sulfonate (PFOS have been identified in milk and dairy products in many regions, knowledge on their occurrence in Xinjiang (China is rare. This study was conducted to measure the levels of PFOA and PFOS in milk and yogurt from Xinjiang and to investigate the average daily intake (ADI of these two compounds. PFOA and PFOS levels were analyzed using ultrasonic extraction with methanol and solid-phase extraction followed by liquid chromatography–mass spectrometry. Retail milk and yogurt samples present higher detection rates (39.6% and 48.1% and mean concentrations (24.5 and 31.8 ng/L of PFOS than those of PFOA (33.0% and 37.0%; 16.2 and 22.6 ng/L, respectively. For raw milk samples, only PFOS was detected. The differences in the levels of the two compounds between samples from the north and south regions were observed, and northern regions showed higher pollution levels than southern regions. On the basis of the retail milk measurements and consumption data, the ADIs of PFOA and PFOS for Xinjiang adults were calculated to be 0.0211 and 0.0318 ng/kg/day, respectively. Furthermore, the estimated intakes of PFOA and PFOS varied among different groupings (age, area, gender, and race and increased with increasing age. Relevant hazard ratios were found to be far less than 1.0, and this finding suggested that no imminent health damages were produced by PFOA and PFOS intake via milk and yogurt consumption in the Xinjiang population.

  16. Validation and optimization of experimental colitis induction in rats using 2, 4, 6-trinitrobenzene sulfonic acid.

    Science.gov (United States)

    Motavallian-Naeini, A; Andalib, S; Rabbani, M; Mahzouni, P; Afsharipour, M; Minaiyan, M

    2012-07-01

    Trinitrobenzene sulfonic acid (TNBS)-induced colitis is one of the most common methods for studying inflammatory bowel disease in animal models. Several factors may, however, affect its reproducibility, rate of animal mortality, and macroscopic and histopathological outcomes. Our aim was to validate the main contributing factors to this method and compare the effects of different reference drugs upon remission of resultant colon injuries. TNBS was dissolved in 0.25 ml of ethanol (50% v/v) and instilled (25, 50, 100 and 150 mg/kg) intracolonically to the male Wistar rats. After determination of optimum dose of TNBS in male rats and assessment of this dose in female rats, they were treated with reference drugs including dexamethasone [1 mg/kg, intraperitoneally (i.p.) and 2 mg/kg, orally (p.o.)], Asacol (mesalazine, 100 mg/kg, p.o.; 150 mg/kg, enema) and hydrocortisone acetate (20 mg/kg, i.p.; 20 mg/kg, enema) which started 2 h after colitis induction and continued daily for 6 consecutive days. Thereafter, macroscopic and microscopic parameters and clinical features were assessed and compared in different groups. We found that the optimum dose of TNBS for the reproducibility of colonic damage with the least mortality rate was 50 mg/kg. Amongst studied reference drugs, hydrocortisone acetate (i.p.), dexamethasone (i.p. and p.o.) and Asacol (p.o.) significantly diminished the severity of macroscopic and microscopic injuries and could be considered effective for experimental colitis studies in rats . Our findings suggest that optimization of TNBS dose is essential for induction of colitis under the laboratory conditions; and gender exerts no impact upon macroscopic and histological characteristics of TNBS-induced colitis in rats. Furthermore, the enema forms of hydrocortisone and Asacol are not appropriate reference drugs. PMID:23181094

  17. Molecular dynamics in conducting polyaniline protonated by camphor sulfonic acid as seen by quasielastic neutron scattering

    International Nuclear Information System (INIS)

    Using incoherent quasielastic neutron scattering techniques, the molecular motions were investigated in fully hydrogenated and partially deuterated polyaniline protonated by camphor sulfonic acid (CSA) conducting samples. The obtained results show that on the 10-9-10-12 s time scale the polymer chains do not exhibit any diffusive motions: the whole observed quasielastic scattering has accordingly to be attributed to motions of CSA ions. From our measurements two molecular movements could be differentiated. A rapid one has been attributed to the three-site rotation of methyl groups present on camphor moieties of CSA and a slower one that has been modeled as a rigid body motion of the whole CSA molecule. Due to the disordered character of the system, the methyl rotors appeared to be dynamically nonequivalent. Their dynamics was then described in terms of a log gaussian distribution of correlation times. This description allowed a good fitting of experimental data and gave an activation energy of 12.5 kJ mol-1. However, two different regimes in temperature could be distinguished. At high temperatures (T>280 K) the width of the distribution is nearly zero and thus, the methyl rotors are dynamically equivalent while it turned larger and larger when temperature is decreased below 250 K revealing that the rotors are more and more sensitive to their local environment. In the conducting samples the slowest motion clearly exists in the 280-330 K temperature range and is blocked at temperatures inferior to 250 K. This transition occurs in the temperature range in which the metal-insulator transition also happens

  18. Covalently bonded sulfonic acid magnetic graphene oxide: Fe3O4@GO-Pr-SO3H as a powerful hybrid catalyst for synthesis of indazolophthalazinetriones.

    Science.gov (United States)

    Doustkhah, Esmail; Rostamnia, Sadegh

    2016-09-15

    Multistep synthesis of covalently sulfonated magnetic graphene oxide was achieved by starting from Hummer's method to produce graphene oxide (GO) from chemical oxidation of graphite. Then, GO nanosheets were applied to support Fe3O4 nanoparticles (Fe3O4@GO) using co-precipitation method in the presence of GO sheets. This strategy led to formation of uniform particles of Fe3O4 on the surface of GO sheets. Then, it was sulfonated (Fe3O4@GO-Pr-SO3H) through modification with 3-mercaptopropyltrimethoxysilane (MPTMS) and subsequent oxidation with hydrogen peroxide (H2O2). In comparison, the covalently bonded propyl sulfonic acid groups were more prevailing rather to sulfonic acids of GO itself. The proposed catalyst was more active and recyclable at least for 11 runs. PMID:27309948

  19. The corrosion inhibition of aluminum and its copper alloys in 1.0 M H{sub 2}SO{sub 4} solution using linear-sodium dodecyl benzene sulfonate as inhibitor

    Energy Technology Data Exchange (ETDEWEB)

    Abd El Rehim, Sayed S.; Amin, Mohammed A. [Chemistry Department, Faculty of Science, Ain Shams University, Abbassia, Cairo (Egypt); Moussa, S.O. [Chemistry Department, Faculty of Science, Ain Shams University, Abbassia, Cairo (Egypt)], E-mail: sherif_m74@yahoo.com; Ellithy, Abdallah S. [Chemistry Department, Faculty of Science, Ain Shams University, Abbassia, Cairo (Egypt)

    2008-12-20

    The corrosion inhibition of Al and its two copper alloys are the subject of tremendous technological importance due to the increased industrial applications of these materials. This paper reports the results of potentiodynamic polarization and electrochemical impedance spectroscopic (EIS) measurements on the corrosion inhibition of Al (Al-2.5% Cu and Al-7.0% Cu) alloys in 1.0 M H{sub 2}SO{sub 4} solution carried out in different concentrations of linear-sodium dodecyl benzene sulfonate as an anionic surfactant (LAS) and temperature range from 10 to 60 deg. C. The data revealed that the inhibition efficiency increases with increasing surfactant concentration and time of immersion, and decreases with solution temperature. Energy dispersion X-ray (EDX) observations of the electrode surface confirmed the existence of LAS adsorbed film on the electrode surface. The surfactant acted mainly as cathodic inhibitor. Maximum inhibition efficiency of the surfactant is observed at concentration around its critical micelle concentration (CMC). The inhibition occurs through adsorption of the surfactant on the metal surface without modifying the mechanism of the corrosion process, which tested by UV-spectroscopy. The potential of zero charge (PZC) of aluminum and Al-7.0% Cu was studied by ac-impedance, and the mechanism of adsorption is discussed. The adsorption isotherm is described by Temkin adsorption isotherm. Thermodynamic functions for activation and adsorption process were determined.

  20. Identification of 6-hydroxy-trans,trans-2,4-hexadienoic acid, a novel ring-opened urinary metabolite of benzene

    Energy Technology Data Exchange (ETDEWEB)

    Kline, S.A.; Robertson, J.F.; Grotz, V.L.; Goldstein, B.D.; Witz, G. (Robert Wood Johnson Medical School, Piscataway, NJ (United States) Environmental and Occupational Health Sciences Institute, Piscataway, NJ (United States))

    1993-09-01

    The authors have studied the in vivo metabolism of benzene in mice to ring-opened compounds excreted in urine. Male CD-1 mice were treated intraperitoneally with benzene (110-440 mg/kg), [[sup 14]C] benzene (220 mg/kg) or trans,trans-muconaldehyde (MUC; 4 mg/kg), a microsomal, hematotoxic metabolite of benzene. Urine, collected over 24 hr, was extracted and analyzed by HPLC with a diode-array detector and by scintillation counting. In addition to trans,trans-muconic acid, previously the only known ring-opened urinary benzene metabolite, a new metabolite, 6-hydroxy-trans,trans-2,4-hexadienoic acid, was detected in urine of mice treated with either benzene or MUC. The authors identified the new metabolite based on coelution of metabolites and UV spectral comparison with authentic standards in unmethylated and methylated urine extracts. Results presented here are consistent with the intermediacy of the ring-opened metabolites.

  1. One-pot Synthesis of Bis(dihydropyrimidinone-4-yl)benzene Using Boric Acid as a Catalyst

    Institute of Scientific and Technical Information of China (English)

    TU Shu-Jiang; ZHU Xiao-Tong; FANG Fang; ZHANG Xiao-Jing; ZHU Song-Lei; LI Tuan-Jie; SHI Da-Qing; WANG Xiang-Shan; JI Shun-Jun

    2005-01-01

    A simple effective synthesis of bis(dihydropyrimidinone-4-yl)benzene derivatives, using boric acid as catalyst,from isophthalic aldehyde or terephthalic aldehyde, 1,3-dicarbonyl compounds and urea or thiourea in glacial acetic acid was described. As the expansion of the classical Biginelli reaction, this method has the advantage of excellent yields 83%-94% and short reaction time 0.5-1.5 h.

  2. Theoretical investigation on the molecular inclusion process of prilocaine into p-sulfonic acid calix[6]arene

    Science.gov (United States)

    de Sousa, Sara M. R.; Fernandes, Sergio A.; De Almeida, Wagner B.; Guimarães, Luciana; Abranches, Paula A. S.; Varejão, Eduardo V. V.; Nascimento, Clebio S., Jr.

    2016-02-01

    The present letter reports, for the first time, results from a theoretical analysis of the inclusion process involving the prilocaine into the p-sulfonic acid calix[6]arene. Structure and stabilization energies were calculated, in both gas and aqueous phases, using a sequential methodology based on semiempirical and Density Functional Theory (DFT) calculations. From the results, a qualitative structure property relationship could be established with some main structural features being relevant for inclusion complex stabilization: (i) the hydrogen bonds established between guest and host molecules, (ii) the dispersion effect and (iii) the inclusion mode of guest molecule into the host cavity.

  3. Silylation of Alcohols and Phenols with Hexamethyldisilazane over Highly Reusable Propyl Sulfonic Acid Functionalized Nanostructured SBA-15

    Institute of Scientific and Technical Information of China (English)

    Daryoush ZAREYEE; Rezvaneh ASGHARI; Mohammad A. KHALILZADEH

    2011-01-01

    Various alcohols and phenols were trimethylsilylated in excellent yields using hexamethyldisilazane in the presence of catalytic amounts of environmentally friendly,hydrophobic,highly thermal stable,and completely heterogeneous sulfonic acid functionalized mesostructured SBA-15 in dichloromethane at ambient temperature.Primary,bulky secondary,tertiary,and phenolic hydroxyl functional groups were transformed to the corresponding trimethylsilyl ethers in excellent yields.The simple experimental procedure was accompanied by easy recovery and the catalyst was reusable (at least 18 reaction cycles); these are attractive features of this protocol.

  4. Extraneous carbon assessment in ultra-microscale radiocarbon analysis using benzene polycarboxylic acids (BPCA)

    Science.gov (United States)

    Hanke, Ulrich M.; McIntyre, Cameron P.; Schmidt, Michael W. I.; Wacker, Lukas; Eglinton, Timothy I.

    2016-04-01

    Measurements of the natural abundance of radiocarbon (14C) concentrations in inorganic and organic carbon-containing materials can be used to investigate their date of origin. Particularly, the biogeochemical cycling of specific compounds in the environment may be investigated applying molecular marker analyses. However, the isolation of specific molecules from environmental matrices requires a complex processing procedure resulting in small sample sizes that often contain less than 30 μg C. Such small samples are sensitive to extraneous carbon (Cex) that is introduced during the purification of the compounds (Shah and Pearson, 2007). We present a thorough radiocarbon blank assessment for benzene polycarboxylic acids (BPCA), a proxy for combustion products that are formed during the oxidative degradation of condensed polyaromatic structures (Wiedemeier et al, in press). The extraneous carbon assessment includes reference material for (1) chemical extraction, (2) preparative liquid chromatography (3) wet chemical oxidation which are subsequently measured with gas ion source AMS (Accelerator Mass Spectrometer, 5-100 μg C). We always use pairs of reference materials, radiocarbon depleted (14Cfossil) and modern (14Cmodern) to determine the fraction modern (F14C) of Cex.Our results include detailed information about the quantification of Cex in radiocarbon molecular marker analysis using BPCA. Error propagation calculations indicate that ultra-microscale samples (20-30 μg) are feasible with uncertainties of less than 10 %. Calculations of the constant contamination reveal important information about the source (F14C) and mass (μg) of Cex (Wacker and Christl, 2011) for each sub procedure. An external correction of compound specific radiocarbon data is essential for robust results that allow for a high degree of confidence in the 14C results. References Shah and Pearson, 2007. Ultra-microscale (5-25μg C) analysis of individual lipids by 14C AMS: Assessment and

  5. Global analysis of myocardial peptides containing cysteines with irreversible sulfinic and sulfonic Acid post-translational modifications

    DEFF Research Database (Denmark)

    Paulech, Jana; Liddy, Kiersten A; Engholm-Keller, Kasper;

    2015-01-01

    Cysteine (Cys) oxidation is a crucial post-translational modification (PTM) associated with redox signaling and oxidative stress. As Cys is highly reactive to oxidants it forms a range of post-translational modifications, some that are biologically reversible (e.g. disulfides, Cys sulfenic acid......) and others (Cys sulfinic [Cys-SO2H] and sulfonic [Cys-SO3H] acids) that are considered "irreversible." We developed an enrichment method to isolate Cys-SO2H/SO3H-containing peptides from complex tissue lysates that is compatible with tandem mass spectrometry (MS/MS). The acidity of these post......-translational modification (pKa Cys-SO3H negative" selection) followed...

  6. Optimization of SPE for Analysis of Mandelic Acid as a Biomarker of Exposure to Ethyl Benzene

    Directory of Open Access Journals (Sweden)

    SJ Shahtaheri, M Abdollahi, F Golbabaei, A Rahimi-Froushani, F Ghamari

    2004-10-01

    Full Text Available Ethyl benzene is an important constituent of widely used solvents in industries and laboratories, causing widespread environmental and industrial pollutions. For evaluation of occupational exposure to such pollutants, biological monitoring is an essential process, in which, preparation of environmental and biological samples is one of the most time-consuming and error-prone aspects prior to chromatographic techniques. The use of solid-phase extraction (SPE has been grown and is a fertile technique of sample preparation as it provides better results than those of liquid-liquid extraction (LLE. In this study, SPE using bonded silica has been optimized with regard to sample pH, sample concentration, elution solvent, elution volume, sorbent type, and sorbent mass. Through experimental evaluation, a strong anion exchange silica cartridge (SAX has been found successful in simplifying sample preparation. The present approach proved that, mandelic acid could be retained on SAX sorbent based on specific interaction. Further study was employed using 10% acetic acid to extract the analyte from spiked urine and gave a clean sample for HPLC-UV system. In this study, a high performance liquid chromatography, using reverse-phase column was used. The isocratic run was done at a constant flow rate of 0.85 ml/min, the mobile phase was water/methanol/acetic acid and a UV detector was used, setting at 225 nm. At the developed conditions the extraction recovery was exceeded 98%. The factors were evaluated statically and also validated with three different pools of spiked urine samples and showed a good reproducibility over six consecutive days as well as six within-day experiments.

  7. Effect of sodium dodecyl benzene sulfonate on reproduction of male mice%十二烷基苯磺酸钠对雄性小鼠生育力的影响

    Institute of Scientific and Technical Information of China (English)

    韩俊娟; 任春娥; 韩海艳; 乔鹏云; 姜俊怡

    2012-01-01

    Objective:To determine the effects of sodium dodecyl benzene sulfonate (SDBS) on reproduction of male mice. Methods: Both 120 Kunming male mice and 120 female mice were randomly divided into four groups and the number of every group was 30. Group A was the female mice which were mated with the male mice gavaged by SDBS for two months; Group B was the female mice which were mated with the male mice gavaged by SDBS for two months and stopped for one month. Group a and group b were the control groups respectively. The pregnancy rates, the average birth number of pregnant rats and the fetal rats of these groups were studied. Results: The pregnancy rates, the average birth number of pregnant rats and the proportion of deaths, malformation and absorbed fetuses in pregnant rats was lower than the control groups, there was significant difference(P 0.05). Conclusion: Sodium dodecyl benzene sulfonate have an significant toxicity effect on the reproduction of male mice and they cannot restore after leaving off being gavaged for a short time.%目的:探讨十二烷基苯磺酸钠(SDBS)对雄性小鼠生育力的影响.方法:分别将120只昆明种雌、雄性小鼠随机分为4组,每组30只.A组为与染毒SDBS两个月后的雄性小鼠交配的雌鼠;B组为与染毒SDBS两个月,停止染毒一个月后的雄鼠交配的雌鼠.A、B两组分别设对照组为a组、b组.对各组怀孕率、孕鼠平均产子数及其胎鼠情况进行比较分析.结果:与对照组相比,A、B两组的怀孕率、孕鼠平均产子数、孕鼠腹中死胎、畸胎与吸收胎比例明显降低,有显著性差异(P<0.05);A、B两组相比,小鼠怀孕率、孕鼠平均产子数、孕鼠腹中死胎、畸胎与吸收胎比例无显著性差异(P>0.05).结论:十二烷基苯磺酸钠对雄性小鼠的生育力有显著影响,并且在停止染毒后的短时期内不能恢复.

  8. Liquid Chromatography-Tandem Mass Spectrometry Analysis of Perfluorooctane Sulfonate and Perfluorooctanoic Acid in Fish Fillet Samples

    Directory of Open Access Journals (Sweden)

    Viviana Paiano

    2012-01-01

    Full Text Available Perfluorooctane sulfonate (PFOS and perfluorooctanoic (PFOA acid are persistent contaminants which can be found in environmental and biological samples. A new and fast analytical method is described here for the analysis of these compounds in the edible part of fish samples. The method uses a simple liquid extraction by sonication, followed by a direct determination using liquid chromatography-tandem mass spectrometry (LC-MS/MS. The linearity of the instrumental response was good, with average regression coefficients of 0.9971 and 0.9979 for PFOS and PFOA, respectively, and the coefficients of variation (CV of the method ranged from 8% to 20%. Limits of detection (LOD were 0.04 ng/g for both the analytes and recoveries were 90% for PFOS and 76% for PFOA. The method was applied to samples of homogenized fillets of wild and farmed fish from the Mediterranean Sea. Most of the samples showed little or no contamination by perfluorooctane sulfonate and perfluorooctanoic acid, and the highest concentrations detected among the fish species analyzed were, respectively, 5.96 ng/g and 1.89 ng/g. The developed analytical methodology can be used as a tool to monitor and to assess human exposure to perfluorinated compounds through sea food consumption.

  9. Benzene Exposure Alters Expression of Enzymes Involved in Fatty Acid β-Oxidation in Male C3H/He Mice

    Directory of Open Access Journals (Sweden)

    Rongli Sun

    2016-10-01

    Full Text Available Benzene is a well-known hematotoxic carcinogen that can cause leukemia and a variety of blood disorders. Our previous study indicated that benzene disturbs levels of metabolites in the fatty acid β-oxidation (FAO pathway, which is crucial for the maintenance and function of hematopoietic and leukemic cells. The present research aims to investigate the effects of benzene on changes in the expression of key enzymes in the FAO pathway in male C3H/He mice. Results showed that benzene exposure caused reduced peripheral white blood cell (WBC, red blood cell (RBC, platelet (Pit counts, and hemoglobin (Hgb concentration. Investigation of the effects of benzene on the expression of FA transport- and β-oxidation-related enzymes showed that expression of proteins Cpt1a, Crat, Acaa2, Aldh1l2, Acadvl, Crot, Echs1, and Hadha was significantly increased. The ATP levels and mitochondrial membrane potential decreased in mice exposed to benzene. Meanwhile, reactive oxygen species (ROS, hydrogen peroxide (H2O2, and malondialdehyde (MDA levels were significantly increased in the benzene group. Our results indicate that benzene induces increased expression of FA transport and β-oxidation enzymes, mitochondrial dysfunction, and oxidative stress, which may play a role in benzene-induced hematotoxicity.

  10. Effect of intrachain sulfonic acid dopants on the solid-state charge mobility of a model radical polymer

    Energy Technology Data Exchange (ETDEWEB)

    Chan, Holly; Wang, Yucheng; Boudouris, Bryan W., E-mail: boudouris@purdue.edu

    2015-02-27

    Radical polymers are an emerging class of non-conjugated, charge-conducting macromolecules that are capable of transporting charge through localized oxidation–reduction (redox) reactions that occur at the stable radical groups present as the pendant groups of the macromolecular chains. The chemical nature and oxidation state of these pendant radical groups are critical to the charge transporting abilities of radical polymers in the solid state. To date, however, the control of this chemistry has been limited to external oxidizing agents, and the concept of intramolecular dopants has not been explored fully. To this end, we have synthesized poly(2,2,6,6-tetramethylpiperidinyloxy methacrylate)-co-poly(vinylsulfonic acid sodium salt) (PTMA-co-PVS). Then, electron paramagnetic resonance spectroscopy and attenuated total reflectance-Fourier transform infrared spectroscopy are implemented to evaluate the exact chemical nature of the pendant groups as a function of the PVS intramolecular dopants and exposure of the materials to external oxidation reactions. We correlate these changes in pendant group chemistry to charge transport ability, and we establish that the inclusion of a moderate amount of PVS dopants can improve the solid-state hole mobility of the material. Conversely, a large amount of sulfonic acidic dopants can be detrimental to the transport of the polymer relative to the homopolymer PTMA. Therefore, refinement of pendant group chemistry and careful addition of intramolecular dopants can enhance the solid-state transport ability of a radical polymer system. These fundamental principles, in turn, provide a vital foothold by which to optimize the solid-state charge transporting ability of current and next-generation radical polymer designs. - Highlights: • Sulfonic acid groups are copolymerized within the backbone of radical polymer chain. • Addition of the sulfonic acid groups alters the pendant group oxidation state. • Exact oxidation states are

  11. Tracer studies of carboxylic acids. VII. Oxygen-18 exchange of propionic acid with solvent water and with surfactant solubilized water in benzene

    Energy Technology Data Exchange (ETDEWEB)

    Lomax, T.D.; O' Connor, C.J.

    1978-08-30

    Oxygen atom exchange between propionic acid/propionate ion and solubilized H/sub 2//sup 18/O has been measured in micellar solutions of dodecylammonium propionate in benzene and in aqueous solutions of ammonium propionate. The size of the solubilized waterpool affects the rate of exchange of carboxylate oxygen atoms in the presence of mineral acid but not in its absence. 3 figures, 1 table.

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

    Directory of Open Access Journals (Sweden)

    V. Kiran

    2015-12-01

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

  13. Characterization, Quantification and Compound-specific Isotopic Analysis of Pyrogenic Carbon Using Benzene Polycarboxylic Acids (BPCA)

    Science.gov (United States)

    Wiedemeier, Daniel B.; Lang, Susan Q.; Gierga, Merle; Abiven, Samuel; Bernasconi, Stefano M.; Früh-Green, Gretchen L.; Hajdas, Irka; Hanke, Ulrich M.; Hilf, Michael D.; McIntyre, Cameron P.; Scheider, Maximilian P. W.; Smittenberg, Rienk H.; Wacker, Lukas; Wiesenberg, Guido L. B.; Schmidt, Michael W. I.

    2016-01-01

    Fire-derived, pyrogenic carbon (PyC), sometimes called black carbon (BC), is the carbonaceous solid residue of biomass and fossil fuel combustion, such as char and soot. PyC is ubiquitous in the environment due to its long persistence, and its abundance might even increase with the projected increase in global wildfire activity and the continued burning of fossil fuel. PyC is also increasingly produced from the industrial pyrolysis of organic wastes, which yields charred soil amendments (biochar). Moreover, the emergence of nanotechnology may also result in the release of PyC-like compounds to the environment. It is thus a high priority to reliably detect, characterize and quantify these charred materials in order to investigate their environmental properties and to understand their role in the carbon cycle. Here, we present the benzene polycarboxylic acid (BPCA) method, which allows the simultaneous assessment of PyC's characteristics, quantity and isotopic composition (13C and 14C) on a molecular level. The method is applicable to a very wide range of environmental sample materials and detects PyC over a broad range of the combustion continuum, i.e., it is sensitive to slightly charred biomass as well as high temperature chars and soot. The BPCA protocol presented here is simple to employ, highly reproducible, as well as easily extendable and modifiable to specific requirements. It thus provides a versatile tool for the investigation of PyC in various disciplines, ranging from archeology and environmental forensics to biochar and carbon cycling research. PMID:27214064

  14. Characterization, Quantification and Compound-specific Isotopic Analysis of Pyrogenic Carbon Using Benzene Polycarboxylic Acids (BPCA).

    Science.gov (United States)

    Wiedemeier, Daniel B; Lang, Susan Q; Gierga, Merle; Abiven, Samuel; Bernasconi, Stefano M; Früh-Green, Gretchen L; Hajdas, Irka; Hanke, Ulrich M; Hilf, Michael D; McIntyre, Cameron P; Scheider, Maximilian P W; Smittenberg, Rienk H; Wacker, Lukas; Wiesenberg, Guido L B; Schmidt, Michael W I

    2016-01-01

    Fire-derived, pyrogenic carbon (PyC), sometimes called black carbon (BC), is the carbonaceous solid residue of biomass and fossil fuel combustion, such as char and soot. PyC is ubiquitous in the environment due to its long persistence, and its abundance might even increase with the projected increase in global wildfire activity and the continued burning of fossil fuel. PyC is also increasingly produced from the industrial pyrolysis of organic wastes, which yields charred soil amendments (biochar). Moreover, the emergence of nanotechnology may also result in the release of PyC-like compounds to the environment. It is thus a high priority to reliably detect, characterize and quantify these charred materials in order to investigate their environmental properties and to understand their role in the carbon cycle. Here, we present the benzene polycarboxylic acid (BPCA) method, which allows the simultaneous assessment of PyC's characteristics, quantity and isotopic composition ((13)C and (14)C) on a molecular level. The method is applicable to a very wide range of environmental sample materials and detects PyC over a broad range of the combustion continuum, i.e., it is sensitive to slightly charred biomass as well as high temperature chars and soot. The BPCA protocol presented here is simple to employ, highly reproducible, as well as easily extendable and modifiable to specific requirements. It thus provides a versatile tool for the investigation of PyC in various disciplines, ranging from archeology and environmental forensics to biochar and carbon cycling research. PMID:27214064

  15. Enhanced bio-decolorization of 1-amino-4-bromoanthraquinone-2-sulfonic acid by Sphingomonas xenophaga with nutrient amendment

    Institute of Scientific and Technical Information of China (English)

    Hong Lu; Xiaofan Guan; Jing Wang; Jiti Zhou; Haikun Zhang

    2015-01-01

    Bacterial decolorization of anthraquinone dye intermediates is a slow process under aerobic conditions.To speed up the process,in the present study,effects of various nutrients on 1-amino-4-bromoanthraquinone-2-sulfonic acid (ABAS) decolorization by Sphingomonas xenophaga QYY were investigated.The results showed that peptone,yeast extract and casamino acid amendments promoted ABAS bio-decolorization.In particular,the addition of peptone and casamino acids could improve the decolorization activity of strain QYY.Further experiments showed that L-proline had a more significant accelerating effect on ABAS decolorization compared with other amino acids.L-Proline not only supported cell growth,but also significantly increased the decolorization activity of strain QYY.Membrane proteins of strain QYY exhibited ABAS decolorization activities in the presence of L-proline or reduced nicotinamide adenine dinucleotide,while this behavior was not observed in the presence of other amino acids.Moreover,the positive correlation between L-proline concentration and the decolorization activity of membrane proteins was observed,indicating that L-proline plays an important role in ABAS decolorization.The above findings provide us not only a novel insight into bacterial ABAS decolorization,but also an L-proline-supplemented bioaugmentation strategy for enhancing ABAS bio-decolorization.

  16. MCM-41 anchored sulfonic acid (MCM-41-R-SO3H): A mild, reusable and highly efficient heterogeneous catalyst for the Biginelli reaction

    Institute of Scientific and Technical Information of China (English)

    2008-01-01

    An efficient three-component synthesis of 3A-dihydropyrimidinones using MCM-41 anchored sulfonic acid (MCM-41-R-SO3H) as a mild, heterogeneous catalyst for Biginelli reaction in CH3CN under reflux condition is described.

  17. Mesomorphic structure of poly(styrene)-block-poly(4-vinylpyridine) with oligo(ethylene oxide)sulfonic acid side chains as a model for molecularly reinforced polymer electrolyte

    NARCIS (Netherlands)

    Kosonen, H; Valkama, S; Hartikainen, J; Eerikainen, H; Torkkeli, M; Jokela, K; Serimaa, R; Sundholm, F; ten Brinke, G; Ikkala, O; Eerikäinen, Hannele

    2002-01-01

    We report self-organized polymer electrolytes based on poly(styrene)-block-poly(4-vinylpyridine) (PS-block-P4VP). Liquidlike ethylene oxide (EO) oligomers with sulfonic acid end groups are bonded to the P4VP block, leading to comb-shaped supramolecules with the PS-block-P4VP backbone. Lithium perchl

  18. Green procedures for the chemoselective synthesis of acylals and their cleavage promoted by recoverable sulfonic acid based nanoporous carbon (CMK-5-SO3H)

    Indian Academy of Sciences (India)

    Daryoush Zareyee; Ehsan Mirzajanzadeh; Mohammad Ali Khalilzadeh

    2015-07-01

    A selective synthesis of gem-diacetates from the reaction of aldehydes and acetic anhydride in the presence of recyclable nanoporous solid sulfonic acid (CMK-5-SO3H) under solvent-free reaction conditions is reported. The catalyst was also found to be highly active for deprotection of resulting acylals in water.

  19. Synthesis, crystal structures and fluorescent properties of two new 7-iodo-8-hydroxyquinoline-5-sulfonic acid-containing polymers

    Science.gov (United States)

    Lu, Yongguang; Cheng, Wei; Meng, Xiangru; Hou, Hongwei

    2008-03-01

    Two new coordination polymers [Zn(IHQS)(4,4'-bipy) 1/2(H 2O) 2] n ( 1) and [Mn(IHQS)(4,4'-bipy) 1/2(H 2O) 2] n ( 2) (IHQS = 7-iodo-8-hydroxyquinoline-5-sulfonic acid) have been synthesized and characterized by single crystal X-ray diffraction. Both of them display one-dimensional chain framework in which the cage-like dimeric units formed by two metal ions, two IHQS anions and four water molecules are bridged by 4,4'-bipy. The hydrogen bonds and weak C--I···X (X = N, O, S) interactions extend the one-dimensional chains into three-dimensional supramolecular frameworks. The fluorescent properties of both polymers and IHQS were measured in solid state at room temperature. The results indicated that the emission spectra of the two polymers could be assigned to intraligand transition.

  20. Spectrofluorimetric Determination of Magnesium ( Ⅱ ) with 7- (8-Hydroxy-3, 6-Disulfonaphthylazo)8-Hydroxyquinoline-5-Sulfonic Acid

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    A new fluorescent reagent, 7- (8-hydroxy-3, 6-disulfonaphthylazo)-8-hydroxyquinoline-5-sulfonic acid (HDNHQ) for the determination of magnesium has been developed. It reacted with magnesium to form a 1: 1 fluorescent complex with λex/λem=356/495 nm immediately at room temperature in ammonia-ammonium chloride buffer (pH 10. 7). A linear relationship was obtained in the magnesium concentration range of 0160 ng@ mL-1 with the detection limit of 0. 04 ng@ mL-1 The proposed method was simple, rapid and sensitive. It has been successfully applied to the determination of trace magnesium in blood serum with recoveries of 103. 75% and 98. 16%, respectively.

  1. Phase II metabolism of benzene.

    OpenAIRE

    Schrenk, D.; Orzechowski, A.; Schwarz, L R; Snyder, R.; Burchell, B; Ingelman-Sundberg, M; K. W. DE BOCK

    1996-01-01

    The hepatic metabolism of benzene is thought to be a prerequisite for its bony marrow toxicity. However, the complete pattern of benzene metabolites formed in the liver and their role in bone marrow toxicity are not fully understood. Therefore, benzene metabolism was studied in isolated rodent hepatocytes. Rat hepatocytes released benzene-1,2-dihydrodiol, hydroquinone (HQ), catechol (CT), phenol (PH), trans-trans-muconic acid, and a number of phase II metabolites such as PH sulfate and PH glu...

  2. Study on the Retention Behavior of Aromatic Carboxylic and Sulfonic acid on a New Anion Exchange Column

    Institute of Scientific and Technical Information of China (English)

    SHI,Ya-Li; CAI,Ya-Qi; MOU,Shi-Fen

    2008-01-01

    Ion chromatography (IC) has gradually developed into a preferred method for the determination of inorganic anions. And in recent years some low molecular aliphatic acid can be also separated in the ion exchange column with the development of stationary phase. But for the determination of aromatic ionic compounds there are some problems. The aromatic anions show enhanced retention due to interaction with the π electrons of the aromatic backbone. Although the addition of an organic modifier can alleviate the difficulty, it is not the ultimate solution.IonPac AS20 column was developed using a unique polymer bonding technology and its substrate coating is aliphatic backbone. The polymer is completely free of any π electron-containing substituents in the AS20 column. In this paper, the retention behavior of aromatic carboxylic and sulfonic acid on two hydroxide-selective columns,IonPac AS11-HC, AS16, and the new column AS20 was also studied. The result showed that the retentions of ten compounds on three columns were different with each other because of their different column characteristics.Among them 4-chlorobenzene sulfonic acid, 3,5-dihydric benzoic acid and salicylic acid obviously exhibited the weakest retention on the IonPac AS20. It was showed that π-π bond function between anion and stationary phases was weakened in AS20 column because its polymer was completely free of any π electron-containing substituents.So in this paper the AS20 was selected as an analytical column to separate ten aromatic ionic compounds, fumaric acid with conjugate bond included. The retention behavior, separation of the ten compounds and effect of temperature on their retention in the anion-exchange column AS20 (2 mm) were studied. The result showed that those compounds could be separated with each other when running in gradient program and the organic modifier was unnecessary during the separation. So it is showed that AS20 column can be used as a separating column because its

  3. Benzene exposure, assessed by urinary trans,trans-muconic acid, in urban children with elevated blood lead levels

    Energy Technology Data Exchange (ETDEWEB)

    Weaver, V.M.; Fitzwilliam, A.; Peters, H.L.; Groopman, J.D. [Johns Hopkins Univ. School of Hygiene and Public Health, Baltimore, MD (United States)] [and others

    1996-03-01

    A pilot study was performed to evaluate the feasibility of using trans, trans-muconic acid (MA) as a biomarker of environmental benzene exposure. A secondary aim was to provide data on the extent of exposure to selected toxicants in a unique population consisting of inner-city children who were already overexposed to one urban hazard, lead. Potential sources of benzene were assessed by a questionnaire. Exposure biomarkers included urinary MA and cotinine and blood lead. Mean MA was 176.6 {plus_minus} 341.7 ng/mg creatinine in the 79 children who participated. A wide range of values was found with as many as 10.1%, depending on the comparison study, above the highest levels reported in adults not exposed by occupation. Mean MA was increased in children evaluated in the afternoon compared to morning, those at or above the median for time spent playing near the street, and those studied in the first half of the investigation. MA levels were not associated with blood lead or, consistently, with either questionnaire environmental tobacco smoke (ETS) data or cotinine. As expected, the mean blood lead level was elevated (23.6 {mu}g/dl). Mean cotinine was also increased at 79.2 ng/mg creatinine. We conclude that the use of MA as a biomarker for environmental benzene exposure is feasible since it was detectable in 72% of subjects with a wide range of values present. In future studies, correlation of MA with personal air sampling in environmental exposure will be essential to fully interpret the significance of these findings. In addition, these inner-city children comprise a high risk group for exposure to environmental toxicants including ETS, lead, and probably benzene, based on questionnaire sources and its presence in ETS. 22 refs., 5 figs., 4 tabs.

  4. Solid-supported sulfonic acid-containing catalysts efficiently promoted one-pot multi-component synthesis of -acetamido carbonyl compounds

    Indian Academy of Sciences (India)

    Mohammad Ali Zolfigol; Ardeshir Khazaei; Abdolkarim Zare; Mohammad Mokhlesi; Tahereh Hekmat-Zadeh; Alireza Hasaninejad; Fatemeh Derakhshan-Panah; Ahmad Reza Moosavi-Zare; Hassan Keypour; Ahmad Ali Dehghani-Firouzabadid; Maria Merajoddin

    2012-03-01

    Silica-functionalized sulfonic acid (SFSA) and sulfuric acid-modified polyethylene glycol-6000 (PEG-OSO3H) efficiently catalysed one-pot multi-component condensation of enolizable ketones or alkyl acetoacetates with arylaldehydes, acetonitrile and acetyl chloride to afford the corresponding -acetamido ketone or ester derivatives in high to excellent yields and in relatively short reaction times. Moreover, in this work, some novel -acetamido carbonyl compounds (i.e., one complex structure) are synthesized.

  5. Application of sulfonic acid functionalized nanoporous silica (SBA-Pr-SO3H in the green one-pot synthesis of triazoloquinazolinones and benzimidazoquinazolinones

    Directory of Open Access Journals (Sweden)

    Ghodsi Mohammadi Ziarani

    2015-01-01

    Full Text Available Sulfonic acid functionalized SBA-15 (SBA-Pr-SO3H with a pore size of 6 nm was proven to be an efficient heterogeneous nanoporous solid acid catalyst in the green one-pot synthesis of triazoloquinazolinones and benzimidazoquinazolinones from the reaction of aromatic aldehydes with 3-amino-1,2,4-triazole (or 2-aminobenzimidazole and dimedone under solvent free conditions.

  6. Sulfonic acid-functionalized ordered nanoporous Na+-montmorillonite as an efficient, eco-benign, and water-tolerant nanoreactor for chemoselective oxathioacetalization of aldehydes

    Science.gov (United States)

    Shirini, Farhad; Atghia, Seyyed Vahid; Mamaghani, Manouchehr

    2013-01-01

    Sulfonic acid-functionalized ordered nanoporous sodium montmorillonite has been found to be a mild and efficient solid acid catalyst for the chemoselective protection of a variety of carbonyl compounds as oxathiolanes in good to excellent yields. The present method offers several advantages such as short reaction times, high yields, simple procedure and mild conditions. Also, the catalyst could be recycled and reused at least for five times without noticeably decreasing the catalytic activity.

  7. Synthesis & application of α-sulfonic acid fatty acid soap collector%α-磺酸基油酸皂捕收剂的应用

    Institute of Scientific and Technical Information of China (English)

    黄齐茂; 蔡坤; 王巍; 罗伍容; 潘志权; 罗惠华; 池汝安

    2012-01-01

    以大豆油酸化油为原料,经磺化、皂化等单元反应合成了α-磺酸基油酸皂浮选捕收剂,用于四川某中低品位胶磷矿的浮选试验.结果表明,该捕收剂实现了胶磷矿与白云石的有效分离,入选原矿P2O5品位23.80%,MgO质量分数6.54%;获得磷精矿P2O5品位33.88%,回收率85.37%,MgO含量1.50%.%A floatation collector, a-sulfonic acid fatty acid soap, was prepared by steps of sulfonated, saponification with soybean oil as raw material. It was used in the floatation of low-and-middle grade Sichuan phosphate ores. Test results show that the collector realizes the effective separation of phosphate and dolomite, the P2O5 content goes up to 33. 88% from 23. 80% of run-of mine with a recovery of 85. 37% , and the MgO content goes down to 1. 50% from 6. 54%.

  8. Catalytic Upgrading of bio-oil using 1-octene and 1-butanol over sulfonic acid resin catalysts

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Zhijun; Wang, Qingwen; Tripathi, Prabhat; Pittman, Charles U.

    2011-02-04

    Raw bio-oil from fast pyrolysis of biomass must be refined before it can be used as a transporation fuel, a petroleum refinery feed or for many other fuel uses. Raw bio-oil was upgraded with the neat model olefin, 1-octene, and with 1-octene/1-butanol mixtures over sulfonic acid resin catalysts frin 80 to 150 degrees celisus in order to simultaneously lower water content and acidity and to increase hydrophobicity and heating value. Phase separation and coke formation were key factors limiting the reaction rate during upgrading with neat 1-octene although octanols were formed by 1-octene hydration along with small amounts of octyl acetates and ethers. GC-MS analysis confirmed that olefin hydration, carboxylic acid esterification, acetal formation from aldehydes and ketones and O- and C-alkylations of phenolic compounds occurred simultaneously during upgrading with 1-octene/1-butanol mixtures. Addition of 1-butanol increased olefin conversion dramatically be reducing mass transfer restraints and serving as a cosolvent or emulsifying agent. It also reacted with carboxylic acids and aldehydes/ketones to form esters, and acetals, respectively, while also serving to stabilize bio-oil during heating. 1-Butanol addition also protected the catalysts, increasing catalyst lifetime and reducing or eliminationg coking. Upgrading sharply increased ester content and decreased the amounts of levoglucosan, polyhydric alcohols and organic acids. Upgrading lowered acidity (pH value rise from 2.5 to >3.0), removed the uppleasant ordor and increased hydrocarbon solubility. Water content decreased from 37.2% to < 7.5% dramatically and calorific value increased from 12.6 MJ kg to about 30.0 MJ kg.

  9. Highly Sulfonated Diamine Synthesized Polyimides and Protic Ionic Liquid Composite Membranes Improve PEM Conductivity

    Directory of Open Access Journals (Sweden)

    Bor-Kuan Chen

    2015-06-01

    Full Text Available A novel sulfonated diamine was synthesized from 1,4-bis(4-aminophenoxy benzene [pBAB]. Sulfonated polyimides (SPIs were synthesized from sulfonated pBAB, 1,4-bis(4-aminophenoxy-2-sulfonic acid benzenesulfonic acid [pBABTS], various diamines and aromatic dianhydrides. Composite proton exchange membranes (PEMs made of novel SPIs and a protic ionic liquid (PIL 1-vinyl-3-H-imidazolium trifluoromethanesulfonate [VIm][OTf] showed substantially increased conductivity. We prepared an SPI/PIL composite PEM using pBABTS, 4,4′-(9-fluorenylidene dianiline (9FDA as diamine, 3,3′,4,4′-diphenylsulfone tetracarboxylic dianhydride (DSDA as dianhydride and 40 wt % [VIm][OTf] with a high conductivity of 16 mS/cm at 120 °C and anhydrous condition. pBABTS offered better conductivity, since the chemical structure had more sulfonated groups that provide increased conductivity. The new composite membrane could be a promising anhydrous or low-humidity PEM for intermediate or high-temperature fuel cells.

  10. Inhibition of lactoperoxidase-catalyzed 2,2'-azino-bis(3-ethylbenzthiazoline-6-sulfonic acid) (ABTS) and tyrosine oxidation by tyrosine-containing random amino acid copolymers.

    Science.gov (United States)

    Clausen, Morten R; Skibsted, Leif H; Stagsted, Jan

    2008-09-24

    Oxidation of 2,2'-azino-bis(3-ethylbenzthiazoline-6-sulfonic acid) by lactoperoxidase was found to be inhibited by tyrosine-containing random amino acid copolymers but not by tyrosine. Both electrostatic effects and polymer size were found to be important by comparison of negatively and positively charged copolymers of varying lengths, with poly(Glu, Tyr)4:1 ([E 4Y 1] approximately 40) as the strongest competitive inhibitor (EC 50 approximately 20 nM). This polymer did not form dityrosine in the presence of lactoperoxidase (LPO) and peroxide. Furthermore, incubation with tert-butyl hydroperoxide, as opposed to hydrogen peroxide, resulted in a peculiar long lag phase of the reaction between the redox intermediate compound II and [E 4Y 1] approximately 40, indicating a very tight association between enzyme and inhibitor. We propose that interactions between multiple positively charged areas on the surface of LPO and the polymer are required for optimal inhibition.

  11. Efficacy of two acidified chlorite postmilking teat disinfectants with sodium dodecylbenzene sulfonic acid on prevention of contagious mastitis using an experimental challenge protocol.

    Science.gov (United States)

    Oura, L Y; Fox, L K; Warf, C C; Kempt, G K

    2002-01-01

    Two acidified sodium chlorite postmilking teat disinfectants were evaluated for efficacy against Staphylococcus aureus and Streptococcus agalactiae by using National Mastitis Council experimental challenge procedures. The effect of these teat dips on teat skin and teat end condition was also determined. Both dips contained 0.32% sodium chlorite, 1.32% lactic, and 2.5% glycerin. Dips differed in the amount of sodium dodecylbenzene sulfonic acid (0.53 or 0.27%) added as a surfactant. Both dips significantly reduced new intramammary infection (IMI) rates compared with undipped controls. The dip containing 0.53% dodecylbenzene sulfonic acid reduced new IMI by Staph. aureus by 72% and Strep. agalactiae by 75%. The dip containing 0.27% dodecylbenzene sulfonic acid reduced new IMI by Staph. aureus by 100% and by Strep. agalactiae by 88%. Changes in teat skin and teat end condition for treatment and control groups varied in parallel over time. Teats treated with either teat dip had higher mean teat skin and teat end scores than control teats at some weeks. However, teat skin and teat end condition did not tend to change from the start to the completion of the trial. Application of the two new postmilking teat dips was effective in reducing new IMI from contagious mastitis pathogens. (Key words: teat dip, contagious mastitis, chlorous acid) PMID:11860118

  12. Mineralization of sulfonated azo dyes and sulfanilic acid by Phanerochaete chrysosporium and Streptomyces chromofuscus.

    OpenAIRE

    Paszczynski, A; Pasti-Grigsby, M B; Goszczynski, S; Crawford, R L; Crawford, D. L.

    1992-01-01

    Five 14C-radiolabeled azo dyes and sulfanilic acid were synthesized and used to examine the relationship between dye substitution patterns and biodegradability (mineralization to CO2) by a white-rot fungus and an actinomycete. 4-Amino-[U-14C]benzenesulfonic acid and 4-(3-sulfo-4-aminophenylazo)-[U-14C]benzenesulfonic acid were used as representative compounds having sulfo groups or both sulfo and azo groups. Such compounds are not known to be present in the biosphere as natural products. The ...

  13. 2-(4-Bromo­benzene­sulfonamido)benzoic acid

    Science.gov (United States)

    Arshad, Muhammad Nadeem; Khan, Islam Ullah; Akkurt, Mehmet; Shafiq, Muhammad; Mustafa, Ghulam

    2009-01-01

    In the title compound, C13H10BrNO4S, the dihedral angle between the benzene rings is 82.75 (15)°. An intra­molecular N—H⋯O hydrogen bond generates an S(6) ring motif. In the crystal structure, two mol­ecules form an R 2 2(8) centrosymmetric dimer through a pair of O—H⋯O hydrogen bonds. Intra- and inter­molecular C—H⋯O hydrogen bonds are also observed. PMID:21582883

  14. Exposure to perfluorooctane sulfonic acid (PFOS) adversely affects the life-cycle of the damselfly Enallagma cyathigerum

    Energy Technology Data Exchange (ETDEWEB)

    Bots, Jessica, E-mail: Jessica.bots@ua.ac.b [Evolutionary Ecology Group, University of Antwerp, Groenenborgerlaan 171, B-2020 Antwerpen (Belgium); De Bruyn, Luc, E-mail: luc.debruyn@ua.ac.b [Evolutionary Ecology Group, University of Antwerp, Groenenborgerlaan 171, B-2020 Antwerpen (Belgium); Research Institute for Nature and Forest (INBO), Kliniekstraat 25, 1070 Brussels (Belgium); Snijkers, Tom, E-mail: tomsnijkers@gmail.co [Evolutionary Ecology Group, University of Antwerp, Groenenborgerlaan 171, B-2020 Antwerpen (Belgium); Van den Branden, Bert, E-mail: bvandenbranden@gmail.co [Department PIH Environment, University College West Flanders (HOWEST), Graaf K. 11 de Goedelaan 5, B-8500 Kortrijk (Belgium); Van Gossum, Hans, E-mail: hans.vangossum@ua.ac.b [Evolutionary Ecology Group, University of Antwerp, Groenenborgerlaan 171, B-2020 Antwerpen (Belgium)

    2010-03-15

    We evaluated whether life-time exposure to PFOS affects egg development, hatching, larval development, survival, metamorphosis and body mass of Enallagma cyathigerum (Insecta: Odonata). Eggs and larvae were exposed to five concentrations ranging from 0 to 10 000 mug/L. Our results show reduced egg hatching success, slower larval development, greater larval mortality, and decreased metamorphosis success with increasing PFOS concentration. PFOS had no effect on egg developmental time and hatching or on mass of adults. Eggs were the least sensitive stage (NOEC = 10 000 mug/L). Larval NOEC values were 1000 times smaller (10 mug/L). Successful metamorphosis was the most sensitive response trait studied (NOEC < 10 mug/L). The NOEC value suggests that E. cyathigerum is amongst the most sensitive freshwater organisms tested. NOEC for metamorphosis is less than 10-times greater than the ordinary reported environmental concentrations in freshwater, but is more than 200-times smaller than the greatest concentrations measured after accidental releases. - Long-term laboratory exposure to perfluorooctane sulfonic acid reduces survival and interferes with metamorphosis of Enallagma cyathigerum (Insecta: Odonata).

  15. A novel voltammetric sensor for citalopram based on multiwall carbon nanotube/(poly(p-aminobenzene sulfonic acid)/β-cyclodextrin).

    Science.gov (United States)

    Gholivand, Mohammad-Bagher; Akbari, Arezoo

    2016-05-01

    Multi-walled carbon nanotube (MWCNTS) coated with poly p-aminobenzene sulfonic acid/β-cyclodextrin (p-ABSA/β-CD) film was used as an effective strategy for modification of the surface of glassy carbon electrode (GCE). Electrochemical study and determination of citalopram (CT) were investigated at the p (p-ABSA)/β-CD/MWCNT/GC using cyclic and differential pulse anodic stripping voltammetric techniques. The results indicate that the p (p-ABSA)/β-CD/MWCNT/GC significantly enhanced the oxidation peak current of CT. The modified electrode was characterized by electrochemical impedance spectroscopy (EIS), scanning electron microscopy(SEM) and cyclic voltammetry (CV).The fabricated electrochemical sensor exhibits a fast and reversible linear response toward CT within the concentration ranges of 90 nM-1 μM, 1-11 μM and 11-100 μM with correlation coefficients greater than 0.99 and detection limit of 44 nM. The resulting functionalized polymer film features interesting electrochemical properties such good recovery, reproducibility and selectivity toward CT. The applicability of the proposed sensor was tested by determination of CT in pharmaceutical combinations and human body fluids. PMID:26952450

  16. Modeling of boldine alkaloid adsorption onto pure and propyl-sulfonic acid-modified mesoporous silicas. A comparative study.

    Science.gov (United States)

    Geszke-Moritz, Małgorzata; Moritz, Michał

    2016-12-01

    The present study deals with the adsorption of boldine onto pure and propyl-sulfonic acid-functionalized SBA-15, SBA-16 and mesocellular foam (MCF) materials. Siliceous adsorbents were characterized by nitrogen sorption analysis, transmission electron microscopy (TEM), scanning electron microscopy (SEM), Fourier-transform infrared (FT-IR) spectroscopy and thermogravimetric analysis. The equilibrium adsorption data were analyzed using the Langmuir, Freundlich, Redlich-Peterson, and Temkin isotherms. Moreover, the Dubinin-Radushkevich and Dubinin-Astakhov isotherm models based on the Polanyi adsorption potential were employed. The latter was calculated using two alternative formulas including solubility-normalized (S-model) and empirical C-model. In order to find the best-fit isotherm, both linear regression and nonlinear fitting analysis were carried out. The Dubinin-Astakhov (S-model) isotherm revealed the best fit to the experimental points for adsorption of boldine onto pure mesoporous materials using both linear and nonlinear fitting analysis. Meanwhile, the process of boldine sorption onto modified silicas was described the best by the Langmuir and Temkin isotherms using linear regression and nonlinear fitting analysis, respectively. The values of adsorption energy (below 8kJ/mol) indicate the physical nature of boldine adsorption onto unmodified silicas whereas the ionic interactions seem to be the main force of alkaloid adsorption onto functionalized sorbents (energy of adsorption above 8kJ/mol). PMID:27612776

  17. Study of polyaniline doped with trifluoromethane sulfonic acid in gas-diffusion electrodes for proton-exchange membrane fuel cells

    Energy Technology Data Exchange (ETDEWEB)

    Gharibi, Hussein; Zhiani, Mohammad; Kheirmand, Mehdi; Kakaei, Karim [Department of Physical Chemistry, Faculty of Science, Tarbiat Modarres University, P.O. Box 14115-175, Tehran (Iran); Entezami, Ali Akbar [Faculty of Chemistry, Tabriz University, Tabriz (Iran); Mirzaie, Rasol Abdullah [Department of Chemistry, Faculty of Science, Shahid Rajaee University, Tehran (Iran)

    2006-04-21

    Polytetrafluoroethylene (PTFE)-bonded gas-diffusion electrodes (GDEs), modified with polyaniline as an electron and proton conductor in the catalyst layer, are prepared and evaluated for use in proton-exchange membrane fuel cells (PEMFCs). Polyaniline is coated on the GDE by electropolymerization of aniline and trifluoromethane sulfonic acid as the proton-conductive monomer. The electrodes are characterized by cyclic voltammetry, current-potential measurements, electrochemical impedance spectroscopy, and chronoamperometry. The polyaniline is found to be homogenously dispersed in the catalyst layer, making it a good candidate proton and electron conductor. Use of polyaniline instead of Nafion in the catalyst layer, increases the utility of the electrocatalyst by 18%. The results are consistent with the presence of polyaniline as a conductive polymer in the reaction layer reducing the polarization resistance of the electrode in comparison with that of a corresponding electrode containing Nafion. Thus, the present results indicate that PEMFCs using polyaniline-containing electrocatalysts should give superior performance to those using catalysts containing traditional ionomers. (author)

  18. One step graft copolymerization of acrylic acid and sodium styrene sulfonate onto high-density polyethylene film by preirradiation method

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    High-density polyethylene (HDPE) films were irradiated by 60Co gamma ray with a dose of 100 kGy in air and then immersed in aqueous solution of acrylic acid (AA) and sodium styrene sulfonate (SSS) at different temperature. The effects of grafting conditions such as temperature, reaction time, Mohr's salt concentration, and total concentration of monomer on grafting yield were studied. Both grafting yield of AA and SSS onto HDPE respectively increases with total concentration of monomers. The highest grafting yield was observed at 3 mol/L monomers where the grafted PE swelled to the largest extent in the monomers mixture. The grafting yield increases with reaction time and then levels off. At higher temperature, the grafting yield decreases with Mohr's salt concentration, but increases at low temperature when Mohr's salt concentration is 0.083%. Which can be interpreted that in the presence of Fe2+ diperoxides and hydroperoxides may decompose at low temperature to form radical which can initiate the grafting. The physical and chemical properties of grafting films were also investigated.

  19. PHOTOPHYSICAL STUDY OF SULFONATED POLYSTYRENE

    Institute of Scientific and Technical Information of China (English)

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

    2004-01-01

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

  20. Covalently anchored sulfonic acid on silica gel (SiO2-R-SO3H) as an efficient and reusable heterogeneous catalyst for the one-pot synthesis of 1,8-dioxooctahydroxanthenes under solvent-free conditions

    Institute of Scientific and Technical Information of China (English)

    Gholam Hossein Mahdavinia; Mohammad A.Bigdeli; Yaser Saeidi Hayeniaz

    2009-01-01

    A highly efficient one-pot synthesis of 1,8-dioxooctahydroxanthenes under solvent-free conditions catalyzed by sulfonic acid covalently anchored onto the surface of silica gel is reported.All types of aldehydes,including aromatic,unsaturated,and heterocyclic,are used.The silica gel/sulfonic acid catalyst (SiO2-R-SO3H) is completely heterogeneous and can be recycled.

  1. 40 CFR 721.10072 - Benzene, 1,1′-methylenebis[4-isocyanato-, polymer with benzenedicarboxylic acid, butyl dialkyl...

    Science.gov (United States)

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Benzene, 1,1â²-methylenebis , .alpha... SUBSTANCES Significant New Uses for Specific Chemical Substances § 721.10072 Benzene, 1,1′-methylenebis... to reporting. (1) The chemical substance identified generically as benzene,...

  2. QSTR studies regarding the ECOSAR toxicity of benzene-carboxylic acid' esters to fathead minnow fish (Pimephales promelas).

    Science.gov (United States)

    Tarko, Laszlo; Putz, Mihai V; Ionascu, Cosmin; Putz, Ana-Maria

    2014-01-01

    The present work employs 152 benzene-carboxylic acid' esters having computed the toxicity within the range [2.251, 10.222] for fathead minnow fish (Pimephales promelas). Calibration set includes many pairs having very similar chemical structure, size, shape and hydrophilicity, but very different value of ECOSAR toxicity or vice versa. The QSTR study, which uses all esters as calibration set, emphasized a large percent (16.2%) of outliers. In this QSTR study most of the estimated values of toxicity for outliers are much lower than ECOSAR toxicity. The LogP and some aromaticity descriptors are predictors. The best QSTR for esters having low value (toxicity and the best QSTR for esters having high value (> 5.5) of ECOSAR toxicity are obtained when the number of outliers is very small. These QSTRs are different enough and highlight opposite influences of certain descriptors on toxicity. The results emphasize two possibilities: (a) the esters having low value of ECOSAR toxicity and the esters having high value of ECOSAR toxicity are included in two different classes from the point of view of structure-toxicity relationship and/or (b) many high values of ECOSAR toxicity are wrong. By comparison, a QSTR using experimental values of toxicity against rats for 37 benzene-carboxylic esters included in the same database gives good correlation experimental/computed values of toxicity, the number of outliers is null and the result of validation test is good. PMID:24724900

  3. Morphological control of layered double hydroxide through a biomimetic approach using carboxylic and sulfonic acids

    Directory of Open Access Journals (Sweden)

    Taishi Yokoi

    2015-09-01

    Full Text Available Layered double hydroxides (LDHs have intercalation properties and are used in various applications. The performances of the LDH materials can be improved by controlling crystal morphology. Morphology of inorganic crystals is controlled by organic molecules in biomineralization. Inspired by biomineralization, we investigated the effect of the addition of mono, di and triacids as morphological control agents on crystal morphology of LDH synthesized by the homogeneous precipitation method. Morphology of LDH was changed from hexagonal plate to stacked disc by addition of monoacids, namely acetic acid and methanesulfonic acid, in the reaction solution. Flower-shaped LDH crystals were formed in the presence of diacids and a triacid, namely succinic acid, 1,2-ethanedisulfonic acid and 1,2,3-propanetricarboxylic acid. We found that the morphology of the LDH crystals was controlled by the number of functional group on the morphological control agent rather than the type of functional group. These findings can contribute for the development of novel and functional LDH materials with precisely controlled morphology.

  4. 2-(4-Acetamido­benzene­sulfonamido)­benzoic acid

    Science.gov (United States)

    Sharif, Shahzad; Khan, Islam Ullah; Mahmood, Tariq; Kang, Sung Kwon

    2011-01-01

    In the title compound, C15H14N2O5S, two similar mol­ecules comprise the asymmetric unit, which are linked by strong inter­molecular C—H⋯π inter­actions. Both mol­ecules are bent, with dihedral angles of 71.94 (16) and 74.62 (15)° between the benzene rings. An intra­molecular N—H⋯O hydrogen bond occurs in each mol­ecule. In the crystal, inter­molecular N—H⋯O and O—H⋯O hydrogen bonds link the mol­ecules into a three-dimensional network. PMID:21836982

  5. Thermotropic liquid crystalline polyesters derived from bis-(4-hydroxybenzoyloxy)-2-methyl-1,4-benzene and aliphatic dicarboxylic acid chlorides

    Indian Academy of Sciences (India)

    Khudbudin Mulani; Mohasin Momin; Nitin Ganjave; Nayaku Chavan

    2015-09-01

    A series of thermotropic liquid crystalline polyesters derived from bis-(4-hydroxybenzoyloxy)-2-methyl-1,4-benzene (BHBOMB) and aliphatic dicarboxylic acid chlorides were investigated. All these polyesters were synthesized by interfacial polycondensation method and characterized by differential scanning calorimetry and wide-angle X-ray diffractometer. These polyesters consist of BHBOMB as a mesogenic diol and aliphatic diacid chlorides were used as flexible spacers. The length of oligomethylene units in polymer was varied from the trimethylene to the dodecamethylene groups. The transition temperatures and thermodynamic properties were studied for all these polymers. All these polyesters were soluble in chlorinated solvents such as chloroform, dichloromethane, dichloroethane, etc. More importantly, all these polyesters exhibited very large mesophase stability.

  6. Synthesis of 2-Aryl-l-arylmethyl-lH-1,3-benzimidazole Derivatives Using Silica-bonded PropyI-S-sulfonic Acid as Recyclable Solid Acid Catalyst

    Institute of Scientific and Technical Information of China (English)

    Ghaem Ahmadi-Ana,Sayed Mohammad; Baghernejad, Mojtaba"; Niknam, Khodabakhsh

    2012-01-01

    A highly selective synthesis of 2-aryl-l-arylmethyl-lH-1,3-benzimidazoles from the reaction of o-phenylene- diamine and aromatic aldehydes in the presence of silica-bonded propyl-S-sulfonic acid (SBSSA) at 80℃ in water in good to excellent yields was developed.

  7. Experimental study of the removal of copper ions using hydrogels of xanthan, 2-acrylamido-2-methyl-1-propane sulfonic acid, montmorillonite: Kinetic and equilibrium study.

    Science.gov (United States)

    Aflaki Jalali, Marzieh; Dadvand Koohi, Ahmad; Sheykhan, Mehdi

    2016-05-20

    In this paper, removal of copper ions from aqueous solution using novel xanthan gum (XG) hydrogel, xanthan gum-graft-2-acrylamido-2-methyl-1-propane sulfonic acid (XG-g-P(AMPS)) hydrogel and xanthan gum-graft-2-acrylamido-2-methyl-1-propane sulfonic acid/montmorillonite (XG-g-P(AMPS)/MMT) hydrogel composite were studied. The structure and morphologies of the xanthan-based hydrogels were characterized by Fourier transform infrared spectroscopy (FTIR) and scanning electron microscope (SEM). Adsorbents comprised a porous crosslink structure with side chains that carried carboxyl, hydroxyl and sulfonate. Maximum adsorption was observed in the pH=5.2, initial concentrations of Cu(2+)=321.8 mg/L, Temperature=45 °C, contact time=5 h with 0.2 g/50 mL of the hydrogels. Adsorption process was found to follow Langmuir isotherm model with maximum adsorption capacity of 24.57, 39.06 and 29.49 mg/g for the XG, XG-g-P(AMPS) and XG-g-P(AMPS)/MMT, respectively. Adsorption kinetics data fitted well with pseudo second order model. The negative ΔG° values and the positive ΔS° confirmed that the adsorption was a spontaneous process. The positive ΔH° values suggested that the adsorption was endothermic in nature. PMID:26917382

  8. Synthesis, Antibacterial and Antitubercular Activities of Some 5H-Thiazolo[3,2-a]pyrimidin-5-ones and Sulfonic Acid Derivatives

    Directory of Open Access Journals (Sweden)

    Dong Cai

    2015-09-01

    Full Text Available A series of 5H-thiazolo[3,2-a]pyrimidin-5-ones were synthesized by the cyclization reactions of S-alkylated derivatives in concentrated H2SO4. Upon treatment of S-alkylated derivatives at different temperatures, intramolecular cyclization to 7-(substituted phenylamino-5H-thiazolo[3,2-a]pyrimidin-5-ones or sulfonation of cyclized products to sulfonic acid derivatives occurred. The structures of the target compounds were confirmed by IR, 1H-NMR, 13C-NMR and HRMS studies. The compounds were evaluated for their preliminary in vitro antibacterial activity against some Gram-positive and Gram-negative bacteria and screened for antitubercular activity against Mycobacterium tuberculosis by the broth dilution assay method. Some compounds showed good antibacterial and antitubercular activities.

  9. Four-component one-pot synthesis of unsymmetrical polyhydroquinoline derivatives using 3-methyl-1-sulfonic acid imidazolium hydrogen sulfate as a catalyst

    Institute of Scientific and Technical Information of China (English)

    Nader Ghaffari Khaligh

    2014-01-01

    3-Methyl-1-sulfonic acid imidazolium hydrogen sulfate has been used as an efficient, halogen-free, and reusable Brönsted acidic ionic liquid catalyst for the synthesis of ethyl-4-aryl/heteryl- hexahy-dro-trimehtyl-5-oxoquinoline-3-carboxylates via the one-pot condensation of dimedone with ar-yl/heteryl aldehydes, ethyl acetoacetate, and ammonium acetate under solvent-free conditions. This method has the advantage of being clean and simple, as well as providing the desired product in high yield over a short reaction time. Furthermore, the catalyst could be recycled and reused four times without any discernible reduction in activity.

  10. The enhancement of fluorescence quantum yields of anilino naphthalene sulfonic acids by inclusion of various cyclodextrins and cucurbit[7]uril

    Science.gov (United States)

    Sueishi, Yoshimi; Fujita, Tomonori; Nakatani, Shinichiro; Inazumi, Naoya; Osawa, Yoshihiro

    2013-10-01

    The association constants (K) for the inclusion complexation of four kinds of cyclodextrins (CDs (β- and γ-), 2,6-di-O-methylated β-CD, and 2,3,6-tri-O-methylated β-CD) and cucurbit[7]uril (CB[7]) with 1,8- and 2,6-anilinonaphthalene sulfonic acids (ANSs) were determined from fluorescence spectra enhanced by inclusion. Various CDs and CB[7] form stable 1:1 inclusion complexes with 1,8- and 2,6-ANSs: K = 80-11 700 M-1 for 2,6-ANS and 50-195 M-1 for 1,8-ANS. The high stability of the inclusion complexes of 2,6-ANS with CB[7] and 2,6-di-O-methylated β-CD is shown. Further, we determined the fluorescence quantum yields (Φ values) for the inclusion complexes of ANSs by using a fluorescence spectrophotometer equipped with a half-moon unit. The Φ values of 1,8- and 2,6-ANSs were largely enhanced by the inclusion of methylated β-CDs and did not correlate with the degree of stability (K) of the inclusion complexes. We characterized the structures of the inclusion complexes by 2D ROESY-NMR measurements. In addition, the microenvironmental polarity inside the hydrophobic CD and CB[7] cavities was evaluated using the fluorescence probe 2,6-ANS. Based on the emission mechanism and the aspect of inclusion in a hydrophobic cavity, we have suggested that the microenvironmental polarity and viscosity for the excited state of ANS plays an important role for the Φ values of inclusion complexes.

  11. Preventive and therapeutic effects of NF-kappaB inhibitor curcumin in rats colitis induced by trinitrobenzene sulfonic acid

    Institute of Scientific and Technical Information of China (English)

    Yan-Ting Jian; Guo-Feng Mai; Ji-De Wang; Ya-Li Zhang; Rong-Cheng Luo; Yong-Xin Fang

    2005-01-01

    AIM: To ascertain the molecule mechanism of nuclear factor-κB (NF-κB) inhibitor curcumin preventive and therapeutic effects in rats' colitis induced by trinitrobenzene sulfonic acid (TNBS).METHODS: Sixty rats with TNBS-induced colitis weretreated with 2.0% curcumin in the diet. Thirty positive control rats were treated with 0.5% sulfasalazine (SASP).Thirty negative control rats and thirty model rats were treated with general diet. Changes of body weight together with histological scores were evaluated. Survival rates were also evaluated. Cell nuclear NF-κB activity in colonic mucosa was evaluated by using electrophoretic mobility shift assay. Cytoplasmic IκB protein in colonic mucosa was detected by using Western Blot analysis.Cytokine messenger expression in colonic tissue was assessed by using semiquantitative reverse-transcription polymerase chain reaction.RESULTS: Treatment with curcumin could prevent and treat both wasting and histopathologic signs of rats with TNBS-induced intestinal inflammation. In accordance with these findings, NF-κB activation in colonic mucosa was suppressed in the curcumin-treated groups. Degradations of cytoplasmic IκB protein in colonic mucosa were blocked by curcumin treatment. Proinfiammatory cytokine messenger RNA expression in colonic mucosa was also suppressed.CONCLUSION: This study shows that NF-κB inhibitor curcumin could prevent and improve experimental colitis in murine model with inflammatory bowel disease (IBD).The findings suggest that NF-κB inhibitor curcumin could be a potential target for the patients with IBD.

  12. Prevention of tri-nitrobenzene of sulfonic acid-induced colitis in chicken by using extract of Aloe vera

    Directory of Open Access Journals (Sweden)

    Motamed Elsayed Mahmoud

    Full Text Available Aim: Aloe vera, species of succulent plant in the genus Aloe, has multiple clinical activities and used routinely to accelerate wound healing. The present study was designed to investigate the anti-inflammatory effect of Aloe vera extracts (AVE in vitro and in vivo. Materials and Methods: The effect of crude AVE on inducible nitric oxide production by LPS/IFNg-stimulated cultured macrophages was evaluated. The therapeutic effect of administering crude Aloe vera extracts (100 mg/kg b.w. on the development of tri-nitrobenzene of sulfonic acid (TNBS-induced colitis (40 mg/kg b. w. in chicken was also investigated. Chicken is a valuable model for this purpose because it showed preference to bitter taste of Aloe vera. Diverse clinical pictures of the colitis including weight loss, diarrhea and histopathological changes were evaluated. Results: Nitrite production by LPS/IFNg-stimulated macrophages was maximally reduced by adding of AVE (100 μg/ml. This result suggests a direct inhibitory effect of AVE on the inflammatory cells. Chicks treated orally with AVE showed improvement of the histological signs with no inflammatory cell infiltrates and reduction of myeloperoxidase (MPO activities when compared with colitis control group. AVE pretreatment ameliorated significantly the clinical and histopathological severity of the TNBS-induced colitis; decreased body weight loss and diarrhea and increased survival. Conclusion: It was concluded that oral administration of AVE represents a valuable therapeutic approach for the treatment of colitis in chicken. [Vet. World 2012; 5(8.000: 469-476

  13. Interaction of multi-walled carbon nanotubes with perfluorinated sulfonic acid ionomers and surface treatment studies

    DEFF Research Database (Denmark)

    Andersen, Shuang Ma; Dhiman, Rajnish; Borghei, Maryam;

    2014-01-01

    equilibrium constant (Keq.) and maximum surface coverage (Γmax) were determined based on the model. In general, the ionomer showed stronger adsorption for MWCNTs (Keq. = 21 − 377 depending on treatment) comparing to Vulcan (Keq. = 18), and slightly lower monolayer coverage. The interaction was found...... efficient, user-friendly and systematic studies based on our earlier experience. In this work, multi-walled carbon nanotubes (MWCNTs) from Showa Denko® and the corresponding acid modified products were explored. The adsorption at low concentration was found to follow a Langmuir isotherm. Adsorption...... to be strongly affected by surface composition, morphology, porosity and oxygen containing functional groups, which are varied with purification and functionalization treatments. The modification of the surface properties was also studied with HR-TEM, BET, porosity measurement, EDXS, XPS, Raman and TG...

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2008-10-15

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

  15. Design, synthesis, and evaluation of 2 beta-alkenyl penam sulfone acids as inhibitors of beta-lactamases.

    Science.gov (United States)

    Richter, H G; Angehrn, P; Hubschwerlen, C; Kania, M; Page, M G; Specklin, J L; Winkler, F K

    1996-09-13

    A general method for synthesis of 2 beta-alkenyl penam sulfones has been developed. The new compounds inhibited most of the common types of beta-lactamase. The level of activity depended very strongly on the nature of the substituent in the 2 beta-alkenyl group. The inhibited species formed with the beta-lactamase from Citrobacter freundii 1205 was sufficiently stable for X-ray crystallographic studies. These, together with UV absorption spectroscopy and studies of chemical degradation, suggested a novel reaction mechanism for the new inhibitors that might account for their broad spectrum of action. The (Z)-2 beta-acrylonitrile penam sulfone Ro 48-1220 was the most active inhibitor from this class of compound. The inhibitor enhanced the action of, for example, ceftriaxone against a broad selection of organisms producing beta-lactamases. The organisms included strains of Enterobacteriaceae that produce cephalosporinases, which is an exceptional activity for penam sulfones.

  16. Effective Liquid-phase Nitration of Benzene Catalyzed by a Stable Solid Acid Catalyst: Silica Supported Cs2.5H0.5PMo12O40

    International Nuclear Information System (INIS)

    Silica supported Cs2.5H0.5PMo12O40 catalyst was prepared through sol-gel method with ethyl silicate-40 as silicon resource and characterized by X-ray diffraction, infrared spectroscopy, scanning electron microscopy, nitrogen adsorption-desorption and potentiometric titration methods. The Cs2.5H0.5PMo12O40 particles with Keggin-type structure well dispersed on the surface of silica, and the catalyst exhibited high surface area and acidity. The catalytic performance of the catalysts for benzene liquid-phase nitration was examined with 65% nitric acid as nitrating agent, and the effects of various parameters were tested, which including temperature, time and amount of catalyst, reactants ratio, especially the recycle of catalyst was emphasized. Benzene was effectively nitrated to mononitro-benzene with high conversion (95%) in optimized conditions. Most importantly, the supported catalyst was proved has excellent stability in the nitration progress, and there were no any other organic solvent and sulfuric acid were used in the reaction system, so the liquid-phase nitration of benzene that we developed was an eco-friendly and attractive alternative for the commercial technology

  17. 2-Chloro-5-(2-iodo­benzene­sulfonamido)­benzoic acid

    Science.gov (United States)

    Arshad, Muhammad Nadeem; Tahir, M. Nawaz; Khan, Islam Ullah; Siddiqui, Waseeq Ahmad; Shafiq, Muhammad

    2009-01-01

    In the mol­ecule of the title compound, C13H9ClINO4S, the coordination around the S atom is distorted tetra­hedral. The aromatic rings are oriented at a dihedral angle of 74.46 (9)°. Intra­molecular C—H⋯O hydrogen bonds result in the formation of two five- and one six-membered rings, which adopt planar, envelope and twisted conformations, respectively. In the crystal structure, inter­molecular N—H⋯O and O—H⋯O hydrogen bonds link the mol­ecules to form R 2 2(8) ring motifs, which are further linked by C—H⋯O hydrogen bonds. π–π contacts between the benzene rings [centroid–centroid distances = 3.709 (3) and 3.772 (3) Å] may further stabilize the structure. The I atom is disordered over two positions, refined with occupancies of ca 0.75 and 0.25. PMID:21581894

  18. Isolation and Characterization of the 2,2'-Azinobis(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS) Radical Cation-Scavenging Reaction Products of Arbutin.

    Science.gov (United States)

    Tai, Akihiro; Ohno, Asako; Ito, Hideyuki

    2016-09-28

    Arbutin, a glucoside of hydroquinone, has shown strong 2,2'-azinobis(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS) radical cation-scavenging activity, especially in reaction stoichiometry. This study investigated the reaction mechanism of arbutin against ABTS radical cation that caused high stoichiometry of arbutin in an ABTS radical cation-scavenging assay. HPLC analysis of the reaction mixture of arbutin and ABTS radical cation indicated the existence of two reaction products. The two reaction products were purified and identified to be a covalent adduct of arbutin with an ABTS degradation fragment and 3-ethyl-6-sulfonate benzothiazolone. A time-course study of the radical-scavenging reactions of arbutin and the two reaction products suggested that one molecule of arbutin scavenges three ABTS radical cation molecules to generate an arbutin-ABTS fragment adduct as a final reaction product. The results suggest that one molecule of arbutin reduced two ABTS radical cation molecules to ABTS and then cleaved the third ABTS radical cation molecule to generate two products, an arbutin-ABTS fragment adduct and 3-ethyl-6-sulfonate benzothiazolone.

  19. Hyaluronic acid as a rescue therapy for trinitrobenzene sulfonic acid-induced colitis through Cox-2 and PGE2 in a Toll-like receptor 4-dependent way

    Institute of Scientific and Technical Information of China (English)

    Huan CHEN; Mahesh MAHASETH; Yah ZHANG

    2011-01-01

    We hypothesized whether systemic administration of high-molecular-weight hyaluronic acid (HMW HA) could rescue trinitrobenzene sulfonic acid (TNBS)-induced colitis through Toll-like receptor 4 (TLR4) signal.C3H/HeN mice and C3H/HeJ mice were used.Mice were divided into four groups:control,50% ethanol treatment group,TNBS treatment group,and TNBS plus HA treatment group.The weight changes,clinical scores,macroscopic scores,and histological scores were recorded.Cyclooxygenase 2 (Cox-2) and prostaglandin E2 (PGE2) expressions were measured both in colons and peritoneal macrophages from these mice.HA was a rescue therapy for the colitis induced by TNBS only in C3H/HeN mice.The clinical score,macroscopic score,and histological score were much lower in C3H/HeN mice receiving TNBS plus HA treatment.Cox-2 and PGE2 expressions only increased in C3H/HeN mice.These Cox-2 expressing cells were macrophages.HA can also promote the production of Cox-2 and PGE2 in peritoneal macrophages from C3H/HeN mice.Our data demonstrated that HMW HA can rescue TNBS-induced colitis through inducing Cox-2 and PGE2 expressions in a TLR4-dependent way.Macrophages may be the effector cells of HMW HA.

  20. Neomycin-loaded poly(styrene sulfonic acid-co-maleic acid) (PSSA-MA)/polyvinyl alcohol (PVA) ion exchange nanofibers for wound dressing materials.

    Science.gov (United States)

    Nitanan, Todsapon; Akkaramongkolporn, Prasert; Rojanarata, Theerasak; Ngawhirunpat, Tanasait; Opanasopit, Praneet

    2013-05-01

    In this study, poly(styrene sulfonic acid-co-maleic acid) (PSSA-MA) blended with polyvinyl alcohol (PVA) was electrospun and then subjected to thermal crosslinking to produce PSSA-MA/PVA ion exchange nanofiber mats. The cationic drug neomycin (0.001, 0.01, and 0.1%, w/v) was loaded onto the cationic exchange fibers. The amount of neomycin loaded and released and the cytotoxicity of the fiber mats were analyzed. In vivo wound healing tests were also performed in Wistar rats. The results indicated that the diameters of the fibers were on the nanoscale (250 ± 21 nm). The ion exchange capacity (IEC) value and the percentage of water uptake were 2.19 ± 0.1 mequiv./g-dry fibers and 268 ± 15%, respectively. The loading capacity was increased upon increasing the neomycin concentration. An initial concentration of 0.1% (w/v) neomycin (F3) showed the highest loading capacity (65.7 mg/g-dry fibers). The neomycin-loaded nanofiber mats demonstrated satisfactory antibacterial activity against both Gram-positive and Gram-negative bacteria, and an in vivo wound healing test revealed that these mats performed better than gauze and blank nanofiber mats in decreasing acute wound size during the first week after tissue damage. In conclusion, the antibacterial neomycin-loaded PSSA-MA/PVA cationic exchange nanofiber mats have the potential for use as wound dressing materials.

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2012-12-15

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

  2. Substrate Effects in the Supramolecular Assembly of 1,3,5-Benzene Tricarboxylic Acid on Graphite and Graphene.

    Science.gov (United States)

    MacLeod, J M; Lipton-Duffin, J A; Cui, D; De Feyter, S; Rosei, F

    2015-06-30

    The behavior of small molecules on a surface depends critically on both molecule-substrate and intermolecular interactions. We present here a detailed comparative investigation of 1,3,5-benzene tricarboxylic acid (trimesic acid, TMA) on two different surfaces: highly oriented pyrolytic graphite (HOPG) and single-layer graphene (SLG) grown on a polycrystalline Cu foil. On the basis of high-resolution scanning tunnelling microscopy (STM) images, we show that the epitaxy matrix for the hexagonal TMA chicken wire phase is identical on these two surfaces, and, using density functional theory (DFT) with a non-local van der Waals correlation contribution, we identify the most energetically favorable adsorption geometries. Simulated STM images based on these calculations suggest that the TMA lattice can stably adsorb on sites other than those identified to maximize binding interactions with the substrate. This is consistent with our net energy calculations that suggest that intermolecular interactions (TMA-TMA dimer bonding) are dominant over TMA-substrate interactions in stabilizing the system. STM images demonstrate the robustness of the TMA films on SLG, where the molecular network extends across the variable topography of the SLG substrates and remains intact after rinsing and drying the films. These results help to elucidate molecular behavior on SLG and suggest significant similarities between adsorption on HOPG and SLG. PMID:25594568

  3. One-pot synthesis of pyrido[2,3-d]pyrimidine derivatives using sulfonic acid functionalized SBA-15 and the study on their antimicrobial activities

    Directory of Open Access Journals (Sweden)

    Ghodsi Mohammadi Ziarani

    2015-11-01

    Full Text Available A simple and clean one-pot method for the preparation of 7-amino-2,4-dioxo-5-aryl-1,2,3,4-tetrahydropyrido[2,3-d]pyrimidine-6-carbonitrile derivatives using 6-amino uracil, various aromatic aldehydes and malononitrile in the presence of sulfonic acid functionalized SBA-15 (SBA-Pr-SO3H is described. Some of synthesized pyrido[2,3-d]pyrimidines showed antimicrobial activities against some fungi and gram positive and negative bacteria.

  4. Preparation and properties of composite membrane of bisphenol A-based sulfonated poly(arylene ether sulfone) and phosphotungstic acid for proton exchange membranes

    Institute of Scientific and Technical Information of China (English)

    ZHANG Ni; LIU Hui-ling; LI Jun-jing; XIA Zhi

    2010-01-01

    A series of bi A-SPAES (Ds=0.4)/phosphotungstic acid (PWA/bi A-SPAES) composite membranes with various contents of PWA were prepared and characterized by FT-IR.Scanning electron microscopy (SEM) images indicated the PWA were well dispersed within polymer matrix.These composite membranes were evaluated for proton exchange membranes (PEM) in direct methanol fuel cell (DMFC).These membranes showed good thermal stability.It was found that the water uptake of these membranes increased with the increase of the PWA content in the hybrid membranes.Meanwhile,the introduction of inorganic particles increased both the proton conductivity and the methanol permeability.The proton conductivities of composite membranes were increased from 0.017 S/cm to 0.045 S/cm at 20 ℃ and from 0.054 S/cm to 0.093 S/cm at 100 ℃ with the increase of PWA content from 0 to 50 %.Especially,all the methanol diffusion coefficients (4.20×10-8-1.05×10-7 cm2/s) of bi A-SPAES/PWA hybrid membranes are much lower than that of Nafion 117 membrane (2.1×10-6 cm2/s).Bi A-SPAES/PWA hybrid membranes were therefore proposed as candidates of material for PEM in DMFC.

  5. 3-[4-(Acetamido)­benzene­sulfonamido]­benzoic acid

    OpenAIRE

    Muhammad Shafiq; Muhammad Zia-ur-Rehman; Islam Ullah Khan; Ghulam Mustafa; Sidra Muzaffar Mirza

    2010-01-01

    In the title compound, C15H14N2O5S, the dihedral angle between the aromatic rings is 63.20 (11) Å. The crystal structure displays classical intermolecular O—H...O hydrogen bonding typical for carboxylic acids, forming centrosymmetric dimers. These dimers are further connected by N—H...O and C—H...O hydrogen bonds to form an extended network.

  6. 3-[4-(Acetamido)­benzene­sulfonamido]­benzoic acid

    Science.gov (United States)

    Mirza, Sidra Muzaffar; Mustafa, Ghulam; Khan, Islam Ullah; Zia-ur-Rehman, Muhammad; Shafiq, Muhammad

    2011-01-01

    In the title compound, C15H14N2O5S, the dihedral angle between the aromatic rings is 63.20 (11) Å. The crystal structure displays classical inter­molecular O—H⋯O hydrogen bonding typical for carb­oxy­lic acids, forming centrosymmetric dimers. These dimers are further connected by N—H⋯O and C—H⋯O hydrogen bonds to form an extended network. PMID:21522739

  7. Sensitive electrochemical determination of trace cadmium on a stannum film/poly(p-aminobenzene sulfonic acid)/electrochemically reduced graphene composite modified electrode

    International Nuclear Information System (INIS)

    In this study, a novel stannum film/poly(p-aminobenzene sulfonic acid)/graphene composite modified glassy carbon electrode (GCE) was prepared by using electrodeposition of exfoliated graphene oxide, electropolymerization of p-aminobenzene sulfonic acid (p-ABSA) and in situ plating stannum fim methods, successively. This sensor was further used for sensitive determination of trace cadmium ions by square wave anodic stripping voltammetry (SWASV). The morphologies and electrochemistry properties of the modified electrode were characterized by scanning electron microscopy, Raman spectroscopy, cyclic voltammetry, electrochemical impedance spectroscopy and linear sweep voltammetry. It was found that the formed graphene layer on the top of GCE could remarkably facilitate the electron transfer and enlarge the specific surface area of the electrode. While the poly(p-ABSA) film could effectively increase the adhesion and stability of graphene layer, enhance ion-exchange capacity and prevent the macromolecule in real samples absorbing on the surface of electrode. By combining co-deposits ability with heavy metals of stannum film, the obtained electrode exhibited a good stripping performance for the analysis of Cd(II). Under the optimum conditions, a linear response was observed in the range from 1.0 to 70.0 μgL−1 with a detection limit of 0.05 μgL−1 (S/N = 3). The sensor was further applied to the determination of cadmium ions in real water samples with satisfactory results

  8. Biocompatibility of polypropylene non-woven fabric membrane via UV-induced graft polymerization of 2-acrylamido-2-methylpropane sulfonic acid

    Energy Technology Data Exchange (ETDEWEB)

    Song Lingjie [State Key Laboratory of Polymer Physics and Chemistry, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022 (China); Graduate University of Chinese Academy of Sciences, Beijing 100049 (China); Zhao Jie; Yang Huawei; Jin Jing; Li Xiaomeng [State Key Laboratory of Polymer Physics and Chemistry, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022 (China); Stagnaro, Paola [Istituto per Io Studio delle Macromolecole, Consiglio Nazionale delle Ricerche, Via de Marini 6, 16149 Genova (Italy); Yin Jinghua, E-mail: yinjh@ciac.jl.cn [State Key Laboratory of Polymer Physics and Chemistry, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022 (China)

    2011-10-15

    This work described the graft polymerization of a sulfonic acid terminated monomer, 2-acrylamido-2-methylpropane sulfonic acid (AMPS), onto the surface of polypropylene non-woven (NWF PP) membrane by O{sub 2} plasma pretreatment and UV-induced photografting method. The chemical structure and composition of the modified surfaces were analyzed by FTIR-ATR and XPS, respectively. The wettability was investigated by water contact angle and equilibrium water adsorption. And the biocompatibility of the modified NWF PP membranes was evaluated by protein adsorption and platelet adhesion. It was found that the graft density increased with prolonging UV irradiation time and increasing AMPS concentration; the water contact angles of the membranes decreased from 124{sup o} to 26{sup o} with the increasing grafting density of poly(AMPS) from 0 to 884.2 {mu}g cm{sup -2}, while the equilibrium water adsorption raised from 5 wt% to 75 wt%; the protein absorption was effectively suppressed with the introduction of poly(AMPS) even at the low grafting density (132.4 {mu}g cm{sup -2}); the number of platelets adhering to the modified membrane was dramatically reduced when compared with that on its virgin surface. These results indicated that surface modification of NWF PP membrane with AMPS was a facile approach to construct biocompatible surface.

  9. Synthesis, characterization and biological evaluation of N-ferrocenylmethyl amino acid benzene carboxamide derivatives and N-ferrocenyl benzoyl amino alkane derivatives as anti-cancer agents.

    OpenAIRE

    Butler, William E.

    2012-01-01

    The aim of this research was to explore the structure-activity relationship (SAR) of ferrocenyl-bioconjugates. A series of N-(ferrocenylmethylamino acid)-fluorinated-benzene carboxamide derivatives and a series of N-(ferrocenyl)-benzoyl-aminoalkane derivatives have been synthesised, structurally characterised and biologically evaluated for their anti-proliferative activity on various cancer cell lines, principally, the (estrogen receptor positive) MCF-7 breast cancer cell line. The anti-c...

  10. Matrix isolation infrared spectra of O-H· · · π Hydrogen bonded complexes of Acetic acid and Trifluoroacetic acid with Benzene

    Indian Academy of Sciences (India)

    PUJARINI BANERJEE; INDRANI BHATTACHARYA; TAPAS CHAKRABORTY

    2016-10-01

    Mid infrared spectra of two O–H· · · π hydrogen-bonded binary complexes of acetic acid (AA) and trifluoroacetic acid (F₃AA) with benzene (Bz) have been measured by isolating the complexes in an argon matrix at ∼8 K. In a matrix isolation condition, the O–H stretching fundamentals (νO−H) of the carboxylic acid groups of the two molecules are observed to have almost the same value. However, the spectral red-shifts of νO−H bands of the two acids on complexation with Bz are largely different, 90 and 150 cm⁻¹ for AA and F₃AA, respectively. Thus, the O–H bond weakening of the two acids upon binding with Bz in a non-interacting environment follows the sequence of their ionic dissociation tendencies (pKa) in aqueous media. Furthermore, ΔνO−H of the latter complex is the largest among the known π-hydrogen bonded binary complexes of prototypical O–H donors reported so far with respect to Bz as acceptor. It is also observed that the spectral shifts (ΔνO−H) of phenol-Bz and carboxylic acid-Bz complexes show similar dependence on the acidity factor (pKa). Electronic structure theory has been used to suggest suitable geometries of the complexes that are consistent with the measured IR spectral changes. Calculation at MP2/6-311++G (d, p) level predicts a T-shaped geometry for both AA-Bz and F₃AA-Bz complexes, and the corresponding binding energies are 3.0 and 4.5 kcal/mol, respectively. Natural Bond Orbital (NBO) analysis has been performed to correlate the observed spectral behavior of the complexes with the electronic structure parameters.

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2007-05-15

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

  12. Preparation and characterization of poly(2-acrylamido-2-methylpropane-sulfonic acid)/Chitosan hydrogel using gamma irradiation and its application in wastewater treatment

    Science.gov (United States)

    Gad, Y. H.

    2008-09-01

    Radiation grafting of chitosan with 2-acrylamido-2-methyl propane sulfonic acid (AMPS) has been successfully performed. The effect of absorbed dose (kGy) and the chitosan:AMPS ratio on graft hydrogelization was studied. The structure of the prepared hydrogel was confirmed using infrared spectroscopy (IR). Thermal properties were simultaneously studied by thermogravimetric analysis (TGA). The effect of the polymerization variables on the swelling % of the prepared hydrogel was investigated. The highest equilibrium degree of swelling (38.6 g/g) and gel % (94.7%) of the prepared chitosan-AMPS hydrogel was at 40% AMPS and absorbed dose of 10 kGy. The removal of methylene blue, acid red dye, Cd (II) and Cr (III) from composed wastewater was also investigated. The effect of pH, the chitosan:AMPS ratio and the concentration of the pollutant on the adsorption process were studied.

  13. Crosslinked sulfonated poly(arylene ether ketone) membranes bearing quinoxaline and acid-base complex cross-linkages for fuel cell applications

    Energy Technology Data Exchange (ETDEWEB)

    Chen, Xinbing; Chen, Pei; An, Zhongwei [Key Laboratory of Applied Surface and Colloid Chemistry, Ministry of Education, School of Chemistry and Materials Science, Shaanxi Normal University, Xi' an 710062 (China); Chen, Kangcheng; Okamoto, Kenichi [Graduate School of Science and Engineering, Yamaguchi University, Tokiwadai 2-16-1, Ube, Yamaguchi 755-8611 (Japan)

    2011-02-15

    A series of crosslinkable sulfonated poly(arylene ether ketone)s (SPAEKs) were synthesized by copolymerization of 4,4'-biphenol with 2,6-difluorobenzil and 5,5'-carbonyl-bis(2-fluorobenzene-sulfonate). A facile crosslinking method was successfully developed, based on the cyclocondensation reaction of benzil moieties in polymer chain with 3,3'-diaminobenzidine to form quinoxaline groups acting as covalent and acid-base ionic crosslinking. The uncrosslinked and crosslinked SPAEK membranes showed high mechanical properties and the isotropic membrane swelling, while the later became insoluble in tested polar aprotic solvents. The crosslinking significantly improved the membrane performance, i.e., the crosslinked membranes had the lower membrane dimensional change, lower methanol permeability and higher oxidative stability than the corresponding precursor membranes, with keeping the reasonably high proton conductivity. The crosslinked membrane (C-B4) with an ion exchange capacity of 2.02 mequiv. g{sup -1} showed a reasonably high proton conductivity of 111 mS cm{sup -1} with a low water uptake of 42 wt% at 80 C. C-B4 exhibited a low methanol permeability of 0.55 x 10{sup -6} cm{sup 2} s{sup -1} for 32 wt% methanol solution at 25 C. The crosslinked SPAEK membranes have potential for PEFC and DMFC applications. (author)

  14. Enhanced conductivity of poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) film by acid treatment for indium tin oxide-free organic solar cells

    Science.gov (United States)

    Lin, Chun-Chiao; Huang, Chih-Kuo; Hung, Yu-Chieh; Chang, Mei-Ying

    2016-08-01

    An acid treatment is used in the enhancement of the conductivity of the conducting polymer poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS) thin film, which is often used as the anode in organic solar cells. There are three types of acid treatment for PEDOT:PSS thin film: hydrochloric, sulfuric, and phosphoric acid treatments. In this study, we examine and compare these three ways with each other for differences in conductivity. Hydrochloric acid results in the highest conductivity enhancement, from 0.3 to 1109 S/cm. We also discuss the optical transmittance, conductivity, surface roughness, surface morphology, and stability, as well as the factors that can influence device efficiency. The devices are fabricated using an acid-treated PEDOT:PSS thin film as the anode. The highest power conversion efficiency was 1.32%, which is a large improvement over that of the unmodified organic solar cell (0.21%). It is comparable to that obtained when using indium tin oxide (ITO) as an electrode, ca. 1.46%.

  15. A complementary electrochromic device based on polyaniline tethered polyhedral oligomeric silsesquioxane and poly(3,4-ethylenedioxythiophene)/poly(4-styrene sulfonic acid)

    Energy Technology Data Exchange (ETDEWEB)

    Xiong, Shanxin [Temasek Laboratories, Nanyang Technological University, 50 Nanyang Drive, Singapore 637553 (Singapore); Ma, Jan; Lu, Xuehong [Temasek Laboratories, Nanyang Technological University, 50 Nanyang Drive, Singapore 637553 (Singapore); School of Materials Science and Engineering, Nanyang Technological University, 50 Nanyang Avenue, Singapore 639798 (Singapore)

    2009-12-15

    A high-contrast complementary electrochromic device based on polyaniline (PANI) tethered polyhedral oligomeric silsesquioxane (POSS) (POSS-PANI) and poly(3,4-ethylenedioxythiophene)/poly(4-styrene sulfonic acid) (PEDOT:PSS) is assembled. The electrochromic properties, cyclic voltammetry behavior and coloration efficiency of the device are studied. Due to the loosely packed structure, POSS-PANI gives rise to a significantly higher electrochromic contrast, coloration efficiency and faster switching speed than PANI. Despite its high contrast, the combination of POSS-PANI with PEDOT:PSS still shows synergy in terms of contrast enhancement, which can be attributed to the additional driving force for the diffusion of dopants into PEDOT:PSS provided by the dedoping of POSS-PANI. (author)

  16. β–Cyclodextrin–Propyl Sulfonic Acid Catalysed One-Pot Synthesis of 1,2,4,5-Tetrasubstituted Imidazoles as Local Anesthetic Agents

    Directory of Open Access Journals (Sweden)

    Yan Ran

    2015-11-01

    Full Text Available Some functionalized 1,2,4,5-tetrasubstituted imidazole derivatives were synthesized using a one-pot, four component reaction involving 1,2-diketones, aryl aldehydes, ammonium acetate and substituted aromatic amines. The synthesis has been efficiently carried out in a solvent free medium using β-cyclodextrin-propyl sulfonic acid as a catalyst to afford the target compounds in excellent yields. The local anesthetic effect of these derivatives was assessed in comparison to lidocaine as a standard using a rabbit corneal and mouse tail anesthesia model. The three most potent promising compounds were subjected to a rat sciatic nerve block assay where they showed considerable local anesthetic activity, along with minimal toxicity. Among the tested analogues, 4-(1-benzyl-4,5-diphenyl-1H-imidazol-2-yl-N,N-dimethylaniline (5g was identified as most potent analogue with minimal toxicity. It was further characterized by a more favourable therapeutic index than the standard.

  17. Camphor-10-sulfonic acid catalyzed condensation of 2-naphthol with aromatic/aliphatic aldehydes to 14-aryl/alkyl-14H-dibenzo[a,j]xanthenes

    Directory of Open Access Journals (Sweden)

    Kundu Kshama

    2014-01-01

    Full Text Available (±-Camphor-10-sulfonic acid (CSA catalyzed condensation of 2-naphthol with both aliphatic/aromatic aldehydes at 80°C yielded 14-alkyl/aryl-dibenzoxanthenes as the sole product in high yields. However, the same condensation with benzaldehyde at 25°C afforded a mixture of intermediate 1,1-bis-(2-hydroxynaphthylphenylmethane and 14-phenyl-dibenzoxanthene while the condensation with aliphatic aldehydes at 25°C furnished the corresponding 14-alkyl-dibenzoxanthenes as the sole product. Moreover, condensation of 2-naphthol with aromatic/aliphatic aldehydes with low catalyst loading (2 mol% was greatly accelerated under microwave irradiation to afford the corresponding 14-aryl/alkyl-dibenzoxanthenes as the sole product in high yields.

  18. Degradation and mineralization of organic UV absorber compound 2-phenylbenzimidazole-5-sulfonic acid (PBSA) using UV-254 nm/H{sub 2}O{sub 2}

    Energy Technology Data Exchange (ETDEWEB)

    Abdelraheem, Wael H.M. [Chemistry Department, Faculty of Science, Sohag University, Sohag 82524 (Egypt); Environmental Engineering and Science Program, University of Cincinnati, Cincinnati, OH 45221-0012 (United States); He, Xuexiang; Duan, Xiaodi [Environmental Engineering and Science Program, University of Cincinnati, Cincinnati, OH 45221-0012 (United States); NIREAS-International Water Research Center, University of Cyprus, Nicosia 1678 (Cyprus); Dionysiou, Dionysios D., E-mail: dionysios.d.dionysiou@uc.edu [Environmental Engineering and Science Program, University of Cincinnati, Cincinnati, OH 45221-0012 (United States); NIREAS-International Water Research Center, University of Cyprus, Nicosia 1678 (Cyprus)

    2015-01-23

    Graphical abstract: - Highlights: • UV-254 nm/H{sub 2}O{sub 2} AOP was utilized for the degradation and mineralization of PBSA and BSA. • Promotion of k{sub obs} with [H{sub 2}O{sub 2}]{sub 0} ≤ 4 mM and inhibition at higher [H{sub 2}O{sub 2}]{sub 0} were observed. • The S and N were released and monitored as SO{sub 4}{sup 2−} and NH{sub 4}{sup +}, respectively. • Br{sup −} inhibited both the degradation and mineralization much more significantly than Cl{sup −}. • There was an increase in [NH{sub 4}{sup +}] at higher [H{sub 2}O{sub 2}]{sub 0} and its further destruction at higher UV fluence. - Abstract: Various studies have revealed the non-biodegradable and endocrine disrupting properties of sulfonated organic UV absorbers, directing people's attention toward their risks on ecological and human health and hence their removal from water. In this study, UV-254 nm/H{sub 2}O{sub 2} advanced oxidation process (AOP) was investigated for degrading a model UV absorber compound 2-phenylbenzimidazole-5-sulfonic acid (PBSA) and a structurally similar compound 1H-benzimidazole-2-sulfonic acid (BSA), with a specific focus on their mineralization. At 4.0 mM [H{sub 2}O{sub 2}]{sub 0}, a complete removal of 40.0 μM parent PBSA and 25% decrease in TOC were achieved with 190 min of UV irradiation; SO{sub 4}{sup 2−} was formed and reached its maximum level while the release of nitrogen as NH{sub 4}{sup +} was much lower (around 50%) at 190 min. Sulfate removal was strongly enhanced by increasing [H{sub 2}O{sub 2}]{sub 0} in the range of 0–4.0 mM, with slight inhibition in 4.0–12.0 mM. Faster and earlier ammonia formation was observed at higher [H{sub 2}O{sub 2}]{sub 0}. The presence of Br{sup −} slowed down the degradation and mineralization of both compounds while a negligible effect on the degradation was observed in the presence of Cl{sup −}. Our study provides important technical and fundamental results on the HO{sup ·} based degradation and

  19. Evaluation of benzene exposure in petrol pump attendants and in mechanics by urinary trans, trans-muconic acid (t, t-MA determination

    Directory of Open Access Journals (Sweden)

    Teresa Cirillo

    2004-12-01

    Full Text Available

    Occupational exposure to benzene in petrol pump attendants and in mechanics was studied by examining the benzene content in both the air breathed and in the urinary metabolite trans,trans-muconic acid (t,t-MA. Thirty petrol pump attendants and thirty mechanics (as exposed workers and thirty adult male office workers (as non exposed workers were involved in the study. Measures were taken at the begin and at the end of the working shifts.

     The benzene concentrations in the breathing air samples varied from 2 to 88 μg m-3, lower than the EU acceptable limit for occupational environment. The average urinary t,t-MA in the petrol pump attendants at the begin and at the end of the working shifts ranged between 133 ± 69 and 255 ± 174 μg g-1 creatinine and in the mechanics between 204 ± 139 and 300 ± 211 μg g-1 creatinine, respectively.

    In all the participants the mean levels of urinary t,t-MA at the end of the working shifts were significantly higher than those at the beginning. In the exposed workers mean levels of urinary t,t-MA were significantly higher than in those of the non-exposed workers. The influence of the smoking was demonstrated by the urinary t,t-MA levels in smoking non-exposed subjects.

  20. Perfluoroalkyl sulfonates and carboxylic acids in liver, muscle and adipose tissues of black-footed albatross (Phoebastria nigripes) from Midway Island, North Pacific Ocean.

    Science.gov (United States)

    Chu, Shaogang; Wang, Jun; Leong, Gladys; Woodward, Lee Ann; Letcher, Robert J; Li, Qing X

    2015-11-01

    The Great Pacific Garbage Patch (GPGP) is a gyre of marine plastic debris in the North Pacific Ocean, and nearby is Midway Atoll which is a focal point for ecological damage. This study investigated 13 C4-C16 perfluorinated carboxylic acids (PFCAs), four (C4, C6, C8 and C10) perfluorinated sulfonates and perfluoro-4-ethylcyclohexane sulfonate [collectively perfluoroalkyl acids (PFAAs)] in black-footed albatross tissues (collected in 2011) from Midway Atoll. Of the 18 PFCAs and PFSAs monitored, most were detectable in the liver, muscle and adipose tissues. The concentrations of PFCAs and PFSAs were higher than those in most seabirds from the arctic environment, but lower than those in most of fish-eating water birds collected in the U.S. mainland. The concentrations of the PFAAs in the albatross livers were 7-fold higher than those in Laysan albatross liver samples from the same location reported in 1994. The concentration ranges of PFOS were 22.91-70.48, 3.01-6.59 and 0.53-8.35 ng g(-1) wet weight (ww), respectively, in the liver, muscle and adipose. In the liver samples PFOS was dominant, followed by longer chain PFUdA (8.04-18.70 ng g(-1) ww), PFTrDA, and then PFNA, PFDA and PFDoA. Short chain PFBA, PFPeA, PFBS and PFODA were below limit of quantification. C8-C13 PFCAs showed much higher composition compared to those found in other wildlife where PFOS typically predominated. The concentrations of PFUdA in all 8 individual albatross muscle samples were even higher than those of PFOS. This phenomenon may be attributable to GPGP as a pollution source as well as PFAA physicochemical properties. PMID:26037817

  1. Polyacrylamido-2-methyl-1-propane sulfonic acid-grafted-natural rubber as bio-adsorbent for heavy metal removal from aqueous standard solution and industrial wastewater.

    Science.gov (United States)

    Phetphaisit, Chor Wayakron; Yuanyang, Siriwan; Chaiyasith, Wipharat Chuachuad

    2016-01-15

    Bio-adsorbent modified natural rubber (modified NR) was prepared, by placing the sulfonic acid functional group on the isoprene chain. This modification was carried out with the aim to prepare material capable to remove heavy metals from aqueous solution. The structures of modified NR materials were characterized by FT-IR and NMR spectroscopies. Thermal gravimetric analysis of modified NR showed that the initial degradation temperature of rubber decreases with increasing amount of polyacrylamido-2-methyl-1-propane sulfonic acid (PAMPS) in the structure. In addition, water uptake of the rubber based materials was studied as a function of time and content of PAMPS. The influence of the amount of PAMPS grafted onto NR, time, pH, concentration of metal ions, temperature, and regeneration were studied in terms of their influence on the adsorption of heavy metals (Pb(2+), Cd(2+) and Cu(2+)). The adsorption isotherms of Pb(2+) and Cd(2+) were fitted to the Freundlich isotherm model, while Cu(2+) was fitted to the Langmuir isotherm. However, the results from these two isotherms resulted in a similar behavior. The adsorption capacity of the modified NR for the various heavy metals was in the following order: Pb(2+)∼Cd(2+)>Cu(2+). The maximum adsorption capacities of Pb(2+), Cd(2+), and Cu(2+) were 272.7, 267.2, and 89.7 mg/g of modified rubber, respectively. Moreover, the modified natural rubber was used for the removal of metal ions in real samples of industrial effluents where the efficiency and regeneration were also investigated.

  2. The impact of hyaluronic acid oligomer content on physical, mechanical, and biologic properties of divinyl sulfone-crosslinked hyaluronic acid hydrogels.

    Science.gov (United States)

    Ibrahim, Samir; Kang, Qian K; Ramamurthi, Anand

    2010-08-01

    In recent studies, we showed that exogenous hyaluronic acid oligomers (HA-o) stimulate functional endothelialization, though native long-chain HA is more bioinert and possibly more biocompatible. Thus, in this study, hydrogels containing high molecular weight (HMW) HA (1 x 10(6) Da) and HA-o mixtures (HA-o: 0.75-10 kDa) were created by crosslinking with divinyl sulfone (DVS). The incorporation of HA-o was found to compromise the physical and mechanical properties of the gels (rheology, apparent crosslinking density, swelling ratio, degradation) and to very mildly enhance inflammatory cell recruitment in vivo; increasing the DVS crosslinker content within the gels in general, had the opposite effect, though the relatively high concentration of DVS within these gels (necessary to create a solid gel) also stimulated a mild subcutaneous inflammatory response in vivo and VCAM-1 expression by endothelial cells (ECs) cultured atop; ICAM-expression levels remained very low irrespective extent of DVS crosslinking or HA-o content. The greatest EC attachment and proliferation (MTT assay) was observed on gels that contained the highest amount of HA-o. The study shows that the beneficial EC response to HA-o and biocompatibility of HA is mostly unaltered by their chemical derivatization and crosslinking into a hydrogel. However, the study also demonstrates that the relatively high concentrations of DVS, necessary to create solid gels, compromise their biocompatibility. Moreover, the poor mechanics of even these heavily crosslinked gels, in the context of vascular implantation, necessitates the investigation of other, more appropriate crosslinking agents. Alternately, the outcomes of this study may be used to guide an approach based on chemical immobilization and controlled surface-presentation of both bioactive HA-o and more biocompatible HMW HA on synthetic or tissue engineered grafts already in use, without the use of a crosslinker, so that improved, predictable, and

  3. Benzene Uptake and Glutathione S-transferase T1 Status as Determinants of S-Phenylmercapturic Acid in Cigarette Smokers in the Multiethnic Cohort

    Science.gov (United States)

    Haiman, Christopher A.; Patel, Yesha M.; Stram, Daniel O.; Carmella, Steven G.; Chen, Menglan; Wilkens, Lynne R.; Le Marchand, Loic; Hecht, Stephen S.

    2016-01-01

    Research from the Multiethnic Cohort (MEC) demonstrated that, for the same quantity of cigarette smoking, African Americans and Native Hawaiians have a higher lung cancer risk than Whites, while Latinos and Japanese Americans are less susceptible. We collected urine samples from 2,239 cigarette smokers from five different ethnic groups in the MEC and analyzed each sample for S-phenylmercapturic acid (SPMA), a specific biomarker of benzene uptake. African Americans had significantly higher (geometric mean [SE] 3.69 [0.2], p<0.005) SPMA/ml urine than Whites (2.67 [0.13]) while Japanese Americans had significantly lower levels than Whites (1.65 [0.07], p<0.005). SPMA levels in Native Hawaiians and Latinos were not significantly different from those of Whites. We also conducted a genome-wide association study in search of genetic risk factors related to benzene exposure. The glutathione S-transferase T1 (GSTT1) deletion explained between 14.2–31.6% (p = 5.4x10-157) and the GSTM1 deletion explained between 0.2%-2.4% of the variance (p = 1.1x10-9) of SPMA levels in these populations. Ethnic differences in levels of SPMA remained strong even after controlling for the effects of these two deletions. These results demonstrate the powerful effect of GSTT1 status on SPMA levels in urine and show that uptake of benzene in African American, White, and Japanese American cigarette smokers is consistent with their lung cancer risk in the MEC. While benzene is not generally considered a cause of lung cancer, its metabolite SPMA could be a biomarker for other volatile lung carcinogens in cigarette smoke. PMID:26959369

  4. Benzene Uptake and Glutathione S-transferase T1 Status as Determinants of S-Phenylmercapturic Acid in Cigarette Smokers in the Multiethnic Cohort.

    Directory of Open Access Journals (Sweden)

    Christopher A Haiman

    Full Text Available Research from the Multiethnic Cohort (MEC demonstrated that, for the same quantity of cigarette smoking, African Americans and Native Hawaiians have a higher lung cancer risk than Whites, while Latinos and Japanese Americans are less susceptible. We collected urine samples from 2,239 cigarette smokers from five different ethnic groups in the MEC and analyzed each sample for S-phenylmercapturic acid (SPMA, a specific biomarker of benzene uptake. African Americans had significantly higher (geometric mean [SE] 3.69 [0.2], p<0.005 SPMA/ml urine than Whites (2.67 [0.13] while Japanese Americans had significantly lower levels than Whites (1.65 [0.07], p<0.005. SPMA levels in Native Hawaiians and Latinos were not significantly different from those of Whites. We also conducted a genome-wide association study in search of genetic risk factors related to benzene exposure. The glutathione S-transferase T1 (GSTT1 deletion explained between 14.2-31.6% (p = 5.4x10-157 and the GSTM1 deletion explained between 0.2%-2.4% of the variance (p = 1.1x10-9 of SPMA levels in these populations. Ethnic differences in levels of SPMA remained strong even after controlling for the effects of these two deletions. These results demonstrate the powerful effect of GSTT1 status on SPMA levels in urine and show that uptake of benzene in African American, White, and Japanese American cigarette smokers is consistent with their lung cancer risk in the MEC. While benzene is not generally considered a cause of lung cancer, its metabolite SPMA could be a biomarker for other volatile lung carcinogens in cigarette smoke.

  5. Novel sulfonated poly (ether ether ketone)/phosphonic acid-functionalized titania nanohybrid membrane by an in situ method for direct methanol fuel cells

    Science.gov (United States)

    Wu, Hong; Cao, Ying; Li, Zhen; He, Guangwei; Jiang, Zhongyi

    2015-01-01

    Sulfonated poly (ether ether ketone)/phosphonic acid-functionalized titania nanohybrid membranes are prepared by an in situ method using titanium tetrachloride (TiCl4) as inorganic precursor and amino trimethylene phosphonic acid (ATMP) as modifier. Phosphonic acid-functionalized titania nanoparticles with a uniform particle size of ∼50 nm are formed and dispersed homogeneously in the SPEEK matrix with good interfacial compatibility. Accordingly, the nanohybrid membranes display remarkably enhanced proton conduction property due to the incorporation of additional sites for proton transport and the formation of well-connected channels by bridging the hydrophilic domains in SPEEK matrix. The nanohybrid membrane with 6 wt. % of phosphonic acid-functionalized titania nanoparticles exhibits the highest proton conductivity of 0.334 S cm-1 at 65 °C and 100% RH, which is 63.7% higher than that of pristine SPEEK membrane. Furthermore, the as-prepared nanohybrid membranes also show elevated thermal and mechanical stabilities as well as decreased methanol permeability.

  6. A highly efficient nano-Fe3O4 encapsulated-silica particles bearing sulfonic acid groups as a solid acid catalyst for synthesis of 1,8-dioxo-octahydroxanthene derivatives

    International Nuclear Information System (INIS)

    The functionalization of silica-coated Fe3O4 magnetic nanoparticles (Fe3O4@SiO2) using chlorosulfonic acid were afforded sulfonic acid-functionalized magnetic Fe3O4 nanoparticles (Fe3O4@SiO2–SO3H) that can be applied as an organic–inorganic hybrid heterogeneous catalyst. The used Fe3O4 magnetic nanoparticles are 18–30 nm sized that was rapidly functionalized and can be used as catalyst in organic synthesis. The prepared nanoparticles were characterized by X-ray diffraction analysis, magnetization curve, scanning electron microscope, dynamic laser scattering, and FT-IR measurements. The resulting immobilized catalysts have been successfully used in the synthesis of 1,8‐dioxo-octahydroxanthene derivatives under solvent free condition. This procedure has many advantages such as; a much milder method, a shorter reaction time, a wide range of functional group tolerance, and absence of any tedious workup or purification. Other remarkable features include the catalyst can be reused at least five times without any obvious change in its catalytic activity. This procedure also avoids hazardous reagents/solvents, and thus can be an eco-friendly alternative to the existing methods.Graphical AbstractA highly efficient nano-Fe3O4 encapsulated-silica particles bearing sulfonic acid groups as a solid acid catalyst for synthesis of 1,8-dioxo-octahydroxanthene derivatives

  7. Silica-based sulfonic acid (MCM-41-SO3H: a practical and efficient catalyst for the synthesis of highly substituted quinolines under solvent-free conditions at ambient temperature

    Directory of Open Access Journals (Sweden)

    Ali Maleki

    2014-06-01

    Full Text Available In this work, a variety of highly substituted quinolines were readily synthesized via Friedlander annulation using Brönsted acid silica-based sulfonic acid as a modified catalyst under solvent-free conditions at room temperature. This efficient procedure has the advantages of giving the target compounds in high yields, short reaction times, simple workup procedure, reusability of the catalyst, and environmentally benign conditions.

  8. Novel Ordered Mesoporous Carbon Based Sulfonic Acid as an Efficient Catalyst in the Selective Dehydration of Fructose into 5-HMF: the Role of Solvent and Surface Chemistry.

    Science.gov (United States)

    Karimi, Babak; Mirzaei, Hamid M; Behzadnia, Hesam; Vali, Hojatollah

    2015-09-01

    Novel ionic liquid derived ordered mesoporous carbons functionalized with sulfonic acid groups IOMC-ArSO3H and GIOMC-ArSO3H were prepared, characterized, and examined in the dehydration reaction of fructose into 5-hydroxymethylfurfural (5-HMF) both in aqueous and nonaqueous systems. To study and correlate the surface properties of these carbocatalysts and some other SBA-15 typed solid acids with 5-HMF yield, hydrophilicity index (H-index) were employed in the fructose dehydration. Our study systematically declared that almost a criterion may be expected for application of solid acids in which by increasing H-index value up to 0.8 the HMF yield enhances accordingly. More increase in H-index up to 1.3 did not change the HMF yield profoundly. Although, it has been shown that the catalyst with larger H-index (∼1.3) resulted in higher activity both in aqueous and 2-propanol systems, during the recycling process deactivation occurs because of more water uptake and the catalysts with optimum amount of H-index (∼0.8) is more robust in the dehydration of fructose. PMID:26259108

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

    Science.gov (United States)

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

    2014-11-12

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

  10. Electrochemical behaviour of benzene on platinum electrodes

    OpenAIRE

    Montilla Jiménez, Francisco; Huerta Arráez, Francisco; Morallón Núñez, Emilia; Vázquez Picó, José Luis

    1999-01-01

    The adsorption and oxidation of benzene in acidic media on platinum electrodes (polycrystalline and single-crystal electrodes) have been studied by cyclic voltammetry and in-situ Fourier transform infrared spectroscopy. The oxidation characteristics of benzene depend on the surface structure of the platinum electrode used. In all platinum electrodes studied, the main reduction product of benzene is cyclohexane, and the oxidation products detected by infrared spectroscopy have been CO2 and ben...

  11. Presence of UV filters in surface water and the effects of phenylbenzimidazole sulfonic acid on rainbow trout (Oncorhynchus mykiss) following a chronic toxicity test.

    Science.gov (United States)

    Grabicova, Katerina; Fedorova, Ganna; Burkina, Viktoriia; Steinbach, Christoph; Schmidt-Posthaus, Heike; Zlabek, Vladimir; Kocour Kroupova, Hana; Grabic, Roman; Randak, Tomas

    2013-10-01

    UV filters belong to a group of compounds that are used by humans and are present in municipal waste-waters, effluents from sewage treatment plants and surface waters. Current information regarding UV filters and their effects on fish is limited. In this study, the occurrence of three commonly used UV filters - 2-phenylbenzimidazole-5-sulfonic acid (PBSA), 2-hydroxy-4-methoxybenzophenone (benzophenone-3, BP-3) and 5-benzoyl-4-hydroxy-2-methoxy-benzenesulfonic acid (benzophenone-4, BP-4) - in South Bohemia (Czech Republic) surface waters is presented. PBSA concentrations (up to 13μgL(-1)) were significantly greater than BP-3 or BP-4 concentrations (up to 620 and 390ngL(-1), respectively). On the basis of these results, PBSA was selected for use in a toxicity test utilizing the common model organism rainbow trout (Oncorhynchus mykiss). Fish were exposed to three concentrations of PBSA (1, 10 and 1000µgL(-1)) for 21 and 42 days. The PBSA concentrations in the fish plasma, liver and kidneys were elevated after 21 and 42 days of exposure. PBSA increased activity of certain P450 cytochromes. Exposure to PBSA also changed various biochemical parameters and enzyme activities in the fish plasma. However, no pathological changes were obvious in the liver or gonads.

  12. Coprecipitation of trace elements with Ni2+/2-Nitroso-1-naphthol-4-sulfonic acid and their determination by flame atomic absorption spectrometry

    International Nuclear Information System (INIS)

    Ni2+/2-Nitroso-1-naphthol-4-sulfonic acid precipitate was used for the coprecipitation of Co, Pb, Cu, Fe and Zn prior to their flame atomic absorption spectrometric (FAAS) determinations in environmental samples. The precipitate could be easily dissolved with concentrated nitric acid. The recovery values for analyte ions were higher than 95%. The parameters including pH, sample volume, centrifuge time, amounts of nickel and matrix effects were optimized for the quantitative recoveries of the analytes. The relative standard deviations of cobalt, lead, copper, iron and zinc were found 4.5, 5.7, 3.8, 6.1 and 7.5%, respectively. The limit of detection was calculated as 1.05, 2.67, 1.30, 1.38, and 0.50 μg L-1 for cobalt, lead, copper, iron and zinc. The validation of the procedure was checked by the analysis of IAEA 336 lichen and SLRS 4 Riverine water standard reference materials were analyzed with satisfactory results. The presented coprecipitation procedure was successfully applied to some environmental samples for determination of analyte ions.

  13. 以弱碱性树脂去除废水中5-氨基-2-氯苯-4-磺酸和盐酸%Removal of 5-Amino-2-chlorotoluene-4-sulfonic and Chlorhydric Acids from Wastewater by Weakly Basic Resin

    Institute of Scientific and Technical Information of China (English)

    李长海; 许振良; 李春平

    2006-01-01

    This research deals with an investigation of the adsorption of two acids, namely, 5-amino-2-chlorotoluene-4-sulfonic and chlorhydric acids from their solution onto weakly basic resin. The screening of resins, kinetics, and isotherm were studied. The results indicate that the D301R is more appropriate for the removal of acids from solution. The adsorption of acids obeys Langmuir isotherm and the first-order kinetics model. Sorptive affinity of the two acids on D301R was found to be in the order of 5-amino-2-chlorotoluene-4-sulfonic acid>chlorhydric acid. Thermodynamic parameters for the adsorption of acids were calculated and discussed. The maximum removal of acids was observed around 97% and 76% at 25℃ for 5-amino-2-chlorotoluene-4-sulfonic acid and chlorhydric acid, respectively.

  14. Probing the Lewis acidity and catalytic activity of the metal-organic framework [Cu3(btc)2] (BTC=benzene-1,3,5-tricarboxylate).

    Science.gov (United States)

    Alaerts, Luc; Séguin, Etienne; Poelman, Hilde; Thibault-Starzyk, Frédéric; Jacobs, Pierre A; De Vos, Dirk E

    2006-09-25

    An optimized procedure was designed for the preparation of the microporous metal-organic framework (MOF) [Cu3(btc)2] (BTC=benzene-1,3,5-tricarboxylate). The crystalline material was characterized by X-ray diffraction, optical microscopy, SEM, X-ray photoelectron spectroscopy, N2 sorption, thermogravimetry, and IR spectroscopy of adsorbed CO. CO adsorbs on a small number of Cu2O impurities, and particularly on the free CuII coordination sites in the framework. [Cu3(btc)2] is a highly selective Lewis acid catalyst for the isomerization of terpene derivatives, such as the rearrangement of alpha-pinene oxide to campholenic aldehyde and the cyclization of citronellal to isopulegol. By using the ethylene ketal of 2-bromopropiophenone as a test substrate, it was demonstrated that the active sites in [Cu3(btc)2] are hard Lewis acids. Catalyst stability, re-usability, and heterogeneity are critically assessed. PMID:16881030

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2011-03-18

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

  16. Visceral hypersensitivity is provoked by 2,4,6-trinitrobenzene sulfonic acid-induced ileitis in rats

    Directory of Open Access Journals (Sweden)

    Manoj Kumar Shah

    2016-07-01

    Full Text Available Background and Aims: Crohn’s Disease (CD, a chronic Inflammatory Bowel Disease, can occur in any part of the gastrointestinal tract, but most frequently in the ileum. Visceral hypersensitivity contributes for development of chronic abdominal pain in this disease. Currently, the understanding of the mechanism underlying hypersensitivity of Crohn’s ileitis has been hindered by a lack of specific animal model. The present study is undertaken to investigate the visceral hypersensitivity provoked by 2,4,6-trinitrobenzene sulfonic (TNBS-induced ileitis rats.Methods: Male Sprague-Dawley rats were anaesthetized and laparotomized for intraileal injection of TNBS (0.6 ml, 80 mg/kg body weight in 30% ethanol, n = 48, an equal volume of 30% Ethanol (n = 24 and Saline (n = 24, respectively. Visceral hypersensitivity was assessed by visceromotor responses (VMR to 20, 40, 60, 80 and 100 mmHg colorectal distension pressure (CRD at day 1, 3, 7, 14, 21 and 28. Immediately after CRD test, the rats were euthanized for collecting the terminal ileal segment for histopathological examinations and ELISA of myleoperoxidase and cytokines (TNF-α, IL-1β, IL-6, and dorsal root ganglia (T11 for determination of calcitonin gene-related peptide by immunohistochemistry, respectively. Results: Among all groups, TNBS-treatment showed transmural inflammation initially at 3 days, reached maximum at 7 days and persisted up to 21 days. The rats with ileitis exhibited (P < 0.05 VMR to CRD at day 7 to day 21. The calcitonin gene-related peptide-immunoreactive positive cells increased (P < 0.05 in dorsal root ganglia at day 7 to 21, which was persistently consistent with visceral hypersensitivity in TNBS-treated rats.Conclusions: TNBS injection into the ileum induced transmural ileitis including granuloma and visceral hypersensitivity. As this model mimics clinical manifestations of CD, it may provide a road map to probe the pathogenesis of gut inflammation and visceral

  17. A highly efficient nano-Fe{sub 3}O{sub 4} encapsulated-silica particles bearing sulfonic acid groups as a solid acid catalyst for synthesis of 1,8-dioxo-octahydroxanthene derivatives

    Energy Technology Data Exchange (ETDEWEB)

    Naeimi, Hossein, E-mail: naeimi@kashanu.ac.ir; Nazifi, Zahra Sadat [University of Kashan, Department of Organic Chemistry, Faculty of Chemistry (Iran, Islamic Republic of)

    2013-11-15

    The functionalization of silica-coated Fe{sub 3}O{sub 4} magnetic nanoparticles (Fe{sub 3}O{sub 4}@SiO{sub 2}) using chlorosulfonic acid were afforded sulfonic acid-functionalized magnetic Fe{sub 3}O{sub 4} nanoparticles (Fe{sub 3}O{sub 4}@SiO{sub 2}–SO{sub 3}H) that can be applied as an organic–inorganic hybrid heterogeneous catalyst. The used Fe{sub 3}O{sub 4} magnetic nanoparticles are 18–30 nm sized that was rapidly functionalized and can be used as catalyst in organic synthesis. The prepared nanoparticles were characterized by X-ray diffraction analysis, magnetization curve, scanning electron microscope, dynamic laser scattering, and FT-IR measurements. The resulting immobilized catalysts have been successfully used in the synthesis of 1,8‐dioxo-octahydroxanthene derivatives under solvent free condition. This procedure has many advantages such as; a much milder method, a shorter reaction time, a wide range of functional group tolerance, and absence of any tedious workup or purification. Other remarkable features include the catalyst can be reused at least five times without any obvious change in its catalytic activity. This procedure also avoids hazardous reagents/solvents, and thus can be an eco-friendly alternative to the existing methods.Graphical AbstractA highly efficient nano-Fe{sub 3}O{sub 4} encapsulated-silica particles bearing sulfonic acid groups as a solid acid catalyst for synthesis of 1,8-dioxo-octahydroxanthene derivatives.

  18. Synthesis of benzo[g]indeno[2,1-b]quinoline derivatives via four-component and one-pot synthesis in presence of 3-methyl-1-sulfonic acid imidazolium hydrogen sulfate

    Institute of Scientific and Technical Information of China (English)

    Nader Ghaffari Khaligh

    2014-01-01

    A simple and facile synthesis of 12-arylbenzo[g]indeno[2,1-b]quinoline-6,11,13-trione deriv-atives was accomplished by the one-pot condensation of 2-hydroxynaphthalene-1,4-dione, aryl aldehydes, 2H-indene-1,3-dione, and ammonium acetate under solvent-free conditions in the presence of a Brönsted ionic liquid catalyst, namely 3-methyl-1-sulfonic acid imidazolium hydrogen sulfate.

  19. Synthesis and Characterization of Sulfonated Poly(Phenylene Containing a Non-Planar Structure and Dibenzoyl Groups

    Directory of Open Access Journals (Sweden)

    Hohyoun Jang

    2016-02-01

    Full Text Available Polymers for application as sulfonated polyphenylene membranes were prepared by nickel-catalyzed carbon-carbon coupling reaction of bis(4-chlorophenyl-1,2-diphenylethylene (BCD and 1,4-dichloro-2,5-dibenzoylbenzene (DCBP. Conjugated cis/trans isomer (BCD had a non-planar conformation containing four peripheral aromatic rings that facilitate the formation of π–π interactions. 1,4-Dichloro-2,5-dibenzoylbenzene was synthesized from the oxidation reaction of 2,5-dichloro-p-xylene, followed by Friedel-Crafts reaction with benzene. DCBP monomer had good reactivity in polymerization affecting the activity of benzophenone as an electron-withdrawing group. The polyphenylene was sulfonated using concentrated sulfuric acid. These polymers without any ether linkages on the polymer backbone were protected from nucleophilic attack by hydrogen peroxide, hydroxide anion, and radicals generated by polymer electrolyte membrane fuel cell (PEMFC operation systems. The mole fraction of the sulfonic acid groups was controlled by varying the mole ratio of bis(4-chlorophenyl-1,2-diphenylethylene in the copolymer. In comparison with Nafion 211® membrane, these SBCDCBP membranes showed ion exchange capacity (IEC ranging from 1.04 to 2.07 meq./g, water uptake from 36.5% to 69.4%, proton conductivity from 58.7 to 101.9 mS/cm, and high thermal stability.

  20. White light emission from Mn2+ doped ZnS nanocrystals through the surface chelating of 8-hydroxyquinoline-5-sulfonic acid

    International Nuclear Information System (INIS)

    White light emitting semiconductor nanocrystals (NCs) have been successfully synthesized from 8-hydroxyquinoline-5-sulfonic acid (HQS) decorated manganese doped ZnS NCs through fine tuning the surface-coordination emission and dopant emission of the NC host. The HQS functionalized manganese doped ZnS NCs (QS-ZnS:Mn), with a cubic crystal structure, have the same diameter of about 4.0 nm as ZnS:Mn NCs without HQS. The intensity of the surface-coordination emission peak increased with increasing HQS content or augmenting excited wavelength. The emission of white light was achieved by carefully controlling the dosage of HQS in NCs and appropriately tuning the excited wavelength. The color coordinates (0.35, 0.34) for the efficient white light emitting NCs were very close to the ideal Commission Internationale de l'Eclairage (CIE) chromaticity coordinates for pure white light (0.33, 0.33). The photoluminescence (PL) decay study revealed that the white light emitting NCs exhibited maximum lifetime values at different emission peaks for different NC samples. The study results also indicated that the HQS molecules were attached to the surface of ZnS:Mn NCs in a single coordination fashion due to the steric hindrance effect of the special spherical surface of NCs, which made the QS-ZnS:Mn NCs possess stable and high fluorescent properties in different organic solvents as compared with the conventional small molecule complexes.

  1. Effect of the intercalated cation-exchanged on the properties of nanocomposites prepared by 2-aminobenzene sulfonic acid with aniline and montmorillonite

    Energy Technology Data Exchange (ETDEWEB)

    Toumi, I. [Laboratoire de Chimie Organique, Macromoleculaire et des Materiaux, Universite de Mascara, Bp 763 Mascara 29000 (Algeria); Benyoucef, A., E-mail: ghani29000@yahoo.fr [Laboratoire de Chimie Organique, Macromoleculaire et des Materiaux, Universite de Mascara, Bp 763 Mascara 29000 (Algeria); Yahiaoui, A. [Laboratoire de Chimie Organique, Macromoleculaire et des Materiaux, Universite de Mascara, Bp 763 Mascara 29000 (Algeria); Quijada, C. [Departamento de Ingenieria Textil y Papelera, Universidad Politecnica de Valencia, Pza Ferrandiz i Carbonel, E-03801 Alcoy, Alicante (Spain); Morallon, E. [Departamento de Quimica Fisica e Instituto Universitario de Materiales, Universidad de Alicante, Apartado 99, E-03080 Alicante (Spain)

    2013-02-25

    Polymer/montmorillonite nanocomposites were prepared. Intercalation of 2-aminobenzene sulfonic acid with aniline monomers into montmorillonite modified by cation was followed by subsequent oxidative polymerization of monomers in the interlayer spacing. The clay was prepared by cation exchange process between sodium cation in (M-Na) and copper cation (M-Cu). XRD analyses show the manifestation of a basal spacing (d-spacing) for M-Cu changes depending on the inorganic cation and the polymer intercalated in the M-Cu structure. TGA analyses reveal that polymer/M-Cu composites is less stable than M-Cu. The conductivity of the composites is found to be 10{sup 3} times higher than that for M-Cu. The microscopic examinations including TEM picture of the nanocomposite demonstrated an entirely different and more compatible morphology. Remarkable differences in the properties of the polymers have also been observed by UV-Vis and FTIR, suggesting that the polymer produced with presence of aniline has a higher degree of branching. The electrochemical behavior of the polymers extracted from the nanocomposites has been studied by cyclic voltammetry which indicates the electroactive effect of nanocomposite gradually increased with aniline in the polymer chain.

  2. Simultaneous determination of caffeine and paracetamol by square wave voltammetry at poly(4-amino-3-hydroxynaphthalene sulfonic acid)-modified glassy carbon electrode.

    Science.gov (United States)

    Tefera, Molla; Geto, Alemnew; Tessema, Merid; Admassie, Shimelis

    2016-11-01

    Poly(4-amino-3-hydroxynaphthalene sulfonic acid)-modified glassy carbon electrode (poly(AHNSA)/GCE) was prepared for simultaneous determination of caffeine and paracetamol using square-wave voltammetry. The method was used to study the effects of pH and scan rate on the voltammetric response of caffeine and paracetamol. Linear calibration curves in the range of 10-125μM were obtained for both caffeine and paracetamol in acetate buffer solution of pH 4.5 with a correlation coefficient of 0.9989 and 0.9986, respectively. The calculated detection limits (S/N=3) were 0.79μM for caffeine and 0.45μM for paracetamol. The effects of some interfering substances in the determination of caffeine and paracetamol were also studied and their interferences were found to be negligible which proved the selectivity of the modified electrode. The method was successfully applied for the quantitative determination of caffeine and paracetamol in Coca-Cola, Pepsi-Cola and tea samples. PMID:27211634

  3. Investigation of the Effects of Perfluorooctanoic Acid (PFOA and Perfluorooctane Sulfonate (PFOS on Apoptosis and Cell Cycle in a Zebrafish (Danio rerio Liver Cell Line

    Directory of Open Access Journals (Sweden)

    Yuan Cui

    2015-12-01

    Full Text Available This study aimed to explore the effects of perfluorooctanoic acid (PFOA and perfluorooctane sulfonate (PFOS on apoptosis and cell cycle in a zebrafish (Danio rerio liver cell line (ZFL. Treatment groups included a control group, PFOA-IC50, PFOA-IC80, PFOS-IC50 and PFOS-IC80 groups. IC50 and IC80 concentrations were identified by cellular modeling and MTT assays. mRNA levels of p53, Bcl-2, Bax, Caspase-3 and NF-κB p65 were detected by qPCR. Cell apoptosis and cell cycle were detected by flow cytometry and the protein levels of p53, Bcl-2, Bax, Caspase-3 and NF-κB p65 were determined by western blotting. Both PFOA and PFOS inhibited the growth of zebrafish liver cells, and the inhibition rate of PFOS was higher than that of PFOA. Bcl-2 expression levels in the four groups were significantly higher than the control group and Bcl-2 increased significantly in the PFOA-IC80 group. However, the expression levels of Bax in the four treatment groups were higher than the control group. The percentage of cell apoptosis increased significantly with the treatment of PFOA and PFOS (p < 0.05. Cell cycle and cell proliferation were blocked in both the PFOA-IC80 and PFOS-IC80 groups, indicating that PFOA-IC80 and PFOS-IC50 enhanced apoptosis in ZFL cells.

  4. A capacitive sensor based on molecularly imprinted polymers and poly(p-aminobenzene sulfonic acid) film for detection of pazufloxacin mesilate

    Institute of Scientific and Technical Information of China (English)

    ZHOU Lu; YE GuangRong; YUAN Ruo; CHAI YaQin; CHEN SuMing

    2007-01-01

    A novel capacitive sensor for pazufloxacin mesilate (pazufloxacin) determination was developed by electropolymerizing p-aminobenzene sulfonic (p-ABSA) and molecularly imprinted polymers (MIPs), which was synthesized through thermal radical copolymerization of metharylic acid (MAA) and ethylene glycol dimethacrylate (EGDMA) in the presence of pazufloxacin template molecules, on the gold electrode surface. Furthermore, 1-dedecanethiol was used to insulate the modified electrode. Alternating current (ac) impedance experiments were carried out with a Model IM6e to obtain the capacitance responses. Under the optimum conditions, the sensor showed linear capacitance response to pazufloxacin in the range of 5ng·Ml-1 to 5μg·mL-1 with a relative standard deviation (RSD) 5.3% (n=7) and a detection limit of 1.8 ng·mL-1. The recoveries for different concentration levels of pazufloxacin samples varied from 94.0% to 102.0%. Electrochemical experiments indicated the capacitive sensor exhibited good sensitivity and selectivity and showed excellent parameters of regeneration and stability.

  5. The Antidotal Effects of High-dosage γ-Aminobutyric Acid on Acute Tetramine Poisoning as Compared with Sodium Dimercaptopropane Sulfonate

    Institute of Scientific and Technical Information of China (English)

    SUN Peng; HAN Jiyuan; WENG Yuying

    2007-01-01

    To investigate the therapeutic effect of high-dosage γ-aminobutyric acid (GABA) on acute tetramine (TET) poisoning, 50 Kunming mice were divided into 5 groups at random and the antidotal effects of GABA or sodium dimercaptopropane sulfonate (Na-DMPS) on poisoned mice in different groups were observed in order to compare the therapeutic effects of high-dosage GABA with those of Na-DMPS. Slices of brain tissue of the poisoned mice were made to examine pathological changes of cells. The survival analysis was employed. Our results showed that both high-dosage GABA and Na-DMPS could obviously prolong the survival time, delay onset of convulsion and muscular twitch, and ameliorate the symptoms after acute tetramine poisoning in the mice.Better effects could be achieved with earlier use of high dosage GABA or Na-DMPS. There was no significant difference in prolonging the survival time between high-dose GABA and Na-DMPS used immediately after poisioning. It is concluded that high-dosage GABA can effectively antagonize acute toxicity of teramine in mice. And it is suggested that high-dosage GABA may be used as an excellent antidote for acute TET poisoning in clinical practice. The indications and correct dosage for clinical use awaits to be further studied.

  6. Congener-specific organic carbon-normalized soil and sediment-water partitioning coefficients for the C1 through C8 perfluoroalkyl carboxylic and sulfonic acids.

    Science.gov (United States)

    Rayne, Sierra; Forest, Kaya

    2009-11-01

    Organic carbon-normalized soil and sediment-water partitioning coefficients (K(oc)) were estimated for all C(1) through C(8) perfluoroalkyl carboxylic (PFCA) and sulfonic (PFSA) acid congeners. The limited experimental K(oc) data set for the straight chain C(7) through C(10) PFCAs and C(8) and C(10) PFSAs was correlated to SPARC and ALOGPS computationally estimated octanol-water partitioning/distribution constants and used to predict K(oc) values for both branched and linear C(1) through C(8) isomers. Branched and linear congeners in this homologue range are generally expected to have K(oc) values > 1, leading to their accumulation in organic matter on sediments and soils, retardation during ground and pore water flow, and the preferential association with dissolved organic matter in aquatic systems. Both increasing perfluoroalkyl chain length and linearity increase K(oc) values with substantial intra- and inter-homologue variation and interhomologue mixing. Variability in K(oc) values among the PFCA and PFSA congeners will likely lead to an enrichment of more linear and longer-chain isomers in organic matter fractions, resulting in aqueous phases fractionated towards shorter-chain branched congeners. The expected magnitude of fractionation will require inclusion in source apportionment models and risk assessments. A comparison of representative established quantitative structure property relationships for estimating K(oc) values from octanol-water partitioning constants suggests that these equilibrium partitioning frameworks may be applicable towards modeling PFCA and PFSA environmental fate processes. PMID:20183495

  7. The Effect of Monosodium Glutamate (MSG On Rat Liver And The Ameliorating Effect Of "Guanidino Ethane Sulfonic acid (GES" (Histological, Histochemical and Electron Microscopy Studies

    Directory of Open Access Journals (Sweden)

    Hanaa F. Waer and *Saleh Edress

    2006-09-01

    Full Text Available Food additives are chemical substances added intentionally to food stuffs to preserve, color, sweeten and flavor food. Monosodium glutamate (MSG is used as a flavor enhancer and found in most soups, salad dressing and processed meat. The use of MSG in food is growing. Irrational fear had increased in the last few years due to the adverse reactions and toxicity of MSG. The present study was designed to investigate the effect of MSG on the rat liver and the ameliorating effect of taurine analog "Guanidinoethane sulfonic acid (GES". Sixty albino rats (2-3 months old were used in the present study. MSG was given orally at a daily dose of 60 mg/1000 g for one month, two months and was given at a daily dose of 100mg/1000gm for one month. The results revealed that the deleterious effects of MSG were dose related and cumulative. In MSG treated rats, the examined sections showed remarkable alterations varied considerably from moderate structural changes to cytoplasmic lysis and signs of degeneration of cellular organelles. The histological changes showed disturbed liver architecture, hemorrhage in the central veins, areas of necrosis, vacuolation and increased inflammatory cells infiltration. The glycogen granules increased as well as the collagen fibers in the liver cells. Ultrastructural changes showed loss of cytoplasmic differentiation, vacuolation, pyknotic nuclei with irregular nuclear membranes and elongated electron dense mitochondria. Conversely, treatment of rats with taurine analog (GES significantly attenuated the cellular toxicity of MSG.

  8. Treatment efficiencies of nitrite nitrogen in industrial wastewater by using amido sulfonic acid; Amido ryusan ni yoru kojo haisuichu no ashosansei chisso no shori koka

    Energy Technology Data Exchange (ETDEWEB)

    Inoue, M. [Kanagawa Environmental Research Center, Kanagawa (Japan); Inamori, Y. [National Inst. for Environmental Studies, Tsukuba (Japan)

    1998-06-10

    Chemical denitrification of NO2-N conducted with amido sulfonic acid was studied to treat NO2-N in both bench and in situ experiments. In bench experiments, following optium conditions for NO2-N removal were obtained. The dosage of amide sulfate was 6.9 times equivalent to NO2-N load, pH value and stirring rate were 2.5 and 50 r.p.m., respectively in the bench reactor, and the period for reaction was more than 60 minutes. Nitrogenous gases like NOx, and N2O, which are causative materials for air pollution and global warming, were not detected in the gas exhaust. In situ experiment was made with wastewater containing NO2-N discharged from a factory and with its operating parameters same as the optimum conditions obtained in the bench experiment. It ran in batch style and was controlled automatically. Results showed that efficient chemical denitrification could be conducted through continuously stirring during treated wastewater discharging, and through covering nitrite sensor to keep it from the nitrogenous gases generated in the reaction. 17 refs., 9 figs., 1 tab.

  9. Self-assembled platinum nanoparticles on sulfonic acid-grafted graphene as effective electrocatalysts for methanol oxidation in direct methanol fuel cells

    Science.gov (United States)

    Lu, Jinlin; Li, Yanhong; Li, Shengli; Jiang, San Ping

    2016-02-01

    In this article, sulfonic acid-grafted reduced graphene oxide (S-rGO) were synthesized using a one-pot method under mild conditions, and used as Pt catalyst supports to prepare Pt/S-rGO electrocatalysts through a self-assembly route. The structure, morphologies and physicochemical properties of S-rGO were examined in detail by techniques such as atomic force microscope (AFM), transmission electron microscopy (TEM) and X-ray photoelectron spectroscopy (XPS). The S-rGO nanosheets show excellent solubility and stability in water and the average particle size of Pt nanoparticles supported on S-rGO is ~3.8 nm with symmetrical and uniform distribution. The electrocatalytic properties of Pt/S-rGO were investigated for methanol oxidation reaction (MOR) in direct methanol fuel cells (DMFCs). In comparison to Pt supported on high surface area Vulcan XC-72 carbon (Pt/VC) and Pt/rGO, the Pt/S-rGO electrocatalyst exhibits a much higher electrocatalytic activity, faster reaction kinetics and a better stability. The results indicate that Pt/S-rGO is a promising and effective electrocatalyst for MOR of DMFCs.

  10. DMFC Performance of Polymer Electrolyte Membranes Prepared from a Graft-Copolymer Consisting of a Polysulfone Main Chain and Styrene Sulfonic Acid Side Chains

    Directory of Open Access Journals (Sweden)

    Nobutaka Endo

    2016-08-01

    Full Text Available Polymer electrolyte membranes (PEMs for direct methanol fuel cell (DMFC applications were prepared from a graft-copolymer (PSF-g-PSSA consisting of a polysulfone (PSF main chain and poly(styrene sulfonic acid (PSSA side chains with various average distances between side chains (Lav and side chain lengths (Lsc. The polymers were synthesized by grafting ethyl p-styrenesulfonate (EtSS on macro-initiators of chloromethylated polysulfone with different contents of chloromethyl (CM groups, and by changing EtSS content in the copolymers by using atom transfer radical polymerization (ATRP. The DMFC performance tests using membrane electrode assemblis (MEAs with the three types of the PEMs revealed that: a PSF-g-PSSA PEM (SF-6 prepared from a graft copolymer with short average distances between side chains (Lav and medium Lsc had higher DMFC performance than PEMs with long Lav and long Lsc or with short Lav and short Lsc. SF-6 had about two times higher PDmax (68.4 mW/cm2 than Nafion® 112 at 30 wt % of methanol concentration. Furthermore, it had 58.2 mW/cm2 of PDmax at 50 wt % of methanol concentration because of it has the highest proton selectivity during DMFC operation of all the PSF-g-PSSA PEMs and Nafion® 112.

  11. A capacitive sensor based on molecularly imprinted polymers and poly(p-aminobenzene sulfonic acid) film for detection of pazufloxacin mesilate

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    A novel capacitive sensor for pazufloxacin mesilate (pazufloxacin) determination was developed by electropolymerizing p-aminobenzene sulfonic (p-ABSA) and molecularly imprinted polymers (MIPs), which was synthesized through thermal radical copolymerization of metharylic acid (MAA) and ethyl-ene glycol dimethacrylate (EGDMA) in the presence of pazufloxacin template molecules, on the gold electrode surface. Furthermore, 1-dedecanethiol was used to insulate the modified electrode. Alter-nating current (ac) impedance experiments were carried out with a Model IM6e to obtain the capaci-tance responses. Under the optimum conditions, the sensor showed linear capacitance response to pazufloxacin in the range of 5 ng·mL-1 to 5 μg·mL-1 with a relative standard deviation (RSD) 5.3% (n=7) and a detection limit of 1.8 ng·mL-1. The recoveries for different concentration levels of pazufloxacin samples varied from 94.0% to 102.0%. Electrochemical experiments indicated the capacitive sensor exhibited good sensitivity and selectivity and showed excellent parameters of regeneration and stabil-ity.

  12. Novel proton-exchange membrane based on single-step preparation of functionalized ceramic powder containing surface-anchored sulfonic acid

    Science.gov (United States)

    Reichman, S.; Burstein, L.; Peled, E.

    2008-05-01

    A novel approach to the synthesis of a low-cost proton-exchange membrane (PEM) based on the single-step preparation of a functionalized ceramic powder containing surface-anchored sulfonic acid (SASA) and a polymer binder, is presented for the first time. The added value of this technique, compared with earlier work published by our group, is the adoption of a direct, single-step synthesis, as opposed to a multiple-step synthesis. The latter requires an oxidation step, in order to convert the thiol group into a sulfonic group. SASA powders of different compositions have been prepared and characterized by means of Brunaur-Emmet-Teller (BET), thermogravimetric analysis-differential thermal analysis (TGA-DTG), differential scanning calorimeter (DSC), Fourier transformation infrared (FT-IR), nuclear magnetic resonance (NMR), X-ray photoelectron spectroscopy (XPS), atomic force microscopy (AFM), scanning electron microscopy (SEM) and electrochemical techniques. The lowest equivalent weight measured for SASA powders is 1281 g equiv.-1. The ionic conductivity of a 100-μm-thick membrane is measured ex situ at room temperature (25 ± 3 °C) and the highest proton conductivity is 48 mS cm-1. The typical pore size, for the SASA powders is less than 10 nm and ranges from 2 to 50 nm for the SASA-based membranes. The membranes are thermally stable up to 250 °C. Direct methanol fuel cells (DMFCs) are assembled with some of the membranes. Preliminary tests showed that the cell resistance for a ∼100-μm-thick membrane ranges between 0.29 and 0.19 Ω cm2 from 80 to 130 °C, respectively, and that the maximum cell power density with a 1 M methanol solution is 127, 208 and 290 mW cm-2 at 80, 110 and 130 °C, respectively, while the corresponding methanol crossover current density is 0.093, 0.238 and 0.281 A cm-2.

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

    Directory of Open Access Journals (Sweden)

    Shimoga D. Ganesh

    2016-01-01

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

  14. Deactivation of sulfonated hydrothermal carbons in the presence of alcohols: Evidences for sulfonic esters formation

    OpenAIRE

    Fraile, José M.; García Bordejé, E.; Roldán, Laura

    2012-01-01

    Sulfonated hydrothermal carbons present high activity for esterification of palmitic acid with alcohols. However, the catalyst is significantly deactivated upon recovery. Leaching of sulfonated species does not account for this deactivation, which is observed even by pretreatment only with the alcohol under reflux. Solid state NMR shows the presence of chemically bound alkyl groups coming from the alcohol, clearly different from strongly physisorbed species obtained by pretreatment at room te...

  15. Alkalized sulfonates (PEP additives); Ueberbasische Sulfonate (PEP-Additive)

    Energy Technology Data Exchange (ETDEWEB)

    Schulz, Joachim [WISURA Mineraloelwerk Goldgrabe und Scheft GmbH und Co., Bremen (Germany)

    2010-05-15

    There are only few additives about which in the last 25 - to 30 were reported as a possible additive group regarding replacement of chlorinated paraffin's. Besides, it concerns around alkalized sulfonic acids which are neutralized with sodium or calcium-hydroxide and contain, in addition, the corresponding carbonate in large quantities. This class of additives should act passively in metalworking under extreme pressure (Passive Extreme Pressure additive). Observations from the field often provide a different picture. The following article offers a literature overview to the reaction behavior and introduces newer lab results. A new model of the (re)action of these additives will be introduced. (orig.)

  16. H2 O2 Generated by Natural Biofilms Under Light Irradiation and Its Effects on Degradation of Sodium Dodecyl Benzene Sulfonate%光照下自然水体生物膜产生 H2O2及其对十二烷基苯磺酸钠降解的影响

    Institute of Scientific and Technical Information of China (English)

    董德明; 李明; 孙家倩; 赵天宇; 花修艺; 郭爱桐; 梁大鹏

    2014-01-01

    In this study, generation of H2 O2(hydrogen peroxide) by natural biofilms of different bioactivities under light irradiation was investigated, and effect of light on sodium dodecyl benzene sulfonate(SDBS) degra-dation in such natural biofilm-water systems was evaluated. The role of H2 O2 in the degradation of SDBS was also verified by SDBS degradation experiments in H2 O2 solution without biofilms. The results indicated that:(1) biofilms with full bio-activity can generate H2 O2 , while biofilms without any bio-activity or bio-activity of photosynthesis can not generate H2 O2; (2) much more SDBS can be degraded under visible light than in darkness; (3) light and Fe2+ can promote the degradation of SDBS in the presence of H2 O2 . H2 O2 produced by natural biofilms should be one of the most important causes of the degradation of SDBS, and the roles of H2 O2 in the degradation should include both direct oxidation of SDBS by H2 O2 and the indirect role in genera-ting active oxygen species.%通过模拟实验研究了不同活性的自然水体生物膜在光照条件下生成过氧化氢(H2 O2)的反应。并研究了光照对自然水体生物膜体系中十二烷基苯磺酸钠(SDBS)降解的影响,结合无生物膜 H2 O2溶液中 SDBS的降解实验,验证了 H2 O2对 SDBS 降解的作用。结果表明,具有生物活性的生物膜可以生成 H2 O2,而无活性和光合作用受到抑制的生物膜则不能生成 H2 O2;光照条件下,生物膜体系中 SDBS 的降解量明显高于无光照条件下的;光照和 Fe2+对 H2 O2降解 SDBS 有促进作用。

  17. An Efficient Solvent Free Synthesis of 1,8-Dioxo-octahydroxanthene Using p-Toluene Sulfonic Acid

    Institute of Scientific and Technical Information of China (English)

    BAYAT, Mohammad; IMANIEH, Hossien; HOSSIENI, Seyydeh Hajar

    2009-01-01

    A simple and efficient method for the synthesis of 1,8-dioxo-octahydroxanthene by using p-toluenesulfonic acid as a catalyst under solvent free conditions is described, which involves cyclizafion of 2,2-arylmethylenebis(3-hydroxy-5,5-dimethyl-2-cyclohexene-1-one) that was obtained firstly by the reaction of dimedone with aromatic aldehydes in water as solvent and catalyst at room temperature. The experimental procedures in the two steps are very simple and the products are formed in excellent yields.

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

    Science.gov (United States)

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

    2015-02-01

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

  19. Analysis of benzene polycarboxylic acids and nitro-benzene polycarboxylic acids as molecular tracers of black carbon by using liquid chromatography-mass spectrometry%液相色谱-质谱法分析黑碳的分子标志物--苯多羧酸和硝基苯多羧酸

    Institute of Scientific and Technical Information of China (English)

    黄国培; 陈颖军; 田崇国; 刘莺

    2016-01-01

    苯多羧酸法是定量检测黑碳和溶解态黑碳的重要分子标志物法,其中苯多羧酸和硝基苯多羧酸的分离和定量是关键环节。本文建立了苯多羧酸和硝基苯多羧酸的液相色谱-质谱分析方法,利用质谱的定性能力解决了部分苯多羧酸和硝基苯多羧酸化合物在缺乏标准品情况下的定性问题。用 Phenomenex Synergi Polar RP 分离柱,柱温为35℃,流动相为0.5%(体积分数)甲酸水溶液和甲醇,流速为0.5 mL/min,梯度洗脱,以电喷雾离子源负离子全扫描和选择扫描模式进行离子阱质谱检测,同时利用串联的二极管阵列检测器采集三维紫外光谱数据。在实际样品检测中,14个含3个及以上羧基的苯多羧酸和硝基苯多羧酸化合物获得良好分离。此方法简化并加快了苯多羧酸法定量黑碳和溶解态黑碳的分析过程,可满足环境样品中黑碳和溶解态黑碳的分析,促进了苯多羧酸法应用的普及。%The benzene polycarboxylic acid( BPCA)method is an important molecular marker method for black carbon and dissolved black carbon quantification while the separation and quantification of benzene polycarboxylic acids and nitro-benzene polycarboxylic acids are the key process. In order to use mass spectrometer to solve the issue of identification of benzene polycarboxylic acids and nitro-benzene polycarboxylic acids due to the lack of the standards of some of the target compounds,a liquid chromatography-mass spectrometry method was pro-posed. It made the experimental procedures easier and faster than using the gas chromatogra-phy mass spectrometry,and would promote the use of the BPCA method. A Phenomenex Syn-ergi Polar RP column was used. The digestion productions of black carbon and dissolved black carbon were gradiently eluted by the mobile phases of 0. 5%( v/v)aqueous formic acid solution and methanol with the flow rate of 0. 5 mL/min at 35 ℃. The determination

  20. Detecting a quasi-stable imine species on the reaction pathway of SHV-1 β-lactamase and 6β-(hydroxymethyl)penicillanic acid sulfone.

    Science.gov (United States)

    Che, Tao; Rodkey, Elizabeth A; Bethel, Christopher R; Shanmugam, Sivaprakash; Ding, Zhe; Pusztai-Carey, Marianne; Nottingham, Michael; Chai, Weirui; Buynak, John D; Bonomo, Robert A; van den Akker, Focco; Carey, Paul R

    2015-01-27

    For the class A β-lactamase SHV-1, the kinetic and mechanistic properties of the clinically used inhibitor sulbactam are compared with the sulbactam analog substituted in its 6β position by a CH2OH group (6β-(hydroxymethyl)penicillanic acid). The 6β substitution improves both in vitro and microbiological inhibitory properties of sulbactam. Base hydrolysis of both compounds was studied by Raman and NMR spectroscopies and showed that lactam ring opening is followed by fragmentation of the dioxothiazolidine ring leading to formation of the iminium ion within 3 min. The iminium ion slowly loses a proton and converts to cis-enamine (which is a β-aminoacrylate) in 1 h for sulbactam and in 4 h for 6β-(hydroxymethyl) sulbactam. Rapid mix-rapid freeze Raman spectroscopy was used to follow the reactions between the two sulfones and SHV-1. Within 23 ms, a 10-fold excess of sulbactam was entirely hydrolyzed to give a cis-enamine product. In contrast, the 6β-(hydroxymethyl) sulbactam formed longer-lived acyl-enzyme intermediates that are a mixture of imine and enamines. Single crystal Raman studies, soaking in and washing out unreacted substrates, revealed stable populations of imine and trans-enamine acyl enzymes. The corresponding X-ray crystallographic data are consonant with the Raman data and also reveal the role played by the 6β-hydroxymethyl group in retarding hydrolysis of the acyl enzymes. The 6β-hydroxymethyl group sterically hinders approach of the water molecule as well as restraining the side chain of E166 that facilitates hydrolysis.

  1. Toxicity of perfluorooctane sulfonate and perfluorooctanoic acid to Escherichia coli: Membrane disruption, oxidative stress, and DNA damage induced cell inactivation and/or death.

    Science.gov (United States)

    Liu, Gesheng; Zhang, Shuai; Yang, Kun; Zhu, Lizhong; Lin, Daohui

    2016-07-01

    Perfluorooctane sulfonate (PFOS) and perfluorooctanoic acid (PFOA) are two widely used polyfluorinated compounds (PFCs) and are persistent in the environment. This study for the first time systematically investigated their toxicities and the underlying mechanisms to Escherichia coli. Much higher toxicity was observed for PFOA than PFOS, with the 3 h half growth inhibition concentrations (IC50) determined to be 10.6 ± 1.0 and 374 ± 3 mg L(-1), respectively, while the bacterial accumulation of PFOS was much greater than that of PFOA. The PFC exposures disrupted cell membranes as evidenced by the dose-dependent variations of cell structures (by transmission electron microscopy observations), surface properties (electronegativity, hydrophobicity, and membrane fluidity), and membrane compositions (by gas chromatogram and Fourier transform infrared spectroscopy analyses). The increases in the contents of intracellular reactive oxygen species (ROS) and malondialdehyde and the activity of superoxide dismutase indicated the increment of oxidative stress induced by the PFCs in the bacterial cells. The fact that the cell growth inhibition was mitigated by the addition of ROS scavenger (N-acetyl cysteine) further evidenced the important role of oxidative damage in the toxicities of PFOS and PFOA. Eighteen genes involved in cell division, membrane instability, oxidative stress, and DNA damage of the exposed cells were up or down expressed, indicating the DNA damage by the PFCs. The toxicities of PFOS and PFOA to E. coli were therefore ascribed to the membrane disruption, oxidative stress, and DNA damage induced cell inactivation and/or death. The difference in the bactericidal effect between PFOS and PFOA was supposed to be related to their different dominating toxicity mechanisms, i.e., membrane disruption and oxidative damage, respectively. The outcomes will shed new light on the assessment of ecological effects of PFCs. PMID:27155098

  2. Effects of co-administration of dietary sodium arsenate and 2,3-dimercaptopropane-1-sulfonic acid (DMPS) on the rat bladder epithelium

    International Nuclear Information System (INIS)

    Inorganic arsenic is a known human carcinogen, inducing tumors of the skin, urinary bladder and lung. It is metabolized to organic methylated arsenicals. 2,3-Dimercaptopropane-1-sulfonic acid (DMPS), a chelating agent, is capable of reducing pentavalent arsenicals to the trivalent state and binding to the trivalent species, and it has been used in the treatment of heavy metal poisoning in humans. Therefore, we investigated the ability of DMPS to inhibit the cytotoxicity and regenerative urothelial cell proliferation induced by arsenate administration in vivo. Female rats were treated for 4 weeks with 100 ppm AsV. DMPS (2800 ppm) co-administered in the diet significantly reduced the AsV-induced cytotoxicity of superficial cells detected by scanning electron microscopy (SEM), and the incidence of simple hyperplasia observed by light microscopy and the bromodeoxyuridine (BrdU) labeling index. It also reduced the total concentration of arsenicals in the urine and the methylation of arsenic. There were no differences in oxidative stress as assessed by immunohistochemical staining for 8-hydroxy-2′-deoxyguanosine (8OHdG) of the bladder urothelium. No differences were detected in urine sediments between groups. These data suggest that DMPS has the ability to inhibit both arsenate-induced acute toxicity and regenerative proliferation of the rat bladder epithelium, most likely by decreasing exposure of the urothelium to trivalent arsenicals excreted in the urine. These data provide additional evidence that the effects of arsenate exposure in vivo do not appear to be related to oxidative effects on dG in DNA.

  3. 苯与双氧水在高效钼钒磷杂多酸催化剂上的羟基化%Hydroxylation of Benzene with Hydrogen Peroxide over Highly Efficient Molybdovanadophosphoric Heteropoly Acid Catalysts

    Institute of Scientific and Technical Information of China (English)

    张富民; 郭麦平; 葛汉青; 王军

    2007-01-01

    Keggin type molybdovanadophosphoric heteropoly acids,H3+nPMo12-nVnO40 (n= 1-3),were prepared by a novel environmentally benign method,and their catalytic performances were evaluated via hydroxylation of benzene to phenol with hydrogen peroxide as oxidant in a mixed solvent of glacial acetic acid and acetonitrile.Various reaction parameters,such as reaction time,reaction temperature,ratio of benzene to hydrogen peroxide,concentration of aqueous hydrogen peroxide,ratio of glacial acetic acid to acetonitrile in solvent and catalyst concentration,were changed to obtain an optimal reaction conditions. H3+nPMo12-nVnO40 (n= 1-3) are revealed to be highly efficient catalyst for hydroxylation of benzene. In case of H5PMo10V2O40,a conversion of benzene of 34.5% with the selectivity of phenol of 100% can be obtained at the optimal reaction conditions.

  4. 微反应器中十二烷基苯液相SO3磺化过程%Process Performance of Dodecylbenzene Sulfonation with Liquid SO3 in a Microreactor

    Institute of Scientific and Technical Information of China (English)

    主凯; 赵玉潮; 张博宇; 陈光文

    2015-01-01

    Petroleum sulfonates and heavy alkyl benzene sulfonates are important anionic surfactants used in tertiary oil recovery and the active components are alkyl benzene sulfonates. In this work, dodecylbenzene (DDB) sulfonation with liquid SO3 inmicroreactors was used as a model reaction and its reaction performance was studied in a microreactor. The effects of some important parameters on the yield of dodecylbenzene sulfonic acid are investigated, including liquid flow rate, reaction temperature, mass fraction of SO3, length of microchannel, molar ratio of SO3 to dodecylbenzene, reactor types and stirring time. The results showed that the sulfonation of dodecylbenzene is controlled by mass transfer and the initial period of sulfonation can be significantly intensified in the microreactor. With a combination of a microreactor and a tank reactor, the yield of dodecylbenzene sulfonic acid can reach 93.7% under the condition of molar ratio of SO3 to dodecylbenzene 1.1:1.%石油磺酸盐和重烷基苯磺酸盐是三次采油用重要阴离子表面活性剂,其主要成分是烷基苯磺酸盐。本研究以十二烷基苯(DDB)液相SO3磺化为模型反应,研究微反应器内的烷基苯磺酸合成反应过程特性,考察了液体流量、反应温度、磺化剂中 SO3含量、反应通道长度、SO3与十二烷基苯物质的量比、微反应器结构、搅拌时间等参数的影响。结果表明,十二烷基苯磺化过程受传质控制,微反应器对反应初始阶段的强化作用明显,在SO3与十二烷基苯物质的量比为1.1时,采用微反应器与釜式反应器串联模式合成十二烷基苯磺酸,收率高达93.7%,为微反应器生产重烷基苯磺酸的路线提供了重要基础。

  5. Crystal Structures of KPC-2[beta]-Lactamase in Complex with 3-Nitrophenyl Boronic Acid and the Penam Sulfone PSR-3-226

    Energy Technology Data Exchange (ETDEWEB)

    Ke, Wei; Bethel, Christopher R.; Papp-Wallace, Krisztina M.; Pagadala, Sundar Ram Reddy; Nottingham, Micheal; Fernandez, Daniel; Buynak, John D.; Bonomo, Robert A.; van den Akker, Focco (Case Western); (Stokes); (SMU)

    2012-08-01

    Class A carbapenemases are a major threat to the potency of carbapenem antibiotics. A widespread carbapenemase, KPC-2, is not easily inhibited by {beta}-lactamase inhibitors (i.e., clavulanic acid, sulbactam, and tazobactam). To explore different mechanisms of inhibition of KPC-2, we determined the crystal structures of KPC-2 with two {beta}-lactamase inhibitors that follow different inactivation pathways and kinetics. The first complex is that of a small boronic acid compound, 3-nitrophenyl boronic acid (3-NPBA), bound to KPC-2 with 1.62-{angstrom} resolution. 3-NPBA demonstrated a Km value of 1.0 {+-} 0.1 {micro}M (mean {+-} standard error) for KPC-2 and blocks the active site by making a reversible covalent interaction with the catalytic S70 residue. The two boron hydroxyl atoms of 3-NPBA are positioned in the oxyanion hole and the deacylation water pocket, respectively. In addition, the aromatic ring of 3-NPBA provides an edge-to-face interaction with W105 in the active site. The structure of KPC-2 with the penam sulfone PSR-3-226 was determined at 1.26-{angstrom} resolution. PSR-3-226 displayed a K{sub m} value of 3.8 {+-} 0.4 {micro}M for KPC-2, and the inactivation rate constant (kinact) was 0.034 {+-} 0.003 s{sup -1}. When covalently bound to S70, PSR-3-226 forms a trans-enamine intermediate in the KPC-2 active site. The predominant active site interactions are generated via the carbonyl oxygen, which resides in the oxyanion hole, and the carboxyl moiety of PSR-3-226, which interacts with N132, N170, and E166. 3-NPBA and PSR-3-226 are the first {beta}-lactamase inhibitors to be trapped as an acyl-enzyme complex with KPC-2. The structural and inhibitory insights gained here could aid in the design of potent KPC-2 inhibitors.

  6. Korelasi paparan benzene melalui pengukuran kadar trans-trans Muconic Acid (t,t-MA) dengan kadar enzim transaminase dan total protein pada pekerja SPBU Pertamina kota Medan

    OpenAIRE

    Musthari

    2016-01-01

    Since evidence of health problems caused by exposure to benzene, then benzene is one of the chemicals that are most harmful to human health. The development of the oil and gas industry in Indonesia can not be separated relevance of the use of a wide range of chemicals. Gasoline is one of the oil products containing benzene (C6H6), which serves to increase the octane rating. Impact of acute benzene exposure in the form of disorders of the nervous system, lack of oxygen supply...

  7. Properties of a novel acid dye 1-amino-4-[(6-nitro-2-benzothiazolyl)amino]-9,10-anthraquinone-2-sulfonic acid with anti-UV capability

    Institute of Scientific and Technical Information of China (English)

    2010-01-01

    A novel acid dye acid was synthesized by the condensation reaction between bromamine acid and 2-amino-6-nitrobenzothiazole and its anti-UV protection properties were evaluated.The results showed that silk dyed with this dye had very good ultraviolet radiation protection capability and excellent dyeing performance.The UV-absorption mechanism of this dye was also discussed.

  8. 磺化腐植酸接枝改性共聚物合成及性能研究%SYNTHESIS AND PROPERTIES RESEARCH OF SULFONATED HUMIC ACID GRAFTED COPOLYMER

    Institute of Scientific and Technical Information of China (English)

    张光华; 刘龙; 李俊国; 尚婷; 徐海龙; 强轶

    2013-01-01

    以腐植酸为基本原料,经过磺化,再以丙烯酸为单体,过硫酸钾为引发剂,采用溶液聚合法,制备磺化腐植酸-丙烯酸接枝共聚物,并检测其对水煤浆的黏度、流变性和稳定性的影响.还研究了不同分散剂用量对水煤浆成浆性能的影响,结果表明,分散剂有效成分为水煤浆总重量的0.12%时,水煤浆具有最低的表观黏度.%To humic acid potassium as basic raw materials, through sulfonation ,was purified humic acid, and then as raw materials, acrylic acid as monomers of copolymerization, potassium persulfate as redox system initiator, the grafted copolymers of sulfonated humic acid and acrylic acid are synthesized by means of aqueous solution of copolymerization. And detect their effect on viscosity, rheology, and stability of coal water slurry. This paper also studies diffefent dispersant dosage on the property of coal water slurry, dispersing agent for coal water slurry of effective components of 0. 12% of the total weight, coal water slurry has minimum apparent viscosity.

  9. Syntheses, structures and fluorescence properties of cadmium coordination polymers with triangular 1,3-bis[2-(4‧-pyridyl)ethenyl]benzene and linear dicarboxylic acids

    Science.gov (United States)

    Liang, Rui; Yue, Fangfang; Wang, Yuting; Guo, Yongkang; Xuan, Xiaopeng

    2016-09-01

    Three new polymeric complexes [Cd3(1,3-BPEB)3(1,4-BDC)3·2H2O]n (1), [Cd2(1,3-BPEB)2(4,4‧-BPDC)2]n (2) and [Cd2(1,3-BPEB)2(4,4‧-STDC)2]n (3) (1,3-BPEB = 1,3-bis[2-(4‧-pyridyl)ethenyl]benzene, 1,4-BDC = 1,4-benzenedicarboxylic acid, 4,4‧-BPDC = 4,4‧-biphenyldicarboxylic acid and 4,4‧-STDC = 4,4‧-stilbenedicarboxylic acid) have been prepared by the solvothermal reaction of 1,3-BPEB, Cd(NO3)2·4H2O and dicarboxylic acids. Single-crystal X-ray diffraction reveals that these complexes have novel complicated structures. Complex 1 is a 3-D network structure by linking Cd atoms with 1,4-BDC and 1,3-BPEB ligands. Complex 2 shows a 3-D interpenetrating layered structure formed by three networks which derived from bridged Cd atoms with 4,4‧-BPDC and 1,3-BPEB ligands. Complex 3 has a fivefold interpenetrating 3-D coordination framework by linking Cd atoms with 4,4‧-STDC and 1,3-BPEB ligands. The dicarboxylic acids afford different coordination modes to bind Cd atoms in these three complexes. Additionally, these compounds were further characterized by PXRD, FT-IR spectroscopy and thermogravimetric (TG) analysis. Their fluorescence spectra were also determined and analyzed in the solid state at room temperature.

  10. Selective removal of Cr(VI) from aqueous solution by polypyrrole/2,5-diaminobenzene sulfonic acid composite.

    Science.gov (United States)

    Kera, Nazia H; Bhaumik, Madhumita; Ballav, Niladri; Pillay, Kriveshini; Ray, Suprakas Sinha; Maity, Arjun

    2016-08-15

    A polypyrrole/2,5-diaminobenzenesulfonic acid (PPy/DABSA) composite, synthesised by the in situ oxidative polymerization of pyrrole in the presence of DABSA, was studied as an adsorbent for the removal of Cr(VI) from aqueous solution. The structure and morphology of the composite were investigated by ATR-FTIR, FE-SEM, EDX, TGA, XRD and XPS studies. The adsorption of Cr(VI) by PPy/DABSA composite was highly pH dependent and optimum removal was achieved at pH 2. Adsorption of Cr(VI) was confirmed by EDX and XPS studies. The isotherm data fitted the linear Langmuir model well, with a maximum adsorption capacity of 303mg/g at 25°C. Thermodynamic parameters (ΔG°, ΔH° and ΔS°) were calculated using isotherm data and confirmed that the adsorption process was spontaneous and endothermic. Adsorption kinetics was best described by the pseudo-second-order model. The activation energy of the adsorption process suggested that Cr(VI) was chemisorbed by PPy/DABSA composite. PPy/DABSA composite could be used for three consecutive adsorption-desorption cycles without loss of its original adsorption capacity. Highly selective removal of Cr(VI) was observed even when co-existing ions such as Cu(2+), Zn(2+), Ni(2+), Cl(-), SO4(2)(-) and NO3(-) were present in the solution. In summary, the potential of PPy/DABSA composite for remediating industrial wastewater contaminated by Cr(VI) has been demonstrated.

  11. Preparation of Sulfuric Acid Sulfonated Modified Starch and Testing Study of Its Scale Inhibition Properties%硫酸磺化改性淀粉制备及阻垢性能试验研究

    Institute of Scientific and Technical Information of China (English)

    刘玉玲; 高升; 刘利

    2011-01-01

    为了减轻和避免目前阻垢剂排放对环境造成的污染,本实验利用浓硫酸氧化淀粉制备改性淀粉,其颜色为棕红色;在不同浓度、温度、Ca2+浓度、pH值下,对硫酸磺化改性淀粉的阻垢性能进行测试.实验结果表明,硫酸磺化改性淀粉高效阻垢的最佳浓度为0.61 mg/L,最佳温度为80℃,对应的阻垢效率为84.7%.其阻垢效率随着Ca2+浓度及pH值的增加而减小,因此Ca2+浓度、pH值是影响阻垢剂阻垢效率的重要因素.对硫酸磺化改性淀粉与其它氧化改性淀粉的阻垢性能进行的比较实验结果表明,硫酸磺化改性淀粉的阻垢性能优于其它改性淀粉.%In order to mitigate and avoid current scale inhibitor pollution emissions on the environment, in this lab, the concentrated sulfuric acid oxidized starch is used to prepare the modified starch, whose color is brown-red.Sulfuric acid sulfonated modified starch is tested in case of different concentrations, temperatures, Ca2+ concentrations, pH values.It has been found that the best concentration of efficient scale of sulfuric acid sulfocated modified starch is 0.61 mg/L, and that the best temperature is 80 ℃, and that under this best concentration and temperature the corresponding inhibition rate is 84.7 %.The inhibition rate of sulfuric acid sulfonated modified starch decreases with an increase in Ca2+ concentration and pH value, thus, indicating that Ca2+ concentration and pH are the important factors that can affect the inhibition rate of scale inhibitor.Finally, the comparison is made of scale performance between sulfuric acid sulfonated modified starch and other oxidized modified starch, with the results showing that the scale inhibition of sulfuric acid sulfonated modified starch is superior to other oxidized modified starch.

  12. Fate and biodegradability of sulfonated aromatic amines

    NARCIS (Netherlands)

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

    2005-01-01

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

  13. Anti-wrinkle and UV protective performance of cotton fabrics finished with 5-(carbonyloxy succinic)-benzene-1,2,4-tricarboxylic acid.

    Science.gov (United States)

    Qi, Huan; Pan, Junbing; Qing, Feng-Ling; Yan, Kelu; Sun, Gang

    2016-12-10

    1,2,3,4-Butane tetracarboxylic acid (BTCA) has been considered as one of the most promising crosslinking agent to replace dimethylol dihydroxy ethylene urea (DMDHEU) for anti-wrinkle finishing on cotton fabrics. However, it could cause significant strength loss of the treated fabrics. In this study, a 5-(carbonyloxy succinic)-benzene-1,2,4-tricarboxylic acid (BSTA) was synthesized and applied as an effective crosslinking agent. The results show that fabrics treated with BSTA present the same or even better anti-wrinkle properties as that with BTCA. FTIR was employed to analyze ester bond formation process on cellulose. Finishing conditions such as agent concentration, curing temperature, and bath pH were also discussed to evaluate crosslinking effect of cellulose. BSTA, as a derivative of photo-active conjugated compound, can absorb ultraviolet lights and offer ultraviolet (UV) protective property on treated materials. The treated fabrics showed excellent UV protection performance due to the addition of aromatic conjugated system on fabrics. PMID:27577923

  14. STUDY ON LIGHTLY SULFONATED SYNDIOTACTIC POLYSTYRENE IONOMERS

    Institute of Scientific and Technical Information of China (English)

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

    2001-01-01

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

  15. 一类磺酸系双子表面活性剂的制备及性能研究%Preparation and properties of a sulfonic acid series gemini surfactants

    Institute of Scientific and Technical Information of China (English)

    宋冬冬; 孙雪丽; 刘方圆; 朱广军

    2012-01-01

    Intermediates, α - sulfostearic acid and α - snlfolauric acid ,were prepared by reacting ehlorosulfonic acid with stearic acid and lauric acid respectively. Five kinds of sulfonic acid gemini surfactant were prepared by reacting α - sulfostearic acid with ethanediol ,1,4- butanediol ,1,6- hexanediol and poly ethanediol respectively as well as α — sulfolauric acid with ethanediol. All the sulfonated intermediates were neutralized to form the corresponding salts and thereby five kinds of sulfonic acid gemini surfactant were prepared. Molecular structures of the gemini surfactants were characterized by FTIR and HNMR. Optimal esterification reaction conditions for preparation of the gemini surfactants were obtained through orthogonal designed experiments. Basic physical - chemical properties of the gemini surfactants were studied. Results showed that following the increase of carbon chain length of the spacing group,its cmc reduces correspondingly. Meanwhile,following the increase of the carbon chain length of the hydrophobic group,its γcmc increases correspondingly. Emulsification and foam properties of the sulfonic acid series gemini surfactants are better than that of the corresponding single body sulfonic acid surfactants.%以氯磺酸为磺化剂,分别与硬脂酸和月桂酸进行磺化反应,制备了中间体α-磺基硬脂酸和α-磺基月桂酸.将中间体α-磺基硬脂酸分别与乙二醇、1,4-丁二醇、1,6-己二醇和聚乙二醇400以及α-磺基月桂酸与乙二醇进行酯化反应,最后中和成盐,制备出5种磺酸系双子表面活性剂.通过FTIR和1HNMR对目标产物进行了表征.通过正交试验对磺酸系双子表面活性剂制备的酯化工艺进行了优化,得到较优的酯化工艺条件.对制备的磺酸系双子表面活性剂的基本物化性能进行了研究,结果表明,临界胶束浓度(cmc)随联结基团长度的增加而降低,同时随着疏水链的增长,γcmc呈增大的

  16. Corrosion inhibition efficiency of linear alkyl benzene derivatives for carbon steel pipelines in 1M HCl

    Directory of Open Access Journals (Sweden)

    A.M. Al-Sabagh

    2011-06-01

    Full Text Available Linear alkyl benzene sulfonic acid (L and three of its ester derivatives (L1, L2, L3 were prepared, followed by quaternization of these esters (L1Q, L2Q, L3Q. The corrosion inhibition effect on carbon steel in 1 M HCl was studied using weight loss and potentiodynamic polarization measurements. The adsorption of the inhibitors on carbon steel surface obeyed the Langmuir’s adsorption isotherm. The associated activation energy of corrosion and other thermodynamic parameters such as enthalpy (ΔH∗, entropy (ΔS∗ of activation, adsorption–desorption equilibrium constant (Kads, standard free energy of adsorption (ΔGoads, heat (ΔHoads, and entropy of adsorption (ΔSoads were calculated to elaborate the corrosion inhibition mechanism.

  17. Ionic Liquid Catalyst Used in Deep Desulfuration of the Coking Benzene for Producing Sulfurless Benzene

    Institute of Scientific and Technical Information of China (English)

    ZHOU Xia-Ping; WANG Yan-Liang; MENG Fan-Wei; FAN Xing-Ming; QIN Song-Bo

    2008-01-01

    For the widening need of benzene used in organic synthesis, ionic liquid catalyst was prepared to study the process of deep desulfuration in the coking benzene. The result shows that the effect of de-thiophene by the ionic liquid catalyst (N-methyl imidazolium hydrogen sulfate [Hmim][HSO4]) is related to its acid function value.Hammett indicator was used to determine the acid function value H0 of the ionic liquid. It can be concluded that while the acid function value is in the range from -4 to -12, the ionic liquid catalyst can make the concentration certain acid quantity and strength, the ionic liquid catalyst helps to form alkyl thiophene through Friedel-Crafts reaction, which differs from the character of benzene and it is absolutely necessary for the separation and refinement of benzene. But overabundant quantity and higher acid value of [Hmim][HSO4] are more suitable for the side copolymerization of benzene, thiophene and alkene, thereby affecting repeated use of the ionic liquid catalyst([Hmim][HSO4]). In our research, thiophene derivant produced by desulfurization in the coking benzene was used as the polymer to provide the passing channel of the charges. The ionic liquid composition in poor performance after repeated use was made to prepare conductive material (resisting to static electricity) as an "electron-receiving" and "electron-giving" doping agent. The result shows that thiophene derivant after desulfuration in the coking benzene can be used to prepare doping conductive materials.

  18. Biochemical toxicity of benzene.

    Science.gov (United States)

    Rana, S V S; Verma, Yeshvandra

    2005-04-01

    Human exposure to benzene in work environment is a global occupational health problem. After inhalation or absorption, benzene targets organs viz. liver, kidney, lung, heart and brain etc. It is metabolized mainly in the liver by cytochrome P450 multifunctional oxygenase system. Benzene causes haematotoxicity through its phenolic metabolites that act in concert to produce DNA strand breaks, chromosomal damage, sister chromatid exchange, inhibition of topoisomerase II and damage to mitotic spindle. The carcinogenic and myelotoxic effects of benzene are associated with free radical formation either as benzene metabolites or lipid peroxidation products. Benzene oxide and phenol have been considered as proheptons. Liver microsomes play an important role in biotransformation of benzene whereas in kidney, it produces degenerative intracellular changes. Cohort studies made in different countries suggest that benzene induces multiple myeloma in petrochemical workers. Though extensive studies have been performed on its toxicity, endocrinal disruption caused by benzene remains poorly known. Transgenic cytochrome P450 IIE1 mice may help in understanding further toxic manifestations of benzene.

  19. Influence of Shenqing Recipe on Morphology and Quantity of Colonic Interstitial Cells of Cajal in Trinitrobenzene Sulfonic Acid Induced Rat Colitis

    Institute of Scientific and Technical Information of China (English)

    Yan-cheng Dai; Zhi-peng Tang; Zhen-nan Wang; Ya-li Zhang; Xin-ying He

    2011-01-01

    Objective To observe the influence of Shenqing Recipe (SQR), a kind of Traditional Chinese Medicine, on the morphology and quantity of colonic interstitial cells of Cajal (ICC) in trinitrobenzene sulfonic acid (TNBS)-induced rat colitis, and to investigate the possible mechanism of SQR in regulating intestinal dynamics. Methods Sixty rats were randomly divided into normal control, model I , model Ⅱ, mesalazine,and high-dose, and low-dose SQR groups with 10 rats in each group. TNBS (10 mg) dissolved in 50% ethanol was instilled into the lumen of the rat colon of the latter five groups to induce colitis. On the 4th day after administration of TNBS, each treatment group was administered one of the following formulations by enteroclysis gavage once a day for 7 days: 600 mg·kg-1·d-1mesalazine, 2.4 g·kg-1·d-1 SQR, and 1.2 g·kg-1·d-1 SQR. Model Ⅱ rats received normal saline solution. After 7 days colonic samples were collected. While the colonic samples of model Ⅰ group were collected on the 3rd day after TNBS administered. Ultrastructure of ICC in the damaged colonic tissues was observed with transmission electron microscope. Expression of c-kit protein in colonic tissue was determined by immunohistochemical staining and Western blot. Results The ultrastructure of colonic ICC in the rat model of TNBS-induced colitis showed a severe injury, and administration of SQR or mesalazine reduced the severity of injury. Similarly, the expression of c-kit protein of TNBS-induced colitis rat model was significantly decreased compared with the normal control group (P<0.05). Treatment with SQR or mesalazine significantly increased the expression of c-kit protein compared with the administration of control formulations (P<0.05), especially the high-dose SQR group.Conclusion SQR could alleviate and repair the injured ICC, and improve its quantity, which might be involved in regulating intestinal motility.

  20. A rapid method for the determination of perfluoroalkyl substances including structural isomers of perfluorooctane sulfonic acid in human serum using 96-well plates and column-switching ultra-high performance liquid chromatography tandem mass spectrometry.

    Science.gov (United States)

    Salihovic, Samira; Kärrman, Anna; Lindström, Gunilla; Lind, P Monica; Lind, Lars; van Bavel, Bert

    2013-08-30

    To facilitate high-throughput analysis suitable for large epidemiological studies we developed an automated column-switching ultra-performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS) method for determination of perfluorocarboxylic acids (PFCAs; C5, C6, C7, C8, C9, C10, C11, C12, and C13), perfluoroalkyl sulfonic acids (PFSAs; C4, C6, C8, and C10), perfluorooctane sulfonamide (PFOSA), and five groups of structural perfluorooctane sulfonic acid (PFOS) isomers in human serum or plasma. The analytical procedure involves rapid protein precipitation using 96-well plates followed by an automated sample clean-up using an on-line trap column removing many potentially interfering sample components while through the mobile phase gradient the target analytes are eluted onto the analytical column for further separation and subsequent mass detection. The method was linear (R(2)method detection limits ranging between 0.01 and 0.17ngmL(-1) depending on the analyte. The developed method was precise, with repeatability (n=7) and reproducibility (n=103) coefficients of variation between 2% and 20% for most compounds including PFOS (2% and 8%) and its structural isomers (2-6% and 4-8%). The method was in conformity with a standard reference material. The column-switching HPLC-MS/MS method has been successfully applied for the determination of perfluoroalkyl substances including structural PFOS isomers in human plasma from an epidemiological study.

  1. Poly(arlyene ether sulfone) based semi-interpenetrating polymer network membranes containing cross-linked poly(vinyl phosphonic acid) chains for fuel cell applications at high temperature and low humidity conditions

    Science.gov (United States)

    Kim, Kihyun; Heo, Pilwon; Ko, Taeyun; Kim, Ki-hyun; Kim, Sung-Kon; Pak, Chanho; Lee, Jong-Chan

    2015-10-01

    Semi-interpenetrating polymer network (semi-IPN) membranes are prepared by in-situ casting and thermal-initiated radical polymerization of vinyl phosphonic acid (VPA) and bis(2-(methacryloyloxy)ethyl) phosphate (BMAEP) in N,N-dimethylacetamide solutions of sulfonated poly(arylene ether sulfone) (SPAES). The incorporation of VPA units into the SPAES membranes improves proton conductivity especially at high temperature and low humidity conditions. In addition the cross-linker, BMAEP, prevents the decrease of the mechanical and chemical stabilities by the aliphatic linear poly(vinyl phosphonic acid) chains in the semi-IPN membranes, and furthermore the phosphonic acid group in BMAEP can prevent the decrease of the proton conductivity by the formation of cross-linked structures. Therefore, the resulting semi-IPN membranes show high proton conductivities up to 15 mS cm-1 at 120 °C and 40% RH. The fuel cell performance (187 mW cm-2 at 120 °C and 40% RH) of membrane-electrode assembly (MEA) from the semi-IPN membrane is found to be superior to that (145 mW cm-2 at 120 °C and 40% RH) of MEA from the SPAES membrane. The durability test result at the operating conditions indicates that the semi-IPN membrane is electrochemically very stable maintaining the low hydrogen cross-over and high power densities.

  2. Benzene from Traffic

    DEFF Research Database (Denmark)

    Palmgren, F.; Berkowicz, R.; Skov, H.;

    The measurements of benzene showed very clear decreasing trends in the air concentrations and the emissions since 1994. At the same time the measurements of CO and NOx also showed a decreasing trend, but not so strong as for benzene. The general decreasing trend is explained by the increasing...... number of petrol vehicles with three way catalysts, 60-70% in 1999. The very steep decreasing trend for benzene at the beginning of the period from 1994 was explained by the combination of more catalyst vehicles and reduced benzene content in Danish petrol. The total amount of aromatics in petrol......, including toluene, increased only weakly. The analyses of air concentrations were confirmed by analyses of petrol sold in Denmark. The concentration of benzene at Jagtvej in Copenhagen is still in 1998 above the expected new EU limit value, 5 µg/m3 as annual average. However, the reduced content of benzene...

  3. Development of Hollow-Fiber Liquid-Phase Microextraction Method for Determination of Urinary trans,trans-Muconic Acid as a Biomarker of Benzene Exposure.

    Science.gov (United States)

    Ghamari, Farhad; Bahrami, Abdulrahman; Yamini, Yadollah; Shahna, Farshid Ghorbani; Moghimbeigi, Abbas

    2016-01-01

    For the first time, hollow-fiber liquid-phase microextraction combined with high-performance liquid chromatography-ultraviolet was used to extract trans,trans-muconic acid, in urine samples of workers who had been exposed to benzene. The parameters affecting the metabolite extraction were optimized as follows: the volume of sample solution was 11 mL with pH 2, liquid membrane containing dihexyl ether as the supporter, 15% (w/v) of trioctylphosphine oxide as the carrier, the time of extraction was 120 minutes, and stirring rate was 500 rpm. Organic phase impregnated in the pores of a hollow fiber was extracted into 24 µL solution of 0.05 mol L(-1) Na2CO3 located inside the lumen of the fiber. Under optimized conditions, a high enrichment factor of 153-182 folds, relative recovery of 83%-92%, and detection limit of 0.001 µg mL(-1) were obtained. The method was successfully applied to the analysis of ttMA in real urine samples. PMID:27660405

  4. Development of Hollow-Fiber Liquid-Phase Microextraction Method for Determination of Urinary trans,trans-Muconic Acid as a Biomarker of Benzene Exposure

    Science.gov (United States)

    Ghamari, Farhad; Bahrami, Abdulrahman; Yamini, Yadollah; Shahna, Farshid Ghorbani; Moghimbeigi, Abbas

    2016-01-01

    For the first time, hollow-fiber liquid-phase microextraction combined with high-performance liquid chromatography–ultraviolet was used to extract trans,trans-muconic acid, in urine samples of workers who had been exposed to benzene. The parameters affecting the metabolite extraction were optimized as follows: the volume of sample solution was 11 mL with pH 2, liquid membrane containing dihexyl ether as the supporter, 15% (w/v) of trioctylphosphine oxide as the carrier, the time of extraction was 120 minutes, and stirring rate was 500 rpm. Organic phase impregnated in the pores of a hollow fiber was extracted into 24 µL solution of 0.05 mol L−1 Na2CO3 located inside the lumen of the fiber. Under optimized conditions, a high enrichment factor of 153–182 folds, relative recovery of 83%–92%, and detection limit of 0.001 µg mL−1 were obtained. The method was successfully applied to the analysis of ttMA in real urine samples. PMID:27660405

  5. Effect of intensity of ultraviolet light on degradation of sodium dodecyl benzene sulfonate by TiO2-bentonite%紫外光光强对TiO2-膨润土降解十二烷基苯磺酸钠的影响

    Institute of Scientific and Technical Information of China (English)

    温淑瑶; 马敏立; 陈素云; 马占青

    2011-01-01

    在室温、电磁搅拌和6W紫外灯(距静止液面距离分别为6.5 cm、18.5 cm、30.5 cm和42.5 cm)的不同光强(在静止液面处的光强分别为700~750 μW/cm2、300~310μW/cm2、200~210 μW/cm2和110~120μW/cm2),及太阳光的不同紫外光强度照射条件下,质量分数为0.5‰的纳米TiO2-膨润土复合光催化剂对初始质量浓度为20 mg/L的十二烷基苯磺酸钠(SDBS)溶液中SDBS的降解反应表明:光强对SDBS降解的影响较大,光强越强SDBS的降解率越高、溶液的COD值降低率越大;不同光强下,TiO2-膨润土对SDBS降解反应为一级反应,符合Langmuir-Hinshelwood方程;随着光强的增大,TiO2-膨润土对SDBS降解的光催化反应速率常数增大.%Different intensities of ultraviolet light (700~750 (μW/cm2 ,300~310μ/W/cm2,200~210μW/cm2 and 110-120 μW/cm2)resulted from different distances(6.5 cm, 18.5 cm,30.5 cm and 42.5 cm ) between 6 W ultraviolet light and still solution surface respectively.Original concentration of sodium dodecyl benzene sulfonate (SDBS) was 20mg/L.Under the same condition (temperature, ultraviolet light shining period, electromagnetic mixing, Ph 6 ) and different intensities of light, the results of degradation reaction of SDBS by 0.5 TiO2-bentonite show that the effect of intensity of light on degradation is obvious.The higher the intensity of ultraviolet light, the more the SDBS was degradated.The higher the intensity of ultraviolet light, the more the chemical oxide demand of solution decreased.The degradation reaction was first-order reaction.Its law of dynamics accorded with Langmuir-Hinshelwood equation.The higher the intensity of ultraviolet light, the bigger the speed coefficient of photocatalytic reaction between SDBS and TiO2-bentonite.

  6. DEVELOPMENT OF OVERBASED CALCIUM SULFONATE FOR SYNTHETIC GREASE%合成润滑脂用高碱值磺酸钙的研制

    Institute of Scientific and Technical Information of China (English)

    刘依农

    2012-01-01

    以5种烷基苯磺酸A,B,C,D,E为原料合成高碱值磺酸钙,并进一步合成润滑脂.结果发现,由C、D合成的磺酸钙转化成的润滑脂性能较好.设计正交试验,考察C、D合成磺酸钙时促进剂、助促进剂、水、二氧化碳等因素的影响,得到优化的工艺条件.在50 L反应器中进行中型放大试验,得到合格产品.其中以C为原料的磺酸钙碱值为396.1 mgKOH/g,100℃运动黏度为134.28mm2/s,以D为原料的磺酸钙碱值为391.6mgKOH/g,100℃运动黏度为92.27mm2/s,二者的碳酸钙均为无定形结构.以上两种磺酸钙进行润滑脂中型试验时发现,磺酸钙转化为润滑脂的时间短、成脂性好,润滑脂高温性能及抗水性能好,其它性能均满足产品指标要求.%5 types of alkyl benzene sulfonic acids (A,B,C,D,E) were used to synthesize overbased sulfonates which were further to be used to prepare sulfonate grease. Test results indicated that sulfon-ate grease samples prepared by calucium sulfonates Ca-C and Ca-D (from sulfonic acids C and D, respectively) exhibited better performance as compared with the others. Orthogonal experiments were designed to investigate the influence of promoter amount, co-promoter, water and carbon dioxide on the properties of calucium sulfonates, and to obtain the optimum preparation conditions. Based on these results, overbased sulfonates Ca-C and Ca-D were prepared in 50 L pilot plant reactor, the TBN of prepared Ca-C and Ca-D was 396. 1 mgKOH/g and 391. 6 mgKOH/g, respectively; their 100℃ kinetic viscosities were 134. 28 mm2/s and 92. 27 mm2/s, respectively, and both having amorphous carbonate. Finally, two sulfonate grease products were prepared by calucium sulfonates Ca-C and Ca-D in pilot plant scale, it was observed that the conversion of calucium sulfonates Ca-C/Ca-D to synthetic grease could be completed in short time. The qualities of these two products met the requirements of relative product specifications, and they exhibited

  7. Densities and Kinematic Viscosities for the Systems Benzene + Methyl Formate, Benzene + Ethyl Formate, Benzene + Propyl Formate, and Benzene + Butyl Formate

    DEFF Research Database (Denmark)

    Emmerling, Uwe; Rasmussen, Peter

    1998-01-01

    Densities and kinematic viscosities have been measured for the system benzene + methyl formate at 20°C and for the systems benzene + ethyl formate, benzene + propyl formate, and benzene + butyl formate from 20°C to 50°C. The results for the system benzene + methyl formate have been correlated using...... a Redlich-Kister type of expression with temperature-independent parameters and the data for the systems benzene + ethyl formate, benzene + propyl formate, and benzene + butyl formate with temperature-dependent parameters. The viscosities have furthermore been compared to values predicted by means of the GC...

  8. Cross-aldol Condensation of Cycloalkanones and Aromatic Aldehydes in the Presence of Nanoporous Silica-based Sulfonic Acid (SiO2-Pr-SO3H) under Solvent Free Conditions

    Institute of Scientific and Technical Information of China (English)

    MOHAMMADI ZIARANI Ghodsi; BADIEI Alireza; ABBASI Alireza; FARAHANI Zahra

    2009-01-01

    The aromatic aldehydes underwent cross aldol condensation with cycloalkanones in the presence of a catalytic amount of nanoporous silica-based sulfonic acid (SiO2-Pr-SO3H) under solvent-free conditions to afford the corresponding a,a'-bis(substituted benzylidene)cycloalkanones in excellent yields with short reaction time without any side reactions.This method is very general,simple and environmentally friendly in contrast with other existing methods.SiO2-Pr-SO3H was proved to be an efficient heterogeneous solid acid catalyst,which could be easily handled and removed from the reaction mixture by simple filtration,and also recovered and reused without loss of reactivity.

  9. Voltammetric determination of dopamine in the presence of uric acid using a 2-hydroxy-1-(1-hydroxynaphthyl-2-azo-naphthalin-4-sulfonic acid modified glassy carbon electrode

    Directory of Open Access Journals (Sweden)

    ALI ASGHAR ENSAF

    2010-12-01

    Full Text Available A polymerized film of 2-hydroxy-1-(1-hydroxynaphthyl-2-azo-naphthalin-4-sulfonic acid (HHNANSA was prepared at the surface of a glassy carbon electrode by electropolymerization. The modified electrode was used for the simultaneous determination of dopamine (DA and uric acid (UA. The electrochemical behaviors of the compounds at the surface of the modified electrode were studied using cyclic voltammetry, chronoamperometry, and square wave voltammetry (SWV. The experimental results indicated that the modified electrode exhibited an efficient electrocatalytic activity towards the oxidation of DA and UA, with a peak separation of about 140 mV at pH 5.0. Using chronoamperometry, the catalytic reaction rate constant was measured and found to equal to 1.23×104 mol-1 L s-1. At pH 5.0, the catalytic peak currents linearly depended on the DA and/or UA concentrations in the range of 1.0–300 µmol L-1 DA (two linear segments with different slopes and 6.7–20 µmol L-1 UA, using SWV. The detection limits for DA and UA were 0.25 and 1.17 µmol L-1, respectively. The RSD % for 40.0 and 140.0 µmol L-1 DA were 1.9 and 2.2 %, respectively, whereas for 10.0 and 20.0 µmol L-1 UA, they were 1.8 and 1.2 %, respectively. The modified electrode showed good sensitivity, selectivity, and stability. It was successfully applied for the determination of DA and UA in real samples, such as drugs and urine.

  10. Bis(tetra­methyl­amonium) bis­(2,4,5-carboxy­benzoate)–benzene-1,2,4,5-tetra­carboxylic acid (1/1)

    OpenAIRE

    Girginova, Penka I.; Tito Trindade; João Rocha; Jacek Klinowski; Almeida Paz, Filipe A.; Luís Cunha-Silva

    2007-01-01

    The asymmetric unit of the title compound, 2C4H12N+·2C10H5O8−·C10H6O8, consists of a tetramethylamonium cation, an anion derived from the singly deprotonated pyromellitic acid anion, 2,4,5-carboxybenzoate (H3bta−), and one-half of a benzene-1,2,4,5-tetracarboxylic acid (H4bta) molecule, which has the centroid of the aromatic ring positioned at a crystallographic centre of inversion. The H4bta and H3bta− residues are involved in an extensive intermolecular O—H...

  11. Catalytic alcoholysis of cellulose into methyl levulinate using sulfonic heteropoly solid acid%磺酸型杂化固体酸催化纤维素醇解为乙酰丙酸甲酯

    Institute of Scientific and Technical Information of China (English)

    杨卫平; 王海军; 李炜; 徐岩杰; 陈仁举

    2016-01-01

    合成了磺酸型杂化固体酸1-(3-磺酸基)丙基-3-烃基咪唑磷钨酸盐(Cn IMPS)3 PW12 O40,并将其应用于催化纤维素的醇解反应之中。与无机酸、对甲苯磺酸(PTSA)以及磷钨酸相比,(C1 IMPS)3 PW12 O40表现出更佳的催化活性。通过单因素法对反应温度、时间、催化剂用量、固液比、加水量等进行考察,结果表明,m((C1 IMPS)3 PW12 O40)∶m(Cellulose)=0.4时,(C1 IMPS)3 PW12 O40在体系中浓度4.00 mg/mL,甲醇和4.0%体积分数的水混合溶剂,反应温度190℃,时间60 min,乙酰丙酸甲酯的产率最大为41.0%。反应结束后将体系置换为水相,调节反应体系的pH值约为2时,催化剂以固体沉淀的方式析出、回收,且经过5次重复利用后仍能保持良好的催化性能。%A kind of sulfonic heteropoly solid acid,(CnIMPS)3PW12O40 (1-(3-sulfonic acid)propyl-3-hy-drocarbon imidazole phosphotungstate),had been synthesized and applied to the catalytic alcoholysis of cellulose.Compared with inorganic acids,p-toluene sulfonic acid (PTSA ) and phosphotungstic acid, (C1IMPS)3PW12O40(1-(3-sulfonic acid)propyl-3-methyl imidazole phosphotungstate)showed better cat-alytic activity.By complete randomalized design,the effect factors of reaction,temperature,time,amount of catalyst,solid-liquid ratio,the amount of water,etc.,had been investigated and optimized in detail as fol-lows∶m ((C1IMPS)3PW12O40):m(Cellulose)=0.4,the concentration of (C1IMPS)3PW12O40 in the sys-tem is 4.00 mg/mL,and 4.0%volume fraction of water mixed methanol,60 min at 190 ℃,and the yield of methyl levulinate reached 41 .0%.After reaction,the solution was replaced with water,then adjusted the pH≈2,the catalyst could be recovered,which was reused for five times with good catalytic perform-ance still maintain.

  12. Facts about Benzene

    Science.gov (United States)

    ... Lab Info Chemical Emergencies A–Z Abrin Adamsite Ammonia Arsenic Arsine Barium Benzene Brevetoxin Bromine BZ Carbon ... used to make some types of lubricants, rubbers, dyes, detergents, drugs, and pesticides. How you could be ...

  13. Improved oral absorption of cilostazol via sulfonate salt formation with mesylate and besylate

    Directory of Open Access Journals (Sweden)

    Seo JH

    2015-07-01

    Full Text Available Jae Hong Seo, Jung Bae Park, Woong-Kee Choi, Sunhwa Park, Yun Jin Sung, Euichaul Oh, Soo Kyung Bae College of Pharmacy and Integrated Research Institute of Pharmaceutical Sciences, The Catholic University of Korea, Bucheon, South Korea Objective: Cilostazol is a Biopharmaceutical Classification System class II drug with low solubility and high permeability, so its oral absorption is variable and incomplete. The aim of this study was to prepare two sulfonate salts of cilostazol to increase the dissolution and hence the oral bioavailability of cilostazol.Methods: Cilostazol mesylate and cilostazol besylate were synthesized from cilostazol by acid addition reaction with methane sulfonic acid and benzene sulfonic acid, respectively. The salt preparations were characterized by nuclear magnetic resonance spectroscopy. The water contents, hygroscopicity, stress stability, and photostability of the two cilostazol salts were also determined. The dissolution profiles in various pH conditions and pharmacokinetic studies in rats were compared with those of cilostazol-free base.Results: The two cilostazol salts exhibited good physicochemical properties, such as nonhygroscopicity, stress stability, and photostability, which make it suitable for the preparation of pharmaceutical formulations. Both cilostazol mesylate and cilostazol besylate showed significantly improved dissolution rate and extent of drug release in the pH range 1.2–6.8 compared to the cilostazol-free base. In addition, after oral administration to rats, cilostazol mesylate and cilostazol besylate showed increases in Cmax and AUCt of approximately 3.65- and 2.87-fold and 3.88- and 2.94-fold, respectively, compared to cilostazol-free base.Conclusion: This study showed that two novel salts of cilostazol, such as cilostazol mesylate and cilostazol besylate, could be used to enhance its oral absorption. The findings warrant further preclinical and clinical studies on cilostazol mesylate and

  14. Benzene Monitor System report

    Energy Technology Data Exchange (ETDEWEB)

    Livingston, R.R.

    1992-10-12

    Two systems for monitoring benzene in aqueous streams have been designed and assembled by the Savannah River Technology Center, Analytical Development Section (ADS). These systems were used at TNX to support sampling studies of the full-scale {open_quotes}SRAT/SME/PR{close_quotes} and to provide real-time measurements of benzene in Precipitate Hydrolysis Aqueous (PHA) simulant. This report describes the two ADS Benzene Monitor System (BMS) configurations, provides data on system operation, and reviews the results of scoping tests conducted at TNX. These scoping tests will allow comparison with other benzene measurement options being considered for use in the Defense Waste Processing Facility (DWPF) laboratory. A report detailing the preferred BMS configuration statistical performance during recent tests has been issued under separate title: Statistical Analyses of the At-line Benzene Monitor Study, SCS-ASG-92-066. The current BMS design, called the At-line Benzene Monitor (ALBM), allows remote measurement of benzene in PHA solutions. The authors have demonstrated the ability to calibrate and operate this system using peanut vials from a standard Hydragard{trademark} sampler. The equipment and materials used to construct the ALBM are similar to those already used in other applications by the DWPF lab. The precision of this system ({+-}0.5% Relative Standard Deviation (RSD) at 1 sigma) is better than the purge & trap-gas chromatograpy reference method currently in use. Both BMSs provide a direct measurement of the benzene that can be purged from a solution with no sample pretreatment. Each analysis requires about five minutes per sample, and the system operation requires no special skills or training. The analyzer`s computer software can be tailored to provide desired outputs. Use of this system produces no waste stream other than the samples themselves (i.e. no organic extractants).

  15. An efficient synthesis of substituted benzene-1,2-dicarboxaldehydes

    Institute of Scientific and Technical Information of China (English)

    ZHU Peter C; WANG Dei-Haw; LU Kaitao; MANI Neelakandha

    2007-01-01

    Substituted-benzene-1,2-dicarbaldehydes were synthesized by the reaction of substituted-1,2-bis (dibromomethyl) benzenes with fuming sulfuric acid, followed by hydrolysis, The yields were significantly improved by introducing solid sodium bicarbonate into the reaction mixture before hydrolysis and workup.

  16. An efficient synthesis of substituted benzene-1,2-dicarboxaldehydes

    Institute of Scientific and Technical Information of China (English)

    ZHU; Peter; C; WANG; Der-Haw; MANI; Neelakandha

    2007-01-01

    Substituted-benzene-1,2-dicarbaldehydes were synthesized by the reaction of substituted-1,2-bis(dibromomethyl) benzenes with fuming sulfuric acid,followed by hydrolysis. The yields were signifi-cantly improved by introducing solid sodium bicarbonate into the reaction mixture before hydrolysis and workup.

  17. Proton-conducting membrane based on epoxy resin-poly(vinyl alcohol)-sulfosuccinic acid blend and its nanocomposite with sulfonated multiwall carbon nanotubes for fuel-cell application

    Science.gov (United States)

    Kakati, Nitul; Das, Gautam; Yoon, Young Soo

    2016-01-01

    A blend of poly(vinyl alcohol) (PVA) with diglycidyl ether of bisphenol-A (DGB) in the presence of sulfosuccinic acid (SSA) was investigated as hydrolytically-stable proton-conducting membrane. The PVA modification was carried out by varying the DGB:SSA ratio (20:20, 10:20, and 5:20). A nanocomposite of the blend (20:20) was prepared with sulfonated multiwall carbon nanotubes (viz., 1, 3 and 5 wt%). The water uptake behavior and the proton conductivity of the prepared membranes were evaluated. The ionic conductivity of the membranes and the water uptake behavior depended on the s-MWCNT and the DGB contents. The ionic conductivity showed an enhancement for the blend and for the nanocomposite membrane as compared to the pristine polymer.

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

    Science.gov (United States)

    Changkhamchom, Sairung; Sirivat, Anuvat

    2012-02-01

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

  19. Sulfonation and characterization of styrene-indene copolymers for the development of proton conducting polymer membranes

    Directory of Open Access Journals (Sweden)

    Cristiane M. Becker

    2012-01-01

    Full Text Available The aim of this work is to obtain polymer precursors based on styrene copolymers with distinct degrees of sulfonation, as an alternative material for fuel cell membranes. Acetyl sulfate was used to carry out the sulfonation and the performance of the polyelectrolyte was evaluated based on the content of acid polar groups incorporated into the macromolecular chain. Polymeric films were produced by blending the sulfonated styrene-indene copolymer with poly(vinylidene fluoride. The degree of sulfonation of the polymer was strongly affected by the sulfonation reaction parameters, with a direct impact on the ionic exchange capacity and the ionic conductivity of the sulfonated polymers and the membranes obtained from them. The films produced with the blends showed more suitable mechanical properties, although the conductivity of the membranes was still lower than that of commercially available membranes used in fuel cells.

  20. Genotoxicity of intermittent co-exposure to benzene and toluene in male CD-1 mice.

    Science.gov (United States)

    Wetmore, Barbara A; Struve, Melanie F; Gao, Pu; Sharma, Sheela; Allison, Neil; Roberts, Kay C; Letinski, Daniel J; Nicolich, Mark J; Bird, Michael G; Dorman, David C

    2008-06-17

    Benzene is an important industrial chemical. At certain levels, benzene has been found to produce aplastic anemia, pancytopenia, myeloblastic anemia and genotoxic effects in humans. Metabolism by cytochrome P450 monooxygenases and myeloperoxidase to hydroquinone, phenol, and other metabolites contributes to benzene toxicity. Other xenobiotic substrates for cytochrome P450 can alter benzene metabolism. At high concentrations, toluene has been shown to inhibit benzene metabolism and benzene-induced toxicities. The present study investigated the genotoxicity of exposure to benzene and toluene at lower and intermittent co-exposures. Mice were exposed via whole-body inhalation for 6h/day for 8 days (over a 15-day time period) to air, 50 ppm benzene, 100 ppm toluene, 50 ppm benzene and 50 ppm toluene, or 50 ppm benzene and 100 ppm toluene. Mice exposed to 50 ppm benzene exhibited an increased frequency (2.4-fold) of micronucleated polychromatic erythrocytes (PCE) and increased levels of urinary metabolites (t,t-muconic acid, hydroquinone, and s-phenylmercapturic acid) vs. air-exposed controls. Benzene co-exposure with 100 ppm toluene resulted in similar urinary metabolite levels but a 3.7-fold increase in frequency of micronucleated PCE. Benzene co-exposure with 50 ppm toluene resulted in a similar elevation of micronuclei frequency as with 100 ppm toluene which did not differ significantly from 50 ppm benzene exposure alone. Both co-exposures - 50 ppm benzene with 50 or 100 ppm toluene - resulted in significantly elevated CYP2E1 activities that did not occur following benzene or toluene exposure alone. Whole blood glutathione (GSH) levels were similarly decreased following exposure to 50 ppm benzene and/or 100 ppm toluene, while co-exposure to 50 ppm benzene and 100 ppm toluene significantly decreased GSSG levels and increased the GSH/GSSG ratio. The higher frequency of micronucleated PCE following benzene and toluene co-exposure when compared with mice exposed to

  1. 21 CFR 573.600 - Lignin sulfonates.

    Science.gov (United States)

    2010-04-01

    ... 21 Food and Drugs 6 2010-04-01 2010-04-01 false Lignin sulfonates. 573.600 Section 573.600 Food... Additive Listing § 573.600 Lignin sulfonates. Lignin sulfonates may be safely used in animal feeds in... feeds, as liquid lignin sulfonate, in an amount not to exceed 11 percent of the molasses. (4) As...

  2. Adsorption mechanism and dispersion efficiency of three anionic additives [poly(acrylic acid), poly(styrene sulfonate) and HEDP] on zinc oxide.

    Science.gov (United States)

    Dange, C; Phan, T N T; André, V; Rieger, J; Persello, J; Foissy, A

    2007-11-01

    Adsorption on ZnO of sodium poly(acrylate) (PAA), sodium poly(styrene sulfonate) (PSS) and a monomer surfactant [hydroxyethylidene diphosphonate (HEDP)] was investigated in suspensions initially equilibrated at pH 7. Results demonstrate interplay in the adsorption mechanism between zinc complexation, salt precipitation, and ZnO dissolution. In the case of PAA, the adsorption isotherm exhibits a maximum attributed to the precipitation of zinc polyacrylate. PSS and HEDP formed high-affinity adsorption isotherms, but the plateau adsorption of HEDP was significantly lower than that of PSS. The adsorption isotherm of each additive is divided into two areas. At low additive concentration (high zinc/additive ratio), the total zinc concentration in the solution decreased and the pH increased upon addition. At a higher additive ratio, zinc concentration and pH increased with the organic concentration. The increase in pH is due to the displacement of hydroxyl ions from the surface and the increase in zinc concentration results from the dissolution of ZnO due to the complexation of zinc ions by the organics. The stability of the ZnO dispersions was investigated by measurement of the particle size distribution after addition of various amounts of polymers. The three additives stabilized the ZnO dispersions efficiently once full surface coverage was reached. PMID:17720181

  3. Synthesis and characterization of sulfonated polyesters derived from glycerol; Sintese e caracterizacao de poliesteres sulfonados obtidos a partir do glicerol

    Energy Technology Data Exchange (ETDEWEB)

    Fiuza, R.A.; Jose, N.M.; Boaventura, J.S. [Universidade Federal da Bahia (IQ/UFBA), Salvador, BA (Brazil). Inst. de Quimica; Fiuza, R.P. [Universidade Federal da Bahia (EP/UFBA), Salvador, BA (Brazil). Escola Politecnica. Curso de Mestrado em Engenharia Quimica

    2010-07-01

    In this work were synthesized polyesters from glycerol and acid sulfonated phthalic previously. The materials were characterized by DSC, TGA, FTIR, SEM, XRD and XRF. The results showed effective sulfonation of phthalic acid. The presence of sulfonic groups promoted strong changes in the crystallinity of the new material makes the lens. The polyesters made from phthalic acid sulfonated combine characteristics such as heat resistance and groups that drivers potentiate the electrolyte for application in fuel cells proton exchange membrane and also for gas separation. (author)

  4. 全氟磺酸类物质在沙质沉积物中的迁移规律%Transport behavior of perfluorinated sulfonic acids in sandy sediment

    Institute of Scientific and Technical Information of China (English)

    宋彦敏; 刘慧; ZAKARI Sissou; 童蕾; 彭月娥

    2016-01-01

    This study aimed to investigate the transport behavior of perfluorinated sulfonic acids (PFSAs) in typical sandy provide sediment,and provide better understanding about the source and control of PFSAs pollution in groundwater.Miscible displacement experiments were conducted,and the breakthrough curves of perfluorohexane sulfonate (PFHxS),perfluoroheptane sulfonate (PFHpS),perfluorooctane sulfonate (PFOS) and its two isomers (iso-PFOS-1 and iso-PFOS-2),were simulated using different models coupled in HYDRUS-1D software.The best simulation model was determined and the transport parameters were computed by inverse estimation.Results showed that the linear first-order two-site non-equilibrium adsorption model was most suitable for the simulation of PFSAs transport in sandy aquifer sediment.And the transport velocities of PFSAs were remarkably different.When water flowed 1000 m,PFHxS,PFHpS,PFOS,iso-PFOS-1,and iso-PFOS-2 moved 457.1,84.4,67.1,250.8,and 280.1 m,respectively.These differences were related to the surface sorption characteristics and molecular diffusion rate of PFSAs due to their different molecular structures.%本工作的目的在于研究全氟磺酸类物质(PFSAs)在典型地下沙质含水层沉积物中的迁移规律,以便于更好地了解地下水中PFSAs的来源和控制措施.通过柱迁移实验获得全氟己烷磺酸(PFHxS)、全氟庚烷磺酸(PFHpS)、全氟辛烷磺酸(n-PFOS)及其两种同分异构体(iso-PFOS-1和iso-PFOS-2)的穿透曲线;用HYDRUS-1D软件中不同的数学模型来模拟穿透曲线,对比确定了最优模拟模型,通过反演推算获取运移参数;并对比了不同PFSAs的迁移规律.研究结果表明,线性一级两位非平衡吸附模型是最优的模拟模型;不同PFSAs的迁移速率有较大的区别:当水流动1000 m时,PFHxS,PFHpS,n-PFOS,iso-PFOS-1和iso-PFOS-2分别迁移了457.1、84.4、67.1、250.8、280.1 m;这种差异与PFSAs分子结构引起的表面吸附特性与分子扩散速率相关.

  5. 卡络磺钠和氨甲环酸治疗肺结核咯血的疗效%Carbazochrome Sodium Sulfonate and Tranexamic Acid for the Treatment of Pulmonary Tuberculosis Hemoptysis

    Institute of Scientific and Technical Information of China (English)

    杜冉

    2013-01-01

    Objective Observation of carbazochrome sodium sulfonate and tranexamic acid in the treatment of hemoptysis of pulmonary tuberculosis the clinical ef ect. Methods In 2010 January~2012 June treated 60 cases of patients with pulmonary tuberculosis hemoptysis as the research object, divide them into two groups, Group A (n=30) patients using carbazochrome sodium sulfonate treatment, B group (n=30) using tranexamic acid treatment, comparative analysis of two groups of patients with clinical ef ects and adverse reactions. Results A group (5.6±3) bleeding time is slightly shorter than the H B group (6±3.3) bleeding time of H, but the two groups of hemostatic time dif erence was not significant, the difference was not statisticaly significant (P>0.05);after treatment, A group total effective rate was 93.5%, total effective rate was 90% in group B the two group, no significant difference, the dif erence was not statisticaly significant (P>0.05); A group did not show any adverse reaction in 7 cases in group B, the occurrence of adverse reactions, between the two groups was significant, with statistical significance (P<0.05). Conclusion For mild hemoptysis of pulmonary tuberculosis, recommended the use of carbazochrome sodium sulfonate treatment, for the more serious hemoptysis of pulmonary tuberculosis, suggested that the preferred tranexamic acid treatment.%  目的观察卡络磺钠和氨甲环酸在治疗肺结核咯血方面的临床效果。方法将2010年1月~2012年6月期间收治的60例肺结核咯血患者为研究对象,将其随机分为两组,A组(n=30)患者采用卡络磺钠治疗,B组(n=30)采用氨甲环酸治疗,对比分析两组患者的临床效果以及不良反应。结果 A组的止血时间(5.6±3.0)h要略短于B组的止血时间(6.0±3.3)h,但两组止血时间差异不显著,不具有统计学意义(P>0.05);经过治疗后,A组总有效率为93.5%, B组总有效率为90.0%,两组差异不显著

  6. 杯[4]芳烃磺酸钠催化合成乙酸正丁酯%Synthesis of n-Butyl Acetate Using Calix[4]arene Sulfonic Acid Sodium as a Catalyst

    Institute of Scientific and Technical Information of China (English)

    刘丽梅; 张岱良; 陈平

    2014-01-01

    以杯[4]芳烃磺酸钠为催化剂,以乙酸与正丁醇为原料,通过酯化反应合成乙酸正丁酯,考察了催化剂用量、原料配比和反应时间对酯化反应的影响,产品进行折光指数检测。结果表明,杯[4]芳烃磺酸钠作为催化剂,乙酸物质的量为0.1 mol,醇酸物质的量比为1.2,催化剂质量为1 g,反应时间为4 h时,酯化率可达81.41%,杯[4]芳烃磺酸钠可以重复使用多次。%Calix[4]arene Sulfonic Acid Sodium was used as a non homogenous catalyst for synthesis of n-Butyl acetate using acetic acid and n-butyl alcohol as raw materials.The effects of reaction conditions,such as the quantity of catalyst,the ratio of the reactants and reaction time were discussed respectively.The product was characterized by index of refraction.The suitable conditions for the reaction were as follows:acetic acid 0.1 mol,molar ratio of n-butyl alcohol to acetic acid 1.2,catalyst amout 1 g,reaction time 4 h,the yield of n-butyl acetate can reach 81.41%.The catalyst could be used repeatedly keeping its initial activity.

  7. 三硝基苯磺酸诱导的慢性胰腺炎模型在疼痛研究中的应用%Application of trinitrobenze sulfonic acid-induced chronic pancreatitis rat model in pain study

    Institute of Scientific and Technical Information of China (English)

    王锋; 沈佳庆; 王兴鹏

    2012-01-01

    Objective To evaluate the application of chronic pancreatitis (CP) model induced by trinitrobenze sulfonic acid (TNBS) in pain study. Methods CP was induced by intraductual infusion of 2% TNBS in rats. Histopathological examination and serum amylase and lipase measurement were performed for the validation of CP. Pain resulting from CP was studied as abdominal sensitivity to Von Frey Filament stimulation on week 1,2,3 and 4 after the induction of CP. Results Progressive fibrosis and parenchyma injury were observed in tissue sections after 4 weeks of TNBS treatment. Abdominal pain was observed in TNBS treated rats and the severity was increased over time. Conclusion The rat CP model induced by TNBS is suitable in pain study.%目的 探讨三硝基苯磺酸(trinitrobenze sulfonic acid,TNBS)建立的慢性胰腺炎(chronic pancreatitis,CP)模型在CP腹痛研究中的适用性.方法 2% TNBS逆行胆胰管灌注建立大鼠CP模型.观察血清淀粉酶、脂肪酶和组织学以评价造模是否成功.Von Frey Filament测试检测不同时间点(1、2、3和4周)大鼠腹部的阳性反应,进而推测大鼠胰腺疼痛的改变.结果 TNBS处理4周后,大鼠胰腺出现实质损伤和进行性纤维化,具有CP的组织病理学改变.Von Frey Filament检测显示CP造模后,随着时间推移,大鼠腹部阳性反应逐渐增加.结论 TNBS不但适用于CP动物模型的建立,而且还适用于CP疼痛的基础研究.

  8. Establishment of biological limit value of urinary S-phenylmercapturic acid for occupational exposure to benzene%职业接触苯尿中苯巯基尿酸生物限值研究

    Institute of Scientific and Technical Information of China (English)

    梅勇; 宋世震; 陈斯琦; 叶玉杰; 叶方立

    2009-01-01

    Objective To establish the biological exposure limit values of urinary S-phenylmercap-turic acid (SPMA) for assessing occupational exposure to benzene. Methods Study participants were selected from 55 workers of benzene exposures below 32.5 mg/m~3. The concentration of personal exposure to benzene was measured by gas chromatography and sampled with personal sampler. The urine samples were collected at the end of work shift and individual internal exposure level was evaluated by determination of SPMA in urine by HPLC/MS method. Comparison of external and internal exposure was assessed by the relative internal expo-sure(RIE) index. Results The benzene exposure level ranged from 0.71 to 32.17 mg/m~3 (geometric mean 6.98 mg/m~3, median 7.50 mg/m~3). The urinary SPMA at the end of the work shift were significantly correlated with benzene exposure, Y (μg/g Cr)=-8.625 + 18.367X (mg/m~3), r=0.8035, (P<0.01). According to the occupational exposure limit for benzene in China and calculation of regression equation, the expected value of urinary SPMA was 101.58 μg/g Cr. Mean level of biotransformation of per mg/m~3 benzene to urinary SPMA was 18.23 μg/g Cr and the metabolic efficiencies of benzene transformation to urinary SPMA decreased with benzene exposure in-creased. Conclusion Based on abroad documents and data, biological limit value for occupational exposure to benzene in China is recommended as follows: 100 μg/g Cr (47 μmol/mol Cr) for SPMA in the urine at the end of shift.%目的 研制我国职业接触苯工人尿中苯巯基尿酸(SPMA)的生物限值.方法 在苯作业车间选择空气中苯浓度在32.5 mg/m~3以下接苯工人55人,应用个体采样器采集空气样品,用气相色谱法检测作业者个体苯接触水平,同时采集当日工人班后尿,应用高压液相色谱/质谱法(HPLC/MS)测定尿中SPMA含量以评价苯接触者的内暴露水平,内外暴露水平的比较用相对内暴露指数(RIE)加以评定.结果 接苯工人工作

  9. Electrical conductivity of sulfonated poly(ether ether ketone) based composite membranes containing sulfonated polyhedral oligosilsesquioxane

    Science.gov (United States)

    Celso, Fabricio; Mikhailenko, Serguei D.; Rodrigues, Marco A. S.; Mauler, Raquel S.; Kaliaguine, Serge

    2016-02-01

    Composite proton exchange membranes (PEMs) intended for fuel cell applications were prepared by embedding of various amounts of dispersed tri-sulfonic acid ethyl POSS (S-Et-POSS) and tri-sulfonic acid butyl POSS (S-Bu-POSS) in thin films of sulfonated poly ether-ether ketone. The electrical properties of the PEMs were studied by Impedance spectroscopy and it was found that their conductivity σ changes with the filler content following a curve with a maximum. The water uptake of these PEMs showed the same dependence. The investigation of initial isolated S-POSS substances revealed the properties of typical electrolytes, which however in both cases possessed low conductivities of 1. 17 × 10-5 S cm-1 (S-Et-POSS) and 3.52 × 10-5 S cm-1 (S-Bu-POSS). At the same time, the insoluble in water S-POSS was found forming highly conductive interface layer when wetted with liquid water and hence producing a strong positive impact on the conductivity of the composite PEM. Electrical properties of the composites were analysed within the frameworks of effective medium theory and bounding models, allowing to evaluate analytically the range of possible conductivity values. It was found that these approaches produced quite good approximation of the experimental data and constituted a fair basis for interpretation of the observed relationship.

  10. 丙烯腈-苯乙烯磺酸共聚物/层状双金属氢氧化物纳米复合质子传导聚合物电解质的制备与表征%Synthesis and characterization of proton-conducting polymer electrolytes based on acrylonitrile-styrene sulfonic acid copolymer/layered double hydroxides nanocomposites

    Institute of Scientific and Technical Information of China (English)

    王盎然; 包永忠; 翁志学; 黄志明

    2008-01-01

    Acrylonitrile-sodium styrene sulfonate copolymer/layered double hydroxides nanocomposites were prepared by in situ aqueous precipitation copolymerization of acrylonitrile (AN) and sodium styrene sulfonate (SSS) in the presence of 4-vinylbenzene sulfonate intercalated layered double hydroxides (MgAl-VBS LDHs) and transferred to acrylonitrile-styrene sulfonic acid (AN-SSA) copolymer/LDHs nanocomposites as a proton-conducting polymer electrolyte. MgAl-VBS LDHs were prepared by a coprecipitation method, and the structure and composition of MgAl-VBS LDHs were determined by X-ray diffraction (XRD), infrared spectroscopy, and elemental analysis. X-ray diffraction result of AN-SSS copolymer/LDHs nanocomposites indicated that the LDHs layers were well dispersed in the AN-SSS copolymer matrix. All the AN-SSS copolymer/LDHs nanocomposites showed significant enhancement of the decomposition temperatures compared with the pristine AN-SSS copolymer, as identified by the thermogravimetric analysis. The methanol crossover was decreased and the proton conductivity was highly enhanced for the AN-SSA copolymer/LDHs nanocomposite electrolyte systems In the case of the nanocomposite electrolyte containing 2% (by mass) LDHs, the proton conductivity of 2.60×10-3 S·m-1 was achieved for the polymer electrolyte.

  11. Synthesis and characterization of sulfonic acid membranes based on interpenetrating polymer networks for application in fuel cells; Sintese e caracterizacao de membranas sulfonadas baseadas em redes polimericas interpenetrantes para aplicacao em celulas a combustivel

    Energy Technology Data Exchange (ETDEWEB)

    Blanco, Lyzed Toloza; Loureiro, Felipe A.M.; Rocco, Ana Maria [Grupo de Materiais Condutores e Energia, Escola de Quimica, Universidade Federal do Rio de Janeiro (UFRJ), RJ (Brazil)], e-mail: amrocco@eq.ufrj.br; Pereira, Robson Pacheco [Instituto de Ciencias Exatas, Universidade Federal Fluminense (UFF), Volta Redonda, RJ (Brazil)

    2011-07-01

    In the present work, the synthesis and characterization of sulfonic membranes based on interpenetrating polymer networks (IPN). In order to obtain such systems, the diglycidyl ether of bisphenol A (DGEBA) was polymerized in presence of polyethyleneimine (PEI). These membranes were submitted to sulfonation reactions, originating IPN-SO{sub 3}H membranes. The characterization by FTIR evidenced the formation of a Semi-IPN structure, while sulfonation reactions resulted in systems containing -SO{sub 3}H groups covalently bonded to the chains. The membranes exhibited water retention up to 200 degree C, in a temperature range sufficient for application in PEMFC under hydration. (author)

  12. HPLC Analysis of Impurity in p-Amino Benzene Sulfonic Acid%高效液相色谱法测定对氨基苯磺酸中的有关杂质

    Institute of Scientific and Technical Information of China (English)

    王燕桓; 高慧; 石志红

    2002-01-01

    用反相高效液相色谱法同时测定工业对氨基苯磺酸中的几种微量杂质 (邻氨基苯磺酸、间氨基苯磺酸、苯胺).以0.1 mol/L 磷酸二氢铵为流动相,采用SUPELCOSIL LC-18-DB(5 μm,150 mm×4.6 mm I.D.)色谱柱,紫外检测波长 205 nm,流速1 mL/min.方法快速准确、灵敏度高、重现性好,测定结果令人满意.

  13. Flame Atomic Absorption Spectrometric Determination of Trace Metal Ions in Environmental and Biological Samples After Preconcentration on a Newly Developed Amberlite XAD-16 Chelating Resin Containing p-Aminobenzene Sulfonic Acid.

    Science.gov (United States)

    Islam, Aminul; Ahmad, Akil; Laskar, Mohammad Asaduddin

    2015-01-01

    Amberlite® XAD-16 was functionalized with p-aminobenzene sulfonic acid via an azo spacer in order to prepare a new chelating resin, which was then characterized by water regain value, hydrogen ion capacity, elemental analyses, and IR spectral and thermal studies. The maximum uptake of Cu(II), Ni(II), Zn(II), Co(II), Cr(III), Fe(III), and Pb(II) ions was observed in the pH range 4.0-6.0 with the corresponding half-loading times of 6.5, 7.0, 8.0, 9.0, 11.0, 8.5, and 16.5 min. The sorption data followed Langmuir isotherms and a pseudo-second-order model. Thermodynamic quantities, ΔH and ΔS, based on the variation of the distribution coefficient with temperature were also evaluated. High preconcentration factors of 60-100 up to a low preconcentration limit of 4.0-6.6 μg/L have been achieved for the metal ions. The validity of the method was checked by analyzing standard reference materials and recoveries of trace metals after spiking. The analytical applications of the method were explored by analyzing natural water, mango pulp, mint leaves, and fish. PMID:25857893

  14. NCX-1015, a nitric-oxide derivative of prednisolone, enhances regulatory T cells in the lamina propria and protects against 2,4,6-trinitrobenzene sulfonic acid-induced colitis in mice

    Science.gov (United States)

    Fiorucci, Stefano; Antonelli, Elisabetta; Distrutti, Eleonora; Del Soldato, Piero; Flower, Roderick J.; Clark, Mark J. Paul; Morelli, Antonio; Perretti, Mauro; Ignarro, Louis J.

    2002-01-01

    NCX-1015 is a nitric oxide (NO)-releasing derivative of prednisolone. In this study we show NCX-1015 protects mice against the S. A. development and induces healing of T helper cell type 1-mediated experimental colitis induced by intrarectal administration of 2,4,6-trinitrobenzene sulfonic acid (TNBS). The beneficial effect of NCX-1015 was reflected in increased survival rates, improvement of macroscopic and histologic scores, a decrease in the mucosal content of T helper cell type 1 cytokines (protein and mRNA), and diminished myeloperoxidase activity in the colon. In contrast to its NO derivative, only very high doses of prednisolone were effective in reproducing these beneficial effects. NCX-1015 was 10- to 20-fold more potent than the parent compound in inhibiting IFN-γ secretion by lamina propria mononuclear cells. Protection against developing colitis correlated with inhibition of nuclear translocation of p65/Rel A in these cells. In vivo treatment with NCX-1015 potently stimulated IL-10 production, suggesting that the NO steroid induces a regulatory subset of T cells that negatively modulates intestinal inflammation. PMID:12427966

  15. Syntheses, structures, and properties of Co(II)/Zn(II) mixed-ligand coordination polymers based on 4-[(3,5-dinitrobenzoyl)amino]benzoic acid and 1,4-bis(1-imidazolyl) benzene

    International Nuclear Information System (INIS)

    Two coordination polymers [Co(dnbab)2(bimb)](H2O)4 (1) and [Zn(dnbab)2(bimb)](H2O)5 (2) (Hdnbab=4-[(3,5-dinitrobenzoyl)amino]benzoic acid, bimb=1,4-bis(1-imidazolyl) benzene) have been solvothermally synthesized. Their structures have been determined by single-crystal X-ray diffraction analyses and further characterized by powder X-ray diffraction (PXRD) and thermogravimetric (TG) analyses. Complexes 1 and 2 are isostructures and each displays an one-dimensional (1D) zigzag chain, which further forms a 3D supramolecular architecture with 1-D channels via inter-chain π–π interactions and hydrogen bonds. Moreover, the magnetic properties of 1 and fluorescent properties of 2 have been investigated. - Graphical abstract: Two coordination supramolecular frameworks [Co(dnbab)2(bimb)](H2O)4(1) and [Zn(dnbab)2(bimb)](H2O)5(2) (Hdnbab=4-[(3,5-dinitrobenzoyl)amino]benzoic acid, bimb=1,4-bis(1-imidazolyl) benzene) have been synthesized and characterized by X-ray single-crystal diffraction. Their thermal, magnetic and fluorescent properties have also been studied. - Highlights: • Two isomorphic Co(II)/Zn(II) complexes with the mixed-ligands have been synthesized. • Hydrogen bonds and π–π stacking interactions directed the final 3-D architecture assembly. • Both Co(II) and Zn(II) complexes show good thermal stability. • Co complex exhibits antiferromagnetic interaction. • The fluorescent property of Zn(II) complex has been investigated in the solid state

  16. Syntheses, structures, and properties of Co(II)/Zn(II) mixed-ligand coordination polymers based on 4-[(3,5-dinitrobenzoyl)amino]benzoic acid and 1,4-bis(1-imidazolyl) benzene

    Energy Technology Data Exchange (ETDEWEB)

    Yin, Fei; Chen, Jing; Liang, Yongfeng [Department of Chemistry, Zhejiang Sci-Tech University, Hangzhou, Zhejiang 310018 (China); Zou, Yang, E-mail: zouyang@zstu.edu.cn [Department of Chemistry, Zhejiang Sci-Tech University, Hangzhou, Zhejiang 310018 (China); Yinzhi, Jiang [Department of Chemistry, Zhejiang Sci-Tech University, Hangzhou, Zhejiang 310018 (China); Xie, Jingli, E-mail: jlxie@mail.zjxu.edu.cn [College of Biological, Chemical Sciences and Engineering, Jiaxing University, Jiaxing, Zhejiang 314001 (China)

    2015-05-15

    Two coordination polymers [Co(dnbab){sub 2}(bimb)](H{sub 2}O){sub 4} (1) and [Zn(dnbab){sub 2}(bimb)](H{sub 2}O){sub 5} (2) (Hdnbab=4-[(3,5-dinitrobenzoyl)amino]benzoic acid, bimb=1,4-bis(1-imidazolyl) benzene) have been solvothermally synthesized. Their structures have been determined by single-crystal X-ray diffraction analyses and further characterized by powder X-ray diffraction (PXRD) and thermogravimetric (TG) analyses. Complexes 1 and 2 are isostructures and each displays an one-dimensional (1D) zigzag chain, which further forms a 3D supramolecular architecture with 1-D channels via inter-chain π–π interactions and hydrogen bonds. Moreover, the magnetic properties of 1 and fluorescent properties of 2 have been investigated. - Graphical abstract: Two coordination supramolecular frameworks [Co(dnbab){sub 2}(bimb)](H{sub 2}O){sub 4}(1) and [Zn(dnbab){sub 2}(bimb)](H{sub 2}O){sub 5}(2) (Hdnbab=4-[(3,5-dinitrobenzoyl)amino]benzoic acid, bimb=1,4-bis(1-imidazolyl) benzene) have been synthesized and characterized by X-ray single-crystal diffraction. Their thermal, magnetic and fluorescent properties have also been studied. - Highlights: • Two isomorphic Co(II)/Zn(II) complexes with the mixed-ligands have been synthesized. • Hydrogen bonds and π–π stacking interactions directed the final 3-D architecture assembly. • Both Co(II) and Zn(II) complexes show good thermal stability. • Co complex exhibits antiferromagnetic interaction. • The fluorescent property of Zn(II) complex has been investigated in the solid state.

  17. Radiolysis of Aqueous Benzene Solutions

    International Nuclear Information System (INIS)

    Aerated and deaerated aqueous solutions of benzene have been irradiated with 60Co γ-rays. The products of radiolysis in deaerated, unbuffered or acid, solutions were phenol, biphenyl, hydrogen and in acid solutions also hydrogen peroxide with the following yields: G(phenol) = 0. 37 (0. 37), G(biphenyl) = 1.3 (1.7), G(H2) = 0.44 (0. 43) and G(H2O2) = 0 (0.60), the figures in brackets giving the results for acid solutions. The results are shown to agree with the conclusion that k(e-aq + H2O2) >> k(H + H2O2). Furthermore, the results indicate that a competition takes place between the reactions: 2 C6H6OH · -> dimer -> biphenyl. C6H7 · + C6H6OH · -> dimer -> biphenyl. The yields in aerated, unbuffered or acid, solutions were: G(phenol) = 2.1 (2.3), G(biphenyl) = 0 (0), and G(H2O2) = 2.2 (3.1), the figures in brackets being valid for acid solutions. The ratio k(H + C6H6)/k(H + O2) was 1.4x10-2. The results indicate that peroxides, or more probably hydroperoxides, take part in the reactions. After the addition of Fe2+ or Fe3+ to aerated acid solutions G(phenol) was increased to 6.6 and 3.4 respectively. Oxygen was consumed more rapidly in the presence of Fe. Reaction mechanisms are discussed

  18. A physiological model for simulation of benzene metabolism by rats and mice.

    Science.gov (United States)

    Medinsky, M A; Sabourin, P J; Lucier, G; Birnbaum, L S; Henderson, R F

    1989-06-15

    Studies conducted by the National Toxicology Program on the chronic toxicity of benzene indicated that B6C3F1 mice are more sensitive to the toxic effects of benzene than are F344 rats. A physiological model was developed to describe the uptake and metabolism of benzene in rats and mice and to determine if the observed differences in toxic effects could be explained by differences in the pathways for metabolism of benzene or by differences in uptake of benzene. Major pathways for elimination of benzene included metabolism to hydroquinone glucuronide or hydroquinone sulfate, phenyl glucuronide or phenyl sulfate, muconic acid, and prephenyl mercapturic acid or phenyl mercapturic acid. Model simulations for total benzene metabolized and for profiles of benzene metabolites were conducted for oral or inhalation exposure and compared to data for urinary excretion of benzene metabolites after exposure of rats and mice to [14C]- or [3H]-benzene by inhalation or gavage. Results for total amount of benzene metabolized, expressed per kilogram body weight, indicated that for inhalation exposure concentrations up to 1000 ppm, mice metabolized at least two to three times as much benzene as did rats. Simulations of oral exposure to benzene resulted in more benzene metabolized per kilogram body weight by rats at oral exposures of greater than 50 mg/kg. Patterns of metabolites formed after either route of exposure were very different for F344/N rats and B6C3F1 mice. Rats primarily formed the detoxification metabolite, phenyl sulfate. Mice formed hydroquinone glucuronide and muconic acid in addition to phenyl sulfate. Hydroquinone and muconic acid are associated with pathways leading to the formation of the putative toxic metabolites of benzene. Metabolic rate parameters, Vmax and Km, were very different for hydroquinone conjugate and muconic acid formation compared to formation of phenyl conjugates and phenyl mercapturic acids. Putative toxication pathways could be characterized as

  19. Benzene exposure: an overview of monitoring methods and their findings.

    Science.gov (United States)

    Weisel, Clifford P

    2010-03-19

    Benzene has been measured throughout the environment and is commonly emitted in several industrial and transportation settings leading to widespread environmental and occupational exposures. Inhalation is the most common exposure route but benzene rapidly penetrates the skin and can contaminant water and food resulting in dermal and ingestion exposures. While less toxic solvents have been substituted for benzene, it still is a component of petroleum products, including gasoline, and is a trace impurity in industrial products resulting in continued sub to low ppm occupational exposures, though higher exposures exist in small, uncontrolled workshops in developing countries. Emissions from gasoline/petrochemical industry are its main sources to the ambient air, but a person's total inhalation exposure can be elevated from emissions from cigarettes, consumer products and gasoline powered engines/tools stored in garages attached to homes. Air samples are collected in canisters or on adsorbent with subsequent quantification by gas chromatography. Ambient air concentrations vary from sub-ppb range, low ppb, and tens of ppb in rural/suburban, urban, and source impacted areas, respectively. Short-term environmental exposures of ppm occur during vehicle fueling. Indoor air concentrations of tens of ppb occur in microenvironments containing indoor sources. Occupational and environmental exposures have declined where regulations limit benzene in gasoline (<1%) and cigarette smoking has been banned from public and work places. Similar controls should be implemented worldwide to reduce benzene exposure. Biomarkers of benzene used to estimate exposure and risk include: benzene in breath, blood and urine; its urinary metabolites: phenol, t,t-muconic acid (t,tMA) and S-phenylmercapturic acid (sPMA); and blood protein adducts. The biomarker studies suggest benzene environmental exposures are in the sub to low ppb range though non-benzene sources for urinary metabolites, differences

  20. Benzene vapor recovery and processing

    International Nuclear Information System (INIS)

    The National Emissions Standards for Hazardous Air Pollutants, or NESHAPs, have provided a powerful motivation for interest in, and attention to, benzene vapor emissions in recent times. Benzene and its related aromatics are volatile organic compounds (VOCs), which marks them for surveillance as potential contributors to air pollution. In addition, benzene is a suspected carcinogen, which applies a special urgency to its control. The regulations governing the control of benzene emissions were issued as Title 40, Code of Federal Regulations, Part 61, subpart Y (Storage Vessels); subpart BB (Transfer Operations); and subpart FF (Waste Operations). These regulations specify very particular emission reduction guidelines for various generating sources. The problem in the hydrocarbon processing industry is to identify significant sources of benzene vapors in plants, and then to collect and process these vapors in an environmentally acceptable manner. This paper discusses various methods for collecting benzene fumes in these facilities

  1. Brain region-specific perfluoroalkylated sulfonate (PFSA) and carboxylic acid (PFCA) accumulation and neurochemical biomarker Responses in east Greenland polar Bears (Ursus maritimus)

    DEFF Research Database (Denmark)

    Pedersen, Kathrine Eggers; Basu, Niladri; Letcher, Robert;

    2015-01-01

    ), acetylcholinesterase (AChE) and glutamine synthetase (GS)) and receptor density (dopamine-2 (D2), muscarinic cholinergic (mAChR) and gamma-butyric acid type A (GABA-A)) along with PFSA and PFCA concentrations. Average brain ∑PFSA concentration was 25ng/g ww where PFOS accounted for 91%. Average ∑PFCA concentration...

  2. CdSe量子点与对氨基苯磺酸偶联反应研究%Coupling reaction of CdSe quantum dots with aminobenzene sulfonic acid

    Institute of Scientific and Technical Information of China (English)

    王伟杰; 俞英; 林碧霞; 梁耀珍

    2011-01-01

    The water soluble CdSe QDs, which were prepared by wrapping nanoparticles of the CdSe QD's with mercapto-propionic acid ( M PA) , were covalently conjugated with ami-nobenzene sulfonic acid ( ABSA) by linker EDC and NHS. The CdSe/MPA/ABSA was characterized using transmission electron microscopy, UV-vis spectrometry, fluorescence spec-trometry, fluorescence decay spectrometry, IR spectrometry, Capillary electrophoregrams. The coupled complex of CdSe QDs with ABSA was proved to be successfully. The results show that CdSe/MPA/ABSA possess fine optical properties.%以巯基丙酸为修饰剂合成水溶性硒化镉量子点(CdSe/MPA),利用碳化二亚胺(EDC)和琥珀酰亚胺(NHS)两种偶联剂,将对氨基苯磺酸与硒化镉量子点进行偶联以制备量子点-对氨基苯磺酸偶合物.通过透射电子显微镜、紫外-可见光谱、荧光光谱、荧光寿命、红外光谱、毛细管电泳对偶合物进行了表征.结果表明:量子点和对氨基苯磺酸偶联成功,该偶合物基本保持了量子点的荧光性能,可以作为研究植物病理的荧光探针.

  3. 脂肪酸甲酯磺酸盐中二钠盐来源分析及改进%Source analysis of dio-sodium salt in fatty acid methyl ester sulfonate and amelioration

    Institute of Scientific and Technical Information of China (English)

    蒋惠亮; 王相明

    2012-01-01

    实验考察了脂肪酸甲酯磺酸盐(MES)合成的各工序中α-磺基脂肪酸二钠(二钠盐)的变化量。其中再酯化阶段二钠盐减少最多,中和阶段二钠盐产生最多,这是由于再酯化阶段引入了部分甲醇以及中和阶段的强碱性环境和较高温度引起的。同时提出了各阶段的改进方法。经过优化实验,得到二钠盐含量最低时,各阶段最佳条件为:漂白温度75℃,再酯化时间6 h,甲醇与脂肪酸甲酯磺酸摩尔比30∶1,中和方式为以碳酸钠粉末干法中和。%The content ofdi-sodium salt ( DSS ) in every step of MES's synthesis was measured, the maximal decrease of DSS is in reesterification stage, the maximal increase of DSS is in neutralization stage. It could be resulted from the methanol introduction in reesterification stage, strong alkaline environment and higher temperature in neutralization stage. Meanwhile, improvement is also proposed for every stage in ameliorated method. By optimizing the experiment, the optimal condition for every stage was obtained as, bleaching temperature 75 ℃, reesterification time 6h, the mole ratio of methanol to fatty acid methyl ester sulfonic acid 30 : 1, neutralization pattern, dry neutralization by sodium carbonate powder when the content of di-sodium salt is the lowest.

  4. Proton conductive membranes based on doped sulfonated polytriazole

    Energy Technology Data Exchange (ETDEWEB)

    Boaventura, M.; Brandao, L.; Mendes, A. [Laboratorio de Engenharia de Processos, Ambiente e Energia (LEPAE), Faculdade de Engenharia da Universidade do Porto, Rua Roberto Frias, 4200-465 Porto (Portugal); Ponce, M.L.; Nunes, S.P. [GKSS Research Centre Geesthacht GmbH, Max Planck Str. 1, D-21502, Geesthacht (Germany)

    2010-11-15

    This work reports the preparation and characterization of proton conducting sulfonated polytriazole membranes doped with three different agents: 1H-benzimidazole-2-sulfonic acid, benzimidazole and phosphoric acid. The modified membranes were characterized by scanning electron microscopy (SEM), infrared spectra, thermogravimetric analysis (TGA), dynamical mechanical thermal analysis (DMTA) and electrochemical impedance spectroscopy (EIS). The addition of doping agents resulted in a decrease of the glass transition temperature. For membranes doped with 85 wt.% phosphoric acid solution proton conductivity increased up to 2.10{sup -3} S cm{sup -1} at 120 C and at 5% relative humidity. The performance of the phosphoric acid doped membranes was evaluated in a fuel cell set-up at 120 C and 2.5% relative humidity. (author)

  5. Detecting a Quasi-stable Imine Species on the Reaction Pathway of SHV-1 β-Lactamase and 6β-(Hydroxymethyl)penicillanic Acid Sulfone

    OpenAIRE

    Che, Tao; Rodkey, Elizabeth A.; Bethel, Christopher R.; Shanmugam, Sivaprakash; Ding, Zhe; Pusztai-Carey, Marianne; Nottingham, Michael; Chai, Weirui; Buynak, John D.; Robert A Bonomo; van den Akker, Focco; Carey, Paul R.

    2014-01-01

    For the class A β-lactamase SHV-1, the kinetic and mechanistic properties of the clinically used inhibitor sulbactam are compared with the sulbactam analog substituted in its 6β position by a CH2OH group (6β-(hydroxymethyl)penicillanic acid). The 6β substitution improves both in vitro and microbiological inhibitory properties of sulbactam. Base hydrolysis of both compounds was studied by Raman and NMR spectroscopies and showed that lactam ring opening is followed by fragmentation of the dioxo...

  6. Exposure to benzene metabolites causes oxidative damage in Saccharomyces cerevisiae.

    Science.gov (United States)

    Raj, Abhishek; Nachiappan, Vasanthi

    2016-06-01

    Hydroquinone (HQ) and benzoquinone (BQ) are known benzene metabolites that form reactive intermediates such as reactive oxygen species (ROS). This study attempts to understand the effect of benzene metabolites (HQ and BQ) on the antioxidant status, cell morphology, ROS levels and lipid alterations in the yeast Saccharomyces cerevisiae. There was a reduction in the growth pattern of wild-type cells exposed to HQ/BQ. Exposure of yeast cells to benzene metabolites increased the activity of the anti-oxidant enzymes catalase, superoxide dismutase and glutathione peroxidase but lead to a decrease in ascorbic acid and reduced glutathione. Increased triglyceride level and decreased phospholipid levels were observed with exposure to HQ and BQ. These results suggest that the enzymatic antioxidants were increased and are involved in the protection against macromolecular damage during oxidative stress; presumptively, these enzymes are essential for scavenging the pro-oxidant effects of benzene metabolites. PMID:27016252

  7. SULFONATED POLYIMIDES CONTAINING PYRIDINE GROUPS AS PROTON EXCHANGE MEMBRANE MATERIALS

    Institute of Scientific and Technical Information of China (English)

    Rui Lei; Chuan-qing Kang; Yun-jie Huang; Xue-peng Qiu; Xiang-ling Ji; Wei Xing; Lian-xun Gao

    2011-01-01

    A series of sulfonated polyimides (SPIs) containing pyridine groups were prepared by direct polycondensation from 1,4,5,8-naphthalenetetracarboxylic dianhydride (NTDA),4,4′-diaminodiphenyl ether-2,2′-disulfonic acid (ODADS) and 4-(4-methoxy)phenyl-2,6-bis(4-aminophenyl)pyridine (DAM).The resulting copolymers displayed good solubility in common organic solvents.Flexible,transparent,tough membranes were obtained via solution casting.All the films showed high thermal stability with desulfonation temperature over 300℃.They exhibited prominent mechanical properties with Young's modulus around 2.0 GPa.High proton conductivity (0.23 S/em at 100% RH) was also observed.More importantly,the new materials exhibited low water uptake (30 wt%-75 wt% at 80℃) and improved water stability,which were attributed to the acid-base interaction between sulfonic acid and pyridine functional groups.

  8. SYNTHESIS AND PROPERTIES OF SULFONATED POLY(ARYLENE ETHER) CONTAINING TRIPHENYL METHANE MOIETIES FROM ISOCYNATE MASKED BISPHENOL

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    A novel sulfonated poly(arylene ether) containing triphenylmethane moieties was synthesized by the sulfonation of a designed parent polymer using chlorosulfonic acid as sulfonation agent. The sulfonation took place at the para position of the pendant phenyl rings because of the specially designed parent polymer. The position and degree of sulfonation were characterized by 1H-NMR and elemental analysis. The sulfonated polymers are highly soluble in common organic solvents, such as dimethylsulfoxide, N,N'-dimethylacetamide, dimethylformamide, ethylene glycol monomethyl ether, and can be readily cast into tough and smooth films from solutions. The films showed good thermal and hydrolysis stabilities. Moreover, Fenton's reagent test revealed that the films exhibited superior stability to oxidation. The proton conductivities of the films were comparable with Nation 117 under same conditions. The membrane electrode assembly (MEA) prepared with the asmade film (706 EW, 100 μm dry thickness) shows better cell performance than Nation 115-MEA in the whole current density range.

  9. Heat-activated persulfate oxidation of PFOA, 6:2 fluorotelomer sulfonate, and PFOS under conditions suitable for in-situ groundwater remediation.

    Science.gov (United States)

    Park, Saerom; Lee, Linda S; Medina, Victor F; Zull, Aaron; Waisner, Scott

    2016-02-01

    PFOA (perfluorooctanoic acid) oxidation (0.121-6.04 μM) by heat-activated persulfate was evaluated at 20-60 °C with 4.2-84 mM [Formula: see text] and in the presence of soluble fuel components to assess feasibility for in-situ remediation of groundwater. 6:2 fluorotelomer sulfonic acid/sulfonate (6:2 FTSA) and PFOS (perfluorooctanesulfonic acid) persulfate oxidation was also evaluated in a subset of conditions given their co-occurrence at many sites. High performance liquid chromatography electron spray tandem mass spectrometry was used for organic analysis and fluoride was measured using a fluoride-specific electrode. PFOA pseudo-1st order transformation rates (k1,PFOA) increased with increasing temperature (half-lives from 0.1 to 7 d for 60 to 30 °C) sequentially removing CF2 groups ('unzipping') to shorter chain perfluoroalkyl carboxylic acids (PFCAs) and F(-). At 50 °C, a 5-fold increase in [Formula: see text] led to a 5-fold increase in k1,PFOA after which self-scavenging by sulfate radicals decreased the relative rate of increase with more [Formula: see text] . Benzene, toluene, ethylbenzene and xylene did not affect k1,PFOA even at 40 times higher molar concentrations than PFOA. A modeling approach to explore pathways strongly supported that for 6:2 FTSA, both the ethyl linkage and CF2-CH2 bond of 6:2 FTSA oxidize simultaneously, resulting in a ratio of ∼25/75 PFHpA/PFHxA. The effectiveness of heat-activated [Formula: see text] on PFOA oxidation was reduced in a soil slurry; therefore, repeated persulfate injections are required to efficiently achieve complete oxidation in the field. However, PFOS remained unaltered even at higher activation temperatures, thus limiting the sole use of heat-activated persulfate for perfluoroalkyl substances removal in the field.

  10. ANALYSIS OF LEACHABLE PERFLUOROOCTANIC ACID AND PERFLUOROOCTANIC SULFONIC IN DISPOSABLE LUNCH BOXES%一次性餐盒材料中全氟辛酸和全氟辛烷磺酸沥出性研究

    Institute of Scientific and Technical Information of China (English)

    潘媛媛; 史亚利; 王亚(韦/华); 蔡亚岐

    2009-01-01

    The leachability of perfluorooctanie acid (PFOA) and perfluorooctanic sulfonic (PFOS) from disposable luneh boxes materials under 4 food stimulant conditions was investigated with the HPLC/MS/MS method, using MPFOA and MPFOS as the internal standard, respectively. Four kinds of solvents were selected to simulate the exposure of food to the plastic materials, which were distilled water, 3% acetic acid (W/W), 15% ethanol (V/V) and n-hexane. The two compounds in the stimulant solvents were extracted using the Supelclean LC-18 SPE (3ec) cartridges. It was indieated that foodstuff can be very likely contaminated by perfluorinated compounds during the usage of disposable lunch boxes, and that mueh higher level of PFOA (about2296 ng· m~(-2))was deteeted in the stimulant solvent of 3% acetic acid after contact with the disposable lunch box for 4 h. Generally, PFOS can hardly be leached out under the four conditions.%利用高效液相色谱-串联质谱检测方法对一次性餐盒材料中可沥出性全氟辛酸(PFOA)和全氟辛烷磺酸(PFPS)进行了研究.分别选取水、3%乙酸(W/W)、15%乙醇(V/V)和正己烷4种浸取液模拟餐盒材料在使用过程中可能接触到的水性、酸性、酒精类和油脂类条件.材料经4种溶液浸提后,浸取液用固相萃取净化和浓缩,目标分析物PFOA和PFOS采用内标法进行定量.研究表明,一次性餐盒材料在模拟条件下中有以PFOA为主的伞氟类化合物从材料中沥出,其中酸性环境对PFOA的浸取率最高(2296 ng·m~(-2)), 为其它3种方法的82.8倍;4种浸提条件下PFPS的沥出率都比较低,浓度仪为0.7 ng·m~(-2)-5.4 ng·m~(-2).

  11. Radiation-induced crosslinking of poly(styrene–butadiene–styrene) block copolymers and their sulfonation

    Energy Technology Data Exchange (ETDEWEB)

    Lee, Sun-Young [Advanced Radiation Technology Institute, Korea Atomic Energy Research Institute, 29 Geumgu-gil, Jeongeup-si, Jeollabuk-do 580-185 (Korea, Republic of); Department of Chemical and Biomolecular Engineering, Yonsei University, 50 Yonsei-ro, Seodaemun-gu, Seoul 120-749 (Korea, Republic of); Song, Ju-Myung; Sohn, Joon-Yong [Advanced Radiation Technology Institute, Korea Atomic Energy Research Institute, 29 Geumgu-gil, Jeongeup-si, Jeollabuk-do 580-185 (Korea, Republic of); Shul, Yong-Gun [Department of Chemical and Biomolecular Engineering, Yonsei University, 50 Yonsei-ro, Seodaemun-gu, Seoul 120-749 (Korea, Republic of); Shin, Junhwa, E-mail: shinj@kaeri.re.kr [Advanced Radiation Technology Institute, Korea Atomic Energy Research Institute, 29 Geumgu-gil, Jeongeup-si, Jeollabuk-do 580-185 (Korea, Republic of)

    2013-12-01

    Highlights: • The c-SBS films were prepared using a gamma ray or electron beam. • The crosslinking degree of the c-SBS films were increased with the irradiation dose. • The prepared c-SBS films were sulfonated with various concentration of CSA. • The sulfonation of the c-SBS film is largely dependent on the concentration of CSA. • The sulfonation process is progressed from the surface to the inner part of c-SBS film. -- Abstract: Several crosslinked poly(styrene–butadiene–styrene) (c-SBS) block copolymer films were prepared using a gamma ray or electron beam with various irradiation doses and the prepared c-SBS film was then subjected to sulfonation using a chlorosulfonic acid (CSA) solution to introduce a sulfonic acid group. To estimate the degree of crosslinking, the gel fractions and FT-IR spectra of the c-SBS films were used and the results indicate that the degree of crosslinking is increased with an increase in the radiation dose. The surface morphology and mechanical property of the c-SBS films were observed using SEM and UTM instruments, respectively. The sulfonated c-SBS films were investigated by measuring the ion exchange capacity (IEC) and by observing the cross-sectional distribution patterns of sulfonic acid group using an SEM-EDX instrument. The IEC and SEM-EDX studies indicate that the sulfonated c-SBS membranes can be successfully prepared through the radiation crosslinking of the SBS film and the subsequent sulfonation with a diluted CSA solution.

  12. Fuel Dependence of Benzene Pathways

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, H; Eddings, E; Sarofim, A; Westbrook, C

    2008-07-14

    The relative importance of formation pathways for benzene, an important precursor to soot formation, was determined from the simulation of 22 premixed flames for a wide range of equivalence ratios (1.0 to 3.06), fuels (C{sub 1}-C{sub 12}), and pressures (20 to 760 torr). The maximum benzene concentrations in 15 out of these flames were well reproduced within 30% of the experimental data. Fuel structural properties were found to be critical for benzene production. Cyclohexanes and C{sub 3} and C{sub 4} fuels were found to be among the most productive in benzene formation; and long-chain normal paraffins produce the least amount of benzene. Other properties, such as equivalence ratio and combustion temperatures, were also found to be important in determining the amount of benzene produced in flames. Reaction pathways for benzene formation were examined critically in four premixed flames of structurally different fuels of acetylene, n-decane, butadiene, and cyclohexane. Reactions involving precursors, such as C{sub 3} and C{sub 4} species, were examined. Combination reactions of C{sub 3} species were identified to be the major benzene formation routes with the exception of the cyclohexane flame, in which benzene is formed exclusively from cascading fuel dehydrogenation via cyclohexene and cyclohexadiene intermediates. Acetylene addition makes a minor contribution to benzene formation, except in the butadiene flame where C{sub 4}H{sub 5} radicals are produced directly from the fuel, and in the n-decane flame where C{sub 4}H{sub 5} radicals are produced from large alkyl radical decomposition and H atom abstraction from the resulting large olefins.

  13. Determination of alachlor and its sulfonic acid metabolite in water by solid-phase extraction and enzyme-linked immunosorbent assay

    Science.gov (United States)

    Aga, D.S.; Thurman, E.M.; Pomes, M.L.

    1994-01-01

    Solid-phase extraction (SPE) and enzyme-linked immunosorbent assay (ELISA) were combined for the trace analysis of the herbicide alachlor and its major soil metabolite, ethanesulfonic acid (ESA). The anti-alachlor antibody cross-reacted with ESA, which produced false-positive detections of alachlor in water samples by immunoassay screens. Alachlor and ESA were isolated from water by SPE on a C18 resin and eluted sequentially with ethyl acetate and methanol. Alachlor is soluble in ethyl acetate while the anionic ESA is not. Thus ESA remained adsorbed on the C18 resin and was eluted later with methanol. The combination of SPE with ELISA effectivety separated and quantified both alachlor and ESA using the same antibody for two ELISA methods. The general method may have applicability for the separation of other herbicides and their ionic metabolites. The SPE-ELISA method has a, detection limit of 0.01 ??g/L for alachlor and 0.05 ??g/L for ESA, with a precision of ?? 10%. Analyses of surface and ground water samples were confirmed by gas chromatography/mass spectrometry and high-performance liquid chromatography with photodiode-array detection. Results showed widespread occurrence of ESA in surface and ground water of the midwestern United States, with concentrations ranging from 10 ??g/L.

  14. Benzaldehyde in cherry flavour as a precursor of benzene formation in beverages.

    Science.gov (United States)

    Loch, Christine; Reusch, Helmut; Ruge, Ingrid; Godelmann, Rolf; Pflaum, Tabea; Kuballa, Thomas; Schumacher, Sandra; Lachenmeier, Dirk W

    2016-09-01

    During sampling and analysis of alcohol-free beverages for food control purposes, a comparably high contamination of benzene (up to 4.6μg/L) has been detected in cherry-flavoured products, even when they were not preserved using benzoic acid (which is a known precursor of benzene formation). There has been some speculation in the literature that formation may occur from benzaldehyde, which is contained in natural and artificial cherry flavours. In this study, model experiments were able to confirm that benzaldehyde does indeed degrade to benzene under heating conditions, and especially in the presence of ascorbic acid. Analysis of a large collective of authentic beverages from the market (n=170) further confirmed that benzene content is significantly correlated to the presence of benzaldehyde (r=0.61, pcherry flavoured beverages, industrial best practices should include monitoring for benzene. Formulations containing either benzoic acid or benzaldehyde in combination with ascorbic acid should be avoided. PMID:27041300

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2011-02-24

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

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

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    Chloromethylated poly(phthalazinone ether sulfone ketone) (CMPPESK) was prepared from poly(phthalazinone ether sulfone ketone) (PPESK) using chloromethyl octyl ethers (CMOE) with lower toxicity as chloromethylated regent. CMPPESK was soluble in N-methyl-2-pyrrolidone (NMP), N,N-dimethylacetamide (DMAc) and chloroform. Quatemized poly(phthalazinone ether sulfone ketone) (QAPPESK) was prepared from CMPPESK by quaternization. QAPPESK had excellent solvent resistance,which was only partly soluble in sulfuric acid (98%) and swollen in N,N-dimethylformamide (DMF). The vanadium redox flow battery (V-RFB) using QAPPESK anion-exchange membrane had better performance with 88.3% of overall energy efficiency.

  17. Lignin Sulfonation - A different Approach

    DEFF Research Database (Denmark)

    Bjørkmann, Anders

    2001-01-01

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

  18. 磺酸官能化的磁性核壳结构的纳米材料用于果糖脱水制备5-羟甲基糠醛%Nanocoating of magnetic cores with sulfonic acid functionalized shells for the catalytic dehydration of fructose to 5-hydroxymethylfurfural

    Institute of Scientific and Technical Information of China (English)

    张晓辰; 王敏; 王业红; 张超峰; 张哲; 王峰; 徐杰

    2014-01-01

    通过反相微乳液法制备了以Fe3O4为核,磺酸官能化的硅基材料为壳层的磁性酸性催化剂.首先制备纳米Fe3O4磁核,然后涂层包覆苯基修饰的纳米级硅层,最后进行苯基磺化修饰,制得固体酸催化剂Fe3O4@Si/Ph-SO3H.在果糖脱水制备5-羟甲基糠醛反应中,该催化剂表现出较好的催化活性,优于传统催化剂A-15,且与均相无机酸催化活性相当.当采用二甲基亚砜作溶剂,在110 oC下反应3 h,果糖转化率达到99%,5-羟甲基糠醛收率为82%.另外,该催化剂经磁法回收后可多次重复使用.%A magnetically recyclable acid catalyst composed of an Fe3O4 core and sulfonic acid functionalized silica shell has been prepared using the reverse microemulsion method. The Fe3O4 core was coated with a phenyl modified silica shell nanolayer, and the phenyl groups were subsequently sulfonated to generate a solid sulfonic acid catalyst. The resulting acid catalyst showed higher activity than the conventional A-15 catalyst and comparable activity to several homogeneous sulfonic acid catalysts for the dehydration of fructose to 5-hydroxymethylfurfural (HMF). This process gave a fructose conversion of 99%with an HMF yield of 82%following 3 h in dimethylsulfoxide at 110 °C. Fur-thermore, the catalyst could be magnetically separated and recycled several times without losing its activity.

  19. Radiation-induced crosslinking of poly(styrene-butadiene-styrene) block copolymers and their sulfonation

    Science.gov (United States)

    Lee, Sun-Young; Song, Ju-Myung; Sohn, Joon-Yong; Shul, Yong-Gun; Shin, Junhwa

    2013-12-01

    Several crosslinked poly(styrene-butadiene-styrene) (c-SBS) block copolymer films were prepared using a gamma ray or electron beam with various irradiation doses and the prepared c-SBS film was then subjected to sulfonation using a chlorosulfonic acid (CSA) solution to introduce a sulfonic acid group. To estimate the degree of crosslinking, the gel fractions and FT-IR spectra of the c-SBS films were used and the results indicate that the degree of crosslinking is increased with an increase in the radiation dose. The surface morphology and mechanical property of the c-SBS films were observed using SEM and UTM instruments, respectively. The sulfonated c-SBS films were investigated by measuring the ion exchange capacity (IEC) and by observing the cross-sectional distribution patterns of sulfonic acid group using an SEM-EDX instrument. The IEC and SEM-EDX studies indicate that the sulfonated c-SBS membranes can be successfully prepared through the radiation crosslinking of the SBS film and the subsequent sulfonation with a diluted CSA solution.

  20. Overbased Calcium sulfonate Detergent Technology Overview

    Institute of Scientific and Technical Information of China (English)

    MA Qing-gao; MUIR Ronald J.

    2009-01-01

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

  1. Hydrothermal Synthesis and Crystal Structure of a Zinc Complex: [Zn2.5(phen)(BDC)2(OH)](phen = 1,10-Phenanthroline, BDC= Benzene-1,4-dicarboxylic Acid)

    Institute of Scientific and Technical Information of China (English)

    WANG Qing-Wei; LI Xiu-Mei; SHI Lin-Fang

    2008-01-01

    A metal-organic coordination polymer [Zn2.5(phen)(BDC)2(OH)]2 (phen = 1,10-phenanthroline, BDC = benzene-1,4-dicarboxylic acid)1 has been hydrothermally synthesized and structurally characterized by single-crystal X-ray diffraction, elemental analyses and IR spectro-scopy. The complex crystallizes in the triclinic system, space group P1 with a = 11.199(2), b =11.593(2), c = 11.865(3) A, α= 99.330(1), β=111.506(1),γ = 104.804(1)°, V= 1328.4(5) A3, Dc=1.722 g/cm3, Z = 1, Mr = 1377.82, F(000) = 692, μ(MoKa) = 2.306 mm-1, S = 1.093, R = 0.0281 and wR= 0.0756 for 4179 observed reflections (Ⅰ 20(Ⅰ)). The coordination polyhedron around Zn(Ⅱ)can be described as a tetrahedron, trigonal bipyramid and octahedron. It is worth noting that the crystal structure of 1 is composed of tetranuclear zinc clusters linked by {ZnO6} units.

  2. 新型砜基聚苯并咪唑的合成%Synthesis of Novel Sulfoned-polybenzimidazole

    Institute of Scientific and Technical Information of China (English)

    徐艺; 常冠军; 张林

    2012-01-01

    Adopted novel synthesis routine, a novel sulfoned-polybenzimidazole was synthesized in sulfolane from monomers of bifluoride and di(benzimidazolyl) benzenes which was prepared by the reaction of 4,4'-dicarboxyl-diphenylsulfone with o-phenylenediamine using polyphosphoric acid(PPA) as the catalysis. The structure was characterized by 'H NMR, IR, MS and elemental analysis.%采用新的合成路线,以多聚磷酸催化4,4′-二羧基二苯砜与邻苯二胺反应制得双苯并咪唑二苯砜(3);以3和4,4′-二氟二苯砜为单体,环丁砜为溶剂,在无水碳酸钾存在下合成了新型砜基聚苯并咪唑,其结构经1H NMR,IR,MS和元素分析表征.

  3. Copolymers of fluorinated polydienes and sulfonated polystyrene

    Science.gov (United States)

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

    2009-11-17

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

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

    Institute of Scientific and Technical Information of China (English)

    Wei Ming XU; Lu Ling WU; Xian HUANG

    2004-01-01

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

  5. Synthesis and characterizations of electrospun sulfonated poly (ether ether ketone) SPEEK nanofiber membrane

    Science.gov (United States)

    Hasbullah, N.; Sekak, K. A.; Ibrahim, I.

    2016-07-01

    A novel electrospun polymer electrolyte membrane (PEM) based on Sulfonated Poly (ether ether ketone) were prepared and characterized. The poly (ether ether ketone) PEEK was sulfonated using concentrated sulfuric acid at room temperature for 60 hours reaction time. The degree sulfonation (DS) of the SPEEK are 58% was determined by H1 NMR using area under the peak of the hydrogen shielding at aromatic ring of the SPEEK. Then, the functional group of the SPEEK was determined using Fourier transfer infrared (FTIR) showed O-H vibration at 3433 cm-1 of the sulfonated group (SO2-OH). The effect of the solvent and polymer concentration toward the electrospinning process was investigated which, the DMAc has electrospun ability compared to the DMSO. While, at 20 wt.% of the polymer concentration able to form a fine and uniform nanofiber, this was confirmed by FESEM that shown electrospun fiber mat SPEEK surface at nano scale diameter.

  6. 4-Aminopyridinium-3-sulfonate monohydrate

    Directory of Open Access Journals (Sweden)

    Zhi-Biao Zhu

    2011-02-01

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

  7. Sulfonates and Organotrophic Sulfite Metabolism

    OpenAIRE

    Cook, Alasdair M.; Theo H. M. Smits; Denger, Karin

    2007-01-01

    One is used to considering sulfite oxidation as part of a lithotrophic process (e.g. SorAB or Sox system), much of which involves neutral or ionic inorganic sulfur species on the outer surface of the cytoplasmic membrane. In contrast, the processes referred to in this chapter involve organic compounds, which (1) include a highly stable sulfonate substituent (C−SO3−), (2) are involved in the organotrophic growth of the organism and (3) much of whose metabolism takes place in the cytoplasm. Man...

  8. Sulfonated graphene oxide as effective catalyst for conversion of 5-(hydroxymethyl)-2-furfural into biofuels.

    Science.gov (United States)

    Antunes, Margarida M; Russo, Patrícia A; Wiper, Paul V; Veiga, Jacinto M; Pillinger, Martyn; Mafra, Luís; Evtuguin, Dmitry V; Pinna, Nicola; Valente, Anabela A

    2014-03-01

    The acid-catalyzed reaction of 5-(hydroxymethyl)-2-furfural with ethanol is a promising route to produce biofuels or fuel additives within the carbohydrate platform; specifically, this reaction may give 5-ethoxymethylfurfural, 5-(ethoxymethyl)furfural diethylacetal, and/or ethyl levulinate (bioEs). It is shown that sulfonated, partially reduced graphene oxide (S-RGO) exhibits a more superior catalytic performance for the production of bioEs than several other acid catalysts, which include sulfonated carbons and the commercial acid resin Amberlyst-15, which has a much higher sulfonic acid content and stronger acidity. This was attributed to the cooperative effects of the sulfonic acid groups and other types of acid sites (e.g., carboxylic acids), and to the enhanced accessibility to the active sites as a result of the 2D structure. Moreover, the acidic functionalities bonded to the S-RGO surface were more stable under the catalytic reaction conditions than those of the other solids tested, which allowed its efficient reuse.

  9. Determination of benzene in different food matrices by distillation and isotope dilution HS-GC/MS

    Energy Technology Data Exchange (ETDEWEB)

    Medeiros Vinci, Raquel [Department of Food Safety and Food Quality, Faculty of Bioscience Engineering, Ghent University, Coupure Links 653, B-9000 Ghent (Belgium); Canfyn, Michael [Food, Medicines and Consumer Safety, Scientific Institute of Public Health, Rue Juliette Wytsmanstraat 14, 1050 Brussels (Belgium); De Meulenaer, Bruno [Department of Food Safety and Food Quality, Faculty of Bioscience Engineering, Ghent University, Coupure Links 653, B-9000 Ghent (Belgium); Schaetzen, Thibault de; Van Overmeire, Ilse; De Beer, Jacques [Food, Medicines and Consumer Safety, Scientific Institute of Public Health, Rue Juliette Wytsmanstraat 14, 1050 Brussels (Belgium); Van Loco, Joris, E-mail: Joris.VanLoco@iph.fgov.BE [Food, Medicines and Consumer Safety, Scientific Institute of Public Health, Rue Juliette Wytsmanstraat 14, 1050 Brussels (Belgium)

    2010-07-05

    Benzene is classified by the IARC as carcinogenic to humans. Several sources may contribute for the occurrence of benzene in foods, such as, environmental contamination and the reaction of benzoate salts with ascorbic acid (naturally present or added as food additives). Matrix effect on benzene recovery (e.g. in fatty foods) and artefactual benzene formation from benzoate during analysis in the presence of ascorbate are some of the challenges presented when determining benzene in a wide range of foodstuffs. Design of experiment (DOE) was used to determine the most important variables in benzene recovery from headspace GC/MS. Based on the results of the DOE, a versatile method for the extraction of benzene from all kind of food commodities was developed. The method which consisted of distillation and isotope dilution HS-GC/MS was in-house validated. Artefactual benzene was prevented by addition of a borate buffer solution (pH 11) under distillation conditions. The method presented in this study allows the use of a matrix-independent calibration with detection limits below the legal limit established by the European Council for benzene in drinking water (1 {mu}g L{sup -1}).

  10. Determination of benzene in different food matrices by distillation and isotope dilution HS-GC/MS.

    Science.gov (United States)

    Vinci, Raquel Medeiros; Canfyn, Michael; De Meulenaer, Bruno; de Schaetzen, Thibault; Van Overmeire, Ilse; De Beer, Jacques; Van Loco, Joris

    2010-07-01

    Benzene is classified by the IARC as carcinogenic to humans. Several sources may contribute for the occurrence of benzene in foods, such as, environmental contamination and the reaction of benzoate salts with ascorbic acid (naturally present or added as food additives). Matrix effect on benzene recovery (e.g. in fatty foods) and artefactual benzene formation from benzoate during analysis in the presence of ascorbate are some of the challenges presented when determining benzene in a wide range of foodstuffs. Design of experiment (DOE) was used to determine the most important variables in benzene recovery from headspace GC/MS. Based on the results of the DOE, a versatile method for the extraction of benzene from all kind of food commodities was developed. The method which consisted of distillation and isotope dilution HS-GC/MS was in-house validated. Artefactual benzene was prevented by addition of a borate buffer solution (pH 11) under distillation conditions. The method presented in this study allows the use of a matrix-independent calibration with detection limits below the legal limit established by the European Council for benzene in drinking water (1 microg L(-1)).

  11. Determination of benzene in different food matrices by distillation and isotope dilution HS-GC/MS

    International Nuclear Information System (INIS)

    Benzene is classified by the IARC as carcinogenic to humans. Several sources may contribute for the occurrence of benzene in foods, such as, environmental contamination and the reaction of benzoate salts with ascorbic acid (naturally present or added as food additives). Matrix effect on benzene recovery (e.g. in fatty foods) and artefactual benzene formation from benzoate during analysis in the presence of ascorbate are some of the challenges presented when determining benzene in a wide range of foodstuffs. Design of experiment (DOE) was used to determine the most important variables in benzene recovery from headspace GC/MS. Based on the results of the DOE, a versatile method for the extraction of benzene from all kind of food commodities was developed. The method which consisted of distillation and isotope dilution HS-GC/MS was in-house validated. Artefactual benzene was prevented by addition of a borate buffer solution (pH 11) under distillation conditions. The method presented in this study allows the use of a matrix-independent calibration with detection limits below the legal limit established by the European Council for benzene in drinking water (1 μg L-1).

  12. APPLICATION OF THE ACID-WASHED COLORIMETRY MEASUREMENT ON LINEAR ALKYL BENZENE (LAB) QUALITY CONTROL%酸洗比色法在直链烷基苯生产质量控制中的应用

    Institute of Scientific and Technical Information of China (English)

    黄爱忠; 胡鹏程; 付在伟; 方绍东; 徐斌; 黄品文; 李丕谊; 祁鸣

    2011-01-01

    Linear Alkyl Benzene(LAB) was widely used as an intermediate to produce the detergents in petrochemical industry. It was selected as an excellent solvent for the Gadolinium-loaded Liquid Scintillator in the Daya Bay reactor neutrino experiment, because of its attractive properties such as appreciable optical yield, high content of protons(13%), security flash point(130℃ ), and environmental friendly. According to some characteristics of LAB mass production from the LAB plant of Jinling petro-chemical, its light attenuation length had only 5-6 m. So that it is necessary to improve the current producing technique, and promote its quality in order to meet the requirement of the Daya Bay experiment successfully. An acid-washed colorimetry method was set up, which was directly used on LAB production procedure, to compare with the results of the attenuation length of some measured LAB samples from our laboratory. It was found that the results of the acid-washed colorimetry measurement corresponded well with the attenuation length of these samples. Therefore, the acid-washed colorimetry method, which is fast and accurate for the on-site measurement, can be used on LAB quality control directly during its producing process, and also would be beneficial to further applications for the LAB producing technique promotion.%对于首次应用于大亚湾中微子物理实验的液体闪烁介质——直链烷基苯( LAB)的工业化生产,其最重要的质量控制指标为光衰减长度,这通常需要在实验室里利用专门仪器进行测量分析.经过对比研究,在LAB工业化生产流程的基础上,建立了相应的测试方法——酸洗比色分析方法,即使直链烷基苯和98.4%的发烟硫酸反应,在波长403 nm处测定其透光率.研究表明:酸洗比色测量值与光衰减长度测量值之间存在着密切相关性,相关系数达到0.9806.利用酸洗比色测定方法可以对生产流程中的LAB进行实时、有效的

  13. Hydroxylation of Benzene to Phenol by H2O2 over an Inorganic-Organic Dual Modified Heteropolyacid☆

    Institute of Scientific and Technical Information of China (English)

    Li Jing; Fumin Zhang; Yijun Zhong; Weidong Zhu

    2014-01-01

    Various catalysts, including the heteropolyacid (HPA) H4PMo11VO40, its cesium salts, and inorganic–organic dual modified HPA catalyst, were prepared and characterized by Fourier transform infrared spectroscopy (FT-IR), nu-clear magnetic resonance (13C NMR), N2 adsorption, acid–base titration, electron spin resonance (ESR) and X-ray diffraction (XRD) techniques as wel as elemental analysis. These prepared catalysts were used in the hydroxyl-ation of benzene to phenol by H2O2 as oxidant. The inorganic–organic dual modified HPA Cs2.5(MIMPS)1.5 PMo11VO40, prepared by partially exchanging Cs+with protons in H4PMo11VO40 and followed by the immobili-zation of 3-(1-methylimidazolium-3-yl)propane-1-sulfonate (MIMPS), led to a liquid–solid biphasic catalysis system in the hydroxylation, which showed the best catalytic performance in terms of reusability and catalytic activity. The high reusability of Cs2.5(MIMPS)1.5PMo11VO40 in the heterogeneous hydroxylation was probably due to its high resistance in leaching of bulk HPA into the reaction medium. The slightly enhanced catalytic activ-ity for the catalyst was due to the acid sites available from MIMPS beneficial to the hydroxylation.

  14. Benzene exposure assessed by metabolite excretion in Estonian oil shale mineworkers: influence of glutathione s-transferase polymorphisms

    DEFF Research Database (Denmark)

    Sørensen, Mette; Poole, Jason; Autrup, Herman;

    2004-01-01

    Measurement of urinary excretion of the benzene metabolites S-phenylmercapturic acid (S-PMA) and trans,trans-muconic acid (t,t-MA) has been proposed for assessing benzene exposure, in workplaces with relatively high benzene concentrations. Excretion of S-PMA and t,t-MA in underground workers...... the last shift of the week. Personal benzene exposure was 114 +/- 35 mug/m(3) in surface workers (n = 15) and 190 +/- 50 mug/m(3) in underground workers (n = 15) in measurements made prior to the study. We found t,t-MA excretion to be significantly higher in underground workers after the end of shifts 1...... of benzene metabolites as biomarkers for assessment of exposure at modest levels and warrant for further investigations of health risks of occupational benzene exposure in shale oil mines....

  15. Species differences in the metabolism of benzene.

    OpenAIRE

    Henderson, R F

    1996-01-01

    The pathways of metabolism of benzene appear to be qualitatively similar in all species studied thus far. However, there are quantitative differences in the fraction of benzene metabolized by the different pathways. These species differences become important for risk assessments based on animal data. Mice have a greater overall capacity to metabolize benzene than rats or primates, based on mass balance studies conducted in vivo using radiolabled benzene. Mice and monkeys metabolize more of th...

  16. 27 CFR 21.97 - Benzene.

    Science.gov (United States)

    2010-04-01

    ... 27 Alcohol, Tobacco Products and Firearms 1 2010-04-01 2010-04-01 false Benzene. 21.97 Section 21... TREASURY LIQUORS FORMULAS FOR DENATURED ALCOHOL AND RUM Specifications for Denaturants § 21.97 Benzene. (a..., Standard No. D 836-77; for incorporation by reference, see § 21.6(b).) When 100 ml of benzene are...

  17. Benzaldehyde in cherry flavour as a precursor of benzene formation in beverages.

    Science.gov (United States)

    Loch, Christine; Reusch, Helmut; Ruge, Ingrid; Godelmann, Rolf; Pflaum, Tabea; Kuballa, Thomas; Schumacher, Sandra; Lachenmeier, Dirk W

    2016-09-01

    During sampling and analysis of alcohol-free beverages for food control purposes, a comparably high contamination of benzene (up to 4.6μg/L) has been detected in cherry-flavoured products, even when they were not preserved using benzoic acid (which is a known precursor of benzene formation). There has been some speculation in the literature that formation may occur from benzaldehyde, which is contained in natural and artificial cherry flavours. In this study, model experiments were able to confirm that benzaldehyde does indeed degrade to benzene under heating conditions, and especially in the presence of ascorbic acid. Analysis of a large collective of authentic beverages from the market (n=170) further confirmed that benzene content is significantly correlated to the presence of benzaldehyde (r=0.61, pbenzaldehyde in combination with ascorbic acid should be avoided.

  18. Mechanoassisted Synthesis of Sulfonated Covalent Organic Frameworks with High Intrinsic Proton Conductivity.

    Science.gov (United States)

    Peng, Yongwu; Xu, Guodong; Hu, Zhigang; Cheng, Youdong; Chi, Chenglong; Yuan, Daqiang; Cheng, Hansong; Zhao, Dan

    2016-07-20

    It is challenging to introduce pendent sulfonic acid groups into modularly built crystalline porous frameworks for intrinsic proton conduction. Herein, we report the mechanoassisted synthesis of two sulfonated covalent organic frameworks (COFs) possessing one-dimensional nanoporous channels decorated with pendent sulfonic acid groups. These COFs exhibit high intrinsic proton conductivity as high as 3.96 × 10(-2) S cm(-1) with long-term stability at ambient temperature and 97% relative humidity (RH). In addition, they were blended with nonconductive polyvinylidene fluoride (PVDF) affording a series of mixed-matrix membranes (MMMs) with proton conductivity up to 1.58 × 10(-2) S cm(-1) and low activation energy of 0.21 eV suggesting the Grotthuss mechanism for proton conduction. Our study has demonstrated the high intrinsic proton conductivity of COFs shedding lights on their wide applications in proton exchange membranes.

  19. 46 CFR 151.05-2 - Compliance with requirements for tank barges carrying benzene and benzene containing cargoes, or...

    Science.gov (United States)

    2010-10-01

    ... benzene and benzene containing cargoes, or butyl acrylate cargoes. 151.05-2 Section 151.05-2 Shipping... Compliance with requirements for tank barges carrying benzene and benzene containing cargoes, or butyl acrylate cargoes. A tank barge certificated to carry benzene and benzene containing cargoes or...

  20. Electronic noses for monitoring benzene occupational exposure in biological samples of Egyptian workers

    Directory of Open Access Journals (Sweden)

    Ehab I. Mohamed

    2013-02-01

    Full Text Available Objectives: Benzene is commonly emitted in several industries, leading to widespread environmental and occupational exposure hazards. While less toxic solvents have been substituted for benzene, it is still a component of petroleum products and is a trace impurity in industrial products resulting in continued higher occupational exposures in industrial settings in developing countries. Materials and Methods: We investigated the potential use of an electronic nose (e-nose to monitor the headspace volatiles in biological samples from benzene-exposed Egyptian workers and non-exposed controls. The study population comprised 150 non-smoking male workers exposed to benzene and an equal number of matching non-exposed controls. We determined biomarkers of benzene used to estimate exposure and risk including: benzene in exhaled air and blood; and its urinary metabolites such as phenol and muconic acid using gas chromatography technique and a portable e-nose. Results: The average benzene concentration measured in the ambient air of the workplace of all studied industrial settings in Alexandria, Egypt; was 97.56±88.12 μg/m3 (range: 4.69–260.86 μg/m3. Levels of phenol and muconic acid were signifi cantly (p < 0.001 higher in both blood and urine of benzene-exposed workers as compared to non-exposed controls. Conclusions: The e-nose technology has successfully classifi ed and distinguished benzene-exposed workers from non-exposed controls for all measured samples of blood, urine and the exhaled air with a very high degree of precision. Thus, it will be a very useful tool for the low-cost mass screening and early detection of health hazards associated with the exposure to benzene in the industry.

  1. Synthesis and Characterization of Sulfonated Poly( phenylene sulfide sulfone)%磺化聚苯硫醚砜的制备和性能表征

    Institute of Scientific and Technical Information of China (English)

    肖慧; 李涛; 胡祥; 李瑞海

    2011-01-01

    This paper studied on sulfonated process of sulfonated poly(phenylene sulfide sulfone) based on sulfuric aid as solvent and oleum as sulfonating agent. By changing the four factors, such as temperature, reaction time, the dosage of sulfuric acid and oleum, the sulfonated conditions were explored. The structures and properties of the obtained polymer were characterized by FT-IR, TGA, testing of solubility, sulfonation degree and reduced inherent viscosity. The results indicated the sulfonation degree was 62. 2% and reduced inherent viscosity was 0. 964 mL/g when the raction temperature was at 15℃, the sulfonated time was for 2 h, sulfuric aid was 8 mL and the ratio of oleum/PPSS was 9. 5. Decomposition temperature of sulfonic aid group and its main chain were 346℃, 534 % , respectively. It can be dissolved improvably in the polar solvent which dialectic constant exceeded 20.7.%以浓硫酸为溶剂,发烟硫酸为磺化剂对聚苯硫醚砜的磺化过程,通过改变温度、反应时间、浓硫酸的用量和发烟硫酸的用量这四个因素来探究磺化反应的条件.利用FTIR、热重分析(TGA)、磺化度、比浓黏度和溶解性测试对其结构和性能进行了表征.结果表明,采用磺化时间为2h,反应温度15℃,浓硫酸8 mL,发烟硫酸与聚苯硫醚砜的质量比为9.5时,可得到磺化度为62.2%,比浓黏度为0.964 mL/g的磺化聚苯硫醚砜.磺酸基的主要分解温度为346℃,主链的分解温度为534℃.其溶解性得到提高,可溶解在介电常数大于20.7的有机溶剂中.

  2. Synthesis, Characterization, and Catalytic Activity of Sulfonated Carbon-Based Catalysts Derived From Rubber Tree Leaves and Pulp and Paper Mill Waste

    Science.gov (United States)

    Janaun, J.; Sinin, E.; Hiew, S. F.; Kong, A. M. T.; Lahin, F. A.

    2016-06-01

    Sulfonated carbon-based catalysts derived from rubber tree leaves, and pulp and paper mill waste were synthesized and characterized. Three types of catalyst synthesized were sulfonated rubber tree leaves (S-RTL), pyrolysed sludge char (P-SC) and sulfonated sludge char (S-SC). Sulfonated rubber tree leaves (S-RTL) and sulfonated sludge char (S-SC) were prepared through pyrolysis followed by functionalization via sulfonation process whereas, P- SC was only pyrolyzed without sulfonation. The characterization results indicated sulfonic acids, hydroxyl, and carboxyl moieties were detected in S-RTL and S-SC, but no sulfonic acid was detected in P-SC. Total acidity test showed S-RTL had the highest value followed by S-SC and P-SC. The thermal stability of S-RTL and S-SC were up to 230oC as the loss was associated with the decomposition of sulfonic acid group, whereas, P-SC showed higher stability than the S-RTL and S-SC. Morphology analysis showed that S-RTL consisted of an amorphous carbon structure, and a crystalline structure for P-SC and S-SC. Furthermore, traces of metal components were also detected on all of the catalysts. The catalyst catalytic activity was tested through esterification of oleic acid with methanol. The results showed that the reaction using S-RTL catalyst produced the highest conversion (99.9%) followed by P-SC (88.4%) and lastly S-SC (82.7%). The synthesized catalysts showed high potential to be used in biodiesel production.

  3. Improving the Conductivity of Sulfonated Polyimides as Proton Exchange Membranes by Doping of a Protic Ionic Liquid

    OpenAIRE

    Bor-Kuan Chen; Jhong-Ming Wong; Tzi-Yi Wu; Lung-Chuan Chen; I-Chao Shih

    2014-01-01

    Proton exchange membranes (PEMs) are a key component of a proton exchange membrane fuel cell. Sulfonated polyimides (SPIs) were doped by protic ionic liquid (PIL) to prepare composite PEMs with substantially improved conductivity. SPIs were synthesized from diamine, 2,2-bis[4-(4-amino-phenoxy)phenyl]propane (BAPP), sulfonated diamine, 4,4'-diamino diphenyl ether-2,2'-disulfonic acid (ODADS) and aromatic anhydride. BAPP improved the mechanical and thermal properties of SPIs, while ODADS enhanc...

  4. Double photoionization of halogenated benzene

    Energy Technology Data Exchange (ETDEWEB)

    AlKhaldi, Mashaal Q. [Institut für Optik und Atomare Physik, Technische Universität Berlin, Hardenbergstr. 36, D-10623 Berlin (Germany); Wehlitz, Ralf, E-mail: rwehlitz@gmail.com [Synchrotron Radiation Center, University of Wisconsin–Madison, Stoughton, Wisconsin 53589 (United States)

    2016-01-28

    We have experimentally investigated the double-photoionization process in C{sub 6}BrF{sub 5} using monochromatized synchrotron radiation. We compare our results with previously published data for partially deuterated benzene (C{sub 6}H{sub 3}D{sub 3}) over a wide range of photon energies from threshold to 270 eV. A broad resonance in the ratio of doubly to singly charged parent ions at about 65 eV appears shifted in energy compared to benzene data. This shift is due to the difference in the bond lengths in two molecules. A simple model can explain the shape of this resonance. At higher photon energies, we observe another broad resonance that can be explained as a second harmonic of the first resonance.

  5. Slow Neutron Scattering by Benzene

    International Nuclear Information System (INIS)

    We have calculated the scattering of slow neutrons by the benzene molecule. The calculations are carried out within the framework of the time dependent formalism of Zemach and Glauber. Detailed account is taken of the effects of the molecular vibrations on the neutron scattering. Among the results explicitly calculated are the slow neutron total scattering cross-section as a function of energy and the energy angular distribution of singly scattered sections. (author)

  6. Retarded acid emulsion

    Energy Technology Data Exchange (ETDEWEB)

    Fast, C.R.; Rixe, F.H.; Duffield, E.L. Jr.

    1972-08-01

    Compositions for use in acidizing hydrocarbon-bearing formations are described. Retarded acid emulsions of prolonged stability make it possible for the acid in this form to be displaced substantial distances out into the formation before becoming spent. The action of acid emulsions for use in acidizing hydrocarbon-bearing formations is prolonged by employing as the principal emulsifying agent an amine salt of dodecylbenzene sulfonic acid. Acid emulsions employing the amine salt of dodecylbenzene sulfonic acid exhibit greater stability than those employing the free acid. (8 claims)

  7. Electrocoagulation of commercial naphthalene sulfonates: process optimization and assessment of implementation potential.

    Science.gov (United States)

    Olmez-Hanci, Tugba; Kartal, Zeynep; Arslan-Alaton, Idil

    2012-05-30

    The commercially important naphthalene sulfonate K-acid (C(10)H(9)NO(9)S(3); 2-naphthylamine 3,6,8-tri sulfonic acid) was subjected to electrocoagulation employing stainless steel electrodes. An experimental design tool was used to mathematically describe and optimize the single and combined influences of major process variables on K-acid and its organic carbon (COD and TOC) removal efficiencies as well as electrical energy consumption. Current density, followed by treatment time were found to be the parameters affecting process responses most significantly, whereas initial K-acid concentration had the least influence on the electrocoagulation performance. Process economics including sludge generation, electrode consumption, and electrochemical efficiency, as well as organically bound adsorbable halogen formation and toxicity evolution were primarily considered to question the feasibility of K-acid electrocoagulation. Considering process economics and ecotoxicological parameters, process implementation appeared to be encouraging. PMID:22318240

  8. Cloning and Characterization of a Sulfonate/α-Ketoglutarate Dioxygenase from Saccharomyces cerevisiae

    OpenAIRE

    Hogan, Deborah A.; Auchtung, Thomas A.; Hausinger, Robert P.

    1999-01-01

    The Saccharomyces cerevisiae open reading frame YLL057c is predicted to encode a gene product with 31.5% amino acid sequence identity to Escherichia coli taurine/α-ketoglutarate dioxygenase and 27% identity to Ralstonia eutropha TfdA, a herbicide-degrading enzyme. Purified recombinant yeast protein is shown to be an Fe(II)-dependent sulfonate/α-ketoglutarate dioxygenase. Although taurine is a poor substrate, a variety of other sulfonates are utilized, with the best natural substrates being is...

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

    Science.gov (United States)

    Staniszewska, Monika; Bondaryk, Małgorzata; Ochal, Zbigniew

    2015-02-01

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

  10. Effects of polymer structure on properties of sulfonated polyimide/protic ionic liquid composite membranes for nonhumidified fuel cell applications.

    Science.gov (United States)

    Yasuda, Tomohiro; Nakamura, Shin-ichiro; Honda, Yoshiyuki; Kinugawa, Kei; Lee, Seung-Yul; Watanabe, Masayoshi

    2012-03-01

    To investigate the effects of polymer structure on the properties of composite membranes including a protic ionic liquid, [dema][TfO] (diethylmethylammonium trifluoromethanesulfonate), for nonhumidified fuel cell applications, we synthesized sulfonated polyimides (SPIs) with different structures as matrix polymers, which have different magnitudes of ion-exchange capacities (IECs), different sequence distributions of ionic groups, and positions of sulfonate groups in the main chain or side chain. Despite having similar IECs, multiblock copolymer SPI and random copolymer SPI having sulfonate groups in the side chain exhibit higher ionic conductivity than random copolymer SPI having sulfonate groups in the main chain, indicating that the flexibility of sulfonic acid groups and the sequence distribution of ionic groups greatly affect the ion conduction. Atomic force microscopy observation revealed that the multiblock copolymer SPI forms more developed phase separation than the others. These results indicate that the flexibility of sulfonic acid groups and the connectivity of the ion conduction channel, which greatly depends on the sequence distribution, affect the ion conduction. PMID:22352958

  11. Sulfonation Process and Desalination Effect of Polystyrene/PVDF Semi-Interpenetrating Polymer Network Cation Exchange Membrane

    Directory of Open Access Journals (Sweden)

    Yin-lin Lei

    2014-07-01

    Full Text Available With the classical sulfonation method of polystyrene-based strongly acidic cation exchange resins, polystyrene/polyvinylidene fluoride (PVDF alloy particles were sulfonated to obtain a cation exchange resin, which was then directly thermoformed to prepare a semi-interpenetrating polymer network (semi-IPN cation exchange membrane. The effects of the swelling agent, sulfonation time and temperature and the relative contents of polystyrene and divinylbenzene (DVB in the alloy particles on the feasibility of the membrane formation are discussed. The results indicate that a favorable sulfonation degree above 80% and a suitable ion exchange capacity of 1.5–2.4 mmol/g can be gained, with concentrated sulfuric acid as the sulfonation agent and 1,2-dichloroethane as the swelling agent. The running electrical resistance and desalination effect of the prepared cation exchange membrane were measured in a pilot-scale electrodialyser and not only obviously exceeded a commercial heterogeneous cation exchange membrane, but was also very close to a commercial homogenous membrane. In this way, the authors have combined the classical sulfonation method of polystyrene-based cation exchange resins with the traditional thermoforming manufacturing process of heterogeneous cation exchange membranes, to successfully develop a novel, low-price, but relatively high-performance polystyrene/PVDF cation exchange membrane with the semi-IPN structure.

  12. Carcinogenic effects of benzene: Cesare Maltoni's contributions.

    Science.gov (United States)

    Mehlman, Myron A

    2002-12-01

    Cesare Maltoni's contributions to understanding, identifying, and characterizing widely used commercial chemicals in experimental animals are among the most important methods developed in the history of toxicology and serve to protect working men and women, the general population, and our environment from hazardous substances. Maltoni developed experimental methods that have reached the "platinum standard" for protection of public health. Benzene was among the 400 or more chemicals that Maltoni and his associates tested for carcinogenicity. In 1976, Maltoni reported that benzene is a potent experimental carcinogen. Maltoni's experiments clearly demonstrated that benzene is carcinogenic in Sprague-Dawley rats, Wistar rats, Swiss mice, and RF/J mice when administered by inhalation or ingestion. Benzene caused carcinomas of the Zymbal gland, oral cavity, nasal cavities; cancers of the skin, forestomach, mammary glands, and lungs; angiosarcomas and hepatomas of the liver; and hemolymphoreticular cancers. Thus, benzene was shown to be a multipotential carcinogen that produced cancers in several species of animals by various routes of administration. On November 2, 1977, Chemical Week reported that Maltoni provided a "bombshell" when he demonstrated the "first direct link" between benzene and cancer. In this paper, I shall summarize early experiments and human studies and reports; Maltoni's experimental contribution to understanding the carcinogenicity of benzene in humans and animals; earlier knowledge concerning benzene toxicity; and benzene standards and permissible exposure levels.

  13. Natural Biological Attenuation of Benzene in Groundwater

    Institute of Scientific and Technical Information of China (English)

    2000-01-01

    Benzene has been found in subsurface unsaturated soil and groundwater beneath a petro-chemical plant. Although the groundwater contained several mg/L of benzene in the area immediately beneath the source, benzene was not detected in monitoring wells approximately 800m down stream. All kinds of physical processes such as adsorption and advection/dispersion are considered to account for the observed attenuation. The results indicated that the attenuation was primarily due to natural biological processes occurring within the aquifer. The evidence for the natural bioremediation of benzene from the groundwater included: (1) analysis of groundwater chemistry, (2) laboratory studies demonstrating benzene biodegradation in aquifer samples, and (3) computer simulations examining benzene transport. Laboratory experiments indicated that for conditions similar to those in the plume, the aerobic degradation of benzene by the naturally occurring microorganisms in the polluted groundwater samples was quite rapid with a half-life time of from 5 to 15 days. In situ analyses indicated the level of dissolved oxygen in the groundwater was over 2mg/L. Thus, oxygen should not limit the biodegradation. In fact, the benzene was also shown to degrade under anaerobic conditions. The results from the modeling simulations indicate that biodegradation is the dominant process influencing attenuation of the benzene.

  14. Albumin Adducts of Electrophilic Benzene Metabolites in Benzene-Exposed and Control Workers

    OpenAIRE

    Lin, Yu-Sheng; Vermeulen, Roel; Tsai, Chin H.; Waidyanatha, Suramya; Lan, Qing; Rothman, Nathaniel; Smith, Martyn T.; Zhang, Luoping; Shen, Min; Li, Guilan; Yin, Songnian; Kim, Sungkyoon; Rappaport, Stephen M.

    2006-01-01

    Background Metabolism of benzene produces reactive electrophiles, including benzene oxide (BO), 1,4-benzoquinone (1,4-BQ), and 1,2-benzoquinone (1,2-BQ), that are capable of reacting with blood proteins to produce adducts. Objectives The main purpose of this study was to characterize relationships between levels of albumin adducts of these electrophiles in blood and the corresponding benzene exposures in benzene-exposed and control workers, after adjusting for important covariates. Because se...

  15. Wine metabolomics reveals new sulfonated products in bottled white wines, promoted by small amounts of oxygen.

    Science.gov (United States)

    Arapitsas, Panagiotis; Ugliano, Maurizio; Perenzoni, Daniele; Angeli, Andrea; Pangrazzi, Paolo; Mattivi, Fulvio

    2016-01-15

    The impact of minute amounts of oxygen in the headspace on the post-bottling development of wine is generally considered to be very important, since oxygen can either damage or improve the quality of wine. This project aimed to gain new experimental evidence about the chemistry of the interaction between wine and oxygen. The experimental design included 216 bottles of 12 different white wines produced from 6 different cultivars (Inzolia, Muller Thurgau, Chardonnay, Grillo, Traminer and Pinot gris). Half of them were bottled using the standard industrial process with inert headspace and the other half without inert gas and with extra headspace. After 60 days of storage at room temperature, the wines were analysed using an untargeted LC-MS method. The use of a detailed holistic analysis workflow, with several levels of quality control and marker selection, gave 35 metabolites putatively induced by the different amounts of oxygen. These metabolite markers included ascorbic acid, tartaric acid and various sulfonated compounds observed in wine for the first time (e.g. S-sulfonated cysteine, glutathione and pantetheine; and sulfonated indole-3-lactic acid hexoside and tryptophol). The consumption of SO2 mediated by these sulfonation reactions was promoted by the presence of higher levels of oxygen on bottling.

  16. Comparison of antioxidant activities of different parts from snow chrysanthemum (Coreopsis tinctoria Nutt.) and identification of their natural antioxidants using high performance liquid chromatography coupled with diode array detection and mass spectrometry and 2,2'-azinobis(3-ethylbenzthiazoline-sulfonic acid)diammonium salt-based assay.

    Science.gov (United States)

    Chen, L X; Hu, D J; Lam, S C; Ge, L; Wu, D; Zhao, J; Long, Z R; Yang, W J; Fan, B; Li, S P

    2016-01-01

    Snow chrysanthemum (Coreopsis tinctoria Nutt.), a world-widely well-known flower tea material, has attracted more and more attention because of its beneficial health effects such as antioxidant activity and special flavor. In this study, a high performance liquid chromatography coupled with diode array detection and mass spectrometry (HPLC-DAD-MS) and 2,2'-azinobis(3-ethylbenzthiazoline-sulfonic acid)diammonium salt (ABTS) based assay was employed for comparison and identification of antioxidants in different samples of snow chrysanthemum. The results showed that snow chrysanthemum flowers possessed the highest while stems presented the lowest antioxidant capacities. Fourteen detected peaks with antioxidant activity were temporarily identified as 3,4',5,6,7-pentahydroxyflavanone-O-hexoside, chlorogenic acid, 2R-3',4',8-trihydroxyflavanone-7-O-glucoside, flavanomarein, flavanocorepsin, flavanokanin, quercetagitin-7-O-glucoside, 3',5,5',7-tetrahydroxyflavanone-O-hexoside, marein, maritimein, 1,3-dicaffeoylquinic acid, coreopsin, okanin and acetyl-marein by comparing their UV spectra, retention times and MS data with standards or literature data. Antioxidants existed in snow chrysanthemum are quite different from those reported in Chrysanthemum morifolium, a well-known traditional beverage in China, which indicated that snow chrysanthemum may be a promising herbal tea material with obvious antioxidant activity.

  17. Comparison of antioxidant activities of different parts from snow chrysanthemum (Coreopsis tinctoria Nutt.) and identification of their natural antioxidants using high performance liquid chromatography coupled with diode array detection and mass spectrometry and 2,2'-azinobis(3-ethylbenzthiazoline-sulfonic acid)diammonium salt-based assay.

    Science.gov (United States)

    Chen, L X; Hu, D J; Lam, S C; Ge, L; Wu, D; Zhao, J; Long, Z R; Yang, W J; Fan, B; Li, S P

    2016-01-01

    Snow chrysanthemum (Coreopsis tinctoria Nutt.), a world-widely well-known flower tea material, has attracted more and more attention because of its beneficial health effects such as antioxidant activity and special flavor. In this study, a high performance liquid chromatography coupled with diode array detection and mass spectrometry (HPLC-DAD-MS) and 2,2'-azinobis(3-ethylbenzthiazoline-sulfonic acid)diammonium salt (ABTS) based assay was employed for comparison and identification of antioxidants in different samples of snow chrysanthemum. The results showed that snow chrysanthemum flowers possessed the highest while stems presented the lowest antioxidant capacities. Fourteen detected peaks with antioxidant activity were temporarily identified as 3,4',5,6,7-pentahydroxyflavanone-O-hexoside, chlorogenic acid, 2R-3',4',8-trihydroxyflavanone-7-O-glucoside, flavanomarein, flavanocorepsin, flavanokanin, quercetagitin-7-O-glucoside, 3',5,5',7-tetrahydroxyflavanone-O-hexoside, marein, maritimein, 1,3-dicaffeoylquinic acid, coreopsin, okanin and acetyl-marein by comparing their UV spectra, retention times and MS data with standards or literature data. Antioxidants existed in snow chrysanthemum are quite different from those reported in Chrysanthemum morifolium, a well-known traditional beverage in China, which indicated that snow chrysanthemum may be a promising herbal tea material with obvious antioxidant activity. PMID:26521095

  18. Mechanisms for selective toxicity of fipronil insecticide and its sulfone metabolite and desulfinyl photoproduct.

    Science.gov (United States)

    Hainzl, D; Cole, L M; Casida, J E

    1998-12-01

    Fipronil, an N-phenylpyrazole with a trifluoromethylsulfinyl substituent, initiated the second generation of insecticides acting at the gamma-aminobutyric acid (GABA) receptor to block the chloride channel. The first generation includes the polychlorocycloalkanes alpha-endosulfan and lindane. In this study, we examine the mechanisms for selective toxicity of the sulfoxide fipronil and its sulfone metabolite and desulfinyl photoproduct relative to their target site interactions in vitro and ex vivo and the importance in fipronil action of biooxidation to the sulfone. Differences in GABA receptor sensitivity, assayed by displacement of 4'-ethynyl-4-n-[2, 3-3H2]propylbicycloorthobenzoate ([3H]EBOB) from the noncompetitive blocker site, appear to be a major factor in fipronil being much more toxic to the insects (housefly and fruit fly) than to the vertebrates (humans, dogs, mice, chickens, quail, and salmon) examined; in insects, the IC50s range from 3 to 12 nM for fipronil and its sulfone and desulfinyl derivatives, while in vertebrates, the IC50 average values are 1103, 175, and 129 nM for fipronil, fipronil sulfone, and desulfinyl fipronil, respectively. The insect relative to the vertebrate specificity decreases in the following order: fipronil > lindane > desulfinyl fipronil > fipronil sulfone > alpha-endosulfan. Ex vivo inhibition of [3H]EBOB binding in mouse brain is similar for fipronil and its sulfone and desulfinyl derivatives at the LD50 dose, but surprisingly, at higher doses fipronil can be lethal without detectably blocking the [3H]EBOB site. The P450 inhibitor piperonyl butoxide, acting in houseflies, increases the metabolic stability and effectiveness of fipronil and the sulfone but not those of the desulfinyl compound, and in mice it completely blocks the sulfoxide to sulfone conversion without altering the poisoning. Thus, the selective toxicity of fipronil and fipronil-derived residues is due in part to the higher potency of the parent compound at

  19. THE EFFECTS OF BENZENE BROMIDE MALONE COMBINED WITH INDAPAMIDE IN THE TREAT-MENT OF BLOOD PRESSURE AND URIC ACID%苯溴马隆与吲达帕胺联合治疗对血压和尿酸的影响

    Institute of Scientific and Technical Information of China (English)

    牛丽霞; 王虹; 李文静

    2015-01-01

    Objective To compare the different action on blood pressure and uric acid effects of the single hypertension treatment drug indapamide and the combination of benzene bromide malone and indapamide. Methods There were 350 patients in the clinical trial,who were divided randomly into two groups.175 patients were in the single drug indapamide treatment group,another 175 patients in the combination of benzene bromide malone and indapamide.The change of blood pressure,blood uric acid and urine uric acid of patients were detected.Results The value of blood uric acid and urine uric acid in the combination group of patients was significantly reduced compared to the single drug group.The amount of blood pressure re-turned to normal in the combination group was improved compared with them in the single drug group. Conclusions The combination of benzene bromide malone and indapamide for treating hypertension and hy-peruricemia is better than the single drug.%目的:比较单纯使用高血压治疗药物吲达帕胺与联合使用苯溴马隆和吲达帕胺对血压和尿酸的影响。方法随机将350例伴高尿酸血症的高血压患者分为二组,其中单纯使用吲达帕胺组175例,苯溴马隆与吲达帕胺联合使用组175例。观察二组患者血压、血尿酸和尿尿酸变化。结果联合用药组患者血尿酸值和尿尿酸值较单纯用药组相比,有显著性降低(P <0.05);联合用药组患者血压值恢复正常的人数与单纯用药组相比,有显著性提高(P <0.05)。结论苯溴马隆与吲达帕胺联合使用对改善高血压和高尿酸血症比单纯使用吲达帕胺疗效好。

  20. 1-(3-sulfonic acid group) propyl piperidinium dodecylbenzenesulfonic acid applied in carbon dioxide capture%1-(3-磺酸基)丙基哌啶十二烷基苯磺酸在CO2捕集中的应用∗

    Institute of Scientific and Technical Information of China (English)

    李工; 丁嘉; 郭剑桥; 徐小军; 王树立; 余益松

    2015-01-01

    A surface active functional ionic liquid, 1⁃(3⁃sulfonic acid group) propyl piperidinium dodecylbenzenesulfonic acid ([ PIPS] DBSA) was synthesized and characterized by 1H NMR, FTIR, and element analysis. [ PIPS] DBSA was used to promote the formation of carbon dioxide hydrate, and its effect on the temperature and pressure was investigated. Experimental results show that, by comparing 300 mg·L-1 [ PIPS ] DBSA solution with the 700 mg·kg-1 sodium dodecylbenzenesulfonate solution( SDBS) , the phase equilibrium pressure of carbon dioxide hydrate was decreased by 13.60% —14.96% in the range of 4℃ —6℃, and the required time for steady CO2 pressure was reduced by 50 min at 4 ℃. The investigation indicated that [ PIPS] DBSA has a good promotion effect on the formation of cardon dioxide hydrate.%合成了一种具有表面活性功能的离子液体1⁃(3⁃磺酸基)丙基哌啶十二烷基苯磺酸([PIPS]DBSA),采用FT⁃IR,1 H NMR 和元素分析等方法对产物进行表征,并将其用于促进 CO2水合物的生成,考察[ PIPS] DBSA对CO2水合物生成过程中温度和压力的影响.实验表明在温度4℃—6℃时,300 mg·L-1[ PIPS] DBSA溶液中CO2的相平衡压力比700 mg·L-1的十二烷基苯磺酸钠( SDBS)溶液的相平衡压力下降了13�6%—14.96%.在4℃时,300 mg·L-1[ PIPS] DBSA溶液中CO2压力稳定所用的时间与700 mg·L-1 SDBS溶液相比减少了50 min,表明[ PIPS] DBSA对CO2水合物的形成具有良好的促进作用.

  1. Chemical of current interest--benzene.

    Science.gov (United States)

    Marcus, W L

    1987-03-01

    Benzene is one of the world's major commodity chemicals. It is derived from petroleum and coal and is used both as a solvent and as a starting material in chemical syntheses. The numerous industrial uses of benzene over the last century need not be recounted here, but the most recent addition to the list of uses of benzene is as a component in a mixture of aromatic compounds added to gasoline for the purpose of replacing lead compounds as anti-knock ingredients. The best known and longest recognized toxic effect of benzene is the depression of bone marrow function seen in occupationally exposed individuals. These people have been found to display anemia, leucopenia, and/or thrombocytopenia. When pancytopenia, i.e., the simultaneous depression of all three cell types, occurs and is accompanied by bone marrow necrosis, the syndrome is called aplastic anemia. In addition to observing this decrease in humans and relating it to benzene exposure, it has been possible to establish animal models which mimic the human disease. The result has been considerable scientific investigation into the mechanism of benzene toxicity. Although the association between benzene exposure and aplastic anemia has been recognized and accepted throughout most of this century, it is only recently that leukemia, particularly of the acute myelogenous type, has been related to benzene. The acceptance of benzene as an etiological agent in aplastic anemia in large measure derives from our ability to reproduce the disease in most animals treated with sufficiently high doses of benzene over the necessary time period. Unfortunately, despite extensive efforts in several laboratories, it has not been possible to establish a reproducible, reliable model for the study of benzene-induced leukemia. The recent demonstration that several animals exposed to benzene either by inhalation or in the drinking water during studies by Drs. B. Goldstein and C. Maltoni suggests that such a model may be forthcoming

  2. Sulfonated graphenes catalyzed synthesis of expanded porphyrins and their supramolecular interactions with pristine graphene

    Indian Academy of Sciences (India)

    Sweta Mishra; Smriti Arora; Ritika Nagpal; Shive Murat Singh Chauhan

    2014-11-01

    A newer synthesis of sulfonic acid functionalized graphenes have been developed, which have been characterized, examined as heterogeneous solid acid carbocatalyst in the synthesis of selected expanded porphyrins in different reaction conditions. This environment-friendly catalyst avoids the use of toxic catalysts and enhances the yields of porphyrinoids. The non-covalent interaction of porphyrinoids has also been studied with exfoliated graphene solution in organic solvents by UV-Visible and fluorescence spectroscopy.

  3. Syntheses and Antibiotic Evaluation of 2-{[(2R,4R-4-Carboxy-2-hydroxypyrrolidin-1-yl]carbonyl}benzene-1,5-dicarboxylic Acids and 2-Carbamoylbenzene-1,5-dicarboxylic Acid Analogues

    Directory of Open Access Journals (Sweden)

    Abdulrazaq Tukur

    2016-01-01

    Full Text Available Our search for new antibiotics led to the syntheses and biological evaluation of new classes of dicarboxylic acid analogues. The syntheses involve nucleophilic addition of different substituted benzylamine, aniline, alkylamine, and 4-hydroxyl-L-proline with carbamoylbenzoic acid. The results of the antimicrobial activity as indicated by the zone of inhibition (ZOI showed that Z10 is the most active against Pseudomonas aeruginosa (32 mm and least active against Candida stellatoidea (27 mm and Vancomycin Resistant Enterococci (VRE (27 mm, while Z7 shows the least zone of inhibition (22 mm against Methicillin Resistant Staphylococcus aureus (MRSA. The minimum inhibition concentration (MIC determination reveals that Z10 inhibits the growth of tested microbes at a low concentration of 6.25 μg/mL, while Z9 and Z12 inhibits the growth of most microbes at a concentration of 12.5 μg/mL, recording the least MIC. The Minimum Bactericidal/Fungicidal Concentration (MBC/MFC results revealed that Z10 has the highest bactericidal/fungicidal effect on the test microbes, at a concentration of 12.5 μg/mL, with the exception of Candida stellatoidea and Vancomycin Resistant Enterococci (VRE with MBC/MFC of 25 μg/mL. The result of this investigation reveals the potential of the target compounds (Z1–3,5,7–12 in the search for new antimicrobial agents.

  4. 聚醚砜酮的磺化及其在异丁烯低聚反应中的应用%Sulfonation of Poly(phthalazinone ether sulfone ketone) and Its Application to Isobutene Oligomerization

    Institute of Scientific and Technical Information of China (English)

    安增建; 周硼; 蹇锡高; 蔡天锡

    2003-01-01

    @@ Concentrated homogeneous mineral acids have been widely used as catalysts in industrial processes for several decades. These catalysts are corrosive to the apparatus, and there are large volumes of chemically reactive waste stream that are difficult to deal with[1]. In order to solve these problems, investigators have replaced these mineral acids with solid acid catalysts. Besides inorganic solid acid catalysts such as zeolite, solid organic polymeric resins containing acid groups, especially sulfuric acid resins such as Amberlyst[2], have attracted much attention. Compared with most inorganic acid catalysts, they have the advantages of their potentially high acidity, controllable surface area and porosity[3]. This article reports a novel sulfonated poly(phthalazinone ether sulfone ketone) (S-PPESK) resin and its application to isobutene oligomerization. S-PPESK exhibits high catalytic activity and excellent dimerization selectivity.

  5. 29 CFR 1926.1128 - Benzene.

    Science.gov (United States)

    2010-07-01

    ... 29 Labor 8 2010-07-01 2010-07-01 false Benzene. 1926.1128 Section 1926.1128 Labor Regulations Relating to Labor (Continued) OCCUPATIONAL SAFETY AND HEALTH ADMINISTRATION, DEPARTMENT OF LABOR (CONTINUED) SAFETY AND HEALTH REGULATIONS FOR CONSTRUCTION Toxic and Hazardous Substances § 1926.1128 Benzene....

  6. 46 CFR 151.50-60 - Benzene.

    Science.gov (United States)

    2010-10-01

    ... 46 Shipping 5 2010-10-01 2010-10-01 false Benzene. 151.50-60 Section 151.50-60 Shipping COAST GUARD, DEPARTMENT OF HOMELAND SECURITY (CONTINUED) CERTAIN BULK DANGEROUS CARGOES BARGES CARRYING BULK LIQUID HAZARDOUS MATERIAL CARGOES Special Requirements § 151.50-60 Benzene. The person in charge of...

  7. 29 CFR 1910.1028 - Benzene.

    Science.gov (United States)

    2010-07-01

    ... safety data sheet (MSDS) which addresses benzene and complies with 29 CFR 1910.1200. (ii) Employers who... the requirements of 29 CFR 1910.1200(h) (1) and (2), and shall include specific information on benzene... and unloading operations, except for the provisions of 29 CFR 1910.1200 as incorporated into...

  8. 29 CFR 1915.1028 - Benzene.

    Science.gov (United States)

    2010-07-01

    ... 29 Labor 7 2010-07-01 2010-07-01 false Benzene. 1915.1028 Section 1915.1028 Labor Regulations Relating to Labor (Continued) OCCUPATIONAL SAFETY AND HEALTH ADMINISTRATION, DEPARTMENT OF LABOR (CONTINUED... Benzene. Note: The requirements applicable to shipyard employment under this section are identical...

  9. 46 CFR 30.25-3 - Benzene.

    Science.gov (United States)

    2010-10-01

    ... 46 Shipping 1 2010-10-01 2010-10-01 false Benzene. 30.25-3 Section 30.25-3 Shipping COAST GUARD, DEPARTMENT OF HOMELAND SECURITY TANK VESSELS GENERAL PROVISIONS Commodities Regulated § 30.25-3 Benzene. The provisions contained in 46 CFR part 197, subpart C, apply to liquid cargoes containing 0.5% or more...

  10. Carbon dioxide sensing with sulfonated polyaniline

    NARCIS (Netherlands)

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

    2012-01-01

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

  11. Selective sorption of perfluorooctane sulfonate on molecularly imprinted polymer adsorbents

    Institute of Scientific and Technical Information of China (English)

    Shubo DENG; Danmeng SHUAI; Qiang YU; Jun HUANG; Gang YU

    2009-01-01

    Perfluorooctane sulfonate (PFOS), as a potential persistent organic pollutant, has been widely detected in water environments, and has become a great concern in recent years. PFOS is very stable and difficult to decompose using conventional techniques. Sorption may be an attractive method to remove it from water. In this study, the molecularly imprinted polymer (MIP) adsorbents were prepared through the polymerization of 4-vinylpyridine under different preparation conditions in order to remove perfluorooctane sulfonate (PFOS) from water. The MIP adsorbents using perfluorooctanoic acid (PFOA) as the template had good imprinting effects and could selectively remove PFOS from aqueous solution. The sorption behaviors including sorption kinetics,isotherms, and effect of pH, salt, and competitive anions were investigated. Experimental results showed that the sorption of PFOS On the MIP adsorbents was very fast, pH-dependent, and highly selective. The achieved fast sorption equilibrium within 1 h was attributed to the surface sorption on the fine adsorbents. The sorption isotherms showed that the sorption selectivity of PFOS on the MIP adsorbents decreased at high PFOS concentrations, which may be due to the double-layer sorption and the formation of PFOS micelles on the sorbent surface. The sorption of PFOS on the MIP adsorbents was mainly dominated by the electrostatic interaction between the protonated vinylpyridine on the adsorbent surface and the anionic PFOS. The prepared MIP adsorbents can potentially be applied in water and wastewater treatment for selective removal of PFOS.

  12. Particle size effects of sulfonated graphene supported Pt nanoparticles on ethanol electrooxidation

    International Nuclear Information System (INIS)

    Highlights: • Pt colloidal nanoparticles with five mean diameters are synthesized. • Size-selected Pt nanoparticles are loaded on sulfonated graphene (sG). • Sulfonic acid functional groups atop graphene donate charge to Pt. • Pt-sG catalysts are used for ethanol oxidation reaction (EOR). • Pt-sG(2.5 nm) has the highest peak current density in EOR. - Abstract: Fuel cells are promising alternative in automobile and stationary power generation. Direct ethanol fuel cells (DEFCs) offer significant advantages due to the non-toxicity and renewability of ethanol as well as its high power density. Development of the efficient catalysts for ethanol oxidation reaction (EOR) has attracted great attention and represents one of the major challenges in electrocatalysis. Graphene, one-atom thick nanocarbon materials, has attracted much attention recently in a variety of applications. The sulfonation of graphene is able to make it hydrophilic, which enhances its dispersibility in aqueous solvents. Furthermore, sulfonation increases the adsorption and uniform distribution of the Pt nanoparticles, which increases both the electrocatalytic activity and the durability. In this study, theoretical calculations demonstrated that the sulfonate functional group can donate charge to Pt, enhanced the adsorption energy of Pt, and then reduce the adsorption energy of CO on Pt. Then experimentally five kinds of Pt/sulfonated-graphene (Pt/sG) catalysts were synthesized via the control of pH values during the preparation of five-selected colloidal nanoparticles. Among all catalysts, Pt-sG(2.5 nm) has the highest peak current density in EOR

  13. Effect of repeated benzene inhalation exposures on benzene metabolism, binding to hemoglobin, and induction of micronuclei.

    Science.gov (United States)

    Sabourin, P J; Sun, J D; MacGregor, J T; Wehr, C M; Birnbaum, L S; Lucier, G; Henderson, R F

    1990-05-01

    Metabolism of benzene is thought to be necessary to produce the toxic effects, including carcinogenicity, associated with benzene exposure. To extrapolate from the results of rodent studies to potential health risks in man, one must know how benzene metabolism is affected by species, dose, dose rate, and repeated versus single exposures. The purpose of our studies was to determine the effect of repeated inhalation exposures on the metabolism of [14C]benzene by rodents. Benzene metabolism was assessed by characterizing and quantitating urinary metabolites, and by quantitating 14C bound to hemoglobin and micronuclei induction. F344/N rats and B6C3F1 mice were exposed, nose-only, to 600 ppm benzene or to air (control) for 6 hr/day, 5 days/week for 3 weeks. On the last day, both benzene-pretreated and control animals were exposed to 600 ppm, 14C-labeled benzene for 6 hr. Individual benzene metabolites in urine collected for 24 hr after the exposure were analyzed. There was a significant decrease in the respiratory rate of mice (but not rats) pretreated with benzene which resulted in lower levels of urinary [14C]benzene metabolites. The analyses indicated that the only effects of benzene pretreatment on the metabolite profile in rat or mouse urine were a slight shift from glucuronidation to sulfation in mice and a shift from sulfation to glucuronidation in rats. Benzene pretreatment also had no effect, in either species, on formation of [14C]benzene-derived hemoglobin adducts. Mice and rats had similar levels of hemoglobin adduct binding, despite the higher metabolism of benzene by mice. This indicates that hemoglobin adduct formation occurs with higher efficiency in rats. After 1 week of exposure to 600 ppm benzene, the frequency of micronucleated, polychromatic erythrocytes (PCEs) in mice was significantly increased. Exposure to the same level of benzene for an additional 2 weeks did not further increase the frequency of micronuclei in PCEs. These results indicate

  14. Study of adjuvant effect of model surfactants from the groups of alkyl sulfates, alkylbenzene sulfonates, alcohol ethoxylates and soaps

    DEFF Research Database (Denmark)

    Clausen, S K; Sobhani, S; Poulsen, O M;

    2000-01-01

    The sodium salts of representatives of anionic surfactants, dodecylbenzene sulfonate (SDBS), dodecyl sulfate (SDS) and coconut oil fatty acids, and a nonionic surfactant, dodecyl alcohol ethoxylate, were studied for adjuvant effect on the production of specific IgE antibodies in mice. The surfact......The sodium salts of representatives of anionic surfactants, dodecylbenzene sulfonate (SDBS), dodecyl sulfate (SDS) and coconut oil fatty acids, and a nonionic surfactant, dodecyl alcohol ethoxylate, were studied for adjuvant effect on the production of specific IgE antibodies in mice...

  15. Reduction of benzene toxicity by toluene.

    Science.gov (United States)

    Plappert, U; Barthel, E; Seidel, H J

    1994-01-01

    BDF1 mice were exposed in inhalation chambers to benzene (900 ppm, 300 ppm) and/or toluene (500 ppm, 250 ppm) 6 hr per day, 5 days per week, for up to 8 weeks. Benzene alone induced a slight anemia after 4 and 8 weeks and a reduction of BFU-E and CFU-E numbers in the marrow. The coexposure to toluene reduced the degree of anemia. These results confirm previous studies where toluene was found to reduce benzene toxicity. This protective effect was most pronounced when DNA damage was studied in peripheral blood cells, bone marrow, and liver using the single cell gel (SCG) assay. With benzene alone, either with 300 or 900 ppm, a significant increase in DNA damage was detected in cells sampled from all three organs. Toluene alone did not induce a significant increase in DNA damage. The coexposure of benzene and toluene reduced the extent of DNA damage to about 50% of benzene alone. This result is considered a clear indication for a protective effect of toluene on the genetic toxicity of benzene.

  16. Development of a new highly conductive and thermomechanically stable complex membrane based on sulfonated polyimide/ionic liquid for high temperature anhydrous fuel cells

    Science.gov (United States)

    Deligöz, Hüseyin; Yılmazoğlu, Mesut

    The paper deals with the synthesis and characterization of a new type of acid doped highly conductive complex membrane based on sulfonated polyimide (sPI) and ionic liquid (IL) for high temperature anhydrous fuel cells. For this purpose, 2,4-diaminobenzene sulfonic acid (2,4-DABSA) is reacted with benzophenontetracarboxylic dianhydride (BTDA) to yield sulfonated poly(amic acid) (sPAA) intermediate. Subsequently, IL is added into sPAA to form an interaction between sulfonic acid and imidazolium group of IL followed by acid doping. The ionic conductivity of acid doped sPI/IL complex polymer membrane is higher than that of IL containing composite membranes reported in the literature (5.59 × 10 -2 S cm -1 at 180 °C). Furthermore, dynamic mechanical analysis (DMA) results of acid doped sPI/IL complex membrane show that the mechanical strength of the complex product is slightly changed until 350 °C due to the formation of ionic interactions between sulfonic acid groups of sPI and imidazolium groups of IL. Consequently, the ionic interaction not only provides high ionic conductivity with excellent thermomechanical properties (the storage module of 0.91 GPa at 300 °C) but also results in a positive effect in long term conductivity stability by blocking IL migration through the membrane.

  17. 臭氧法降解水中对甲基苯磺酸的动力学研究%Kinetics of p-toluene sulfonic acid degradation by ozone in aqueous solutions

    Institute of Scientific and Technical Information of China (English)

    张凌; 陶莹; 常志显; 李德亮

    2011-01-01

    The degradation kinetics of p-Toluene sulfonic acid(p-TSA) oxidized by ozone in aqueous solutions was studied.The factors that affected the reaction rate,including the initial concentration of p-TSA,pH value,ozone flux,reaction temperature and common inorganic anions and cations,were investigated.Experimental results showed that the degradation ratio could amount to 99.0% under the reaction conditions of the initial concentration of pTSA 0.29 mmol.L-1,pH 9.0,ozone flux 3.75 × 10-6 mol.s-1,reaction time 60 min and temperature 25 ℃.The degradation process was found to follow pseudo first-order kinetics and the kinetics equation was calculated as C = C0exp(-0.6868exp(-24464.8/RT)Q0O.39 293C0-1.7712[OH-]0.1248t)%采用臭氧法降解对甲基苯磺酸废水,研究了对甲基苯磺酸降解的影响因素和动力学.考察了反应液初始浓度、初始pH值、臭氧投量、反应温度、常见无机离子等因素对臭氧氧化降解对甲基苯磺酸反应速率的影响.结果表明,对甲基苯磺酸初始浓度0.29mmol.L-1,pH9.0,臭氧投量3.75×10-6mol.s-1,控制温度25℃,反应60min后,对甲基苯磺酸降解率达99.0%;对甲基苯磺酸在臭氧氧化下的降解符合表观一级动力学,采用幂指数方程描述反应动力学,得到方程:C=C0exp(-0.6868exp(-24464.8/RT)Q0O.39293C0-1.7712[OH-]0.1248t).

  18. Excited state of protonated benzene and toluene

    Energy Technology Data Exchange (ETDEWEB)

    Esteves-López, Natalia; Dedonder-Lardeux, Claude; Jouvet, Christophe, E-mail: Christophe.jouvet@univ-amu.fr [Aix-Marseille Université, CNRS, UMR-7345, Physique des Interactions Ioniques et Moléculaires (PIIM), Marseille (France)

    2015-08-21

    We present photo-fragmentation electronic spectra of the simplest protonated aromatic molecules, protonated benzene and toluene, recorded under medium resolution conditions and compared with the photo-fragmentation spectrum of protonated pyridine. Despite the resolution and cold temperature achieved in the experiment, the electronic spectra of protonated benzene and toluene are structure-less, thus intrinsically broadened. This is in agreement with the large geometrical changes and the fast dynamic toward internal conversion predicted by ab initio calculations for protonated benzene [Rode et al., J. Phys. Chem. A 113, 5865–5873 (2009)].

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

    Science.gov (United States)

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

    2015-07-01

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

  20. Catalytic transformation of methyl benzenes over zeolite catalysts

    KAUST Repository

    Al-Khattaf, S.

    2011-02-01

    Catalytic transformation of three methyl benzenes (toluene, m-xylene, and 1,2,4-trimethyl benzene) has been investigated over ZSM-5, TNU-9, mordenite and SSZ-33 catalysts in a novel riser simulator at different operating conditions. Catalytic experiments were carried out in the temperature range of 300-400 °C to understand the transformation of these alkyl benzenes over large pore (mordenite and SSZ-33) in contrast to medium-pore (ZSM-5 and TNU-9) zeolite-based catalysts. The effect of reaction conditions on the isomerization to disproportionation product ratio, distribution of trimethylbenzene (TMB) isomers, and p-xylene/o-xylene ratios are reported. The sequence of reactivity of the three alkyl benzenes depends upon the pore structure of zeolites. The zeolite structure controls primarily the diffusion of reactants and products while the acidity of these zeolites is of a secondary importance. In the case of medium pore zeolites, the order of conversion was m-xylene > 1,2,4-TMB > toluene. Over large pore zeolites the order of reactivity was 1,2,4-TMB > m-xylene > toluene for SSZ-33 catalyst, and m-xylene ∼ 1,2,4-TMB > toluene over mordenite. Significant effect of pore size between ZSM-5 and TNU-9 was observed; although TNU-9 is also 3D 10-ring channel system, its slightly larger pores compared with ZSM-5 provide sufficient reaction space to behave like large-pore zeolites in transformation of aromatic hydrocarbons. We have also carried out kinetic studies for these reactions and activation energies for all three reactants over all zeolite catalysts under study have been calculated. © 2011 Elsevier B.V.

  1. Brain met-enkephalin immunostaining after subacute and subchronic exposure to benzene

    Energy Technology Data Exchange (ETDEWEB)

    Gandarias, J.M. de; Echevarria, E.; Martinez-Millan, L.; Casis, L. [Univ. of the Basque Country, Bilbao (Spain); Martinez-Garcia, F. [Univ. of Valencia (Spain)

    1994-01-01

    Benzene is used in a wide variety of domestic and occupational activities, and due to its lipophilic nature, it accumulates in lipid-rich tissues like the brain. In this sense, neurotoxic action has long been associated with organic solvent exposure and it has been shown that benzene, injected in a single dose or during a prolongued administration, modifies the content of dopamine, noradrenaline, serotonin and its main metabolite 5-hydroxy indolacetic acid, in several brain regions of the rat, then revealing a stimulating action on brain monoamine synthesis and turnover. However, information concerning neurotoxic action of benzene exposure in vivo on peptidergic neuromodulatory systems is still lacking. Nevertheless, it has been recently described that subacute benzene exposure in rats generates regional changes in brain aminopeptidase activity. These proteolytic enzymes have been widely associated with metabolic control of neuropeptides and it has been suggested that they could play a role in benzene neurotoxic mechanism by hypothetically changing regional neuropeptide levels. This being the case, we focused on analyzing met-enkephalin immunostaining in different brain regions of the rat after subacute and subchronic administration of benzene. 12 refs., 3 figs.

  2. Degradation of Benzene by Using a Silent-Packed Bed Hybrid Discharge Plasma Reactor

    Science.gov (United States)

    Jiang, Nan; Lu, Na; Li, Jie; Wu, Yan

    2012-02-01

    In this work, a novel gas phase silent-packed bed hybrid discharge plasma reactor has been proposed, and its ability to control a simulative gas stream containing 240 ppm benzene is experimentally investigated. In order to optimize the geometry of the reactor, the benzene conversion rate and energy yield (EY) were compared for various inner electrode diameters and quartz tube shapes and sizes. In addition, benzene removal efficiency in different discharge regions was qualitatively analyzed and the gas parameter (space velocity) was systematically studied. It has been found that silent-packed bed hybrid discharge plasma reactor can effectively decompose benzene. Benzene removal proved to achieve an optimum value of 60% with a characteristic energy density of 255 J/L in this paper with a 6 mm bolt high-voltage electrode and a 13 mm quartz tube. The optimal space velocity was 188.1 h-1, which resulted in moderate energy yield and removal efficiency. Reaction by-products such as hydroquinone, heptanoic acid, 4-nitrocatechol, phenol and 4-phenoxy-phenol were identified by mean of GC-MS. In addition, based on these organic by-products, a benzene destruction pathway was proposed.

  3. Degradation of Benzene by Using a Silent-Packed Bed Hybrid Discharge Plasma Reactor

    Institute of Scientific and Technical Information of China (English)

    姜楠; 鲁娜; 李杰; 吴彦

    2012-01-01

    In this work, a novel gas phase silent-packed bed hybrid discharge plasma reactor has been proposed, and its ability to control a simulative gas stream containing 240 ppm benzene is experimentally investigated. In order to optimize the geometry of the reactor, the benzene conversion rate and energy yield (EY) were compared for various inner electrode diameters and quartz tube shapes and sizes. In addition, benzene removal efficiency in different discharge regions was qualitatively analyzed and the gas parameter (space velocity) was systematically studied. It has been found that silent-packed bed hybrid discharge plasma reactor can effectively decompose benzene. Benzene removal proved to achieve an optimum value of 60% with a characteristic energy density of 255 J/L in this paper with a 6 mm bolt high-voltage electrode and a 13 mm quartz tube. The optimal space velocity was 188.1 h^-1, which resulted in moderate energy yield and removal efficiency. Reaction by-products such as hydroquinone, heptanoic acid, 4-nitrocatechol, phenol and 4-phenoxy-phenol were identified by mean of GC-MS. In addition, based on these organic by-products, a benzene destruction pathway was proposed.

  4. Sulfonated polyvinyl chloride fibers for cation-exchange microextraction.

    Science.gov (United States)

    Xu, Li; Lee, Hian Kee

    2009-09-18

    Polyvinyl chloride (PVC) fiber was derivatized by concentrated sulfuric acid to yield sulfonated PVC (PVC-SO3H). The PVC-SO3H fiber had dual properties as a sorbent, based on cation-exchange and hydrophobicity. In the present study, the novel fiber was used directly as an individual device for extraction purposes in the cation-exchange microextraction of anaesthetics, followed by high-performance liquid chromatography-UV analysis. The results demonstrated that this PVC-SO3H fiber-based microextraction afforded convenient operation and cost-effective application to basic analytes. The limits of detection for four anaesthetics ranged from 1.2 to 6.0 ng/mL. No carryover (because of its disposable usage), and no loss of sorbent phase (which normally occurs in stir-bar sorptive extraction) during extraction were observed.

  5. 46 CFR 197.565 - Notifying personnel of benzene hazards.

    Science.gov (United States)

    2010-10-01

    ... appendices A and B of this subpart or a MSDS on benzene meeting the requirements of 29 CFR 1910.1200(g) is... 46 Shipping 7 2010-10-01 2010-10-01 false Notifying personnel of benzene hazards. 197.565 Section... AND HEALTH STANDARDS GENERAL PROVISIONS Benzene § 197.565 Notifying personnel of benzene hazards....

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

    Indian Academy of Sciences (India)

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

    2013-08-01

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

  7. Printing properties of the red reactive dyes with different number sulfonate groups on cotton fabric.

    Science.gov (United States)

    Xie, Kongliang; Gao, Aiqin; Li, Min; Wang, Xiao

    2014-01-30

    Cellulose fabric is an important printing substrate. Four red azo reactive dyes based on 1-naphthol-8-amino-3,6-disulfonic acid for cotton fabric printing were designed. Their UV-Vis spectra and printing properties for cotton were investigated. The relationship between the chemical structures of the dyes and their printing properties on cotton fabric was discussed. The results show that the color yield (K/S) values of the printed fabrics decreased with the increase of sulfonate groups, but the fixation and penetration of the reactive dyes on cotton fabric increased. The reactive dyes with fewer number sulfonate groups were sensitive to alkaline and urea. Whereas, the reactive dyes with numerous sulfonate groups were not sensitive to urea and had good leveling properties, penetration uniformity, and good wet fastness for cotton fabric. Surface wettability of all cotton fabrics printed with four dyes was excellent. It is possible to print cotton fabric urea-free using the reactive dyes with numerous sulfonate groups.

  8. Neuroendocrine effects of perfluorooctane sulfonate in rats.

    OpenAIRE

    Austin, Maureen E; Kasturi, Badrinarayanan S.; Barber, Matthew; Kannan, Kurunthachalam; MohanKumar, Puliyur S.; MohanKumar, Sheba M.J.

    2003-01-01

    Perfluorooctane sulfonate (PFOS) is a degradation product of sulfonyl-based fluorochemicals that are used extensively in industrial and household applications. Humans and wildlife are exposed to this class of compounds from several sources. Toxicity tests in rodents have raised concerns about potential developmental, reproductive, and systemic effects of PFOS. However, the effect of PFOS on the neuroendocrine system has not been investigated thus far. In this study, adult female rats were inj...

  9. Anaerobic degradation of linear alkylbenzene sulfonate

    DEFF Research Database (Denmark)

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

    2003-01-01

    Linear alkylbenzene sulfonate (LAS) found in wastewater is removed in the wastewater treatment facilities by sorption and aerobic biodegradation. The anaerobic digestion of sewage sludge has not been shown to contribute to the removal. The concentration of LAS based on dry matter typically increa...... under thermophilic conditions was 37% with LAS as sole carbon source. Benzaldehyde was produced in the UASB reactor during LAS transformation....

  10. Benzene and lead exposure assessment among occupational bus drivers in Bangkok traffic.

    Science.gov (United States)

    Muttamara, S; Leong, Shing Tet; Arayasiri, M

    2004-01-01

    Four environmental and biological monitoring sites were strategically established to evaluate benzene and lead exposure assessment at various traffic zones of Bangkok Metropolitan Region(BMR). Biological measurement of 48 non air-conditioned, male bus drivers was carried to study the relationship between individual exposure levels and exposure biomarkers. The study group was further subdivided into four age groups(16-25, 26-35, 36-45 and 46-55 years old) to monitor the age-related exposure effects. A total of 12 unexposed persons were deliberately chosen as the control group. Measurement of unmetobolized benzene in blood and analysis of urinary tt-Muconic acid urine and urinary creatinine are recommended as biomarkers of benzene exposure. Measurement of lead in blood and urine is also recommended for the biological monitoring of lead exposure. During the monitoring period, benzene and lead levels at Yaowarat Road was C6H6: 42.46 +/- 3.88 microg/m3 , Pb: 0.29 +/- 0.03 microg/m3 and decreased to C6H6: 33.5 +/- 1.35 microg/m3, Pb: 0.13 +/- 0.01 microg/m3 at Phahonyothin Road. Significant difference was established between the nonsmoking exposed group and nonsmoking control group for blood benzene concentrations (P < 0.001, two-tailed, Mann-Whiteney U test). Strong correlations were also found between trans-trans-Muconic acid concentrations in post shift samples and atmospheric benzene concentrations. Similarly, good correlation between all of biomarkers and lead level in air is established from automobile emissions. The analysis revealed that among the occupational population in the urban sites, the driver groups were found to have the highest risk of benzene and lead exposures derived from automobile emission. PMID:14971454

  11. Benzene and lead exposure assessment among occupational bus drivers in Bangkok traffic

    Institute of Scientific and Technical Information of China (English)

    SHING TET LEONG; PREECHA LAORTANAKUL

    2004-01-01

    Four environmental and biological monitoring sites were strategically established to evaluate benzene and lead exposure assessment at various traffic zones of Bangkok Metropolitan Region(BMR). Biological measurement of 48 non air-conditioned, male bus drivers was carried to study the relationship between individual exposure levels and exposure biomarkers. The study group was further subdivided into four age groups( 16-25, 26-35, 36-45 and 46-55 years old) to monitor the age-related exposure effects. A total of 12unexposed persons were deliberately chosen as the control group. Measurement of unmetobolized benzene in blood and analysis of urinary tt-Muconic acid urine and urinary creatinine are recommended as biomarkers of benzene exposure. Measurement of lead in blood and urine is also recommended for the biological monitoring of lead exposure.During the monitoring period, benzene and lead levels at Yaowarat Road was C6H6: 42.46 + 3.88 μg/m3 , Pb: 0.29 + 0.03 μg/m3 and decreased to C6 H6: 33.5 ± 1.35 μg/m3 , Pb: O. 13 + 0.01 μg/m3 at Phahonyothin Road. Significant difference was established between the nonsmoking exposed group and nonsmoking control group for blood benzene concentrations ( P < 0.001, two-tailed, Mann-Whiteney U test). Strong correlations were also found between trans-trans-Muconic acid concentrations in post shift samples and atmospheric benzene concentrations. Similarly, good correlation between all of biomarkers and lead level in air is established from automobile emissions.The analysis revealed that among the occupational population in the urban sites, the driver groups were found to have the highest risk of benzene and lead exposures derived from automobile emission.

  12. SYNTHESIS AND CHARACTERIZATION O F SODIUM METHYL ESTER SULFONATE FOR CHEMICALLY-ENHANCED OIL RECOVERY

    OpenAIRE

    Babu, K.; N. K. Maurya; Mandal, A.; Saxena, V. K.

    2015-01-01

    AbstractAttention has been given to reduce the cost of surfactant by using castor oil as an alternative natural source of feedstock. A new surfactant, sodium methyl ester sulfonate (SMES) was synthesised using ricinoleic acid methyl ester, which is obtained from castor oil, for enhanced oil recovery in petroleum industries. The performance of SMES was studied by measuring the surface tension with and without sodium chloride and its thermal stability at reservoir temperature. SMES exhibited go...

  13. SEPARATION OF CHOLESTEROL ESTERS BY SILVER ION CHROMATOGRAPHY USING HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY OR SOLID-PHASE EXTRACTION COLUMNS PACKED WITH A BONDED SULFONIC-ACID PHASE

    NARCIS (Netherlands)

    HOVING, EB; MUSKIET, FAJ; CHRISTIE, WW

    1991-01-01

    Two methods for the separation of cholesterol esters, based on the number of double bonds in their fatty acid moieties, are presented. Silver ion chromatography, usually performed on thin-layer chromatographic plates, was made suitable for high-performance liquid chromatography (HPLC) and solid-phas

  14. Sulfonated graphene nanosheets as a superb adsorbent for various environmental pollutants in water.

    Science.gov (United States)

    Shen, Yi; Chen, Baoliang

    2015-06-16

    Graphene nanosheets, as a novel nanoadsorbent, can be further modified to optimize the adsorption capability for various pollutants. To overcome the structural limits of graphene (aggregation) and graphene oxide (hydrophilic surface) in water, sulfonated graphene (GS) was prepared by diazotization reaction using sulfanilic acid. It was demonstrated that GS not only recovered a relatively complete sp(2)-hybridized plane with high affinity for aromatic pollutants but also had sulfonic acid groups and partial original oxygen-containing groups that powerfully attracted positively charged pollutants. The saturated adsorption capacities of GS were 400 mg/g for phenanthrene, 906 mg/g for methylene blue and 58 mg/g for Cd(2+), which were much higher than the corresponding values for reduced graphene oxide and graphene oxide. GS as a graphene-based adsorbent exhibits fast adsorption kinetic rate and superior adsorption capacity toward various pollutants, which mainly thanks to the multiple adsorption sites in GS including the conjugate π region sites and the functional group sites. Moreover, the sulfonic acid groups endow GS with the good dispersibility and single or few nanosheets which guarantee the adsorption processes. It is great potential to expose the adsorption sites of graphene nanosheets for pollutants in water by regulating their microstructures, surface properties and water dispersion.

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

    Directory of Open Access Journals (Sweden)

    Chulsung Bae

    2011-01-01

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

  16. Simultaneous Determination of Benzene Series and Phthalate Acid Esters in the Nail Polish by Gas Chromatography%气相色谱法同时测定指甲油中的苯系物和邻苯二甲酸酯类化合物

    Institute of Scientific and Technical Information of China (English)

    陈琨; 姚媛艳

    2011-01-01

    建立指甲油中苯系物、邻苯二甲酸酯类化合物(DMP,DEP,DBP,BBP,DEHP,DNOP)多种有毒有害成分同时检测技术:用毛细管柱气相色谱分离,外标法定量,苯系物的线性范围为1×10-2~100μg,邻苯二甲酸酯类为5×10-2~20μg;苯系物的回收率为90%~102%,相对标准偏差(RSD)的范围为0.13%~0.92%;邻苯二甲酸酯类的回收率为92%~109%,相对标准偏差(RSD)的范围为0.44%~2.54%.结果表明,该方法简便、快速、灵敏、精密度好.%In this paper, the technology method for detecting a variety of toxic and harmful components simultaneously in the nail polish, such as benzene series and phthalate acid esters (DMP, DEP,DBP, BBP,DEHP, DNOP), was established. This method uses capillary column gas chromatography to separate substances and quantifies by external standard. Linear range of benzene series is 1 × 10-2 ~ 100μg and PAEs is 5 × 10-2 ~20μg. The recovery rate of benzene series is 90% ~ 102% and the relative standard deviation (RSD) ranges from 0.13% to 0. 92%. The recovery rate of PAEs is 92% ~ 109% and the relative standard deviation (RSD) ranges from 0. 44% to 2.54%. The results show that this method is simple, rapid, sensitive and good precision.

  17. Differences in the pathways for metabolism of benzene in rats and mice simulated by a physiological model.

    Science.gov (United States)

    Medinsky, M A; Sabourin, P J; Henderson, R F; Lucier, G; Birnbaum, L S

    1989-07-01

    Studies conducted by the National Toxicology Program on the chronic toxicity of benzene indicated that B6C3F1 mice were more sensitive to the carcinogenic effects of benzene than were F344 rats. A physiological model was developed to describe the uptake and metabolism of benzene in rats and mice. Our objective was to determine if differences in toxic effects could be explained by differences in pathways for benzene metabolism or by differences in total uptake of benzene. Compartments incorporated into the model included liver, fat, a poorly perfused tissue group, a richly perfused tissue group, an alveolar or lung compartment and blood. Metabolism of benzene was assumed to take place only in the liver and to proceed by four major competing pathways. These included formation of hydroquinone conjugates (HQC), formation of phenyl conjugates (PHC), ring-breakage and formation of muconic acid (MUC), and conjugation with glutathione with subsequent mercapturic acid (PMA) formation. Values for parameters such as alveolar ventilation, cardiac output, organ volumes, blood flow, partition coefficients, and metabolic rate constants were taken from the literature. Model simulations confirmed that during and after 6-hr inhalation exposures mice metabolized more benzene on a mumole per kilogram body weight basis than did rats. After oral exposure, rats metabolized more benzene than mice at doses above 50 mg/kg because of the more rapid absorption and exhalation of benzene by mice. Model simulations for PHC and PMA, generally considered to be detoxification metabolites, were similar in shape and dose-response to those for total metabolism.(ABSTRACT TRUNCATED AT 250 WORDS)

  18. Synthesis and properties of novel multiblock copolyimides consisting of benzimidazole-groups-containing sulfonated polyimide hydrophilic blocks and non-sulfonated polyimide hydrophobic blocks as proton exchange membranes

    International Nuclear Information System (INIS)

    A series of novel multiblock copolymers consisting of benzimidazole-groups-containing sulfonated polyimide hydrophilic blocks (averaged block length = 20) and non-sulfonated polyimide hydrophobic blocks (averaged block length = 5 or 10) have been synthesized via two-pot synthetic procedures. The anhydride-terminated hydrophilic oligomer is synthesized by copolymerization of excess 1,4,5,8-naphthalelnetetracarboxylic dianhydride (NTDA) with amine-terminated polybenzimidazole (PBI-NH2) and 4,4′-bis(4-aminophenoxy) biphenyl-3,3′-disulfonic acid (BAPBDS), while the amine-terminated hydrophobic oligomers are synthesized by polymerization of excess non-sulfonated diamines with NTDA or a fluorinated dianhydride. The resulting multiblock copolymers can be cast into tough membranes indicating that reasonably high molecular weights block copolymers have been obtained. The block SPIs exhibit microphase-separated structure, whereas the random one is amorphous. Fenton’s test reveals that the block copolymer membranes, in particular, those consisting of fluorinated hydrophobic blocks, are fairly stable toward radical oxidation. Preliminary fuel cell tests are performed to evaluate the fuel cell performance of the block copolymer membranes. The single cell equipped with the block copolymer membrane of which hydrophobic block is prepared from NTDA and a fluorinated diamine (averaged block length = 5) exhibits a peak output power density of 0.70 W/cm2 at 90 °C and 92% relative humidity for H2/air which is comparable to that of Nafion 112

  19. Improving the Conductivity of Sulfonated Polyimides as Proton Exchange Membranes by Doping of a Protic Ionic Liquid

    Directory of Open Access Journals (Sweden)

    Bor-Kuan Chen

    2014-10-01

    Full Text Available Proton exchange membranes (PEMs are a key component of a proton exchange membrane fuel cell. Sulfonated polyimides (SPIs were doped by protic ionic liquid (PIL to prepare composite PEMs with substantially improved conductivity. SPIs were synthesized from diamine, 2,2-bis[4-(4-amino-phenoxyphenyl]propane (BAPP, sulfonated diamine, 4,4'-diamino diphenyl ether-2,2'-disulfonic acid (ODADS and aromatic anhydride. BAPP improved the mechanical and thermal properties of SPIs, while ODADS enhanced conductivity. A PIL, 1-vinylimidazolium trifluoromethane-sulfonate ([VIm][OTf], was utilized. [VIm][OTf] offered better conductivity, which can be attributed to its vinyl chemical structure attached to an imidazolium ring that contributed to ionomer-PIL interactions. We prepared sulfonated polyimide/ionic liquid (SPI/IL composite PEMs using 50 wt% [VIm][OTf] with a conductivity of 7.17 mS/cm at 100 °C, and in an anhydrous condition, 3,3',4,4'-diphenyl sulfone tetracarboxylic dianhydride (DSDA was used in the synthesis of SPIs, leading to several hundred-times improvement in conductivity compared to pristine SPIs.

  20. Enhancing the phase segregation and connectivity of hydrophilic channels by blending highly sulfonated graft copolymers with fluorous homopolymers

    DEFF Research Database (Denmark)

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

    2013-01-01

    The influence of tuning the ionic content of membranes by blending, as opposed to varying the degree of sulfonation, is evaluated. Membranes of fully sulfonated poly(vinylidene fluoride-co-chlorotrifluoroethylene)-g-poly(styrene sulfonic acid) blended with PVDF were prepared and investigated for...... morphology, water sorption, and proton transport properties. The blend membranes exhibit conductivities superior to pure graft copolymers under fully humidified conditions despite their lower water uptake. Transmission electron microscopy images of the blends reveal that the membranes comprise a combination...... of macro-phase segregated regions of ion-rich and PVDF-rich domains, and, at higher PVDF contents, ion-rich nano-scale domains within fluorine-rich domains. © 2013 The Royal Society of Chemistry....

  1. Alkylation mechanism of benzene with 1-dodecene catalyzed by Et3NHCl-AlCl3

    Institute of Scientific and Technical Information of China (English)

    2010-01-01

    The isotope exchange method was employed to investigate the catalytic mechanism of ionic liquid in alkylation of benzenes with olefins.It is proposed that alkylation was induced by the Lewis acid AlCl3 which attracted π electrons of 1-dodecene to shift toward 1-carbon,thus forming a carbonium ion.The carbonium ion further reacted with benzenes to form a complex.Due to unstabilit of the complex,a deuterated ring proton was transferred into an electronegative 1-carbon of the side chain to substitute for the AlCl3,accordingly 2-phenyldodecane was generated.

  2. Three-component synthesis of pyrano[2,3-d]-pyrimidine dione derivatives facilitated by sulfonic acid nanoporous silica (SBA-Pr-SO3H and their docking and urease inhibitory activity

    Directory of Open Access Journals (Sweden)

    Ziarani Ghodsi Mohammadi

    2013-01-01

    Full Text Available Abstract Background A straightforward and efficient method for the synthesis of pyrano[2,3-d]pyrimidine diones derivatives from the reaction of barbituric acid, malononitrile and various aromatic aldehydes using SBA-Pr-SO3H as a nanocatalyst is reported. Results Reactions proceed with high efficiency under solvent free conditions. Urease inhibitory activity of pyrano[2,3-d]pyrimidine diones derivatives were tested against Jack bean urease using phenol red method. Three compounds of 4a, 4d and 4l were not active in urease inhibition test, but compound 4a displayed slight urease activation properties. Compounds 4b, 4k, 4f, 4e, 4j, 4g and 4c with hydrophobic substitutes on phenyl ring, showed good inhibitory activity (19.45-279.14 μM. Discussion The compounds with electron donating group and higher hydrophobic interaction with active site of enzyme prevents hydrolysis of substrate. Electron withdrawing groups such as nitro at different position and meta-methoxy reduced urease inhibitory activity. Substitution of both hydrogen of barbituric acid with methyl group will convert inhibitor to activator.

  3. Three-component synthesis of pyrano[2,3-d]-pyrimidine dione derivatives facilitated by sulfonic acid nanoporous silica (SBA-Pr-SO3H and their docking and urease inhibitory activity

    Directory of Open Access Journals (Sweden)

    Ghodsi Mohammadi Ziarani

    2013-01-01

    Full Text Available A straightforward and efficient method for the synthesis of pyrano[2,3-d]pyrimidine diones derivatives from the reaction of barbituric acid, malononitrile and various aromatic aldehydes using SBA-Pr-SO3H as a nanocatalyst is reported.ResultsReactions proceed with high efficiency under solvent free conditions. Urease inhibitory activity of pyrano[2,3-d]pyrimidine diones derivatives were tested against Jack bean urease using phenol red method. Three compounds of 4a, 4d and 4l were not active in urease inhibition test, but compound 4a displayed slight urease activation properties. Compounds 4b, 4k, 4f, 4e, 4j, 4g and 4c with hydrophobic substitutes on phenyl ring, showed good inhibitory activity (19.45-279.14 muM.DiscussionThe compounds with electron donating group and higher hydrophobic interaction with active site of enzyme prevents hydrolysis of substrate. Electron withdrawing groups such as nitro at different position and meta-methoxy reduced urease inhibitory activity. Substitution of both hydrogen of barbituric acid with methyl group will convert inhibitor to activator.

  4. Analysis of recycled poly (styrene-co-butadiene) sulfonation: a new approach in solid catalysts for biodiesel production.

    Science.gov (United States)

    Aguilar-Garnica, Efrén; Paredes-Casillas, Mario; Herrera-Larrasilla, Tito E; Rodríguez-Palomera, Felicia; Ramírez-Arreola, Daniel E

    2013-01-01

    The disposal of solid waste is a serious problem worldwide that is made worse in developing countries due to inadequate planning and unsustainable solid waste management. In Mexico, only 2% of total urban solid waste is recycled. One non-recyclable material is poly (styrene-co-butadiene), which is commonly used in consumer products (like components of appliances and toys), in the automotive industry (in instrument panels) and in food services (e.g. hot and cold drinking cups and glasses). In this paper, a lab-scale strategy is proposed for recycling poly (styrene-co-butadiene) waste by sulfonation with fuming sulfuric acid. Tests of the sulfonation strategy were carried out at various reaction conditions. The results show that 75°C and 2.5 h are the operating conditions that maximize the sulfonation level expressed as number of acid sites. The modified resin is tested as a heterogeneous catalyst in the first step (known as esterification) of biodiesel production from a mixture containing tallow fat and canola oil with 59% of free fatty acids. The preliminary results show that esterification can reach 91% conversion in the presence of the sulfonated polymeric catalyst compared with 67% conversion when the reaction is performed without catalyst. PMID:24098857

  5. Interfacial behavior of pure surfactants for enhanced oil recovery. Part 1. A study on the adsorption and distribution of cetylbenzene sulfonate

    Energy Technology Data Exchange (ETDEWEB)

    Weihong Qiao; Liangjun Dong; Zhongkui Zhao; Jie Yang; Huamin Li; Zongshi Li [Dalian Univ. of Technology (China)

    2003-04-01

    The contents of pure alkyl benzene sulfonate surfactants in both the aqueous and oil phases were determined. The diffusion, adsorption and distribution of the surfactants in the oil and aqueous phases were studied at dynamic equilibrium and the effects of different structures on diffusion were investigated. N-nonane was used as the oil phase. The results indicate that the contents of the surfactants on both sides of the interface tend to increase with increasing sodium hydroxide and sodium chloride concentrations. The corresponding interfacial tensions, however, decrease gradually, and the quantities adsorbed at the oil-water interface reach a maximum value. The content of surfactant at the interface tends to be higher when the benzene ring is located near the middle of the carbon chain, so resulting in ultralow interfacial tension. (orig.)

  6. QENS investigation of proton confined motions in hydrated perfluorinated sulfonic membranes and self-assembled surfactants

    Directory of Open Access Journals (Sweden)

    Berrod Quentin

    2015-01-01

    Full Text Available We report on QuasiElastic Neutron Scattering (QENS investigations of the dynamics of protons and water molecules confined in nanostructured perfluorinated sulfonic acid (PFSA materials, namely a commercial Aquivion membrane and the perfluorooctane sulfonic acid (PFOS surfactant. The former is used as electrolyte in low-temperature fuel cells, while the latter forms mesomorphous self-assembled phases in water. The dynamics was investigated as a function of the hydration level, in a wide time range by combining time-of-flight and backscattering incoherent QENS experiments. Analysis of the quasielastic broadening revealed for both systems the existence of localized translational diffusive motions, fast rotational motions and slow hopping of protons in the vicinity of the sulfonic charges. The characteristic times and diffusion coefficients have been found to exhibit a very similar behaviour in both membrane and surfactant structures. Our study provides a comprehensive picture of the proton motion mechanisms and the dynamics of confined water in model and real PFSA nanostructures.

  7. Enhancement of proton conductivity of sulfonated polystyrene membrane prepared by plasma polymerization process

    Indian Academy of Sciences (India)

    Bhabesh Kumar Nath; Aziz Khan; Joyanti Chutia; Arup Ratan Pal; Heremba Bailung; Neelotpal Sen Sarma; Devasish Chowdhury; Nirab Chandra Adhikary

    2014-12-01

    This work reports the achievement of higher proton conductivity of polystyrene based proton exchange membrane synthesized in a continuous RF plasma polymerization process using two precursors, styrene (C8H8) and trifluoromethane sulfonic acid (CF3SO3H). The chemical composition of the developed membranes is investigated using Fourier transform infrared spectroscopy and energy dispersive spectroscopy. Scanning electron microscopy has been used for the study of surface morphology and thickness measurement of the membrane. The membranes deposited in the power range from 0.114 to 0.318 Wcm-2 exhibit a lot of variation in the properties like proton transport, water uptake, sulfonation rate, ion exchange capacity and thermal behaviour. The proton conductivity of the membranes is achieved up to 0.6 Scm-1, measured with the help of potentiostat/galvanostat. The thermogravimetric study of the plasma polymerized membrane shows the thermal stability up to 140 °C temperature.

  8. Sulfonate-grafted porous polymer networks for preferential CO2 adsorption at low pressure.

    Science.gov (United States)

    Lu, Weigang; Yuan, Daqiang; Sculley, Julian; Zhao, Dan; Krishna, Rajamani; Zhou, Hong-Cai

    2011-11-16

    A porous polymer network (PPN) grafted with sulfonic acid (PPN-6-SO(3)H) and its lithium salt (PPN-6-SO(3)Li) exhibit significant increases in isosteric heats of CO(2) adsorption and CO(2)-uptake capacities. IAST calculations using single-component-isotherm data and a 15/85 CO(2)/N(2) ratio at 295 K and 1 bar revealed that the sulfonate-grafted PPN-6 networks show exceptionally high adsorption selectivity for CO(2) over N(2) (155 and 414 for PPN-6-SO(3)H and PPN-6-SO(3)Li, respectively). Since these PPNs also possess ultrahigh physicochemical stability, practical applications in postcombustion capture of CO(2) lie well within the realm of possibility.

  9. Oil-soluble metal containing sulfonated polymers useful as oil additives

    Energy Technology Data Exchange (ETDEWEB)

    Miller, H.N.

    1983-02-08

    This invention relates to oil soluble, metal containing sulfonated polymers useful as additives for lubricating oils or hydrocarbon fuels and which are effective as dispersants. Such polymers of high molecular weight are also useful as viscosityindex improvers for the lubricating oils. The polymeric dispersant additives are ionic polymers which comprise a backbone substantially soluble in the fuel or lubricant, and pendant ionic groups which are sulfonic acid groups neutralized with a metal compound. Polymeric dispersant additives of this type may be made which are also capable of imparting excellent viscosity improvement, varnish inhibition, oxidation inhibition and detergency to the lubricant. These additives may also impart rust preventive properties to the oil or fuel, and as V.I. improvers they can be formed to have particularly good low temperature viscosity effects in lubricating oil.

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

    Institute of Scientific and Technical Information of China (English)

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

    1997-01-01

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

  11. Organic chemistry. A rhodium catalyst for single-step styrene production from benzene and ethylene.

    Science.gov (United States)

    Vaughan, Benjamin A; Webster-Gardiner, Michael S; Cundari, Thomas R; Gunnoe, T Brent

    2015-04-24

    Rising global demand for fossil resources has prompted a renewed interest in catalyst technologies that increase the efficiency of conversion of hydrocarbons from petroleum and natural gas to higher-value materials. Styrene is currently produced from benzene and ethylene through the intermediacy of ethylbenzene, which must be dehydrogenated in a separate step. The direct oxidative conversion of benzene and ethylene to styrene could provide a more efficient route, but achieving high selectivity and yield for this reaction has been challenging. Here, we report that the Rh catalyst ((Fl)DAB)Rh(TFA)(η(2)-C2H4) [(Fl)DAB is N,N'-bis(pentafluorophenyl)-2,3-dimethyl-1,4-diaza-1,3-butadiene; TFA is trifluoroacetate] converts benzene, ethylene, and Cu(II) acetate to styrene, Cu(I) acetate, and acetic acid with 100% selectivity and yields ≥95%. Turnover numbers >800 have been demonstrated, with catalyst stability up to 96 hours.

  12. Organic chemistry. A rhodium catalyst for single-step styrene production from benzene and ethylene.

    Science.gov (United States)

    Vaughan, Benjamin A; Webster-Gardiner, Michael S; Cundari, Thomas R; Gunnoe, T Brent

    2015-04-24

    Rising global demand for fossil resources has prompted a renewed interest in catalyst technologies that increase the efficiency of conversion of hydrocarbons from petroleum and natural gas to higher-value materials. Styrene is currently produced from benzene and ethylene through the intermediacy of ethylbenzene, which must be dehydrogenated in a separate step. The direct oxidative conversion of benzene and ethylene to styrene could provide a more efficient route, but achieving high selectivity and yield for this reaction has been challenging. Here, we report that the Rh catalyst ((Fl)DAB)Rh(TFA)(η(2)-C2H4) [(Fl)DAB is N,N'-bis(pentafluorophenyl)-2,3-dimethyl-1,4-diaza-1,3-butadiene; TFA is trifluoroacetate] converts benzene, ethylene, and Cu(II) acetate to styrene, Cu(I) acetate, and acetic acid with 100% selectivity and yields ≥95%. Turnover numbers >800 have been demonstrated, with catalyst stability up to 96 hours. PMID:25908817

  13. Catalytic Synthesis of Isopropyl Benzene over SO42-/ZrO2 -MCM-41

    Institute of Scientific and Technical Information of China (English)

    2006-01-01

    Super acid catalyst SO2-4-/ZrO2 was introduced into pure silicone MCM-41 via the impregnation method and the catalyst samples obtained at different temperatures were characterized by means of XRD, IR, and Py-IR techniques.The selectively catalytic gas-phase flow reactions of benzene with propene over the catalyst samples were carried out in a made-to-measure high-pressure flow reactor equipped with a thermostat and a condenser. Effect of the preparative condition on the catalytic synthesis of isopropyl benzene over the catalyst samples was tested. The results show that SO2-4/ZrO2-MCM-41 (SZM-41) can be used as a catalyst for the title reaction, in which there are a higher conversion (97%) for the propene and a higher selectivity(93%) for the isopropyl benzene.

  14. PERVAPORATION FOR SEPARATING BENZENE/CYCLOHEXANE MIXTURE BY P(AA-MA) COPOLYMER MEMBRANES

    Institute of Scientific and Technical Information of China (English)

    Gao-fei Xu; Wei-pu Zhu

    2011-01-01

    P(AA-MA) copolymers composed of acrylic acid and methyl acrylate with different molecular weights and sequence structures were synthesized by combination of ATRP and selective hydrolysis. These copolymers were used as membrane materials to separate benzene/cyclohexane mixture by pervaporation. The effects of molecular weight and sequence structure of the copolymers on the pervaporation performance were investigated in detail. For the random copolymers, the permeate flux decreased rapidly with the increasing of molecular weight. The separation factor was also influenced by the molecular weight, which was changed from no selectivity to cyclohexane selectivity with increasing the molecular weight. Contrarily, the block copolymer membrane showed good benzene selectivity with separation factor of 4.3 and permeate flux of 157 g/(m2h) to 50 wt% benzene/cyclohexane mixture.

  15. Determination of glucose at poly(p-aminobenzene sulfonic acid)/graphene composite modified glassy carbon electrode%聚对氨基苯磺酸/石墨烯复合膜修饰玻碳电极测定葡萄糖

    Institute of Scientific and Technical Information of China (English)

    许春萱; 宋力; 余萌; 蔡翠玲

    2011-01-01

    制备了对氨基苯磺酸/石墨烯复合膜修饰电极,研究了葡萄糖在该修饰电极上的电化学行为.在0.1 moL/L NaOH溶液中,峰电流与葡萄糖的浓度在1 ×1O-6 ~5 ×1O-4 mol/L的范围内呈良好的线性关系,检出限为2×10-7 mol/L(S/N =3).实验结果表明对氨基苯磺酸/石墨烯复合膜显著提高了方法的检测灵敏度.利用该传感器测定了人血清中的葡萄糖,回收率在97.2%~104.1%之间.%A poly (p-aminobenzene sulfonic acid)/graphene composite film modified glassy carbon electrode was fabricated for glucose determination. In 0. 1 mol/L NaOH solution, the peak currents varied linearly with the concentration of glucose in the range of 1x10-6 ~5x10-4 mol/L with the detection limit of 2x10-7 mol/L(S/N =3). It indicated that the composite fibs obviously improved the sensitivity for the glucose determination. The biosensor was used in the determination of glucose in serum with recoveries ranging from 97. 2 % to 104.1%.

  16. 高吸水性树脂丙烯酰胺-丙烯酸-对苯乙烯磺酸钠三元共聚物的合成%Synthesis of super absorbent resin acrylamide - acrylic acid - sodium p - styrene sulfonate terpolymer

    Institute of Scientific and Technical Information of China (English)

    余巧玲; 杨燕; 张杰

    2012-01-01

    以丙烯酰胺(AM)、丙烯酸(AA)和对苯乙烯磺酸钠(SSS)为单体,过硫酸钾为引发剂,N,N'-亚甲基双丙烯酰胺为交联剂,采用溶液聚合法制备出AM - AA - SSS三元共聚物.结果表明,聚合最佳条件为:AA用量10 mL,AM用量3.3g,SSS用量0.5 g,引发剂用量0.040 g,交联剂用量0.010 g,反应温度60℃.在此条件下,试样的吸蒸馏水倍率为259g/g,吸盐水倍率为42 g/g.%Aciylamide (AM) - acrylic acid (AA) - sodium p - styrene sulfonate ( SSS) terpoly-mer was synthesized by solution polymerization with AM,AA and SSS as monomers,potassium persulfate as initiator, N, N' - methylene bisacrylamide as crosslinking agent. The results showed that the optimum synthetic conditions were AA 10 mL, AM 3.3 g, SSS 0.5 g, initiator 0.040 g, crosslinkingagent 0.010 g, reaction temperature 60 °C . Under these conditions, the water absorption rate of the polymer was 259 g/g,the salt water absorption rate of the polymer was 42 g/g.

  17. Synthesis and properties of poly(aryl sulfone benzimidazole) and its copolymers for high temperature membrane electrolytes for fuel cells

    DEFF Research Database (Denmark)

    Yang, Jingshuai; Li, Qingfeng; Cleemann, Lars Nilausen;

    2012-01-01

    Poly(aryl sulfone benzimidazole) (SO2PBI) and its copolymers with poly[2,2′-p-(phenylene)-5,5′-bibenzimidazole] (pPBI), termed as Co-SO2PBI, were synthesized with varied feeding ratios of 4,4′-sulfonyldibenzoic acid (SDBA) to terephthalic acid (TPA). Incorporation of the stiff para-phenylene and ......Poly(aryl sulfone benzimidazole) (SO2PBI) and its copolymers with poly[2,2′-p-(phenylene)-5,5′-bibenzimidazole] (pPBI), termed as Co-SO2PBI, were synthesized with varied feeding ratios of 4,4′-sulfonyldibenzoic acid (SDBA) to terephthalic acid (TPA). Incorporation of the stiff para...

  18. Detection of Sperm DNA Damage in Workers Exposed to Benzene by Modified Single Cell Gel Electrophoresis

    Institute of Scientific and Technical Information of China (English)

    Bo SONG; Zhi-ming CAI; Xin LI; Li-xia DENG; Qiao ZHANG; Lu-kang ZHENG

    2005-01-01

    Objective To assess the effect of benzene on sperm DNA damageMethods Twenty-seven benzene-exposed workers were selected as exposed groupand 35 normal sperm donors as control group. Air concentration of benzene series inworkshop was determined by gas chromatography. As an internal exposure dose ofbenzene, the concentration of trans, trans-muconic acid (ttMA) was determined byhigh performance liquid chromatography. DNA was detected by modified single cellgel electrophoresis (SCGE).Results The air concentrations of benzene, toluene and xylene at the workplace were86.49 ± 2.83 mg/m3, 97.20 ±3.52 mg/m3 and 97.45 ±2.10 mg/m3, respectively.Urinary ttMA in exposed group (1.040 ± 0.617 mg/L) was significantly higher thanthat of control group (0.819 ± 0.157 mg/L). The percentage of head DNA, determinedby modified SCGE method, significantly decreased in the exposed group (n=13, 70.18%± 7.36%) compared with the control (n=16, 90.62% ± 2.94%)(P<0.001).Conclusion The modified SCGE method can be used to investigate the damage ofsperm DNA. As genotoxin and reprotoxins, benzene had direct effect on the germ cellsduring the spermatogenesiss.

  19. An analytical model for the conductivity of polymeric sulfonated membranes

    Energy Technology Data Exchange (ETDEWEB)

    Pisani, L.; Valentini, M.; Hofmann, D.H.; Kuleshova, L.N.; D' Aguanno, B. [CRS4, Parco Scientifico e Tecnologico, Polaris, 09010, Pula (Italy)

    2008-06-15

    In this work, we present a new approach to model the conductivity of polymeric sulfonated membranes. In the first part, we develop a model for the proton conductivity in a bulk acid solution. The model describes the vehicular and structural diffusion mechanisms at different proton concentrations as a function of four parameters with well defined physical meanings. These parameters are adjusted by fitting the experimental proton conductivity in a hydrochloric acid solution. In the second part, the effects of the presence of the porous membrane on the proton conductivity are added to the model. As a result, the model predicts the membrane conductivity as a function of its hydration level and porous structure. In the absence of experimental data on the membrane porous structure, the model can be used to predict the membrane porous structure once membrane conductivities are experimentally known. In this scope, in the third part, we provide a simple analytical description of the porous membrane based on the percolation theory depending on two structure parameters. A side result of the conductivity model is to provide analytical expressions for the drag coefficient, pore diameters and water permeability. All obtained results compare very well with experimental data. (author)

  20. Ways of reducing the bromine numbers of benzene for nitration with the use of the piperylene additive

    Energy Technology Data Exchange (ETDEWEB)

    Kolyandr, L.Ya.; Litvinenko, A.M.; Mastyukov, V.A.; Potapchenko, A.A.; Savikkova, M.T.; Shoherbakova, T.G.; Shuzhenko, E.A.; Titarenko, V.G.; Tkachenko, L.A.

    1981-01-01

    To study the diminution of the bromine numbers of benzene for nitration, an investigation has been made of the impurities according to the fractions of the tests of benzene production of three coke and chemical works: the works in Makeev-a, ka, Bagleisk and Yenakievo. It has been found that when the piperylene additive is used, the value of the bromine numbers of benzene for nitration is determined, in the main, not by the piperylenes removed during purification. When the intermediate BT fractions are not sufficiently clearly selected, the value of the bromine numbers of benzene is influenced also by the impurities which are concentrated in its terminal fractions. To radically remove piperylenes, it is necessary to improve the contact between the acid and the fraction being purified; this is attained by intensifying mixing and lengthening the purification process.

  1. Evidence for strain-specific differences in benzene toxicity as a function of host target cell susceptibility.

    Science.gov (United States)

    Neun, D J; Penn, A; Snyder, C A

    1992-01-01

    It has long been recognized that benzene exposure produces disparate toxic responses among different species or even among different strains within the same species. There is ample evidence that species- or strain-dependent differences in metabolic activity correlate with the disparate responses to benzene. However, bone marrow cells (the putative targets of benzene toxicity) may also exhibit species- or strain-dependent differences in susceptibility to the toxic effects of benzene. To investigate this hypothesis, two sets of companion experiments were performed. First, two strains of mice, Swiss Webster (SW) and C57B1/6J (C57), were exposed to 300 ppm benzene via inhalation and the effects of the exposures were determined on bone marrow cellularity and the development of bone marrow CFU-e (Colony Forming Unit-erythroid, an early red cell progenitor). Second, bone marrow cells from the same strains were exposed in vitro to five known benzene metabolites (1,4 benzoquinone, catechol, hydroquinone, muconic acid, and phenol) individually and in binary combinations. Benzene exposure, in vivo, reduced bone marrow cellularity and the development of CFU-e in both strains; however, reductions in both these endpoints were more severe in the SW strain. When bone marrow cells from the two strains were exposed in vitro to the five benzene metabolites individually, benzoquinone, hydroquinone, and catechol reduced the numbers of CFU-e in both strains in dose-dependent responses, phenol weakly reduced the numbers of the C57 CFU-e only and in a non-dose-dependent manner, and muconic acid was without effect on cells from either strain.(ABSTRACT TRUNCATED AT 250 WORDS)

  2. Behavioral changes in mice following benzene inhalation.

    Science.gov (United States)

    Evans, H L; Dempster, A M; Snyder, C A

    1981-01-01

    Although benzene is an important occupational health hazard and a carcinogen, the possibility that behavioral changes may forewarn of the later-occurring hematological changes has not been investigated. A time-sampling protocol was used to quantify the occurrence of 7 categories of behavior in the homecage following daily 6-hr exposures to two strains of adult mice (CD1 and C57BL/6J). The behavioral categories were stereotypic behavior, sleeping, resting, eating, grooming, locomotion, and fighting. The inhalation exposures were designed to reflect occupational exposure. Dynamic vapor exposure techniques in standard inhalation chambers were employed. Exposure to 300 or 900 ppm benzene increased the occurrence of eating and grooming and reduced the number of mice that were sleeping or resting. The responses to benzene of both the CD1 and the C57 strains were similar. The positive findings with benzene inhalation indicate the utility of behavioral investigations into the toxicology of inhaled organic solvents. The methods described herein illustrate an objective observation of animal behavior that is capable of documenting toxicity and of guiding detailed follow-up studies aimed at mechanism of action.

  3. 46 CFR 153.1060 - Benzene.

    Science.gov (United States)

    2010-10-01

    ... 46 Shipping 5 2010-10-01 2010-10-01 false Benzene. 153.1060 Section 153.1060 Shipping COAST GUARD, DEPARTMENT OF HOMELAND SECURITY (CONTINUED) CERTAIN BULK DANGEROUS CARGOES SHIPS CARRYING BULK LIQUID, LIQUEFIED GAS, OR COMPRESSED GAS HAZARDOUS MATERIALS Operations Special Cargo Procedures § 153.1060...

  4. Formation of Benzene in the Interstellar Medium

    Science.gov (United States)

    Jones, Brant M.; Zhang, Fangtong; Kaiser, Ralf I.; Jamal, Adeel; Mebel, Alexander M.; Cordiner, Martin A.; Charnley, Steven B.; Crim, F. Fleming (Editor)

    2010-01-01

    Polycyclic aromatic hydrocarbons and related species have been suggested to play a key role in the astrochemical evolution of the interstellar medium, but the formation mechanism of even their simplest building block-the aromatic benzene molecule-has remained elusive for decades. Here we demonstrate in crossed molecular beam experiments combined with electronic structure and statistical calculations that benzene (C6H6) can be synthesized via the barrierless, exoergic reaction of the ethynyl radical and 1,3- butadiene, C2H + H2CCHCHCH2 --> C6H6, + H, under single collision conditions. This reaction portrays the simplest representative of a reaction class in which aromatic molecules with a benzene core can be formed from acyclic precursors via barrierless reactions of ethynyl radicals with substituted 1,3-butadlene molecules. Unique gas-grain astrochemical models imply that this low-temperature route controls the synthesis of the very first aromatic ring from acyclic precursors in cold molecular clouds, such as in the Taurus Molecular Cloud. Rapid, subsequent barrierless reactions of benzene with ethynyl radicals can lead to naphthalene-like structures thus effectively propagating the ethynyl-radical mediated formation of aromatic molecules in the interstellar medium.

  5. Preparation of sulfonic-functionalized graphene oxide as ion-exchange material and its application into electrochemiluminescence analysis.

    Science.gov (United States)

    Chen, Guifen; Zhai, Shengyong; Zhai, Yanling; Zhang, Ke; Yue, Qiaoli; Wang, Lei; Zhao, Jinsheng; Wang, Huaisheng; Liu, Jifeng; Jia, Jianbo

    2011-03-15

    Graphene oxide (GO) obtained from chemical oxidation of flake graphite was derivatized with sulfonic groups to form sulfonic-functionalized GO (GO-SO(3)(-)) through four sulfonation routes: through amide formation between the carboxylic group of GO and amine of sulfanilic acid (AA-GO-SO(3)(-)), aryl diazonium reaction of sulfanilic acid (AD-GO-SO(3)(-)), amide formation between the carboxylic group of GO and amine of cysteamine and oxidation by H(2)O(2) (CA-GO-SO(3)(-)), and alkyl diazonium reaction of cysteamine and oxidation by H(2)O(2) (CD-GO-SO(3)(-)). Results of Fourier transform infrared spectroscopy and X-ray photoelectrospectrocopy showed that -SO(3)(-) groups were attached onto GO. Thermo gravimetric analysis showed that derivatization with sulfonic groups improved thermo stability of GO. X-ray diffraction results indicated that GO-SO(3)(-) had more ordered π-π stacking structure than the original GO. GO-SO(3)(-) and cationic polyelectrote, poly (diallyldimethylammoniumchloride) (PDDA) were adsorbed at indium tin oxide (ITO) glass surface through layer-by-layer assembling to form (GO-SO(3)(-)/PDDA)(n)/ITO multilayers. After tris-(2,2'-bipyridyl) ruthenium (II) dichloride (Ru(bpy)(3)(2+)) was incorporated into the multilayers, the obtained Ru(bpy)(3)(2+)/(GO-SO(3)(-)/PDDA)(n)/ITO electrodes can be used as electrochemiluminescence sensors for detection of organic amine with high sensitivity (limit of detection of 1 nM) and stability.

  6. Contrastive Analysis of the Raman Spectra of Polychlorinated Benzene: Hexachlorobenzene and Benzene

    Directory of Open Access Journals (Sweden)

    Zhengjun Zhang

    2011-12-01

    Full Text Available Detection of persistent pollutants such as polychlorinated benzene in environment in trace amounts is challenging, but important. It is more difficult to distinguish homologues and isomers of organic pollutantd when present in trace amounts because of their similar physical and chemical properties. In this work we simulate the Raman spectra of hexachlorobenzene and benzene, and figure out the vibration mode of each main peak. The effect on the Raman spectrum of changing substituents from H to Cl is analyzed to reveal the relations between the Raman spectra of homologues and isomers of polychlorinated benzene, which should be helpful for distinguishing one kind of polychlorinated benzene from its homologues and isomers by surface enhanced Raman scattering.

  7. 40 CFR 721.1187 - Bis(imidoethylene) benzene.

    Science.gov (United States)

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Bis(imidoethylene) benzene. 721.1187... Substances § 721.1187 Bis(imidoethylene) benzene. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance bis(imidoethylene)benzene (PMN P-93-1447) is subject to...

  8. 40 CFR 721.1350 - Benzene, (1-methylethyl)(2-phenylethyl)-.

    Science.gov (United States)

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Benzene, (1-methylethyl)(2-phenylethyl... Substances § 721.1350 Benzene, (1-methylethyl)(2-phenylethyl)-. (a) Chemical substances and significant new uses subject to reporting. (1) The chemical substance identified as benzene,...

  9. 40 CFR 721.1210 - Benzene, (2-chloroethoxy)-.

    Science.gov (United States)

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Benzene, (2-chloroethoxy)-. 721.1210... Substances § 721.1210 Benzene, (2-chloroethoxy)-. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified as benzene, (2-chloroethoxy)- (PMN P-87-1471) is subject...

  10. 40 CFR 721.10028 - Disubstituted benzene metal salts (generic).

    Science.gov (United States)

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Disubstituted benzene metal salts... Specific Chemical Substances § 721.10028 Disubstituted benzene metal salts (generic). (a) Chemical... as disubstituted benzene metal salts (PMNs P-01-901 and P-01-902) are subject to reporting under...

  11. Benzene oxide is a substrate for glutathione S-transferases.

    Science.gov (United States)

    Zarth, Adam T; Murphy, Sharon E; Hecht, Stephen S

    2015-12-01

    Benzene is a known human carcinogen which must be activated to benzene oxide (BO) to exert its carcinogenic potential. BO can be detoxified in vivo by reaction with glutathione and excretion in the urine as S-phenylmercapturic acid. This process may be catalyzed by glutathione S-transferases (GSTs), but kinetic data for this reaction have not been published. Therefore, we incubated GSTA1, GSTT1, GSTM1, and GSTP1 with glutathione and BO and quantified the formation of S-phenylglutathione. Kinetic parameters were determined for GSTT1 and GSTP1. At 37 °C, the putative Km and Vmax values for GSTT1 were 420 μM and 450 fmol/s, respectively, while those for GSTP1 were 3600 μM and 3100 fmol/s. GSTA1 and GSTM1 did not exhibit sufficient activity for determination of kinetic parameters. We conclude that GSTT1 is a critical enzyme in the detoxification of BO and that GSTP1 may also play an important role, while GSTA1 and GSTM1 seem to be less important.

  12. Toward 5 V Li-Ion Batteries: Quantum Chemical Calculation and Electrochemical Characterization of Sulfone-Based High-Voltage Electrolytes.

    Science.gov (United States)

    Wu, Feng; Zhou, Hang; Bai, Ying; Wang, Huali; Wu, Chuan

    2015-07-15

    In seeking new sulfone-based electrolytes to meet the demand of 5 V lithium-ion batteries, we have combined the theoretical quantum chemistry calculation and electrochemical characterization to explore several sulfone/cosolvent systems. Tetramethylene sulfone (TMS), dimethyl sulfite (DMS), and diethyl sulfite (DES) were used as solvents, and three kinds of lithium salts including LiBOB, LiTFSI, and LiPF6 were added into TMS/DMS [1:1, (v)] and TMS/DES [1:1, (v)] to form high-voltage electrolyte composites, respectively. All of these electrolytes display wide electrochemical windows of more than 5.4 V, with the high electrolyte conductivities being more than 3 mS/cm at room temperature. It is indicated that to achieve the best ionic conductivity in TMS/DMS cosolvent, the optimized concentrations of lithium salts LiBOB, LiTFSI, and LiPF6 were 0.8, 1, and 1 M, respectively. Furthermore, the vibrational changes of the molecular functional groups in the cosolvents were evaluated by Fourier transform infrared spectroscopy. It is found that lithium salts show strong interaction with the main functional sulfone groups and sulfonic acid ester group, thus playing a vital role in the enhancement of the ionic conductivity and electrochemical stability of the solvent system. These sulfone-based solvents with high electrochemical stability are expected to become a new generation of a high-voltage organic electrolytic liquid system for lithium-ion batteries. PMID:26087246

  13. L benzene sulfonic acid amlodipine and enalaprilat in elderly patients with ischemic stroke compared analysis of blood pressure regulation%苯磺酸左旋氨氯地平与依那普利对老年缺血性脑卒中患者血压调控的对比分析

    Institute of Scientific and Technical Information of China (English)

    周健

    2013-01-01

      Objective To investigate the correlation of senile cerebral arterial thrombosis patients using the Levamlodipine and enalapril treatment on blood pressure regulation. Methods The object of this study selected 100 cases in our hospital in 2010 June to 2012 June were elderly cerebral arterial thrombosis patients, randomized, were treated with Levamlodipine besylate (group A) and enalapril (group B), review the clinical data of two groups. Results Within 1 weeks of treatment, two groups with the passage of time, the blood pressure decreased to normal level at 7d, but the A group decreased significantly than that in B group, the difference was statistical y significant (P0.05). A mean of 9 months of fol ow-up, the A group of acute cerebral infarction rate was 10%, 14% in B group, no significant difference (P>0.05). There were no serious adverse reactions of the two groups. Conclusion The elderly cerebral arterial thrombosis patients with Levamlodipine besylate tablets treatment, concrete with high safety and effectiveness, can effectively control blood pressure level, accelerate the rehabilitation process, improve the quality of life of patients.%  目的探讨老年缺血性脑卒中患者采用苯磺酸左旋氨氯地平与依那普利治疗对血压调控的对比。方法本次研究选择的对象共100例,均为我院2010年6月至2012年6月收治的老年缺血性脑卒中患者,随机分组,分别给予苯磺酸左旋氨氯地平(A 组)和依那普利(B 组),回顾两组临床资料。结果治疗1周内,两组随时间推移,血压在第7天均降至正常水平,但 A 组下降幅度显著高于 B 组,差异有统计学意义(P<0.05)。与治疗前比较,治疗后 A 组24h动态血压水平下降幅度高于 B 组,A 组24h 动态血压合格率为88%,对照组为78%,A 组明显高于 B 组,差异均有统计学意义(P<0.05)。两组治疗后颈动脉 IMT 均显著降低,与治疗前比较差异有统计学意义(P<0.05)。A 组斑块面积与治疗前比较,明显缩小,差异有统计学意义(P<0.05),B 组斑块面积与治疗前比较无明显变化(P>0.05)。行平均9个月随访,A 组急性脑梗死率为10%,B 组为14%,无明显差异(P>0.05)。两组均无严重不良反应。结论老年缺血性脑卒中患者采用苯磺酸左旋氨氯地平片治疗,具有较高安全性和有效性,可有效控制血压水平,加快疾病康复进程,改善患者生活质量。

  14. Investigation into Variation of Endogenous Metabolites in Bone Marrow Cells and Plasma in C3H/He Mice Exposed to Benzene

    Directory of Open Access Journals (Sweden)

    Rongli Sun

    2014-03-01

    Full Text Available Benzene is identified as a carcinogen. Continued exposure of benzene may eventually lead to damage to the bone marrow, accompanied by pancytopenia, aplastic anemia or leukemia. This paper explores the variations of endogenous metabolites to provide possible clues for the molecular mechanism of benzene-induced hematotoxicity. Liquid chromatography coupled with time of flight-mass spectrometry (LC-TOF-MS and principal component analysis (PCA was applied to investigate the variation of endogenous metabolites in bone marrow cells and plasma of male C3H/He mice. The mice were injected subcutaneously with benzene (0, 300, 600 mg/day once daily for seven days. The body weights, relative organ weights, blood parameters and bone marrow smears were also analyzed. The results indicated that benzene caused disturbances in the metabolism of oxidation of fatty acids and essential amino acids (lysine, phenylalanine and tyrosine in bone marrow cells. Moreover, fatty acid oxidation was also disturbed in plasma and thus might be a common disturbed metabolic pathway induced by benzene in multiple organs. This study aims to investigate the underlying molecular mechanisms involved in benzene hematotoxicity, especially in bone marrow cells.

  15. Surfactant-modified fatty acid composition of Citrobacter sp. SA01 and its effect on phenanthrene transmembrane transport.

    Science.gov (United States)

    Li, Feng; Zhu, Lizhong

    2014-07-01

    The effects of the surfactants, Tween 80 and sodium dodecyl benzene sulfonate (SDBS) on a membrane's fatty acid composition and the transmembrane transport of phenanthrene were investigated. The results indicated that both surfactants could modify the composition of fatty acids of Citrobacter sp. Strain SA01 cells, 50 mg L(-1) of both surfactants changed the composition of the fatty acids the most, increasing the amount of unsaturated fatty acids. The comparison of fatty acid profiles with diphenylhexatriene fluorescence anisotropy, a probe for plasma membrane fluidity, suggested that an increased amount of unsaturated fatty acids corresponded to greater membrane fluidity. In addition, increased unsaturated fatty acids promoted phenanthrene to partition from the extracellular matrix to cell debris, which increased reverse partitioning from the cell debris to the cytochylema. The results of this study were expected in that the addition of a surfactant is a simple and effective method for accelerating the rate-limiting step of transmembrane transport of hydrophobic organic compounds (HOCs) in bioremediation.

  16. Efficient and selective adsorption of multi-metal ions using sulfonated cellulose as adsorbent.

    Science.gov (United States)

    Dong, Cuihua; Zhang, Fulong; Pang, Zhiqiang; Yang, Guihua

    2016-10-20

    Contamination of heavy metal in wastewater has caused great concerns on human life and health. Developing an efficient material to eliminate the heavy metal ions has been a popular topic in recent years. In this work, sulfonated cellulose (SC) was explored as efficient adsorbent for metal ions in solution. Thermo gravimetric analyzer (TGA), X-ray diffraction (XRD) and Fourier-transform infrared spectrometer (FTIR) first analyzed the characterizations of SC. Subsequently, effects of solution pH, adsorbent loading, temperature and initial metal ion concentration on adsorption performance were investigated. The results showed that sulfonated modification of cellulose could decrease the crystallinity and thermostability of cellulose. Due to its excellent performance of adsorption to metal ions, SC could reach adsorption equilibrium status within as short as 2min. In multi-component solution, SC can orderly removes Fe(3+), Pb(2+) and Cu(2+) with excellent selectivity and high efficiency. In addition, SC is a kind of green and renewable adsorbent because it can be easily regenerated by treatment with acid or chelating liquors. The mechanism study shows that the sulfonic group play a major role in the adsorption process. PMID:27474562

  17. Blends of a Polymer of Intrinsic Microporosity and Partially Sulfonated Polyphenylenesulfone for Gas Separation.

    Science.gov (United States)

    Yong, Wai Fen; Lee, Zhi Kang; Chung, Tai-Shung; Weber, Martin; Staudt, Claudia; Maletzko, Christian

    2016-08-01

    Polyphenylenesulfone (PPSU) and sulfonated polyphenylenesulfone (sPPSU) are widely used for liquid separations in the medical and food industries. However, their potential applications for gas separation have not been studied extensively owing to their low intrinsic gas permeability. We report here for the first time that blending with sPPSU can significantly improve the gas separation performance of highly permeable polymers of intrinsic microporosity (PIMs), specifically PIM-1, because of the strong molecular interactions of the sulfonic acid groups of sPPSU with CO2 and O2 . In addition, a novel co-solvent system has been discovered to overcome the immiscibility of these polymers. The presence of a higher degree of sulfonation in sPPSU results in better gas separation performance of the blend membranes close to or above the Robeson upper bound lines for O2 /N2 , CO2 /N2 and CO2 /CH4 separations. Interestingly, the blend membranes have comparable gas selectivity to sPPSU even though their sPPSU content is only 5-20 wt %. Moreover, they also display improved anti-plasticization properties up to 30 atm (3 MPa) using a binary CO2 /CH4 feed gas. The newly developed PIM-1/sPPSU membranes are potential candidates for air separation, natural gas separation, and CO2 capture. PMID:27332951

  18. Remediation of textile azo dye acid red 114 by hairy roots of Ipomoea carnea Jacq. and assessment of degraded dye toxicity with human keratinocyte cell line.

    Science.gov (United States)

    Jha, Pamela; Jobby, Renitta; Desai, N S

    2016-07-01

    Bioremediation has proven to be the most desirable and cost effective method to counter textile dye pollution. Hairy roots (HRs) of Ipomoea carnea J. were tested for decolourization of 25 textile azo dyes, out of which >90% decolourization was observed in 15 dyes. A diazo dye, Acid Red 114 was decolourized to >98% and hence, was chosen as the model dye. A significant increase in the activities of oxidoreductive enzymes was observed during decolourization of AR114. The phytodegradation of AR114 was confirmed by HPLC, UV-vis and FTIR spectroscopy. The possible metabolites were identified by GCMS as 4- aminobenzene sulfonic acid 2-methylaniline and 4- aminophenyl 4-ethyl benzene sulfonate and a probable pathway for the biodegradation of AR114 has been proposed. The nontoxic nature of the metabolites and toxicity of AR114 was confirmed by cytotoxicity tests on human keratinocyte cell line (HaCaT). When HaCaT cells were treated separately with 150 μg mL(-1) of AR114 and metabolites, MTT assay showed 50% and ≈100% viability respectively. Furthermore, flow cytometry data showed that, as compared to control, the cells in G2-M and death phase increased by 2.4 and 3.6 folds respectively on treatment with AR114 but remained unaltered in cells treated with metabolites.

  19. (Liquid + liquid) equilibria for (benzene + cyclohexane + dimethyl sulfoxide) system at T = (298.15 or 303.15) K: Experimental data and correlation

    International Nuclear Information System (INIS)

    Graphical abstract: The selectivity of DMSO, is usually high. At 25 °C and atmospheric pressure, the selectivity coefficient can reach beyond 14, which means that DMSO can compete with some ionic liquids for extracting benzene from cyclohexane. So, DMSO has large potential to separate benzene from cyclohexane as a new extractant. - Highlights: • The highest selectivity coefficient is beyond 14 of DMSO at T = (298.15 or 303.15) K. • The data’s reliability is approved by the correlation of Othmer–Tobias equation. • NRTL model is in good agreement with the experimental data. - Abstract: (Liquid + liquid) equilibrium (LLE) data were measured experimentally at T = (298.15 or 303.15) K and atmospheric pressure for the (benzene + cyclohexane + dimethyl sulfone (DMSO)) system. The Othmer–Tobias equation was applied to verify the reliability of the data. Based on the data, the selectivity of DMSO was estimated and compared with that of ionic liquids. The highest selectivity coefficient of DMSO can reach beyond 14, which means it is able to compete with some ionic liquids and it would be a good extractant to separate benzene from cyclohexane. At the same time, the NRTL model was used to correlate the data and the results show that the model agrees on the experimental data very well

  20. Effects of electrode geometry on the performance of dielectric barrier/packed-bed discharge plasmas in benzene degradation

    International Nuclear Information System (INIS)

    Highlights: • Benzene was successfully degraded by dielectric barrier/packed-bed discharge plasmas. • Different electrode geometry has distinct effect on plasmas oxidation performance. • Benzene degradation and energy performance were enhanced when using the coil electrode. • The reaction products were well determined by online FTIR analysis. -- Abstract: In this study, the effects of electrode geometry on benzene degradation in a dielectric barrier/packed-bed discharge plasma reactor with different electrodes were systematically investigated. Three electrodes were employed in the experiments, these were coil, bolt, and rod geometries. The reactor using the coil electrode showed better performance in reducing the dielectric loss in the barrier compared to that using the bolt or rod electrodes. In the case of the coil electrode, both the benzene degradation efficiency and energy yield were higher than those for the other electrodes, which can be attributed to the increased role of surface mediated reactions. Irrespective of the electrode geometry, the packed-bed discharge plasma was superior to the dielectric barrier discharge plasma in benzene degradation at any specific applied voltage. The main gaseous products of benzene degradation were CO, CO2, H2O, and formic acid. Discharge products such as O3, N2O, N2O5, and HNO3 were also detected in the outlet gas. Moreover, the presence of benzene inhibited the formation of ozone because of the competing reaction of oxygen atoms with benzene. This study is expected to offer an optimized approach combining dielectric barrier discharge and packed-bed discharge to improve the degradation of gaseous pollutants

  1. Preparation and properties of copolymer of graphene oxide and methyl acrylic acid and sodium methallyl sulfonate%氧化石墨烯与甲基丙烯酸和烯丙基磺酸钠共聚物的制备与性能∗

    Institute of Scientific and Technical Information of China (English)

    吕生华; 崔亚压; 杨文强; 周庆芳; 孙世彧

    2015-01-01

    The nanometer dispersion solution of graphene oxide (GO)was prepared by oxidation and ultrasoni-cation,followed carried out the free-radical copolymerization with methylacrylic acid (MAA)and sodium allyl-sulfonate (SAS)to synthesize the copolymer of GO,MAA and SAS (p(GO-MAA-SAS)).The copolymer was prepared by the weight ratios of MAA,SAS and GO of 1 3∶6∶1 .The FT-IR results indicated that the copoly-merization of GO and vinyl monomers was taken placed and GO naosheets were dispersed uniformly with thick-ness of 4 nm and size of 5-10 nm.The applied results indicated that the shrinkage temperature of the leather tanned with the 10% copolymer could reach 84 ℃,and the tanning function come from the synergistic effect of nano effects and functional groups.The research result has positive meaning to preparation of leather by green and clearning process.%通过氧化和超声波作用制备了氧化石墨烯(GO)纳米相片层分散液,再与甲基丙烯酸(MAA)和烯丙基磺酸钠(SAS)进行自由基共聚反应制备了氧化石墨烯与甲基丙烯酸和烯丙基磺酸钠的共聚物 P (GO-MAA-SAS),各组分的质量比为 m (MAA)∶m(SAS)∶m(GO)=13∶6∶1.FT-IR 检测结果表明GO 与单体之间发生了共聚反应,AFM检测结果表明共聚物中GO 片层的厚度为4 nm、长宽在5~10 nm范围.应用结果表明用10%的 P(GO-MAA-SAS)鞣制皮革的收缩温度为84℃,GO 的鞣制作用与 GO 的纳米效应和与胶原纤维的键合作用及其二者之间的协同作用有关,研究结果 GO 纳米片层可以鞣制皮革并且GO 的分散状态是影响鞣制效果的主要因素.

  2. 21 CFR 173.395 - Trifluoromethane sulfonic acid.

    Science.gov (United States)

    2010-04-01

    .... Neutralization equivalent, 147-151. Water, 1 percent maximum. Fluoride ion, 0.03 percent maximum. Heavy metals... esterification reaction is quenched with steam and water and the catalyst is removed with the aqueous phase... detection limit of 0.2 part per million fluoride as determined by the method described in “Official...

  3. Nonlinear diffusion in Acetone-Benzene Solution

    CERN Document Server

    Obukhovsky, Vjacheslav V

    2010-01-01

    The nonlinear diffusion in multicomponent liquids under chemical reactions influence has been studied. The theory is applied to the analysis of mass transfer in a solution of acetone-benzene. It has been shown, that the creation of molecular complexes should be taken into account for the explanation of the experimental data on concentration dependence of diffusion coefficients. The matrix of mutual diffusivities has been found and effective parameters of the system have been computed.

  4. PROCESS SIMULATION OF BENZENE SEPARATION COLUMN OF LINEAR ALKYL BENZENE (LABPLANT

    Directory of Open Access Journals (Sweden)

    Zaid A. AbdelRahman

    2013-05-01

    Full Text Available       CHEMCAD process simulator was used for the analysis of existing benzene separation column in LAB plant(Arab Detergent Company/Beiji-Iraq.         Simulated column performance curves were constructed. The variables considered in this study are the thermodynamic model option, top and bottom temperatures, feed temperature, feed composition & reflux ratio. Also simulated columns profiles for the temperature, vapor & liquid flow rates compositions, were constructed. Four different thermodynamic models options (SRK, TSRK, PR, and ESSO were used, affecting the results within 1-25% variation for the most cases.            For Benzene Column (32 real stages, feed stage 14, the simulated results show that bottom temperature above 200 oC the weight fractions of top components, except benzene, increases sharply, where as benzene top weight fraction decreasing sharply. Also, feed temperature above 180 oC  shows same trends. The column profiles remain fairly constant from tray 3 (immediately below condenser to tray 10 (immediately above feed and from tray 15 (immediately below feed to tray 25 (immediately above reboiler. Simulation of the benzene separation column in LAB production plant using CHEMCAD simulator, confirms the real plant operation data. The study gives evidence about a successful simulation with CHEMCAD.

  5. Sulfonated copolyimide membranes derived from a novel diamine monomer with pendant benzimidazole groups for fuel cells

    DEFF Research Database (Denmark)

    Li, Wei; Guo, Xiaoxia; Aili, David;

    2015-01-01

    Sulfonated polyimides are among the most interesting proton exchange membrane materials with high proton conductivity and good mechanical characteristics. As a major challenge the hydrolytic instability of the polymer backbone is addressed by introducing basic moieties in the polymer main chain......(4-aminophenoxy)biphenyl-3,3'-disulfonic acid (BAPBDS) at different diamine molar ratios (BAPBDS/BIPOB, 4/1, 6/1, 9/1 and 12/1). With ion exchange capacities in the range of 1.60-2.24 meq g(-1), transparent and ductile membranes are obtained by solution casting. The incorporation of benzimiclazole...

  6. Quinolinium 8-hydroxy-7-iodoquinoline-5-sulfonate 0.8-hydrate

    OpenAIRE

    Graham Smith

    2012-01-01

    In the crystal structure of the title hydrated quinolinium salt of ferron (8-hydroxy-7-iodoquinoline-5-sulfonic acid), C9H7N+·C9H5INO4S−·0.8H2O, the quinolinium cation is fully disordered over two sites (occupancy factors fixed at 0.63 and 0.37) lying essentially within a common plane and with the ferron anions forming π–π-associated stacks down the b axis [minimum ring centroid separation = 3.462 (6) Å]. The...

  7. Polarized synchronous light scattering characterization of the interaction of proteins with sodium dodecyl sulfonate

    Institute of Scientific and Technical Information of China (English)

    ZHAO XiaoHui; HUANG ChengZhi

    2007-01-01

    In acid buffer solution, proteins with positive charge can react with anion surfactant and result in a great enhancement of synchronous light scattering (SLS) signals. In this contribution, the correlative experiment was made to compare the interaction of human serum albumin (HAS) and immunoglobulin G (IgG) with sodium dodecyl sulfonate (SDS). Based on the measurements of the polarization light scattering signals, a new method of scattering polarization was constituted to distinguish these two interaction systems with molecular weight difference (HAS 66 kDa; IgG 150 kDa). The results were consistent with the data measured by dynamic light scattering (DLS) technique.

  8. Analyses of nitrobenzene,benzene and aniline in environmental water samples by headspace solid phase micro-extraction coupled with gas chromatography-mass spectrometry

    Institute of Scientific and Technical Information of China (English)

    CHEN Ming; YIN Yongguang; TAI Chao; ZHANG Qinghua; LIU Jiyan; HU Jingtian; JIANG Guibin

    2006-01-01

    A headspace solid phase microextraction coupled with gas chromatography mass spectrometry (HS-SPME/GC-MS) method was established for analyzing nitrobenzene, benzene and aniline in environmental water samples simultaneously.Factors affecting extraction efficiency (SPME fiber selection, acidity, temperature, salt addition, extraction time, headspace, etc) were verified. Under optimal extraction conditions, the detection limits are 0.50, 0.11 and 1.00 μg/L for nitrobenzene, benzene and aniline, respectively. The results indicate that this method is capable of making sensitive and accuracy analyses on nitrobenzene, benzene and aniline in environmental water samples.

  9. Synthesis and Characterization of Poly(arylene ether sulfone)s for Reverse Osmosis Water Purification and Gas Separation Membranes

    OpenAIRE

    Sundell, Benjamin James

    2014-01-01

    Crosslinking is an effective technique for increasing the salt rejection of water purification membranes and the selectivity of gas separation membranes. An abundance of monomers, telechelic oligomers, and novel polymers were synthesized for use as separation membranes. These materials were often imbued with crosslinking functionalities to increase their performance during testing at the University of Texas-Austin. Crosslinking of sulfonated poly(arylene ether sulfone) oligomers was stud...

  10. Synthesis and Characterization of trans-1,4-Cyclohexylene Ring Containing Poly(arylene ether sulfone)s

    OpenAIRE

    ZHANG Bin

    2012-01-01

    Poly(arylene ether sulfone)s (PAES) are important commercial polymers and have been extensively studied due to their excellent thermal and mechanical properties. However, some applications are still limited when good solvent resistance and low thermal expansion coefficient are required. There has been a continuous interest in developing new PAES based on new monomers or polymer modifications to obtain new properties or to enhance existing properties. In this dissertation, the synthesis, chara...

  11. At-line benzene monitor for measuring benzene in precipitate hydrolysis aqueous

    International Nuclear Information System (INIS)

    A highly accurate and repeatable at-line benzene monitor (ALBM) has been developed to measure the benzene concentration in precipitate hydrolysis aqueous (PHA) in the DWPF. This analyzer was conceived and jointly developed within SRTC by the Analytical Development and the Defense Waste Process Technology Sections with extensive support from the Applied Statistics Group and the TNX Operations Section. It is recommended that an ALBM specifically adapted to DWPF analytical requirements be used to measure benzene in PHA; calibrations be performed using a 10% methanol solution matrix (for standard stability); and based on experience gained in development at TNX, the services of ADS and ASG be employed to both adapt the ALBM to DWPF requirements and develop statistical control procedures

  12. At-line benzene monitor for measuring benzene in precipitate hydrolysis aqueous

    Energy Technology Data Exchange (ETDEWEB)

    Jenkins, W.J.

    1992-10-14

    A highly accurate and repeatable at-line benzene monitor (ALBM) has been developed to measure the benzene concentration in precipitate hydrolysis aqueous (PHA) in the DWPF. This analyzer was conceived and jointly developed within SRTC by the Analytical Development and the Defense Waste Process Technology Sections with extensive support from the Applied Statistics Group and the TNX Operations Section. It is recommended that an ALBM specifically adapted to DWPF analytical requirements be used to measure benzene in PHA; calibrations be performed using a 10% methanol solution matrix (for standard stability); and based on experience gained in development at TNX, the services of ADS and ASG be employed to both adapt the ALBM to DWPF requirements and develop statistical control procedures.

  13. Neuroendocrine effects of perfluorooctane sulfonate in rats.

    Science.gov (United States)

    Austin, Maureen E; Kasturi, Badrinarayanan S; Barber, Matthew; Kannan, Kurunthachalam; MohanKumar, Puliyur S; MohanKumar, Sheba M J

    2003-09-01

    Perfluorooctane sulfonate (PFOS) is a degradation product of sulfonyl-based fluorochemicals that are used extensively in industrial and household applications. Humans and wildlife are exposed to this class of compounds from several sources. Toxicity tests in rodents have raised concerns about potential developmental, reproductive, and systemic effects of PFOS. However, the effect of PFOS on the neuroendocrine system has not been investigated thus far. In this study, adult female rats were injected intraperitoneally with 0, 1, or 10 mg PFOS/kg body weight (BW) for 2 weeks. Food and water intake, BW, and estrous cycles were monitored daily. At the end of treatment, PFOS levels in tissues were measured by high-performance liquid chromatography (HPLC) interfaced with electrospray mass spectrometry. Changes in brain monoamines were measured by HPLC with electrochemical detection, and serum corticosterone and leptin were monitored using radioimmunoassay. Treatment with PFOS produced a dose-dependent accumulation of this chemical in various body tissues, including the brain. PFOS exposure decreased food intake and BW in a dose-dependent manner. Treatment with PFOS affected estrous cyclicity and increased serum corticosterone levels while decreasing serum leptin concentrations. PFOS treatment also increased norepinephrine concentrations in the paraventricular nucleus of the hypothalamus. These results indicate that exposure to PFOS can affect the neuroendocrine system in rats. PMID:12948888

  14. New pathway for degradation of sulfonated azo dyes by microbial peroxidases of Phanerochaete chrysosporium and Streptomyces chromofuscus.

    OpenAIRE

    Goszczynski, S; Paszczynski, A; Pasti-Grigsby, M B; Crawford, R L; Crawford, D. L.

    1994-01-01

    Pathways for the degradation of 3,5-dimethyl-4-hydroxy-azobenzene-4'-sulfonic acid (I) and 3-methoxy-4-hydroxyazobenzene-4'-sulfonamide (II) by the manganese peroxidase and ligninase of Phanerochaete chrysosporium and by the peroxidase of Streptomyces chromofuscus have been proposed. Twelve metabolic products were found, and their mechanisms of formation were explained. Preliminary oxidative activation of the dyes resulted in the formation of cationic species, making the molecules vulnerable ...

  15. Pd(II/HPMoV-Catalyzed Direct Oxidative Coupling Reaction of Benzenes with Olefins

    Directory of Open Access Journals (Sweden)

    Yasutaka Ishii

    2010-03-01

    Full Text Available The direct aerobic coupling reaction of arenes with olefins was successfully achieved by the use of Pd(OAc2/molybdovanadophosphoric acid (HPMoV as a key catalyst under 1 atm of dioxygen. This catalytic system could be extended to the coupling reaction of various substituted benzenes with olefins such as acrylates, aclrolein, and ethylene through the direct aromatic C-H bond activation.

  16. Investigation on Molecular Non-covalent Interaction in the Sodium Dodecyl Benzene Sulfonatepolychrome Blue B-protein Replacement Reaction

    Institute of Scientific and Technical Information of China (English)

    GAO,Hong-Wen(郜洪文); WU,Ji-Rong(邬继荣); SHEN,Rong(沈荣)

    2004-01-01

    The molecular non-covalent interaction often originates from the electrostatic attraction and accords with the Langmuir isothermal adsorption. The sodium dodecyl benzene sulfonate (SDBS)-polychrome blue B (PCB)-protein [bovine serum albumin (BSA), ovalbumin (OVA) and myoglobin (MB)] ternary reaction has been investigated at Ph 3.88. Protein to replace PCB from the PCB-SDBS binding product was used to characterize the assembly of an invisible-spectral compound, SDBS, on proteins by measuring the variation of PCB light-absorption by the microsurface adsorption-spectral correction (MSASC) technique. The effect of ionic strength and temperature on the aggregation was studied. Results showed that the aggregates SDBS92·BSA, SDBS58·OVA and SDBS15·MB at 30 ℃ and SDBS83·BSA, SDBS39·OVA and SDBS10·MB at 50 ℃ are formed.

  17. Enhancement of proton conductivity of chitosan membrane enabled by sulfonated graphene oxide under both hydrated and anhydrous conditions

    Science.gov (United States)

    Liu, Yahua; Wang, Jingtao; Zhang, Haoqin; Ma, Chuanming; Liu, Jindun; Cao, Shaokui; Zhang, Xiang

    2014-12-01

    In this study, sulfonated graphene oxide (SGO) nanosheets with controllable sulfonic acid group loading are synthesized via the facile distillation-precipitation polymerization, and then incorporated into chitosan (CS) matrix to prepare nanohybrid membranes. The microstructure and physicochemical properties of the resulting membranes are extensively investigated. Compared with CS control and GO-filled membranes, SGO-filled membranes attain enhanced thermal and mechanical stabilities due to the strong electrostatic attractions between -SO3H of SGO and -NH2 of CS, which inhibit the mobility of CS chains. Additionally, the inhibited mobility reduces the area swellings of SGO-filled membranes, reinforcing their structural stabilities. The incorporation of SGO generates acid-base pairs along CS-SGO interface, which work as facile proton-hoping sites and thus construct continuous and wide proton transfer pathways, yielding enhanced proton conductivities under both hydrated and anhydrous conditions. Meanwhile, the conductivity can be elevated by increasing the sulfonic acid group loading and content of SGO. Particularly, incorporating 2.0% S4GO can afford the nanohybrid membrane a 122.5% increase in hydrated conductivity and a 90.7% increase in anhydrous conductivity when compared with CS control membrane. The superior conduction properties then offered a significant enhancement in H2/O2 cell performances to the nanohybrid membranes, guaranteeing them to be promising proton exchange membranes.

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2009-11-15

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

  19. Covalently Cross-Linked Sulfone Polybenzimidazole Membranes with Poly(Vinylbenzyl Chloride) for Fuel Cell Applications

    DEFF Research Database (Denmark)

    Yang, Jingshuai; Aili, David; Li, Qingfeng;

    2013-01-01

    Covalently cross-linked polymer membranes were fabricated from poly(aryl sulfone benzimidazole) (SO(2) PBI) and poly(vinylbenzyl chloride) (PVBCl) as electrolytes for high-temperature proton-exchange-membrane fuel cells. The cross-linking imparted organo insolubility and chemical stability against...... radical attack to the otherwise flexible SO(2) PBI membranes. Steady phosphoric acid doping of the cross-linked membranes was achieved at elevated temperatures with little swelling. The acid-doped membranes exhibited increased mechanical strength compared to both pristine SO(2) PBI and poly[2,2'-(m......-phenylene)-5,5'-bibenzimidazole] (mPBI). The superior characteristics of the cross-linked SO(2) PBI membranes allowed higher acid doping levels and, therefore, higher proton conductivity. Fuel-cell tests with the cross-linked membranes demonstrated a high open circuit voltage and improved power performance...

  20. Benzene exposure: An overview of monitoring methods and their findings

    OpenAIRE

    Weisel, Clifford P.

    2010-01-01

    Benzene has been measured throughout the environment and is commonly emitted in several industrial and transportation settings leading to widespread environmental and occupational exposures. Inhalation is the most common exposure route but benzene rapidly penetrates the skin and can contaminant water and food resulting in dermal and ingestion exposures. While less toxic solvents have been substituted for benzene, it still is a component of petroleum products, including gasoline, and is a trac...

  1. Annulation Reactions of Donor-Acceptor Cyclopropanes with (1-Azidovinyl)benzene and 3-Phenyl-2H-azirine.

    Science.gov (United States)

    Curiel Tejeda, Joanne E; Irwin, Lauren C; Kerr, Michael A

    2016-09-16

    Under the influence of heat and Lewis acid, donor/acceptor cyclopropanes underwent annulation reactions with (1-azidovinyl)benzene and 3-phenyl-2H-azirine to form an unusual azabicyclic scaffold with an imbedded aziridine. The mechanism of reaction is believed to proceed via a vinyl nitrene intermediate. PMID:27598518

  2. Nafion/SiO2 Nanocomposites: High Potential Catalysts for Alkylation of Benzene with Linear C9-C13 Alkenes

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    High surface area Nafion/SiO2 nanocomposites with nano-sized Nafion resin particles entrapped and dispersed within the highly porous silica matrix exhibited significantly enhanced activity, high selectivity and long-term stability for the alkylation of benzene with linear C9-C13 alkenes owing to the increased accessibility of Nafion resin-based acid sites to reactants.

  3. Physiological and phylogenetic characterization of a stable chlorate-reducing benzene-degrading microbial community

    NARCIS (Netherlands)

    Weelink, S.A.B.; Tan, N.C.G.; Broeke, ten H.; Doesburg, van W.C.J.; Langenhoff, A.A.M.; Gerritse, J.; Stams, A.J.M.

    2007-01-01

    stable anoxic enrichment culture was obtained that degraded benzene with chlorate as an electron acceptor. The benzene degradation rate was 1.65 mM benzene per day, which is similar to reported aerobic benzene degradation rates but 20¿1650 times higher than reported for anaerobic benzene degradation

  4. 40 CFR 80.1230 - What are the gasoline benzene requirements for refiners and importers?

    Science.gov (United States)

    2010-07-01

    ... 40 Protection of Environment 16 2010-07-01 2010-07-01 false What are the gasoline benzene... Benzene Gasoline Benzene Requirements § 80.1230 What are the gasoline benzene requirements for refiners and importers? (a) Annual average benzene standard. (1) Except as specified in paragraph (c) of...

  5. Physiological and phylogenetic characterization of a stable benzene-degrading, chlorate-reducing microbial community

    NARCIS (Netherlands)

    Weelink, S.A.B.; Tan, N.C.G.; Broeke, H. ten; Doesburg, W. van; Langenhoff, A.A.M.; Gerritse, J.; Stams, A.J.M.

    2007-01-01

    A stable anoxic enrichment culture was obtained that degraded benzene with chlorate as an electron acceptor. The benzene degradation rate was 1.65 mM benzene per day, which is similar to reported aerobic benzene degradation rates but 20-1650 times higher than reported for anaerobic benzene degradati

  6. Acid monolayer functionalized iron oxide nanoparticle catalysts

    Science.gov (United States)

    Ikenberry, Myles

    Superparamagnetic iron oxide nanoparticle functionalization is an area of intensely active research, with applications across disciplines such as biomedical science and heterogeneous catalysis. This work demonstrates the functionalization of iron oxide nanoparticles with a quasi-monolayer of 11-sulfoundecanoic acid, 10-phosphono-1-decanesulfonic acid, and 11-aminoundecanoic acid. The carboxylic and phosphonic moieties form bonds to the iron oxide particle core, while the sulfonic acid groups face outward where they are available for catalysis. The particles were characterized by thermogravimetric analysis (TGA), transmission electron microscopy (TEM), potentiometric titration, diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS), inductively coupled plasma optical emission spectrometry (ICP-OES), X-ray photoelectron spectrometry (XPS), and dynamic light scattering (DLS). The sulfonic acid functionalized particles were used to catalyze the hydrolysis of sucrose at 80° and starch at 130°, showing a higher activity per acid site than the traditional solid acid catalyst Amberlyst-15, and comparing well against results reported in the literature for sulfonic acid functionalized mesoporous silicas. In sucrose catalysis reactions, the phosphonic-sulfonic nanoparticles (PSNPs) were seen to be incompletely recovered by an external magnetic field, while the carboxylic-sulfonic nanoparticles (CSNPs) showed a trend of increasing activity over the first four recycle runs. Between the two sulfonic ligands, the phosphonates produced a more tightly packed monolayer, which corresponded to a higher sulfonic acid loading, lower agglomeration, lower recoverability through application of an external magnetic field, and higher activity per acid site for the hydrolysis of starch. Functionalizations with 11-aminoundecanoic acid resulted in some amine groups binding to the surfaces of iron oxide nanoparticles. This amine binding is commonly ignored in iron oxide

  7. Experimental Emulsified Diesel and Benzen Investigation

    Directory of Open Access Journals (Sweden)

    Suleiman Abu-Ein

    2010-05-01

    Full Text Available This study presents an experimental investigation of emulsified fuels as an operating material for vehicle engines. Water in fuel blends is still relatively unknown and unaccepted by the majority of people. Introducing water into the combustion chamber has been around for more than one time, through water injection systems and emulsification of water into fuel. Adding water to fules will reduce bad emissions of the vehicles. It is found that brake power, engine power and also the engine torque have been improved with the emulsified fuels for both diesel and benzen till 25% water percentage addition.

  8. ANALYSIS OF SULFONATES IN AQUEOUS SAMPLES BY ION-PAIR LC/ESI-MS/MS WITH IN-SOURCE CID FOR ADDUCT PEAK ELIMINATION

    Energy Technology Data Exchange (ETDEWEB)

    OUYANG,S.; VAIRAVAMURTHY,M.A.

    1999-06-13

    Determination of low-molecular-weight organic sulfonates (e.g. taurine and cysteic acid) in aqueous solutions is important in many applications of biological, environmental and pharmaceutical sciences. These compounds are difficult to be determined by commonly used reversed-phase liquid chromatographic separation combined with UV-Visible detection because of their high solubility and the lack chromophoric moieties. Here the authors report a method combining ion-pair liquid chromatography and electrospray ionization tandem mass spectrometry (IPLC/ESI-MS/MS)for determining sulfonates. The ability of low-molecular-weight sulfonates to form ion-pairs with quaternary ammonium cations in aqueous solutions allowed LC separation with a C{sub 18} column. Detection of the sulfonates was accomplished with ESI-MS that lends a universal mode of mass detection for polar, water soluble compounds. An in-source collision induced dissociation (CID) was applied to eliminate the adduct peaks in mass spectra. Characteristic marker ions showed in the second stage mass spectra lent a method for identifying sulfonates.

  9. Neurotoxicity of perfluorooctane sulfonate to hippocampal cells in adult mice.

    Directory of Open Access Journals (Sweden)

    Yan Long

    Full Text Available Perfluorooctane sulfonate (PFOS is a ubiquitous pollutant and found in the environment and in biota. The neurotoxicity of PFOS has received much concern among its various toxic effects when given during developing period of brain. However, little is known about the neurotoxic effects and potential mechanisms of PFOS in the mature brain. Our study demonstrated the neurotoxicity and the potential mechanisms of PFOS in the hippocampus of adult mice for the first time. The impairments of spatial learning and memory were observed by water maze studies after exposure to PFOS for three months. Significant apoptosis was found in hippocampal cells after PFOS exposure, accompanied with a increase of glutamate in the hippocampus and decreases of dopamine (DA and 3,4-dihydrophenylacetic acid (DOPAC in Caudate Putamen in the 10.75 mg/kg PFOS group. By two-dimensional fluorescence difference in gel electrophoresis (2D-DIGE analysis, seven related proteins in the hippocampus that responded to PFOS exposure were identified, among which, Mib1 protein (an E3 ubiquitin-protein ligase, Herc5 (hect domain and RLD 5 isoform 2 and Tyro3 (TYRO3 protein tyrosine kinase 3 were found down-regulated, while Sdha (Succinate dehydrogenase flavoprotein subunit, Gzma (Isoform HF1 of Granzyme A precursor, Plau (Urokinase-type plasminogen activator precursor and Lig4 (DNA ligase 4 were found up-regulated in the 10.75 mg/kg PFOS-treated group compare with control group. Furthermore, we also found that (i increased expression of caspase-3 protein and decreased expression of Bcl-2, Bcl-XL and survivin proteins, (ii the increased glutamate release in the hippocampus. All these might contribute to the dysfunction of hippocampus which finally account for the impairments of spatial learning and memory in adult mice.

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

    NARCIS (Netherlands)

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

    2011-01-01

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

  11. Comparative metabolism of [14C]benzene to excretable products and bioactivation to DNA-binding derivatives in maternal and neonatal mice

    International Nuclear Information System (INIS)

    Lactating adult female mice treated with a single dose of 880 mg/kg i.p. [14C]benzene, and their 2-day-old sucklings similarly treated or nursed by their treated dams were compared in terms of their ability to metabolize benzene to urinary products or reactive intermediates as assessed by covalently-bound benzene derivatives in whole blood or liver DNA. Six metabolite fractions were identified in the urine of sucklings by high performance liquid chromatographic (HPLC) analysis at 5 h following intraperitoneal (direct) treatment with benzene. Three of the metabolite fractions co-chromatographed with authentic phenol, phenyl glucuronide, and muconic acid, and contributed 11, 6.9 and 0.6%, respectively, to the total urinary benzene metabolites. Two of the fractions were unidentified. The sixth and most polar fraction consisted of multiple metabolites, 21% of which were conjugates, and accounted for 72% of the total urinary metabolites. A similar metabolite profile was observed in 24-h urine samples from treated dams with the exception that one of the unidentified fractions in the sucklings was absent and levels of the metabolites were quantitatively higher than those observed in sucklings 5 h following their treatment with benzene. Furthermore, 78% of the most polar fraction from the dams consisted of conjugates compared with 21% of that from the sucklings. The metabolite pattern in urine of sucklings nursed by treated dams was qualitatively similar to, but quantitatively different from the pattern in treated dams. Five hours following intraperitoneal treatment with benzene, covalent binding of the compound to DNA (expressed as pmol benzene equivalents/mg DNA) in sucklings was slightly higher in whole blood (1.15±0.07) than in liver (0.77±0.07), whereas in the dam, it was slightly lower in whole blood (0.88±0.48) than in liver (1.63±0.61). Twenty four hours following benzene exposure in sucklings of benzene-treated dams, DNA binding by the compound in whole blood

  12. Fe-ZSM-5分子筛酸性和Fe离子对苯一步氧化制苯酚反应的影响%Effects of Acidity and Fe-ions for Benzene to Phenol Oxidation over Fe-ZSM-5 Zeolite

    Institute of Scientific and Technical Information of China (English)

    郭泉辉; 李娟; 李建伟

    2013-01-01

    离子交换法制备的Fe-ZSM-5和K-Fe-ZSM-5分子筛,经不同温度水热处理后作为催化剂应用于N2O为氧化剂的苯一步氧化制取苯酚反应中.实验中,采用XRD、N2-吸附仪、NH3-TPD、27A1 MAS NMR、FT-IR、UV-vis和H2-TPR等方法对催化剂进行表征.结果显示:离子交换制备的Fe-ZSM-5分子筛,部分Fe离子以Fe2O3形式负载于分子筛的孔道中.经水热处理,分子筛骨架脱铝导致Brφnsted酸性位减少,而Fe2O3离子发生迁移形成活性Fe离子位.在苯一步氧化制苯酚反应中,N2O分子吸附于Fe离子位生成α-O.活性评价结果显示,水热处理前后,催化剂分解N2O性能不变,但苯酚选择性随水热处理温度的升高而逐渐降低.此外,K离子的引入将导致催化剂选择性的降低.%Fe-ZSM-5 and K-Fe-ZSM-5 zeolites were prepared by ion-exchange,followed by hydrothermal treatment at different temperature.After characterization by means of XRD,nitrogen adsorption/desorption,NH3-TPD,27A1 MAS NMR,FT-IR,UV-vis and H2-TPR,the samples have been investigated as catalysts for the one step oxidation of benzene to phenol by N2O as oxidizing agent.The results show that part of Fe2O3 particles are loaded on the surface and the pore of the Fe-ZSM-5 zeolite by ion-exchange.After hydrothermal treatment,Fe-ZSM-5 zeolite occurs framework dealumination and Brφnsted acid sites is decreased; The amounts of Fe2O3 particles decrease and iron-ions can be migrates to form highly active Fe3+ sites.These result in that N2O molecules can be adsorbed on these highly active Fe3+ sites and decompound to α-O.Before and after hydrothermal treatment,N2O conversion is almost unchanged in one step oxidation of benzene to phenol.Phenol selectivity is gradually increased with increasing temperature of hydrothermal treatment.However,the phenol selectivity is decreased because kalium ion is introduced into Fe-ZSM-5 zeolite.

  13. Steady-state inhibition model for the biodegradation of sulfonated amines in a packed bed reactor.

    Science.gov (United States)

    Juárez-Ramírez, Cleotilde; Galíndez-Mayer, Juvencio; Ruiz-Ordaz, Nora; Ramos-Monroy, Oswaldo; Santoyo-Tepole, Fortunata; Poggi-Varaldo, Héctor

    2015-05-25

    Aromatic amines are important industrial products having in their molecular structure one or more aromatic rings. These are used as precursors for the synthesis of dyes, adhesives, pesticides, rubber, fertilizers and surfactants. The aromatic amines are common constituents of industrial effluents, generated mostly by the degradation of azo dyes. Several of them are a threat to human health because they can by toxic, allergenic, mutagenic or carcinogenic. The most common are benzenesulfonic amines, such as 4-ABS (4-aminobenzene sulfonic acid) and naphthalene sulfonic amines, such as 4-ANS (4-amino naphthalene sulfonic acid). Sometimes, the mixtures of toxic compounds are more toxic or inhibitory than the individual compounds, even for microorganisms capable of degrading them. Therefore, the aim of this study was to evaluate the degradation of the mixture 4-ANS plus 4-ABS by a bacterial community immobilized in fragments of volcanic stone, using a packed bed continuous reactor. In this reactor, the amines loading rates were varied from 5.5 up to 69 mg L(-1) h(-1). The removal of the amines was determined by high-performance liquid chromatography and chemical oxygen demand. With this information, we have studied the substrate inhibition of the removal rate of the aromatic amines during the degradation of the mixture of sulfonated aromatic amines by the immobilized microorganisms. Experimental results were fitted to parabolic, hyperbolic and linear inhibition models. The model that best characterizes the inhibition of the specific degradation rate in the biofilm reactor was a parabolic model with values of RXM=58.15±7.95 mg (10(9) cells h)(-1), Ks=0.73±0.31 mg L(-1), Sm=89.14±5.43 mg L(-1) and the exponent m=5. From the microbial community obtained, six cultivable bacterial strains were isolated and identified by sequencing their 16S rDNA genes. The strains belong to the genera Variovorax, Pseudomonas, Bacillus, Arthrobacter, Nocardioides and Microbacterium. This

  14. Associations of in Utero Exposure to Perfluorinated Alkyl Acids with Human Semen Quality and Reproductive Hormones in Adult Men

    DEFF Research Database (Denmark)

    Vested, Anne; Ramlau-Hansen, Cecilia Høst; Olsen, Sjurdur Frodi;

    2013-01-01

    Perfluorinated alkyl acids (PFAAs), persistent chemicals with unique water-, dirt-, and oil-repellent properties, are suspected of having endocrine-disrupting activity. The PFAA compounds perfluorooctanoic acid (PFOA) and perfluorooctane sulfonic acid (PFOS) are found globally in humans; because...

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

    Institute of Scientific and Technical Information of China (English)

    杨根生; 施介华; 等

    2002-01-01

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

  16. Synthesis, Characterization and Adsorption Studies of Sulfonated Poly(Styrene)

    International Nuclear Information System (INIS)

    Poly(styrene) was synthesized by suspension polymerization of styrene. Molar mass of poly(styrene) was determined by viscosity method. Sulfonated poly(styrene) was synthesized by direct sulfonation of poly(styrene) at 40 degree C. These products were identified by using IR spectroscopic technique. Cation exchange properties of sulfonated poly(styrene) have been determined for some metal ions such as Ni/sup 2+/, Zn/sup 2+/, Cu/sup 2+/ and Ca/sup 2+/. The distribution co-efficient and apparent adsorption capacities show that selectivity order of the metals as follow: Ni/sup 2+/ > Zn/sup 2+/ > Cu/sup 2+/ > Ca/sup 2+/. It was found that by increasing the pH of solution, the distribution Co-efficients (Kd) value also increased. (author)

  17. New ionic polyiodo benzene derivatives useful as X-ray contrast media

    International Nuclear Information System (INIS)

    New ionic polyiodo benzene derivatives are described for use as X-ray contrast media. The basic structure of these compounds has two trio-iodo-benzene nuclei and a single carboxylic group; in addition the possible structures of four different R groupings are described in detail. The general process for the preparation of these compounds by reacting an amine with an acid chloride is given. Examples of the preparation of five specific compounds are also described, i.e. (1) 2,4,5-triiodo-3-hydroxymethyl-5-(2,4,6-triiodo-3-N-methylcarbamoyl-5-N-methyl-N-acetylamino-benzoyl)glycylamino-benzoic acid, (2) 2,4,6-triiodo-3-hydroxymethyl-5-(2,4,6-triiodo-3-N-methyl-N-acetylamino-benzoyl)glycylamino-benzoic acid, (3) 2,4,6-triiodo-3-hydroxymethyl-5-(2,4,6-triiodo-3-amino-5-N-methyl-N-acetylamino-benzoyl)glycylamino-benzoic acid, (4) 2,4,6-triiodo-3-hydroxymethyl-5-(2,4,6-triiodo-3-N-methylcarbamoyl-5-N-methyl-N-acetylamino-benzoyl)β-aminopropionyl-amino-benzoic acid and (5) 2,4,6-triiodo-3-hydroxymethyl-5-(2,4,6-triiodo-3-amino-5-N-methylcarbamoyl-benzoyl)glycyl-N-methylamino-benzoic acid. These X-ray contrast media are in the form of aqueous solutions of pharmaceutically acceptable salts. (UK)

  18. Hydroxylation of Benzene to Phenol via Hydrogen Peroxide in Hydrophilic Triethylammonium Acetate Ionic Liquid

    Institute of Scientific and Technical Information of China (English)

    HU Xiao-ke; ZHU Liang-fang; GUO Bin; LIU Qiu-yuan; LI Gui-ying; HU Chang-wei

    2011-01-01

    A new Fenton-like system in a medium of hydrophilic triethylammonium type of ionic liquid(IL) was used for the hydroxylation of benzene to phenol. The triethylammonium acetate([Et3NH][CH3COO]) IL exhibited retardation performance for the decomposition of H2O2 and protection performance for the further oxidation of phenol,thus the yield and selectivity to phenol were promoted greatly. The acidity of the system was proved to be an important factor for the selectivity to phenol. The utilization of H2O2 and the selectivity to phenol, as well as the Turnover number(TON) of the catalyst were effectively enhanced by a benzene-[Et3NH][CH3COO] bi-phase system. The catalyst with [Et3NH][CH3COO] IL was recycled with stable catalytic performance.

  19. Hexaaquamagnesium(II bis(d-camphor-10-sulfonate

    Directory of Open Access Journals (Sweden)

    Dejan Jeremić

    2008-07-01

    Full Text Available The structure of the title complex, [Mg(H2O6](C10H15O4S2, consists of regular octahedral [Mg(H2O6]2+ cations and d-camphor-10-sulfonate anions. A three-dimensional supramolecular architecture is formed via hydrogen-bond interactions [O—H...O = 2.723 (2–2.833 (2 Å] to give alternating layers of [Mg(H2O6]2+ cations and d-camphor-10-sulfonate anions. The title compound is isomorphous with the zinc, copper, cadmium and nickel analogues.

  20. The excited state antiaromatic benzene ring: a molecular Mr Hyde?

    Science.gov (United States)

    Papadakis, Raffaello; Ottosson, Henrik

    2015-09-21

    The antiaromatic character of benzene in its first ππ* excited triplet state (T1) was deduced more than four decades ago by Baird using perturbation molecular orbital (PMO) theory [J. Am. Chem. Soc. 1972, 94, 4941], and since then it has been confirmed through a range of high-level quantum chemical calculations. With focus on benzene we now first review theoretical and computational studies that examine and confirm Baird's rule on reversal in the electron count for aromaticity and antiaromaticity of annulenes in their lowest triplet states as compared to Hückel's rule for the ground state (S0). We also note that the rule according to quantum chemical calculations can be extended to the lowest singlet excited state (S1) of benzene. Importantly, Baird, as well as Aihara [Bull. Chem. Soc. Jpn. 1978, 51, 1788], early put forth that the destabilization and excited state antiaromaticity of the benzene ring should be reflected in its photochemical reactivity, yet, today these conclusions are often overlooked. Thus, in the second part of the article we review photochemical reactions of a series of benzene derivatives that to various extents should stem from the excited state antiaromatic character of the benzene ring. We argue that benzene can be viewed as a molecular "Dr Jekyll and Mr Hyde" with its largely unknown excited state antiaromaticity representing its "Mr Hyde" character. The recognition of the "Jekyll and Hyde" split personality feature of the benzene ring can likely be useful in a range of different areas. PMID:25960203