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Sample records for ironiii pvc membrane

  1. PVC waterproofing membranes and alkali-aggregated reaction in dams

    SciTech Connect

    Scuero, A.M.

    1995-12-31

    A waterproofing polyvinylchloride (PVC) based geocomposite was installed on two dams subject to alkali-aggregate reaction, to eliminate water intrusion and to protect the facing from further deterioration. The installation system allows drainage of the infiltrated water, thus accomplishing dehydration of the dam body. On one dam, the membrane also provided protection for future slot cutting.

  2. Celluloses filled ENR/PVC membranes for palm oil mill effluent (POME) treatment

    NASA Astrophysics Data System (ADS)

    Shamsuddin, Mohd Razali; Abdullah, Ibrahim; Othaman, Rizafizah

    2013-11-01

    Membranes from composite materials have been used especially in water treatment applications. In this paper the composite membranes of celluloses filled ENR/PVC were successfully prepared for POME treatment application. The preparation of the membrane involves solution blending, casting, phase inversion and drying methods. Two types of fillers, cellulose (Cell) and cellulose grafting polymethyl methacrylate (Cell-g-PMMA) were added into ENR/PVC matrix in various compositions (1, 5, 10, 15 and 20 wt%) to determine the effect of the filler to the performance of the membrane. The membranes were characterized by using FTIR and SEM. Membrane properties in terms of porosity and water flux were examined using mathematical calculation. FTIR spectrum shows the existence of stretching vibration from the functional group of ester carbonyl, -C=O at peak 1725 cm-1 that belongs to Cell-g-PMMA filler in ENR/PVC/Cell-g-PMMA membrane which makes the membranes slightly hydrophobic. SEM micrographs exhibit that pores were formed on both ENR/PVC/Cell and ENR/PVC/Cell-g-PMMA membranes. Water flux test indicates that ENR/PVC/Cell-20% was the highest because the addition of Cell increases the hydrophilicity of the membrane. In POME treatment, ENR/PVC/Cell-20% and ENR/PVC/Cell-g-PMMA-10% showed the highest decolorization.

  3. Reverse osmosis membrane composition, structure and performance modification by bisulphite, iron(III), bromide and chlorite exposure.

    PubMed

    Ferrer, O; Gibert, O; Cortina, J L

    2016-10-15

    Reverse osmosis (RO) membrane exposure to bisulphite, chlorite, bromide and iron(III) was assessed in terms of membrane composition, structure and performance. Membrane composition was determined by Rutherford backscattering spectrometry (RBS) and membrane performance was assessed by water and chloride permeation, using a modified version of the solution-diffusion model. Iron(III) dosage in presence of bisulphite led to an autooxidation of the latter, probably generating free radicals which damaged the membrane. It comprised a significant raise in chloride passage (chloride permeation coefficient increased 5.3-5.1 fold compared to the virgin membrane under the conditions studied) rapidly. No major differences in terms of water permeability and membrane composition were observed. Nevertheless, an increase in the size of the network pores, and a raise in the fraction of aggregate pores of the polyamide (PA) layer were identified, but no amide bond cleavage was observed. These structural changes were therefore, in accordance with the transport properties observed. PMID:27470468

  4. Effect of radiation on properties of ENR/PVC/SiO2 membrane

    NASA Astrophysics Data System (ADS)

    Ismail, Nur Farahein Hadina; Abdullah, Ibrahim; Daik, Rusli; Ahmad, Ishak; Jamil, Suzereen; Lazim, Mohammad Azwan Mat; Othaman, Rizafizah

    2015-09-01

    In this study epoxidised natural rubber (ENR)/polyvinyl chloride (PVC) matrix was prepared by melt blending. The matrix was swelled in THF and silica as a filler was introduced to the solution to generate pore formation. The ENR/PVC/10 % SiO2 membrane was prepared using a casting knife technique. The membrane was irradiated using 2 MeV electron beam accelerator at a dose range of 10-100 kGy. The effect of electron beam irradiation of the membrane was studied by undergo characterization of Scanning electron microscope (SEM) and Fourier transform infra red (FTIR). Morphological studies showed that pores generated in ENR/PVC/10 % SiO2 membrane increased with the dosage of radiation. While FTIR analysis showed the presence of peak of Si-O-Si asymmetric stretching at 834 cm-1. There are no significant changes in the functional group before and after radiation.

  5. Effect of radiation on properties of ENR/PVC/SiO{sub 2} membrane

    SciTech Connect

    Ismail, Nur Farahein Hadina; Abdullah, Ibrahim; Daik, Rusli; Ahmad, Ishak; Jamil, Suzereen; Lazim, Mohammad Azwan Mat; Othaman, Rizafizah

    2015-09-25

    In this study epoxidised natural rubber (ENR)/polyvinyl chloride (PVC) matrix was prepared by melt blending. The matrix was swelled in THF and silica as a filler was introduced to the solution to generate pore formation. The ENR/PVC/10 % SiO{sub 2} membrane was prepared using a casting knife technique. The membrane was irradiated using 2 MeV electron beam accelerator at a dose range of 10-100 kGy. The effect of electron beam irradiation of the membrane was studied by undergo characterization of Scanning electron microscope (SEM) and Fourier transform infra red (FTIR). Morphological studies showed that pores generated in ENR/PVC/10 % SiO{sub 2} membrane increased with the dosage of radiation. While FTIR analysis showed the presence of peak of Si-O-Si asymmetric stretching at 834 cm{sup −1}. There are no significant changes in the functional group before and after radiation.

  6. Use of PVC plasticized membranes for uptake of radioactive cesium and strontium

    SciTech Connect

    Rais, J.; Mason, C.V.; Abney, K.D.

    1997-03-01

    A new type of sorbent for the selective uptake of elements based on the use of PVC plasticized membranes, commonly used in electrochemistry as ion selective (ISE) membranes, is described. It is theoretically derived that the material acting as a selective ion sensor of ISE must be also effective as a sorbent. In experimental verification of the hypothesis, the cobalt dicarbollide and sodium tetraphenylborate with the addition of a synergist of the polyethyleneglycol type were dissolved in several solvents mixed with a tetrahydrofurane solution of 5% PVC and evaporated to produce a membrane used for the sorption experiments. It was found that PVC, besides functioning as a solid support, does not influence significantly the behavior of the prepared materials; however, the kinetics are slower than for the analogous solvent extraction techniques. Practical applications of such membranes for the isolation of radioactive cesium and strontium from acidic and alkaline solutions with a high of Na{sup +} ions content are shown, with emphasis on nontoxic solvents as substitutes for the toxic nitrobenzene. 25 refs., 3 figs., 6 tabs.

  7. Plasticizer Effects in the PVC Membrane of the Dibasic Phosphate Selective Electrode

    PubMed Central

    Carey, Clifton

    2016-01-01

    The PVC membrane of an ion-selective electrode (ISE) sensitive to dibasic phosphate ions (HPO4-ISE) has not been optimized for maximum selectivity, sensitivity, and useable ISE lifetime and further work was necessary to improve its performance. Two areas of investigation are reported here: include the parameters for the lipophilicity of the plasticizer compound used and the amount of cyclic polyamine ionophore incorporated in the PVC membrane. Six candidate plasticizers with a range of lipophilicity were evaluated for their effect on the useable lifetime, sensitivity, and selectivity of the ISE against 13 different anions. Selectivity was determined by a modified fixed interferent method, sensitivity was determined without interferents, and the usable lifetime evaluated at the elapsed time where 50% of the HPO4-ISE failed (L50). The results show that choosing a plasticizer that has a lipophilicity similar to the ionophore's results in the best selectivity and sensitivity and the longest L50. PMID:27347487

  8. Portable e-Tongue based on Multi-channel LAPS Array with PVC Membrane for Rapid Environment Detection

    NASA Astrophysics Data System (ADS)

    Ha, D.; Yu, H.; Hu, N.; Wu, C. X.; Zhou, J.; Kirsanov, Dmitry; Legin, Andrey; Wang, P.

    2011-09-01

    A new kind of portable e-Tongue based on multi-channel LAPS array with PVC membrane has been designed for the rapid detection of environment situation, especially the seawater. It has the great advantages of depositing membranes which are offered by Chemistry Department, Saint-Petersburg State University on the sensors artificially with convenience and efficiency. To detect various heavy metal ions (Pb2+, Cd2+, Zn2+) simultaneously, respective Polyvinyl Chloride (PVC) membrane could be prepared on the surface of the silicon-based sensor in different channel.

  9. An oxalate selective electrode based on modified PVC-membrane with tetra-butylammonium--Clinoptilolite nanoparticles.

    PubMed

    Hoseini, Zohre; Nezamzadeh-Ejhieh, Alireza

    2016-03-01

    A modified PVC-membrane electrode with tetra-butylammonium bromide - Clinoptilolite nano-particles (TBA-NCP) showed good Nernstian slope (29.9±0.6 mV per decade of oxalate concentration) in concentration range of 3.1×10(-7)-8.3×10(-1) mol L(-1) with a detection limit of 1.5×10(-7) mol L(-1). The best performance was obtained with a membrane composition of 31.5% PVC, 62.5% DOP and 6% TBA-NCP in the temperature range of 20-35 °C and the pH range of 4-9. The fast response time and good reproducibility over a period of 3 months are other characteristics of the sensor. The proposed electrode was successfully used as an indicator electrode in titration of oxalate ions with CaCl2 solution. The proposed electrode was also used in direct potentiometric determination of oxalate in many real samples such as: mushroom, black and green tea, spinach and beet. PMID:26706514

  10. Immobilization of tris(2 pyridyl) methylamine in a PVC-Membrane Sensor and Characterization of the Membrane Properties

    PubMed Central

    2012-01-01

    Background Due to the increasing industrial use of titanium compounds, its determination is the subject of considerable efforts. The ionophore or membrane active recognition is the most important component of any polymeric membrane sensor. The sensor’s response depends on the ionophore and bonding between the ionophore and the target ion. Ionophores with molecule-sized dimensions containing cavities or semi-cavities can surround the target ion. The bond between the ionophore and target ion gives different selectivity and sensitivity toward the other ions. Therefore, ionophores with different binding strengths can be used in the sensor. Results In the present work, poly (vinyl chloride) (PVC) based membrane incorporating tris (2 pyridyl) methylamine (tpm) as an ionophore has been prepared and explored as a titanium(III) selective sensor. Conclusions The strengths of the ion–ionophore (Ti(OH)2+-tpm) interactions and the role of ionophore on membrane were tested by various techniques such as elemental analysis, UV–vis, Fourier transform infrared (FTIR) spectroscopy, scanning electron microscopy (SEM), and powder X-ray diffraction (XRD). All data approved the successful incorporation of organic group via covalent bond. PMID:22564322

  11. Dielectric behavior of different nanofillers incorporated in PVC-PMMA based polymer electrolyte membranes

    NASA Astrophysics Data System (ADS)

    Sowmya, G.; Pradeepa, P.; Kalaiselvimary, J.; Edwinraj, S.; Prabhu, M. Ramesh

    2016-05-01

    The Poly (methyl methacrylate) (PMMA)-Poly (vinyl chloride) (PVC) based polymer electrolytes were prepared by solvent casting technique. The prepared polymer electrolytes were subjected to conductivity studies by using electrochemical impedance spectroscopy and the maximum ionic conductivity value was found to be 0.8011 × 10-3 Scm-1 at 303K for PVC (17.5wt%) - PMMA (7.5wt %) - LiClO4 (8wt %) - PC (67wt %) - BaTiO3 (8wt%) electrolyte system. The dielectric behavior of the samples also studied.

  12. Construction of Uranyl Selective Electrode Based on Complex of Uranyl Ion with New Ligand Carboxybenzotriazole in PVC Matrix Membrane

    NASA Astrophysics Data System (ADS)

    Abu-Dalo, M. A.; Al-Rawashdeh, N. A. F.; Al-Mheidat, I. R.; Nassory, N. S.

    2015-10-01

    In the present study uranyl selective electrodes in polyvinyl chloride (PVC) matrix membrane were prepared based on a complex of uranyl ion (UO2) with carboxybenzotriazole (CBT) as ligand. The effect of the nature of plasticizer in PVC matrix were evaluated using three different plasticizers, these are dibutyl phthalate (DBP), dioctyl phthalate (DOP) and bis(2-ethylhexyl) sebacate (BHS). The results of this study indicated that the best plasticizer could be used is the DBP, which may be attributed to its lowest viscosity value compared to DOP and BHS. The electrodes with DBP as plasticizer exhibits a Nernstian response with a slope of 28.0 mV/ decade, over a wide range of concentration from 3.0×10-5-6.0×10-2 M and a detection limit of 4.0×10-6 M. It can be used in the pH range of 4.0-10.0 with a response time of less than 10 s for DBP and 25 s for both DOP and BHS. The effects of ions interferences on the electrode response were evaluated. The di- and tri-valent cations were found to interfere less than univalent cations, which was attributed to the high diffusion and the exchange rate between the univalent ions and the uranyl ion solution. The electrodes were characterized by Fourier Transform Infrared Spectroscopy (FTIR) and Scanning Electron microscopy (SEM). The results of the standard addition method were satisfactory with errors less than 7%. The developed electrode was found to be fast, sensitive and reliable indicated its potential use in measuring the uranly ion concentration in the field.

  13. A novel sensor for monitoring of iron(III) ions based on porphyrins.

    PubMed

    Vlascici, Dana; Fagadar-Cosma, Eugenia; Popa, Iuliana; Chiriac, Vlad; Gil-Agusti, Mayte

    2012-01-01

    Three A(3)B porphyrins with mixed carboxy-, phenoxy-, pyridyl-, and dimethoxy-substituent functionalization on the meso-phenyl groups were obtained by multicomponent synthesis, fully characterized and used as ionophores for preparing PVC-based membrane sensors selective to iron(III). The membranes have an ionophore:PVC:plasticizer composition ratio of 1:33:66. Sodium tetraphenylborate was used as additive (20 mol% relative to ionophore). The performance characteristics (linear concentration range, slope and selectivity) of the sensors were investigated. The best results were obtained for the membrane based on 5-(4-carboxyphenyl)-10,15,20-tris(4-phenoxyphenyl)-porphyrin plasticized with bis(2-ethylhexyl)sebacate, in a linear range from 1 × 10(-7)-1 × 10(-1) M with a slope of 21.6 mV/decade. The electrode showed high selectivity with respect to alkaline and heavy metal ions and a response time of 20 s. The influence of pH on the sensor response was studied. The sensor was used for a period of six weeks and the utility has been tested for the quantitative determination of Fe(III) in recovered solutions from spent lithium ion batteries and for the quantitative determination of Fe(III) in tap water samples. PMID:22969395

  14. Selective sensing of mercury(II) using PVC-based membranes incorporating recently synthesized 1,3-alternate thiacalix[4]crown ionophore.

    PubMed

    Mahajan, Rakesh Kumar; Kamal, Ajar; Kumar, Naresh; Bhalla, Vandana; Kumar, Manoj

    2013-05-01

    The construction and electrodes characteristics of poly(vinylchloride) (PVC)-based polymeric membrane electrode (PME) and coated graphite electrode (CGE), incorporating 1,3-alternate thiacalix[4]crown as ionophore for estimation of Hg(II) ions, are reported here. The best potential response was observed for PME-1 having membrane composition of: ionophore (6.2 mg), PVC (100.0 mg), 2-nitrophenyl octyl ether (2-NPOE; 200.0 mg), and sodium tetraphenyl borate (NaTPB; 2.0 mg); for CGE-1 with the membrane composition: ionophore (3.5 mg), PVC (40.0 mg), 2-NPOE (80.0 mg), and NaTPB (2.0 mg). The electrodes exhibits Nernstian slope of 29.16 mV/decade with PME-1 and 30.39 mV/decade with CGE-1 for Hg(II) ions over wide concentration range, i.e., 1.0 × 10(-1) to 5.0 × 10(-6) M with PME-1 and 1.0 × 10(-1) to 5.0 × 10(-7) M with CGE-1. Lower detection limits were found to be 9.77 × 10(-6) M for PME-1 and 7.76 × 10(-7) M for CGE-1 with response time varying from 10 to 20 s. Also, these electrodes work within pH range of 2.0-6.0 for PME-1 and 1.5-6.5 for CGE-1. Overall, CGE-1 has been found to be better than PME-1. CGE-1 has been used as indicator electrode for the potentiometric titration of Hg(II) ions with EDTA as well as successfully applied for determination of Hg(II) content in wastewater, insecticide, dental amalgam, and ayurvedic medicines samples with very good performance (0.9974 correlation coefficient in the comparison against volumetric method). PMID:23054787

  15. Extraction of Gold(III) from Hydrochloric Acid Solutions with a PVC-based Polymer Inclusion Membrane (PIM) Containing Cyphos® IL 104

    PubMed Central

    Bonggotgetsakul, Ya Ya Nutchapurida; Cattrall, Robert W.; Kolev, Spas D.

    2015-01-01

    Abstract: Poly(vinyl chloride) (PVC) based polymer inclusion membranes (PIMs), with different concentrations of Cyphos® IL 104 as the membrane extractant/carrier, were studied for their ability to extract Au(III) from hydrochloric acid solutions. Some of the PIMs also contained one of the following plasticizers or modifiers: 2-nitrophenyloctyl ether, dioctylphthalate, 1-dodecanol, 1-tetradecanol, or tri(2-ethylhexyl) phosphate. The best performance, in terms of extraction rate and amount of Au(III) extracted, was exhibited by a PIM consisting of 25 wt% Cyphos® IL 104, 5 wt% 1-dodecanol, and 70 wt% PVC. An almost complete back-extraction of the Au(III) extracted from this membrane was achieved by using a 0.10 mol L−1 Na2SO3 receiver solution at pH 8. The stoichiometry of the extracted Au(III)/Cyphos® IL 104 adduct was determined as [P]+ [AuCl4]− H+ [PO2]− where [P]+ and [PO2]− represent trihexyl(tetradecyl) phosphonium and bis(2,4,4-trimethylpentyl) phosphinate ions, respectively. Back-extraction of Au(III) is suggested to occur by reduction of Au(III) to Au(I), with the formation of the species [Au(SO3)2]3− in the aqueous receiver solution. Loss of 1-dodecanol from the newly developed PIM to the aqueous solutions in contact with it was observed, which indicated that this membrane was suitable for single use in the efficient recovery of Au(III) from hydrochloric acid solutions of electronic scrap or recycled jewelry. PMID:26670259

  16. Comparison of physicochemical and electrochemical characterization of PVC incorporated ZT and ZM composite membranes and their applicability on TMS theoretical equation

    NASA Astrophysics Data System (ADS)

    Arsalan, Mohd; Zeeshan, Mohd; Rafiuddin

    2015-10-01

    PVC incorporated ZT/ZM composite materials have been synthesized via qualitative sol-gel method of material synthesis. Both the composite materials have the combination of inorganic ion-exchanger of different metal salt as well as same organic polymers, which is used to design a new class of organic-inorganic composite ion exchange membrane with much better chemical and mechanical properties, good ion-exchange capacity, higher thermal stability, reproducibility, selectivity etc. The physicochemical, electrochemical, mechanical and thermal properties of both the membranes were characterized by SEM, XRD, FTIR and simultaneous TGA-DTA studies were carried out to understand the ion exchange behavior of materials. The above analysis demonstrated the functional groups, material nature, thermal stability, surface structure, porosity, elemental percentages, ion transportation etc. The electrochemical properties have been studied by TMS theoretical approach which easily determined the important parameters of membranes like transport number, mobility ratio, charge density, charge effectiveness etc. The observed ionic potential and graphical fixed-charge density of both the membranes follows KCl < NaCl < LiCl and KCl > NaCl > LiCl order respectively.

  17. The facts about PVC.

    PubMed

    Hansen, O G

    1997-10-01

    Poly(vinyl chloride) (PVC) continually arouses debate, but it remains the most widely used polymer in the industry. Important decisions about the use of materials should be based on scientific fact. This article provides the latest data on the use of PVC and describes how Denmark, the most environmentally radical country in Europe, is handling the issues. PMID:10174272

  18. PC and PVC Acoustics Demonstrations.

    ERIC Educational Resources Information Center

    Luzader, Stephen

    1990-01-01

    Described are four musical instruments constructed from polyvinyl chloride (PVC) pipe. The use of computerized synthesizers to play scales and chords is discussed. Suggestions for other illustrations of acoustics are included. (CW)

  19. Electrospinning of PVC with natural rubber

    NASA Astrophysics Data System (ADS)

    Othman, Muhammad Hariz; Mohamed, Mahathir; Abdullah, Ibrahim

    2013-11-01

    Polyvinyl chloride (PVC) was mixed with natural rubbers which are liquid natural rubber (LNR), liquid epoxidised natural rubber (LENR) and liquid epoxidised natural rubber acrylate (LENRA) for a preparation of a fine non-woven fiber's mat. PVC and each natural rubbers(PVC:LENR, PVC:LNR and PVC:LENRA) were mixed based on ratio of 70:30. Electrospinning method was used to prepare the fiber. The results show that the spinnable concentration of PVC/ natural rubber/THF solution is 16 wt%. The morphology, diameter, structure and degradation temperature of electrospun fibers were investigated by scanning electron microscopy (SEM) and thermogravimetric analysis (TGA). SEM photos showed that the morphology and diameter of the fibers were mainly affected by the addition of natural rubber. TGA results suggested that PVC electrospun fiber has higher degradation temperature than those electrospun fibers that contain natural rubber.

  20. Electrospinning of PVC with natural rubber

    SciTech Connect

    Othman, Muhammad Hariz; Abdullah, Ibrahim; Mohamed, Mahathir

    2013-11-27

    Polyvinyl chloride (PVC) was mixed with natural rubbers which are liquid natural rubber (LNR), liquid epoxidised natural rubber (LENR) and liquid epoxidised natural rubber acrylate (LENRA) for a preparation of a fine non-woven fiber’s mat. PVC and each natural rubbers(PVC:LENR, PVC:LNR and PVC:LENRA) were mixed based on ratio of 70:30. Electrospinning method was used to prepare the fiber. The results show that the spinnable concentration of PVC/ natural rubber/THF solution is 16 wt%. The morphology, diameter, structure and degradation temperature of electrospun fibers were investigated by scanning electron microscopy (SEM) and thermogravimetric analysis (TGA). SEM photos showed that the morphology and diameter of the fibers were mainly affected by the addition of natural rubber. TGA results suggested that PVC electrospun fiber has higher degradation temperature than those electrospun fibers that contain natural rubber.

  1. Thermal degradation of PVC: A review.

    PubMed

    Yu, Jie; Sun, Lushi; Ma, Chuan; Qiao, Yu; Yao, Hong

    2016-02-01

    This review summarized various chemical recycling methods for PVC, such as pyrolysis, catalytic dechlorination and hydrothermal treatment, with a view to solving the problem of energy crisis and the impact of environmental degradation of PVC. Emphasis was paid on the recent progress on the pyrolysis of PVC, including co-pyrolysis of PVC with biomass/coal and other plastics, catalytic dechlorination of raw PVC or Cl-containing oil and hydrothermal treatment using subcritical and supercritical water. Understanding the advantage and disadvantage of these treatment methods can be beneficial for treating PVC properly. The dehydrochlorination of PVC mainly happed at low temperature of 250-320°C. The process of PVC dehydrochlorination can catalyze and accelerate the biomass pyrolysis. The intermediates from dehydrochlorination stage of PVC can increase char yield of co-pyrolysis of PVC with PP/PE/PS. For the catalytic degradation and dechlorination of PVC, metal oxides catalysts mainly acted as adsorbents for the evolved HCl or as inhibitors of HCl formation depending on their basicity, while zeolites and noble metal catalysts can produce lighter oil, depending the total number of acid sites and the number of accessible acidic sites. For hydrothermal treatment, PVC decomposed through three stages. In the first region (T<250°C), PVC went through dehydrochlorination to form polyene; in the second region (250°C

  2. Studies of Iron(III) Porphyrinates Containing Silylthiolate Ligands

    PubMed Central

    Meininger, Daniel J.; Caranto, Jonathan D.; Arman, Hadi D.

    2014-01-01

    The chemistry of several iron(III) porphyrinates containing silylthiolate ligands is described. The complexes are prepared by protonolysis reactions of silanethiols with the iron(III) precursors, [Fe(OMe)(TPP)] and [Fe(OH)(H2O)(TMP)] (TPP = dianion of meso-tetraphenylporphine; TMP = dianion of meso-tetramesitylporphine). Each of the compounds has been fully characterized in solution and the solid state. The stability of the silylthiolate complexes versus other iron(III) porphyrinate complexes containing sulfur-based ligands allows for an examination of their reactivity with several biologically relevant small molecules including H2S, NO, and 1-methylimidazole. Electrochemically, the silylthiolate complexes display a quasi-reversible one-electron oxidation event at potentials higher than that observed for an analogous arylthiolate complex. The behavior of these complexes versus other sulfur-ligated iron(III) porphyrinates is discussed. PMID:24138018

  3. Low Temperature Flow of PVC Chains

    NASA Astrophysics Data System (ADS)

    Chen, Wei; Xue, Gi

    2011-03-01

    PVC is usually processed at temperature above 180& circ; C, however, it starts to degrade at 130& circ; C. If PVC can flow at temperatures below glass transition temperature (Tg), the manufacturing procedure will be energy-conserving and environment-friendly. We find that PVC powders with controlled inter-segment van der Waals attraction can be compressed into a transparent pellet with high modulus at low temperatures. The molecular mechanism underlying this phenomenon involves shear-induced unjamming transition. PVC chains are unjammed by cold-pressing freeze-dried powder with decreased packing density. Because the Tg of freeze-dried PVC is dramatically reduced to the test temperatures under compression, PVC chains are able to flow by applying pressure solely. These results help us better understanding glass transition and can possible to develop a theory for cold processes.

  4. Bags of toys: the demise of PVC.

    PubMed

    Williams, D

    1999-01-01

    Poly(vinyl chloride) (PVC) is a widely used commodity plastic that has many applications in medical devices. Recent concerns over the oestrogenic activity of some of the phthalate plasticizers used in PVC, and the hazards associated with dioxin that may be produced during the incineration of PVC waste have initiated an assessment of the future role of this material. This article addresses some of the underlying toxicological and risk assessment issues. PMID:10623344

  5. Australia slaps duties on PVC imports

    SciTech Connect

    Young, I.

    1992-12-02

    The Australian Anti-Dumping Authority (ADA0) has imposed dumping duties on imports of polyvinyl chloride (PVC) resin from seven countries and on certain expanded polystyrene (EPS) beads from Korea and Singapore. The decisions come at the end of two separate investigations begun earlier this year. In its first finding, the ADA concluded that there has been dumping of PVC resin from Canada, China, France, Japan, Norway, Saudi Arabia, and Thailand, which has caused and threatens to cause material injury to the domestic PVC industry. An eighth country, Romania, was found not to have been exporting PVC to Australia. The case is the second of its kind in Australia focusing on PVC. In December 1991 the ADA found in favor of local producer sin a dumping complaint against Argentina, Brazil, Hungary, Israel, Korea, Mexico, Poland, Singapore, Taiwan, and the US.

  6. PVC flexible liners as corrosion protection for brine treatment tanks in chlor-alkali plants

    SciTech Connect

    Perez-de-Obanos, M.; Marin, S.

    1999-11-01

    Three flexible PVC sheets were evaluated to determine their suitability as liners to protect existing steel tanks handling treated brine at 55 C in a membrane technology Chlor-Alkali plants. The evaluation included: characterization of liners and plasticizers (by Soxhlet technique, Infrared Spectroscopy (IRS), Secondary Ion Mass Spectroscopy (SIMS) and Gel Permeation Chromatography (GPC)); quantification of brine pollutants by Atomic Emission Spectroscopy (AES) and weight-loss/volume ratios; observation of the superficial damage produced by extended immersion in acid hot brine by Scanning Electron Microscopy (SEM); and the estimation of remaining properties in high temperature oxidative atmospheres (per ASTM D 3045). As a result of this evaluation, remaining property curves as a function of time and temperature are presented for high temperature atmospheric exposure. These curves are related to actual service and to changes in liner hardness. Economics of using flexible PVC liners are compared to flakeglass filled thermosetting coatings. The conclusions are that, even though flexible PVC linings are disposable, they protect steel against hot acid brine corrosion, and they are economically attractive compared to flakeglass filled coatings. In addition PVC linings may be more reliable because remaining PVC properties can be measured using nondestructive hardness measurements. PVC linings are not recommended above 65 C in corrosive service because life is notably reduced.

  7. Liquefaction of commingled waste plastics containing PVC

    SciTech Connect

    Huffman, G.P.; Feng, Zhen; Bailey, D.; Rockwell, J.

    1996-12-31

    Direct liquefaction studies were conducted on a washed, commingled waste plastic (CWP), as received from the American Plastics Council and after addition of 5 wt.% of polyvinyl chloride (PVC). Both non-catalytic and catalytic experiments were performed the catalytic experiments utilized 1 wt.% of HZSM-5. The experiments on the CWP-PVC mixture were conducted with and without the addition of 5 wt.% of calcium hydroxide. The effect of PVC on product yields was evaluated. Oil quality was examined by GC simulated distillation. The forms of occurrence of chlorine in the liquefaction products were determined by x-ray absorption fine structure (XAFS) spectroscopy utilizing the X-ray absorption near edge structure (XANES).

  8. Rapid quenching effects in PVC films

    NASA Technical Reports Server (NTRS)

    Lee, H. D.; Mandell, J. F.; Mcgarry, F. J.

    1981-01-01

    Using a specially constructed microbalance for hydrostatic weighing, density changes in PVC thin films (with no additives, 30-100 micrometers thick), due to rapid quenching (approximately 300 C/sec) through the glass transition temperature, have been observed. The more severe the quench, the greater is the free volume content. Isobaric volume recovery of PVC has also been studied by volume dilatometry. Both show aging of relaxing molecular rearrangements takes place as a linear function of logarithmic aging time at room temperature. Distribution of retardation times and Primak's distributed activation energy spectra have been applied to the volume recovery data. The concomitant changes in mechanical properties of PVC after quenching have been monitored by tensile creep and stress-strain to failure. All reflect the presence of excess free volume content, due to rapid quenching.

  9. Structure and magnetic properties of an unusual homoleptic iron(III) thiocyanate dimer.

    PubMed

    Dinsdale, D R; Lough, A J; Lemaire, M T

    2015-06-28

    We describe the structural and variable temperature magnetic susceptibility properties of an unusual homoleptic bimetallic iron(III) thiocyanate tetraanion. This work represents the first structurally characterized bis(μ-1,3-thiocyanato) dimer of iron(III). A weak antiferromagnetic exchange interaction is observed between the two iron(III) ions, which is supported by broken symmetry density functional theory (DFT) calculations. PMID:25996241

  10. PVC (polyvinylchloride) pipe reliability and failure modes

    SciTech Connect

    Carroll, M.M.

    1984-06-01

    This report is narrowed to one variety of plastic pipe, polyvinylchloride (PVC), because of its common and extensive industrial, commercial and residential applications. There are certain disadvantages which must also be considered. PVC pipe is essentially brittle in nature, and it is relatively easily damaged by mechanical means such as being struck by tools or other materials; being weakened or fractured by gouging, abrasion or rough handling such as commonly occurs when pipe sections are thrown or walked on by workers. Excessive heat, welding slag, sunlight, and certain chemicals adversely affect it. There is also some concern about manufacturing processes which can affect product quality and integrity.

  11. Superhydrophobic Materials Technology-PVC Bonding Techniques

    SciTech Connect

    Hunter, Scott R.; Efird, Marty

    2013-05-03

    The purpose of the technology maturation project was to develop an enhanced application technique for applying diatomaceous earth with pinned polysiloxane oil to PVC pipes and materials. The oil infiltration technique is applied as a spray of diluted oil in a solvent onto the superhydrophobic diatomaceous earth substrate. This makes the surface take on the following characteristics: wet-cleanable; anti-biofouling; waterproof; and anti-corrosion. The project involved obtaining input and supplies from VeloxFlow and the development of successful techniques that would quickly result in a commercial license agreement with VeloxFlow and other companies that use PVC materials in a variety of other fields of use.

  12. Effect of disinfectants on pseudomonads colonized on the interior surface of PVC pipes.

    PubMed Central

    Anderson, R L; Holland, B W; Carr, J K; Bond, W W; Favero, M S

    1990-01-01

    We investigated the effect of disinfectants on microbial contamination present on the interior surface of polyvinyl chloride (PVC) pipes filled with 600 ml of water contaminated with Pseudomonas pickettii and P. aeruginosa. After eight weeks, water was removed, and the test pipes exposed to various types of aqueous disinfectants. Disinfectant samples were removed, neutralized, and examined for recovery of microorganisms by membrane filtration. After seven-days exposure, disinfectant solutions were removed and pipes filled with sterile distilled water. Water was examined by membrane filtration at seven-day intervals to determine whether the organisms had survived in the pipes. Colonization of PVC surfaces were examined during each study phase by scanning electron-microscopy (SEM). P. aeruginosa was isolated directly from iodophor disinfectant, phenolic germicide, and iodophor antiseptic solutions. After addition of sterile water, P. aeruginosa was recovered from PVC pipes previously exposed to chlorine, phenolic, quaternary-ammonium, and iodophor disinfectants; P. pickettii was recovered from water in pipes treated with iodophor disinfectant, chlorine, and ethanol. The existence of glycocalyx-like cellular masses on the interior wall of PVC pipes most likely protected embedded organisms from the microbicidal action of some of the disinfectants tested and served as the reservoir for continuous contamination. Images FIGURE 1 PMID:2293797

  13. Conversion of waste polyvinyl chloride (PVC) to useful chemicals

    SciTech Connect

    Kamo, T.; Yamamoto, Y.; Miki, K.; Sato, Y.

    1995-12-01

    Combustion and pyrolysis of plastics have been studyed for thermal energy recycling. In this study, hydrogen chloride was removed from PVC, then liquefied the chloried free PVC in hydrogen donor solvent.

  14. a Mossbauer Effect Study of Iron(iii) Dithiocarbamates.

    NASA Astrophysics Data System (ADS)

    Fiddy, Judith Mary

    Available from UMI in association with The British Library. Ever since the pioneering work of Cambi iron(III) trisdithiocarbamates, which have the formula Fe(R _2NCS_2]_3 where R is an alkyl or an aryl group, have formed the basis for understanding spin-state equilibria in iron(III) complexes. Magnetic and infrared studies clearly indicate equilibrium between the high-spin and low-spin states. The Mossbauer spectra, however, show only a single component, indicating rapid relaxation between the two spin states on the Mossbauer timescale. It has been assumed that the spectral parameters are therefore a function of the relative spin-state populations. In this thesis, the results of Mossbauer experiments carried out on a series of iron(III) trisdithiocarbamates with various organic substituents, known to give a range of high-spin and low-spin state populations at room temperature, are presented. An iron(III) bisdithiocarbamate complex, Fe^{57} ((C_5 H_{10})_2NCS _2]_2NCS, was also investigated. The samples were studied at temperatures from 1.3K to 295K, and at pressures between atmospheric pressure and 80kbar at room temperature only. It was found that, in fact, the spin-equilibrium plays only a minor role in determining the Mossbauer spectra of the trisdithiocarbamate compounds. The effects of spin -state relaxation on the temperature dependence of the spectra are, in general, masked by those of slow paramagnetic relaxation which, in contrast to the effects of the spin-equilibrium, are marked and different for each compound. By fitting the spectra to models of paramagnetic relaxation the temperature dependence of the relaxation rates and possible directions of the magnetic hyperfine field relative to the major axis of the electric field gradient were found. The pressure dependence of the spectra was found to be rather similar for all the compounds, the main differences being in the widths and in the asymmetry of the areas of the spectral lines. Both these effects can

  15. Properties of lightweight aggregate concrete prepared with PVC granules derived from scraped PVC pipes.

    PubMed

    Kou, S C; Lee, G; Poon, C S; Lai, W L

    2009-02-01

    This paper aims to investigate the fresh and hardened properties of lightweight aggregate concretes that are prepared with the use of recycled plastic waste sourced from scraped PVC pipes to replace river sand as fine aggregates. A number of laboratory prepared concrete mixes were tested, in which river sand was partially replaced by PVC plastic waste granules in percentages of 0%, 5%, 15%, 30% and 45% by volume. Two major findings are identified. The positive side shows that the concrete prepared with a partial replacement by PVC was lighter (lower density), was more ductile (greater Poisson's ratios and reduced modulus of elasticity), and had lower drying shrinkage and higher resistance to chloride ion penetration. The negative side reveals that the workability, compressive strength and tensile splitting strength of the concretes were reduced. The results gathered would form a part of useful information for recycling PVC plastic waste in lightweight concrete mixes. PMID:18691863

  16. Polarizing PVC — A Discrepant Event

    NASA Astrophysics Data System (ADS)

    Headly, David; Karabatek, Mohamed

    2016-01-01

    Each year when teaching polarization phenomena and the Triboelectric Series in a unit on electrostatics, I would balance some rods (2-3 ft in length) made from wood, aluminum, PVC, and Plexiglas on an inverted watch glass and demonstrate to the class how a party balloon rubbed with fake rabbit fur (charging the balloon negative) would always attract the uncharged rods, causing them to rotate towards the balloon (see Fig. 1). The fact that a charged object always attracts a neutral object due to the induced dipole in the latter is a great way to test if something is in fact charged. Surprisingly, the PVC pipe would usually, but not always, repel the charged balloon and rotate away! Repulsion means that neither of the objects are electrically neutral. In a separate test, after rubbing together a Plexiglas rod with a polyethylene grocery bag (making the rod positively charged and the bag negatively charged), the PVC usually attracts the rod. With the help of a student as part of his senior project, I finally decided to investigate further the source of the negative charge that exists on PVC. Specifically, is it nothing more than static charge that builds up on the pipe from unavoidable contact with its surroundings, or is it somehow intrinsic to the manufacturing process?

  17. Polarizing PVC--A Discrepant Event

    ERIC Educational Resources Information Center

    Headly, David; Karabatek, Mohamed

    2016-01-01

    This article describes an experiment teaching polarization phenomena and the Triboelectric Series in a unit on electrostatics. Using rods (2-3 ft in length) made from wood, aluminum, PVC, and Plexiglas on an inverted watch glass, these items demonstrated to the class how a party balloon rubbed with fake rabbit fur (charging the balloon negative)…

  18. Conversion of waste polyvinyl chloride (PVC) to useful chemicals

    SciTech Connect

    Kamo, T.; Yamamoto, Y.; Miki, K.; Sato, Y.

    1995-12-31

    Developments of recycling technologies are expected one of the most important keys for saving energy and resources, and minimization impact for environment. For instance, combustion of waste for power generation and conversion of plastics into liquid fuels have been studying for thermal energy recycling. However, PVC has been excepted from the most of these experiments. Because, heat of combustion of PVC is almost a half of other plastics, hydrogen chloride, which is produced at low temperature, corrodes the combustion chamber, and PVC causes coking reaction during pyrolysis of plastics. Numerous investigations have been conducted on degradation of PVC. However, most of these experiments were done to improve heat resistance of PVC or to study reaction mechanism of PVC degradation. Pyrolysis of PVC into liquid products have been studying since 1960`s from a view of environmental protection. Recently, Y. Maezawa et al. reported PVC was converted into oil at 600 T with sodium hydroxide. However, more than 50 % of hydrocarbon fraction of PVC was converted to residue and gas in their experiment. We are going to develop a new technology to convert of PVC into useful chemicals or liquid fuels at high efficiency by using hydrogen donor solvent.

  19. A novel PVC-membrane optical sensor for highly sensitive and selective determination of UO 22+ ion based on a recently synthesized benzo-substituted macrocyclic diamide and dibenzoylmethane

    NASA Astrophysics Data System (ADS)

    Shamsipur, Mojtaba; Zargoosh, Kiomars; Mizani, Farhang; Eshghi, Hossein; Rostami, Faramarz

    2010-09-01

    A highly sensitive ion-selective bulk optode membrane for sensing UO 22+ ion based on plasticized poly(vinyl chloride) containing 6,7,9,10,12,13,15,16,23,24,25,26-dodecahydrodibenzo[n,v][1,4,7,10,13,17,20]pentaoxa-diazacyclotricosine-22,27-dione as ionophore, dibenzodylmethane as chromoionophore and sodium tetraphenylborate as an ionic additive was prepared. In addition to its high stability, reproducibility and relatively long lifetime, the proposed optical sensor revealed good selectivity for uranyl ion over a large number of alkali, alkaline earth, transition, and heavy metal ions. The proposed sensor displays a calibration response for UO 22+ over a concentration range of 4.3 × 10 -6 to 2.5 × 10 -8 M with a limit of detection of 8.0 × 10 -9 M and a response time of less than 12 min. The proposed optical sensor was applied successfully to the determination of UO 22+ ion in tap water and Khoshumi mine concentrated solution samples.

  20. Poly(vinyl alcohol)/poly(vinyl chloride) composite polymer membranes for secondary zinc electrodes

    NASA Astrophysics Data System (ADS)

    Yang, Chun-Chen; Yang, Jen Ming; Wu, Cheng-Yeou

    A microporous composite polymer membrane composed of poly(vinyl alcohol) (PVA) and poly(vinyl chloride) (PVC), was prepared by a solution casting method and a partial dissolution process. The characteristic properties of microporous PVA/PVC composite polymer membranes containing 2.5-10 wt.% PVC polymers as fillers were characterized by thermogravimetric analysis (TGA), X-ray diffraction (XRD), scanning electron microscopy (SEM), capillary flow porometry (CFP), micro-Raman spectroscopy, dynamic mechanical analyzer (DMA) and the AC impedance method. The electrochemical properties of a secondary Zn electrode with the PVA/PVC composite polymer membrane were studied using the galvanostatic charge/discharge method. The PVA/PVC composite polymer membrane showed good thermal, mechanical and electrochemical properties. As a result, the PVA/PVC composite polymer membrane appears to be a good candidate for use on the secondary Zn electrodes.

  1. Polyaniline nanorods/PVC composites with antistatic properties

    NASA Astrophysics Data System (ADS)

    Tao, Yulun; Feng, Weitao; Ding, Guoxin; Cheng, Guojun

    2015-08-01

    Novel antistatic polyaniline/poly(vinyl chloride) (PVC) composite materials are prepared. This study focuses on modification of PVC matrix with different content of polyaniline nanorods. Polyaniline nanorods can reduce the volumn resistivity of PVC/polyaniline composites 1016 Ω cm from to 1011 Ω cm five orders of magnitude at low content of 2 wt %. Moreover, the mechanical performance of the composite material is also good. Based on the results, we have confidence in the new antistatic composites.

  2. A selective optical chemosensor based on a thia-containing Schiff-base iron(III) complex for thiocyanate ion.

    PubMed

    Ershad, Sohrab; Sagathforoush, Lotf-Ali; Karim-Nezhad, Ghasem

    2009-05-01

    A new optode membrane for the sensitive and selective determination of thiocyanate ion, based on a change in the absorption spectrum of a polymer film, is proposed. A membrane composed of plasticized poly vinyl chloride (PVC), an Fe(III) Schiff-base complex as a chromoionophore and hexadecyl trimethyl ammonium bromide (HDTMABr) as a cationic additive was prepared. The influence of different plasticizers was studied concerning the sensitivity, linear range and selectivity of the membrane film. Satisfactory analytical sensing characteristics for determining thiocyanate ion were obtained in terms of the selectivity, reversibility and reproducibility with a good detecting range. In addition, the optical film responds to thiocyanate ion reversibly over a wide dynamic range 1.0 x 10(-8) to 1.0 x 10(-3) M with fast response and recovery times. The optode membrane has been applied to determine the thiocyanate ion in urine samples. PMID:19430150

  3. Structure and activity of the anticaking agent iron(iii) meso-tartrate.

    PubMed

    Bode, Arno A C; Granneman, Sanne J C; Feiters, Martin C; Verwer, Paul; Jiang, Shanfeng; Meijer, Jan A M; van Enckevort, Willem J P; Vlieg, Elias

    2016-04-12

    Iron(iii) meso-tartrate, a metal-organic complex, is a new anticaking agent for sodium chloride. A molecular structure in solution is proposed, based on a combination of experimental and molecular modelling results. We show that the active complex is a binuclear iron(iii) complex with two bridging meso-tartrate ligands. The iron atoms are antiferromagnetically coupled, resulting in a reduced paramagnetic nature of the solution. In solution, a water molecule coordinates to each iron atom as a sixth ligand, resulting in an octahedral symmetry around each iron atom. When the water molecule is removed, a flat and charged site is exposed, matching the charge distribution of the {100} sodium chloride crystal surface. This charge distribution is also found in the iron(iii) citrate complex, another anticaking agent. This gives a possible adsorption geometry on the crystal surface, which in turn explains the anticaking activity of the iron(iii) meso-tartrate complex. PMID:26974191

  4. Cell Adhesion to Plasma-Coated PVC

    PubMed Central

    Rangel, Elidiane C.; de Souza, Eduardo S.; de Moraes, Francine S.; Duek, Eliana A. R.; Lucchesi, Carolina; Schreiner, Wido H.; Durrant, Steven F.; Cruz, Nilson C.

    2014-01-01

    To produce environments suitable for cell culture, thin polymer films were deposited onto commercial PVC plates from radiofrequency acetylene-argon plasmas. The proportion of argon in the plasmas, PAr, was varied from 5.3 to 65.8%. The adhesion and growth of Vero cells on the coated surfaces were examined for different incubation times. Cytotoxicity tests were performed using spectroscopic methods. Carbon, O, and N were detected in all the samples using XPS. Roughness remained almost unchanged in the samples prepared with 5.3 and 28.9% but tended to increase for the films deposited with PAr between 28.9 and 55.3%. Surface free energy increased with increasing PAr, except for the sample prepared at 28.9% of Ar, which presented the least reactive surface. Cells proliferated on all the samples, including the bare PVC. Independently of the deposition condition there was no evidence of cytotoxicity, indicating the viability of such coatings for designing biocompatible devices. PMID:25247202

  5. PET and PVC Separation with Hyperspectral Imagery

    PubMed Central

    Moroni, Monica; Mei, Alessandro; Leonardi, Alessandra; Lupo, Emanuela; La Marca, Floriana

    2015-01-01

    Traditional plants for plastic separation in homogeneous products employ material physical properties (for instance density). Due to the small intervals of variability of different polymer properties, the output quality may not be adequate. Sensing technologies based on hyperspectral imaging have been introduced in order to classify materials and to increase the quality of recycled products, which have to comply with specific standards determined by industrial applications. This paper presents the results of the characterization of two different plastic polymers—polyethylene terephthalate (PET) and polyvinyl chloride (PVC)—in different phases of their life cycle (primary raw materials, urban and urban-assimilated waste and secondary raw materials) to show the contribution of hyperspectral sensors in the field of material recycling. This is accomplished via near-infrared (900–1700 nm) reflectance spectra extracted from hyperspectral images acquired with a two-linear-spectrometer apparatus. Results have shown that a rapid and reliable identification of PET and PVC can be achieved by using a simple two near-infrared wavelength operator coupled to an analysis of reflectance spectra. This resulted in 100% classification accuracy. A sensor based on this identification method appears suitable and inexpensive to build and provides the necessary speed and performance required by the recycling industry. PMID:25609050

  6. PET and PVC separation with hyperspectral imagery.

    PubMed

    Moroni, Monica; Mei, Alessandro; Leonardi, Alessandra; Lupo, Emanuela; Marca, Floriana La

    2015-01-01

    Traditional plants for plastic separation in homogeneous products employ material physical properties (for instance density). Due to the small intervals of variability of different polymer properties, the output quality may not be adequate. Sensing technologies based on hyperspectral imaging have been introduced in order to classify materials and to increase the quality of recycled products, which have to comply with specific standards determined by industrial applications. This paper presents the results of the characterization of two different plastic polymers--polyethylene terephthalate (PET) and polyvinyl chloride (PVC)--in different phases of their life cycle (primary raw materials, urban and urban-assimilated waste and secondary raw materials) to show the contribution of hyperspectral sensors in the field of material recycling. This is accomplished via near-infrared (900-1700 nm) reflectance spectra extracted from hyperspectral images acquired with a two-linear-spectrometer apparatus. Results have shown that a rapid and reliable identification of PET and PVC can be achieved by using a simple two near-infrared wavelength operator coupled to an analysis of reflectance spectra. This resulted in 100% classification accuracy. A sensor based on this identification method appears suitable and inexpensive to build and provides the necessary speed and performance required by the recycling industry. PMID:25609050

  7. Selective extraction and separation of iron(III) with 4-methylpentan-2-ol.

    PubMed

    Gawali, S B; Shinde, V M

    1974-11-01

    4-methylpentan-2-ol is used for quantitative extraction of iron(III) from 5.5-6M hydrochloric acid. The iron(III) is then stripped with water and determined titrimetrically. Te(IV), Se(IV), ascorbate, fluoride and thiocyanate interfere must be absent. Mo(VI), W(VI) and Au(III) are co-extracted but do not interfere in the determination. PMID:18961587

  8. Sorption of iron(III) from chromate solution by the aminocarboxylic ion exchanger ANKB-2

    SciTech Connect

    Stoyanova, O.F.; Izmailova, D.R.; Kurolap, N.S.; Uglyanskaya, V.A.

    1986-12-20

    The possibility of iron(III) sorption by the amphoteric ion exchanger ANKB-2 from chromate solution and its superiority over the cation exchanger KU-23 (10/60) have been demonstrated. By means of IR spectroscopy it has been shown that iron(III) sorption from chromate solution by ANKB-2 proceeds via both ionic and coordination reactions. The proportion of these kinds of reaction does not depend on the Cr(VI) content of the initial solution.

  9. Spectroscopic and structural investigations of iron(III) isothiocyanates. A comparative theoretical and experimental study.

    PubMed

    Elijošiutė, Erika; Eicher-Lorka, Olegas; Griškonis, Egidijus; Kuodis, Zenonas; Jankūnaitė, Dalia; Denafas, Gintaras

    2014-08-14

    A combined experimental and theoretical study on the molecular structure and vibrational spectra of [Fe(NCS)](2+) complex in the aqueous solution at the pH∼2 ± 0.1 have been performed. Experimental Raman spectra of the iron(III) isothiocyanate with higher coordination number in the acidic aqueous solution have been analyzed. Molecular modeling of the iron(III) monoisothiocyanate complex was accomplished by the density functional theory (DFT) method using B3LYP and PBE1PBE functionals. Theoretical vibrational spectra of the iron(III) monoisothiocyanate were interpreted by means of the potential energy distributions (PEDs). The influence of different solvation models and position of SO4(2)(-) ligand vs. NCS(-) ligand upon its geometry and vibrational frequencies have been evaluated. The effect of H2O/D2O isotopic substitution on the experimental and calculated Raman spectra of iron(III) isothiocyanates has been examined. Procedures of Raman spectra subtraction have been applied for the extractions of weak and/or obscured Raman signals. As a result, the presence of bound SO4(2)(-) ion and water molecules in the first coordination sphere in the acidic aqueous iron(III) isothiocyanate solution was confirmed. The vibrational assignments for the investigated iron(III) isothiocyanates were proposed here for the first time. PMID:24721282

  10. Chloride contamination of concrete by interaction with PVC combustion gases

    SciTech Connect

    Climent-Llorca, M.A.; Viqueira-Perez, E.; Vera-Almenar, G. de; Lopez-Atalaya, M.M.

    1998-02-01

    Chloride contamination of concrete by interaction with PVC combustion gases has been studied in a small-scale testing chamber, which allows simulating the conditions probably prevailing in PVC fires of different magnitude through variation of the quotient between mass of burnt PVC and exposed concrete surface (PVC/S). In all cases, a steep gradient of chloride concentration with depth is found after the fire: most chloride is detected in the outermost layer at depths below 5 mm. Surface chloride contents (within 5 mm) for prestressed and reinforced concretes, tested with a high (PVC/S) ratio, are as high as 2.5 and 5% by weight of cement, respectively. Chloride concentrations in concrete near the steels are below the corrosion thresholds after the fire, but they can rise by diffusion to values able to induce rebar corrosion, especially if concrete is exposed to a humid atmosphere.

  11. Risks and benefits of PVC in medical applications.

    PubMed

    Fanelli, R; Zuccato, E

    2002-01-01

    The safety of using PVC in the medical field has been recently challenged due to the toxic activity it allegedly exerts on exposed patients. The environmental repercussions of disposing of PVC, once its use has terminated, represent an additional point of debate, used to sustain the advisability of abolishing PVC. The reasons that have led some to request the abolition of PVC involve valid questions of principle, perhaps, but they lack a technical evaluation of the benefit-risk ratio and the possible consequences this action would have on patients and on healthcare personnel. The purpose of this paper is therefore to help bring the terms of the question back into the realm of evidence and proof, attempting to formulate a brief picture of what is known, in terms of PVC uses in the clinical field, evaluating the benefits and risks to human health and to the environment, also in relation to possible alternatives, and discussing the margins of uncertainty that emerge. Evidence supports the conclusion that PVC is an important weapon in the complex arsenal medicine has at its disposal to care for patients and cure diseases. Though its use can be considered safe, recent surveys have identified in some patients possibility of risks associated with DEHP, the principal plasticizer of PVC for medical applications. Studies are in progress to eliminate these margins of risk and increase the safety for patients. PMID:12426816

  12. Spectrophotometric determination of trace amounts of iron(III) with norfloxacin as complexing reagent.

    PubMed

    Issopoulos, P B

    1989-05-01

    The complexation of iron(III) with norfloxacin in acidic solution at 25 degrees C, at an ionic strength of about 0.3 M and a pH of 3.0 has been studied. The water-soluble complex formed, which exhibits an absorption maximum at 377 nm, was used for the spectrophotometric determination of trace amounts of iron(III). The molar absorptivity was 9.05 x 10(3) I mol-1 cm-1 and the Sandell sensitivity 6.2 ng cm-2 of iron(III) per 0.001 A. The formation constant (Kf) was determined spectrophotometrically and was found to be 4.0 x 10(8) at 25 degrees C. The calibration graph was rectilinear over the range 0.25-12.0 p.p.m. of iron(III) and the regression line equation was A = 0.163c - 0.00042 with a correlation coefficient of 0.9998 (n = 9). Common cations, except cerium (IV), did not interfere with the determination. The results obtained for the determination of iron(III) using the described procedure and the thiocyanate method were compared statistically by means of the Student t-test and no significant difference was found. PMID:2757232

  13. Binding of Iron(III) to Organic Soils: Exafs Spectroscopy And Chemical Equilibrium Modeling

    SciTech Connect

    Gustafsson, J.P.; Persson, I.; Kleja, D.B.; Schaik, J.W.J.van

    2007-07-09

    The complexation of iron(III) to soil organic matter is important for the binding of trace metals in natural environments because of competition effects. In this study, we used extended X-ray absorption fine structure (EXAFS) spectroscopy to characterize the binding mode for iron(III) in two soil samples from organic mor layers, one of which was also treated with iron(III). In most cases the EXAFS spectra had three significant contributions, inner-core Fe-O/N interactions at about 2.02(2) angstroms, Fe-C interactions in the second scattering shell at 3.00(4) angstroms, and a mean Fe-Fe distance at 3.37(3) angstroms. One untreated sample showed features typical for iron (hydr)oxides; however, after treatment of iron(III) the EXAFS spectrum was dominated by organically complexed iron. The presence of a Fe-Fe distance in all samples showed that the major part of the organically complexed iron was hydrolyzed, most likely in a mixture of complexes with an inner core of (O{sub 5}Fe){sub 2}O and (O{sub 5}Fe){sub 3}O. These results were used to constrain a model for metal-humic complexation, the Stockholm Humic Model (SHM). The model was able to describe iron(III) binding very well at low pH considering only one dimeric iron(III)-humic complex. The competition effect on trace metals was also well described.

  14. 42. VIEW EAST OF PLASTIC STACK (PROBABLY PVC) WHICH VENTED ...

    Library of Congress Historic Buildings Survey, Historic Engineering Record, Historic Landscapes Survey

    42. VIEW EAST OF PLASTIC STACK (PROBABLY PVC) WHICH VENTED FUMES FROM THE DIPPING OPERATIONS IN BUILDING 49A; BUILDING 49 IS AT THE LEFT OF THE PHOTOGRAPH - Scovill Brass Works, 59 Mill Street, Waterbury, New Haven County, CT

  15. Hoechst and Wacker plan joint venture in PVC

    SciTech Connect

    Young, I.

    1992-12-02

    Restructuring of Europe's petrochemical industry has taken a further step with the announcement that Hoechst (Frankfurt) and Wacker Chemie (Munich) are planning a joint venture in polyvinyl chloride (PVC). The venture would include production, R D, sales and marketing, plus both companies' PVC recycling activities. However, their vinyl chloride monomer (VCM) plants, and Hoechst's Kalle PVC film business, have been left out. Erich Schnitzler, head of Hoechst's PVC business unit, does not anticipate problems with the European Community's competition directorate. We are both among the middle-sized European PVC producers, and together we would have a 9%-10% market share. Our joint venture would not limit competition. Both partners are hoping for approval from Brussels in first-quarter 1993. Hoechst has 255,000 m.t./year of PVC capacity at Gendorfand Knapsack, while Wacker has 365,000 m.t./year at Burghausen and Cologne. All the units, except Wacker's Cologne plant, are back integrated to VCM. The joint venture would buy VCM from the two parent companies and on the merchant market.

  16. Calix(6)arene carboxylate derivative for solvent extraction separation of iron(III).

    PubMed

    Khandwe, R M; Khopkar, S M

    1998-08-01

    Hexaacetatocalix(6)arene was used for the solvent extraction of iron(III). About 7.5x10(-2) M extractant was used at pH 7.0 for the quantitative extraction of iron(III). The metal from the organic phase was stripped with 1.0 M hydrochloric acid and determined spectrophotometrically as its thiocyanate complex at 480 nm. Iron(III) was separated from large excesses of alkali and alkaline earths in the ratio 1:20. The transition and main group elements were tolerated in the ratio 1:10. The method was extended for the analysis of iron from its mineral, alloy and pharmaceutical preparation. The method is reproducible with SD+/-1.10%. PMID:18967172

  17. Development of NH4+-sensitive polymer membranes for long-term performance microsensors

    NASA Astrophysics Data System (ADS)

    Brzozka, Zbigniew; Dawgul, Marek; Pijanowska, Dorota; Torbicz, Wladislaw

    1997-02-01

    This paper describes the development of NH4+- sensitive membranes based on various polymer materials incorporating nonactine as the ionophore for long-term performance CHEMFETs. Different composition of membranes based on plasticized PVC, carboxylated PVC, plasticized PVC modified by decylmethacrylate, polysiloxane and Siloprene were studied. Although polysiloxane membrane presented the most improved adhesion to the chip surface, the Siloprene membrane was successfully applied to design durable NH4+-sensitive CHEMFETs. These sensors showed NH4+-responses with good selectivity even after 14 months of continuous exposure to conditioning electrolyte.

  18. Stabilizing effects of estertins mercaptide (methyl acrylate) for PVC degradation

    NASA Astrophysics Data System (ADS)

    Zhang, S. H.; Liu, T. M.; Li, J. L.; Wang, C. R.; Li, C.; Wang, Z. Q.

    2016-07-01

    The thermal and UV light (ultraviolet light) stability of PVC films with estertins mercaptide (methyl acrylate), methyltins mercaptide and the compound consisted of estertins mercaptide (methyl acrylate) and hydrotalcite (2:2.5) were investigated by ageing in a circulation oven at 190 °C and irradiating with 72W UV light for 96h, respectively, and then the yellowness and transmission rate were tested by Color Quest XE. Hydrotalcite was proved to have good synergies with estertins mercaptide (methyl acrylate) on improving the thermal stability and UV light stability. The retarding effects of the heat stabilizers to PVC degradation were tested by TGA from 50°C to 600°C. The results show that temperature of HCl evolution from PVC film was improved obviously by compounding with estertins mercaptide(methyl acrylate) and hydrotalcite and estertins mercaptide(methyl acrylate) was found to have a better long term stability. Sn4+ consistence of water and seawater in which films before and after UV light irradiation were soaked for 60 days was analyzed by ICP; the results indicate that the Sn4+ consistence from the films with estertins mercaptide(methyl acrylate) as thermal stabilizer was lower than that from the film with methyltins mercaptide. The crosslink moderately by UV irradiation for PVC films can hold back the dissolution of organotin heat stabilizers from PVC products into water and seawater.

  19. Solubility and durability of cardanol derived plasticizers for soft PVC

    NASA Astrophysics Data System (ADS)

    Greco, Antonio; Ferrari, Francesca; Velardi, Rosario; Frigione, Mariaenrica; Maffezzoli, Alfonso

    2015-12-01

    This work is aimed to study the suitability of cardanol derivatives as primary plasticizer for PVC. The innovative plasticizer is obtained by chemical modification of cardanol, a natural, renewable resource, obtained as a by-product of the cashew nut shell industry. Cardanol derived plasticizers (CDP) were prepared by following various procedures, that allow obtaining different degrees of conversion of cardanol. Rheological and ageing tests were made on soft PVC produced by the addition of CDP;results obtained were compared to soft PVC attained by the use of di-ethyl-hexyl-phthalate (DEHP) and other natural derived plasticizers already used in PVC industry (epoxidated soybean oil, ESBO, and acetic acid ester, AAE).A high dependence on the degree of conversion was found: CDP with a good degree of conversion have similar gelation temperature and diffusion coefficient compared to DEHP based plastisols. Otherwise,CDP with a low degree of conversionshow a higher diffusion coefficient, index of a fast migration of the plasticizer from soft PVC.

  20. Recycling of PVC Waste via Environmental Friendly Vapor Treatment

    NASA Astrophysics Data System (ADS)

    Cui, Xin; Jin, Fangming; Zhang, Guangyi; Duan, Xiaokun

    2010-11-01

    This paper focused on the dechlorination of polyvinyl chloride (PVC), a plastic which is widely used in the human life and thereby is leading to serious "white pollution", via vapor treatment process to recycle PVC wastes. In the process, HCl emitted was captured into water solution to avoid hazardous gas pollution and corruption, and remaining polymers free of chlorine could be thermally degraded for further energy recovery. Optimal conditions for the dechlorination of PVC using vapor treatment was investigated, and economic feasibility of this method was also analyzed based on the experimental data. The results showed that the efficiency of dechlorination increased as the temperature increased from 200° C to 250° C, and the rate of dechlorination up to 100% was obtained at the temperature near 250° C. Meanwhile, about 12% of total organic carbon was detected in water solution, which indicated that PVC was slightly degraded in this process. The main products in solution were identified to be acetone, benzene and toluene. In addition, the effects of alkali catalysis on dechlorination were also studied in this paper, and it showed that alkali could not improve the efficiency of the dechlorination of PVC.

  1. A spin-crossover ionic liquid from the cationic iron(III) Schiff base complex.

    PubMed

    Okuhata, Megumi; Funasako, Yusuke; Takahashi, Kazuyuki; Mochida, Tomoyuki

    2013-09-01

    A thermochromic magnetic ionic liquid containing a cationic iron(III) Schiff-base complex has been developed, whose color and magnetic moment change with temperature because of spin crossover in the liquid state. This spin-crossover behavior closely resembles that of a solid having the same cation. PMID:23872624

  2. Kinetics and Mechanism of Iodide Oxidation by Iron(III): A Clock Reaction Approach

    ERIC Educational Resources Information Center

    Bauer, Jurica; Tomisic, Vladislav; Vrkljan, Petar B. A.

    2008-01-01

    A simple method for studying the kinetics of a chemical reaction is described and the significance of reaction orders in deducing reaction mechanisms is demonstrated. In this student laboratory experiment, oxidation of iodide by iron(III) ions in an acidic medium is transformed into a clock reaction. By means of the initial rates method, it is…

  3. Spectral characterization of iron(III) complexes of 2-benzoylpyridine N(4)-substituted thiosemicarbazones

    NASA Astrophysics Data System (ADS)

    Joseph, Marthakutty; Sreekanth, Anandaram; Suni, V.; Kurup, M. R. Prathapachandra

    2006-06-01

    Three iron(III) complexes (1-3) of 2-benzoylpyridine N(4)-phenyl thiosemicarbazone (HL 1) and one iron(III) complex (4) of 2-benzoylpyridine N(4)-cyclohexyl thiosemicarbazone (HL 2) were synthesized and characterized by means of different physicochemical techniques viz., molar conductivity measurements, magnetic susceptibility studies and electronic, infrared and EPR spectral studies. The analytical data and the molar conductance measurements of the complexes reveal that two molecules of the ligand and the anion are coordinated to the metal atom in all the four complexes. The magnetic moments of the complexes suggest that they are of low spin. From the infrared spectra of the ligands and the complexes it is confirmed that the ligands coordinate to iron(III) as an anion coordinating via the azomethine nitrogen, pyridyl nitrogen, and the thiolate sulphur. The EPR spectra of the complexes in the polycrystalline state at 298 and 110 K and in DMF solution at 110 K were recorded and all the spectra show three g values indicating that these complexes have rhombic distortion. All the iron(III) complexes in DMF solution at 110 K have similar anisotropic spectra with almost the same gav values, indicating that the bonding in all the complexes is similar and is unaffected by the coordination of the anion.

  4. Nucleotide sequences of the fecBCDE genes and locations of the proteins suggest a periplasmic-binding-protein-dependent transport mechanism for iron(III) dicitrate in Escherichia coli.

    PubMed Central

    Staudenmaier, H; Van Hove, B; Yaraghi, Z; Braun, V

    1989-01-01

    The fec region of the Escherichia coli chromosome determines a citrate-dependent iron(III) transport system. The nucleotide sequence of fec revealed five genes, fecABCDE, which are transcribed from fecA to fecE. The fecA gene encodes a previously described outer membrane receptor protein. The fecB gene product is formed as a precursor protein with a signal peptide of 21 amino acids; the mature form, with a molecular weight of 30,815, was previously found in the periplasm. The fecB genes of E. coli B and E. coli K-12 differed in 3 nucleotides, of which 2 gave rise to conservative amino acid exchanges. The fecC and fecD genes were found to encode very hydrophobic polypeptides with molecular weights of 35,367 and 34,148, respectively, both of which are localized in the cytoplasmic membrane. The fecE product was a rather hydrophilic but cytoplasmic membrane-bound protein of Mr 28,189 and contained regions of extensive homology to ATP-binding proteins. The number, structural characteristics, and locations of the FecBCDE proteins were typical for a periplasmic-binding-protein-dependent transport system. It is proposed that after FecA- and TonB-dependent transport of iron(III) dicitrate across the outer membrane, uptake through the cytoplasmic membrane follows the binding-protein-dependent transport mechanism. FecC and FecD exhibited homologies to each other, to the N- and C-terminal halves of FhuB of the iron(III) hydroxamate transport system, and to BtuC of the vitamin B12 transport system. FecB showed some homology to FhuD, suggesting that the latter may function in the same manner as a binding protein in iron(III) hydroxamate transport. The close homology between the proteins of the two iron transport systems and of the vitamin B12 transport system indicates a common evolution for all three systems. Images PMID:2651410

  5. Experimental and computational evidence for the mechanism of intradiol catechol dioxygenation by non-heme iron(III) complexes.

    PubMed

    Jastrzebski, Robin; Quesne, Matthew G; Weckhuysen, Bert M; de Visser, Sam P; Bruijnincx, Pieter C A

    2014-11-24

    Catechol intradiol dioxygenation is a unique reaction catalyzed by iron-dependent enzymes and non-heme iron(III) complexes. The mechanism by which these systems activate dioxygen in this important metabolic process remains controversial. Using a combination of kinetic measurements and computational modelling of multiple iron(III) catecholato complexes, we have elucidated the catechol cleavage mechanism and show that oxygen binds the iron center by partial dissociation of the substrate from the iron complex. The iron(III) superoxide complex that is formed subsequently attacks the carbon atom of the substrate by a rate-determining C-O bond formation step. PMID:25322920

  6. PVC makers study expansions to meet demand growth

    SciTech Connect

    Hunter, D.; Coeyman, M.

    1993-02-10

    As prospects for the polyvinyl chloride (PVC) industry continue to improve, the next batch of capacity increases is being studied. Vista Chemical (Houston) sees an opportunity to achieve what company president James R. Ball calls the lowest-cost capacity addition in the market, by debottlenecking its PVC plants at Aberdeen, MS and Oklahoma City. That would increase capacity 40%, adding 300 million lbs/year to Vista's 830 million lbs/year. US demand for PVC grew 12.5% through the first 10 months of 1992, to 7.3 billion lbs, according to the latest figures available from the Society of the Plastics Industry. Alan Bailey, Oxy-Chem's executive v.p./polymers and plastics, predicts a good demand year in 1993 - better even than 1992, driven by an upward trend in housing starts and a recovering economy.

  7. Properties of rigid films made of PVC nanocomposites

    NASA Astrophysics Data System (ADS)

    Obloj-Muzaj, Maria; Abramowicz, Agnieszka; Kumosinski, Marcin; Zielecka, Maria; Kozakiewicz, Janusz; Gorska, Agnieszka

    2016-05-01

    PVC nanocomposites containing 0.5 wt. %/VCM of either nanosilica or hybrid core/shell type nanofiller were produced in-situ in suspension polymerisation and rigid films were prepared. The composites obtained were applied in the blends for rigid films. The properties of them were checked and showed advantageous differences in tear resistance and tensile impact properties. It appeared the composites properties let reduce the amount of impact modifiers in the blends at least 40 %. The PVC/SiO2 composite shows the best properties. Even for the blend containing 0.7 part of standard amount of impact modifier (suitable for this formulation) all the properties (except tensile impact strength crosswise) are significantly better than those of PVC blend with full amount of impact modifier.

  8. PET and PVC separation system based on optical sensors

    NASA Astrophysics Data System (ADS)

    Pérez-Sánchez, G. G.; Álvarez Chávez, J. A.; Pérez-Torres, J. R.; Gómez-Vieyra, A.

    2015-08-01

    In this work, we present experimental results of a cost-efficient photonic system capable to discriminate Polyvinyl Chloride (PVC) bottles from those made of Polyethylene Terephthalate (PET). The proposed array uses a semiconductor laser emitting at 810 nm, whose output is diverged employing a line lens in order to obtain a line light pattern. Given the lower attenuation coefficient of the PVC in comparison to PET at this wavelength, the received optical power is higher for the PVC than for the PET, which results in higher photogenerated current and, consequently, higher voltage after the transimpedance amplifier. Experiments considering several samples reveal an average voltage difference of 10% between materials, probing its feasibility for future industrial applications.

  9. PVC removal from mixed plastics by triboelectrostatic separation.

    PubMed

    Park, Chul-Hyun; Jeon, Ho-Seok; Park, Jai-Koo

    2007-06-01

    Ever increasing oil price and the constant growth in generation of waste plastics stimulate a research on material separation for recycling of waste plastics. At present, most waste plastics cause serious environmental problems due to the disposal by reclamation and incineration. Particularly, polyvinyl chloride (PVC) materials among waste plastics generates hazardous HCl gas, dioxins containing Cl, and so on, which lead to air pollution and shorten the life of incinerator, and it makes difficultly recycling of other plastics. Therefore, we designed a bench scale triboelectrostatic separator for PVC removal from mixed plastics (polyvinyl chloride/polyethylene terephthalate), and then carried out material separation tests. In triboelectrostatic separation, PVC and PET particles are charged negatively and positively, respectively, due to the difference of the work function of plastics in tribo charger of the fluidized-bed, and are separated by means of splitter through an opposite electric field. In this study, the charge efficiency of PVC and PET was strongly dependent on the tribo charger material (polypropylene), relative humidity (below 30%), air velocity (over 10 m/s), and mixture ratio (PET:PVC=1:1). At the optimum conditions (electrode potential of 20 kV and splitter position of -2 cm), PVC rejection and PET recovery in PET products were 99.60 and 98.10%, respectively, and the reproducibility of optimal test was very good (+/-1%). In addition, as a change of splitter position, we developed the technique to recover high purity PET (over 99.99%) although PET recovery decreases by degrees. PMID:17161526

  10. Recommendation to replace PVC disposable shoe cover with alternative materials

    SciTech Connect

    Slaughter, A.E.; Rankin, W.N.

    1992-01-17

    An alternative for disposable shoe covers presently fabricated from PVC (polyvinyl chloride) was investigated to minimize disposal costs. Plans are to incinerate these items for disposal. The exhaust from the incineration of PVC must be processed through a sodium hydroxide scrubber to remove the chlorides. A substantial cost savings ($70OK/yr) would be expected from replacing these supplies with similar items fabricated from a material that contains no chlorides. This report contains evaluations of submitted to the Savannah River Laboratory for testing.

  11. Predicting the Migration Rate of Dialkyl Organotins from PVC Pipe into Water

    EPA Science Inventory

    Organotins (OTs) are additives widely used as thermal and light stabilizers in polyvinyl chloride (PVC) plastics. OTs can leach into water flowing through PVC pipes. This work examines the leaching rates of two neurotoxic OTs, dimethyl tin (DMT) and dibutyl tin (DBT), from PVC pi...

  12. Experimental Research on Pyromagnetic Effect of PVC Sheet

    NASA Astrophysics Data System (ADS)

    Luo, Yingshe; Su, Jianxin; Zhang, Yongzhong; Deng, Xuhua; Chen, Shengming; Deng, Ruiji; Yang, Zhanyu; Ma, Minwei

    2008-07-01

    Experimental Research on PVC sheet with defects was conducted under tensile load. In the region of viscoplastic damage a deformation heat was given out and the temperature was increased and measured by instrument named HX8600. Using the surveying system exploited by authors, a heat-force coupling pyromagnetic effect in the process zone of rheologically damaged fracture was measured.

  13. ADULT AND DEVELOPMENTAL NEUROTOXICITY AND IMMUNOTOXICITY OF ORGANOTIN PVC LEACHATES

    EPA Science Inventory

    The primary source of organotins in drinking water is believed to be PVC leachates. Limited occurrence data from residential surveys indicate as much as 300 ng/l of monomethyltin can be detected. Noland et al., (1982) reported that exposure of rats to monomethyltin (12, 40, 120 m...

  14. Properties of irradiated PVC plasticized with non-endocrine disruptor

    NASA Astrophysics Data System (ADS)

    Hutzler, Beatriz W.; Machado, Luci D. B.; Lugão, Ademar B.; Villavicencio, Anna.-Lucia C. H.

    2000-03-01

    Polyvinylchloride (PVC) is under heavy attack from environmentalist groups due to the use of plasticizers and its recycling difficulties. Chloro-organics and phtalates are considered now as ubiquitous global contaminants due to their potential as weak endocrine disruptor and huge consumption. In order to make PVC acceptable for the irradiation processing industry in the long term, non-toxic plasticizers should be used. PVC was added with dioctyl phtalate (DOP) and epoxy soybean oil (ESO) and irradiated up to 50 kGy. Mechanical properties, optical properties and viscosity were measured and compared. The elongation and mechanical strength were under the usual range and they didn't show any significant change in the studied range of irradiation dose. All the samples showed a weak yellowing effect after irradiation and the molecular weight measured by viscosimetry showed only negligible changes. In conclusion, DOP and ESO were shown to be effective in stabilizing the radiolytic abstraction of HCl from PVC. Both plasticizers imparted good color stability and overall properties to the products.

  15. IMMUNOTOXICITY OF ORGANOTINS USED AS STABILIZERS IN PVC PIPE

    EPA Science Inventory

    Organotins, used as stabilizers in the production of PVC drinking water supply pipe, are known to leach into water, particularly from new pipe. Certain organotins (dibutyl-, dioctyl- and tributyltins) are known to suppress immune function following acute and subchronic exposure o...

  16. ORGANIC AND ORGANOTIN COMPOUNDS LEACHED FROM PVC AND CPVC PIPE

    EPA Science Inventory

    The primary objective of this research program was to determine whether organotins, contained in heat stabilizers of polyvinyl chloride (PVC) and chlorinated polyvinyl chloride (CPVC) pipe, and other organics present in pipe sealing cement solvents may leach into potable water su...

  17. Emission of phthalates from PVC and other materials.

    PubMed

    Afshari, A; Gunnarsen, L; Clausen, P A; Hansen, V

    2004-04-01

    The main objective of this study was to generate quantitative and qualitative emission data on phthalates from different materials. To achieve this the existing (Chamber for Laboratory Investigations of Materials, Pollution and Air Quality) Climpaq-based procedure for simplified measurements of emissions of plasticizer from PVC and other plasticized materials was modified. It was applied to a range of products. Some of them were suspected of contributing to the indoor concentration of plasticizers. The emissions from PVC flooring, polyolefine flooring, a refrigerator list, two electric cables, PVC skirting and floor wax were studied in separate Climpaqs. The emission from the PVC flooring in the Climpaq was compared with results from the ultra-small chamber Field and Laboratory Emission Cell (FLEC). Sampling and analysis methods were optimized to measure plasticizers. Samples were taken in exhaust air from the chambers after 6, 35, 62, 105, and 150 days from the start of the experiment. PVC flooring was tested for an additional 100 days. Polyolefine covered with wax resulted in an air concentration of 22 microg/m3 of dibutylphthalate (DBP), which is two orders of magnitude larger than any other materials, but did not emit di(2-ethylhexyl)phthalate (DEHP). The other materials resulted in max concentration of approximately 1 microg/m3 of DEHP and low emissions of DBP. The concentration of DEHP in each chamber increased slowly to a rather stable level which was reached after 150 days. DBP concentrations in the chambers with PVC skirting, PVC flooring, polyolefine and floor wax reached their quasi-static equilibrium after 60 days. The modified method did not create sufficient data for the calculation of emission rates. Adsorption of emission on chamber surfaces made it impossible to use the first part of the experiment for emission rate calculation. When the concentration had stabilized, it was found to be almost identical and independent of chamber and ventilation

  18. Zeta-Fe2O3--A new stable polymorph in iron(III) oxide family.

    PubMed

    Tuček, Jiří; Machala, Libor; Ono, Shigeaki; Namai, Asuka; Yoshikiyo, Marie; Imoto, Kenta; Tokoro, Hiroko; Ohkoshi, Shin-ichi; Zbořil, Radek

    2015-01-01

    Iron(III) oxide shows a polymorphism, characteristic of existence of phases with the same chemical composition but distinct crystal structures and, hence, physical properties. Four crystalline phases of iron(III) oxide have previously been identified: α-Fe2O3 (hematite), β-Fe2O3, γ-Fe2O3 (maghemite), and ε-Fe2O3. All four iron(III) oxide phases easily undergo various phase transformations in response to heating or pressure treatment, usually forming hexagonal α-Fe2O3, which is the most thermodynamically stable Fe2O3 polymorph under ambient conditions. Here, from synchrotron X-ray diffraction experiments, we report the formation of a new iron(III) oxide polymorph that we have termed ζ-Fe2O3 and which evolved during pressure treatment of cubic β-Fe2O3 (Ia3 space group) at pressures above 30 GPa. Importantly, ζ-Fe2O3 is maintained after pressure release and represents the first monoclinic Fe2O3 polymorph (I2/a space group) that is stable at atmospheric pressure and room temperature. ζ-Fe2O3 behaves as an antiferromagnet with a Néel transition temperature of ~69 K. The complex mechanism of pressure-induced transformation of β-Fe2O3, involving also the formation of Rh2O3-II-type Fe2O3 and post-perovskite-Fe2O3 structure, is suggested and discussed with respect to a bimodal size distribution of precursor nanoparticles. PMID:26469883

  19. Zeta-Fe2O3 - A new stable polymorph in iron(III) oxide family

    NASA Astrophysics Data System (ADS)

    Tuček, Jiří; Machala, Libor; Ono, Shigeaki; Namai, Asuka; Yoshikiyo, Marie; Imoto, Kenta; Tokoro, Hiroko; Ohkoshi, Shin-Ichi; Zbořil, Radek

    2015-10-01

    Iron(III) oxide shows a polymorphism, characteristic of existence of phases with the same chemical composition but distinct crystal structures and, hence, physical properties. Four crystalline phases of iron(III) oxide have previously been identified: α-Fe2O3 (hematite), β-Fe2O3, γ-Fe2O3 (maghemite), and ɛ-Fe2O3. All four iron(III) oxide phases easily undergo various phase transformations in response to heating or pressure treatment, usually forming hexagonal α-Fe2O3, which is the most thermodynamically stable Fe2O3 polymorph under ambient conditions. Here, from synchrotron X-ray diffraction experiments, we report the formation of a new iron(III) oxide polymorph that we have termed ζ-Fe2O3 and which evolved during pressure treatment of cubic β-Fe2O3 ( space group) at pressures above 30 GPa. Importantly, ζ-Fe2O3 is maintained after pressure release and represents the first monoclinic Fe2O3 polymorph (I2/a space group) that is stable at atmospheric pressure and room temperature. ζ-Fe2O3 behaves as an antiferromagnet with a Néel transition temperature of ~69 K. The complex mechanism of pressure-induced transformation of β-Fe2O3, involving also the formation of Rh2O3-II-type Fe2O3 and post-perovskite-Fe2O3 structure, is suggested and discussed with respect to a bimodal size distribution of precursor nanoparticles.

  20. Functional initiators for both ATRP and ROP catalyzed by iron(III) catalyst

    NASA Astrophysics Data System (ADS)

    Li, J.; Yang, C.; Cheng, C. J.

    2016-07-01

    α-Trichloromethyl benzyl alcohol was successfully used as initiators for both AGET ATRP and ROP reactions, which was catalyzed by only one non-toxic and very cheap catalyst iron(III) chloride. The corresponding polymers PMMA and PCL were characterized by 1H NMR, and their molecular mass were calculated as 7.53 kDa and 10.08 kDa, respectively.

  1. Immobilized metal affinity chromatography on collapsed Langmuir-Blodgett iron(III) stearate films and iron(III) oxide nanoparticles for bottom-up phosphoproteomics.

    PubMed

    Gladilovich, Vladimir; Greifenhagen, Uta; Sukhodolov, Nikolai; Selyutin, Artem; Singer, David; Thieme, Domenika; Majovsky, Petra; Shirkin, Alexey; Hoehenwarter, Wolfgang; Bonitenko, Evgeny; Podolskaya, Ekaterina; Frolov, Andrej

    2016-04-22

    Phosphorylation is the enzymatic reaction of site-specific phosphate transfer from energy-rich donors to the side chains of serine, threonine, tyrosine, and histidine residues in proteins. In living cells, reversible phosphorylation underlies a universal mechanism of intracellular signal transduction. In this context, analysis of the phosphoproteome is a prerequisite to better understand the cellular regulatory networks. Conventionally, due to the low contents of signaling proteins, selective enrichment of proteolytic phosphopeptides by immobilized metal affinity chromatography (IMAC) is performed prior to their LC-MS or -MS/MS analysis. Unfortunately, this technique still suffers from low selectivity and compromised analyte recoveries. To overcome these limitations, we propose IMAC systems comprising stationary phases based on collapsed Langmuir-Blodgett films of iron(III) stearate (FF) or iron(III) oxide nanoparticles (FO) and mobile phases relying on ammonia, piperidine and heptadecafluorooctanesulfonic acid (PFOS). Experiments with model phosphopeptides and phosphoprotein tryptic digests showed superior binding capacity, selectivity and recovery for both systems in comparison to the existing commercial analogs. As evidenced by LC-MS/MS analysis of the HeLa phosphoproteome, these features of the phases resulted in increased phosphoproteome coverage in comparison to the analogous commercially available phases, indicating that our IMAC protocol is a promising chromatographic tool for in-depth phosphoproteomic research. PMID:27016113

  2. The effects of thermally reversible agents on PVC stability properties

    NASA Astrophysics Data System (ADS)

    Wang, J.; Yao, J.; Xiong, X. H.; Jia, C. X.; Ren, R.; Chen, P.; Liu, X. M.

    2016-07-01

    One kind of thermally reversible cross-linking agents for improving PVC thermally stability was synthesized. The chemical structure and thermally reversible characteristics of cross-linking agents were investigated by FTIR and DSC analysis, respectively. FTIR results confirmed that the cyclopentadienyl barium mercaptides ((CPD-C2H4S)2Ba) were successfully synthesized. DSC results showed it has thermally reversible characteristics and the depolymerization temperature was between 170 °C and 205 °C. The effects of cross-linking reaction time on gel content of Poly(vinyl chloride) compounds was evaluated. The gel content value arrived at 42% after being cross-linked for 25 min at 180 C. The static thermally stability measurement proved that the thermally stability of PVC compounds was improved.

  3. Selective flotation of PVC using gelatin and lignin alkali.

    PubMed

    Yenial, Unzile; Kangal, Olgaç; Güney, Ali

    2013-06-01

    Recycling has become one of the most important issues as a result of increasing waste mass in present day. This is especially important for polymer wastes as they are hard to degenerate in nature. Today, most of the practical methods used for the recycling of waste mass, such as hand sorting, gravity separation, etc., cannot be performed successfully owing to close densities of polymers. Froth flotation can be used successfully and economically for this purpose. The main objective of this study was to investigate the effect of plasticizer reagents and the success of froth flotation at plastic recycling. In this study, lignin alkali and gelatin were used as plasticizer reagents. The effect of these reagents was searched with the parameters of pH, concentration, conditioning and flotation time. In the case of post-consumed polyethylene terephthalate and polyvinyl chloride (PVC), 98.9% purity of PVC was obtained at optimum conditions. PMID:23439876

  4. The Three-Dimensional Structures of Pseudomonas aeruginosa PvcA and PvcB, Two Proteins Involved in the Synthesis of 2-Isocyano-6,7-dihydroxycoumarin†

    PubMed Central

    Drake, Eric J.; Gulick, Andrew M.

    2008-01-01

    Summary The pvcABCD operon of Pseudomonas aeruginosa encodes four proteins (PA2254, PA2255, PA2256, and PA2257) that form a cluster that is responsible for the synthesis of a cyclized isocyano derivative of tyrosine. These proteins, which were originally identified as being responsible for a step in the maturation of the chromophore of the peptide siderophore pyoverdine, have recently been identified as belonging to a family of proteins that produce small organic isonitriles. We report that strains harboring a disruption in the pvcA or pvcB genes are able to grow in iron depleted conditions and to produce pyoverdine. Additionally, we have determined the three dimensional crystal structures of PvcA and PvcB. The structure of PvcA demonstrates a novel enzyme architecture that is built upon a Rossmann fold. We have analyzed the sequence conservation of enzymes within this family and identified six conserved motifs. These regions of the protein cluster around a putative active site cavity. The structure of the PvcB protein confirms it is a member of the Fe2+/α-ketoglutarate dependent oxygenase family of enzymes. The active site of PvcB is compared to the structures of other family members and suggests that a conformational change to order several loops will accompany the binding of ligands. PMID:18824174

  5. The Three-Dimensional Structures of Pseudomonas Aeruginosa PvcA And PvcB, Two Proteins Involved in the Synthesis of 2-Isocyano-6,7-Dihydroxycoumarin

    SciTech Connect

    Drake, E.J.; Gulick, A.M.

    2009-05-12

    The pvcABCD operon of Pseudomonas aeruginosa encodes four proteins (PA2254, PA2255, PA2256, and PA2257) that form a cluster that is responsible for the synthesis of a cyclized isocyano derivative of tyrosine. These proteins, which were identified originally as being responsible for a step in the maturation of the chromophore of the peptide siderophore pyoverdine, have been identified recently as belonging to a family of proteins that produce small organic isonitriles. We report that strains harboring a disruption in the pvcA or pvcB genes are able to grow in iron-depleted conditions and to produce pyoverdine. Additionally, we have determined the three-dimensional crystal structures of PvcA and PvcB. The structure of PvcA demonstrates a novel enzyme architecture that is built upon a Rossmann fold. We have analyzed the sequence conservation of enzymes within this family and identified six conserved motifs. These regions of the protein cluster around a putative active site cavity. The structure of the PvcB protein confirms it is a member of the Fe2+/alpha-ketoglutarate-dependent oxygenase family of enzymes. The active site of PvcB is compared to the structures of other family members and suggests that a conformational change to order several loops will accompany the binding of ligands.

  6. Imaging PVC gas pipes using 3-D GPR

    SciTech Connect

    Bradford, J.; Ramaswamy, M.; Peddy, C.

    1996-11-01

    Over the years, many enhancements have been made by the oil and gas industry to improve the quality of seismic images. The GPR project at GTRI borrows heavily from these technologies in order to produce 3-D GPR images of PVC gas pipes. As will be demonstrated, improvements in GPR data acquisition, 3-D processing and visualization schemes yield good images of PVC pipes in the subsurface. Data have been collected in cooperation with the local gas company and at a test facility in Texas. Surveys were conducted over both a metal pipe and PVC pipes of diameters ranging from {1/2} in. to 4 in. at depths from 1 ft to 3 ft in different soil conditions. The metal pipe produced very good reflections and was used to fine tune and optimize the processing run stream. It was found that the following steps significantly improve the overall image: (1) Statics for drift and topography compensation, (2) Deconvolution, (3) Filtering and automatic gain control, (4) Migration for focusing and resolution, and (5) Visualization optimization. The processing flow implemented is relatively straightforward, simple to execute and robust under varying conditions. Future work will include testing resolution limits, effects of soil conditions, and leak detection.

  7. Reconciling kinetic and equilibrium observations of iron(III) solubility in aqueous solutions with a polymer-based model

    NASA Astrophysics Data System (ADS)

    Rose, Andrew L.; David Waite, T.

    2007-12-01

    Due to hydrolysis reactions, iron(III) forms oxyhydroxide precipitates in natural waters that minimise its availability to living organisms. Thermodynamic studies have established equilibrium concentrations of dissolved iron at various pH values, however these studies offer no insight into the kinetics of iron(III) polymerisation and subsequent precipitation. In recent work, the kinetics of iron(III) precipitation and dissolution of the precipitate have been investigated, but there are apparent discrepancies between the equilibrium solubility of iron(III) calculated from the kinetic parameters and its solubility measured by separation of the solid and dissolved phases at equilibrium. In this work, we reconcile kinetic and thermodynamic measurements using a polymer-based mechanistic model of the processes responsible for iron(III) precipitation in aqueous solutions based on a variety of previously published experimental data. This model is used to explain the existence of a solubility limit, including the effect of precipitate ageing on its solubility. We suggest that the model provides a unified approach for examining aqueous systems containing dissolved, solid-phase and surface species.

  8. A novel EIS field effect structures coated with TESUD-PPy-PVC-dibromoaza[7]helicene matrix for potassium ions detection.

    PubMed

    Tounsi, Moncef; Ben Braiek, Mourad; Barhoumi, Houcine; Baraket, Abdoullatif; Lee, Michael; Zine, Nadia; Maaref, Abderrazak; Errachid, Abdelhamid

    2016-04-01

    In this work, we describe the development of new Aza[7]helicene-containing PVC-based membranes for the K(+) ions quantification. Here, silicon nitride-based structures (Si-p/SiO2/Si3N4) were developed and the surface was activated, functionalized with an aldehyde-silane (11-(Triethoxysilyl)undecanal (TESUD)), functionalized with polypyrrole (PPy), and coated with the polyvinylchloride (PVC)-membrane containing the Aza[7]helicene as ionophore. All stages of functionalization process have been thoroughly studied by contact angle measurements (CAMs) and atomic force microscopy (AFM). The developed ion-selective electrode (ISE) was then applied using electrochemical impedance spectroscopy (EIS) for the detection of potassium ions. A linear range was observed between 1.0 × 10(-8) M to 1.0 × 10(-3) M and a detection limit of 1.0 × 10(-8) M was observed. The EIS results have showed a good sensitivity to potassium ion using this novel technique. The target helicene exhibited good solubility and excellent thermal stability with a high decomposition temperature (Td > 300 °C) and it indicates that helicene may be a promising material as ionophore for ion-selective electrodes (ISEs) elaboration. PMID:26838889

  9. Strontium (II)-Selective Potentiometric Sensor Based on Ester Derivative of 4-tert-butylcalix(8)arene in PVC Matrix

    PubMed Central

    Jain, Ajay K.; Gupta, Vinod K.; Raisoni, Jitendra R.

    2004-01-01

    Membranes of 4-tert-butylcalix(8)arene-octaacetic acid octaethyl ester (I) as an electroactive material, sodium tetraphenyl borate (NaTPB) as an anion excluder, and tri-n-butyl phosphate (TBP) as a solvent mediator in poly(vinyl chloride) (PVC) matrix have been tried for a strontium-selective sensor. The best performance was exhibited by the membrane having a composition 5:100:150:2 (I: PVC: TBP: NaTPB (w/w)). This sensor exhibits a good potentiometric response to Sr2+ over a wide concentration range (3.2 × 10 –5 –1.0 × 10 –1 M) with a Nernstian slope (30 mV/ decade). The response time of the sensor is 10 s and it has been used for a period of four months without any drift in potentials. The selectivity coefficient values are in the order of 0.01 for mono-, bi-, and trivalent cations which indicate a good selectivity for Sr2+ over a large number of cations. The useful pH range for the sensor was found to be 3-10 and it works well in mixtures with non-aqueous content up to 25 % (v/v). The sensor has been used as an indicator electrode in the potentiometric titration of Sr2+ against EDTA.

  10. Benzyl and Methyl Fatty Hydroxamic Acids Based on Palm Kernel Oil as Chelating Agent for Liquid-Liquid Iron(III) Extraction

    PubMed Central

    Haron, Md Jelas; Jahangirian, Hossein; Silong, Sidik; Yusof, Nor Azah; Kassim, Anuar; Rafiee-Moghaddam, Roshanak; Mahdavi, Behnam; Peyda, Mazyar; Abdollahi, Yadollah; Amin, Jamileh

    2012-01-01

    Liquid-liquid iron(III) extraction was investigated using benzyl fatty hydroxamic acids (BFHAs) and methyl fatty hydroxamic acids (MFHAs) as chelating agents through the formation of iron(III) methyl fatty hydroxamate (Fe-MFHs) or iron(III) benzyl fatty hydroxamate (Fe-BFHs) in the organic phase. The results obtained under optimized conditions, showed that the chelating agents in hexane extract iron(III) at pH 1.9 were realized effectively with a high percentage of extraction (97.2% and 98.1% for MFHAs and BFHAs, respectively). The presence of a large amount of Mg(II), Ni(II), Al(III), Mn(II) and Co(II) ions did affect the iron(III) extraction. Finally stripping studies for recovering iron(III) from organic phase (Fe-MFHs or Fe-BFHs dissolved in hexane) were carried out at various concentrations of HCl, HNO3 and H2SO4. The results showed that the desired acid for recovery of iron(III) was 5 M HCl and quantitative recovery of iron(III) was achieved from Fe(III)-MFHs and Fe(III)-BFHs solutions in hexane containing 5 mg/L of Fe(III). PMID:22408444

  11. Formation and fluidity measurement of supported lipid bilayer on polyvinyl chloride membrane

    SciTech Connect

    Kobayashi, Takuji Kono, Akiteru Sawada, Kazuaki; Futagawa, Masato; Tero, Ryugo

    2014-02-20

    We prepared an artificial lipid bilayer on a plasticized poly(vinyl chloride) (PVC) membrane on a Si3N4 layer deposited on a Si wafer. We optimized the experimental condition for the fabrication of the PVC membrane, and obtained a PVC membrane with a flat and uniform surface on the scale of several hundreds of micrometer suitable for a substrate for supported lipid bilayers (SLBs). The SLB of 1,2-dioleoyl-sn-glycero-3-phosphocholine (DOPC) was formed on the PVC membrane by the vesicle fusion method. The observation with a conventional epi-fluorescence microscope and a confocal laser scanning microscope gave geometrically uniform images of the SLB on the PVC membrane. The fluidity and the mobile fraction of the SLB was evaluated by the fluorescence recovery after photobleaching method, and compared with that on a thermally oxidized SiO{sub 2}/Si substrate. The SLB on the PVC membrane contained immobile fraction ∼30%, but the diffusion in the mobile fraction was two times faster than that in the SLB on SiO{sub 2}/Si, which had little immobile fraction.

  12. Formation and fluidity measurement of supported lipid bilayer on polyvinyl chloride membrane

    NASA Astrophysics Data System (ADS)

    Kobayashi, Takuji; Kono, Akiteru; Futagawa, Masato; Sawada, Kazuaki; Tero, Ryugo

    2014-02-01

    We prepared an artificial lipid bilayer on a plasticized poly(vinyl chloride) (PVC) membrane on a Si3N4 layer deposited on a Si wafer. We optimized the experimental condition for the fabrication of the PVC membrane, and obtained a PVC membrane with a flat and uniform surface on the scale of several hundreds of micrometer suitable for a substrate for supported lipid bilayers (SLBs). The SLB of 1,2-dioleoyl-sn-glycero-3-phosphocholine (DOPC) was formed on the PVC membrane by the vesicle fusion method. The observation with a conventional epi-fluorescence microscope and a confocal laser scanning microscope gave geometrically uniform images of the SLB on the PVC membrane. The fluidity and the mobile fraction of the SLB was evaluated by the fluorescence recovery after photobleaching method, and compared with that on a thermally oxidized SiO2/Si substrate. The SLB on the PVC membrane contained immobile fraction ˜30%, but the diffusion in the mobile fraction was two times faster than that in the SLB on SiO2/Si, which had little immobile fraction.

  13. TG/FTIR analysis on co-pyrolysis behavior of PE, PVC and PS.

    PubMed

    Wu, Jingli; Chen, Tianju; Luo, Xitao; Han, Dezhi; Wang, Zhiqi; Wu, Jinhu

    2014-03-01

    The pyrolysis and co-pyrolysis behaviors of polyethylene (PE), polystyrene (PS) and polyvinyl chloride (PVC) under N2 atmosphere were analyzed by Thermal gravimetric/Fourier transform infrared (TG/FTIR). The volatile products were analyzed to investigate the interaction of the plastic blends during the thermal decomposition process. The TGA results showed that the thermal stability increased followed by PVC, PS and PE. The pyrolysis process of PE was enhanced when mixed with PS. However, PS was postponed when mixed with PVC. As for PE and PVC, mutual block was happened when mixed together. The FTIR results showed that the free radical of the decomposition could combine into a stable compound. When PE mixed with PVC or PS, large amount of unsaturated hydrocarbon groups existed in products while the content of alkynes was decreased. The methyl (-CH3) and methylene (-CH2-) bonds were disappeared while PVC mixed with PE. PMID:24411064

  14. I-TiO2/PVC film with highly photocatalytic antibacterial activity under visible light.

    PubMed

    Deng, Weihua; Ning, Shangbo; Lin, Qianying; Zhang, Hualei; Zhou, Tanghua; Lin, Huaxiang; Long, Jinlin; Lin, Qun; Wang, Xuxu

    2016-08-01

    Iodine-modified TiO2(I-TiO2) film were coated on medical-grade PVC material by impregnation-deposition method and subsequently characterized by XRD, SEM, TEM, AFM, DRS and XPS. The photocatalytic anti-bacterial activity of I-TiO2/PVC was investigated both by in vitro anti-bacterial experiments and by clinical study. The results revealed that I-TiO2/PVC exhibit excellent photocatalytic antibacterial activity, which can destroy the propagation of the Escherichia coli and cause the deactivation and death of most E. coli bacteria within 30min visible light illumination. Clinical study on animals showed that I-TiO2 coated on PVC decrease the formation of biofilm on PVC surface in the mechanical ventilation. Furthermore, I-TiO2/PVC can effectively reduce inflammation of tracheal tissue of bam suckling pig and prevents the occurrence of VAP. PMID:27088189

  15. Different arsenate and phosphate incorporation effects on the nucleation and growth of iron(III) (Hydr)oxides on quartz.

    PubMed

    Neil, Chelsea W; Lee, Byeongdu; Jun, Young-Shin

    2014-10-21

    Iron(III) (hydr)oxides play an important role in the geochemical cycling of contaminants in natural and engineered aquatic systems. The ability of iron(III) (hydr)oxides to immobilize contaminants can be related to whether the precipitates form heterogeneously (e.g., at mineral surfaces) or homogeneously in solution. Utilizing grazing incidence small-angle X-ray scattering (GISAXS), we studied heterogeneous iron(III) (hydr)oxide nucleation and growth on quartz substrates for systems containing arsenate and phosphate anions. For the iron(III) only system, the radius of gyration (Rg) of heterogeneously formed precipitates grew from 1.5 to 2.5 (± 1.0) nm within 1 h. For the system containing 10(-5) M arsenate, Rg grew from 3.6 to 6.1 (± 0.5) nm, and for the system containing 10(-5) M phosphate, Rg grew from 2.0 to 4.0 (± 0.2) nm. While the systems containing these oxyanions had more growth, the system containing only iron(III) had the most nucleation events on substrates. Ex situ analyses of homogeneously and heterogeneously formed precipitates indicated that precipitates in the arsenate system had the highest water content and that oxyanions may bridge iron(III) hydroxide polymeric embryos to form a structure similar to ferric arsenate or ferric phosphate. These new findings are important because differences in nucleation and growth rates and particle sizes will impact the number of available reactive sites and the reactivity of newly formed particles toward aqueous contaminants. PMID:25232994

  16. Different Arsenate and Phosphate Incorporation Effects on the Nucleation and Growth of Iron(III) (Hydr)oxides on Quartz

    SciTech Connect

    Neil, Chelsea W.; Lee, Byeongdu; Jun, Young-Shin

    2014-10-21

    Iron(III) (hydr)oxides play an important role in the geochemical cycling of contaminants in natural and engineered aquatic systems. The ability of iron(III) (hydr)oxides to immobilize contaminants can be related to whether the precipitates form heterogeneously (e.g., at mineral surfaces) or homogeneously in solution. Utilizing grazing incidence small-angle X-ray scattering (GISAXS), we studied heterogeneous iron(III) (hydr)oxide nucleation and growth on quartz substrates for systems containing arsenate and phosphate anions. For the iron(III) only system, the radius of gyration ( R g ) of heterogeneously formed precipitates grew from 1.5 to 2.5 ( ± 1.0) nm within 1 h. For the system containing 10-5 M arsenate, R g grew from 3.6 to 6.1 ( ± 0.5) nm, and for the system containing 10-5 M phosphate, R g grew from 2.0 to 4.0 ( ± 0.2) nm. While the systems containing these oxyanions had more growth, the system containing only iron(III) had the most nucleation events on substrates. Ex situ analyses of homogeneously and heterogeneously formed precipitates indicated that precipitates in the arsenate system had the highest water content and that oxyanions may bridge iron(III) hydroxide polymeric embryos to form a structure similar to ferric arsenate or ferric phosphate. These new fi ndings are important because di ff erences in nucleation and growth rates and particle sizes will impact the number of available reactive sites and the reactivity of newly formed particles toward aqueous contaminants.

  17. Quality control in the recycling stream of PVC from window frames by hyperspectral imaging

    NASA Astrophysics Data System (ADS)

    Luciani, Valentina; Serranti, Silvia; Bonifazi, Giuseppe; Di Maio, Francesco; Rem, Peter

    2013-05-01

    Polyvinyl chloride (PVC) is one of the most commonly used thermoplastic materials in respect to the worldwide polymer consumption. PVC is mainly used in the building and construction sector, products such as pipes, window frames, cable insulation, floors, coverings, roofing sheets, etc. are realised utilising this material. In recent years, the problem of PVC waste disposal gained increasing importance in the public discussion. The quantity of used PVC items entering the waste stream is gradually increased as progressively greater numbers of PVC products approach to the end of their useful economic lives. The quality of the recycled PVC depends on the characteristics of the recycling process and the quality of the input waste. Not all PVC-containing waste streams have the same economic value. A transparent relation between value and composition is required to decide if the recycling process is cost effective for a particular waste stream. An objective and reliable quality control technique is needed in the recycling industry for the monitoring of both recycled flow streams and final products in the plant. In this work hyperspectral imaging technique in the near infrared (NIR) range (1000-1700 nm) was applied to identify unwanted plastic contaminants and rubber present in PVC coming from windows frame waste in order to assess a quality control procedure during its recycling process. Results showed as PVC, PE and rubber can be identified adopting the NIR-HSI approach.

  18. Mixed anion (phosphate/oxalate) bonding to iron(III) materials.

    PubMed

    Kizewski, Fiona R; Boyle, Paul; Hesterberg, Dean; Martin, James D

    2010-02-24

    A novel phosphate/oxalate inorganic-organic hybrid material has been prepared to elucidate synthesis and bonding characteristics of iron(III) with both phosphate and organic matter (OM). Such mixed anion bonding of inorganic oxyanions and OM to iron(III) and aluminum(III) in environmental systems has been proposed but not proven, mainly because of the complexity of natural geochemical matrices. The compound reported here with the molecular formula of [C(3)H(12)N(2)](2)[Fe(5)(C(2)O(4))(2)(H(x)PO(4))(8)] (I) was hydrothermally synthesized and characterized by single crystal X-ray diffraction and X-ray absorption spectroscopy (XAS). In this new structure, Fe-O octahedra and P-O tetrahedra are connected by corner-sharing to form a 2-D network in the a-b plane. Oxalate anions cross-link these Fe-P layers constructing a 3-D anionic framework. A diprotonated structure-directing template, DAP (1,3-diaminopropane), resides in the oxalate layer of the structure and offsets the negative charge of the anionic framework. Iron K-edge XANES spectra confirmed that the iron in I is Fe(III). The crystal structure of I is used to successfully fit its Fe K-edge EXAFS spectrum, which exhibits spectral signatures that unambiguously identify iron-phosphate and iron-OM bonding. Such molecular spectroscopic features will be invaluable for the evaluation of complex environmental systems. Furthermore, syntheses demonstrated the critical role of the templating amine to mediate whether or not the iron(III) is reduced by the organic acid. PMID:20121236

  19. Mixed Anion (Phosphate/Oxalate) Bonding to Iron(III) Materials

    SciTech Connect

    Kizewski, F.; Boyle, P; Hesterberg, D; Martin, J

    2010-01-01

    A novel phosphate/oxalate inorganic-organic hybrid material has been prepared to elucidate synthesis and bonding characteristics of iron(III) with both phosphate and organic matter (OM). Such mixed anion bonding of inorganic oxyanions and OM to iron(III) and aluminum(III) in environmental systems has been proposed but not proven, mainly because of the complexity of natural geochemical matrices. The compound reported here with the molecular formula of [C{sub 3}H{sub 12}N{sub 2}]{sub 2}[Fe{sub 5}(C{sub 2}O{sub 4}){sub 2}(H{sub x}PO{sub 4}){sub 8}] (I) was hydrothermally synthesized and characterized by single crystal X-ray diffraction and X-ray absorption spectroscopy (XAS). In this new structure, Fe-O octahedra and P-O tetrahedra are connected by corner-sharing to form a 2-D network in the a-b plane. Oxalate anions cross-link these Fe-P layers constructing a 3-D anionic framework. A diprotonated structure-directing template, DAP (1,3-diaminopropane), resides in the oxalate layer of the structure and offsets the negative charge of the anionic framework. Iron K-edge XANES spectra confirmed that the iron in I is Fe(III). The crystal structure of I is used to successfully fit its Fe K-edge EXAFS spectrum, which exhibits spectral signatures that unambiguously identify iron-phosphate and iron-OM bonding. Such molecular spectroscopic features will be invaluable for the evaluation of complex environmental systems. Furthermore, syntheses demonstrated the critical role of the templating amine to mediate whether or not the iron(III) is reduced by the organic acid.

  20. Occupational hazards in the VC-PVC industry

    SciTech Connect

    Nicholson, W.J.; Henneberger, P.K.; Seidman, H.

    1984-01-01

    Overall, the results of the analysis of 12 studies of VC production and polymerization workers demonstrate an enormously elevated risk of liver malignancies, the possibility of a twofold increased risk of brain and central nervous system tumors and perhaps, also, of malignancies of the lymphatic and hematopoietic system. However, the role of other agents cannot be excluded in the etiology of nonhepatic malignancies. Bronchogenic carcinoma does not appear to be increased from exposures to VC monomer, although a relationship to PVC dust was suggested in one study. These conclusions must be considered in light of limited data on workers followed more than 25 years from onset of exposure. Considering the numbers of observed and expected deaths in all studies, it would appear that the excess of malignancies at nonhepatic sites is less than the excess of liver tumors. Data presented elsewhere suggest that exposure reductions in 1974 may have virtually eliminated the VC-associated risk of liver cancer if the current U.S. standard is met. To the extent that VC exposure is associated with other cancers, a similar risk reduction would be expected. Raynaud's phenomenon, acroosteolysis, scleroderma-like skin lesions, hepato- and splenomegaly with noncirrhotic hepatic fibrosis, and severe portal hypertension have been associated with past heavy exposures to VC. Evidence exists that the liver disease and portal hypertension may progress following cessation of exposure. However, all of the above syndromes were found largely in heavily exposed individuals. Their occurrence would be much less likely in workers exposed only to concentrations currently allowed. Pulmonary deficits, X-ray abnormalities, and, perhaps, lung cancer have been associated with VC/PVC exposure. Because of the possible contribution of PVC dust to these findings, engineering controls during polymer drying, bagging and usage are warranted.

  1. Flow-injection simultaneous determination of iron(III) and copper(II) and of iron(III) and palladium(II) based on photochemical reactions of thiocyanato-complexes.

    PubMed

    Oguma, Koichi; Yoshioka, Osamu

    2002-12-01

    The flow injection analysis systems have been developed for the simultaneous determination of iron(III) and copper(II) and of iron(III) and palladium(II) based on the photochemical reactions of their thiocyanato-complexes. In the first system, a sample solution was injected in to nitric acid solution and mixed with ammonium thiocyanate solution, followed by spectrophotometric monitoring of the thiocyanato-complexes formed. Another aliquot of the same sample solution was injected and the thiocyanato-complexes formed in the same way were irradiated by UV light before spectrophotometric monitoring. In another system, the absorbance of thiocyanato-complexes formed by each sample injection was monitored with two flow cells aligned with the same optical path before and after UV irradiation. The difference in the extent of photochemical decomposition of the thiocyanato-complexes enabled simultaneous determinations of iron(III) and copper(II) and of iron(III) and palladium(II) at levels of several mugml(-1) to some tens mugml(-1) in their admixtures. Sample throughputs are 40 and 20 h(-1) by the former and latter systems, respectively. PMID:18968842

  2. PVC biodeterioration and DEHP leaching by DEHP-degrading bacteria

    PubMed Central

    Latorre, Isomar; Hwang, Sangchul; Sevillano, Maria; Montalvo-Rodriguez, Rafael

    2012-01-01

    Newly isolated, not previously reported, di-(2-ethylhexyl) phthalate (DEHP)-degraders were augmented to assess their role in polyvinyl chloride (PVC) shower curtain deterioration and DEHP leaching. The biofilms that developed on the surfaces of the bioaugmented shower curtains with Gram-positive strains LHM1 and LHM2 were thicker than those of the biostimulated and Gram-negative strain LHM3-augmented shower curtains. The first derivative thermogravimetric (DTG) peaks of the bioaugmented shower curtains with the Gram-positive bacteria were observed at ~287°C, whereas the control and Gram-negative strain LHM3-augmented shower curtains were detected at ~283°C. This slight delay in the first DTG peak temperature is indicative of lower plasticizer concentrations in the shower curtains that were bioaugmented with Gram positive bacteria. Despite bioaugmentation with DEHP-degraders, aqueous solutions of the bioaugmentation reactors were not DEHP-free due probably to the presence of co-solutes that must have supported microbial growth. Generally, the bioaugmented reactors with the Gram-positive strains LHM1 and LHM2 had greater aqueous DEHP concentrations in the first-half (<3 wk) of the biodeterioration experiment than the biostimulated and strain LHM3-augmented reactors. Therefore, strains LHM1 and LHM2 may play an important role in DEHP leaching to the environment and PVC biodeterioration. PMID:22736894

  3. On the Radial Breathing Mode in SWCNTs dispersed within PVC

    NASA Astrophysics Data System (ADS)

    Flor, Fernando; Ajayan, Pullickel; Chipara, Alin; Lozano, Karen; Chipara, Dorina; Vajtai, Robert; Chipara, Mircea; Utrgv-Rice Collaboration

    The Radial Breathing Mode (RBM) is an unique set of Raman lines, characterized by shifts smaller than 500 cm-1, assigned to vibrations that affect the diameter of carbon nanotubes. The position of the RBM lines is inversely proportional to the diameter of nanotubes. RBM was reported in Single Walled Carbon Nanotubes (SWCNTs) and Double Walled Carbon Nanotubes. This mode is very sensitive being frequently used to obtain information regarding the stress transfer from the polymeric matrix. Nanocomposites have been prepared by loading the polyvinylchloride (PVC) purchased from Sigma Aldrich with SWCNTs from Cheap Tubes Inc., by melt mixing, using Haake Rheomix equipped with two counter rotating screws. The concentration of SWCNTs dispersed within PVC ranged from 0 % wt. up to 20 % wt. The as recorded spectra have been deconvoluted into several individual lines characterized by an extended Breit-Wigner-Fano line shape. A full analysis of the Raman spectra of the polymeric matrix and of the matrix is reported with emphasize on the RBM features. The spectra have been recorded by using a Renishaw InVia spectrometer equipped with Eclipse filters that allow the recording of Raman lines starting from about 25 cm-1.

  4. Comparative Fatigue Lives of Rubber and PVC Wiper Cylindrical Coatings

    NASA Technical Reports Server (NTRS)

    Vlcek, Brian L.; Hendricks, Robert C.; Zaretsky, Erwin V.; Savage, Michael

    2002-01-01

    Three coating materials for rotating cylindrical-coated wiping rollers were fatigue tested in 2 Intaglio printing presses. The coatings were a hard, cross-linked, plasticized PVC thermoset (P-series); a plasticized PVC (A-series); and a hard, nitryl rubber (R-series). Both 2- and 3-parameter Weibull analyses as well as a cost-benefit analysis were performed. The mean value of life for the R-series coating is 24 and 9 times longer than the P- and A-series coatings, respectively. Both the cost and replacement rate for the R-series coating was significantly less than those for the P- and A-series coatings. At a very high probability of survival the R-series coating is approximately 2 and 6 times the lives of the P- and A-series, respectively, before the first failure occurs. Where all coatings are run to failure, using the mean (life) time between removal (MTBR) for each coating to calculate the number of replacements and costs provides qualitatively similar results to those using a Weibull analysis.

  5. Self-Propelled and Long-Time Transport Motion of PVC Particles on a Water Surface.

    PubMed

    Wang, Lei; Yuan, Bin; Lu, Jinrong; Tan, Sicong; Liu, Fujun; Yu, Lujia; He, Zhizhu; Liu, Jing

    2016-06-01

    Driven by the Marangoni effect, a poly(vinyl chloride) (PVC) particle runs in its orbit (a) with high velocity due to the release of surfactant and heat. The PVC particles are also able to efficiently drive an aluminum bulk and to induce spinning and quick runs on a water surface (b). PMID:27031683

  6. Fluorescence quenching and bonding properties of some hydroxamic acid derivatives by iron(III) and manganese(II).

    PubMed

    Senthilnithy, R; De Costa, M D P; Gunawardhana, H D

    2009-01-01

    Spectrophotometric investigations of highly fluorescent metal chelating molecules are of relevance due to their potential application in novel, selective fluorescence-based sensors. Benzene and naphthalene chromophores are highly fluorescent while hydroxamic acids are widely used as ligands for complexation of transition metals. In order to develop fluorescence probes, several phenyl derivatives of N-phenylbenzohydroxamic acid and an aminodihydroxamic acid linked with a naphthalene chromophore were synthesized and their selective ionophoric properties towards iron(III) and manganese(II) ions were investigated using fluorescence and absorption spectroscopy. Both methods confirm the formation of 1:1 and 1:2 complexes for iron(III) and a 1:1 complex for manganese(II). The complex that is formed depends on the concentration of the ligand and pH of the medium. The amino dihydroxamic acid exhibits a prominent selectivity towards iron(III) with a two-step 1:1 and 1:2 quenching mechanism at pH 3 and towards manganese(II) with a 1:1 quenching mechanism at a probe concentration of 1 x 10(-5) mol dm(-3) at pH 9.5 The logarithm of overall formation constants of 1:1 and 1:2 complexes of iron(III) were estimated as 3.30 and 9.05, respectively. PMID:18800360

  7. Salicylate Detection by Complexation with Iron(III) and Optical Absorbance Spectroscopy: An Undergraduate Quantitative Analysis Experiment

    ERIC Educational Resources Information Center

    Mitchell-Koch, Jeremy T.; Reid, Kendra R.; Meyerhoff, Mark E.

    2008-01-01

    An experiment for the undergraduate quantitative analysis laboratory involving applications of visible spectrophotometry is described. Salicylate, a component found in several medications, as well as the active by-product of aspirin decomposition, is quantified. The addition of excess iron(III) to a solution of salicylate generates a deeply…

  8. Influence of Ionic Liquids on an Iron(III) Catalyzed Three-Component Coupling/Hydroarylation/Dehydrogenation Tandem Reaction.

    PubMed

    Muntzeck, Maren; Wilhelm, René

    2016-01-01

    A three-component oxidative dehydrogenation tandem reaction via the coupling and hydroarylation of benzaldehyde, aniline and phenylacetylene to a quinoline derivate was catalyzed by an iron-containing ionic liquid. The reaction was air mediated and could be performed under neat conditions. The iron(III) of the ionic liquid was the oxidizing species. PMID:27258264

  9. Influence of Ionic Liquids on an Iron(III) Catalyzed Three-Component Coupling/Hydroarylation/Dehydrogenation Tandem Reaction

    PubMed Central

    Muntzeck, Maren; Wilhelm, René

    2016-01-01

    A three-component oxidative dehydrogenation tandem reaction via the coupling and hydroarylation of benzaldehyde, aniline and phenylacetylene to a quinoline derivate was catalyzed by an iron-containing ionic liquid. The reaction was air mediated and could be performed under neat conditions. The iron(III) of the ionic liquid was the oxidizing species. PMID:27258264

  10. Investigation on the thermal stability of PVC filled with hydrotalcite by the UV-vis spectroscopy

    NASA Astrophysics Data System (ADS)

    Zhang, Qiang; Li, Hancheng

    2008-01-01

    The thermal stability of the polyvinyl chloride (PVC) filled with hydrotalcite was studied in this paper. It was found that the stability of the PVC resin mixed with organic Sn and hydrotalcite was better than that of the PVC resin mixed with organic Sn alone. The UV-vis spectra showed that under certain heat treatment conditions, the sample without hydrotalcite embodied relatively high content of the conjugated double bonds with the chain length of about 3-5, however, the content of the conjugated double bond with the chain length of about 7 was greatly increased when the hydrotalcite was filled into the PVC resin. The hydrotalcite could inhibit the thermal degradation process of PVC resin in ionic mechanism.

  11. Study of mechanical properties of polyvinyl chloride (PVC) and polystyrene (PS) polymers and their blends

    NASA Astrophysics Data System (ADS)

    Agarwal, Shalini; Saxena, N. S.; Agrawal, R.; Saraswat, Vibhav K.

    2013-06-01

    Presented work is an effort to observe the variation in mechanical properties of two thermoplastic materials PVC, PS and their blends. PVC and PS are taken in the ratio of 100:0, 70:30, 50:50, and 0:100. Mixing of PVC and PS is carried out by solution casting method using tetra hydro furan as solvent. Dynamical mechanical analyzer (DMA) is used to study mechanical properties. The storage modulus, loss modulus and mechanical loss factor (tan δ) are determined with temperature. The pallets of pure PS, PVC and their blends are scanned over a temperature range from room to 140 °C. The variation of modulus, tan δ of pure PVC & pure PS and their blends with temperature were studied. The observed variation in modulus and tan δ could be accounted for their thermal behavior and compositions.

  12. Characterization of the surface and the interphase of PVC-copper amine-treated wood composites

    NASA Astrophysics Data System (ADS)

    Jiang, Haihong; Kamdem, D. Pascal

    2010-05-01

    Contact angles and surface energy of wood, as well as interfacial shear strength between wood and polyvinyl chloride (PVC) were investigated and used to monitor the modifications generated on the surfaces of wood treated with a copper ethanolamine solution. An increase in surface energy of wood after treatments promotes wetting of PVC on wood surfaces. Improved interfacial shear strength between treated wood and PVC matrix can be attributed to the formation of a stronger wood-PVC interphase. This suggests that treatment may be used to improve the adhesion between wood surface and PVC in the formulation of wood fiber composites to yield products with enhanced mechanical properties and better biological and physical performance against decay and insect destroying wood.

  13. Tuning of spin crossover behaviour in iron(III) complexes involving pentadentate Schiff bases and pseudohalides.

    PubMed

    Nemec, Ivan; Herchel, Radovan; Boča, Roman; Trávníček, Zdeněk; Svoboda, Ingrid; Fuess, Hartmut; Linert, Wolfgang

    2011-10-21

    Investigations on a series of eight novel mononuclear iron(III) Schiff base complexes with the general formula [Fe(L(5))(L(1))]·S (where H(2)L(5) = pentadentate Schiff-base ligand, L(1) = a pseudohalido ligand, and S is a solvent molecule) are reported. Several different aromatic 2-hydroxyaldehyde derivatives were used in combination with a non-symmetrical triamine 1,6-diamino-4-azahexane to synthesize the H(2)L(5) Schiff base ligands. The consecutive reaction with iron(III) chloride resulted in the preparation of the [Fe(L(5))Cl] precursor complexes which were left to react with a wide range of the L(1) pseudohalido ligands. The low-spin compounds were prepared using the cyanido ligand: [Fe(3m-salpet)(CN)]·CH(3)OH (1a), [Fe(3e-salpet)(CN)]·H(2)O (1b), while the high-spin compounds were obtained by the reaction of the pseudohalido (other than cyanido) ligands with the [Fe(L(5))Cl] complex arising from salicylaldehyde derivatives: [Fe(3Bu5Me-salpet)(NCS)] (2a), [Fe(3m-salpet)(NCO)]·CH(3)OH (2b) and [Fe(3m-salpet)(N(3))] (2c). The compounds exhibiting spin-crossover phenomena were prepared only when L(5) arose from 2-hydroxy-1-naphthaldehyde (H(2)L(5) = H(2)napet): [Fe(napet)(NCS)]·CH(3)CN (3a, T(1/2) = 151 K), [Fe(napet)(NCSe)]·CH(3)CN (3b, T(1/2) = 170 K), [Fe(napet)(NCO)] (3c, T(1/2) = 155 K) and [Fe(napet)(N(3))], which, moreover, exhibits thermal hysteresis (3d, T(1/2)↑ = 122 K, T(1/2)↓ = 117 K). These compounds are the first examples of octahedral iron(III) spin-crossover compounds with the coordinated pseudohalides. We report the structure and magnetic properties of these complexes. The magnetic data of all the compounds were analysed using the spin Hamiltonian formalism including the ZFS term and in the case of spin-crossover, the Ising-like model was also applied. PMID:21904754

  14. Burning Characteristics and Flammability of PVC Cables in Groups

    NASA Technical Reports Server (NTRS)

    Mikado, T.; Akita, K.

    1988-01-01

    Because burning cables represent a danger of increasing secondary damage it is of utmost importance for disaster prevention to correctly evaluate the combustion characteristics of cable. However, in many cases cable is laid out in bundles complicating the combustion characteristics. A situation has developed where group cable characteristics are not completely understood. A new method is developed for testing the combustion of high polymer type cable and earlier reports gave comparative combustion measurement results. It was learned that there is considerable difference between the combustion characteristics of the grouped cables and those of single cables. This study is supplemental research concerning the special behavior of group PVC cables, throwing some light on their combustion characteristics.

  15. Upgrading of PVC rich wastes by magnetic density separation and hyperspectral imaging quality control.

    PubMed

    Luciani, Valentina; Bonifazi, Giuseppe; Rem, Peter; Serranti, Silvia

    2015-11-01

    Polyvinylchloride (PVC) is one of the most produced polymers in Europe, with a share of 11% in terms of mass (8 milliontons) of total polymer consumption, but in 2010 only 5% of the total PVC production came from recycled materials, where other polymer recycling achieves a level of 15% on average. In order to find an innovative process to extract PVC from window frames waste, a combination of two innovative technologies was tested: magnetic density separation (MDS) and hyperspectral imaging (HSI). By its nature, MDS is a flexible high precision density separation technology that is applicable to any mixture of polymers and contaminants with non-overlapping densities. As PVC has a very distinctive high density, this technology was tested to obtain high-grade PVC pre-concentrates from window frame waste. HSI was used to perform a quality control of the products obtained by MDS showing that PVC was clearly discriminated from unwanted rubber particles of different colors. The results showed that the combined application of MDS and HSI techniques allowed to separate and to check the purity of PVC from window frame waste. PMID:25458764

  16. Space Charge Formation and Electrical Breakdown at High Temperature Region in PVC for Electrical Wiring Assembly

    NASA Astrophysics Data System (ADS)

    Miura, Masakazu; Fukuma, Masumi; Kishida, Satoru

    The Polyvinyl chloride (PVC), the most popular insulating material, is used as an insulating material of various electric products. When using an electrical wiring assembly code over the power capacity, PVC could melt by the joule heating and cause an electrical breakdown. Therefore, it is necessary to clarify the electrical breakdown phenomena near the melting point (170°C) in PVC. In this paper, space charge distribution and conduction current have been measured in PVC sheets up to the electrical breakdown in the range from room temperature to 200°C under DC electric field. The breakdown strength decreases with temperature in PVC. Small hetero-space charges are accumulated near both of the electrodes at room temperature region. At high temperature region above 100°C, it is observed that positive charges are injected from anode and move toward the cathode; the electric field is emphasized near the cathode due to the packet-like positive charge in PVC. It shows a thermal breakdown process of the electric fields due to positive charge behavior and conduction current increase with temperature near the melting point in PVC.

  17. Effect of PVC and iron materials on Mn(II) deposition in drinking water distribution systems.

    PubMed

    Cerrato, José M; Reyes, Lourdes P; Alvarado, Carmen N; Dietrich, Andrea M

    2006-08-01

    Polyvinyl chloride (PVC) and iron pipe materials differentially impacted manganese deposition within a drinking water distribution system that experiences black water problems because it receives soluble manganese from a surface water reservoir that undergoes biogeochemical cycling of manganese. The water quality study was conducted in a section of the distribution system of Tegucigalpa, Honduras and evaluated the influence of iron and PVC pipe materials on the concentrations of soluble and particulate iron and manganese, and determined the composition of scales formed on PVC and iron pipes. As expected, total Fe concentrations were highest in water from iron pipes. Water samples obtained from PVC pipes showed higher total Mn concentrations and more black color than that obtained from iron pipes. Scanning electron microscopy demonstrated that manganese was incorporated into the iron tubercles and thus not readily dislodged from the pipes by water flow. The PVC pipes contained a thin surface scale consisting of white and brown layers of different chemical composition; the brown layer was in contact with the water and contained 6% manganese by weight. Mn composed a greater percentage by weight of the PVC scale than the iron pipe scale; the PVC scale was easily dislodged by flowing water. This research demonstrates that interactions between water and the infrastructure used for its supply affect the quality of the final drinking water. PMID:16765409

  18. Layered and intercalated hydrotalcite-like materials as thermal stabilizers in PVC resin

    NASA Astrophysics Data System (ADS)

    Lin, Yanjun; Wang, Jianrong; Evans, David G.; Li, Dianqing

    2006-05-01

    In the light of the accepted mechanism of thermal stabilization of PVC by layered double hydroxides (LDHs), the layer cations and interlayer counterions in LDHs were tailored to give MgZnAl-CO3-LDH and MgZnAl-maleate-LDH. These materials were characterized by XRD, FT-IR, and TG DTA. The thermal stability of PVC composites containing different LDH additives was tested in sheets having a thickness of about 1 mm. The results showed that compared with MgAl-CO3-LDH, MgZnAl-CO3-LDH enhances the thermal stability of PVC in terms of both long-term stability and early coloring. After intercalation of maleate in the LDH by reaction of maleic acid with the MgZnAl-CO3-LDH precursor, the interlayer distance increases from 0.75 to 1.11 nm. Since Cl- promotes the autocatalytic dehydrochlorination of PVC, which is responsible for its degradation, an increased interlayer distance should facilitate entry of Cl- into the interlayer galleries and inhibit the decomposition of PVC. In addition, maleic acid has a conjugated C=C double bond which can react with double bond formed in the dehydrochlorination of PVC and thus further inhibit the autocatalytic degradation reaction. The results show that the early coloring of PVC is markedly improved and the long-term stability slightly reduced by addition of the MgZnAl-maleate-LDH.

  19. N-butylamine functionalized graphene oxide for detection of iron(III) by photoluminescence quenching.

    PubMed

    Gholami, Javad; Manteghian, Mehrdad; Badiei, Alireza; Ueda, Hiroshi; Javanbakht, Mehran

    2016-02-01

    An N-butylamine functionalized graphene oxide nanolayer was synthesized and characterized by ultraviolet (UV)-visible spectrometry, Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, and transmission electron microscopy. Detection of iron(III) based on photoluminescence spectroscopy was investigated. The N-butylamine functionalized graphene oxide was shown to specifically interact with iron (III), compared with other cationic trace elements including potassium (I), sodium (I), calcium (II), chromium (III), zinc (II), cobalt (II), copper (II), magnesium (II), manganese (II), and molybdenum (VI). The quenching effect of iron (III) on the luminescence emission of N-butylamine functionalized graphene oxide layer was used to detect iron (III). The limit of detection (2.8 × 10(-6)  M) and limit of quantitation (2.9 × 10(-5)  M) were obtained under optimal conditions. PMID:26016610

  20. Determination of tungsten with iron(III) after reduction with mercury in thiocyanate medium.

    PubMed

    Yatirajam, V; Dhamija, S

    1976-01-01

    Tungsten(V) is formed by shaking for 2 min sodium tungstate solution in 0.4 M potassium thiocyanate-4M hydrochloric acid medium, with mercury. It is titrated with standard iron(III) solution. The thiocyanate present stabilizes W(V) to aerial oxidation and also acts as indicator. The W(V) can also be titrated potentiometrically in 7M hydrochloric acid, a tungsten wire electrode being used. Fe, Ni, Cr, Zr, Bi, Sb, Ce, Al, Pb, Ca and U do not interfere. Cu, V and As can be tolerated up to 5 mg. Co, Mo, Re, Nb and Mn interfere, but not in the potentiometric determination. The method is direct, simple, rapid, accurate and reproducible. PMID:18961802

  1. Gallium(iii) and iron(iii) complexes of quinolone antimicrobials.

    PubMed

    Mjos, Katja Dralle; Cawthray, Jacqueline F; Polishchuk, Elena; Abrams, Michael J; Orvig, Chris

    2016-08-16

    Iron is an essential nutrient for many microbes. According to the "Trojan Horse Hypothesis", biological systems have difficulties distinguishing between Fe(3+) and Ga(3+), which constitutes the antimicrobial efficacy of the gallium(iii) ion. Nine novel tris(quinolono)gallium(iii) complexes and their corresponding iron(iii) analogs have been synthesized and fully characterized. Quinolone antimicrobial agents from three drug generations were used in this study: ciprofloxacin, enoxacin, fleroxacin, levofloxacin, lomefloxacin, nalidixic acid, norfloxacin, oxolinic acid, and pipemidic acid. The antimicrobial efficacy of the tris(quinolono)gallium(iii) complexes was studied against E. faecalis and S. aureus (both Gram-positive), as well as E. coli, K. pneumonia, and P. aeruginosa (all Gram-negative) in direct comparison to the tris(quinolono)iron(iii) complexes and the corresponding free quinolone ligands at various concentrations. For the tris(quinolono)gallium(iii) complexes, no combinational antimicrobial effects between Ga(3+) and the quinolone antimicrobial agents were observed. PMID:27315225

  2. Properties of blends for profiles and semi-rigid films made of PVC nanocomposites produced in pilot scale

    NASA Astrophysics Data System (ADS)

    Obloj-Muzaj, Maria; Abramowicz, Agnieszka; Kumosinski, Marcin; Zielecka, Maria; Kozakiewicz, Janusz; Gorska, Agnieszka

    2016-05-01

    PVC nanocomposites containing 0.5 wt. %/VCM of either nanosilica or hybrid core/shell type nanofiller were produced in-situ in suspension polymerisation. Significant increase in impact strength of PVC composites obtained was observed (higher 25 - 60 % in comparison with PVC). The amount of impact modifier in selected rigid PVC blends (e.g. in window profiles) could be significantly reduced (≥ 50 %). Tensile and flexural properties of nanocomposites were similar to PVC, however, at smaller amount of impact modifier other mechanical properties improve. Tear resistance of rigid films was better.

  3. Molecular surface structural changes of plasticized PVC materials after plasma treatment.

    PubMed

    Zhang, Xiaoxian; Zhang, Chi; Hankett, Jeanne M; Chen, Zhan

    2013-03-26

    In this research, a variety of analytical techniques including sum frequency generation vibrational spectroscopy (SFG), coherent anti-Stokes Raman spectroscopy (CARS), and X-ray photoelectron spectroscopy (XPS) have been employed to investigate the surface and bulk structures of phthalate plasticized poly(vinyl chloride) (PVC) at the molecular level. Two types of phthalate molecules with different chain lengths, diethyl phthalate (DEP) and dibutyl phthalate (DBP), mixed with PVC in various weight ratios were examined to verify their different surface and bulk behaviors. The effects of oxygen and argon plasma treatment on PVC/DBP and PVC/DEP hybrid films were investigated on both the surface and bulk of films using SFG and CARS to evaluate the different plasticizer migration processes. Without plasma treatment, SFG results indicated that more plasticizers segregate to the surface at higher plasticizer bulk concentrations. SFG studies also demonstrated the presence of phthalates on the surface even at very low bulk concentration (5 wt %). Additionally, the results gathered from SFG, CARS, and XPS experiments suggested that the PVC/DEP system was unstable, and DEP molecules could leach out from the PVC under low vacuum after several minutes. In contrast, the PVC/DBP system was more stable; the migration process of DBP out of PVC could be effectively suppressed after oxygen plasma treatment. XPS results indicated the increase of C═O/C-O groups and decrease of C-Cl functionalities on the polymer surface after oxygen plasma treatment. The XPS results also suggested that exposure to argon plasma induced chemical bond breaking and formation of cross-linking or unsaturated groups with chain scission on the surface. Finally, our results indicate the potential risk of using DEP molecules in PVC since DEP can easily leach out from the polymeric bulk. PMID:23445444

  4. Isolation of microorganisms involved in reduction of crystalline iron(III) oxides in natural environments.

    PubMed

    Hori, Tomoyuki; Aoyagi, Tomo; Itoh, Hideomi; Narihiro, Takashi; Oikawa, Azusa; Suzuki, Kiyofumi; Ogata, Atsushi; Friedrich, Michael W; Conrad, Ralf; Kamagata, Yoichi

    2015-01-01

    Reduction of crystalline Fe(III) oxides is one of the most important electron sinks for organic compound oxidation in natural environments. Yet the limited number of isolates makes it difficult to understand the physiology and ecological impact of the microorganisms involved. Here, two-stage cultivation was implemented to selectively enrich and isolate crystalline iron(III) oxide reducing microorganisms in soils and sediments. Firstly, iron reducers were enriched and other untargeted eutrophs were depleted by 2-years successive culture on a crystalline ferric iron oxide (i.e., goethite, lepidocrocite, hematite, or magnetite) as electron acceptor. Fifty-eight out of 136 incubation conditions allowed the continued existence of microorganisms as confirmed by PCR amplification. High-throughput Illumina sequencing and clone library analysis based on 16S rRNA genes revealed that the enrichment cultures on each of the ferric iron oxides contained bacteria belonging to the Deltaproteobacteria (mainly Geobacteraceae), followed by Firmicutes and Chloroflexi, which also comprised most of the operational taxonomic units (OTUs) identified. Venn diagrams indicated that the core OTUs enriched with all of the iron oxides were dominant in the Geobacteraceae while each type of iron oxides supplemented selectively enriched specific OTUs in the other phylogenetic groups. Secondly, 38 enrichment cultures including novel microorganisms were transferred to soluble-iron(III) containing media in order to stimulate the proliferation of the enriched iron reducers. Through extinction dilution-culture and single colony isolation, six strains within the Deltaproteobacteria were finally obtained; five strains belonged to the genus Geobacter and one strain to Pelobacter. The 16S rRNA genes of these isolates were 94.8-98.1% identical in sequence to cultured relatives. All the isolates were able to grow on acetate and ferric iron but their physiological characteristics differed considerably in

  5. Photostabilizing Efficiency of PVC in the Presence of Schiff Bases as Photostabilizers.

    PubMed

    Yousif, Emad; Al-Amiery, Ahmed A; Kadihum, Abdulhadi; Kadhum, Abdul Amir H; Mohamad, Abu Bakar

    2015-01-01

    The photostabilization of polyvinyl chloride (PVC) films by Schiff bases was investigated. Polyvinyl chloride films containing 0.5 wt % Schiff bases were produced using the same casting method as that used for additive-free PVC films from tetrahydrofuran (THF) solvent. The photostabilization activities of these compounds were determined by monitoring the carbonyl, polyene and hydroxyl indices with irradiation time. The changes in viscosity average molecular weight of PVC with irradiation time were also monitored using THF as a solvent. The quantum yield of chain scission (Φcs) for the studied complexes in PVC was estimated to range between 4.72 and 8.99 × 10(-8). According to the experimental results, several mechanisms were suggested, depending on the structure of the additive. Ultra violet (UV) absorption, peroxide decomposition and radical scavenging were suggested as the photostabilizing mechanisms. PMID:26556323

  6. Modification of medical grade PVC with N-vinylimidazole to obtain bactericidal surface

    NASA Astrophysics Data System (ADS)

    Meléndez-Ortiz, H. Iván; Alvarez-Lorenzo, Carmen; Concheiro, Angel; Jiménez-Páez, Víctor M.; Bucio, Emilio

    2016-02-01

    N-vinylimidazole (VIm) was grafted onto medical-grade poly(vinyl chloride) (PVC) catheters in order to provide a bactericidal surface that make them less susceptible to microbial colonization. The grafting of VIm was carried out by means of gamma rays using the direct method, which demonstrated to be an efficient and fast procedure for obtaining PVC-g-VIm copolymers. These copolymers could be quaternized in a second step using methyl iodide (CH3I). The effects of solvent nature, absorbed dose, and monomer concentration on the grafting yield were investigated. Modified PVC catheters were characterized by means of Fourier transform infrared spectroscopy (FT-IR), thermogravimetry (TGA), and swelling studies. PVC-g-VIm copolymers both before and after quaternization showed good hemocompatibility, while quaternization was required to inhibit the growth of Staphylococcus aureus.

  7. Gallium(III) Tetraphenylporphyrinates Containing Hydrosulfide and Thiolate Ligands: Structural Models for Sulfur-Bound Iron(III) Hemes.

    PubMed

    Meininger, Daniel J; Chee-Garza, Max; Arman, Hadi D; Tonzetich, Zachary J

    2016-03-01

    Gallium(III) tetraphenylporphyrinates (TPP) containing anionic sulfur ligands have been prepared and characterized in the solid state and solution. The complexes serve as structural models for iron(III) heme sites containing sulfur coordination that otherwise prove challenging to synthesize due to the propensity for reduction to iron(II). The compounds prepared include the first well-characterized example of a trivalent metalloporphyrinate containing a terminal hydrosulfide ligand, [Ga(SH)(TPP)], as well as [Ga(SEt)(TPP)], [Ga(SPh)(TPP)], and [Ga(SSi(i)Pr3)(TPP)]. The stability of these compounds toward reduction has permitted an investigation of their solid-state structures and electrochemistry. The structural features and reaction chemistry of the complexes in relation to their iron(III) analogs is discussed. PMID:26872092

  8. Prebiotic polymerization: Oxidative polymerization of 2, 3-dimercapto-1-propanol on the surface of iron(III) hydroxide oxide

    NASA Technical Reports Server (NTRS)

    Weber, Arthur L.

    1995-01-01

    The oxidation of 2, 3-dimercapto-1-propanol by ferric ions on the surface of iron(III) hydroxide oxide (Fe(OH)O) yielded polydisulfide oligomers. This polymerization occurred readily at low dithiol concentration under mild aqueous conditions. Polydisulfide polymers up to the 15-mer were synthesized from 1 mM dithiol in 5 ml water reacted with iron(III) hydroxide oxide (20 mg, 160 micromole Fe) for 3 days under anaerobic conditions at 40 C and pH 4. About 91% of the dithiol was converted to short soluble oligomers and 9% to insoluble larger oligomers that were isolated with the Fe(OH)O phase. Reactions carried out at the same ratio of dithiol to Fe(OH)O but at higher dithiol concentrations gave higher yields of the larger insoluble oligomers. The relationship of these results to prebiotic polymer synthesis is discussed.

  9. Prebiotic Polymerization: Oxidative Polymerization of 2,3 Dimercapto-1- Propanol on the Surface of Iron(III) Hydroxide Oxide

    NASA Technical Reports Server (NTRS)

    Weber, Arthur L.

    1995-01-01

    The oxidation of 2,3-dimercapto-1-propanol by ferric ions on the surface of iron(III) hydroxide oxide (Fe(OH)O) yielded polydisulfide oligomers. This polymerization occurred readily at low dithiol concentration under mild aqueous conditions. Polydisulfide polymers up to the 15-mer were synthesized from 1 mM dithiol in 5 ml water reacted with iron(III) hydroxide oxide (20 mg, 160 micromole Fe) for 3 days under anaerobic conditions at 40 C and pH 4. About 91% of the dithiol was converted to short soluble oligomers and 9% to insoluble larger oligomers that were isolated with the FE(OH)O phase. Reactions carried out at the same ratio of dithiol to FE(OH)O but at higher dithiol concentrations gave higher yields of the larger insoluble oligomers. The relationship of these results to prebiotic polymer synthesis is discussed.

  10. Ion-exchange extraction of platinum(II,IV) from chloride solutions in the presence of iron(III)

    NASA Astrophysics Data System (ADS)

    Kononova, O. N.; Duba, E. V.; Karplyakova, N. S.; Krylov, A. S.

    2015-08-01

    The sorption concentration of platinum(II,IV) in the presence of iron(III) is studied on new samples of domestically produced ionites of the CYBBER brand. In comparing the sorption and kinetic properties of the new ionites to those of sorbents of the Purolite brand studied earlier, the higher effectiveness of the former is demonstrated via the extraction of platinum(II,IV) ions from strongly and weakly acidic chloride solutions. It is found that the sorbed platinum ions can be completely separated from iron(III) ions through separate elution using 0.01-0.001 M HCl (iron ions) and a thiourea solution (80 g/L) in 0.3 M H2SO4 (platinum ions).

  11. Performance enhancement of polyvinyl chloride ultrafiltration membrane modified with graphene oxide.

    PubMed

    Zhao, Yuanyuan; Lu, Jiaqi; Liu, Xuyang; Wang, Yudan; Lin, Jiuyang; Peng, Na; Li, Jingchun; Zhao, Fangbo

    2016-10-15

    A novel polyvinyl chloride (PVC) membrane was modified with graphene oxide (GO) via phase inversion method to improve its hydrophilicity and mechanical properties. The GO presented a large amount of hydrophilic groups after the modification through the modified Hummers method. It was observed that with the addition of low fraction of GO powder, the GO/PVC hybrid membranes exhibited a significant enhancement in hydrophilicity, water flux, and mechanical properties. With optimal dosage (0.1wt%), the pure water flux of GO/PVC membrane increased from 232.6L/(m(2)hbar) to 430.0L/(m(2)hbar) and the tensile strength increased from 231.3cN to 305.3cN. The improved properties of the PVC/GO hybrid membranes are mainly attributed to the strong hydrophilicity of functional groups on the GO surface, indicating that GO has a promising candidate for modification of PVC ultrafiltration membranes in wastewater treatment. PMID:27399613

  12. Study on the recycling of waste PVC compounds from electrical wires

    SciTech Connect

    Roman Jr, Celso Zattera, Ademir José

    2014-05-15

    The good mechanical, thermal and electrical properties of poly (vinyl chloride) (PVC) make it a polymer used in many applications, among which is the coating of wires and cables. The processing of PVC for this application is made using the extrusion process. The PVC waste resulting from extrusion can be recycled or placed on landfills. The objective of this work is to develop recycling methods to decrease the amount of PVC stored in landfills. This work evaluated the influence of successive processing of PVC on the final properties of the obtained compound, which will be used in the process of coating wire and cable by extrusion. The mechanical properties of the electrical wires were assessed according to the Brazilian Association of Technical Standards (ABNT NBR 6251). Tests of tensile strength, elongation at break, before and after thermal aging in an oven with air circulation for a period of 168 hours at 100 °C were performed. The degradation of the PVC compound was carried out through Fourier transform infrared spectroscopy (FTIR) and mechanical properties evaluation. The results showed that the compound can be reprocessed five times keeping the minimum requirements of the ABNT NBR 6251 Standard. Reprocessing was stopped upon color changing (yellowing) of the compound. Yellowing is a characteristic degradation behavior by dehydrochlorination of PVC. FTIR analysis showed changes at 1600 cm{sup −1}, 1430 cm{sup −1}, 685 cm{sup −1} and 614 cm{sup −1} bands. The performance of the PVC compound for coating electrical wire and cable was fair, meeting the requirements of the ABNT NBR 6251 Standard even after five reprocessing cycles.

  13. Study on the recycling of waste PVC compounds from electrical wires

    NASA Astrophysics Data System (ADS)

    Roman, Celso, Jr.; Zattera, Ademir José

    2014-05-01

    The good mechanical, thermal and electrical properties of poly (vinyl chloride) (PVC) make it a polymer used in many applications, among which is the coating of wires and cables. The processing of PVC for this application is made using the extrusion process. The PVC waste resulting from extrusion can be recycled or placed on landfills. The objective of this work is to develop recycling methods to decrease the amount of PVC stored in landfills. This work evaluated the influence of successive processing of PVC on the final properties of the obtained compound, which will be used in the process of coating wire and cable by extrusion. The mechanical properties of the electrical wires were assessed according to the Brazilian Association of Technical Standards (ABNT NBR 6251). Tests of tensile strength, elongation at break, before and after thermal aging in an oven with air circulation for a period of 168 hours at 100 °C were performed. The degradation of the PVC compound was carried out through Fourier transform infrared spectroscopy (FTIR) and mechanical properties evaluation. The results showed that the compound can be reprocessed five times keeping the minimum requirements of the ABNT NBR 6251 Standard. Reprocessing was stopped upon color changing (yellowing) of the compound. Yellowing is a characteristic degradation behavior by dehydrochlorination of PVC. FTIR analysis showed changes at 1600 cm-1, 1430 cm-1, 685 cm-1 and 614 cm-1 bands. The performance of the PVC compound for coating electrical wire and cable was fair, meeting the requirements of the ABNT NBR 6251 Standard even after five reprocessing cycles.

  14. Extracellular polymeric substances mediate bioleaching/biocorrosion via interfacial processes involving iron(III) ions and acidophilic bacteria.

    PubMed

    Sand, Wolfgang; Gehrke, Tilman

    2006-01-01

    Extracellular polymeric substances seem to play a pivotal role in biocorrosion of metals and bioleaching, biocorrosion of metal sulfides for the winning of precious metals as well as acid rock drainage. For better control of both processes, the structure and function of extracellular polymeric substances of corrosion-causing or leaching bacteria are of crucial importance. Our research focused on the extremophilic bacteria Acidithiobacillus ferrooxidans and Leptospirillum ferrooxidans, because of the "simplicity" and knowledge about the interactions of these bacteria with their substrate/substratum and their environment. For this purpose, the composition of the corresponding extracellular polymeric substances and their functions were analyzed. The extracellular polymeric substances of both species consist mainly of neutral sugars and lipids. The functions of the exopolymers seem to be: (i) to mediate attachment to a (metal) sulfide surface, and (ii) to concentrate iron(III) ions by complexation through uronic acids or other residues at the mineral surface, thus, allowing an oxidative attack on the sulfide. Consequently, dissolution of the metal sulfide is enhanced, which may result in an acceleration of 20- to 100-fold of the bioleaching process over chemical leaching. Experiments were performed to elucidate the importance of the iron(III) ions complexed by extracellular polymeric substances for strain-specific differences in oxidative activity for pyrite. Strains of A. ferrooxidans with a high amount of iron(III) ions in their extracellular polymeric substances possess greater oxidation activity than those with fewer iron(III) ions. These data provide insight into the function of and consequently the advantages that extracellular polymeric substances provide to bacteria. The role of extracellular polymeric substances for attachment under the conditions of a space station and resulting effects like biofouling, biocorrosion, malodorous gases, etc. will be discussed

  15. Catalytic oxidation of water and alcohols by a robust iron(iii) complex bearing a cross-bridged cyclam ligand.

    PubMed

    Tan, Peng; Kwong, Hoi-Ki; Lau, Tai-Chu

    2015-08-01

    An iron(iii) complex bearing a cross-bridged cyclam ligand (4,11-dimethyl-1,4,8,11-tetraazabicyclo[6.6.2]hexadecane) is an efficient catalyst for the oxidation of both water and alcohols using sodium periodate as the oxidant. In catalytic water oxidation a maximum turnover number (TON) of 1030 is achieved, while in catalytic alcohol oxidation >95% conversions and yields can be obtained. PMID:26126521

  16. Zeta-Fe2O3 – A new stable polymorph in iron(III) oxide family

    PubMed Central

    Tuček, Jiří; Machala, Libor; Ono, Shigeaki; Namai, Asuka; Yoshikiyo, Marie; Imoto, Kenta; Tokoro, Hiroko; Ohkoshi, Shin-ichi; Zbořil, Radek

    2015-01-01

    Iron(III) oxide shows a polymorphism, characteristic of existence of phases with the same chemical composition but distinct crystal structures and, hence, physical properties. Four crystalline phases of iron(III) oxide have previously been identified: α-Fe2O3 (hematite), β-Fe2O3, γ-Fe2O3 (maghemite), and ε-Fe2O3. All four iron(III) oxide phases easily undergo various phase transformations in response to heating or pressure treatment, usually forming hexagonal α-Fe2O3, which is the most thermodynamically stable Fe2O3 polymorph under ambient conditions. Here, from synchrotron X-ray diffraction experiments, we report the formation of a new iron(III) oxide polymorph that we have termed ζ-Fe2O3 and which evolved during pressure treatment of cubic β-Fe2O3 ( space group) at pressures above 30 GPa. Importantly, ζ-Fe2O3 is maintained after pressure release and represents the first monoclinic Fe2O3 polymorph (I2/a space group) that is stable at atmospheric pressure and room temperature. ζ-Fe2O3 behaves as an antiferromagnet with a Néel transition temperature of ~69 K. The complex mechanism of pressure-induced transformation of β-Fe2O3, involving also the formation of Rh2O3-II-type Fe2O3 and post-perovskite-Fe2O3 structure, is suggested and discussed with respect to a bimodal size distribution of precursor nanoparticles. PMID:26469883

  17. Effect of UV and gamma radiation on Rn222 permeation through polyvinyl chloride (PVC). Application to the packaging of radium sources for the purpose of storage

    NASA Astrophysics Data System (ADS)

    Tomasella, E.; Labed, V.; Klein, D.; Robé, M. C.; Cetier, Ph.; Chambaudet, A.

    1995-11-01

    Mining of uranium and thorium, as well as the use of radioactive sources in radiotherapy, have caused, during the 20th century, the production of waste with a varying concentration in long-lived radionucleides (particularly radium). This waste cannot be stored in traditional storage sites which will return to the public domain after 300 years, due to, on the one hand, the radium period (1620 years) and, on the other hand, the build-up of radon, its gaseous daughter. One solution, in order to optimize the packaging and storage of such products, could be to use successive barriers, made of polymer membranes, intended to limit radon emission. Laboratory tests have shown that polyvinyl chloride (PVC) greatly reduces radon emission from a radium source. However one should take into account the damage of the polymer in time, due to radioactive waste storage itself over long periods of time. Therefore, in order to check the durability of such barriers, PVC samples have been subjected to different accelerated ageing processes by exposure to ultra-violet (UV) radiations or gamma rays. We have determined the effect of such radiation of the samples using two approaches: — demonstration of structural changes using analytical method (Infra-red with Fourier Transform or IRTF), — study of variations in the radon permeation factor. In the first analysis, it seems that the UV irradiation, causes structural changes in the PVC as a function of the irradiation length of time. This leads first to an increase in the efficiency of the polymer as a "radon barrier", i.e. a reduction in its permeation factor (2.41 × 10 -12m 2s -1 for a non exposed membrane, against 3.30 × 10 -13m 2.s -1 for a membrane exposed during 284 hours, with an exposure rate of 62.5 W.m -2, thus a reduction by a factor 10 of the radon emission) then to a long-term weakness. The gamma irradiation (dose rate: 1.05 kGy.h -1, dose: 0.71 MGy) also causes a reduction in the permeation factor of PVC, but only by a

  18. Comparison of VOC and ammonia emissions from individual PVC materials, adhesives and from complete structures.

    PubMed

    Järnström, H; Saarela, K; Kalliokoski, P; Pasanen, A-L

    2008-04-01

    Emission rates of volatile organic compounds (VOCs) and ammonia measured from six PVC materials and four adhesives in the laboratory were compared to the emission rates measured on site from complete structures. Significantly higher specific emission rates (SERs) were generally measured from the complete structures than from individual materials. There were large differences between different PVC materials in their permeability for VOCs originating from the underlying structure. Glycol ethers and esters from adhesives used in the installation contributed to the emissions from the PVC covered structure. Emissions of 2-ethylhexanol and TXIB (2,2,4-trimethyl-1,3-pentanediol diisobutyrate) were common. High ammonia SERs were measured from single adhesives but their contribution to the emissions from the complete structure did not appear as obvious as for VOCs. The results indicate that three factors affected the VOC emissions from the PVC flooring on a structure: 1) the permeability of the PVC product for VOCs, 2) the VOC emission from the adhesive used, and 3) the VOC emission from the backside of the PVC product. PMID:17997159

  19. Tertiary recycling of PVC-containing plastic waste by copyrolysis with cattle manure.

    PubMed

    Duangchan, Apinya; Samart, Chanatip

    2008-11-01

    The corrosion from pyrolysis of PVC in plastic waste was reduced by copyrolysis of PVC with cattle manure. The optimization of pyrolysis conditions between PVC and cattle manure was studied via a statistical method, the Box-Behnken model. The pyrolysis reaction was operated in a tubular reactor. Heating rate, reaction temperature and the PVC:cattle manure ratio were optimized in the range of 1-5 degrees C/min, 250-450 degrees C and the ratio of 1:1-1:5, respectively. The suitable conditions which provided the highest HCl reduction efficiency were the lowest heating rate of 1 degrees C/min, the highest reaction temperature of 450 degrees C, and the PVC:cattle manure ratio of 1:5, with reliability of more than 90%. The copyrolysis of the mixture of PVC-containing plastic and cattle manure was operated at optimized conditions and the synergistic effect was studied on product yields. The presence of manure decreased the oil yield by about 17%. The distillation fractions of oil at various boiling points from both the presence and absence of manure were comparable. The BTX concentration decreased rapidly when manure was present and the chlorinated hydrocarbon was reduced by 45%. However, the octane number of the gasoline fraction was not affected by manure and was in the range of 99-100. PMID:18314324

  20. Tertiary recycling of PVC-containing plastic waste by copyrolysis with cattle manure

    SciTech Connect

    Duangchan, Apinya Samart, Chanatip

    2008-11-15

    The corrosion from pyrolysis of PVC in plastic waste was reduced by copyrolysis of PVC with cattle manure. The optimization of pyrolysis conditions between PVC and cattle manure was studied via a statistical method, the Box-Behnken model. The pyrolysis reaction was operated in a tubular reactor. Heating rate, reaction temperature and the PVC:cattle manure ratio were optimized in the range of 1-5 deg. C/min, 250-450 deg. C and the ratio of 1:1-1:5, respectively. The suitable conditions which provided the highest HCl reduction efficiency were the lowest heating rate of 1 deg. C/min, the highest reaction temperature of 450 deg. C, and the PVC:cattle manure ratio of 1:5, with reliability of more than 90%. The copyrolysis of the mixture of PVC-containing plastic and cattle manure was operated at optimized conditions and the synergistic effect was studied on product yields. The presence of manure decreased the oil yield by about 17%. The distillation fractions of oil at various boiling points from both the presence and absence of manure were comparable. The BTX concentration decreased rapidly when manure was present and the chlorinated hydrocarbon was reduced by 45%. However, the octane number of the gasoline fraction was not affected by manure and was in the range of 99-100.

  1. Investigation on the mechanical and physical properties of TPU/PVC blend as potential material of bedpan

    NASA Astrophysics Data System (ADS)

    Hakim, M. I.; Shahnaz, S. S. B.; Luqman, M.; Anis, N. I.; Shuhaida, Y.; Zaharah, S. A.; Baidi, M. B.; Yu, C. W.; Kathiresan, V. S.

    2016-06-01

    The purpose of this study is to determine the impact properties, chemical resistance and morphology of TPU/PVC blend in order to be used as potential material to fabricate bedpan. TPU and incorporation of PVC in TPU was done by melt-mixing method. The blends of TPU/PVC from melt mixing were then undergoing hot press compression moulding to produce sample with 3mm thickness. The blend sample was subjected to drop weight impact test, chemical resistance test and SEM test. Results from impact test showed that 30/70 TPU/PVC has recorded the maximum velocity impacted by 6 J of 1.8 m/s at 97ms while 50/50 TPU/PVC has the highest force (impact strength) of 0.95kN compared with other samples. The result also found that 50/50 TPU/PVC blend has lowest weight change, indicated that the blend has good resistance toward NaOH. HCl has a stronger effect on TPU/PVC blend compared to NaOH for all blend composition where 10/90 TPU/PVC showed highest resistance towards HCl. The micrograph shows that 50/50 TPU/PVC exhibited both smooth surface, indicating the brittleness of PVC and rough and the plasticity fractured surface, indicating the ductility of TPU features.

  2. CHARACTERIZATION OF CLEAN AND FOULED PERFORATED MEMBRANE DIFFUSERS

    EPA Science Inventory

    Laboratory analyses were conducted on plasticized PVC perforated membrane tube diffusers after varying periods in service at two different municipal wastewater treatment facilities. One set of diffusers from Cedar Creek, NY, was in service for 26 months. The other set from the ...

  3. Isolation of microorganisms involved in reduction of crystalline iron(III) oxides in natural environments

    PubMed Central

    Hori, Tomoyuki; Aoyagi, Tomo; Itoh, Hideomi; Narihiro, Takashi; Oikawa, Azusa; Suzuki, Kiyofumi; Ogata, Atsushi; Friedrich, Michael W.; Conrad, Ralf; Kamagata, Yoichi

    2015-01-01

    Reduction of crystalline Fe(III) oxides is one of the most important electron sinks for organic compound oxidation in natural environments. Yet the limited number of isolates makes it difficult to understand the physiology and ecological impact of the microorganisms involved. Here, two-stage cultivation was implemented to selectively enrich and isolate crystalline iron(III) oxide reducing microorganisms in soils and sediments. Firstly, iron reducers were enriched and other untargeted eutrophs were depleted by 2-years successive culture on a crystalline ferric iron oxide (i.e., goethite, lepidocrocite, hematite, or magnetite) as electron acceptor. Fifty-eight out of 136 incubation conditions allowed the continued existence of microorganisms as confirmed by PCR amplification. High-throughput Illumina sequencing and clone library analysis based on 16S rRNA genes revealed that the enrichment cultures on each of the ferric iron oxides contained bacteria belonging to the Deltaproteobacteria (mainly Geobacteraceae), followed by Firmicutes and Chloroflexi, which also comprised most of the operational taxonomic units (OTUs) identified. Venn diagrams indicated that the core OTUs enriched with all of the iron oxides were dominant in the Geobacteraceae while each type of iron oxides supplemented selectively enriched specific OTUs in the other phylogenetic groups. Secondly, 38 enrichment cultures including novel microorganisms were transferred to soluble-iron(III) containing media in order to stimulate the proliferation of the enriched iron reducers. Through extinction dilution-culture and single colony isolation, six strains within the Deltaproteobacteria were finally obtained; five strains belonged to the genus Geobacter and one strain to Pelobacter. The 16S rRNA genes of these isolates were 94.8–98.1% identical in sequence to cultured relatives. All the isolates were able to grow on acetate and ferric iron but their physiological characteristics differed considerably in

  4. Hydration effects and antifouling properties of poly(vinyl chloride-co-PEGMA) membranes studied using molecular dynamics simulations

    NASA Astrophysics Data System (ADS)

    Shaikh, Abdul Rajjak; Rajabzadeh, Saeid; Matsuo, Ryuichi; Takaba, Hiromitsu; Matsuyama, Hideto

    2016-04-01

    Polyvinyl chloride (PVC) membranes are widely used in water treatment because of their low cost and chemical stability. However, PVC membranes can become fouled, and this restricts their applications in membrane technology. In order to enhance the antifouling property of PVC membranes, copolymers such as poly(vinyl chloride-co-poly(ethylene glycol)methyl ether methacrylate) (poly(VC-co-PEGMA)) with different PEGMA segment percentages were synthesized in our previous work. Experimentally, it was observed that the poly(VC-co-PEGMA) copolymer has better antifouling properties than those of PVC membranes. Here, we explore effect of the PEGMA segment percentage on the surface hydration properties of poly(VC-co-PEGMA) copolymers. Density functional theory calculations and molecular dynamics simulations were carried out to understand the interactions between PVC and PEGMA. Model structures of these systems were validated by comparing the simulated values of their volumetric properties with the experimental values. MD studies showed that increasing PEGMA percentage in the copolymer increases the interaction with water molecules, leading to improved resistance to fouling. The antifouling mechanism is also discussed with respect to surface hydration and water dynamicity. This study could form a basis for the systematic studies of polymeric membranes as well as their stability from the extent of solvent-polymer, solvent-solvent, and polymer-polymer interactions.

  5. Greater fibroblast proliferation on an ultrasonicated ZnO/PVC nanocomposite material.

    PubMed

    Maschhoff, Paul M; Geilich, Benjamin M; Webster, Thomas J

    2014-01-01

    There has been a significant and growing concern over nosocomial medical device infections. Previous studies have demonstrated that embedding nanoparticles alone (specifically, zinc oxide [ZnO]) in conventional polymers (eg, polyvinyl chloride [PVC]) can decrease bacteria growth and may have the potential to prevent or disrupt bacterial processes that lead to infection. However, little to no studies have been conducted to determine mammalian cell functions on such a nanocomposite material. Clearly, for certain medical device applications, maintaining healthy mammalian cell functions while decreasing bacteria growth is imperative (yet uncommon). For this reason, in the presented study, ZnO nanoparticles of varying sizes (from 10 nm to >200 nm in diameter) and functionalization (including no functionalization to doping with aluminum oxide and functionalizing with a silane coupling agent KH550) were incorporated into PVC either with or without ultrasonication. Results of this study provided the first evidence of greater fibroblast density after 18 hours of culture on the smallest ZnO nanoparticle incorporated PVC samples with dispersion aided by ultrasonication. Specifically, the greatest amount of fibroblast proliferation was measured on ZnO nanoparticles functionalized with a silane coupling agent KH550; this sample exhibited the greatest dispersion of ZnO nanoparticles. Water droplet tests showed a general trend of decreased hydrophilicity when adding any of the ZnO nanoparticles to PVC, but an increase in hydrophilicity (albeit still below controls or pure PVC) when using ultrasonication to increase ZnO nanoparticle dispersion. Future studies will have to correlate this change in wettability to initial protein adsorption events that may explain fibroblast behavior. Mechanical tests also provided evidence of the ability to tailor mechanical properties of the ZnO/PVC nanocomposites through the use of the different ZnO nanoparticles. Coupled with previous

  6. Iron(III) coordination chemistry of alterobactin A: a siderophore from the marine bacterium Alteromonas luteoviolacea.

    PubMed

    Holt, Pamela D; Reid, Richard R; Lewis, Brent L; Luther, George W; Butler, Alison

    2005-10-17

    Alterobactin A is a siderophore produced by the oceanic bacterium Alteromonas luteoviolacea. The thermodynamic stability constant of the ferric alterobactin A (Alt-A) complex was estimated from electrochemical measurements on the basis of a previously reported linear relationship between the reduction potentials and the pH-independent stability constants for known iron(III) complexes. The reduction potential of the ferric alterobactin A complex determined by square wave voltammetry is -0.972 V vs SCE and reversible, corresponding to a thermodynamic stability constant of 10(51+/-2). Potentiometric titration of Fe(III)-Alt-A shows the release of six protons on complexation of Fe(III) to Alt-A. The 1H NMR resonances of the Ga(III)-Alt-A complex show that the C-4, C-5, and C-6 catecholate protons and the C(alpha) and C(beta) protons of both beta-hydroxyaspartate moieties are shifted downfield relative to the free ligand, which along with the potentiometric titration data is consistent with a complex in which Fe(III) is coordinated by both catecholate oxygen atoms and both oxygen atoms of each beta-hydroxyaspartate. The UV-vis spectrum of Fe(III)-Alt-A is invariant over the pH range 4-9, indicating the coordination does not change over a wide pH range. In addition, in the absence of a coordinated metal ion, the serine ester of Alt-A hydrolyzes forming Alt-B. PMID:16212394

  7. Electron Shuttles Enhance Anaerobic Ammonium Oxidation Coupled to Iron(III) Reduction.

    PubMed

    Zhou, Guo-Wei; Yang, Xiao-Ru; Li, Hu; Marshall, Christopher W; Zheng, Bang-Xiao; Yan, Yu; Su, Jian-Qiang; Zhu, Yong-Guan

    2016-09-01

    Anaerobic ammonium oxidation coupled to iron(III) reduction, termed Feammox, is a newly discovered nitrogen cycling process. However, little is known about the roles of electron shuttles in the Feammox reactions. In this study, two forms of Fe(III) (oxyhydr)oxide ferrihydrite (ex situ ferrihydrite and in situ ferrihydrite) were used in dissimilatory Fe(III) reduction (DIR) enrichments from paddy soil. Evidence for Feammox in DIR enrichments was demonstrated using the (15)N-isotope tracing technique. The extent and rate of both the (30)N2-(29)N2 and Fe(II) formation were enhanced when amended with electron shuttles (either 9,10-anthraquinone-2,6-disulfonate (AQDS) or biochar) and further simulated when these two shuttling compounds were combined. Although the Feammox-associated Fe(III) reduction accounted for only a minor proportion of total Fe(II) formation compared to DIR, it was estimated that the potentially Feammox-mediated N loss (0.13-0.48 mg N L(-1) day(-1)) was increased by 17-340% in the enrichments by the addition of electron shuttles. The addition of electron shuttles led to an increase in the abundance of unclassified Pelobacteraceae, Desulfovibrio, and denitrifiers but a decrease in Geobacter. Overall, we demonstrated a stimulatory effect of electron shuttles on Feammox that led to higher N loss, suggesting that electron shuttles might play a crucial role in Feammox-mediated N loss from soils. PMID:27494694

  8. Iron(III) Fluorinated Porphyrins: Greener Chemistry from Synthesis to Oxidative Catalysis Reactions.

    PubMed

    Rebelo, Susana L H; Silva, André M N; Medforth, Craig J; Freire, Cristina

    2016-01-01

    Iron(III) fluorinated porphyrins play a central role in the biomimetics of heme enzymes and enable cleaner routes to the oxidation of organic compounds. The present work reports significant improvements in the eco-compatibility of the synthesis of 5,10,15,20-tetrakis-pentafluorophenylporphyrin (H₂TPFPP) and the corresponding iron complex [Fe(TPFPP)Cl], and the use of [Fe(TPFPP)Cl] as an oxidation catalyst in green conditions. The preparations of H₂TPFPP and [Fe(TPFPP)Cl] typically use toxic solvents and can be made significantly greener and simpler using microwave heating and optimization of the reaction conditions. In the optimized procedure it was possible to eliminate nitrobenzene from the porphyrin synthesis and replace DMF by acetonitrile in the metalation reaction, concomitant with a significant reduction of reaction time and simplification of the purification procedure. The Fe(III)porphyrin is then tested as catalyst in the selective oxidation of aromatics at room temperature using a green oxidant (hydrogen peroxide) and green solvent (ethanol). Efficient epoxidation of indene and selective oxidation of 3,5-dimethylphenol and naphthalene to the corresponding quinones is observed. PMID:27077840

  9. Mechanism of photoreductive stripping of iron(III) in a liquid-liquid extraction system and its application for a hydrometallurgical process

    SciTech Connect

    Nishihama, Syouhei; Hirai, Takayuki; Komasawa, Isao

    1999-12-01

    The mechanism of the photoreductive stripping of iron(III) in the liquid-liquid extraction process was investigated by employing (2-ethylhexyl)phosphonic acid mono(2-ethylhexyl) ester (EHPNA) and bis(2-ethylhexyl)phosphoric acid (D2EHPA) as extractants, n-dodecane and kerosene as diluents, and a xenon lamp as the light source. The photoreductive stripping of iron(III) progressed by photoirradiation following an initial induction period caused by dissolved oxygen in the extraction system. The iron(III)-extractant complex was photoexcited in the organic phase and photoreduced to the iron(II) complex by electron donation from the water at the aqueous/organic interface. A kinetic study of the photoreductive stripping of iron(III) revealed that the photochemical reduction of iron(III) was the rate-determining step. The removal of iron from a simulated zinc refinery residue solution by using liquid-liquid extraction combined with photochemical reduction of iron was also investigated, showing that the rare metals in the refinery residue, gallium and indium, were recovered effectively and leaving almost all iron(III) in the aqueous phase.

  10. Change Spectroscopic, thermal and mechanical studies of PU/PVC blends

    NASA Astrophysics Data System (ADS)

    Hezma, A. M.; Elashmawi, I. S.; Rajeh, A.; Kamal, Mustafa

    2016-08-01

    Blends of polyurethane (PU) and polyvinyl chloride (PVC) with different concentrations were prepared by casting method. The effects of PU on PVC blends was examined by Fourier transform-infrared (FTIR), Ultra-violet visible studies (UV/VIS.), X-ray diffraction (XRD), Thermogravimetric (TGA), Differential scanning calorimetry (DSC), and mechanical properties (stress-strain curve). The interaction between PU and PVC was examined by FT-IR through the absorbance of the N-H groups and was correlated to mechanical/thermal properties. Ultra-violet visible said that optical energy gap decrease with increasing concentration of PU. Differential scanning calorimetry results was observed a single glass transition temperature (Tg) for blends this confirming existence miscibility within the blends. The causes for best thermal stability of some blends may be described by measurements of interactions between C=O groups of PU and the α-hydrogen of PVC or a dipole-dipole -C=O..Cl-C- interactions. Significant alterations in FTIR, X-ray and DSC examination shows an interactions between blends had good miscibility. X-ray shows some alterations in the intensity with additional PU. PU change the mechanical behavior of PVC through of the blends. When polyurethane content increase causes polyvinyl chloride tensile strength decreases and elongation at break increase.

  11. Comparative study of the sorption of clomipramine and viloxazine hydrochlorides in Stedim 6 and PVC bags.

    PubMed

    Airaudo, C B; Gayte-Sorbier, A; Bianchi, C

    1998-01-01

    The stability of two antidepressant drugs, clomipramine and viloxazine hydrochlorides, was studied as was their possible sorption on Stedim 6, a new multilayer polyethylene-lined film, which was considered comparatively to polyvinyl chloride (PVC) and glass surfaces. Appropriate amounts of the drugs were added to 500 ml of 5% dextrose and 0.9% sodium chloride solutions in Stedim 6 and PVC bags, and in glass flasks, in order to obtain the concentrations currently used in clinical practice. All the containers were stored at room temperature in daylight for 72 hours. Samples were taken at various times and evaluated for remaining drug concentrations by UV spectrometry. The two drugs appeared stable under the given conditions. No concentration decrease was observed in glass flasks. Viloxazine hydrochloride showed an excellent compatibility with the PVC bags, but a slight concentration decrease (about 6-7% in 72 hours) was observed for clomipramine hydrochloride, depending on the contact duration. The compatibility of the two drugs with the new material Stedim 6 was found to be perfect. The behavioral differences observed between the two drugs with regard to PVC are explained in terms of differences of lipophilicity of the drugs. Those observed for a given drug with regard to the two materials are due to the crystalline structure of polyethylene and the amorphous one of PVC. PMID:10081591

  12. Microwave treatment of electric arc furnace dust with PVC: dielectric characterization and pyrolysis-leaching.

    PubMed

    Al-Harahsheh, Mohammad; Kingman, Sam; Al-Makhadmah, Leema; Hamilton, Ian E

    2014-06-15

    Microwave treatment of electric arc furnace dust (EAFD) with poly(vinyl chloride) (PVC) was studied in this work. A comprehensive characterization of the dust as well as assessing the suitability of using the thermal de-chlorination of the common plastic (PVC) under inert atmosphere was carried out to assess the possibility of Zn and other heavy metals extraction (Pb and Cd) from EAFD. The dielectric and thermal properties of EAFD, PVC and their mixtures were measured. Once combined and heated the metal oxides present in the dust reacted with HCl released from PVC during thermal de-chlorination, forming metal chlorides which were subsequently recovered by leaching with water. It was found that zinc chloride could be almost completely recovered in the leaching stage, with the overall recovery of Zn reaching 97% when the EAFD:PVC ratio was 1:2. The investigation highlighted that franklinite, the most refractory mineral to leaching, was completely destroyed. The leaching residue was found to compose mainly of magnetite and hematite. PMID:24769846

  13. A Computational Study of the Factors Influencing the PVC-Triggering Ability of a Cluster of Early Afterdepolarization-Capable Myocytes

    PubMed Central

    Zimik, Soling; Nayak, Alok Ranjan; Pandit, Rahul

    2015-01-01

    Premature ventricular complexes (PVCs), which are abnormal impulse propagations in cardiac tissue, can develop because of various reasons including early afterdepolarizations (EADs). We show how a cluster of EAD-generating cells (EAD clump) can lead to PVCs in a model of cardiac tissue, and also investigate the factors that assist such clumps in triggering PVCs. In particular, we study, through computer simulations, the effects of the following factors on the PVC-triggering ability of an EAD clump: (1) the repolarization reserve (RR) of the EAD cells; (2) the size of the EAD clump; (3) the coupling strength between the EAD cells in the clump; and (4) the presence of fibroblasts in the EAD clump. We find that, although a low value of RR is necessary to generate EADs and hence PVCs, a very low value of RR leads to low-amplitude EAD oscillations that decay with time and do not lead to PVCs. We demonstrate that a certain threshold size of the EAD clump, or a reduction in the coupling strength between the EAD cells, in the clump, is required to trigger PVCs. We illustrate how randomly distributed inexcitable obstacles, which we use to model collagen deposits, affect PVC-triggering by an EAD clump. We show that the gap-junctional coupling of fibroblasts with myocytes can either assist or impede the PVC-triggering ability of an EAD clump, depending on the resting membrane potential of the fibroblasts and the coupling strength between the myocyte and fibroblasts. We also find that the triggering of PVCs by an EAD clump depends sensitively on factors like the pacing cycle length and the distribution pattern of the fibroblasts. PMID:26675670

  14. Synthesis and characterization of oxalate-bridged binuclear iron(III) complex: [(N)2(O)2Fe(μ-ox)Fe(N)2(O)2

    NASA Astrophysics Data System (ADS)

    Karimpour, Touraj; Safaei, Elham; Wojtczak, Andrzej; Cotič, Patricia

    2013-04-01

    In the present work, a novel oxalate-bridged binuclear iron(III) complex of aminophenol derivative, (μ-ox-FeLNEM), where LNEM is deprotonated form of a tetradentate aminophenol ligand and ox stands for oxalate, was synthesized. The iron complex has been characterized by X-ray crystallography, infrared spectroscopy, UV-Vis, magnetic susceptibility studies and cyclic voltammetry techniques. X-ray structure analysis has revealed that each iron(III) is coordinated by two oxygen atoms of the oxalate group, two amine nitrogen's and two oxygen atoms of phenolate ligand in an octahedral arrangement. The temperature variable magnetic susceptibility exhibits quite strong antiferromagnetic coupling between the two iron(III) centers. Cyclic voltammograms of the complex in dichloromethane at low temperatures showed two quasi-reversible cathodic peaks, corresponding to FeIIIsbnd FeIII to FeIIIsbnd FeII followed by FeIIIsbnd FeII to FeIIsbnd FeII process.

  15. Comparison of the kinetic laws of the dissolution of bauxite and aluminum and iron(III) oxides and hydroxides in hydrochloric acid

    NASA Astrophysics Data System (ADS)

    Gololobova, E. G.; Gorichev, I. G.; Lainer, Yu. A.; Kozlov, K. V.

    2013-07-01

    The influence of the temperature and concentration of a hydrochloric acid solution on the dissolution kinetics of aluminum and iron(III) oxides and hydroxides and a natural sample of aluminum-containing raw materials, bauxite, is studied. The rate W of the transition of iron(III) ions from bauxite is higher than the rate of aluminum ion transition. The dependence of the fraction of a dissolved solid phase on time τ of dissolution of the oxides and hydroxides is determined, α = 1 — exp(- Asinh( Wτ)). The solubility of iron(III) chloride increases and that of aluminum chloride decreases as the HCl concentration increases. An empirical equation is proposed for the description of the dependence of the process rate on a series of parameters,.

  16. Lysozyme immobilization onto PVC catheters grafted with NVCL and HEMA for reduction of bacterial adhesion

    NASA Astrophysics Data System (ADS)

    Guadarrama-Zempoalteca, Yesica; Díaz-Gómez, Luis; Meléndez-Ortiz, H. Iván; Concheiro, Angel; Alvarez-Lorenzo, Carmen; Bucio, Emilio

    2016-09-01

    The aim of the present work was to functionalize poly(vinyl chloride) (PVC) urinary catheters with grafted copolymers that can improve the biocompatibility and serve as binding points of lysozyme. PVC catheters were modified by grafting a mixture of N-vinylcaprolactam (NVCL) and 2-hydroxyethylmethacrylate (HEMA) applying a gamma-ray pre-irradiation method. The effect of absorbed dose, monomer concentration, temperature, and reaction time on the grafting percentage was evaluated. The grafted catheters were characterized regarding surface composition (FTIR-ATR spectroscopy), thermal properties (DSC and TGA) and swelling in aqueous medium. Lysozyme was directly coupled onto PVC-g-(NVCL/HEMA) previously activated using carbonyldiimidazole. Antimicrobial lytic activity of the modified catheters over time was tested against Micrococcus lysodeikticus. Lysozyme diminished the adhesion of Staphylococcus aureus onto the functionalized catheters, which may be suitable to prevent biofilm formation.

  17. [Cytotoxicity of PVC tubes sterilized in ethylene oxide after gamma radiation exposure].

    PubMed

    de Souza, Rafael Queiroz; Graziano, Kazuko Uchikawa; Ikeda, Tamiko Ichikawa; Gonçalves, Cláudia Regina; Cruz, Aurea Silveira

    2013-04-01

    Do materials sterilized using gamma rays become toxic when re-sterilized in ethylene oxide? This question guided the objective of this study, which was to investigate the potential cytotoxic effect of PVC sterilized by gamma radiation and re-sterilized with EO by the agar diffusion method in cell cultures. Nine PVC tubes were subjected to gamma radiation sterilization and were re-sterilized in EO. The tubes were divided into a total of 81 units of analysis that were tested so as to represent the internal and external surfaces and mass of each tube. It was concluded that the PVC materials sterilized in gamma radiation and re-sterilized in EO are not cytotoxic. PMID:23743920

  18. Model fire tests on polyphosphazene rubber and polyvinyl chloride (PVC)/nitrile rubber foams

    NASA Technical Reports Server (NTRS)

    Widenor, W. M.

    1978-01-01

    A video tape record of model room fire tests was shown, comparing polyphosphazene (P-N) rubber and polyvinyl chloride (PVC)/nitrile rubber closed-cell foams as interior finish thermal insulation under conditions directly translatable to an actual fire situation. Flashover did not occur with the P-N foam and only moderate amounts of low density smoke were formed, whereas with the PVC/nitrile foam, flashover occurred quickly and large volumes of high density smoke were emitted. The P-N foam was produced in a pilot plant under carefully controlled conditions. The PVC/nitrile foam was a commercial product. A major phase of the overall program involved fire tests on P-N open-cell foam cushioning.

  19. Synthesis, crystal structure and magnetic properties of a novel tetranuclear oxo-bridged iron(III) butterfly

    NASA Astrophysics Data System (ADS)

    Arizaga, Livia; Gancheff, Jorge S.; Faccio, Ricardo; Cañón-Mancisidor, Walter; González, Ricardo; Kremer, Carlos; Chiozzone, Raúl

    2014-01-01

    A novel carboxylate/picolinate oxo-bridged iron(III) cluster, namely [Na2(H2O)8][Fe4(μ-O)2(O2CPh)7(pic)2]2·2H2O (1) where pic = picolinate, has been obtained by reacting "basic iron benzoate" [Fe3O(O2CPh)6(H2O)3](O2CPh) with sodium picolinate in acetonitrile. The compound has been characterized by elemental analysis and IR spectroscopy and its crystal structure has been determined by single-crystal X-ray diffraction.

  20. Self-reported short- and long-term respiratory effects among PVC-exposed firefighters

    SciTech Connect

    Markowitz, J.S. )

    1988-10-01

    Firefighters exposed to burning polyvinyl chloride (PVC) were studied to assess respiratory effects at 5-6 wk post-incident and again 22 mo following the fire. Exposed subjects reported significantly more frequent and severe respiratory symptoms at both time points than did firefighter controls. In longitudinal analyses, a number of symptoms persisted over time, and acute symptom scores were significantly correlated with chronic scores. At Time 2, approximately 18% of exposed firefighters, compared with none of the controls, reported that since the time of the PVC exposure, a physician had told them that they had either asthma and/or bronchitis.

  1. Kinetics of thermal de-chlorination of PVC under pyrolytic conditions

    SciTech Connect

    Castro, Alexandra; Soares, Delfim; Vilarinho, Candida; Castro, Fernando

    2012-05-15

    Highlights: Black-Right-Pointing-Pointer Several tests were performed in DTA/TGA for understanding the thermal behavior of pure PVC. Black-Right-Pointing-Pointer We did a kinetic model for the de-chlorination of PVC molecule. Black-Right-Pointing-Pointer A temperature of 340 Degree-Sign C was defined as the optimum temperature for breaking the bond of chlorine in the PVC molecule. Black-Right-Pointing-Pointer The experimental validation of this temperature, led to a removal rate of 99.9% chlorine. - Abstract: Although PVC-containing wastes are an important potential source of energy they are frequently disposed in landfill. In thermal treatment processes such as pyrolysis and gasification, the presence of poly(vinyl chloride) (PVC), a compound with 56.7% of chlorine, may cause problems concerned with environmental protection, as consequence of the formation of hydrochloric acid, chlorine gas and dioxins, as well as corrosion phenomena of the reactor/equipment materials. Thus, a possible solution may involve a previous removal of the chlorine from PVC containing waste through a pyrolysis process at low temperatures before the material being submitted to a subsequent thermal treatment, for energetic valorization. In this work, a kinetic model for the thermal decomposition of PVC has been developed, in view of its de-chlorination. DTA/TGA testing at different temperatures indicated a first order reaction and an activation energy of 133,800 J/mol. An almost completed de-chlorination reaction was obtained at 340 Degree-Sign C under an inert atmosphere. The resulted material is a C{sub n}H{sub n} type polymer with potential to be used in an energy recovery process. Validation test performed at laboratory scale indicate that the temperature of 340 Degree-Sign C enables the removal of {approx}99.9% of the chlorine present in PVC. The chloride can be fixed in the form of an aqueous solution of HCl or calcium chloride, driving to an alternative full process with

  2. Experimental investigations on PVC-LiAsF 6-DBP polymer electrolyte systems

    NASA Astrophysics Data System (ADS)

    Rajendran, S.; Uma, T.

    Poly(vinyl chloride) (PVC)-LiAsF 6 polymer electrolytes plasticized with dibutyl phthalate in different mole ratios have been studied by means of X-ray diffraction (XRD), infrared spectroscopy (IR) and a.c. impedance spectroscopy. The complexation has been confirmed from XRD and IR studies. A maximum room temperature conductivity (3.938×10 -5 S cm -1) has been observed for PVC: LiAsF 6: DBP (10:5:85 mol%) complex. The log σ vs. 1/ T plots ( σ=electrical conductivity; T=temperature) show Arrhenius behaviour. The activation energy is estimated and the results are discussed.

  3. Research on the property improvement of PVC using red mud in industrial waste residue

    NASA Astrophysics Data System (ADS)

    Nie, Xiaopeng; Li, Xingang; Shuai, Songxian

    2015-07-01

    Red mud is a red solid power waste that is discharged in the aluminium refinery industry during production. It is a strong alkali and can be categorized as polluting industrial residue. How to make comprehensive use of red mud has become a worldwide issue. In this paper, we put red mud into PVC (polyvinyl chloride polymer), taking advantage of the complicated chemical properties of red mud derived from the Bayer process. The results are compared with silica fume, coal ash and calcium carbonate under the same experimental conditions, which shows that improvement of PVC plastication can be achieved by adding red mud.

  4. Radon 222 permeation through different polymers (PVC, EVA, PE and PP) after exposure to gamma radiation or surface treatment by cold plasma

    NASA Astrophysics Data System (ADS)

    Klein, D.; Tomasella, E.; Labed, V.; Meunier, C.; Cetier, Ph.; Robé, M. C.; Chambaudet, A.

    1997-08-01

    In order to limit radon emission during the storage of radioactive wastes and to comply with the different regulations in the storage facility, the packaging used for these types of wastes should include intermediate enclosures, such as polymer membranes used as radon barriers. However, the membrane would be subjected to different types of radiation during long periods of storage, it would have to be regularly monitored for damage. The first aim of this study is to check the efficiency and the continuity of such polymer membranes subjected to different accelerated ageing processes by exposure to gamma radiation. PolyVinyl Chloride (PVC) and Ethylene Vinyl Acetate (EVA) membranes were studied after gamma exposures. Thus, we evaluated the effects of the gamma radiations on the radon permeation coefficient, and the degradation of these polymers due to this exposure. The second objective of this study is to evaluate the modifications of the polymer surface by cold plasma. PolyEthylene (PE) and PolyPropylene (PP) membranes were studied. Exposure of a polymer to a plasma creates reactive sites on the polymer's surface. Different modifications in the surface composition (chemical composition, molecular weight, etc.) can be obtained. The advantage of the plasma process is that it acts within seconds and does not produce any noticeable effects on the bulk properties. The obtained results show that this treatment increases the polymer's efficiency as a radon barrier.

  5. Determination of water uptake of polymeric ion-selective membranes with the coulometric Karl Fischer and FT-IR-attenuated total reflection techniques.

    PubMed

    He, Ning; Lindfors, Tom

    2013-01-15

    The water uptake of plasticized poly(vinyl chloride) (PVC) and silicone rubber (SR) based calcium-selective membranes which are commonly used in solid-contact and coated-wire ion-selective electrodes (SC-ISEs and CWEs) was quantified with the oven based coulometric Karl Fischer (KF) technique. Two different membrane types were studied: (1) the plasticized PVC or SR (RTV 3140) membrane matrix without other added membrane components and (2) the full Ca(2+)-selective membrane formulation consisting of the membrane matrixes, potassium tetrakis[3,5-bis(trifluoromethyl)phenyl]borate and calcium ionophore IV (ETH 5234) or calcium ionophore I (ETH 1001). The membranes were contacted for 24 h either asymmetrically from one side or symmetrically from both sides with deionized water (DIW) or 0.1 M solutions of CaCl(2), KCl, or NaCl. It was found that the water uptake was higher for symmetrically contacted membranes. The highest water uptake (0.15-0.17 wt %) was obtained for the plasticized PVC based Ca(2+)-selective membranes in DIW, whereas the water uptake was lower in 0.1 M electrolyte solutions. Symmetrically contacted Ca(2+)-selective SR membranes had much lower water uptake in 0.1 M CaCl(2) (0.03 wt %) than their plasticized PVC counterparts (0.1 wt %). However, the (noncontacted) SR membranes contained initially much more water (0.09-0.15 wt %) than the PVC membranes (0.04-0.07 wt %). Furthermore, in good accordance with the KF measurements, it was verified with FT-IR-attenuated total reflection (ATR) spectroscopy that the water content at the substrate/membrane interface and consequently in the whole membrane was influenced by the electrolyte solution. PMID:23249325

  6. Diazepam sorption to PVC- and non-PVC-based tubes in administration sets with quantitative determination using a high-performance liquid chromatographic method.

    PubMed

    Jin, Su-Eon; You, Siwon; Jeon, Seungho; Hwang, Sung-Joo

    2016-06-15

    Diazepam is highly sorbed to the plastic materials of administration sets for intravenous infusion. This can be detrimental as it should be delivered to the patient at the administered amount for efficacy and safety. We report here the sorption levels of diazepam onto various types of tubes in administration sets. The tube materials of the administration sets included polyvinylchloride (PVC) and the non-PVC materials such as polyurethane (PU) and polyolefin (PO) were used. Two conditions of diazepam administered in preclinical and clinical settings were tested using an infusion pump. Injections were prepared by diluting diazepam to 20mg/500mL and 10mg/100mL in 5% dextrose. Diluted diazepam solutions at the concentrations of 10mg/100mL and 20mg/500mL were separately delivered through 1m of tubing at 1mL/min for 1.05 and 4.05h. Samples were analyzed using a high-performance liquid chromatography with UV detection. PVC- and PU-based tubes showed higher sorption of diazepam than did PO-based tubes. PO-based tubes delivered more than 90% of the administered diazepam. The results showed that PO-based tubes of administration sets have a promising potential to deliver hydrophobic drugs like diazepam with minimal sorption levels. In addition, the tube materials in administration sets may be one of the critical factors to ensure drug efficacy and safety. PMID:27091292

  7. Construction and evaluation of PVC conventional and tubular tripelennamine-selective electrodes: their application in pharmaceutical preparations.

    PubMed

    Lima, J L; Montenegro, M C; Sales, M G

    1996-06-01

    The construction and evaluation of tripelennamine conventionally-shaped ion-selective electrodes and tubular detectors for the determination of this compound in pharmaceutical formulations are described. Electrodes with conventional configuration have been constructed without an internal reference solution, using several types of immobilized ionic sensors in PVC. The different electrode membranes were prepared by using tripelennamine tetraphenylborate as ionic-exchanger, dissolved in 2-nitrophenyl octyl ether (type A), dibutylphthalate (type B) and bis-(2-ethylhexyl)sebacate (type C) as plasticizer solvents. The general working characteristics of the different types of conventional electrodes were evaluated in tripelennamine solutions, with adjusted ionic strength, showing a linear response in the concentration range of about 4 x 10(-5) - 1 x 10(-1) M and a slope near the theoretical value. The electrodes presented a fast response (> 20 s) and a high reproducibility (> or = 0.2 mV per day). The electrode selectivity in the presence of some interferents, such as sodium, potassium, lithium, ammonium, chlorpheniramine, diphenydramine, promethazine, meclizine and pentazocine, was good, particularly for those whose sensor membrane was prepared with tripelennamine tetraphenylborate dissolved in 2-nitrophenyl octyl ether (type A). Tubular detectors were also prepared using the same sensor membrane and were evaluated in a low-dispersion flow-injection manifold. Under these conditions the detectors presented response characteristics similar to those of the corresponding conventionally-shaped electrodes. The analysis of different pharmaceutical forms (creams, syrups and gels) gave good results with mean recoveries of 99.8-100.6% when the experiments were conducted by direct potentiometry and 99.9-100.4% where the same determinations were conducted by flow-injection analysis with tubular detectors. PMID:8817997

  8. Effect of oxygen plasma treatment on surface charge and wettability of PVC blood bag—In vitro assay

    NASA Astrophysics Data System (ADS)

    Khorasani, M. T.; Mirzadeh, H.

    2007-06-01

    Wettability and zeta potential studies were performed to characterize the hydrophobicity and surface charge of PVC blood bag samples and evaluate the effect of these properties on fibroblast cells growth. The surface properties of PVC and plasma treated PVC were compared by water drop contact angle and zeta potential measurement. Light microscopy was used to study the behavior of cell attachment and growth on these surfaces. Water drop contact angle measurement shows that the plasma treated PVC becomes more hydrophilic and wettability increased. Zeta potential and in vitro cell culture measurements noticed that the plasma treated PVC surface is more negatively charge and consequently attachment of the L929 fibroblast cells decreased on this surface.

  9. Polypyrrole–titanium(IV) doped iron(III) oxide nanocomposites: Synthesis, characterization with tunable electrical and electrochemical properties

    SciTech Connect

    Nandi, Debabrata; Ghosh, Arup Kumar; Gupta, Kaushik; De, Amitabha

    2012-08-15

    Highlights: ► Synthesis and characterization of polymer nanocomposite based on titanium doped iron(III) oxide. ► Electrical conductivity increased 100 times in composite with respect to polymer. ► Electrochemical capacitance of polymer composites increased with nanooxide content. ► Thermal stability of the polymer enhanced with nano oxide content. -- Abstract: Titanium(IV)-doped synthetic nanostructured iron(III) oxide (NITO) and polypyrrole (PPy) nanocomposites was fabricated by in situ polymerization using FeCl{sub 3} as initiator. The polymer nanocomposites (PNCs) and pure NITO were characterized by X-ray diffraction, Föurier transform infrared spectroscopy, scanning electron microscopy, electron dispersive X-ray spectroscopy, transmission electron microscopy, etc. Thermo gravimetric and differential thermal analyses showed the enhancement of thermal stability of PNCs than the pure polymer. Electrical conductivity of the PNCs had increased significantly from 0.793 × 10{sup −2} S/cm to 0.450 S/cm with respect to the PPy, and that had been explained by 3-dimensional variable range hopping (VRH) conduction mechanisms. In addition, the specific capacitance of PNCs had increased from 147 F/g to 176 F/g with increasing NITO content than that of pure NITO (26 F/g), presumably due to the growing of mesoporous structure with increasing NITO content in PNCs which reduced the charge transfer resistance significantly.

  10. Paerucumarin, a new metabolite produced by the pvc gene cluster from Pseudomonas aeruginosa.

    PubMed

    Clarke-Pearson, Michael F; Brady, Sean F

    2008-10-01

    The pvc gene cluster from Pseudomonas aeruginosa has been linked to the biosynthesis of both the pyoverdine chromophore and pseudoverdine. Our reinvestigation of the role this gene cluster plays in P. aeruginosa secondary metabolite biosynthesis shows that its major product is actually paerucumarin, a novel isonitrile functionalized cumarin. PMID:18689486

  11. Paerucumarin, a New Metabolite Produced by the pvc Gene Cluster from Pseudomonas aeruginosa▿ †

    PubMed Central

    Clarke-Pearson, Michael F.; Brady, Sean F.

    2008-01-01

    The pvc gene cluster from Pseudomonas aeruginosa has been linked to the biosynthesis of both the pyoverdine chromophore and pseudoverdine. Our reinvestigation of the role this gene cluster plays in P. aeruginosa secondary metabolite biosynthesis shows that its major product is actually paerucumarin, a novel isonitrile functionalized cumarin. PMID:18689486

  12. Selective separation of virgin and post-consumer polymers (PET and PVC) by flotation method.

    PubMed

    Burat, Firat; Güney, Ali; Olgaç Kangal, M

    2009-06-01

    More and more polymer wastes are generated by industry and householders today. Recycling is an important process to reduce the amount of waste resulting from human activities. Currently, recycling technologies use relatively homogeneous polymers because hand-sorting waste is costly. Many promising technologies are being investigated for separating mixed thermoplastics, but they are still uneconomical and unreliable. At present, most waste polymers cause serious environmental problems. Burning polymers for recycling is not practiced since poisonous gases are released during the burning process. Particularly, polyvinyl chloride (PVC) materials among waste polymers generate hazardous HCl gas, dioxins containing Cl, etc., which lead to air pollution and shorten the life of the incinerator. In addition, they make other polymers difficult to recycle. Both polyethylene terephthalate (PET) and PVC have densities of 1.30-1.35g /cm(3) and cannot be separated using conventional gravity separation techniques. For this reason, polymer recycling needs new techniques. Among these techniques, froth flotation, which is also used in mineral processing, can be useful because of its low cost and simplicity. The main objective of this research is to recycle PET and PVC selectively from post-consumer polymer wastes and virgin polymers by using froth flotation. According to the results, all PVC particles were floated with 98.8% efficiency in virgin polymer separation while PET particles were obtained with 99.7% purity and 57.0% efficiency in post-consumer polymer separation. PMID:19155169

  13. Leaching of lead from new unplasticized polyvinyl chloride (uPVC) pipes into drinking water.

    PubMed

    Zhang, Yuanyuan; Lin, Yi-Pin

    2015-06-01

    Unplasticized polyvinyl chloride (uPVC) pipes have been used in the premise plumbing system due to their high strength, long-term durability, and low cost. uPVC pipes, however, may contain lead due to the use of lead compounds as the stabilizer during the manufacturing process. The release of lead from three locally purchased uPVC pipes was investigated in this study. The effects of various water quality parameters including pH value, temperature, and type of disinfectant on the rate of lead release were examined. The elemental mapping obtained using scanning electron microscopy-energy dispersive X-ray spectroscopy (SEM-EDX) confirmed the presence of lead on the inner surfaces of the uPVC pipes and their surface lead weight percentages were determined. The leachable lead concentration for each pipe was determined using high strength acidic EDTA solutions (pH 4, EDTA = 100 mg/L). Lead leaching experiments using tap water and reconstituted tape water under static conditions showed that the rate of lead release increased with the decreasing pH value and increasing temperature. In the presence of monochloramine, lead release was faster than that in the presence of free chlorine. PMID:25539706

  14. CORRELATION OF THE GLASS TRANSITION TEMPERATURE OF PLASTICIZED PVC USING A LATTICE FLUID MODEL

    EPA Science Inventory

    A model has been developed to describe the composition dependence of the glass transition temperature (Tg) of polyvinyl chloride (PVC) + plasticizer mixtures. The model is based on Sanchez-Lacombe equation of state and the Gibbs-Di Marzio criterion, which states that th...

  15. Selective separation of virgin and post-consumer polymers (PET and PVC) by flotation method

    SciTech Connect

    Burat, Firat; Gueney, Ali; Olgac Kangal, M.

    2009-06-15

    More and more polymer wastes are generated by industry and householders today. Recycling is an important process to reduce the amount of waste resulting from human activities. Currently, recycling technologies use relatively homogeneous polymers because hand-sorting waste is costly. Many promising technologies are being investigated for separating mixed thermoplastics, but they are still uneconomical and unreliable. At present, most waste polymers cause serious environmental problems. Burning polymers for recycling is not practiced since poisonous gases are released during the burning process. Particularly, polyvinyl chloride (PVC) materials among waste polymers generate hazardous HCl gas, dioxins containing Cl, etc., which lead to air pollution and shorten the life of the incinerator. In addition, they make other polymers difficult to recycle. Both polyethylene terephthalate (PET) and PVC have densities of 1.30-1.35 g/cm{sup 3} and cannot be separated using conventional gravity separation techniques. For this reason, polymer recycling needs new techniques. Among these techniques, froth flotation, which is also used in mineral processing, can be useful because of its low cost and simplicity. The main objective of this research is to recycle PET and PVC selectively from post-consumer polymer wastes and virgin polymers by using froth flotation. According to the results, all PVC particles were floated with 98.8% efficiency in virgin polymer separation while PET particles were obtained with 99.7% purity and 57.0% efficiency in post-consumer polymer separation.

  16. Influence of Water Content on the Flow Behaviour of PVC-Plastisols

    NASA Astrophysics Data System (ADS)

    Hochstein, B.; Willenbacher, N.

    2008-07-01

    PVC-Plastisols are used as stone-chipping and corrosion protection. To process plastisols, they have to show special rheological properties. The influence of water content on viscosity and yield stress of PVC-Plastisols was analyzed by using a simplified but relevant formulation with several PVC-particles. When only 0.5-1% of water was added, the viscosity increased by a factor of round about ten and the yield stress increased by a factor of round about one hundred. On the one hand, this shows us, how carefully we have to work during the establishing of the plastisols and the conditioning of the particular ingredients. On the other hand, it allows us to control the rheological properties by the use of water. Neither the particle size distribution nor the structure of the agglomerates is the primary reason for the extreme influence of water content on the rheological properties of plastisols. We assume an adsorption of water on the contact area between adjacent PVC particles and thus an increase of the contact forces between the particles.

  17. Irreversible deformation processes in PVC and its short glass fiber reinforced composites

    SciTech Connect

    Yuan, J.Y.

    1985-01-01

    The tensile mechanical behavior of PVC and its short glass fiber reinforced composites under superimposed hydrostatic pressure was studied up to 3 x 10/sup 8/ Pa. For rigid PVC, the brittle-to-ductile transition was observed at a pressure between 1 x 10/sup 7/ Pa and 2 x 10/sup 7/ Pa. This pressure-induced brittle-to-ductile transition was controlled by the competitive microdeformation processes of crazing and shear banding. Deformation in the post-yield region occurred by neck formation and subsequent drawing to produce chain orientation. A strong environmental stress-cracking effect was observed when PVC samples were exposed to the pressure-transmitting fluid, silicone oil. Three types of pressure dependent deformation processes was observed for the short glass fiber reinforced composites of PVC. Type I behavior shows debonding at the interface between fiber and matrix followed by brittle fracture of the matrix. Type II behavior, which was observed for the first time, exhibits a sharp stress drop due to debonding at the interface followed by matrix shear yielding. In Type III behavior, only upper shear yielding of matrix was observed. The transitional behavior from Type I and Type II was controlled by the pressure induced brittle to ductile transition of the matrix, while the Type II-III transition was strongly affected by debonding at the interface.

  18. Synthesis of AzPhchitosan-bifenthrin-PVC to protect cables against termites.

    PubMed

    Zhang, Lingkun; Cai, Weiwei; Chen, Wu-Ya; Zhang, Li; Hu, Kaikai; Guan, Yan-Qing

    2016-03-30

    The destruction of PVC cables by termites is a continuing and long-standing problem, which can lead to power leakage and power cut. Given the environmental demerits of insecticide overuse, alternative methods of addressing this problem are a highly desirable goal. In this study, we used photo-immobilization to develop a chitosan carrier system to help bifenthrin immobilize on the surface of the PVC substrate. The immobilization was analyzed using nuclear magnetic resonance (NMR), UV absorption, reverse-phase high-performance liquid chromatography (RP-HPLC), Raman absorption spectroscopy, and thermal gravimetric analysis (TGA). The surface structure and biological activity of the embedded and immobilized bifenthrin were examined using scanning electron microscopy (SEM), atomic force microscopy (AFM), and X-ray photon-electron spectroscopy (XPS). Its efficacy was assessed in pest experiments. The results indicate a successful embedding and immobilization of bifenthrin. Furthermore, the chemical bonding network between AzPhchitosan, bifenthrin, and PVC is stable, guaranteeing no environmental release of bifenthrin, and also providing more efficacious protection against termites. The evidence suggests that this photo-immobilization of bifenthrin-embedded chitosan on the surface of PVC substrates is a novel and environmentally friendly technique for termite control. This paper also reports a modification of chitosan with respect to its novel application in environmental protection. PMID:26794946

  19. Electrical Detection of Nucleic Acid Amplification Using an On-Chip Quasi-Reference Electrode and a PVC REFET

    PubMed Central

    2015-01-01

    Electrical detection of nucleic acid amplification through pH changes associated with nucleotide addition enables miniaturization, greater portability of testing apparatus, and reduced costs. However, current ion-sensitive field effect transistor methods for sensing nucleic acid amplification rely on establishing the fluid gate potential with a bulky, difficult to microfabricate reference electrode that limits the potential for massively parallel reaction detection. Here we demonstrate a novel method of utilizing a microfabricated solid-state quasi-reference electrode (QRE) paired with a pH-insensitive reference field effect transistor (REFET) for detection of real-time pH changes. The end result is a 0.18 μm, silicon-on-insulator, foundry-fabricated sensor that utilizes a platinum QRE to establish a pH-sensitive fluid gate potential and a PVC membrane REFET to enable pH detection of loop mediated isothermal amplification (LAMP). This technique is highly amendable to commercial scale-up, reduces the packaging and fabrication requirements for ISFET pH detection, and enables massively parallel droplet interrogation for applications, such as monitoring reaction progression in digital PCR. PMID:24940939

  20. The Effect of Temperature and Ionic Strength on the Oxidation of Iodide by Iron(III): A Clock Reaction Kinetic Study

    ERIC Educational Resources Information Center

    Bauer, Jurica; Tomisic, Vladislav; Vrkljan, Petar B. A.

    2012-01-01

    A laboratory exercise has recently been reported in which the students use the initial rates method based on the clock reaction approach to deduce the rate law and propose a reaction mechanism for the oxidation of iodide by iron(III) ions. The same approach is used in the exercise proposed herein; the students determine the dependence of the…

  1. Charge transfer of iron(III) monomeric and oligomeric aqua hydroxo complexes: semiempirical investigation into photoactivity.

    PubMed

    Lopes, Ludovic; de Laat, Joseph; Legube, Bernard

    2002-05-01

    Aqueous hydrolyses of iron(III) solutions were studied using electronic spectroscopy. Complete spectra from 200 to 800 nm were obtained for the four ferric aqua hydroxo complexes: Fe(H(2)O)(6)(3+), Fe(OH)(H(2)O)(5)(2+), Fe(OH)(2)(H(2)O)(4)(+), and the dimer Fe(2)(mu-Omicron Eta)(2)(H(2)O)(8)(4+). Semiempirical Zindo/s calculations were employed to assign which types of electronic transfers are involved so that the photoactivity as regards the photoreduction dissociation Fe(III)(aq) Fe(II)(aq) + OH* can be discussed. Fe(3+) exhibits two LMCT from non-bonding p orbitals (nLp) located at 190 and 240 nm. Fe(OH)(2+) shows two major nLp(OH) --> d transitions at 205 and 295 nm. As regards its geometry, computed investigations using an Fe-OH distance of 2.05 A better fit than using a shorter distance ( approximately 1.8 A); the same conclusion remains constant for all hydroxo complexes. The dihydroxo form's spectrum was confronted to its common cis and trans expectable isomers plus an unusual pentacoordinate one. Even if the trans isomer is supposed to be the lowest Gibbs free energy species in solution, there is some evidence of the presence of the cis form; hence, both species must be close in energy. Other isolated nLp(OH) --> d transfer wavelengths are 235, 245, and 335 nm. As for the dimer, this study provides some clue in favor of the bis(mu-hydroxo)) description. Both water and hydroxo ligands are involved along the electronic transitions toward only d(1) metal-centered orbitals at 220 and 260 nm for H(2)O, 335 and 470 nm for OH(-), and 205 nm for both. Charge transfers for the hydrogen oxide bridge form Fe(2)(mu-Eta(3)Omicron(2))(H(2)O)(8)(5+) were also computed. Finally predictions about the two bis(mu-hydroxo) bridge trimer Fe(3)(OH)(4)(H(2)O)(10)(5+) enable one to foresee a huge and broad charge transfer in the UV region (approximately 240 nm) followed by a multi nLp(OH) --> d(1) transfer extending up to approximately 650 nm. PMID:11978119

  2. A Stopped-Flow Kinetics Experiment for Advanced Undergraduate Laboratories: Formation of Iron(III) Thiocyannate

    NASA Astrophysics Data System (ADS)

    Clark, Charles R.

    1997-10-01

    A series of 15 stopped-flow kinetic experiments relating to the formation of iron(III)- thiocyanate at 25.0 °C and I = 1.0 M (NaClO4) is described. A methodology is given whereby solution preparation and data collection are able to be carried out within the time scale of a single laboratory period (3-4 h). Kinetic data are obtained using constant [SCN-], and at three H+ concentrations (0.10, 0.20, 0.30 M) for varying concentrations of Fe3+ (ca. 0.0025 - 0.020 M). Rate data (450 nm) are consistent with rate laws for the forward and reverse reactions: kf = (k1 + k2Ka1/[H+])[Fe3+] and kr = k-1 + k-2Ka2/[H+] respectively, with k1,k-1 corresponding to the rate constants for formation and decay of FeSCN2+, k2, k-2 to the rate constants for formation and decay of the FeSCN(OH)+ ion and Ka1,Ka2 to the acid dissociation constants (coordinated OH2 ionization) of Fe3+ and FeSCN2+. Using literature values for the latter two quantities ( Ka1 = 2.04 x 10-3 M, Ka2 = 6.5 x 10-5 M) allows values for the four rate constants to be obtained. A typical data set is analyzed to give k1 = 109(10) M-1s-1, k-1 = 0.79(0.10) s-1, k2= 8020(800) M-1s-1, k-2 = 2630(230) s-1. Absorbance change data for reaction (DeltaA) follow the expression: DeltaA = Alim.Kf.[Fe3+]/(1 + Kf.[Fe3+]), with Alim corresponding to the absorbance of fully formed FeSCN2+ (i.e. free SCN- absent) and Kf to the formation constant of this complex (value in the example 112(5) M-1, c.f. 138(29) M-1 from the kinetic data).

  3. Mercury transformation and distribution across a polyvinyl chloride (PVC) production line in China.

    PubMed

    Ren, Wen; Duan, Lei; Zhu, Zhenwu; Du, Wen; An, Zhongyi; Xu, Lingjun; Zhang, Chi; Zhuo, Yuqun; Chen, Changhe

    2014-02-18

    The production of polyvinyl chloride (PVC) via the calcium carbide process utilizes a catalyst containing large amounts of mercury (Hg) and is therefore one of the most important sources of anthropogenic Hg in China. To measure the emission of Hg from PVC production, we established a flowchart for the calcium carbide process, for which we quantified the Hg content of the material/product at each step. Results indicated that 71.5% of the total Hg (Hg(T)) was lost from the catalyst, most of which was recovered by the Hg remover, accounting for 46.0% of the total Hg (Hg(T)). We determined that 3.7% of the Hg(T) was released into the environment, mostly in solid wastes and byproducts such as hydrochloric acid. Furthermore, no Hg has been detected in the PVC end product. However, we were only able to account for 78.1% of the Hg across the whole system, leaving 21.7% unaccounted for in the mass balance. A rough estimation indicates that most of the "missing" Hg had accumulated in deposits on the inner surface of converters and downstream pipelines; however, the emission to the atmosphere was ≤ 1% of the Hg(T). For a PVC production line equipped with a Hg remover, emissions of Hg to the atmosphere have been estimated to be 4.9 g per tonne PVC. Currently, almost all calcium carbide facilities have been equipped with a Hg remover, which may reduce the release of Hg in China by ∼ 500 t/year. PMID:24428761

  4. Structural and spectral studies of an iron(III) complex [Fe(Pranthas) 2][FeCl 4] derived from 2-acetylpyridine- N(4), N(4)-(butane-1, 4-diyl) thiosemicarbazone (HPranthas)

    NASA Astrophysics Data System (ADS)

    Sreekanth, A.; Fun, Hoong-Kun; Prathapachandra Kurup, M. R.

    2005-02-01

    A novel iron(III) complex of 2-acetylpyridine N(4), N(4)-(butyl-1, 4-diyl) thiosemicarbazone (HPranthas), [Fe(Pranthas) 2]FeCl 4 was synthesized and physico-chemically characterized by means of partial elemental analysis, magnetic measurements (polycrystalline state), UV-Vis and IR spectroscopies. The presence of spin-paired iron(III) cation with dxz2dyz2dxy1 ground state is revealed by the EPR and Mössbauer spectral data. Structure of the free ligand HPranthas and the complex [Fe(Pranthas) 2]FeCl 4 were solved by single crystal X-ray diffraction. The framework of iron(III) complex consists of a discrete monomeric cationic entity containing low spin iron(III) in a slightly distorted octahedral environment. The metal ion is bonded to one sulfur and two nitrogens of each thiosemicarbazone molecule. The tetrachloroferrate(III) ion acts as counterion.

  5. Determination of thermooptical and transport parameters of ε iron(III) oxide-based nanocomposites by beam deflection spectroscopy

    NASA Astrophysics Data System (ADS)

    Korte, Dorota; Carraro, Giorgio; Maccato, Chiara; Franko, Mladen

    2015-04-01

    In this work, photothermal beam deflection (PBD) experiments have been used to characterize the thermooptical and transport properties of ε-Fe2O3-based nanocomposites. In particular, iron(III) nanostructures have been functionalized with Au, Ag and Cu nanoparticles, tailoring both their nano-organization and their chemical state. In order to elucidate the correlation between the thermooptical and transport parameters, the structural, compositional and morphological properties of Fe2O3-based systems were studied by field emission scanning electron microscopy (FE-SEM), X-ray photoelectron spectroscopy (XPS) and X-ray diffraction (XRD). It was observed that the optothermal and transport parameters were influenced by the nature and oxidation state of the nanoparticles, which can serve as a key tool to master the material properties for their application in light-assisted processes.

  6. Structural and transport properties of PVC blend PEG doped with Mg(ClO4)2 solid polymer electrolyte

    NASA Astrophysics Data System (ADS)

    Ramesh, C. H.; Reddy, M. Jaipal; Kumar, J. Siva; Reddy, K. Narasimha

    2014-04-01

    An attempt was made to investigate the effect of Mg(ClO4)2 concentration in PVC-PEG blend polymer electrolyte system. Solid polymer electrolyte films of PVC-PEG-Mg(ClO4)2 have been prepared by using solution - casting process. Structural and transport properties have been studied by employing experimental tools like XRD, FT-IR and DC electrical conductivity. The XRD, FTIR studies were confirmed the formation of a polymer-salt complex. The conductivity results indicated that the incorporation of Mg(ClO4)2 salt into PVC-PEG polymer; at low concentrations the increase in the conductivity is large, but at higher concentrations the increase in conductivity is modest. Using this electrolyte, an electrochemical cells have been fabricated with the configuration Mg/ (PVC-PEG-Mg(ClO4)2) electrolyte / (I2 + C + electrolyte) and its discharge characteristics were determined.

  7. Simultaneous measurement of the orthogonal components of thermal diffusivity in PVC sheet

    SciTech Connect

    Doss, D.J.; Wright, N.T.

    2000-02-01

    An extension of the flash method is described that measures simultaneously the three orthogonal components of thermal diffusivity in specimens of moderate thermal diffusivity. Only part of the top face of the specimen is illuminated and the temperature histories are recorded at three points on the bottom face. A Marquardt parameter estimation algorithm coupled with a finite difference model of the diffusion equation analyzes these temperature histories to determine the components of thermal diffusivity. Illustrative measurements in stainless steel, glass, and PVC demonstrate that accurate three-dimensional thermal diffusivity measurements can be made in this way. The in-plane components of thermal diffusivity of as-supplied PVC sheet are shown to be about 20% greater than the out-of-plane component. This anisotropy appears to be due to the manufacturing process and exemplifies the need for such measurements.

  8. Speed of Sound Versus Temperature Using PVC Pipes Open at Both Ends

    NASA Astrophysics Data System (ADS)

    Bacon, Michael E.

    2012-09-01

    In this paper we investigate the speed of sound in air as a function of temperature using a simple and inexpensive apparatus. For this experiment it is essential that the appropriate end corrections be taken into account. In a recent paper the end corrections for 2-in i.d. (5.04-cm) PVC pipes open at both ends were investigated. The air column resonance was excited using a paddle as in Blue Man Group® pipes.2 The "open end" end correction is given by 0.6133r in accordance with recent experiments3 and detailed theoretical calculations.4 This correction amounted to 1.56 cm for the 2-in PVC pipe used. However, the paddle end correction was found to be influenced by the transient position of the paddle during the excitation process. The paddle end correction was found to be 1.94 cm.

  9. Fate of plasticised PVC products under landfill conditions: a laboratory-scale landfill simulation reactor study.

    PubMed

    Mersiowsky, I; Weller, M; Ejlertsson, J

    2001-09-01

    The long-term behaviour of plasticised PVC products was investigated in laboratory-scale landfill simulation reactors. The examined products included a cable material and a flooring with different combinations of plasticisers. The objective of the study was to assess whether a degradation of the PVC polymer or a loss of plasticisers occurred under landfill conditions. A degradation of the polymer matrix was not observed. The contents of plasticisers in aged samples was determined and compared to the respective original products. The behaviour of the various plasticisers was found to differ significantly. Losses of DEHP and BBP from the flooring were too low for analytical quantification. No loss of DIDP from the cable was detectable, whereas DINA in the same product showed considerable losses of up to 70% compared to the original contents. These deficits were attributable to biodegradation rather than leaching. There was no equivalent release of plasticisers into the leachate. PMID:11487101

  10. Experimental Studies on (PVC+LiCIO4+DMP) Polymer Electrolyte Systems for Lithium Battery

    NASA Astrophysics Data System (ADS)

    Subba Reddy, Ch. V.; Qi, Y. Y.; Zhu, Q. Y.; Liu, H. X.; Zhao, X. J.; Chen, W.

    2006-06-01

    Poly (vinyl chloride)(PVC)-based solid polymer electrolyte films with LiClO4+plasticizer (dimethyl phthalate) have been prepared by the solution -cast technique. Various experimental techniques have been used, such as X-ray diffraction (XRD) and infrared spectroscopy (IR), a.c. impedance spectroscopy and transport number measurements, to characterize these polymer electrolyte films. The complexation has been confirmed from XRD and IR studies. A maximum room temperature conductivity (1.1 × 10-4S/cm) has been observed for (PVC+LiClO4+DMP)(20:5:75) complex. The temperature dependent conductivity plots show Arrhenius behaviour. The activation energy is estimated and the results are discussed. The transference number data indicated that the conducting species in these electrolytes are the anions. Using this electrolyte, electrochemical cells are fabricated and their discharge profiles are studied under constant load.

  11. EFFECT OF THE CLAY MODIFICATION ON THE THERMAL PROPERTIES OF PVC

    SciTech Connect

    Zykova, J.; Kalendova, A.; Kovarova, L.; Malac, J.

    2010-06-02

    The intercalation of organic compound is necessary to functionalize the montmorillonite surface. So, the intercalation of diethylene glycol and polyethylene glycol and the influence of plasticizer, namely tricresyl phosphate and isodecyldiphenyl phosphate as co-intercalating agents were studied. For the PVC/clay nanocomposites the suspension type of PVC was used and the compound was prepared by the melt intercalation method. Two kinds of MMT (Cloisite registered Na{sup +}, Cloisite registered 30B) and laboratory modified MMT by intercalation (diethylene glycol, polyethylene glycol) and co-intercalation (tricresyl phosphate and isodecildifenyl phosphate) agents were used for the set of nanocomposite samples. The thermal stability of nanocomposite specimens was tested using of thermo gravimetric analysis, DMA and pH method.

  12. The pvc operon regulates the expression of the Pseudomonas aeruginosa fimbrial chaperone/usher pathway (cup) genes.

    PubMed

    Qaisar, Uzma; Luo, Liming; Haley, Cecily L; Brady, Sean F; Carty, Nancy L; Colmer-Hamood, Jane A; Hamood, Abdul N

    2013-01-01

    The Pseudomonas aeruginosa fimbrial structures encoded by the cup gene clusters (cupB and cupC) contribute to its attachment to abiotic surfaces and biofilm formation. The P. aeruginosa pvcABCD gene cluster encodes enzymes that synthesize a novel isonitrile functionalized cumarin, paerucumarin. Paerucumarin has already been characterized chemically, but this is the first report elucidating its role in bacterial biology. We examined the relationship between the pvc operon and the cup gene clusters in the P. aeruginosa strain MPAO1. Mutations within the pvc genes compromised biofilm development and significantly reduced the expression of cupB1-6 and cupC1-3, as well as different genes of the cupB/cupC two-component regulatory systems, roc1/roc2. Adjacent to pvc is the transcriptional regulator ptxR. A ptxR mutation in MPAO1 significantly reduced the expression of the pvc genes, the cupB/cupC genes, and the roc1/roc2 genes. Overexpression of the intact chromosomally-encoded pvc operon by a ptxR plasmid significantly enhanced cupB2, cupC2, rocS1, and rocS2 expression and biofilm development. Exogenously added paerucumarin significantly increased the expression of cupB2, cupC2, rocS1 and rocS2 in the pvcA mutant. Our results suggest that pvc influences P. aeruginosa biofilm development through the cup gene clusters in a pathway that involves paerucumarin, PtxR, and different cup regulators. PMID:23646138

  13. The pvc Operon Regulates the Expression of the Pseudomonas aeruginosa Fimbrial Chaperone/Usher Pathway (Cup) Genes

    PubMed Central

    Qaisar, Uzma; Luo, Liming; Haley, Cecily L.; Brady, Sean F.; Carty, Nancy L.; Colmer-Hamood, Jane A.; Hamood, Abdul N.

    2013-01-01

    The Pseudomonas aeruginosa fimbrial structures encoded by the cup gene clusters (cupB and cupC) contribute to its attachment to abiotic surfaces and biofilm formation. The P. aeruginosa pvcABCD gene cluster encodes enzymes that synthesize a novel isonitrile functionalized cumarin, paerucumarin. Paerucumarin has already been characterized chemically, but this is the first report elucidating its role in bacterial biology. We examined the relationship between the pvc operon and the cup gene clusters in the P. aeruginosa strain MPAO1. Mutations within the pvc genes compromised biofilm development and significantly reduced the expression of cupB1-6 and cupC1-3, as well as different genes of the cupB/cupC two-component regulatory systems, roc1/roc2. Adjacent to pvc is the transcriptional regulator ptxR. A ptxR mutation in MPAO1 significantly reduced the expression of the pvc genes, the cupB/cupC genes, and the roc1/roc2 genes. Overexpression of the intact chromosomally-encoded pvc operon by a ptxR plasmid significantly enhanced cupB2, cupC2, rocS1, and rocS2 expression and biofilm development. Exogenously added paerucumarin significantly increased the expression of cupB2, cupC2, rocS1 and rocS2 in the pvcA mutant. Our results suggest that pvc influences P. aeruginosa biofilm development through the cup gene clusters in a pathway that involves paerucumarin, PtxR, and different cup regulators. PMID:23646138

  14. Beam Damage of Poly(Vinyl Chloride) [PVC] Film as Observed by X-ray Photoelectron Spectroscopy

    SciTech Connect

    Engelhard, Mark H.; Krishna, Abhilash; Kulkarni, Pranita B.; Lee, Chi-Ying M.; Baer, Donald R.

    2003-03-08

    XPS spectra of a spin-coated film poly(vinyl chloride) (PVC) were collected over a period of 243 minutes at 303 K to determine specimen damage during long exposures to monochromatic Al Ka x-rays. For this PVC film we measured the loss of chlorine as a function of time by rastering a focused 104.6 w 100 um diameter x-ray beam over a 1.4 mm x 0.2 mm area on the sample.

  15. Speed of Sound versus Temperature Using PVC Pipes Open at Both Ends

    ERIC Educational Resources Information Center

    Bacon, Michael E.

    2012-01-01

    In this paper we investigate the speed of sound in air as a function of temperature using a simple and inexpensive apparatus. For this experiment it is essential that the appropriate end corrections be taken into account. In a recent paper the end corrections for 2-in i.d. (5.04-cm) PVC pipes open at both ends were investigated. The air column…

  16. Application of electrostatic separation to the recycling of plastic wastes: separation of PVC, PET, and ABS.

    PubMed

    Park, Chul-Hyun; Jeon, Ho-Seok; Yu, Hyo-Shin; Han, Oh-Hyung; Park, Jai-Koo

    2008-01-01

    Plastics are widely used in everyday life as a useful material, and thus their consumption is growing at a rate of about 5% per year in Korea. However, the constant generation of plastic wastes and their disposal generates environmental problems along with economic loss. In particular, mixed waste plastics are difficult to recycle because of their inferior characteristics. A laboratory-scale triboelectrostatic separator unit has been designed and assembled for this study. On the basis of the control of electrostatic charge, the separation of three kinds of mixed plastics, polyvinyl chloride (PVC), poly(ethylene terephthalate) (PET), and acrylonitrile-butadiene-styrene (ABS), in a range of similar gravities has been performed through a two-stage separation process. Polypropylene (PP) and high-impact polystyrene (HIPS) were found to be the most effective materials for a tribo-charger in the separation of PVC, PET, and ABS. The charge-to-mass ratio (nC/g) of plastics increased with increasing air velocity in the tribo charger. In the first stage, using the PP cyclone charger, the separation efficiency of particles considerably depended on the air velocity (10 m/s), the relative humidity (< 30%), the electrode potential (> 20 kV), and the splitter position (+2 cm from the center) in the triboelelctrostatic separator unit. At this time, a PVC grade of 99.40% and a recovery of 98.10% have successfully been achieved. In the second stage, using the HIPS cyclone charger, a PET grade of 97.80% and a recovery of 95.12% could be obtained under conditions of 10 m/s, over 25 kV, a central splitter position, and less than 40% relative humidity. In order to obtain 99.9% PVC grade and 99.3% PET grade, their recoveries should be sacrificed by 20.9% and 27%, respectively, with moving the splitter from the center to a (+)6 cm position. PMID:18350904

  17. Corrosion failure of duplex stainless steel equipment in a PVC plant

    SciTech Connect

    Davies, M.; Potgieter, G.

    2000-05-01

    After <9 months of operation in a polyvinyl chloride (PVC) manufacturing plant, alloy 2205 duplex stainless steel (UNS 31803) columns and spiral heat exchangers (HXs) were corroding and cracking. The columns were repaired and remained in service but the HXs needed to be replaced. Candidate materials for the HXs were assessed, and it was found that the super-austenitic alloys containing 6% molybdenum would be more appropriate for this application.

  18. Flame treatment for the selective wetting and separation of PVC and PET

    SciTech Connect

    Pascoe, R.D.; O'Connell, B

    2003-07-01

    Flame treatment has been used for many years to modify the surface of plastics to allow coatings to be added. The effect of the treatment is to produce hydrophilic species on the surface of the plastic making it water-wettable. The production of hydrophilic plastic surfaces is also required in the selective separation of plastics by froth flotation. For the process to be selective one plastic must be rendered hydrophilic while another remains hydrophobic. In this study the potential for separation of PVC and PET has been investigated. Flame treatment was shown to be very effective in producing a hydrophilic surface on both plastics, although the process was not selective under the conditions investigated. Raising the temperature of the plastics above their softening point produced a hydrophobic recovery. As the softening point of PVC was significantly lower than for PET it was possible to produce a significant difference in hydrophobicity, as judged using contact angle measurement. When immersed in water the contact angle of the PVC was found to be strongly dependent on the pH. Good separation efficiency of the two plastics was achieved by froth flotation from pH 4 to 9. One particular advantage of the technique is that no chemical reagents may be required in the flotation stage. The practicalities of designing a flake treatment system however have to be addressed before considering it to be a viable industrial process.

  19. Cold Heading of Cylindrical PVC Billets: An Experimental and Theoretical Investigation

    NASA Astrophysics Data System (ADS)

    Alves, L. M.; Martins, P. A. F.

    2010-12-01

    The design of upset forged metal parts by cold heading is presently well established. Major operating parameters are identified and the typical modes of deformation that may occur during the process are fully characterized. In contrast to metals, there is no research work and no practical design rules in the specialized literature concerning the cold heading of polymer parts. This paper is concerned with the abovementioned lack of knowledge and is a contribution toward the application of cold heading to polymers. The experimental research work makes use of polyvinyl chloride (PVC) and the overall findings are interpreted in the light of an innovative extension of the flow formulation that is capable of modeling cold forming of pressure-sensitive materials under a nonassociated flow rule. Emphasis is placed on the deformation mechanics of cold heading applied to PVC and on the influence of the major operating parameters on the overall formability limits of the process. Results show that cold heading of PVC can be successfully utilized for producing upset forged parts.

  20. On the Nd:YAG pulsed laser processing of rigid PVC

    NASA Astrophysics Data System (ADS)

    Hernández, L. C.; Arronte, M.; Ponce, L.; Flores, T.; Guerrero, J.; de Posada, E.; Rodríguez, E.

    2009-09-01

    The potential of Nd:YAG pulsed laser to processing PVC sheets minimizing HCl gases emission is investigated. We studied the gas emission when the PVC is cut by either CO2 or Nd:YAG pulsed laser by using FTIR Spectroscopy. Optical microscopy of laser treated PVC samples was performed in order to demonstrate the carbonization. On the other hand, LIBS spectroscopy for two different ranges of pulse duration was employed in order to investigate the plume composition during the Nd:YAG pulsed laser ablation process. The experiments shows that Cl atoms are emitted during the Nd:YAG pulsed laser ablation although the HCl gases are produced at low levels. In order to explain the sub-surface irregularities detected for Nd:YAG laser irradiation, a one-dimensional model is developed to study the temperature evolution inside the sample. We demonstrate that the ablation mechanisms prevail on thermally drive emission until 70 μm, afterwards the thermal expansion process is already observed.

  1. Migration of plasticizers from PVC medical devices: Development of an infusion model.

    PubMed

    Bernard, L; Cueff, R; Chagnon, Mc; Abdoulouhab, F; Décaudin, B; Breysse, C; Kauffmann, S; Cosserant, B; Souweine, B; Sautou, V

    2015-10-15

    Alternatives to DEHP plasticizers are used in various PVC medical devices (MD) for infusion. As they are able to migrate from these MDs into infused solutions, they may come into contact with patient. Different and specific clinical parameters influence their migration in at-risk situations such as infusion. In contrast to the regulations for Food Contact Materials (MCDA), there is currently no acceptable migration limits for the use of these plasticizers in clinical situations. In order to assess their migration, and thus control the risks linked to these MDs, we developed a migration model for the plasticizers in MDs. To this end, we applied a cross-disciplinary methodological process similar to that used in the food-processing industry, taking into account the MDs' conditions of use in clinical practice. The simulation model is simple and includes the following conditions: MD should be tested with a dynamic method that respects our established clinical assumption (2 L of infused solutions via 13 dm(2) of plasticized PVC), at a temperature of 25 °C and during 24 h of contact, using a 50/50 (v/v) ethanol/water simulant. This model could be proposed as a tool for the safety evaluation of the patients' exposure risk to plasticizers from PVC medical devices for infusions. PMID:26278488

  2. Migrability of PVC plasticizers from medical devices into a simulant of infused solutions.

    PubMed

    Bernard, L; Cueff, R; Breysse, C; Décaudin, B; Sautou, V

    2015-05-15

    Medical devices (MD) for infusion and artificial nutrition are essentially made of plasticized PVC. The plasticizers in the PVC matrix can leach out into the infused solutions and may enter into contact with the patients. In order to assess the risk of patient exposure to these plasticizers we evaluated the migration performance of DEHP, DEHT, DINCH, and TOTM using a model adapted to the clinical use of the MDs. Each PVC tubing sample was immersed in a simulant consisting of a mixture of ethanol/water (50/50v/v) at 40°C and migration tests were carried out after 24h, 72h, and 10 days.DEHP had the highest migration ability, which increased over time. The amount of TOTM released was more than 20 times less than that of DEHP, which makes it an interesting alternative. DEHT is also promising, with a migration level three times smaller than DEHP. However, the migration ability of DINCH was similar to DEHP, with the released amounts equaling 1/8th of the initial amount in the tubing after 24h of contact. Taking into account the available toxicological data, TOTM and DEHT appear to be of particular interest. However, these data should be supplemented and correlated with clinical and toxicological studies on plasticizers and their metabolites. PMID:25796128

  3. Sensing property of thin film optical waveguide sensor based on PVC copolymer

    NASA Astrophysics Data System (ADS)

    Kim, Kyungho; Minamitani, Haruyuki; Matsumoto, Kunihiro; Kang, Shin-Won

    1998-01-01

    In this report, an active PVC thin film waveguide sensor which can select a specific ion and measure its concentrations is proposed. In order to investigate the applicability of this sensor, we measured calcium ion. The waveguide layer was fabricated with plasticized poly (vinyl chloride) (PVC) co-polymer matrix containing a neutral ionophore for calcium dioctyl phthalate, and chromoionophore, which plays important roles both in incident light propagation and in selective ion sensing. For this purpose, we applied the sensor to the sample solution whose CaCl2 was gradually altered. In this study, we found that this thin film waveguide possessed good light propagation. In addition, it showed enough chemical reaction to Ca2+ to select Ca2+ and to measure its concentration. These findings suggested that the proposed active PVC optical thin film waveguide sensor was very effective in selecting Ca2+ and measuring its concentration. Also, it will be expected that this sensor is applicable to various ions other than Ca2+.

  4. Flame treatment for the selective wetting and separation of PVC and PET.

    PubMed

    Pascoe, R D; O'Connell, B

    2003-01-01

    Flame treatment has been used for many years to modify the surface of plastics to allow coatings to be added. The effect of the treatment is to produce hydrophilic species on the surface of the plastic making it water-wettable. The production of hydrophilic plastic surfaces is also required in the selective separation of plastics by froth flotation. For the process to be selective one plastic must be rendered hydrophilic while another remains hydrophobic. In this study the potential for separation of PVC and PET has been investigated. Flame treatment was shown to be very effective in producing a hydrophilic surface on both plastics, although the process was not selective under the conditions investigated. Raising the temperature of the plastics above their softening point produced a hydrophobic recovery. As the softening point of PVC was significantly lower than for PET it was possible to produce a significant difference in hydrophobicity, as judged using contact angle measurement. When immersed in water the contact angle of the PVC was found to be strongly dependent on the pH. Good separation efficiency of the two plastics was achieved by froth flotation from pH 4 to 9. One particular advantage of the technique is that no chemical reagents may be required in the flotation stage. The practicalities of designing a flake treatment system however have to be addressed before considering it to be a viable industrial process. PMID:14583247

  5. Oil palm empty fruit bunch (OPEFB) fiber reinforced PVC/ENR blend-electron beam irradiation

    NASA Astrophysics Data System (ADS)

    Ratnam, Chantara Thevy; Raju, Gunasunderi; Yunus, Wan Md Zin Wan

    2007-12-01

    The effect of irradiation on the tensile properties of oil palm empty fruit bunch (OPEFB) fiber reinforced poly(vinyl chloride)/epoxidized natural rubber (PVC/ENR) blends were studied. The composites were prepared by mixing the fiber and the PVC/ENR blend using HAAKE Rheomixer at 150 °C. The composites were then irradiated by using a 3.0 MeV electron beam machine at doses ranging from 0 to 100 kGy in air and room temperature. The tensile strength, Young's modulus, elongation at break and gel fraction of the composites were measured. Comparative studies were also made by using poly(methyl acrylate) grafted OPEFB fiber in the similar blend system. An increase in tensile strength, Young's modulus and gel fraction, with a concurrent reduction in the elongation at break (Eb) of the PVC/ENR/OPEFB composites were observed upon electron beam irradiation. Studies revealed that grafting of the OPEFB fiber with methyl acrylate did not cause appreciable effect to the tensile properties and gel fraction of the composites upon irradiation. The morphology of fractured surfaces of the composites, examined by a scanning electron microscope showed an improvement in the adhesion between the fiber and the matrix was achieved upon grafting of the fiber with methyl acrylate.

  6. Influence of hydroxylation on fabrication of PVC/CaSO4 composite

    NASA Astrophysics Data System (ADS)

    Chen, H. Y.; Wang, J.; Ma, P. Y.; Liang, J.; Xiang, L.

    2015-12-01

    The influences of hydroxylation on grafting of aminopropyltrimethoxysilane ((CH3O)3sbnd Sisbnd CH2sbnd CH2sbnd CH2sbnd NH2, abbreviated as APS) and fabrication of CaSO4/PVC composite were investigated in this paper. The experimental results indicated that the pre-treatment of CaSO4 particles by NaOH promoted the formation of OH-, which enhanced the grafting of APS on CaSO4 surface and improved the interfacial adhesion between CaSO4 and PVC matrix. Compared with the use of CaSO4 with sole APS modification, the use of the CaSO4 with NaOH and APS modification led to the increase of the impact strength of the CaSO4/PVC composite from 36.5 kJ m-2 to 50.2 kJ m-2 and the flexural strength from 48.7 MPa to 62.1 MPa.

  7. Optical absorption depth profiling of photodegraded poly(vinylchloride) (PVC) films by quantitative photothermal deflection technique

    NASA Astrophysics Data System (ADS)

    Fu, S.-W.; Power, J. F.; Nepotchatykh, O. V.

    2000-05-01

    An improved photothermal beam deflection technique is applied for optical absorption depth profiling of UV photodegraded PVC films, for nondestructive evaluation of their decomposition mechanism. A new model-based on diffraction theory is used to describe the photothermal response (with bicell recording), induced by impulse irradiation of a depth dependent array of thin planar optical absorbers approximating the sample's depth profile. Improved techniques of alignment, sample preparation and quantitative deconvolution of the bicell impulse response have increased the signal repeatability and reduced the principal bias errors affecting this ill posed problem. By this technique and a stable solution of the inverse problem, the absorption coefficient depth profile is accurately reconstructed in PVC films. Experimental depth profiles were confirmed against destructive techniques run on identical samples of the degraded material. An excellent agreement was found between depth profiles recovered using the mirage effect and these reference methods. Observed absorption profiles were fully consistent with known patterns of depth dependent PVC degradation under nitrogen and oxygen atmospheres.

  8. Tiered environmental risk assessment of methyltins from heat stabilizers in rigid PVC in Sweden.

    PubMed

    van Dokkum, Henno P; Huwer, Sherri L

    2005-02-01

    The methyltins, methyltin 2-ethylhexyl mercaptoacetate and methyltin-2-mercaptoethyloleate sulfide, are used as heat stabilizers in rigid PVC. The degradation products monomethyltintrichloride (MMTTC) and dimethyltindichloride (DMTDC) may leach from the PVC, and enter the environment. A risk assessment was executed for the use of these products in Sweden, with the double aim to (a) assess the potential environmental risks, and (b) explore the possibilities of a tiered risk assessment. An initial assessment was executed with EUSES 1.0. The initial assessment showed no significant environmental risks on a regional scale. On a local scale however, emissions from a sewage treatment plant to the surface water pose a potential risk for the near proximity. In a second tier, this critical exposure route was studied in more detail; an improved exposure scenario was drawn up; and an additional sorption experiment was performed. This refinement resulted in much lower predicted environmental concentrations (PVC in Sweden are of no concern. PMID:15649829

  9. Electroless plating of PVC plastic through new surface modification method applying a semi-IPN hydrogel film

    NASA Astrophysics Data System (ADS)

    Wang, Ming-Qiu; Yan, Jun; Du, Shi-Guo; Li, Hong-Guang

    2013-07-01

    A novel palladium-free surface activation process for electroless nickel plating was developed. This method applied a semi-Interpenetrating Polymer Network (semi-IPN) hydrogel film to modify the poly(vinyl chloride) (PVC) surface by chemical bonds. The activation process involved the formation of semi-IPN hydrogel film on the PVC surface and the immobilization of catalyst for electroless plating linking to the pretreated substrate via Nsbnd Ni chemical bond. The hydrogel layer was used as the chemisorption sites for nickel ions, and the catalyst could initiate the subsequent electroless nickel plating onto the PVC surface. Finally, a Ni-P layer was deposited on the nickel-activated PVC substrate by electroless plating technique. The composition and morphology of nickel-plated PVC foils were characterized by scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), energy dispersive X-ray spectroscopy (EDS) and X-ray diffraction (XRD). The results of SEM and XRD show that a compact and continuous Ni-P layer with amorphous nickel phase is formed on the PVC surface. EDS shows that the content of the nickel and the phosphorus in the deposits is 89.4 wt.% and 10.6 wt.%, respectively.

  10. Unentangled star-shape poly(ε-caprolactone)s as phthalate-free PVC plasticizers designed for non-toxicity and improved migration resistance.

    PubMed

    Choi, Woohyuk; Chung, Jae Woo; Kwak, Seung-Yeop

    2014-07-23

    We develop a nontoxic unentangled star-shape poly(ε-caprolactone) (UESPCL) plasticizer with excellent migration resistance for the production of phthalate-free flexible poly(vinyl chloride) (PVC) by means of the ring-opening polymerization of ε-caprolactone, initiated from the multifunctional core, combined with end-capping, and vacuum purification processes. UESPCL is a transparent liquid at room temperature and exhibits unentangled Newtonian behavior because of its extremely short branched segments. UESPCL is biologically safe without producing an acute toxicity response. Torque analysis measurements reveals that UESPCL offers a faster fusion rate and a higher miscibility with PVC compared to a typical plasticizer, di(2-ethylhexyl) phthalate (DEHP). The solid-state (1)H nuclear magnetic resonance (NMR) spectrum reveals that PVC and UESPCL are miscible with an average domain size of less than 8 nm. The flexibility and transparency of the PVC/UESPCL mixture, that is, phthalate-free flexible PVC, are comparable to the corresponding properties of the PVC/DEHP mixture, and the stretchability and fracture toughness of PVC/UESPCL are superior to the corresponding properties of the PVC/DEHP system. Most of all, PVC/UESPCL shows excellent migration resistance with a weight loss of less than 0.6% in a liquid phase, whereas DEHP migrated out of PVC/DEHP into a liquid phase with a weight loss of about 10%. PMID:24955769

  11. Synthesis, antioxidant activities of the nickel(II), iron(III) and oxovanadium(IV) complexes with N2O2 chelating thiosemicarbazones

    NASA Astrophysics Data System (ADS)

    Bal-Demirci, Tülay; Şahin, Musa; Özyürek, Mustafa; Kondakçı, Esin; Ülküseven, Bahri

    The nickel(II), iron(III) and oxovanadium(IV) complexes of the N2O2 chelating thiosemicarbazones were synthesized using 4-hydroxysalicyladehyde-S-methylthiosemicarbazone and R1-substitute-salicylaldehyde (R1: 4-OH, H) in the presence of Ni(II), Fe(III), VO(IV) ions by the template reaction. The structures of the thiosemicarbazone complexes were characterized by FT-IR, 1H NMR, elemental, ESI-MS and APCI-MS analysis. The synthesized compounds were screened for their antioxidant capacity by using the cupric reducing antioxidant capacity (CUPRAC) method. Trolox equivalent antioxidant capacity (TEAC) of iron(III) complex, 1c, was measured to be higher than that of the other complexes. Other parameters of antioxidant activity (scavenging effects on rad OH, O2rad - and H2O2) of these compounds were also determined. All the compounds have shown encouraging ROS scavenging activities.

  12. 4-Nitrocatecholato iron(III) complexes of 2-aminomethyl pyridine-based bis(phenol) amine as structural models for catechol-bound 3,4-PCD

    NASA Astrophysics Data System (ADS)

    Safaei, Elham; Heidari, Sima; Wojtczak, Andrzej; Cotič, Patricia; Kozakiewicz, Anna

    2016-02-01

    Two nitrocatecholato(HNC) iron(III) complexes, [FeLAMPX(H-NC)]. NEt3, of the tetradendate ligand (2-aminomethylpyridine)bis(2-pyridylmethyl)amine (H2LAMPX) were synthesized and structurally characterized. These structural models for catechol-bound 3,4-PCD were characterized by IR, UV-vis, elemental analysis and magnetic measurements. X-ray crystallography studies revealed that in both complexes the iron(III) centers are distorted octahedral and coordinated by two phenolate oxygen's, two amine nitrogen's of the ligand and mono anionic nitrocatecholate group (HNC). The variable-temperature magnetic susceptibility studies revealed paramagnetic properties of the reported complexes. The effective magnetic moments for the complexes lie between 5.3 and 5.4 BM correspond to the reported values for high spin Fe(III) center. The ligand-centered oxidation and metal-centered reduction of complexes was studies using cyclic voltammetry (CV) technique.

  13. Synthesis, antioxidant activities of the nickel(II), iron(III) and oxovanadium(IV) complexes with N2O2 chelating thiosemicarbazones.

    PubMed

    Bal-Demirci, Tülay; Sahin, Musa; Ozyürek, Mustafa; Kondakçı, Esin; Ulküseven, Bahri

    2014-05-21

    The nickel(II), iron(III) and oxovanadium(IV) complexes of the N2O2 chelating thiosemicarbazones were synthesized using 4-hydroxysalicyladehyde-S-methylthiosemicarbazone and R1-substitute-salicylaldehyde (R1: 4-OH, H) in the presence of Ni(II), Fe(III), VO(IV) ions by the template reaction. The structures of the thiosemicarbazone complexes were characterized by FT-IR, (1)H NMR, elemental, ESI-MS and APCI-MS analysis. The synthesized compounds were screened for their antioxidant capacity by using the cupric reducing antioxidant capacity (CUPRAC) method. Trolox equivalent antioxidant capacity (TEAC) of iron(III) complex, 1c, was measured to be higher than that of the other complexes. Other parameters of antioxidant activity (scavenging effects on •OH, O2(•-) and H2O2) of these compounds were also determined. All the compounds have shown encouraging ROS scavenging activities. PMID:24656797

  14. Forensic utility of the carbon isotope ratio of PVC tape backings

    NASA Astrophysics Data System (ADS)

    Stern, L. A.; Thompson, A. H.; Mehltretter, A. H.; McLaskey, V.; Parish, A.; Aranda, R.

    2008-12-01

    Forensic interest in adhesive tapes with PVC-backings (polyvinyl chloride, electrical tapes) derives from their use in construction of improvised explosive devices, drug packaging and in a variety of other illicit activities. Due to the range of physical characteristics and chemical compositions of such tapes, traditional microscopic and chemical analysis of the tape backings and adhesives offer a high degree of discrimination between tapes from different manufacturers and products. To evaluate whether carbon isotope ratios may be able to increase discrimination of electrical tapes, particularly with regards to different tapes of the same product, we assessed the PVC-backings of 87 rolls of black electrical tape for their δ13C values. The adhesive on these tapes was physically removed with hexane, and plasticizers within the PVC tape backings were removed by three-20 minute extractions with chloroform. The δ13C values of the PVC tape backings ranged between -23.8 and -41.5 (‰ V-PDB). The carbon isotopic variation within a product (identical brand and product identification) is significant, based on five products with at least 3 rolls (ranges of 7.4‰ (n=3), 10.0‰ (n=6), 4.2‰ (n=16), 3.8‰ (n=6), and 11.5‰ (n=8), respectively). There was no measurable carbon isotope variation in regards to the following: a) along the length of a roll (4 samples from 1 roll); b) between the center and edge of a strip of tape (1 pair); c) between rolls assumed to be from the same lot of tape (2 pairs); d) between different rolls from the same batch of tape (same product purchased at the same time and place; 5 pairs); and e) between samples of a tape at room temperature, heated to 50° C and 80° C for 1 week. For each sample within the population of 87 tapes, carbon isotopes alone exclude 80 to 100% of the tapes as a potential match, with an average exclusion power of 92.5%, using a window of ± 0.4‰. Carbon isotope variations originate from variations in starting

  15. The effect of the synthetic route on the structural, textural, morphological and catalytic properties of iron(iii) oxides and oxyhydroxides.

    PubMed

    Oulego, Paula; Villa-García, María A; Laca, Adriana; Diaz, Mario

    2016-06-21

    A variety of iron(iii) oxides and oxyhydroxides were synthesised and characterised using three distinct methods of preparation: microemulsion, precipitation and sol-gel. The results clearly showed that the structure, textural properties, crystal morphology and catalytic performance of the phases obtained were highly dependent on the chemical routes used for the synthesis. Precipitation and microemulsion methods allowed obtaining mesoporous nanostructured iron(iii) oxides with mean particle sizes of 4 nm (amorphous hematite) and 7 nm (ferrihydrite), which exhibited a high surface area (291.4 m(2) g(-1) and 192.3 m(2) g(-1), respectively) and a very good catalytic behaviour in the advanced oxidation of highly non-biodegradable wastewaters. The different conditions employed in the synthesis of these materials through the sol-gel method yielded two goethites with practically the same catalytic properties, but dissimilar morphologies and texture. When soft agitation and slow addition of the precipitating agent were used, the resulting material (G1) was made up of shorter and finer particles, markedly acicular, with an average length of 400 ± 50 nm and width of 15 ± 5 nm. However, vigorous agitation and rapid addition of the precipitating agent led to the formation of longer and coarser particles, moderately acicular, the average length and width being 950 ± 100 nm and 140 ± 20 nm, respectively. The use of the sol-gel technique also resulted in the formation of a solid consisting of a mixture of hematite as the main crystalline phase and goethite particles dispersed among the hematite particles. This solid presented a low specific surface area (13.2 m(2) g(-1)) and lower catalytic activity. Therefore, precipitation and microemulsion proved to be the most suitable techniques to synthesise catalytically active disordered iron(iii) oxide nanoparticles, due to the presence of highly reactive non-stoichiometric iron(iii) ions, a higher surface area and smaller particle

  16. Anion selective membrane. [ion exchange resins and ion exchange membrane electrolytes for electrolytic cells

    NASA Technical Reports Server (NTRS)

    Alexander, S. S.; Geoffroy, R. R.; Hodgdon, R. B.

    1975-01-01

    Experimental anion permselective membranes were prepared and tested for their suitability as cell separators in a chemical redox power storage system being developed at NASA-Lewis Research Center. The goals of long-term (1000 hr) oxidative and thermal stability at 80 C in FeCl3 and CrCl3 electrolytes were met by most of the weak base and strong base amino exchange groups considered in the program. Good stability is exhibited by several of the membrane substrate resins. These are 'styrene' divinylbenzene copolymer and PVC film. At least four membrane systems produce strong flexible films with electrochemical properties (resistivity, cation transfer) superior to those of the 103QZL, the most promising commercial membrane. The physical and chemical properties of the resins are listed.

  17. Iron(III) complexes of bis (benzimidazol-2-yl) methyl) thiophene-2,5-dicarboxamide: synthesis, spectral and oxidation of o-phenylenediamine.

    PubMed

    Tyagi, Nidhi; Mathur, Pavan

    2012-10-01

    Iron(III) complexes of a potentially pentadentate ligand N(2), N(5)-bis ((1H-benzo [d] imidazol-2-yl) methyl) thiophene-2,5-dicarboxamide are synthesized with an exogenous anion X=Cl(-), NO(3)(-). Mössbauer and EPR spectroscopy indicates axially distorted complexes. These complexes were utilized for the oxidation of o-phenylenediamine to 2,3-diaminophenazine in presence of H(2)O(2). The initial rate of reaction is dependent on the concentration of o-phenylenediamine as well as the iron(III) complex. Rates of reaction were found to be at least five times higher for the Cl(-) bound complex. The effect of an added anion like acetate, azide and citrate is found to inhibit the rate of reaction. This suggests that one of the factors affecting the rate determining step is the binding of these anions on a vacant site at the iron(III) centre. The oxidation of o-phenylenediamine to 2,3-diaminophenazine is reminiscent of the functioning of horse radish peroxidase. PMID:22885893

  18. Iron(III) complexes of bis (benzimidazol-2-yl) methyl) thiophene-2,5-dicarboxamide: Synthesis, spectral and oxidation of o-phenylenediamine

    NASA Astrophysics Data System (ADS)

    Tyagi, Nidhi; Mathur, Pavan

    2012-10-01

    Iron(III) complexes of a potentially pentadentate ligand N2, N5-bis ((1H-benzo [d] imidazol-2-yl) methyl) thiophene-2,5-dicarboxamide are synthesized with an exogenous anion X = Cl-, NO3-. Mössbauer and EPR spectroscopy indicates axially distorted complexes. These complexes were utilized for the oxidation of o-phenylenediamine to 2,3-diaminophenazine in presence of H2O2. The initial rate of reaction is dependent on the concentration of o-phenylenediamine as well as the iron(III) complex. Rates of reaction were found to be at least five times higher for the Cl- bound complex. The effect of an added anion like acetate, azide and citrate is found to inhibit the rate of reaction. This suggests that one of the factors affecting the rate determining step is the binding of these anions on a vacant site at the iron(III) centre. The oxidation of o-phenylenediamine to 2,3-diaminophenazine is reminiscent of the functioning of horse radish peroxidase.

  19. A new iron(III) complex of glycine derivative of amine-chloro substituted phenol ligand: Synthesis, characterization and catechol dioxygenase activity

    NASA Astrophysics Data System (ADS)

    Saberikia, Iraj; Safaei, Elham; Kowsari, Mohammad Hossein; Lee, Yong-Ill; Cotic, Patricia; Bruno, Giuseppe; Rudbari, Hadi Amiri

    2012-12-01

    A new iron(III) complex of the glycine derivative of amine-chloro substituted phenol ligand (H3LGDC) has been prepared and characterized by IR, 1H NMR, UV-Vis spectroscopic techniques, cyclic voltammetry, ESI-MS and magnetic susceptibility studies. X-ray analysis reveals that in iron complex of FeLGDC the iron(III) center has a distorted trigonal bipyramidal coordination sphere and is surrounded by an amine nitrogen, a carboxylate, a water and two phenolate oxygen atoms. The DFT calculations with the UB3LYP/6-311++G** level optimized structure of the complex are in good agreement with experimental X-ray structural data. The variable-temperature magnetic susceptibility indicates that FeLGDC is the paramagnetic high spin iron(III) complex. It has been shown that electrochemical oxidation of this complex is ligand-centered due to the oxidation of phenolate to the phenoxyl radicals. This enzyme mimic utilized molecular oxygen in carrying out the oxidative cleavage of catechols with complete conversion at room temperature.

  20. Effect of tris(3-hydroxy-4-pyridinonate) iron(III) complexes on iron uptake and storage in soybean (Glycine max L.).

    PubMed

    Santos, Carla S; Carvalho, Susana M P; Leite, Andreia; Moniz, Tânia; Roriz, Mariana; Rangel, António O S S; Rangel, Maria; Vasconcelos, Marta W

    2016-09-01

    Iron deficiency chlorosis (IDC) is a serious environmental problem affecting the growth of several crops in the world. The application of synthetic Fe(III) chelates is still one of the most common measures to correct IDC and the search for more effective Fe chelates remains an important issue. Herein, we propose a tris(3-hydroxy-4-pyridinonate) iron(III) complex, Fe(mpp)3, as an IDC corrector. Different morphological, biochemical and molecular parameters were assessed as a first step towards understanding its mode of action, compared with that of the commercial fertilizer FeEDDHA. Plants treated with the pyridinone iron(III) complexes were significantly greener and had increased biomass. The total Fe content was measured using ICP-OES and plants treated with pyridinone complexes accumulated about 50% more Fe than those treated with the commercial chelate. In particular, plants supplied with compound Fe(mpp)3 were able to translocate iron from the roots to the shoots and did not elicit the expression of the Fe-stress related genes FRO2 and IRT1. These results suggest that 3,4-HPO iron(III) chelates could be a potential new class of plant fertilizing agents. PMID:27156133

  1. VizieR Online Data Catalog: Pulkovo Photographic Vertical Circle (PVC96) (Gontcharov+ 1998)

    NASA Astrophysics Data System (ADS)

    Gontcharov, A. G.; Bagildinsky, B. K.; Kornilov, E. V.; Polojentsev, D. D.; Shkutov, V. D.

    1996-10-01

    The Pulkovo photographic vertical circle catalogue, the first version, PVC96, gives accurate declinations of 760 stars from the FK5 () and FK5 () Extension north of declination -15deg. In 1987-1995 the Photographic vertical circle of the Pulkovo observatory (PVC) carried out programme of observations of declinations of Mars, Jupiter and FK5 stars. Stars with declination higher than 45 deg were observed at both culminations. 8250 observations of 1345 stars and 49 ones of 2 planets have been treated and used to establish an instrumental coordinate frame conform to the DE200. The first version of the catalogue, PVC96, has been constructed on the basis of 6821 observations of 760 stars with at least 4 observations at upper culmination. For the stars with declination higher than 70 deg the observations at both culminations were used in the catalogue, for the rest of the stars only observations at upper culmination were used. The mean observational epoch is 1991.5. The internal mean error of one observation at zenith is 0.14 arcsec. The declinations of the stars are obtained with mean precision of 0.07 arcsec. The classical method of observations with vertical circle was used. Each meridian transit observation includes two exposures of 40 seconds each separated by a reversal of the entire instrument taking about one minute. During the period of the observations the PVC had a photographic-photoelectric micrometer including a photographic camera at the eyepiece end of the tube, and a special visual-photoelectric measuring machine. Readings of two divided vertical circles of glass were registered by photoelectric microscopes. A tilt of the instrument with respect to the vertical line was measured by two bubble levels. All the measuring devices of the PVC were calibrated and investigated externally (i.e., independently of observations). The flexure of the tube investigated at various zenith distances proves to be a function of zenith distance and temperature

  2. Determination of bisphenol A in, and its migration from, PVC stretch film used for food packaging.

    PubMed

    López-Cervantes, J; Paseiro-Losada, P

    2003-06-01

    Bisphenol A (BPA) is used as an additive in polyvinyl chloride (PVC) products, including stretch films used for food packaging. The BPA contents were investigated of several brands of stretch film bought locally but marketed internationally or throughout Spain and which were presumably produced at different manufacturing plants. Their major components were identified by FTIR (Fourier Transform Infrared Spectrometry) and horizontal attenuated total reflectance, and the migration of BPA from these materials into the standard European Union food simulants was determined by high-performance liquid chromatography (HPLC) using both fluorescence (FL) and ultraviolet (UV) detection, the identity of the analyte being confirmed by gas chromatography-mass spectrometry (GC-MS) and liquid chromatography-mass spectrometry (LC-MS). The two HPLC detection methods had different detection limits (30 microg x l(-1) for UV, 3 microg x l(-1) for FL), but afforded virtually identical BPA determinations for the samples tested. BPA contents ranging from 40 to 100 mg x kg(-1) were found in three of the five PVC-based films analysed, and a content of 500 mg x kg(-1) was found in a fourth; for these determinations, extraction into acetonitrile was used. In standard tests of migration into water, 3% acetic acid and olive oil over 10 days at 40 degrees C, migration from a given film was in all cases greatest into olive oil. Migration from the films with non-zero BPA contents ranged from 3 to 31 microg x dm(-2), values higher than those reported for many other food-contact materials, but lower than the European Union specific migration limit for BPA. PVC stretch film nevertheless may make a significant contribution to contamination of foodstuffs by BPA, and should be taken into account in estimating BPA intake or exposure to this substance. PMID:12881134

  3. Migration of DEHP and DINP into dust from PVC flooring products at different surface temperature.

    PubMed

    Jeon, Seunghwan; Kim, Ki-Tae; Choi, Kyungho

    2016-03-15

    Phthalates are important endocrine disrupting chemicals that have been linked to various adverse human health effects. Phthalates are ubiquitously present in indoor environment and could enter humans. Vinyl or PVC floorings have been recognized as one of important sources of phthalate release to indoor environment including house dust. In the present study, we estimated the migration of di(2-ethylhexyl)phthalate (DEHP) and di-isononyl phthalate (DINP) from the flooring materials into the dust under different heating conditions. For this purpose, a small chamber specifically designed for the present study and a Field and Laboratory Emission Cell (FLEC) were used, and four major types of PVC flooring samples including two UV curing paint coated, an uncoated residential, and a wax-coated commercial type were tested. Migration of DEHP was observed for an uncoated residential type and a wax-coated commercial type flooring. After 14 days of incubation, the levels of DEHP in the dust sample was determined at room temperature on average (standard deviation) at 384 ± 19 and 481 ± 53 μg/g, respectively. In contrast, migration of DINP was not observed. The migration of DEHP was strongly influenced by surface characteristics such as UV curing coating. In the residential flooring coated with UV curing paint, migration of DEHP was not observed at room temperature. But under the heated condition, the release of DEHP was observed in the dust in the FLEC. Migration of DEHP from flooring materials increased when the flooring was heated (50 °C). In Korea, heated flooring system, or 'ondol', is very common mode of heating in residential setting, therefore the contribution of PVC flooring to the total indoor DEHP exposure among general population is expected to be greater especially during winter season when the floor is heated. PMID:26824397

  4. PVC/CaCO3 Nanocomposites: Influence of nanoparticle surface treatment on properties

    NASA Astrophysics Data System (ADS)

    Bonadies, Irene; Avella, Maurizio; Avolio, Roberto; Carfagna, Cosimo; Emanuela Errico, Maria; Gentile, Gennaro

    2010-06-01

    The influence of nanosized calcium carbonate on the gelation process, thermal stability and mechanical properties of rigid poly(vinyl chloride) has been studied. The gelation time of rigid PVC/calcium carbonate nanocomposites depends on the percentage and superficial treatment of CaCO3. The results of thermogravimetric analysis underline an improvement of the thermal stability as a function of the surface modifier. Finally, the flexural modulus, the flexural strength as well as the critical stress intensity factor increase with the addition of poly(acrylic acid) (PAA) or poly(butadiene-co-acrilonitrile-co-acrylic acid) (PBAA) coated nanoparticles.

  5. A creep apparatus to explore the quenching and ageing phenomena of PVC films

    NASA Technical Reports Server (NTRS)

    Lee, H. H. D.; Mcgarry, F. J.

    1991-01-01

    A creep apparatus has been constructed for an in situ determination of length and length change. Using this apparatus, the creep behavior of PVC thin films associated with quenching and aging was studied. The more severe the quench through the glass transition temperature, the greater is the instantaneous elastic deformation and the subsequent creep behavior. As aging proceeds, the quenched films gradually lose the ductility incurred by quenching. These results agree well with the well-known phenomena of physical aging. Thus, the changes reflecting molecular mobilities due to quenching and aging can be properly monitored by such a creep apparatus.

  6. [Effectiveness of a PVC ear tag impregnated with the insecticide flucythrinate].

    PubMed

    Sol, J; Prijs, H J; Counotte, G H; Kommerij, R

    1987-04-01

    A PVC ear tag containing the synthetic pyrethroid flucythrinate was tested in seventeen herds including 218 heifers. There was a comparable control group of twelve herds including 157 heifers. The ear tags were more effective against sucking flies than they were against sticking flies. Varying with the species of the fly, the effectiveness ranged from 36.2 per cent to 95.7 per cent. The effectiveness also varied between the herds. The active constituent was still released within approximately 5 1/2 months after introduction. PMID:3576578

  7. UHV deposition and characterization of a mononuclear iron(III) β-diketonate complex on Au(111)

    PubMed Central

    Cimatti, Irene; Ninova, Silviya; Lanzilotto, Valeria; Malavolti, Luigi; Rigamonti, Luca; Cortigiani, Brunetto; Mannini, Matteo; Magnano, Elena; Bondino, Federica; Totti, Federico; Cornia, Andrea

    2014-01-01

    Summary The adsorption of the sterically hindered β-diketonate complex Fe(dpm)3, where Hdpm = dipivaloylmethane, on Au(111) was investigated by ultraviolet photoelectron spectroscopy (UPS) and scanning tunnelling microscopy (STM). The high volatility of the molecule limited the growth of the film to a few monolayers. While UPS evidenced the presence of the β-diketonate ligands on the surface, the integrity of the molecule on the surface could not be assessed. The low temperature STM images were more informative and at submonolayer coverage they showed the presence of regular domains characterized by a flat morphology and height of ≈0.3 nm. Along with these domains, tetra-lobed features adsorbed on the kinks of the herringbone were also observed. DFT-simulated images of the pristine molecule and its possible decomposition products allowed to assess the partial fragmentation of Fe(dpm)3 upon adsorption on the Au(111) surface. Structural features with intact molecules were only observed for the saturation coverage. An ex situ prepared thick film of the complex was also investigated by X-ray magnetic circular dichroism (XMCD) and features typical of high-spin iron(III) in octahedral environment were observed. PMID:25551042

  8. Synthesis and spectroscopic investigations of iron(III) complexes with chlorides and dianionic, symmetrically halogen substituted phthalocyanines as ligands.

    PubMed

    Somashekarappa, M P; Keshavayya, J; Sherigara, B S

    2003-03-01

    The synthesis of iron(III) complexes of general formula FeCl(R-pc), where R-pc are dianionic, symmetrically halogen substituted phthalocyanines at the positions 2,9,16,23 or 1,8,15,22, from the corresponding amino substituted derivatives is described (R=Cl, Br, I). The complexes are characterized by UV-visible and infrared spectra, powder X-ray diffraction and magnetic susceptibility measurements. The effect of substituents at the periphery and the basicity of the solvents used on the electronic spectra are discussed. The Q band of the electronic spectra for symmetrically halogen substituted derivatives are redshifted and the substituents at 2,9,16,23- positions are more effective in redshifting the Q bands than those at 1,8,15,22-positions. Depending upon the basicity of the solvents, the ligand-to-metal charge transfer (LMCT) transitions on Q band envelop shift to the higher energy region in the order of pyridine>DMF>DMSO. The infrared absorption signals for C-H and metal-ligand vibrations appear to be sharper for 1,8,15,22 substituted derivatives than for 2,9,16,23 substituted ones. PMID:12609638

  9. Spin Crossover, Polymorphism and Porosity to Liquid Solvent in Heteroleptic Iron(III) {Quinolylsalicylaldimine/Thiosemicarbazone-Salicylaldimine} Complexes.

    PubMed

    Phonsri, Wasinee; Davies, Casey G; Jameson, Guy N L; Moubaraki, Boujemaa; Murray, Keith S

    2016-01-22

    Heteroleptic iron(III) complexes of formula [Fe(qsal)(thsa)]⋅solvent have been synthesized: [Fe(qsal)(thsa)]⋅0.4 BuOH (1), [Fe(qsal)(thsa)]⋅0.5 MeCN (2) and [Fe(qsal)(thsa)]⋅0.5 THF, (3). The latter two show partial solvent loss at room temperature to yield [Fe(qsal)(thsa)]⋅0.1 MeCN (2') and [Fe(qsal)(thsa)]⋅0.1 THF (3'), respectively. This family maintains a structural integrity which is analogous over different degrees of solvation, a rare occurrence in discrete molecular species. Uniquely, removal of MeCN from compound 2 leads to retention of crystallinity yielding the isostructural, fully desolvated compound [Fe(qsal)(thsa)] (2'') and a new high spin polymorph, 4. To the best of our knowledge, this is the first compound that forms polymorphs through a desolvation process. The desolvated mixture, 2'' and 4, is porous and can reabsorb MeCN and give rise to 2' again. This illustrates the reversible single-crystal-to-single-crystal transformation of two polymorphs back to a purely original phase, 2''+4↔2'. The structural, magnetic and Mőssbauer features of the various samples are described in terms of spin crossover. PMID:26662933

  10. 5-Aminotetrazole induces spin crossover in iron(III) pentadentate Schiff base complexes: experimental and theoretical investigations.

    PubMed

    Herchel, Radovan; Trávníček, Zdeněk

    2013-12-14

    A series of novel mononuclear iron(III) complexes [Fe(saldpt)(atz)] (1) and [Fe(Rsalpet)(atz)] (2a-d) involving 5-aminotetrazole (Hatz) and pentadentate Schiff base ligands (H2saldpt = N,N'-bis(2-hydroxybenzyliden)-1,7-diamino-4-azaheptane, H2salpet = N,N'-bis(2-hydroxybenzyliden)-1,6-diamino-3-azahexane, H25Cl-salpet = N,N'-bis(5-chloro-2-hydroxybenzylidene)-1,6-diamino-3-azahexane, H25Br-salpet = N,N'-bis(5-bromo-2-hydroxybenzylidene)-1,6-diamino-3-azahexane and H23,5Br-salpet = N,N'-bis(3,5-dibromo-2-hydroxybenzylidene)-1,6-diamino-3-azahexane) was prepared and characterized by elemental analysis, FTIR spectroscopy, mass spectrometry, single crystal X-ray analysis, magnetic measurements and (57)Fe Mössbauer spectroscopy. In contrast to the high-spin magnetic properties of [Fe(saldpt)(atz)] (1), the complexes [Fe(Rsalpet)(atz)] (2a-d) undergo spin crossover with critical temperatures above 416 K. Furthermore, DFT calculations with the B3LYP functional were employed to investigate the effect of the conductor-like screening model (COSMO) and van der Waals corrections (VDW) as well as relativistic effects with the scalar relativistic second-order Douglas-Kroll-Hess Hamiltonian (DKH2) on low-spin and high-spin molecular geometries and thus on spin crossover parameters (enthalpy, entropy and critical temperature). PMID:24121719

  11. Influence of Al2O3 on the ionic conductivity of plasticized PVC-PEG blend polymer electrolytes

    NASA Astrophysics Data System (ADS)

    Ravindran, D.; Vickraman, P.

    2016-05-01

    Polymer electrolytes with PVC-PEG blend as host matrix and LiClO4 as dopant salt was prepared through conventional solution casting method. To enhance the conductivity propylene carbonate (PC) was used as plasticizer. The influence of ceramic filler Al2O3 on the conductivity of the electrolyte films were studied by varying the (PVC: Al2O3) ratio. The films were subjected to XRD, complex impedance analysis and SEM analysis. The XRD studies reveal a marginal increase in the amorphous phase of the electrolyte films due to the incorporation of filler. The AC impedance analysis shows the dependency of ionic conductivity on the content (wt %) of filler and exhibit a maximum at 4 wt% filler. The SEM analysis depicts the occurrence of phase separation in electrolyte which is attributed to the poor solubility of polymer PVC in the liquid electrolyte.

  12. Production of Laccase by Cochliobolus sp. Isolated from Plastic Dumped Soils and Their Ability to Degrade Low Molecular Weight PVC

    PubMed Central

    Sumathi, Tirupati; Sri Lakshmi, Akula; SaiGopal, D. V. R.

    2016-01-01

    One of the utmost man-made problems faced today has been the ever-increasing plastic waste filling the world. It accounts for an estimated 20–30% (by volume) of municipal solid waste in landfill sites worldwide. Research on plastic biodegradation has been steadily growing over the past four decades. Several fungi have been identified that produce enzymes capable of plastic degradation in various laboratory conditions. This paper presents a study that determined the ability of fungi to degrade low molecular weight polyvinyl chloride (PVC) by the enzyme laccase. We have isolated a fungal species, Cochliobolus sp., from plastic dumped soils and they were cultured on Czapek Dox Agar slants at 30°C. The effectiveness of this fungal species on the degradation of commercial low molecular weight polyvinyl chloride (PVC) was studied under laboratory conditions. Significant differences were observed from the FTIR, GC-MS, and SEM results in between control and Cochliobolus sp. treated PVC. PMID:27293894

  13. Production of Laccase by Cochliobolus sp. Isolated from Plastic Dumped Soils and Their Ability to Degrade Low Molecular Weight PVC.

    PubMed

    Sumathi, Tirupati; Viswanath, Buddolla; Sri Lakshmi, Akula; SaiGopal, D V R

    2016-01-01

    One of the utmost man-made problems faced today has been the ever-increasing plastic waste filling the world. It accounts for an estimated 20-30% (by volume) of municipal solid waste in landfill sites worldwide. Research on plastic biodegradation has been steadily growing over the past four decades. Several fungi have been identified that produce enzymes capable of plastic degradation in various laboratory conditions. This paper presents a study that determined the ability of fungi to degrade low molecular weight polyvinyl chloride (PVC) by the enzyme laccase. We have isolated a fungal species, Cochliobolus sp., from plastic dumped soils and they were cultured on Czapek Dox Agar slants at 30°C. The effectiveness of this fungal species on the degradation of commercial low molecular weight polyvinyl chloride (PVC) was studied under laboratory conditions. Significant differences were observed from the FTIR, GC-MS, and SEM results in between control and Cochliobolus sp. treated PVC. PMID:27293894

  14. Direct observation by laser scanning confocal microscopy of microstructure and phase migration of PVC gels in an applied electric field.

    PubMed

    Xia, Hong; Ueki, Takamitsu; Hirai, Toshihiro

    2011-02-01

    The fluorescent probe lucigenin was incorporated in poly(vinyl chloride) (PVC) gels, and laser scanning confocal microscopy (LSCM) was used to clarify the internal structures of the gels. From the two-dimensional and three-dimensional information by LSCM, we first observed the internal structure of the PVC gel at a wet status, where the PVC gels comprised a polymer-rich phase and a polymer-poor phase uniformly with a three-dimensional network structure. After an electric field was applied, an effect of the electric field resulted in the change of internal structure in the gels. The polymer-poor phase moved from the cathode to the anode and the polymer-rich phase formed linelike arrangement between electrodes due to the attraction force. On the other hand, the freeze-dried PVC gels with/without in-situ dc voltage casting were particularly fabricated to confirm above results by the field emission scanning electron microscopy (FE-SEM). It was found that many craters remained on the surface of the gel near the anode due to sublimation in freeze-drying. This phenomenon did not appear on the surface near the cathode. The results of in-situ dc voltage casting also suggested that a substantial amount of polymer-poor phase was moved and fixed at the anode. Thus, results of both LSCM and in-situ dc voltage casting corresponded to the effect of electric field on PVC gels and provided a convincing evidence for the interpretation of the deformation mechanism of PVC gel actuators by an applied electric field. PMID:21174424

  15. Recovery of copper from PVC multiwire cable waste by steam gasification.

    PubMed

    Zabłocka-Malicka, Monika; Rutkowski, Piotr; Szczepaniak, Włodzimierz

    2015-12-01

    Screened multiwire, PVC insulated tinned copper cable was gasified with steam at high temperature (HTSG) under atmospheric pressure for recovery of cooper. Gases from the process were additionally equilibrated at 850°C on the bed of calcined clay granules and more than 98% of C+H content in the cable was transformed to non-condensing species. Granules prepared from local clay were generally resistant for chlorination, there was also almost no deposition of metals, Cu and Sn, on the catalytic bed. It was found that 28% of chlorine reacted to form CaCl2, 71% was retained in aqueous condensate and only 0.6% was absorbed in alkaline scrubber. More than 99% of calcium existed in the process solid residue as a mixture of calcium chloride and calcium oxide/hydroxide. PVC and other hydrocarbon constituents were completely removed from the cable sample. Copper was preserved in original form and volatilization of copper species appeared insignificant. Tin was alloying with copper and its volatilization was less than 1%. Fractionation and speciation of metals, chlorine and calcium were discussed on the basis of equilibrium model calculated with HSC Chemistry software. High temperature steam gasification prevents direct use of the air and steam/water is in the process simultaneously gaseous carrier and reagent, which may be recycled together with hydrocarbon condensates. PMID:26282888

  16. Determination of the Composition and Quantity of Phthalate Ester Additives in PVC Children's Toys. Greenpeace Research Laboratories Technical Note 06/97.

    ERIC Educational Resources Information Center

    Stringer, Ruth; Labounskaia, Irina; Santillo, David; Johnston, Paul; Siddorn, John; Stephenson, Angela

    Polyvinyl chloride (vinyl or PVC) is widely used in toys and other children's products. This study, conducted by Greenpeace, examined the composition and quantity of phthalate ester additives in children's PVC toys, used to give the toys added flexibility. Drawn from 17 countries, a total of 71 toys designed to be chewed by babies and young…

  17. Membrane stabilizer

    DOEpatents

    Mingenbach, William A.

    1988-01-01

    A device is provided for stabilizing a flexible membrane secured within a frame, wherein a plurality of elongated arms are disposed radially from a central hub which penetrates the membrane, said arms imposing alternately against opposite sides of the membrane, thus warping and tensioning the membrane into a condition of improved stability. The membrane may be an opaque or translucent sheet or other material.

  18. The Pseudomonas aeruginosa extracellular secondary metabolite, Paerucumarin, chelates iron and is not localized to extracellular membrane vesicles.

    PubMed

    Qaisar, Uzma; Kruczek, Cassandra J; Azeem, Muhammed; Javaid, Nasir; Colmer-Hamood, Jane A; Hamood, Abdul N

    2016-08-01

    Proteins encoded by the Pseudomonas aeruginosa pvcA-D operon synthesize a novel isonitrile functionalized cumarin termed paerucumarin. The pvcA-D operon enhances the expression of the P. aeruginosa fimbrial chaperone/usher pathway (cup) genes and this effect is mediated through paerucumarin. Whether pvcA-D and/or paerucumarin affect the expression of other P. aeruginosa genes is not known. In this study, we examined the effect of a mutation in pvcA-D operon the global transcriptome of the P. aeruginosa strain PAO1-UW. The mutation reduced the expression of several ironcontrolled genes including pvdS, which is essential for the expression of the pyoverdine genes. Additional transcriptional studies showed that the pvcA-D operon is not regulated by iron. Exogenously added paerucumarin enhanced pyoverdine production and pvdS expression in PAO1-UW. Iron-chelation experiments revealed that purified paerucumarin chelates iron. However, exogenously added paerucumarin significantly reduced the growth of a P. aeruginosa mutant defective in pyoverdine and pyochelin production. In contrast to other secondary metabolite, Pseudomonas quinolone signal (PQS), paerucumarin is not localized to the P. aeruginosa membrane vesicles. These results suggest that paerucumarin enhances the expression of iron-controlled genes by chelating iron within the P. aeruginosa extracellular environment. Although paerucumarin chelates iron, it does not function as a siderophore. Unlike PQS, paerucumarin is not associated with the P. aeruginosa cell envelope. PMID:27480638

  19. Pyochelin, a siderophore of Pseudomonas aeruginosa: physicochemical characterization of the iron(III), copper(II) and zinc(II) complexes.

    PubMed

    Brandel, Jérémy; Humbert, Nicolas; Elhabiri, Mourad; Schalk, Isabelle J; Mislin, Gaëtan L A; Albrecht-Gary, Anne-Marie

    2012-03-01

    Pseudomonas aeruginosa is an opportunistic pathogen, synthesizing two major siderophores, pyoverdine (Pvd) and pyochelin (Pch), to cover its needs in iron(III). If the high affinity and specificity of Pvd toward iron(III) (pFe = 27.0) was well described in the literature, the physicochemical and coordination properties of Pch toward biologically relevant metals (Fe(III), Cu(II) or Zn(II)) have been only scarcely investigated. We report a thorough physico-chemical investigation of Pch (potentiometry, spectrophotometries, ESI/MS) that highlighted its moderate but significantly higher affinity for Fe(3+) (pFe = 16.0 at p[H] 7.4) than reported previously. We also demonstrated that Pch strongly chelates divalent metals such as Zn(II) (pZn = 11.8 at p[H] 7.4) and Cu(II) (pCu = 14.9 at p[H] 7.4) and forms predominantly 1 : 2 (M(2+)/Pch) complexes. Kinetic studies revealed that the formation of the ferric Pch complexes proceeds through a Eigen-Wilkins dissociative ligand interchange mechanism involving two protonated species of Pch and the Fe(OH)(2+) species of Fe(III). Our physico-chemical parameters supports the previous biochemical studies which proposed that siderophores are not only devoted to iron(III) shuttling but most likely display other specific biological role in the subtle metals homeostasis in microorganisms. This work also represents a step toward deciphering the role of siderophores throughout evolution. PMID:22261733

  20. NMR Investigation of beta-Substituted High-Spin and Low-Spin Iron(III) Tetraphenylporphyrins.

    PubMed

    Wojaczynski, Jacek; Latos-Grazynski, Lechoslaw; Hrycyk, Witold; Pacholska, Ewa; Rachlewicz, Krystyna; Szterenberg, Ludmila

    1996-11-01

    The NMR spectra of a series of beta-substituted iron(III) tetraphenylporphyrin (2-X-TPP) complexes have been studied to elucidate the relationship between the electron donating/withdrawing properties of the 2-substituent and the (1)H NMR spectral pattern. The electronic nature of the substituent has been significantly varied and covered the -0.6 to 0.8 Hammett constant range. Both high-spin and low-spin complexes of the general formula (2-X-TPP)Fe(III)Cl and [(2-X-TPP)Fe(III)(CN)(2)](-) have been investigated. The (1)H NMR data for the following substituents (X) have been reported: py(+), NO(2), CN, CH(3), BzO (C(6)H(5)COO), H, D, Br, Cl, CH(3), NH(2), NH(3)(+), NHCH(3), OH, and O(-). The (1)H NMR resonances for low-spin dicyano complexes have been completely assigned by a combination of two-dimensional COSY and NOESY experiments. In the case of selected high-spin complexes, the 3-H resonance has been identified by the selective deuteration of all but the 3-H position. The pattern of unambiguously assigned seven pyrrole resonances reflects the asymmetry imposed by 2-substitution and has been used as an unique (1)H NMR spectroscopic probe to map the spin density distribution. The pyrrole isotropic shifts of [(2-X-TPP)Fe(III)(CN)(2)](-) are dominated by the contact term. In order to quantify the substituent effect, the dependence of isotropic shift of all low-spin pyrrole resonances and 3-H high-spin pyrrole resonance versus Hammett constants has been studied. The electronic effect is strongly localized at the beta-substituted pyrrole. The major change of the isotropic shift has also been noted for only one of two adjacent pyrrole rings, i.e., at 7-H and 8-H positions. These neighboring protons, located on a single pyrrole ring, experienced opposite shift changes when electron withdrawing/donating properties were modified. Two other pyrrole rings for all investigated derivatives revealed considerably smaller, substituent related, isotropic shift changes. A long

  1. Lead exposure in the lead-acid storage battery manufacturing and PVC compounding industries.

    PubMed

    Ho, S F; Sam, C T; Embi, G B

    1998-09-01

    This study was conducted as part of the Human Exposure Assessment Location (HEAL) Project which comes under the United Nations Environment Programme/World Health Organisation (UNEP/WHO) Global environmental Monitoring System (GEMS). The objective of the study was to evaluate workers' exposure to lead in industries with the highest exposure. All subjects were interviewed about their occupational and smoking histories, the use of personal protective equipment and personal hygiene. The contribution of a dietary source of lead intake from specified foods known to contain lead locally and personal air sampling for lead were assessed. A total of 61 workers from two PVC compounding and 50 workers from two lead acid battery manufacturing plants were studied together with 111 matched controls. In the PVC compounding plants the mean lead-in-air level was 0.0357 mg/m3, with the highest levels occurring during the pouring and mixing operations. This was lower than the mean lead-in-air level of 0.0886 mg/m3 in the lead battery manufacturing plants where the highest exposure was in the loading of lead ingots into milling machines. Workers in lead battery manufacturing had significantly higher mean blood lead than the PVC workers (means, 32.51 and 23.91 mcg/100 ml respectively), but there was poor correlation with lead-in-air levels. Among the lead workers, the Malays had significantly higher blood lead levels than the Chinese (mean blood levels were 33.03 and 25.35 mcg/100 ml respectively) although there was no significant difference between the two ethnic groups in the control group. There were no significant differences between the exposed and control group in terms of dietary intake of specified local foods known to contain lead. However, Malays consumed significantly more fish than the Chinese did. There were no ethnic differences in the hours of overtime work, number of years of exposure, usage of gloves and respirators and smoking habits. Among the Malays, 94.3% eat with

  2. Forensic utility of carbon isotope ratio variations in PVC tape backings.

    PubMed

    Dietz, Marianne E; Stern, Libby A; Mehltretter, Andria Hobbs; Parish, Ashley; McLasky, Velvet; Aranda, Roman

    2012-03-01

    Forensic interest in adhesive tapes with polyvinyl chloride (PVC) backings (electrical tape) derives from their use in a variety of illicit activities. Due to the range of physical characteristics, chemical compositions, and homogeneity within a single roll of tape, traditional microscopic and chemical analyses can offer a high degree of discrimination between tapes, permitting the assessment of potential associations between evidentiary tape samples. The carbon isotope ratios of tapes could provide additional discrimination among tape samples. To evaluate whether carbon isotope ratios may be able to increase discrimination of electrical tapes, particularly with regards to different rolls of tape of the same product, we assessed the δ(13)C values of backings from 87 rolls of PVC-based black electrical tape (~20 brands, >60 products) Prior to analysis, adhesives were removed to prevent contamination by adhering debris, and plasticizers were extracted because of concern over their potential mobility. This result is consistent with each of these tapes having approximately the same plasticizer δ(13)C value and proportion of carbon in these plasticizers. The δ(13)C values of the 87 PVC tape backings ranged between -23.5 and -41.3 (‰, V-PDB), with negligible carbon isotopic variation within single rolls of tape, yet large variations among tape brands and tape products. Within this tape population, carbon isotope ratios permitted an average exclusion power of 93.7%, using a window of +/-0.3‰; the combination of carbon isotope ratio measurement with additional chemical and physical analyses raises the discrimination power to over 98.9%, with only 41 out of a possible 3741 pairs of tape samples being indistinguishable. There was a linear relationship between the δ(13)C value of tape backings and the change in δ(13)C value with the extraction of plasticizers. Analyses of pre- and post-blast tape sample pairs show that carbon isotope signatures are within 0.3‰ of

  3. sup 1 H nuclear magnetic resonance studies of the reduction of paramagnetic iron(III) alkyl porphyrin complexes to diamagnetic iron(II) alkyl complexes

    SciTech Connect

    Balch, A.L.; Cornman, C.R.; Safari, N. ); Latos-Grazynski, L. )

    1990-09-01

    Reaction of (TPP)Fe{sup III}Cl in dichloromethane with LiHBEt{sub 3} yields (TPP)Fe{sup III}Et. Reduction of (TPP)Fe{sup III}R to ((TPP)Fe{sup II}R){sup {minus}} (R = n-propyl, ethyl) by either LiHBEt{sub 3} or KHB(i-Bu){sub 3} can be accomplished in benzene/tetrahydrofuran solution, where electron exchange between the iron(III) and iron(II) alkyls is rapid. ((TPP)Fe{sup II}R){sup {minus}} is diamagnetic and is reoxidized by dioxygen by (TPP)Fe{sup III}R.

  4. Ferrate(VI)-induced arsenite and arsenate removal by in situ structural incorporation into magnetic iron(III) oxide nanoparticles.

    PubMed

    Prucek, Robert; Tuček, Jiří; Kolařík, Jan; Filip, Jan; Marušák, Zdeněk; Sharma, Virender K; Zbořil, Radek

    2013-04-01

    We report the first example of arsenite and arsenate removal from water by incorporation of arsenic into the structure of nanocrystalline iron(III) oxide. Specifically, we show the capability to trap arsenic into the crystal structure of γ-Fe2O3 nanoparticles that are in situ formed during treatment of arsenic-bearing water with ferrate(VI). In water, decomposition of potassium ferrate(VI) yields nanoparticles having core-shell nanoarchitecture with a γ-Fe2O3 core and a γ-FeOOH shell. High-resolution X-ray photoelectron spectroscopy and in-field (57)Fe Mössbauer spectroscopy give unambiguous evidence that a significant portion of arsenic is embedded in the tetrahedral sites of the γ-Fe2O3 spinel structure. Microscopic observations also demonstrate the principal effect of As doping on crystal growth as reflected by considerably reduced average particle size and narrower size distribution of the "in-situ" sample with the embedded arsenic compared to the "ex-situ" sample with arsenic exclusively sorbed on the iron oxide nanoparticle surface. Generally, presented results highlight ferrate(VI) as one of the most promising candidates for advanced technologies of arsenic treatment mainly due to its environmentally friendly character, in situ applicability for treatment of both arsenites and arsenates, and contrary to all known competitive technologies, firmly bound part of arsenic preventing its leaching back to the environment. Moreover, As-containing γ-Fe2O3 nanoparticles are strongly magnetic allowing their separation from the environment by application of an external magnet. PMID:23451768

  5. Surfactant-Assisted Nanodrop Spectrophotometer Determination of Iron(III) in a Single Drop of Food, Biological, and Environmental Samples

    NASA Astrophysics Data System (ADS)

    Sharma, A.; Tapadia, K.; Sahin, R.; Shrivas, K.

    2016-01-01

    A surfactant-assisted nanodrop spectrophotometric (NDS) method has been developed for the determination of the iron(III) content in single drops (1 μ L) of food, biological, and or environmental sample using disodium 1-nitroso-2-naphthol-3,6-sulfonate (Nitroso-R salt) as a complexing agent and Tween-80 as non-ionic surfactant at pH 4.0. This method is based on the formation of a complex between the Fe(III) present in a sample and the Nitroso-R-salt in the presence of a surfactant to form a green-colored Fe(III)-Nitroso-R salt complex, which can be measured using a NDS method at a λ max = 710 nm. This system was found to obey Beer's law at concentrations in the range of 50-5000 μ g/L with slope, intercept and correlation coefficient values of 0.683, 0.102, and 0.986, respectively. The molar absorptivity of the complex in terms of the Fe(III) content was determined to be 4.86 × 10 5 L· mol -1 · cm -1 . The detection limit and %RSD values of the method were found to be 17 × 10-3 mg/L and ±1.3706%, respectively. This newly developed method was successfully applied to the determination of the Fe(III) content in single drops of food, biological, and environmental samples, and the results were compared with those obtained by atomic absorption spectrometry.

  6. Reaction mechanism for the highly efficient catalytic decomposition of peroxynitrite by the amphipolar iron(III) corrole 1-Fe.

    PubMed

    Avidan-Shlomovich, Shlomit; Gross, Zeev

    2015-07-21

    The amphipolar iron(III) corrole 1-Fe is one of the most efficient catalysts for the decomposition of peroxynitrite, the toxin involved in numerous diseases. This research focused on the mechanism of that reaction at physiological pH, where peroxynitrite is in equilibrium with its much more reactive conjugated acid, by focusing on the elementary steps involved in the catalytic cycle. Kinetic investigations uncovered the formation of a reaction intermediate in a process that is complete within a few milliseconds (k1 ∼ 3 × 10(7) M(-1) s(-1) at 5 °C, about 7 orders of magnitude larger than the first order rate constant for the non-catalyzed process). Multiple evidence points towards iron-catalyzed homolytic O-O bond cleavage to form nitrogen dioxide and hydroxo- or oxo-iron(iv) corrole. The iron(iv) intermediate was found to decay via multiple pathways that proceed at similar rates (k2 about 10(6) M(-1) s(-1)): reaction with nitrogen dioxide to form nitrate, nitration of the corrole macrocyclic, and dimerization to binuclear iron(iv) corrole. Catalysis in the presence of substrates affects the decay of the iron intermediate by either oxidative nitration (phenolic substrates) or reduction (ascorbate). A large enough excess of ascorbate accelerates the catalytic decomposition of PN by 1-Fe by orders of magnitude, prevents other decay routes of the iron intermediate, and eliminates nitration products as well. This suggests that the beneficial effect of the iron corrole under the reducing conditions present in most biological media might be even larger than in the purely chemical system. The acquired mechanistic insight is of prime importance for the design of optimally acting catalysts for the fast and safe decomposition of reactive oxygen and nitrogen species. PMID:25747957

  7. Microbiological safety of household membrane water filter.

    PubMed

    Zhang, Yongli; Wang, Qing; Lou, Wei; Wang, Yuxin; Zhu, Xuan

    2013-04-01

    Waterborne pathogens outbreaks are major reasons of diarrhea disease worldwide. Detecting and monitoring emerging waterborne pathogens (EWPs) is important for drinking water microbiological safety. The microbiological safety of household water hollow fiber membrane filter which is the end of drinking water treatment process was studied with heterotrophic plate count (HPC) and real-time PCR method. The effect of the flow rate, idle time and washing fashion were investigated. Among the selected filters from three manufacturers, only the PVDF membrane water filter (Brand B) could achieve a good water purification criteria. Brand A was found a certain degree of EWPs in its effluent. The lowest bacteria-removing efficiency of the PVC membrane water filter was found Brand C. Our study showed that the microorganisms could reach up to 10(6) CFU ml(-1) and the 16s rDNA could reach up to 10(6) copies ml(-1) in the initial filtrate of Brand C. More species and amounts of EWPs were detected in the washing water. These results suggested that the popular household membrane filters might cause microbiological risks at certain circumstances such as the shock load of EWPs and leakage of the membranes in the case of abnormal source water or poor membrane filter quality. PMID:24620621

  8. Studying DEHP migration in plasticized PVC used for blood bags by coupling Raman confocal microscopy to UV spectroscopy.

    PubMed

    Al Salloum, H; Saunier, J; Tfayli, A; Yagoubi, N

    2016-04-01

    Plasticized PVC is widely used to make medical devices such as tubing, perfusion bags and blood bags. By using confocal Raman microscopy on a PVC sheet plasticized with around 40% of di-(2-ethylhexyl)phthalate (DEHP), we propose a simple and sensitive approach to studying and understanding the diffusion of plasticizers from polymers into the surrounding media. Moreover, we sought to correlate our findings to standard measurements conducted by UV spectroscopy. This study showed differences in the concentration gradient observed due to the diffusion of the plasticizer inside a PVC sheet. We can thus follow the critical DEHP ratios that can impact the diffusion process. Water and ethanol were chosen as storage media: in ethanol, the lowest concentration of DEHP was observed at the surface resulting in the formation of a less plasticized layer near the interface; unlike ethanol, PVC sheets stored in water showed a greater concentration of DEHP on the film surface as an exudation of DEHP onto the surface. PMID:26838824

  9. Roles of ionic strength and biofilm roughness on adhesion kinetics of Escherichia coli onto groundwater biofilm grown on PVC surfaces

    PubMed Central

    Janjaroen, Dao; Ling, Fangqiong; Monroy, Guillermo; Derlon, Nicolas; Mogenroth, Eberhard; Boppart, Stephen A.; Liu, Wen-Tso; Nguyen, Thanh H.

    2013-01-01

    Mechanisms of Escherichia coli attachment on biofilms grown on PVC coupons were investigated. Biofilms were grown in CDC reactors using groundwater as feed solution over a period up to 27 weeks. Biofilm physical structure was characterized at the micro- and meso-scales using Scanning Electron Microscopy (SEM) and Optical Coherence Tomography (OCT), respectively. Microbial community diversity was analyzed with Terminal Restricted Fragment Length Polymorphism (T-RFLP). Both physical structure and microbial community diversity of the biofilms were shown to be changing from 2 weeks to 14 weeks, and became relatively stable after 16 weeks. A parallel plate flow chamber coupled with an inverted fluorescent microscope was also used to monitor the attachment of fluorescent microspheres and E. coli on clean PVC surfaces and biofilms grown on PVC surfaces for different ages. Two mechanisms of E. coli attachment were identified. The adhesion rate coefficients (kd) of E. coli on nascent PVC surfaces and 2-week biofilms increased with ionic strength. However, after biofilms grew for 8 weeks, the adhesion was found to be independent of solution chemistry. Instead, a positive correlation between kd and biofilm roughness as determined by OCT was obtained, indicating that the physical structure of biofilms could play an important role in facilitating the adhesion of E. coli cells. PMID:23497979

  10. Ag+-sensitive membranes for electrochemical and optical sensors

    NASA Astrophysics Data System (ADS)

    Wroblewski, Wojciech; Dybko, Artur; Rozniecka, Ewa; Brzozka, Zbigniew

    1999-04-01

    The paper is focused on lipophilic acyclic thioethers as neutral ionophores for heavy-metals cations. Membranes based on plasticized PVC containing these carriers exhibited high selectivity toward silver cations over transition metal ions (log KAgM < -4.5) except mercury ions. Membrane containing the ionophore II (with l-naphtyl pendant group) was used to design silver-selective ISE which shows linear response in the range 3 - 6 pAg with a slope of 51.5 mV/pAg. The addition of the pH chromoionophore to the membrane composition allowed to obtain a silver-sensitive optrode membrane, responding in the concentration range 0.01 - 1 mM Ag+.

  11. Parameter optimization of nanosecond laser for microdrilling on PVC by Taguchi method

    NASA Astrophysics Data System (ADS)

    Canel, Timur; Kaya, A. Uğur; Çelik, Bekir

    2012-11-01

    Formation of cavities having maximum aspect ratio (depth-to-width (D/W) ratio) on PVC during laser drilling has several undesirable outcomes with regard to cavity quality. Hence it is essential to select optimum drilling process parameters to maximize aspect ratio and minimize Heat Affected Zone (HAZ) and circularity. This paper presents application of the Taguchi optimization method to obtain cavities possessing maximum aspect ratio influenced by drilling conditions such as wavelength, fluence and frequency. In the present work, the effects of laser processing parameters, including laser fluence, laser frequency and wavelength were investigated in relation to the aspect ratio, HAZ and circularity. Then the optimal values of wavelength, fluence and frequency were determined. According to the result of the confirmation experiment using optimum parameters, it was observed that experimental results were compatible with Taguchi method with 93% rate. The details of experimentation analysis and analysis of variance are presented in this paper.

  12. Reduced adhesion of Staphylococcus aureus to ZnO/PVC nanocomposites

    PubMed Central

    Geilich, Benjamin M; Webster, Thomas J

    2013-01-01

    In hospitals and clinics worldwide, medical device surfaces have become a rapidly growing source of nosocomial infections. In particular, patients requiring mechanical ventilation (and, thus, intubation with an endotracheal tube) for extended lengths of time are faced with a high probability of contracting ventilator-associated pneumonia. Once inserted into the body, the endotracheal tube provides a surface to which bacteria can adhere and form a biofilm (a robust, sticky matrix that provides protection against the host immune system and antibiotic treatment). Adding to the severity of this problem is the spread of bacterial genetic tolerance to antibiotics, in part demonstrated by the recent and significant increase in the prevalence of methicillin-resistant Staphylococcus aureus. To combat these trends, different techniques in biomaterial design must be explored. Recent research has shown that nanomaterials (materials with at least one dimension less than 100 nm) may have the potential to prevent or disrupt bacterial processes that lead to infections. In this study, polyvinyl chloride (PVC) taken from a conventional endotracheal tube was embedded with varying concentrations of zinc oxide (ZnO) nanoparticles. S. aureus biofilms were then grown on these nanocomposite surfaces during a 24-hour culture. Following this, biofilms were removed from the surfaces and the number of colony forming units present was assessed. Bacterial proliferation on the samples embedded with the highest concentration of ZnO nanoparticles was 87% less when compared to the control, indicating that this technique is effective at reducing biofilm formation on PVC surfaces without the use of antibiotics. PMID:23658484

  13. Molecular Signatures for the PVC Clade (Planctomycetes, Verrucomicrobia, Chlamydiae, and Lentisphaerae) of Bacteria Provide Insights into Their Evolutionary Relationships.

    PubMed

    Gupta, Radhey S; Bhandari, Vaibhav; Naushad, Hafiz Sohail

    2012-01-01

    The PVC superphylum is an amalgamation of species from the phyla Planctomycetes, Verrucomicrobia, and Chlamydiae, along with the Lentisphaerae, Poribacteria, and two other candidate divisions. The diverse species of this superphylum lack any significant marker that differentiates them from other bacteria. Recently, genome sequences for 37 species covering all of the main PVC groups of bacteria have become available. We have used these sequences to construct a phylogenetic tree based upon concatenated sequences for 16 proteins and identify molecular signatures in protein sequences that are specific for the species from these phyla or those providing molecular links among them. Of the useful molecular markers identified in the present work, six conserved signature indels (CSIs) in the proteins Cyt c oxidase, UvrD helicase, urease, and a helicase-domain containing protein are specific for the species from the Verrucomicrobia phylum; three other CSIs in an ABC transporter protein, cobyrinic acid ac-diamide synthase, and SpoVG protein are specific for the Planctomycetes species. Additionally, a 3 aa insert in the RpoB protein is uniquely present in all sequenced Chlamydiae, Verrucomicrobia, and Lentisphaerae species, providing evidence for the shared ancestry of the species from these three phyla. Lastly, we have also identified a conserved protein of unknown function that is exclusively found in all sequenced species from the phyla Chlamydiae, Verrucomicrobia, Lentisphaerae, and Planctomycetes suggesting a specific linkage among them. The absence of this protein in Poribacteria, which branches separately from other members of the PVC clade, indicates that it is not specifically related to the PVC clade of bacteria. The molecular markers described here in addition to clarifying the evolutionary relationships among the PVC clade of bacteria also provide novel tools for their identification and for genetic and biochemical studies on these organisms. PMID:23060863

  14. Identification and quantification of 14 phthalates and 5 non-phthalate plasticizers in PVC medical devices by GC-MS.

    PubMed

    Gimeno, Pascal; Thomas, Sébastien; Bousquet, Claudine; Maggio, Annie-Françoise; Civade, Corinne; Brenier, Charlotte; Bonnet, Pierre-Antoine

    2014-02-15

    A GC/MS method was developed for the identification and quantification of 14 phthalates: 8 phthalates classified H360 (DBP, DEHP, BBP, DMEP, DnPP, DiPP, DPP and DiBP), 3 phthalates proposed to be forbidden in medical devices (DnOP, DiNP and DiDP) and 3 other phthalates none regulated (DMP, DCHP and DEP) which may interfere with hormone function. In order to identify and quantify other plasticizers that are commonly used in PVC medical devices such as DEHP substitute, 5 non-phthalate plasticizers (ATBC, DEHA, DEHT, TOTM, and DINCH) were included in this study. Analyses are carried out on a GC/MS system with electron impact ionization mode (EI). The separation of plasticizers is obtained on a cross-linked 5%-phenyl/95%-dimethylpolysiloxane capillary column 30m×0.25mm (i.d.)×0.25μm film thickness using a gradient temperature. Compounds quantification is performed by external calibration using an internal standard. Validation elements on standard solutions were determined using the ISO 12787 standard approach. Plasticizers are extracted from PVC medical devices using THF for dissolving the PVC part of the sample followed by precipitation of the PVC by addition of ethanol. The supernatant is injected into a GC/MS system after dilution in ethanol. Different validation elements, including extraction recoveries for all compounds or for DEHP a cross-validation of the extraction process using the European pharmacopoeia monograph 3.1.14 as reference method, are discussed. Results obtained on 61 medical devices in PVC and 12 raw materials used as plasticizers are given. PMID:24480330

  15. Molecular Signatures for the PVC Clade (Planctomycetes, Verrucomicrobia, Chlamydiae, and Lentisphaerae) of Bacteria Provide Insights into Their Evolutionary Relationships

    PubMed Central

    Gupta, Radhey S.; Bhandari, Vaibhav; Naushad, Hafiz Sohail

    2012-01-01

    The PVC superphylum is an amalgamation of species from the phyla Planctomycetes, Verrucomicrobia, and Chlamydiae, along with the Lentisphaerae, Poribacteria, and two other candidate divisions. The diverse species of this superphylum lack any significant marker that differentiates them from other bacteria. Recently, genome sequences for 37 species covering all of the main PVC groups of bacteria have become available. We have used these sequences to construct a phylogenetic tree based upon concatenated sequences for 16 proteins and identify molecular signatures in protein sequences that are specific for the species from these phyla or those providing molecular links among them. Of the useful molecular markers identified in the present work, six conserved signature indels (CSIs) in the proteins Cyt c oxidase, UvrD helicase, urease, and a helicase-domain containing protein are specific for the species from the Verrucomicrobia phylum; three other CSIs in an ABC transporter protein, cobyrinic acid ac-diamide synthase, and SpoVG protein are specific for the Planctomycetes species. Additionally, a 3 aa insert in the RpoB protein is uniquely present in all sequenced Chlamydiae, Verrucomicrobia, and Lentisphaerae species, providing evidence for the shared ancestry of the species from these three phyla. Lastly, we have also identified a conserved protein of unknown function that is exclusively found in all sequenced species from the phyla Chlamydiae, Verrucomicrobia, Lentisphaerae, and Planctomycetes suggesting a specific linkage among them. The absence of this protein in Poribacteria, which branches separately from other members of the PVC clade, indicates that it is not specifically related to the PVC clade of bacteria. The molecular markers described here in addition to clarifying the evolutionary relationships among the PVC clade of bacteria also provide novel tools for their identification and for genetic and biochemical studies on these organisms. PMID:23060863

  16. Discoloration of polyvinyl chloride (PVC) tape as a proxy for water-table depth in peatlands: validation and assessment of seasonal variability

    USGS Publications Warehouse

    Booth, Robert K.; Hotchkiss, Sara C.; Wilcox, Douglas A.

    2005-01-01

    Summary: 1. Discoloration of polyvinyl chloride (PVC) tape has been used in peatland ecological and hydrological studies as an inexpensive way to monitor changes in water-table depth and reducing conditions. 2. We investigated the relationship between depth of PVC tape discoloration and measured water-table depth at monthly time steps during the growing season within nine kettle peatlands of northern Wisconsin. Our specific objectives were to: (1) determine if PVC discoloration is an accurate method of inferring water-table depth in Sphagnum-dominated kettle peatlands of the region; (2) assess seasonal variability in the accuracy of the method; and (3) determine if systematic differences in accuracy occurred among microhabitats, PVC tape colour and peatlands. 3. Our results indicated that PVC tape discoloration can be used to describe gradients of water-table depth in kettle peatlands. However, accuracy differed among the peatlands studied, and was systematically biased in early spring and late summer/autumn. Regardless of the month when the tape was installed, the highest elevations of PVC tape discoloration showed the strongest correlation with midsummer (around July) water-table depth and average water-table depth during the growing season. 4. The PVC tape discoloration method should be used cautiously when precise estimates are needed of seasonal changes in the water-table.

  17. Development of a pH sensing membrane electrode based on a new calix[4]arene derivative.

    PubMed

    Kormalı Ertürün, H Elif; Demirel Özel, Ayça; Sayın, Serkan; Yılmaz, Mustafa; Kılıç, Esma

    2015-01-01

    A new pH sensing poly(vinyl chloride) (PVC) membrane electrode was developed by using recently synthesized 5,17-bis(4-benzylpiperidine-1-yl)methyl-25,26,27,28-tetrahydroxy calix[4]arene as an ionophore. The effects of membrane composition, inner filling solution and conditioning solution on the potential response of the proposed pH sensing membrane electrode were investigated. An optimum membrane composition of 3% ionophore, 67% o-nitrophenyl octyl ether (o-NPOE) as plasticizer, 30% PVC was found. The electrode exhibited a near-Nernstian slope of 58.7±1.1 mV pH(-1) in the pH range 1.9-12.7 at 20±1 °C. It showed good selectivity for H(+) ions in the presence of some cations and anions and a longer lifetime of at least 12 months when compared with the other PVC membrane pH electrodes reported in the literature. Having a wide working pH range, it was not only applied as a potentiometric indicator electrode in various acid-base titrations, but also successfully employed in different real samples. It has good reproducibility and repeatability with a response time of 6-7s. Compared to traditional glass pH electrode, it exhibited excellent potentiometric response after being used in fluoride-containing media. PMID:25476362

  18. Iron(III) complex of N-phenylethylenediamine derivative of amine bis(phenol) ligand as model for catechol dioxygenase: Synthesis, characterization and complexation studies

    NASA Astrophysics Data System (ADS)

    Poureskandari, Maryam; Safaei, Elham; Maryam Sajjadi, S.; Karimpour, Touraj; Jaglicic, Zvonko; Lee, Yong-Ill

    2015-08-01

    A new amine bis(phenol) ligand (HLPEA), was synthesized and characterized by IR, 1H NMR spectroscopic techniques and elemental analyses. The mononuclear iron(III) complex (FeLPEA) of this ligand has been prepared and characterized by IR and UV-Vis spectroscopic techniques, ESI-MS, elemental analyses and magnetic susceptibility studies. The molecular mass of complex was determined by ESI-MS which is corresponding to a mononuclear iron(III) complex consist of amine bis(phenolate) ligand coordinated to Fe(III) including chlorine atoms and solvent molecule. The variable temperature magnetic susceptibility indicates paramagnetic character of complex. To determine the formation constant of the complex, multivariate hard modeling method was applied on spectral data collected throughout the titration of Fe(III) with ligand. FeLPEA shows good catalytic activity in cleavage oxygenation of 3,5-di-tert-butyl catechol in the presence of dioxygen at room temperature with a nearly complete conversion and particularly extradiol cleavage mechanism.

  19. Membrane stabilizer

    DOEpatents

    Mingenbach, W.A.

    1988-02-09

    A device is provided for stabilizing a flexible membrane secured within a frame, wherein a plurality of elongated arms are disposed radially from a central hub which penetrates the membrane, said arms imposing alternately against opposite sides of the membrane, thus warping and tensioning the membrane into a condition of improved stability. The membrane may be an opaque or translucent sheet or other material. 10 figs.

  20. Investigation into the sorption of nitroglycerin and diazepam into PVC tubes and alternative tube materials during application.

    PubMed

    Treleano, Anna; Wolz, Gerd; Brandsch, Rainer; Welle, Frank

    2009-03-18

    Plastic bags and tubes are increasingly used for the storage and application of pharmaceutical formulations. The most common polymer material for drug application sets is plasticized poly(vinylchloride) (PVC). During application of pharmaceutical drug solution through PVC tubes, the polymer and the contact media interact which leads to leaching out of polymer additives or sorption of ingredients of the drug solution. Whereas the discussion of leaching of plasticizers is focussed on the toxicological properties of a drug packaging system, the sorption of drug formulation compounds has an influence on the dosage of the active pharmaceutical ingredient resulting in a reduced drug delivery to the patient. Therefore sorption has an influence on the effectiveness and success of the therapy. Within the study, the concentration profiles of nitroglycerin and diazepam solutions were determined after pumping the solutions through infusion administration sets. The study includes plasticized PVC tubes with different plasticizers (DEHP, DEHA, DEHT, TEHTM, DINCH, poly adipate), PVC (DEHP) tubes with different shore hardness as well as alternative polymer materials like EVA, TPE, PUR, silicone, LDPE and PP. From the experimental concentration curves it could be shown, that in the first minutes of the application of the drug solution the sorption of the active compound is at its maximum, resulting in the lowest concentration in the applied pharmaceutical solution. For a PVC tube with DEHP as plasticizer and a shore hardness of 80 only about 57% of the initial nitroglycerin concentration in the solution is applied to the patient in the first minutes of the application. For PVC tube (DEHP, shore 80) the experimental data were simulated using mathematical diffusion models. The concentration profiles during application could be well simulated using the partition coefficient K=50 (nitroglycerin) and K=300 (diazepam), respectively. However, the experimental results indicate, that the

  1. Miniaturizable Ion-Selective Arrays Based on Highly Stable Polymer Membranes for Biomedical Applications

    PubMed Central

    Mir, Mònica; Lugo, Roberto; Tahirbegi, Islam Bogachan; Samitier, Josep

    2014-01-01

    Poly(vinylchloride) (PVC) is the most common polymer matrix used in the fabrication of ion-selective electrodes (ISEs). However, the surfaces of PVC-based sensors have been reported to show membrane instability. In an attempt to overcome this limitation, here we developed two alternative methods for the preparation of highly stable and robust ion-selective sensors. These platforms are based on the selective electropolymerization of poly(3,4-ethylenedioxythiophene) (PEDOT), where the sulfur atoms contained in the polymer covalently interact with the gold electrode, also permitting controlled selective attachment on a miniaturized electrode in an array format. This platform sensor was improved with the crosslinking of the membrane compounds with poly(ethyleneglycol) diglycidyl ether (PEG), thus also increasing the biocompatibility of the sensor. The resulting ISE membranes showed faster signal stabilization of the sensor response compared with that of the PVC matrix and also better reproducibility and stability, thus making these platforms highly suitable candidates for the manufacture of robust implantable sensors. PMID:24999717

  2. Miniaturizable ion-selective arrays based on highly stable polymer membranes for biomedical applications.

    PubMed

    Mir, Mònica; Lugo, Roberto; Tahirbegi, Islam Bogachan; Samitier, Josep

    2014-01-01

    Poly(vinylchloride) (PVC) is the most common polymer matrix used in the fabrication of ion-selective electrodes (ISEs). However, the surfaces of PVC-based sensors have been reported to show membrane instability. In an attempt to overcome this limitation, here we developed two alternative methods for the preparation of highly stable and robust ion-selective sensors. These platforms are based on the selective electropolymerization of poly(3,4-ethylenedioxythiophene) (PEDOT), where the sulfur atoms contained in the polymer covalently interact with the gold electrode, also permitting controlled selective attachment on a miniaturized electrode in an array format. This platform sensor was improved with the crosslinking of the membrane compounds with poly(ethyleneglycol) diglycidyl ether (PEG), thus also increasing the biocompatibility of the sensor. The resulting ISE membranes showed faster signal stabilization of the sensor response compared with that of the PVC matrix and also better reproducibility and stability, thus making these platforms highly suitable candidates for the manufacture of robust implantable sensors. PMID:24999717

  3. Spectroscopic and Theoretical Study of Spin-Dependent Electron Transfer in an Iron(III) Superoxo Complex.

    PubMed

    Stout, Heather D; Kleespies, Scott T; Chiang, Chien-Wei; Lee, Way-Zen; Que, Lawrence; Münck, Eckard; Bominaar, Emile L

    2016-06-01

    It was shown previously (J. Am. Chem. Soc. 2014, 136, 10846) that bubbling of O2 into a solution of Fe(II)(BDPP) (H2BDPP = 2,6-bis[[(S)-2-(diphenylhydroxymethyl)-1-pyrrolidinyl]methyl]pyridine) in tetrahydrofuran at -80 °C generates a high-spin (SFe = (5)/2) iron(III) superoxo adduct, 1. Mössbauer studies revealed that 1 is an exchange-coupled system, [Formula: see text], where SR = (1)/2 is the spin of the superoxo radical, of which the spectra were not well enough resolved to determine whether the coupling was ferromagnetic (S = 3 ground state) or antiferromagnetic (S = 2). The glass-forming 2-methyltetrahydrofuran solvent yields highly resolved Mössbauer spectra from which the following data have been extracted: (i) the ground state of 1 has S = 3 (J < 0); (ii) |J| > 15 cm(-1); (iii) the zero-field-splitting parameters are D = -1.1 cm(-1) and E/D = 0.02; (iv) the major component of the electric-field-gradient tensor is tilted ≈7° relative to the easy axis of magnetization determined by the MS = ±3 and ±2 doublets. The excited-state MS = ±2 doublet yields a narrow parallel-mode electron paramagnetic resonance signal at g = 8.03, which was used to probe the magnetic hyperfine splitting of (17)O-enriched O2. A theoretical model that considers spin-dependent electron transfer for the cases where the doubly occupied π* orbital of the superoxo ligand is either "in" or "out" of the plane defined by the bent Fe-OO moiety correctly predicts that 1 has an S = 3 ground state, in contrast to the density functional theory calculations for 1, which give a ground state with both the wrong spin and orbital configuration. This failure has been traced to a basis set superposition error in the interactions between the superoxo moiety and the adjacent five-membered rings of the BDPP ligand and signals a fundamental problem in the quantum chemistry of O2 activation. PMID:27159412

  4. Experimental and Theoretical Investigations of Magnetic Exchange Pathways in Structurally Diverse Iron(III) Schiff-Base Complexes.

    PubMed

    Herchel, Radovan; Nemec, Ivan; Machata, Marek; Trávníček, Zdeněk

    2015-09-01

    The synthesis, and the structural and magnetic properties, of the following new iron(III) Schiff base complexes with the {O',N,O″}-chelating ligand H2L (2-hydroxyphenylsalicylaldimine) are reported: K[FeL2]·H2O (1), (Pr3NH)[FeL2]·2CH3OH (2), [FeL(bpyO2) (CH3OH)][FeL2]·CH3OH (3), [Fe2L3(CH3OH)]·2CH3OH·H2O (4), and [{Fe2L2}(μ-OH)2{FeL(bpyO2)}2][BPh4]2·2H2O (5), where Pr3NH(+) represents the tripropylammonium cation and bpyO2 stands for 2,2'-bipyridine-N-dioxide. A thorough density functional theory (DFT) study of magnetic interactions (the isotropic exchange) at the B3LYP/def-TZVP level of theory was employed, and calculations have revealed superexchange pathways through intramolecular/intermolecular noncovalent contacts (π-π stacking, C-H···O and O-H···O hydrogen bonds, diamagnetic metal cations) and/or covalent bonds ((μ-O(Ph), μ-OH) or bis(μ-O(Ph)) bridging modes), which helped us to postulate trustworthy spin Hamiltonians for magnetic analysis of experimental data. Within the reported family of compounds 1-5, the mediators of the antiferromagnetic exchange can be sorted by their increasing strength as follows: π-π stacking (J(DFT) = -0.022 cm(-1)/J(mag) = -0.025(4) cm(-1) in 2) < C-H···O contacts and π-π stacking (J(DFT) = -0.19 cm(-1)/J(mag) = -0.347(9)cm(-1) in 1) < O-H···O hydrogen bonds (J(DFT) = -0.53 cm(-1)/J(mag) = -0.41(1) cm(-1) in 3) < bis(μ-O(Ph)) bridge (J(DFT) = -13.8 cm(-1)/J(mag) = -12.3(9) cm(-1) in 4) < (μ-O(Ph), μ-OH) bridge (J(DFT) = -18.0 cm(-1)/J(mag) = -17.1(2) cm(-1) in 5), where J(DFT) and J(mag) are the isotropic exchange parameters derived from DFT calculations, and analysis of the experimental magnetic data, respectively. The good agreement between theoretically calculated and experimentally derived isotropic exchange parameters suggests that this procedure is applicable also for other chemical and structural systems to interpret magnetic data properly. PMID:26262499

  5. Membrane tension and membrane fusion.

    PubMed

    Kozlov, Michael M; Chernomordik, Leonid V

    2015-08-01

    Diverse cell biological processes that involve shaping and remodeling of cell membranes are regulated by membrane lateral tension. Here we focus on the role of tension in driving membrane fusion. We discuss the physics of membrane tension, forces that can generate the tension in plasma membrane of a cell, and the hypothesis that tension powers expansion of membrane fusion pores in late stages of cell-to-cell and exocytotic fusion. We propose that fusion pore expansion can require unusually large membrane tensions or, alternatively, low line tensions of the pore resulting from accumulation in the pore rim of membrane-bending proteins. Increase of the inter-membrane distance facilitates the reaction. PMID:26282924

  6. Characterization of emissions of dioxins and furans from ethylene dichloride (EDC), vinyl chloride (VCM) and polyvinylchloride (PVC) facilities in the United States.

    SciTech Connect

    Carroll, W.F. Jr.; Borrelli, F.E.; Garrity, P.J.; Jacobs, R.A.; Lewis, J.W.; McCreedy, R.L.; Weston, A.F.; Ledvina, J.C.

    1997-12-31

    Members of The Vinyl Inst., under the auspices of its Dioxin Characterization Program have analyzed for potential dioxin/furan (PCDD/F) concentrations in polyvinylchloride (PVC) resins, treated wastewater effluent, ethylene dichloride (EDC) product and wastewater sludge at EDC, vinyl chloride (VCM) and PVC facilities. No 2,3,7,8-TCDD was detected in any sample analyzed under the program to date. Results from wastewater sludge analysis are pending. Trace concentrations (low pg/g) of PCDD/F were detected in only a few samples of PVC resins and ethylene dichloride (EDC) product. Treated wastewater contained low ppq concentrations of PCDD/F. All concentrations are expressed as Toxicity Equivalents (TEQ). Extrapolation of these data shows that the contribution of EDC/VCM/PVC manufacturing via these media constitutes less than 1 percent of the US annual dioxin emission to the environment.

  7. Scintillation proximity assay using polymeric membranes

    SciTech Connect

    Mansfield, R.K.

    1992-01-01

    Liquid scintillation counting (LSC) is typically used to quantify electron emitting isotopes. In LSC, radioactive samples are dissolved in an organic fluor solution (scintillation cocktail) to ensure that the label is close enough to the fluor molecules to be detected. Although efficient, scintillation cocktail is neither specific or selective for samples labeled with the same radioisotope. Scintillation cocktail is flammable posing significant health risks to the user and is expensive to purchase and discard. Scintillation Proximity Assay (SPA) is a radioanalytical technique where only those radiochemical entities (RCE's) bound to fluor containing matrices are detected. Only bound RCE's are in close enough proximity the entrapped fluor molecules to induce scintillations. Unbound radioligands are too far removed from the fluor molecules to be detected. The research in this dissertation focused on the development and evaluation of fluor-containing membranes (scintillation proximity membranes, SP membranes) to be used for specific radioanalytical techniques without using scintillation cocktail. Polysulfone and PVC SP membranes prepared in our laboratory were investigated for radioimmunossay (RIA) where only bound radioligand is detected, thereby eliminating the separation step impeding the automation of RIA. These SP membranes performed RIA where the results were nearly identical to commercial SP microbeads. SP membranes functionalized with quaternary ammonium hydroxide moieties were able to trap and quantify [sup 14]CO[sub 2] without using liquid scintillation cocktail. RCE's bound in the pore structure of SP membranes are intimate with the entrapped fluor providing the geometry needed for high detection efficiencies. Absorbent SP membranes were used in radiation surveys and were shown to be as effective as conventional survey techniques using filter paper and scintillation cocktail.

  8. Compositional GC-FID analysis of the additives to PVC, focusing on the gaskets of lids for glass jars.

    PubMed

    Biedermann-Brem, Sandra; Biedermann, Maurus; Fiselier, Katell; Grob, Koni

    2005-12-01

    A gas chromatographic (FID) method is described which aims at the quantitative compositional analysis of the additives in plasticized PVC, particularly the plastisols used as gaskets for lids of glass jars. An extract of the PVC is analysed directly as well as after transesterification to ethyl esters. Transesterification enables the analysis of epoxidized soya bean and linseed oil (ESBO and ELO) as well as polyadipates. For most other additives, the shifts in the chromatogram resulting from transesterification is used to confirm the identifications made by direct analysis. In the gaskets of 69 lids from the European market used for packaging oily foods, a broad variety of plastisol compositions was found, many or possibly all of which do not comply with legal requirements. In 62% of these lids, ESBO was the principal plasticizer, whereas in 25% a phthalate had been used. PMID:16356892

  9. Beam damage of poly(vinyl chloride) [PVC] as observed by x-ray photoelectron spectroscopy at 143 K, 303 K and 373 K.

    SciTech Connect

    Engelhard, Mark H.; Baer, Donald R.; Lea, Alan S.

    2003-03-08

    X-ray beam damage is often observed during surface analysis of beam sensitive materials as indicated in the introduction to this issue and in a wide variety of references. While damage occurs in a wide range of materials, those that are most susceptible to damage are materials that contain low energy covalent bonds such as polymers or other organic materials. Even amongst the relatively easily damaged polymers, there is a wide range of damage rates. The data reported in this submission was collected in the interest of comparing the rates of damage produced by x-ray and electron irradiation of different materials. The focus of this submission is x-ray damage of bulk poly(vinyl chloride) PVC since it is a readily available material. The temperature of the sample holder was controlled during irradiation of the PVC in order to determine the extent to which localized sample heating affects the rate of damage. PVC degrades by photoionization, resulting in the production of HCl through H and Cl bond cleavage. Bulk PVC has previously been the focus of an x-ray damage study involving many laboratories throughout the world. For comparison to the bulk PVC data, damage rates for thin films of poly(2-chloroethyl methacrylate) (PCEMA) are also reported for the same three temperatures. Measurements of several relatively common materials on one instrument can provide a data base that allows damage rates on one instrument to be linked or compared to other damage data in the literature. In addition to the PCEMA films and bulk PVC, other data collected at the same x-ray parameters include thin films of PVC (for which damage rates are essentially identical to the bulk material) and of poly(acrylonitrile) PAN which is more stable that either PCEMA or PVC. An additional set of PVC data for a different instrument is also included in the volume. X-ray beams used for XPS produce less damage in materials than electrons used for AES analysis. This is due to both th e weaker interaction

  10. Membrane tethering

    PubMed Central

    Chia, Pei Zhi Cheryl

    2014-01-01

    Membrane trafficking depends on transport vesicles and carriers docking and fusing with the target organelle for the delivery of cargo. Membrane tethers and small guanosine triphosphatases (GTPases) mediate the docking of transport vesicles/carriers to enhance the efficiency of the subsequent SNARE (soluble N-ethylmaleimide-sensitive factor attachment protein receptor)-mediated fusion event with the target membrane bilayer. Different classes of membrane tethers and their specific intracellular location throughout the endomembrane system are now well defined. Recent biochemical and structural studies have led to a deeper understanding of the mechanism by which membrane tethers mediate docking of membrane carriers as well as an appreciation of the role of tethers in coordinating the correct SNARE complex and in regulating the organization of membrane compartments. This review will summarize the properties and roles of membrane tethers of both secretory and endocytic systems. PMID:25343031

  11. (Nitro)Iron(III) Porphyrins. EPR Detection of a Transient Low-Spin Iron(III) Complex and Structural Characterization of an O Atom Transfer Product.

    PubMed

    Munro, Orde Q.; Scheidt, W. Robert

    1998-05-01

    The reaction of BF(3).OEt(2) with the bis(nitro) complex of iron(III) picket-fence porphyrin, [K(18C6)(OH(2))][Fe(TpivPP)(NO(2))(2)], leads to the formation of a transient porphyrin intermediate, assigned on the basis of its rhombic low-spin EPR spectrum as the five-coordinate N-bound mono(nitro) iron(III) derivative, [Fe(TpivPP)(NO(2))]. This species is reactive and readily undergoes oxygen atom transfer to form [Fe(III)(TpivPP)(NO(3))] and [Fe(II)(TpivPP)(NO)]. The reactions have been followed by EPR and IR spectroscopy. [Fe(TpivPP)(NO(2))] has a rhombic EPR spectrum (g = 2.60, 2.35, and 1.75) in chlorobenzene and CH(2)Cl(2) and is spectroscopically distinct from the bis(nitro) starting material (g = 2.70, 2.50, and 1.57). Oxidation of the nitrosyl species to [Fe(TpivPP)(NO(3))] proceeds via an intermediate assigned as [Fe(TpivPP)(NO(2))] on the basis of its EPR spectrum. The crystal structure of one of the reaction products, [Fe(TpivPP)(NO(3))], has been determined. The nitrate ion of [Fe(TpivPP)(NO(3))] is bound to the iron(III) ion in a "symmetric" bidentate fashion within the ligand-binding pocket of the porphyrin pickets. Individual Fe-O distances are 2.123(3) and 2.226(3) Å. The dihedral angle between the plane of the nitrate ion and the closest N(p)-Fe-N(p) plane is 10.0 degrees. The Fe-N(p) bonds (and trans N(p)-Fe-N(p) angles) perpendicular and parallel to the plane of the axial ligand average to 2.060(5) Å (154.84(9) degrees ) and 2.083(3) Å (146.14(9) degrees ), respectively. Crystal data for [Fe(TpivPP)(NO(3))]: a = 23.530(2) Å, b = 10.0822(5) Å, c = 48.748(3) Å, beta = 92.145(5) degrees, monoclinic, space group I2/a, V = 11556.4(14) Å(3), Z = 8, FeN(9)O(7)C(64)H(64), 8798 observed data, R(1) = 0.0606, wR(2) = 0.1313, all observations at 127(2) K. PMID:11670389

  12. Surface morphology changes of polymer membrane and carbon paste sertraline sensors.

    PubMed

    Khater, M M; Hassib, H B; Issa, Y M; Mohammed, S H

    2015-03-01

    Polymer membrane and chemically modified carbon paste (CMCP) sensors for determination of sertraline HCl (Ser-Cl) incorporating sertraline tetraphenylborate (Ser-TPB) as an electro-active material were constructed. They showed a rapid and linear response for Ser-ion over the concentration range 0.01-10.00 mmol L(-1). The limits of detection were 2.80 and 9.55 μmol L(-1), and Nernastian slopes were 56.60, 59.60 mV decade(-1) for membrane and CMCP sensors for batch method. In flow injection analysis (FIA), the electrodes revealed comparatively good selectivity for Ser-ion with regard to a wide variety of different cations, sugars, and amino acids. The addition of different anionic additives, namely sodium tetraphenylborate (NaTPB), potassium tetraphenylborate (KTPB), potassium tetrakis[3,5-bis-(triflouromethyl)phenyl]borate (KTFMPB), and sodium tetrakis[3,5-bis(trifluoro-methyl)phenyl]borate (NaTFMPB), to the prepared mixture improved their response characteristics. The surface morphologies of membrane films containing PVC only (blank), plasticizer+PVC, Ser-TPB+plasticizer+PVC, and Ser-TPB +plasticizer+PVC+additive were studied using scanning and atomic force electron microscopes. These sensors had been used in the potentiometric titration of Ser-ion against NaTPB. Standard addition method for the pure raw material and some of its pharmaceutical tablets was used for Ser-Cl determination. The obtained results were tested for their repeatability and reproducibility and were statistically treated by F- and t- tests. PMID:25618706

  13. Effects of TiO2 addition on ionic conductivity of PVC/PEMA blend based composite polymer electrolyte

    NASA Astrophysics Data System (ADS)

    Subban, R. H. Y.; Sukri, Nursyazwani

    2015-08-01

    PVC/PEMA blend based polymer electrolytes with lithium bistrifluoromethane sulfonimide (LiN(CF3SO2)2) and PVC/PEMA/(LiN(CF3SO2)2-TiO2 films were prepared by solution cast technique. The sample containing 35 wt. % LiN(CF3SO2)2 exhibited the highest conductivity of 1.75 × 10-5 Scm-1. The conductivity of the sample increased to 2.12 × 10-5 Scm-1 and 4.61 × 10-5 Scm-1 when 4 wt. % and 10 wt. % of titanium dioxide (TiO2) was added to the sample at 65 wt. % PVC/PEMA-35 wt. % LiN(CF3SO2)2 composition respectively. The low increase in conductivity is attributed to two competing factors: increase in crystallinity as accounted by X-Ray diffraction (XRD) and decrease in glass transition temperature as accounted by differential scanning calorimetry (DSC).

  14. Effects of TiO{sub 2} addition on ionic conductivity of PVC/PEMA blend based composite polymer electrolyte

    SciTech Connect

    Subban, R. H. Y.; Sukri, Nursyazwani

    2015-08-28

    PVC/PEMA blend based polymer electrolytes with lithium bistrifluoromethane sulfonimide (LiN(CF{sub 3}SO{sub 2}){sub 2}) and PVC/PEMA/(LiN(CF{sub 3}SO{sub 2}){sub 2}-TiO{sub 2} films were prepared by solution cast technique. The sample containing 35 wt. % LiN(CF{sub 3}SO{sub 2}){sub 2} exhibited the highest conductivity of 1.75 × 10{sup −5} Scm{sup −1}. The conductivity of the sample increased to 2.12 × 10{sup −5} Scm{sup −1} and 4.61 × 10{sup −5} Scm{sup −1} when 4 wt. % and 10 wt. % of titanium dioxide (TiO{sub 2}) was added to the sample at 65 wt. % PVC/PEMA-35 wt. % LiN(CF{sub 3}SO{sub 2}){sub 2} composition respectively. The low increase in conductivity is attributed to two competing factors: increase in crystallinity as accounted by X-Ray diffraction (XRD) and decrease in glass transition temperature as accounted by differential scanning calorimetry (DSC)

  15. Preparation and testing of a solid secondary plasticizer for PVC produced by chemical degradation of post-consumer PET.

    PubMed

    Amaro, Lucía Pérez; Coiai, Serena; Ciardelli, Francesco; Passaglia, Elisa

    2015-12-01

    Post-consumer poly(ethylene therephthalate) (PET) obtained from milled water bottles was chemically degraded by glycolysis, using suitable amounts of diethylene glycol (DEG) and Ca/Zn stearate as catalyst system. The process was carried out by employing a melt mixer as the chemical reactor, which is the facility generally used for plastic compounding. The degraded PET products were first characterized from structural and thermal point of view by Fourier transform infrared spectroscopy (FTIR), Proton nuclear magnetic resonance ((1)H NMR), Size exclusion chromatography (SEC) Differential scanning calorimetry (DSC) and Thermogravimetric analysis (TGA), and thereafter used alone or together with di(2-ethylhexyl) phthalate (DEHP) in poly(vinyl chloride) PVC formulations. The plasticization was, in fact, accomplished by using a binary system consisting of DEHP as primary plasticizer and a degraded PET product as secondary plasticizer (SP). The obtained materials were characterized through the main methods used to assess flexible PVC compounds: hardness in Shore A scale, thermal properties and quantitative migration of the plasticizer. The solid secondary plasticizer obtained from post-consumer PET improves both the processing characteristics and the thermal stability of the final flexible PVC compounds while maintaining their hardness within the top values of the Shore A scale. In addition, a considerable reduction of the plasticizers migration (23%) was obtained by optimizing the formulation. PMID:26376120

  16. Development of new generation of copolymers via reactive extrusion in a twin screw extruder and application in various PVC blends

    NASA Astrophysics Data System (ADS)

    Kim, In

    Polymerization in twin screw extruders has largely involved homopolymers. Here we generalize this and polymerize a range of copolymers and terpolymers including epsilon-caprolactam(CA), o-lauryl lactam(LA), epsilon-caprolactone(CL), and gamma-butyrolactone(GBL) in a modular intermeshing co-rotating twin screw extruder. We considered different types of copolymer structures (di-block, tri-block, and random-block) and different backbones of copolymer(lactams-lactones) as well as the variables of temperature profile, screw speed, monomer feed rate, the ratio of monomer to initiator, and feeding order of co-monomers on reactive extrusion of polyamides-polylactones based (co)polymers. Specially designed block copolymers have played a role as compatibilizing agents in the system of immiscible polymer blends. We apply the di-block copolymer(P(LA-b-CL)) and random block copolymer (P(LA/CA-b-CL)) produced by reactive extrusion as a compatibilizing agent in immiscible polymer blend systems: (i) poly(vinyl chloride) (PVC)/polyamide 12 (PA12), (ii) PVC/polypropylene(PP), and (iii) PVC/Ethylene-propylene-non-conjugated diene elastomer(EPDM).

  17. Increasing heavy metal emissions due to PVC-derived chlorine in simulated MSW incineration

    SciTech Connect

    Wang, K.S.; Chiang, K.Y.; Sun, C.J.; Lin, K.L.; Tsai, C.C.

    1999-07-01

    The effect of PVC-derived chlorine on heavy metal emissions in MSW incineration was investigated using a tubular furnace and simulated MSW spiked with PVCs and heavy metals (Cd, Cr, Cu, and Zn). The authors varied the molar ratio of the chlorine content to that of the heavy metal (Cl/M ratio) from 3--200 as one parameter. The results indicated that the major species found in the fly ash were chlorides of alkaline and alkali-earth metals, whereas those identified in the bottom ash were MgSiO{sub 3}, SiO{sub 2} and some complex aluminates and silicates. The emission of heavy metals and/or their compounds, with extreme and medium volatility, tended to be enhanced within the lower Cl/M range, whereas those with a refractory volatility were likely to be affected within the higher Cl/M range. However, those with an extremely refractory volatility were less affected by an increase of the Cl/M ratio. The variation of speciation and partitioning in MSW combustion as affected by the Cl/M ratio are discussed.

  18. Survey of phthalate levels in Italian oily foods contained in glass jars with PVC gaskets.

    PubMed

    Sannino, A

    2009-01-01

    A method based on gas chromatography/tandem mass spectrometry was used to assess levels of twelve phthalates in 50 samples of oily foods packed in glass jars with metal closure obtained from a retail market. The amounts of di-methyl phthalate, di-ethyl phthalate, di-propyl phthalate, di-butyl phthalate, di-pentyl phthalate, benzyl butyl phthalate, di-cyclohexyl phthalate, di-n-octyl phthalate, di-isononyl phthalate and di-isodecyl phthalate in all samples analysed were less than the limit of quantification (LOQ). Di-(2-ethylhexyl) phthalate was detected in 20 samples in the range from 0.1 to 6 mg kg(-1) with an average of 1.0 mg kg(-1), and it exceeded the specific migration limit (SML) of 1.5 mg kg(-1) in five cases with an average of 3.0 mg kg(-1). Di-isobutyl phthalate was found in four samples at 0.1-0.4 mg kg(-1). The PVC gaskets used for the lids were negative for all tested phthalates, suggesting that the contamination of the foods originated from other sources, e.g. olive oil. PMID:24785180

  19. Co-occurrence of invasive Cuban Treefrogs and native treefrogs in PVC pipe refugia

    USGS Publications Warehouse

    Elston, Laura M.; Waddle, J. Hardin; Rice, Kenneth G.; Percival, H. Franklin

    2013-01-01

    The Cuban Treefrog (Osteopilus septentrionalis) was first introduced to Florida at Key West. Since this introduction, Cuban Treefrogs have spread to Miami and are now established throughout most of peninsular Florida. Cuban Treefrogs can become very abundant in areas they colonize. Several reasons contribute to their success, including a generalist diet, high fecundity and the ability to reproduce year-round, and use of disturbed or human-modified habitats. Scientists and managers are concerned that Cuban Treefrogs may contribute to the decline of native treefrogs. Cuban Treefrogs may exclude native treefrogs through both competition and predation. Because the evidence from our study and others suggests that Green and Squirrel Treefrogs do not alter their behavior to avoid Cuban Treefrogs, there is cause for concern that sampling with PVC pipes may increase the vulnerability of the native species to predation. This possibility needs further research, including whether other species of native treefrogs sympatric to where Cuban Treefrogs have invaded are also naïve to the possible threat posed by these frogs, and also if native treefrogs eventually learn to avoid Cuban Treefrogs.

  20. Analysis of toxic effluents released from PVC carpet under different fire conditions.

    PubMed

    Stec, A A; Readman, J; Blomqvist, P; Gylestam, D; Karlsson, D; Wojtalewicz, D; Dlugogorski, B Z

    2013-01-01

    A large number of investigations have been reported on minimising the PAH and PCDD/F yields during controlled combustion, such as incineration. This study is an attempt to quantify acute and chronic toxicants including PAH and PCDD/F in conditions relating to unwanted fires. This paper investigates distribution patterns of fire effluents between gas and aerosol phase, and the different particle size-ranges produced under different fire conditions. PVC carpet was selected as the fuel as a precursor for both PAH and PCDD/F. In order to generate fire effluents under controlled fire conditions, the steady-state tube furnace, was chosen as the physical fire model. Fire scenarios included oxidative pyrolysis, well-ventilated and under-ventilated fires. Fire effluent measurements included: carbon monoxide, carbon dioxide, hydrogen chloride, polycyclic aromatic hydrocarbons, chlorinated dibenzo-dioxins and furans and soot. The distribution patterns between gas and particle phase, and the size-ranges of the particles produced in these fires together with their chemical composition is also reported. Significant quantities of respirable submicron particles were detected, together with a range of PAHs. Lower levels of halogenated dioxins were detected in the fire residue compared with those found in other studies. Nevertheless, the findings do have implications for the health and safety of fire and rescue personnel, fire investigators, and other individuals exposed to the residue from unwanted fires. PMID:22960058

  1. Simulated neonatal exposure to DEHP and MEHP from PVC enteral nutrition products.

    PubMed

    Takatori, Satoshi; Okamoto, You; Kitagawa, Yoko; Hori, Shinjiro; Izumi, Shun-Ichiro; Makino, Tsunehisa; Nakazawa, Hiroyuki

    2008-03-20

    The leaching of di(2-ethylhexyl)phthalate (DEHP) and mono(2-ethylhexyl)phthalate (MEHP) from medical products made of polyvinyl-chloride (PVC) to enteral nutrition (EN) for neonatal patients was determined in a simulated study. The study simulated a typical case of EN administration to a neonatal patient (body weight, 3 kg) in a neonatal care unit (temperature, 25 degrees C); the medical products used were an irrigator and catheter containing DEHP (9.1-31.8%, w/w) as a plasticizer. The worst-case daily exposures of the neonatal patient to DEHP and MEHP by the administration of EN were estimated to be 148 and 3.72 microg/(kg day), respectively, as assessed from the levels of these compounds leaching from the medical products to the EN. The use of DEHP-free medical products reduced the exposure of DEHP and MEHP to the minimum levels contained in the EN at preparation. A transition to DEHP-free medical products for neonatal patients would be effective in reducing the exposure of neonatal patients to DEHP via EN administration. PMID:18063492

  2. Novel Organic Membrane-based Thin-film Microsensors for the Determination of Heavy Metal Cations

    PubMed Central

    Arida, Hassan A.; Kloock, Joachim P.; Schöning, Michael J.

    2006-01-01

    A first step towards the fabrication and electrochemical evaluation of thin-film microsensors based on organic PVC membranes for the determination of Hg(II), Cd(II), Pb(II) and Cu(II) ions in solutions has been realised. The membrane-coating mixture used in the preparation of this new type of microsensors is incorporating PVC as supporting matrix, o-nitrophenyloctylether (o-NPOE) as solvent mediator and a recently synthesized Hg[dimethylglyoxime(phene)]2+ and Bis-(4-hydroxyacetophenone)-ethylenediamine as electroactive materials for Hg(II) and Cd(II), respectively. A set of three commercialised ionophores for Cd(II), Pb(II) and Cu(II) has been also used for comparison. Thin-film microsensors based on these membranes showed a Nernstian response of slope (26-30 mV/dec.) for the respective tested cations. The potentiometric response characteristics (linear range, pH range, detection limit and response time) are comparable with those obtained by conventional membranes as well as coated wire electrodes prepared from the same membrane. The realisation of the new organic membrane-based thin-film microsensors overcomes the problem of an insufficient selectivity of solid-state-based thin-film sensors.

  3. Behaviour of Steel Arch Stabilized by a Textile Membrane

    NASA Astrophysics Data System (ADS)

    Svoboda, O.; Machacek, J.

    2015-11-01

    Behaviour of the slender steel arch supporting textile membranes in a membrane structure with respect to in-plane and out-of plane stability is investigated in the paper. In the last decades the textile membranes have been widely used to cover both common and exclusive structures due to progress in new membrane materials with eminent properties. Nevertheless, complex analysis of such membranes in interaction with steel structure (carbon/stainless steel perimeter or supporting elements) is rather demanding, even with specialized software. Laboratory model of a large membrane structure simulating a shelter roof of a concert stage was tested and the resulting stress/deflection values are presented. The model of a reasonable size was provided with prestressed membrane of PVC coated polyester fabric Ferrari® Précontraint 702S and tested under various loadings. The supporting steel structure consisted of two steel arch tubes from S355 grade steel and perimeter prestressed cables. The stability behaviour of the inner tube was the primary interest of the investigation. The SOFiSTiK software was used to analyse the structural behaviour in 3D. Numerical non-linear analysis of deflections and internal forces of the structure under symmetrical and asymmetrical loadings covers various membrane prestressing and specific boundary conditions. The numerical results are validated using test results. Finally, the preliminary recommendations for appropriate numerical modelling and stability design of the supporting structure are presented.

  4. Efficient cross-coupling of aryl Grignard reagents with alkyl halides by recyclable ionic iron(III) complexes bearing a bis(phenol)-functionalized benzimidazolium cation.

    PubMed

    Xia, Chong-Liang; Xie, Cun-Fei; Wu, Yu-Feng; Sun, Hong-Mei; Shen, Qi; Zhang, Yong

    2013-12-14

    A novel bis(phenol)-functionalized benzimidazolium salt, 1,3-bis(3,5-di-tert-butyl-2-hydroxybenzyl)benzimidazolium chloride (H3LCl, 1), was designed and used to prepare ionic iron(III) complexes of the type [H3L][FeX4] (X = Cl, 2; X = Br, 3). Both 2 and 3 were characterized by elemental analysis, Raman spectroscopy, electrospray ionization mass spectrometry and X-ray crystallography. The catalytic performances of 2 and 3 in cross-coupling reactions using aryl Grignard reagents with primary and secondary alkyl halides bearing β-hydrogens were studied. This analysis shows that complex 2 has good potential for alkyl chloride-mediated coupling. In comparison, complex 3 showed slightly lower catalytic activity. After decanting the product contained in the ethereal layer, complex 2 could be recycled at least eight times without significant loss of catalytic activity. PMID:24145602

  5. Iron(III) tartrate as a potential precursor of light-induced oxidative degradation of white wine: studies in a model wine system.

    PubMed

    Clark, Andrew C; Dias, Daniel A; Smith, Trevor A; Ghiggino, Kenneth P; Scollary, Geoffrey R

    2011-04-27

    The potential for iron(III) tartrate to act as a photoactivator in light-induced oxidative degradation of white wine is described. Using a tartaric-acid-based model wine system containing 5 mg/L iron, exposure to light from a xenon arc lamp led to the oxidative degradation of tartaric acid and the production of glyoxylic acid. The critical wavelength of light for the degradation process was found to be below 520 nm. No glyoxylic acid was formed in the absence of iron and/or light. Flint glass offered little protection from the light-induced photodegradation of tartaric acid. Antique Green glass offered more protection but did not stop the photodegradation process. PMID:21381783

  6. The ground states of iron(III) porphines: role of entropy-enthalpy compensation, Fermi correlation, dispersion, and zero-point energies.

    PubMed

    Kepp, Kasper P

    2011-10-01

    Porphyrins are much studied due to their biochemical relevance and many applications. The density functional TPSSh has previously accurately described the energy of close-lying electronic states of transition metal systems such as porphyrins. However, a recent study questioned this conclusion based on calculations of five iron(III) porphines. Here, we compute the geometries of 80 different electronic configurations and the free energies of the most stable configurations with the functionals TPSSh, TPSS, and B3LYP. Zero-point energies and entropy favor high-spin by ~4kJ/mol and 0-10kJ/mol, respectively. When these effects are included, and all electronic configurations are evaluated, TPSSh correctly predicts the spin of all the four difficult phenylporphine cases and is within the lower bound of uncertainty of any known theoretical method for the fifth, iron(III) chloroporphine. Dispersion computed with DFT-D3 favors low-spin by 3-53kJ/mol (TPSSh) or 4-15kJ/mol (B3LYP) due to the attractive r(-6) term and the shorter distances in low-spin. The very large and diverse corrections from TPSS and TPSSh seem less consistent with the similarity of the systems than when calculated from B3LYP. If the functional-specific corrections are used, B3LYP and TPSSh are of equal accuracy, and TPSS is much worse, whereas if the physically reasonable B3LYP-computed dispersion effect is used for all functionals, TPSSh is accurate for all systems. B3LYP is significantly more accurate when dispersion is added, confirming previous results. PMID:21855825

  7. Selective oxidation catalysts obtained by immobilization of iron(III) porphyrins on thiosalicylic acid-modified Mg-Al layered double hydroxides.

    PubMed

    de Freitas Castro, Kelly Aparecida Dias; Wypych, Fernando; Antonangelo, Ariana; Mantovani, Karen Mary; Bail, Alesandro; Ucoski, Geani Maria; Ciuffi, Kátia Jorge; Cintra, Thais Elita; Nakagaki, Shirley

    2016-09-15

    Nitrate-intercalated Mg-Al layered double hydroxides (LDHs) were synthesized and exfoliated in formamide. Reaction of the single layer suspension with thiosalicylic acid under different conditions afforded two types of solids: LDHA1, in which the outer surface was modified with the anion thiosalicylate, and LDHA2, which contained the anion thiosalicylate intercalated between the LDH layers. LDHA1 and LDHA2 were used as supports to immobilize neutral (FeP1 and FeP2) and anionic (FeP3) iron(III) porphyrins. For comparison purposes, the iron(III) porphyrins (FePs) were also immobilized on LDH intercalated with nitrate anions obtained by the co-precipitation method. Chemical modification of LDH facilitated immobilization of the FePs through interaction of the functionalizing groups in LDH with the peripheral substituents on the porphyrin ring. The resulting FePx-LDHAy solids were characterized by X-ray diffraction (powder) and UV-Vis and EPR spectroscopies and were investigated as catalysts in the oxidation of cyclooctene and cyclohexane. The immobilized neutral FePs and their homogeneous counterparts gave similar product yields in the oxidation of cyclooctene, suggesting that immobilization of the FePs on the thiosalicylate-modified LDHs only supported the catalyst species without interfering in the catalytic outcome. On the other hand, in the oxidation of cyclohexane, the thiosalicylate anions on the outer surface of LDHA1 or intercalated between the LDHA2 layers influenced the catalytic activity of FePx-LDHAy, leading to different efficiency and selectivity results. FeP1-LDHA2 performed the best (29.6% alcohol yield) due to changes in the polarity of the surface of the support and the presence of FeP1. Interestingly, FeP1 also performed better in solution as compared to the other FePs. Finally, it was possible to recycle FeP1-LDHA2 at least three times. PMID:27322950

  8. Dinuclear and 1D iron(III) Schiff base complexes bridged by 4-salicylideneamino-1,2,4-triazolate: X-ray structures and magnetic properties.

    PubMed

    Herchel, Radovan; Pavelek, Lubomír; Trávníček, Zdeněk

    2011-11-28

    Four new iron(III) complexes were obtained by the reaction of 4-salicylideneamino-1,2,4-triazole (Hsaltrz) and selected dinuclear μ-oxo-bridged iron(III) Schiff base complexes [{FeL(4)}(2)(μ-O)], where L(4) represents a terminal tetradentate dianionic Schiff-base ligand. X-ray structural analysis revealed a novel bridging mode of κN,κO of the saltrz ligand to form dinuclear complexes [{Fe(salen)(μ-saltrz)}(2)]·CH(3)OH (1) (H(2)salen = N,N'-ethylenebis(salicylimine)) and [{Fe(salpn)(μ-saltrz)}(2)] (2) (H(2)salpn = N,N'-1,2-propylenbis(salicylimine)), whereas one-dimensional (1D) zig-zag chains were formed in the case of [{Fe(salch)(μ-saltrz)}·0.5CH(3)OH](n) (3) (H(2)salch = N,N'-cyclohexanebis(salicylimine)) and [Fe(salophen)(μ-saltrz)](n) (4) (H(2)salophen = N,N'-o-phenylenebis(salicylimine)). It was also shown that the rigidity of the terminal ligand L(4) can be considered as the key factor for the molecular dimensionality of the products. The thorough magnetic analysis based on SQUID experiments, including the isotropic exchange and the zero-field splitting of both temperature and field dependent data, was performed for dimeric (1 and 2) and also for polymeric compounds (3 and 4) and revealed weak antiferromagnetic exchange mediated by the saltrz anions with much larger D-parameter (|D|≫|J|). PMID:21968851

  9. Radiation-grafted, chemically modified membranes part I - Synthesis of a selective aluminum material

    NASA Astrophysics Data System (ADS)

    Bazante-Yamaguishi, Renata; Moura, Eduardo; Manzoli, José E.; Geraldo, Aurea B. C.

    2014-01-01

    Polymeric membranes were styrene grafted by irradiation methods and the obtained material was chemically modified to become aluminum selective. For this purpose, polymeric substrates of PVC (polyvinyl chloride) and PP (polypropylene) were styrene grafted mutually by gamma and electron beam irradiation. The modification process includes three basic reaction paths: Friedel-Crafts acylation, 2-methylanisole coupling and a final oxidation to achieve aluminum selectivity. Although this specific chemical modification in derivatives of polystyrene is not new, the new challenge is to obtain a selective material where original membrane characteristics (physical shape and mechanical resistance) are minimally conserved after such an aggressive treatment.

  10. Membrane Processes.

    PubMed

    Pellegrin, Marie-Laure; Sadler, Mary E; Greiner, Anthony D; Aguinaldo, Jorge; Min, Kyungnan; Zhang, Kai; Arabi, Sara; Burbano, Marie S; Kent, Fraser; Shoaf, Robert

    2015-10-01

    This review, for literature published in 2014, contains information related to membrane processes for municipal and industrial applications. This review is a subsection of the Treatment Systems section of the annual Water Environment Federation literature review and covers the following topics: pretreatment, membrane bioreactor (MBR) configuration, design, nutrient removal, operation, industrial treatment, fixed film and anaerobic membrane systems, reuse, microconstituents removal, membrane technology advances, membrane fouling, and modeling. Other sub-sections of the Treatment Systems section that might relate to this literature review include: Biological Fixed-Film Systems, Activated Sludge and Other Aerobic Suspended Culture Processes, Anaerobic Processes, Water Reclamation and Reuse. The following sections might also have related information on membrane processes: Industrial Wastes, Hazardous Wastes, and Fate and Effects of Pollutants. PMID:26420079

  11. Membrane Processes.

    PubMed

    Pellegrin, Marie-Laure; Burbano, Marie S; Sadler, Mary E; Diamond, Jason; Baker, Simon; Greiner, Anthony D; Arabi, Sara; Wong, Joseph; Doody, Alexandra; Padhye, Lokesh P; Sears, Keith; Kistenmacher, Peter; Kent, Fraser; Tootchi, Leila; Aguinaldo, Jorge; Saddredini, Sara; Schilling, Bill; Min, Kyungnan; McCandless, Robert; Danker, Bryce; Gamage, Neranga P; Wang, Sunny; Aerts, Peter

    2016-10-01

    This review, for literature published in 2015, contains information related to membrane processes for municipal and industrial applications. This review is a subsection of the Treatment Systems section of the annual Water Environment Federation literature review and covers the following topics: pretreatment, membrane bioreactor (MBR) configuration, design, nutrient removal, operation, industrial treatment, anaerobic membrane systems, reuse, microconstituents removal, membrane technology advances, membrane fouling, and modeling. Other sub-sections of the Treatment Systems section that might relate to this literature review include: Biological Fixed-Film Systems, Activated Sludge and Other Aerobic Suspended Culture Processes, Anaerobic Processes, Water Reclamation and Reuse. The following sections might also have related information on membrane processes: Industrial Wastes, Hazardous Wastes, and Fate and Effects of Pollutants. PMID:27620084

  12. Adsorption and Fenton regeneration of SBA-15 for di-(2-ethylhexyl) phthalate leached from PVC sheets by Gram-positive strains LHM1 and LHM2

    NASA Astrophysics Data System (ADS)

    Hwang, S.; Latorre, I.; Caban, M.; Soto, B.; Montalvo-Rodríguez, R.; Hernández-Maldonado, A.

    2012-12-01

    Bioleaching of Di-(2-ethylhexyl) phthalate (DEHP) from PVC sheets was studied with newly isolated, Gram-positive strains LHM1 and LHM2 capable of growing on DEHP as the sole carbon source. According to 16S rRNA gene analysis, strains LHM1 and LHM2 were closely related (more than 97% similarity) to Chryseomicrobium imtechense MW 10(T) and Lysinibacillus fusiformis NBRC 15717(T), respectively. The biodeteriorated PVC sheets by the strains LHM1 and LHM2 had thicker biofilm development. Despite their metabolic capability of degrading DEHP as the sole carbon source, the strains LHM1 and LHM2 did not metabolize all DEHP leached out of the PVC sheets. Thermogravimetric analysis (TGA) showed that the biodeterioration by strains LHM1 and LHM2 resulted in less amount of and weakly bonded DEHP present in PVC sheets, in comparison to the virgin PVC sheet. Therefore, PVC biodeterioration by strains LHM1 and LHM2 might play an important role in stability of PVC sheets and fate and effect of leached DEHP on the environmental receptors. In response to this, an advanced adsorption with SBA-15 was assessed as a potential alternative DEHP remediation with arsenic as a co-contaminant. SBA-15 had an excellent arsenic adsorption showing >90% arsenic removal when arsenic was present as a singular contaminant. Adsorption effectiveness was irrelevant to the solid/liquid (S/L) ratio. However, when arsenic was present together with DEHP, arsenic adsorption to bare SBA-15 was reduced by 10 - 40%, with lesser S/L ratio having greater arsenic removal. On the contrary, bare SBA-15 only adsorbed ~30% of DEHP on average. When DEHP was present as a co-solute with arsenic, DEHP adsorption to bare SBA-15 was increased. For SBA-15 regeneration, adsorbed arsenic was recovered with EDTA elution, whereas adsorbed DEHP was destructed with Fenton oxidation.

  13. Multicomponent membranes

    DOEpatents

    Kulprathipanja, Santi; Kulkarni, Sudhir S.; Funk, Edward W.

    1988-01-01

    A multicomponent membrane which may be used for separating various components which are present in a fluid feed mixture comprises a mixture of a plasticizer such as a glycol and an organic polymer cast upon a porous organic polymer support. The membrane may be prepared by casting an emulsion or a solution of the plasticizer and polymer on the porous support, evaporating the solvent and recovering the membrane after curing.

  14. Mycelial fungi completely remediate di(2-ethylhexyl)phthalate, the hazardous plasticizer in PVC blood storage bag.

    PubMed

    Pradeep, S; Benjamin, Sailas

    2012-10-15

    This pioneering work describes how simply, inexpensively and efficiently novel fungi utilize the alarming plasticizer, di(2-ethylhexyl)phthalate (DEHP) blended in PVC blood storage bags (BB). In order to quantify total DEHP (33.5%, w/w) present in BB, it was extracted using n-hexane and confirmed by GC-MS. Three mycelial fungi, viz., Aspergillus parasiticus, Fusarium subglutinans and Penicillium funiculosum isolated in our laboratory form heavily plastics-contaminated soil - either singly or in consortium - completely consumed intact DEHP physically bound to BB by static submerged growth (28 °C) in simple basal salt medium (BSM). A two-stage cultivation strategy was adopted for the complete removal of DEHP from BB in situ. During the first growth stage, almost 70% DEHP contained in the BB was consumed in 2 weeks, accompanied by increased fungal biomass (~0.15-0.35 g/g BB; OD ~7 at 600 nm) and a sharp declining (3.3) of initial pH (7.2). Spent BSM was replaced at this stagnant growth state (low pH), thus in the second stage, remaining DEHP bound to BB utilized completely (over 99%). Furthermore, A. parasiticus and F. subglutinans also grew well on scrapes of PVC water pipes in BSM. F. subglutinans was as efficient independently as consortium in completely utilizing the DEHP bound to BB, and these fungi offer great potentials for the inexpensive and eco-friendly bioremediation of phthalates in medical and allied PVC wastes on a large scale through a batch process in alleviating the plactics waste management issue. PMID:22858127

  15. Unique anisotropic optical properties of a highly stable metal-organic framework based on trinuclear iron(iii) secondary building units linked by tetracarboxylic linkers with an anthracene core.

    PubMed

    Vinogradov, A V; Milichko, V A; Zaake-Hertling, H; Aleksovska, A; Gruschinski, S; Schmorl, S; Kersting, B; Zolnhofer, E M; Sutter, J; Meyer, K; Lönnecke, P; Hey-Hawkins, E

    2016-05-01

    A highly stable metal-organic framework, [{Fe3(ACTBA)2}X·6DEF]n (1; X = monoanion), based on trinuclear iron(iii) secondary building units connected by tetracarboxylates with an anthracene core, 2,6,9,10-tetrakis(p-carboxylatophenyl)anthracene (ACTBA), is reported. Depending on the direction of light polarisation, crystals of 1 exhibit anisotropic optical properties with birefringence Δn = 0.3 (λ = 590 nm). PMID:26906040

  16. Novel and selective procedure for Cr(VI) determination by X-ray fluorescence analysis after membrane concentration

    NASA Astrophysics Data System (ADS)

    Fontàs, Clàudia; Queralt, Ignasi; Hidalgo, Manuela

    2006-04-01

    A new, simple and selective method for the determination of Cr(VI) in aqueous samples has been developed by using a combination of membrane preconcentration and energy dispersive X-ray fluorescence spectrometry. The enrichment of Cr in the membranes is accomplished by the addition of the commercial anion-exchanger extractant Aliquat 336. Two different types of membranes have been investigated: the so-called impregnated membranes, where an organic solution of the extractant fills the pores of commercial polymeric membranes, and polymer inclusion membranes, prepared by physical inclusion of Aliquat 336 in the matrix formed by either cellulose triacetate or poly(vinyl chloride) and the plasticizer 2-nitrophenyl octyl ether. Both types of membranes were found to be stable and efficient for the preconcentration of Cr, but polymeric membranes made of PVC showed a higher degree of homogeneity in terms of metal distribution. Determination of the Cr collected on the membranes was performed by means of a commercial energy dispersive X-ray fluorescence spectrometer. Parameters affecting the performance of the preconcentration method as well as the analysis of the membranes have been investigated, and a linear response has been obtained between the Cr present in the aqueous solutions and the metal extracted on the membrane. The calibration curve obtained when using PVC-based membranes was linear over the concentration range 0.3-8.8 mg L - 1 with a detection limit of 0.3 mg L - 1 . The selectivity of the proposed method has been evaluated, and also, it has successfully been applied to the analysis of chromium present in real samples of electroplating water from galvanic baths.

  17. Functionalized polymer nanofibre membranes for protection from chemical warfare stimulants

    NASA Astrophysics Data System (ADS)

    Ramaseshan, Ramakrishnan; Sundarrajan, Subramanian; Liu, Yingjun; Barhate, R. S.; Lala, Neeta L.; Ramakrishna, S.

    2006-06-01

    A catalyst for the detoxification of nerve agents is synthesized from β-cyclodextrin (β-CD) and o-iodosobenzoic acid (IBA). Functionalized polymer nanofibre membranes from PVC polymer are fabricated with β-CD, IBA, a blend of β-CD+IBA, and the synthesized catalyst. These functionalized nanofibres are then tested for the decontamination of paraoxon, a nerve agent stimulant, and it is observed that the stimulant gets hydrolysed. The kinetics of hydrolysis is investigated using UV spectroscopy. The rates of hydrolysis for different organophosphate hydrolyzing agents are compared. The reactivity and amount of adsorption of these catalysts are of higher capacity than the conventionally used activated charcoal. A new design for protective wear is proposed based on the functionalized nanofibre membrane.

  18. Crystalline Membranes

    NASA Technical Reports Server (NTRS)

    Tsapatsis, Michael (Inventor); Lai, Zhiping (Inventor)

    2008-01-01

    In certain aspects, the invention features methods for forming crystalline membranes (e.g., a membrane of a framework material, such as a zeolite) by inducing secondary growth in a layer of oriented seed crystals. The rate of growth of the seed crystals in the plane of the substrate is controlled to be comparable to the rate of growth out of the plane. As a result, a crystalline membrane can form a substantially continuous layer including grains of uniform crystallographic orientation that extend through the depth of the layer.

  19. Covalent organic/inorganic hybrid proton-conductive membrane with semi-interpenetrating polymer network: Preparation and characterizations

    NASA Astrophysics Data System (ADS)

    Fu, Rong-Qiang; Woo, Jung-Je; Seo, Seok-Jun; Lee, Jae-Suk; Moon, Seung-Hyeon

    2008-05-01

    A series of new covalent organic/inorganic hybrid proton-conductive membranes, each with a semi-interpenetrating polymer network (semi-IPN), for direct methanol fuel cell (DMFC) applications is prepared through the following sequence: (i) copolymerization of impregnated styrene (St), p-vinylbenzyl chloride (VBC) and divinylbenzene (DVB) within a supporting polyvinyl chloride (PVC) film; (ii) reaction of the chloromethyl group with 3-(methylamine)propyl-trimethoxysilane (MAPTMS); (ii) a sol-gel process under acidic conditions; (iv) a sulfonation reaction. The developed membranes are characterized in terms of Fourier transform infrared/attenuated total reflectance (FTIR/ATR), scanning electron microscopy/energy-dispersive X-ray analysis (SEM/EDXA), elemental analysis (EA) and thermogravimetric analysis (TGA), which confirm the formation of the target membranes. The developed copolymer chains are interpenetrating with the PVC matrix to form the semi-IPN structure, and the inorganic silica is covalently bound to the copolymers. These features provide the membranes with high mechanical strength. The effect of silica content is investigated. As the silica content increases, proton conductivity and water content decrease, whereas oxidative stability is improved. In particular, methanol permeability and methanol uptake are reduced largely by the silica. The ratio of proton conductivity to methanol permeability for the hybrid membranes is higher than that of Nafion 117. All these properties make the hybrid membranes a potential candidate for DMFC applications.

  20. A study on the combustion characteristics of PVC, poly(styrene), poly(ethylene), and poly(propylene) particles under high heating rates

    SciTech Connect

    Panagiotou, T.; Levendis, Y. . Dept. of Mechanical Engineering)

    1994-10-01

    The combustion characteristics of four commonly encountered plastics: poly(styrene), PVC, poly(ethylene) and poly(propylene) were studied under conditions pertinent to incinerators, that is, high heating rates (in the order of 10,000 K/s) and elevated gas temperatures (1,200--1,500 K). Batches of spherical and monodisperse particles of these plastics were generated in the size range of 53--300 [mu]m. Combustion of single particles, of known size and mass, was conducted in a laminar-flow drop-tube furnace, at controlled atmospheres. The radiation emitted from burning particles was monitored, along their flight path, by simultaneous three-color optical pyrometry and high-speed cinematography. Results indicate that polymer particles (plastics) burned expediently with burntimes similar to those of light oil drops such as kerosene, hexadecane, etc. Both PVC and poly(styrene) burned with very luminous yellow flames, which were attributed to high soot loadings. The flame combustion of PVC was the brightest and fastest with steadily decreasing temperature and flame diameter, while that of poly(styrene) occurred mostly at constant flame diameter and mildly decreasing temperature. Combustion of both poly(ethylene) and poly(propylene) was dimmer and somewhat lengthier. Furthermore, in this temperature region, it is argued herein that the combustion of poly(styrene), poly(ethylene), and poly(propylene) occurred concurrently with, and was partially controlled by, pyrolysis reactions. PVC seemed to undergo significant pyrolysis prior to ignition; thereafter, combustion occurred in a premixed-like flame mode and, finally, dimly glowing combustion of the remaining char was observed. PVC exhibited the highest soot volume fraction in its flame, followed by poly(styrene); poly(propylene), and poly(ethylene). Moreover, it was observed that the rate of burning was the highest for PVC particles and the lowest for poly(ethylene).

  1. Development of an improved membrane for a vapor diffusion water recovery process. [onboard manned spacecraft

    NASA Technical Reports Server (NTRS)

    Rich, T. R.; Mix, T. W.

    1974-01-01

    Recovery of potable water from urine on manned space missions of extended duration was the objective of work aimed at the improvement of membrane performance for the vapor diffusion process (VDR). Kynar, Teflon, PVC, and polysulfone candidate membranes were evaluated from chemical, thermal, mechanical, and fabricating standpoints to determine their suitability for operation in the VDR pervaporation module. Pervaporation rates and other performance characteristics were determined in a breadboard pervaporator test rig. Kynar and Teflon membranes were demonstrated to be chemically stable at pervaporation temperatures in urine pretreated with chromic acid bactericide. The separation of the pervaporator and condenser modules, the use of a recirculating sweep gas to conduct pervaporate to the condenser, and the selection of a hollow fiber membrane configuration for pervaporator module design is recommended as a result of the investigation.

  2. Isolation and molecular identification of landfill bacteria capable of growing on di-(2-ethylhexyl) phthalate and deteriorating PVC materials

    PubMed Central

    Latorre, Isomar; Hwang, Sangchul; Montalvo-Rodriguez, Rafael

    2012-01-01

    Waste materials containing Di-(2-ethylhexyl) phthalate (DEHP), a suspected endocrine disruptor and reasonably anticipated human carcinogen, are typically disposed of in landfills. Despite this, very few studies had been conducted to isolate and identify DEHP-degrading bacteria in landfill leachate. Therefore, this study was conducted to isolate and characterize bacteria in landfill leachate growing on DEHP as the sole carbon source and deteriorating PVC materials. Four strains LHM1, LHM2, LHM3 and LHM4, not previously reported as DEHP-degraders, were identified via 16S rRNA gene sequence. Gram-positive strains LHM1 and LHM2 had a greater than 97% similarity with Chryseomicrobium imtechense MW 10(T) and Lysinibacillus fusiformis NBRC 15717(T), respectively. Gram-negative strains LHM3 and LHM4 were related to Acinetobacter calcoaceticus DSM 30006(T) (90.7% similarity) and Stenotrophomonas pavanii ICB 89(T) (96.0% similarity), respectively. Phylogenetic analysis also corroborated these similarities of strains LHM1 and LHM2 to the corresponding bacteria species. Strains LHM2 and LHM4 grew faster than strains LHM1 and LHM3 in the enrichment where DEHP was the sole carbon source. When augmented to the reactors with PVC shower curtains containing DEHP, strains LHM1 and LHM2 developed greater optical densities in the solution phase and thicker biofilm on the surfaces of the shower curtains. PMID:22934997

  3. Study on microwave absorbing properties of carbonyl-iron composite coating based on PVC and Al sheet

    NASA Astrophysics Data System (ADS)

    Yuping, Duan; Guangli, Wu; Shuchao, Gu; Shuqing, Li; Guojia, Ma

    2012-05-01

    To suppress the increasingly terrible electromagnetic pollution, microwave absorption coatings based on polyvinyl chloride (PVC) sheet have been fabricated, employing polyurethane varnish (PU) as matrix and carbonyl-iron particle (CIP) as absorbent. The morphology, static magnetic and microwave absorption properties of CIP were characterized by scanning electron microscope (SEM), vibrating sample magnetometer (VSM) and vector network analyzer (VNA), respectively. Bruggeman's equation was introduced to calculate the electromagnetic parameters of materials in the frequency range of 2-18 GHz and the loss mechanisms were discussed. Furthermore, the microwave absorption properties of composite coatings with different component content and thickness were investigated. The results show that the electromagnetic properties of the composite heavily depended on the particle loadings. The minimum reflection peaks of the coatings shift towards the lower frequency region with the increase of CIP content or coating thickness. PVC-based coatings with a component content of 1:7 (PU:CIP mass ratio) in CIP/PU layer, exhibit a minimum reflection loss value of -29 dB at 4 GHz and a permissible reflection loss (RL ≤ -10 dB) frequency band of 2-6 GHz, which is much better than the performance of the common metal-based coatings in the lower frequency.

  4. Biological membranes

    PubMed Central

    Watson, Helen

    2015-01-01

    Biological membranes allow life as we know it to exist. They form cells and enable separation between the inside and outside of an organism, controlling by means of their selective permeability which substances enter and leave. By allowing gradients of ions to be created across them, membranes also enable living organisms to generate energy. In addition, they control the flow of messages between cells by sending, receiving and processing information in the form of chemical and electrical signals. This essay summarizes the structure and function of membranes and the proteins within them, and describes their role in trafficking and transport, and their involvement in health and disease. Techniques for studying membranes are also discussed. PMID:26504250

  5. Membranous nephropathy

    MedlinePlus

    ... to reduce cholesterol and triglyceride levels (most often statins) may be recommended. A low-salt diet may ... of membranous nephropathy Your symptoms get worse or don't go away You develop new symptoms You have ...

  6. Synthesis of lithium iron phosphate/carbon microspheres by using polyacrylic acid coated iron phosphate nanoparticles derived from iron(III) acrylate.

    PubMed

    Xu, Dongwei; He, Yan-Bing; Chu, Xiaodong; Ding, Zhaojun; Li, Baohua; He, Jianfu; Du, Hongda; Qin, Xianying; Kang, Feiyu

    2015-03-01

    Lithium iron phosphate/carbon (LiFePO4 /C) microspheres with high rate and cycling performance are synthesized from iron phosphate/polyacrylic acid (FePO4 /PAA) nanoparticles. Iron(III) acrylate is used as a precursor for both the iron and carbon sources. FePO4 nanoparticles are first produced by a coprecipitation reaction. The byproduct, acrylic acid ions, is polymerized in situ to form a uniform PAA layer on the surface of the FePO4 nanoparticles. The as-prepared LiFePO4 /C microspheres are composed of primary nanoparticles with sizes of 40-50 nm. The nanoparticles are fully coated with a thin, uniform carbon layer derived from the decomposition of the PAA layer. The uniform carbon-coating layer cooperates with interstitial and boundary carbon derived from sucrose successfully to construct an excellent interconnecting conductive network in the microspheres. As a result of the unique structure, the as-prepared LiFePO4 /C microspheres display both high electronic and ionic conductivities, which contribute to their high rate performance (162.9 mAh g(-1) at 0.1C and 126.1 mAh g(-1) at 5C) and excellent cycling stability (97.1% of capacity retention after 500 cycles at 5C/5C). PMID:25469674

  7. Pseudo-solubilities of potassium sulfate in water in the presence of crystal-growth and -dissolution suppressor iron(III) impurities

    NASA Astrophysics Data System (ADS)

    Kubota, Noriaki; Fujisawa, Yoriko; Yokota, Masaaki; Mullin, J. W.

    1999-02-01

    Iron(III) is a growth and dissolution suppressor for potassium sulfate crystals in aqueous solutions. An excess amount of potassium sulfate crystal powder was agitated for 2 h at 40°C in water contaminated with Fe(III) (10 and 100 ppm (=g Fe/m 3 water)). The resulting concentration of dissolved potassium sulfate was significantly lower than the true equilibrium solubility and changes with initial pH of the contaminated solvent water and the Fe(III) concentration. The decreased concentration (pseudo-solubility) is attributed to stoppage of the dissolution process by the adsorption of Fe(III) on the potassium sulfate crystals. Four salts (FeCl 3·6H 2O, Fe 2(SO 4) 2· nH 2O, FeNH 4(SO 4) 2·12H 2O, FeC 6H 5O 7· nH 2O) were examined as Fe(III) sources, among which the citrate had no effect, but the others had the same effect. An active species for the effect is speculated to be the first hydrolysis product, [Fe(H 2O) 5(OH)] 2+, of Fe(III) aqua-complexes.

  8. Selective sensing of submicromolar iron(III) with 3,3‧,5,5‧-tetramethylbenzidine as a chromogenic probe

    NASA Astrophysics Data System (ADS)

    Zhang, Lufeng; Du, Jianxiu

    2016-04-01

    The development of highly selective and sensitive method for iron(III) detection is of great importance both from human health as well as environmental point of view. We herein reported a simple, selective and sensitive colorimetric method for the detection of Fe(III) at submicromolar level with 3,3,‧5,5‧-tetramethylbenzidine (TMB) as a chromogenic probe. It was observed that Fe(III) could directly oxidize TMB to form a blue solution without adding any extra oxidants. The reaction has a stoichiometric ratio of 1:1 (Fe(III)/TMB) as determined by a molar ratio method. The resultant color change can be perceived by the naked eye or monitored the absorbance change at 652 nm. The method allowed the measurement of Fe(III) in the range 1.0 × 10- 7-1.5 × 10- 4 mol L- 1 with a detection limit of 5.5 × 10- 8 mol L- 1. The relative standard deviation was 0.9% for eleven replicate measurements of 2.5 × 10- 5 mol L- 1 Fe(III) solution. The chemistry showed high selectivity for Fe(III) in contrast to other common cation ions. The practically of the method was evaluated by the determination of Fe in milk samples; good consistency was obtained between the results of this method and atomic absorption spectrophotometry as indicated by statistical analysis.

  9. Spectrophotometric method for the determination of sorbic acid in various food samples with iron(III) and 2-thiobarbituric acid as reagents.

    PubMed

    Lau, O W; Luk, S F; Lam, R K

    1989-02-01

    A simple, rapid and accurate spectrophotometric method has been developed for the determination of sorbic acid in various food samples based on the oxidation of sorbic acid by iron(III) at 100 degrees C to malonaldehyde, which then reacts with 2-thiobarbituric acid to form a reddish brown product. The optimum experimental conditions for colour development have been assessed. Absorbance measurements were made at 529 nm in the presence of 0.4% m/V citric acid. The calibration graph was linear for 0-6 micrograms ml-1 of sorbic acid with a slope of 0.131 A micrograms-1 ml. The recoveries of sorbic acid at concentrations of 164-557 micrograms ml-1 ranged from 96 to 103%. The relative standard deviations of ten replicate determinations of sorbic acid in a synthetic cream soda sample spiked with 573 micrograms ml-1 of sorbic acid and in an onion juice sample containing 82 micrograms ml-1 of sorbic acid were 1.6 and 1.9%, respectively. Interferences from several common food additives can be minimised by extracting sorbic acid with diethyl ether and then back-extracting the acid with sodium hydrogen carbonate. The method has been applied successfully to the determination of sorbic acid in a wide range of food samples including beverages, cake, cake mate, garlic bread sprinkle, onion juice, oyster flavoured sauce and grenadine syrup. PMID:2712320

  10. Mössbauer spectroscopic study on valence-detrapping and trapping of mixed-valence trinuclear iron(III, III, II) fluorine-substituted benzoate complexes

    NASA Astrophysics Data System (ADS)

    Sakai, Yoichi; Onaka, Satoru; Takahashi, Masashi; Ogiso, Ryo; Takayama, Tsutomu; Nakamoto, Tadahiro

    2012-03-01

    Four mixed-valence trinuclear iron(III, III, II) fluorine-substituted benzoate complexes were synthesized; Fe3O(C6F5COO)6(C5H5N)3·CH2Cl2 ( 1), Fe3O(C6F5COO)6(C5H5N)3 ( 2), Fe3O(2H-C6F4COO)6(C5H5N)3 ( 3), and Fe3O(4H-C6F4COO)6(C5H5N)3 ( 4), in which valence-detrapping and trapping phenomena have been investigated by 57Fe- Mössbauer spectroscopy. The valence state of the three iron ions is trapped at lower temperatures while it is fully detrapped at higher temperatures for 1. Valence detrapping is not observed for 2, 3, and 4 even at room temperature, although Mössbauer spectra for 3 and 4 show complicated temperature dependence.

  11. Studies on solvent extraction of iron(III) as a step for conversion of a waste effluent to a value added product.

    PubMed

    Agrawal, Archana; Kumari, S; Sahu, K K

    2011-12-01

    Solvent extraction of iron(III) from actual sulphate waste pickle liquor was investigated using trialkylphosphine oxide diluted with kerosene. The waste pickle liquor was procured from a local company which deals with the manufacturing of pipes and tubes made of iron and steel. Various parameters were studied to optimise a suitable condition for the maximum extraction of iron. The composition of the aqueous feed used in the experiment was 60.88 g/L Fe(III), 53 g/L acid with traces of Cu, Ni and Co. An ambient extraction at 30 °C yielded acceptable kinetics and loading efficiency for 40% trialkylphosphine oxide with a saturated loading capacity of 51.85 g/L in four contacts at O/A ratio of 1/1 in a multiple contact mode. Iron from the loaded organic was stripped using various strippants such as distilled water, H(2)SO(4) and oxalic acid. Since only 32% of loaded Fe could be stripped with 2 M H(2)SO(4) in five contacts, further stripping was done with 5% oxalic acid which showed a very promising result. It was found that almost 100% of Fe(III) could be stripped out with 5% oxalic acid at O/A of 1/1 in five contacts. PMID:21862202

  12. Preparation and Properties of Double-Sided AgNWs/PVC/AgNWs Flexible Transparent Conductive Film by Dip-Coating Process.

    PubMed

    Chen, Cui-Yu; Jing, Mao-Xiang; Pi, Zhi-Chao; Zhu, Sheng-Wen; Shen, Xiang-Qian

    2015-12-01

    The double-sided transparent conductive films of AgNWs/PVC/AgNWs using the silver nanowires and PVC substrate were fabricated by the dip-coating process followed by mechanical press treatment. The morphological and structural characteristics were investigated by scanning electron microscope (SEM) and atomic force microscope (AFM), the photoelectric properties and mechanical stability were measured by ultraviolet-visible spectroscopy (UV-vis) spectrophotometer, four-point probe technique, 3M sticky tape test, and cyclic bending test. The results indicate that the structure and photoelectric performances of the AgNWs films were mainly affected by the dipping and lifting speeds. At the optimized dipping speed of 50 mm/min and lifting speed of 100 mm/min, the AgNWs are evenly distributed on the surface of the PVC substrate, and the sheet resistance of AgNWs film on both sides of PVC is about 60 Ω/sq, and the optical transmittance is 84.55 % with the figure of merit value up to 35.8. The film treated with the 10 MPa pressure shows excellent adhesion and low surface roughness of 17.8 nm and maintains its conductivity with the sheet resistance change of 17 % over 10,000 cyclic bends. PMID:26245859

  13. The Effect of Zn-Al-Hydrotalcites Composited with Calcium Stearate and β-Diketone on the Thermal Stability of PVC

    PubMed Central

    Tong, Mengliang; Chen, Hongyan; Yang, Zhanhong; Wen, Runjuan

    2011-01-01

    A clean-route synthesis of Zn-Al-hydrotalcites (Zn-Al-LDHs) using zinc oxide and sodium aluminate solution has been developed. The as-obtained materials were characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), and scanning electron microscopy (SEM). The effects of metal ions at different molar ratios on the performance of hydrotalcites were discussed. The results showed that the Zn-Al-hydrotalcites can be successfully synthesized at three different Zn/Al ratios of 3:1, 2:1 and 1:1. Thermal aging tests of polyvinyl chloride (PVC) mixed with Zn-Al-LDHs, calcium stearate (CaSt2) and β-diketone were carried out in a thermal aging test box by observing the color change. The results showed that Zn-Al-LDHs can not only enhance the stability of PVC significantly due to the improved capacity of HCl-adsorption but also increase the initial stability and ensure good-initial coloring due to the presence of the Zn element. The effects of various amounts of Zn-Al-LDHs, CaSt2 and β-diketone on the thermal stability of PVC were discussed. The optimum composition was determined to be 0.1 g Zn-Al-LDHs, 0.15 g CaSt2 and 0.25 g β-diketone in 5 g PVC. PMID:21673921

  14. Preparation and Properties of Double-Sided AgNWs/PVC/AgNWs Flexible Transparent Conductive Film by Dip-Coating Process

    NASA Astrophysics Data System (ADS)

    Chen, Cui-yu; Jing, Mao-xiang; Pi, Zhi-chao; Zhu, Sheng-wen; Shen, Xiang-qian

    2015-08-01

    The double-sided transparent conductive films of AgNWs/PVC/AgNWs using the silver nanowires and PVC substrate were fabricated by the dip-coating process followed by mechanical press treatment. The morphological and structural characteristics were investigated by scanning electron microscope (SEM) and atomic force microscope (AFM), the photoelectric properties and mechanical stability were measured by ultraviolet-visible spectroscopy (UV-vis) spectrophotometer, four-point probe technique, 3M sticky tape test, and cyclic bending test. The results indicate that the structure and photoelectric performances of the AgNWs films were mainly affected by the dipping and lifting speeds. At the optimized dipping speed of 50 mm/min and lifting speed of 100 mm/min, the AgNWs are evenly distributed on the surface of the PVC substrate, and the sheet resistance of AgNWs film on both sides of PVC is about 60 Ω/sq, and the optical transmittance is 84.55 % with the figure of merit value up to 35.8. The film treated with the 10 MPa pressure shows excellent adhesion and low surface roughness of 17.8 nm and maintains its conductivity with the sheet resistance change of 17 % over 10,000 cyclic bends.

  15. A MIXTURE OF ORGANOTINS FOUND IN POLYVINYL CHLORIDE (PVC) PIPE IS NOT IMMUNOTOXIC TO SPRAGUE-DAWLEY RATS WHEN GIVEN IN DRINKING WATER

    EPA Science Inventory

    Organotin compounds used in PVC pipe production are of concern to the U.S. EPA because they leach from supply pipes into drinking water and are reported multisystem toxicants. We assessed immune functions in male Sprague-Dawley rats exposed to the mixture of organotins used in P...

  16. The effect of Zn-Al-hydrotalcites composited with calcium stearate and β-diketone on the thermal stability of PVC.

    PubMed

    Tong, Mengliang; Chen, Hongyan; Yang, Zhanhong; Wen, Runjuan

    2011-01-01

    A clean-route synthesis of Zn-Al-hydrotalcites (Zn-Al-LDHs) using zinc oxide and sodium aluminate solution has been developed. The as-obtained materials were characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), and scanning electron microscopy (SEM). The effects of metal ions at different molar ratios on the performance of hydrotalcites were discussed. The results showed that the Zn-Al-hydrotalcites can be successfully synthesized at three different Zn/Al ratios of 3:1, 2:1 and 1:1. Thermal aging tests of polyvinyl chloride (PVC) mixed with Zn-Al-LDHs, calcium stearate (CaSt(2)) and β-diketone were carried out in a thermal aging test box by observing the color change. The results showed that Zn-Al-LDHs can not only enhance the stability of PVC significantly due to the improved capacity of HCl-adsorption but also increase the initial stability and ensure good-initial coloring due to the presence of the Zn element. The effects of various amounts of Zn-Al-LDHs, CaSt(2) and β-diketone on the thermal stability of PVC were discussed. The optimum composition was determined to be 0.1 g Zn-Al-LDHs, 0.15 g CaSt(2) and 0.25 g β-diketone in 5 g PVC. PMID:21673921

  17. Ion-selective charge separation at the phase boundary of ionophore-incorporated liquid membranes as studied by optical second-harmonic generation

    NASA Astrophysics Data System (ADS)

    Tohda, Koji; Yoshiyagawa, Shinji; Umezawa, Yoshio

    1997-06-01

    Optical second-harmonic generation (SHG) in various plasticized poly(vinyl chloride) (PVC)-based ion-selective membranes was observed. The SHG signal from the ionophore-incorporated membranes in contact with an aqueous solution of selective cation chloride salts generally increased with increase of the cation concentration and then levelled off. This result was explained by the formation of oriented and therefore SHG-active cation-ionophore complexes at the membrane surface. The fact that the membrane potential and SHG signal changed in parallel revealed that the observed membrane potentials were primarily governed by SHG-active oriented complex cations at the membrane surface. The effect of the ionophore structures and their cation selectivities on the SHG responses was also examined and discussed.

  18. Membrane magic

    SciTech Connect

    Buecker, B.

    2005-09-01

    The Kansas Power and Light Co.'s La Cyne generating station has found success with membrane filtration water pretreatment technology. The article recounts the process followed in late 2004 to install a Pall Aria 4 microfilter in Unit 1 makeup water system at the plant to produce cleaner water for reverse osmosis feed. 2 figs., 2 photos.

  19. Schiff's Bases and Crown Ethers as Supramolecular Sensing Materials in the Construction of Potentiometric Membrane Sensors

    PubMed Central

    Faridbod, Farnoush; Ganjali, Mohammad Reza; Dinarvand, Rassoul; Norouzi, Parviz; Riahi, Siavash

    2008-01-01

    Ionophore incorporated PVC membrane sensors are well-established analytical tools routinely used for the selective and direct measurement of a wide variety of different ions in complex biological and environmental samples. Potentiometric sensors have some outstanding advantages including simple design and operation, wide linear dynamic range, relatively fast response and rational selectivity. The vital component of such plasticized PVC members is the ionophore involved, defining the selectivity of the electrodes' complex formation. Molecular recognition causes the formation of many different supramolecules. Different types of supramolecules, like calixarenes, cyclodextrins and podands, have been used as a sensing material in the construction of ion selective sensors. Schiff's bases and crown ethers, which feature prominently in supramolecular chemistry, can be used as sensing materials in the construction of potentiometric ion selective electrodes. Up to now, more than 200 potentiometric membrane sensors for cations and anions based on Schiff's bases and crown ethers have been reported. In this review cation binding and anion complexes will be described. Liquid membrane sensors based on Schiff's bases and crown ethers will then be discussed.

  20. Lead-selective membrane potentiometric sensor based on a recently synthesized bis(anthraquinone) sulfide derivative

    SciTech Connect

    Pouretedal, H.R.; Forghaniha, A.; Sharghi, H.; Shamsipur, M.

    1998-12-01

    The need for monitoring of toxic heavy metal ions in environmental samples has prompted the development of ion-selective electrodes for these ions. A new PVC membrane electrode for lead ions, based on bis[(1-hydroxy-9,10-anthraquinone)-2-methyl]sulfide as membrane carrier, was prepared. The sensor exhibits a Nernstian response for Pb{sup 2+} over a wide concentration range (5.6 {times} 10{sup {minus}3}--4.0 {times} 10{sup {minus}6} M). It has a response time of about 30 s and can be used for at least 3 months without any divergence in potentials. The proposed membrane sensor revealed good selectivities for Pb{sup 2+} over a wide variety of other metal ions. It was used as an indicator electrode in potentiometric titration of lead ion.

  1. Iron(III) complexes of sterically hindered tetradentate monophenolate ligands as functional models for catechol 1,2-dioxygenases: the role of ligand stereoelectronic properties.

    PubMed

    Velusamy, Marappan; Mayilmurugan, Ramasamy; Palaniandavar, Mallayan

    2004-10-01

    The iron(III) complexes of the monophenolate ligands 2-(bis(pyrid-2-ylmethyl)aminomethyl)-4-nitrophenol [H(L1)], N,N-dimethyl-N'-(pyrid-2-ylmethyl)-N'-(2-hydroxy-4-nitrobenzyl)ethylenediamine [H(L2)], N,N-dimethyl-N'-(6-methyl-pyrid-2-ylmethyl)-N'-(2-hydroxy-4-nitrobenzyl)ethylenediamine [H(L3)], and N,N-dimethyl-N'-(1-methylimidazole-2-ylmethyl)-N'-(2-hydroxy-4-nitrobenzyl)ethylenediamine [H(L4)] have been obtained and studied as structural and functional models for the intradiol-cleaving catechol dioxygenase enzymes. The complexes [Fe(L1)Cl(2)].CH(3)CN (1), [Fe(L2)Cl(2)] (2), [Fe(L3)Cl(2)] (3), and [Fe(L4)Cl(2)] (4) have been characterized using absorption spectral and electrochemical methods. The single crystal X-ray crystal structures of 1 and 2 have been successfully determined. Both the complexes possess a rhombically distorted octahedral coordination geometry for the FeN(3)OCl(2) chromophore. In 2, the phenolate oxygen, the pyridine nitrogen, an amine nitrogen, and a chloride ion are located on the corners of a square plane with the nitrogen atom of a -NMe(2) group and the other chloride ion occupying the axial positions. In 1, also the equatorial plane is constituted by the phenolate oxygen, the pyridine nitrogen, an amine nitrogen atom, and a chloride ion; however, the axial positions are occupied by the second pyridine nitrogen and the second chloride ion. Interestingly, the Fe-O-C angle of 136.1 degrees observed for 2 is higher than that (128.5 degrees ) in 1; however, the Fe-O(phenolate) bond distances in both the complexes are the same (1.929 A). This illustrates the importance of the nearby sterically demanding coordinated -NMe(2) group and implies similar stereochemical constraints from the other ligated amino acid moieties in the 3,4-PCD enzymes, the enzyme activity of which is traced to the difference in the equatorial and axial Fe-O(tyrosinate) bonds (Fe-O-C, 133 degrees, 148 degrees ). The nature of heterocyclic rings of the ligands and the

  2. [Membranous nephropathy].

    PubMed

    Mercadal, Lucile

    2013-12-01

    Membranous nephropathy is characterized by immune complex deposits on the outer side of the glomerular basement membrane. Activation of complement and of oxidation lead to basement membrane lesions. The most frequent form is idiopathic. At 5 and 10 years, renal survival is around 90 and 65% respectively. A prognostic model based on proteinuria, level and duration, progression of renal failure in a few months can refine prognosis. The urinary excretion of C5b-9, β2 and α1 microglobuline and IgG are strong predictors of outcome. Symptomatic treatment is based on anticoagulation in case of nephrotic syndrome, angiotensin conversion enzyme inhibitors, angiotensin II receptor blockers and statins. Immunosuppressive therapy should be discussed for patients having a high risk of progression. Corticoids alone has no indication. Treatment should include a simultaneous association or more often alternating corticoids and alkylant agent for a minimum of 6 months. Adrenocorticoid stimulating hormone and steroids plus mycophenolate mofetil may be equally effective. Steroids plus alkylant decrease the risk of end stage renal failure. Cyclosporine and tacrolimus decrease proteinuria but are associated with a high risk of recurrence at time of withdrawal and are nephrotoxic. Rituximab evaluated on open studies needs further evaluations to define its use. PMID:24315535

  3. Reduction of Toxoplasma gondii Development Due to Inhibition of Parasite Antioxidant Enzymes by a Dinuclear Iron(III) Compound

    PubMed Central

    Portes, J. A.; Souza, T. G.; dos Santos, T. A. T.; da Silva, L. L. R.; Ribeiro, T. P.; Pereira, M. D.; Horn, A.; Fernandes, C.; DaMatta, R. A.; de Souza, W.

    2015-01-01

    Toxoplasma gondii, the causative agent of toxoplasmosis, is an obligate intracellular protozoan that can infect a wide range of vertebrate cells. Here, we describe the cytotoxic effects of the dinuclear iron compound [Fe(HPCINOL)(SO4)]2-μ-oxo, in which HPCINOL is the ligand 1-(bis-pyridin-2-ylmethyl-amino)-3-chloropropan-2-ol, on T. gondii infecting LLC-MK2 host cells. This compound was not toxic to LLC-MK2 cells at concentrations of up to 200 μM but was very active against the parasite, with a 50% inhibitory concentration (IC50) of 3.6 μM after 48 h of treatment. Cyst formation was observed after treatment, as indicated by the appearance of a cyst wall, Dolichos biflorus lectin staining, and scanning and transmission electron microscopy characteristics. Ultrastructural changes were also seen in T. gondii, including membrane blebs and clefts in the cytoplasm, with inclusions similar to amylopectin granules, which are typically found in bradyzoites. An analysis of the cell death pathways in the parasite revealed that the compound caused a combination of apoptosis and autophagy. Fluorescence assays demonstrated that the redox environment in the LLC-MK2 cells becomes oxidant in the presence of the iron compound. Furthermore, a reduction in superoxide dismutase and catalase activities in the treated parasites and the presence of reactive oxygen species within the parasitophorous vacuoles were observed, indicating an impaired protozoan response against these radicals. These findings suggest that this compound disturbs the redox equilibrium of T. gondii, inducing cystogenesis and parasite death. PMID:26392498

  4. Reduction of Toxoplasma gondii Development Due to Inhibition of Parasite Antioxidant Enzymes by a Dinuclear Iron(III) Compound.

    PubMed

    Portes, J A; Souza, T G; dos Santos, T A T; da Silva, L L R; Ribeiro, T P; Pereira, M D; Horn, A; Fernandes, C; DaMatta, R A; de Souza, W; Seabra, S H

    2015-12-01

    Toxoplasma gondii, the causative agent of toxoplasmosis, is an obligate intracellular protozoan that can infect a wide range of vertebrate cells. Here, we describe the cytotoxic effects of the dinuclear iron compound [Fe(HPCINOL)(SO4)]2-μ-oxo, in which HPCINOL is the ligand 1-(bis-pyridin-2-ylmethyl-amino)-3-chloropropan-2-ol, on T. gondii infecting LLC-MK2 host cells. This compound was not toxic to LLC-MK2 cells at concentrations of up to 200 μM but was very active against the parasite, with a 50% inhibitory concentration (IC50) of 3.6 μM after 48 h of treatment. Cyst formation was observed after treatment, as indicated by the appearance of a cyst wall, Dolichos biflorus lectin staining, and scanning and transmission electron microscopy characteristics. Ultrastructural changes were also seen in T. gondii, including membrane blebs and clefts in the cytoplasm, with inclusions similar to amylopectin granules, which are typically found in bradyzoites. An analysis of the cell death pathways in the parasite revealed that the compound caused a combination of apoptosis and autophagy. Fluorescence assays demonstrated that the redox environment in the LLC-MK2 cells becomes oxidant in the presence of the iron compound. Furthermore, a reduction in superoxide dismutase and catalase activities in the treated parasites and the presence of reactive oxygen species within the parasitophorous vacuoles were observed, indicating an impaired protozoan response against these radicals. These findings suggest that this compound disturbs the redox equilibrium of T. gondii, inducing cystogenesis and parasite death. PMID:26392498

  5. Lipid membranes for membrane proteins.

    PubMed

    Kukol, Andreas

    2015-01-01

    The molecular dynamics (MD) simulation of membrane proteins requires the setup of an accurate representation of lipid bilayers. This chapter describes the setup of a lipid bilayer system from scratch using generally available tools, starting with a definition of the lipid molecule POPE, generation of a lipid bilayer, energy minimization, MD simulation, and data analysis. The data analysis includes the calculation of area and volume per lipid, deuterium order parameters, self-diffusion constant, and the electron density profile. PMID:25330959

  6. Omniphobic Membrane for Robust Membrane Distillation

    SciTech Connect

    Lin, SH; Nejati, S; Boo, C; Hu, YX; Osuji, CO; Ehmelech, M

    2014-11-01

    In this work, we fabricate an omniphobic microporous membrane for membrane distillation (MD) by modifying a hydrophilic glass fiber membrane with silica nanoparticles followed by surface fluorination and polymer coating. The modified glass fiber membrane exhibits an anti-wetting property not only against water but also against low surface tension organic solvents that easily wet a hydrophobic polytetrafluoroethylene (PTFE) membrane that is commonly used in MD applications. By comparing the performance of the PTFE and omniphobic membranes in direct contact MD experiments in the presence of a surfactant (sodium dodecyl sulfate, SDS), we show that SDS wets the hydrophobic PTFE membrane but not the omniphobic membrane. Our results suggest that omniphobic membranes are critical for MD applications with feed waters containing surface active species, such as oil and gas produced water, to prevent membrane pore wetting.

  7. Organophosphorus reagents as extractants-part 3. Synergic effect of triphenyl phosphine oxide and bis(diphenyl phosphinyl) alkanes on extraction of iron(III) from thiocyanate medium with 2,4-pentdione.

    PubMed

    Lobana, T S; Bhatia, P K

    1992-06-01

    The extraction of iron(III) from thiocyanate medium was carried out with a synergic combination of 2,4-pentdione (Hacac) and either triphenyl phosphine oxide (Ph(3) PO) or bis (diphenylphosphinyl) alkanes, Ph(2)P(O)(CH(2))(n).P(O)PH(2) [ligand abbreviation, n: dpeO(2), 2; dpbO(2), 4]. Iron(III) was quantitatively separated from its binary mixture with chromium(III), manganese(III), cobalt(II), nickel(II), zinc(II), cadmium(II), mercury(II), lead(II), magnesium(II) and from steel samples. Copper(II) and silver(I) however, interfered. The percentage extraction was 99.0%. The respective extraction constants, K(HA), K(L) or K(syn), for the extracted species, [Fe(NCS)(acac)(2)(H(2)O)] (HA Hacac), Fe(NCS)(3)L(2) [L b Ph(3)PO, dpeO(2) or dpbO(2)], or Fe(NCS)(acac)(2)L were found to be: K(HA), 1.48 x 10(3), K(L), 1.80 x 10(2) (L Ph(3)PO), 2.02 x 10(2) (L dpeO(2) or dpbO(2)) and K(syn), 1.87 x 10(6) (L Ph(3)PO), 2.56 x 10(6) [L dpeO(2) or dpbO(2)]. PMID:18965433

  8. An application of enhanced 3D-CAD methods with integrated geometry creation algorithms for PVC-seams in automotive body in white design

    NASA Astrophysics Data System (ADS)

    Frener, Gernot; Thum, Katharina; Hirz, Mario; Harrich, Alexander

    2012-06-01

    State of the art automotive development processes are based on virtual product models, which include a digital representation of complete vehicle geometry and structures. Increasing computation performance and continuously growing demands on virtual development processes lead to the application of precise product representation within common CAD software packages. A specific challenge represents the creation of PVC-seams, which are used for corrosion protection of sheet metal components in automotive body in white design. Besides the high requirements of accurate geometric modeling in digital representation, modern development processes call for an increasing level of design automation. To fit both, the present approach introduces a method for an automatic generation of PVC-seams using the functionalities of commercial CAD software. [Figure not available: see fulltext.

  9. Synergistic anti-biofouling effect of Ag-exchanged zeolite and D-Tyrosine on PVC composite against the clinical isolate of Acinetobacter baumannii.

    PubMed

    Milenkovic, Jelena; Hrenovic, Jasna; Goic-Barisic, Ivana; Tomic, Milos; Djonlagic, Jasna; Rajic, Nevenka

    2014-09-01

    Due to their susceptibility to bacterial biofilm formation, commercial tubes for medical use are one of the main sources of hospital infections with Acinetobacter baumannii. The anti-biofouling activity of novel composites against the clinical isolate of the multi-drug resistant A. baumannii is reported here. The composites were prepared by addition of micronised silver-exchanged natural zeolite (Ag-NZ) into poly(vinyl chloride) (PVC), followed by coating of the composites with D-Tyrosine (D-Tyr). The Ag-NZ composites (containing 1-15 wt% of Ag-NZ) coated with D-Tyr (Ag-NZ-Tyr) showed a bactericidal effect (100% or a 6.9 log CFU reduction) towards immobilised bacterial cells. The uncoated Ag-NZ composites showed a reduction of up to 70% (4.4 log CFU) of immobilised bacteria in comparison with the original PVC. Rheological testing of the composites revealed that the addition of Ag-NZ slightly affected processability and formability of the PVC and increased the elasticity of the polymer matrix. PMID:25237773

  10. Emission of di-2-ethylhexyl phthalate from PVC flooring into air and uptake in dust: emission and sorption experiments in FLEC and CLIMPAQ.

    PubMed

    Clausen, Per Axel; Hansen, Vivi; Gunnarsen, Lars; Afshari, Alireza; Wolkoff, Peder

    2004-05-01

    The emission of di-2-ethylhexyl phthalate (DEHP) from a PVC flooring was studied for up to 472 days in both the FLEC (Field and Laboratory Emission Cell) and the CLIMPAQ (Chamberfor Laboratory Investigations of Materials, Pollution, and Air Quality). The loading of the CLIMPAQs was varied but was constant in the FLECs. The sorption properties of FLEC and CLIMPAQ were investigated using different methods. In addition, the uptake of DEHP by office floor dust on the PVC flooring was studied in CLIMPAQ experiments. The concentration versus time curves in both FLECs and CLIMPAQs increased slowly over about 150 days and reached a quasi-static equilibrium at 1 microg m(-3). The main conclusions were that (i) the emission rate of DEHP was limited by gas-phase mass transport and (ii) the dust layer increased the emission rate by increasing the external concentration gradient above the surface of the PVC. These conclusions were based on the facts that the specific emission rate was inversely proportional to the loading and that the dust had sorbed about four times as much DEHP over a 68-day period as emitted in the gas-phase experiments. About one-half of the emitted DEHP was deposited on the internal surfaces of both the FLEC and the CLIMPAQ. PMID:15180047

  11. Electrodriven selective transport of Cs+ using chlorinated cobalt dicarbollide in polymer inclusion membrane: a novel approach for cesium removal from simulated nuclear waste solution.

    PubMed

    Chaudhury, Sanhita; Bhattacharyya, Arunasis; Goswami, Asok

    2014-11-01

    The work describes a novel and cleaner approach of electrodriven selective transport of Cs from simulated nuclear waste solutions through cellulose tri acetate (CTA)/poly vinyl chloride (PVC) based polymer inclusion membrane. The electrodriven cation transport together with the use of highly Cs+ selective hexachlorinated derivative of cobalt bis dicarbollide, allows to achieve selective separation of Cs+ from high concentration of Na+ and other fission products in nuclear waste solutions. The transport selectivity has been studied using radiotracer technique as well as atomic emission spectroscopic technique. Transport studies using CTA based membrane have been carried out from neutral solution as well as 0.4 M HNO3, while that with PVC based membrane has been carried out from 3 M HNO3. High decontamination factor for Cs+ over Na+ has been obtained in all the cases. Experiment with simulated high level waste solution shows selective transport of Cs+ from most of other fission products also. Significantly fast Cs+ transport rate along with high selectivity is an interesting feature observed in this membrane. The current efficiency for Cs+ transport has been found to be ∼100%. The promising results show the possibility of using this kind of electrodriven membrane transport methods for nuclear waste treatment. PMID:25299942

  12. The relationship between the strength of hydrogen bonding and spin crossover behaviour in a series of iron(III) Schiff base complexes.

    PubMed

    Nemec, Ivan; Herchel, Radovan; Trávníček, Zdeněk

    2015-03-14

    X-ray crystal structures and magnetic properties of an isostructural series of iron(III) Schiff base complexes with the general formula [Fe(L(5))(NCX)]·Solv (where H2L(5) = N,N'-bis(2-hydroxy-naphthylidene)-1,6-diamino-4-azahexane, X = S, Solv = tetrahydrofuran, 1a; X = S, Solv = methanol and 0.5 pyrazine, 1b; X = S, Solv = butanone, 1c; Solv = N,N'-dimethylformamide, X = S (1d) or X = Se (1d'); X = S, Solv = dimethyl sulfoxide, 1e) are reported. In the crystals, the individual [Fe(L(5))(NCX)] molecules are connected through weak C-H···O, C-H···π or C-H···S non-covalent contacts into 2D supramolecular networks, while the guest-solvent (Solv) molecules are trapped in the cavities between two adjacent layers, which are furthermore stabilized by N-H···O hydrogen bonds connecting the Solv oxygen atom with the amine group of the [Fe(L(5))(NCX)] molecule, with the N···O distances varying from 2.921(6) Å (in 1d') to 3.295(2) Å (in 1a). The magnetic properties of the complexes were tuned by the different Solv molecules and as a result of this, four new spin crossover (SCO) compounds with cooperative spin transitions are reported, which are accompanied by thermal hysteresis in two cases (1d and 1e): , T1/2 = 84 K; 1d, T1/2↓ = 232 K, T1/2↑ = 235 K and 1e, T1/2↓ = 127 K, T1/2↑ = 138 K. The role of the N-H···O hydrogen bonding in the occurrence and tuning of SCO was also computationally studied using a topological analysis, and also by evaluation of non-covalent interaction (NCI) indexes. Both theoretical approaches showed a clear relationship between the strength of the N-H···O hydrogen bonds and T1/2, as already inferred from X-ray structural and magnetic data. PMID:25645590

  13. Selective Iron(III) ion uptake using CuO-TiO2 nanostructure by inductively coupled plasma-optical emission spectrometry

    PubMed Central

    2012-01-01

    Background CuO-TiO2 nanosheets (NSs), a kind of nanomaterials is one of the most attracting class of transition doped semiconductor materials due to its interesting and important optical, electrical, and structural properties and has many technical applications, such as in metal ions detection, photocatalysis, Chemi-sensors, bio-sensors, solar cells and so on. In this paper the synthesis of CuO-TiO2 nanosheets by the wet-chemically technique is reported. Methods CuO-TiO2 NSs were prepared by a wet-chemical process using reducing agents in alkaline medium and characterized by UV/vis., FT-IR spectroscopy, X-ray photoelectron spectroscopy (XPS), powder X-ray diffraction (XRD), and field-emission scanning electron microscopy (FE-SEM) etc. Results The structural and optical evaluation of synthesized NSs were measured by XRD pattern, Fourier transform infrared (FT-IR) and UV–vis spectroscopy, respectively which confirmed that the obtained NSs are well-crystalline CuO-TiO2 and possessing good optical properties. The morphological analysis of CuO-TiO2 NSs was executed by FE-SEM, which confirmed that the doped products were sheet-shaped and growth in large quantity. Here, the analytical efficiency of the NSs was applied for a selective adsorption of iron(III) ion prior to detection by inductively coupled plasma-optical emission spectrometry (ICP-OES). The selectivity of NSs towards various metal ions, including Au(III), Cd(II), Co(II), Cr(III), Fe(III), Pd(II), and Zn(II) was analyzed. Conclusions Based on the selectivity study, it was confirmed that the selectivity of doped NSs phase was the most towards Fe(III) ion. The static adsorption capacity for Fe(III) was calculated to be 110.06 mgg−1. Results from adsorption isotherm also verified that the adsorption process was mainly monolayer-adsorption onto a surface containing a finite number of CuO-TiO2 NSs adsorption sites. PMID:23244218

  14. Kinetics and {sup 13}C NMR study of oxygen incorporation into PVC- and pitch-derived materials

    SciTech Connect

    Gisele F. Altoe; Jair C.C. Freitas; Alfredo G. Cunha; Francisco G. Emmerich; Mark E. Smith

    2009-03-15

    The kinetics of oxygen incorporation into a PVC-derived material with pitch-like characteristics was studied by isothermal thermogravimetric analysis at temperatures ranging from 200 to 270{sup o}C. Activation energy, E{sub a}, pre-exponential factor, A, and rate constants, kT, were obtained from the weight-gain curves recorded during reactions of the material with molecular oxygen, which were analyzed following a kinetic first-order model. The numerical values obtained were E{sub a} = 100.5 kJ/mol and A = 1.6 x 1010 h{sup -1}. The extent of the oxidation at a fixed temperature was monitored by elemental analysis, and the chemical changes in the materials were followed by solid-state {sup 13}C NMR. The study was next extended to the chars obtained from three coal tar pitches with different softening points (55, 85, and 110{sup o}C). Comparisons were then established between the determined kinetic parameters and the chemical/structural aspects and compositions of each analyzed material. 23 refs., 7 figs., 3 tabs,

  15. Solid state self-healing system: Effects of using PDGEBA, PVC and PVA as linear healing agents

    NASA Astrophysics Data System (ADS)

    Muhamad, Noor Nabilah; Jamil, Mohd. Suzeren Md.; Abdullah, Shahrum

    2014-09-01

    The solid state self-healing system was obtained by employing a thermosetting epoxy resin, into which a thermoplastic is dissolved. In this study, the effect of healing efficiency was investigated by using different thermoplastic polymers which are poly(bisphenol-A-co-epichlorohydrin), polyvinyl chloride and polyvinyl alcohol as healing agents. Healing was achieved by heating the fractured resins to a specific temperature i.e. above their glass transition temperature (Tg) which obtained from dynamic mechanical analysis (DMA) to mobilize the polymeric chains of the healing agent. The curing reaction in the epoxy resins were characterized by means of Fourier transform infrared spectroscopy (FTIR). Izod impact test was been performed to demonstrate self-healing of the different specimens. Under test, it was found that healable resin with PDGEBA has highest healing efficiency followed by PVC and PVA, with 63%, 35% and 18% of average percentage healing efficiencies respectively. These results are due to the different solubility parameters of the thermoset/network and thermoplastic polymer which led to the phase separation. Morphological studies prove the fracture-healing process and morphological properties of the resins.

  16. Experimental, Theoretical and Numerical Investigation of the Flexural Behaviour of the Composite Sandwich Panels with PVC Foam Core

    NASA Astrophysics Data System (ADS)

    Mostafa, A.; Shankar, K.; Morozov, E. V.

    2014-08-01

    This study presents the main results of an experimental, theoretical and numerical investigation on the flexural behaviour and failure mode of composite sandwich panels primarily developed for marine applications. The face sheets of the sandwich panels are made up of glass fibre reinforced polymer (GFRP), while polyvinylchloride (PVC) foam was used as core material. Four-point bending test was carried out to investigate the flexural behaviour of the sandwich panel under quasi static load. The finite element (FE) analysis taking into account the cohesive nature of the skin-core interaction as well as the geometry and materials nonlinearity was performed, while a classical beam theory was used to estimate the flexural response. Although the FE results accurately represented the initial and post yield flexural response, the theoretical one restricted to the initial response of the sandwich panel due to the linearity assumptions. Core shear failure associate with skin-core debonding close to the loading points was the dominant failure mode observed experimentally and validated numerically and theoretically.

  17. Adenovirus, MS2 and PhiX174 interactions with drinking water biofilms developed on PVC, cement and cast iron.

    PubMed

    Helmi, K; Menard-Szczebara, F; Lénès, D; Jacob, P; Jossent, J; Barbot, C; Delabre, K; Arnal, C

    2010-01-01

    Biofilms colonizing pipe surfaces of drinking water distribution systems could provide habitat and shelter for pathogenic viruses present in the water phase. This study aims (i) to develop a method to detect viral particles present in a drinking water biofilm and (ii) to study viral interactions with drinking water biofilms. A pilot scale system was used to develop drinking water biofilms on 3 materials (7 cm(2) discs): PVC, cast iron and cement. Biofilms were inoculated with viral model including MS2, PhiX174 or adenovirus. Five techniques were tested to recover virus from biofilms. The most efficient uses beef extract and glycine at pH = 9. After sonication and centrifugation, the pH of the supernatant is neutralized prior to viral analysis. The calculated recovery rates varied from 29.3 to 74.6% depending on the virus (MS2 or PhiX174) and the material. Applying this protocol, the interactions of virus models (MS2 and adenovirus) with drinking water biofilms were compared. Our results show that adsorption of viruses to biofilms depends on their isoelectric points, the disc material and the hydrodynamic conditions. Applying hydrodynamic conditions similar to those existing in drinking water networks resulted in a viral adsorption corresponding to less than 1% of the initial viral load. PMID:20555217

  18. Improved ion-selective detection method using nanopipette with poly(vinyl chloride)-based membrane.

    PubMed

    Kang, Eun Ji; Takami, Tomohide; Deng, Xiao Long; Son, Jong Wan; Kawai, Tomoji; Park, Bae Ho

    2014-05-15

    Ion-selective electrodes (ISEs) are widely used to detect targeted ions in solution selectively. Application of an ISE to a small area detection system with a nanopipette requires a special measurement method in order to avoid the enhanced background signal problem caused by a cation-rich layer near the charged inner surface of the nanopipette and the selectivity change problem due to relatively fast saturation of the ISE inside the nanopipette. We developed a novel ion-selective detection system using a nanopipette that measures an alternating current (AC) signal mediated by saturated ionophores in a poly(vinyl chloride) (PVC) membrane located at the conical shank of the nanopipette to solve the above problems. Small but reliable K(+) and Na(+) ionic current passing through a PVC membrane containing saturated bis(benzo-15-crown-5) and bis(12-crown-4) ionophore, respectively, could be selectively detected using the AC signal measurement system equipped with a lock-in amplifier. PMID:24766420

  19. Anion permselective membrane

    NASA Technical Reports Server (NTRS)

    Hodgdon, R. B.; Waite, W. A.

    1980-01-01

    The efforts on the synthesis of polymer anion redox membranes were mainly concentrated in two areas, membrane development and membrane fabrication. Membrane development covered the preparation and evaluation of experimental membranes systems with improved resistance stability and/or lower permeability. Membrane fabrication covered the laboratory scale production of prime candidate membranes in quantities of up to two hundred and sizes up to 18 inches x 18 inches (46 cm x 46 cm). These small (10 in x 11 in) and medium sized membranes were mainly for assembly into multicell units. Improvements in processing procedures and techniques for preparing such membrane sets lifted yields to over 90 percent.

  20. Selecting a Roof Membrane.

    ERIC Educational Resources Information Center

    Waldron, Larry W.

    1990-01-01

    Offers a brief synopsis of the unique characteristics of the following roof membranes: (1) built-up roofing; (2) elastoplastic membranes; (3) modified bitumen membranes; (4) liquid applied membranes; and (5) metal roofing. A chart compares the characteristics of the raw membranes only. (MLF)

  1. Magnetic Membrane System

    DOEpatents

    McElfresh, Michael W.; ; Lucas, Matthew S.

    2004-12-30

    The present invention provides a membrane with magnetic particles. In one embodiment the membrane is created by mixing particles in a non-magnetic base. The membrane may act as an actuator, a sensor, a pump, a valve, or other device. A magnet is operatively connected to the membrane. The magnet acts on and changes the shape of the membrane.

  2. Membrane Systems in Cyanobacteria

    SciTech Connect

    Liberton, Michelle L.; Pakrasi, Himadri B.

    2008-01-01

    Cyanobacteria are photosynthetic prokaryotes with highly differentiated membrane systems. In addition to a Gram-negative-type cell envelope with plasma membrane and outer membrane separated by a periplasmic space, cyanobacteria have an internal system of thylakoid membranes where the fully functional electron transfer chains of photosynthesis and respiration reside. The presence of different membrane systems lends these cells a unique complexity among bacteria. Cyanobacteria must be able to reorganize the membranes, synthesize new membrane lipids, and properly target proteins to the correct membrane system. The outer membrane, plasma membrane, and thylakoid membranes each have specialized roles in the cyanobacterial cell. Understanding the organization, functionality, protein composition and dynamics of the membrane systems remains a great challenge in cyanobacterial cell biology.

  3. Rapid detection of nitroaromatic and nitramine explosives on chromatographic paper and their reflectometric sensing on PVC tablets.

    PubMed

    Erçağ, Erol; Uzer, Ayşem; Eren, Sule; Sağlam, Sener; Filik, Hayati; Apak, Reşat

    2011-09-30

    Rapid and inexpensive sensing of explosive traces in soil and post-blast debris for environmental and criminological purposes with optical sensors has recently gained importance. The developed sensing method for nitro-aromatic and nitramine-based explosives is based on dropping an acetone solution of the analyte to an adsorbent surface, letting the solvent to dry, spraying an analytical reagent to produce a persistent spot, and indirectly measuring its reflectance by means of a miniature spectrometer. This method proved to be useful for on-site determination of nitro-aromatics (trinitrotoluene (TNT), 2,4,6-trinitrophenylmethylnitramine (tetryl) and dinitrotoluene (DNT)) and nitramines (1,3,5-trinitro-1,3,5-triazacyclohexane (RDX) and octahydro-1,3,5,7-tetranitro-1,3,5,7-tetrazocine (HMX)) pre-adsorbed on a poly vinyl chloride (PVC) surface, with the use of different spray reagents for each group of explosives producing different colors. The calibration equations of the tested compounds as reflectance vs. concentration showed excellent linearity (correlation coefficient: 0.998-0.999). The linear quantification interval in terms of absolute quantity of analyte was 0.1-0.5 μg. The developed method was successfully tested for the analysis of military explosives Comp B and Octol, and was validated against high performance liquid chromatography (HPLC). The reflectometric sensing method could also be used for qualitative identification of the nitrated explosives on a chromatographic paper. The reagent-impregnated paper could also serve as sensor, enabling semi-quantitative determinations of TNT and tetryl. PMID:21872082

  4. Composite sensor membrane

    DOEpatents

    Majumdar, Arun; Satyanarayana, Srinath; Yue, Min

    2008-03-18

    A sensor may include a membrane to deflect in response to a change in surface stress, where a layer on the membrane is to couple one or more probe molecules with the membrane. The membrane may deflect when a target molecule reacts with one or more probe molecules.

  5. Preparation and analytical application of the novel Hg(II)-selective membrane electrodes based on oxime compounds.

    PubMed

    Sardohan-Koseoglu, Tugba; Kir, Esengul; Dede, Bulent

    2015-04-15

    Novel Hg(II)-selective poly(vinyl) chloride (PVC) membrane electrodes based on oxime compounds of (4-(4-methylphenylaminoisonitrosoacetyl)biphenyl, I1; 4-(4-clorophenylaminoisonitrosoacetyl)biphenyl, I2; N,N-bis[1-(4-phenylphenyl)-2-hydroxyimino-2-(4-chloroaniline)-1-ethylidene]-diethylenetriamine, I3 and N,N-bis[1-(4-phenylphenyl)-2-hydroxyimino-2-(4-chloroaniline)-1-ethylidene]- 1,3-propanediamine), I4 were developed. Effects of the species and ratios of ionophore, plasticizer, PVC and lipophilic additive on the potentiometric response of electrodes were investigated in order to determine the electrode specifications. Overall results revealed that the optimum membrane composition was: 4% ionophore, 64% plasticizer (o-NPOE), 31% PVC, and 1% lipophilic additive (NaTPB). Obtained results showed that the electrodes have detection limit of 1.76×10(-6), 1.68×10(-6), 2.35×10(-6) and 2.44×10(-6) and have linear responses of 34.2, 33.4, 35.9 and 37.6 mV/pHg(2+) for a wide concentration range of Hg(II) ions. According to durability studies, the electrodes can be used for approximately 1 month without any considerable divergence in potential values. Analytical applications of the electrodes were performed and it was found that developed electrodes can successfully be used as indicator electrodes for the potentiometric titration of Hg(II) ion with EDTA solution. PMID:25585282

  6. Determination of six phthalic acid esters in orange juice packaged by PVC bottle using SPE and HPLC-UV: application to the migration study.

    PubMed

    Guo, Zhiyong; Wei, Danyi; Wang, Meili; Wang, Sui

    2010-10-01

    A high-performance liquid chromatographic assay is described for the determination of six phthalic acid esters (PAEs) in orange juice packaged in polyvinyl chloride (PVC) bottle. Samples were extracted by solid-phase extraction (SPE) cartridges and separated by a C₁₈ column. The calibration curves were all linear with a correlation coefficient r > 0.9900. The limits of detection for the assay ranged from 2.6 to 13.8 ng/mL. Expressed as the within- and between-day coefficient of variation (CV), precision was 1.4-13.4% and 1.9-13.3%, respectively, and relative errors were 7.6-12.8% and -9.0-14.2%, respectively. The recovery ranged from 76.8 to 112.3% with the CV from 0.3 to 11.3%. The proposed methodology was applied for studing the migration of the selected PAEs into orange juice packaged in PVC bottle. Di-ethyl phthalate (DEP) and di-(2-ethylhexyl) phthalate (DEHP) were detected in the orange juice without the other four PAEs. Concentrations would increase with the storage time and reach up to 0.385 μg/mL and 0.662 μg/mL, respectively, when the expiration date arrived. The level of DEHP was about 110 times higher than the limiting one in drink water (6 ppb) regulated by U.S. EPA. Results suggest that PVC plasticized by DEHP should not be used as the packaging material for orange juice. PMID:20875239

  7. Covalent immobilization of lipase, glycerol kinase, glycerol-3-phosphate oxidase & horseradish peroxidase onto plasticized polyvinyl chloride (PVC) strip & its application in serum triglyceride determination

    PubMed Central

    Chauhan, Nidhi; Narang, Jagriti; Pundir, Chandra Shekhar

    2014-01-01

    Background & objectives: Reusable biostrip consisting enzymes immobilized onto alkylamine glass beads affixed on plasticized PVC strip for determination of triglyceride (TG) suffers from high cost of beads and their detachments during washings for reuse, leading to loss of activity. The purpose of this study was to develop a cheaper and stable biostrip for investigation of TG levels in serum. Methods: A reusable enzyme-strip was prepared for TG determination by co-immobilizing lipase, glycerol kinase (GK), glycerol-3-phosphate oxidase (GPO) and peroxidase (HRP) directly onto plasticized polyvinyl chloride (PVC) strip through glutaraldehyde coupling. The method was evaluated by studying its recovery, precision and reusability. Results: The enzyme-strip showed optimum activity at pH 7.0, 35°C and a linear relationship between its activity and triolein concentration in the range 0.1 to 15 mM. The strip was used for determination of serum TG. The detection limit of the method was 0.1 mM. Analytical recovery of added triolein was 96 per cent. Within and between batch coefficients of variation (CV) were 2.2 and 3.7 per cent, respectively. A good correlation (r=0.99) was found between TG values by standard enzymic colrimetric method employing free enzymes and the present method. The strip lost 50 per cent of its initial activity after its 200 uses during the span of 100 days, when stored at 4°C. Interpretation & conclusions: The nitrating acidic treatment of plasticized PVC strip led to glutaraldehyde coupling of four enzymes used for enzymic colourimetric determination of serum TG. The strip provided 200 reuses of enzymes with only 50 per cent loss of its initial activity. The method could be used for preparation of other enzyme strips also. PMID:24927348

  8. Effects of oxygen, catalyst and PVC on the formation of PCDDs, PCDFs and dioxin-like PCBs in pyrolysis products of automobile residues.

    PubMed

    Joung, Hyun-Tae; Seo, Yong-Chil; Kim, Ki-Heon; Seo, Yong-Chan

    2006-11-01

    End-of-life vehicles are dismantled to recover reusable parts and then sent to a shredding facility for steel material recovery. The residue generated from the shredding process, so-called automobile shredder residue, is now being mostly disposed in landfill, however landfill will be prohibited in the near future. More recycling and energy recovery must be made by the regulation. The most appropriate method is the thermal treatment that will produce various forms of fuels and less volume of vitrified residue. In this research, an automobile shredder residue was simulated with considering the residue from a shredding factory based on the new vehicle and thermally treated by pyrolysis or gasification to observe the yields of gas, oil and char. In the temperature range of 400-800 degrees C, the yields of gas, oil, and char were 38.7-45.8%, 12.3-18.2%, and 36.0-49.0%, respectively. The optimum pyrolyzing temperature for more oil production was around 600 degrees C. Emission characteristics of the byproducts, PCDDs, PCDFs and dioxin-like PCBs were studied at the temperature of 600 degrees C. The analysis on the concentration and distribution of the isomers in various forms of the products were completed with and without oxygen, PVC, and catalytic metals, in order to observe how the existence of oxygen, PVC, and catalytic metals affect the formation of PCDDs, PCDFs, and dioxin-like PCBs from pyrolysis or gasification process. Without PVC, no PCDDs, PCDFs and dioxin-like PCBs were found in any products. PCDFs were predominant in any conditions. Catalyst and oxygen were found to affect to form more PCDDs, PCDFs, and dioxin-like PCBs. Effects of catalyst and oxygen on the byproduct formation seemed to be similar in oil and gas while that was different in char. PMID:16740293

  9. Study of hydrophilic electrospun nanofiber membranes for filtration of micro and nanosize suspended particles.

    PubMed

    Asmatulu, Ramazan; Muppalla, Harish; Veisi, Zeinab; Khan, Waseem S; Asaduzzaman, Abu; Nuraje, Nurxat

    2013-01-01

    Polymeric nanofiber membranes of polyvinyl chloride (PVC) blended with polyvinylpyrrolidone (PVP) were fabricated using an electrospinning process at different conditions and used for the filtration of three different liquid suspensions to determine the efficiency of the filter membranes. The three liquid suspensions included lake water, abrasive particles from a water jet cutter, and suspended magnetite nanoparticles. The major goal of this research work was to create highly hydrophilic nanofiber membranes and utilize them to filter the suspended liquids at an optimal level of purification (i.e., drinkable level). In order to overcome the fouling/biofouling/blocking problems of the membrane, a coagulation process, which enhances the membrane's efficiency for removing colloidal particles, was used as a pre-treatment process. Two chemical agents, Tanfloc (organic) and Alum (inorganic), were chosen for the flocculation/coagulation process. The removal efficiency of the suspended particles in the liquids was measured in terms of turbidity, pH, and total dissolved solids (TDS). It was observed that the coagulation/filtration experiments were more efficient at removing turbidity, compared to the direct filtration process performed without any coagulation and filter media. PMID:24957063

  10. The novel approach to Cd(II) extraction by polymer inclusion membrane using TIOA as carrier

    NASA Astrophysics Data System (ADS)

    Polat, Cüneyt; Eyüpoǧlu, Volkan; Sara, Osman Nuri

    2016-04-01

    In the present study, the novel approach for the extraction of Cd(II) from acidic iodide solutions was achieved by using PVC based polymer inclusion membrane (PIM) technique containing triisooctyl amine (TIOA) as a carrier. PIMs were prepared according to the literature (1) and characterized by in aspects of thickness and surface morphology and molecular characterization. PIM composition was varied to find optimum membrane formation on Cd(II) transport. The effective parameters like thickness, plasticizer type and rate and carrier rate were investigated. Also, as a useful parameter, the concentration in the feed phase was examined to assess the effect on optimized membrane compositions. It was found that the concentration was the most useful parameter in the aqueous phase of Cd(II) transport because the remained I- in the aqueous feed phase unreacted with Cd(II). We recognize that by the time free I- concentration in the feed, the accumulation of the membrane increases and loading capacity of the membrane with CdI42- decreases because of the limited amount of carrier molecules in the PIM. As a result, it is concluded that extraction and separation of Cd(II) from simulated Ni/Cd leach solutions was carried out with higher initial mass transfer and permeation coefficients as 9,07×10-7 mol/m2s and 1,02×10-5 m/s at the optimum conditions respectively.

  11. Sheet Membrane Spacesuit Water Membrane Evaporator

    NASA Technical Reports Server (NTRS)

    Bue, Grant; Trevino, Luis; Zapata, Felipe; Dillion, Paul; Castillo, Juan; Vonau, Walter; Wilkes, Robert; Vogel, Matthew; Frodge, Curtis

    2013-01-01

    A document describes a sheet membrane spacesuit water membrane evaporator (SWME), which allows for the use of one common water tank that can supply cooling water to the astronaut and to the evaporator. Test data showed that heat rejection performance dropped only 6 percent after being subjected to highly contaminated water. It also exhibited robustness with respect to freezing and Martian atmospheric simulation testing. Water was allowed to freeze in the water channels during testing that simulated a water loop failure and vapor backpressure valve failure. Upon closing the backpressure valve and energizing the pump, the ice eventually thawed and water began to flow with no apparent damage to the sheet membrane. The membrane evaporator also serves to de-gas the water loop from entrained gases, thereby eliminating the need for special degassing equipment such as is needed by the current spacesuit system. As water flows through the three annular water channels, water evaporates with the vapor flowing across the hydrophobic, porous sheet membrane to the vacuum side of the membrane. The rate at which water evaporates, and therefore, the rate at which the flowing water is cooled, is a function of the difference between the water saturation pressure on the water side of the membrane, and the pressure on the vacuum side of the membrane. The primary theory is that the hydrophobic sheet membrane retains water, but permits vapor pass-through when the vapor side pressure is less than the water saturation pressure. This results in evaporative cooling of the remaining water.

  12. Methanotroph outer membrane preparation.

    PubMed

    Karlsen, Odd A; Berven, Frode S; Jensen, Harald B; Fjellbirkeland, Anne

    2011-01-01

    All presently known methanotrophs are gram-negative bacteria suggesting that they are surrounded by a two-layered membrane: an inner or cytoplasmic membrane and an outer membrane. In the methanotroph Methylococcus capsulatus (Bath), separation of the two membranes has allowed studies on protein and lipid composition of the outer membrane. Its outer membrane can be isolated from purified cell envelopes by selective solubilization of the inner membranes with the detergent Triton X-100. The proteins associated with the outer membrane can further be fractionated into integral and tightly associated proteins and peripheral loosely associated proteins. We present here protocols for this fractionation and show how the proteins associated with the outer leaflet of the outer membrane can be isolated and identified by whole-cell biotin surface labeling. PMID:21419921

  13. A Ho(III) potentiometric polymeric membrane sensor based on a new four dentate neutral ion carrier.

    PubMed

    Zamani, Hassan Ali; Zanganeh-Asadabadi, Abbas; Rohani, Mitra; Zabihi, Mohammad Saleh; Fadaee, Javad; Ganjali, Mohammad Reza; Faridbod, Farnoush; Meghdadi, Soraia

    2013-03-01

    In this research, we report a new Ho(3+)-PVC membrane electrode based on N-(4,5-dimethyl-2-(picolinamido)phenyl)picolinamide (H(2)Me(2)bpb) as a suitable ion carrier. Poly vinylchloride (PVC)-based membrane composed of H(2)Me(2)bpb with oleic acid (OA) as anionic additives, and o-nitrophenyloctyl ether (NPOE) as plasticized solvent mediator. The sensor exhibits a Nernstian slope of 20.1 ± 0.2 mV decade(-1) over the concentration range of 1.0 × 10(-6) to 1.0 × 1(-2) mol L(-1), and a detection limit of 5.0 × 10(-7) mol L(-1) of Ho(3+) ions. The potentiometric response of the sensor is independent of the solution pH in the range of 3.5-9.4. It has a very short response time, in the whole concentration range (<10s), and can be used for at least eight weeks. The proposed electrode shows a good selectivity towards Ho(3+) ions over a wide variety of cations, including alkali, alkaline earth, transition and heavy metal ions. To assess its analytical applicability the proposed Ho(3+) sensor was successfully applied as an indicator electrode in the titration of Ho(3+) ion solutions in certified reference materials, alloy samples and for the determination of the fluoride ion in two mouthwash preparations. PMID:25427515

  14. Enhanced performance of mixed-matrix membranes through a graft copolymer-directed interface and interaction tuning approach.

    PubMed

    Chi, Won Seok; Kim, Sang Jin; Lee, Seung-Joon; Bae, Youn-Sang; Kim, Jong Hak

    2015-02-01

    Herein, a high performance mixed-matrix membrane (MMM) is reported with simultaneously large improvements in the CO2 permeability by 880 % from 70.2 to 687.7 Barrer (1 Barrer=1×10(-10)  cm(3)  cm cm(-2)  s(-1)  cmHg(-1) ) and CO2 /N2 selectivity by 14.4 % from 30.5 to 34.9. These findings represent one of the most dramatic improvements ever reported for MMMs. These improvements are obtained through an interface and interaction tuning approach based on an amphiphilic grafted copolymer. Poly(vinyl chloride)-g-poly(oxyethylene methacrylate) (PVC-g-POEM) graft copolymer plays a key role as a soft organic matrix to provide good permeation properties, uniform distribution of zeolite imidazole frameworks-8 (ZIF-8), and better interfacial contact with inorganic compounds. In particular, the CO2 /C3 H8 and CO2 /C3 H6 selectivities reached 10.5 and 42.7, respectively, for PVC-g-POEM/ZIF (40 %) MMMs; this indicates that it could be a promising membrane material for the purification of C3 hydrocarbons. PMID:25393936

  15. Developments in the Field of Conducting and Non-conducting Polymer Based Potentiometric Membrane Sensors for Ions Over the Past Decade

    PubMed Central

    Faridbod, Farnoush; Ganjali, Mohammad Reza; Dinarvand, Rassoul; Norouzi, Parviz

    2008-01-01

    Many research studies have been conducted on the use of conjugated polymers in the construction of chemical sensors including potentiometric, conductometric and amperometric sensors or biosensors over the last decade. The induction of conductivity on conjugated polymers by treating them with suitable oxidizing agents won Heeger, MacDiarmid and Shirakawa the 2000 Nobel Prize in Chemistry. Common conjugated polymers are poly(acetylene)s, poly(pyrrole)s, poly(thiophene)s, poly(terthiophene)s, poly(aniline)s, poly(fluorine)s, poly(3-alkylthiophene)s, polytetrathiafulvalenes, poly-napthalenes, poly(p-phenylene sulfide), poly(p-phenylenevinylene)s, poly(3,4-ethylene-dioxythiophene), polyparaphenylene, polyazulene, polyparaphenylene sulfide, poly-carbazole and polydiaminonaphthalene. More than 60 sensors for inorganic cations and anions with different characteristics based on conducting polymers have been reported. There have also been reports on the application of non-conducting polymers (nCPs), i.e. PVC, in the construction of potentiometric membrane sensors for determination of more than 60 inorganic cations and anions. However, the leakage of ionophores from the membranes based on these polymers leads to relatively lower life times. In this article, we try to give an overview of Solid-Contact ISE (SCISE), Single-Piece ISE (SPISE), Conducting Polymer (CP)-Based, and also non-conducting polymer PVC-based ISEs for various ions which their difference is in the way of the polymer used with selective\\ membrane. In SCISEs and SPISEs, the plasticized PVC containing the ionophore and ionic additives govern the selectivity behavior of the electrode and the conducting polymer is responsible of ion-to-electron transducer. However, in CPISEs, the conducting polymer layer is doped with a suitable ionophore which enhances the ion selectivity of the CP while its redox response has to be suppressed.

  16. Membrane selectivity in pervaporation

    SciTech Connect

    Kujawski, W.

    1996-06-01

    A qualitative description is presented of pervaporation which discusses the initial preferential sorption into the membrane, diffusion of liquid, phase transition from liquid to vapor phase, followed by diffusion of vapors and fast desorption from the other side of the membrane. The overall separation of each pervaporation step was calculated in terms of separation factor {alpha}. The results show that in the case of hydrophilic membranes (i.e., dense polyamide-6 membrane and ion-exchange membrane PESS-1) and water-ethanol mixtures, the phase transition step decreases the overall separation. Also, diffusion through the membrane is unfavorable to water at a low concentration range.

  17. Stabilization of gamma-irradiated poly(vinyl chloride) by epoxy compounds. III. Conjugated double bonds and degree of unsaturation in gamma-irradiated PVC-stabilizer mixtures

    SciTech Connect

    Lerke, G.; Lerke, I.; Szymanski, W.

    1983-01-01

    The concentration of conjugated polyene sequences was studied in ..gamma..-irradiated PVC with 4% admixture of four epoxy stabilizers: diglycidyl ether of 2,2-bis(4-hydroxy-3-methylphenyl)propane (I), styrene oxide (1,2-epoxy ethyl benzene) (IV), epoxidized ricinus oil (VI), and epoxidized soybean oil (Drapex 6.8) (VII). As in the former investigations (Papers I and II), the process of the formation of the polyenes occurs in two stages. The concentration of polyene sequences with n double bonds, H/sub n/ the total amount of polyene sequences, ..sigma..H/sub n/, the average length of the polyene sequence, n, and the extents of reaction x and p, were computed. The stabilizing effect of all compounds used agrees with the increasing content of epoxy groups. The addition of stabilizers diminishes the value of n. The decrease of the fraction of long sequences and the increase of short ones occurs. Apart from the binding of evolved HCl, the protective effect towards the macromolecules of PVC consists mainly in the inhibition of growth of chain dehydrochlorination by the epoxy groups.

  18. Migration of epoxidised soybean oil from PVC gaskets of commercial lids: simulation of migration under various conditions and screening of food products from Czech markets.

    PubMed

    Hanušová, Kristýna; Vrbík, Karel; Rajchl, Aleš; Dobiáš, Jaroslav; Sosnovcová, Jitka

    2015-01-01

    Previous studies have shown that a large number of polyvinylchloride (PVC) lid gaskets exceed the existing migration limits for epoxidised soybean oil (ESBO) and correct prediction of ESBO release into food therefore appears to be a difficult issue. ESBO migration from PVC gaskets of metal closures into food simulants and food products from the Czech market is evaluated during a survey in 2009 and subsequently one in 2012 to assess progress in lid manufacturing and official testing conditions. ESBO migration from lids into various food simulants was studied at various temperatures (25, 40 and 60°C) during storage times up to 12 months. ESBO released into food simulants or food products was transmethylated, derivatised and analysed by GC-MS. The levels of ESBO migration in foodstuffs in 2012 exceeded the specific migration limit (SML) in fewer products in comparison with the previous survey. However, most of the products were analysed at a time far from the expiry date and exceedance of the SML at the end of the product shelf life is not therefore excluded. More severe test conditions (60°C for 10 days) for specific migration given by the current European Union legislation (Regulation (EU) No. 10/2011) still seem to be insufficient for the simulation of ESBO migration during long-term storage. PMID:25685888

  19. Molecular characterization of natural biofilms from household taps with different materials: PVC, stainless steel, and cast iron in drinking water distribution system.

    PubMed

    Lin, Wenfang; Yu, Zhisheng; Chen, Xi; Liu, Ruyin; Zhang, Hongxun

    2013-09-01

    Microorganism in drinking water distribution system may colonize in biofilms. Bacterial 16S rRNA gene diversities were analyzed in both water and biofilms grown on taps with three different materials (polyvinyl chloride (PVC), stainless steel, and cast iron) from a local drinking water distribution system. In total, five clone libraries (440 sequences) were obtained. The taxonomic composition of the microbial communities was found to be dominated by members of Proteobacteria (65.9-98.9 %), broadly distributed among the classes Alphaproteobacteria, Betaproteobacteria, and Gammaproteobacteria. Other bacterial groups included Firmicutes, Acidobacteria, Bacteroidetes, Cyanobacteria, and Deinococcus-Thermus. Moreover, a small proportion of unclassified bacteria (3.5-10.6 %) were also found. This investigation revealed that the bacterial communities in biofilms appeared much more diversified than expected and more care should be taken to the taps with high bacterial diversity. Also, regular monitor of outflow water would be useful as potentially pathogenic bacteria were detected. In addition, microbial richness and diversity in taps ranked in the order as: PVC < stainless steel < cast iron. All the results interpreted that PVC would be a potentially suitable material for use as tap component in drinking water distribution system. PMID:23143469

  20. Sorbents based on asbestos with a layer of an hydroxyethylcyclam derivative of PVC containing aquacomplexes of sulfuric acid or sodium hydroxide with aza-crown groups

    NASA Astrophysics Data System (ADS)

    Tsivadze, A. Yu.; Fridman, A. Ya.; Morozova, E. M.; Sokolova, N. P.; Voloshchuk, A. M.; Petukhova, G. A.; Bardyshev, I. I.; Gorbunov, A. M.; Polyakova, I. Ya.; Titova, V. N.; Yavich, A. A.; Novikov, A. K.; Petrova, N. V.

    2016-07-01

    Aquacomplexes of sulfuric acid and sodium hydroxide with aza-crown groups are synthesized in cavities of a sorbent from the porous layer of a PVC cyclam-derivative grafted onto fibers of asbestos fabric. The structure of sorbents with complexes is studied and their adsorption characteristics are determined. It is shown that the affinity of the developed surface toward ethanol, benzene, and hexane depends on the nature of complexes in the pore walls, and the volume of cavities formed as a result of the pores on the developed asbestos surface being coated with networks of aza-crown groups is larger than that of cavities with walls of aza-crown groups in the layers of a PVC cyclam derivative. Indicators of H+- and OH--conductivity of sorbents with complexes as electrochemical bridges are determined. It is shown that the major part of H+- and OH--ions moves through complexes with aza-crown groups in the region of cavities formed of pores on the surface of asbestos.

  1. Ionene membrane battery separator

    NASA Technical Reports Server (NTRS)

    Moacanin, J.; Tom, H. Y.

    1969-01-01

    Ionic transport characteristics of ionenes, insoluble membranes from soluble polyelectrolyte compositions, are studied for possible application in a battery separator. Effectiveness of the thin film of separator membrane essentially determines battery lifetime.

  2. Composite zeolite membranes

    DOEpatents

    Nenoff, Tina M.; Thoma, Steven G.; Ashley, Carol S.; Reed, Scott T.

    2002-01-01

    A new class of composite zeolite membranes and synthesis techniques therefor has been invented. These membranes are essentially defect-free, and exhibit large levels of transmembrane flux and of chemical and isotopic selectivity.

  3. Hybrid adsorptive membrane reactor

    DOEpatents

    Tsotsis, Theodore T.; Sahimi, Muhammad; Fayyaz-Najafi, Babak; Harale, Aadesh; Park, Byoung-Gi; Liu, Paul K. T.

    2011-03-01

    A hybrid adsorbent-membrane reactor in which the chemical reaction, membrane separation, and product adsorption are coupled. Also disclosed are a dual-reactor apparatus and a process using the reactor or the apparatus.

  4. Supertubes and Superconducting Membranes

    SciTech Connect

    Cordero, Ruben; Miguel-Pilar, Zelin

    2007-02-09

    We show the equivalence between configurations that arise from string theory of type IIA, called supertubes, and superconducting membranes at the bosonic level. We find equilibrium and oscillating configurations for a tubular membrane carrying a current along its axis.

  5. Premature rupture of membranes

    MedlinePlus

    ... When the water breaks early, it is called premature rupture of membranes (PROM). Most women will go ... th week of pregnancy, it is called preterm premature rupture of membranes (PPROM). The earlier your water ...

  6. Hybrid adsorptive membrane reactor

    NASA Technical Reports Server (NTRS)

    Tsotsis, Theodore T. (Inventor); Sahimi, Muhammad (Inventor); Fayyaz-Najafi, Babak (Inventor); Harale, Aadesh (Inventor); Park, Byoung-Gi (Inventor); Liu, Paul K. T. (Inventor)

    2011-01-01

    A hybrid adsorbent-membrane reactor in which the chemical reaction, membrane separation, and product adsorption are coupled. Also disclosed are a dual-reactor apparatus and a process using the reactor or the apparatus.

  7. Supported inorganic membranes

    DOEpatents

    Sehgal, Rakesh; Brinker, Charles Jeffrey

    1998-01-01

    Supported inorganic membranes capable of molecular sieving, and methods for their production, are provided. The subject membranes exhibit high flux and high selectivity. The subject membranes are substantially defect free and less than about 100 nm thick. The pores of the subject membranes have an average critical pore radius of less than about 5 .ANG., and have a narrow pore size distribution. The subject membranes are prepared by coating a porous substrate with a polymeric sol, preferably under conditions of low relative pressure of the liquid constituents of the sol. The coated substrate is dried and calcined to produce the subject supported membrane. Also provided are methods of derivatizing the surface of supported inorganic membranes with metal alkoxides. The subject membranes find use in a variety of applications, such as the separation of constituents of gaseous streams, as catalysts and catalyst supports, and the like.

  8. Composite fuel cell membranes

    DOEpatents

    Plowman, Keith R.; Rehg, Timothy J.; Davis, Larry W.; Carl, William P.; Cisar, Alan J.; Eastland, Charles S.

    1997-01-01

    A bilayer or trilayer composite ion exchange membrane suitable for use in a fuel cell. The composite membrane has a high equivalent weight thick layer in order to provide sufficient strength and low equivalent weight surface layers for improved electrical performance in a fuel cell. In use, the composite membrane is provided with electrode surface layers. The composite membrane can be composed of a sulfonic fluoropolymer in both core and surface layers.

  9. Composite fuel cell membranes

    DOEpatents

    Plowman, K.R.; Rehg, T.J.; Davis, L.W.; Carl, W.P.; Cisar, A.J.; Eastland, C.S.

    1997-08-05

    A bilayer or trilayer composite ion exchange membrane is described suitable for use in a fuel cell. The composite membrane has a high equivalent weight thick layer in order to provide sufficient strength and low equivalent weight surface layers for improved electrical performance in a fuel cell. In use, the composite membrane is provided with electrode surface layers. The composite membrane can be composed of a sulfonic fluoropolymer in both core and surface layers.

  10. Meniscus membranes for separations

    DOEpatents

    Dye, Robert C.; Jorgensen, Betty; Pesiri, David R.

    2004-01-27

    Gas separation membranes, especially meniscus-shaped membranes for gas separations are disclosed together with the use of such meniscus-shaped membranes for applications such as thermal gas valves, pre-concentration of a gas stream, and selective pre-screening of a gas stream. In addition, a rapid screening system for simultaneously screening polymer materials for effectiveness in gas separation is provided.

  11. Meniscus Membranes For Separation

    DOEpatents

    Dye, Robert C.; Jorgensen, Betty; Pesiri, David R.

    2005-09-20

    Gas separation membranes, especially meniscus-shaped membranes for gas separations are disclosed together with the use of such meniscus-shaped membranes for applications such as thermal gas valves, pre-concentration of a gas stream, and selective pre-screening of a gas stream. In addition, a rapid screening system for simultaneously screening polymer materials for effectiveness in gas separation is provided.

  12. Cadmium sulfide membranes

    DOEpatents

    Spanhel, Lubomir; Anderson, Marc A.

    1992-07-07

    A method is described for the creation of novel q-effect cadmium sulfide membranes. The membranes are made by first creating a dilute cadmium sulfide colloid in aqueous suspension and then removing the water and excess salts therefrom. The cadmium sulfide membrane thus produced is luminescent at room temperature and may have application in laser fabrication.

  13. Cadmium sulfide membranes

    DOEpatents

    Spanhel, Lubomir; Anderson, Marc A.

    1991-10-22

    A method is described for the creation of novel q-effect cadmium sulfide membranes. The membranes are made by first creating a dilute cadmium sulfide colloid in aqueous suspension and then removing the water and excess salts therefrom. The cadmium sulfide membrane thus produced is luminescent at room temperature and may have application in laser fabrication.

  14. Polyphosphazene semipermeable membranes

    DOEpatents

    Allen, Charles A.; McCaffrey, Robert R.; Cummings, Daniel G.; Grey, Alan E.; Jessup, Janine S.; McAtee, Richard E.

    1988-01-01

    A semipermeable, inorganic membrane is disclosed; the membrane is prepared from a phosphazene polymer and, by the selective substitution of the constituent groups bound to the phosphorous in the polymer structure, the selective passage of fluid from a feedstream can be controlled. Resistance to high temperatures and harsh chemical environments is observed in the use of the phosphazene polymers as semipermeable membranes.

  15. Water vapor diffusion membranes

    NASA Technical Reports Server (NTRS)

    Holland, F. F., Jr.; Smith, J. K.

    1974-01-01

    The program is reported, which was designed to define the membrane technology of the vapor diffusion water recovery process and to test this technology using commercially available or experimental membranes. One membrane was selected, on the basis of the defined technology, and was subjected to a 30-day demonstration trial.

  16. Tracking Membrane Protein Association in Model Membranes

    PubMed Central

    Reffay, Myriam; Gambin, Yann; Benabdelhak, Houssain; Phan, Gilles; Taulier, Nicolas; Ducruix, Arnaud; Hodges, Robert S.; Urbach, Wladimir

    2009-01-01

    Membrane proteins are essential in the exchange processes of cells. In spite of great breakthrough in soluble proteins studies, membrane proteins structures, functions and interactions are still a challenge because of the difficulties related to their hydrophobic properties. Most of the experiments are performed with detergent-solubilized membrane proteins. However widely used micellar systems are far from the biological two-dimensions membrane. The development of new biomimetic membrane systems is fundamental to tackle this issue. We present an original approach that combines the Fluorescence Recovery After fringe Pattern Photobleaching technique and the use of a versatile sponge phase that makes it possible to extract crucial informations about interactions between membrane proteins embedded in the bilayers of a sponge phase. The clear advantage lies in the ability to adjust at will the spacing between two adjacent bilayers. When the membranes are far apart, the only possible interactions occur laterally between proteins embedded within the same bilayer, whereas when membranes get closer to each other, interactions between proteins embedded in facing membranes may occur as well. After validating our approach on the streptavidin-biotinylated peptide complex, we study the interactions between two membrane proteins, MexA and OprM, from a Pseudomonas aeruginosa efflux pump. The mode of interaction, the size of the protein complex and its potential stoichiometry are determined. In particular, we demonstrate that: MexA is effectively embedded in the bilayer; MexA and OprM do not interact laterally but can form a complex if they are embedded in opposite bilayers; the population of bound proteins is at its maximum for bilayers separated by a distance of about 200 Å, which is the periplasmic thickness of Pseudomonas aeruginosa. We also show that the MexA-OprM association is enhanced when the position and orientation of the protein is restricted by the bilayers. We

  17. Elastic membranes in confinement

    NASA Astrophysics Data System (ADS)

    Bostwick, Joshua; Miksis, Michael; Davis, Stephen

    2014-11-01

    An elastic membrane stretched between two walls takes a shape defined by its length and the volume of fluid it encloses. Many biological structures, such as cells, mitochondria and DNA, have finer internal structure in which a membrane (or elastic member) is geometrically ``confined'' by another object. We study the shape stability of elastic membranes in a ``confining'' box and introduce repulsive van der Waals forces to prevent the membrane from intersecting the wall. We aim to define the parameter space associated with mitochondria-like deformations. We compare the confined to `unconfined' solutions and show how the structure and stability of the membrane shapes changes with the system parameters.

  18. Separation membrane development

    SciTech Connect

    Lee, M.W.

    1998-08-01

    A ceramic membrane has been developed to separate hydrogen from other gases. The method used is a sol-gel process. A thin layer of dense ceramic material is coated on a coarse ceramic filter substrate. The pore size distribution in the thin layer is controlled by a densification of the coating materials by heat treatment. The membrane has been tested by permeation measurement of the hydrogen and other gases. Selectivity of the membrane has been achieved to separate hydrogen from carbon monoxide. The permeation rate of hydrogen through the ceramic membrane was about 20 times larger than Pd-Ag membrane.

  19. A robust multisyringe system for process flow analysis. Part II. A multi-commuted injection system applied to the photometric determination of free acidity and iron(III) in metallurgical solutions.

    PubMed

    Albertús, F; Cladera, A; Cerda, V

    2000-12-01

    A new software-controlled volume-based system for sample introduction in process flow injection analysis was developed. By using a multi-syringe burette coupled with one or two additional commutation valves, the multi-commuted injection of precise sample volumes was accomplished. Characteristics and performance of the injection system were studied by injecting an indicator in a buffered carrier. Three configurations were implemented in order to achieve two different tasks: the single injection of a sample in a two- or three-channels manifold, and the dual injection into different streams. The two channel flow system using the single injection was applied to the determination of free acidity in diluted samples containing high levels of iron(III), by employing the single point titration methodology. The precipitation of ferric hydroxide was prevented using the ammonium and sodium salts of oxalate and acetate as buffer titrant. Methyl Red was employed as indicator. The procedure allows determination of acid concentration in solutions with a Fe(III)/H+ molar ratio up to 0.2. Samples with higher Fe(III)/H+ molar ratios were spiked with a known strong acid at dilution. The three-channel configuration was applied to the determination of ferric ions, using, as reagent, a merging mixture of sulfuric acid and potassium thiocyanate. The double injection system was implemented in series in a single (three-channel) manifold in such a way that a different injection volume and a changed reagent were used for each analyte. It was applied to the separated or sequential determination of free acidity and ferric ions. In this configuration, iron(III) was determined using 0.5-0.7% (w/v) sodium salicylate solution as reagent. The systems can operate at up to 100, 84 and 78 injections per hour, respectively. Determinations on synthetic and process samples compared well with the reference values and procedures. Recoveries of 95-102% with a maximum RSD value of 5.4% were found for acidity

  20. Migration of epoxidised soya bean oil into foods from retail packaging materials and from plasticised PVC film used in the home.

    PubMed

    Castle, L; Mayo, A; Gilbert, J

    1990-01-01

    Epoxidised soya bean oil (ESBO) is used as a plasticiser and heat stabiliser in a number of feed contact materials, in particular in poly(vinyl chloride) (PVC) films and gaskets. The level of ESBO migration into foods has been determined using a combined gas chromatographic/mass spectrometric (GC/MS) analytical procedure. The study has included both the use of ESBO-containing materials for retail packaged foods and the domestic use of plasticised PVC films for applications such as wrapping food and covering food for re-heating in a microwave oven. Levels of ESBO in fresh retail meat samples wrapped in film ranged from less than 1 to 4 mg/kg, but were higher (max. 22 mg/kg) in retail cooked meat. Migration into sandwiches and rolls from 'take-away' outlets ranged from less than 1 to 27 mg/kg depending on factors such as the type of filling and the length of the contact time prior to analysis. The levels of migration of ESBO into cheese and cakes were consistent with previous experience with plasticiser migration--direct contact with fatty surfaces leading to the highest levels. When the film was used for microwave cooking in direct contact with food, levels of ESBO from 5 to 85 mg/kg were observed, whereas when the film was employed only as a splash cover for re-heating foods, ESBO levels ranged from 0.1 to 16 mg/kg. For a variety of baby foods there was no significant difference in ESBO levels between foods packaged in glass jars with PVC gaskets and foods in cans containing ESBO in the can lacquer. In both cases ESBO levels were low, ranging from less than 0.1 to 7.6 mg/kg. It is not clear for these retail samples, if the low levels observed (average 1.9 mg/kg) result solely from migration or contain some contribution from naturally occurring epoxides. PMID:2307263

  1. New molecularly-imprinted polymer for carnitine and its application as ionophore in potentiometric selective membranes.

    PubMed

    Moret, Joséphine; Moreira, Felismina T C; Almeida, Sofia A A; Sales, M Goreti F

    2014-10-01

    Carnitine (CRT) is a biological metabolite found in urine that contributes in assessingseveral disease conditions, including cancer. Novel quick screening procedures for CRT are therefore fundamental. This work proposes a novel potentiometric device where molecularly imprinted polymers (MIPs) were used as ionophores. The host-tailored sites were imprinted on a polymeric network assembled by radical polymerization of methacrylic acid (MAA) and trimethylpropane trimethacrylate (TRIM). Non-imprinted polymers (NIPs) were produced as control by removing the template from the reaction media. The selective membrane was prepared by dispersing MIP or NIP particles in plasticizer and poly(vinyl chloride), PVC, and casting this mixture over a solid contact support made of graphite. The composition of the selective membrane was investigated with regard to kind/amount of sensory material (MIP or NIP), and the need for a lipophilic additive. Overall, MIP sensors with additive exhibited the best performance, with near-Nernstian response down to ~1×10(-4)mol L(-1), at pH5, and a detection limit of ~8×10(-5)mol L(-1). Suitable selectivity was found for all membranes, assessed by the matched potential method against some of the most common species in urine (urea, sodium, creatinine, sulfate, fructose and hemoglobin). CRT selective membranes including MIP materials were applied successfully to the potentiometric determination of CRT in urine samples. PMID:25175239

  2. Membrane Flotation Assay

    PubMed Central

    Vogt, Dorothee A; Ott, Melanie

    2016-01-01

    Many postitive-stranded RNA viruses, such as Hepatitis C virus (HCV), highjack cellular membranes, including the Golgi, ER, mitchondria, lipid droplets, and utilize them for replication of their RNA genome or assembly of new virions. By investigating how viral proteins associate with cellular membranes we will better understand the roles of cellular membranes in the viral life cycle. Our lab has focused specifically on the role of lipid droplets and lipid-rich membranes in the life cycle of HCV. To analyze the role of lipid-rich membranes in HCV RNA replication, we utilized a membrane flotation assay based on an 10–20–30% iodixanol density gradient developed by Yeaman et al. (2001). This gradient results in a linear increase in density over almost the entire length of the gradient, and membrane particles are separated in the gradient based on their buoyant characteristics. To preserve membranes in the lysate, cells are broken mechanically in a buffer lacking detergent. The cell lysate is loaded on the bottom of the gradient, overlaid with the gradient, and membranes float up as the iodixanol gradient self-generates. The lipid content of membranes and the concentration of associated proteins will determine the separation of different membranes within the gradient. After centrifugation, fractions can be sampled from the top of the gradient and analyzed using standard SDS-PAGE and western blot analysis for proteins of interest.

  3. Water Membrane Evaporator

    NASA Technical Reports Server (NTRS)

    Ungar, Eugene K.; Almlie, Jay C.

    2010-01-01

    A water membrane evaporator (WME) has been conceived and tested as an alternative to the contamination-sensitive and corrosion-prone evaporators currently used for dissipating heat from space vehicles. The WME consists mainly of the following components: An outer stainless-steel screen that provides structural support for the components mentioned next; Inside and in contact with the stainless-steel screen, a hydrophobic membrane that is permeable to water vapor; Inside and in contact with the hydrophobic membrane, a hydrophilic membrane that transports the liquid feedwater to the inner surface of the hydrophobic membrane; Inside and in contact with the hydrophilic membrane, an annular array of tubes through which flows the spacecraft coolant carrying the heat to be dissipated; and An inner exclusion tube that limits the volume of feedwater in the WME. In operation, a pressurized feedwater reservoir is connected to the volume between the exclusion tube and the coolant tubes. Feedwater fills the volume, saturates the hydrophilic membrane, and is retained by the hydrophobic membrane. The outside of the WME is exposed to space vacuum. Heat from the spacecraft coolant is conducted through the tube walls and the water-saturated hydrophilic membrane to the liquid/vapor interface at the hydrophobic membrane, causing water to evaporate to space. Makeup water flows into the hydrophilic membrane through gaps between the coolant tubes.

  4. Catalytic membranes beckon

    SciTech Connect

    Caruana, C.M.

    1994-11-01

    Chemical engineers here and abroad are finding that the marriage of catalysts and membranes holds promise for faster and more specific reactions, although commercialization of this technology is several years away. Catalytic membrane reactors (CMRs) combine a heterogeneous catalyst and a permselective membrane. Reactions performed by CMRs provide higher yields--sometimes as much as 50% higher--because of better reaction selectivity--as opposed to separation selectivity. CMRs also can work at very high temperatures, using ceramic materials that would not be possible with organic membranes. Although the use of CMRs is not widespread presently, the development of new membranes--particularly porous ceramic and zeolite membranes--will increase the potential to improve yields of many catalytic processes. The paper discusses ongoing studies, metal and advanced materials for membranes, the need for continued research, hydrogen recovery from coal-derived gases, catalytic oxidation of sulfides, CMRs for water purification, and oxidative coupling of methane.

  5. Stabilization of gamma-irradiated poly(vinyl chloride) by epoxy compounds. II. Production of hydroperoxides in gamma-irradiated PVC-stabilizer mixtures

    SciTech Connect

    Lerke, I., Szymanski, W.

    1983-01-01

    The concentration of hydroperoxides,produced in the process of radiolysis, was studied in ..gamma..-irradiated PVC samples with 4% admixture of four epoxy stabilizers: diglycidyl ether of 2.2-bis(4-hydroxy-3-methyl phenyl)propane (I), styrene oxide (1,2-epoxy ethyl benzene) (IV), epoxidized ricinus oil (VI), and epoxidized soybean oil (Drapex 6.8) (VII). The results indicate that the process of radiation oxidation occurs in two stages. Only the stabilizers with benzene ring demonstrate the antioxidative action. The stabilizers VI and VII do not act as the antioxidants, and, moreover, as a consequence of their plasticizing properties, they facilitate the penetration of the oxygen to polymer. The epoxy groups have no influence upon the oxidation process, in the case of compounds VI and VII.

  6. Layers of cyclam-substituted PVC with sodium hydroxide aqua complexes with aza-crown ligands on cellulose tissue filled with active coal

    NASA Astrophysics Data System (ADS)

    Fridman, A. Ya.; Tsivadze, A. Yu.; Morozova, E. M.; Sokolova, N. P.; Voloshchuk, A. M.; Petukhova, G. A.; Bardyshev, I. I.; Gorbunov, A. M.; Novikov, A. K.; Polyakova, I. Ya.; Titova, V. N.; Yavich, A. A.; Petrova, N. V.

    2016-03-01

    A material with an electrically OH--conductive porous layer of cyclam-substituted PVC filled with active coal containing NaOH aqua complexes with aza-crown ligands and cross-linked with the surface of cellulose tissue fibers has been synthesized. The structure of the material was studied. Its sorption capacity in vapors and liquid benzene and hexane, specific resistance, potential of OH- transfer from solution to layer, and rate constants of OH- travel in the layer of the material as an electrochemical bridge in vapors and liquid benzene and hexane were determined. The aqua complexes decomposed in the layer with formation of H2 during the cathodic polarization of the bridge and O2 during the anodic polarization; the composition of the complexes was regenerated due to the motion of OH-.

  7. Electrically conductive PVC layers filled with active carbon containing H+-conducting porous structures of sulfuric acid complexes of cyclams on fabrics

    NASA Astrophysics Data System (ADS)

    Tsivadze, A. Yu.; Fridman, A. Ya.; Morozova, E. M.; Sokolova, N. P.; Voloshchuk, A. M.; Petukhova, G. A.; Bardyshev, I. I.; Gorbunov, A. M.; Novikov, A. K.; Polyakova, I. Ya.; Titova, V. N.; Yavich, A. A.; Petrova, N. V.; Krasil'nikova, O. K.

    2015-07-01

    Electrically conductive PVC layers are synthesized. The layers are filled with active carbons containing porous H+-conductive structures of hydroxyethylcyclam/sulfuric acid complexes crosslinked with cellulose fabric. They are interlaid with layers based on the same structures containing added benzene and hexane adsorbates and solvates. It is found that upon anode or cathode polarization of the layers as H+-conductive electrochemical bridges in air and in the vapor and liquid phases of benzene and hexane, either the electroreduction of H+ to H2 or the electrooxidation of H2O to O2 occurs in the areas of contact between active carbon particles and the complexes. The dependences of rates of H2 and O2 formation on the voltage are studied. The magnitudes of overvoltage and the constants of electrochemical reactions are found to depend on the composition of a layer.

  8. Polymers at membranes

    NASA Astrophysics Data System (ADS)

    Breidenich, Markus

    2000-11-01

    The surface of biological cells consists of a lipid membrane and a large amount of various proteins and polymers, which are embedded in the membrane or attached to it. We investigate how membranes are influenced by polymers, which are anchored to the membrane by one end. The entropic pressure exerted by the polymer induces a curvature, which bends the membrane away from the polymer. The resulting membrane shape profile is a cone in the vicinity of the anchor segment and a catenoid far away from it. The perturbative calculations are confirmed by Monte-Carlo simulations. An additional attractive interaction between polymer and membrane reduces the entropically induced curvature. In the limit of strong adsorption, the polymer is localized directly on the membrane surface and does not induce any pressure, i.e. the membrane curvature vanishes. If the polymer is not anchored directly on the membrane surface, but in a non-vanishing anchoring distance, the membrane bends towards the polymer for strong adsorption. In the last part of the thesis, we study membranes under the influence of non-anchored polymers in solution. In the limit of pure steric interactions between the membrane and free polymers, the membrane curves towards the polymers (in contrast to the case of anchored polymers). In the limit of strong adsorption the membrane bends away from the polymers. Die Oberfläche biologischer Zellen besteht aus einer Lipidmembran und einer Vielzahl von Proteinen und Polymeren, die in die Membran eingebaut sind. Die Beeinflussung der Membran durch Polymere, die mit einem Ende an der Membran verankert sind, wird im Rahmen dieser Arbeit anhand eines vereinfachten biomimetischen Systems studiert. Der entropische Druck, den das Polymer durch Stöße auf die Membran ausübt, führt dazu, dass sich die Membran vom Polymer weg krümmt. Die resultierende Membranform ist ein Kegel in der Nähe des Ankers und ein Katenoid in grossem Abstand vom Ankerpunkt. Monte Carlo-Simulationen best

  9. Uranium Adsorbent Fibers Prepared by Atom-Transfer Radical Polymerization (ATRP) from Poly(vinyl chloride)- co -chlorinated Poly(vinyl chloride) (PVC- co -CPVC) Fiber

    DOE PAGESBeta

    Brown, Suree; Yue, Yanfeng; Kuo, Li-Jung; Mehio, Nada; Li, Meijun; Gill, Gary; Tsouris, Costas; Mayes, Richard T.; Saito, Tomonori; Dai, Sheng

    2016-03-11

    The need to secure future supplies of energy attracts researchers in several countries to a vast resource of nuclear energy fuel: uranium in seawater (estimated at 4.5 billion tons in seawater). In this study, we developed effective adsorbent fibers for the recovery of uranium from seawater via atom-transfer radical polymerization (ATRP) from a poly-(vinyl chloride)-co-chlorinated poly(vinyl chloride) (PVC-co-CPVC) fiber. ATRP was employed in the surface graft polymerization of acrylonitrile (AN) and tert-butyl acrylate (tBA), precursors for uranium-interacting functional groups, from PVC-co-CPVC fiber. The [tBA]/[AN] was systematically varied to identify the optimal ratio between hydrophilic groups (from tBA) and uranyl-binding ligandsmore » (from AN). The best performing adsorbent fiber, the one with the optimal [tBA]/[AN] ratio and a high degree of grafting (1390%), demonstrated uranium adsorption capacities that are significantly greater than those of the Japan Atomic Energy Agency (JAEA) reference fiber in natural seawater tests (2.42 3.24 g/kg in 42 days of seawater exposure and 5.22 g/kg in 49 days of seawater exposure, versus 1.66 g/kg in 42 days of seawater exposure and 1.71 g/kg in 49 days of seawater exposure for JAEA). Lastly, adsorption of other metal ions from seawater and their corresponding kinetics were also studied. The grafting of alternative monomers for the recovery of uranium from seawater is now under development by this versatile technique of ATRP.« less

  10. Genome-Wide Influence of Indel Substitutions on Evolution of Bacteria of the PVC Superphylum, Revealed Using a Novel Computational Method

    PubMed Central

    Kamneva, Olga K.; Liberles, David A.; Ward, Naomi L.

    2010-01-01

    Whole-genome scans for positive Darwinian selection are widely used to detect evolution of genome novelty. Most approaches are based on evaluation of nonsynonymous to synonymous substitution rate ratio across evolutionary lineages. These methods are sensitive to saturation of synonymous sites and thus cannot be used to study evolution of distantly related organisms. In contrast, indels occur less frequently than amino acid replacements, accumulate more slowly, and can be employed to characterize evolution of diverged organisms. As indels are also subject to the forces of natural selection, they can generate functional changes through positive selection. Here, we present a new computational approach to detect selective constraints on indel substitutions at the whole-genome level for distantly related organisms. Our method is based on ancestral sequence reconstruction, takes into account the varying susceptibility of different types of secondary structure to indels, and according to simulation studies is conservative. We applied this newly developed framework to characterize the evolution of organisms of the Planctomycetes, Verrucomicrobia, Chlamydiae (PVC) bacterial superphylum. The superphylum contains organisms with unique cell biology, physiology, and diverse lifestyles. It includes bacteria with simple cell organization and more complex eukaryote-like compartmentalization. Lifestyles range from free-living organisms to obligate pathogens. In this study, we conduct a whole-genome level analysis of indel substitutions specific to evolutionary lineages of the PVC superphylum and found that indels evolved under positive selection on up to 12% of gene tree branches. We also analyzed possible functional consequences for several case studies of predicted indel events. PMID:21048002

  11. Membrane with supported internal passages

    NASA Technical Reports Server (NTRS)

    Gonzalez-Martin, Anuncia (Inventor); Salinas, Carlos E. (Inventor); Cisar, Alan J. (Inventor); Hitchens, G. Duncan (Inventor); Murphy, Oliver J. (Inventor)

    2000-01-01

    The invention provides an improved proton exchange membrane for use in electrochemical cells having internal passages parallel to the membrane surface comprising permanent tubes preferably placed at the ends of the fluid passages. The invention also provides an apparatus and process for making the membrane, membrane and electrode assemblies fabricated using the membrane, and the application of the membrane and electrode assemblies to a variety of devices, both electrochemical and otherwise. The passages in the membrane extend from one edge of the membrane to another and allow fluid flow through the membrane and give access directly to the membrane.

  12. Poxvirus Membrane Biogenesis

    PubMed Central

    2015-01-01

    Poxviruses differ from most DNA viruses by replicating entirely within the cytoplasm. The first discernible viral structures are crescents and spherical immature virions containing a single lipoprotein membrane bilayer with an external honeycomb lattice. Because this viral membrane displays no obvious continuity with a cellular organelle, a de novo origin was suggested. Nevertheless, transient connections between viral and cellular membranes could be difficult to resolve. Despite the absence of direct evidence, the intermediate compartment (ERGIC) between the endoplasmic reticulum (ER) and Golgi apparatus and the ER itself were considered possible sources of crescent membranes. A break-through in understanding poxvirus membrane biogenesis has come from recent studies of the abortive replication of several vaccinia virus null mutants. Novel images showing continuity between viral crescents and the ER and the accumulation of immature virions in the expanded ER lumen provide the first direct evidence for a cellular origin of this poxvirus membrane. PMID:25728299

  13. Poxvirus membrane biogenesis.

    PubMed

    Moss, Bernard

    2015-05-01

    Poxviruses differ from most DNA viruses by replicating entirely within the cytoplasm. The first discernible viral structures are crescents and spherical immature virions containing a single lipoprotein membrane bilayer with an external honeycomb lattice. Because this viral membrane displays no obvious continuity with a cellular organelle, a de novo origin was suggested. Nevertheless, transient connections between viral and cellular membranes could be difficult to resolve. Despite the absence of direct evidence, the intermediate compartment (ERGIC) between the endoplasmic reticulum (ER) and Golgi apparatus and the ER itself were considered possible sources of crescent membranes. A break-through in understanding poxvirus membrane biogenesis has come from recent studies of the abortive replication of several vaccinia virus null mutants. Novel images showing continuity between viral crescents and the ER and the accumulation of immature virions in the expanded ER lumen provide the first direct evidence for a cellular origin of this poxvirus membrane. PMID:25728299

  14. Substituted polyacetylene separation membrane

    DOEpatents

    Pinnau, Ingo; Morisato, Atsushi

    1998-01-13

    A separation membrane useful for gas separation, particularly separation of C.sub.2+ hydrocarbons from natural gas. The invention encompasses the membrane itself, methods of making it and processes for using it. The membrane comprises a polymer having repeating units of a hydrocarbon-based, disubstituted polyacetylene, having the general formula: ##STR1## wherein R.sub.1 is chosen from the group consisting of C.sub.1 -C.sub.4 alkyl and phenyl, and wherein R.sub.2 is chosen from the group consisting of hydrogen and phenyl. In the most preferred embodiment, the membrane comprises poly(4-methyl-2-pentyne) ›PMP!. The membrane exhibits good chemical resistance and has super-glassy properties with regard to separating certain large, condensable permeant species from smaller, less-condensable permeant species. The membranes may also be useful in other fluid separations.

  15. Substituted polyacetylene separation membrane

    DOEpatents

    Pinnau, I.; Morisato, Atsushi

    1998-01-13

    A separation membrane is described which is useful for gas separation, particularly separation of C{sub 2+} hydrocarbons from natural gas. The invention encompasses the membrane itself, methods of making it and processes for using it. The membrane comprises a polymer having repeating units of a hydrocarbon-based, disubstituted polyacetylene, having the general formula shown in the accompanying diagram, wherein R{sub 1} is chosen from the group consisting of C{sub 1}-C{sub 4} alkyl and phenyl, and wherein R{sub 2} is chosen from the group consisting of hydrogen and phenyl. In the most preferred embodiment, the membrane comprises poly(4-methyl-2-pentyne) [PMP]. The membrane exhibits good chemical resistance and has super-glassy properties with regard to separating certain large, condensable permeant species from smaller, less-condensable permeant species. The membranes may also be useful in other fluid separations. 4 figs.

  16. Anion permselective membrane

    NASA Technical Reports Server (NTRS)

    Alexander, S.; Hodgdon, R. B.

    1977-01-01

    The objective of NAS 3-20108 was the development and evaluation of improved anion selective membranes useful as efficient separators in a redox power storage cell system being constructed. The program was divided into three parts, (a) optimization of the selected candidate membrane systems, (b) investigation of alternative membrane/polymer systems, and (c) characterization of candidate membranes. The major synthesis effort was aimed at improving and optimizing as far as possible each candidate system with respect to three critical membrane properties essential for good redox cell performance. Substantial improvements were made in 5 candidate membrane systems. The critical synthesis variables of cross-link density, monomer ratio, and solvent composition were examined over a wide range. In addition, eight alternative polymer systems were investigated, two of which attained candidate status. Three other alternatives showed potential but required further research and development. Each candidate system was optimized for selectivity.

  17. Anion permselective membrane

    NASA Technical Reports Server (NTRS)

    Hodgdon, R. B.; Waite, W. A.; Alexander, S. S.

    1984-01-01

    Two polymer ion exchange membranes were synthesized to fulfill the needs of both electrical resistivity and anolyte/catholyte separation for utility load leveling utilizing the DOE/NASA mixed electrolyte REDOX battery. Both membranes were shown to meet mixed electrolyte utility load leveling criteria. Several modifications of an anion exchange membrane failed to meet utility load leveling REDOX battery criteria using the unmixed electrolyte REDOX cell.

  18. Anion permselective membrane

    NASA Astrophysics Data System (ADS)

    Hodgdon, R. B.; Waite, W. A.; Alexander, S. S.

    1984-07-01

    Two polymer ion exchange membranes were synthesized to fulfill the needs of both electrical resistivity and anolyte/catholyte separation for utility load leveling utilizing the DOE/NASA mixed electrolyte REDOX battery. Both membranes were shown to meet mixed electrolyte utility load leveling criteria. Several modifications of an anion exchange membrane failed to meet utility load leveling REDOX battery criteria using the unmixed electrolyte REDOX cell.

  19. Siloxane-grafted membranes

    DOEpatents

    Friesen, Dwayne T.; Obligin, Alan S.

    1989-01-01

    Composite cellulosic semipermeable membranes are disclosed which are the covalently bonded reaction product of an asymmetric cellulosic semipermeable membrane and a polysiloxane containing reactive functional groups. The two reactants chemically bond by ether, ester, amide or acrylate linkages to form a siloxane-grafted cellulosic membrane having superior selectivity and flux stability. Selectivity may be enhanced by wetting the surface with a swelling agent such as water.

  20. Polyarylether composition and membrane

    DOEpatents

    Hung, Joyce; Brunelle, Daniel Joseph; Harmon, Marianne Elisabeth; Moore, David Roger; Stone, Joshua James; Zhou, Hongyi; Suriano, Joseph Anthony

    2010-11-09

    A composition including a polyarylether copolymer is provided. The copolymer includes a polyarylether backbone; and a sulfonated oligomeric group bonded to the polyarylether suitable for use as a cation conducting membrane. Method of bonding a sulfonated oligomeric group to the polyarylether backbone to form a polyarylether copolymer. The membrane may be formed from the polyarylether copolymer composition. The chain length of the sulfonated oligomeric group may be controlled to affect or control the ion conductivity of the membrane.

  1. Siloxane-grafted membranes

    DOEpatents

    Friesen, D.T.; Obligin, A.S.

    1989-10-31

    Composite cellulosic semipermeable membranes are disclosed which are the covalently bonded reaction product of an asymmetric cellulosic semipermeable membrane and a polysiloxane containing reactive functional group. The two reactants chemically bond by ether, ester, amide or acrylate linkages to form a siloxane-grafted cellulosic membrane having superior selectivity and flux stability. Selectivity may be enhanced by wetting the surface with a swelling agent such as water.

  2. Proteins causing membrane fouling in membrane bioreactors.

    PubMed

    Miyoshi, Taro; Nagai, Yuhei; Aizawa, Tomoyasu; Kimura, Katsuki; Watanabe, Yoshimasa

    2015-01-01

    In this study, the details of proteins causing membrane fouling in membrane bioreactors (MBRs) treating real municipal wastewater were investigated. Two separate pilot-scale MBRs were continuously operated under significantly different operating conditions; one MBR was a submerged type whereas the other was a side-stream type. The submerged and side-stream MBRs were operated for 20 and 10 days, respectively. At the end of continuous operation, the foulants were extracted from the fouled membranes. The proteins contained in the extracted foulants were enriched by using the combination of crude concentration with an ultrafiltration membrane and trichloroacetic acid precipitation, and then separated by two-dimensional polyacrylamide gel electrophoresis (2D-PAGE). The N-terminal amino acid sequencing analysis of the proteins which formed intensive spots on the 2D-PAGE gels allowed us to partially identify one protein (OmpA family protein originated from genus Brevundimonas or Riemerella anatipestifer) from the foulant obtained from the submerged MBR, and two proteins (OprD and OprF originated from genus Pseudomonas) from that obtained from the side-stream MBR. Despite the significant difference in operating conditions of the two MBRs, all proteins identified in this study belong to β-barrel protein. These findings strongly suggest the importance of β-barrel proteins in developing membrane fouling in MBRs. PMID:26360742

  3. Anion exchange membrane prepared from simultaneous polymerization and quaternization of 4-vinyl pyridine for non-aqueous vanadium redox flow battery applications

    NASA Astrophysics Data System (ADS)

    Maurya, Sandip; Shin, Sung-Hee; Sung, Ki-Won; Moon, Seung-Hyeon

    2014-06-01

    A simple, single step and environmentally friendly process is developed for the synthesis of anion exchange membrane (AEM) by simultaneous polymerization and quaternization, unlike the conventional membrane synthesis which consists of separate polymerization and quaternization step. The membrane synthesis is carried out by dissolving polyvinyl chloride (PVC) in cyclohexanone along with 4-vinyl pyridine (4VP) and 1,4-dibromobutane (DBB) in the presence of thermal initiator benzoyl peroxide, followed by film casting to get thin and flexible AEMs. The membrane properties such as ion exchange capacity, ionic conductivity and swelling behaviour are tuned by varying the degree of crosslinking. These AEMs exhibit low vanadium permeability, while retaining good dimensional and chemical stability in an electrolyte solution, making them appropriate candidates for non-aqueous vanadium acetylacetonate redox flow battery (VRFB) applications. The optimized membrane displays ion exchange capacity and ionic conductivity of 2.0 mequiv g-1 and 0.105 mS cm-1, respectively, whereas the efficiency of 91.7%, 95.7% and 87.7% for coulombic, voltage and energy parameter in non-aqueous VRFB, respectively. This study reveals that the non-aqueous VRFB performance is greatly influenced by membrane properties; therefore the optimal control over the membrane properties is advantageous for the improved performance.

  4. Biomolecular membrane protein crystallization

    NASA Astrophysics Data System (ADS)

    Reddy Bolla, Jani; Su, Chih-Chia; Yu, Edward W.

    2012-07-01

    Integral membrane proteins comprise approximately 30% of the sequenced genomes, and there is an immediate need for their high-resolution structural information. Currently, the most reliable approach to obtain these structures is X-ray crystallography. However, obtaining crystals of membrane proteins that diffract to high resolution appears to be quite challenging, and remains a major obstacle in structural determination. This brief review summarizes a variety of methodologies for use in crystallizing these membrane proteins. Hopefully, by introducing the available methods, techniques, and providing a general understanding of membrane proteins, a rational decision can be made about now to crystallize these complex materials.

  5. Plant cell membranes

    SciTech Connect

    Packer, L.; Douce, R.

    1987-01-01

    The contents of this book are: Cells, Protoplasts, Vacuoles and Liposomes; Tonoplasts; Nuclei, Endolplasmic Reticulum, and Plasma Membrane; Peroxisomes; Plastids; Teneral Physical and Biochemical Methods; and Mitochondira.

  6. Drugging Membrane Protein Interactions.

    PubMed

    Yin, Hang; Flynn, Aaron D

    2016-07-11

    The majority of therapeutics target membrane proteins, accessible on the surface of cells, to alter cellular signaling. Cells use membrane proteins to transduce signals into cells, transport ions and molecules, bind cells to a surface or substrate, and catalyze reactions. Newly devised technologies allow us to drug conventionally "undruggable" regions of membrane proteins, enabling modulation of protein-protein, protein-lipid, and protein-nucleic acid interactions. In this review, we survey the state of the art of high-throughput screening and rational design in drug discovery, and we evaluate the advances in biological understanding and technological capacity that will drive pharmacotherapy forward against unorthodox membrane protein targets. PMID:26863923

  7. Membrane Tension Control

    NASA Technical Reports Server (NTRS)

    Su, Ji (Inventor); Harrison, Joycelyn S. (Inventor)

    2005-01-01

    An electrostrictive polymer actuator comprises an electrostrictive polymer with a tailorable Poisson's ratio. The electrostrictive polymer is electroded on its upper and lower surfaces and bonded to an upper material layer. The assembly is rolled tightly and capped at its ends. In a membrane structure having a membrane, a supporting frame and a plurality of threads connecting the membrane to the frame, an actuator can be integrated into one or more of the plurality of threads. The electrostrictive polymer actuator displaces along its longitudinal axis, thereby affecting movement of the membrane surface.

  8. Gas separation membranes

    DOEpatents

    Schell, William J.

    1979-01-01

    A dry, fabric supported, polymeric gas separation membrane, such as cellulose acetate, is prepared by casting a solution of the polymer onto a shrinkable fabric preferably formed of synthetic polymers such as polyester or polyamide filaments before washing, stretching or calendering (so called griege goods). The supported membrane is then subjected to gelling, annealing, and drying by solvent exchange. During the processing steps, both the fabric support and the membrane shrink a preselected, controlled amount which prevents curling, wrinkling or cracking of the membrane in flat form or when spirally wound into a gas separation element.

  9. Anion exchange membrane

    DOEpatents

    Verkade, John G; Wadhwa, Kuldeep; Kong, Xueqian; Schmidt-Rohr, Klaus

    2013-05-07

    An anion exchange membrane and fuel cell incorporating the anion exchange membrane are detailed in which proazaphosphatrane and azaphosphatrane cations are covalently bonded to a sulfonated fluoropolymer support along with anionic counterions. A positive charge is dispersed in the aforementioned cations which are buried in the support to reduce the cation-anion interactions and increase the mobility of hydroxide ions, for example, across the membrane. The anion exchange membrane has the ability to operate at high temperatures and in highly alkaline environments with high conductivity and low resistance.

  10. Development of a passive sampler based on a polymer inclusion membrane for total ammonia monitoring in freshwaters.

    PubMed

    Almeida, M Inês G S; Silva, Adélia M L; Coleman, Rhys A; Pettigrove, Vincent J; Cattrall, Robert W; Kolev, Spas D

    2016-05-01

    A passive sampler for determining the time-weighted average total ammonia (i.e. molecular ammonia and the ammonium cation) concentration (C TWA) in freshwaters, which incorporated a polymer inclusion membrane (PIM) as a semi-permeable barrier separating the aqueous source solution from the receiving solution (i.e. 0.8 mol L(-1) HCl), was developed for the first time. The PIM was composed of dinonylnaphthalene sulfonic acid (DNNS) as a carrier, poly (vinyl chloride) (PVC) as a base polymer and 1-tetradecanol as a modifier. Its optimal composition was found to be 35 wt% commercial DNNS, 55 wt% PVC and 10 wt% 1-tetradecanol. The effect of environmental variables such as the water matrix, pH and temperature were also studied using synthetic freshwaters. The passive sampler was calibrated under laboratory conditions using synthetic freshwaters and exhibited a linear response within the concentration range 0.59-2.8 mg L(-1) NH4(+) (0.46-2.1 mg N L(-1)) at 20 °C. The performance of the sampler was further investigated under field conditions over 7 days. A strong correlation between spot sampling and passive sampling was achieved, thus providing a proof-of-concept for the passive sampler for reliably measuring the C(TWA) of total ammonia in freshwaters, which can be used as an indicator in tracking sources of faecal contamination in stormwater drains. PMID:26873214

  11. Transportation and Accumulation of Redox Active Species at the Buried Interfaces of Plasticized Membrane Electrodes.

    PubMed

    Sohail, Manzar; De Marco, Roland; Jarolímová, Zdeňka; Pawlak, Marcin; Bakker, Eric; He, Ning; Latonen, Rose-Marie; Lindfors, Tom; Bobacka, Johan

    2015-09-29

    The transportation and accumulation of redox active species at the buried interface between glassy carbon electrodes and plasticized polymeric membranes have been studied using synchrotron radiation X-ray photoelectron spectroscopy (SR-XPS), near edge X-ray absorption fine structure (NEXAFS), in situ electrochemical Fourier transform infrared-attenuated total reflectance (FTIR-ATR) spectroscopy, cyclic voltammetry (CV), chronoamperometry (CA), and electrochemical impedance spectroscopy (EIS). Ferrocene tagged poly(vinyl chloride) [FcPVC], ferrocene (Fc), and its derivatives together with tetracyanoquinodimethane (TCNQ) doped plasticized polymeric membrane electrodes have been investigated, so as to extend the study of the mechanism of this reaction chemistry to different time scales (both small and large molecules with variable diffusion coefficients) using a range of complementary electrochemical and surface analysis techniques. This study also provides direct spectroscopic evidence for the transportation and electrochemical reactivity of redox active species, regardless of the size of the electrochemically reactive molecule, at the buried interface of the substrate electrode. With all redox dopants, when CA electrolysis was performed, redox active species were undetectable (<1 wt % of signature elements or below the detection limit of SR-XPS and NEXAFS) in the outermost surface layers of the membrane, while a high concentration of redox species was located at the electrode substrate as a consequence of the deposition of the reaction product (Fc(+)-anion complex) at the buried interface between the electrode and the membrane. This reaction chemistry for redox active species within plasticized polymeric membranes may be useful in the fashioning of multilayered polymeric devices (e.g., chemical sensors, organic electronic devices, protective laminates, etc.) based on an electrochemical tunable deposition of redox molecules at the buried substrate electrode beneath

  12. Anion permselective membrane

    NASA Technical Reports Server (NTRS)

    Hodgdon, R. B.; Waite, W. A.

    1982-01-01

    The synthesis and fabrication of polymeric anion permselective membranes for redox systems are discussed. Variations of the prime candidate anion membrane formulation to achieve better resistance and/or lower permeability were explored. Processing parameters were evaluated to lower cost and fabricate larger sizes. The processing techniques to produce more membranes per batch were successfully integrated with the fabrication of larger membranes. Membranes of about 107 cm x 51 cm were made in excellent yield. Several measurements were made on the larger sample membranes. Among the data developed were water transport and transference numbers for these prime candidate membranes at 20 C. Other work done on this system included characterization of a number of specimens of candidate membranes which had been returned after service lives of up to sixteen months. Work with new polymer constituents, with new N.P.'s, catalysts and backing fabrics is discussed. Some work was also done to evaluate other proportions of the ingredients of the prime candidate system. The adoption of a flow selectivity test at elevated temperature was explored.

  13. Membrane in cancer cells

    SciTech Connect

    Galeotti, T.; Cittadini, A.; Neri, G.; Scarpa, A.

    1988-01-01

    This book contains papers presented at a conference on membranes in cancer cells. Topics covered include Oncogenies, hormones, and free-radical processes in malignant transformation in vitro and Superoxide onion may trigger DNA strand breaks in human granulorytes by acting as a membrane target.

  14. Microporous alumina ceramic membranes

    DOEpatents

    Anderson, M.A.; Guangyao Sheng.

    1993-05-04

    Several methods are disclosed for the preparation microporous alumina ceramic membranes. For the first time, porous alumina membranes are made which have mean pore sizes less than 100 Angstroms and substantially no pores larger than that size. The methods are based on improved sol-gel techniques.

  15. Microporous alumina ceramic membranes

    DOEpatents

    Anderson, Marc A.; Sheng, Guangyao

    1993-01-01

    Several methods are disclosed for the preparation microporous alumina ceramic membranes. For the first time, porous alumina membranes are made which have mean pore sizes less than 100 Angstroms and substantially no pores larger than that size. The methods are based on improved sol-gel techniques.

  16. Polymide gas separation membranes

    DOEpatents

    Ding, Yong; Bikson, Benjamin; Nelson, Joyce Katz

    2004-09-14

    Soluble polyamic acid salt (PAAS) precursors comprised of tertiary and quaternary amines, ammonium cations, sulfonium cations, or phosphonium cations, are prepared and fabricated into membranes that are subsequently imidized and converted into rigid-rod polyimide articles, such as membranes with desirable gas separation properties. A method of enhancing solubility of PAAS polymers in alcohols is also disclosed.

  17. Membrane module assembly

    DOEpatents

    Kaschemekat, Jurgen

    1994-01-01

    A membrane module assembly adapted to provide a flow path for the incoming feed stream that forces it into prolonged heat-exchanging contact with a heating or cooling mechanism. Membrane separation processes employing the module assembly are also disclosed. The assembly is particularly useful for gas separation or pervaporation.

  18. Membrane module assembly

    DOEpatents

    Kaschemekat, J.

    1994-03-15

    A membrane module assembly is described which is adapted to provide a flow path for the incoming feed stream that forces it into prolonged heat-exchanging contact with a heating or cooling mechanism. Membrane separation processes employing the module assembly are also disclosed. The assembly is particularly useful for gas separation or pervaporation. 2 figures.

  19. Membrane Transport Phenomena (MTP)

    NASA Technical Reports Server (NTRS)

    Mason, Larry W.

    1996-01-01

    The development of the seal between the membrane and the Fluid Optical Cells (FOC) has been a high priority activity. This seal occurs at an interface in the instrument where three key functions must be realized: (1) physical membrane support, (2) fluid sealing, and (3) unobscured optical transmission.

  20. Permeable membrane experiment

    NASA Technical Reports Server (NTRS)

    Slavin, Thomas J.; Cao, Tuan Q.; Kliss, Mark H.

    1993-01-01

    The purpose of the Permeable Membrane Experiment is to gather flight data on three areas of membrane performance that are influenced by the presence of gravity. These areas are: (1) Liquid/gas phase separation, (2) gas bubble interference with diffusion through porous membranes and (3) wetting characteristics of hydrophilic membrane surfaces. These data are important in understaning the behavior of membrane/liquid/gas interfaces where surface tension forces predominate. The data will be compared with 1-g data already obtained and with predicted micrograviity behavior. The data will be used to develop designs for phase separation and plant nutrient delivery systems and will be available to the life support community for use in developing technologies which employ membranes. A conceptual design has been developed to conduct three membrane experiments, in sequence, aboard a single Complex Autonomous Payload (CAP) carrier to be carried in the Shuttle Orbiter payload bay. One experiment is conducted for each of the three membrane performance areas under study. These experiments are discussed in this paper.

  1. Viral Membrane Scission

    PubMed Central

    Rossman, Jeremy S.; Lamb, Robert A.

    2014-01-01

    Virus budding is a complex, multistep process in which viral proteins make specific alterations in membrane curvature. Many different viral proteins can deform the membrane and form a budding virion, but very few can mediate membrane scission to complete the budding process. As a result, enveloped viruses have developed numerous ways of facilitating membrane scission, including hijacking host cellular scission machinery and expressing their own scission proteins. These proteins mediate scission in very different ways, though the biophysical mechanics underlying their actions may be similar. In this review, we explore the mechanisms of membrane scission and the ways in which enveloped viruses use these systems to mediate the release of budding virions. PMID:24099087

  2. Ion-conducting membranes

    DOEpatents

    Masel, Richard L.; Chen, Qingmei; Liu, Zengcai; Kutz, Robert

    2016-06-21

    An ion conducting polymeric composition mixture comprises a copolymer of styrene and vinylbenzyl-R.sub.s. R.sub.s is selected from the group consisting of imidazoliums and pyridiniums. The composition contains 10%-90% by weight of vinylbenzyl-R.sub.s. The composition can further comprise a polyolefin comprising substituted polyolefins, a polymer comprising cyclic amine groups, a polymer comprising at least one of a phenylene group and a phenyl group, a polyamide, and/or the reaction product of a constituent having two carbon-carbon double bonds. The composition can be in the form of a membrane. In a preferred embodiment, the membrane is a Helper Membrane that increases the faradaic efficiency of an electrochemical cell into which the membrane is incorporated, and also allows product formation at lower voltages than in cells without the Helper Membrane.

  3. Anton permselective membrane

    NASA Technical Reports Server (NTRS)

    Alexander, S. S.; Hodgdon, R. B.; Waite, W. A.

    1979-01-01

    Experimental composite membranes were synthesized on a lab scale consisting of a thin layer of anion permselective resin supported by and bonded to a porous physically strong and conductive substrate film. These showed good selectivity and also substantially lower electrical resistivities than the homogenous candidate membranes optimized in the previous contract. A wide range of resin porosities were examined for three candidate membrane systems, CDIL, CP4L, and A3L to identify the formulation giving the best overall redox cell performance. Candidate anion membranes showed large increases in resistivity after a short time of immersion in concentrated FeCl/HCl solution. Largely on the basis of resistance stability the CDIL formulation was selected as prime candidate and about thirty-five membranes (one foot square) were produced for experimental static and dynamic evaluation.

  4. Elastic membranes in confinement.

    PubMed

    Bostwick, J B; Miksis, M J; Davis, S H

    2016-07-01

    An elastic membrane stretched between two walls takes a shape defined by its length and the volume of fluid it encloses. Many biological structures, such as cells, mitochondria and coiled DNA, have fine internal structure in which a membrane (or elastic member) is geometrically 'confined' by another object. Here, the two-dimensional shape of an elastic membrane in a 'confining' box is studied by introducing a repulsive confinement pressure that prevents the membrane from intersecting the wall. The stage is set by contrasting confined and unconfined solutions. Continuation methods are then used to compute response diagrams, from which we identify the particular membrane mechanics that generate mitochondria-like shapes. Large confinement pressures yield complex response diagrams with secondary bifurcations and multiple turning points where modal identities may change. Regions in parameter space where such behaviour occurs are then mapped. PMID:27440257

  5. OXYGEN TRANSPORT CERAMIC MEMBRANES

    SciTech Connect

    Dr. Sukumar Bandopadhyay; Dr. Nagendra Nagabhushana

    2002-04-01

    This report covers the following tasks: Task 1--Design, fabricate and evaluate ceramic to metal seals based on graded ceramic powder/metal braze joints; Task 2--Evaluate the effect of defect configuration on ceramic membrane conductivity and long term chemical and structural stability; Task 3--Determine materials mechanical properties under conditions of high temperatures and reactive atmospheres; Task 4--Evaluate phase stability and thermal expansion of candidate perovskite membranes and develop techniques to support these materials on porous metal structures; Task 5--Assess the microstructure of membrane materials to evaluate the effects of vacancy-impurity association, defect clusters, and vacancy-dopant association on the membrane performance and stability; and Task 6--Measure kinetics of oxygen uptake and transport in ceramic membrane materials under commercially relevant conditions using isotope labeling techniques.

  6. Membrane projection lithography

    DOEpatents

    Burckel, David Bruce; Davids, Paul S; Resnick, Paul J; Draper, Bruce L

    2015-03-17

    The various technologies presented herein relate to a three dimensional manufacturing technique for application with semiconductor technologies. A membrane layer can be formed over a cavity. An opening can be formed in the membrane such that the membrane can act as a mask layer to the underlying wall surfaces and bottom surface of the cavity. A beam to facilitate an operation comprising any of implantation, etching or deposition can be directed through the opening onto the underlying surface, with the opening acting as a mask to control the area of the underlying surfaces on which any of implantation occurs, material is removed, and/or material is deposited. The membrane can be removed, a new membrane placed over the cavity and a new opening formed to facilitate another implantation, etching, or deposition operation. By changing the direction of the beam different wall/bottom surfaces can be utilized to form a plurality of structures.

  7. Ammonium across a Selective Polymer Inclusion Membrane: Characterization, Transport, and Selectivity.

    PubMed

    Casadellà, Anna; Schaetzle, Olivier; Loos, Katja

    2016-05-01

    The recovery of ammonium from urine requires distinguishing and excluding sodium and potassium. A polymer inclusion membrane selective for ammonium is developed using an ionophore based on pyrazole substituted benzene. The interactions of the components are studied, as well as their effect on transport and selectivity. Spectroscopic and thermogravimetric measurements show no extensive physical interactions of the components, and that the plasticizer reduces the intermolecular forces (rigidity) of the membrane. The ionophore turns the membrane more rigid, although it increases its swelling degree and therefore the affinity of cations. A ratio of plasticizer (DEHP) and polymer (PVC) of 1:3 in mass gives the highest ammonium flux. Tested contents of ionophore (2 and 5 wt%) show that the higher the content of the ionophore, the fastest the flux is (7.5 × 10(-3) mmol cm(-2) h(-1) ). Selectivity of NH4 (+) over Na(+) and over K(+) is reduced from 13.07 to 9.33 and from 14.15 to 9.57 correspondingly. PMID:27062504

  8. Development of a portable taste sensor with a lipid/polymer membrane.

    PubMed

    Tahara, Yusuke; Nakashi, Kenichi; Ji, Ke; Ikeda, Akihiro; Toko, Kiyoshi

    2013-01-01

    We have developed a new portable taste sensor with a lipid/polymer membrane and conducted experiments to evaluate the sensor's performance. The fabricated sensor consists of a taste sensor chip (40 mm × 26 mm × 2.2 mm) with working and reference electrodes and a portable sensor device (80 mm × 25 mm × 20 mm). The working electrode consists of a taste-sensing site comprising a poly(hydroxyethyl)methacrylate (pHEMA) hydrogel layer with KCl as the electrolyte layer and a lipid/polymer membrane as the taste sensing element. The reference electrode comprises a polyvinyl chloride (PVC) membrane layer with a small hole and a pHEMA layer with KCl. The whole device is the size of a USB memory stick, making it suitable for portable use. The sensor's response to tannic acid as the standard astringency substance showed good accuracy and reproducibility, and was comparable with the performance of a commercially available taste sensing system. Thus, it is possible for this sensor to be used for in-field evaluations and it can make a significant contribution to the food industry, as well as in various fields of research. PMID:23325168

  9. In vitro clearance of intravenous acetaminophen in extracorporeal membrane oxygenation.

    PubMed

    Gillogly, A; Kilbourn, C; Waldvogel, J; Martin, J; Annich, G; Wagner, D

    2013-03-01

    Extracorporeal membrane oxygenation (ECMO) is a life support system used as a bridge to transplantation in critically ill patients who suffer from acute respiratory or cardiac failure with resultant hypoxemia and tissue hypoxia. This is not amendable to conventional support intervention. Previous studies have shown significant drug losses in the components of an ECMO circuit, leading to decreased plasma drug levels. An in vitro study was conducted to determine: (1) changes in intravenous acetaminophen levels over time and (2) changes in concentration observed between different sites of the ECMO circuit. A single bolus dose of intravenous (IV) acetaminophen was injected into a standard blood-primed ECMO circuit. Plasma drug concentrations in the circuit were then measured at specific time points at three different locations to determine concentrations of the drug at time 0, 15, 30, 60, 240 and 360 minutes. The three samples were drawn pre- and post-membrane oxygenator and the polyvinyl chloride (PVC) tubing. A second bolus dose was administered 24 hours after the first in order to compare "new" and "old" circuits. This entire process was repeated a total of three times. The results show that acetaminophen concentrations do not change significantly over time, with consistent levels seen in both new and old circuits (N=9). Average old circuit concentrations were approximately two times greater than the average new circuit concentrations after the circuit was re-dosed at 24 hours. Drug sequestration in the circuit was not significant in any of the three sites measured. It appears that, while acetaminophen levels remain relatively constant over a six hour period, dosing adjustments may be required for use in a circuit beyond the initial 24 hour period, depending on physiologic clearance of the drug. Assuming a six-hour dosing interval, levels should remain constant. PMID:23201817

  10. Ordered ceramic membranes

    SciTech Connect

    Anderson, M.A.; Hill, C.G. Jr.; Zeltner, W.A.

    1991-10-01

    Ceramic membranes have been formed from colloidal sols coated on porous clay supports. These supported membranes have been characterized in terms of their permeabilities and permselectivities to various aqueous test solutions. The thermal stabilities and pore structures of these membranes have been characterized by preparing unsupported membranes of the correpsonding material and performing N{sub 2} adsorption-desorption and X-ray diffraction studies on these membranes. To date, membranes have been prepared from a variety of oxides, including TiO{sub 2}, SiO{sub 2}, ZrO{sub 2}, and Al{sub 2}O{sub 3}, as well as Zr-, Fe-, and Nb-doped TiO{sub 2}. In many of these membranes pore diameters are less than 2 nm, while in others the pore diameters are between 3 and 5 nm. Procedures for fabricating porous clay supports with reproducible permeabilities for pure water are also discussed. 30 refs., 59 figs., 22 tabs.

  11. Hollow fiber catalytic membranes

    SciTech Connect

    Ma, Yi Hua; Moser, W.; Shelekhin, A.; Pien, Shyhing

    1993-09-01

    The objective of the present research is to investigate the possibility of the enhancement of the H{sub 2}S thermal decomposition in the IGCC system by employing the hollow fiber catalytic membrane reactor. To accomplish the objective, the following major components in the analysis of the high temperature membrane reactor must be investigated: high-temperature stability of the porous glass membrane; catalytic properties of MoS{sub 2} and of the porous glass membrane; catalytic decomposition of H{sub 2}S in a packed bed reactor; catalytic decomposition of 100%, 8.6%, and 1.1% H{sub 2}S gas mixtures in the membrane reactor. The study has been shown that the conversion of the H{sub 2}S can be increased in the packed bed membrane reactor compared to the equilibrium conversion on the shell side. The development of a mathematical model for the proposed process is in progress. The model will enable optimization of the H{sub 2}S decomposition. These conditions include selectivity factors and pressure drop across the membrane.

  12. Supported double membranes

    PubMed Central

    Murray, David H.; Tamm, Lukas K.; Kiessling, Volker

    2009-01-01

    Planar model membranes, like supported lipid bilayers and surface-tethered vesicles, have been proven to be useful tools for the investigation of complex biological functions in a significantly less complex membrane environment. In this study, we introduce a supported double membrane system that should be useful for studies that target biological processes in the proximity of two lipid bilayers such as the periplasm of bacteria and mitochondria or the small cleft between pre-and postsynaptic neuronal membranes. Large unilamellar vesicles (LUV) were tethered to a preformed supported bilayer by a biotin-streptavidin tether. We show from single particle tracking (SPT) experiments that these vesicle are mobile above the plane of the supported membrane. At higher concentrations, the tethered vesicles fuse to form a second continuous bilayer on top of the supported bilayer. The distance between the two bilayers was determined by fluorescence interference contrast (FLIC) microscopy to be between 16 and 24 nm. The lateral diffusion of labeled lipids in the second bilayer was very similar to that in supported membranes. SPT experiments with reconstituted syntaxin-1A show that the mobility of transmembrane proteins was not improved when compared with solid supported membranes. PMID:19236921

  13. Electroporation of cell membranes.

    PubMed

    Tsong, T Y

    1991-08-01

    Electric pulses of intensity in kilovolts per centimeter and of duration in microseconds to milliseconds cause a temporary loss of the semipermeability of cell membranes, thus leading to ion leakage, escape of metabolites, and increased uptake by cells of drugs, molecular probes, and DNA. A generally accepted term describing this phenomenon is "electroporation." Other effects of a high-intensity electric field on cell membranes include membrane fusions, bleb formation, cell lysis... etc. Electroporation and its related phenomena reflect the basic bioelectrochemistry of cell membranes and are thus important for the study of membrane structure and function. These phenomena also occur in such events as electric injury, electrocution, and cardiac procedures involving electric shocks. Electroporation has found applications in: (a) introduction of plasmids or foreign DNA into living cells for gene transfections, (b) fusion of cells to prepare heterokaryons, hybridoma, hybrid embryos... etc., (c) insertion of proteins into cell membranes, (d) improving drug delivery and hence effectiveness in chemotherapy of cancerous cells, (e) constructing animal model by fusing human cells with animal tissues, (f) activation of membrane transporters and enzymes, and (g) alteration of genetic expression in living cells. A brief review of mechanistic studies of electroporation is given. PMID:1912274

  14. Electroporation of cell membranes.

    PubMed Central

    Tsong, T Y

    1991-01-01

    Electric pulses of intensity in kilovolts per centimeter and of duration in microseconds to milliseconds cause a temporary loss of the semipermeability of cell membranes, thus leading to ion leakage, escape of metabolites, and increased uptake by cells of drugs, molecular probes, and DNA. A generally accepted term describing this phenomenon is "electroporation." Other effects of a high-intensity electric field on cell membranes include membrane fusions, bleb formation, cell lysis... etc. Electroporation and its related phenomena reflect the basic bioelectrochemistry of cell membranes and are thus important for the study of membrane structure and function. These phenomena also occur in such events as electric injury, electrocution, and cardiac procedures involving electric shocks. Electroporation has found applications in: (a) introduction of plasmids or foreign DNA into living cells for gene transfections, (b) fusion of cells to prepare heterokaryons, hybridoma, hybrid embryos... etc., (c) insertion of proteins into cell membranes, (d) improving drug delivery and hence effectiveness in chemotherapy of cancerous cells, (e) constructing animal model by fusing human cells with animal tissues, (f) activation of membrane transporters and enzymes, and (g) alteration of genetic expression in living cells. A brief review of mechanistic studies of electroporation is given. PMID:1912274

  15. Catalytic nanoporous membranes

    DOEpatents

    Pellin, Michael J; Hryn, John N; Elam, Jeffrey W

    2013-08-27

    A nanoporous catalytic membrane which displays several unique features Including pores which can go through the entire thickness of the membrane. The membrane has a higher catalytic and product selectivity than conventional catalysts. Anodic aluminum oxide (AAO) membranes serve as the catalyst substrate. This substrate is then subjected to Atomic Layer Deposition (ALD), which allows the controlled narrowing of the pores from 40 nm to 10 nm in the substrate by deposition of a preparatory material. Subsequent deposition of a catalytic layer on the inner surfaces of the pores reduces pore sizes to less than 10 nm and allows for a higher degree of reaction selectivity. The small pore sizes allow control over which molecules enter the pores, and the flow-through feature can allow for partial oxidation of reactant species as opposed to complete oxidation. A nanoporous separation membrane, produced by ALD is also provided for use in gaseous and liquid separations. The membrane has a high flow rate of material with 100% selectivity. Also provided is a method for producing a catalytic membrane having flow-through pores and discreet catalytic clusters adhering to the inside surfaces of the pores.

  16. Nanoengineered membrane electrode assembly interface

    DOEpatents

    Song, Yujiang; Shelnutt, John A

    2013-08-06

    A membrane electrode structure suitable for use in a membrane electrode assembly (MEA) that comprises membrane-affixed metal nanoparticles whose formation is controlled by a photochemical process that controls deposition of the metal nanoparticles using a photocatalyst integrated with a polymer electrolyte membrane, such as an ionomer membrane. Impregnation of the polymer membrane with the photocatalyst prior to metal deposition greatly reduces the required amount of metal precursor in the deposition reaction solution by restricting metal reduction substantially to the formation of metal nanoparticles affixed on or near the surface of the polymer membrane with minimal formation of metallic particles not directly associated with the membrane.

  17. Potassium monopersulfate oxidation of 2,4,6-tribromophenol catalyzed by a SiO2-supported iron(III)-5,10,15,20-tetrakis(4-carboxyphenyl)porphyrin.

    PubMed

    Zhu, Qianqian; Mizutani, Yusuke; Maeno, Shohei; Nishimoto, Ryo; Miyamoto, Takafumi; Fukushima, Masami

    2013-01-01

    Iron(III)-porphyrin complexes are generally regarded as green catalysts, since they mimic the catalytic center of cytochrome-P450 and widely used as green catalysts for degrading halogenated phenols in wastewater, such as landfill leachates. However, iron(III)-porphyrins are deactivated by self-oxidation in the presence of an oxygen donor, such as KHSO5. In the present study, to enhance the reusability of an iron(III)-porphyrin catalyst, iron(III)-5,10,15,20-tetrakis(4-carboxyphenyl) porphyrin (FeTCPP) was immobilized on a functionalized silica gel. The oxidative degradation of 2,4,6-tribromophenol (TrBP), a widely used brominated flame retardant that is found in landfill leachates, was examined using the prepared catalyst. In addition, the influence of humic substances (HSs), major components of leachates, on the TrBP oxidation was investigated. Concerning the effect of pH, more than 90% of the TrBP was degraded in the pH range of 3-8 in the absence of HS, while the optimal pH for the reaction was in the range of pH 5-7 in the presence of HS. Although the oxidation of TrBP was inhibited in the presence of HSs, more than 90% of the TrBP was degraded in the presence of 50 mg L(-1) of HS. Thus, the prepared catalyst, SiO2-FeTCPP, showed a high catalytic activity and could be reused up to 10 times even in the presence of HS. PMID:23947696

  18. INO-4885 [5,10,15,20-tetra[N-(benzyl-4'-carboxylate)-2-pyridinium]-21H,23H-porphine iron(III) chloride], a peroxynitrite decomposition catalyst, protects the heart against reperfusion injury in mice.

    PubMed

    Jiao, Xiang-Ying; Gao, Erhe; Yuan, Yuexin; Wang, Yajing; Lau, Wayne Bond; Koch, Walter; Ma, Xin-Liang; Tao, Ling

    2009-03-01

    Oxidative/nitrative stress caused by peroxynitrite, the reaction product of superoxide (O2(.-)) and nitric oxide (NO), is the primary cause of myocardial ischemia/reperfusion injury. The present study determined whether INO-4885 [5,10,15,20-tetra[N-(benzyl-4'-carboxylate)-2-pyridinium]-21H,23H-porphine iron(III) chloride], a new peroxynitrite decomposition catalyst, may provide cellular protection and protect heart from myocardial ischemia/reperfusion injury. Adult male mice were subjected to 30 min of ischemia and 3 or 24 h of reperfusion. Mice were randomized to receive vehicle, INO-4885 without catalytic moiety, or INO-4885 (3-300 microg/kg i.p.) 10 min before reperfusion. Infarct size, apoptosis, nitrotyrosine content, NO/O2(.-) production, and inducible nitric-oxide synthase (iNOS)/NADPH oxidase expression were determined. INO-4885 treatment reduced ischemia/reperfusion-induced protein nitration and caspase 3 activation in a dose-dependent fashion in the range of 3 to 100 microg/kg. However, doses exceeding 100 microg/kg produced nonspecific effects and attenuated its protective ability. At the optimal dose (30 microg/kg), INO-4885 significantly reduced infarct size (p < 0.01), decreased apoptosis (p < 0.01), and reduced tissue nitrotyrosine content (p < 0.01). As expected, INO-4885 had no effect on ischemia/reperfusion-induced iNOS expression and NO overproduction. To our surprise, this compound significantly reduced superoxide production and partially blocked NADPH oxidase overexpression in the ischemic/reperfused cardiac tissue. Additional experiments demonstrated that INO-4885 provided better cardioprotection than N-(3-(aminomethyl)benzyl)acetamidine (1400W, a selective iNOS inhibitor), apocynin (an NADPH oxidase inhibitor), or Tiron (a cell-permeable superoxide scavenger). Taken together, our data demonstrated that INO-4885 is a cardioprotective molecule that attenuates myocardial reperfusion injury by facilitating peroxynitrite decomposition and

  19. CENTRIFUGAL MEMBRANE FILTRATION

    SciTech Connect

    Daniel J. Stepan; Bradley G. Stevens; Melanie D. Hetland

    1999-10-01

    The overall project consists of several integrated research phases related to the applicability, continued development, demonstration, and commercialization of the SpinTek centrifugal membrane filtration process. Work performed during this reporting period consisted of Phase 2 evaluation of the SpinTek centrifugal membrane filtration technology and Phase 3, Technology Partnering. During Phase 1 testing conducted at the EERC using the SpinTek ST-IIL unit operating on a surrogate tank waste, a solids cake developed on the membrane surface. The solids cake was observed where linear membrane velocities were less than 17.5 ft/s and reduced the unobstructed membrane surface area up to 25%, reducing overall filtration performance. The primary goal of the Phase 2 research effort was to enhance filtration performance through the development and testing of alternative turbulence promoter designs. The turbulence promoters were designed to generate a shear force across the entire membrane surface sufficient to maintain a self-cleaning membrane capability and improve filtration efficiency and long-term performance. Specific Phase 2 research activities included the following: System modifications to accommodate an 11-in.-diameter, two-disk rotating membrane assembly; Development and fabrication of alternative turbulence promoter designs; Testing and evaluation of the existing and alternative turbulence promoters under selected operating conditions using a statistically designed test matrix; and Data reduction and analysis; The objective of Phase 3 research was to demonstrate the effectiveness of SpinTek's centrifugal membrane filtration as a pretreatment to remove suspended solids from a liquid waste upstream of 3M's WWL cartridge technology for the selective removal of technetium (Tc).

  20. Membrane photobiophysics and photochemistry

    NASA Astrophysics Data System (ADS)

    Ti Tien, H.

    Life, as we know it, depends on solar energy, in particular in the visible range of the solar spectrum. However, visible light alone is useless to the living organism unless a means is available for its capture, transformation, and utilization. Nature, through its long evolution, has perfected a process known as photosynthesis by which visible light is transduced into electrical/ chemical energy. However, the heart of Nature's energy transducer is the thylakoid membrane whose molecular organization was not known until early in the 1960s. Then it was established that the bilayer lipid membrane was central to the design of the thylakoid membrane. To explain the light-driven reactions from water oxidation to carbon dioxide reduction, the so-called Z-scheme was proposed. Concurrent with the establishment of Mitchell's Chemiosmotic Hypothesis for electron transfer and phosphorylation, the experimental bilayer lipid membrane (BLM) system was developed in 1960. But what are the fundamental biophysical mechanisms involved in the phototransduction via pigmented bilayer lipid membrane-based transducers? One of the main purposes of this review is to consider these questions. A second main purpose is to introduce to the reader the experimental aspects of lipid bilayers in the investigation of photoactive biomembranes. The areas covered in this review include a brief summary of the laws of photochemistry relevant to membrane photobiophysics and photobiology. The current exploitation of the BLM system in relation to the thylakoid membrane and to the visual receptor membrane will be considered in turn. The purple membrane of H. Halobium is then discussed. Consideration will also be given to dye-sensitized BLMs, semiconducting BLMs, and BLMs formed from liquid crystals. A common characteristic in the topics covered in this review is the desire to stimulate further studies in the use of the BLM system, not only for the fundamental understanding of biomembranes, but also towards

  1. Cyclic membrane separation process

    DOEpatents

    Bowser, John

    2004-04-13

    A cyclic process for controlling environmental emissions of volatile organic compounds (VOC) from vapor recovery in storage and dispensing operations of liquids maintains a vacuum in the storage tank ullage. In one of a two-part cyclic process ullage vapor is discharged through a vapor recovery system in which VOC are stripped from vented gas with a selectively gas permeable membrane. In the other part, the membrane is inoperative while gas pressure rises in the ullage. Ambient air is charged to the membrane separation unit during the latter part of the cycle.

  2. Rotating bubble membrane radiator

    DOEpatents

    Webb, Brent J.; Coomes, Edmund P.

    1988-12-06

    A heat radiator useful for expelling waste heat from a power generating system aboard a space vehicle is disclosed. Liquid to be cooled is passed to the interior of a rotating bubble membrane radiator, where it is sprayed into the interior of the bubble. Liquid impacting upon the interior surface of the bubble is cooled and the heat radiated from the outer surface of the membrane. Cooled liquid is collected by the action of centrifical force about the equator of the rotating membrane and returned to the power system. Details regarding a complete space power system employing the radiator are given.

  3. Cholesterol dynamics in membranes.

    PubMed Central

    Yeagle, P L; Albert, A D; Boesze-Battaglia, K; Young, J; Frye, J

    1990-01-01

    Time-resolved fluorescence anisotropy of the sterol analogue, cholestatrienol, and 13C nuclear magnetic resonance (NMR) spin lattice relaxation time (T1c) measurements of [13C4] labeled cholesterol were exploited to determine the correlation times characterizing the major modes of motion of cholesterol in unsonicated phospholipid multilamellar liposomes. Two modes of motion were found to be important: (a) rotational diffusion and (b) time dependence of the orientation of the director for axial diffusion, or "wobble." From the time-resolved fluorescence anisotropy decays of cholestatrienol in egg phosphatidylcholine (PC) bilayers, a value for tau perpendicular, the correlation time for wobble, of 0.9 x 10(-9) s and a value for S perpendicular, the order parameter characterizing the same motion, of 0.45 s were calculated. Both tau perpendicular and S perpendicular were relatively insensitive to temperature and cholesterol content of the membranes. The T1c measurements of [13C4] labeled cholesterol did not provide a quantitative determination of tau parallel, the correlation time for axial diffusion. T1c from the lipid hydrocarbon chains suggested a value for tau perpendicular similar to that for cholesterol. Steady-state anisotropy measurements and time-resolved anisotropy measurements of cholestatrienol were used to probe sterol behavior in a variety of pure and mixed lipid multilamellar liposomes. Both the lipid headgroups and the lipid hydrocarbons chains contributed to the determination of the sterol environment in the membrane, as revealed by these fluorescence measurements. In particular, effects of the phosphatidylethanolamine (PE) headgroup and of multiple unsaturation in the lipid hydrocarbon chains were observed. However, while the steady-state anisotropy was sensitive to these factors, the time-resolved fluorescence analysis indicated that tau perpendicular was not strongly affected by the lipid composition of the membrane. S perpendicular may be increased

  4. Neural Membrane Signaling Platforms

    PubMed Central

    Wallace, Ron

    2010-01-01

    Throughout much of the history of biology, the cell membrane was functionally defined as a semi-permeable barrier separating aqueous compartments, and an anchoring site for proteins. Little attention was devoted to its possible regulatory role in intracellular molecular processes and neuron electrical signaling. This article reviews the history of membrane studies and the current state of the art. Emphasis is placed on natural and artificial membrane studies of electric field effects on molecular organization, especially as these may relate to impulse propagation in neurons. Implications of these studies for new designs in artificial intelligence are briefly examined. PMID:20640161

  5. Composite metal membrane

    DOEpatents

    Peachey, Nathaniel M.; Dye, Robert C.; Snow, Ronny C.; Birdsell, Stephan A.

    1998-01-01

    A composite metal membrane including a first metal layer of Group IVB met or Group VB metals, the first metal layer sandwiched between two layers of an oriented metal of palladium, platinum or alloys thereof is provided together with a process for the recovery of hydrogen from a gaseous mixture including contacting a hydrogen-containing gaseous mixture with a first side of a nonporous composite metal membrane including a first metal of Group IVB metals or Group VB metals, the first metal layer sandwiched between two layers of an oriented metal of palladium, platinum or alloys thereof, and, separating hydrogen from a second side of the nonporous composite metal membrane.

  6. Composite metal membrane

    DOEpatents

    Peachey, N.M.; Dye, R.C.; Snow, R.C.; Birdsell, S.A.

    1998-04-14

    A composite metal membrane including a first metal layer of Group IVB met or Group VB metals, the first metal layer sandwiched between two layers of an oriented metal of palladium, platinum or alloys thereof is provided together with a process for the recovery of hydrogen from a gaseous mixture including contacting a hydrogen-containing gaseous mixture with a first side of a nonporous composite metal membrane including a first metal of Group IVB metals or Group VB metals, the first metal layer sandwiched between two layers of an oriented metal of palladium, platinum or alloys thereof, and, separating hydrogen from a second side of the nonporous composite metal membrane.

  7. Cyclic membrane separation process

    DOEpatents

    Nemser, Stuart M.

    2005-05-03

    A cyclic process for controlling environmental emissions of volatile organic compounds (VOC) from vapor recovery in storage and dispensing operations of liquids maintains a vacuum in the storage tank ullage. In the first part of a two-part cyclic process ullage vapor is discharged through a vapor recovery system in which VOC are stripped from vented gas with a selectively gas permeable membrane. In the second part, the membrane is inoperative while gas pressure rises in the ullage. In one aspect of this invention, a vacuum is drawn in the membrane separation unit thus reducing overall VOC emissions.

  8. PERSISTENT PUPILLARY MEMBRANE OR ACCESSORY IRIS MEMBRANE?.

    PubMed

    Gavriş, Monica; Horge, Ioan; Avram, Elena; Belicioiu, Roxana; Olteanu, Ioana Alexandra; Kedves, Hanga

    2015-01-01

    Frequently, in literature and curent practice, accessory iris membrane (AIM) and persistant pupillary membrane (PPM) are confused. Both AIM and PPM are congenital iris anomalies in which fine or thick iris strands arrise form the collarette and obscure the pupil. AIM, which is also called iris duplication, closely resembles the normal iris tissue in color and thickness and presents a virtual second pseudopupil aperture in the centre while PPM even in its extreme forms presents as a translucent or opaque membranous structure that extends across the pupil and has no pseudopupil. Mydriatiscs, laser treatment or surgery is used to clear the visual axis and optimize visual development. Surgical intervention is reserved for large, dense AIMs and PPMs. Our patient, a 29 year old male, has come with bilateral dense AIM, bilateral compound hyperopic astigmatism, BCVA OD = 0.6, BCVA OS = 0.4, IOP OU = 17 mmHg. To improve the visual acuity of the patient we decided to do a bilateral membranectomy, restoring in this way transparency of the visual axis. After surgery, the visual acuity improved to BCVA OD= 0.8, BCVA OS=0.8. PMID:26978889

  9. Novel Catalytic Membrane Reactors

    SciTech Connect

    2009-02-01

    This factsheet describes a research project that will focus on the development and application of nonporous high gas flux perfluoro membranes with high temperature rating and excellent chemical resistance.

  10. Hydrogen transport membranes

    DOEpatents

    Mundschau, Michael V.

    2005-05-31

    Composite hydrogen transport membranes, which are used for extraction of hydrogen from gas mixtures are provided. Methods are described for supporting metals and metal alloys which have high hydrogen permeability, but which are either too thin to be self supporting, too weak to resist differential pressures across the membrane, or which become embrittled by hydrogen. Support materials are chosen to be lattice matched to the metals and metal alloys. Preferred metals with high permeability for hydrogen include vanadium, niobium, tantalum, zirconium, palladium, and alloys thereof. Hydrogen-permeable membranes include those in which the pores of a porous support matrix are blocked by hydrogen-permeable metals and metal alloys, those in which the pores of a porous metal matrix are blocked with materials which make the membrane impervious to gases other than hydrogen, and cermets fabricated by sintering powders of metals with powders of lattice-matched ceramic.

  11. Protein mediated membrane adhesion

    NASA Astrophysics Data System (ADS)

    Carlson, Andreas; Mahadevan, L.

    2015-05-01

    Adhesion in the context of mechanical attachment, signaling, and movement in cellular dynamics is mediated by the kinetic interactions between membrane-embedded proteins in an aqueous environment. Here, we present a minimal theoretical framework for the dynamics of membrane adhesion that accounts for the kinetics of protein binding, the elastic deformation of the membrane, and the hydrodynamics of squeeze flow in the membrane gap. We analyze the resulting equations using scaling estimates to characterize the spatiotemporal features of the adhesive patterning and corroborate them using numerical simulations. In addition to characterizing aspects of cellular dynamics, our results might also be applicable to a range of phenomena in physical chemistry and materials science where flow, deformation, and kinetics are coupled to each other in slender geometries.

  12. Ultrasonic Membrane Processing

    NASA Astrophysics Data System (ADS)

    Kentish, Sandra; Ashokkumar, Muthupandian

    A membrane is a sermipermeable material that permits the passage of some molecules while retaining others. Ultrasound can enhance membrane operation through the asymmetric collapse of cavitating bubbles and through the turbulence associated with acoustic streaming. The added turbulence can lead to a looser, more porous fouling cake layer and may agglomerate fine particles, reducing pore blockage and cake compaction.These effects are dependent upon the ultrasonic intensity, the operating pressure, crossflow velocity and solids concentration.Membrane cleaning can also be enhanced by the use of ultrasound, but this application may not be economic when used in isolation. One of the greatest challenges facing the technology is the generation of a uniform acoustic field across the entire membrane surface in a full-scale module.

  13. Membrane separation technology

    SciTech Connect

    Stookey, D.J.; Patton, C.J.; Malcolm, G.L.

    1986-01-01

    Membrane separations of interest here are not to be confused with barrier separations of the type employed in the uranium enrichment plant at Oak Ridge, Tennessee. There isotopes of uranium hexafluoride were separated by the free-molecular or Knudsen flow of the gas mixture through the pores and orifices created within a porous nickel media which was sometimes referred to as a membrane. In barrier separation, an enrichment of gases of differing molecular weights is accomplished by the differing gaseous diffusion rates within the porous media. By contrast the membranes of interest here are thin, dense, continuous films, typically formed from polymers. The separation of species is accomplished by the dissolution of the gases in the polymer and their diffusion across the solid film thickness under a concentration gradient according to Fick's law. This process is commonly referred to as membrane permeation.

  14. Drugging Membrane Protein Interactions

    PubMed Central

    Yin, Hang; Flynn, Aaron D.

    2016-01-01

    The majority of therapeutics target membrane proteins, accessible on the surface of cells, to alter cellular signaling. Cells use membrane proteins to transduce signals into cells, transport ions and molecules, bind the cell to a surface or substrate, and catalyze reactions. Newly devised technologies allow us to drug conventionally “undruggable” regions of membrane proteins, enabling modulation of protein–protein, protein–lipid, and protein–nucleic acid interactions. In this review, we survey the state of the art in high-throughput screening and rational design in drug discovery, and we evaluate the advances in biological understanding and technological capacity that will drive pharmacotherapy forward against unorthodox membrane protein targets. PMID:26863923

  15. Evaporative Cooling Membrane Device

    NASA Technical Reports Server (NTRS)

    Lomax, Curtis (Inventor); Moskito, John (Inventor)

    1999-01-01

    An evaporative cooling membrane device is disclosed having a flat or pleated plate housing with an enclosed bottom and an exposed top that is covered with at least one sheet of hydrophobic porous material having a thin thickness so as to serve as a membrane. The hydrophobic porous material has pores with predetermined dimensions so as to resist any fluid in its liquid state from passing therethrough but to allow passage of the fluid in its vapor state, thereby, causing the evaporation of the fluid and the cooling of the remaining fluid. The fluid has a predetermined flow rate. The evaporative cooling membrane device has a channel which is sized in cooperation with the predetermined flow rate of the fluid so as to produce laminar flow therein. The evaporative cooling membrane device provides for the convenient control of the evaporation rates of the circulating fluid by adjusting the flow rates of the laminar flowing fluid.

  16. Structures of membrane proteins

    PubMed Central

    Vinothkumar, Kutti R.; Henderson, Richard

    2010-01-01

    In reviewing the structures of membrane proteins determined up to the end of 2009, we present in words and pictures the most informative examples from each family. We group the structures together according to their function and architecture to provide an overview of the major principles and variations on the most common themes. The first structures, determined 20 years ago, were those of naturally abundant proteins with limited conformational variability, and each membrane protein structure determined was a major landmark. With the advent of complete genome sequences and efficient expression systems, there has been an explosion in the rate of membrane protein structure determination, with many classes represented. New structures are published every month and more than 150 unique membrane protein structures have been determined. This review analyses the reasons for this success, discusses the challenges that still lie ahead, and presents a concise summary of the key achievements with illustrated examples selected from each class. PMID:20667175

  17. Fuel cell membrane humidification

    DOEpatents

    Wilson, Mahlon S.

    1999-01-01

    A polymer electrolyte membrane fuel cell assembly has an anode side and a cathode side separated by the membrane and generating electrical current by electrochemical reactions between a fuel gas and an oxidant. The anode side comprises a hydrophobic gas diffusion backing contacting one side of the membrane and having hydrophilic areas therein for providing liquid water directly to the one side of the membrane through the hydrophilic areas of the gas diffusion backing. In a preferred embodiment, the hydrophilic areas of the gas diffusion backing are formed by sewing a hydrophilic thread through the backing. Liquid water is distributed over the gas diffusion backing in distribution channels that are separate from the fuel distribution channels.

  18. Supported membrane nanodevices.

    PubMed

    Anrather, Dorothea; Smetazko, Michaela; Saba, Miriam; Alguel, Yilmaz; Schalkhammer, Thomas

    2004-01-01

    Supported membrane nanodevices are based on natural or artificial ion channels embedded in a lipid membrane deposited on a chip wafer. Membrane conductance is modulated by biorecognitive events, with the use of intrinsic binding sites of the ion channel or via artificial sites fused to the channel protein. Artificial ion gates are constructed by coupling a specific ligand for the analyte near the channel entrance or a site important to triggering channel conformation. The binding event leads to the closure of the ion channel or induces a conformational change of the channel, reducing the ion flux. The signal transduced from the device is the decrease in the ion flux-induced electron current at a silver-silver chloride electrode at ultimate single-molecule sensitivity. Among the natural ion channels, gramicidin A, a transport antibiotic, was found to be most suitable, and thus was used by AMBRI, Australia, to set up prototypes of membrane biochips, using self-association of the dimer. Covalent dimerization-based devices, developed by the Vienna group, make use of the down-regulation of the permanently open membrane-spanning bisgramicidine ion channel. The reactive group at the C-terminus, a hydroxy group, allows precise coupling of the analyte-binding moiety in gramicidin as well as bisgramicidin. The device is set up with bilayer membranes deposited on apertures of a hydrophobic frame structure produced via microlithography, facing an aqueous or hydro-gel micro-environment on both sides, constructing black lipid membranes or patch-clamp devices "on chip." The setup of the device needs gel membrane supports that allow membrane formation and contribute to the stability of the bilayer by exposure of functional groups that promote electrostatic interaction and formation of hydrogen bridges and enable the introduction of covalent spacers and anchors. Photo-cross-linked polyvinylpyrrolidone and polyacrylamide, electropolymerized polydiaminobenzene and coated agarose, as

  19. Experimental investigation on the large-area fabrication of micro-pyramid arrays by roll-to-roll hot embossing on PVC film

    NASA Astrophysics Data System (ADS)

    Deng, Yujun; Yi, Peiyun; Peng, Linfa; Lai, Xinmin; Lin, Zhongqin

    2014-04-01

    Large-area polymeric components with micro-pyramids have been widely applied in the fields of optics, optoelectronics, biology and chemistry, etc. Roll-to-roll (R2R) hot embossing is regarded as a promising approach to fulfil high throughput fabrication of patterned polymeric films. In this study, an R2R hot embossing system has been developed in-house and effective and continuous production of the polymeric component with micro-pyramids is demonstrated by R2R hot embossing. The influence of processing parameters has been firstly investigated by using the one-variable-at-a-time method. Afterwards, a series of experiments based on the central composite design approach have been conducted for the analysis of variance and the establishment of empirical models of the R2R hot embossing process. As a result, a 90 mm × 90 mm PVC sample with a feature height of 65 µm was successfully fabricated and the height consistency reached 94.5%. Additionally, a process window with a mold temperature of 150-160 °C, an applied force of 18-25 kgf and a feeding speed of 0.3-0.5 m min-1, was established to achieve 100% passable micro-pyramid arrays. The processing rules and the concrete ranges of parameter values can guide the process production of large-area micro-pyramids.

  20. Dinuclear copper(II) octaazamacrocyclic complex in a PVC coated GCE and graphite as a voltammetric sensor for determination of gallic acid and antioxidant capacity of wine samples.

    PubMed

    Petković, B B; Stanković, D; Milčić, M; Sovilj, S P; Manojlović, D

    2015-01-01

    A novel efficient differential pulse voltammetric (DPV) method for determination gallic acid (GA) was developed by using an electrochemical sensor based on [Cu2tpmc](ClO4)4 immobilized in PVC matrix and coated on graphite (CGE) or classy carbon rod (CGCE). The proposed method is based on the gallic acid oxidation process at formed [Cu2tpmcGA](3+) complex at the electrode surface. The complexation was explored by molecular modeling and DFT calculations. Voltammograms for both sensors, recorded in a HNO3 as a supporting electrolyte at pH 2 and measured in 2.5×10(-7) to 1.0×10(-4) M of GA, resulted with two linear calibration curves (for higher and lower GA concentration range). The detection limit at CGE was 1.48×10(-7) M, while at CGCE was 4.6×10(-6) M. CGE was successfully applied for the determination of the antioxidant capacity based on GA equivalents for white, rosé and red wine samples. PMID:25476338

  1. Ion-conducting porous layers of sodium hydroxide complexes with hydroxyethylated cyclams on modified surfaces of a PVC coating for fabrics

    NASA Astrophysics Data System (ADS)

    Tsivadze, A. Yu.; Fridman, A. Ya.; Morozova, E. M.; Sokolova, N. P.; Voloshchuk, A. M.; Petukhova, G. A.; Bardyshev, I. I.; Novikov, A. K.; Gorbunov, A. M.; Polyakova, I. Ya.; Titova, V. N.; Yavich, A. A.; Petrova, N. V.

    2015-02-01

    Layers of polynuclear NaOH complexes with aza-crown groups are synthesized using a NaOH solution on porous layers with internal voids of macromolecular hydroxyethylated cyclams on a chemically modified PVC coating that encapsulates the fibers of a cellulose fabric. The porous structure of the layers is studied along with the adsorption of solvent vapors (benzene, hexane) and liquid solvents. The OH- conductivity of layers that act as electrochemical bridges is examined in air and the vapor and liquid phases of the solvent. It is established that the complexes occupy the voids and have a developed system of hydrogen bonds. The pores are filled during adsorption. Molecules of the solvent are connected by the macrocyclic groups of pore walls into a host-guest complex as the structural system of hydrogen bonds changes. It is observed that the motions of OH- ions start at a certain value of potential E over. An expression describing the dependence of velocity of voltage is obtained: v' = K 1( E - E over) + K 2( E - E over)2, where K 1 is the conductivity constant of a layer and K 2 is the constant of transfer acceleration, determined by the structural changes in the layer in a field of moving OH- ions. It is shown that the values of E over, K 1, and K 2 depend on the composition of the complex and the nature of solvents.

  2. Removal of caffeine from aqueous solution by indirect electrochemical oxidation using a graphite-PVC composite electrode: A role of hypochlorite ion as an oxidising agent.

    PubMed

    Al-Qaim, Fouad F; Mussa, Zainab H; Othman, Mohamed R; Abdullah, Md P

    2015-12-30

    The electrochemical oxidation of caffeine, a widely over-the-counter stimulant drug, has been investigated in effluent wastewater and deionized water (DIW) using graphite-poly vinyl chloride (PVC) composite electrode as anode. Effects of initial concentration of caffeine, chloride ion (Cl(-)) loading, presence of hydrogen peroxide (H2O2), sample volume, type of sample and applied voltage were determined to test and to validate a kinetic model for the oxidation of caffeine by the electrochemical oxidation process. The results revealed that the electrochemical oxidation rates of caffeine followed pseudo first-order kinetics, with rate constant values ranged from 0.006 to 0.23 min(-1) depending on the operating parameters. The removal efficiency of caffeine increases with applied voltage very significantly, suggesting a very important role of mediated oxidation process. However, the consumption energy was considered during electrochemical oxidation process. In chloride media, removal of caffeine is faster and more efficiently, although occurrence of more intermediates takes place. The study found that the adding H2O2 to the NaCl solution will inhibit slightly the electrochemical oxidation rate in comparison with only NaCl in solution. Liquid chromatography-time of flight-mass spectrometry (LC-TOF-MS) technique was applied to the identification of the by-products generated during electrochemical oxidation, which allowed to construct the proposed structure of by-products. PMID:26218306

  3. Materials based on carbon-filled porous layers of PVC cyclam derivatives cross-linked with the surfaces of asbestos fabric fibers

    NASA Astrophysics Data System (ADS)

    Tzivadze, A. Yu.; Fridman, A. Ya.; Morozova, E. M.; Sokolova, N. P.; Voloshchuk, A. M.; Petukhova, G. A.; Bardishev, I. I.; Gorbunov, A. M.; Novikov, A. K.; Polyakova, I. Ya.; Titova, V. N.; Yavich, A. A.; Petrova, N. V.

    2016-08-01

    The synthesis of bilayer materials with porous upper layers composed of PVC hydroxyethylcyclam derivatives filled with carbon and a layer consisting of hydroxyethylcyclam, cross-linked via Si-O-C groups with the silica chains of a developed surface of asbestos fabric, is described. The aza-crown groups in these materials are bound with aqua complexes of H2SO4 or NaOH. The structure of the materials is examined, their adsorption characteristics are determined, and the rate of motion of H+ or OH- ions in electrochemical bridges is measured, while the formation of H2 and O2 in their cathodic and anodic polarization is determined as a function of voltage. It is shown that the upper layer of these materials is adsorption-active and electronand H+- or OH-- conductive, while the bottom layer is only H+- or OH-- conductive; through it, the upper layer is supplied with the H+ or OH- ions needed for the regeneration of the aqua complexes broken down to H2 and O2 on carbon particles.

  4. Microprobes aluminosilicate ceramic membranes

    DOEpatents

    Anderson, Marc A.; Sheng, Guangyao

    1993-01-01

    Methods have been developed to make mixed alumina-silicate and aluminosilicate particulate microporous ceramic membranes. One method involves the making of separate alumina and silica sols which are then mixed. Another method involves the creation of a combined sol with aluminosilicate particles. The resulting combined alumina and silica membranes have high surface area, a very small pore size, and a very good temperature stability.

  5. [Candidiasis of mucous membranes].

    PubMed

    Khmel'nitskiĭ, O K

    2000-01-01

    The author presents a new concept of complex relationship between the organism and Candida. According to this concept there is transformation of Candida carriage into invasive candidiasis of the mucous membranes. The idea is formulated on mixed-mycocenosis as association of fungal, bacterial, protozoic and viral biota. For the first time the notion of intermediate preinvasive form of candidiasis is given and clinical, morphological criteria of differential diagnosis between candida carriage, preinvasive and invasive candidiasis of mucous membranes are presented. PMID:11198119

  6. Membrane separation of hydrocarbons

    DOEpatents

    Funk, Edward W.; Kulkarni, Sudhir S.; Chang, Y. Alice

    1986-01-01

    Mixtures of heavy oils and light hydrocarbons may be separated by passing the mixture over a polymeric membrane which comprises a polymer capable of maintaining its integrity in the presence of hydrocarbon compounds at temperature ranging from about ambient to about 100.degree. C. and pressures ranging from about 50 to about 1000 psi. The membranes which possess pore sizes ranging from about 10 to about 500 Angstroms are cast from a solvent solution and recovered.

  7. Membrane reference electrode

    DOEpatents

    Redey, L.; Bloom, I.D.

    1988-01-21

    A reference electrode utilizes a small thin, flat membrane of a highly conductive glass placed on a small diameter insulator tube having a reference material inside in contact with an internal voltage lead. When the sensor is placed in a non-aqueous ionic electrolytic solution, the concentration difference across the glass membrane generates a low voltage signal in precise relationship to the concentration of the species to be measured, with high spatial resolution. 2 figs.

  8. Battery utilizing ceramic membranes

    DOEpatents

    Yahnke, Mark S.; Shlomo, Golan; Anderson, Marc A.

    1994-01-01

    A thin film battery is disclosed based on the use of ceramic membrane technology. The battery includes a pair of conductive collectors on which the materials for the anode and the cathode may be spin coated. The separator is formed of a porous metal oxide ceramic membrane impregnated with electrolyte so that electrical separation is maintained while ion mobility is also maintained. The entire battery can be made less than 10 microns thick while generating a potential in the 1 volt range.

  9. Highly selective thiocyanate poly(vinyl chloride) membrane electrode based on a cadmium-Schiff's base complex.

    PubMed

    Ganjali, M R; Poursaberi, T; Basiripour, F; Salavati-Niassari, M; Yousefi, M; Shamsipur, M

    2001-08-01

    A PVC membrane electrode based on a cadmium-salen (N,N'-bis-salicylidene-1,2-ethylenediamine) complex as an anion carrier is described. The electrode has an anti-Hofmeister selectivity sequence with a preference for thiocyanate at pH 1.5-11.0. It has a linear response to thiocyanate from 1.0 x 10(-6) to 1.0 x 10(-1) mol L(-1) with a slope of 59.1 +/- 0.2 mV per decade, and a detection limit of 7 x 10(-7) mol L(-1). This electrode has high selectivity for thiocyanate relative to many common organic and inorganic anions. The proposed sensor has a fast response time of approximately 15 s. It was applied to the determination of thiocyanate in a milk sample. PMID:11583093

  10. Exploring membrane respiratory chains.

    PubMed

    Marreiros, Bruno C; Calisto, Filipa; Castro, Paulo J; Duarte, Afonso M; Sena, Filipa V; Silva, Andreia F; Sousa, Filipe M; Teixeira, Miguel; Refojo, Patrícia N; Pereira, Manuela M

    2016-08-01

    Acquisition of energy is central to life. In addition to the synthesis of ATP, organisms need energy for the establishment and maintenance of a transmembrane difference in electrochemical potential, in order to import and export metabolites or to their motility. The membrane potential is established by a variety of membrane bound respiratory complexes. In this work we explored the diversity of membrane respiratory chains and the presence of the different enzyme complexes in the several phyla of life. We performed taxonomic profiles of the several membrane bound respiratory proteins and complexes evaluating the presence of their respective coding genes in all species deposited in KEGG database. We evaluated 26 quinone reductases, 5 quinol:electron carriers oxidoreductases and 18 terminal electron acceptor reductases. We further included in the analyses enzymes performing redox or decarboxylation driven ion translocation, ATP synthase and transhydrogenase and we also investigated the electron carriers that perform functional connection between the membrane complexes, quinones or soluble proteins. Our results bring a novel, broad and integrated perspective of membrane bound respiratory complexes and thus of the several energetic metabolisms of living systems. This article is part of a Special Issue entitled 'EBEC 2016: 19th European Bioenergetics Conference, Riva del Garda, Italy, July 2-6, 2016', edited by Prof. Paolo Bernardi. PMID:27044012

  11. Catalytic nanoporous membranes

    DOEpatents

    Pellin, Michael J.; Hryn, John N.; Elam, Jeffrey W.

    2009-12-01

    A nanoporous catalytic membrane which displays several unique features including pores which can go through the entire thickness of the membrane. The membrane has a higher catalytic and product selectivity than conventional catalysts. Anodic aluminum oxide (AAO) membranes serve as the catalyst substrate. This substrate is then subjected to Atomic Layer Deposition (ALD), which allows the controlled narrowing of the pores from 40 nm to 10 nm in the substrate by deposition of a preparatory material. Subsequent deposition of a catalytic layer on the inner surfaces of the pores reduces pore sizes to less than 10 nm and allows for a higher degree of reaction selectivity. The small pore sizes allow control over which molecules enter the pores, and the flow-through feature can allow for partial oxidation of reactant species as opposed to complete oxidation. A nanoporous separation membrane, produced by ALD is also provided for use in gaseous and liquid separations. The membrane has a high flow rate of material with 100% selectivity.

  12. The Excitable Membrane

    PubMed Central

    Offner, Franklin F.

    1972-01-01

    The model of the excitable membrane assumes common channels for Na+ and K+; the two ion species interact within the pores through their electrostatic forces. The electric field varies across the membrane and with time, as a result of ionic redistribution. Ionic flow is primarily controlled by energy barriers at the two interfaces and by Ca++ adsorption at the external interface. When the membrane is polarized, the high electric field at the external interface acting on the membrane fixed charge keeps the effective channel diameter small, so that only dihydrated ions can cross the interface. The higher energy required to partially dehydrate Na+ accounts for its lower permeability when polarized. Depolarized, the channel entrance can expand, permitting quadrihydrated ions to pass; the large initial Na+ flow is the result of the large concentration ratio across the interface. The effect at the internal interface is symmetric; Na+ crosses with greater difficulty when the membrane is depolarized. Na+ inactivation occurs when the ion distribution within the membrane has assumed its new steady-state value. Calculations based on parameters consistent with physicochemical data agree generally with a wide range of experiments. The model does not obey the two fundamental Hodgkin-Huxley (HH) postulates (independence principle, ion flow proportional to thermodynamic potential). In several instances the model predicts experimental results which are not predicted by the HH equations. ImagesFIGURE 12 PMID:4655662

  13. OXYGEN TRANSPORT CERAMIC MEMBRANES

    SciTech Connect

    Dr. Sukumar Bandopadhyay; Dr. Nagendra Nagabhushana

    2000-10-01

    This is the third quarterly report on oxygen Transport Ceramic Membranes. In the following, the report describes the progress made by our university partners in Tasks 1 through 6, experimental apparatus that was designed and built for various tasks of this project, thermodynamic calculations, where applicable and work planned for the future. (Task 1) Design, fabricate and evaluate ceramic to metal seals based on graded ceramic powder/metal braze joints. (Task 2) Evaluate the effect of defect configuration on ceramic membrane conductivity and long term chemical and structural stability. (Task 3) Determine materials mechanical properties under conditions of high temperatures and reactive atmospheres. (Task 4) Evaluate phase stability and thermal expansion of candidate perovskite membranes and develop techniques to support these materials on porous metal structures. (Task 5) Assess the microstructure of membrane materials to evaluate the effects of vacancy-impurity association, defect clusters, and vacancy-dopant association on the membrane performance and stability. (Task 6) Measure kinetics of oxygen uptake and transport in ceramic membrane materials under commercially relevant conditions using isotope labeling techniques.

  14. Fractal reconstruction of rough membrane surface related with membrane fouling in a membrane bioreactor.

    PubMed

    Zhang, Meijia; Chen, Jianrong; Ma, Yuanjun; Shen, Liguo; He, Yiming; Lin, Hongjun

    2016-09-01

    In this paper, fractal reconstruction of rough membrane surface with a modified Weierstrass-Mandelbrot (WM) function was conducted. The topography of rough membrane surface was measured by an atomic force microscopy (AFM), and the results showed that the membrane surface was isotropous. Accordingly, the fractal dimension and roughness of membrane surface were calculated by the power spectrum method. The rough membrane surface was reconstructed on the MATLAB platform with the parameter values acquired from raw AFM data. The reconstructed membrane was much similar to the real membrane morphology measured by AFM. The parameters (including average roughness and root mean square (RMS) roughness) associated with membrane morphology for the model and real membrane were calculated, and a good match of roughness parameters between the reconstructed surface and real membrane was found, indicating the feasibility of the new developed method. The reconstructed membrane surface can be potentially used for interaction energy evaluation. PMID:27318159

  15. Composite membranes for fluid separations

    DOEpatents

    Blume, Ingo; Peinemann, Klaus-Viktor; Pinnau, Ingo; Wijmans, Johannes G.

    1991-01-01

    A method for designing and making composite membranes having a microporous support membrane coated with a permselective layer. The method involves calculating the minimum thickness of the permselective layer such that the selectivity of the composite membrane is close to the intrinsic selectivity of the permselective layer. The invention also provides high performance membranes with optimized properties.

  16. Composite membranes for fluid separations

    DOEpatents

    Blume, Ingo; Peinemann, Klaus-Viktor; Pinnau, Ingo; Wijmans, Johannes G.

    1992-01-01

    A method for designing and making composite membranes having a microporous support membrane coated with a permselective layer. The method involves calculating the minimum thickness of the permselective layer such that the selectivity of the composite membrane is close to the intrinsic selectivity of the perselective layer. The invention also provides high performance membranes with optimized properties.

  17. Composite membranes for fluid separations

    DOEpatents

    Blume, Ingo; Peinemann, Klaus-Viktor; Pinnau, Ingo; Wijmans, Johannes G.

    1990-01-01

    A method for designing and making composite membranes having a microporous support membrane coated with a permselective layer. The method involves calculating the minimum thickness of the permselective layer such that the selectivity of the composite membrane is close to the intrinsic selectivity of the permselective layer. The invention also provides high performance membranes with optimized properties.

  18. Stability-indicating electrochemical methods for the determination of meclophenoxate hydrochloride and pyritinol dihydrochloride using ion-selective membrane electrodes.

    PubMed

    El-Bardicy, Mohammad Galal; Lotfy, Hayam Mahmoud; El-Sayed, Mohammad Abdalla; El-Tarras, Mohammad Fayez

    2007-01-01

    The construction and electrochemical response characteristics of polyvinyl chloride (PVC) membrane sensors for the determination of meclophenoxate hydrochloride (I) and pyritinol dihydrochloride (II) in presence of their degradation products are described. The sensors are based on the use of the ion-association complexes of (I) and (II) cation with sodium tetraphenyl borate and ammonium reineckate counteranions as ion-exchange sites in the PVC matrix. In addition beta-cyclodextrin (beta-CD) membranes were used in the determination of I and II. These ion pairs and beta-CD were then incorporated as electroactive species with ortho nitrophenyl octyl ether (oNPOE) as a plasticizer. Three PVC sensors were fabricated for each drug, i.e. meclophenoxate tetraphenyl borate (meclo-TPB), meclophenoxate reineckate (meclo-RNC) and meclophenoxate beta-cyclodextrin (meclo-beta-CD), and the same was done for pyritinol (pyrit-TPB), (pyrit-RNC) and (pyrit-beta-CD). They showed near Nernestian responses for meclophenoxate over the concentration range 10(-5)-10(-2) with slopes of 52.73, 51.64 and 54.05 per concentration decade with average recoveries of 99.92+/-1.077, 99.96+/-0.502 and 100.03+/-0.763 for meclo-TPB, meclo-RNC and meclo-beta-CD respectively. Pyritinol also showed near Nernestian responses over the concentration range of 3.162 x 10(-6) - 3.162 x 10(-4) for pyrit-TPB and pyrit-RNC, and 10(-6) - 3.162 x 10(-4) for pyrit-beta-CD with slopes of 30.60, 31.10 and 32.89 per concentration decade and average recoveries of 99.99+/-0.827, 100.00+/-0.775 and 99.99+/-0.680 for pyrit-TPB, pyrit-RNC and pyrit-beta-CD respectively. The sensors were used successfully for the determination of I and II in laboratory prepared mixtures with their degradation products, in pharmaceutical dosage forms and in plasma. PMID:17202801

  19. Handbook of industrial membrane technology

    SciTech Connect

    Porter, M.C.

    1989-01-01

    This book emphasizes the use of synthetic membranes for separations involving industrial or municipal process streams. In addition to the classic membrane processes-microfiltration, ultrafiltration, reverse osmosis, gas separation, and electrodialysis-chapters on enzyme membrane reactors, membrane fermentors and coupled transport membranes are included. The preparation of synthetic membranes and process design and optimization are also covered. Most of the membrane processes are pressure driven, the notable exception being electrodialysis, by which ions are separated under the influence of an electric field. In addition, coupled transport covers processes driven under the influence of a concentration gradient.

  20. Oxygen Transport Ceramic Membranes

    SciTech Connect

    S. Bandopadhyay; T. Nithyanantham; X.-D Zhou; Y-W. Sin; H.U. Anderson; Alan Jacobson; C.A. Mims

    2005-11-01

    The present quarterly report describes some of the investigations on the structural properties of dense OTM bars provided by Praxair and studies on newer composition of Ti doped LSF. In the current research, the electrical conductivity and Seebeck coefficient were measured as a function of temperature in air. Based on these measurements, the charge carrier concentration, net acceptor dopant concentration, activation energy of conduction and mobility were estimated. The studies on the fracture toughness of the LSFT and dual phase membranes at room temperature have been completed and reported previously. The membranes that are exposed to high temperatures at an inert and a reactive atmosphere undergo many structural and chemical changes which affects the mechanical properties. To study the effect of temperature on the membranes when exposed to an inert environment, the membranes (LAFT and Dual phase) were heat treated at 1000 C in air and N{sub 2} atmosphere and hardness and fracture toughness of the membranes were studied after the treatment. The indentation method was used to find the fracture toughness and the effect of the heat treatment on the mechanical properties of the membranes. Further results on the investigation of the origin of the slow kinetics on reduction of ferrites have been obtained. The slow kinetics appears to be related to a non-equilibrium reduction pathway that initially results in the formation of iron particles. At long times, equilibrium can be reestablished with recovery of the perovskite phase. 2-D modeling of oxygen movement has been undertaken in order to fit isotope data. The model will serve to study ''frozen'' profiles in patterned or composite membranes.

  1. Tectorial Membrane Stiffness Gradients

    PubMed Central

    Richter, Claus-Peter; Emadi, Gulam; Getnick, Geoffrey; Quesnel, Alicia; Dallos, Peter

    2007-01-01

    The mammalian inner ear processes sound with high sensitivity and fine resolution over a wide frequency range. The underlying mechanism for this remarkable ability is the “cochlear amplifier”, which operates by modifying cochlear micromechanics. However, it is largely unknown how the cochlea implements this modification. Although gradual improvements in experimental techniques have yielded ever-better descriptions of gross basilar membrane vibration, the internal workings of the organ of Corti and of the tectorial membrane have resisted exploration. Although measurements of cochlear function in mice with a gene mutation for α-tectorin indicate the tectorial membrane's key role in the mechanoelectrical transformation by the inner ear, direct experimental data on the tectorial membrane's physical properties are limited, and only a few direct measurements on tectorial micromechanics are available. Using the hemicochlea, we are able to show that a tectorial membrane stiffness gradient exists along the cochlea, similar to that of the basilar membrane. In artificial perilymph (but with low calcium), the transversal and radial driving point stiffnesses change at a rate of –4.0 dB/mm and −4.9 dB/mm, respectively, along the length of the cochlear spiral. In artificial endolymph, the stiffness gradient for the transversal component was –3.4 dB/mm. Combined with the changes in tectorial membrane dimensions from base to apex, the radial stiffness changes would be able to provide a second frequency-place map in the cochlea. Young's modulus, which was obtained from measurements performed in the transversal direction, decreased by −2.6 dB/mm from base to apex. PMID:17496047

  2. Iron(III) oxidized nucleophilic coupling of catechol with o-tolidine/p-toluidine followed by 1,10-phenanthroline as new and sensitivity improved spectrophotometric methods for iron present in chemicals, pharmaceutical, edible green leaves, nuts and lake water samples

    NASA Astrophysics Data System (ADS)

    Shyla, B.; Bhaskar, C. Vijaya; Nagendrappa, G.

    2012-02-01

    A nucleophile formed from iron(III) oxidized catechol in 0.1 M hydrochloric acid couple with o-tolidine, system 1/p-toluidine, system 2 to produce dye product, λ max 520 nm. The system 1/2 obeys Beer's law in the range 0.08-8.0 μg ml -1 with molar absorptivity, Sandell sensitivity and regression coefficient values, 4.225 × 10 3/3.140 × 10 3 l mol -1 cm -1, 0.0132/0.0178 μg cm -2 and 0.9987/0.9981. Iron(II) formed from iron(III) in system 1/2 reacts with 1,10-phenanthroline, λ max 510 nm, will constitute sensitivity improved iron determinations with values 0.08-1.6 μg ml -1, 2.4136 × 10 4/2.2511 × 10 4 l mol -1 cm -1, 0.0023/0.0025 μg cm -2 and 0.9980/0.9997 corresponding to range, molar absorptivity, Sandell sensitivity and regression coefficient. The results of the systems for iron present in chemicals, pharmaceutical, edible green leaves, nuts and lake water samples are satisfactory since they are comparable with the results of iron determined separately from 1,10-phenanthroline method.

  3. Membrane Bending by Protein Crowding

    NASA Astrophysics Data System (ADS)

    Stachowiak, Jeanne

    2014-03-01

    From endosomes and synaptic vesicles to the cristae of the mitochondria and the annulus of the nuclear pore, highly curved membranes are fundamental to the structure and physiology of living cells. The established view is that specific families of proteins are able to bend membranes by binding to them. For example, inherently curved proteins are thought to impose their structure on the membrane surface, while membrane-binding proteins with hydrophobic motifs are thought to insert into the membrane like wedges, driving curvature. However, computational models have recently revealed that these mechanisms would require specialized membrane-bending proteins to occupy nearly 100% of a curved membrane surface, an improbable physiological situation given the immense density and diversity of membrane-bound proteins, and the low expression levels of these specialized proteins within curved regions of the membrane. How then does curvature arise within the complex and crowded environment of cellular membranes? Our recent work using proteins involved in clathrin-mediated endocytosis, as well as engineered protein-lipid interactions, has suggested a new hypothesis - that lateral pressure generated by collisions between membrane-bound proteins can drive membrane bending. Specifically, by correlating membrane bending with quantitative optical measurements of protein density on synthetic membrane surfaces and simple physical models of collisions among membrane-bound proteins, we have demonstrated that protein-protein steric interactions can drive membrane curvature. These findings suggest that a simple imbalance in the concentration of membrane-bound proteins across a membrane surface can drive a membrane to bend, providing an efficient mechanism by which essentially any protein can contribute to shaping membranes.

  4. CENTRIFUGAL MEMBRANE FILTRATION

    SciTech Connect

    William A. Greene; Patricia A. Kirk; Richard Hayes; Joshua Riley

    2005-10-28

    SpinTek Membrane Systems, Inc., the developer of a centrifugal membrane filtration technology, has engineered and developed a system for use within the U.S. Department of Energy (DOE) Environmental Management (EM) Program. The technology uses supported microporous membranes rotating at high rpm, under pressure, to separate suspended and colloidal solids from liquid streams, yielding a solids-free permeate stream and a highly concentrated solids stream. This is a crosscutting technology that falls under the Efficient Separations and Processing Crosscutting Program, with potential application to tank wastes, contaminated groundwater, landfill leachate, and secondary liquid waste streams from other remediation processes, including decontamination and decommissioning systems. SpinTek II High Shear Rotary Membrane Filtration System is a unique compact crossflow membrane system that has large, demonstrable advantages in performance and cost compared to currently available systems: (1) High fluid shear prevents membrane fouling even with very high solids content; hazardous and radioactive components can be concentrated to the consistency of a pasty slurry without fouling. (2) Induced turbulence and shear across the membrane increases membrane flux by a factor of ten over existing systems and allows operation on fluids not otherwise treatable. (3) Innovative ceramic membrane and mechanical sealing technology eliminates compatibility problems with aggressive DOE waste streams. (4) System design allows rapid, simple disassembly for inspection or complete decontamination. (5) Produces colloidal- and suspended-solids-free filtrate without the addition of chemicals. The first phase of this project (PRDA maturity stage 5) completed the physical scale-up of the SpinTek unit and verified successful scale-up with surrogate materials. Given successful scale-up and DOE concurrence, the second phase of this project (PRDA maturity stage 6) will provide for the installation and

  5. Small scale membrane mechanics

    PubMed Central

    Rangamani, Padmini; Benjamini, Ayelet; Agrawal, Ashutosh; Smit, Berend; Oster, George

    2014-01-01

    Large scale changes to lipid bilayer shapes are well represented by the Helfrich model. However, there are membrane processes that take place at smaller length scales that this model cannot address. In this work, we present a one-dimensional continuum model that captures the mechanics of the lipid bilayer membrane at the length scale of the lipids themselves. The model is developed using the Cosserat theory of surfaces with lipid orientation, or ‘tilt’, as the fundamental degree of freedom. The Helfrich model can be recovered as a special case when the curvatures are small and the lipid tilt is everywhere zero. We use the tilt model to study local membrane deformations in response to a protein inclusion. Parameter estimates and boundary conditions are obtained from a coarse-grained molecular model using dissipative particle dynamics (DPD) to capture the same phenomenon. The continuum model is able to reproduce the membrane bending, stretch and lipid tilt as seen in the DPD model. The lipid tilt angle relaxes to the bulk tilt angle within 5–6 nm from the protein inclusion. Importantly, for large tilt gradients induced by the proteins, the tilt energy contribution is larger than the bending energy contribution. Thus, the continuum model of tilt accurately captures behaviors at length scales shorter than the membrane thickness. PMID:24081650

  6. Halogen-free ionic liquid as an additive in zinc(II)-selective electrode: surface analyses as correlated to the membrane activity.

    PubMed

    Al-Asousi, Maryam F; Shoukry, Adel F; Bu-Olayan, Abdul Hadi

    2012-05-30

    Two conventional Zn(II) polyvinyl chloride (PVC) membrane electrodes have been prepared and characterized. They were based on dibenzo-24-crown-8 (DBC) as a neutral carrier, dioctyl phthalate (DOP) as a plasticizer, and potassium tetrakis (p-chlorophenyl) borate, KTpClPB or the halogen-free ionic liquid, tetraoctylammonium dodecylbenzene sulfonate [TOA][DBS] as an additive. The use of ionic liquid has been found to enhance the selectivity of the sensor. For each electrode, the surfaces of two membranes were investigated using X-ray photoelectron, ion-scattering spectroscopy and atomic force microscopy. One of the two membranes was conditioned by soaking it for 24 h in a 1.0×10(-3) M Zn(NO(3))(2) solution and the second was soaked in bi-distilled water for the same interval (24 h). Comparing the two surfaces indicated the following: (a) the high selectivity in case of using [TOA][DBS] as an additive is due to the extra mediation caused by the ionic liquid and (b) the working mechanism of the electrode is based on phase equilibrium at the surface of the membrane associated with ion transport through the bulk of the membrane. PMID:22608433

  7. Yeast Golgi-localized, gamma-Ear-containing, ADP-ribosylation factor-binding proteins are but adaptor protein-1 is not required for cell-free transport of membrane proteins from the trans-Golgi network to the prevacuolar compartment.

    PubMed

    Abazeed, Mohamed E; Fuller, Robert S

    2008-11-01

    Golgi-localized, gamma-Ear-containing, ADP-ribosylation factor-binding proteins (GGAs) and adaptor protein-1 (AP-1) mediate clathrin-dependent trafficking of transmembrane proteins between the trans-Golgi network (TGN) and endosomes. In yeast, the vacuolar sorting receptor Vps10p follows a direct pathway from the TGN to the late endosome/prevacuolar compartment (PVC), whereas, the processing protease Kex2p partitions between the direct pathway and an indirect pathway through the early endosome. To examine the roles of the Ggas and AP-1 in TGN-PVC transport, we used a cell-free assay that measures delivery to the PVC of either Kex2p or a chimeric protein (K-V), in which the Vps10p cytosolic tail replaces the Kex2p tail. Either antibody inhibition or dominant-negative Gga2p completely blocked K-V transport but only partially blocked Kex2p transport. Deletion of APL2, encoding the beta subunit of AP-1, did not affect K-V transport but partially blocked Kex2p transport. Residual Kex2p transport seen with apl2Delta membranes was insensitive to dominant-negative Gga2p, suggesting that the apl2Delta mutation causes Kex2p to localize to a compartment that precludes Gga-dependent trafficking. These results suggest that yeast Ggas facilitate the specific and direct delivery of Vps10p and Kex2p from the TGN to the PVC and that AP-1 modulates Kex2p trafficking through a distinct pathway, presumably involving the early endosome. PMID:18784256

  8. Yeast Golgi-localized, γ-Ear–containing, ADP-Ribosylation Factor-binding Proteins Are but Adaptor Protein-1 Is Not Required for Cell-free Transport of Membrane Proteins from the Trans-Golgi Network to the Prevacuolar Compartment

    PubMed Central

    Abazeed, Mohamed E.

    2008-01-01

    Golgi-localized, γ-Ear–containing, ADP-ribosylation factor-binding proteins (GGAs) and adaptor protein-1 (AP-1) mediate clathrin-dependent trafficking of transmembrane proteins between the trans-Golgi network (TGN) and endosomes. In yeast, the vacuolar sorting receptor Vps10p follows a direct pathway from the TGN to the late endosome/prevacuolar compartment (PVC), whereas, the processing protease Kex2p partitions between the direct pathway and an indirect pathway through the early endosome. To examine the roles of the Ggas and AP-1 in TGN–PVC transport, we used a cell-free assay that measures delivery to the PVC of either Kex2p or a chimeric protein (K-V), in which the Vps10p cytosolic tail replaces the Kex2p tail. Either antibody inhibition or dominant-negative Gga2p completely blocked K-V transport but only partially blocked Kex2p transport. Deletion of APL2, encoding the β subunit of AP-1, did not affect K-V transport but partially blocked Kex2p transport. Residual Kex2p transport seen with apl2Δ membranes was insensitive to dominant-negative Gga2p, suggesting that the apl2Δ mutation causes Kex2p to localize to a compartment that precludes Gga-dependent trafficking. These results suggest that yeast Ggas facilitate the specific and direct delivery of Vps10p and Kex2p from the TGN to the PVC and that AP-1 modulates Kex2p trafficking through a distinct pathway, presumably involving the early endosome. PMID:18784256

  9. Viral membrane fusion

    PubMed Central

    Harrison, Stephen C.

    2015-01-01

    Membrane fusion is an essential step when enveloped viruses enter cells. Lipid bilayer fusion requires catalysis to overcome a high kinetic barrier; viral fusion proteins are the agents that fulfill this catalytic function. Despite a variety of molecular architectures, these proteins facilitate fusion by essentially the same generic mechanism. Stimulated by a signal associated with arrival at the cell to be infected (e.g., receptor or co-receptor binding, proton binding in an endosome), they undergo a series of conformational changes. A hydrophobic segment (a “fusion loop” or “fusion peptide”) engages the target-cell membrane and collapse of the bridging intermediate thus formed draws the two membranes (virus and cell) together. We know of three structural classes for viral fusion proteins. Structures for both pre- and postfusion conformations of illustrate the beginning and end points of a process that can be probed by single-virion measurements of fusion kinetics. PMID:25866377

  10. Altering morphology of membranes

    SciTech Connect

    Narayan, R.S.

    1987-01-01

    The use of membranes in industrial gas processing and separation has been on the increase in the last eight years, especially since the successful introduction and commercialization of PRISM separators by Monsanto in 1979. Since that time, a number of gas separation applications have been successfully applied on an industrial scale. Separation of hydrogen from N/sub 2/ and hydrocarbons using membranes have become commonplace, and separation of carbon dioxide from hydrocarbons is gaining increasing acceptance. More recently, the separation of nitrogen from oxygen from air has been gaining considerable attention. The economic benefits of using membranes for on-site generation of N/sub 2/ containing less than 5% O/sub 2/ for inert blanketing such as, product storage, packaging, on board ships, airplanes and oil/gas production platforms, etc., are demonstrated to be significant.

  11. Permeability across lipid membranes.

    PubMed

    Shinoda, Wataru

    2016-10-01

    Molecular permeation through lipid membranes is a fundamental biological process that is important for small neutral molecules and drug molecules. Precise characterization of free energy surface and diffusion coefficients along the permeation pathway is required in order to predict molecular permeability and elucidate the molecular mechanisms of permeation. Several recent technical developments, including improved molecular models and efficient sampling schemes, are illustrated in this review. For larger penetrants, explicit consideration of multiple collective variables, including orientational, conformational degrees of freedom, are required to be considered in addition to the distance from the membrane center along the membrane normal. Although computationally demanding, this method can provide significant insights into the molecular mechanisms of permeation for molecules of medical and pharmaceutical importance. This article is part of a Special Issue entitled: Biosimulations edited by Ilpo Vattulainen and Tomasz Róg. PMID:27085977

  12. Outer membrane protein purification.

    PubMed

    Arigita, C; Jiskoot, W; Graaf, M R; Kersten, G F

    2001-01-01

    The major outer membrane proteins (OMPs) from Neisseria meningitidis, which are expressed at high levels, are subdivided in five classes based on molecular weight (1,2) (see Table 1). Table 1 Major Meningococcal Outer-Membrane Proteins Outer-membrane proteins Name Molecular maass Function/characteristics Class 1 PorA 44-47 kDa Porin Class 2/3 PorB 37-42 kDa Porin Class 4 Rmp Reductionmodifiableprotein, unknown Class 5 Opa 26-30 kDa Adhesion,opacity protein Opc 25 kDa Invasion, opacity protein Iron-regulated proteins Mirp 37 kDa Iron acquisition (?);majoriron-regulatedprotein FrpB 70 kDa Ferric enterobactin receptor (also FetA) Adapted from ref. (1). PMID:21336748

  13. Oxygen Transport Ceramic Membranes

    SciTech Connect

    S. Bandopadhyay; T. Nithyanantham; X.-D Zhou; Y-W. Sin; H.U. Anderson; Alan Jacobson; C.A. Mims

    2006-05-01

    In this quarter a systematic analysis on the decomposition behavior of the OTM membranes at air and nitrogen were initiated to understand the structural and stoichiometric changes associated with elevated temperatures. Evaluation of the flexural strengths using 4-point bend test was also started for the dual phase membranes. Initial results on the synthesis of dual phase composite materials have been obtained. The measurements have focused on the compatibility of mixed conductors with the pure ionic conductors yttria stabilized zirconia (YSZ) and gadolinium doped ceria (GDC). The initial results obtained for three different mixed conductors suggest that (GDC) is the better choice. A new membrane permeation system has been designed and tested and sintering studies of biphasic systems are in progress.

  14. Performance Evaluation of a Novel Potentiometric Membrane Sensor for Determination of Atorvastatin in Pharmaceutical Preparations

    PubMed Central

    Ahmadi, Farhad; Asaadi, Nasim

    2013-01-01

    A novel potentiometric ion-selective PVC membrane sensor for analysis of atorvastatin (AT) in pharmaceutical preparations based on atorvastatin-(tetraphenyl borate), (AT-(TPB)2) as sensing element, tetraphenyl borate as additive and tris-2-ethyl-hexyl phosphate (TOP) as plasticizer solvent was prepared. The electrode shows a good Nernestian response over the concentration range of 0.09–5586 μg mL-1of AT with slope of 30.1±0.1 mV/decade and limit of detection0.056μg mL-1.The response time of sensor is fats (less than 10 sec) and could be used for about one month in the pH range of 4.5–8.0. The electrode exhibit good selectivity for the AT in the presence of large amount of co-drugs and inorganic cations. The method is precise and accurate with mean relative standard deviation of <2%.Atorvastatin is determined successfully in several tablets by the proposed membrane. PMID:24523744

  15. Hybrid Filter Membrane

    NASA Technical Reports Server (NTRS)

    Laicer, Castro; Rasimick, Brian; Green, Zachary

    2012-01-01

    Cabin environmental control is an important issue for a successful Moon mission. Due to the unique environment of the Moon, lunar dust control is one of the main problems that significantly diminishes the air quality inside spacecraft cabins. Therefore, this innovation was motivated by NASA s need to minimize the negative health impact that air-suspended lunar dust particles have on astronauts in spacecraft cabins. It is based on fabrication of a hybrid filter comprising nanofiber nonwoven layers coated on porous polymer membranes with uniform cylindrical pores. This design results in a high-efficiency gas particulate filter with low pressure drop and the ability to be easily regenerated to restore filtration performance. A hybrid filter was developed consisting of a porous membrane with uniform, micron-sized, cylindrical pore channels coated with a thin nanofiber layer. Compared to conventional filter media such as a high-efficiency particulate air (HEPA) filter, this filter is designed to provide high particle efficiency, low pressure drop, and the ability to be regenerated. These membranes have well-defined micron-sized pores and can be used independently as air filters with discreet particle size cut-off, or coated with nanofiber layers for filtration of ultrafine nanoscale particles. The filter consists of a thin design intended to facilitate filter regeneration by localized air pulsing. The two main features of this invention are the concept of combining a micro-engineered straight-pore membrane with nanofibers. The micro-engineered straight pore membrane can be prepared with extremely high precision. Because the resulting membrane pores are straight and not tortuous like those found in conventional filters, the pressure drop across the filter is significantly reduced. The nanofiber layer is applied as a very thin coating to enhance filtration efficiency for fine nanoscale particles. Additionally, the thin nanofiber coating is designed to promote capture of

  16. Transient formation of the oxo-iron(IV) porphyrin radical cation during the reaction of iron(III) tetrakis-5,10,15,20-(N-methyl-4-pyridyl)porphyrin with hydrogen peroxide in aqueous solution.

    PubMed

    Saha, Tapan Kumar; Karmaker, Subarna; Tamagake, Keietsu

    2003-01-01

    The reaction of iron(III) tetrakis-5,10,15,20-(N-methyl-4-pyridyl)porphyrin (Fe(III)TMPyP) with hydrogen peroxide (H(2)O(2)) and the catalytic activity of the reaction intermediates on the luminescent peroxidation of luminol in aqueous solution were studied by using a double-mixing stopped-flow system. The observed luminescence intensities showed biphasic decay depending on the conditions. The initial flashlight decayed within <1 s followed by a sustained emission for more than 30 s. Computer deconvolution of the time-resolved absorption spectra under the same conditions revealed that the initial flashlight appeared during the formation of the oxo-iron(IV) porphyrin, TMPyPFe(IV) = O, which is responsible for the sustained emission. The absorption spectra 0.0-0.5 s did not reproduce well by a simple combination of the two spectra of Fe(III)TMPyP and TMPyPFe(IV) = O, indicating that transient species was formed at the initial stage. Addition of uric acid (UA) caused a significant delay in the initiation of the luminol emission as well as in the formation of the TMPyPFe(IV) = O. Both of them were completely diminished in the presence of UA equimolar with H(2)O(2), while mannitol had no effect at all. The delay of the light emission as well as the appearance of TMPyPFe(IV) = O was directly proportional to the [UA](0) but other kinetic profiles were not changed significantly. Based on these observations and the kinetic analysis, we confirmed the involvement of the oxo-iron(IV) porphyrin radical cation, (TMPyP)(.+)Fe(IV) = O, as an obligatory intermediate in the rate-determining step of the overall reaction, Fe(III)TMPyP + H(2)O(2) --> TMPyPFe(IV) = O, with a rate constant of k = 4.3 x 10(4)/mol/L/s. The rate constants for the reaction between the (TMPyP)(.+)Fe(IV) = O and luminol, and between the TMPyPFe(IV) = O and luminol were estimated to be 3.6 x 10(6)/mol/L/s and 1.31 x 10(4)/mol/L/s, respectively. PMID:12701092

  17. Functional membranes. Present and future

    NASA Technical Reports Server (NTRS)

    Kunitake, T.

    1982-01-01

    The present situation and the future development of the functional membrane are discussed. It is expected that functional membranes will play increasingly greater roles in the chemical industry of the coming decade. These membranes are formed from polymer films, liquid membranes or bilayer membranes. The two most important technologies based on the polymeric membrane are reverse osmosis and ion exchange. The liquid membrane is used for separation of ionic species; an extension of the solvent extraction process. By using appropriate ligands and ionophores, highly selective separations are realized. The active transport is made possible if the physical and chemical potentials are applied to the transport process. More advanced functional membranes may be designed on the basis of the synthetic bilayer membrane.

  18. Supported microporous ceramic membranes

    DOEpatents

    Webster, E.; Anderson, M.

    1993-12-14

    A method for the formation of microporous ceramic membranes onto a porous support includes placing a colloidal suspension of metal or metal oxide particles on one side of the porous support and exposing the other side of the porous support to a drying stream of gas or a reactive gas stream so that the particles are deposited on the drying side of the support as a gel. The gel so deposited can be sintered to form a supported ceramic membrane useful for ultrafiltration, reverse osmosis, or molecular sieving having mean pore sizes less than 100 Angstroms. 4 figures.

  19. Supported microporous ceramic membranes

    DOEpatents

    Webster, Elizabeth; Anderson, Marc

    1993-01-01

    A method for permformation of microporous ceramic membranes onto a porous support includes placing a colloidal suspension of metal or metal oxide particles on one side of the porous support and exposing the other side of the porous support to a drying stream of gas or a reactive gas stream so that the particles are deposited on the drying side of the support as a gel. The gel so deposited can be sintered to form a supported ceramic membrane useful for ultrafiltration, reverse osmosis, or molecular sieving having mean pore sizes less than 100 Angstroms.

  20. Battery utilizing ceramic membranes

    DOEpatents

    Yahnke, M.S.; Shlomo, G.; Anderson, M.A.

    1994-08-30

    A thin film battery is disclosed based on the use of ceramic membrane technology. The battery includes a pair of conductive collectors on which the materials for the anode and the cathode may be spin coated. The separator is formed of a porous metal oxide ceramic membrane impregnated with electrolyte so that electrical separation is maintained while ion mobility is also maintained. The entire battery can be made less than 10 microns thick while generating a potential in the 1 volt range. 2 figs.